EPA/600/R-93/071
IRRIGATED WETLANDS OF THE COLORADO PLATEAU:

  INFORMATION SYNTHESIS AND HABITAT EVALUATION METHOD
                          by:
                     Paul R. Adamus
            ManTech Environmental Technology Inc.
           USEPA Environmental Research Laboratory
                     200 SW 35th St.
                   Corvallis, OR 97333
                    EPA Project Officer:
                     Mary E. Kentula
          USEPA Environmental Research Laboratory
                     200 SW 35th St.
                    Corvallis, OR 97333
                       April 1993

-------
                                         DISCLAIMER

This project has been funded by the U.S. Environmental Protection Agency (EPA) and conducted through
contract #68-C8-0006 to ManTech Environmental Technology Inc. This document has been subjected to the
Agency's peer and administrative review and has been approved for publication. The opinions expressed
herein are those of the author and do not necessarily reflect those of EPA  The official endorsement of the
Agency should not be inferred.
This document should be cited as:

Adamus, P.R.   1993.   Irrigated Wetlands of the Colorado  Plateau: Information  Synthesis  and Habitat
Evaluation Method. EPA/600/R-93/071.  U.S. Environmental Protection Agency Environmental Research
Laboratory, Corvallis, Oregon.

-------
                                             SUMMARY

Wetlands of the Colorado Plateau that receive water from irrigation can, by their functions, support several
societal values. For example, their capacity for removing nitrate and perhaps pesticides from nonpoint source
runoff might be considerable. However, relatively little research has been conducted in irrigated wetlands, and
their ability to alter water quality in particular remains relatively unknown.

Much more documentation exists concerning the importance of irrigated wetlands as habitat.  About 72% of
all reptiles, 77% of all amphibian species, 80% of all mammals, and 90% of all bird species which occur
regularly in the Colorado Plateau region routinely use irrigated wetlands and riparian areas.  About 30% of
the region's bird species use wetlands and other aquatic areas to  the exclusion of upland habitats. Wetland
and  riparian habitats also support a disproportionate number of species that are of concern because they
migrate to neotropical areas, have small continental populations, or are declining.  Virtually all wetland and
riparian habitats in agricultural areas of the Colorado Plateau are sustained to some degree by runoff and
seepage from  irrigation.
No single characteristic (i.e., "indicator") reliably predicts which irrigated wetlands comprise the best habitat.
Rather, habitat quality is associated with various combinations of the conditions of several indicators, at
several scales.  The most predictive indicators are probably patch size, water regime, vegetation form and
species, aquatic organism abundance, and landscape context.   However, attempts to identify indicators of
"good" irrigated wetland habitat encounter a problem of defining "good for which species?" The importance
of each indicator, or of each unique combination of indicator conditions, depends on the values placed on the
species associated with it. Many indicator conditions are ideal for only a few species, but if these species are
particularly valued (e.g., because they are regionally rare,  declining, or hunted), then the indicator conditions
can be considered important.

To help address the need for an explicit, integrated, local-scale approach to biodiversity assessment, this report
introduces a new procedure for  rapidly evaluating wetland and riparian habitat.  In  contrast to existing
methods,  it does  not require  the user to judge a habitat  based on the habitat's  suitability for just  a few
"indicator species."  Rather, the  procedure addresses the question, "good for which species" by estimating
explicitly  the quality  of a  habitat for all wetland/riparian species of the region's most diverse vertebrate
taxonomic group -- birds.  The procedure estimates the number  of species likely to occur regularly in a
particular wetland and uses this to assign importance to the wetland. The user can employ the procedure to
evaluate a wetland using any subset of the species, and to select combinations of wetlands that will maximize
avian diversity  at local and regional scales.  The procedure's emphasis on biodiversity and an ecosystems
approach  is consistent with current shifts in scientific thinking and the mandates and  operations of many
resource agencies. The procedure requires less than 30 minutes per wetland to implement.  Information from
systematic field testing has been  used to improve the procedure and its supporting database.  Additional
validation, by comparing evaluation scores with actual species  richness as measured by direct multitemporal
surveys of birds and other vertebrates, is desirable.

-------
                                    ACKNOWLEDGMENTS

This effort was conceived by Gene Reetz and David Ruiter of EPA Region 8.  Mary E. Kentula and Richard
Sumner of the Wetlands Research Program,  USEPA Environmental Research Laboratory - Corvallis, were
instrumental in helping focus the study objectives and quality assurance program, in providing administrative
support, and in providing many excellent suggestions that helped clarify the text. Brooke Abbruzzese was the
project manager for ManTech Environmental Technology, Inc.  Kristina Miller helped  prepare the figures.
The report benefitted greatly from the review comments of David Cooper, Natasha Kotliar, Ronald Lambeth,
Steve McCall, and Claudia Rector.

This report would  not have been possible without the gracious assistance of many resource managers in
Colorado and Utah, who provided background information and opinions on the wetland resource, irrigation
practices, and local wildlife habitat requirements.  In particular, I thank those who  assisted with the field-
testing of the habitat evaluation method and/or showed me irrigated wetlands in their locality: Nelson Boschen
(Moab, UT), Brent Draper (Soil Conservation Service (SCS), Roosevelt, UT), Dave Galinat (Olathe, CO),
Ron Lambeth (U.S. Bureau of Land Management (BLM), Grand Junction, CO), Steve McCall (U.S. Bureau
of Reclamation (USER), Grand Junction, CO), Doug Meaghley (SCS, Grand Junction, CO), Ed Neilson, Jr.
(SCS, Grand Junction, CO), Paul Obert (SCS, Delta, CO), Maple Taylor (SCS, Montrose, CO), and Steve
Woodis (SCS, Montrose, CO). Jim Gamer (Colorado Division of Wildlife (CDW), Montrose, CO) and Wes
Johnson (Utah Division of Wildlife Resources (UDWR), Salt Lake City, UT) kindly shared and facilitated
transfer of computerized species databases of their agencies, which were helpful for developing the habitat
relationships database for the Colorado Plateau. Michael Carter of the Colorado Bird Observatory generously
shared his computerized database on conservation characteristics of neotropical migrants.  More than 50 other
persons were contacted and provided information for this study. I thank them all.
                                               111

-------
                                        CONTENTS

SUMMARY  	  ii
ACKNOWLEDGMENTS	  iii

1.0 INTRODUCTION 	  1
       1.1 Problem Statement and Definitions  	  1
       1.2 Study Background and Report Purpose  	  2

2.0 CHARACTERIZATION OF IRRIGATED WETLANDS	  4
       2.1 Geographic Distribution  	  4
       2.2 Classification by Size and Type	  4
       2.3 Within-Region Differences	  6

3.0 NON-HABITAT FUNCTIONS AND VALUES OF IRRIGATED WETLANDS	  10
       3.1 Water Quality Functions and Values  	  10
       3.2 Hydrologic Functions and Values	  13
       3.3 Recreation and Harvest Values	  14
       3.4 Multiple Use Considerations  	  15

4.0 HABITAT FUNCTIONS AND VALUES OF IRRIGATED WETLANDS	  16
       4.1 Definitions of "Good" Habitat 	  16
       4.2 Results of Previous Assessments of Irrigated Wetland Habitat	  16
       4.3 Habitat "Indicators" and Evaluation Procedures  	  23
       4.4 Which Indicators Predict "Good" Habitat?	  24
              4.4.1 Wetland Size and Related Indicators	  24
              4.4.2 Surface Water Regime ("Wetness")	  28
              4.4.3 Vegetation  Characteristics	  35
              4.4.4 Other Animals and Wetland Water Quality	  37
              4.4.5 Landscape Land Cover and Seclusion	  39
       4.5 Summary of Remaining Information  Needs  	  40

5.0  AVIAN  RICHNESS  EVALUATION METHOD   (AREM) FOR THE  COLORADO
       PLATEAU	  41
       5.1 AREM and What It Can Do  	  41
       5.2 Conceptual Basis for AREM  	  41
       5.3 How AREM Works	  45
       5.4 Results of Initial Testing	  52
              5.4.1 Comparability	  52
              5.4.2 Replicability	  55
              5.4.3 Practicality	  55
              5.4.4 Field Testing Conclusions	  55

6.0 STUDY CONCLUSIONS	  57

7.0 LITERATURE CITED .	  58
                                             IV

-------
                                        LIST OF TABLES

Table 1.   Acreage estimates for irrigated wetlands by location, wetland type, and water source	  7
Table 2.   Mean acreage of various wetland types in the Lower Gunnison and Big Sandy Valleys	  8
Table 3.   Number of bird species  in each wetland dependency category by seasonal
          abundance and neotropical migrant status	   17
Table 4.   Estimates of avian richness from prior surveys of riparian or wetland areas in
          Colorado and eastern Utah	   20
Table 5.   Number of wetland bird species, by habitat type and wetland dependency category.	   26
Table 6.   Number of neotropical migrants in various wetland dependency categories,
          by conservation characteristics	   30
Table 7.   Number of bird species  in various wetland dependency categories,
          by taxonomic uniqueness, harvest status, and official conservation designations	   31
Table 8.   Wetland and riparian birds whose abundance during the breeding period
          is significantly changing	   33
Table 9.   Advantages of using AREM  	   42
Table 10.  Limitations and assumptions of AREM 	   43
Table 11.  The context for properly using AREM  	   44
Table 12.  Meaning of codes used in the AREM species habitat relationships database  	   46
Table 13.  Example of a species model defined by AREM database coding  	   47
Table 14.  Example of calculation of synthesis scores  	   51
Table 15.  Use of AREM to select wetland combinations that optimize
          protection of regional avian diversity  	   53
Table 16.  Comparison of rankings of wetlands by SCS method, AREM,
          local avian experts, and  field biologists  	   54

-------
                                       LIST OF FIGURES
Figure 1. Subregions of the Colorado Plateau addressed by this report	   5
Figure 2. Comparison of avian richness among seasons and habitats in the Grand Valley, Colorado.  .   21
                                               VI

-------

-------
                                        1.0  INTRODUCTION

1.1 Problem Statement and Definitions

Many areas of the American West have been irrigated for almost a century to support agriculture.  Water
diverted from rivers is routed through pipes and canals to disperse it among agricultural lands in adjoining
valleys.  Traditionally, this river water has been used to flood fields, for about a day at a time, several times
during the growing season. Water is applied in amounts and according to schedules that are not the same as
natural  precipitation.  Much of the applied water leaves irrigated fields as groundwater from deep percolation
and as surface runoff.  As a result, the hydrologic,  soil, and vegetation conditions that technically define
wetlands have sometimes been unintentionally created, both within the on-farm areas which are irrigated
directly, and  particularly within many off-farm areas that receive irrigation runoff or seepage.  These are
termed  "irrigated wetlands."  Thousands of acres of irrigated wetlands that did not exist before this century
have arisen on the landscape. In some instances the subsidizing irrigation water has extended the boundaries
of the relatively few, historically present wetlands or increased the permanency of their water regime, to create
what is  termed "enhanced wetlands."  In other instances irrigation water has caused wetland conditions to
develop in soils that historically did not support wetlands, to  create "induced wetlands."

As acreage of some wetland types has expanded regionally, wildlife species that once occurred seldom, if at
all, in the region have become more widespread and dependent on irrigated wetlands.  An example is the long-
tailed vole (Ecology Consultants 1976).  In some areas, the dependence of wildlife on irrigated wetlands has
grown in  proportion  to loss  of the very  limited  acreage of the few historically present, naturally formed
wetlands or  other natural land covers.   Wildlife dependence on  wetlands and other  structurally intact
vegetation also has increased as the quality or suitability of other  wetlands and natural land cover has been
diminished by artificial  drainage, overgrazing, water  diversions, water table  drawdown, contamination, and
other factors. In addition to sustaining wildlife, wetlands are capable of benefitting society in many other ways.
Recent  evidence from other regions in the U.S. points to the key role some wetlands ~ whether natural or
"artificial" - can passively play in removing certain contaminants from farm runoff, reducing river flood peaks,
maintaining water tables and low flows, and supporting recreation and tourism.

At the same time, concern exists over the fact that  irrigation water, when it comes in contact with certain salt-
rich soils at the land surface or in underlying aquifers,  dissolves the  salts and severely increases the water's salt
content. Traditionally, fields  in the region have been  flooded as much to dilute and leach out the excess salts
(which inhibit crop production) as to provide moisture for crops.  As a result, at least 10% more water is
applied  than is needed to satisfy crop moisture requirements, and up to 60% of the applied water drains into
rivers and wetlands downslope, bearing with  it up to 70% of the salt once  contained in the irrigated soil.
Attempts to reuse this salt-enriched water at downriver locations for domestic, agricultural, or industrial needs
are thwarted  by the impalatability, toxicity, and corrosivity associated with high salt content.

Facilities are  sometimes constructed at downstream locations to concentrate and remove  the salt from river
water, but they are costly. Attention has increasingly focused on introducing salt-tolerant crop strains, and
reducing the introduction of salts at the source. Managers have begun to implement practices that reduce the
amount of water leaving agricultural lands, and thus, the salt-loading of downriver areas.  These practices
involve  adjusting  the  amount, timing, duration, and  spatial distribution  of irrigation water as it comes in
contact  with soils with high salt leaching potential.  This is accomplished in many ways,  such as lining dirt
canals and stock ponds with concrete or other sealers, moving water through pipes instead of open ditches,
and distributing water with sprinkler systems rather than by flooding fields. Government technical assistance
and funding  for these efforts has been facilitated by the Colorado River  Salinity Control Act of 1974.
Assistance is provided to farmers primarily by the U.S. Department of Agriculture's Soil Conservation Service
(SCS) and the U.S. Bureau of Reclamation (USER). Where the resulting improvements in on-farm efficiency
of water use require less water to be drawn initially from rivers for irrigation use, aquatic ecosystems of the

                                                  1

-------
rivers might benefit from increased base flows as well as reduced salinity, and the acreage of riparian wetlands
might increase toward levels historically present, perhaps compensating partly for whatever losses of irrigated
nonriparian wetlands occur.  However, flow regulation by dams, water rights restrictions, and institutional
factors often prevent the realization of these potential benefits.

Reducing the amount of water that leaves irrigated fields surely reduces the amount of water available to
sustain the functions of thousands of acres of wetlands that are located downslope from fields and supported
by field runoff or seepage. In some instances, wetland hydrologic conditions in these wetlands have altogether
ceased to exist.  Wetlands that formerly existed along miles of canals and ditches can become dominated by
upland plant species or other non-wetland land cover.  Functions and values formerly provided to society by
these wetlands could be lost or replaced by functions more typical of the nonwetland systems that prevail in
the region. The long-term changes in vegetation species composition and dominance that occur with salinity
control  projects are being  monitored by the USER and SCS along permanent transects  (pers. comm., S.
McCall, USSR, Grand Junction, Colorado). Declines in wildlife associated with such vegetation changes were
documented by Colorado Division of Wildlife (CDW) in a four-year, before-after, treatment-control study in
the Grand Valley (CDW 1984). The study primarily addressed the effects on wildlife of lining the irrigation
canals with concrete or other mostly impermeable material.

1.2 Study Background and Report Purpose

Despite these earlier efforts at identifying irrigation effects, it became apparent to EPA that a closer scrutiny
and documentation of the possible functions and values of different types of irrigated wetlands was needed to
strengthen wetland  decision-making,  especially in the  context  of mitigation  planning and  evaluation.
Accordingly,  this project was initiated and funded by EPA Region 8. The work was administered by EPA's
Wetlands Research Program, headquartered at the Environmental Research Laboratory in Corvallis, Oregon.
This report represents the first phase of an anticipated two-phase study, and primarily seeks to address the
question:

        Are some of the irrigation-induced and -enhanced wetlands in  EPA Region 8 capable of
        passively providing many of the functions attributed to wetlands generally? If so, which types
        of these wetlands are most capable of doing so, and which functions are they supporting?

This question is addressed through a review of key literature, interviews with scientists from both within and
beyond Region 8 who are familiar with wetland functions, and the experience and professional judgement of
the report's author.  It has been beyond the scope of this project to employ field research and monitoring
methods to determine the degree to which wetland functions occur in irrigated wetlands. One function is an
exception - the ability of irrigated wetlands to provide habitat that sustains  avian (bird) diversity.  In the
context of this project, avian diversity is emphasized because (a) birds comprise the largest  portion of the
region's vertebrate diversity, and appear to be highly sensitive to irrigation inputs in this arid landscape, (b)
avian diversity can be measured directly and cost-effectively, and (c) threats to biodiversity in general are a
growing  concern within EPA and other  agencies.  A second phase of the current EPA project may be
implemented to address this topic more rigorously by collecting avian data from a series of irrigated wetlands.
The project phase  reported here has focused on literature review and analysis of existing regional data, and
has covered hydrologic and water quality functions of wetlands (Section 3.0), as well as  habitat functions
(Section  4.0).

This report contains both a review of literature and expert judgement, and a description of a new, technically-
documented procedure for rapidly evaluating wetland habitat (Section 5.0).  Both are intended for use as one
of several possible inputs to decision-making, where government actions attempt to mitigate the loss of
wetland functions  as caused by salinity control projects.  Such government  actions may  involve decisions
regarding (a) the desirable amount and type of replacement habitats or habitat enhancement measures, (b)
methods  used to measure and compile information on these, and (c) evaluations of their success. This report

-------
does not propose a classification system for irrigated wetlands or methods for distinguishing the degree to
which a wetland is dependent on irrigation. Being a technical background report, this document uses the term
"wetland" broadly and without specific definition, to include riparian, shallow water, and saturated soil habitats
that contain woody or herbaceous hydrophytic vegetation.

-------
                     2.0 CHARACTERIZATION OF IRRIGATED WETLANDS

2.1 Geographic Distribution

This report addresses irrigated wetlands that are associated with major salinity control projects of the Colorado
Plateau (Figure 1) 1.  These wetlands are located primarily in the following five areas, termed "subregions"
in this report:

Colorado
1. Grand Valley: the irrigated area surrounding the towns of Grand Junction and Fruita.
2. Lower Gunnison Valley: includes  the Uncompahgre Valley and  irrigated areas surrounding towns of
Montrose and Delta.
3. Cortez: includes irrigated areas surrounding McElmo Creek and in the Mancos Valley.

Utah
4. Includes the Uinta Basin (irrigated areas surrounding towns of Vernal, Roosevelt, and Duchesne) and the
Price-San Rafael area (irrigated areas  surrounding towns of Price, Castle Dale, and Huntington)2.

Wyoming
5. Includes the Big Sandy area (irrigated areas surrounding the town of Parson).

No comprehensive  inventory exists of the wetlands in these subregions.  Where information on  wetland
location or acreage  exists, it is often of unknown or questionable quality. This is caused by several factors,
including (1) a complete lack of National Wetland Inventory maps that  are prepared by the U.S. Fish and
Wildlife  Service (USFWS) using  standard methods,  (2) changing  government  procedural  definitions of
"wetland," (3) changing acreage of wetlands as a result of ongoing irrigation management programs, and (4)
lack of documentation and/or justification for methods used to arrive at previously published estimates of
wetlands in some salinity control areas or subregions.  In some areas, wetlands are being mapped on an ad
hoc basis, farm-by-farm,  as a salinity  control contract with each farmer is  considered. Digitization of all
irrigated lands in the Upper Colorado Basin will be completed by USER in 1993 (Henricksen and Hall 1992).
All wetlands and land cover were digitized by USER in the western half of the Grand Valley (Crane et al.
1986) and by SCS and others in the Uinta Basin (Ridd and Christensen 1980). However, neither of these data
sets were made available to us for this report, and their quality is unknown.

Elsewhere in the United States, soil surveys sometimes are used to estimate the acreage of wetlands historically
present.  This approach cannot be used in the Colorado Plateau because only a very few soil series in  the
region are exclusively "hydric," whereas many span a gradient of hydric (wetland) to nonhydric (nonwetland).
This occurs partly because hydric conditions often develop in a nonhydric soil after only a few years of direct
application of water, or even of exposure  to indirect irrigation seepage. Thus, any estimation based only on
soils that are officially-designated as hydric is likely to severely underestimate the current acreage of wetlands.

2.2 Classification by Size and Type

As shown in Table 1, irrigated wetlands have not  been classified in a systematic manner.  This greatly
complicates attempts to make comparisons among subregions.  The most commonly applied classification
      Geographers differ with regard to the exact boundaries of the area considered to be the Colorado Plateau.
Thus,  the  term is used loosely  in this report,  to  include areas  of Wyoming and Utah  that  some geographers
consider to belong to other physiographic provinces.

      Irrigated  areas also exist near Moab, Spanish Valley, and perhaps other places.

-------
Figure 1. Subregions of the Colorado Plateau addressed by this report.
                                                           Legend
                                                             = State border
                                                             = County border
                                                        S.C.A. = Salinity Control
                                                                Area
            - • WYOMING SUBREGION
                  Big Sandy S.C.A.
                      SWEETWATER

                       WYOMI
                               COLORADO

                               MOFFAT
 Uinta Basin S.C.A.
DUCHESNE
  	   /UTAH
           UfcREGION
           ice-San
         Rafael S.C.A.
                       GRAND VALLEY... -r\ P1™N

                       SUBREGIQN
                               .**""  I"M=I TA   !
                       MESA    .'

-------
systems are based on wetland location, vegetation form, water depth and seasonal duration, and water source.
Location (on-farm vs. off-farm, in-field vs. off-field), vegetation form, and water regime of irrigated wetlands
are relatively easy to estimate during site visits. However, even after visiting a site it is difficult to determine
conclusively the primary source of water that sustains  a wetland.  "Irrigated wetlands," as considered by this
project, can range from wetlands that are completely supported by irrigation runoff at all seasons, to wetlands
that exist naturally but for which any measurable amount of their water originates from irrigation, however
indirectly (e.g., through seepage or raised water tables). In this sense, virtually all wetlands in irrigated regions
could be considered "irrigated wetlands." However, determining whether the primary water source of a wetland
is irrigation-related in many cases requires considerable judgement, and no highly replicable approach exists
that is applicable  to all situations.   For  distinguishing  natural wetlands from  those recently created by
irrigation, analyses of sediments to determine seed bank species richness might be used.  However, judging
from seed bank data from other regions (Weinhold and van der Valk 1988), this approach would be unable
to distinguish irrigated wetlands older than a few decades from natural wetlands. Similarly, soil organic matter
may not be a suitable indicator of the origin, primary water source, or maturation rate of irrigated wetlands,
because it probably does not accumulate consistently over time in most irrigated wetlands, but is probably
mineralized to a large degree at the end of each growing season. In some wetlands, the presence of large
cottonwood or willow stands, and resulting development of a soil litter layer, suggests considerable ecological
maturity of the wetland. However, the lack of such woody vegetation does not necessarily mean a wetland is
young because trees might have been cut or for other reasons might  never have become established.

Most irrigated wetlands lack permanent water, are  relatively small, are located near ditches and canals, and
are dominated by just a few emergent (herbaceous) species of vegetation.  Many are located on steep slopes,
where seepage from irrigated fields in upslope plateau or mesa areas  re-emerges at the land surface. This is
in contrast to apparently "natural" wetlands of the same areas, which more often contain permanent water, are
larger and mostly  located in river bottomlands, and are often dominated by shrub and forested (riparian)
vegetation.  Anecdotal  information suggests that few irrigated wetlands experience  normal cottonwood
regeneration  because of overgrazing  and the degree and manner in which river flooding is  regulated
throughout the region.

The mean size of  irrigated  wetlands along canals was about 24 acres  in the Big Sandy,  Wyoming, salinity
control area, and about 4 acres in the Lower Gunnison salinity control area (Table 2).  Forested wetlands that
typically occur in  bottomlands  are  generally much larger than emergent  and shrub wetlands.  However,
estimates of the characteristics of irrigated wetlands are difficult to compare among studies. For example, in
a rather comprehensive survey of the wetlands of the Lower Gunnison Valley, Rector et. al. (1979) reported
more woody than emergent wetlands.  Among the wetlands with woody vegetation, more were forested than
shrub. Conversely, from a  3% sample of wetlands in the same area (mostly wetlands near canals), USER
(1991) reported shrub wetlands to cover a larger total area than forested wetlands. USSR (1991) also found
forested wetlands in their sample to be generally smaller (mean of 1.3 acres, range 0.1-4.2 acres) than shrub
wetlands (mean of 2.9 acres, range 0.1-12.1  acres) and especially emergent wetlands (mean of 5.2 acres, range
of 0.1 to 22.3 acres).

2.3  Within-Region Differences

Land use and  wetland data have not been collected in a manner that would allow comparisons among the
subregions (Table 1). Thus, the following information is anecdotal, based entirely on the author's visit to each
of the subregions during November 1992. The purpose of those visits was to ensure that the habitat evaluation
method  being  developed (Section  5.0) included indicators appropriate for each subregion.  Photographs of
wetlands in each subregion are on file at the USEPA Environmental Research Laboratory, Corvallis, Oregon.
The five subregions are characterized as follows:

1. Grand Valley subregion.  Compared with the other subregions, wetlands here are more often surrounded
by row crops (especially corn), are closer to human dwellings, and are smaller  (mostly less than 20 acres).

-------
Table 1.  Acreage estimates for irrigated wetlands by location, wetland type, and water source.

Methods used to define, locate, and classify wetlands and estimate their acreage varied greatly among locations.
Totals in each of the three blocks below should add independently to the Total Wetland Acres Identified" on
line two. Sources of discrepancies are unknown; the data are reproduced as given in original reports. Grand
Valley data are from U.S. Fish and Wildlife Service (1984) and Crane et al. (1986).  Lower Gunnison Valley
data are  from Rector et al. (1979).  Uncompahgre Valley data are from a sample of wetlands in the Lower
Gunnison area, as reported by the U.S. Bureau of Reclamation (USER 1991).  Cortez data are from SCS
(1989).   Utah data pertain only to the Price-San Rafael area and are from USER and Soil Conservation
Service  (SCS 1991).  Although other data exist for Utah (Uinta  Basin  wetland inventory by Ridd and
Christensen 1980) they were not included because they were not received. Wyoming subregion data pertain
to the Big Sandv salinity control area jind are from the SCS (1989).
    Salinity Control Area:            Grand Valley  Lower Gunnison Uncompahgre  Cortez  Utah    Uyoning
Acreage of Area Surveyed 63156
Total Wetland Acres Identified 3546
Total On Farm Acreage
o In Field
o Off Field
o Bottomland
179889
21670
13350
29100
751 4254
3775

25250
15059
10293
3577
1189

10171

Total Off Farm Acreage
o Canals
o River/Bottomland
Total Woody Acreage
o shrub
o forested

1970
1377
593
8320
613
7707
10970
2376
8595

222
182
40
217
262

10191
3620
    Total Emergent Acreage             1576

    Emergent  Wetland Acreage:
    o narrow-leaved
    o water interspersed
    o vegetated flat

    o pasture/hay
    o sedge/grass
    o cattail/rush

    o Type 1  (seasonally flooded)
    o Type 2  (fresh meadows)
    o Type 3  (shallow fresh marshes)
    o Type 4  (deep fresh marshes)
    o Type 9  (saline flats)

    Open Water Acreage                  697
    o Type 5  (open fresh water)
    o Type 10 (saline marshes)
 9625
 5933
  785
  247
529
11439
                                   9015
                                   1993
                                    431
                                            254
                                           3771
                                             29
                                            152
                                           2378
                                           3410
                                            177
    By Estimated Source of  Water:
    o Natural
    o Field Runoff
    o Canals
    o Reservoir Seepage
    o Natural  + Fields
    o Natural  + Canals
    o Natural  + Fields + Canal
    o Fields + Canals
    o Fields + Canals + Reservoir
13014
 3315
  378

 4157
  178
   22
  605
                          2538
                          5211
                           143
                          3857
                          1010

                          1269

-------
Table 2.  Mean acreage of various wetland types in the Lower Gunnison and Big Sandy Valleys.

Methods used to define, locate, and classify wetlands and estimate their acreage varied greatly among locations.
Data are reproduced as given in original reports.  Under the heading "By Water Source," each wetland was
assigned to only one category.  Lower Gunnison data are from Rector et al. (1979). The Wyoming data are
from the Big Sandy area, as reported in Soil Conservation Service (1989).
Subregion:
Mean Wetland Size
On Farm, mean size
Off Farm, mean size
o Canals
o River/Bottomland
Woody Wetlands:
o shrub, mean size
o forested, mean size
Emergent Wetlands:
o narrow- leaved
o water interspersed
o vegetated flat
By Water Source:
o Natural, mean size
o Field, mean size
o Canal, mean size
o Reservoir, mean size
o Natural + Fields
o Natural + Canals
o Natural + Fields + Canals
o Fields + Canals
Lower Gunnison
27
23

4
249

14
69

20
14
8

63
17
4

21
4
2
14
Wyoming













2538
14
24
32





-------
Tamarisk (salt cedar) and Russian olive are prominent features of the irrigated wetlands located in washes.
Salinity management consists mainly of lining and burying water delivery ditches.

2. Lower Gunnison subregion.  These wetlands are most similar to those of the Grand Valley, but fewer
wetlands are located close to human dwellings. Pinyon-juniper vegetation is encountered along the edge of
some wetlands.

3. Cortez subregion. Wetlands here are more often surrounded by or contain pastureland and alfalfa. Willows
are prevalent.  Several wetlands are  large (>40 acres) and dominated by cattail and/or cottonwood-Russian
olive.  Pinyon-juniper borders wetlands at higher elevations within the subregion.  Salinity management
consists mainly of converting from field-flooding to sprinkler systems.

4. Utah subregion.  These wetlands  are generally similar to those of the Cortez subregion.  Some wetlands
have extensive stands of Russian olive.

5. Wyoming subregion. Wetlands here are largely pastureland. There is little wooded riparian or wash habitat.
Willows are moderately prevalent but heavily grazed. There appears to be a greater density of small (<5 acre),
seasonal ponds here than in the other subregions.

-------
          3.0 NON-HABITAT FUNCTIONS AND VALUES OF IRRIGATED WETLANDS

Wetlands, including ones artificially created by irrigation water, function in ways that have the potential to
greatly benefit society. Probably the most widely recognized funtion of irrigated wetlands is their ability to
support wildlife by providing habitat. This function (habitat) is the subject of a separate section of the report
(4.0) and is the focus of a new evaluation method that is described in Section 5.0. To a large extent, habitat
is supported by hydrological and biogeochemical functions of wetlands. These functions support other values,
including but not limited to: improvement of water quality, maintenance of watershed hydrology, recreation,
and production  of harvested products.  This section discusses these functions in  the context of irrigated
wetlands.

3.1 Water Quality Functions and Values

Hundreds of studies have documented the ability  of wetlands, as a whole, to purify water.  However, no
credible studies have examined the water quality role specifically of irrigated wetlands or, for that matter, any
lowland wetlands in the  Colorado Plateau.  If these wetlands serve the same functions as many wetlands
elsewhere, they could be important in reducing nonpoint source pollution and maintaining watershed water
quality in a variety of ways, such as:

        1. Irrigated wetlands could be important for removing excessive nutrients (nitrogen and phosphorus)
        that cause algae problems in livestock watering ponds and dissolved oxygen deficits in lakes and river
        systems.  For example, a Wyoming study  (Hussey et al. 1985) found that riparian areas, compared to
        desert scrub areas, have much higher densities of microorganisms that remove nitrogen from runoff.
        Irrigated wetlands would be expected to play a greater role in removing  nitrogen than retaining
        phosphorus, because of their relatively high soil organic content and the likelihood that much
        phosphorus is adsorbed by the clay-rich upland soils of the region before it reaches wetlands in runoff.
        Increases in irrigation efficiency, by reducing field runoff, can reduce off-farm export of phosphorus
        in runoff but might, by reducing wetland area, increase nitrate export to downslope rivers and
        reservoirs.

        2. Pesticides and other toxic substances  are often  degraded and detoxified in areas that  have high
        levels of organic detritus. The expected high plant production in irrigated wetlands probably supports
        a seasonally high level of organic detritus.  Thus, irrigated wetlands, compared with other regional
        land cover types, might be particularly capable of degrading pesticides, and  in some instances might
        do so without increasing the accumulation  of pesticides in wetland food chains.

        3. Irrigated wetlands, especially on grazed slopes, could be important to retaining and stabilizing
        runoff-borne sediment, at least temporarily. Such sediment otherwise diminishes the storage capacity
        of stock ponds and flood storage reservoirs, blocks light, and lessens the biological productivity of
        some waters.

        4. Irrigated wetlands  are likely to  maintain water quality and reduce  the  toxicity  of various
        contaminants by maintaining or reducing summertime water temperature, just as any plant cover does.

It is probable that many aridland wetlands, especially those that historically lacked permanent water but are
located within washes, are located at sites where groundwater is naturally recharged  (Heath 1982, Wood and
Osterkamp 1984, Loken 1991). However, there is probably nothing about an irrigated wetland that encourages
infiltration and recharge of groundwater; rather, some wetlands just happen to occur in places where recharge
would occur  regardless of wetland  presence.  Moreover, even if irrigated wetlands facilitate  recharge  of
groundwater, the benefits of their doing so are seldom apparent in this region. In contrast to many other
regions, only a small portion of the domestic drinking water in the Colorado Plateau  is drawn from wells.
Thus, even if some of the region's irrigated wetlands are capable of recharging groundwater, the benefits  to

                                                 10

-------
the local welfare and economy would be relatively small. Ecological benefits are also unclear.  Infiltration of
runoff through soils in many parts of the Colorado Plateau is ecologically and economically undesirable,
because such infiltration can increase salinity in wetlands and other receiving waters farther downslope.

Apparently only one study (Fannin et al. 1985) has attempted to statistically examine the natural landscape
factors that influence  nonpoint source pollution across the region.  That study found  that phosphorus
concentration in rivers to be correlated with watershed soil credibility, and nitrate concentration was correlated
with the extent of Cretaceous rock formations.  However, the role of wetlands was not examined.

It is difficult to speculate as to which characteristics of a particular irrigated wetland would make it more
capable than others for retaining sediment, and for removing nutrients and pesticides. Processes that occur
in irrigated wetlands and that are important to improving water quality include the following:

       Water  Deceleration/Storage:   Wetlands, more than other landscape types, delay the downslope
       movement of water  and increase pollutant processing time.  They do so by increasing frictional
       resistance to runoff and focusing infiltration.  Irrigated wetlands most capable of this might include
       those that lack outlets (e.g., farm ponds) or, to a lesser degree, those that have flat gradients with
       dense perennial vegetation and low hydraulic loading (i.e.,  large wetland area relative to amount of
       incoming runoff, such as wetlands fed mainly by groundwater).

       Filtration, Settling, Burial, and Stabilization:  Wetlands can physically confine suspended sediments
       or chemicals, causing their settling by physical processes (e.g., gravity), and their possible burial by
       erosion-resistant, accumulating layers of sediment or precipitate.  Irrigated wetlands are most likely
       to cause filtering, settling, burial, and longer-term stabilization of incoming sediment where (a) such
       sediment is relatively coarse-particled, (b) the wetland is relatively sheltered from wind turbulence
       (e.g., deep, permanent water overlies the accumulating sediment layer), and (c) warm, hypersaline
       conditions (which otherwise can keep fine sediments buoyant and inhibit growth of stabilizing plants)
       are not present.

       Deoxygenation:  Partly because wetlands occur in flat terrain, water that passes  through them
       experiences little turbulence and as a result, the water in wetlands typically has the lowest dissolved
       oxygen concentrations of any landscape  type.   This facilitates retention of some substances that
       influence water quality but mobilizes others.  Irrigated wetlands having the least dissolved oxygen
       might be those that have the greatest potential to decelerate and store runoff (see paragraph above).
       In addition,  irrigated wetlands that are  highly saline, sheltered from wind turbulence (e.g.,  ponds
       recessed within washes), subject to warmer temperatures (because of elevation or exposure), and/or
       which have fine sediments and high primary production would be most likely to experience oxygen
       deficits.

       Adsorption and Physico-chemical Precipitation: Wetlands  typically retain finer-particled sediments
       and more organic detritus than upland sites. This is important because many incoming contaminants
       can become chemically bound to the fine sediments and detritus.  Irrigated wetlands most capable of
       this might include those on soils having a  high content of clay, organic carbon, iron, or aluminum; and
       ones whose salinity is approximately 5 ppt, which promotes deposition through chemical flocculation
       (Akhurst and Breen 1988).

       Uptake and  Accumulation:  Wetland organisms directly take up and/or  transform  chemicals and
       sediments as part of their normal metabolic processes.  This is usually of minor importance  in the
       long-term, but can be an important determinant of water quality seasonally.  The ability of a particular
       irrigated wetland to  purify water through uptake and accumulation depends on the contaminant of
       concern.  Uptake can increase with increases in growing season  length (as affected by elevation,
       latitude, etc.).   Accumulation  can increase  with  increases  in the  resistance  of plant litter  to

                                                 11

-------
        decomposition (as indicated by plant species, acidic or saline conditions, cool water temperatures, lack
        of water circulation, and other factors).

        Denitrification: Wetlands are the most favorable sites on the landscape for the types of bacteria that
        remove (by transforming to a gas)  the nitrogen in nonpoint source runoff (Groffman and Tiedje
        1989a,b, Groffman et al. 1992). In one experiment, irrigated wetlands (flooded meadows) in Gunnison
        and Jackson Counties, Colorado, probably removed 50-85% of the applied nitrogen (Rumberg 1969,
        Ludwick et al. 1978).  Artificial wetlands elsewhere have been documented as removing nitrate via
        denitrification (Stengel et al. 1987).  Irrigated wetlands that are likeliest to have high denitrification
        rates are those that (a) are fed mainly by runoff, not groundwater, and especially runoff from alfalfa
        fields or feedlots, (b)  have the highest soil organic content (as usually  associated with high plant
        production and ungrazed, nonsaline conditions), (c) remain flooded or moist for the longest duration
        of the growing season, (d) warm up the soonest in spring (or never freeze over), and (e) are not highly
        saline. Wetlands having such conditions are also those most likely to support microbial populations
        capable of detoxifying many pesticides and other contaminants.  Literature that documents  the
        purification capacity of wetlands or other carbon-rich systems in agricultural areas, especially in arid
        regions, includes: Rice and Smith 1982, Gersberg et al.  1983, Linn and Doran 1984,  Schimel et al.
        1985, Lemme 1988, Fraser et al.  1988, Neely and Baker  1989, and Parkin and Meisinger 1989.

        Consumption by Wide-Ranging Animals, and Combustion:  Wetlands of the Colorado Plateau are a
        focal point for concentrations of migratory animals, as well as livestock that link several ecosystem
        types.  Nutrients and other chemicals contained in wetland food sources are both imported to and
        exported from wetlands by these animals. Burning of wetlands also exports chemicals beyond wetland
        boundaries as smoke.

In the absence of any regional studies, hypotheses about the ability of particular variables to predict any water
quality process, or about the net effect of the various processes on concentration of a particular contaminant,
would be highly speculative.  For example, wetlands that contain dense vegetation normally would seem better
able to purify water. However, in the Colorado Plateau region, the irrigated wetlands that are more sparsely
vegetated might be better purifiers than those that are more densely vegetated, for  the following theoretical
reasons:

o       Vegetation in the densely vegetated wetlands produces large amounts of detritus.  Detritus causes
        oxygen deficits in sediments and water3. Deoxygenated conditions can facilitate remobilization (not
        retention)  of phosphorus and many contaminants.

o       Vegetation reduces  sunlight and wind, and thus reduces open water evaporation.  Consequently,
        sheltered wetlands might stay wetter longer during the season than unsheltered wetlands.  If  the
        wetland substrate is constantly saturated, it has less storage space for additional runoff than if it is
        periodically and partially dried out.   Whatever pollution-bearing runoff  then enters the wetland is
        quickly shunted through, rather than being slowly processed.

o       Densely vegetated wetlands are often those that have been less heavily grazed.  Grazing  has  the
        potential to increase denitrification  rates by increasing the  availability of nitrogen to microbial
        denitrifiers.
      However,  limited evidence from measurements of Colorado wetlands (Smith  1989) suggests that chemically
reducing conditions are generally not present at the sediment surface or in the water column, except  in the most
stagnant wetlands.


                                                 12

-------
Literature from other regions could be cited to support any of the above arguments. The point here is not
to suggest that sparsely vegetated wetlands provide more water quality benefits, but rather, to emphasize the
complexity of the issue and the fact that we just don't know how various competing processes balance out in
irrigated wetlands.  Vegetation is just one  of several factors of potential use as indicators of water quality
function.  There would be equally frustrating paradoxes to resolve in considering other indicators, such as
many of those associated with processes described earlier in this section.  If this uncertainty is not understood
and articulated, unwarranted credibility can be attached  to the results of rapid methods intended to evaluate
wetland water quality functions.

3.2 Hydrologic Functions and Values

As is true for water quality functions, many studies have documented the ability of wetlands, as a whole, to
reduce flood peaks and, in more limited instances, to  sustain summertime low flows and soil moisture of
surrounding cropland. But again, no credible studies have examined the hydrologic role specifically of irrigated
wetlands or, for that matter, any lowland wetlands in the Colorado Plateau. Wetlands can either remove water
from local surface flow systems (sink function) or conserve water and  sustain  the moisture of local areas
(source function).  Various processes that control the water budget within a wetland determine whether sink
or source functions prevail.  Sink functions  prevail  where runoff entering wetlands infiltrates or is converted
to water vapor by  means of transpiring vegetation. Source functions usually prevail where wetlands act as
conduits for discharging groundwater, or where water inputs are increased or conserved because wetlands are
good at intercepting precipitation, detaining drifting snow, or reducing open water evaporation.

Processes that  occur in an irrigated wetland and that determine whether it is a hydrologic source or sink
include:

        Water  Loading:   The amount and rate at which  water is introduced or becomes  available to an
        irrigated wetland determines how much can be assimilated. Most irrigated wetlands are fed mainly
        by lateral subsurface seepage and overland runoff, but other sources of water include direct inputs
        from channels, ditches, and pipes, direct precipitation, condensation, and  groundwater discharge. For
        wetlands fed entirely by natural sources, the extent of their  upslope drainage area  -- weighted by
        slope, soil permeability, local precipitation, land cover type, shape, and other factors ~ is frequently
        used to estimate water loading.

        Water Removal:  Some irrigated wetlands are more able than others to significantly delay or stop the
        downslope movement of water. They do so by facilitating the processes of evaporation, transpiration,
        infiltration, and recharge.  Indicators of these processes include number of ice-free days, vegetation
        density and type,  wind and sun exposure, soil type, depth  to  water table,  open water area, and
        landscape position.

        Water Deceleration/Storage:  Irrigated wetlands  can also delay the downslope movement of water by
        increasing a landscape's frictional  resistance and sometimes the storage of water above ground.
        Irrigated wetlands most able to perform this process are probably those  that lack outlets (e.g., stock
        ponds). Among open-ended wetlands, those that lack well-defined channels and  are almost totally
        vegetated (especially with dense stands of robust vegetation)  are most likely to decelerate runoff.

        Water Routing: The spatial arrangement of irrigated wetlands within the landscape also influences
        their cumulative capacity to affect the timing and amount of downstream flow or  soil moisture, but
        in ways that are not predictable without sophisticated computer models calibrated to  a particular
        watershed.

Although irrigated wetlands that  are sinks  for runoff (e.g., stock pond wetlands) are most able to control
downstream flooding, almost any irrigated wetland contains vegetation that offers resistance (quantified by a

                                                 13

-------
 "roughness coefficient")  at points in the landscape where  runoff is usually concentrated.  For example,
 Burkham (1976) reported that the removal of riparian vegetation  in an Arizona floodplain lowered the
 roughness coefficient 0.026 and resulted in a velocity increase of 0.8 ft/s velocity during floods. An increase
 in the roughness coefficient of only 0.008, following vegetation reestablishment, caused a 0.2-ft/s reduction in
 velocity.

 The slowing of runoff by wetlands that are dispersed throughout a watershed has the potential for reducing
 flood peaks by staggering runoff arrival in downstream areas.  Such deceleration also reduces channel erosion
 and allows greater time  for processing of waterborne contaminants.  This could be particularly important
 because irrigation, by increasing the antecedent moisture condition of soils, makes irrigated watersheds more
 "flashy" (sharp, steep runoff response to summer rainfall) and  prone to  channel erosion and downcutting,
 which removes the edges of valuable farmland and degrades water quality.  Major (e.g., 100-year) flood events
 are, in contrast,  less a concern in the region now than historically, because most large floods are now largely
 controlled by regulated impoundments.

 Evidence of wetlands performing as passive sources of water  to streams and adjoining cropland is limited. If
 a study of the watershed role of stockponds in Arizona is any indication, the  cumulative role of irrigated
 wetlands  on baseflow might  not  be great.  In that study, Milne and  Young (1989)  reported virtually no
 measurable effect on streamflow of stockponds that were present in a river basin at a density of 0.2 ponds per
 km2 (and having an average storage capacity of 1,803 m^). Nonetheless, some studies of western restoration
 projects  suggest that certain  headwater riparian wetlands can promote water conservation (Winegar 1977,
 Stabler 1985, Van Haveren 1986, Debano and Schmidt 1990, Ponce and Lindquist 1990). These wetlands do
 so partly by reducing wind, channel erosion, and water temperature, increasing infiltration of runoff, and
 reducing stream velocity.  If some irrigated wetlands do serve such a function, and if the water they conserve
 and export is not highly saline, then their potential value to other ecosystems and cropland in this arid region
 could be considerable. However, it is difficult to speculate as to which characteristics of a particular irrigated
 wetland would make it more capable than others for conserving water or influencing downstream floods.

 3.3 Recreation and Harvest Values

 As a whole, wetlands can provide opportunities for many recreational activities, such as hunting,  fishing,
 trapping, swimming,  canoeing, birding, hiking, foraging, photography, and ice skating. Wetlands in  general
 can also provide opportunities for education, research, and simple enjoyment of open space and natural beauty.
 Commercially, wetlands  can provide income to their  owners  through  hunting and grazing  leases, and
 sustainable harvest of hay, timber, furbearers, bait animals, and  decorative plants.

 The extent to which these activities occur in irrigated wetlands is, again, unknown. Foraging for wild asparagus
 is  popular in  some irrigated wetlands (Rector et  al. 1979).  Most irrigated wetlands are  too  shallow for
 activities such as canoeing and swimming.   Fishing is generally poor because of the lack of much  natural
 reproduction in these drastically manipulated systems. Probably no irrigated wetlands have sufficient timber
 to allow sustainable logging.  Irrigated wetlands support only  the occasionaly harvest of  fallen limbs for
 firewood. Of greater importance in limiting the recreational use of irrigated wetlands is the fact that nearly
 all are located on private property. Because most owners prohibit public trespass, recreational and  harvest
values of the wetlands are realized most directly,  if at all, by the private landowners.  Nonetheless, large
 numbers of migratory birds that depend on  irrigated wetlands are later enjoyed by visitors  to non-irrigated
wetlands that are open to the public, both locally and in other regions. Also, many citizens who never visit
wetlands appreciate the resource simply for its existence and heritage values.

The greatest commercial values of irrigated wetlands are probably related to opportunities  for hunting and
grazing leases and the harvest of hay and furbearers (mainly muskrat). Communications with local biologists
indicated that hunting leases, primarily for irrigated wetlands and adjoining farmlands that have been stocked
with captive-raised pheasants, are selling for several hundred dollars each.  In Utah, commercial hunting areas

                                                 14

-------
must be between 160 and 1280 acres in size and at least one mile apart.  Lining of canals and conversion to
sprinkler systems would be expected to have little effect on the area of natural hay in wetlands that is available
for harvest.

3.4 Multiple Use Considerations

It is unlikely that any single irrigated wetland is optimal for all functions. More often, functions are likely to
be in conflict with one another.  For example, irrigated wetlands that retain contaminants and sediments can,
in some instances, be hazardous to wildlife. Recreation sometimes is incompatible with habitat values (e.g.,
jogging trails  through riparian habitat), but also fosters increased public awareness  and appreciation of
wetlands.   Riparian restoration programs can  degrade water quality if new vegetation attracts excessive
numbers of shade- and forage-seeking livestock (or wild herbivores) to streams, degrading water quality with
their wastes (unless fences are simultaneously installed to exclude livestock). Such considerations must enter
into decisions  based on the relative values  of various types of irrigated wetlands.
                                                  15

-------
             4.0  HABITAT FUNCTIONS AND VALUES OF IRRIGATED WETLANDS

4.1 Definitions of "Good" Habitat

Wetlands support plants and animals partly by providing habitat.  That is, they provide conditions that are
suitable for sustaining the reproduction, growth, and dispersal of natural populations. Of course, virtually all
land and water provides habitat for some species.  Specifically, how are wetlands important?  Many studies
in the Colorado Plateau region have compared the suitability of wetland habitats with that of nonwetland
habitats. A few have specifically compared irrigated wetlands with nonwetlands and with wetlands not highly
influenced by irrigation.

In examining these studies, it is crucial to first define some endpoints that comprise "good" (or "high-quality")
habitat.  Most ecologists define quality habitat operationally as habitat which:

        (a) contains a large number of species, or species per unit area (i.e., richness4);

        (b) contains a large number of individuals, or individuals per unit area (density);

        (c) contains species having special status because of their rarity5, narrow environmental tolerance,
        key influence on  other ecosystem components, or  recreational/commercial value, especially if the
        wetland supports  high production of these species;,  and/or

        (d) supports conditions a, b, or c indirectly, i.e., the wetland has features that support high species
        richness, density,  or important species in surrounding habitats, although the wetland itself may not
        be so characterized.

Of these various  habitat endpoints, species richness was chosen as the main focus of this project.  Species
richness was chosen because (a) it is a component of "biodiversity," which is a theme of growing interest among
resource agencies and the public, (b) its prediction (in relative terms) for any irrigated wetland is believed
possible within the constraints of this project, and (c) it can be quantified as a real number, rather than as an
ordinal rating (sealer).  The  endpoint is narrowed even further to "avian species  richness"  because, in the
Colorado Plateau region, (a) wetland data are much more available for birds than for mammals, amphibians,
or other  animals or plants, and (b) birds are the most diverse terrestrial vertebrate group in the region.

4.2 Results of Previous Assessments of Irrigated Wetland Habitat

In the five combined subregions of the Colorado Plateau, approximately 183 bird species occur regularly, i.e.,
are not considered accidental, rare, or casual (Kingery 1988). Of these, 165 (90%) occur regularly in wetland
or riparian habitats during at least one season of the year (Appendices A, B, C). Of these 165 species, about
15% require water as a substrate, another 20% occur only in wetland, riparian, or deepwater habitats, and the
remaining 65% use uplands as well as wetlands and riparian areas, but occur much less often in uplands (Table
3).  For this report, I used the following procedure to arrive  at these estimates. I began by creating a source
list of regional birds from Kingery (1988). All species listed in that report as occurring in aquatic, riparian,
      In this report, the term "diversity" is sometimes used interchangeably with "richness," although strictly
speaking, richness  is only one  component of diversity, the other being "evenness" or "equitability."

       Wetlands  containing such species  are often said to be most  important as contributors  to "gamma"
(regional) diversity, whereas wetlands containing the most species, regardless of the rarity of the species,
are said to have the most "alpha" (within-wetland) diversity.

                                                 16

-------
Table 3. Number of bird species in each wetland dependency category by seasonal abundance and neotropical
migrant status.
                         Number of  Colorado Plateau  Species, by Dependency Category:
                         Highly  ?                                       TOTAL
                         Dependent        Intermediate    Dependent        Wetland
Total Species

# of Breeding Species:
   Abundant
   Common
   Fairly Common
   Uncommon
   TOTAL

# of Migrating Species:
   Abundant
   Common
   Fairly Common
   Uncommon
   TOTAL

   Type A8
   Type B
   TOTAL

# of Wintering Species:
   Abundant
   Common
   Fairly Common
   Uncommon
   TOTAL
25
 2
 3
 7
 6
18

 0
 0
 0
33
                 0
                 4
                 3
                 4
                 11
 0
 3
 1
21
25

 2
 5
 7
107
                 6
                 13
                 19
                 16
                 54
 8
 8
32
32
80

31
28
59
                                  8
                                  3
                                 10
                                 19
                                 30
165
                  6
                  18
                  24
                  22
                  70
 10
 14
 40
 59
123

 33
 33
 66
                                  10
                                   6
                                  12
                                  26
                                  54
       Based on knowledge of the author and interviewed local experts.  Numbers  of species are those occurring
in the Grand Valley subregion;  other  subregions would differ only slightly.  Terms for abundance are as used
in Kingery (1988).

       "Highly Dependent" means that surface water is the species' primary substrate: e.g., common goldeneye.
"Intermediate" means the species occurs only where water/wetland is present:  e.g.,  spotted sandpiper.
"Dependent" means  species also  uses uplands, but uses wetlands frequently:  e.g.,  warbling  vireo.

     o
       Type A species breed only in the United States and/or Canada and migrate to  the Neotropics.   Type B
species also breed  in the Neotropics.   Other regional species generally do not migrate to Neotropics.  Species
were also counted  in the total  for "Migration."   Information on neotropical migrant status is as compiled in
Carter and Barker  (1992).
                                                    17

-------
or wetland habitats of Colorado were included. Next, I added three species to the Kingery list9 on the advice
of local ornithologists: savannah sparrow (use of lowland riparian in migration), and western meadowlark and
Gambel's quail (use of lowland riparian in winter).  The degree of dependence on wetland/riparian habitats
varies greatly among the listed species, but all would experience population declines at least locally, if these
aquatic habitats were diminished. Only regularly-occurring species are included, because they are perhaps the
most reliable indicators of habitat quality. I excluded species that were categorized as "occasional" or "rare"
in USFWS refuge lists for the region, or "rare" (or even less regular) by Dexter and Lavad (1992), because few
such species occur regularly.  I also excluded species occurring in the local area, but only at higher elevations
(>7000 ft) where irrigated wetlands are uncommon.  Finally, I excluded seven species that probably are little-
affected by irrigation water inputs because they use only large reservoirs, lakes, and rivers: common loon, eared
grebe, horned grebe, western grebe, tundra swan, snow goose, and common merganser.

Within  the Colorado Plateau region, the  Cortez  subregion appears to have the richest wetland and riparian
avifauna, whereas the Wyoming subregion  seems to have the poorest10.  The number of species  that use
wetland and riparian habitats for nesting appears to be greatest in the Utah subregion and least in the Grand
Valley.  Seasonally, the number of wetland/riparian species is greatest during migration (May and September),
secondary during the breeding season (June-July), and least in winter (Table 3). Of the Colorado Plateau's
165 regularly occurring wetland and riparian species, a greater percentage of uncommon species occur during
winter and migration than during the breeding season (Table 3, p. 17). Avian densities probably follow the
same seasonal pattern (Ecology Consultants 1976, Somers 1979).  Although density and diversity are low in
winter compared with the rest of the year,  wetlands in winter provide wildlife with shelter unavailable in much
of the surrounding landscape, and thus at this season may be the most important landscape component for
regional wildlife. Also, some of the irrigated wetlands that receive water mainly from warmer, more saline
subsurface seepage (e.g., wetlands  recessed  within washes or at  the toe of escarpments)  seem  to remain
unfrozen longer in winter than other wetlands, thus providing habitat for lingering waterbirds.  Studies  that
have compared bird diversity in irrigated wetland habitats (marshes, cottonwoods, tamarisk) with diversity in
nonirrigated habitats have generally supported the greater importance of wetlands.  For example, Ecology
Consultants (1976) surveyed birds at several seasons in various Grand  Valley habitats - saltbush, greasewood,
greasewood-saltbush, cottonwood,  tamarisk, and marsh.  Based on a single  transect in each habitat, they
estimated that the most songbird species during May and August occurred in the riparian cottonwood habitat
(Figure 2).  In January, greasewood had  the most species but cottonwood was ranked second.  The marsh
habitat in May and August had nearly as many species as the riparian cottonwoods. Wintertime avian diversity
of the marsh was termed "intermediate" among the habitat types sampled. Also in the Grand Valley, the four-
year study  by CDW (1984) found more species along the  marsh transect than along transects in either the
       I also compared the Kingery (1988) designations of wetland and riparian species with similar designations
in a list for eastern Utah by Dalton et al. (1990),  which categorizes wetland/riparian habitat as "critical,"
"high-priority," or "substantially used" for each of 178 regularly occurring birds.  In general, the Dalton et
al. (1990)  list is more inclusive.  That  list  agreed that all  but four of the 165  species which I  had  listed
as  wetland/riparian  are,  indeed,  dependent  on wetland/riparian  habitat  (i.e.,  such  habitat was  labeled
"critical" or "high-priority").  The four exceptions to my list were Brewer's sparrow and western meadowlark,
which Dalton et al. did not list at all for wetland/riparian habitats, and pinyon jay and plain titmouse, for
which Dalton et al. nonetheless considered wetland/riparian habitat to be "substantially  used."  The Dalton et
al.  list includes 15  species  which  I  did not  include.   For these  15  species,  Dalton  et al.  consider
wetland/riparian habitat to be "critical" for four (rough-legged hawk, chukar, mountain bluebird, sage sparrow),
"high-priority" for seven  (prairie falcon,  sage grouse, Say's phoebe,  scrub jay, canyon wren, sage thrasher,
vesper sparrow), and "substantially used" by four  (burrowing owl, common poorwill,  white-throated swift, rock
wren).

         Total  numbers of bird  species that occur regularly in  wetlands and/or riparian  habitats are as
follows:  Cortez  subregion, 147 (78 nesting,  135  migrants,  50 wintering);  Grand  Valley subregion, 133 (70
nesting,  123 migrants, 54  wintering); Utah subregion,  121 (86 nesting,  112 migrants,  28 wintering); Wyoming
subregion, 114 (72 nesting, 107 migrants, 22 wintering).  Apparent differences among regions are probably not
biologically  meaningful because they likely  reflect  differences in the  extent of  inventory  efforts among
subregions, rather than actual differences  in species richness.

                                                  18

-------
greasewood or saltbush stands. A species richness of from 10 to 50 species appears to be typical of individual
irrigated wetlands (Table 4).  The potential for discovering even greater avian diversity, given more frequent
or long-term surveys of large wetlands with considerable open water and forested acreage, is indicated by the
results of surveys of a river bottomland site in the Grand Valley (Dexter 1992), where 225 species have been
recorded so far, and from a similar site farther downriver -- the Moab Slough (Boschen 1992), where more
than 170 species have been recorded to date.

Various studies (e.g., Knopf 1985) also have documented the density of birds to be greater in forested riparian
wetlands than in upland habitats in Colorado. Although by itself avian density does not necessarily reflect
habitat quality (Van Home 1983), it can be a useful reflection of habitat quality when paired with other
endpoints, such as species richness and community composition. The Ecology Consultants (1976) study found
greater densities of songbirds in the riparian cottonwood habitat than in the  other habitats during May.  In
January and August, greasewood had the greatest densities, but cottonwoods were ranked second.  In May the
marsh habitat was second only to the riparian cottonwoods in density of individuals, but that density was only
half that of the cottonwoods.  Wintertime avian diversity and density in both the marsh and the tamarisk
habitat was termed "intermediate" among the habitat types sampled. Also  in the Grand Valley, the four-year
study by CDW (1984) reported greater bird densities along the marsh transect than along transects in either
the greasewood or saltbush stands.

Regardless of whether wetlands have many species or dense populations, they nonetheless are critical for
supporting particular species.  An individual wetland that  is ranked lower than other wetlands or upland
habitats (because it lacks large numbers of individuals or a high species total) may nonetheless be important
to maintaining regional biodiversity if the species that are present are ones that occur seldom, if at all, in the
other habitats.

Categorizing species according to  their "wetland dependence" is difficult.  Some species clearly would vanish
from local areas within the Colorado Plateau if all wetlands in these areas were eliminated, even if rivers and
lakes  remained.  This is sometimes apparent from their life  history characteristics.  More typical are species
that seem to use wetland and riparian areas extensively, but  are also found regularly in nonwetland areas. If
wetlands were locally eliminated, some of these species might survive in the nonwetland habitats, although at
diminished population levels, but such determinations are difficult to make. One study (Szaro and Jakle 1985)
reported that the number of typically upland species that used Arizona riparian areas was much less than the
number of riparian species that used upland areas.  In the Grand Valley, of the habitats surveyed by Ecology
Consultants (1976) in January, the cottonwood, marsh, and tamarisk habitats each  contained one species that
was found in no other habitat at this season (yellow-rumped warbler, song sparrow,  and Bewick's wren,
respectively). When the six habitats were surveyed in May, the cottonwood habitat had the most exclusively
occurring species (11), followed by the marsh (5).  In August, both the cottonwood and marsh habitats had
more  exclusively occurring species (7)  than any of the six habitats surveyed.  Another  Grand Valley study
(CDW 1984) covered a smaller number of habitats (marsh,  saltbush, and greasewood), but  more intensively
and over a four-year period.  Of these three habitat types, "marsh" contained 17 breeding bird species that did
not occur in the other two habitats.  Neither of the other habitats contained more  than two species that were
absent from the marsh.  Considering the data from all seasons pooled together, 19 species  occurred only in
the marsh, whereas only 7 occurred exclusively in greasewood and  none occurred only in saltbush.   The 19
marsh species represent 39% of the 49 species found in the marsh over the 4-year period.

In summary, it is apparent  that Colorado's irrigated wetlands,  like most wetlands elsewhere, support the
greatest diversity and density of  birds of  all habitat types within their landscape.  Their  importance is
highlighted further by the fact that their avifauna is composed largely of species that do not occur regularly
in other habitat types.

Much less is known about the amphibians, mammals, and reptiles that  regularly use wetland or  riparian
habitats of the Colorado Plateau, but their diversity is less than that of birds. Appendices D and E show that

                                                 19

-------
Table 4.  Estimates of avian richness from prior surveys of riparian or wetland areas in Colorado and eastern
Utah.
Habitat Type/Location

Irrigated marsh, Grand Valley
         in May
         in August
         in January

Irrigated marsh. Grand Valley

About 20 irrigated wetlands
(emergent, shrub, forested),
Grand Valley, Colorado

30 irrigated wetlands
(emergent, shrub, forested),
Lower Gunmson Valley, Colorado

Irrigated marsh, Cortez area

Irrigated marsh with pond,
Cortez area,  Colorado

3 riparian areas (relatively
undisturbed watersheds), e. Utah

Floodplain (Colorado River)
forested wetland, Grand Valley

Riparian areas, Douglas Cr.,
northwestern Colorado

Cottonwood willow creekbottom
(20 acres),  El Paso County,
eastern Colorado

Semi-wooded riverbottom pasture,
eastern Colorado

Urban cattail marsh and
cottonwood woodland (8 acres).
El Paso Co.,  eastern Colorado

Floodplain cottonwood forest,
129 acres, Weld Co.,
eastern Colorado

Floodplain pond, 21 acres.
Weld Co., eastern Colorado
# of SPP.


11
12
 4

49

11-27



 2-26



27

42


22-37


45
16



27


17



18
Source  Method/Coverage

(1)     0.5 mi EmIen strip census, 3 visits/month,
        one year (1975)
(2)     0.25 mi transect, weekly Apr.-June, 4 yrs.

(3)     Roadside point counts 0.5 mi apart; monthly
        except not Jan, Feb, July,  Aug.; 40 points
                per month,  for 4 years

(4)     Emlen strip census,  April 18-July 22, 1977,
        3 hours per morning
(5)     Unstructured survey, 11/77-10/78

(6)     Unstructured survey, 11/77-10/78
(7)     Point counts, 10 per site, 8 minutes/count,
        twice during June 1992

(8)     Emlen strip census on 5/77; 3,5/79;
        4,6,10/81; 3,7/82; 5/83; 8/85; 9/88
93 total         (9)
47-76 per seg.
        Variable circular plots, 11 stream
        segments, 16 visits during June 1991-1992
(10)    June 1980
(11)    6-year June average, 1973-1979
(12)    2-year June average
(13)    21-year June average, 1971-1986
                 (14)     5-year June average
Sources:
1. Ecology Consultants 1976
2. Colorado Division of Wildlife (CDW)  1984
3. Colorado Division of Wildlife (CDW)  1984
4. Rector et al. 1979
5. Somers 1979
6. Somers 1979
7. Utah Division of Wildlife Resources  1992
8. U.S. Bureau of Land Management (USBLM)  1992
9. Baker et al. 1992
10-13. Breeding Bird Census database, Laboratory of Ornithology, Cornell Univ., Ithaca, NY
                                                    20

-------
Figure 2.  Comparison of avian richness among seasons and habitats in the Grand Valley,
Colorado.
                    Source: Ecological Consultants (1976)
                    W-1: Desert Shrub (sattbush) transect
                    W-2: Riparian Woodland (cottonwood) transect
                    W-3: Marsh transect
                    W-4: Phreatophytic Shrub transect (greasewood)
                    W-5: Phreatophytic Shrub transect (tamarisk)
                    W-6: Desert Shrub transect (saltbush-greasewood)
         20


         18


         16

         14


         12
      •o  -8
      VI
             ^lil
                       I
                       m.
                I
                W-1
               August
                            W-2
                                        W-3
                                                    W-4
                                                                W-5
                                                                            W-6
                                            TRANSECTS1
I . 'I January
May
                                           21

-------
10 amphibian, 26 reptile, and 85 mammal species use wetland/riparian areas, as compared with 165 bird
species. This represents about 77% of all amphibian species, 72% of all reptiles, and 80% of all mammals
occurring  in  the  region (Dalton et al.  1990).   Information  on use of irrigated wetlands by mammals,
amphibians, and reptiles is  limited to a very few reports (McCoy 1962,  Ecology Consultants 1976, Somers
1976a, 1976b, 1977,1979,1980, CDW 1984). In the Cortez area, the surveys by Somers (1979) revealed a few
species that used emergent wetlands almost exclusively: chorus frog, Western harvest mouse, and montane vole.

Information on fish and invertebrates of irrigated wetlands appears to be even scarcer. According to Dalton
et al. (1990), only 12 of the 42 fish species in the region are  native (i.e., not exotic/introduced)  Limited
sampling by CDW (1984) of four natural washes receiving irrigation water in the Grand Valley revealed a total
of 13 fish  species. This represents about  31% of all fish species inhabiting the region (Dalton et al. 1990).
All four washes contained two species ~  flannelmouth sucker (Catostomus latapinnis)  and roundtail chub
(Gila robusta).  Three of  the four washes  contained another species - bluehead sucker (Catostomus
discobolus^ Species occurring in only one wash were rainbow trout (Oncorhvnchus gairdneri). red shiner
(Notropis  lutrensis). black bullhead (Ictaluris melas). channel catfish (Ictalurus punctatus). and black crappie
(Pomoxis nigromaculatus).  The wash with the most fish (as collected by wintertime electrofishing) had 11 of
the 13 species as pooled from all washes; 5 of these species (and 50 individuals) occurred within one 50-ft
reach.

Sampling  the  same four natural washes, the CDW (1984) study found 21  taxa of invertebrates.   Even
considering the infrequency of sampling and the fact that few of the invertebrates were keyed to genus  or
species, by comparison with other studies this represents an extremely low species richness. No sample from
the wash  having the most  taxa  had more than 8 of the  21  taxa as pooled from all washes, and  many
summertime efforts failed completely to  collect any invertebrates.  The largest number of invertebrates
collected (about 1138 individuals per ft2) was  collected in winter. Dominant invertebrates included midges
(Chironomidae), blackfiies (Simuliidae), and the caddisfly, Hvdropsyche. Another study from the Grand Valley
(Hayes and Nielsen 1978) reported on mosquitoes in irrigated wetlands as a possible vector of deadly equine
encephalitis, although the number of documented cases of this disease in the region is relatively  few. Risks
are perhaps greatest in  irrigated wetlands  of the Uinta Basin, where pasture and horses  are most prevalent.
Elsewhere in the western part of EPA Region 8, most invertebrate studies have focused on streams and lakes,
but a few (USFWS 1979, Severn 1992) have addressed wetlands. Literature from other regions has sometimes
documented high  densities of invertebrates important to wildlife in some irrigated, agricultural, or created
emergent wetlands (Broschart and Linder 1986, Scheffer et al. 1984, Kreil and Crawford 1986, Stephens et al.
1988, Euliss et al. 1991, Severn 1992).

Although not comparative, many other studies and literature reviews document considerable wildlife use  of
irrigated wetlands, agricultural wetlands, and created ("artificial") wetlands. These include the following
(* indicates information from Colorado or eastern Utah):

       Wildlife Use of Irrigated Wetlands:
       Earl 1950, Harris 1953, Ecology Consultants 1976*,  Dalton et al.  1978*, Rector et al.  1979*, Guthery
       et al. 1982, Colorado Division of Wildlife  1984*, Gatz et al. 1984, Ohmart et al. 1985, Lewis and
       Bockelman 1988, Boschen 1992*.

       Wildlife Use of Wetlands and Riparian Areas in Irrigated Regions:
       Twomey 1942*, Copelin 1953, Austin 1970, Bottorff 1974*, Gaines 1974,  Carothers et al.  1974,
       Carothers and  Johnson 1975, Lewke  1975, Logan  1975, Whitmore 1975, Somers 1976a*, 1976b*,
       1977*, 1980*, Tolle  1977*, Stevens et al. 1977, Conine et al. 1978, Henke and Stone 1978, Tubbs 1980,
       Hobaugh  and Teer 1981, Briggs 1982,  Cook 1984*, Stinnett and Klebenow 1986, Hunter et al. 1987,
       Faber et al. 1989, Dalton et al. 1990*, Peterson and Cooper 1991, Dexter 1992*, U.S. Bureau of Land
       Management 1992*, Utah Division of Wildlife Resources 1992*.
                                                22

-------
        Wetland Wildlife Use of Western Croplands:
        Glover 1956, Gates 1965, Evans  1967, Duebbert and Lokemoen 1976, Higgins 1977, Kantrud 1981,
        1986, Cowan 1982, Baldassarre et al. 1983, Duebbert and Frank 1984, Guthery et al. 1984, Baldassarre
        and Bolen  1984, Baldassarre and Fischer 1984, Balsore et al. 1986, Duebbert and Kantrud 1987,
        LaGrange and Dinsmore 1989, Budeau and Snow 1992.

        Wildlife Use of Stockponds and Other Created Emergent Wetlands:
        Nelson  1953*, Smith 1953, Nelson  1954, Berg 1956, Yeager and Swope  1956,  Hopper 1972*,
        Lokemoen  1973, Schroeder  et al.  1976*, Evans  and Kerbs 1977, Flake et al.  1977, Ruwalt 1979,
        Rossiter and Crawford 1981, Hudson 1983, Kreil and Crawford 1986, Belanger and Couture 1988,
        Buckner 1988*, Matter and Mannan 1988, Payne 1992, Taylor and Trost 1992.

4.3 Habitat "Indicators" and Evaluation Procedures: Definition and Historical Uses

Many biologists use the term "indicator" to describe species that indicate the suitability of a habitat for many
other species, or that tell us something about a habitat's ecological "health."  In the following pages I use the
term in a much broader sense, to refer not  only to biological features, but also to the physical and chemical
features (or variables) of a habitat, at both site-specific and landscape scales, that can be estimated rapidly and
that relate, either empirically or deterministically, to the habitat's suitability for supporting individual species
and/or avian diversity in general.  The characteristics of a particular indicator are termed the indicator
conditions.  For example,  one indicator of  avian diversity in irrigated wetlands is the extent of woody
vegetation.  Acreage categories of "0.1-1" and ">1" represent two conditions of this indicator.  The use of
indicators is a popular practice because indicators can be estimated rapidly, whereas it is seldom practical to
directly observe wildlife use of all wetlands in an area.  To be credible, direct surveys require  lengthy visits to
all wetlands during carefully specified seasonal periods.

Indicators have  often been organized into  standardized evaluation procedures  (e.g., questionnaires  or
checklists) and models that are used to evaluate wetlands. Examples are the Habitat Evaluation Procedures
(HEP) of the U.S. Fish and Wildlife Service (1980) and others reviewed by Adamus (1992). When indicators
are organized in standardized procedures and used to classify or rank wetlands, it can promote  efficiency in
government.  This  is because the classification and ranking process can quickly focus  management and
regulatory policies and effort on the wetlands that are likely to be most important.  Moreover, organizing the
indicators in a standardized protocol allows different persons evaluating the same wetland to more often arrive
at the same conclusion regarding the relative habitat quality of a particular wetland.  Such  consistency and
comparability is  important  to help ensure public confidence in the evaluations, rankings, and management
decisions.

Specifying the best indicators of habitat suitability begs the question, "best habitat for what?" Wetland features
that are good indicators of habitat suitable for some species are often less useful for other species.  HEP
addresses this dilemma by requiring that the user determine habitat suitability for just a few species presumed
to be representative of the larger set.  The Golet-Larson (Golet 1972) and Colorado SCS method (Rector et
al. 1979, SCS 1992a) do not clearly specify which habitat endpoint is being evaluated. These methods imply
that their indicators describe "good" habitat, leaving the user to wonder if "good" habitat means species-rich
habitat, habitat with high vertebrate densities (which groups? which seasons?), habitat productive mainly for
open-water, recreational, or rare species, or (improbably) all of these endpoints.  Many of the indicators that
they use (e.g., ratio  of open water to vegetation) are based mainly on research documenting importance to
waterfowl production, not necessarily to the conservation of biodiversity.

Within the study region, perhaps the  first habitat evaluation method to be widely used on irrigated wetlands
was one sponsored  by SCS and USER,  and developed  and used by Rector et al. (1979) for the Lower
Gunnison area.  That method was based  largely on work in Massachusetts wetlands (Golet 1972), and was
revised  several times by Paul  Obert and others of the SCS (SCS 1992a).   Variations of the  model have

                                                 23

-------
subsequently been used to evaluate a statistical sample of Uncompahgre Valley wetlands (USBR 1991) and
all irrigated wetlands of the Cortez subregion (SCS 1989).

4.4 Which Indicators Predict "Good" Habitat?

I identified five major indicators of the habitat suitability of irrigated wetlands:

        1. Wetland Size and Related Indicators
        2. Water Regime ("Wetness")
        3. Vegetation Characteristics
        4. Other Animals and Water Quality
        5. Landscape Land Cover and Seclusion

Various formulations of these indicators are applied collectively as a part of a new method for evaluating
wetland habitat -- the avian richness evaluation method (AREM) -- described in Section 5.0.  The importance
of these indicators and their general relationship to the evaluation method are documented in the following
sections. I identified these indicators of bird diversity mainly from personal experience and through interviews
with local avian experts11.  In these interviews, habitat requirements of all local species listed in Appendices
A-C were  discussed, species-by-species.  This was the primary approach because it appears that only two
published studies (Rector  et al. 1979 in the Lower Gunnison Valley, Ohmart et al. 1985  along the lower
Colorado River in Arizona) have tried to systematically relate avian species richness, or the presence/absence
of particular species, to habitat variables (indicators) in irrigated wetlands.

I considered other indicators but found the local information insufficient to link them to bird habitat quality
or avian richness. In particular, I considered using "water source" as an indicator because of its potential
relevance to wetland policies and frequent use in previous classifications of irrigated wetlands.  However, as
noted earlier, determining the primary water  source of an irrigated wetland is a subjective process, and other
indicators  are  likely  to be more  directly  linked to habitat quality.  If statistical relationships could be
established between the more direct indicators and "water source," and if a consistent method for determining
"water source" could be developed, then "water source" might be validly used.  One study (Rector et al. 1979)
did attempt to relate wildlife use of irrigated wetlands to apparent water sources.  In the Lower Gunnison
Valley, they reported greatest diversity of spring and summer birds in "natural" wetlands, followed by "canal"
wetlands,  "irrigation management  wetlands,"  and an "open drain" (ditch).  Small mammal diversity did not
differ among the  types, but small mammal density (trap catch) was greatest in natural wetlands, followed by
irrigation management wetlands and canal wetlands. Bird densities were similar among natural and irrigation
management wetlands, but canal wetlands had much lower densities.

4.4.1 Wetland Size and Related Indicators

The importance of wetland size as a positive indicator of habitat suitability is suggested by its common use
in rapid evaluation methods.  For example, of nine wetland evaluation methods reviewed by Adamus (1992),
all used wetland size or related morphologic  features to indicate suitable habitat.
        I spent two full days with each of the following avian experts who were recommended to me by several
biologists in the region:
Ronald Lambeth (Grand Valley  area) has been a birder  for over 20 years,  13  of  which have been in the  Grand
Valley.  He has an M.S.  in Wildlife Biology and is employed as a biologist by the Bureau  of Land Management,
where he conducts bird surveys and is developing BLM's agency strategy for conservation of neotropical migrants.
David Galinat (Lower Gunnison area) has been  a birder for  25  years, including 10  in  the  Lower Gunnison area
(Olathe) and 10 in the Grand Valley.   He has a B.S.  in Wildlife Science and has served  on the Colorado  Field
Ornithologists Records Committee.

                                                 24

-------
Species vary greatly in the habitat patch sizes that they regularly use (Opdam et al. 1985).  No species in the
Colorado Plateau region appears to  favor or use relatively small wetlands disproportionately.  In some
agricultural landscapes, relatively large wetlands have more species than relatively small wetlands (Brown and
Dinsmore 1986, 1988, Gutzwiler and Anderson 1987, Budeau and Snow 1992).  This is partly because large
wetlands normally contain a wide range of vegetation types and water depths, and a larger "core" area that
shields birds from predators and disturbances such as people on foot.  However, regular use by waterbirds of
agricultural wetlands (mainly pools of open water) smaller than 0.1 acre was documented by Budeau and Snow
(1992) in Oregon. In prairie regions where small ponds are abundant, many species nest in wetlands smaller
than an acre (Rumble and Rake 1983). I estimate that of the 165 wetland species in the Colorado Plateau
region, 13 are unlikely to use open water patches  smaller than about one acre (Table 5).  The minimum sizes
of vegetated patches used by most species are unknown.  Irrigated wetlands in the Colorado Plateau range in
size from less than 0.1 acre to several hundred acres.  Mean size of the Lower Gunnison on-farm wetlands is
about 22 acres (Table 2,  p. 8).

However, wetland size is not a consistent indicator of avian  diversity. Many other indicators confound the
relationship. One of these confounding indicators is wetland location.  In a survey of 30 wetlands in the Lower
Gunnison Valley, Rector et al. (1979)  tended to find more bird species and greater densities of individuals in
relatively large wetlands.  These large wetlands also tended to be forested and located in off-farm, river bottom
sites.  They also had relatively great densities of small mammals and slightly greater mammalian diversity.
However, it was unclear whether they had more species because of their large size, their bottomland location,
their woody vegetation, or the  likelihood that they received proportionately less irrigation water inflow than
wetlands farther upslope.  Local avian experts whom I interviewed indicated that many species occur only in
wetlands along major rivers, such as the Colorado, and on major lakes. Based on these discussions, I estimate
that about 19% of the region's wetland/riparian habitats species are almost totally restricted to habitats close
to major rivers or lakes, and another 19% probably occur more regularly in such habitats than in drier areas.
Such bottomland habitats are required or preferred by 44% of species that require water as a substrate, 55%
of the species that use only wetland/riparian habitats, and 30% of the species that use upland habitats as well
(Table 5).

Another indicator that confounds the prediction of avian diversity from wetland size is wetland width. Large
wetlands probably are less useful to some birds  and small mammals if they are narrow.  Linearly  shaped,
narrow wetlands, such as  the canal wetlands in the Lower Gunnison Valley (Rector et al. 1979), and riparian
strips in Arizona (Carothers and Johnson 1975), California  (Henke and Stone 1978), Iowa (Stauffer and Best
1980), and Pennsylvania (Croonquist and Brooks 1993) have relatively few species and sometimes relatively
few individuals, even if with their great length they have large area.  In Arizona riparian habitats, forested
patch forested patch size was not a statistically significant indicator of breeding-season avian richness, perhaps
because none of the forested strips exceeded 50 m width  (Strong and Bock 1990). Narrow wetlands provide
less protection from wind and  sun, and the linear corridors that  they form  might  facilitate  movements of
mammalian predators (e.g., Peterson and Cooper 1991).  Nests of many songbirds, if located within forested
riparian patches narrower than about 0.5 mi (Wilcove 1985), are highly susceptible to loss from cowbird
parasitism.  Some computer simulations (Henein and Merriam 1990) suggest that increasing the number of
"high quality" (e.g., wide) corridors can benefit small mammals in habitat patches, but increasing the number
of "low quality" corridors (beyond just one) can have a negative effect.

Although some ducks in  the Grand Valley nest in the larger, unlined canals and natural washes, especially
where elevated spoil banks and dense vegetation are present, they seldom use narrower canals  or sides of
drains and laterals, where nests are probably more vulnerable to predation (CDW 1984). Vegetation along
the laterals is frequently disturbed by burning, weed control, and other agricultural activities.  In Arizona
croplands, waterbirds  that particularly shun irrigation canals  included geese, sandhill crane, and white-faced
ibis (Ohmart et al. 1985).  Narrow wetlands are  not, however, unsuitable as habitat to  all species.  If they
contain at least minimal vegetative cover, irrigation canals  might provide travel corridors for mammals
                                                25

-------
Table 5.  Number of wetland bird species, by habitat type and wetland dependency category.
                                 Highly
                                 Dependent
                Number of Colorado Plateau Species
                 12
Total Species
       13
Require   large water bodies
Prefer large water bodies
        25

        10
         1
Seldom use small (<1 acre) ponds 13
Mudflats required
Mudflats used

Woody vegetation required
Woody vegetation used
14
   Trees required
   Trees used
        Big trees especially
        Snags especially

   Shrubs required
   Shrubs used

   Willow required
   Willow preferred
   Russian olive preferred
   Tamarisk preferred
   Pinyon-juniper preferred
   Greasewood preferred
                              16
Herbaceous vegetation required
Herbaceous vegetation used
   Robust emergents preferred
   Other wet emergents preferred
   Drier grasses preferred
   Broad-leaved forbs preferred
   Aquatic plants preferred
 0
 1

 1
 1

 1
 1
 1
 1

 0
 0

 0
 0
 0
 0
 0
 0

 4
11
 0
 0
 0
 0
 8
                 Intermediate

                 33

                 16
                 3
15
 0

 1
 4

 1
 3
 1
 0

 0
 2

 0
 1
 0
 0
 0
 0

 8
 8
 6
 2
 0
 0
 0
                Dependent

                107

                  5
                 27
 0
 9

85
13

26
 5
24
20

24
43

 2
 4
19
 4
 7
 1

20
13
 1
 2
 0
 7
 0
13

15
10

87
18

28
 9
26
21

24
45

 2
 5
19
 4
 7
 1

32
32
 7
 4
 0
 7
 8
     1 ?
           "Highly Dependent"  means that surface  water is  the  species'  primary  substrate,   e.g.:  common
goldeneye.   "Intermediate"  means the  species  occurs only  where water/wetland is  present,   e.g.:  spotted
sandpiper.  "Dependent" means species also uses uplands, but uses wetlands frequently,  e.g.:  warbling vireo.
All estimates of wetland dependence and  use of particular habitats  were based on the author's judgement and that
of interviewed local  experts.  A species  can be counted  in more.than one row in this table,  but is counted in
only one column.

     13 In this and the subsequent categorizations of "required" and "used" habitat, the tally of  species for
"used" habitat does NOT include species  that "require" the habitat.  All  determinations of "required" vs. "used"
(or "preferred")  are  based on the author's knowledge of the species  and on interviews with local experts.  The
habitat terms correspond to similar  terms on  the  field form;  refer  to Appendix  F for  precise definitions.
     14
        Tallies for woody vegetation include tallies for species requiring/using  trees  and shrubs,  as listed
under tree and shrub headings.
     15
        Tallies include,  but  are  not  limited to, bird species tallied for the individual  shrub species in the
subsequent block.

        Tallies for herbaceous vegetation include,  but are not  limited to,  tallies  of  bird species occurring
in the individual  types listed in the subsequent  block.
                                                    26

-------
Table 5.  (continued)

                                          Number  of  Colorado  Plateau  Species:
                                 Highly
                                 Dependent        Intermediate    Dependent        TOTAL

Fish required                     14                 05
Dirt banks required               01                 34

Strongly avoid areas grazed/
   burned/mowed in spring         8               10               14               32
Avoid such areas (less strongly)  0                0               12               20
Benefitted by grazing             0459
Benefitted by cropland            1                8               23               32
Benefitted by enriched runoff     9                6               10               25
Benefitted by clear water        12                5                 0               17

Prefer highly secluded areas     23               22               11               56
Strongly avoid predation-
   vulnerable wetlands            0                3               24               27
Avoid such areas (less strongly) 25               30               83              138

TOTAL SPECIES                    25               33              107              165
                                                    27

-------
 (Bennett 1990). Rector et al. (1979) hypothesized that canal wetlands might still be important because they
 could provide a protected corridor for wildlife traveling among larger, wider patches of natural habitat.

 A third factor that confounds the prediction of avian diversity from wetland size concerns the manner in which
 "wetland size" is measured. For many species, the overall wetland size (i.e., acreage including large stands of
 contiguous unflooded wetland vegetation) is a weaker indicator of wetland quality than the size of a particular
 habitat within a wetland (e.g., open water area).  For others, especially those with large home ranges, overall
 wetland size is probably a weaker indicator than cumulative (landscape-level) acreage of the wetland plus that
 of contiguous or closely accessible, structurally similar, upland habitat. Thus, "scale" is an important qualifier
 in any description of species-area relationships  of Colorado Plateau species (Gutzwiler and Anderson  1987,
 Van Home and Wiens 1991).

 In summary,  it is apparent that "wetland size" should be used as an indicator of habitat suitability only (a) if
 it is related to the  particular species that could occur in an area, (b) if other indicators ~ particularly wetland
 width and landscape position ~ are used simultaneously, and (c) if it is represented not as total wetland size,
 but as the size of particular habitat types relevent to named species within a wetland.

 Accordingly,  these recommendations have been incorporated into the design of the new  avian  richness
 evaluation  method (AREM)  described in Section 5.0. Specifically:

        (a) A wetland score  that results from using AREM reflects the collective  results from component
        species models. These models in turn have addressed the effect of habitat size individually for each
        species. The overall size of a wetland is not used as an  indicator;  rather,  the  collective area of
        particular  cover type(s) within the wetland is used.  The particular area  required is stipulated by
        species. For some species, patches of suitable habitat larger than 1 acre are considered better than
        smaller ones, whereas for other species, patches larger than 10, 20, or 40 acres are considered even
        better.  For a few species, patch size is  not used at all as an indicator.

        (b) A wetland score that results from using AREM reflects the confounding effects of other indicators.
        Wetland size is  not used as the sole indicator for any species.  For most species, other indicators are
        addressed  simultaneously.  For example, AREM assigns the same or higher scores to small wetlands
        containing otherwise optimal habitat than large wetlands with habitat that is suboptimal because of
        narrow patch width, landscape location, or conditions of other indicators.

4.4.2 Surface Water Regime ("Wetness")

If "wetness" is used as the only indicator of bird diversity, "wetter" is often - but not always ~ better.  That
is, wetlands with water regimes characterized by relatively deep, seasonally permanent water can often support
many species.  Partly to provide a greater area  of open water and permanently flooded wetland habitat for
water-dependent species, more than 100 wetlands in the Colorado Plateau have been intentionally altered, or
have been created  from  upland by excavation or damming of intermittent drainageways (database from SCS
1992b). These projects  have  been completed voluntarily by farmers on their own land, in cooperation with
salinity control projects that provide subsidies  and  technical assistance (from the  U.S. Department  of
Agriculture, as  provided by various public laws).  Priorities for these projects, and the particular enhancement
or creation practices that are employed, are established by biologists in local SCS offices.  Some completed
projects are monitored annually using habitat evaluation methods, primarily HEP. Actual wildlife use, species
richness, and productivity has been systematically monitored in few if any of these projects.

Part of the reason why  "wetter" wetlands seem to support many species is because they  are likelier to be
flooded more predictably and for longer duration. This allows additional invertebrate species with long aquatic
development  times (e.g., some dragonflies) to be present (Driver 1977, Ebert and Balko 1987). These types
of invertebrates in turn help support additional species of  birds.   In  Oregon, agricultural wetlands that

                                                 28

-------
remained flooded longer in spring  had greater species richness of waterbirds (Budeau and Snow 1992).
Grazing of a wetland's upslope drainage area can sometimes increase the amount of runoff delivered to the
wetland and thus, its flooding duration and waterbird diversity (Guthery and Stormer 1984).  However, in the
Colorado Plateau, intensive grazing of vegetation overlying some soils can exacerbate salinity problems that
are potentially detrimental to aquatic diversity (see p. 37).

Little is known about the effects on wildlife of shifting from a regime of periodic  flooding by lateral ditch
overflows (about 5 times per growing season, 12-24 hr at a time), to continuous and less intense watering from
sprinklers. Direct flooding from ditch overflows, as well as plowing, can drive some soil invertebrates to the
surface of plowed fields (Edwards and Lofty 1975), and can distribute over the exposed field whatever
organisms were contained in the river source water. This probably attracts a few species (e.g., gulls, white-
faced ibis, killdeer, swallows, American pipit, American robin, blackbirds) for short periods. But unlike  in
some other regions where "backflood  irrigation" or natural seasonal  flooding of agricultural land provides
major feeding opportunities and/or territorial areas for shorebirds and waterfowl (Wishart et al. 1984, Ohmart
et al. 1985, LaGrange and Dinsmore 1989), in the Colorado Plateau, the overflow water usually infiltrates so
quickly, even where soils have the lowest permeability, that bird use is  ephemeral. When sprinklers are used,
even less water "ponds" on the fields.

Many wildlife species colonize and begin to use ephemerally flooded or newly created wetlands almost as soon
as they arise on the  landscape, if they are otherwise suitable as indicated by the soil development rate and
vegetative community maturation rate (Spencer 1963, Lathwell et al.  1969, 1973, Danell and Sjoberg  1982,
Hudson 1983, Kadlec and Smith  1984, Weller et al. 1991).  Wildlife densities and  perhaps species richness
continue to increase for a period of years while a new wetland  "matures," i.e., while vegetation develops,
diverse seeds are transported in by animals and wind, and an organic soil layer important to invertebrates is
deposited by annual plant production. However, instances have been documented (Heitmeyer and Vohs 1984)
of birds continuing to prefer using natural wetlands despite the availability of many created wetlands.

To some people, the "drier" wetlands that lack surface water are "not really wetlands" because when observed
casually they may not appear to support much wildlife. However, their importance  to individual species can
be considerable. In the San Luis  Valley of south-central Colorado, wetlands  having the greatest diversity of
herbaceous plants are not the permanently inundated or saline ones, but rather seasonal ones that have low
salinity (conductivity < 1000 ^mhos/cm2) and high water tables (located at or  within 24 inches below  the soil
surface)(Cooper and Severn 1992). In the Colorado Plateau region, at least 113 bird species (68% of the total
wetland/riparian species) use such wetlands regularly (Table 5, p. 26).  For some of these species, deep open
surface water occupies space that,  if alternatively occupied by woody  vegetation or even by emergent
vegetation, would provide habitat to more species, especially species that are of highest conservation interest.
This group of "drier end" species comprise a greater proportion of uncommon species during winter and
migration  , as compared with wetland/riparian species that require water as a substrate. As shown in Tables
6 and 7, they also comprise a higher proportion of neotropical migrants18, and a higher proportion of species
        For  example, although 48% of all the region's wintering   wetland/riparian species  are  considered
uncommon  (by Dexter  and  Lavad  1992), only  33%  of  those  that  require  water  as  a  substrate  are  uncommon.
Similarly, although 48% of  all the region's  migrant species  are considered uncommon, only 38% of  those  that
require  water  as  a substrate are uncommon.   At  all seasons, many more uncommon species  are  classified as
"dependent"  (prefer wetlands but do not require open water) than "highly dependent"  (require open  water  as a
substrate).  See Table  3.

     18
       None of the region's species which require water  as a substrate are neotropical migrants.  Of 33 species
that occur only where water  or wetlands are present, 7 (21%) are neotropical migrants.  Of the 107 species  that
prefer wetlands but occur  in uplands as well,  59 (55%) are neotropical  migrants. About 61% of all species  that
regularly occur in the  Colorado  Plateau are neotropical  migrants, and 86% of these are  species that regularly
occur in  irrigated wetlands (Table 6).  The importance of conserving neotropical migrants in  particular is
emphasized by EPA's signing of an interagency memorandum of agreement in support  of  an  international  program
focusing on  these species (Partners in Flight Information and Education Working Group 1992).

                                                 29

-------
Table 6.  Number  of neotropical  migrants in  various wetland dependency categories,  by conservation
characteristics.
                                                                                                  ..19.
Total Neotropical   Migrants
                                          Number  of Colorado Plateau Species, by Dependency Category
                                          Highly                                    Total
                                          Dependent        Intermediate     Depend.  Wetland      Upland
                                                  0               8        78       86              14
# of species with threats to breeding areas (species breeding in and/or visiting  region):
   No known threat, "generalist" species          0               1        10        11
   Minor threat, moderate generalists             0               2        21        23
   Moderate threat, "specialist" species          0               0        33        33
   Extensive threat, specialists                  0               5        11_.      16
   Extirpation likely, extreme specialists        0               033

# of species with threats to breeding areas (only species breeding in Colorado Plateau):
   No known threat, "generalist" species          0               189
   Minor threat, moderate generalists             0               088
   Moderate threat, "specialist" species          0               0        15        15,-
   Extensive threat, specialists                  0               43         r
   Extirpation likely, extreme specialists        0               011

# of species with threats to wintering areas (species breeding in and/or visiting region):
   No known threat, "generalist" species          0               1        14        15
   Minor threat, moderate generalists             0               2        33        35
   Moderate threat, "specialist" species          0               3        24        27
   Extensive threat, specialists                  0               279
   Extirpation likely, extreme specialists        0               000

# of species with threats to wintering areas (only species wintering  in Colorado  Plateau):
   No known threat, "generalist" species          0               099
   Minor threat, moderate generalists             0               145
   Moderate threat, "specialist" species          0               1        6         7.,
   Extensive threat, specialists                  0               202
   Extirpation likely, extreme specialists        0               000
Breeding Range Sizes of Component Species
   Very widespread (>75% of N.  America)           0
   Widespread (51-75% of N. America)              0
   Intermediate (26-50% of N.  America)            0
   Local (11-25% of N. America)                   0
   Very local (<11% of N. America)                0
                                                                           26
                                                                           21
                                                                           24
                                                                            6
                                                                            1
31
21
27,
  2*
                                                                                                     2
                                                                                                     7
                                                                                                     2
                                                                                                     3
                                                                                                     1
                                                                                                     2
                                                                                                     7
                                                                                                     2
                                                                                                     3
                                                                                                     1
        Dependence categories are based on the author's judgement  and  interviews with  local  experts.
"Highly Dependent" means that surface water is the species'  primary substrate,  e.g.:  common goldeneye.
"Intermediate" means the species occurs only where water/wetland  is present,  e.g.: spotted  sandpiper.
"Dependent" means species also uses uplands,  but  uses  wetlands  frequently,  e.g.:  warbling vireo.
        Neotropical migrants are species  that  spend  the winter in Central and South America.   Conservation
biologists consider neotropical  migrants to be  of critical concern because of the long distances they migrate
and the rapid loss of  their  wintering habitat.  This table was prepared with information from the database of
Carter and Barker (1992).

     21
     22
        yellow-billed cuckoo,  loggerhead shrike,  willow flycatcher

        peregrine  falcon,  short-eared  owl,  band-tailed  pigeon,  loggerhead shrike,  marsh wren,  Hammond's
flycatcher, olive-sided flycatcher

        northern harrier,  marsh wren

        rufuous hummingbird, Cordilleran flycatcher, dusky flycatcher,  Hammond's  flycatcher,  MacQillivray's
warbler, green-tailed towhee

        Virginia's warbler
                                                    30

-------
Table 7. Number of bird species in various wetland dependency categories, by taxonomic uniqueness, harvest
status, and official conservation designations.


                                         Number of Species of Colorado Plateau, by Dependency   Category:
                                 Highly                                            Wetland
                                 Dependent        Intermediate     Dependent        Total            Upland

Probable Taxonomic Uniqueness
of Component Species
   Very High (only species of
      its genus in region)               1                3                7        11                1
   High (one of 2 species of its
      genus in region)                   0                2                35                1
   Moderate (one of 3 species of
      its genus in region)               1                2                8        11                1
   Low (one of 4 species of its
      genus in region)                   1                6                9        16                2
   Very Low (one of >4 species
      of its genus in region)           22                20              80       122               19

Hunted Species                          18                4                3        25                2

Official Designations
   Endangered                                                                      1                 0
   Threatened                                                                      2                 0
   Candidate for T/E listing                                                       2                 1
   G3 ("rare/uncommon globally but
        not imperiled")                                                            2                 0
   G4 ("not rare; apparently secure but
        cause for longterm concern")                                                6                 2
   S1 (rare statewide, CO)                                                         1                 0
   S2 (uncommon statewide,  CO)                                                     1                 1
   S3 (fairly comnon statewide, CO)                                                19                4
   "Watch List" (Colorado)                                                         11                4
        Dependency of  each  species  was  based on the author's judgement and interviews with local experts.
"Highly Dependent" means  that  surface water is the species' primary substrate: e.g., common goldeneye.
"Intermediate" means  the  species  occurs only where water/wetland is present: e.g., spotted sandpiper.
"Dependent" means species also uses uplands, but uses wetlands frequently: e.g., warbling vireo.
Lists of species assigned official  designations were provided by the Colorado Natural Heritage Program.


        These tallies  include  some  regional species that occur so irregularly that they were not included in
the habitat database or in  tallies  of previous characteristics.  Wetland species include:
   Endangered (nonbreeding): bald eagle
   Threatened (nonbreeding): Arctic peregrine falcon, sandhill crane
   Candidate species  (breeding):  ferruginous hawk, loggerhead shrike
   G3:  (nonbreeding): Arctic  peregrine falcon, bald eagle
   G4:  American bittern, Cooper's  hawk,  ferruginous hawk,  loggerhead shrike, merlin, northern goshawk
   S1:  yeI low-billed cuckoo
   S2:  Arctic peregrine  falcon,  gray vireo,  least bittern,  long-billed curlew, snowy egret, wood duck
   S3:  American bittern, black-throated sparrow, bobolink, Cassin's kingbird.  Cooper's hawk,  eared grebe,
        ferruginous hawk, golden eagle, grasshopper sparrow, gray catbird, great blue heron, indigo bunting,
        long-eared owl, loggerhead shrike, marsh wren, northern harrier, red-eyed vireo,  red-headed woodpecker,
        sage sparrow,  sharp-shinned hawk, short-eared owl,  snow goose, sora
                                                    31

-------
 that contribute importantly to regional genetic diversity because of their relative taxonomic uniqueness28.
 Also, it is notable that many of the bird species that prefer the drier types of wetlands seem to be declining
 in the region (Table 8). Conceivably, the conversion of drier emergent and wooded wetlands  to wetter open
 water habitats could fragment the drier wetland habitats so much that it might reduce the suitability of the
 remaining dry-wetland patches for many of their characteristic species.

 Moreover, the habitat suitability of many of the wetter wetlands declines over time.  This is most likely to
 happen (a) if these wetlands never receive any overflow flooding from rivers or tributaries, (b) if their water
 levels are kept relatively constant, and/or (c) most of their sediment is seldom exposed to the air.  Natural
 water exchange  rates and fluctuations are  needed to help remobilize nutrients bound  chemically to the
 substrate and to trigger the germination of seeds lying dormant  in  the sediment (Welling et al.  1988).
 Consequently, dynamic water conditions are needed in wetter wetlands to increase the food resources for a
 wide variety of animals and stimulate invertebrate production  (Severn 1992).  Overbank flooding can also
 increase plant and animal production (and perhaps diversity) in normally isolated wetlands by diluting the high
 salinity and  accumulated toxicants, resuspending  excessive  accumulations  of  sediment,  scouring and
 rejuvenating dense homogeneous stands of emergent vegetation, and facilitating recolonization by crayfish,
 other noninsect invertebrates,  fish, and waterborne seeds.  For example, stock ponds that  are created by
 damming washes (and which therefore receive outside waters) probably support more waterfowl than isolated,
 pit-type stock ponds (Tolle 1977).

 The seasonal timing of surface water is at least as important as its amount (Sangster 1977).  Wetlands that
 contain the most surface water during freezing months naturally receive less use by water-dependent species
 at that time.  Few Colorado Plateau wetlands have such a flooding regime.  Most irrigated wetlands of the
 region receive surface runoff or subsurface inputs from approximately April to October. This permits their
 use by many wetland species.  Use by shorebirds, however, is not great.  This is  partly because water levels do
 not begin to drop until at least October, when most migrating shorebirds have already passed through the
 region.  Dropping water levels in canals at this season do, however, cause stranding of some fish, making them
 more available to eagles, corvids, and mammalian scavengers. Shorebirds along inland migration routes prefer
 large flats of mud rather than sand, clay, or  rock (Taylor and Trost  1992).

 In summary, water regime clearly has a major influence on avian diversity in irrigated wetlands, and "wetter"
wetlands generally support more species.  However, actions based solely on a philosophy of "wetter is better"
may neglect the needs of some species. More appropriate is  an  approach that takes a landscape and species-
specific perspective, considering the relative scarcity of open water vs. other wetland types within a local area,
the conservation characteristics of open water species vs. other wetland species, the seasonal and daily timing
and duration of flooding, and  the need  for periodic disturbance (e.g., drawdowns, overbank flooding) to
maintain the avian productivity of the wetter wetlands.

Accordingly, these findings have been incorporated into the design of the new avian richness evaluation
method (AREM) described in Section 5.0.  Specifically:

        (a) A wetland score that results from using AREM addresses the collective results from component
        species models, which in turn have addressed the effect of water regime individually for each species.
        Water regime is not used as an indicator for some species, whereas for others, wetlands lacking surface
        water are considered more suitable, and for still others, wetlands containing open water or flooded
        vegetation are considered more suitable;
       Of the region's 165 wetland/riparian species, 16 (10%) contribute highly to genetic diversity because
of their taxonomic uniqueness.   That is, their genus is represented by only one or two species in the region.
Of these 16 species,  10  (63%) occur sometimes in uplands,  although they prefer wetlands.   Only  one requires
water as a substrate.  See Table 7.   The importance of focusing conservation efforts on the more taxonomically
(and presumably,  genetically) unique species is  explained,  for example, by Vane-Wright  et  al.  (1991).

                                                 32

-------
Table 8.  Wetland and riparian birds whose abundance during the breeding period is significantly changing.

These species are either declining (D) in significantly (p<.10) more areas within the named state than areas
where they are increasing, or are increasing (I) in significantly (p<.10) more areas of the named state than
areas where they are declining. Species found fewer than 14 times in the survey area during the survey years
were not included, following recommendations of the source of these data (the Breeding Bird Survey, U.S. Fish
and Wildlife Service 1991). Notations in the last column denote wetland/riparian species (W) or species that
use upland habitat almost exclusively (U).
         Species                     State  Trend 1982-1991  Trend 1966-1991  Wetland or MonWetland Sp.
AMERICAN GOLDFINCH

AMERICAN KESTREL
AUOUBON'S WARBLER
BARN SWALLOW
BEWICK'S WREN
BLACK-BILLED MAGPIE
BLACK-CAPPED CHICKADEE
BLACK- HEADED GROSBEAK
BLUE-WINGED TEAL

BREWER'S BLACKBIRD
BREWER'S SPARROW
BROAD-TAILED HUMMINGBIRD
BULLOCK'S ORIOLE
CANADA GOOSE
CHIPPING SPARROW

CLIFF SWALLOW

COMMON CRACKLE
COMMON RAVEN
COMMON YELLOWTHROAT

DUSKY FLYCATCHER


EUROPEAN STARLING

GREAT BLUE HERON

GREEN-TAILED TOWHEE
HOUSE FINCH
HOUSE SPARROW
KILLDEER
LARK SPARROW
LOGGERHEAD SHRIKE
MACGILLIVRAY'S WARBLER
MOUNTAIN BLUEBIRD

MOURNING DOVE

NORTHERN HARRIER

CO
WY
WY
UT
UT
CO
WY
WY
CO
CO
WY
UT
WY
CO
WY
WY
UT
WY
CO
WY
CO
WY
CO
WY
CO
UT
WY
CO
UT
CO
WY
CO
WY
UT
UT
UT
CO
WY
CO
UT
UT
WY
CO
UT

I
I

D





I
D
D


I
D

I






I

D
D


D

D
D




I

I


I


I
D
I
D
D
I
I
I
D
D
I
D
I
D
D
I
I
I
D
I
D
I

I


I
I

D
D

I
I
I
I

D

D
D
W
W
U
W
W
W
W
W
W
W
W
W
W
W
W
W
W
W
W
W
W
U
W
W
W
W
W
W
W
W
W
W
W
U
W
W
W
W
U
U
W
W
W
W
                                                33

-------
Species                      State  Trend 1982-1991  Trend 1966-1991  Wetland or NonWetland Sp.
PIED-BILLED GREBE
PINE SISKIN
PRAIRIE FALCON

RED-BREASTED NUTHATCH
RED-SHAFTED FLICKER
RED-TAILED HAWK

RING-NECKED PHEASANT
ROCK DOVE
RUFOUS-SIDED TOUHEE
SAGE THRASHER
SAY'S PHOEBE
SWAINSON'S HAWK
TOWNSEND'S SOLITAIRE
TREE SWALLOW

TURKEY VULTURE


WESTERN MEADOWLARK

WHITE-THROATED SWIFT
WILLOW FLYCATCHER
YELLOW WARBLER
YELLOW-HEAD, BLACKBIRD
WY
CO
UT
WY
WY
UT
CO
WY
CO
CO
CO
WY
WY
WY
WY
CO
UT
CO
UT
WY
CO
UT
CO
WY
UT
WY

D


I
D
I
I
D




D

I




D
D

I
D
I
I

I
I
I

I

D
D
I
D
I

I

D
I
I
I
D

D
I

I
W
W
u
u
W
W
W
W
u
u
W
u
u
W
W
W
W
W
W
W
W
W
u
W
W
W
                                              34

-------
        (b) A wetland score that results  from using AREM addresses  the  confounding effects of other
        indicators by including other indicators simultaneously. A wetland's "wetness" is not used as the sole
        indicator for any species.  For  example,  for some species  the scores that AREM  assigns to dry
        wetlands which contain otherwise optimal habitat are the same or greater than scores it assigns to
        wetter wetlands that have habitat which is suboptimal because of other specified factors;

        (c) For many specieva wetland score that results from using  AREM is higher in a surface-water
        wetland that experiences periodic disturbance of its water regime, than in one that does not, other
        factors being equal.

4.4.3 Vegetation Characteristics

Vegetation provides the physical substrate for many birds that nest in irrigated wetlands.  In addition,
vegetation provides food  directly  (e.g., seeds, berries) and indirectly  (e.g., serving  as a  substrate for
invertebrates), and shelters wildlife from strong winds, sun, and predators. The physical form of the dominant
plant species  in a wetland, the number of different vegetation forms present in a wetland,  and/or the co-
occurrence of vegetation with open  water are used as habitat suitability indicators in all nine wetland
evaluation methods reviewed by Adamus (1992).

Wetland vegetation is commonly categorized according to its form as woody (includes trees and shrubs) or
herbaceous (includes emergent, floating-leaved, and submersed vascular plants).  Wetlands of the Colorado
Plateau that are most visibly supported by irrigation water tend to be dominated by emergent vegetation, and
seldom are dominated by floating-leaved or submersed vegetation. From the information provided partly by
the interviewed experts, of the 165 bird species regularly occurring in irrigated wetlands  of the Colorado
Plateau, I  calculated that  19% require herbaceous vegetation and an  additional 19% prefer (but do not
require) wetlands containing herbaceous vegetation. In contrast,  many more wetland/riparian species require
or use woody vegetation29.

However, wetlands containing the greatest number of bird species are usually not those that contain a single
vegetation form in abundance, but rather  are those that contain a  mixture of many types and also some
unvegetated open water.  For example, the Rector et al. (1979) study of the Lower Gunnison Valley found
that whereas forested wetlands, shrub wetlands, and many emergent wetlands had similar bird density (and to
a lesser degree bird diversity), diversity was greatest in wetlands  where open water, in addition to emergent
vegetation, was  present.   The avian  density and diversity such wetlands also surpassed that of wetlands
dominated by shrub or tree vegetation30.  Even for small mammals, wetlands where both open water and
emergent vegetation were present together had greater density and diversity than wetlands dominated by trees
or shrubs, or where emergent vegetation occurred in the absence of open water. The importance of wetlands
containing both open water and vegetation is recognized by most existing wetland evaluation  methods. For
example, when Rector  and others (1979) applied their evaluation method to 30 Lower Gunnison wetlands,
it tended to give highest ranks to emergent wetlands that contained some open water, followed by forested
wetlands, shrub wetlands, and emergent wetlands without open water.  When SCS applied a similar version
of the evaluation method to the Cortez subregion's wetlands  (SCS 1989), it tended to rank forested wetlands
     29
       About 53% of the  species require  woody vegetation and an additional 11% prefer (but do not require)
wetlands  containing woody vegetation.  More specifically, 15% require shrubs  and  an  additional  27% prefer
wetlands  containing shrubs.  About 17% require trees and an  additional 5% prefer wetlands  containing trees.
Cavity-nesting species comprise 13% of all the  region's wetland/riparian species.  See Table 5.

       Also, several  studies  from other  regions  (Kaminski  and Prince  1981, Harris et al. 1983,  Murkin and
Kadlec 1986) and other parts of Colorado and Utah  (Weller et  al.  1958, Hooper  1962, Robinson 1971, Rector et
al.  1979) demonstrate that wetland use by  some bird groups, notably waterfowl,  increases when both open water
and  emergent vegetation are present.   In  dense cattail  stands, water openings of 0.37 acre were found to be
preferred by mallards (Ball and Nudds 1989).

                                                 35

-------
the highest, followed by cattail, shrub, and sedge-dominated wetlands. A similar version that was applied to
a subset of the Lower Gunnison wetlands rated forested wetlands the highest, followed by emergent wetlands
and shrub wetlands (USER 1991).

Perhaps almost as important as open water to bird diversity is the presence in a wetland of exposed mud.
Fifteen (9%) of the region's 165 species that regularly occur in irrigated wetland/riparian habitats require
mudflats as a substrate, and an additional 10 (6%) regularly use or prefer such habitats (Table 5, p. 26).

Avian  use of wetlands is related not only to the area of various vegetation forms, but to vegetation species,
density, and height.  In fact, contrary to findings from  studies of forests, at least one study of southwestern
riparian habitats (Rice et al. 1983) suggests that the species of dominant tree or shrub can influence avian
richness and the presence of many individual species to at least as great an extent as the diversity of vegetative
life forms (i.e., foliage height diversity).

Willow and cottonwood appear to be at least as capable as open water in their ability to increase the avian
diversity of an emergent wetland. Describing irrigated valley wetlands of the Cortez subregion, Somers (1979)
commented:

       "We found that marshes dominated by short, resistant grasses are least productive of birds
       and mammals.  Those dominated by cattails and rushes are only slightly more productive.
       But those  with even small willow thickets [emphasis mine] harbor many birds."

Willows,  particularly when forming tall, broad stands, seem to be used preferentially by wintering sparrows,
migrant passerines, and nesting willow flycatchers and yellow warblers. Cottonwoods, because of their larger
size, provide much better sites for cavity-nesting species and perching hawks than most shrubs.  As long as
water continues to be present, wetlands dominated by exotic plant species are not necessarily species-poor for
birds, and in many cases have greater species richness31. Russian olive, for example, greatly increases habitat
suitability for at least 38 (23%) of the 165 wetland/riparian species of the region, and is specifically preferred
by 19 (12%). The much-maligned tamarisk (salt cedar) tolerates conditions inhospitable for many other trees
and appears to be used preferentially during some seasons by long-eared owls, mourning doves, western
meadowlarks, blue grosbeaks, and perhaps some other  species (Hunter et al. 1985).

Among emergent wetlands, those dominated by robust plants with stiff, persistent stems (e.g., cattail, common
reed, bulrush) are  used preferentially by several species (e.g., rails, marsh wren, blackbirds, pheasant; Glahn
1974, Sather-Blair and Under 1980, Guthery and Stormer  1984); bulrush in Colorado requires less than 2
months of flooding to become established (Cooper and Severn 1992).  Wetlands with weedy forbs attract
sparrows and other finches, especially if located near trees or brushy cover (Strong and Bock 1990). Flowering
forbs attract hummingbirds. Wetlands with submerged  sago pondweed or coontail are particularly attractive
to wigeon, canvasback, coot, and  some other Colorado  waterfowl (Gorenzel  et al. 1981, Kantrud 1990).
Irrigated wetlands with beds of watercress attract many invertebrate-feeding marsh birds (e.g., common snipe).
The type of crop present in a flooded field also influences aquatic insect density  and thus, probably the
occurrence of nighthawks, swallows, and other insect-hawking species. A study in the Grand Valley indicated
that irrigated pasture supported greater density of some aquatic insects than irrigated alfalfa, corn, or orchards
(Hayes and Nielsen 1978). Density and height of wetland vegetation are often influenced by grazing, mowing,
and burning. Ditches in some wetlands in all subregions are burned, generally in the spring, to increase the
capacity of ditches to convey water and reduce weed sources.  This can adversely affect wetland habitat of many
        However, some woody exotic plants  are  capable of  severely drawing down the water  table  in  their
immediate vicinity.   If  this results in loss  of  the only local  wetland habitat that  contains surface  water
during much of  the growing season,  then gains to some species might be offset  by losses  of other species (e.g.,
common snipe) which  are more restricted in their  habitat selection.

                                                 36

-------
species (Fritzell 1975, Gorenzel et al. 1981, Kantrud 1986). Herbicides are also sometimes used to remove
vegetation along irrigation canals.

Grazing and mowing are most prevalent in wetlands of the Utah subregion, where pasture is a predominant
land use.  Limited evidence from  other  western regions  suggests that moderate grazing of wetlands, by
increasing visibility of predators and access to food sources, might increase habitat suitability for perhaps nine
of the region's wetland/riparian species, e.g., some shorebirds, geese, barn owl, American robin, Brewer's
blackbird (Table 5, p. 26).  However, partly by altering ground cover density and causing clumping of shrubs
(Crouch 1961, Cannon and Knopf 1984, Knopf et al. 1988), grazing can decrease suitability for at least 52
others32.  Grazed  riparian areas also can have fewer  mammal species (Medin and Clary 1989). Especially
among the forested types of irrigated wetlands, those with dense canopy might be more important to wintering
wildlife (for shelter), whereas those with individually large  trees might  be more important  in summer
(Anderson and Ohmart 1977, Morrison et al. 1986).

The season of grazing, mowing, or burning probably influences avian communities more than the intensity of
these activities (Wiens 1973). Adverse effects on birds are probably greatest when grazing, mowing, or burning
are conducted during the nesting season (May through mid-July). Moderate, late-fall grazing appears to have
minimal effect on the use of some riparian  habitats during the following breeding season (Sedgwick and Knopf
1987).  Late-season mowing can increase wetland invertebrate biomass and waterfowl use (Beck et al. 1987,
Ball and Nudds  1989).

In summary, no single vegetation type is "best" for  bird communities. Rather, irrigated wetlands that are most
similar to  natural  bottomland  (river)  wetlands (e.g., presence of open  water, extensive trees  and shrubs,
multispecies emergent vegetation, etc.) probably  support the largest  number of species.  Human  activities
potentially alter the density, height, and species composition of wetland vegetation, and consequently affect
bird diversity.  As a result of these findings, the following features have been incorporated into the design of
the avian richness  evaluation method (AREM) described in Section 5.0.  Specifically:

        (a) A wetland score that results from using AREM reflects the collective results from  component
        species  models, which  in turn  have addressed the suitability of each  vegetation form  (and some
        dominant vegetation species) for each species.  Vegetation form or species is used as an indicator for
        a majority of bird species, as are the effects of vegetation height and density.  The effects specifically
        of burning, mowing, or intensively grazing wetlands during the springtime are reflected in the models
        for 61 species.

        (b) A wetland score that results from using AREM reflects  the confounding effects of other indicators.
        A wetland's vegetation form or species is seldom used as the sole indicator for any species. For most
        species,  other indicators - particularly the presence of open water - are incorporated simultaneously
        and, in some cases, independently.

4.4.4 Other Animals and Wetland Water Quality

Use of wetlands by many bird groups is strongly influenced by the amount  of aquatic invertebrates and  fish
supported by the wetland, and the seasonal timing of their availability (Joyner 1980, Ball  and Nudds 1989,
Hands  et al. 1991). The abundance of invertebrates and fish is, in turn, influenced by water quality and by the
     32
       Literature reports adverse grazing impacts on the following: northern harrier, great horned owl, broad-
tailed hummingbird, house wren, eastern and western kingbirds, western wood pewee, willow flycatcher, blue-gray
gnatcatcher, yellow warbler,  common yellowthroat, yeI low-breasted chat, orange-crowned warbler, white-crowned
sparrow, song sparrow, dark-eyed junco, green-tailed towhee, red-winged blackbird, and northern oriole (Kantrud
1981, Taylor  1986,  Sedgwick  and  Knopf 1987, Szaro and Rinne  1988, Szaro 1991,  Schultz and Leininger 1991,
Krueper 1992, Baker et al. 1992).

                                                 37

-------
indicators described above, such as water regime (Driver 1977, Broschart and Linder 1986, Euliss et al. 1991)
and vegetation type/interspersion (Scheffer et al. 1984).

Irrigated wetlands appear to be deficient in fish and noninsect invertebrates (as discussed previously on p. 22).
This is partly because all surface water disappears from most irrigated wetlands at some time of the year
(usually in winter). Surface water that is reintroduced to wetlands in the spring contains whatever small fish,
amphibians, and invertebrates happened to be in the water source (i.e., river) at the time, and that are capable
of surviving turbulent conditions while being transported through miles of canals, ditches, diversion pipes, and
(sometimes) holding ponds before reaching the wetland.

Habitat quality and bird diversity of irrigated wetlands are also affected by water quality. The high salinity and
turbidity of some wetlands undoubtedly limits the production and presence of some wetland plants (Kauskik
1963, McKnight and Low 1969, Christiansen and Low 1970, Cooper and Severn 1992). Of the region's 165
wetland/riparian species, at least 17 (10%, see Table 5, p. 26) can suffer reduced feeding capacity as a result
of high turbidity visually obscuring their prey and perhaps limiting the production of aquatic prey. When plant
production is reduced, so are the numbers of invertebrates that depend heavily on aquatic plants (Rawson and
Moore 1944), and which themselves  provide  essential foods for many waterbirds.  Such a situation has been
documented in irrigated wetlands of the San  Luis Valley (Severn 1992). High salinity can also limit directly
the abundance of invertebrates and some fish and amphibians.  Consequently,  most isolated, saline, irrigated
wetlands are not used heavily by piscivorous  birds (e.g., kingfisher, loons, grebes, herons, egrets)33.

Because heavy sediment loads, high salinity, winter freezing of sediments, and the frequent lack of permanent
water hinder the maturation of many  species (Adamus and Brandt 1990), the aquatic insect fauna of most
irrigated wetlands probably consists mainly of opportunistic species with short life cycles (e.g., midges), rather
than long-lived species (e.g., dragonflies).  Studies of western river segments receiving irrigation return waters
have shown they have more aquatic worms and leeches, and fewer mayflies,  caddisflies, water beetles, and
isopods, than  unaffected waters (Kreis and Johnson 1968).

In localized areas of the Colorado Plateau, selenium and possibly other trace metals have sometimes become
concentrated in irrigation tailwaters  (Stephens et al. 1988) and have killed wetland birds and possibly other
aquatic life. Pesticides are widely used in this agricultural region. Studies of isolated prairie wetlands have
demonstrated  severe impacts on invertebrate  populations and wetland birds from regular pesticide use (Grue
et al. 1988), but apparently this potential threat to wetland wildlife remains uninvestigated in salinity control
areas.  A more obvious threat is the great turbidity of irrigation tailwater. Highly erodible, clayey soils become
suspended in water running off flooded fields and into wetlands.  In many parts of the region this severely
impedes light  penetration and limits the establishment and growth of submerged aquatic plants valuable to
waterfowl.  It  also raises questions about the long-term sustainability of wetland creations or enhancements
in this  heavily  agricultural region. In many areas, heavy sediment runoff combines with the effects of intensive
springtime grazing, severe eutrophication, local water table disruption, and possible contamination with metals
and pesticides to cumulatively threaten the functional longevity of created wetlands, as much or more so than
natural wetlands.

In summary, it is apparent that water quality in  irrigated wetlands can affect the amount and availability of
aquatic plants and animals important as food to birds. Salinity and sediment are  the most obvious pollutants
of concern to  birds, and they probably affect some species more than others.  In response to these  findings,
           A review of primary production by Hammer (1981) concluded that the most productive saline lakes have
high alkalinity, are not  highly saline (<30mS/cm ), and are rich  in soluble phosphorus.  A few bird species
(e.g.,  red-necked phalarope,  American  white  pelican, American avocet)  are  heavy  users  of  alkali  lakes or
wetlands, and some invertebrates (e.g.,  brine flies) can reach very high densities in saline lakes (Timms 1981,
Vareschi  1987).  However, salinity  greater  than about 1.5  dS/m causes  digestive stress  in some  birds, and
salinity greater than 5.0 dS/m is considered unsatisfactory for livestock (National Academy of Sciences 1974).

                                                  38

-------
the new avian richness evaluation method (AREM) described in Section 5.0 takes a species-specific approach.
Excessive turbidity (from suspended sediment) is assumed to have the greatest influence in wetlands containing
surface water.  The primary impact is assumed to be to species that feed visually on subsurface  prey (e.g.,
kingfisher on small fish) and on submersed plants, and a secondary impact is assumed for species that depend
largely on aquatic insects (e.g., swallows). The AREM models for shorebird species reflect the likely reduced
suitability of highly saline mudflats.

4.4.5 Landscape Land Cover and Seclusion

Birds are highly mobile. Thus the suitability of a wetland's habitat for many species depends as much or more
on the suitability of the surrounding nonwetland land cover. Land cover in the Colorado Plateau is influenced
by elevation, which ranges from under 5000 ft in the southern part of the Utah subregion to slightly over 7000
ft in the Wyoming subregion. Most irrigated wetlands are surrounded by cropland or desert scrub ~ mainly
greasewood, saltbush, and sagebrush.  None are surrounded by upland forest, although above the valley floors
(e.g., parts of Uinta Basin and Uncompahgre Valley), pinyon-juniper scrub becomes slightly more  prevalent.
When large patches of pinyon-juniper scrub are present, at least seven wetland/riparian species which seem
to require both the scrub and wetlands become more regular, e.g., Townsend's solitaire, plain titmouse (Table
5, p. 26).

Within the agricultural areas, wetland use by geese and mallards seems to be influenced the most by proximity
to cropland, especially  the proximity to partly-harvested corn. Of the region's 165 wetland/riparian species,
about 32 (19%) tend to occur in wetlands that have fields with grain nearby (Table 5, p. 26).  In Arizona,
wetlands (cottonwood  stands) adjacent  to agricultural lands  had  greater densities  of birds than  those
surrounded by pinyon-juniper or other woody vegetation (Carothers 1977).  However, species richness can
decline in relict stands  following  agricultural conversion of surrounding natural habitat (Conine et al. 1978).
Crop type and height also can affect use of adjoining irrigated cropland by some waterbird species (Ohmart
et al. 1985).  A study of narrow woodlots in Pennsylvania suggested that breeding bird diversity can be greater
in woodlots  adjoining croplands  than in those adjoining pastureland (Yahner 1983).

Surrounding land uses can also  affect the trophic condition of  a  wetland.  Some wetlands that have been
enriched by fertilizer runoff, livestock waste,  or domestic wastewater have  shown high levels of  waterfowl
production (Piest and Sowls 1985,  Wilhelm et al.  1988, Hoffman et al. 1990), at least partly in response to
elevated invertebrate production.  About 25  (15%) of the region's 165 wetland/riparian species  appear to
prefer such situations; examples  include barn  owls and Brewer's blackbirds. Enrichment of saline wetlands
also can increase the production of some characteristic plants (Loveland  and Ungar 1983).

Some species appear to avoid small irrigated wetlands that are deeply recessed within washes or are completely
surrounded by tall, woody vegetation.  For example, most species  of shorebirds, loons, grebes, cormorant, and
geese avoid wetlands where ground-level visibility of the surrounding land (and predators) is restricted and
space is too confining for their running take-offs (Dwyer 1970, Evans and Kerbs  1977). On the other hand,
some species that use wetlands in more heavily developed areas appear to favor wetlands surrounded by dense,
moderately tall  vegetation that provides a visual buffer against disturbance (Milligan 1985). Of the region's
165 wetland/riparian species, about 56 (34%) appear to benefit from a high degree of visual seclusion (Table
5).  About 23 of these are species that require water as a substrate, i.e., are categorized as "highly dependent."
Greatest disturbance is usually caused by people on foot (LaGrange and Dinsmore 1989).  Species  that seem
most wary of approaching humans are generally the larger-bodied ones, e.g., herons, egrets, waterfowl, raptors
(Dahlgren and Korschgen 1992),  and  long-distance migrants that feed in large flocks at the ground or water
level (Burger 1981)34. Reduced use of human-visited wetlands by waterfowl or nongame waterbirds has been
       Of the region's 165 wetland/riparian species, about 56 (34%) appear to benefit from a high degree  of
visual seclusion.  About 23 of these are species that require water as a substrate.

                                                39

-------
demonstrated by Kaiser and Fritzell (1984) and Hoy (1987).  Seclusion (i.e., distance from human dwellings)
is also important to many songbird species because it reduces harrassment and predation by domestic animals,
notably house cats.  Constant presence of cattle in wetlands during the nesting season can also reduce nesting
success  of some species (Tolle 1977). Of the region's 165 wetland/riparian species, at least 27 (16%) avoid
wetland habitats where predation pressures are likely to be great.

Other landscape variables that might influence bird use of wetlands in western regions include watershed size
and orientation (Dobkin and Wilcox  1986, Gutzwiler and Anderson 1992).  Evidence of the importance of
these indicators has, to date, been limited to a few species that occur  in wooded wetlands.

In summary, wetland habitat suitability should not be judged independently of the habitat suitability of the
surrounding landscape. No particular surrounding habitat type is optimal for all species, or always results in
higher avian diversity  of adjoining wetland/riparian  areas.  Although (other factors being equal) secluded
wetlands might be likelier to be visited by more species, the response  of birds to disturbance is probably
species- or group-specific. Accordingly, the new avian richness evaluation method  (AREM) described in
Section 5.0 takes a species-specific approach.  The fact that certain surrounding land covers benefit some
species  but not others  is factored into the method.  At a species level, the method accounts for the varying
effects of the presence of  cropland, other wetlands, land uses that add high concentrations of nutrients, and
secluded areas.  When  assessing habitat acreage for some wide-ranging wetland species, the AREM user also
is asked to include the acreage of continguous, structurally similar habitat even if such habitat is not within
the evaluated wetland.

4.5 Summary of Remaining Information Needs

As  a result of the foregoing review of habitat indicators, it appears that several questions, all of possible
interest to EPA because of their regulatory/mitigation implications, require further research and clarification.
These are presented in no particular order, and should not be considered comprehensive:

o       Do wetlands that  support a diverse avifauna  also support a high diversity of vertebrates, plants, and
        invertebrates?

o       Are the wetlands that have the greatest species richness (or that contribute the  most to regional
        biodiversity) the same ones that are highest-functioning for hydrologic and water quality functions?

o       Can  avian species richness,  or  at least the  occurrence  of some component species,  be predicted
        accurately and consistently through use of rapid indicators?

o       Can statistically sound relationships be defined between habitat indicators, avian richness, and simple
        management classifications (e.g., on-farm vs. off-farm)?

o       Do wetlands that  have more permanent water regimes have more species, and/or more species that
        are of conservation concern (e.g., neotropical migrants, regionally declining species, habitat specialists,
        etc.)? Or are riparian fringe and irrigated emergent wetlands more important?

o       To what degree do birds use  various types of irrigated wetlands in Utah and/or Wyoming?  Is the
        relative importance of various types of irrigated wetlands the same as found previously in the Lower
        Gunnison Valley in  Colorado?

Although some previous studies have provided clues to the above questions, or  answered them for particular
wetlands, sufficient data  have not been  collected in a systematic manner that would permit a  general
extrapolation of findings to irrigated wetlands of the Colorado Plateau. Such data are essential to ensure the
credibility of any evaluation  method or classification  system applied to these wetlands.

                                                 40

-------
5.0 AVIAN RICHNESS EVALUATION METHOD (AREM) FOR THE COLORADO PLATEAU

5.1 AREM and What It Can Do

I used the indicators documented in Section 4.0 to formulate a procedure for rapidly evaluating the suitability
of irrigated wetland  habitat for  birds.  This procedure, termed the "Avian  Richness Evaluation Method"
(AREM), can:

o   Assign a score to each evaluated wetland, which represents the number of bird species that could occur
    in the wetland, multiplied by an estimate of the suitability of the wetland for each.

o   List the species likely to occur in a particular wetland.  Such a list can be combined with lists predicted
    for other wetlands, to identify minimum combinations  of wetlands  that will provide habitat for all bird
    species in an area.

o   Tally the  number of species likely to occur in the wetland and which have particular characteristics, e.g.,
    neotropical migrants, uncommon or game species.  If desired, the  user can  assign scores to these
    characteristics and use them  as "weights" in deriving the wetland score.

The following pages introduce AREM by describing its conceptual basis and demonstrating how it works. Its
advantages are  summarized in Table 9, its  limitations and assumptions are summarized in Table 10, and
recommendations for identifying its proper context of use are presented in Table 11.

5.2 Conceptual  Basis for AREM

Biodiversity is the organizing theme and endpoint of AREM.  Biodiversity can be defined as the variety of
biological material at any or all levels of organization: genetic, species, community, and function.  Biodiversity
is of fundamental concern for scientific, economic, and aesthetic reasons.  Scientific evidence suggests that,
in some situations, balanced and diverse (species-rich) biological communities  are better able than nondiverse
communities to endure environmental change with minimal loss of function. It is important to minimize loss
of wetland function  because increased costs to society can be incurred to  replace  products and services
otherwise supplied passively and at no direct cost by wetlands.  For example, loss of a wetland's natural ability
to purify runoff can pose a burden on users of lakes and rivers that depend  on wetlands to maintain water
quality.  When  this happens, there is often a demand to alleviate the pollution by investing in construction
of wastewater treatment facilities. Moreover, because diverse natural communities (as well as some productive
ones) are aesthetically attractive to many people, regions with high biodiversity often enjoy greater economic
benefits from tourism. Recognizing the importance of biodiversity, EPA's Science Advisory Board in 1990
recommended that biodiversity be accorded highest priority in the Agency's programs. EPA is not alone in
this concern; the U.S. Forest Service, U.S. Fish and Wildlife Service, and other agencies have legal mandates
for maintaining biodiversity, and the concept of a National Biological Survey that will focus on biodiversity
using ecosystem approaches is currently under discussion within the U.S. Department of the Interior.

Some wetland evaluation methods may have included biodiversity as an endpoint, but seldom say so explicitly.
For example, the Golet method, which is used as the  basis for SCS's current (1992) wetland evaluation
method, rates habitat without stating what species a "good"  habitat would contain, or even whether it will be
biodiverse.  Another method - WET (Adamus et al. 1987) -- assigns highest ratings to habitats that indicators
presumably predict will be "diverse and/or productive," but does not document this assumption by quantifying
the number of species or listing them. The Habitat Evaluation Procedure, or "HEP" (USFWS 1980), is often
used to evaluate irrigated wetlands, and its users sometimes assume, without any documented basis, that
habitat which HEP shows is highly suitable for a few selected indicator species will be suitable for supporting
a high  diversity of species.  "Bottom-up" attempts have been made to aggregate HEP's individual species
models into a general model for a particular habitat type (e.g., Bain and Robinson 1988), or to take a "top-

                                                41

-------
Table 9. Advantages of using AREM.

1. Using AREM is relatively simple and rapid. Field data collection requires less than 15 minutes
per wetland.  Data entry and analyses require less than 30 minutes per wetland.

2. Models used to predict habitat suitability for individual species are mathematically simpler than
those used by HEP (the Habitat Evaluation Procedure), so may be  easier to understand and
explain.

3. The synthesis  scores that result from an AREM evaluation (see Section 5.3) have a high level
of accountability. Users can call up the database for any species in order to closely examine the
habitat model supporting that species. Users can also call up any indicator condition, to identify
all species predicted by that condition. This is of potential use in predicting a species' response
to wetland change, e.g., for impact analysis or planning of wetland enhancements.

4. Users with little computer knowledge can interactively edit the database and revise models for
any species. AREM provides this capacity while ensuring that the original database is not erased.
This also allows  users to adapt AREM for  other regions and wetland/riparian types, provided
habitat requirements of  all bird  species in  these areas are known or can be determined with
sufficient accuracy.

5. AREM is perhaps the only rapid habitat evaluation method whose major organizing theme and
endpoint is biodiversity.  This is of interest because many government agencies are  mandated
to account for the impacts of their activities on biodiversity, and public concern over the global
and regional loss of biodiversity appears to be growing.

6. In contrast to HEP, AREM does not  require  the user to base  a wetland's score on  a few
presumed "indicator species." Users do not need to assume that habitats which are found to be
optimum for a few species will also be suitable for many species, i.e., be biodiverse.

7. Species lists predicted by AREM for various wetlands can be combined in any local area or
subregion to  determine which  particular combination of wetlands cumulatively supports the
greatest number of species (see Table 15 for an example). This "optimization process" can be
further focused  by  applying constraints related to  species characteristics, land ownership,
management costs, or other factors. As such, use of AREM can provide a complementary, local
refinement of the "gap analysis" approach currently being applied at state and regional levels by
the U.S. Fish and Wildlife Service (Scott  et al. 1987).

8. AREM's synthesis scores may be less subject than  those of other rapid methods to bias from
imperfect science.  This  is because the  synthesis scores are a composite of both a wetland's
number of species and its suitability rating for each species.

9. One of AREM's outputs - the "unweighted richness" score -  is the actual number of species
predicted to occur in a wetland. As such, this is an ecological parameter that can be validated
empirically.

10. AREM does not require the user to conduct bird surveys or, for that matter, be an expert on
birds or other wildlife.

-------
Table 10.  Limitations and assumptions of AREM.
1.  AREM has not been validated scientifically, either in total, or in terms of its habitat relationship
models for individual  species.  This is true of probably all  other rapid methods for habitat
assessment.

2. AREM is a compromise between convenience and technical certainty.  The technical certainty
of many of the species habitat models that comprise AREM might be increased, and details and
assumptions  explained  at greater length,  but probably  only at  the  expense  of  speed  of
application, replicability, and clarity. AREM is intended to be intermediate in complexity between
the simple,  few-indicator wildlife  habitat  relationship (WHR)  models  used  in  landscape
classification and the multi-indicator, few-species HEP models used for site evaluations. It shares
many of the limitations of WHR's as described by Morrison et al. (1992) and limitations of HEP
described by  Van Home and Wiens (1991), but avoids others.

3. Indicator conditions used in AREM's species models in some cases are related to a species'
presence in a loosely deterministic manner, but in other instances are related only empirically, i.e.,
they correlate with a species'  presence but have necessarily been  shown to control use of
habitats through explicit  effects on food, cover, or reproduction.

4. Wetlands are dynamic systems, and scores assigned by any evaluation method can change
as a result of natural vegetative succession, flood or drought, management actions,  and other
factors.

5. AREM pertains only to avian biodiversity. We do not know if wetlands that contain a relatively
great  number of bird  species usually also  have a relatively great number of plants,  insects,
amphibians, or whatever.

6. It cannot be assumed that wetlands that are species-diverse will always be diverse at genetic,
community, or functional levels, although this is often the case.

7. It cannot be assumed that wetlands that are species-diverse will always have greater ecological
"integrity,"  "health," or "sustainability," although this is usually the case.
                                         43

-------
Table 11.  The context for properly using AREM.
1. AREM is intended for application only to lowland irrigated wetlands and riparian areas larger
than 0.1 acre, and located within the Colorado Plateau region of western Colorado, eastern Utah,
and southwestern Wyoming.

2. Users should be capable of recognizing all indicator conditions specified in the field forms
(Appendix F). When evaluating a wetland, note situations in which you feel information requested
by the field forms  has required considerable judgement, and report this with the results.

3. As is true of other rapid methods for habitat assessment, AREM's habitat relationship models
for individual species cannot be used to estimate the relative or absolute abundance or density
of these species' populations. Many factors not included  in the species models, e.g., weather,
determine population size and even presence/absence in  a given wetland.

4. AREM should not be used to compare wetland/riparian  habitats with other habitats.  Species
habitat scores from AREM estimate the suitability of a wetland or riparian habitat relative only to
the suitability of other irrigated wetlands and riparian habitats of the Colorado Plateau.  In some
circumstances, some species included in AREM might find nonwetland habitats more suitable.

5. Scores from AREM should not be used in lieu of species occurrence data from actual surveys
of a wetland, provided such data  have been  collected with  sufficient  intensity and  using
appropriate methods.

6. Scores from AREM should be considered as only one of several possible inputs used in the
decision-making process. Under most circumstances it is inappropriate to use AREM as the only
means for deciding whether mitigation  should be required.  A habitat index, defined as the
product of an AREM score and wetland acreage, can be computed if desired. The values from
such an  index can potentially be used as one input in mitigation deliberations, monitoring of
restoration/enhancement projects, and description of the future biodiversity consequences of
specified impacts  to the indicator conditions.  However, the commonly associated practice of
using values from such indices to rationalize a decision to offset the  loss of a collectively large
acreage of low-quality wetlands with the creation of a small acreage of high-quality wetlands must
be viewed cautiously.  As is true of other methods, caution is needed because use of simple
multiplication presumes that species richness is  related to habitat acreage (wetland size) in a
direct, linear manner.  This is not necessarily valid  because (a)  the effect of wetland size  on
richness  can vary by species composition, season, surrounding landscape characteristics,
wetland size and  shape, and other factors, (b) wetland size  is "double-counted,' first as it is
included in individual species models,  and second as it is  applied as a multiplier, and  (c)
"enhanced" habitat quality does not necessarily compensate for lost habitat space.
                                          44

-------
down" approach in which a series of general statements about a system are used to focus and incorporate more
specific detail only as needed (e.g., Schroeder 1986). Both of these approaches produce an ordinal score rather
than a real variable (species richness) and contain many implicit assumptions (Van Home and Wiens 1991).
Another method, the Habitat Assessment Technique (HAT, Cable et al. 1991), does equate wetland habitat
suitability directly with species richness but is time-consuming to use because it requires that birds be surveyed
directly rather than estimating their presence through use of indicators. Finally, wildlife habitat relationship
(WHR) models or matrices have been developed by many government agencies (Morrison et al. 1992). WHR's
can be aggregated, in what is called "gap analysis," to estimate species richness of a  habitat area or region
(Scott et al. 1987).  However, the WHR models are crude and seldom use more than a few indicators, e.g.,
gross land cover type. Conventional WHR models typically do not differentiate among various wetland types.
Thus, applying such models to a series of wetlands would  result in all wetlands having the same species
composition and richness.

5.3 How AREM Works

When you use AREM, how does the information you collect on a wetland's indicators get converted to scores
and species lists for a wetland?  First, understand that the tools AREM uses to generate the products are:

o      The data that you enter from your completed field form (Appendix F), representing the indicator
       conditions of the evaluated wetland;

o      Three databases that are used to match the data from your field  form with information  on each
       species' habitat requirements, geographic/seasonal distribution, and conservation characteristics; and

o      A computer program that does the matching described above.

These tools interact  sequentially to generate scores and species lists.  A wetland evaluation using AREM
proceeds in the following manner. First, you briefly visit the wetland and check off habitat indicators observed,
using a standardized checklist (the field form, Appendix F). Next, you take your completed data form indoors
to a computer, where  a menu-driven program explains how to  generate scores and species lists for  the
evaluated wetland. It instructs you to compare the list  of indicator conditions you noted on your field form
(Appendix F) with a similar list on the  computer screen, and mark the conditions that are common to both
lists.  Then, the computer program compares the marked conditions with the databases. Finally, it calculates
three types of scores for the wetland, based on sums of the scores for all the individual species.

The main database that is the foundation of AREM is a habitat relationships matrix which I prepared from
literature, professional experience, and especially, from interviews with local avian experts.  When developing
the database, the literature that I found to be most relevant included the citations in Chapter 4.0, as well as
various Habitat Suitability Index (HSI) models (Schroeder 1982,1983a, b, Prose 1985, Short 1985, Short and
Cooper 1985, Sousa 1987, Schroeder and Allen 1992), and the following journal papers, books, and reports:
Provost 1947, Johnsgard 1956, Johnson and Ryder 1977, Whitmore 1977, Thomas 1979, Faanes 1982, Bull and
Skovlin 1982, Rice et al. 1983, and Ehrlich et al. 1988.

One axis  of AREM's supporting database matrix is a list of all 71 indicator conditions that are contained on
the field form (Appendix F). The other axis contains a list of the 165 bird species that regularly use irrigated
wetlands  in the region (p. 16 explains the basis for this list).  I assigned one of the codes shown in Table 12
to each cell in the matrix. When used together, these codes form a simple habitat relationship model for each
species.  Table 13 shows an example.
                                                45

-------
Table 12.  Meaning  of codes used in the species habitat relationships
database.
X           means  the  species requires that indicator condition  (i.e.,
            habitat feature)

f           means the species requires either that condition or another
            one (or more), also pre-labeled in the database with an "f1

1           a number (could also be 2, 3, or 4) representing the species'
            preference  for that indicator condition,  relative  to other
            indicator conditions for that species in the database  (4=
            more important, 1 = less important)

+2         a number (could also be +2 or +3, or could be preceded by
            a minus sign) that  describes a condition that is not essential
            to the species, but influences its probability of occurrence in
            a particular  area (+2 = more influential than +1)

(blank)      means the indicator condition is  not sufficiently  relevant to
            predicting the suitability for the species (i.e., other indicator
            conditions are more predictive)
                                 46

-------
Table 13.  Example of the marsh wren species model, as defined by database
coding.
For marsh wren, the database includes characters in 10 data fields1 as follows:

Data Field Name   Code  Brief Description of Data Field
Anywater:

Drawdown:


Emln:


RbMuchDens:

RbMuchOpen:

RbSomeDens:

RbSomeOpen:

WEMuchDens:

PredHPot:


GrazBurnMo:
 +1    Wetland has >2 inches of surface water

. +1    Wetland sediments  are occasionally  exposed,  or
       wetland receives floodwater input from a major river

 X    Wetland  has  >0.1   acre  herbaceous,  emergent
       vegetation

 3    Wetland has >1 acre robust, dense vegetation

 2    Wetland has >1 acre robust, open vegetation

 2    Wetland has 0.1-1.0 acre robust, dense vegetation

 1     Wetland has 0.1-1.0 acre robust, open vegetation

 1     Wetland has >1 acre wet, grassy, dense vegetation

 -1     Wetland is likely  to  be subject to  high  predation
       pressure

 -2    Wetland is intensely grazed, mowed, or burned during
       nesting season
     The terms "data field" and "indicator condition" are used interchangeably because each indicator
condition is allocated to one data field in the habitat relationships database.  In this example, the
other 60 fields of  the database  are blank  because their indicator conditions  were judged to be
insufficiently relevant to estimating the habitat suitability of Colorado Plateau irrigated wetlands
for the marsh wren.  At least one other species is associated with each of the 71  data fields in the
database.
                                      47

-------
A unique feature of the computer program that supports AREM is that it allows users (regardless of their
computer skills) to edit the main database.  For example, users can (a) add or delete species, e.g., to reflect
a different opinion regarding a species' dependence on wetland/riparian habitats, or to narrow the analysis just
to game species, (b) change the indicator conditions (from the current set of 71 in Appendix F) which support
the habitat model for any species,  and (c) change  the  manner in which a particular indicator condition
contributes to a model. Moreover, AREM provides this capacity while ensuring that the original database is
not erased.

To demonstrate how the AREM analysis program works, consider one species ~ marsh wren — whose habitat
is defined by the model in Table 13.  The computer program compares the model (as defined by the database)
with data you entered from your field form. The analysis proceeds in the following sequence:

Step 1.  Before evaluating the suitability of the habitat for marsh wren, it is necessary to determine if the
geographic range of the marsh wren during a specified season includes the evaluation area. To determine this,
the computer program scans  a database that has  cataloged the within-region geographic  and seasonal
distribution of each of the region's 165 wetland/riparian birds.  If the database shows the marsh wren does not
occur in  the  season and  subregion marked  on the field form,  then  the marsh wren is  dropped  from
consideration and the program proceeds to the next species on the seasonal list of regionally-occurring species.
If marsh wren does occur in the subregion during  the season of interest, the analysis of the wetland using the
marsh wren's habitat model proceeds.

Step 2. Next, it is essential to determine if the wetland is minimally acceptable to the marsh wren. To do this,
the program scans the marsh wren model in the database. If the database contains an "X" or an T in one of
the data  fields that you checked  off on  your field  form, then  the program  considers  the wetland  to be
minimally acceptable, because a required condition is  present. The program assigns marsh wren a "base score"
of 5. If neither an "X" nor an T are present, further analysis is considered  moot and marsh wren is assigned
a score of 0.   For marsh wren, the  database considers a minimally acceptable wetland to be any one that
contains at least 0.1 acre of herbaceous vegetation (Emln). That is, data field Emln is marked with an "X"
or "f."

Step 3. Next,  it is important to determine if conditions are present that would make the wetland more than
minimally acceptable for the  marsh wren.  The manner in which the program does this is  described here and
in Step 4. Initially, the program identifies  beneficial, compensatory indicator conditions  that are defined by
the marsh wren model and are also present in the wetland. "Compensatory" means that if more than one of
these conditions is present, their effects are not additive. For example, marsh wrens usually prefer robust
vegetation that is dense, but benefit somewhat from robust vegetation even if it is relatively open.  In the
database, the best compensatory indicator condition  has been assigned the largest number, generally on a 1
to 3 scale. From  the numbers for marsh wren in the database, the computer program selects the maximum
value for any indicator that is also present in the  evaluation wetland.  The maximum rather than the sum is
used because the sum would erroneously imply that habitat is optimal when both dense and open robust
vegetation stands are present, i.e., the two density conditions would be  treated as if they were functionally
additive.

To demonstrate, the marsh wren model part of the database contains  the following compensatory indicator
conditions:
                                                48

-------
  Data Field Name  Code     Brief Description of Data Field
  RbMuchDens:    3   Wetland has > 1 acre robust, dense vegetation
  RbMuchOpen:    2   Wetland has > 1 acre robust, open vegetation
  RbSomeDens:    2   Wetland has 0.1-1.0 acre robust, dense vegetation
  RbSomeOpen:    1   Wetland has 0.1-1.0 acre robust, open vegetation
  WEMuchDens:   1   Wetland has >1 acre wet, grassy, dense vegetation

If you showed (on the field form) that the wetland contains only RbSomeDens and RbSomeOpen, then the
program will select RbSomeDens because its number (2) is larger than the value for RbSomeOpen (1). The
program then adds this number (2) to the base score (5) determined in Step 2, giving a total of 7, and the
analysis continues.  If the  base score had been  0, nothing  would have been added because the analysis for
marsh wren would have been terminated at Step 2.

Step 4. The program also determines if one or more cumulative indicator conditions are present.  As with
compensatory conditions,  these are conditions  that are not required by marsh wren, but which  alter its
probability of occurrence in a wetland.  "Cumulative" means that if more than one of these conditions is
present, their individual effects  are  combined.  For this reason  they  must be treated differently from
compensatory conditions  in the calculations.   Each cumulative indicator  condition in the database is
represented by a number preceded by a sign (+ or -) indicating whether that condition tends to increase (+)
or decrease (-) the probability of that species occurring in a wetland. This cues the computer to recognize that
it is a cumulative condition, not a compensatory condition. A number (+1 to +3, or -1 to -3) indicates the
intensity of the effect, with larger positive or negative numbers indicating stronger effects.

Consider again the marsh  wren.  According to  the database, the chances of the wren using an herbaceous
wetland with dense, robust vegetation increase if:
    (a) the wetland also contains at least 2 inches of surface water (i.e., the indicator condition "Anywater"
    was checked on the field form), and/or
    (b)  the wetland's sediments are occasionally exposed,  or the wetland receives floodwater input from a
    major river  (i.e., the indicator condition "Drawdown" was checked on the field form).

At the same time, the probability of the wren using  the wetland  decreases if:
    (c) the wetland is likely to be subject to high predation pressure, and/or
    (d) the wetland is intensely grazed, mowed,  or burned during nesting season.

In the database, the above statements are coded in the marsh wren model in the following manner:

  Data Field Name
  Anywater:
  Drawdown:
  PredHPot:
  GrazBurnMo:

In this  case, the database considers the negative effect (-2) of nesting-season grazing, mowing, or burning to
be greater than the effects  of any of the other indicator conditions (+1 or -1).

At this point the program adds to the sum (7) from Step 3 all of the cumulative indicator conditions present
in the evaluated wetland. For example, if this wetland contains just two of these conditions ~ Anywater (+1)
and GrazBurnMo (-2) ~ their sum (-1) is added to the sum (7) from Step 3.  If none of the cumulative
indicator conditions are present, the sum (7) is brought forward  and the analysis continues.

                                                49

-------
Step 5.  Next, it is crucial that the species scores be standardized, so that no species is implicitly given more
weight.  If the scores are not standardized, species whose models specified many indicator conditions would
be implicitly biased toward higher scores and would contribute disproportionately to the total, whereas species
having models that specified fewer indicator conditions would artificially tend to score lower. To standardize
the species scores, the program divides the total by a "potential maximum"  (PotMax) number,  which is the
largest point total the marsh wren could theoretically receive.  That number represents the optimum habitat
suitability as  defined by the marsh wren model ("optimum" meaning that these conditions represent the best
habitat  likely to be currently available within any  Colorado Plateau irrigated wetland).  Because different
species models use different numbers of indicator conditions, each species has its own value for PotMax.  In
the example of the marsh wren, the Step 4 total (6) is divided by a PotMax value of 10, to give  a final score
(termed the species habitat score) for marsh wren of 0.6. By dividing by PotMax, the program  ensures that
no species' score  can exceed 1.0, so that if a wetland's habitat were optimum for all species, they would be
counted equally and the sum of all the species habitat scores would equal the number of species.

Step 6.  Having assigned the wetland a score for marsh wren, the computer program now proceeds in similar
manner to assign scores to the other 164 potentially occurring species. The sum of the scores from all species
is the unweighted habitat score. An example is shown in Table 14. The unweighted habitat score represents
both the number of species for which the wetland is minimally suitable, and the degree of suitability for each
species.  This type of score, based on the individual scores of many species, is termed a synthesis score.  In
theory, the maximum value for the unweighted habitat score would be 165 (the number of species potentially
occurring  in irrigated wetlands at any season, multiplied by 1.0, which is the maximum species habitat score
of each).  However, because habitat conditions that  are optimal for some  groups of species are less than
optimal for other groups  (i.e., are mutually exclusive), the actual habitat score usually will be much less than
165.

Step 7.  At this point the analysis can be stopped and the unweighted habitat score can be used  to represent
the wetland.  Or, users can choose to use one or both of two other types of synthesis scores to represent the
wetland.  Although probably correlated with each other,  each  synthesis score represents a conceptually
different evaluation of the wetland's potential to support biodiversity.

The unweighted richness score is simply the number of species that have scores above a certain threshold score
(>0, >0.25, >0.50, >0.75) that the program prompts you to select. For example, if you specify the threshold
of ">0," the  program will count the number of species for which the  wetland is even minimally suitable,
whereas if you specify "0.75," the program will produce a more conservative (lower) tally comprised just of
species for that the evaluation wetland's conditions resulted in a species  habitat score exceeding 0.75.  An
example is shown in Table 14.  The purpose of the unweighted richness score is to  provide an estimate of
avian species richness that is more suitable for use in later validation testing, because species richness can be
determined empirically (e.g., by conducting  an appropriate bird survey).  Users are given the option of
specifying different probability levels because at this point in the development of AREM, the level which most
often corresponds to actual species richness is unknown. The maximum value for the unweighted richness
score at a  cutoff level of >0 is, like the unweighted habitat  score, 165 (i.e., the number of species potentially
occurring  in irrigated wetlands at any season).  Again, because habitat conditions that are optimal for some
groups of species are less than optimal for other groups, the actual habitat score usually will be much less than
165. Initial experience using AREM suggests that the maximum values would be approximately 104,104,102,
and 89 at  the >0,  >0.25, >0.50, and >0.75 cutoff levels, respectively.

To obtain the weighted habitat score, the computer program multiplies  the habitat score of each species by
a conservation priority weight for that species, and the products are then summed as shown in Table 14. The
"conservation priority weights" are preassigned numbers, on a 1 to 10 scale,  that represent categories of a

                                                50

-------
        Table 14. Example of calculation of synthesis scores.


        WETLAND #1:
                              Species Habitat       Conservation
        Species              Score (calculated)36   Priority Weight37       Score X Weight

        Downy Woodpecker   0.77                       2                    1.54
        American Crow        0.63                       2                    1.26
        Black-billed  Magpie    0.27                       2                    0.54
        Lewis'Woodpecker    0.18                       2                    0.36
        Marsh Wren          0.60                       6                    1.20
        Wilson's Phalarope    0.31                       6                    0.62
        Pied-billed Grebe      0.84                       10                   8.40
        Bonaparte's Gull      0.22                       10                   2.20
        Common Goldeneye   0.43                       10                   4.30


        Unweighted Habitat Score: 4.25 ( =sum of the species habitat scores)

        Unweighted Richness Scores:
                @ species habitat score cutoff of >0.75 =  2
                    (2 species: downy woodpecker (.77), pied-billed grebe (.84))
                @ species habitat score cutoff of > 0.50 =  4
                    (above 2 species, plus American crow (.63), marsh wren (.60) = 4 species)
                @ species habitat score cutoff of >0.25 =  7
                    (above 4 species, plus magpie, phalarope, goldeneye =7 species)
                @ species habitat score cutoff of >0   = 9
                    (all species above, = 9 species)

        Weighted Habitat Scores (weighting factor= "water dependence"):
                @ species habitat score cutoff of >0.75 =  9.94
                    (add downy woodpecker (1.54) to  pied-billed grebe (8.40))
                @ species habitat score cutoff of >0.50 = 12.40
                    (above, + American crow (1.26) + marsh wren (1.20))
                @ species habitat score cutoff of >0.25 = 17.86
                    (above, + magpie (0.54) + phalarope (0.62) + goldeneye (4.30)
                @ species habitat score cutoff of >0  = 20.42
                    (sum of all Score x Weight)
       Species having a score of 0 are not included in this example. Also, expect that species lists
from most wetlands will be longer than this example.

       In this example, weights  in the database that define each species' relative dependence on water
are used (these weights are defined further in the  footnote to Table 10).  Users have the option to
select other  conservation characteristics for which the database contains a weight for each species
fp-g-, rplativp reginnal ahundarvi^  status ag  a npntropi'ral migrant^.


                                               51

-------
species characteristic that could be important to the conservation of biodiversity, e.g., relative abundance,
water-dependence. From a list of these weighting characteristics for which the database contains information
(i.e., the weight of 1-10) for each species, the program prompts you to select and mark characteristics of
greatest relevance to your objectives.  You may also redefine the preassigned weights  (e.g., make the lowest
weight a 0 instead of a 1).  In addition to (or in lieu of) summing the products for all species as just described
(i.e., all species with habitat score >0) the user can choose to sum the products only for species having a
specified minimum habitat score (>0.75, >0.50, >0.25,  >0, as before). Table 14 shows this.  The purpose of
the weighted habitat score is to allow the user to emphasize  species of greatest interest because of agency
mandates, management goals, or other reasons.  The option of specifying thresholds is  provided so that users
can focus mainly on species most likely to occur in a wetland.

In addition to providing up to three synthesis scores, AREM also provides the option of printing out the list
of (a) species that were tallied to produce the score, (b) the species habitat scores associated with each species,
as calculated for the evaluation wetland, and/or (c) the weighted habitat scores for all species. These options
are provided to  facilitate field testing of AREM (e.g.,  Do the particular species predicted  to occur in the
wetland actually occur in it?) and to generally document the basis for any generated score.  In addition, users
have the option of using  the output to define which particular combination of wetlands or wetland types
cumulatively supports the  greatest  number of species (see example, Table 15).

Although no testing has yet been conducted to characterize the sensitivity of AREM's three synthesis scores
to different  types of  irrigated wetlands, knowledge of the species suggests that the  unweighted habitat and
unweighted  richness  scores might  be highest for large (>40 acre), wide, secluded, ungrazed, periodically
desiccated or flooded wetlands that adjoin lakes or rivers within agricultural landscapes, and contain multiple
water depths and multiple vegetation life forms and species.  Such wetlands are usually, but not necessarily,
"natural" in origin.

5.4 Results of Initial Testing

I applied an early version of AREM during visits in November 1992 to 20 irrigated wetlands in the Grand and
Lower Gunnison Valleys,  Colorado.  AREM was evaluated through  a  quality assurance  (QA)  protocol
designed to estimate AREM's replicability, practicality, and comparability.  Comparability refers to the extent
to which AREM rated a series of wetlands the same as local avian experts. Local experts checked off species
they believed likely to be seen in each wetland, based on personal knowledge of habitat requirements.  The
wetland score from this approach was the number of species that-the experts checked off.  The expert's results
and those obtained from using  AREM also were compared with results from using the SCS method (SCS
1992a). Replicability was measured as the frequency with  which different users responded the same to  a
particular indicator question (see Appendix F for a similar series of questions). Practicality was assessed by
measuring the time required to evaluate a wetland and by asking users to identify questions they felt were most
subjective or difficult to answer.

5.4.1 Comparability

With regard to comparability, the results (Table 16) suggest limited congruence among scores based on expert
opinion, the SCS  (1992a) method, and the early version of AREM.  In no case did two or more of these three
approaches agree on which wetland was the most important or least important. Of the five wetlands that were
ranked highest based on the avian expert's species list, only  two were in the top five based on AREM score
and only two were in the top five based on the SCS method.  Of the five wetlands that were ranked lowest
based on the avian expert's species list, only one was in AREM's bottom five and none were in SCS's bottom
five.  Conversely, of the five wetlands ranked highest by this early version of AREM, only two were in the

                                                52

-------
  Table 15. Use of AREM to select wetland combinations that optimize protection of regional avian
  diversity.

  This simplified  example demonstrates the importance of using AREM (or other methods) to
  consider wetland functions and values at a cumulative, regional basis as well as individually3", If
  the only basis for a wetland decision was the scores for individual wetlands, then wetlands A and
  B below would be selected because they individually have the most species (i.e., highest unweighted
  richness score) of any of the wetlands. However, if the objective is to maintain biodiversity at a
  regional level rather than exclusively at  an individual site  level, then wetlands C and D,  which
  individually are the poorest in species, would be the best  choice because together they have a
  larger species list  (8 species)  than the two  richer wetlands combined  (6 species), or the
  combination of either poorer wetland (C  or D) with either of  the richer  wetlands  (A or B).
  Wetlands C and D also would usually be chosen if the unweighted habitat score were used instead
  of the unweighted richness score.  These selection principles can be applied to more than two
  wetlands at a time, although for large sets of wetlands use of a computer greatly facilitates the
  calculations. In instances where one or both members of an "optimal pair" (as determined by this
  process) cannot be protected because of cost or other reasons, a next-best pairing of sites can be
  determined; some authors have  even proposed that cost-per-species-protected be  calculated and
  used to optimize conservation strategies, i.e., by calculating and comparing for all possible wetland
  combinations both the number of species protected and the associated land stewardship costs.  Of
  course, sustaining the populations of all  species requires some amount of redundancy of species
  composition among wetlands.
                                                Occurs in Wetland:
                 Species                 A      B      C      D
                 Mallard                x        x               x
                 Mourning Dove        x        x               x
                 Black-billed Magpie    x        x       x
                 European Starling      x        x       x
                 Song Sparrow          x        x       x
                 Killdeer                x                       x
                 Sora                                  x
                 Yellow-headed  Blackbird                       x
                 TOTAL Species
                 (Unweighted Richness)  6544

                 Collective # of Species,  by Combination of Wetlands:
                        Wetlands A + B =  6 (all species but Killdeer are  redundant)
                        Wetlands A + C =  7
                        Wetlands A + D = 7
                        Wetlands B + C =  6
                        Wetlands B + D =  7
                        Wetlands C + D =  8 (no species are redundant)
    •70
       Despite a continuing and necessary focus of resource agencies on the individual site level when
setting wetland priorities,  the cumulative assessment principles upon which this example is based are
also relevant and  have been noted for years by conservation biologists (e.g., Samson and Knopf 1982,
           Proasey and Mii-hnlls 198<»-	

                                             53

-------
Table 16.
biologists.
Comparison of rankings of wetlands by SCS method, AREM, local avian experts, and field
Wetlands 1-10 are located in the Grand Valley subregion and the local expert who was consulted was Ronald
Lambeth. The local biologists were Meaghley, McCall, and Neilson. Wetlands 11-25 are located in the Lower
Gunnison subregion and the local expert who was consulted was David Galinat  Local biologists in this
subregion were Obert, Taylor, and Woodis. The "SCS Method" is SCS (1992). "AREM" is the November 1992
draft of the Avian Richness Evaluation Method; the score is the unweighted number of species predicted.  The
score, in the "Expert" column is the unweighted number of species predicted by the expert to occur.  Numbers
in the remaining columns are the ranks (1= best habitat, 5= poorest habitat) assigned  within each series of
wetlands by the biologists.
       Wetland No.  SCS Method  AREM    Expert  Meaghley  McCall  Neilson  Obert  Taylor Woodis
01
02
03
04
05
06
07
08
09
10
11
12
13
14
15
16
17
18
19
20
21
22
25
6.4
5.2
4.2
6.8
8.0
5.6
6.0
6.4
7.2
6.8
6.4
8.0
7.2
6.4
7.2
7.2
6.8
7.2
7.6
7.6
6.8
6.4

72
68
59
54
42
35
35
50
35
59

53
44


43
42
35
46
57
48
68
46
45
47
40
38
55
42
44
53
41
40
36
37
61
40






23
41

3
2
4
5
1
2
5
3
4
1













3
4
5
2
1
2
4
3
5
1













1
3
5
4
2
2
5
1
4
3



























5 6
4 5
1 4
6 3
3 2
2 1
2 2
1 1















6
3
2
5
4
1
2
1

                                               54

-------
expert's top five; of the five wetlands ranked lowest by AREM, only one was in the expert's bottom five.
Similarly, of the five wetlands ranked highest by the SCS method, only two were in the expert's  top five; of
the wetlands ranked lowest by the SCS method, none were in the expert's bottom five.

Also, the scores were compared statistically, two  methods at a time, using two nonparametric  tests -- the
Spearman rank-correlation test and the Kendall Tau-b rank correlation test. At a one-tailed significance level
of p<.01, none of the approaches were correlated.  That is, no two methods ranked the series of wetlands in
approximately the same order.

In addition to the above, I asked each of three local government biologists to independently rank two series
of wetlands, five per series, according to  "habitat quality" as they perceived it.  In both series of wetlands, two
of the three biologists selected the same wetland as representing the "best habitat," and the other biologist
rated it second.  Also, two of the three biologists agreed on the wetland representing "poorest habitat," and
the other biologist ranked it next-to-poorest. Comparing the biologists' rankings with those based on species
richness (as predicted by the local avian expert), I found that for the first series of wetlands, the biologists
mostly agreed with  the avian expert and the SCS  method, but not AREM, on which wetland would be the
lowest- and highest-ranking. However, for the second series of wetlands, the wetland which the  expert
predicted to have highest species richness was considered the best habitat by only one of the three biologists.
The wetland that most of the biologists and AREM believed represented the best habitat was predicted by the
avian expert to actually have the lowest  species richness. The wetland that the SCS method ranked highest
was ranked next-to-lowest by most of the biologists and  the avian expert.  Because of the small sample size,
none of these  data were analyzed statistically.

5.4.2 Replicability

For 22 (75%) of the 30 main questions, users concurred in the majority (>9) of the wetlands evaluated.  This
was considered a reasonable level of replicability. Still, some questions nave since been modified to increase
replicability even further.

5.4.3 Practicality

Users took between 4 to 13 minutes per wetland  to complete the evaluation.  Longer times were mostly
associated with the use of the "long form" (see Appendix F). After becoming familiar with the method through
use of the long  form, users instead began  using the "short form."  Users indicated  that they believed all
questions were reasonably practical to answer. Those which they sensed were most likely to require judgement,
because of difficulty of onsite estimation, were the questions asking about land cover or habitat features in
the general landscape rather than the wetland. In some instances, this information could  be obtained from
aerial photographs.

5.4.4 Field Testing Conclusions

Results from the initial field testing indicated that AREM, although not perfect, is generally practical to use
and results are reasonably replicable.  AREM's disadvantages are mostly ones shared with other methods for
rapidly evaluating wetland habitat. Results of testing AREM's comparability are difficult  to interpret because
it is uncertain, when various methods give different results, which method is the "correct"  method.  Therefore,
future validation should occur not through comparison with other methods, but by comparing AREM results
with data from actual bird surveys.  In such a study, a list of birds found to occur in a series of irrigated
wetlands should be compared with a list of birds predicted to occur based on a simultaneous evaluation of each
of the wetlands using  AREM.  A professional statistician and field ornithologist should be involved in the

                                                 55.

-------
design and execution of the study.  Data from the study should be used to examine the following questions,
at a minimum.  These questions should be examined sequentially in the order listed.  The order reflects
decreasing probability of successful validation.

o       Is there a statistically significant difference in the ranking of the study wetland sites based on AREM
        synthesis scores vs. actual measurement of bird species richness?

o       Which type of AREM synthesis score, when used to rank the wetlands, produces a pattern of ranks
        closest to those based on the measured species richness?

o       Is there a statistically significant difference between the number of species predicted by AREM (at
        each of the probability levels) and absolute number of species as determined by the field inventory?

o       Which species are most consistently underpredicted or overpredicted, and what types of irrigated
        wetlands are associated with such errors?  Based on previous experience, I would expect there to be
        more Type I errors (species predicted by AREM to be present but were absent) than Type II errors
        (species found by surveys but not predicted by AREM to be present).

A field survey of this type is essential to further define the validity of AREM and situations in which its use
is most and least appropriate.  However, in the meantime it is essential to understand that the results reported
above were based on an early  version of AREM. The version of AREM contained in Appendix F represents
a major revision of the  earlier  version,  largely reflecting what was learned from the local expert.  The
supporting database also has been extensively revised, taking into account knowledge gained through the initial
field-testing.
                                                56

-------
                                    6.0 STUDY CONCLUSIONS

No single characteristic (i.e., "indicator") reliably predicts which irrigated wetlands comprise the best habitat.
Rather, habitat  quality is  associated with various combinations  of the conditions  of  several indicators,
measured at several scales.  The most predictive indicators are probably patch size, water regime, vegetation
form  and species, aquatic organism abundance, and  landscape context.  However, attempts to identify
indicators of "good" irrigated wetland habitat encounter a problem of defining "good for which species?" The
importance of each indicator, or of each unique combination of indicator conditions, depends on the values
placed on the species associated with  it. Many indicator conditions are ideal for only a few species, but if these
species are particularly valued (e.g., because they are regionally rare, declining, or hunted), then the indicator
conditions can be considered important.   For this reason, it became essential to develop a new evaluation
method (AREM) that would allow flexibility in selecting which species are used to define habitat quality, and
that could identify indicators important  to  the "most" species.  Initial testing has demonstrated  AREM's
general replicability and practicality.  Future validation should involve a  comparison of AREM results with
results from appropriately designed and executed field surveys. Additional research on water quality functions
of irrigated  wetlands,  particularly their  potential for removing nitrate from agricultural runoff, is also
warranted.
                                                 57

-------
                                        7.0 LITERATURE CITED


Adarnus, P.R.   1992.  Data  sources and evaluation methods  for  addressing  wetland issues,   pp.  171-224 In:
Statewide Wetlands Strategies.  World Wildlife Fund,  Washington, D.C.  and Island Press,  Washington,  D.C.

Adamus, P.R., E.J.  Clairain, Jr., D.R. Smith, and R.E. Young.  1987.  Wetland Evaluation Technique (WET). Volume
II.  Technical Report Y-87.  U.S. Army Corps of  Engineers, Waterways Experiment Station, Vicksburg, Mississippi.

Adamus, P.R. and K. Brandt.   1990.   Impacts on Quality of  Inland Wetlands  of the United States:  A Survey of
Indicators,  Techniques,  and Applications  of  Community Level Biomonitoring  Data.   EPA/600/3-90/073.   U.S.
Environmental Protection Agency, Cincinnati,  Ohio.

Akhurst, E.G.J. and C.H.  Breen.  1988.  Ionic content  as a factor influencing turbidity in two  floodplain  lakes
after a flood.  Hydrobiologia 160:19-31.

Anderson, B.W., A.  Higgins,  and  R.D. Ohmart.   1977.  Avian use of salt  cedar communities  in the lower Colorado
River valley,   pp.  128-136  In:  R.R.  Johnson and D.A.  Jones  (tech.  coords.).   Importance,  Preservation, and
Management of Riparian Habitat: A Symposium. Gen. Tech. Rep. RM-43.  USDA Forest Serv., Fort Collins, Colorado.

Andrews, R.  and R.  Righter.   1992.  Colorado Birds:  A Reference to Their  Distribution  and  Habitat.  Denver
Museum of Natural History, Denver, Colorado.   442 pp.

Austin, G.T.  1970.  Breeding birds of desert  riparian habitat in southern  Nevada.   Condor 72:431-436.

Bain, M.B. and C.L. Robinson.   1988.   Structure, Performance,  and Assumptions of Riverine Habitat Suitability
Index Models.  Aq.  Resour. Res.  Ser.  Rep.  88-3.   Coop. Fish & Wildl. Res. Unit,  Auburn,  Alabama.

Baker, B.W., D.L. Hawksworth,  and J.G. Graham.  1992.  Wildlife habitat  response to riparian restoration on the
Douglas Creek watershed,  pp. 62-70 In: Proceedings of Fourth Annual  Convention, Colorado Riparian Association,
Boulder, Colorado.

Baldassarre, G.A.,  R.J.  Whyte,  E.E.  Quintan, and E.G. Bolen.   1983.  Dynamics  and quality of  waste  corn
available to postbreeding waterfowl in Texas.  Wildl. Soc.  Bull. 11:25-31.

Baldassarre, G.A. and E.G. Bolen.  1984. Field-feeding  ecology of waterfowl  wintering on  the south High Plains
of Texas.  J. Wildl. Manage. 48:63-71.

Baldassarre, G.A. and D.H. Fischer.  1984.  Food habits of fall  migrant shorebirds on the Texas High Plains.
J. Field Ornith. 55:220-229.

Ball, J.P. and T.D. Nudds.  1989.  Mallard habitat selection: An experiment and implications for management.
pp. 659-671  In:  R.R.  Sharitz and J.W. Gibbons  (eds.).   Freshwater  Wetlands  and Wildlife.   CONF-8603101,
Symposium Series No. 61.   U.S. Dept.  Energy, Oak  Ridge, Tennessee.

Balsore, N.S., L.B. Best, and J.B. Wooley.  1986.  Bird nesting in Iowa no-tillage and  tilled cropland.  J.
Wildl. Manage. 50:19-28.

Beck, D.A.,  D.E. Hubbard,  and K.F. Higgins.   1987.    Effects of  Haying  on Seasonal Wetland Hydrophyte and
Invertebrate Populations  in  South Dakota.  Completion Report, PR  W-75-R, Job 4, Study 7529.  South Dakota  Div.
Wildlife, Pierre.

Behle, W.H.   1981.  The Birds of  Northeastern Utah.  Occas. Publ.  2, Utah Mus. Nat. Hist.,  Univ. Utah, Salt  Lake
City.

Belanger, L. and R. Couture.  1988. Use of man-made ponds by dabbling duck broods.   J. Wildl. Manage.  52:718-
723.

Bennett, A.F.   1990.    Habitat  corridors and  the  conservation  of  small  mammals  in  a fragmented  forest
environment.  Landscape Ecol.  4:109-122.

Berg, P.F.  1956.   A study of  waterfowl  broods in eastern Montana with special reference to movements and the
relationship of reservoir fencing to  production.   J.  Wildl.  Manage.  20:253-262.

Bissell, S.J. (ed.).   1978.   Colorado  Mammal Distribution  Latilong Study.  Colorado Division of  Wildlife,
Denver.

Boschen, N.   1992.  Birds of the Moab Slough of the Colorado River floodplain, Moab, Utah.  (Detailed notes of
monthly surveys).


                                                     58

-------
Bottorff, R.L.  1974.  Cottonwood habitat for birds in Colorado.  Am. Birds 28:975-979.

Briggs, R.  1982.  Avian Use of Small Aquatic Habitats in South Texas.  M.S. thesis. College of Agriculture,
Texas A & I University, Kingsville.

Broschart, M.R. and R.L.  Linder.   1986.  Aquatic invertebrates in level ditches  and adjacent emergent marsh in
a South Dakota wetland.  Prairie Nat. 18:167-178.

Brown, M. and J.J. Oinsmore.  1988.  Habitat  islands and the equilibrium theory of  island biogeography: testing
some predictions.  Oecologia 75:426-429.

Brown, M. and J.J. Dinsmore.  1986.  Implications of marsh size and isolation for marsh bird management.  J.
Uildl. Manage. 50(3):392-397.

Buckner, D.L.  1988.   Construction  of cattail wetlands along  the  East Slope of the Front Range of Colorado.
pp. 126-131 In: K.M. Mutz, D.J. Cooper, M.L.  Scott, and L.K. Miller (tech. coords). Restoration, Creation, and
Management of Wetland and Riparian Ecosystems of the American West.   PIC Technologies,  Denver.

Budeau, D. and P. Snow.  1992. Wildlife Use of Agriculturally Disturbed Wetland Sites in  the Willamette Valley,
Oregon.  Oregon Fish & Wildlife Dept., Salem.

Bull, E.L. and J.M. Skovlin.  1982.   Relationships between avifauna and  streamside vegetation.  Trans. N. Am.
Wildl. Nat. Resour. Conf. 47:496-505.

Burdick, H.E.  1979.  Wildlife Inventory: McElmo Creek Project,  Colorado.  Colorado Div.  Wildlife,  Durango.

Burger, J.  1981.  The effect of human activity on birds  at  a coastal bay.   Biol. Conserv.  32:231-241.

Burkham, D.E.  1976.   Hydraulic Effects  of Changes in Bottomland Vegetation on Three Major Floods, Gila River
in Southeastern Arizona.   Prof. Paper 655-J, U.S.  Geol. Surv., Reston, Virginia.

Cable, T.T., V. Brack,  Jr.,  and V.R.  Holmes.  1989.  Simplified method for wetland habitat assessment.  Envir.
Manage. 13: 207-213.

Cannon, R.W. and F.L.  Knopf.   1984.   Species composition of  a willow community relative to seasonal grazing
histories in Colorado.  Southwest. Nat.  29:234-237.

Carothers, S.W.  1977.  Importance, preservation, and management  of riparian habitat: an  overview,  pp. 2-4 In:
R.R. Johnson, C.D.  Ziebell,  D.R.  Patton,  P.F. Ffolliott,  R.H.  Hamre (tech. coords.).  Riparian Ecosystems and
Their Management:  Reconciling  Conflicting Uses.  Gen. Tech.  Rep.  RM-120,  USDA  Forest Serv.,  Fort Collins,
Colorado.

Carothers, S.W.,  R.R.  Johnson, and  S.W.  Aitchison.   1974.  Population  structure and social  organization of
Southwestern riparian birds.  Amer. Zool. 14:97-108.

Carothers, S.W. and R.R. Johnson.  1975.  Water management  practices and their effects on  nongame birds in range
habitats,  pp. 210-222 In:  D.R.  Smith (tech. coord.).  Proceedings on  Management  of Forest and Range Habitats
for Nongame Birds.  Gen.  Tech. Rep. WO-1.  USDA Forest  Serv.,  Washington, D.C.

Carter, M.  and K.  Barker.    1991.   An interactive  database  for setting  conservation priorities  for western
neotropical migrants.  Colorado Bird Observatory,  Brighton,  Colorado.

Christiansen, J.E.  and J.B.  Low.   1970.   Water Requirements  of Waterfowl Marshlands in Northern Utah.  Publ.
69-12.  Utah Div. Fish & Game, Salt Lake City.

Colorado Division of Wildlife (CDU).  1984.  Colorado River Basin Salinity Control Project, Grand Valley Unit,
Stage One.  Wildlife Monitoring,  Final Report 1984.  Colorado  Division of Wildlife, Grand Junction, Colorado.

Conine, K.H.,  B.W.  Anderson,  R.D. Ohmart, and J.F. Drake.   1978.  Responses of riparian species to agricultural
habitat conversions,  pp. 248-263 In: R.R. Johnson and J.F. McCormick (tech.  coord.), Strategies for Protection
and Management of FLoodplain, Wetlands and Other  Riparian  Ecosystems.  USDA Forest  Serv. Gen. Tech. Rep. WO-12,
Washington, D.C.

Cook, A.G.  1984.  Birds  of  the desert region of Uintah County,  Utah.   Great Basin  Nat. 44:584-620.

Cooper, D.J. and  C. Severn.  1992.  Wetlands  of the San Luis Valley,  Colorado:  An Ecological Study and Analysis
of the Hydrotogic  Regime, Soil Chemistry, Vegetation,  and the Potential Effects of a  Water  Table Drawdown.
Report to Colorado Division of Wildlife,  Denver.



                                                    59

-------
 Copelin, F.F.  1953.  Waterfowl inventory on small flood prevention reservoirs in western Oklahoma.  Proc. Okla.
 Acad. Sci. 42:260-263.

 Cowan, W.F.   1982.  Waterfowl production on zero tillage farms.  Wildl. Soc. Bull. 10:305-308.

 Crane, M.P.,  M.J.  Pucherelli, and S.K.  McCall.   1986.   Determining impacted wildlife resources in the Grand
 Valley by remote sensing techniques,   pp. 51-57  In: R.D. Comer (ed.).  Issues and  Technology in the Management
 of  Impacted Western Wildlife.  Thorne Ecological Inst., Boulder, Colorado.

 Croonquist, M.J.  and R.P. Brooks.   1993.   Effects  of  habitat disturbance on bird  communities in riparian
 corridors.  J. Soil Water Conserv. 48:65-70.

 Crouch, G.L.   1961.  Wildlife Populations  and Habitat Conditions on Grazed  and Ungrazed Bottomlands in Logan
 County, Colorado.  M.S. thesis, Colorado St. Univ., Fort Collins.

 Dahlgren, R.B. and C.E.  Korschgen.  1992.  Human Disturbances of Waterfowl: An Annotated Bibliography.  Resour.
 Publ. 188.  U.S. Fish & Wildl. Serv., Washington, D.C.

 Dalton, L.B., R.S. Smith, and R.B. Wilson.   1978.   Inventory of Terrestrial  Vertebrate Wildlife  in Carbon and
 Emery Counties of Utah that Inhabit or Utilize Irrigated Farmland, Potentially Irrigable RangeI and,  and Wetland
 in  the Price-San Rafael  River Drainages of  the Colorado  River.   Div. Wildl.  Resour., Utah Dept. Nat. Resour.,
 Salt Lake City.

 Dalton, L.B.,  J.S.  Price, and L.A. Romin. 1990.  Fauna of Southeastern Utah and Life Requisites  Regarding Their
 Ecosystems.  Publ. No. 90-11.  Div. Wildlife Resour., Utah Dept. Nat.  Resour., Salt Lake City.

 Dane11, K.  and K. Sjoberg.  1982.   Successional patterns of  plants,  invertebrates, and ducks in a man-made lake.
 J.  Appl. Ecol. 19:395-409.

 Debano, L.F. and L.J. Schmidt.   1990.   Potential  for enhancing riparian habitats in the southwestern United
 States with watershed practices.  Forest Ecol. & Manage.  33/34:385-403.

 Dexter, C.   1992.   Birds of the  Colorado  River floodplain wetland, Clifton, Colorado.   (Computer database
 containing weekly counts).

 Dexter, C. and R.  Lavad.   1992.   Bird check list for the Grand Valley and  surrounding high country of Mesa
 County, Colorado.  Grand Valley Audubon Society, Grand Junction, Colorado.

 Dobkin, D.S.  and B.A. Wilcox.   1986.   Analysis of  natural  forest fragments: riparian  birds  in the Toiyabe
 Mountains,  Nevada,  pp.  293-299 In: J. Verner, M.L. Morrison , and C.J.  Ralph.  Wildlife 2000: Modeling Habitat
 Relationships of Terrestrial  Vertebrates.  Univ. Wisconsin Press,  Madison, Wisconsin.

 Driver, E.A.   1977.  Chironomid communities in small prairie ponds: some characteristics and  controls.  Freshw.
 Biol. 7:121-133.

 Duebbert, H.F. and  H.A.  Kantrud.   1987.  Use of no-till winter wheat by nesting ducks in North Dakota.  J. Soil
 Water Conserv. 42:50-53.

 Duebbert, H.  F.,  and  A.  M.  Frank.  1984.  Value of prairie wetlands to duck broods. Wildl. Soc. Bull. 12:27-34.

 Duebbert, H.  F.,  and J. T. Lokemoen. 1976. Duck nesting in fields of undisturbed grass-legume cover.  J. Wildl.
 Manage. 40:39-49.

 Dwyer,  T.J.  1970.  Waterfowl  breeding habitat in agricultural and nonagricultural  land in Manitoba.  J. Wildl.
 Manage. 34:130-136.

 Earl, J.P.   1950.  Production of mallards on irrigated land in the Sacramento Valley,  California.   J.  Wildl.
 Manage. 14:332-342.

 Ebert,  T.A.  and M.L.  Balko.  1987.  Temporary pools as islands  in space  and time:  the biota  of vernal pools in
 San Diego,  Southern California.   Archiv fur Hydrobiologie  110:101-123.

 Ecology Consultants,  Inc.   1976.   Final Report on Flora and Terrestrial  Vertebrate Studies of the Grand Valley
Unit.   U.S.  Bureau of Reclamation, Grand Junction,  Colorado.

 Edwards,  C.A.  and J.F. Lofty.  1975.   The influence of cultivation on animal populations,  pp. 399-408 In:  J.
Vanek (ed.).  Progress in Soil  Zoology.  Academia Publ.,  Prague.

 Ehrlich,  P.R., D.S. Dobkin, D.  Wheye.  1988.  The Birder's Handbook: A  Field Guide to the Natural  History of


                                                    60

-------
North American Birds.  Simon & Schuster Inc., New York.  785 pp.

Euliss, N.H., R.H.  Jarvis,  and D.S. GUmer.  1991.  Standing  crops  and ecology of aquatic invertebrates  in
agricultural drain water ponds in California.  Wetlands 11:179-190.

Evans, R.D. and  C.W. Wolfe, Jr.  1967.  Waterfowl production in the Rainwater Basin area of Nebraska.  J. Wildl.
Manage. 31:788-794.

Evans, K.E. and  R.R. Kerbs.  1977.  Avian use of  livestock watering poinds in western South Dakota.  Gen. Tech.
Rep. RH-35.  USDA Forest Serv., St. Paul, Minnesota.

Faanes, C.A.  1982.  Avian Use of Sheyenne Lake and Associated Habitats in Central North Dakota.  Resour. Publ.
144.  U.S. Fish & Wildl. Serv., Washington, D.C.

Faber, P.M., E.  Keller, A. Sands,  and B.M.  Massey.   1989.   The Ecology of Riparian Habitats of the Southern
California Coastal Region: A Community Profile.   Biol.  Rep. 85(7.27).  U.S. Fish & Wildl. Serv., Washington,
D.C.

Fannin, T.E., M. Parker, and T.J.  Maret.   1985.  Multiple regression  analysis for evaluating non-point source
contributions to  water quality in  the Green River, Wyoming,   pp.  201-205  In: R.R.  Johnson  et  al. (eds.).
Riparian Ecosystems and Their Management.   Gen.  Tech. Rep.  RM-120, USDA  Forest  Serv.,  Ft. Collins, Colorado.

Flake, L.D., G.L.  Peterson, and W.L. Tucker.  1977.   Habitat relationships of breeding waterfowl  of  stock ponds
in northwestern South Dakota.  Proc. South Dakota Acad. Sci.  56:135-151.

Fraser, D.G., J.W. Doran,  W.W.  Sahs, and G.W. Lesoing.  1988,   Soil microbial populations  and activities under
conventional and organic management.  J.  Envir.  dual. 17:585-590.

Fritzell,  K.E.  1975.   Effects of agricultural burning  on nesting waterfowl.   Can.  Field-Nat.  89:27-37.

Gaines, D.A.  1974.  A new look at the nesting riparian avifauna of the  Sacramento Valley, California.  West.
Birds 5:61-80.

Gates, J.M.  1965.  Duck nesting and production  on Wisconsin farmlands.   J.  Wildl.  Manage.  29:515-523.

Gatz, T.A., G. Brucker, W. Otto, S. Rothe,  and D.  Orthmeyer.  1984.  Wildlife use of irrigation canal rights-of-
way  in the  prairie  pothole  region of  North Dakota.   pp.  630-639 In:  Proceedings of  the Symposium on
Environmental Concerns in Rights-of-Way Management.

Gersberg,  R.M.,  B.V. Elkins, and C.R. Goldman.  1983.  Nitrogen removal  inartificial  wetlands.  Water Resour.
Res. 17:1009-1014.

Glahn, J.F.  1974.  Study of breeding rails with recorded calls  in north-central Colorado.  Wilson Bull. 86:206-
214.

Glover, F.   1956.  Nesting  and  production  of  the  blue-winged teal in northwest  Iowa.    J.  Wildl. Manage.
20:28-46.

Golet, F.C.  1973.  Classification and Evaluation  of Freshwater Wetlands as Wildlife  Habitat in the Glaciated
Northeast.  PhD  dissertation,  Univ. Massachusetts,  Amherst.

Gorenzal,  W.P.,  R.A. Ryder, and C.E. Braun.   1981.   American coot response to habitat change on a Colorado
marsh.  Southwestern Nat.  26:59-65.

Groffman,  P.M.,  J.M. Tiedje, D. L. Mokma,  and S. Simkins.   1992.  Regional scale analysis of denitrification
in north temperate forest soils.   Landscape Ecol.  7:45-53.

Groffman,  P.M. and J.M.  Tiedje.  1989a.  Denitrification in north temperate forest soils:  Spatial and temporal
patterns at the  landscape and seasonal  scales.  Soil Biol.  Biochem.  21:613-620.

Groffman,  P.M. and J.M. Tiedje.  1989b.  Denitrification in north temperate forest soils: Relationships between
denitrification  and environmental  factors  at the landscape  scale.  Soil  Biol.  Biochem. 21:621-626.

Grue, C.E., M.W. Tome,  G.A.  Swanson, S.M.  Borthwick,  and L.R. DeWeese.   1988.  Agricultural chemicals and the
quality of prairie pothole wetlands for adult and juvenile waterfowl: What are the concerns?  p. 55-64 In: P.J.
Stuber (coord.).  Proc.  Nat.  Sympos.  on  the Protection of  Wetlands from Agricultural Impacts.   Biol.  Rep.
88(16).  U.S. Fish & Wildl.  Serv., Fort  Collins,  Colorado.

Guthery,  F.S. and  F.A.  Stormer.  1984.   Wildlife  management  scenarios  for playa  management.  Wildl. Soc.  Bull.


                                                    61

-------
12:227-234.

Guthery, F.S.  , J.M. Pates,  and  F.A.  Stormer.   1982.   Characterization of playas of the north-central Llano
Estacado in Texas.  Trans. N. Am. Wildl. Nat. Resour. Conf. 47:516-527.

Guthery, F.S., S.M. Obenberger,  and F.A. Stormer.   1984.   Predictors  of site use by ducks on the Texas High
Plains.  Wildl. Soc. Bull. 12:35-40.

Gutzwiler, K.J. and S.H. Anderson.  1992.   Interception of  moving organisms:  influences of patch shape, size,
and orientation on community structure.  Landscape Ecol. 6:293-303.

Gutzwiler, K.J. and S.H. Anderson.  1987a.   Multiscale  associations between cavity-nest ing birds and features
of Wyoming streamside woodlands.   Condor 89:534-548.

Gutzwiler, K.J. and S.H. Anderson. 1987b.  Short-term dynamics of cavity-nesting  bird communities  in disjunct
floodplain habitats.  Condor 89:710-720.

Hammer, U.T.  1981.  Primary production in saline lakes.  Hydrobiologia 81:47-57.

Hands,  H.M.,  M.R.  Ryan, and  J.W. Smith.    1991.   Migrant shorebird  use of marsh, moist-soil,  and flooded
agricultural habitats.   Wildl. Soc. Bull.  19:457-464.

Harris, S.W.  1954. An  ecological  study of the waterfowl of the Potholes Area, Grant County, Washington.  Am.
Midi. Nat. 52:403-432.

Harris, H.J., M.S. Hilligan,  and  G.A.  Fewless.   1983.   Diversity: Quantification  and ecological evaluation in
freshwater marshes.  Biol. Conserv. 27:99-110.

Hayes, R.O. and R.L. Nielsen.  1978.  Irrigation management service and mosquito control.  ASCE J. Irriga. &
Drainage Div. 104(IR2):153-163,

Hayward, C.L.  1967.  Birds of the Upper Colorado River  Basin.  Biological Series Vol. 9, No.  2.  Brigham Young
University, Provo, Utah.

Heath, R.C.  1982.  Classification of  groundwater systems of the United States.   Ground Water 20:393-401.

Heitmeyer, M.E. and P.A. Vohs.   1984.  Distribution and habitat use of waterfowl wintering in Oklahoma.   J.
Wildl. Manage. 48:51-62.

Henein, K. and G.  Merriam.  1990.  The elements of connectivity where corridor quality is variable.  Landscape
Ecol. 4:157-170.

Henke, M.  and C.P.  Stone.  1978.  Value of riparian vegetation to avian populations along the Sacramento River
system.   In:  R.R.  Johnson and J.F. McCormick  (tech.  coord.).   Strategies for Protection  and Management  of
Floodplain Wetlands and  Other Riparian Ecosystems.  Gen. Tech. Rep. WO-12.  USDA Forest Serv., Washington, D.C.

Henriksen, C. and  L. Hall.  1992.  CIS measures water use in the arid west.  Geo Info Systems July/August,  pp.
63-67.

Higgins, K.F.  1977.  Duck nesting in intensively farmed areas of North Dakota.  J. Wildl. Manage. 41:232-242.

Hobaugh, W.C. and  J.G. Teer.   1981.  Waterfowl  use characteristics of flood-prevent ion lakes in north-central
Texas.  J. Wildl.  Manage. 45:16-26.

Hoffman, R.J.,  R.J.  Hallock, T.G.  Rowe,  M.S.  Lico,  H.L.  Burge,  and  S.P.  Thompson.  1990.   Reconnaissance
investigation of water  quality,  bottom  sediment,  and biota associated with  irrigation drainage  in and near
Stillwater Wildlife Management Area,   Churchill  County, Nevada,  1986-1987.    U.S.  Geological Survey Water
Resources Investigations Report 89-4105.   Carson City,  Nevada.

Hooper, R.M.   1962.  Relationships of Certain Characteristics of Small  Wetlands and Waterfowl  Abundance  in
Northeastern Colorado.   M.S.  thesis, Colorado State Univ.,  Fort Collins.   101 pp.

Hopper, R.M.  1972. Waterfowl use in  relation to size and cost of  potholes.   J.  Wildl. Manage. 36:459-468.

Hoy, M.D.   1987.   Waterfowl  Use of a Northcentral  Texas Reservoir.   M.S. thesis, Texas A&M  Univ.,  College
Station.

Hudson, M.S.  1983. Waterfowl production on three age-classes of  stock ponds in Montana.   J. Wildl.  Manage.
47:112-117.


                                                    62

-------
Hunter, W.C., R.D. Ohmart, and B.W. Anderson.  1987.  Status of breeding riparian obligate birds in southwestern
riverine systems.  Western Birds 18:10-18.

Hunter, W.C., B.W. Anderson, and R.D. Ohmart.  1985.  Summer avian community composition of Tamarix habitats
in three southwestern desert riparian systems,  pp. 128-134 In: R.R. Johnson, C.D.Ziebell, D.R. Patton, P.P.
Ffolliott, R.H.  Hamre (tech. coords.). Riparian Ecosystems and their Management:  Reconciling Conflicting Uses.
Gen. Tech. Rep. RM-120, USDA Forest Serv., Fort Collins, Colorado.

Hussey, M.R., Q.D.  Skinner,  J.C. Adams, and A.J.  Harvey.   1985.   Denitrification and  bacterial  numbers in
riparian soils of a Wyoming mountain watershed.  J. Range Manage.  38(6):492-496.

Johnsgard, P.A.  1956.  Effects of water fluctuation and vegetation change on bird populations, particularly
waterfowl.  Ecology 37:689-701.

Johnson, B.R. and R.A. Ryder.   1977.  Breeding densities  and migration  periods of common snipe in Colorado.
Wilson Bull. 89:116-121.

Joyner, D.E.   1980.   Influence of invertebrates on pond  selection  by ducks in Ontario.   J. Wildl. Manage.
44:700-705.

Kadlec, J.A. and L.M.  Smith.  1984.  Marsh plant establishment  on newly flooded  salt flats.  Wildl. Soc. Bull.
12:388-394.

Kaiser, M.S. and E.K. Fritzell.   1984.   Effects  of river  recreationists on green-backed heron behavior.  J.
Wildl. Manage. 48:561-568.

Kaminski, R.M. and H.H. Prince.  1981.  Dabbling duck and aquatic  macroinvertebrate responses to manipulated
wetland habitat.  J. Wildl. Manage. 45:1-15.

Kantrud, H.A.   1981.  Grazing  intensity effects  on the  breeding avifauna of  North Dakota native grasslands.
Can. Field-Nat. 95:404-417.

Kantrud, H.A.   1986.   Effects of Vegetation Manipulation on  Breeding  Waterfowl  in Prairie Wetlands  --  A
Literature Review.  Fish  and Wildlife Tech.  Rep.  No. 3,  U.S. Fish  &  Wildl. Serv.,  Washington, D.C.

Kantrud, H.A.   1990.   Sago  Pondweed:  A Literature Review.   Resour.  Publ.  176,  U.S.  Fish  & Wildl.  Serv.,
Washington, D.C.

Kauskik, I.K.   1963.   The Influence of  Salinity  on the  Growth  and Rejuvenation of Marsh  Plants.   Ph.D.
dissertation, Utah State  Univ., Logan, UT.  123 pp.

Kingery, H.E. (ed.).  1988.  Colorado Bird Distribution Latilong Study.   Revised Edition.  Colorado Division
of Wildlife, Denver.

Knopf, F.L.  1985.  Significance of riparian vegetation to breeding birds across  an  altitudinal  dine, pp. 105-
111.   In:  R.R.  Johnson,  C.D.  Ziebell,  D.R.  Patton,  P.F.  Ffolliott,  R.H. Hamre  (tech.  coords.).   Riparian
Ecosystems and Their Management: Reconciling Conflicting  Uses.  Gen. Tech. Rep. RM-120.   USDA Forest Serv., Fort
Collins, Colorado.

Knopf, F.L.  1986.  Changing landscapes  and  the cosmopolitism of the eastern Colorado avifauna.  Wildl. Soc.
Bull. 14(2):132-142.

Knopf, F.L.,  J.A. Sedgwick, and R.W. Cannon.  1988.  Guild structure of a riparian avifauna relative to seasonal
cattle grazing.  J.  Wildl. Manage. 52:280-290.

Kreis, R.D. and W.C. Johnson.  1968.  The response of macrobenthos to irrigation  return water.   J. Water Pollu.
Contr. Fed. 40:1614-1621.

Krueper, D.J.   1992.  Birds  and habitat in  the San Pedro  Riparian National  Conservation Area.   Partners in
Flight 2(1):10.

Kreil, K.L. and R.D. Crawford.   1986.  Evaluation of Constructed Ponds  as a Means of Replacing Natural Wetland
Habitat Affected by  Highway Projects in North  Dakota - Phase II.  Final Rep. FHWA-ND-RD-(2)-81A,  Dept. of Biol.,
Univ. of North Dakota,  Grand Forks, North Dakota.

LaGrange, T.G.  and J.J. Dinsmore.  1989.   Habitat  use by mallards during spring migration  through central Iowa.
J. Wildl. Manage. 53:1076-1081.

Langlois, D. (ed.).   1978.   Colorado  Reptile  and  Amphibian  Distribution  Latilong Study.  Colorado Division of


                                                    63

-------
Wildlife, Denver.

Lathwell, H.F. Mulligan, and O.R. Bouldin.   1969.   Chemical properties, physical properties, and plant growth
in twenty artificial wildlife marshes.  N.Y. Fish and Game J. 16:158-183.

Lathwell, D.J., J.D.R. Bouldin, and E.A. Gayetter.  1973.  Growth and chemical composition of aquatic plants
in twenty artificial marshes.  N.Y. Fish and Game J. 20:108-128.

Lemme,  T.H.    1988.   Denitrification and  Tillage Relationships on  Two Eastern  South  Dakota Soils.   Ph.D
dissertation, South Dakota St. Univ., Brookings.

Lewis, G.L. and R.J. Bockelman.  1988.  Wetland impacts of large scale center-pivot irrigation in Nebraska's
Sandhills: hydrologic and habitat  issues,   pp.  30-37 In : P.J. Stuber (coord.).   Proc.  Nat.  Sympos. on the
Protection of Wetlands from Agricultural  Impacts.  Biol. Rep.  88(16).   U.S.  Fish &  Wildl. Serv., Fort Collins,
Colorado.

Lewke, R.E.  1975.  Pre-impoundment Study of Vertebrate  Populations and Riparian Habitat Behind Lower Granite
Dam on  the Snake River  in  Southeastern Washington.   Ph.D.  dissertation,  Washington State  Univ.,  Pullman,
Washington.

Linn, D.M. and J.W. Doran.   1984.   Aerobic  and  anaerobic microbial populations  in no-till and plowed soils.
Soil Sci. Soc. Am. J. 48:794-799.

Logan, T.H.  1975.  Characteristics of Small  Impoundments in Western Oklahoma,  Their Value as Waterfowl Habitat
and Potential for Management.  M.S. thesis,  Oklahoma St. Univ., Stillwater.

Lokemoen, J.T.  1973.  Waterfowl production  on stock-watering poinds in the  Northern Plains.  J. Range Manage.
26:179-184.

Loken, L.G.   1991.   Wetland Soil  Characteristics  of  Basins  in Closed Groundwater Catchment  Systems.   M.S.
thesis. North Dakota St. Univ., Fargo.

Loveland, D.G. and I.A.  Ungar.  1983.  The effect of nitrogen  fertilization  on the  production of halophytes in
an inland salt marsh.  Am. Midi.  Nat.  109(2):346-354.

Ludwick, A.E., C.B.  Rumburg, and  E.G.  Siemer. 1978.   Nitrogen  sources for  hay production on flooded meadows.
Soil Sci. Soc. Am. J. 42:509-512.

Matter, W.J.  and  R.W. Mannan.   1988.  Sand and  Gravel  Pits  as Fish  and Wildlife Habitat  in the Southwest.
Resour. Publ. 171, U.S.  Fish & Wildl. Serv., Washington, D.C.  11  pp.

McCoy, C.C.   1962.    Herpetofaunal dispersal in  the  Grand Valley of  Colorado.    J.  Colorado-Wyoming  Acad.
Sci.4:41-42.

McKnight, D.E. and J.B.  Low.  1969.  Factors  affecting  waterfowl production of  a spring-fed  salt marsh in Utah.
Trans. N. Am. Wildl. Nat. Resour. Conf.  34:307-314.

Medin, D.E. and W.P.  Clary.  1989.   Small  Mammal  Populations  in  a Grazed and Ungrazed Riparian Habitat in
Nevada.  Res. Pap. INT-413,  USDA  Forest  Serv., Ogden,  Utah.   6  pp.

Milligan, D.A.  1985.  The Ecology  of Avian Use of Urban Freshwater Wetlands in King County, Washington.  M.S.
thesis, Univ. Washington, Seattle.

Milne, M.M. and D.W. Young.  1989.  The impact of stockwatering ponds (stockponds) on runoff from large Arizona
watersheds.  Water Resour. Bull.  25:165-173.

Morrison, M.L., K.A. With, and I.C. Timossi.   1986.  The  structure of a forest  bird  community during summer and
winter.  WiIson Bull.  98:214-130.

Morrison, M.L., B.C.  Marcot,  and R. W. Mannan.  1992.   Wildlife-Habitat Relationships.  Univ. Wisconsin Press,
Madison, Wisconsin.   243 pp.

Murkin, H.R. and J.A. Kadlec.  1986b.  Relationships  between waterfowl  and macroinvertebrate densities in a
northern prairie marsh.   J.  Wildl. Manage.  50:212-217.

National Academy  of  Sciences.   1974.   Nutrients and Toxic  Substances  in  Water  for  Livestock  and  Poultry.
National Academy of  Sciences, Washington, D.C.

Neely, R.K. and J. Baker.  1989.  Nitrogen and phosphorus dynamics and the fate of agricultural  runoff,  p. 92-


                                                    64

-------
131 In: A.G. van der Valk (ed.).  Northern Prairie Wetlands.  Iowa St. Univ. Press,
Ames.

Nelson, N.F.  1953.  Marsh development and management on artificial impoundments in Utah.  Proc. Conf. Western
Assoc. State Game & Fish Commissioners 32:207-209.

Nelson, N.F.  1954.  Factors in the development and restoration of waterfowl habitat at Ogden Bay Refuge, Weber
County, Utah.  Utah State Dept. Fish & Game, Pub. # 6.  87 pp.

Ohmart, R.D.,  B.W.  Anderson,  and  W.C.  Hunter.   1985.   Influence  of agriculture on  waterbird,  wader,  and
shorebird use along the lower Colorado River,  pp. 123-127 In:  R.R. Johnson, C.D. Ziebell, D.R. Patton, P.P.
Ffolliott, R.H. Hamre (tech. coords.).  Riparian Ecosystems and Their Management: Reconciling Conflicting Uses.
Gen. Tech. Rep. RM-120, USDA Forest Serv.,  Fort Collins, Colorado.

Opdam, P., G. Rijsdijk, and  F. Hustings.  1985.  Bird communities in small  woods in an agricultural landscape:
effects of area and isolation.  Biol. Conserv. 34:333-352.

Parkin, T.B. and  J.J.  Meisinger.   1989.   Denitrification below the crop  rooting zone as influenced by soil
tillage.  J. Envir. Qual. 18:12-16.

Partners in Flight Information and Education Working Group.  1991 Annual Report.  National Fish and Wildlife
Foundation, Washington, D.C.

Payne, N.F.  1992.  Techniques of Wildlife Habitat Management of Wetlands.  McGraw-Hill,  Inc.   549 pp.

Peterson,  T.L.  and J.A. Cooper.  1991.' Impacts of center pivot irrigation systems on birds  in prairie wetlands.
J. Wildl.  Manage.  51:238-247.

Piest, L.A. and L.K.  Sowls.  1985.  Breeding duck use of a sewage marsh in  Arizona.  J. Wildl. Manage. 49:580-
585.

Ponce, V.M. and D.S. Lindquist.  1990.  Management of baseflow augmentation: a review.  Water  Resources Bulletin
26:259-268.

Pressey, R.L.  and A.O. Nicholls.   1989.   Efficiency  in conservation evaluation: scoring versus iterative
approaches.  Biol. Conserv.  50:199-218.

Prose, B.L.  1985.  Habitat  Suitability  Index Models:  Belted  Kingfisher.   Biol. Rep.  82 (10.87).  U.S. Fish &
Wildl. Serv., Fort Collins,  Colorado.

Provost, M.W.  1947.   Nesting  of birds in the marshes of northwest Iowa. Amer.  Midi.  Nat. 38:485-503.

Rawson, D.S. and J.E. Moore.  1944.  The saline lakes of Saskatchewan.  Can. J. Res.  Ser. D 22:141-201.

Rector, C.D.,  E.W.  Mustard,  and  J.T.  Windell.   1979.   Lower  Gunnison  River Basin Wetland  Inventory  and
Evaluation.  USDA Soil Conservation Serv.,  Denver, Colorado.

Rice,  C.W.  and M.S. Smith.  1982.  Denitrification in no-till  and plowed soils.  Soil Sci.  Soc. Am. J. 46:1168-
1173.

Rice,   J.,  R.D.  Ohmart, and B.W.  Anderson.    1983.   Habitat selection attributes of an avian  community:  a
discriminant analysis investigation.   Ecol.  Monogr. 53:263-290.

Ridd,  M.K. and J.G. Christensen.   1980.  Uinta  Basin Wetland/Land Use Study.   Center for Remote Sensing  and
Cartography, Univ. Utah, Salt  Lake City.

Robinson,  G.G.W.   1971.  Vegetation  and  Physical Factors  Influencing  Waterfowl Production.    M.S.  thesis,
Colorado St. Univ., Ft. Collins.

Rossiter,  J.A. and R.D.  Crawford.   1981.   Evaluation  of Constructed  Ponds as a  Means of  Replacing Natural
Wetland Habitat Affected by  Highway Projects in North Dakota.  State Study  (2)-79(A),  Biol. Dept., Univ. North
Dakota, Grand Forks,  North Dakota.

Rumble, M.A. and  L.D.  Flake.   1983.   Management  considerations  to enhance use of stock ponds  by waterfowl
broods.  J. Range Manage.  36:691-694.

Rumburg, C.B.   1969.  Yield and concentration of meadow hay fertilized with  three N sources.  Agron. J. 61:824-
825.
                                                    65

-------
Ruwalt, J.J., L.D. Flake,  and J.M.  Gates.  1979.  Waterfowl pair use of natural  and man-made wetlands  in South
Dakota.  J. Uildl. Manage. 43:375-383.

Sangster, M.E.  1977.  Spring waterfowl migration in the Uinta Basin of northeastern Utah.  Great Basin Nat.
37:274-278.

Samson, F.B. and  F.L. Knopf.  1982.   In  search  of  a diversity ethic for wildlife management.   Trans. N. Am.
Wildl. Resour. Conf. 47:421-431.

Sather-Blair, S. and R.L.  Linder.   1980.  Pheasant use of South Dakota wetlands during the winter.  Proc. South
Dakota Acad. Sci. 59:147-155.

Scheffer, M., A.A. Achterberg, and B. Beltman.  1984.  Distribution of macroinvertebrates in a ditch in  relation
to the vegetation.  Freshw. Biol. 14:367-370.

Schimel, D.S., D.C.  Coleman,  and K.A. Norton.   1985.  Soil organic matter  dynamics in paired rangeIand and
cropland toposequences in North Dakota.  Geoderma 36:201-214.

Schroeder, R.L.   1982.  Habitat Suitability Index Models: Yellow-headed Blackbird.  FwS/OBS-82/10.26.  U. S.
Fish Wildl. Serv., Fort Collins, Colorado.

Schroeder, R.L. 1983a.  Habitat  Suitability Index Models:  Black-capped  Chickadee.  FWS/OBS-82/10.37.  U.S. Fish
& Wildl. Serv., Fort Collins, Colorado.

Schroeder, R.L.   1983b.  Habitat SuitabiIity Index Models: Downy Woodpecker.  FWS/OBS-82/10.38.  U.S. Fish &
Wildl. Serv., Fort Collins, Colorado.

Schroeder, R.L. 1986.  Habitat Suitability Index Models: Wi Idlife Species Richness in Shelterbelts.  Biol. Rep.
82 (10.128).  U.S. Fish & Wildt. Serv., Fort Collins, Colorado.

Schroeder, R.L. and  A.W.  Allen.   1992.  Assessment  of Habitat of Wildlife Communities  on  the Snake River,
Jackson, Wyoming.  Resour. Publ. 190, U.S. Fish & Wildl.  Serv.,  Washington,  D.C.

Schroeder, L.D., D.R. Anderson,  R.D.  Pospahala, G.W. Robinson,  and F.A. Glover.  1976.   Effects of early water
application on waterfowl production.  J.  Wildl.  Manage. 40:226-232.

Schultz, T.T. and W.C. Leininger.  1991.   Nongame wildlife communities  in grazed and ungrazed riparian sites.
Great Basin Nat. 51: 286-292.

Scott,  J.M.,  B.  Csuti, J.D.  Jacobi, and J.E.  Estes.    1987.   Species  richness:  a geographic approach  to
protecting future biological diversity.  BioScience 37:782-788.

Sedgwick, J.A. and F.L.  Knopf.  1986.  Cavity-nest ing birds and  the cavity-tree resource  in plains cottonwood
bottomlands.  J. Wildl. Manage.  50:247-252.

Sedgwick, J.A. and F.L. Knopf.   1987.  Breeding  bird response to cattle grazing  of  a cottonwood bottomland.
J. Wildl. Manage.  51:230-237.

Severn, C.  1992.  Distribution  of  Aquatic Insects Along a Hydrologic Gradient in the Russell Lakes Area, San
Luis Valley, Colorado.  M.S. thesis, Colorado School of Mines, Golden,  Colorado.

Short, H.   1985.  Habitat Suitability Index Models: Red-winged Blackbird.  FWS/OBS-82/10.95. U.S. Fish  & Uildl.
Serv., Fort Collins, Colorado.

Short, H. and R. Cooper.   1985.   Habitat  Suitability Index Models: Great Blue Heron.   FUS/OBS-82/10.26.  U.S.
Fish & Uildl. Serv., Fort Collins,  Colorado.

Smith, B.  1989.  Phosphorus Retention Functions and Interactions at the Chatfield Arboretum Wetlands.  M.S.
thesis, Colorado School of Mines, Golden, Colorado.

Smith, N.F.  1979.  Aquatic Inventory: McElmo Creek Project, Colorado.   Colorado  Div. Wildlife, Durango.

Smith, R.H.  1953.  A study  of  waterfowl production on artificial  reservoirs  in  eastern Montana.   J. Wildl.
Manage. 17:276-291.

Soil Conservation Service (SCS).   1987.   Big  Sandy River Unit,  Colorado  Salinity Control  Program,  Final
Environmental Impact Statement.   USDA Soil Conservation Serv.,  Casper,  Wyoming.

Soil Conservation Service (SCS).  1989.  Environmental  Impact  Statement for  On-farm Irrigation Improvements.


                                                     66

-------
McElmo Creek Unit Salinity Control Study.  USDA Soil Conservation Serv.,  Lakewood,  Colorado.

Soil Conservation Service (SCS).  1991.  Wildlife Habitat Monitoring and Evaluation: Lower Gunnison Salinity
Unit.  USDA Soil Conservation Serv., Montrose, Colorado.

Soil Conservation Service (SCS).  1992a.  Colorado SCS Wetland Evaluation Procedures  Worksheet.  September 1992
Version.  USDA Soil Conservation Serv., Denver, Colorado.

Soil Conservation  Service (SCS).   1992b.   Wetland and  Wildlife  Habitat  Tracking  System (WET).   USDA Soil
Conservation Serv., Cortez, Colorado.

Sommers, P.   1976a.   Fauna Inventory of the  Am mas -  La Plata Project Area.   Fort Lewis College, Durango,
Colorado.

Sommers, P.  1976b.  Fauna Inventory of the Paradox Valley Unit.  Fort Lewis College, Durango,  Colorado.

Sommers, P.  1977.  Fauna Inventory of the San Miguel  Project Area.  Fort  Lewis College,  Durango,  Colorado.

Somers, P.  1979.   Inventory of Terrestrial  Nongame Animals of the McElmo Creek Unit  Area, Colorado River Basin
Salinity Control Project.  Fort Lewis College, Durango, Colorado.

Somers, P.   1980.   McElmo Creek Fauna Analysis,  Nongame Inventory  Number 2.   Fort Lewis College, Durango,
Colorado.

Sousa, P.  1987.  Habitat Suitability Index Models:  Hairy Woodpecker.  FWS/OBS-82/10.146.  U.S. Fish & Wildl.
Serv., Fort Collins, Colorado.

Spencer, H.E.   1963.   Man-made Marshes for Maine  Waterfowl.   Bull.  No.  9.   Maine Dept.  Inland  Fisheries &
Wildl., Augusta.

Stabler, D.F.  1985.  Increasing summer flow in small streams through  management of riparian areas and adjacent
vegetation: a synthesis,   pp.  206-210 In: R.R.  Johnson,  C.D. Ziebell, D.R. Patton,  P.F. Ffolliott, R.H. Hamre
(tech. coords.).  Riparian Ecosystems and Their Management: Reconciling Conflicting  Uses.   Gen. Tech. Rep. RM-
120, USDA Forest Serv., Fort Collins, Colorado.

Stauffer, D.F. and L.B. Best.   1980.   Habitat  selection  by birds of riparian communities:  Evaluating effects
of habitat alterations.  J. Wildl.  Manage.  44:1-15.

Stengel, E.,  W.  Carduck, and C. Jebsen.  1987.  Evidence  for denitrification in artificial  wetlands,  p. 543-550
In: K.R. Reddy  and W.H.  Smith (eds.).   Aquatic Plants  for Water  Treatment and  Resource Recovery.   Magnolia
Publishing Inc.

Stephens, D.W., B. Waddell, and  J.B. Miller.   1988.  Reconnaissance  Investigation of Water  Quality,  Bottom
Sediment, and Biota Associated with Irrigation Drainage  in the Middle Green River  Basin.  Water-Resour. Invest.
Rep. 88-4011.  U.S. Geol. Surv.,  Washington, D.C.

Stevens, L.E.,  B.T.  Brown, J.M. Simpson and R.R.  Johnson.   1977.    The  importance of riparian  habitat to
migrating birds,  pp. 156-164 In: Johnson,  R.R. and D.A. Jones (tech. coord.).  Importance,  Preservation and
Management of Riparian Habitat: A Symposium..  Gen.  Tech. Rep.  RM-42.   USDA Forest Serv., Washington, D.C.

Stinnett, D.P. and D.A. Klebenow.  1986.  Habitat use of  irrigated lands by California quail. J. Wildl. Manage.
50:368-372.

Strong, T.R. and C.E. Bock.   1990.   Bird species distribution  patterns  in riparian habitats  in southeastern
Arizona.  Condor 92:866-885.

Szaro, R.C.  1991.  Wildlife communities of southwestern riparian ecosystems,   pp. 173-201  In: J.E. Rodiek and
E.G. Bolen (eds.).   Wildlife and Habitats in Managed Landscapes.   Island  Press,  Washington, D.C.

Szaro, R.C.  and M.D.  Jakle.   1985.   Avian  use of  a desert  riparian island and  its adjacent  scrub habitat.
Condor 87:511-519.

Szaro, R.C. and J.N. Rinne.   1988.   Ecosystem approach  to management of  Southwestern  riparian communities.
Trans. N. Am. Wildl.  Nat. Resour. Conf.  53:502-511.

Taylor, D.M.   1986.  Effects of cattle grazing on passerine birds nesting in riparian  habitat.  J. Range Manage.
39:254-258.

Taylor, D.M.  and C.H. Trost.   1992.   Use of  lakes  and reservoirs by migrating shorebirds in  Idaho.  Great Basin


                                                    67

-------
Nat. 52:179-184.

Thomas, J.W.  (tech.  ed.).   1979.   Wildlife Habitats in Managed  Forests:  The Blue Mountains  of  Oregon and
Washington.  Agric. Handbook No. 553, USDA Forest Serv.,  Portland, Oregon.

Timtns, B.V.  1981.  Animal  communities in three Victorian lakes of differing salinity.  Hydrobiotogia 81:181-
193.

Tolle, D.A.  1977.  A  survey of breeding and migratory birds southwest  of  Farmington, New Mexico.  Great Basin
Nat. 37:489-500.

Tubbs, A.A.  1980.  Riparian bird communities of the Great  Plains.   In: Proceedings on the Management of Western
Forests and Grasslands for Nongame Birds.  Gen.  Tech. Rep.  INT-86.  USDA  Forest  Serv.,  Washington, D.C.

Twomey, A.C.  1942.  The birds of the Uinta Basin, Utah.  Ann.  Carnegie Mus.  28:341-490.

U.S. Bureau of Land Management (USBLM).  1992.  Emlen transect data for riparian and other habitats of western
Colorado.   Data on file.  U.S.  Bureau of Land Management  Office,  Grand Junction,  Colorado.

U.S. Bureau  of  Reclamation (USBR).   1991.  Wetlands  Inventory  and Evaluation, Uncompahgre  Project System
Optimization/Joint Use, U.S. Bureau of Reclamation, Upper Colorado Region,  Grand Junction,  Colorado.

U.S. Bureau of Reclamation (USBR) and USOA Soil Conservation  Service (SCS).  1991.  Price - San Rafael Rivers
Unit, Utah.  Planning Report/Draft Environmental  Impact Statement.  U.S.  Bureau  of  Reclamation,  Provo, Utah.

U.S. Fish and Wildlife Service (USFWS).  1979.  A study of  macroinvertebrate populations on Arapaho National
Wildlife Refuge.  U.S. Fish & Wildl. Serv., Arapaho National  Wildlife  Refuge,  Waiden, Colorado.

U.S. Fish  and Wildlife Service (USFWS).  1980.  Habitat Evaluation Procedures (HEP) Manual  (102ESM).  U.S.  Fish
& Wildl. Serv.,  Washington, D.C.

U.S. Fish and Wildlife Service  (USFWS).   1984.  Fish  and Wildlife Coordination Act Report, Grand Valley Unit,
Colorado River Basin Salinity Control Project.  U.S.  Fish & Wildl.  Serv., Salt Lake City,  Utah.

U.S. Fish  and Wildlife Service  (USFWS).   1991.  Breeding Bird Survey: Summary of Trends, 1966-1991.  Patuxent
Research Laboratory, Laurel,  Maryland.

U.S. Fish and Wildlife Service (USFWS).  n.d.   Bird List, Seedskadee National  Wildlife  Refuge,  Wyoming.

U.S. Fish and Wildlife Service (USFWS).  n.d.   Bird List, Ouray National  Wildlife Refuge,  Utah.

Usher, M.B. (ed.).  1986.  Wildlife Conservation  Evaluation.  London:   Chapman and  Hall.

Utah Division of  Wildlife  Resources (UDWR).   1992.  Inventories of Neotropical  Birds  in Riparian Habitats:
Vernal, Westwater, Seep Ridge.   Utah Division of  Wildlife Resources, Salt Lake City, Utah.

Van Haveren, B.P.   1986.  Management of  instream  flows through runoff detention and retention.  Water Resour.
Bull. 22:399-404.

Van Home, B.  1983.  Density as a misleading indicator of  habitat quality.   J.  Wildl.  Manage.  47:893-901.

Van Home, B. and J.A. Wiens.   1991.   Forest Bird Habitat  Suitability Models  and the Development  of General
Habitat Models.   Fish and Wildlife Research Rep.  8.  U.S. Fish  &  Wildl. Serv., Washington,  D.C.

Vane-Wright, R.I., C.J. Humphries,  and P.H.  Williams.  1991.  What to protect? -  systematics and the agony of
choice.  Biol. Conserv. 55:235-254.

Vareschi,  E.  1987.   Saline lake ecosystems,  pp.  347-364 In: E.D. Schulze and H. Zwolfer (eds.).  Potentials
and Limitations of Ecosystem Analysis.  Ecological Studies,  Vol.  61.   Springer-Verlag,  New York.

Weinhold,  C.E. and A.G. van der Valk.  1988.  The impact of  duration of drainage on the seed banks of  northern
prairie wetlands.   Can. J.  Bot.  67:1878-1884.

Waller, M.W., B.H. Wingfield, and J.B.  Low.  1958.  Effects of habitat deterioration on bird populations  of a
small Utah marsh.   Condor 60:220-226.

Ueller, M.W., G.W. Kaufmann, and P.A. Vohs, Jr.  1991.  Evaluation of wetland development and waterbird response
at Elk Creek Wildlife Management Area, Lake Mills, Iowa,  1961 to  1990.  Wetlands  11:245-262.
                                                    68

-------
Welling, C.H., R.L.  Pederson, and A.G. van der Valk.   1988.  Recruitment from the seed bank and the development
of zonal ion of emergent vegetation during a drawdown in a prairie wetland.   J.  Ecol. 76:483-496.

Whitmore, R.C.  1975.  Habitat  ordination  of  passerine  birds  of  the Virgin River Valley,  southwestern Utah.
Wilson Bull. 87:65-74.

Whitmore, R.C.  1977.  Habitat partitioning in a community of  passerine birds.   Wilson Bull. 89:253-265.

Wiens, J.A.  1973.  Pattern and process in grassland bird conmunities.   Ecol. Monogr. 43:237-270.

Wilcove, D.S.   1985.  Nest predation in forest  tracts  and the decline of  migratory songbirds.  Ecology 66:1211-
1214.

Wilhelm, M., S.R.  Lawry,  and D.D. Hardy.  1988.  Creation and management of wetlands using municpal wastewater
in northern Arizona: A status  report,   pp.  154-159 In: J. Zelazny and J.S. Feierabend (eds.).  Proceedings of
Conference: Increasing Our Wetland Resources.   National  Wildlife  Federation, Washington, D.C.

Uinegar, H.H.   1977.  Camp Creek channel fencing: plant, wildlife,  soil, and water  response.   Rangemen's J.
4:10-12.

Uishart, R.A.,  J.W.  Nelson,  and P.J.  Caldwell.  1984.   Needs for  private  sector   wetland research:  Ducks
Unlimited's perspective.   Trans. N. Am. Wildl. Nat.  Resour. Conf.  49:297-303

Wood, W.W. and W.R. Osterkamp.  1984.   Recharge to the  Ogallala aquifer from playa  lake basins in the Llano
Estacado.  pp.337-349 In: G.A. Whetstone (ed.).  Proc.  Ogallala Aquifer Sympos.  II.   Texas Tech  University,
Lubbock.

Yahner, R.H.   1983.   Seasonal dynamics,  habitat  relationships,  and  management of avifauna in  farmstead
shelterbelts.   J.  Wildl.  Manage. 47:85-104.

Yeager, L.E. and H.M.  Swope.   1956.  Waterfowl production during wet and dry years in north-central Colorado.
J. Wildl. Manage.  20:442-446.
                                                    69

-------
Appendix A.  Relative abundance, by subregion, of birds that regularly breed in lowland riparian and wetland
habitats of the Colorado Plateau.

Species are listed in phylogenetic order. Codes are reproduced from the original information sources, which
seldom define the relative terms, and are as follows: A= abundant, C= common, F= fairly common, U=
uncommon.  A blank means the species does not regularly occur in, and/or is not dependent on, wetlands and
riparian habitats of the specified subregion during its breeding period.  Asterisks (*) in the Utah column
indicate the species was reported specifically from irrigated wetlands of the Price-San Rafael salinity control
area (USER and SCS 1991).

Information for the Grand Valley is mostly from Dexter and Lavad (1992) and secondarily from Andrews and
Righter (1992) and Dexter (1992).  The Grand Valley information is probably the most accurate because of
the relatively high intensity of coverage in this subregion. No similar information was available for the Lower
Gunnison subregion, but bird abundance can probably be assumed to be identical to the nearby Grand Valley
area. Information for the Cortez subregion is mostly from Sommers 1979,1980, and secondarily from Andrews
and Righter (1992).  The Cortez list, although based on surveys of irrigated wetlands  and probably quite
complete, does not discriminate relative abundance as finely as the Grand Valley list. The Utah and Wyoming
lists also do not discriminate well, categorizing most species only as common  or uncommon.  The  Utah
information is mainly derived from the  Ouray National Wildlife Refuge list  (USFWS n.d.).  Although this
refuge contains wetlands and is in the same subregion, most irrigated wetlands of the subregion are probably
smaller and their avifauna has not  been inventoried.  Other sources for the Utah list were Twomey  1942,
Hayward 1967, Behle 1981, Cook  1984, Boschen 1992, and Dalton et al. 1978,1990.  The Wyoming subregion
list is probably the least comprehensive and accurate, because few birders have visited the Big Sandy area. The
information is mainly from the bird list  of the Seedskadee National Wildlife Refuge (USFWS n.d.), located
about 30 miles southwest of the Big Sandy  area and containing somewhat different habitat.

    Common Name                   Grand Valley,  CO  Cortez, CO        Utah             Wyoming

    PIED-BILLED  GREBE                             C                C                C
    AMERICAN BITTERN                              U                                U
    GREAT BLUE HERON              C               C                C                C
    BLACK-CROWNED NIGHT-HERON                      C                C                U
    WHITE-FACED  IBIS                              U
    CANADA GOOSE                 C               C                C                C
    WOOD DUCK                    U
    GREEN-WINGED TEAL             F               U                C                C
    MALLARD                      C               C                C                A
    NORTHERN PINTAIL                              U                C                C
    CINNAMON TEAL                 U               C                C                C
    NORTHERN SHOVELER                             U                                C
    GADWALL                                      U                C                C
    RUDDY DUCK                                   U                C                C
    TURKEY VULTURE                FCC
    NORTHERN HARRIER                              C                C                C
    RED-TAILED HAWK               F               C                C                C
    AMERICAN KESTREL              C               C                C                C
    RING-NECKED  PHEASANT           FCC
    GAMBEL'S QUAIL                F               C
    VIRGINIA RAIL                 U               C                C
    SORA                         U               C                C                U
    AMERICAN COOT                 U               C                C                C
    KILLDEER                     C               C                C                C
    SPOTTED SANDPIPER             F               C                U                C
    COMMON SNIPE                 F               C                U                C
    WILSON'S PHALAROPE                            U                C                U
                                               70

-------
Cannon Name                    Grand Valley,  CO  Cortez,  CO        Utah              Wyoming
BAUD-TAILED PIGEON
MOURNING DOVE
BARN OWL
WESTERN SCREECH-OWL
GREAT HORNED OWL
LONG -EARED OWL
COMMON NIGHTHAWK
BLACK-CHINNED HUMMINGBIRD
BROAD-TAILED HUMMINGBIRD
BELTED KINGFISHER
LEWIS' WOODPECKER
DOWNY WOODPECKER
HAIRY WOODPECKER
NORTHERN FLICKER
WESTERN WOOD -PE WEE
ASH-THROATED FLYCATCHER
WESTERN KINGBIRD
TREE SWALLOW
VIOLET-GREEN SWALLOW
NORTHERN ROUGH-WINGED SWALLOW
BANK SWALLOW
CLIFF SWALLOW
BARN SWALLOW
BLACK-BILLED MAGPIE
AMERICAN CROW
BLACK-CAPPED CHICKADEE
WHITE-BREASTED NUTHATCH
BEWICK'S WREN
HOUSE WREN
BLUE -GRAY GNATCATCHER
AMERICAN ROBIN
GRAY CATBIRD
LOGGERHEAD SHRIKE
EUROPEAN STARLING
WARBLING VIREO
ORANGE-CROWNED WARBLER
VIRGINIA'S WARBLER
YELLOW WARBLER
COMMON YELLOWTHROAT
YELLOW-BREASTED CHAT
BLACK- HEADED GROSBEAK
BLUE GROSBEAK
LAZULI BUNTING
GREEN-TAILED TOWHEE
RUFOUS-SIDED TOWHEE
CHIPPING SPARROW
LARK SPARROW
SONG SPARROW
RED-WINGED BLACKBIRD
YELLOW-HEADED BLACKBIRD
BREWER'S BLACKBIRD
COMMON CRACKLE
NORTHERN ORIOLE
PINE SISKIN
LESSER GOLDFINCH
AMERICAN GOLDFINCH

A
U
U
U
U
c
F

U
U
U

F
F
F
C
U
U
U
C
A
A
A
U
U
U
U
U
F
C

U
A
C


C
U
U
F
F
F

C
U
F
U
A
C
F
U
F

U
U
C
C


C

C
C
C
C
C
C
C
C
C
C
C
C
c
c

c
c
c
c
c
c
c
c
c
c
c
c
c
U
c
c
c
c
U
c
c
c
c
c
c
c
c
c
c
c
c
c
U
c
c

c


c

c
c
c

c
U
U
c
U

c
U
U
U
U
c
c
c

c


c
U
c

U
c
U
U
U
c
U
U
U
U
U

U

U
c
c
c
c

U


c

c


c

c

U

U
U
U
c
U

U
A
A

A
A
A
c

U
U
c
c

c

U
c
U


A
c

c


c

c

c
c
c
c


c


                                                    71

-------
Appendix B.  Relative abundance, by subregion, of birds that regularly winter in lowland riparian and wetland
habitats of the Colorado Plateau.

See Appendix A for explanation of abbreviations and information sources.
                      Common Name                  Grand Valley Cortez  Utah  Wyoming
GREAT BLUE HERON
CANADA GOOSE
WOOD DUCK
GREEN-WINGED TEAL
MALLARD
NORTHERN PINTAIL
GADWALL
AMERICAN WIGEON
CANVASBACK
RING- NECKED DUCK
LESSER SCAUP
COMMON GOLDENEYE
BARROW'S GOLDENEYE
BUFFLEHEAD
BALD EAGLE
NORTHERN HARRIER
SHARP-SHINNED HAWK
COOPER'S HAWK
NORTHERN GOSHAWK
RED-TAILED HAWK
FERRUGINOUS HAWK
AMERICAN KESTREL
PEREGRINE FALCON
RING- NECKED PHEASANT
GAMBEL'S QUAIL
AMERICAN COOT
COMMON SNIPE
MOURNING DOVE
BARN OWL
WESTERN SCREECH-OWL
GREAT HORNED OWL
LONG-EARED OWL
BELTED KINGFISHER
DOWNY WOODPECKER
HAIRY WOODPECKER
NORTHERN FLICKER
PINYON JAY
BLACK-BILLED MAGPIE
AMERICAN CROW
BLACK-CAPPED CHICKADEE
PLAIN TITMOUSE
BUSHTIT
RED-BREASTED NUTHATCH
WHITE-BREASTED NUTHATCH
BROWN CREEPER
BEWICK'S WREN
MARSH WREN
TOWNSEND'S SOLITAIRE
AMERICAN ROBIN
AMERICAN PIPIT
CEDAR WAXWING

C
A
F
C
A
U

U

C
U
F


U
U
U
U

F
U
F

F
F

U
A
U
U
U
U
U
U

C
F
A
F
F
U
U
U
U

U
U
U
A
U
F
72
U
C

U
C


U



C


C
C
C
C
U
C

C
U
C
C

U
C


C

U
C
C
C
C
C
C
C
C
C

C
C
C
C
C
C

C

U
C






U
U

U

U
C
C



C

U

C

U




C




C

C

C





U







U

U
C

U
U



A
U
C
C



U

U









C






C

C

U
U
U






C


-------
Common Name                    Grand Valley  Cortez  Utah  Wyoming

NORTHERN SHRIKE                U             U       U     U
LOGGERHEAD SHRIKE              U             U       U     U
EUROPEAN STARLING              A             C       C     C
RUFOUS-SIDED TOWHEE            U             C
AMERICAN TREE SPARROW          U             C       U*
SONG SPARROW                   C             C       U
WHITE-CROWNED SPARROW          A             C       U
DARK-EYED JUNCO                A             C       U
RED-WINGED BLACKBIRD           A             C       U
WESTERN MEADOWLARK             C             C       U
BREWER'S BLACKBIRD                                   U
CASSIN'S FINCH                               U
HOUSE FINCH                    A             C
PINE SISKIN                    U             C
AMERICAN GOLDFINCH             F             C       U
EVENING GROSBEAK               FCC
                               73

-------
Appendix C.  Relative abundance, by subregion, of birds that regularly occur during migration in lowland
riparian and wetland habitats of the Colorado Plateau.

See Appendix A for explanation of abbreviations and information sources.
Common Name
PIED-BILLED GREBE
DOUBLE-CRESTED CORMORANT
AMERICAN BITTERN
GREAT BLUE HERON
SNOWY EGRET
BLACK-CROWNED NIGHT-HERON
WHITE-FACED IBIS
CANADA GOOSE
WOOD DUCK
GREEN-WINGED TEAL
MALLARD
NORTHERN PINTAIL
BLUE-WINGED TEAL
CINNAMON TEAL
NORTHERN SHOVELER
GADWALL
AMERICAN WIGEON
CANVASBACK
REDHEAD
RING-NECKED DUCK
GREATER SCAUP
LESSER SCAUP
COMMON GOLDENEYE
BARROW'S GOLDENEYE
BUFFLEHEAD
RUDDY DUCK
TURKEY VULTURE
OSPREY
BALD EAGLE
NORTHERN HARRIER
SHARP-SHINNED HAWK
COOPER'S HAWK
NORTHERN GOSHAWK
SWAINSON'S HAWK
RED-TAILED HAWK
FERRUGINOUS HAWK
AMERICAN KESTREL
MERLIN
PEREGRINE FALCON
RING-NECKED PHEASANT
GAMBEL'S QUAIL
VIRGINIA RAIL
SORA
AMERICAN COOT
SANDHILL CRANE
SEMIPALMATED PLOVER
KILLDEER
BLACK- NECKED STILT
AMERICAN AVOCET
GREATER YELLOWLEGS
LESSER YELLOWLEGS
Grand Valley
U


C
U

U
C
U
A
A
U
U
C
F
F
F

U
C

F
F

F
F
F

U
U
U
U


F
U
C


F
F
U
U
C
F

C

U
U
U
Cortez
C
U
U
C
C
C
C
C

C
C
C
C
C
C
C
C

C
C

C
C

C
C
C
U
C
C
C
C


C

C

U
C
C
C
C
C

U
C
U
C
U
U
Utah
C
U

C*
C*
C*
C*
C*

C*
C*
C*
C*
C*
C
C*
C
U*
C*
U

C
U

U
C
C*


C*
U
U*

U
C*

C*


C*

U
U
A
C

C*
C*
C*

U*
Wyoming
C


C
U
U
C
C

C
A
A
C
C
A
C
C
C
C
C
U
C
C
U

C

U
U
C
U
U
U
C
C
U
C
U




U
C
U

C
U
U
U
U
                                               74

-------
Conmon
Grand Valley Cortex
                                                        Utah
Wyoming
SOLITARY SANDPIPER
WILLET
SPOTTED SANDPIPER
MARBLED GOOUIT
WESTERN SANDPIPER
LEAST SANDPIPER
LONG-BILLED DOWITCHER
COMMON SNIPE
WILSON'S PHALAROPE
RED-NECKED PHALAROPE
FRANKLIN'S GULL
BONAPARTE'S GULL
RING-BILLED GULL
CALIFORNIA GULL
FORSTER'S TERN
BLACK TERN
BAND-TAILED PIGEON
MOURNING DOVE
YELLOW-BILLED CUCKOO
BARN OWL
WESTERN SCREECH-OWL
GREAT HORNED OWL
LONG-EARED OWL
SHORT-EARED OWL
COMMON NIGHT HAWK
BLACK-CHINNED HUMMINGBIRD
BROAD-TAILED HUMMINGBIRD
RUFOUS HUMMINGBIRD
BELTED KINGFISHER
LEWIS' WOODPECKER
RED-NAPED SAPSUCKER
DOWNY WOODPECKER
HAIRY WOODPECKER
NORTHERN FLICKER
OLIVE-SIDED FLYCATCHER
WESTERN WOOD-PEWEE
WILLOW FLYCATCHER
HAMMOND'S FLYCATCHER
DUSKY FLYCATCHER
CORDILLERAN FLYCATCHER
ASH-THROATED FLYCATCHER
WESTERN KINGBIRD
EASTERN KINGBIRD
TREE SWALLOW
VIOLET-GREEN SWALLOW
NORTHERN ROUGH-WINGED SWALLOW
BANK SWALLOW
CLIFF SWALLOW
BARN SWALLOW
PINYON JAY
BLACK-BILLED MAGPIE
AMERICAN CROW


F

U
U
U
U
U

U
U
U
U



A

U
U
U
U

A
f
F
f
U
U

U
U
C

U


F
U
U


F
F
U
F
F
C
F
A
F
U
C
C
C
C
C
C
C
C
U
U
U
C

U
U
C
C



C


C
C
C
C
C
C
C
C
C
C

C
U
U
U
C



C
C
C
U
C
C
C
C
C

U
U*
U


U
U*
C*
U*
U

C
C*
U*
U

A*



C*

U*
U*
U
U

U
U
U
U
U
C*

U


U


U*
U*
U*
U*
U*
u*
U*
u*

C*

u
C
C
C



C
C




C



C
u


C




u
u

u
u
u
u
C
u
u
C
u
u
u

u

C
C

C
C
C

C
u
                                          75

-------
Common Name
BLACK-CAPPED CHICKADEE
RED-BREASTED NUTHATCH
WHITE-BREASTED NUTHATCH
BROUN CREEPER
BEWICK'S WREN
HOUSE WREN
MARSH WREN
RUBY-CROWNED KINGLET
BLUE-GRAY GNATCATCHER
WESTERN BLUEBIRD
TOWNSEND'S SOLITAIRE
HERMIT THRUSH
AMERICAN ROBIN
GRAY CATBIRD
NORTHERN MOCKINGBIRD
AMERICAN PIPIT
CEDAR WAXWING
LOGGERHEAD SHRIKE
EUROPEAN STARLING
SOLITARY VIREO
WARBLING VIREO
ORANGE-CROWNED WARBLER
VIRGINIA'S WARBLER
YELLOW WARBLER
YELLOW-RUMPED WARBLER
BLACK-THROATED GRAY WARBLER
TOWNSEND'S WARBLER
MACGILLIVRAY'S WARBLER
COMMON YELLOWTHROAT
WILSON'S WARBLER
YELLOW-BREASTED CHAT
WESTERN TANAGER
BLACK- HEADED GROSBEAK
BLUE GROSBEAK
LAZULI BUNTING
GREEN-TAILED TOWHEE
RUFOUS-SIDED TOWHEE
CHIPPING SPARROW
BREWER'S SPARROW
LARK SPARROW
SAVANNAH SPARROW
SONG SPARROW
LINCOLN'S SPARROW
WHITE-CROWNED SPARROW
DARK- EYED JUNCO
RED-WINGED BLACKBIRD
YELLOW- HEADED BLACKBIRD
BREWER'S BLACKBIRD
COMMON CRACKLE
NORTHERN ORIOLE
CASSIN'S FINCH
PINE SISKIN
Grand Valley
U

U

F
F
U
F
F
U
U
U
C

U
U
F
U
A
U
U
F
F
F
A
U

U
U
F

F
U
F
U
F
F
C
F

U
C
F
A
A
A
U
F
f
U

C
Cortez
C

C
C
C
C
C
C
C
C
C
C
C
U
U
C
C
C
C
C
C
C
C
C
C
U

C
C
C
C
C
C
C
C
C
C
C
C

C
C
C
C
C
C
C
C
C
C

C
Utah
C*




C
C*
U
U



C*


U

U*
C*
U
U
U
U
U
C*
U
U
U
U*

U

U
U
U
U
U
U
U*
C*
U*
C*
U*
U*
C*
C*
C*
C*

U

U*
Wyoming
U
U
U

U
C
U
U




C


U
U
U
C
U
U


A
A


C
C
C

C
U


C

C
C

C
C
C
A
A
C
C
A


C
C
76

-------
Gomroon Name                    Grand Valley  Cortex        Utah          Wyoming

LESSER GOLDFINCH               U             C
AMERICAN GOLDFINCH             C             C             C
EVENING GROSBEAK               DC                           C
                                       77

-------
Appendix D.  Amphibians and reptiles that use riparian and wetland areas of the Colorado Plateau.

Species are listed alphabetically by genus and species.  The  column "Wet/Rip" lists species  that occur in
Colorado wetland or riparian habitats according to Langlois 1978 (L).  Species not so categorized by Langlois
(1978) but which are considered to depend on wetland or riparian  habitats in Utah by Dalton et al. 1990 (D)
or the Colorado State Heritage Program's (HP) Vertebrate Characterization Abstracts (HP) are also marked.
An "O" in a subregion column indicates the species regularly occurs in wetlands and riparian habitats of the
specified subregion.  A blank means the  species does not regularly occur in, and/or is not dependent  on,
wetland/riparian areas of  that subregion.  For the Grand Valley,  Lower  Gunnison, and Cortez subregions,
occurrence information is mainly from Langlois (1978).  Utah information  is from Dalton  et al.  (1990).
Species  occurring  in   the  Wyoming  subregion  were inferred  from  Langlois's  (1978)  list  for   the
northwesternmost part  of Colorado.  Entries with an asterisk (*) indicate  the species was  found within
irrigated wetlands in the  Grand Valley by Ecology Consultants (1976), in the Lower Gunnison Valley by
Rector et al. (1979), or  the Cortez area by Somers  et al. (1979).  In the next-to-last column, the abundance
codes pertain only to Colorado, and are reproduced from the original  information source (Langlois 1978) as
follows:  A= abundant,  C= common,  F=  fairly common, U= uncommon, ?=  unknown abundance.
  Genus and Species
                             Wet/Rip  Grand Valley  L. Gunnison  Cortez  Utah  Wyoming Abund.  Cannon Name
  AMBYSTOMA TIGRINUM (subspecies)  L       0
  AM8YSTOMA TIGRINUM (subspecies).  I       0
  BUFO COGNATUS                 0
  BUFO PUNCTATUS                L       0*
  BUFO UOOO HOUSE I               L       0*
  CNEHIDOPHOROUS VELOX           L       0*
  CNEM1DOPHORUS TIGRIS           L       0*
  COLUBER CONSTRICTOR            L       0
  CROTAUS VIRIDIS (subspecies)    L       0
  CROTALUS VIRIDIS (subspecies)    HP
  CROTALUS VIRIDIS (subspecies)    L
  CROTAPHYTUS COLLAR IS           I       0*
  CROTAPHYTUS WISL1ZEHI           HP      0*
  OIADOLPHIS PUNCTATUS           NR
  ELAPHE GUTTATA                HP      0
  EUHECES HULTIVIRGATUS           L
  HOLBROOKIA MACULATA            HP
  HYLA ARENltOLOR               L       0
  HYPSIGLENA TOROUATA            HP      0
  LAMPROPELTIS TRIANGULUM (subsp)   HP      0
  LAMPROPELTIS TRIANGULUM (subsp)   L
  LAMROPELTIS GETULUS            L
  HASTICOPHIS TAENIATUS           L       0
  OPHEOORYS VERNAL IS             L
  PHRYNOSOMA DOUGLASS! {subsp.)    HP      0
  PHRYNOSOHA DOUGLASS I (subsp.)    L       0
  PITUOPHIS MELANOLEUCUS          L       0
  PSEUDACRIS TRISERIATA           L       0
  RAMA CATESBIANA               L       0
  RANA PIPIENS                 L       0*
  RHINOCHEILUS LECONTEI          NR
  SCAPHIOPUS HAMHOMOI            L
  SCAPHIOPUS INTERNONTANUS       L       0
  SCELOPORUS GRACIOSUS           L       0*
  SCELOPORUS HAGISTER            L
  SCELOPORUS UNOULATUS           L       0*
  TANTILLA UTAHENSIS             HP      0
  THAMNOPHIS CYRTOPSIS           HP      0
  THAMNOPHIS ELEGANS             L       0
 UROSAURUS OfiNATUS              L       0
 UTA  STANSBURIANA              L       0*
                       0      A      BLOTCHED TIGER SALAMANDER
 0         0      0    0      A      ARIZONA TIGER SALAMANDER
                  0           C      GREAT PLAINS TOAD
 0         0*     0           ?      RED-SPOTTED TOAD
 0*         0*     0    0      A      WOOOHOUSE'S TOAD
 0         0                  7      PLATEAU WHIPTAIL
 0*         0           0      ?      NORTHERN WHIPTAIL
                  0           7      WESTERN YELLOW-BELLIED RACER
 0                0           U      MIDGET FADED RATTLESNAKE
 0         0           OF      PRAIRIE RATTLESNAKE
           0                  7      HOPI RATTLESNAKE
 0         0                  7      YELLOW-HEADED COLLARED LIZARD
           0                  7      LONG-NOSED LEOPARD LIZARD
                  0           U      RING-NECK SNAKE
 0                            7      GREAT PLAINS RAT SNAKE
           0                  1      SOUTHERN MANY-LINED SKINK
           0*                 7      SPECKLED EARLESS LIZARD
 0                0           7      CANYON TREE FROG
           00           U      MESA VERDE NIGHT SNAKE
 0                07-      UTAH MILK SNAKE
           0                  7      NEW MEXICO MILK SNAKE
           0                  7      CALIFORNIA KINGSNAKE
 0         0007      DESERT STRIPED WHIPSNAKE
           0                  7      WESTERN SMOOTH GREEN SNAKE
 00                  7      MOUNTAIN SHORT-HORNED LIZARD
 0         0      0    0       F      DESERT SHORT-HORNED LIZARD
 0         0      0    0       F      GREAT BASIN GOPHER SNAKE
 0         0*     0    0       A      BOREAL CHORUS FROG
                              F      BULLFROG
 0*         0      0    0       A      LEOPARD FROG
                  0           U      LONG-NOSED SNAKE
 0         00           A      WESTERN SPAOEFOOT
 0                 0           A      GREAT BASIN SPAOEFOOT
 0          0*           OF       NORTHERN SAGEBRUSH LIZARD
           00           7       TWIN-SPOTTED LIZARD
 °*         0           OF       NORTHERN PLATEAU  LIZARD
                              7       UTAH  BLACK-HEADED SNAKE
 0                             7       W. BLACK-NECKED GARTER SNAKE
°*         0*      0     0       F       WANDERING  GARTER  SNAKE
0          0       0     0       F       NORTHERN TREE LIZARD
0          0007       NORTHERN SIDE-BLOTCHED LIZARD
                                                       78

-------
Appendix E.  Mammals that use riparian and wetland areas of the Colorado Plateau.

Species are listed alphabetically by genus and species.  The column "Wet/Rip" indicates whether a species was
listed as occurring regularly in wetland or riparian habitats in Utah by Dalton et al. 1990 (D), in Colorado by
Bissell 1978 (B), or in Colorado by the State Heritage Program's Vertebrate Characterization Abstracts (HP).
A "B" in a subregion column indicates the species regularly breeds in wetlands and riparian habitats of the
specified subregion, and an "M" indicates that it uses  such habitats during migration, but probably does not
breed in them.  A blank means the species does not regularly occur in, and/or is not dependent on,
wetland/riparian areas of  that subregion. For the Grand Valley, Lower Gunnisoo, and Cortez subregions,
information is mainly from Bissell (1978). Utah information is from Dalton et al. (1990).  Species occurring
in the Wyoming subregion were inferred from BisselTs (1978) list for the northwesternmost part of Colorado.
Entries with an asterisk (*) indicate the species was found within irrigated wetlands in the Grand Valley by
Ecology Consultants (1976) or CDW (1984), in the Lower Gunnison Valley by Rector et al. (1979), in the
Cortez area by Somers et al. (1979), or in the Price-San Rafael salinity control area by USER and SCS (1991).
In the next-to-last  column, the abundance  codes pertain only to  Colorado, and are reproduced  from the
original information source (Bissell 1978) as follows:  A= abundant, C= common, F= fairly common, U=
uncommon, ?= unknown  abundance.
   Genus and Specie*
Wet/Rip Grand Valley L. Gunnison  Cortex Utah Uyooing  Abend. Cannon Na*e
AHMOSPERMOPHILUS LEUCURUS
ANTILOCAPRA AMERICANA
ANTROZOUS PALLIDUS
BASSARISCUS ASTUTUS
CASTOR CANADENSIS
CERVUS ELAPHUS
CYNOMYS GUNNISONI
CYNOMYS LEUCURUS
DIPCOOMYS OROII
EPTESICUS FUSCUS
ERETHIZON DORSATUN
EUDERMA MACULATLM
EUTAMIAS MINIMUS
EUTAMIAS QUADRIVITTATUS
EUTAMIAS UMBRINUS
FELIS CONCOLOR
LAGURUS CURTATUS
LASIONYCTERIS NOCTIVAGANS
LASIURUS CINEREUS
LEPUS CALIFORNICUS
LEPUS TOUNSENOI1
LUTRA CANADENSIS
LYNX RUFUS
MARMOTA FLAVIVENTRIS
MEPHITIS MEPHITIS
HICROTUS LONGICALOUS
HICROTUS MONTANUS
HICROTUS PENNSYLVANICUS
MUS MUSCULUS
HUSTELA ERMINEA
MUSTELA FREHATA
HUSTELA VI SON
MYOTIS CALIFORNICUS
MYOTIS CILIOLABRUH
MYOTIS EVOTIS
MYOTIS LEI8II
MYOTIS LUCIFUGUS
MYOTIS THYSANOOES
MYOTIS VOLANS
MYOTIS YUMANENSIS
NEOTOMA ALBIGULA
NEOTOMA CINEREA
NEOTOHA LEPIDA
NEOTOMA MEXICAHA
HP
HP
HP
HP
B
HP
B
HP
HP
HP
HP
D
HP
HP
HP
HP
HP
HP
HP
HP
HP
D
. B
HP
B
HP
HP
B
HP
HP
B
B
HP
D
HP
HP
HP
HP
HP
HP
HP
HP
HP
HP
B*
B
B
B
B*
B*

B*
B
B
B

B
B
B
B
B
M
M
B*
B*

B*
B
B*
B*
B

B*
B
B»
B*
B

B
B
B

B
B

B
B
B
B
B
B
B
B*
B
B

B
B
B

B*
8

B

M

B*
B*

B
8
8*
B
B*
*
*

B

B

B
B
B

B

B
B

B
B

B
' B
B
B
B«

B
B
B

B
8

B


M
B


B

8
B
B*


B
B
B
B

B
B

B
B

t*
B

1
B
B
B
B
B
B


B
B
B
B



B


M
B*
B
B
B

B*
B
8*
B*
B

B*

B
B


B
B
B
B

B
B

8
B
B
B
B
B

B
B
B
B

B
8

B
B

M

B

B
B
B
B




B
B


B
B


B
B

B
B

R
C
7
7
C
C
C
C
A
C
C
R
C
C
C
R
7
7
C
C
A
R
C
C
C
C
A
7
C
7
C
7
7
U
C
C
7
R
R
7
C
C
R
C
WHITE-TAILED ANTELOPE SQUIRREL
PRONGHORN ANTELOPE
PALLID BAT
RINGTAIL
BEAVER
AMERICAN ELK
GUMN ISDN'S PRAIRIE DOG
WHITE-TAILED PRAIRIE DOG
ORO'S KANGAROO RAT
BIG BROUN BAT
PORCUPINE
SPOTTED BAT
LEAST CHIPMUNK
COLORADO CHIPMUNK
UINTA CHIPMUNK
MOUNTAIN LION
SAGE-BRUSH VOLE
SILVER-HAIRED BAT
HOARY BAT
BLACK-TAILED JACKRABBIT
WHITE-TAILED JACKRABBIT
RIVER OTTER
BOBCAT
YELLOW-BELLIED MARMOT
STRIPED SKUNK
LONG-TAILED VOLE
MONTANE VOLE
MEADOW VOLE
HOUSE MOUSE
ERMINE
LONG-TAILED WEASEL
MINK
CALIFORNIA MYOTIS
SMALL-FOOTED MYOTIS
LONG-EARED MYOTIS
SMALL-FOOTED MYOTIS
LITTLE BROUN BAT
FRINGED MYOTIS
LONG-LEGGED MYOTIS
YUMA MYOTIS
WHITE-THROATED WOOD RAT
BUSHY -TAILED WOOD RAT
DESERT WOOD RAT
MEXICAN WOOD RAT
                                               79

-------
Genus and Species
Wet/Rip  Grand Valley  L. Gumison  Cortez  Utah  Wyoming  Abend.  Cannon Mama
ODOCOILEUS HEHIONUS            8        B"
ONDATRA ZI8ETH1OJS             B        B*
ONOCHOHYS IEUCOGASTER          HP       B*
OVIS CANAOENSIS                0
PEROGNATHUS APACHE             HP       B
PEROGNATHUS FASCIATUS          HP
PEROGNATHUS FLAWS             HP
PEROMYSCUS BOYLII              HP
PEROHYSCUS CRIHITUS            HP       B
PEROMYSCUS MANICULATUS         B        8*
PERCHYSCUS TRUE!               HP       B
PIPISTRELLUS HESPERUS          HP       B*
PLECOTUS TOWNSEHOI1            HP
PROCYOH LOTOS                  8        B*
REITHRODONTOHYS HEGALOT1S      B        8*
SOREX CINEREUS                 B        B
SOREX HERR1AM1                 HP       B
SOREX MONTICOUIS               B
SOREX HANUS                    0
SOREX PALUSTRIS                B
SOREX VAGRANS                  B        B
SPERHOPHILUS LATERAL IS         HP       B
SPERMOPHILUS RICHARDSON 11      B        B
SPERMOPHILUS SPILOSOHA         HP
SPERHOPHILUS TRIOECEHLIHEATUS  HP       B
SPERMOPHILUS VARIEGATUS        B        B*
SPILOGALE PUTORIUS             B        B
SYLVILAGUS AUOUBONII           HP       B*
SYLVILAGUS NUTTALLII           HP       B
TAOARIDA BRASIL1ENS1S          HP
TAOARIOA MACROTIS              HP       M
TAMIAS DORSALIS                0
TAWIAS UMBRIMUS                D
TAX IDEA TAXUS                  B        B*
THOHCMYS BOTTAE                HP       B*
THONOMYS TALPOIOES             HP       B
UROCYON CINEREOARGENTEUS       8        B*
URSUS AMERICANUS               B        B*
VULPES MACROTIS                HP       B*
VULPES VULPES                  B        B*
ZAPOS PRIHCEPS                 B        B
                       B*
                       B*
                       B
                       B

                       B*
                       B*
                       B
                       B*
                       B
B*      B*    8        C       MULE DEER
B*      B*    B        C       HUSKRAT
8             B        C       NORTHERN GRASSHOPPER MOUSE
        B              C       BIGHORN SHEEP
B             B        7       APACHE POCKET MOUSE
              B        7       OLIVE-BACKED POCKET MOUSE
B                      C       SILKY POCKET HOUSE
B       B              7       BRUSH MOUSE
8       B     B        C       CANYON MOUSE
B*      B*    B        A       DEER MOUSE
B       B     B        C       PINON MOUSE  •
B       B     B        C       WESTERN PIPISTRELLE
B       B     B        C       TOUNSEND'S BIG-EARED BAT
B*      B              C       RACCOON
B*      B*    8        A       WESTERN HARVEST MOUSE
B                      C       MASKED SHREW
B       B              7       HERRIAM'S SHREW
        B              7       MONTANE (DUSKY) SHREW
        B                      DWARF SHREW
B       B              C       WATER SHREW
B*      B              C       WANDERING SHREW
B       B     B        A       GOLDEN-MANTLED GROUND SQUIRREL
              B        C       RICHARDSON'S GROUND SQUIRREL
8                      C       SPOTTED GROUND SQUIRREL
        B     B        C       THIRTEEN-LINED GROUND SQUIRREL
8*      B              C       ROCK SQUIRREL
B       B     B        C       SPOTTED SKUNK
B       8     B        A       DESERT COTTONTAIL
B             B        C       NUTTALL'S COTTONTAIL
MM              7       BRAZILIAN FREE-TAILED BAT
                       7       BIG FREE-TAILED BAT
        B              U       CLIFF CHIPMUNK
                               UINTAN CHIPMUNK
                               BADGER
        B                      VALLEY POCKET GOPHER
        B     B                NORTHERN POCKET GOPHER
        8     B                GRAY FOX
        B     B        C     .  BLACK BEAR
        B              7       KIT FOX
        B     B        C       RED FOX
                       C       WESTERN JUMPING MOUSE
                                                             80

-------
                                      APPENDIX F.

Table F-1.  AREM field form: Documenting information
Table F-2.  AREM field form: Long form
Table F-3.  AREM field form: Short form
                                          81

-------
 Table F-1.  AREM field form: Documenting information

 I. DOCUMENTING INFORMATION (not used in the analysis):

 Wetland Name:	  Date Evaluated:

 Name of Associated Computer File (assign one, having 8 characters):	

 Evaluator (s):	

 Type of Wetland (check one):
        	  On-farm	 Off-farm

 Wetland Water Source (check one or more):
        	Subsurface seepage - Mostly Natural
        	Subsurface seepage - Mostly Irrigation-related
        	Overland runoff - Mostly Natural
        	Overland runoff - Mostly Irrigation-related
        	Channel or lake overflow - Mostly Natural
        	Channel or lake overflow - Mostly Irrigation-related
WETLAND SCORES
Unweighted Habitat Score
Unweighted Richness Score
Habitat Score Weighted1 By Species':
Relative Dependency on Wetlands
Relative Abundance
Taxonomic Uniqueness
Neotropical Migrant Status
Official Conservation Designations
Hunted Status
(insert here after completing the data analysis):
Cutoff Level for
>0%
(all possible sp








Species Habi
>25%
3.)








at Scores
>50%








>75%
(most conservative)








          For "Dependency on Wetlands,"  largest weights are assigned  to species using water as a substrate;
smallest weights to species that regularly use upland habitat.   For "Relative Abundance," largest weights are
assigned to uncommon species,  smallest to abundant species.  For "Taxonomic  Uniqueness," largest weights are
assigned to  species that are  the  only ones of  their genus in the  region;  smallest to species having many
congeners.  For  Neotropical Migrant Status, largest weights are assigned to species breeding only in the U.S.
or Canada and migrating to the Neotropics; smallest weights to norxnigratory species.  For "Official Conservation
Designations," largest weights are assigned species with  state, federal,  or Heritage  Program designations;
smallest weights to others.  For "Hunted Status," largest weights are assigned species that are  legally hunted;
smallest weights to others.
                                                 82

-------
Table F-2.  AREM long form

II. FIELD DATA
For each  numbered item, check only one response  unless noted otherwise.  Then
proceed to the next question unless noted otherwise.  Parenthetical file names are the
names of fields in the supporting database.

1. LOCATION. Is the wetland part of, or is it within 0.5 mile of, a major* river or lake?
* River wider than 100 ft or lake larger than 40 acres
	  Yes (file BigWater)       	  No

2. SURFACE WATER. Is there at least 0.1 acre* of surface water in the wetland during
most of the growing season?
* See Figure F-1  for guidance in estimating acreage categories.
	  Yes (file AnyWater).  Go to next question.
	  No.  Skip to question #5.

3. OPEN WATER.  How much open* water is present in the wetland during the growing
season?
* Water deeper than 2 inches and mostly lacking vegetation (except submerged plants).
	  > 20 acres and it is mostly wider than 500 ft (file OpenBig)
	  < 1 acre, or, >1  acre but mostly narrower than 3 ft (file OpenSmall)
	  Other conditions (file OpenOther)

4. SPECIFIC AQUATIC CONDITIONS
Check all that apply:
	  > 0.1 acre of the surface water is still, i.e., usually flows at  less than  1 ft/s (file
      StillWater)
	  Wetland can be assumed to contain fish (file Fish)
	  Wetland can be  assumed to contain frogs, salamanders, and/or crayfish  (file
      Amphibs)
	  Water transparency in the deepest part of the wetland is (or would be, if depth is
      shallow) sufficient to see an object 10 inches below the surface, and wetland is not
      known to have problems with metal contamination  (file Clear)
	  Wetland is highly enriched by  direct fertilizer applications,  water from nearby
      feedlots, or other sources (file Enriched)
	  Most of the normally-flooded part of the wetland goes dry at least one year in five,
      or, is subject to flooding from a river at  least as often (file Drawdown)

5. MUD. Is there at least 0.1 acre of exposed  mud*, which contains water before any
week in the period April 15-May 30,  or July 10-Sept. 10, and then goes dry?
* "Mud" can include tilled, sandy, alkali, or very sparsely vegetated soil.
	  Yes (file Mud). Go to next question.
	  No.  Skip to question #7.


                                      83

-------
                                  SHAPE
                               (Not to Scale)
0.1 acre:
(4350 ft2)
  Square

Dee ft
 10fL
                                                 435ft.
1 acre:
(43,500 ft2)
    208ft.
 10ft.
                                                 4350 ft. (~0.8mi)
10 acres:
(435,000 ft2)
     660ft.
 80ft.
                                                 5438ft. (~1mi)
20 acres:
(870,000 ft2)
40 acres:
(1,740,0000 ft2)
       993ft.
          1319ft.
160ft.
                                                 5438ft. (~1mi)
                           320ft.
                                                 5438ft. (~1mi)
Rgure F-1. Examples of wetland dimensions for various wetland shapes and acreages.

                                    84

-------
6. LARGE MUDFLAT.  Does the mud habitat have all these features?:
   o   At least 1  acre in size
   o   Maximum dimension is greater than 100 ft
   o   Salt crust or salt stains are not apparent
   o   Not recessed within a wash  or  canal whose depth (relative  to surrounding
      landscape) is greater than half its width.
	  Yes (file MudBig)        	 No

7. TREES. Are there at least 3 trees*:
* Cottonwood, Chinese elm, ash, or other plants taller than 20 ft.
	  within 1000 ft of the wetland  (including the wetland itself)? (file TreelnBy)
	  in the wetland or within 300 ft? (file Treeln)
(Both of the above may be checked if appropriate)
	  Neither of the above. Skip to #11.

8. TREE COVER. Add the tree acreage within 300 ft of the wetland, to the tree acreage
actually within the wetland. Then check  the  response below that best represents the
overall extent of tree cover:
      	 >1  acre,  dense*,  with  maximum  tree-stand dimension  >300  ft  (file
            ForestDens)
      	 >1  acre,  open,  with  maximum  tree-stand  dimension  >300  ft  (file
            ForestOpen)
      	 0.1-1  acre, dense*,  or greater acreage but narrower than  300 ft  (file
            Wood Dens)
      	 0.1-1  acre,  open, or  greater acreage  but narrower than  300  ft  (file
            WoodOpen)
      	 <0.1 acre
* Dense =  the tree canopy, viewed from the ground during midsummer,  appears at least
50% closed, as averaged across an area that is at least as large as the acreage specified.

9. BIG TREES. Are there at least three trees of >12 inch diameter within the wetland or
within 300 ft of its perimeter?
	  Yes (file TreesBig)        	  No

10. SNAGS. Are there  at least three snags, or trees with dead limbs with diameter >5
inches, within the wetland or within 300 ft of its perimeter?
	  Yes (file Snags)          	  No

11. SHRUBS.  Is there  at least 0.1 acre of shrubs*:
* Tamarisk, willow,  Russian olive, greasewood, or others 2-20 ft in height.
	  within 1000 ft of the wetland (including  the wetland itself)? (file ShrublnBy)
	  in the wetland or within 300 ft? (file Shrubln)
(Both  of the above  may be checked if appropriate).
	  Neither of the above. Skip to #13.

                                      85

-------
12. SHRUB SPECIES AND DENSITY. For each shrub type listed below, add the acreage
of the same shrub within 300 ft of the wetland, to the acreage within the wetland. Then
check the response below that best represents the overall condition for that shrub:

      Willow:
      	  >1 acre, dense (file WwMuchDens)
      	  >1 acre, open or very clumped (file WwMuchOpen)
      	  0.1-1 acre, dense* (file WwSomeDens)
      	  0.1-1 acre, open or very clumped (file WwSomeOpen)

      Greasewood or other tall desert shrubs:
      	  >1 acre (file GreaseMuch)
      	  0.1-1 acre (file GreaseSome)

      Russian olive or others with succulent fruit:
      	  >1 acre, dense (file OvMuchDens)
      	  >1 acre, open (file OvMuchOpen)
      	  0.1-1 acre, dense (file OvSomeDens)
      	  0.1-1 acre, open (file OvSomeOpen)

      Tamarisk (salt cedar):
      	  >1 acre, dense (file TmMuchDens)
      	  >1 acre, open (file TmMuchOpen)
      	  0.1-1 acre, dense (file TmSomeDens)
      	  0.1-1 acre, open (file TmSomeOpen)

      Pinyon - juniper:
      	  >1 acre (file PJMuch)
      	  0.1-1 acre (file PJSome)

* Dense= the shrub canopy, as viewed from a height of 100 ft during midsummer,
appears to be >50% closed,  as averaged across an area that is at least as large as the
acreage specified.

13. HERBACEOUS VEGETATION.  Is there at least 0.1 acre of emergent vegetation*:
* Nonwoody cattail, bulrush, sedges, grasses, and forbs.
	  within  1000 ft of the wetland (including the wetland itself)? (file EmlnBy)
	  in the wetland or within 300 ft? (file Em In)
(Both of the above may be checked if appropriate).
	  Neither of the above. Skip to #15.
                                    86

-------
14. HERBACEOUS SPECIES. For each cover type listed below, add the acreage of the
same cover within 300 ft of the wetland, to that present within the wetland.  Then check
the response below that best represents the overall condition for that cover type:

      Robust emergents (e.g., cattail, phragmites)
      	  >1 acre, dense* (file RbMuchDens)
      	  >1 acre, open  (file RbMuchOpen)
      	  0.1-1 acre, dense (file RbSomeDens)
      	  0.1-1 acre, open (file RbSomeOpen)
      Other wet** emergents (e.g., bulrush, sedge)
      	  >1 acre, dense*, height >4 in (file WEMuchDens)
      	  >1 acre, open, height >4 in (file WEMuchOpen)
      	  >1 acre and height <4 in (file  WEMuchShrt)
      	  0.1-1 acre, dense, height >4 in (file WESomeDens)
      	  0,1-1 acre, open, height >4 in  (file  WESomeOpen)
      	  0.1-1 acre, height <4 in (file WESomeShrt)
      Drier emergents (e.g., grasses)
      	  >1 acre, dense* (file DEMuchDens)
      	  >1 acre, open  (file DEMuchOpen)
      	  0.1-1 acre, dense (file DESomeDens)
      	  0.1-1 acre, open (file DESomeOpen)
      Broad-leaved Forbs (e.g., milkweed, thistle, alfalfa)
      	  >1 acre (file ForbMuch
      	  0.1-1 acre (file ForbSome)
      Aquatic plants (e.g., watercress, sago pondweed, duckweed)
      	  >10 acres (file AqMuch)
      	  0.1-10 acres (file AqSome)

*  Dense = these plants are at least 4 inches high  and mostly obscure  the soil or
underlying water, as viewed from a height of 100 ft during midsummer.
** Wet =  at least 2 inches  of surface water underlay the plants during most of the
growing season.

15. SURROUNDING LAND COVER. Within 0.5 mi of the wetland, is the land cover >60%
pasture, alfalfa, grain crops, row crops, other wetlands, grass lawns, and/or weed fields?
	  Yes (file SurrCover).  Skip to #17.
	  No. Go to next question.

16. LOCAL LAND COVER. Within 3 mi of the wetland, is the land cover >60% pasture,
alfalfa, grain crops, row crops, other wetlands, grass lawns, and/or weed fields?
	  Yes (file LocalCover).
      No
                                     87

-------
17. VISUAL SECLUSION
Check only one:
	  Both of the following: (a) wetland is seldom visited by people on foot or boat (less
      than once  weekly),  (b) there are no paved roads within 600 ft, or if there are,
      wetland is not visible from the roads (file SeclusionH).
	  Either (a) or (b) above (file Seclusion M).
	  Other condition.

18. PREDATION POTENTIAL
Check only one:
	  Wetland adjoins a heavily-traveled road (usual maximum of > 1 car/minute), and/or
      is in a high-density housing area  (>1 house/5 acres), and/or
      is linear (i.e., no more than  10% of the wetland is farther than 25 ft from a road,
      canal, or other artificially linear feature) (file  PredHPot)
	  Wetland adjoins a less-traveled road, and/or
      is in an area with sparser  housing density  but is closer than 1000 ft from a
      normally-occupied building  (file PredMPot)
	  Other condition.

19. GRAZED, BURNED, MOWED.  Is the wetland mowed,  burned, or intensively grazed
between April and mid-July?
	  Yes (file GrazBurnMo)
	  No

20. NESTING LOCATIONS
Check all that apply:
	  Semi-open  structures (bridges, barns)  suitable for  nesting swallows are present
      within 300 ft (file SwallNest)
	  Platforms suitable for nesting  geese are present in the  wetland or along  its
      perimeter (file GooseNest)
	  Vertical, mostly bare dirt banks at least 15  ft high  are present within 0.5 mi., of
      potential use to nesting kingfishers, barn owls, and swallows (file Banks)
This concludes the initial evaluation.  If you intend to infer the value of this wetland at
seasons  or  years  other than  the  present one,  you should go back over  all  your
responses and, on a new form, change the responses that would be different at that
season/year.  Then, proceed to the analysis. Refer to Section 5.0 for instructions on how
to convert the above information into wetland  scores and a species list.
                                      88

-------
Table F-3.  AREM short form
(A= acre, ft= feet, in= inches, mi= miles)

1. Location: river/lake <0.5 mi?
	BigWater

2. Surface Water: >0.1 A in growing season?
	AnyWater  [skip to #5 if no]

3. Open Water:  in growing season:
	OpenBig:  >20 A and width mostly >500 ft
	OpenSmall:  < 1 A, or >1 A but width <3 ft
	OpenOther:  all other

4. Specific Aquatic Conditions:
	StillWater:  >0.1 A that flows at <1 ft/s
	Fish
	Amphibs: crayfish, frogs, salamanders
	Clear: 10 inch visibility and no metals problem
	Enriched: feedlots etc.
	Drawdown: most of wetland dries out or floods from river 1 year in 5

5. Mud: >0.1 A  of exposed mud is wet-then-dry, April 15 - May 30, or July 10- Sept. 10
	Mud [skip to 7 if no]

6. Large Mudflat: >1 A + width > 100 ft + no salt + not recessed
	MudBig

7. Trees: >2 trees...
	TreelnBy: within 1000 ft, or in
	Treeln: in wetland
[skip to 11  if no]

8. Tree Cover: tree acres within 300 ft + acres in wetland
	ForestDens:  >1 A, closed canopy, and  >300 ft wide
	ForestOpen:  >1 A, open, and >300 ft wide
	WoodDens: 0.1-1.0 A closed, or larger but  narrower than 300 ft
	WoodOpen:  0.1-1.0 A open, or larger but narrower than  300 ft

9. Big Trees: >2 trees, >12 inch diameter within 300 ft or in?
	TreesBig

10-Snags: >2 snags (>5 inch diameter), within 300 ft or in wetland?
	Snags

                                     89

-------
 11.Shrubs: >0.1 acre of shrubs (2-20 ft height)...
 	ShrublnBy: within 1000 ft, or in
 	Shrubln: in wetland
 [skip to 13 if no]

 12.Shrub Species and Density: shrub acres within 300 ft + in wetland:
 __WwMuchDens: willow >1 A, closed
 __WwMuchOpen: willow >1 A, open or clumped
 	WwSomeDens: willow 0.1 - 1.0 A, closed
 	WwSomeOpen: willow 0.1  - 1.0 A, open or clumped
 	GreaseMuch: greasewood >1 A
 	GreaseSome: greasewood 0.1 - 1.0 A
 	OvMuchDens: Russian olive >1 A, closed
 	OvMuchOpen: Russian olive >1 A, open or clumped
 	OvSomeDens: Russian olive 0.1 - 1.0 A, closed
 	OvSomeOpen: Russian olive 0.1 - 1.0 A, open or clumped
  _TmMuchDens: tamarisk >1 A, closed
  _TmMuchOpen: tamarisk >1 A, open or clumped
  _TmSomeDens: tamarisk 0.1 - 1.0 A, closed
  _TmSomeOpen: tamarisk 0.1 - 1.0 A, open or clumped
  _PJMuch: pinyon-juniper >1 A
  _PJSome: pinyon-juniper 0.1 - 1 A
13. Herbaceous Vegetation: >0.1 A of herbaceous
	EmlnBy: within 1000 ft, or in wetland
	Emln: in wetland

14. Herbaceous Species and Density: herbaceous acres within 300 ft + in wetland:
	RbMuchDens: robust cattail etc. >1 A, dense
	RbMuchOpen: robust cattail etc. >1 A, open
	RbSomeDens: robust cattail etc. 0.1 - 1.0 A, dense
	RbSomeOpen: robust cattail etc. 0.1 - 1.0 A, open
	WEMuchDens: wet emergents (sedge, bulrush)  >1 A, dense, >4 in tall
	WEMuchOpen: wet emergents  (sedge, bulrush) >1 A, open tall
	WEMuchShrt: wet emergents (sedge, bulrush) >1 A, short <4 in
	WESomeDens: wet emergents  (sedge, bulrush) 0.1 - 1.0 A, dense, >4 in tall
	WESomeOpen: wet emergents (sedge, bulrush) 0.1 - 1.0 A, open tall
  _WESomeShrt: wet emergents (sedge, bulrush) 0.1 - 1.0 A, short <4 in
	DEMuchDens: dry emergents (grasses etc.) >1 A, dense, >4 in tall
	DEMuchOpen: dry emergents (grasses etc.) >1 A, open
	DESomeDens: dry emergents (grasses etc.) 0.1 - 1.0 A, dense, >4 in tall
	DESomeOpen: dry emergents (grasses etc.) 0.1 - 1.0 A, open
                                   90

-------
14 (continued). Herbaceous Species and Density: acres within 300 ft + in wetland:
	ForbMuch: alfalfa, milkweed, etc.  > 1 A
	ForbSome: alfalfa, milkweed, etc. 0.1 -  1.0 A
	AqMuch: watercress, sago, duckweed  etc. >  1 A
   _AqSome: watercress, sago, duckweed etc. 0.1 - 1.0 A
15. Surrounding Land Cover: within 0.5 mi...
	SurrCover: >60% pasture, alfalfa, grain, row crops, other wetlands, weeds, grass
[skip to 17 if yes]

16. Local Land Cover: within 3.0 mi of wetland...
	LocalCover: >60% pasture, etc.

17. Visual Seclusion: check ONLY ONE:
	SeclusionH: no road within 600 ft or not visible if road present, and <1 visit/week on
foot
	SeclusionM: EITHER of above
	other

18. Predation Potential: check ONLY ONE:
	PredHPot: major road, urban, or linear
	PredMPot: other road or building within 1000 ft
   other

19. Burned, mowed, or intensively grazed, April to mid-July?
	GrazBurnMo

20. Nesting Locations:
	SwallNest: swallow sites -- barns, bridges within 300 ft
	GooseNest: goose platforms, in wetland or on perimeter
	Banks: within 0.5 mi, height >15 ft, vertical
                                      91

-------
                                                                  Ri
                                                                         17
May 12, 1993
Fred Weinmann
USEPA Region 10 - Wetlands
1200 Sixth Ave.
Seattle, WA 98101

Dear Mr. Weinmann:

The enclosed report describes a new method ("AREM") which assesses biodiversity by
assessing habitat. Although this method may in some ways be less sophisticated than
HEP (the Habitat  Evaluation Procedure of the U.S. Fish and Wildlife Service), it is faster
and simpler to use (<30 minutes per wetland).   Most importantly, it is  relatively
comprehensive in addressing wildlife diversity. Its current focus is on wetland habitats
and birds, which  are the richest group of terrestrial vertebrates in most regions of the
U.S., but  it can be adapted for other resources and regions.  Given a  list of  habitat
features, AREM predicts the number  of species present, their identities, and relative
suitability of habitat for each. If desired, users can assign greater weight  to species of
particular interest  (e.g., neotropical migrants) and less weight to less desirable species
(e.g., abundant habitat-generalists).  Initial tests of the method's accuracy are ongoing.
It is understood that habitat values are just one of several potential values of wetlands,
the others possibly including (for example) purification of nonpoint source pollution, flood
storage, and open space/recreation.  These would need to be addressed by methods
other than AREM.

When adapted for other regions and resources, AREM might be useful as a local-level
complement to region-level biological surveys, Gap Analysis, and ecosystems planning;
or as a complement to HEP in watershed assessments, impact analyses, and monitoring
of mitigation/restoration projects. The enclosed report describing AREM has already
undergone review by  many scientists  from  outside  EPA, and I continue to appreciate
comments and  suggestions from any source.

The software and  instruction manual that support AREM are nearing completion and will
be publicly available at no cost later this year.  If you are interested in receiving a copy
at that time, please let me know of your interest.
Sincerely,
Paul R. Adamus,
Wildlife Biologist
                             ManTech Environmental Technology, Inc.
            200 Southwest 35th Street, Corvallis, Oregon 97333  503-754-4664 FAX 503-754-4799 or 503-754-4335

-------