CATALOG DOCUMENTATION
EMAP-GREAT LAKES PROGRAM LEVEL DATABASE
1994 LAKE MICHIGAN NEARSHORE
CHLOROPHYLL DATA

TABLE OF CONTENTS

1.	DATA SET IDENTIFICATION

2.	INVESTIGATOR INFORMATION

3.	DATA SET ABSTRACT

4.	OBJECTIVES AND INTRODUCTION

5.	DATA ACQUISITION AND PROCESSING METHODS

6.	DATA MANIPULATIONS

7.	DATA DESCRIPTION

8.	GEOGRAPHIC AND SPATIAL INFORMATION

9.	QUALITY CONTROL/QUALITY ASSURANCE

10.	DATA ACCESS

11.	REFERENCES

12.	TABLE OF ACRONYMS

13.	PERSONNEL INFORMATION

1. DATA SET IDENTIFICATION

1.1	Title of Catalog document

EMAP-Great Lakes Program Level Database
1994 Lake Michigan Nearshore
Chlorophyll Data

1.2	Authors of the Catalog entry
Jenny Kysely, ILS

1.3 Catalog revision date
29 November 1996

1.4	Data set name
LMCHL94

1.5	Task Group
Great Lakes

1.6	Data set identification code
501


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1.7 Version

001

1.8 Requested Acknowledgment

These data were produced as part of the U.S. EPA's Environmental Monitoring
and Assessment Program (EMAP). If you plan to publish these data in any way,
EPA requires a standard statement for work it has supported:

"Although the data described in this article has been funded wholly or in part
by the U.S. Environmental Protection Agency through its EMAP-Great Lakes
Program, it has not been subjected to Agency review, and therefore does not
necessarily reflect the views of the Agency and no official endorsement
should be inferred."

2.	INVESTIGATOR INFORMATION

2.1	Principal Investigator
Stephen Lozano

U.S. Environmental Protection Agency
NHEERL-MED

2.2	Investigation Participant - Sample Collection
Floyd Boetcher

U.S. Environmental Protection Agency
NHEERL-MED

2.3	Investigation Participant - Sample Collection
Gary Phipps

U.S. Environmental Protection Agency
NHEERL-MED

2.4	Investigation Participant - Sample Collection

James Gangl
SAIC

(Currently, University of Minnesota)

2.5	Investigation Participant - Sample Processing
Jill Scharold

U.S. Environmental Protection Agency
NHEERL-MED

3.	DATA SET ABSTRACT

3.1	Abstract of the Data Set

The Lake Michigan Chlorophyll data set provides chlorophyll concentrations
at thirty-nine sampling stations located in the nearshore region of Lake
Michigan. Chlorophyll analysis was conducted on water samples collected
from the surface, approximately at the 1 meter depth.

Samples were filtered and pigments were solvent extracted with an acetone-DMSO
solvent. Spectrophotometric analysis was performed using the monochromatic
method for determination of chlorophyll a.

3.2	Keywords for the Data Set

Chlorophyll, nearshore region, spectrophotometric analysis, Great Lakes,

Lake Michigan


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4. OBJECTIVES AND INTRODUCTION

4.1	Program Objective

The Environmental Monitoring and Assessment Program (EMAP) was designed to
periodically estimate that status and trends of the Nation's ecological
resources on a regional basis. EMAP provides a strategy to identify and
bound the extent, magnitude and location of environmental degradation and
improvement on a regional scale based on station sites randomly located in the
Great Lakes. Base grid and three-fold enhanced sampling sites from the
nearshore region of Lake Michigan are included in this data set.

4.2	Data Set Objective

The primary objective of the chlorophyll data set is to characterize the
trophic status endpoint by providing estimates of phytoplankton biomass
and serving as an indicator of aquatic productivity in the Great Lakes.
Chlorophyll measurements were also used to calibrate an in situ fluorometer
and interpret remotely-sensed AVHRR data.

4.3	Background Discussion

Condition indicators provide important information about ecological condition
of a sampling site. Chlorophyll a is an important factor addressing the
trophic status of an ecosystem. Chlorophyll a is the primary photosynthetic
pigment of algae and provides an estimate of algal biomass, which can be
used as an indication of productivity. Consequently, its absorbance is
measured most frequently.

The amount of chlorophyll in an algal cell can change depending on ambient
conditions. It readily responds to natural and anthropogenic influenced
stressors such as nutrient levels and light attenuation characteristics.
Turbidity levels, particularly from increases in suspended solids, can affect
light penetration depth and intensity. This can cause an effect on the
algal community to carry out photosynthesis. Since algal abundance and
productivity is the energy base for an autochthonous system, any changes
can have impacts on the food web dynamics. Other water chemistry and
abiotic parameters were measured which will be helpful with chlorophyll a
data interpretation.

4.4	Summary of Data Set Parameters

Chlorophyll a using the monochromatic method is reported for surface
(1 meter) conditions for each sampling station.

5. DATA ACQUISITION AND PROCESSING METHODS

5.1 Data Acqui si ti on

5.1.1	Sampling Objective

To collect water samples from 39 sampling sites from the nearshore region
of Lake Michigan. A sampler was used to collect water samples from the
surface, approximately at the 1 meter depth.

5.1.2	Sample Collection Methods Summary

At all stations, an 8 L sampler was used to collect water samples.

The water samples were subsampled for chlorophyll measurements by obtaining
a 9 L liter sample from the surface and placing the subsample into separate
opaque polyethylene bottles and refrigerated for filtration. Each sample was
filtered through a 0.45 membrane filter (Millipore type HA, 47 mm diameter).
Using a vacuum filtration apparatus, pressure was maintained at no more
than 0.5 atms. The filters were folded into quarters, wrapped in aluminum
foil, and frozen for storage until laboratory analysis.


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5.1.3	Beginning Sampling Date
18 July 1994

5.1.4	Ending Sampling Date
5 August 1994

5.1.5	Platform

Sampling was conducted from a 28 meter research vessel, the R/V Explorer,
owned and operated by the U.S. EPA, NHEERL-MED.

5.1.6	Sampling Equipment

An 8 L water sampler was used to collect water samples. Opaque polyethylene
containers were used for subsamples. A 2000 Liter graduated cylinder was
used for measuring subsample volume for filtering. A filtering apparatus
with a vacuum pump was used for filtering samples. Millipore type HAWP
(0.45 membrane filters, 47 mm diameter) were used for collecting the
algal biomass.

5.1.7	Manufacturer of Instrument

5.1.8	Key Variables

This data set contains surface (1 meter) water sample values. Replicate
samples were taken from each site and averaged values are reported.

5.1.9	Collection Method Calibration

The sampling gear required no calibration.

5.1.10	Collection Quality Control

5.1.11	Sample Collection Method Reference

Strobel, C.J. and S.C. Schimmel, 1991. Environmental Monitoring and
Assessment Program-Near Coastal. 1991 Virginian Province, Field Operations
and Safety Manual. U.S. EPA, NHEERL-AED, Narragansett, RI. June 1991.

5.2 Data Processing and Sample Processing

5.2.1	Sample Processing Objective

To process chlorophyll samples to characterize algal biomass in terms of
chlorophyll a.

5.2.2	Sample Processing Methods Summary

The chlorophyll samples were stored as frozen filters wrapped in aluminum
foil until analysis. Spectrophotometric analysis was used for chlorophyll
determination, and the monochromatic method was used for detection of
chlorophyll a. The filters were placed in 20 ml scintillation vials and
solvent extracted for 20-24 hours. The solvent used was an acetone-DMSO
mixture. Analysis was performed in subdued light using a Perkin Elmer Lambda
2S Spectrophotometer with 5 cm path length cell. Blanks and standards were
run prior to and at the end of analysis for background correction. Samples
were acidified with 1 N HCL for phaeophytin correction.

5.2.3	Sample Processing Method Calibration

Analysis of chlorophyll samples, standards, and blanks were performed in
subdued light. Samples were allowed to warm to room temperature. An initial


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blank was analyzed prior to sample analysis for background correction. Solvent
absorbances were read to verify zero readings. If zero readings were not
obtained, the sequence was repeated. If zero readings were obtained, solvent
was drawn into the cell and read to verify a stable reading of zero.

5.2.4	Sample Processing Quality Control

Blanks and standards were analyzed before, during, and at end of analysis.

5.2.5	Sample Processing Method Reference

Standard methodology was used with DMSO extraction procedure. Reference
follows:

Shoaf, W.T. and B.W. Lium. 1976. Improved extraction of chlorophyll a and
b from algae using dimethyl sulfoxide. Limnol. Oceanogr. 21:926-928.

5.2.6	Sample Processing Method Deviations
6. DATA ANALYSIS AND MANIPULATIONS

6.1 Name of New or Modified Values

6.2 Data Manipulation Description

The formulas used for calculating chlorophyll a using the monochromatic
procedure follows:

Monochromatic Method (Lorenzen, 1967):

(k) (F) (E6650 E665a) (v)

Chi a ( g/L or mg/m ) = (V) (Z)

where

E6650 = turbidity-corrected absorption at 665 nm before acidification

= A6650 A7500, where A = the absorption value
E665a = turbidity-corrected absorption at 665 nm after acidification
= A665a - A750a
k = absorption coefficient of chlorophyll a, = 11.0
F = factor to equate the reduction in absorbency to initial chlorophyll

concentration, 1.7:0.7, or = 2.43
R = maximum ration of E6650:E665a in the absence of phaeopigments, = 1.7

v = volume of extract in ml
V = volume of water filtered in liters
Z = length of light path through cuvette or cell in cm.

6.3 Data Manipulation Examples

7. DATA DESCRIPTION

7.1 Description of Parameters

#

Name

Type

Length

Format Parameter Label

1

STA NAME

Char

8

8. Station Name

2

DATE

Num

8

YYMMDD8. Date the sample was collected

3

DEPTH C

Char

1

1. Depth category of sample (S-surface)

4

DEPTH

Num

5

5. Depth (m)

5

AVG CHLA M

Num

6

6.2 Average chlorophyll a ( g/L),

monochromatic method

7.1.1 Precision to which values are reported

The number of decimal places for each value reflects the precision of
the spectrophotometer.


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7.1.2	Minimum Value in Data Set
AVG CHLA_M 0.67

7.1.3	Maximum Value in Data Set
AVG CHLA_M 9.81

7.2 Data Record Example

7.2.1	Column Names for Example Records
STA_NAME, DATE, DEPTH_C, DEPTH, AVG CHLA_M

7.2.2	Example Data Records

STA_NAME	DATE DEPTH_C DEPTH AVG CHLA_M

LM94-73452 940725 S 1 2.61
LM94-73472 940725 S 1 1.27
LM94-73492 940726 S 1 0.74

8.	GEOGRAPHIC AND SPATIAL INFORMATION

8.1	Minimum Longitude
-79 deg 21' 17"

8.2	Maximum Longitude
-76 deg 20' 04"

8.3. Minimum Latitude

42	deg 27' 29"

8.4	Maximum Latitude

43	deg 53' 49"

8.5	Name of Area or Region
Nearshore Lake Michigan

Stations were located within the Nearshore resource class of Lake Michigan.
The nearshore sites were located within the 85 meter contour.

9.	QUALITY CONTROL/QUALITY ASSURANCE
9.1 Measurement Quality Objectives
9.2. Data Quality Assurance Procedures

9.3	Actual Measurement Quality

10.	DATA ACCESS

10.1	Data Access Procedures

Data can be downloaded from the EMAP Website.

10.2	Data Access Restrictions
Not applicable.


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10.3 Data Access Contact Persons

Stephen J. Lozano
U.S. E.P.A. NHEERL-MED
(218)529-5205
(218)529-5003 (FAX)
lozano.stephen@epa.gov

10.4	Data Set Format

Data from the Website are in ASCII fixed format.

10.5	Information Concerning Anonymous FTP
Not accessible.

10.6	Information Concerning WWW

Data can be downloaded from the EMAP Website.

10.7	EMAP CD-ROM Containing the Data Set
Data are not available on CD-ROM.

11.	REFERENCES

Lorenzen, C.J. 1967 Determination of chlorophyll and pheopigments:
spectrophotometric equations, Limnol. Oceanogr. 12:343-346.

Hedtke, S., A. Pilli, D. Dolan, G. McRae, B. Goodno, R. Kreis, G. Warren,
D. Swackhamer, and M. Henry. 1992. Great Lakes Monitoring and Research
Strategy: Environmental Monitoring and Assessment Program. USEPA, Office
Research and Development, ERL-Duluth, Duluth, Minnesota. EPA/602/R-92/001
204 p.

12.	TABLE OF ACRONYMS
NA

13.	PERSONNEL INFORMATION

Stephen J. Lozano

U.S. Environmental Protection Agency

NHEERL-MED

6201 Congdon Blvd

Duluth, MN 55804

(218)529-5205

(218)529-5003 (FAX)

lozano.stephen@epa.gov

Gary L. Phipps

U.S. Environmental Protection Agency

NHEERL-MED

6201 Congdon Blvd

Duluth, MN 55804

(218)529-5205

(218)529-5003 (FAX)

phipps.gary@epa.gov


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Jill V. Scharold

U.S. Environmental Protection Agency

NHEERL-MED

6201 Congdon Blvd

Duluth, MN 55804

(218)529-5205

(218)529-5003 (FAX)

scharold.jill@epa.gov

Floyd L. Boettcher

U.S. Environmental Protection Agency

NHEERL-MED

6201 Congdon Blvd

Duluth, MN 55804

(218)529-5205

(218)529-5003 (FAX)

boetcher.floyd@epa.gov


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