C'/3
                                                       902R82001
                        F.INAL  REPORT
BASELINE SEDIMENT STUDIES TO DETERMINE  DISTRIBUTION, PHYSICAL
     PROPERTIES, SEDIMENTATION  BUDGETS  AND RATES IN THE
        ,   VIRGINIA PORTION OF  THE  CHESAPEAKE BAY
                        UNITED  STATES
               ENVIRONMENTAL  PROTECTION AGENCY
                   GRANT  NUMBER R806001010
                       Robert  J.  Byrne
                     Carl  H. Hobbs,  III
                      Michael  J.  Carron
            Virginia  Institute of Marine Science
                  College  of  William and Mary
              Gloucester  Point, Virginia  23062
                                      Library
                         U. S. Environmental Protection Agency
                                    Region 111
                             Central Regional Laboratory
                                 839 Bestgate Koad
                             Annapolis, Maryland 21401

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                                DISCLAIMER

     This report has been reviewed by "the Chesapeake Bay Program Office,
U.S. Environmental Protection Agency, and approved for publication.
Approval does not signify that the contents necessarily reflect the views
and policies of the U.S. Environmental Protection Agency, nor does mention
of trade names or commercial products constitute endorsement or
recommendation for use.
                                      ii

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                                 ABSTRACT

     The distribution of the physical 'properties, patterns of deposition
and rates of accumulation of sediments provide an integrating framework for
investigations of the concentration and distribution of toxic substances.
Over 2,000 grab samples of surface-sediment (1.4 km grid) reveal  that  the
bottom of the Virginia portion of Chesapeake Bay is significantly sandier
than hitherto reported.  About 65% of the area is sand.  The number  of
samples in this study is an order to magnitude greater  (2,000 versus 200)
then previous studies allowing a significantly better delineation of
sedimentary characteristics.

     Distribution of sediment size is, in large part, a function  of
geomorphology, there being an apparently good correlation between depth and
sediment type; the finer grained sediments are usually  confined to the
deeper channels.  The exceptions to the depthisize relationship are  the
presence of fines in the shallow, marginal embayments such as Mobjack  Bay
and the absence of fines in the deep channel in the southeastern  section of
the Bay.  The occurrence of sands here is a function of infilling with
sands from the area of the Bay mouth and, perhaps, of scour into  older
(Pliocene?) materials.  Sediment distribution also reflects the local
source with the shallow-water, marginal sands derived from erosion of  the
banks and relict features.

     Several large geomorphic features are distinguishable on the maps of
sediment characteristics.  These features include the deep channels, a
large sand-shield near Tangier Island, relict spits, and the zone of
influence of the Bay mouth.

     Nine hundred samples, selected to avoid the coarser sands, were
analyzed for total carbon, organic carbon, and sulfur contents.   There are
strong correlations between these characteristics and sediment  type,
especially weight-percent clay.  Additionally, there is a good  relationship
between the organic carbon and sulfur contents.  Although total carbon
content reached 10% in some samples; the average was 1.5%.  Average  organic
carbon and sulfur contents were 1.0 and 0.34%.

     Comparisons of the bathymetry on boat sheets from  the 1850"s and
1950's were used to delineate the patterns and volumes  of cut and fill in
the Virginia portion of the Chesapeake Bay.  The comparisons were adjusted
for relative sea level change and monthly variations in mean tide level.
In addition, propagation of the error was evaluated and the results
applied.  Coupled with the data concerning the character of the surface
sediments and adjusted for water content, the volumes of. sediment shown by
the bathymetric changes to have been deposited were converted to  the masses
                                    ill

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of sand, silt, and clay deposited in a 100-year period.  The patterns of
deposition and erosion, particularly when coupled with grain-size
information, provide very important insights into the sedimentation
processes within the Bay.  The main Bay-axial channel from Maryland and the
transition to the Virginia basin are the principal deposition sites for
clay.  Silt-sized materials are somewhat more uniformly distributed
throughout the stem; however, about 33% of the silt accumulates  in the
transition region, an area of relatively low tidal-current energy.  The Bay
mouth may be a principal source.  The -pattern of deposition of  sand
suggests that the Bay mouth source is very significant as very  fine sands
penetrate much further into the Bay than has heretofore been suspected.
The patterns are consistent with present understanding of circulation
within the Bay.

     The project includes an attempt at constructing a sediment  budget
using published values for silt and clay estuarine advection and
contributions from shore erosion measured against the bottom residual
accumulations.  The residual accumulation of silt and clay is an order of
magnitude larger than previously estimated.  No previous work has
considered the sand budget but the general assumption has been  that the
contribution  from shore  erosion would be the principal source.   This  study
indicates the residue bottom accumulation of sand is greater than  the shore
erosion contribution by  a factor of 40.  It  is evident that additional
understanding of the flux of sediment through the Bay mouth and  the mouths
flanking of the tributaries is required.
                                     iv

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                                  CONTENTS

                                                                        Page

' Abstract    	    iii
, Contents  	      v
 List of Figures	    vii
 List of Tables	      x
 Acknowledgements	     xi

   I.  Introduction  	  .....      1
  II.  Conclusions   	      3
 III.  Recommendations   	      6
          A.  Management Recommendations   	      6
          B.  Research Needs   	      7
  IV.  Background  of the Study	      8
          A.  Geological History of  the Chesapeake Bay   	      8
          B. Recent  Sedimentological Work  	     13
   V.  Methods	     16
       A.  Characterization of Sediments	     16
             1.  Sample Collection 	     16
             2.  Analysis of Sediments	     19
                   a. water content	     21
                   b. grain-size  analysis   	     21
                   c. clay mineralogy	     27
                   d. carbon and  sulphur analysis   	     27
             3.  Quality Assurance 	     28
                i  a. shared and  duplicate  samples  	     28    i
                   b. calibration of  the rapid  sediment  analyzer  ...     28
                |  c. comparison  of RSA's at VIMS and MGS	     36    |
                   d. comparison  of analyzer by pipette  and Coulter            i
                       Counter	     40
                   e. Coulter Counter precision  	     42
                   f. carbon and  sulfur analyses  	     45
       B.  Formulation of Sediment Budget  	     46
             1.  Bathymetric Comparison  	     49
             2.  Conversion of  Sedimentation Rate to Mass
                   Accumulation  Rate	     57
             3.  Sources   	     64
                   a. shoreline erosion  	     64
                   b. biogenic  sediment  	     67
       C.  Data  Storage	     67
  VI.  Results and Discussion    	     72

 —    A.  Sedimentology	     72

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            1.  Description of Sediments	      72
            2.  Comparison with earlier surveys of bottom
                  sediments	      83
            3.  Clay Mineralogy	      92
            4.  Carbon and Sulphur in the Sediments	      95
                 a. previous work	      95
                 b. results	      98
                 c. discussion	     104
                 d. conclusions  ..."	     107
      B.  Patterns and Rate of Sediment Accumulation	     107
            1.  Patterns of Erosion and Deposition	     107
                 a. the nearfield mouth belt	     108
                 b. the central southern bay belt	     108
               i  c. the upper southern bay belt	     114
               ;  d. the lower middle bay belt	     115
            2.  Sediment Budget	     116

References Cited 	     137
Appendices .	     144
 -1. Loran C Correction Data . .-	   -  144
  2. Mass of Sediment Eroded from the Shoreline	     149
                                     vi

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                               LIST  OF  FIGURES
                                        *
 Number                                                                 Page

  1.  A plot of sea-level  fluctuations  during the  Quaternary ....      11

  2.  Location of major paleochannels in  the subbottom of  the
      Virginia portion of  the Chesapeake  Bay  ............      12

  3.  Rates of change in crustal elevation  in the  Chesapeake
      Bay region  .......................  ...      14

  4.  Map showing location of sample stations and  subareas  .....      17

  5.  Photograph  of  sample scoops  fabricated  for  this  project   ...      13

  6.  Photograph  of  the R/V  Captain  John  Smith  ...........      20

  7.  Flow chart  for the analysis  of sediments  ...........      22

  8.  The Rapid Sediment Analyzer  (RSA) as  constructed at  VIMS  ...      25

  9.  Ternary plot of sand: silt relay ratios of  samples analyzed
      at both VIMS and the MGS  ...................      31

 10.  Plots of cumulative  a  grain-size  frequency  distribution  as
      determined  by  both sieve and RSA  techniques   .........      37

 11.  Comparison  of  frequency distributions as  determined  by
      both pipette and Coulter Counter  ...............      41

j 12.  A plot of the  envelope described  by 20  replicate analyses
      using a Coulter Counter   ...................      43

 13.  A plot of the  cumulative  frequency  percents  at  1 0
      intervals for  20 replicates  of each of  2  aliquots of the
      same sample  .........................      44
  14.   Location  of  6-second  cells  with  bathymetric  comparisons
       and  Bay Sub  segments
  15.  Flow  chart  for  residual  mass  estimates  ............     5Q

'  16.  Index map of  bathymetric surveys  for 1849-1856 ........     51
                                      vii

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17.   Index map of bathymetric surveys for 1948-1961 ........       52

18.   Tidal variations used in the reduction of sea-level data ...       53

19.   Schematic diagram of corrections applied to bathymetric
     change data  .........................       55
20.  Map showing locations of short cores .............       59
                                      *
21.  Vertical profiles of water content ..............       60

22.  Vertical profiles of water content, normalized to a common
     origin ............................       61

23.  Nomogram for the determination of depth averaged water
     content  ...........................       62

24.  A plot of the mass of dry sediment in one cubic meter of
     bottom material as a function of water content ........       65

25.  Histogram of the mass of material eroded from the
     shoreline  ..........................       66

26.  A sketch of the profile of an eroding shore depicting
     material not included in the calculation .......  ....       68

27.  Subareas used in estimating the biological contribution to
     bottom sediment  .......................
28.  Isopleth map of weight-percent  sand   .............       74

29.  Isopleth map of mean grain-size   ...............       75

30.  Map of the distribution of sediment  types   ..........       76

31.  Histogram of depths at sample sites   .............       77

32.  Bathymetric Map   ........  ...............       70

33.  Isopleth map of weight-percent  clay   .............       70

34.  Isopleth map of graphic mean  grain-size  of  the  sand
     fraction ...........................       gQ

35.  Ternary diagrams  of sand:silt :clay ratios of  sediments  at
     different depths  .......................        2
36.   Scatter  plot  of mud  versus  water  content
37.   Isopleth map  of mean  grain-size  of sands  from Shideler
  .    (1975)  ............................      86
                                    viii

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38.  Location map of samples from earlier studies  .........        87

39 A,B,C  Comparison of weight percent mud or profiles  from
     earlier studies  .......................        88

40.  Histogram of values of total carbon, organic  carbon,  and
     sulfur content ........................        99

41.  Isopleth map of total carbon content .............       101

42.  Isopleth map of organic carbon content  ............       102

43.  Isopleth map of sulfur content ................       103

44.  Histogram of depths at sample sites for which there  are
     carbon analyses  .......................       105

45.  Scatter plot of organic carbon versus sulfur  content  .....       106

46.  Bathymetric changes during the past 100 years  in the
     Virginia portion of the Chesapeake Bay  ............       109

47.  Bathymetry and generalized bathymetric changes  in  the
     Virginia portion of the Chesapeake Bay  ............       HO

48.  The mass of sand accumulated per square meter per  century
     in the Virginia portion of the Chesapeake Bay  ........       HI

49.  The mass of silt accumulated per square meter per  century
     in the Virginia portion of the Chesapeake Bay  ........       H2

50.  The mass of clay accumulated per square meter per  century
     in the Virginia portion of the Chesapeake Bay  ........       H3

51.  Cumulative mass accumulation as a function of latitude  ....       125

52.  Total sediment mass accumulation per unit area per century
     as a function of depth interval  ...............       ^29

53a. Sand, mass accumulation per unit area per century  as  a
     function of depth interval ..................
53b. Silt, mass accumulation per unit  area  per  century  as  a
     function of depth interval
53c. Clay, mass accumulation  per unit  area  per  century  as  a
     function of depth interval ..................       -j.32
                                     ix

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                              LIST OF TABLES

Table                                 *                                Page

 1.  Schedule of sampling	      19
 2.  Grain-size nomenclature  	      23
 3A&B. Grain-size characteristics of samples analyzed at both
     VIMS and MGS	      29
  '   Summary of RSA calibration data	      33
 5.  Comparison of expected and observed diameters of
     calibration spheres  	      34
 6.  Comparison of percent errors in fall velocity and mid
     class diameter	      35
 7.  Determination of average water content with depth   	      63
 8.  Calculation of the ash weight of biogenic sediment  by
     subareas	      69
 9.  Distribution of sediment types 	      73
10.  Approximate proportions of specific clay minerals   	      93
11.  Table of R^ values for various regressions and  subareas   .  .  .
12.  Suspended sediment budget after Schubel and Carter  (1976).  .  .
13.  Comparison between nearshore sand  accumulation  on the
     western shore with sand from shore erosion	     120
14.  Bottom deposition of combined sand, silt and  clay	     122
15.  Comparison of sediment budget terms   	     123
16A. Sand accumulation as a function of latitude zone	     126
16B. Silt accumulation as a function of latitude zone	     127
16C. Clay accumulation as a function of latitude zone	
 ; ^  Sediment mass accumulation rate as a  function of  zone  and
     depth interval for ± 0.57 m level  of  estimation	
18.  Sediment mass accumulation rate per unit area as  a
     function of zone and depth interval for ± 0.57  m  level
     of estimation	     134
                                      x

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                             ACKNOWLEDGEMENTS

     In a project as large as this, it" is impossible to credit even  all  the
major contributors as authors.  We thank the following individuals and
acknowledge that the project could not have been completed without their
labors.  J. Zeigler wrote the section on the Geologic History of  the
Chesapeake Bay and was constantly available for discussion.  P. Peebles
wrote the section on the statistical comparison of  the Rapid Sediment
Analyzers.  Additionally, she drafted most of the maps and figures and
participated in several other program areas.  0. Bricker, originally with
the Maryland Geological Survey, later our E.P.A. Project Monitor, and now
of the U.S. Geological Survey, provided much assistance and encouragement.
R. Kerhin, J. Halka, and J. Hill of the Maryland Geological Survey assisted
with technical development, inter-state coordination, and general
discussion.  C. Sutton and D. Owen did much of the  computer work.  G.
Thomas, L. Morgan, D. Owen, S. Fenstermacher, K. Worrell, J. Cumbee, S.
Synder, M. Mitchell, A. Frisch, K. Farrell, and G.  Chianakas collected  the
samples.  W. Athearn did much of the early logistical work.  G. Pongonis
and D. Ward, Captain and Mate of the R/V Captain John Smith, provided
encouragement, assistance, and excellent service under often trying
circumstances.  A. Haywood, E. Travelstead, C. Fischler, M. Mitchell, L.
Zellmer, R. Bowles, G. Chianakas, C. Lukin, M. Fedosh, B. Savage, H. Byrne,
and B. Comyns did laboratory analyses and data reduction.  L. Kilch
assisted with the quality assurance program for carbon and sulfur analyses.
J. Boon provided guidance and discussion on error analysis.  M. Nichols  and
B. Nelson provided valuable assistance and discussion.  B. Marshall, C.
Gaskins, and the staff of the V.I.M.S. Word Processing Center prepared  the
various drafts.  J. Gilley drafted some of the maps and figures.  0.
Bricker, C. Strobel, J. Klein, and D. Wilding, among others at E.P.A.,
assisted with technical coordination.  The Chesapeake Bay Program, U.S.
Environmental Protection Agency funded the program.
                                     XI

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                                     I

                               INTRODUCTION

     The basic reason for the study of the physical characteristics of  the
bottom sediments of the Chesapeake Bay is that the sediment is the locus of
interaction between toxic substances that have been introduced into the Bay
system and the biological communities that use the same system.  Whether
the biological elements make permanent use of the Bay by residing in  it, or
temporary use through migration or seasonal habitation, they all are  to
some extent dependent on the sediments and the sediment-formed strata which
form the physical structure over and through which the biota are
distributed.  If, as often has been postulated, there are discrete
relationships between the substances of concern and specific types of
sediment, knowledge of the sediments is critical to the understanding of
the toxic substances problem.  Thus, the first objective was to discern the
sedimentological characteristics of the bottom sediment at a sufficient
sample density so that reasonable interpolations may be made from a sample
subset which is analyzed for various toxic substances and other related
parameters.

     Other tasks within the Environmental Protection Agency's Chesapeake
Bay Program are concerned with the transport and transformation of toxic
substances and upon the recent sedimentation history of the Bay.  A very
important element in the analyses of these problems are detailed maps of
the characterization of the surface sediments.  Thus, a second objective
was to supply maps of the characteristics of the bottom sediments to
support  interpretations made in other phases of the EPA-Chesapeake Bay
Program, specifically those phases dealing with the transportation of
materials and with the history of recent sedimentation.

     As  one of the long term goals of the entire Chesapeake Bay Program is
to develop a system by which changes in the status of the Bay  could be
monitored, a third objective of this project was to provide a  comprehensive
statement of the "condition" of the bottom sediments of the Virginia
portion  of the Chesapeake Bay against which future sediment samples and
characteristics could be compared.

     Similarly, the study of sedimentation budgets and  rates benefits both
the theoretical and practical understanding of the Bay's workings.  Areas
of deposition might be expected to be reservoirs of existing or  potential
pollutants which are related to the sediment.  Areas of bottom erosion
would be very poor sites for disposal of dredged materials.

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     Thus the objectives of Sediment Budgets and Rates subtask were
     1.  to identify the principal sites of deposition in the Virginia
         portion of the Bay,
     2.  to establish sedimentation rate as a function of position in the
         Virginia portion of the Bay, and
     3.  to formulate a sediment budget for the Virginia portion of the Bay
         which incorporates the sedimentation rates from 2 and available
         estimates of sediment supply from the tributaries of the Bay, the
         ocean, and from shoreline eroeion.

     The attainment of the objectives of both subtasks should be of benefit
in making management decisions concerning the fate of the entire Chesapeake
Bay.  This study was integrated with a similar study in the Maryland
portion of the Bay conducted by the Maryland Geological Survey, thus
compatible Bay-wide data will be available to those persons making
interpretations and decisions affecting the region.  An equally important
product of the project(s) is information leading to further basic research
problems which will augment the ultimate thrust of the EPA-Chesapeake Bay
Program and the general understanding of estuaries.

     This report is organized with separate, generally complete discussions
of the sedimentology of the Virginia portion of the Bay and of the
volumetric cut and fill within that area.  The discussion of the overall
sediment budget draws the sedimentology together with the volumetric
changes in the quantity of the surface sediment and additional information
in an attempt to determine and to rank the various sediment sources.  The
several large sets of data which were created during the life of the
project and which were used in the intrepretations are included as separate
appendices or are available from Virginia's State Water Control Board and
its files in E.P.A.'s STORET data system.

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                                    II

                                CONCLUSIONS

     1.)  The bottom sediments of the Virginia portion of the Chesapeake
Bay are significantly sandier than has been previously reported.  The
difference is attributed to the much higher sampling density used in this
study rather than to gross changes in sediment characteristics through
time.  However, there are locations where transitions may have occurred
during extreme events.

     The high sampling density disclosed that grain-size gradients are very
steep in the transverse sections, generally a reflection of bathymetry.
The very fine grained sediments (mud) are generally restricted to the
deeper channels or the lower energy environments associated with shallow,
marginal embayments.  The principal floor areas with mud sediments are the
axial channel and basin between the Potomac and Rappahannock tributary
estuaries.  In addition the channels leading to the James and York
tributaries are mud as are the entrance channels and basins of the
embayments of Mobjack, and Pocomoke, and Tangier Sounds.

     This study corroborates the strong correlations between total carbon,
organic carbon, and sulfur content of the sediment and the weight-percent
clay as previously has been found.

     2.)  The patterns of deposition and erosion, calculated by comparing
bathymetric data of the 1850's with that of the 1950's, provide very
important insights into the sedimentation processes within the Bay,
particularly when coupled with grain-size information.  The deposition
patterns suggest that there is appreciable advection of fine sand  from the
Bay-mouth region to at least thirty-five kilometers up the Bay.  This is
represented by significant fine-sand and silt deposition in the Wolf Trap
Light region.  This locus of deposition is argued to occur as a consequence
of net up-Bay estuarine circulation through the deep channel along the
Eastern Shore (Cape Charles Deep) mediated by the relatively strong tidal
current energies.  As well, the contribution of fine and very fine sand  to
the broad central basin north of this region is most reasonably
attributable  to a Bay mouth source.  Thus, the Bay mouth may contribute
very fine sand to as  far north as the latitude of the Rappahannock River
entrance.

     The immediate Bay mouth region, known to be a zone of active  bedload
movement, is  characterized by a pattern of "alternating" erosion and
deposition areas as expressed by slowly shifting shoals and intershoal

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 deeps.  This pattern  is consistent with earlier  studies  of  individual
 components of the system.

      The second region of particular  interest  is  the  transition  area
 between Potomac and Rappahannock tributaries.  This region  contains  the
 junction of the deep  axial  channel leading  from Maryland waters  which
 flares into the central basin of the  Virginia  Bay, and the  junction  of  the
 channels leading to Tangier and Pocomoke Sounds.  The main  axial channel
 and the channel system of the Sounds  are separated by the sand shield
 containing Tangier and Smith Islands.  The  western and southern  fringes of
 the sand shield exhibit appreciable deposition.   This is attributed  to  sand
 encroachment over the "edge" of the shield  induced by net down-bay
 circulation of the surface water layer augmented  by wind drift currents and
 wave driven resuspension accompanying strong north and northwest winds, a
. dominant component in fall and winter.

      The main Bay axial channel from  Maryland  and the transition to  the
 Virginia basin is the principal deposition  site  for clay in the  Virginia
 portion of the Bay.   The clay/silt deposition  area is pronounced where  the
 axial channel flares  in cross-section leading  into the broad central basin.
 Approximately 50% of  the total clay accumulation  in the  Virginia Bay occurs
 between the Potomac and Rappahannock  tributaries.  Silt-sized materials are
 somewhat more uniformly distributed throughout the stem; however,  about 33%
 of the silt accumulates in  this transition  region, an area  of relatively
 low tidal-current energy.

      The distribution of the fractional accumulations of sand, silt  and
 clay suggest that the principal clay  sources are  from the northern Bay
 followed by the Bay mouth,  that the principal  sources of silt are the Bay
 mouth followed by the northern Bay, and that the  Bay  mouth  is the principal
 sand source.

      3.)  The estimates of  a sediment budget were constructed for the
] Virginia portion of the Bay using measured  values for the contribution  from
; shore erosion and residual  bottom accumulation,  and literature values  for
i silt and clay importation from Maryland waters.   The  residual bottom
I accumulation of silt  and clay exceeds the values  from the estimated  sources
 by a factor of 12.  The measured values of  the silt and  clay contribution
1 from shore erosion are an order of magnitude less than previously
 estimated.  Bottom accumulation of sand exceeds  that  contributed from shore
 erosion by a factor of 40.

      Previous attempts at constructing a sediment budget have dealt  solely
 with suspended sediments and with shore erosion  as the sole contributor of
 sand.  The patterns of deposition and the magnitudes  of  the sand
 accumulation clearly  indicate that there is a  strong  advection of nearshore
 sands into the Bay mouth and up the Bay stem.  Previous  estimates of the
 sediment budget using only  the suspended component have  concluded, using
 salt budget arguments, that the tributaries are  sinks for materials
 transported from the  Bay.   If indeed  the tributaries  are sinks for
 materials transported from  the Bay, then the apparent discrepancies  between
 -bottom accumulation and the previous  estimates of source strength are

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enlarged.  If the tributaries are sources rather than sinks,  and  if  the  Bay
mouth is a stronger source than hitherto estimated, then  the  order of
magnitude discrepancy for silt and clay accumulation would be reduced.

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                                    Ill

                              RECOMMENDATIONS

A.  MANAGEMENT RECOMMENDATIONS.

     The parameters addressed in this report are not amenable  to  control  by
environmental management agencies.  Rather, this study has provided
baseline information on the character of the sediments of the  Bay  stem, an
identification of the patterns of deposition with an interpretation of the
transporting agents involved, and, finally, an attempt at balancing the
residual sediment accumulation on the Bay floor with potential sources.
However, this does not mean the information portrayed is without  utility  to
management agencies.  Quite the contrary, these results form a foundation
from which many management decisions will be founded when used in
conjunction with other components of the EPA/Bay Program.  In  particular,
the integration of the results of grain-size patterns and bottom  mass
accumulation patterns will allow determination of the spatial  accumulation
of trace metals and toxic organic compounds and estimates of their mass
accumulation.

     In addition, the results of this study, when coupled with other
components of the EPA/Bay Program, should appreciably improve  the
management of the disposal of dredged material.

     Heretofore, the selection of sites for the disposal of dredge material
within the Bay stem has been made on economic considerations and  on very
scanty information concerning the environmental character and  operative
processes.  As a result of the EPA/Bay Program, several very important
elements may be integrated to choose disposal sites:

     1.)  The patterns of deposition may be used to  identify areas of
natural accumulation and therein sites where the dredged materials are
likely to be relatively stable.

     2.)  The bottom-sediment grain-size information may be compared with
that expected for the dredged material and the sites may then  be  evaluated
as to whether the benthic community colonizing the disposal area  have
greater or lesser resource values.

     3.)  The expected tidal currents and residual circulation at  the
potential sites may be estimated from the finite element hydrodynamic model
generated in the Eutrophication Program.  When the aforementioned elements
are combined with bottom slope, salinity, water depth and expected wave
energy, potential disposal sites may be ranked relative to expected short

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and long term stability, and whether the areas, when recolonized, are
likely to have an altered benthic community as well as their relative
resource value.

B.  RESEARCH NEEDS

     1.)  It is evident that considerable additional study  is needed to
gain improvements in construction of a sediment budget.  In particular,
research must be focused on the question of the flux suspended sediment
through the mouths of the major tributary estuaries with emphasis on fate
of materials discharged from the Potomac and the Rappahannock.  The results
reported herein suggest that the Bay mouth may be a strong  source for  silt
as well as fine sand; further study is needed to evaluate the strength of
this source.

     2.)  To date there have been three major studies  on the grain  size
characteristics of bottom sediments of the Virginia portion of the  Bay
stem.  This report provides a comparison of these studies with a resulting
interpretation that the gross patterns are generally invariant with time.
Since the previous studies utilized very sparse sampling densities,
additional periodic sampling at a subset of the grid sites  sampled  in  this
study should be undertaken to test the hypothesis that the  patterns are
stable.  Since it is the reservoir characteristics of  the fine-grained
sediment are of principal interest, the subset of stations  should be
focused in the areas of primarily fine-grained sediments.

     Particular attention is warranted on flood events as deposition of
fine-grained sediments may be more widespread during these  events.  If such
widespread deposition does occur, then follow-on sampling should be
conducted to investigate the fate of the "thin" layer.  The object  would be
to determine how much of the material is "folded" into the  sediment column
by bioturbation and how much is simply resuspended and advected  into the
principal regions of deposition of muddy sediments.

     3.)  The  interpretation of patterns of deposition and  associated
grain-size characteristics has been based upon heuristic arguments  about
estuarine circulation and dominant pathways of flow.   Such  interpretation
is tenuous until tested with a comprehensive  set of measurements  of the
vertical distribution of currents and density.  An important contribution
toward  that goal will be met through the ongoing study of circulation  in
Bay conducted  by NOAA/NOS.  Analysis of this  data set  will  provide  the
framework to  test the interpretation of the gross patterns.  As  well,  it
will provide  the background necessary to design further specific  studies of
particulate resuspension and transportation in the various  subareas.

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                                    IV

                          BACKGROUND OF THE STUDY

     The main stem of the Bay and its tributary estuaries form a  system;
the physical characteristics of the system have evolved through time with
the current circumstances representative of conditions only slowly changing
over the last two or three thousand years.  As viewed today the system
represents a trap for sediments entering the system from the  fluvial
drainage and, as well, for materials entering the mouth of the Bay by an
impressed estuarine circulation.

     It is important that the management strategies formulated for the Bay
incorporate the realization of a naturally changing system.   The  purpose of
this chapter is to review the geologic history of the Bay region  and to
review the status of understanding of its sedimentological characteristics
prior to this study.

A.  GEOLOGIC HISTORY OF THE CHESAPEAKE BAY REGION

     The geologic history of the Chesapeake Bay spans time scales that
differ by orders of magnitude.  The region is related to happenings
hundreds of million years ago and to modern sedimentation that sometimes is
governed by man-induced changes that occur within a
decade.  Nevertheless, the parts can be fitted into a single, internally
consistent narrative.

     Five to six hundred million years ago North America consisted only of
a low continent centered around what is now Hudsons Bay.  The shoreline ran
approximately through the present day Great Lakes and southern Ontario.
The region that was to become the Chesapeake Bay lay hundreds of  miles
offshore near the edge of the continental shelf where thick sequences of
muds and sands were being deposited (Hallam, 1974).

     While this was taking place the continents of North America, Africa,
and Europe were drifting together.  By the end of Permian time,
approximately 225 million years ago, the continents had been  forced
together.  The sediments caught between these huge plates were folded,
faulted, and metamorphosed into the schists, gneisses, slates, and other
crystalline rocks which now form the Piedmont and on which the coastal
plain sediments have since been deposited.

     The collision was to be temporary, for during the Triassic the
continents began to drift apart.  Huge faults cracked the continental edges
dropping blocks of the continental downward to form enormous  rift valleys,

-------
similar to those in east Africa today, where the same process  is  taking
place.  Sediments worn from the mountains, lava flows and ash  poured  into
the basins and, in some cases such as the basin which had formed  near what
is now Richmond, coal swamps formed.  These deposits, stacked  in  their
ancient valleys, are the Triassic "red beds" which can be found in basins
from the Maritime Provinces and New England to the Carolinas.

     Ultimately the cracks between continents widened and the  sea invaded
to form the beginning of the Atlantic Ocean.  Rivers from the  Appalachian
regions spread fresh water deposits over the low area at the continental
edge.  These are the non-marine sands and silts of the Potomac Group  of
Cretaceous age.

     The widening continued.  Local and regional uplifting  and downwarping
took place as the continent adjusted to new loads of sediment  and to  forces
associated with continental drift.  The sea inundated the area of the
mid-Atlantic states with the result that the non—marine sediments of  the
Cretaceous grade upward into the younger marine late Cretaceous and early
Tertiary materials from about 65 million years to perhaps 25 million  years
age.

     As formations of early Miocene age are missing, we infer  that the  sea
must have withdrawn until about the middle Miocene, perhaps 15 to 18
million years ago, after which time the sea returned and layers of marine
sands, sandy clays, clays, and shell beds were deposited as the Chesapeake
Group (Calvert, Choptank, St. Marys, and Yorktown formations of
Miocene-Pliocene age).  This continued until perhaps 2 million years  before
the  present.

     It is during this middle Miocene-Pliocene episode that the broad
outlines of the Chesapeake Bay are  thought to have formed.   Stephenson,
Cooke, and Mansfield (1933) pointed out that uplift  took place during
Calvert time beginning in, or north of, Maryland, and spread southward
until the seas of Yorktown time receded. Contemporaneously  with  the
tipping-off of the seas, sands and  gravels poured from the  Delaware,
Susquehanna, and Potomac Rivers over the newly emerged coastal plain,
forming the land mass of what is now New Jersey and  the Eastern-Shore of
Maryland, and Delaware.  The rivers themselves adjusted their  courses
around the sands and gravels, the Delaware ultimately  flowing  between the
coarse outwash plains of New Jersey and Maryland-Delaware,  and the
Susquehanna and Potomac into the basin between the Maryland Eastern Shore
and  the eroded uplands of  the western  shore.

      We have sketched a history which  shows that  the basin  which  was  to
become the Chesapeake Bay had  formed before the Pleistocene and  extended at
least as  far seaward as the  last Pliocene  sea.  The  Virginia's Eastern
Shore, the  lower portion of  the Delmarva Peninsula,  had not yet  formed.

      This brings us  to the most recent  geologic acts which  formed the Bay;
namely, the glacially  induced  sea-level changes of  the Pleistocene.   The
Chesapeake  Bay  fills a broad,  shallow  valley which was  cut, or in our
opinion modified, by Pleistocene  rivers during multiple  lowered  sea  levels

-------
and subsequently flooded by the rise of the sea during the past  ten
thousand years to produce the modern Bay.  This clearly seems to have
happened.  However, the complete story is more complicated.

     In general, sea level remained reasonably close to present  sea  level
between 2 x 10  and 1.5 x 10° years ago when a very high stand
approximately 30 meters (100 feet) above the present occurred.   This
elevation coincides with that of the Surry Scarp, a prominent geomorphic
feature in Virginia's coastal plain.  Following that very high stand,  the
sea was close to or slightly above the present level for the next  500,000
years.  Belknap and Wehmiller (1980) believe the core of lower Delmarva
formed during this million years between 2 x 10° and 1 x 10" years B.P.  If
this be true, then the basin enclosing the Chesapeake Bay was virtually
formed and was filled with marine water to approximately its modern  shores
by about 1 million years ago.  Figure 1 is a composite of sea-level  changes
based upon the work of Shackelton an Opdyke (1973) and van Donk  (1976), as
modified by Zellmer (1979).

     It is not the purpose of this paper to attempt to unravel the details
of these multiple lowerings except in a general way.  However it is  clear
that when sea level was so low that the entire Bay was drained,  the  basin
must have been occupied by rivers in deep channels.  Each time sea level
rose above these channel margins the rivers were essentially lifted  out of
their channels.  When sea level dropped the rivers did not necessarily
settle back into their old channels but to one side or the other,  except
where the basin was narrow.

     The evidence for this is widespread.  Schubel and Zabawa (1972, 1973)
reported a major buried channel they took to be an old channel of  the
Susquehanna which connects the lower reaches of the Chester, Miles,  and
Choptank estuaries.  Drilling and seismic studies connected with
construction of the Bay-mouth bridge-tunnel reported by Harrison et  al.
(1965) showed three large buried channels.  Later a cross-section  of the
bridge-tunnel crossing was refined and presented by Meisburger (1972).
Carron (1979) presented a map showing his interpretation of the  old
drainage lines (Figure 2).  Inasmuch as our main interest is in  the  most
recent or Holocene blanket of sediment, we need not concern ourselves  with
unravelling the drainage network of the Pleistocene unless in some way it
impacts modern sedimentation.

     A knowledge of the most recent rise of sea level is an important  tool
in the understanding of the Holocene sedimentation.  Approximately 17,500
years ago the shoreline of the Atlantic Ocean was about 100 km (65 miles)
east of the Chesapeake Bay mouth along the break in slope of the
continental shelf.  Sea level was approximately 100 meters (300  feet)  below
the present level.  Much of the shelf was dry land or swamp over which the
river systems draining the Bay area spread sand and gravels.  The  basin of
the Bay was traversed by rivers confined within their valleys.

     If we accept the erosion-deposition model of river activity by  Jordan
(1974), the height of the glacial advance would have been a time of  river
stability with a tendency for deposition as the glacial age began  to end.

                                     10

-------
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-------
Sea level rose approximately 80 meters (250 feet) in the first 7500 years
of deglaciation (17,500-10,000 B.P.), or 1 meter (3.3 feet) per century
(Shackleton and Updyke, 1973).  The Bay would have started to flood at a
sea level of minus 15 meters (50 feet) and sediments would have begun to
fill the old channels rapidly.  Although the rate of rise of sea  level
slowed during the next 6500 years, from 10,000 B.P. to 3500 years B.P., it
still rose approximately 12 meters (40 feet), or about 18 cm (0.6 feet) per
century.  The Bay 3500 years ago must have been very nearly the size it is
today.  Sea level at that time was aboat 3 meters (10 feet) below the
present.  Sea level has risen at an average rate of only 10 cm (0.3 feet)
per century in the past 3500 years (Newman and Rusnack, 1965).

     It is perhaps self-evident that the level of the sea with respect to
the land can change because the volume of the sea increases or decreases,
or because the land rises or falls, or because of some combination of the
two.  On the other hand, it is usually impossible to know which is the
mechanism at any one place, unless of course eustatic or world wide
sea-level is unchanging.  For purposes of this discussion it is not
critical that we know the cause but it is very important to know  the rate.
Mariner (1949) reported that sea level, as reported on tide gauges, was
rising along the entire east coast.  Hicks and Crosby (1974) reported that
sea level at Hampton Roads and Portsmouth, Virginia, had been rising at a
rate of approximately 30 cm (1 foot) per century, 3 mm (0.01 foot) per
year, since 1928.  Further confirmation that sea level is rising  over the
region of the Chesapeake Bay comes from precise re-levelling between first
order benchmarks in the Bay area coupled with tidegage data, Figure 3
(Hohldahl and Morrison, 1974).  The authors attempted to remove the
eustatic effects by substracting an assumed world wide rise of 1.0 mm per
year from their measurements.  If correct, the entire Bay area appears to
be sinking tectonically but not everywhere at the same rate.

B.  RECENT SEDIMENTOLOGICAL WORK

     The earliest survey of the bottom sediment characteristics was that of
Ryan (1953) wherein he obtained 209 samples along transverse sections of
the Bay and the river mouths.  Eighty-six of those stations were  in the
Virginia section of the Bay.  From the skeleton framework Ryan inferred the
spatial patterns of texture on the basis of an implied depth-texture
association.  An improved portrayal of the spatial patterns in the Virginia
part of the Bay resulted from the work of Shideler (1975) who occupied 200
stations, again along transverse sections.  This work provided clearer
definition of the areas dominated by mud.  He observed the sands  to be
relatively coarse in shallow water and to be very fine in deeper  water in
association with mud.  The differentiation of the sand sizes was
interpreted to be the result of wave energy with the coarser, fringing
sands representing a lag deposit from shoreline erosion and the very fine
sand in deeper waters representing the wave-winnowed fraction transported
into deeper water.  In the lower portion of the Bay, from the York River to
the Bay mouth, were stringers of medium-grained sands which did not appear
to be depth controlled.  These deposits were interpreted as being partially
reworked relict materials.
                                     13

-------
„

-------
     There are no previous attempts at constructing a sediment budget which
includes the sand component for the Virginia portion of the Chesapeake Bay.
Schubel and Carter (1976) formulated a suspended sediment budget for the
entire Bay stem utilizing a salt budget argument and field measurements of
Bay axial suspended sediment distributions during 1969-1970.  They argued
that in the lower Bay shore erosion may be the largest source of inorganic
sediment.  In addition they calculated that the input of suspended sediment
through the Bay mouth was a strong source and that the tributary estuaries
were, in fact, sinks for sediment materials in the Bay.
                                     15

-------
                                     V

                                  METH6DS

     The methods used in this study matched, to the extent possible, those
of the Maryland Geological Survey's (MGS) parallel study of the Maryland
portion of the Bay.  The two studies used essentially identical protocols
for the analyses of sediment characteristics and chemistry.  However, the
treatment of the rates of deposition and the information derived therefrom
were somewhat different due to differences in the availability of data  from
bathymetric surveys and in the formatting for automatic data processing.

A.  CHARACTERIZATION OF SEDIMENTS

     1.  Sample Collection.  Two basic considerations, providing sufficient
coverage to delineate gradients in grain size and efficient utilization of
the time available, drove the design of the sampling density and pattern.
Moreover, the Virginia grid was designed to be as compatible as with the  1
square kilometer grid that the MGS already had established for their
project.  The resulting "diamond shaped" sampling pattern in Virginia is
based upon the Universal Transverse Mercator (UTM) 1,000 meter grid.  The
sample sites were at the intersections of even numbered rows with even
numbered columns and odd numbered rows with odd numbered columns.  This
plan resulted in a nominal, minimum spacing of 1.4 km.  The total field
collection was 2,172 sample sets from 2,018 locations (Figure 4).

     Bottom samples were acquired with a stainless steel Smith-MacIntyre
grab sampler which has a volume of approximately 0.01 m .  When the  sampler
was on deck at least two subsamples were taken from the sediment surface.
Surface samples were skimmed from the top centimeter for the carbon-sulfur
analysis.  These were placed in a labeled plastic vial and promptly
refrigerated or iced.  The second subsamples were several hundred grams of
material from the top 4 to 6 centimeters.  These were placed in large
plastic envelopes with top fasteners and, although not refrigerated, care
was taken to avoid long exposure to environmental extremes.  Special scoops
were designed and fabricated (Figure 5) for the two sample sets so that a
uniform rectangular cross-section was plugged from the larger sample.
Using these devices avoided the bias introduced by inserting a circular
cross-section sampler into a sediment with vertical gradients in any
parameter of interest.

     As part of the Quality Assurance Program, discussed later, so as  to
minimize the possibility of losing the sampling information, two logs were
maintained.  A "sample log" contained the date, sample code number as
recorded on the sample container, and nominal site location.  The "cruise


                                     16

-------
Figure 4.   A map of the Virginia portion  of the  Chesapeake  Bay  showing
           the location of subareas  and sample stations.

-------
Figure 5.   Photograph of sample scoops that were fabricated for use in
           this project.  The larger device, shown with sample bag, was
           used to collect the large, bulk sample of the top 6 cm of
           sediment for grain-size and water-content analyses.  The
           smaller device was used to skim a sample from the top 1 cm
           of the sample for carbon and sulfur analyses.

-------
 log"  contained,  in  addition  to  this  information,  the  time  of collection,
 water depth  from an echosounder,  name  of  the  sampler,  and  a description of
 the sediment  surface  and  of  the materials  recovered.   All  sampling was
 conducted  from the  Research  Vessel Captain John Smith (Figure 6).

      Sample  stations  were located by navigating the research vessel to
 points defined by LORAN C signals; the predetermined  values for the LORAN C
 signals  being obtained  from  tables supplied by the Defense Mapping Agency
 through  EPA  and  by  applying  a "Bias  Correction Factor" to  the listed
 values.  The  tabulated  values are theoretical and do  not consider
 variations in electromagnetic signal propagation across land masses and
 across the land-water interface.  Bias correction values were determined by
 comparing  the observed  LORAN C  values  for  known points with the theoretical
 values for the same locations.  The  correction data is given in Appendix 1.
 Once  on  station,  LORAN  C  readings were automatically  printed on paper tape.
 The tapes  were attached to the  sample  log-sheets.  Later the readings for
 each  station  were averaged,  "un-corrected", and entered into a computer
 program  which yielded the latitude and longitude of the actual station.

      In  order to check  the ability to  return  to actual sample sites, at the
 conclusion of the sampling program,  nineteen  sample sites  were relocated to
 the averaged  LORAN  coordinates.  Comparison of the calculated latitudes and
 longitudes for the  nineteen  pairs of stations yielded an average return to
 within 30  meters of the original  location.  With the  ability to return to
 sample sites  as  located by the  observed LORAN or by latitude and longitude
 as determined by other  means, future researchers should be able to very
 closely  approximate the locations of the  sites sampled.

      Samples  were collected  on  75 days spread over eight months in 1978 and
 1979.  Sampling  was very  slow during the  winter months when days were
 short, windy, and icy.  Milder  spring  weather brought with it a great
 increase in  productivity; Table 1 details  the specifics of sampling.

                                  TABLE 1

                           Schedule  of Sampling

           Year	Month	Days     Samples Per  Month
1978

1979





November
December
January
February
March
April
May
June
13
5
10
5
12
13
15
2
160
104
238
112
462
525
547
26
      2.   Analysis  of  the  Sediments.   As  mentioned previously,  two sample
 subsets  were  collected  at  each  station (aside from replicates).   The
-smaller  subsample,  for  carbon and sulfur analyses, was taken from the

                                     19

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cruise on ice and then frozen and held until pretreatment  for  analysis.
The larger subsample, secured for water content and size analyses,  upon
delivery to the laboratory was mixed and split into at  least three
subsamples.  One was labeled for the archive, another was  stored  pending
granulometric analysis, and the third was promptly analyzed for bulk water
content.  Figure 7 is a flow chart of the analytical procedures.

a.  Water Content.  The water contents were determined  by  placing the
sample in a preweighed beaker, weighing it, drying it at 65°C  and weighing
again; the weight difference being the weight of  the water.  The  percent
water content was calculated with the formula
          u
     u  = "w   ,nn
     wc   77- x 100,
          WT
where Wc is percent water content, Ww weight of the water, and W>j the
weight of the sediment-water mixture.  No attempt was made to  compensate
for the weight of salts from evaporation.

b.  Grain-Size Analysis.  As the sediments range  from granules to clays,  it
is necessary to employ different analytical techniques  on  different
fractions of the sample.  The sand fraction was analyzed in a  Rapid
Sediment Analyzer (settling tube), the granules by conventional sieving,
and the fines by Coulter Counter.  The different  data sets from each sample
were then joined in a miscegnatious marriage by the computer.

     All the samples received the same pretreatment, separate  digestions
with HC1 and I^C^, washing, fluid removal through filter candles, dispersal
in an ultrasonic bath, and wet sieving through a  4 0 (63 ym) screen.

     Table 2 is a listing of phi, 0, classes and  the equivalent metric
sizes.  Phi, a logarithmic transformation of the  linear metric measurement,
is calculated with the formula 0 = -Iog2 (diameter in millimeters).
Because phi is logarithmic and is, in one sense,  a measure of  the interval
between classes (McManus, 1982) it is inappropriate to  compare phi  and
metric standard deviations.

     The material passing the screen was transferred to a  1,000 ml  cylinder
and processed by conventional pipette techniques, including dispersants,
for total weight of material, and percents silt and clay.  An  additional
withdrawal of the total sample was taken and kept for analysis on a Coulter
Counter Model TA or, later in the project, TA II.  This analysis  was
performed using standard 2-tube (140 ym and 30 ym apertures) techniques
(Coulter Electronics, 1975 and revisions).  Shideler (1976) discusses  the
differences between standard pipette data and Coulter Counter  data.
Further discussion is provided in the section on  Quality Assurance.  It
should, however, be remembered that neither pipette nor Coulter methods
give direct measurement of grain size.  The former yields  grain by
equivalence in fall velocities of the natural particles and spheres of  a
given specific weight.  The latter converts electronically estimated
particle volumes to spheres of equal volume.
                                    21

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                                                    FLOW CHART
                                               SEDIMENT  ANALYSIS
                                VIRGINIA CHESAPEAKE  BAY  BOTTOM  SEDIMENTS
                                                   | GRAB SAMPLE |
          LARGE PLUG OF TOP
          4 -6 cm INTO LARGE
             WHIRLPAK
                I
           STORE OUT OF
            DIRECT SUN
                1
          TRANSFER TO LAB
                                                          SCRAPING OF TOP
                                                           Icm INTO VIAL
                                                                I
                                                           REFRIGERATE
                                                                I
                                                         TRANSFER TO LAB
                                                           REFRIGERATE
                                                     DISCARD OVERBOARD OR
                                                      USE FOR "DUPLICATE"
                                                  SAMPLE (QUALITY ASSURANCE)
            HOMOGENIZE
                I
              SPLIT
          INTO PREWEIGHED
             BEAKER
    ARCHIVE
    WEIGH
      I
     DRY
      I
    WEIGH

  CALCULATE
WATER CONTENT
              DISCARD
                                                                        POWDER
                                                                        SPLIT
                                                                            I
                              HCL
                            DIGESTION
                              WASH
                                I
                              LECO
                           PROCEDURES

                         ORGANIC CARBON
                            CONTENT
     I
   LECO
 PROCEDURES

TOTAL CARBON
  CONTENT
                                                                                                       LECO
                                                                                                   PROCEDURES
                                                                                                  SULFUR CONTENT
                                       REMOVE LARGE
                                      SHELL FRAGMENTS

                                        DIGEST WITH HCL
                                             I
                                            WASH

                                        FILTER CANDLE
                                                            WEIGHTS OF GRANULE, SANDS, SILTS, AND
                                                            CLAYS, AS DETERMINED IN THE SEPARATE
                                                            ANALYSES ARE SUMMED  TO YIELD THE TOTAL
                                                            WEIGHT OF THE DRY SAMPLE  THIS TOTAL
                                                            WEIGHT IS USED IN THE CALCULATIONS OF
                                                            THE RATIOS OF THE SIZE GROUPS AND THE
                                                            WEIGHT PERCENT  OF EACH SIZE CLASS.
                      IF MOSTLY SAND
                           I
                       DIGEST  WITH
                  APPROXIMATELY 8% M,O,
                                                           IF MOSTLY FINE
                                               DIGEST WITH 15% H20,
                                           HOT PLATE
                                               I
                                             WASH
                                               I
                                         FILTER CANDLE
                                               I
                                           ADO OISPERSANT
                                               I
                                     ULTRASONIC DISPERSAL
                                               I
                                       WETSEIVE THROUGH
                                       63 MICRON SCREEN
                                        INTO lOOOml CYL,
                         SAND AND GRANULE
                        INTO FILTER PAPER
                        AND EVAPORATIN6 DISH
                               I
                              DRY
                   GRANULE
                           DRY SIEVE
                           2mm SCREEN

                           _J  1	
                           SAND
                  I
                WEIGH
                  I
          CALCULATE WEIGHT
            OF GRANULES
                 J;
                                                         IF FLOCCULATION
                                                         ~\
                                                        HEAT
                                                     DO NOT BOIL
                      DRY SIEVE FOR
                    SIZE DISTRIBUTION
                        ARCHIVE
       I
     WEIGH
       I
CALCULATE WEIGHT
     OF SAND
       J;
                                                                BRING UP TO 1000 ml

                                                                     AGITATE
                                                                        I
                                                                  COVER CYLINDER
                                                             TO PREVENT EVAPORATION
                                                             	1	
                                                              LET STAND AND VISUALLY
                                                              CHECK FOR FLOCCULATION
                                  ARCHIVE
                                                     RSA
                                                  PROCEDURES
                                                   PER GRAIN
                                                 SIZE ANALYSIS
                                                                             PIPETTE ANALYSIS
                                                                             FOR TOTAL WEIGHT
                                                                             OF FINES AND SILT
                                                                                          COUNTER ANALYSIS
                                                                                              FOR GRAIN
                                                                                           SIZE DISTRIBUTION
Figure  7.   The  flow chart  for the  analysis of  sediments.

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                  Table 2
       Grain-Size
Nomenclature
                                      m
-2
-1
f
0
1
1.5
2
2.5
3
3.5
4
4.5
5
6
7
8
9
10
Granule
Very coarse
Coarse sand
Medium sand
Fine sand




1/2

1/4

1/8

1/16

1/32
1/64
1/128
1/256
1/512
1/1024

sand



Very fine sand
Silt
Clay


4
2

1
0.5
0.35
0.25
0.177
0.125
0.088
0.0625
0.044




i

-20 - -10
-10 - 00
00 - 10
10 - 20
20 - 30
30 - 40
40 - 80
80




500
350
250
177
125
88
625
44
31
15.6
7.8
3.9
20
0.98








Some researchers use 90 as the silt-clay
boundary.

Sediments finer than 40, that is both silt
and clay, are muds.
                         23

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     If the sample were less than 10% mud (silt + clay), the analysis by
Coulter Counter was omitted, leaving only the 4 0 and 8 0 pipette data  to
describe the distribution of the fine tail of the distribution.  The 10%
cutoff was used for the first thousand or so samples; 5% was used for the
remainder.

     The sand-size portions of the samples, that is the material held on
the 4 0 wet sieve and passing a -1 0 dry-sieve, were weighed, and passed
through a microsplitter until a 0.5 to 1.0 gram subsample was obtained.
This subsample was for analysis on the" Rapid Sediment Analyzer  (RSA)
(Figure 8).  The remainder was packaged and stored to be available  for
other researchers.  The RSA has a 1.5 m fall distance and is similar in
design to that described by Gibbs (1974) and is essentially identical to
the device used by the Maryland Geological Survey.  The data delivered  by
the RSA is in the form of a strip chart depicting proportion of sediment
fallen versus time since introduction of the sample to the system.  The
strip chart was then processed on a Numonics 1224 Graphics Calculator which
served to put the fall velocity data onto computer compatible magnetic
tape.  This information was converted to size data by a computer
application of the Gibbs, Mathews, and Link (1971) formula

r = 0.055804 V2 pf +  [0.003114 V4  pf2 + (g(ps - pf)  (4.5 V + 0.008705  V2ps))]1/2
                                 g (ps - pf)


where r   is sphere radius  in cm,

       V   is fall velocity in cm/sec.,

       Pf  is fluid density in g/cm  ,

       ps  is density of the sphere in g/cnH, 2.65 gm/cm-* was assumed,

       g   is the acceleration of gravity  in cm/sec.2, 980 cm/sec2  was
           used,                      ,                                        ;

         •H is the dynamic viscosity of the  fluid  in poises.                   :

As  the fluid density  and dynamic viscosity  vary with  temperature,
appropriate values from  tables for distilled water were used.

      If the sample were more than 5% granule,  the particles  coarser than -1
0 were sieved at  1/4  0 intervals  in  the  conventional  manner.

      All  the procedures  and methods were,  in so  far  as  possible,
standardized with  those  used in  a parallel  project  conducted  by the
Maryland  Geological  Survey.

      The  weights  of  each major size  class,  granule,  sand,  silt, clay,  were
summed and the  ratios were  calculated.   As  each  separate  class  analysis,
Coulter Counter,  RSA,  sieve, was  referenced to  100%,  it was  necessary to
multiply  each separate phi-class  by  the  respective  granule,  sand,  or mud

                                     24

-------
Figure 8.   The Rapid Sediment Analyzer (RSA) as constructed at V.I.M.S.

-------
ratio to obtain the proportion of each class relative  to  the entire  sample.
Similarly, phi classes common to two modes of analysis were algebraically
summed in a form of splined fit.

     The standard graphic measures of Folk or Folk and Ward (Folk, 1974)
and the first four moments plus moment skewness and moment kurtosis  were
computer calculated for each sample.

                             Graphic Measures
                                      <*

Median = 05Q

Graphic Mean

     M  = 016 + 050 + 084
      L*          -    	
Graphic Standard Deviation

     G = 084 - 016
             2


Inclusive Graphic Standard Deviation

     I = 084 - 016 + 095 - 05
             4          6.6           ;


Inclusive Graphic Skewness

     SK  = 016 + 084 - 2050 + 05 + 095 -  2050
             2(084 - 016)2(095 - 05)
               i                       I
                                      i
Graphic Kurtosis

     KO =    095 - 05                 ;
          2.44(075 - 025)


                              Moment  Measures

 1st Moment = 	
              100
 where  f  is frequency percent  of  each  0 class,  m0  is midpoint of each
 class.   By definition  the  first  moment equals  the  mean,  X,  of the
 distribution.

 2nd Moment =  f(m0 - X)2
                 100

                                     26

-------
The  2nd moment  is  the  square  of the standard deviation.

3rd  Moment  (mean cubed  deviation)  = f(m0 -
                                        Too

4th  Moment  =  f(m0  - X)4
                 100

Moment Skewness =         3rd  Moment
                   standard deviation cubed

Moment  Kurtosis  =               4th Moment
                   standard deviation to the 4th power


 c.   Clay Mineralogy.   The methods  used for the semi-quantitative
 determination  of  the  clay mineral  contents of the sediment were quite
 simple.  A subset of  the 2 pm (9 0)  and smaller sediments was obtained by
 standard pipette  methods based  on Stokes"  Law fall velocity.   The particles
 were concentrated by  centrifuge.  This material was pipetted  onto glass
 slides  and dried  at 60°C.  Another set of  slides was dried then heated over
 glycol.  Finally, a third set of some slides was heated to higher
 temperatures.   The slides were  analyzed in a General Electric X-Ray
 diffractometer at approximately 43 KV and  30 ma.  The analyses used a 2"
 aperture silt  and a 2° 20 per minute scan  speed.  Each slide  was scanned
 from 2° 20 to  approximately 28° 26.   The data was recorded on 10-inch wide
 chart paper at 1° 2   per inch.   The  relative proportions of the various
 major clay minerals was estimated by the ratios of the heights of the
 diffraction peaks for each mineral.

 d.   Carbon and Sulfur Analysis.  Approximately 900 samples were selected
 for  carbon and sulfur analyses.  As  the primary interest was  in the
 chemical alliances with the finer grained  sediments, the samples were
 selected on the basis of an inferred minimum of 15% mud by weight.  It was
 necessary  to use  percent water content to  infer mud content because while
 the  water  content analyses were complete for most samples, the
 granulometric  work had just begun.  On the basis of 500 samples there was a
 strong  correlation, r = 0.96, between mud  and water contents.  Also, as all
 the  carbon and sulfur analyses were to be  in at least duplicate, it was
 necessary  to reduce the number of samples  to a manageable level.

      The  frozen samples were thawed, oven dried at 50°C, powdered with a
 mortar  and pestle, and divided into several aliquots with a microsplitter.
 The  aliquots were weighed and placed in small vials.  The subsamples for
 sulfur  and total  carbon analysis received  no additional pretreatment.  The
 samples to be  analyzed for organic carbon were treated with 10% HC1 until
 evidence of continuing reaction ceased, then they were washed with
 distilled, deionized  water, decanted, oven dried, and weighed.  Final
 analyses were  done in at least duplicate on a LEGO Gasometric Carbon
 Analyzer,  Model 572-100 and a LEGO 532-000 Titrator for sulfur.  Both
 analytical instruments were operated in conjunction with a LEGO 523-300
-Induction  Furnace. The averages of the duplicate analyses are the reported

                                     27

-------
values.  Inorganic carbon may be calculated as the difference between  total
and organic carbon.  Samples with differences between paired readings  that
were outside acceptable limits were re-analyzed with the result of  the
multiple values showing less variation than the initial pair.

     The LEGO carbon analysis equipment is relatively common and has been
discussed elsewhere in the literature (Leventhal and Shaw, 1980).   The
method for determination of sulfur, however, is not so common, and  is
described as follows (LEGO, 1975).

     "The sample is burned in a stream of oxygen at a sufficiently  high
     temperature to convert about 90 to 97 percent of the sulfur to sulfur
     dioxide.  A standardization factor is employed to obtain accurate
     results.  The combustion products are passed into a dilute acid
     solution containing potassium iodate, potassium iodide and starch
     indicator.  The blue starch iodine complex thus formed is bleached  by
     the SC>2.  As combustion proceeds, bleaching the blue color, more
     iodate is added to return to the original blue color.  The amount of
     standard iodate consumed during the combustion is a measure of the
     sulfur content of the sample."

     3.  Quality Assurance.  All aspects of the laboratory work were
subjected to a quality assurance program.  The following text describes
some of that program.

a.  Shared and Duplicate Samples.  Several samples were split so that
analyses could be performed in the sediment laboratories of both the
Maryland Geological Survey and the Virginia Institute of Marine Science.
The primary data, sand:silt:clay ratios agree quite closely  (Table  3A&B  and
Figure 9).   In all cases except one, No. 7, VCB 1626, the samples  fall in
the same class.  In the single exception, the ratios are very close, but
fall along the sandrsilty-sand boundary.  With the samples  for which  there
are graphic data from both labs, the measures generally agree quite
closely.  The exceptions are the very fine grained samples, No. 2,  VCB 784
and No. 3, VCB 785, where very minor differences in measurement, in both
cases  0.003 mm in the  graphic mean, appear disproportionately large on the
0 scale.       •                       i

     Additionally duplicate samples were collected at 135 stations.  These
samples were packaged  as ordinary samples and returned to the laboratory
for routine  analysis;  the  laboratory  staff not being aware  which samples
were the check samples.  Although the data on the duplicates have  not  been
subjected to a rigorous statistical examination, a qualitative review
indicates a  very close and satisfactory agreement between duplicate
analysis.

b.  Calibration of the Rapid Sediment Analyzer.  The calibration of the  RSA
constructed  at VIMS followed procedures that were described  by the Maryland
Geological Survey  (Halka,  et al.).  The MGS provided VIMS with a  set  of
glass  beads  of known diameters and densities.  Members of  the staff at the
MGS had  inspected  the  beads  for  sphericity, sieved  them  at  1/4 0  intervals
for size classification, and floated  them  in various heavy  liquids to

                                      28

-------
                                 Table 3A




Samples from the Virginia Portion "Of the Bay Analyzed by Both VIMS  and  MGS




     Plotted     %       %      %      %    Graphic   Mean   Graphic    Std  Dev
Sample
783 M
; v
784 M
V
785 M
V
786 M
V
1624 M
V
1625 M
V
1626 M
V
' 1627 M
! v
as
1
2
3
4
5
6
7
8
Gran. Sand
39.3
33.5
0.5 4.0
1.5
92.2
87.9
97.5
97.3
88.2
7.3 82.3
74.0
0.4 72.9
67.2
1.2 57.0
Silt
31.5
36.5
42.3
44.9
41.4
42.0
3.3
4.8
2.0
1.3
6.3
6.2
14.2
17.8
2.3
31.6
Clay
29.2
29.9
57.7
50.6
58.6
56.5
4.5
7.2
0.6
1.3
5.5
4.2
11.8
8.9
9.8
10.1
0
6.3
5.7
8.7
7.5
8.9
7.5
2.2
2.3
1.9
1.9
1.3
1.2
4.3
3.9
4.2
4.1
nun.
0.013
0.019
0.0024
0.0055
0.0021
0.0055
0.22
0.20
0.27
0.27
0.41
0.44
0.051
0.067
0.054
0.058
0
3.3
2.3
2.7
1.8
2.8
1.8
1.1
1.3
0.6
0.5
1.9
1.7
2.0
1.3
2.0
1.5
mm.
0.10
0.20
0.15
0.29
0.14
0.29
0.47
0.41
0.66
0.71
0.27
0.31
0.25
0.41
0.25
0.35
                                 29

-------
                                Table 3B




Samples from the Maryland Portion of the Bay Analyzed by Both VIMS and MGS
Sample
R G
1148.51
1162.52
1138.03
1175.85
; 1191.14
1164.09
1269.09
| 1180.58
i
; 1113.06
1092.45
1071.10
1253.96
1908.50 M
i V
1912.50 M
V
1922.02 M
V
1846.02 M
V
1853.56 M
V
1861.80 M
V
1831.49 M
V
1867.00 M
: V
1815.95 M
V
1845.50 M
V
1764.94 M
V
1825.15 M
V
Plotted
as
9
10
11
12
13
14
15
16
17
18
19
20
% %
Gran. Sand
2.1
4.7 1.8
0.5
0.4
0 6.1
1.0 1.7
15.5
11.0
7.8
6.6
5.3
4.2
78.9
83.1
83.7
83.4
89.9
90.4
94.0
93.5
95.8
90.7
99.2
97.9
%
Silt
23.2
24.8
24.2
24.6
23.7
24.6
29.4
39.5
39.7
44.5
31.6
37.3
15.9
9.8
5.8
6,4
- 10.
4.1
- 6.
2.1
- 4.
0.2
- 0.
0.7
%
Clay
74.7
68.7
75.3
75.0
70.2
72.7
55.1
49.5
52.5
48.9
63.1
58.5
5.2
7.1
10.5
10.1
0 -
5.6
0 -
4.3
2 -
3.2
8 -
1.3
                                    30

-------
o
2
_
>

 O
             2

             •
                                 31

-------
determine their density.  The expected fall velocity of the spheres, as
predicted by the equation published by Gibbs, Mathews, and Link  (1971),
served as a standard to which the observed velocities could be compared.
Several aliquots of very nearly 0.5 gram of each separate size class of
spheres were processed through the RSA.  (Because of a limited quantity,
the aliquots of the 4 0 spheres were roughly 0.45 and 0.28 gram.)  The
elapsed fall time for 50% by weight of the sample to fall through  the
column was used as the time for the calculation of the observed  velocity  of
the mid-class size.  Table 4 is a summary of those comparisons.  The data
from the test samples of the range 0.25 0 through 2.25 0 agree quite
satisfactorily with the expected values and appear to have good
repeatability.  The very coarse and very fine particles, however,  pose a
question as the differences between observed and expected values are
significant.  The greatest errors occur with the 3.25 0 and 4.0  0  spheres.

     Aside from operator and machine errors, there are three  possible
sources of error associated with the spheres themselves:  1)  that  the size
distribution of the sphere within a size class is not as assumed,  2) that
the particle density is not as specified, and 3) that size distribution
errors were introduced in "splitting" the collection of spheres  into
smaller samples for analysis.  The following example demonstrates  the
impact of small differences in size and density on fall velocity as
predicted by the equation referred to above.

     In the 3.25 0 class, the radius of the mid-class particle is  3.125 0,
0.00578 cm, and the given density is 2.49 g/cm^.  The expected fall
velocity is 0.88 cm/sec., the observed 1.127 cm/sec,  for a 28 "percent
error."  If the mid-class size were 1/8 0 different, 3.0 0 instead of 3.125
0, the expected velocity would be 1.01 cm/sec, and the error  a more
respectable 11.6%.  Or if the size assumptions were correct but  the density
was 2.92 g/cva-  instead of the given 2.49 g/cnr, the expected  velocity would
be 1.09 cm/sec, and the error 2.9%.  Similar examples of the  roles played
by density and  size assumptions can be demonstrated with the  other size
classes.  It should be noted that the size class with the greatest error,
4.00 0, is the  one most subject to errors in density measurement due  to
particle-surface air bubbles, and to size distribution assumptions.  At
small  particle  sizes, a small diameter change yields  a large  relative
change in fall  velocity.

     As a partial test of the likelihood of  a size error, optical
measurements were made of the diameters of  10 spheres from each  size  class.
Table  5 is a  listing of the data.  Although  10 observations probably  is  not
a sufficiently  large sample to give a highly significant mean, the sign  of
the difference  most likely  is correct.  Table 6 is a  comparison  of the
percent errors, or differences, between expected and  observed fall
velocities and  sphere diameters.  As can be  seen,  in  most cases, the  sense
of the errors are the same, perhaps explaining some of the discrepancies  in
fall velocity.

     Although machine and operator errors are very difficult  to  assess,
there  are specific mechanical problems  in introducing  the  larger test
spheres into  the RSA.   The  size  and extreme  spherecity of  the particles,  as

                                    32

-------



























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-------
                               Table 5

                 Comparison of Expected and Observed

                   Diameter of Calibration Spheres
0
-1.0
-0.75
-0.5
-0.25
0.25
0.5
1.25
1.75
2.25
3.25
4.0
Expected
Diameter (mm)
2.190
1.840
1.545
1.30
0.920
0.775
0.460
0.325
0.230
0.115
0.06825
Observer
Mean (mm)
2.1008
1.7248
1.5408
1.2224
0.9048
0.7956
0.4684
0.3192
0.2348
0.1148
0.0684
Standard
Deviation (mm)
0.0784
0.0544
0.0830
0.1026
0.0334
0.0262
0.0204
0.0110
0.0103
0.0103
0.0091
% Error
4.1
6.3
0.3
5.8
1.7
2.7
1.8
1.8
2.1
0.2
0.2
NOTES:  Predicted diameter is taken as the mid-point  for  each  0
          interval.

        Percent errors was calculated as
          (100(Vexpectecj - V0bservecj)/Vexpecte(j).

        Column 3 is the mean of  10 measurements.

        -1 0 through 1.75 0 45 x magnification.

        2.25 0 through 4.0 0 90  x magnification.
                                  34

-------
                     Table 6

          Comparison of Percent Errors

     In Fall Velocity and Mid-Class Diameter
0
Class
-1.00
-0.75 .
-0.50
-0.25
0.25
0.50
1.25
1.75
2.25
3.25
4.0
% Error
Fall Velocity % Error
MGS VIMS Mid-Class Diameter
1.9
4.9
1.8
1.5
3.7*
3.8*
0.9
5.2
2.2
3.2*
19.1*
13.4
12.2
~ 7.1
9.2
1.0
1.5*
3.8*
1.6
3.3*
28.1*
45.1*
4.1
6.3
0.3
5.8
1.7
2.7*
1.8*
1.8
2.1*
0.2
0.2*
* Observed greater than expected.

NOTES:  4 0 velocity error, VIMS, is average of
           2 sets of observations.

        MGS fall velocity erro data from draft
           reports by Kerhin, Halka, and
           others.
                     35

-------
compared to natural sediments, severely limits the retention of  the  spheres
on the wetted, convex plate used to introduce the sample in the  analytical
procedure.  Additionally, there are possible errors associated with  the
values for fluid density and viscosity.  The values used were published,
tabulated values for pure water, not values measured  from  the water  in the
RSA.  Thus, while maintaining a continuing check on the reproducibility of
the RSA data, we accept the RSA calibration and data  as satisfactory.

     Even though rapid sediment analyzers or settling tubes have been used
for over two decades (Zeigler, Whitney, and Hayes, 1960) to determine the
grain-size frequency distribution of sands, questions still arise
concerning the comparison of analyses done by RSA and by sieves.   Because
the two measure different properties, one resulting from a set of  variables
concerning both grain and fluid, and other resulting  from  various  facets of
both grain and mesh sizes and shapes, it would be expected that  the
distributions depicted by each would differ.  This does not state  that one
method if better than the other, just that they differ.  Sanford and Swift
(1971) published a comparison of data from sieving and settling  techniques
in which they found that the results of the two techniques were  quite
similar.  As a check of the Chesapeake Bay samples, cumulative frequency
plots were made of data from both sieve and RSA of splits  of each  of 20
sand samples.  Figure 10 is an example of one of the  comparative plots.

     In general, the plot of the RSA data indicates a slightly better
sorted sample than does the sieve data.  This difference primarily occurs
in the "tails" of the distributions, usually the first and last  5% or  less,
and would note be reflected in the calculated graphic-measures.  In the
Chesapeake Bay samples there is no consistent relationship of  coarser or
finer as was found by Sanford and Swift.  This probably  is due to  the
differences between the methods used to convert fall  velocity, which is
what an RSA measures, to equivalent hydraulic diameter.  Sanford and Swift
used Schlee's (1966) fall times as a basis for their  work  whereas  the
present study used Gibbs, Mathews and Links' (1971) formula.

     Although the plots do differ, they are quite similar, showing
inflections  in slope at similar grain  sizes when plotted on probability
paper.  This indicates that each method discerns similar mixings of
sediment  populations with only minor differences in interpreting the means
and modes of those distributions.

c.  Comparison of RSA's at VIMS and MGS.   In order  to determine  whether  or
not the measurements made on  the RSA at the Maryland  Geological  Survey,  it
was necessary to develop a method for  characterizing  the  precision of an
RSA.  It  should be remembered that precision is not the  same  as  accuracy.
EPA (1979) defines precision  as "the degree of mutual agreement  among
individual measurements made  under prescribed,  like conditions," whereas
accuracy  is  a measure of the  proximity  of  a measurement  to a  true  value.
The problem  at hand is compounded by the  fact  that  there  is  a neither a
standard  sediment nor a  standard RSA agains which  to  gauge accuracy.  The
individual calibration process  for each RSA, described  elsewhere,  is an
approximation of an accuracy  determination.  This  section  presents a
                                     36

-------
  I00-i
  99-
  90-

  80
  70
  60
  50
  40
  30
  20

   10
   5

  '2
    I
   0.1-
       COMPARISON OF SAND SIZE DISTRIBUTION
       OF  SAMPLE VCB 0288 BY  BOTH
                            *
       RSA AND  SIEVE
   -1/2
                SIEVE /
1/2    I    I  1/2   2    21/2   3   3 1/2   4
               0
Figure 10.  Plots of cumulative grain-size frequency distributions of
          the sand portion of a sample as determined by both sieve   /
          and RSA techniques.

-------
 characterization of the precision of the RSAs based upon the traditional
 model of normal grain size frequency distributions.

      To accomplish this characterization, 42 aliquots of the same  sandy
 sediment (Whitemarsh No. 2 quarry sand, supplied by the MGS) were  analyzed
 on each RSA.  The resulting quarter-phi grain-size-frequency distribution
 data were used to calculate the first and second moments of each of  the 84
 separate grain size distributions.  The mean vectors of these  two
 parameters for each RSA were determined and compared.  The method  of
 comparison was the Retelling T^ test which is a statistical test of  the
 equality of mean vectors.

      The formulae for the calculation of the moment measures,  where  the
 mean is equal to the first moment and the standard deviation equal to  the
 square root of the second moment, were taken from Friedman and Sanders
 (1978).  The first moment is calculated as

      Hi = zfM0
            100,

 where f is the frequency percent  in each 1/4 0 size class, and M0  is the

 mid-point of the class.  The second moment, M2, is

      Zf(M0 --X)
<          100

 where the mean, X, is the first moment.  This then is a distribution with
• two variables  (bivariate) on each of many samples from the larger  overall
 sample.

      For all practical purposes,  the RSAs at VIMS and at the MGS are
 mechanically identical.  The methods of  treating the data vary slightly.
 At the MGS, the instrument is wired to a microprocessor and the  conversion
: of cumulative weight percent and  fall time to grain size is
: "instantaneous," whereas at VIMS  it is a two step procedure.   The  data
I product of the RSA is a paper strip chart which has to be digitized  in
: order to allow computer  transformation of distance to time, to velocity,  to
 grain size.

      Eighty-four  subsamples, each of approximately 0.5 gram, were  split
 from a homogeneous "archive" sample, half were analyzed at each  sediment
 lab.  The  frequency distribution  data  for the quarter phi  classes  from -1.0
 0 through 4.0  0 (very coarse through very fine sand) were  used to  calculate
 moment means and  moment  standard  deviations  of each  subsample.

      The measurement error, precision, herein considered  is that which
 occurs within  each variate among  all the samples measured.  Because  there
 are many samples, we can assume  the measurement error follows
 the  central  limit  thereon, which  states, "If random  samples of fixed size
 are  drawn  from a  population whose theoretical distribution  is  of arbitrary
 •shape, but with a finite mean  and variance,  the distribution  of. the  sample

                                      38

-------
 mean  tends  more  and  more  toward  a normal  frequency distribution as the size
 of  the  sample  increases"  (Koch and Link,  1970).   Thus,  one can use the
 Retelling T2 test  as a  statistical means  of comparison  between the
 population  of  measurements  generated  by each RSA.   This test  is used to
 judge  the hypothesis that  the  two mean vectors  are equal.   The mean vectors
 of  each variate  of the  data from the  RSA  at VIMS is tested against the
 corresponding  mean vector  of the MGS  data.

      The Hotelling T2 statistic  is calculated as

                           -  x2]  • [s2]-i •  [xx - x2]
                nj  + n2


 with  (nj  + n2  ~  2) degress  of  freedom.   [Xj  - X2]  is  the difference between
 the two mean vectors.   [Xj  - X2]l  ^s  c^e  transpose of that  difference and
 [S2,] ~1  is the  inverse  of  the pooled estimate of  the variance-covariance
 matrix.   The test is the  multivariant equivalent  of the  univariate t test,

  .  -      t =      Xj - X2
               bp


 where Xj  and  X2  are  sample  means,  Sp  is  the  pooled  estimate of the standard
 deviation (based on  both  samples),  and n^  and  n2  are  the  number of
 observations  in  each sample.

      For  the  Hotelling  test,  the  calculated  T2 is compared to tables of T2
 distribution  for a particular  level of significance,  based upon the number
. of variates and  the  degrees of freedom.   If  the calculated value exceeds
 the tabulated value,  the  test  supports rejection  of the hypothesis of
 equivalence.  If the calculated T2 is less than the listed value,  the
 Hotelling T2  test supports  the acceptance  of the  hypothesis that the mean
 vectors are equivalent  at the  specified  level  of  significance.  If this is
' the case,  the information yielded by  the two RSAs can be  considered
I equivalent.

      Computer programs  in the  Statistical  Analysis  System and SAS Users
 Guide (1979)  were used  to determine the  variance-covariance matrices and
 the Hotelling T2.  The  difference of  the two mean vectors was computed by
 determining the  mean of each of the two  variates, and arranging those means
 in a 1 x  2 matrix (a vector) for  each data set, and finally subtracting the
 VIMS mean vector from the MGS  mean vector.

      The  Hotelling T2 statistic was computed to be  0.442.  The value listed
 in tables of  T2  distribution (Kramer, 1972)  at the  0.05  level of
 significance  with p  = 2 and 82 degrees of  freedom is  6.303.  Therefore, as
 the calculated value is less than the tabulated value, the Hotelling T2
 test indicates equivalence between the precision  of MGS  and VIMS Rapid
 Sediment  Analyzers.   In turn this encourages the  acceptance of the
 assumption that  data from the  two RSAs may be used  interchangeably.
                                      39

-------
d.  Comparison of Analyses by Pipette and Coulter Counter.  As most of the
grain size distribution analyses reported in the literature for silt and
clay particles utilize the pipette-Stokes Law procedures (Folk, 1974;
Galehouse, 1971), it is advantageous to this report to compare the results
obtained using a Coulter Counter with those of the more traditional method.
Swift, Schubel, and Sheldon (1972), Shideler (1976), and Behrens  (1978) all
present dicussions bearing on the subject.

     Results obtained by the two methods are not expected to be identical.
Each measures a different characteristic and uses that to infer the
diameter of a sphere having the same characteristic.  The pipette method
indirectly measures fall velocity which, when with certain assumptions is
used in the equation for Stokes" Law, yields the diameter (or radius) of a
sphere that has the same fall velocity.  Fall velocity is influenced by,
among other things, both the specific gravity and shape of the particle.
As fine particles are platelike, the shape factor is quite important as  it
results in fall velocities much lower than that of a sphere of equivalent
volume.  The Coulter Counter makes an indirect measurement of particle
volume and assuming that as the volume of a sphere, determines the
diameter.  The other significant difference between the methods is the
nature of the distribution each observes.  The pipette distribution is open
ended; that is, given proper laboratory conditions, it is possible to
analyze through the full range of silt and clay sizes.  Pipette results
yield the cumulative percent-coarser-than, thus if the procedure  is not
carried to completion, the results may terminate at appreciably less than
100 percent.  The Coulter Counter uses only a limited size range
(approximately 4 0 through 10 0 in this study) and the results are given
relative to the range used.  The contribution of the particles outside the
machine's range is omitted from consideration.  Thus the distribution as
defined by the Coulter Counter always closes at 100 percent.

     With these considerations, one would expect that the distribution
depicted by the Coulter Counter would be  coarser and better  sorted than
that shown by pipette analysis.  Indeed this is noted by both  Shideler and
Behrens and is apparent  in comparisons made for this study (Figure 11).   In
addition to the two reasons just discussed, Shideler offers  a  third  factor
contributing to the Coulter-pipette difference.  This is  the error that
occurs when two or more  particles simultaneously pass through  the Coulter
Counter's aperture and are sensed as a  single,  larger particle.   With
proper sediment concentrations, this "coincidence error"  should be less
than  3 percent.  Behrens maintains that the most significant contribution
to the difference in results between the  two methods is  the  omission
artifact resulting from  the arbitrary  truncation of  the  distribution  by  the
Coulter Counter.

      Analysis  of 20, or  approximately  1 percent, of  the  Chesapeake Bay
sediment samples by both methods yields results which display  the expected
differences.   Figure  11  depicts the  grain size  distributions as  determined
by both methods  of the mud portion of  one of the samples.  The  figure  also
shows  a plot of  the pipette data adjusted or normalized  to  the Coulter
Counter end point.  The  Coulter Counter and adjusted pipette data are
nearly  identical, agreeing with Behren's  statement.  Although  not all  of

                                     40

-------
 DC.
 UJ
 O
 o
 UJ
 o
 DC.
 UJ
 Q.
    99.99 -i
     99.9
     99.8
ADJUSTED
 PIPETTE
    0.01
                                                             10
Figure 11.  Comparison of frequency distributions as determined by
            pipette and Coulter Counter techniques.  The distribution
            as determined by pipette but adjusted or normalized to
            the Coulter Counter's end point is also shown.

-------
the plots for the 20 pairs are as close as the example, none vary
significantly.  Assumedly, the difference between the end of the unaltered
pipette data and 100 percent is the material finer than 10 0.

     The reasons for using the Coulter Counter in preference to the more
traditional pipette method are several.  Using the Coulter Counter,
individual analyses can be completed in a fraction of an hour, whereas  the
pipette method is much more time-consuming.  Although several pipette
analyses can be run concurrently, analysis to 10 0 takes upwards of 15
hours with dramatically greater times required for finer sizes.  Galehouse
(1971) states that pipette analysis probably should be ended at 8  or 9  0
unless laboratory conditions can be maintained stable for long periods.
Swift, Schubel, and Sheldon (1972) speak of the advantage of the short  time
required for complete analyses by Coulter Counter.  It is possible to
interpolate the distribution from the end point of the pipette analysis  to
100 percent at 14 0 (Folk; 1974), there is question as to the validity  of
the data so obtained (Galehouse, 1971).  Also, as the pipette analysis
requires a great number of finely timed, carefully executed steps,  there
are a number of opportunities for error.  Although the Coulter Counter  also
is subject to operator error, there are few separate phases in the analysis
and possibly a lesser opportunity for operator caused errors.  Shideler
makes reference to other  studies (Interagency Committee on Water Resources,
1964; Allen, 1968) which  "indicate that the accuracy of electronic sensing
is probably superior to that of any other commonly used technique  suitable
for routine analysis."  If the Coulter Counter were not available,  it would
have been impossible to perform the number of analyses reported for this
study.

e.  Coulter Counter Precision.  The precision, or reproducibility, of the
Coulter Counter is, within limits, quite acceptable.  Shideler (1976)
stated that comparison of the curves from triplicate analyses of  two
samples each analyzed by  both Coulter Counter and pipette suggested a
greater precision for the more modern technique.  A similar procedure,  20
replicates of each of two aliquots of the same sample, also indicates the
relative precision of the technique.  Figure  12 is a plot of  the  envelope
of one set.  When superimposed on the similar plot for the other  20
replicates, the two are indistinguishable from one another, indicating  a
high degree of reproducibility.  The thickness of the envelopes, however,
detracts somewhat from the confidence one might have in the precision.

     This aspect of the precision perhaps is  explained by the data in
Figure 13.  For the first 10 or  so replicates, the reproducibility appears
very satisfactory with no apparent trends in  the data.  The later
observations, however, tend towards decreasing values, especially  for  the
coarser particles.  This  most likely is an artifact of the sample  size  and
not of the instrument or  operator.  As  successive small quantities of  the
dilute sediment-water mixture are withdrawn  from the vial for analysis, the
remaining suspension is progressively  less representative of  the  whole.
Also, as the coarser particles are relatively fewer  in number,  their
progressive depletion may have a pronounced  impact on  the overall  remaining
particle-size distribution.
                                     42

-------
                SAMPLE VCB  937F
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                                                9        10

                               *

Figure 12.  Plot of the envelope described by the cumulative frequency

          distribution of 20 replicate Coulter Counter analyses

          and a table of the means and standard deviations  of the

          cumulative  frequency at whole # intervals for  2 sets of
          20  replicates of the same sample.


-------
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      Therefore,  it  appears that the precision of the Coulter Counter
 analyses  is  quite  satisfactory as long as care is maintained to assure that
 the  sample  analyzed is representative of the whole.

 f.   Quality  Assurance - Carbon and Sulfur Analyses.   There were four major
 elements  to  the  quality assurance program which was  developed and
 implemented  for  the analyses of the carbon and sulfur content of sediments.
 These elements were 1) personnel and procedures, 2)  reagents and other
 supplies,  3) records, and 4) the statistical interpretation of the quality
 assurance  statistics.  A brief discussion of each of these areas follows.

      Personnel:   The majority of the analytical work was performed by
 technicians  and/or  graduate assistants.   Prior to initiating analyses, all
 the  equipment operators reviewed both the manufacturer's operations manuals
 and  the laboratory's protocol and operating guides.
 Then they  followed  a "hands on" learning process working directly with
 experienced  technicians.

      Reagents and Supplies:  All reagents, chemicals, gases, and standards
 used were  of analytical quality and were purchased from appropriate
 manufacturers or supply houses.

      Records: Several, sometimes redundant, formats were used to record
 and  track  the hundreds of samples and analyses.  A master log was used to
 list each  sample and record the various procedures or analyses that had
 been performed on each sample.  A second set of records was kept to record
 the  specific analytical data and results for each sample.  Additionally,
 another log  was  kept to record the results of instrument calibrations and
 standards.   Finally the statistical comparisons of sample pairs were
 calculated  and plotted to see if the duplicate analyses fall within
 satisfactory limits.

      Interpretation:  Statistical interpretation of the quality assurance
 information  was  accomplished in two forms.  Accuracy was checked using a
 percent recovery technique which utilized known standards.  Precision, or
 the  ability  to obtain consistent results, was monitored with an industrial
 control statistic,
                       /A - B/
                   I = /A + B/,

 where A and  B are the values from duplicate analyses of aliquots of the
 same sample.  As the total carbon and organic carbon analyses are
 identical,  only  total carbon and sulfur were tracked for accuracy.  Both
 procedures  follows  EPA (1979) formats.

      The  percent recovery was calculated as the ratio of the observed value
 to  the actual value of the commercially purchased standards.  The results
 of  the first 50  analyses of standards were used to establish the general
 control limits  for  future analyses.  The mean and standard deviation of the
 carbon analyses  were 98.5% and 1.4% respectively.  The EPA (1979)
 procedures  set  the  control limits as plus or minus 3 standard deviations
-about the  mean;  hence the accuracy control limits for the carbon analyses


                                      45

-------
were 102.7 and 94.3 percent recovery.  Less than 10% of the observations
were outside the control limits.  The majority of these observations were
traced to procedural errors or instrument malfunction.  All observations
were plotted promptly and there were no consistencies or trends apparent in
the out-of-control samples.

     The average percent recovery of the first 50 sulfur standards was
90.2% with a standard deviation of 5.5%; thus the control limits were
106.7% and 73.7%.  All observations fell within two standard deviations of
the mean, well within the control limits.

     The control limit for the industrial statistics used in the evaluation
of precision is equal to the average range of the absolute value of  the
differences between duplicate determinations multiplied by 3.27, the
Shubart factor calculated for duplicate analyses.  If the difference
between duplicates of a particular sample exceed the control limit,  the
analysis is repeated until duplicate determinations are within  control
limits.  The control limits, calculated on the basis of the first  25
duplicates, were 0.339 for total carbon, 0.268 for organic carbon, and
0.095 for sulfur.  Due to the great number of analyses, several persons
assisted with the visual examinations of the graphs of the industrial
statistic for each set of analyses in order to assure that all
out-of—control samples were noticed and corrected.

B.  FORMULATION OF SEDIMENT BUDGET

     The estimation of the sediment budget for the Virginia portion  of  the
main-stem of the Chesapeake Bay involves the comparison of the  residual
sediment mass as determined for a 100-year period.  This estimation  treats
the Bay as a "sink" for sediments derived from various "sources."  The
determination of the residual sediment mass utilizes the method of
comparing corrected bathymetric data from the 100-year interval of
(approximately) 1850 to 1950 to discern  the patterns of sedimentation  and
erosion.  This information, coupled with the data obtained from the  2,000
samples of  the surface sediment, enables one to estimate the mass  of
sediment deposited in the Bay, both in total and in terms of the  separate
masses of sand, silt, and clay.  The calculations require the  synthesis of
several sets of data and the acceptance  of several assumptions.  The most
important of these assumptions  are:

     1.  That the  surficial sediments  sampled are representative  of  the
sediment column beneath.  As such, we  assume the sand:silt:clay ratios
observed at  the  surface are constant over  the sedimentation  lengths
calculated  for the 100-year period.  This  is a necessary assumption  for the
estimation  of residual  sediment mass.

     2.  That the  sense of  the  depth difference reflected  in  the
bathymetric  comparison  are  representative  of conditions  at  the time  of
sediment sampling  (1979-1980).  For  example, at a given point  the
bathymetric  comparisons between 1850 and 1950 may  indicate  a  net  loss of
sediment  (a  net erosional  condition).   In  such a circumstance  we  would
expect a reduced water  content  in  a  surface  sediment  sample  due to

                                     46

-------
 compaction.  In  fact, however, we may  find  that  the  sample  station
 exhibited a high water content indicative of recent  deposition.   This  is
 ignored in our calculations as the conversion  from sediment  volume  to  mass
 would use the "high" water content and thus underestimated  the mass  of
 sediment "eroded".  Again, we have utilized a  necessary assumption.  It  is
 particularly noteworthy that the sedimentation dynamics associated with  the
 passage of the high, fresh water discharge  due to Hurricane  Agnes in 1972
 may have temporarily switched an area  of erosion to  one of  deposition.  Or,
 even more dramatically, there may have-been erosion  followed by  deposition
 at a given site  during the respective  onset and relaxation  of the event.

      In order to array the bathymetric and  sedimentological  data at  a
 common level, the information was smoothed  to  a 0.5  minute  grid  using  a
 pseudo-two-dimensional, bicubic, spline-fitting program.  This program was
; used separately with the roughly 40,000 corrected bathymetric-comparisons
 (Figure 14) and with the sediment information  from the 2,000 or  so  sediment
 samples.

      Thus, at the center of each 0.5 minute grid cell there  were
 interpolated values of sedimentation rates  (based upon corrected water
 depth comparison), surface sediment water content, and percentages  of  sand,
 gravel, silt, and clay.  The surface water  content was used  to estimate  the
 average water content over the sedimentation distance.  Then the average
 water content was used to convert the  sedimentation  rate  to  total mass
 accumulation rate which, in turn, could be  partitioned to component  values
 of sand, silt, and clay.  The depositional  patterns  of the  sand,  silt, clay
 components might be expected to be depth dependent and, as  well,
 latitudinally variable.  Accordingly the final tabulation was arrayed  into
 66 one-minute north-south intervals (38°00' to 37°59' = zone 1)  with depth
 stratification into eight depth zones  (0-6  ft.,  6-12 ft., 12-18  ft.  18-24
 ft., 24-30 ft.,  30-36 ft., 36-42 ft.,  and > 42 ft.).*  Finally,  as  the
 western part of  the Bay may exhibit different  behavior than  the  eastern
 part, the array  was further divided into six sub-segments:   the  western
; shore and eastern shore divided by the Bay  thalweg,  eastern  and  western
 sides of Smith-Tangier Islands, Pocomoke Sound,  and  Mobjack  Bay  (Figure


      Within a given one-minute, depth-bounded  latitude slice:

          a.  the area was approximated as the  surae of the elemental  0.5
              minute cells with centerpoints within the depth limits.
 *Because  the  original  bathymetry  is  in  feet,  or  fathoms, many  of the
 calculations  were  performed  using feet.   Thus some  of  the  intermediate
 results discussed  in  this  report  are presented in English  units, 1  meter
 equals 3.28 feet,  1 inch equals 2.54 centimeters,  1 metric ton equals 1.1
 English tons.
                                      47

-------
 I
I
                          LOCATION OF SIX-SECOND CELLS
                          WITH COMPARISON BATHYMETRY
Figure 14.  Location of 6-second cells with bathymetric
           comparisons and bay sub-segments.

-------
         b.  the average sedimentation  length  (and  rate) was  computed  by
             dividing the cumulative  5.0 minute cell volumes,  prorated to
             100 years, by  the  total  area.

         c.  the accumulated masses of  sand, silt,  and  clay were  calculated
             from the sum of the  contributions  from each 0.5  minute call to
             yield mass of  sand (and  gravel),  silt,  and clay  per  100 years.

The process  flow chart  is shown in Figure  15 and  the details  of the
calculations of depth difference, and conversion  of sediment  volume to
sediment mass follow.

     1.  Bathymetric Comparisons.  The  elemental  information  available
consisted of the most recent bathymetric information (circa 1950) available
from NOAA (EDS) wherein the average depth  within  six-second (approximately
150 x 200 m) cells were listed  on magnetic tape,  and the bathymetric "boat
sheets" of circa 1850.  The latter were partitioned into identical
six-second rectangles and the depths  within were  algebraically averaged.
Thus, the basic data set for bathymetric comparisons were  those six-second
cells for which there were  recorded depth  data  for  both survey periods.
The boundaries of the respective  surveys are shown  in Figures 16  and 17.
Approximately 40,000 grid points  (out of a possible 420,000)  were obtained
(Figure 14).  The time  difference between  surveys ranged from 85  to 110
years but the preponderance was between 95 and  100  years.

     In order to rectify the two  data sets to  the same  mean-low-water
datum, it was necessary to  consider three  corrections  (Carron, 1979);

         a.  eustatic sea level change,

         b.  crustal changes, and

         c.  semi-annual and annual tidal  variations.

     Eustatic sea level change  was assumed to  be  1  mm per  year.  The
correction was applied  to the number  of years  between  the  center  of the
1950 tidal epoch (1950) and the survey  date for the 1850 series survey.

     Crustal changes which  would  appear to be  bottom erosion  (all changes
were downward), when in fact no mass  balance change took place, were
accounted for by applying a fifth order trend  surface equation to the  data
of Holdahl and Morrison (1974)  (Figure  3), giving vertical crustal movement
rates for the same period used  in this  sedimentation and erosion  study.

     Semi-annual and annual tidal variation (Figure 18) corrections were
applied to the 1850-series  data to correct for seasonal deviations of
observed mean low water from long-term  mean low-water.

     However, it is  important ot  note that no  corrections  were attempted to
estimate the depth differences  solely due  to compaction of the bottom
sediments.   While negligible for  sandy  sediments, the  effect  of compaction
•in fine-grained sediments over  one hundred years  could  be  significant.

                                     49

-------
                                 FIGURE 15

                  FLOW CHART FOR RESIDUAL MASS ESTIMATES
           (1)

 "Corrected" Bathymetric
       Comparisons
40,000-6 sec. grid points
   with associated #t
     between surveys
         (2)

 Sediment Parameter
     Information
2,000 grid points at
   1.4 km spacing
                                           Surface Water Content
                                           % Sand, Gravel
                                           % Silt
                                           % Clay
                Array to 0,5 Minute Grid'
              Using Pseudo-Two-Dimensional
                     Bi-Cubic Spline
         For each grid point, calculate average
           water content as a function of surface
           water content and observed corrected
           depth difference.
         Calculate total mass  accumulation  rate
           using average water content, grain
           density, and sedimentation  length,  D,
           over survey period,  t and  normalized
           to  100 years.
         Partition  total mass  accumulation  rate
            to  component  sand  and  gravel,  silt,
            and  clay (m - tons/M^/100  years).
 Map
     Tabulate  for  one
     minute  latitude
     slices, depth
     stratified.
                                     50

-------
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     In addition, no corrections were attempted to compensate for the fact
that lead-line methods were used in the surveys of the 1800s whereas echo
sounding techniques were employed in the 1950s surveys.  Again the
difference would depend upon the grain-size characteristics of the bottom
sediments.  In sandy materials and at shallow to moderate depths, the two
techniques would be comparable.  In muddy sediments, significant
differences might exist (Watts, 1954), and these errors would be
particularly sensitive in areas of very high water content, such as where
fluid muds are encountered.  Other studies have not disclosed such
conditions within the main stem of the Bay in Virginia (Nichols, personal
communication).  Moreover, as the larger survey vessels calibrate the echo
sounder against lead-line determinations, the differences would be
partially rectified in sediments with intermediate water contents.

     The corrections applied are shown schematically in Figure 19 and given
as follows:

         a.  We assume the 1850 surveys have not been  rectified for monthly
variation in MIL (or MLW).  This correction is applied from Figure 18 as
follows (Figure 19A):

              DO = DO' - T                                              
-------
The  sedimentation  rate,  S,  normalized to a 100-year period is then

          S = D  • 100  = D0'  - Dn  + E  • At + C •  At - T                  (4)
 The  above  noted  "corrections"  take  into account  depth difference biases
 which may  amount  to  about  0.6  meter.

     As  previously mentioned,  the  corrections  do not include the effects of
 sediment compaction  as  shown in Figure  19B  for an otherwise rectified
 situaiton.   Layer 1,  deposited in  1850, may have become thinner due to
 expulsion  of water through time and due to  overburden of new sediment.  The
 bathymetric  comparison  would yield  AD and thereby underestimate the total
 sedimentation  by  AS,  the component  due  to compaction.  The thickness of the
 layer A  would  depend  upon  the  vertical, water-content profile and the rate
 of sedimentation.

     In  addition  to  the corrections noted above, the propagation of error
 in the sounding  comparisons must be considered.   Each of the separate
 surveys  contains  error, and, as well, the comparison between surveys
 embodies error.   For  a  given survey,  the principal errors are in accuracy
 of locating  a  hypothetical site, and the variability of repetitive
 soundings  at a fixed  site.

     The surveyors were aware  of the problem of  accuracy and, as a check on
 their data,  ran  crossing survey lines.   If  the differences of the crossing
 vlues  for  particular  water depths  were  within given limits (Sallenger et
 a1., 1975),  the  bathymetry was acceptable.   For  example, criteria adopted
 in 1955  quote  a  maximum allowable  difference between depth measurements at
 0.3  m  for  water  depth less than 20  m.

     As  a  means  of quantifying absolute sounding error, we examined the
 crossing differences  from  both the  1850s and 1950s data.  The crossing
 differences  are  the  absolute values of  the differences in depth from two
 lines of bathymetry where  the  lines cross.   Because soundings from separate
 lines were seldom coincidental, crossing values  were derived from linear
 interpolation  along  the separate lines.  In neither survey were crossing
 differences  related  to  depth.

     For two soundings  at  the  "same location" (i.e. a crossing) we have

     a = d + Ea

     b = d + Eb

 where  a  and  be are the  soundings at a crossing,  d is the true depth, and
 Ea,  Eb are the respective  errors from d.  The difference is

     a - b = Ea  - Eb  and

, "   (a  -  b)2  =  Ea2  - 2EaEb +  Eb2

                                      55

-------
                                     A
•^'0


-------
 For comparisons at a  large number  of  locations  we  assume  EaE^  is  small
 compared to the squared terms and  that  aEa2  =  SE^2.   Furthermore,  if Ea and
 Ejj are random deviations with zero mean and  the same  standard  deviation
 then the variance is  approximated  as:
          *2=(1/2)(a-b)2
      Calculations for the  1850's  and  1950's  survey  series  give,
 respectively, cr.  = 3.03 ft2 and  a_ = 0.52 ft2  for  sample  sizes  of
 N£ = 351 and N2 = 691.

      The pooled variance arising  from the comparison  of  individual
 soundings at a given location  is:

i      al,2  = ?l + a2 = 3'55 ft2'  and

 the standard deviation

      Slj2 = ± 1.88 ft (± 0.57 m)

      The 95% confidence interval  is 1.96  Sij2 or  ±  3-68  ft (± 1>12 m^-
 Thus, for a comparison between co-located individual  depths  on separate
 surveys, a depth difference greater ± 1.12 m has  a  5% probability of being
 to survey error.
t
      While the above applies to the comparison  of individual co-located
 depths, our comparison procedures  should  reduce the error  as the average
 depths within co-located six-second sedon grid  cells  are compared.
 Furthermore, this grid cell sampling  density is further  smoothed by
 application of the bi-cubic spline.   However, the degree of  potential error
 reduction has not been evaluated.

      2.  Conversion of Sedimentation  Rate to Mass Accumulation Rate.
: Recall that each 0.5 minute grid  point  had interpolated  values of the
| sedimentation length (E corrected comparative depth difference), surface
; water content, and the percentages of sand,  silt, and clay.   The
! sedimentation length (+ as accumulation,  - as erosion) when  applied to unit
1 area, a square meter, yields cubic meters of change in sediment volume per
 square meter of surface.   Once the volume of deposition  or erosion per unit
 area at a site has been calculated, the problem is  to convert the volume, a
 mix of solid (mineral) sediments,  shell,  organic  sediments,  and water to
 the mass of dry, mineral sediment.  In  order to arrive at  the number of
 metric tons of dry, non-organic sediment  deposited  per square meter, it is
 necessary to discount the  volume  of water and the mass of  organic material
 from the volume of material deposited.

      The most significant  problem in  the  procedure  for conversion from wet
 volume to dry mass is estimation  of a value  for the average  water content
 over the estimated sedimentation  length when given  only  the  surface water
 content.  Although an exponential-like  decrease in  water content with depth
 may be expected for uniform sediment  material,  the  exact form of the
-equation cannot generally  be stated since the water content  (or porosity)


                                     57

-------
gradient is also dependent upon the uniformity and rate of sediment
accumulation.

     In this study, the water content gradient with depth, as a  function  of
surface-sediment water-content, was estimated using approximately  fifty
(50) short (1 meter) gravity cores obtained in 1978 and 1979 by  the MGS for
study of interstitial water chemistry (Figure 20).  Their analysis included
determination of the water content gradient and a log of sediment  type.
The surface water content of these cores varied from over 80% to less  than
20%.  The water content profiles were then grouped into 10 percentum
surface water content classes.  These class groupings are exemplified  in
Figure 21 where it may be noticed that most of the profiles fall within an
envelope monotonically decreasing values of water content with depth.
However, some of the profiles depart from the envelope with either a
dramatically nonmonotonic behavior or otherwise wide departure from the
general grouping (i.e. VA 78).

     The second step was to shift all of the profiles exhibiting "normal"
behavior within a class group to a common surface origin (Figure 22).  An
"average" profile for the class group was then drawn.  At this stage  in the
process any profile with a surface water content within a particular  10
percentum class interval would be estimated by the averaged profile for
that class.

     The depth averaged water content was then determined at  10  cm depth
increments for each "average" water content profile.  For any
given depth  in the core, the depth-averaged water content of  the overlying
material could then be expressed as a deficit relative to the value of the
surface water content.  A nomogram  (Figure 23) was prepared for  this
purpose.  Values for water content at between 1 and  2 meters  are
extrapolations.  Observation indicated that when  the surface  water content
in  a core was less than about 30% there was little variation  with  depth,
and have thus been treated as constant.

     Again,  recall that each 0.5 minute grid point had an associated  value
for sedimentation length (+ or -),  and a value  for surface water content.
The nomogram  (Figure 23) was applied in tabular form (Table 7) at  each
point wherein the sedimentation length, AD, and surface water content, were
used to calculate an average water  content  for  the pertinent  AD, value.

     If we  assume zero  gas content  and ignore  the  salt evaporate,  the dry
mass of sediment per unit volume of wet sediment  may be expressed  as:

         M  = ps (1 - Wr)
              (pS -  pf)(Wc +  1)

where  ps    = sediment grain  density,

        ps   = water density,

        Wc  = average water content.
                                     58

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                                     Table 7

                Determination of Average Water Content with Depth


   Surface
Water Content   x, Deficit in water content relative to surface water content.
  AD in cm      < 30     30-39.9     40-49.9     50-59.9     60-69.9     >  70
10
20
30
40
50
60
70
80
90
100
110
120
130
140
150
160
170
180
190
200+
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
2.5
4.0
4.5
5.0
5.0
5.0
5.0
5.0
5.0
5.0
5.0
5.0
5.0
5.0
5.0
5.0
5.0
5.5
5.5
5.5
4.5
6.5
8.0
8.5
9.0
9.5
9.5
9.5
9.5
9.5
10.0
10.0
10.0
10.0
10.0
10.0
10.0
10.0
10.0
10.0
6.0
9.0
11.0
12.5
13.0
13.5
14.0
14.0
14.0
14.0
14.0
14.5
14.5
14.5
14.5
14.5
15.0
15.0
15.0
15.0
7.0
11.0
14.0
16.0
17.0
17.5
17.0
17.5
18.0
18.0
18.0
18.5
18.5
18.5
18.5
19.0
19.0
19.0
19.5
19.5
8.0
13.0
17.0
19.0
20.0
21.0
21.5
21.5
22.0
22.0
22.5
22.5
23.0
23.0
23.5
24.0
24.0
24.0
24.5
24.5
For a given  AD and surface water content, Wc,  subtract  the values  taken  from the
table_from the surface water-content  to  obtain the  depth  averaged  water  content,
Wc:  Wc = Wc - x.

-------
It should be noted that this expression differs from the saturated unit
weight generally used in geotechnical studies (Bennett and Lambert,  1971).
Consistent with the assumption of zero salt evaporate, we have  assumed  the
density of pore water is 1.0 g per cm^.  The range of salinities  in  the
pore water of cores from the Virginia portion of the Bay ranges  from 12  to
32 °/oo (James Hill, Maryland Geologial Survey, personal communication).
At 0°C, these salinities yield densities of 1.0096 and 1.025 g  per crn^
(Knudsen, 1959).  Dry grain density was taken as 2.7 g per cnH  following
the findings of Harrison, Lynch and Alfcschaeffle (1964).  This  assumption
is valid for the mineral component, and nearly so for shell, but  invalid
for the small component of other organic materials.  A sensitivity analysis
indicates about a 2% error in dry mass calculation for the extreme of pf =
1.02 g per cm^ and ps varying between 2.65 and 2.75 g per cnr*.   Figure  24
displays the graph of dry mass (m-tons per nH) as a function average water
content.

     The preceding paragraphs explained the procedures for determination of
the average water content, Wc, over the sedimentation length, and the
determination of dry mass of sediment per cubic meter given the  average
water content.  Multiplication of the latter value by the length  of  the
sedimentation column, AD, then gives the mass accumulation between the
survey periods, At.  Further multiplication by 100/At then gives  the final
result of total sediment mass accumulation normalized to a 100  year  period.

     3.  Sources
a.  Sediment Mass Derived From Shoreline Erosion.   The  estimation of the
mass of material supplied to the Virginia  portion  of  the  Chesapeake Bay
from erosion of  the  shoreline utilized  published data concerning areal loss
(Byrne and Anderson,  1977), field observations  of  shoreline  geology and
geomorphology, and sediment samples.  Byrne  and Anderson  determined the
area of shoreline change by comparing shoreline positions for  the period
1850-1950.  These estimates of area were converted to volume by multiplying
them by observed shoreline heights.  The volumes,  in  turn, were converted
to mass using data on the unit dry weight  of different  sediment types from
Terzaghi  and Peck (1948).  The most frequently  used values were 90 lb/ft3
(1.43 gm/cra^) and 99  Ib/ft3 (1.99 gm/cm3)  for uniform and mixed grained,
loose sands, respectively.

     In addition to  the  general  observation  of  sediment type,  samples were
taken at  approximately 1 mile intervals along the  main  shoreline of the
Bay.  At  each site,  samples of the beach and and  fastland sediments were
obtained.  The fastland  samples  were collected  so  as  to be representative
of the stratigraphy.   Thus, the  sandrsiltrelay  ratios of  the samples of the
(eroding) sediments,  coupled with the calculated mass of  the material
eroded for each  shore segment yielded information  on  the  separate masses of
sand, silt, and  clay  supplied to the Lower Bay. Appendix 2  is a tabulation
by minute-of-latitude of the mass of material attributable to  shoreline
changes.  Figure 25  depicts both the mass  of sediment per
rainute-of-latitutde  and  the areas of the Bay shoreline that  were included
in the calculation.
                                     64

-------
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Figure 25.   Histogram of the mass of material eroded from the shoreline
            for each minute of latitude.   The areas used in the calcula-
            tions are shown on the map with bold lines.

-------
     The sum, approximately 42.3 x 10° metric tons, 90% of which  is  sand,
is probably a conservative, or low, figure.  The calculated areas  and
volumes of shore change use only data from approximately mean high water
and above.  Sediment eroded from below MHW as part of normal shoreline
retreat is not included in the calculations (Figure 26).  The quantity  of
this material is a function of both the rate of retreat and tide  range.  In
areas of low shore elevations and gently nearshore slopes, the  quantity of
material not considered could approach the calculated supratidal  amounts.
                                      *
b.  Calculation of the Mass of Biogenic Sediment.  Jacobs (1978)  presented
basic data on the distribution of zooplankton through a large portion of
the Lower Chesapeake Bay.  His data stems from two years of monthly  samples
from each of eight subareas.  The samples were collected by careful  tows of
202 ym mesh nets and were later concentrated through  110 ym strainers in
order to retain broken specimens.  Hence the mass of material deposited
from zooplankton and phytoplankton less than 202 ym in life size  is  not
included.  Because this data is to be integrated with data on sediments
that have been digested in HC1 and H2C>2, only the ash weights of  the
plankton samples are used in the calculations as the ash weight is
representative of the mass that would remain after the digestion  process.

     Table 8 shows the path of the calculations from the determination  of
the monthly average ash weight of the zooplankton in a cubic meter of water
in each of the eight subareas through the total ash weight for  a  100-year
period.  The calculations use the assumption that all the potential,
zooplankton derived, ash material settles to the bottom and is  incorporated
in the sediment.  Figure 27 depicts the subareas.  It should be noted that
subareas G and H extend north only to 37°40' latitude, not to the state
line, approximately 38°00'.

     The calculated total ash, from Table 8 is 81.4 x 10^ metric  tons per
100 years.  If the contribution of subareas G and H are doubled,  to  extend
the area to include all of the Virginia portion of the Bay, the total of
the ash weight of the fraction of the biogenic sediment in the  study area
is 1.252 x 106 metric tons.           ;

C.  DATA STORAGE

     Several very large data sets were constructed to provide  for the
logical storage of the information derived as part of this project.   These
data sets can be divided into two groups.  The first  is the data  associated
with the bathymetric changes.  The other is the information concerned with
the two thousand bottom samples.

     The raw bathymetric data is available on magnetic tape at  the Virginia
Institute of Marine Science.  This data includes digitized sounding  data
from both the 1850 and 1950 bathymetric survey series.  The latter
informaiton was obtained from NOAA.  Additionally, bathymetric  changes,
adjusted to compensate for the parameters noted section also are  available
on tape.
                                      67

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-------
     The data on the individual sediment samples are comprehensive and are
available from several sources.  The data include the latitude and
longitude, water depth, water content, weight percents total carbon,
organic carbon, and sulfur (not all samples), weight percents gravel, sand,
silt, and clay, tabulated, 1/4 0 interval grain-size-frequency
distribution, and the several calculated statistics.  This information was
submitted on magnetic tape to the Virginia State Water Control Board  for
transferral to the EPA STORET data system and should be available through
both agencies.  Additionally, both magnetic tape and paper tabulations of
the data are filed at VIMS.
                                     71

-------
                                    VI

                          RESULTS AND DISCUSSION

A.  SEDIMENTOLOGY

     1.  Description of Sedimentology.  One of  the most  striking  attributes
of the bottom sediments of the Virginia portion of the Chesapeake Bay  is
the dominance of sand over mud.  Over 65% of  the  samples  are  75%  or  more
sand (Table 9).  The mean of the graphic mean grain size  for  over 2,000
samples is 3.17 0 (0.11 mm).  Table 9 displays  sediment  type  from Shepard's
(1954) ternary classification.  The data is grouped by 5  minute bands  of
latitude for the main stem and by fringing subarea.  On most  maps of
sediment characteristics, such as weight percent  sand, mean grain size, or
sediment type (Figures 28, 29, and 30), the great extent  of the sands  is
clear.  With few exceptions, the finer-grained  sediments  are  confined  to
the deeper portions of the Bay.  Indeed the patterns of  the various
sediment maps echo the bathymetry.  However so  little of  the  Bay  is  deep,
approximately 80% of the study area is less than  42 feet  (13  meters) deep
(Figures 31 and 32) that silts and clays in shallow areas such as Mobjack
Bay and the sands in the deep channel near the  lower Eastern  Shore destroy
any significant correlation between grain size  and depth.  R^ for 2,018
depth versus percent mud samples is 0.13.  Figure 33 depicts  clay content.
Although the visual correlation between depth and clay content is strong,
the R^ value is only 0.11 for the entire suite  of samples.  Again this poor
quantitative relationship is, in part, a function of the  hypsometric
distribution.

     On all the above sediment characteristic maps the channels  into
Pocomoke and Tangier Sound, the channel in the  main stem that runs north
from near the mouth of the Rappahannock, and  the  York and Rappahannock
channels are clearly shown.  Only the deep channel in the southeastern Bay
is  lost.  The presence of coarser grained sediments in this deep  portion
probably is due to erosion of a sand  substrate, or, locally,  to  the
transport of sediment into the channel from the region of the Bay mouth.

     The qualitative depth versus grain size  relationship is  very well
depicted in Figure 34 which is a map  of the graphic mean of the  sand
portion of the samples.  The distribution of  the  very fine sands, 3 to 4  0
(0.125 to 0.0625 mm), marks all the deeper areas  of the  Lower Bay including
the channel near Cape Charles.  This  map, as  well as the others,  depicts  a
band of finer-grained sediments running southeast from  the mouth  of Mobjack
Bay.  Although this area is in slightly deeper  water than the surrounding
region, the bathymetry is not nearly  so pronounced  as with the York River
channel which the Mobjack band parallels.  It is  possible that  this band  is


                                      72

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           WEIGHT PERCENT SAND
             :ONTOUR INTERVAL 20%
Figure 28.  Isopleth map of weight percent sand.

-------
                     GRAIN SIZE
              CONTOUR INTERVAL  I*
Figure 29.   Isopleth map of mean grain size.

-------
               VT.1—^-4v.
                 r?
                S|C SEDIMENT TYPES
Figure 30.  Map of the distribution of sediment  types.

-------
          DISTRIBUTION  OF DEPTHS

               FOR THE ENTIRE BAY
  60 H
   50-
  40-
u
o
CE
u
o.
  20-
   10-
         15  27  39  51  63  75  87 99

                        "DEPTH
                          T T T T T 1—i—i—i—I—i—i—i—r
123 135 147
      Figure 31. Histogram of depths at sample locations.
                       77

-------
Figure 32.   Map showing the bathymetry of the  Virginia portion  of the
            Chesapeake Bay,  10-foot contour interval.

-------
Figure 33.   Isopleth map of weight percent clay.
                   CONTOUR INTERVAL 20%

-------
Figure 34.   Isopleth map of the graphic mean grain size  of the sand
            portion of the sediment samples.

-------
 the surface representation of a channel filling with material derived  from
 the Mobjack Bay upland drainage.

      The explanation of the distribution of the medium and coarse  sands  is
 complementary to that for the very fine sands.  Whereas the very fine  sands
 are deposited in the deeper portions of the Bay,  the medium and coarse
 sands are found in the shallower areas that are subject to agitation by
 waves.  It is arguable from site to site whether  the coarser sands  are the
 lag deposit left behind as the shallow sediments  have been reworked and
 winnowed of the fines by waves or are relict, palimpsest, materials.
 Indeed the two explanations are not mutually exclusive and often may both
 be true.  Dramatic shoreline retreat has accompanied the Holocene  rise or
 sea level.  Rosen (1976) cited evidence for the shallow, 3.6 meters (12
 foot) and less, flat terraces being the erosional platform created  during
 the relatively slow sea level rise of the past 3,000 years.  Using  the work
 of Brunn (1962), Rosen related the change in bottom slope to the change  in
 the rate of sea-level rise that occurred approximately thirty centuries
 ago.  Thus the roughly shore-parallel zones of coarser sediment adjacent to
 Accoraack and Mathews Counties may be the lag deposits of Rosen's erosional
 terraces.  The southeast-northwest trending coarse zones adjacent  to the
 York River channel, extending from southern Mathews County, and just north
 of Windmill Point at the mouth of the Rapphannock may be the sediment  of
 the eroded morphology and not exclusively a "lag" material.  These  features
 are likely to be the remnants of fossil spits formed during an earlier,
. lower stand of sea level.  The large sandy-shield around Tangier and Smith
 Islands also probably is a relict feature as there are insufficient modern
 sources for this material.

      The classification of sediments according to Shepard's (1954)  ternary
 scheme provides additional data.  Figure 30, clearly shows the dominance of
 sands and silty sands.  The finer sediments, particularly the sandy- and
 clayey-silts, describe the major channels and, as previously noted, Mobjack
 Bay.  The thin band of fines extending southeast  from Mobjack Bay  also
 appears on this map.

      The sample data, when plotted on sand:silt relay ternary diagrams
i (Figure 35) also illustrate the depth-sediment relationship.  The  samples
 all fall in a swath running from pure sand to clayer silt.  Although the
 width of the swath remains nearly constant from depth to depth, indicating
 a mixture of the same general sediment types, the distribution within  the
 swaths changes with the proportion of fines increasing with depth.  This
 pattern is very similar to that shown by Kerhin,  Halka, and Wells  (1979) in
 the Maryland portion of the Bay except that the trend of their swath is
 somewhat finer, running from sands to silty clays and having a greater
 percentage of the samples falling on the silt-clay axis with little or no
 sand.  They also show the general trend of an increasing percentage of
 fines with depth.

      The generally finer nature of the sediments  upstream in the Bay is  not
 surprising.  The proximity to the mouth of the Susquehanna and the  presence
 of  the  turbidity maximum in the upper Bay work toward the resultant
 presence of an abundance of fines.  Also the general phenomenon of

                                      81

-------
CLAY
                  to 12 FEET
                 335 SAMPLES
SAND
             SILT
SAND
                 131o 24 FEET
                 404 SAMPLES
             SILT
 CLAY
                  25 to 36 FEET
                  547 SAMPLES
CLAY
                 37 FEET AND
                   GREATER
                 674 SAMPLES
SAND
             SILT
 SAND
             SILT
Figure 35.   Ternary diagrams of sand:silt relay ratios  of  sediments at
            different depths.

-------
 down-estuary coarsening has been noted by Nichols  (personal  communication)
 in the James River.  Nelson (personal communication) has demonstrated  it
 with successive down stream sand:silt:clay plots of sediments  from  the
 Rappahannock.

      Water content is closely related to sediment  type.  For mud  (x) versus
 water content (y) the R^ for 2,018 samples is 0.91 with the  equation y =
 0.459x + 18.6.  The R^ values for mean grain size  versus water  content and
 weight percent clay versus water contetit are only  slightly less significant
 at 0.881 and 0.879.  Figure 36 is a scatter plot of the mud-water data.

      As will be discussed later, these descriptions are somewhat  similar  to
 those of Ryan (1953) and Shideler (1975).  The present study demonstrates
 that the sands are more widespread than was thought by the earlier  works.
, Although some of the difference may be real, reflecting a change  in bottom
 sediment through time, much of the difference is due to the  better  detail
 that results from the near order-of-magnitude greater sampling  density of
 the present study.  A comparison of isopleth maps  of the mean grain size  of
 the sand fraction (Shideler's Figure  3, this study's Figure  37)
 demonstrates the different levels of detail.  As an example, where  Shideler
 depicts a small shield of very fine sand near the  mouth of the  York River,
 the present study shows two discrete band, one from the York connecting
 with the main, central Bay bands fines, the other  running from  Mobjack Bay
: toward, but not connected to, the mid-Bay band.
      2.  Comparison With Earlier Surveys of Bottom Sediments.  As  the  work
 done through the course of this study covers some of  the  same ground that
 was touched by the work of Ryan (1953), Harrison and  others  (1964), and
 Shideler (1975), it is appropriate to discuss  the differences in observed
 characteristics and among results.  This is especially  important as the
 major physical events of the 1962 Ash Wednesday storm and the floods of
 Hurricane Agnes in 1972 occurred during the interval  between these studies
• and it may be possible to discern changes in the bottom sediments  results
 from these events.  Broadly speaking there are two distinct  types  of
| differences that could exist between studies.  The first  are real  or actual
: differences that result from true changes in the bottom.   The second group
i is due to such causes as dissimilar sampling and analytical  techniques,
, including sample pretreatment, errors in site  location, differences in
 sample spacing, and differences in the subjective interpretation of the
 data.  Although it is only the changes in bottom sediment which should be
 compared across studies, it is difficult to isolate these differences  from
 those that are artifacts of the methods and techniques  of the individual
 projects.

      Analytical differences can be minimized by using comparisons  of the
 weight percent mud (or sand) as the wet-sieving technique used to  separate
 sand from mud are standard.  The major remaining places for  variation  are
 in obtaining the sample and pretreatment.  In  the present study, the top 6
 cm of sediment were sampled.  Shideler used the top 10  cm, Harrrison et al.
 the top 20 cm, and Ryan the whole "snapper" sample or the top 15 to 20 cm
 of each core.  None of the earlier reports indicated  any  pretreatment  of
 the samples.  The VCB samples were pretreated  by digestion with HC1 and

                                      83

-------
             WATER VS PERCENT  MUD
                    FOR THE  ENTIRE  BAY
       c
       o

         80 H
         70-
         6CH
         50-
         40-
         30-
         20-
               ** .•
              •.% • *
                  .. .  • :•.-  ••".-
                ' .v.  '.'\..:-''';. .*:.•$,V:
                       '.  -''•'  ..:••  . '

                    ..—.. !:/' V'^'->'-"
0      20      40      60      80

           Weight Percent  Mud
                                                 100
'Figure  36.  Scatter plot of weight percent mud versus water content.
                            84

-------
     to remove carbonate and organics.  Although not typical of  the VCB
samples, a laboratory study of 22 samples from a separate project  in  the
Elizabeth River indicated that the weight percent mud averaged  1.1% greater
(weight percent sand 1.1% less) for the digested samples.  This  suggests
that the difference due to the pretreatment is not significant.   (The
differences in weight percent clay were significant, though, with  the
digested samples having an average of a 9.3% greater clay content  (less
silt) than the undigested).  The other possible source of variation is the
wet sieve itself.  Although the 4 0 separation of sand and mud  is  62.5 ym,
sieves with nominal openings of 60 to 64 ym are commonly used.   This  plus
variations due to the condition of the sieve contribute to minor
differences in the final result.  Thus if one accepts that analytical
differences are minimal, the remaining differences are due either  to  sample
position, sample thickness or true changes.

     Ryan had approximately 200 stations through the entire Chesapeake Bay.
Shideler also had about 200 samples, but just from the Virginia  portion of
the Bay.  The present study has over 2,000 samples from the Virginia
portion of Bay including Mobjack Bay and Pocomoke and Tangier Sounds.
Harrison and others studied only a small section of the area.   Figure 38
shows the location of the samples from those three studies and  Figure 4
shows the locations of the 2,000 samples analyzed for this study.  The
profile lines A through G on Figure 38 are the transects along which
comparisons of weight percent mud were made.  These profile comparisons are
shown in Figure 39A,B,C.  As samples were seldom exactly on the  line, any
falling within a half kilometer were used.  If the sediment distributions
were "patchy", this would be a source of error in the comparison.  The
profiles shown in the figure depict the west to east variations  in weight
percent mud for the present study (VCB) and Ryan, Shideler, and  Harrison
and others where applicable.

     The VCB data and Shideler's generally are similar.  Profiles  E
adjacent to the mouth of the York and G near the Bay mouth are  especially
interesting as they show the differences in gradient that can result  from
different sample spacings.  The VCB data has steeper gradients  and more
variations than the "smoother" data from Shideler.  It is probably a  result
of this greater detail that the present interpretations show much  less
fine-grained material than the earlier studies.

     Harrison's samples appear only on Profile B and show reasonable
correspondence with both Ryan's and the VCB data.

     On Profile F the VCB sample which is almost 90% mud has been
identified as being taken from a spoil area.

     Although in some instances, Profiles A and D, Ryan's data  indicate a
greater mud content than either the present or Shideler's works, it  is
difficult to assess the variations as either being due to the "patchiness"
of the  sediment types or due to an actual change in sediment type  through
time.  As strong gradients of sediment properties are apparent,  it is
desirable to have a great number of closely spaced samples.  However
                                     85

-------
   40'N
37 00 N
           SAND MEAN  SIZE
                                    0'
76°00'W
 Figure 37.   Isopleth map of the mean grain size of the sand fraction.
             Reprinted, with permission of the publisher,  from
             Shideler,  1975.

-------
                                v  v * ~i  v  i  v r  r  T  :
Figure 38.  Location of sample stations from Ryan  (1953),  Harrison and
            others (1964), and Shideler (1975).

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 factors  such as  time,  funding level,  and logistics often necessitate the
 acquisition of  fewer  samples  than might otherwise be desirable.

      The concept of the nature of the bottom sediments changing with time
 should  not  be discounted.   In considering this possibility it is worth
 while to look at the  dates of sampling and their relationship .to specific
 physical events:

 Ryan (1953)
                                       «\
      Samples collected     1950,  1951
                            March  1962             Ash Wednesday Storm

 Harrison et_ aJL  (1964)

      Samples collected     June 1962, April 1963
                            June 1972               Agnes floods

 Shideler (1975)

      Samples collected     April-September 1973

 This study

      Samples collected     November 1978-June 1979

      The Ash Wednesday 1962 storm lasted several days and was accompanied
 by greatly  elevated water levels  and  heavy wave agitation.  Hurricane
 Agnes,  1972, provided all the elements necessary for the maximum transport
 of sediments from the upper Bay and tributary rivers into the lower Bay.
 It should be noted that two studies,  Harrison et al. and Shideler, follow
 within a year of the  significant  storms while the other two studies fall
 during periods  of "normal" processes.  This then presents the questions of
 both the nature and duration of the storm impacts on the bottom sediment.

      The profile comparison between the information from Shideler and the
 present (VCB) studies are somewhat ambiguous.  In the profiles and plots of
 weight  percent  mud are generally  parallel and exhibit the greatest
 differences in places where sample location, or rather lack of co-location,
 could account for the differences.  That is the "spikes" in one plot occur
 between samples on the other indicating that, perhaps, the second study
 failed  to sample the  "spike" area.  However, if in the laboratory, one
 plots both  complete sets of mud-content data on the same map, another
 interpretation becomes possible.   In  some areas Shideler observed bottom
 sediments that  were 10 to 15% muddier than the bottom sediments of the most
 recent  study.  The greatest differences are immediately south of Tangier
 Island  in Shideler"s  northernmost line of samples and in the lines adjacent
 to and  below the Rappahannock. A possible explanation is that the muddier
 sediments are material that entered the Bay as a result of the major floods
 that followed Hurricane Agnes in  1972.  The sediments coming from either
 the Maryland portion  of the Bay the Potomac, and the Rappahannock.  During
~the years between the two studies, the "normal" processes would have

                                      91

-------
altered the immediate post-storm surface sediments by both redistribution
and burial.  Unfortunately a similar comparison using Harrison et al.
post-Ash Wednesday storm data is in-conclusive.

     The map comparison of Shideler's with the present study's data
suggests that there may have been unusually high loads of fine-grained
sediment deposited within the Virginia portion of the Bay as a result of
the Agnes floods and that five years of "normal" processes are sufficient
to "mask" the event.  The profile comparisons of the several data sets
demonstrate, or at least very strongly suggest, that the distribution of
the sediment is quite patchy and that significant gradients may be lost to
a wide sample spacing.  Indeed if sediment types can vary across an  area of
one or two hundred meters width the relatively "close" spacing of the
present study gives only a slightly better picture than the less close
spacing of Shideler's work.

     3.  Clay Mineralogy.  Little work has been done with the details of
the clay mineralogy of the Chesapeake Bay.  A quarter century ago Powers
(1954) studies the diagenesis of clays in the Bay and reported the
formation of a thermally stable, clorite-like mineral that increases with
salinity and depth of burial.  Hathaway (1972) had fewer than a dozen
samples from the lower Bay in his study of east coast clay-mineral facies,
although he does indicate the Bay as a transition area between glaciated
and non-glaciated sources.  Nelson (1960) discussed some of the aspects of
the clays of the Rappahannock.  Nichols (1972) examined the sediment of a
portion of the lower James River.  Harrison, Lynch, and Altschaeffl  (1964)
briefly mention the clay mineralogy of sediments in the portion of the Bay
roughly between the Potomac and Rappahannock Rivers.  More recently,
Feuillet and Fleischer (1980) studies the clay mineralogy of the lower
James River and the extreme southern portion of the Bay.  There has  been no
comprehensive investigation of the clay mineralogy of the Chesapeake Bay.
This study slightly increases the body of knowledge in two ways.  First, it
defines the distribution of clays as a size class (Figure 33) and second it
reports the clay-mineral composition of approximately 20 samples (Table
10).

     The original intent of the investigation was to test three hierarchial
or nested hypotheses.  1) That there are mappable variations in the
clay-mineral assemblages of the lower Chesapeake Bay, 2) that the major
cause of the variations are differences in the material supplied by  the
several sources, and 3) that  the mapped pattern of clay-mineral assemblages
can be explained by logical processes, e.g. currents.  This set of
hypotheses can be recast as the following questions.  Do the major  sources
of sediment to the  Bay, the several rivers, the ocean, and shoreline
erosion contribute  different, definable suites of clay minerals to  the Bay?
Do those clay-mineral assemblages remain as identifiable units coding
deposited  sediments as to  their source?  What  processes govern the
distribution and physical  form of the deposits?  The reconaissance work  is
only semi-quantitative in  nature using ratios  of peak heights of both
untreated  glycolated sediment from the 9 0  (2  pm) and finer fraction of  the
sample.  As with  the previous researchers, chlorite,  illite, kaolinite and
montmorillonite,  and vermiculite are the major clay minerals.

                                     92

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     However the relative paucity of sediments with even moderate  clay
contents raises questions about the significance and validity of the data.
If the samples analyzed are chosen only from those with appreciable clay
contents, the spatial distribution is quite limited, hence greatly
restricting the inference of broad processes.  If, on the other hand,
samples are chosen as a random subset of the large sample grid, the data
from samples with minimal clay contents might be sufficiently suspect as  to
invalidate specific conclusions.
                                      *
     Using both the new and published data though, there is evidence to
suggest that the hypotheses may be valid.  Much of the published evidence
is summarized by Hathaway (1972), but other sources include Powers (1954),
Meade (1969), Nelson (1960), Harrison and others (1964), and Feuillet and
Fleischer (1980).  The Susquehanna River, the Bay's major tributary, is  the
only one of the Bay's tributaries which drains a glaciated region.  The
potential availability of rock flour in addition to the clay products of
more conventional weathered bedrock should give the Susquehanna borne clay
assemblage different and differentiable characteristics.  Similarly the
rivers draining non-glaciated areas transport sediment eroded from more
deeply weathered bedrock of the piedmont.  Although Hathaway"s (1972) map
of kaolinite distribution in the Chesapeake Bay shows a mid-Bay peak, this
would be expected as a result of the upstream estuarine bottom circulation.
Indeed, Hathaway indicates that the kaolinite concentration of the James,
York, and Rappahannock Rivers is 4 to 5 parts in 10, with far and  away  the
greatest quantity contributed by the James, whereas the Potomac and
Susquehanna have 2 to 3 and 1 part in 10 kaolinite respectively.   The
greatest concentrations in the Bay's clays away from the immediate river
mouths, however, are north of the Rappahannock.  It should be noted that
Hathaway depicts 10 stations in the lower Bay and fewer than a dozen and  a
half in the entire Chesapeake Bay.  The progressively deeper and more
intense weathering of the southern areas is perhaps an explanation of the
increased kaolinite content of the more southerly rivers.

     Other patterns outlined by Hathaway include increasing montmorillonite
content in the rivers away  from the Susquehanna, but a relatively  uniform
distribution in the mid and lower Bay, a definite progressive down-Bay
increase in chlorite, even  though the mineral was not detected  in  the
rivers south of the Potomac, and an extensive area of illite concentration
surrounding a  small island  of lesser concentration adjacent  to  the mouth of
the Potomac.   The present work echos the down Bay chlorite trend.   The  Bay
mouth changes  which he notes can be attributed  to the contributions  of
sediment from  outside the Chesapeake.  Indeed,  in a separate figure  (his
Figure  14), he depicts a definite bottom transport of clay  into  the
Chesapeake during the Holocene.

     Powers (1954 and other dates) attributed the lower Bay  increase  in
chlorite to the diagenetic  formation of chlorite in  increasingly  saline
waters.  Nelson (I960) also reported a downstream increase  of  chlorinte in
the Rappahannock but was unwilling to  ignore  causes oter  than  diagenesis
and withheld  judgment.
                                      94

-------
     Meade (1969) drawing on the works of many others presents a  strong
case for the "landward transport of bottom sediments."  And as noted  above,
the patterns depicted by Hathaway (1972) infer the presence of such a
process.

     Harrison et_ ajU (1964) state that most of the clays  in this  area were
primarily illite (50%), chlorite (30%), and a mixed layer clay (20%);  the
later being illite-montmorillonite and chlorite-montmorillonite.  They
reported only a trace of kaolinite.
                                      •>

     Feuillet's and Fleischer's work  in the James is primarily concerned
with along-river trends in varying concentrations of various clay minerals.
In the extreme lower Bay between Hampton Roads and Cape Henry, they record
illite (approximately 50%), montmorillonite (12%), chlorite (8%), and
lesser quantities of kaolinite, vermiculite, and dioctahedral vermiculite.

     4.  Carbon and Sulfur in the Sediments.  The spatial distribution of
the carbon, organic carbon, and sulfur contents, as weight percents,  of  the
sediments of the bottom of the Virginia portion of the Chesapeake Bay are
the major concern of this section.  The delineation of relationships  of
these distributions with one another  and with physical characteristics,
such as water depth or sediment type, makes a contribution toward the
understanding of the processes active within the Bay.

     The gross chemical attributes of the modern sediments provide
information of potentially broad use.  When compared to the analyses
necessary for the determination of the presence of various complex organic
pollutants, the cost of the laboratory analyses performed for this study is
relatively small.  It may possible, when data from the more complex
analyses become available, to correlate indices derived from the  relatively
simple analyses with the different levels or aspects of pollution.  If such
were the case, index values could be  used to screen areas in order to
identify zones of possible concentration of contaminants.  Additionally,
index data developed from samples taken on a tight grid might be  used to
extend maps of more difficulty obtained data from a coarser grid.

a.  Previous Work.  Shideler (1975) discussed the total organic content  of
the sand-gravel fractions of the sediments of the Lower Bay.  The weight
percent organic content as determined by heating the greater than 63   m
sediments at 400°C and acid digestion ranged from 0% to 43% with  most
values less than 5%.  Shell material  was the dominant component.  He  mapped
areas of concentration adjacent to but offset to the south of the mouths of
the Rappahannock and York Rivers, perhaps reflecting areas of sediment
enriched in nutrients by material supplied from the rivers.  Harrison et
al. (1964), reporting on an area between the Potomac and  Rappahannock
Rivers noted organic and inorganic carbon contents ranging up to  1.9% and
0.42% respectively.

     Biggs (1967) reported on the organic carbon content  of 120 samples
taken from the mid-Bay in the vicinity of the mouth of the Patuxent River.
The values range from 0.95% to 3.4% (organic) carbon, with the lower  values
from shallow-water silty-sands, the higher from the finer sediments of the

                                      95

-------
deeper waters.  Biggs, working with relatively short cores, also reported  a
general decrease in organic matter with depth of burial, confirming
observations of earlier workers.  He related the increase in organic carbon
of the surface sediments with increasing water depth to four phenomena:  1)
a higher rate of sedimentation in shallow water which would serve to dilute
the organic matter with detrital material; 2) the higher oxygen content of
the shallow waters and the greater grain size (thus permeability) of the
shallow water sediments; 3) the scavenging activity or organisms in shallow
areas; and 4) the greater physical energy of the shallow areas.

     Folger (1972) related organic carbon content to sediment texture and
cited the organic carbon content as an index to the level of pollution.  He
stated that the organic matter in estuarine sediments is derived from plant
detritus carried to the estuary by rivers, from the debris of estuarine
plants and animals, and from various anthropogenic effluents.  Referring
back to the earlier work of Trask (1932), he states, "concentrations of
organic matter vary inversely with sediment grain size."  As did Biggs
(1967), Folger (1972) also found the sediment-organic matter relationship
to be a complex one including the settling characteristics of the particles
and permeability of the sediment, in addition to water chemistry and
microbiology.  In a brief discussion of the Chesapeake Bay, he found the
organic carbon content to be as would be expected for the grain size; that
is, generally below 1% for sands, below 5% for silts and clays.  In
reviewing the organic carbon content of estuarine sediments in general,
citing Whitewater Bay, Florida, and Deep Inlet, Alaska, as examples, he
stated that areas where the bottom waters are anaerobic (swamps and fjords)
there may be higher concentrations of natural organic carbon.

     Although the impact on his paper probably is not great, Folger's
(1972) work has a synthesis of  the work of several researchers who used  a
number of different analytical  techniques.  Leventhal and Shaw (1980),
working with a shale, showed that precision within individual techniques to
determine carbon content is good  (± 3%), but there can be significant  (24%
or more) variations among techniques.  Obviously this necessitates  that
researchers carefully document  and describe analytical procedures.

     Mencher et al. (1968) reported very high organic-carbon-contents  in
the surficial sediments of Boston Harbor, Massachusetts.  The enormously
high values, however, are explained by the high level of pollution  in  the
harbor.  The  sandier  sediments  contained wind-carried fragments  of  coal  and
coke;  raw sewage was  the probable prime contributor to the organic  content
of  the less  than 62   m  sediments.

     Rashid  and Reinson (1979)  noted the  relationship of organic-carbon
content and  fine-grained sediments with an average 4.8% organic-carbon
content  in muds and 3.6% in  sandy muds of  the Miramichi Estuary  of  New
Brunswick.   They further state  that "The  sediments of the Miramichi  contain
a much higher quantity  of  organic carbon  than would be  expected  to  occur
naturally  in  a shallow, well-mixed estuary", and attribute  this  apparent
anomaly  to  the discharge of  pulpmills.
                                      96

-------
LORAN-C INTERVALS

Chart
27318.4
27314.2
27340.8
27283.0
27223.2
27230.4
27203.1
27237.2
27275.1














9960-X
Theoretical
27321.56
27316.99
27343.38
27285.93
27226.48
27233.39
27206.18
27239.91
27278.01
27228.83
27221.93
27306.60
27271.34
27192.80
27260.17
27244.46
27255.68
27296.79
27190.93
27208.75
27222.25
27272.41
27194.55
27250.33

Actual Chart
27318.88 41634.6
27314.67 41719.2
•t
27341.30 41925.9
27283.53 41904.0
27223.69 41987.1
27230.80 41841.5
27203.63 41840.6
27237.49 41703.8
27275.77 41575.8
27226.20
27219.71
27303.63
27268.75
27464.99
. 27257.46
27241.72
27252.97
27293.64
27188.49
27206.29
27219.53
27269.18
27191.98
27247.41
9960-Y
Theoretical
41636.81
41720.41
41926.90
41905.88
41989.74
41843.29
41842.76
41705.67
41577.68
41595.64
41497.59
41449.50
41443.50
41405.09
41366.01
41307.17
41280.57
41256.82
41300.78
41287.70
41267.81
41242.21
41247.25
41212.49
i
Actual !
41636.34
41720.06
41926.74
41905.26
41988.46
41842.49
[
41842.14
41705.07
41577.32
41594.59
41497.79 '
41448.44
41442.95
41404.32
41365.84
41306.50
41280.05 ;
i
41255.73
41300.63 !
\
41287.45
i
41267.52
41241.54
i
41246.94
41212.14

-------
LORAN-C INTERVALS

Chart
53476.9
53388.4
53208.4
53172.1
53028.9
53181.8

53326.4
53492.4
53425.3
53616.0
53516.7
53649.1
53619.8
53579.5
53685.9
53729.1
53767.3

53681.9
53712.0
53746.2

53739.0

9930-Y
Theoretical
53477.72
53389.54
53209.45
53173.02
53029.71
53183.07
53156.40
53327.22
53493.30
53426.16
53616.54
53517.31
53650.06
53620.81
53580.68
53687.13
53730.27
53768.08
53832.94
53683.12
53714.02
53747.41
53823.17
53740.27
53830.81

Actual
53475.63
53387.80
53207.93
53171.55
53028.40
53181.62
53154.65
53325.74
53491.92
53424.96
53614.99
53515.25
53648.40
53619.17
53578.97
53684.97
53728.52
53766.31
53831.33
53681.14
53712.21
53745.24
53821.02
53738.25
53828.74

Chart
70565.2
70528.5
70409.2
70464.3
70467.4
70533.8

70597.6
70631.2
70661.5
70666.6
70716.9
70670.4
70704.2
70788.4
70753.0
70797.4
70801.5

70845.0
70837.0
70836.7

70870.6

9930-Z
Theoretical
70563.26
70526.59
70407.26
70462.35
70465.40
70532.14
70552.11
70595.61
70629.16
70659.70
70665.19
70715.41
70668.84
70702.52
70786.73
70751.88
70795.95
70800.23
70775.83
70843.61
70836.12
70835.49
70805.54
70869.36
70840.76

Actual
70564.51
70527.90
70408.58
70463.77
70466.70
70533.74
70553.33
70597.00
70630.49
70661.26
70666.52
70715.94
70670.05
70703.74
70788.00
70752.93
70797.23
70801.17
70777.05
70844.67
70837.22
70836.55
70806.80
70870.47
70841.83

-------
      Jones  and  Jordan  (1979)  report  concentrations of organic carbon in the
estuary  of  the  River Liffey,  Dublin,  ranging  from 1.7% at  the mouth of the
estuary  to  25.4%.   The River  Liffey  flows  through the urban environment of
Dublin and  the  greatest levels  of  organic  carbon occur at  the upper limits
of  sea-water  incursion (the zone of  the  turbidity maximum),  perhaps
reflecting  the  deposition  of  particulate wastes  from paper mills and other
sources.

      In  a discussion of the 1 cm surface  sediments from Lakes Ontario,
Erie, and Huron, Kemp  (1971)  reported that  carbonate carbon was  usually
less  than 1%.   Higher  values, up to  5%, were  attributed to bottom materials
that  were locally  derived  from  carbonate  sediments.   Organic carbon ranged
upward to 5%.   Kemp also noted  the strong  relationship between organic
carbon and  clay contents and  an apparently  equally strong  correlation
between  organic carbon and nitrogen.   As  in Chesapeake Bay,  basin
morphology  in the  lakes is a  factor  in the  distribution of sediment sizes
and,  hence,  in  the spatial distribution  of  organic carbon.

      Thomas (1969) addressed  the relationship of organic-carbon  content and
grain size  and  suggested that,  partially  as a function of  the great surface
area  of  clays,  carbon  is associated  with  clay particles.   He further stated
that  environmental conditions might  also  have an influence.

      Young  (1968)  addressed the chemistry  of  the sediments of a  portion of
the Lower Chesapeake Bay.  His  reported  values or organic  carbon, 0.15% to
2.01% agree with the ranges noted  in the  present study. Young's procedures
included using  a LEGO  carbon  analyzer to  determine carbon  content and by
digesting the sample in 10% HC1 to remove  carbonate ("inorganic" carbon).
As  Young's  samples were short cores  he provided some information on the
vertical trends.   At most  sites, the highest  organic carbon contents were
between  the 10  and 20  cm depths.   In only 1 of the 19 stations was there an
increase in organic carbon below 20  cm.   He found no trend with  depth of
burial in the inorganic carbon. The highest  organic carbon contents were
found in the  deep  water stations.  He found a good correlation (R = 0.82)
between  total iron and organic  carbon content and noted that although
clayey sediment contained  larger amounts  of organic carbon than  sandier
sediments,  the  percent organic  carbon to  percent clay correlation was not
significant (R  = 0.40).

      The literature on sulfur in estuarine sediments in relatively scant
when  compared to that  on organic carbon.   Dunham (1961, cited in Goldhaber
and Kaplan, 1974)  lists river estuaries  and tidal lagoons  among  a limited
set of environments wherein the sediments  may contain authigenically formed
reduced  sulfur  compounds.  There  is, however, a reasonable body  of
literature  on sulfur  in marine  sediments  including, among  others, the
summary  work  of Goldhaber  and Kaplan (1974) and Berner (1970, 1981, 1982).
Goldhaber and Kaplan  (1974) in  tabulating the work of several other marine
researchers show sulfur contents ranging from 0.02% to 2.0% in marine
sediments.

      The incorporation of  sulfur in  the sediments depends  upon the
-reduction of  sulfate  to H2S and HS  by bacteria.  This process requires

                                      97

-------
anoxic conditions, which, even if not present in the water column may  exist
below the sediment-water interface.  Although the sediments may have been
deposited through oxygen-rich water, the dissolved oxygen of the
interestial water is removed as it is used by the organisms inhabiting the
sediment (Goldhaber and Kaplan, 1974).  Berner (1981),  in a discussion of
sulfidic sediments, states that the occurrance of sulfides in marine
sediments is common because of the sulfate available from seawater  and
nearly universal presence of organic matter in the sediments.  Berner
(1969), however, sites local differences in the content of organic  matter
as causing local differences in the sulfur content of anaerobic sediments.
Berner (1970), using a field example from the Connecticut shore of  Long
Island Sound, further states that the availability of organic matter that
can be metabolized by sulfate-reducing bacteria is a factor limiting the
formation of pyrite in marine sediment.  This relationship is depicted in  a
plot of weight percent organic carbon, a rough indicator of the content of
organic matter, versus weight percent sulfur.  The data points show very
little scatter about a line of best fit.  Goldhaber and Kaplan (1974),
using data from several sources, present a similar plot.  They state that
the relationship is approximated by a line with a slope of 0.36 but admit
to "a good deal if scatter the data."  The scatter is due to a number  of
causes, including the great range of depths (0 to 500 cm) below the
sediment-water interface from which the samples were taken.

b.  Results.  The ranges of values of total carbon, organic carbon, and
sulfur contents (Figure 40) present no anomalies.  The  values of  organic
carbon up to a maximum of 3.9% with a mean of 1.0% are  consistent with
literature values (Shidler, 1975; Folger, 1972; Kemp, 1971).  Total carbon
contents are slightly greater, with mean 1.3% and are generally under  4%
but with a few samples reaching 9 or 10%.  These very high values are  from
areas where  shell fragments constitute a significant portion of the
sediment.  Although little was known to predict the values of sulfur
content, the distribution and range are not unreasonable with a maximum of
approximately 2% and a mean of 0.35%.

     Although the samples were chosen with a bias toward  finer sediments,
this bias is not significantly represented in the statistical correlations
of the various parameters (Table  11).  The strongest correlations of  the
chemical contents with a sedimentological factor are of the organic carbon
and sulfur contents with the percentage of clay  in  the  sediments.   The
table  is a listing  of R^ values from the SAS, GLM calculations of
regressions  of  the  chemical contents against mean and median grain  sizes,
mud and clay contents and water depth, and each other.  The table has
values  for the  entire sample set  and  for sets of  samples  within  subareas
because study of the spatial distributions  (Figures 41, 42  and 43)  seemed
to indicate  a general trend of  relationships between carbon or  sulfur
contents and depth  or clay  content  except  in shallow and/or restricted
areas  such as Mobjack Bay or Pocomoke Sound.  In  these  areas  the  patterns
differed from those in  the  Chesapeake  Bay  proper.   The  several  subareas
represent different physical environments  and deserve  separate
consideration.
                                     98

-------
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-------
Figure 41.   Isopleth map of the total carbon content of the sediments
            of the Virginia portion of the Chesapeake Bay.

                          CONTOUR INTERVAL  I %

-------
                        ORGANIC CARBON CONTENT
                            CONTOUR INTERVAL  1%
Figure  42.
Isopleth map of the organic carbon of the sediments of the
Virginia portion of the Chesapeake Bay.

-------
                                                                        JS'OO1
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                                 SULFUR CONTENT

                               CONTOUR INTERVAL 0.5%
Figure 43.   Isopleth map of the sulfur of the sediments of the Virginia

            portion of the Chesapeake Bay.

-------
 c.  Discussion.  Because the visual tie between depth and the various other
 parameters, both sedimentological and chemical, is so appealing, the very
 poor statistical correlations, maximum R^ of 0.47 and common values of 0.1,
 is surprising.  It most probably is explained by the frequency distribution
 of depths (Figure 44).  The distribution is decidedly asymetrical, with
 most depths being quite shallow.  Hence there are very few locations of
 greater depth with high clay contents to offset the locations of shallow
 depth and high clay content which results from the very sheltered nature of
 the location.                         ••

      Of the several characteristics used to describe the sediment type, the
 percentage of clay has the most significant relationship to the carbon and
 sulfur contents.  This agrees with the conclusion of Thomas (1969), based
 on the work of others, that "(organic) carbon is predominantly absorbed by
 clay particles (Bader, 1962), the quantity of which is related to clay
 surface area...".  The poor percent-clay with total carbon correlation is
 probably a function of shell material found in sandy sediments.  The close
 parallel between the clay-organic carbon and clay-sulfur relationships is a
 further expression of the good organic carbon-sulfur (Figure 45)
 correlation.  R^ for the entire system 0.76, range for subareas exclusive
 of Hampton Roads, 0.63 to 0.84.  Figure 45 is very similar to Goldhaber and
 Kaplan's (1974) plot.   The very low organic carbon-sulfur correlation in
 Hampton Roads  is most likely the result of several factors including the
 vast quantities of coal moved through the port and the industrial and urban
 nature of the  surrounding lands.  The measures of the central tendencies of
 the grain size distributions, mean and median, and the mud content of the
 sediment are  less well correlated than the percentage of clay.  This points
 out that the  governing processes are the great surface area and
 (potentially) active nature of clay particles and not purely grain size.
 Hence the quantity of clay in the sediment is more important than an
 integrating measure of the grain-size distribution.

      The interrelationship of the various characteristics within  individual
: subareas is a function of the local, physical environment of the  subareas.
' Relatively shallow, semi-enclosed and  little populated Mobjack Bay,  from
i which roughly 35 of a possible 55 samples were selected  for chemical
i analysis is the site of the strongest  interrelationships.  R^ values  for
 percent clay  versus total carbon, organic carbon, and sulfur contents  are
 0.97, 0.96, and 0.90 respectively.  The quality of the interrelationships
 reflects the  relatively simple nature  of the set  of processes active within
 Mobjack Bay.   There is only a minimum of fresh water inflow; the  mean  tidal
 range is low,  approximately 0.75 m; and  fetches are limited as  the bay  is
 open only to  the southeast.

      The York and Rappahannock River mouths, with 13 and 21 samples,  also
 exhibit reasonably good correlations reflecting the uniform nature of  the
 processes  active  across the  limited areas of  the  river mouths.   The
 information from  the other subareas indicates  some of the differences
 between  them.

      Pocomoke Sound is  shallow  and has  a small drainage  basin  and
-freshwater  inflow when compared  to the  rivers  of  the western  shore.   This

                                      104

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^  5/
                         ^^
                         63  75


                           DEPTH
                            l23
                                     147
44

  '
            c.:r
    105

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is reflected in the relatively poor relationship of organic to total
carbon.  This is probably due both to the less polluted waters of Pocomoke
Sound and to the abundance of shell material in the clean sediments.
Tangier Sound, which has a great range of depths, also has an abundance of
shell material.  Also there is no freshwater inflow, hence no indirect
mechanism for the inward transportation of organic materials derived from
terrestrial sources.

d.  Conclusions.  There is a strong relationship between the clay content
and the total carbon, organic carbon, and sulfur contents of the sediments
of the lower Chesapeake Bay.  This relationship probably is due to  the
great surface-area presented by a large volume of clay particles and to the
chemically active nature of the clays.  The ratio of organic to total
carbon is most strongly controlled by the presence or absence of shell
material and must equal one in the absence of shell.

     Several subareas of the Bay are affected by different processes which,
in turn, influence the chemical and sedimentological relationships.  The
urban, industrial surroundings of Hampton Roads create an environment quite
different from that in Tangier Sound or Mobjack Bay.  The volume of
fresh-water inflow, the nature of the drainage basin, and the local energy
regime, in the form of waves and currents, all contribute to local
variations.

B.  PATTERNS AND RATES OF SEDIMENT ACCUMULATION

     1.  Patterns of Erosion and Deposition.  The patterns of erosion and
deposition in the Bay fit, with minor modifications, the physiographic
segmentation offered by Ryan (1953) based upon the Bay geomorphology:

          Northern Bay:  Susquehanna River to south of the Patapsco
          River mouth.

          Middle Bay:  Patapsco River to the mouth of the Rappahannock
          River.

          Southern Bay:  Rappahannock River mouth  to the Bay entrance.

Within the Virginia portion of  the Bay  stem,  the patterns of erosion  and
deposition suggest  a further zonation:

          Middle Bay:

              Lower belt:  37°55'  to  37*35'

          Southern  Bay;

              Upper  (transitional  belt):  37°35'  to 37°25'
              Central (farfield  Bay mouth) belt:  37°25'  to  37°15'
              Lower  (nearfield Bay mouth belt:   37*15' to  36°55'
                                     107

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     The principal loci of deposition and erosion  are  shown  in Figure  46.
The generalized pattern is superimposed on bathymetry  in Figure 47.  The
patterns of deposition/erosion are displayed in terms  of the  rate  of mass
accumulation in Figures 48, 49 and 50 showing, respectively,  the sand,
silt, and clay components.

a.  The Nearfield Bay mouth belt is characterized  by a pattern of
"alternating" erosion/deposition areas across the  Bay  mouth  entrance,  and
depositional zones on the flanks of the Tail of the Horseshoe Shoal and
Thimble Shoal Channel (Figure 4).  Erosion is pronounced off  of Cape Henry,
and in False Channel and North Channel separating  Middle Ground, Inner
Middle Ground and Latimer Shoals on the northern part  of the  entrance.  The
shoal areas themselves are characteristically depositional,  while  the
location of the alternating cut and fill pattern suggests a  migration  of
the Inner Middle Ground and Middle Ground Shoals to the southwest.  The
migration is consistent with the results of Granat (1976) who studied
Middle Ground Shoal and presented bathymetric comparisons of  five  surveys
between 1852 and 1975.  The principal surface sediment type  (> 80% by
weight) within this zone is fine sand although there are fingers of medium
and very fine sand (Figure 48).

     The Chesapeake Channel is indicated as depositional throughout the
reach from the entrance to the latitude of Cape Charles.  The surface
sediments are predominately fine and very fine sand with up  to 40% silt.

     The lower part of Old Plantation Flats Channel is included in this
belt.  The deeper areas of the channel are erosional as is the eastern
flank; the bottom sediments are very fine sand with up to 30% silt in  the
deep area while the eastern flank is composed of fine  to medium sand.  The
western flank, indicated as depositional, is very  fine sand  (> 607, by
weight) and silt.

     Horseshoe Shoal, which forms the western portion  of the  Bay mouth
nearfield belt, is indicated as an area of relatively  low deposition with
areas of erosion in the nearshore zone.  This sand shield (>  80% sand) is
characterized by fine sand on the southern part whereas the  region flanking
York Spit Channel is medium sand with patches of coarse sand.  The latter
areas fronting Poquoson Flats are indicated as non-deposition or erosional.
This is consistent with independent observations from  a coring study which
show only a veneer of sand over Pliocene sediments.

     The Bay bottom south of Thimble Shoals Channel is indicated as
depositional near the seaward part of the channel, and erosional within the
inner segment (dredging zone).  The Crumps Bank area is expressed  as non-
to slightly depositional with fine and very fine sand  and local areas  of
silt.  The nearshore zone along the southern Bay shore and Willoughby  Bank
is indicated as being a relatively weak depositional zone with erosional
spots in the nearshore.  Surface sediments are fine to medium sands.

b.  The Central Southern Bay belt is considered a  portion of  the Bay mouth
system because of the presence of a pronounced depositional  area (Figures
46 and 47) to which we attribute a Bay mouth source.   This depositional

                                    108

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                                                                 37-00'
                                                      E3 >l METER "FILL"
                                                          .5 METER "CUT"
                          BATHYMETRIC CHANGES
                       CONTOUR INTERVAL 0.5 METER
Figure 46.  Bathymetric changes during the past 100 years in the Virginia
           portion of the  Chesapeake Bay.

-------
                                                             "r—ii i "
                                                   Q >l METER  FILL
                                                     >Q5 METER "CUT"
                 BATHYMETRY,  CONTOUR INTERVAL 10 FEET
Figure 47.   Bathymetry and generalized bathymetric changes in the Virginia
           portion of the Chesapeake Bay.

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Figure 48.
        MASS ACCUMULATION OF  SAND
     CONTOUR ^NTERVAL  I M-TON / M'/CENTURY


The mass of sand accumulation per square meter per century
in the Virginia portion of the Chesapeake Bay.

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Figure  49.
         MASS ACCUMULATION  OF SILT
      CONTOUR (NTERVAL .2 M-TONS/M*/CENTURY


The mass of silt accumulation per square meter per century
in the Virginia portion  of the Chesapeake Bay.

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                    MASS ACCUMULATION OF CLAY
                 CONTOUR INTERVAL .2 M-TONS /M1/CENTURY
Figure  50.  The mass  of clay accumulation per square meter per century
           in the Virginia portion of the Chesapeake Bay.

-------
 area,  centered  at  37"20',  includes  the northern ramp of the Old Plantation
 Flats  Channel.   Our  hypothesis  is  that this  depositional lobe (> 60% sand;
 the  remainder  silt)  results  from transport  from the Bay entrance through
 the  channel  and  up onto  the  ramp as  the channel cross-sectional area
 increases.   The  driving  force  for  the transport is argued to be the net
 up-Bay bottom-water  circulation which is strongest along the eastern side
 of the Bay.  The recovery  of bottom drifters (Harrison, et al., 1967)
 released  in  the  vicinity of  the Bay mouth fortifies the hypothesis; one of
 the  strongest  recovery zones within the Bay, and incidentally the
 northernmost zone, was the shoreline west of the deposition lobe.

     The  eastern flank of  the  channel and the adjacent shallow terrace have
 erosional loci  of  fine and medium  sands (total sand > 80% by weight).

     There are  two additional  zones of deposition in the western part of
 the  belt.  The  westernmost of  the  two is the nearshore terrace (water
 depths generally less  than 6 meters (20 feet) fringing Mathews County.  For
 the  most  part,  the bottom  sediments are medium sands (Figure 30) which may
 represent bedload  migration  from the more northerly nearshore terrace which
 is  indicated,  in part, to  be erosional.  In  these shallow waters, the net
 bottom flows could be  expected  to  be down-bay.  During strong northeast
 wind events, the southerly wind-drift currents and wind wave driven bottom
 agitation could, as  well,  play  a significant role.  To the east of the
 terrace depositional area  is a  narrow erosional zone which is coincident
 with the  western flank of  the  spit-like shoal upon which Wolf Trap Light is
 situated.

     The  second locus  of deposition on the western side is directly east of
 the  Wolf  Trap  Shoal.  The  bottom materials  are predominately fine and very
 fine sand with  pockets containing more silt.  This depositional lobe may
 represent an admixture of  materials from the adjacent "Bay mouth derived"
 depositional area  and  the  western terrace.   According to Firek (1975) and
 Firek  et  al. (1977)  the  eastern lobe has relatively high concentrations of
 garnet in the  heavy  mineral  suite  compared to the western lobe which has a
 higher concentration of  tourmaline  and zircon which he considered to be
 representative  of  western  shore source.

 c.   The Upper  Southern Bay belt is  indicated as being generally
 depositional  (0 to 0.5 m/cent)  but  no strong depositional loci are
 expressed.   Erosional  loci are  indicated in  the channel trough on the
 eastern side of the  Bay.  As well,  the nearshore terrace along the Eastern
 shore  has patchy erosional areas.   A strong  erosional locus is indicated on
 the  western shore  terrace  below the Rappahannock River.  When the
 depositional patterns  are  viewed in conjunction with bottom sediment type
 (Figure 30),  this  belt appears  as  a transitional region .between the
 predominately  sandy  regions  to  the  south and the finer grained sediments to
 the  north.

     Within the channel  along  the Eastern Shore, indicated as erosional,
 the  bottom is  composed of  fine  sands with up to 25% silt.  The erosional
 areas  on the western shore terrace  are composed of medium and coarse sands.
-Zircon is a strongly dominate  heavy mineral  in the fine fraction (Firek,

                                     114

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 1975,  Firek  et^ al^. ,  1977),  which  in terms of hydraulic equivalence is
 consistent with the  relatively coarse sand population.

      The  Bay floor area  between the fringing terraces, without strong
 depositional loci, may be  roughly divided longitudinally.  The area in the
 central part is characterized  as  about 50% very fine sand, less than 20%
 clay,  and the  remainder  silt.   In contrast, the western area,  a confluence
 of the Rappahannock  Tributary  and the main channel leading to Maryland
 waters, is characteized  by increasing dilution of very fine sand with
 increasing contributions of clay  and silt (Figure 28 and 33).

 d.  The Lower  Middle Bay belt, ranging in latitude from the mouth of the
 Rappahannock River to the Virginia boundary at the mouth of the Potomac, is
 the most  complex segment in the Virginia portion of the Bay stem.  The
 clearly defined deep channel which extends through most of the Maryland
 portion of the Bay terminates  in  this section.  The channel is flanked on
 the east  by  the large sand-shield containing Tangier and Smith Islands.  As
 well,  the segment contains the junction of the channels leading into
 Tangier  and  Pocomoke Sounds.

      The  channel floor,  except in the deepest parts and associated flanks,
 are indicated  as depositional.  The sand component, very fine sand, is a
 relatively minor constituent of the channel and lower flank, and the clay
 fraction  exceeds 40%.  The deepest parts of the channel, with essentially
 the same  sediment constituents, are erosional loci.  These erosional sites
 include  parts  of the eastern channel flank where the sediments rapidly
 grade into sands.

      At  approximately 37°40' latitude, the channel begins to flare in width
 and cross-sectional  area.   The flaring section is associated with sites of
 pronounced deposition.  In this section sand  (very fine sand) is a very
 minor constituent « 5%) and clay exceeds 40%.  The western boundary of
 this section follows closely the 30-foot (10 meter) bathymetric contour,
 shoreward of which  sand  sized  materials dominate (> 90%).  The
 Tangier-Smith Island sand shield terminates at 37°40' (following the 10-13
 m contours)  so the  channel flare is not bathymetrically bounded on the
 eastern  side.   However,  between 37°40' and 37°35' the dilution with the
 clay constituent rapidly decreases to the east such that the mud component
 increases to 25-30%  with silt  generally dominating.

      Most of the surface sediments with significant clay fractions
 (> 20%)  are  contained within  the latitude  range 37°35' to 37°55'.  This
 band apparently represents the principal residual deposits of material
 delivered to the Virginia Bay stem from Maryland waters  including  the
 Potomac  River and,  perhaps, the Rappahannock  River.

      The sand shield containing Tangier and Smith Islands is  indicated  as
 null to  mild deposition in water depths less  than  7 meters.  However,  there
 are erosional loci in very  shallow waters.  The western  and southern  limits
 of the shield have strong depositional loci.  On the  west,  fringing the
 main Bay channel, deposition  extends  to water depths  of  greater  than  17
.meters (50  feet) while on the southern terminus the depositional  lobes

                                      115

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 extend to depths greater than 12-14 meters (36 feet).  The shield is
 generally greater than 90% sand with the deposttional loci composed of fine
 to medium sand.   The depositional nature of the deeper fringes of the belt
 is attributed to encroachment of sand over the edge of the shield induced
 by the net down-bay circulation in "surface" waters, augmented (or perhaps
 dominated) by wind drift current with wave driven resuspension accompanying
 strong north and northwest winds, a dominant component in fall and winter.

      2.  Sediment Budget.  Previous work addressing sediment budgets for
 the Bay has dealt only with the suspended sediment component.  Moreover,
 with one notable exception (Schubel and Carter, 1976), attention has
 previously focused on the Maryland portion of the Bay.  Observations of
 suspended sediment concentrations in the Virginia part of the Bay are
 relatively scanty.
!
      A complete sediment budget for the inorganic constituents of the
 Virginia portion of the system would include several terms for sources and
 sinks:

   - -  1.)  the Maryland portion of the system (Bay stem and the Potomac
           estuary) (probably a source),

      2.)  the principal Virginia tributary estuaries (Rappahannock,
           Piankatank, York, and James), and minor fringing creeks (could be
           either sources or sinks),

      3.)  the Bay mouth and near continental shelf waters (probably
           sources),

      4.)  Shore eros.ion of the margin of the Virginia Bay stem (source),

      5.)  skeletal remains from primary production (source),

 i     6.)  carbonates from shell (source), and
 I
 i     7.)  accumulation of material on the Bay floor  (treated as a sink).

 ;     As ensuing discussion will indicate, current knowledge  is
 insufficiently developed to address all of the requisite contributions.
 Our attempt at a sediment budget utilizes the reported values for estimates
 of suspended sediment (clay plus silt) for items 1, 2, 3 (Schubel and
 Carter, 1976; Biggs, 1970), and 5, and information derived from this study
 for items 4, 6 and 7.  No estimates of influx of sand from the Bay mouth
 have been reported.  The strategy is to ask whether the observed sediment
 accumulation on the Bay floor is consistent with the existing best
 estimates of the contributions from various sources.

      The most comprehensive evaluation of the relative sources (inorganic
 and organic) within the Maryland portion of the Bay is that  of Biggs
 (1970).  Utilizing estimates for the annual yield of silt and clay from
 shoreline erosion, of skeletal material derived from plankton, and a
 comprehensive set of suspended sediment measurements taken over a one-year

                                       116

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(1967) period, he concluded that 10% of the total input of  inorganic
material was transported, by estuarine circulation, into the regions  south
of the Patuxent River.

     Schubel and Carter (1976) advanced a suspended sediment budget  for  the
entire main stem of the Chesapeake Bay.  They formulated this budget  from a
single-segment, two-layer model using the salt balance equations  to  infer
net movement of suspended sediment.  Axial distributions of vertical
salinity and inorganic suspended sediments down the Bay stem during  a
twelve month period, 1969-1970, provided the primary data for the model.
They concluded that there is a net movement of suspended sediment into the
Bay from the ocean, and that the tributary estuaries are sinks  for
suspended sediment from the Bay (summarized in Table 12).   The  results in
Table 12 display several interesting points aside from the  conclusion that
the tributaries act as sinks for sediments from the Bay.  In order of rank,
the sources of suspended sediment are the Susquehanna River, silt and clay
derived from shore erosion, and, then the ocean.  The tributaries are
relatively weak sinks and, by subtraction, the remainder is deposition onto
the Bay bottom.

     Whether the Bay stem responds as a net source or sink  for  suspended
sediments to the principal estuaries remains a question demanding detailed
investigation.  Nichols (1977), in a study of the response  of the
Rappahannock estuary to the flooding of the 1972 tropical storm,  Agnes
calculated that over the sixteen days encapsulating the event,  10%  (11,000
tons) of the suspended load escaped into the Bay.  Officer  and  Nichols
(1980) applied a two dimensional box-model formulation to four  sets  of
suspended sediment concentration in the James and Rappahannock  estuaries,
one of which was the Rappahannock response to Agnes.  In the  latter,  the
estuary was found to export sediment to the Bay.  However,  in another data
set (spring, 1978) the estuary was found to be a sink for Bay materials  and
the magnitude was the same order of the sediment input from the river.   For
the James data sets, the estuary was found to be an exporter  of sediment
during very high discharge but an importer of sediments from  the Bay during
moderate river discharge conditions.  Ludwick (1981) argued that the
relatively high deposition rate of fine grained sediments in  Thimble Shoals
Channel exiting the James estuary is due,  in part,  to the deposition of
sediments from the ebb plume of the James.  This in itself  does not
constitute sufficient evidence that the James is a  net sediment exporter,
but it does suggest tha James River sediments are deposited in  the  Bay.
The strength of the oceanic source could however be stronger  than the
amount deposited with a net importation resulting.  Feuillet  and Fleischer
(1980) documented  the mixing of clay minerals from  the ocean  source  within
the James estuary.

      It is  important  to  recognize  that  none of  these  studies  were
specifically designed to address  the question of net  flux.  Rather  than
investigation  of transverse variations  in  salinity,  flow,  and sediment
concentrations at  a cross-section, these studies have emphasized the
vertical distribution along the estuary axis.   For  example, in  the  1978
series of measurements at  the  Rappahannock estuary  mouth  (Nichols et al.,
1981) a single vertical  array  of  current meters  on  the  northern side of  the

                                    117

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                       Table 12




               Suspended Sediment Budget




           (after Schubel and Carter, 1976)
Sources




Susquehanna River




Shore Erosion, Md.




               Va.




Ocean




TOTAL







Sinks




Tributaries




  Potomac




  Rappahanncok




  York




  James




All Others




TRIBUTARY TOTAL




Deposition




TOTAL
   Mass/Year




1.07 X 106 tons




0.40 X 106 tons




0.20 X 106 tons




0.22 X 106 tons




1.89 X 106 tons
0.04 X 106 tons




0.02 X 106 tons




0.02 X 106 tons




0.05 X 106 tons




0.03 X 106 tons




0.16 X 106 tons




1.73 X 106 tons




1.89 X 106 tons
                       118

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channel indicated a net landward flow at all depths.  Prior measurements
indicated a net bayward flow at all depths on the south  side of  the
channel.  Estimates of the flux at a cross-section would require sufficient
sampling to capture these pronounced transverse variations.

     While the evidence that the tributary estuaries are effective  traps
for riverine sediment is incontestable, considerably more detailed
measurements will be required to settle the claim that the Bay stem  acts  as
a net source for sediments to the tributary estuaries.   The availability  of
sediments from tidal resuspension would be a controlling factor.  The
suspended materials "leaking" into the Bay stem from the tributaries may,
upon settling, arrive in regions where tidal currents are not strong enough
for appreciable resuspension.

     The present attempt at a sediment budget does not attempt to resolve
whether the tributaries are net sources or sinks.  Before venturing  into
the evaluation of the sources, it is necessary to consider the residual
sediment accumulation derived from the treatment of bathymetric  comparisons
(see section V B for the details of calculation).  Taking into
consideration the errors in bathymetric comparison, the  data are presented
at three levels of estimation; for data cells (1 minute, depth bounded,
latitude slice) with changes greater than ± 1.10 m, ± 0.57 m, and finally
treating the data as if there were no error, that is ± 0.00 m.   Application
of ± 0.57 m and ± 1.10 m cutoff criteria is very conservative as these
values were derived from the error associated with comparison of individual
depth measurements.  Here they are applied to information which  has
undergone three levels of smoothing, each of which would be expected to
reduce the propagated error of the bathymetric comparison.

     There are no reliable independent ways to ascertain the reasonableness
of the three levels of estimation.  The approach herein  used is  to  make  a
comparison between sand derived from erosion and the mass of sand
"accumulated" in the nearshore zone.  The sediment distribution  maps show
the nearshore to be dominated by coarse sand.  The test  is applied  to  the
western side of the Bay as it is reasonable to argue that the major
tributaries act as barriers to sand transport and that  the Bay's western
shore is isolated from sand sources other than shore erosion.  Table 13
displays the correspondence between the mass of  sand derived from shore
erosion and the "accumulated" mass for eight relatively  isolated coastal
segments along the western shore of the Bay.  Comparisons are made  for two
outer-depth limits, 12 feet  (3.7 m) and 18  feet  (5.5 m). For  the wave
height and period conditions  found in  the Bay, the  12  foot (3.7  meter)
depth is a reasonable  limit for normal active wave induced movement of the
bottom sediment.  The  18  foot (5.5 meter) depth-limit  is taken  as the
maximum depth to which appreciable sand from shore erosi-on  is  likely to  be
dispersed.  Zone 4 displays relatively large sand accumulations  out to the
18 foot  (5.5 meter) depth and beyond.  Previous  discussion has  noted that
this zone, between the Piankatank River and  the  entrance to Mobjack Bay,  is
at the latitude of appreciable deposition argued to have a Bay-mouth
source.  Furthermore,  this  shore  zone  was  the  recovery area  for a number of
seabed drifters  (Harrison, et_ al_. ,  1967).   Comparison  within  this zone may
thus be  "contaminated" with  sands derived  from a source other  than shore

                                    119

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 erosion.   Thus,  the total without Zone 4 is of final interest.   Both the ±
 0.00 m and ± 1.10 m estimation levels for accumulation show poor
 correspondence with the shore-erosion source.   The ± 0.57 m level, however,
 displays  a correspondence within a factor ranging between one-half and to
 one for the two depth limits.   The individual  zones show a better
 correspondence for the 12-foot depth limit.  Based upon this comparison,
 the estimation level using depth changes greater than ± 0.57 m appears to
 be the most reasonable.  Ludwick (1981) used,  without explanation, ± 0.61 m
 as the level of significant change in his study of bathymetric change in
 the Thimble Shoals area.

      The values of accumulated sediment mass of sand, silt, and clay are
 shown in Table 14 for the three levels of estimation.  Only the Bay stem
 excluding fringing sounds, embayments, and tributary mouths is included in
 this discussion.  Sand-sized materials clearly dominate the sediment mass
 accumulation.  Given the dominance of sand-sized materials in the surficial
 sediments, and the method of calculating mass  accumulation, this result is
 not surprising.  However, the summary values of Table 14 do provide an
 estimation of the magnitude of the dominance.   Given the mass of residual
 accumulation, we may draw the first comparison between the strength of the
 known sources and the residual accumulation, a sink, shown in Table 15.
 The bottom accumulation dramatically exceeds the source terms for both the
 silt and clay and the sand comparisons.  The contribution of silt and clay
 from Maryland waters (0.147 X 10°" m-tons/100 years) is taken from Table 12
 as the contribution of the Susquehanna and shore erosion reduced by 90% as
 argued by Biggs (1970).  This value is uncompensated for any deposition
 between the Patuxent River and Smith Point or any source or sink value for
 the Potomac.  The value of 0.025 X 10° m-tons/100 years for silt and clay
 from shore erosion in Virginia, obtained in this study, is an order of
 magnitude less than that value estimated by Schubel and Carter (1976).  The
 inorganic constituent from zooplankton is relatively small.  The value for
 oceanic source, also taken from Table 12, appears as a stronger source for
 silt and clay than the estuarine contribution from the Maryland portion of
 the Bay.
                '                       :
      If the ^_ 0.57 m average depth change  is accepted as the appropriate
 basis for calculation of mass accumulation, the bottom accumulation of silt
 and clay (4.9 X 10° m-tons/100 years) exceeds the value from the estimated
 sources (0.4 X 10** m-tons/100 years) by a factor of 12.  This formulation
 does not include the major Virginia tributaries as either  sources or sinks.
 Bottom accumulation of sand (16.9 X 10° m-tons/100 years)  exceeds shore
 erosion source by a factor of 40.  Inspection of the axial  trends of sand,
 silt, and clay bottom accumulation may offer some insight  toward explaining
 the discrepancy.

      The patterns of accumulation (Figures 48, 49, and 50)  indicate that
 the principal locus of clay deposition is between the Potomac and
 Rappahannock Rivers.  The  silt accumulation occurs throughout the central
 basin between the York River and the confluence of the channels to Tangier
 and Pocomoke Sounds as well as within  the  axial channel  leading into the
 Maryland portion of the  Bay.  Sand accumulations are most  pronounced at  the
-Bay mouth  area with secondary loci at  about 37°20" latitude, and  on the

                                     121

-------
Table 14
Bottom Deposition of Combined Sand, Silt and Clay;
Values are cumulative from north to south
SAND, SILT, AND CLAY
(X 108 m-tons/100 years)
Zone
7
10
15
20
25
30
35
40
45
50
55
60
64



Latitude
37°54'
37°51'
37°46'
37°41'
37°36'
37"31' >
H
37°21' o
37°16'
37°11'
37°06'
37°01'
36°57'
TOTALS
SAND
SILT
CLAY
±
•
1.
5.
7.
10.
11.
12.
15.
17.
20.
21.
26.
27.
22.
3.
2.
0
3544
5002
1092
6834
1408
2542
2022
4840
8967
2808
5884
2558
6047
1038
2958
2051
± 0.57 m

1
3
6
7
7
8
12
14
15
17
20
21
16
3
1
.3291
.2860
.6093
.0761
.3292
.7420
.9009
.6242
.1358
.1037
.6011
.8609
t
.0685
.9074
.0594
.8409
±


1
1
2
2
2
4
4
5
6
8
8
7
1
0
1.10 m Geographic Location
.0527 Smith Point
.2800
.1247
.9129
.0970 Rappahannock Spit
.1527 Cherry Point
.2496 Wolf Trap Light
.1704
.8951 Entrance Mob jack Bay
.2419 Poquoson River
.1397 Fisherman Island
.4071 Old Point Comfort ;
1
.9523 Cape Henry j
i
.1685
.1017
.6821
 122

-------
                                  Table 15

                     Comparison of Sediment Budget Terms
Source



Maryland

Shore Erosion, Va.

Zooplankton, Va.
      ash

Ocean


TOTAL SOURCE
   SILT PLUS CLAY

X 108 m-tons/100 years

       0.147

       0.025

       0.008


       0.220
       0.400
         SAND

X 108 m-tons/100 years

         ?

       0.400
       0.400
BOTTOM
±
±
±
RESIDUAL
0 m
0.57 m
1.10 m '

5
4
1

.500
.900
.784

22
16
7

.104
.907
.168
                                     123

-------
 'fringes of the Tangier-Smith Island sand-shield.  These  patterns  are
 rendered in quantitative form in Figure 51 and Table  16  which  indicates
 cumulative mass accumulation as a  function of latitude.

      The curves for sand accumulation indicate that about  25%  of  the  total
 accumulation occurs between Smith  Point (37°51') and  the fringes  of the
 Tangier Smith Islands shield (37°43').  Between 37°43' and 37°25'  there  is
 relatively small additional accumulation of  sand.  For the intermediate
 level of estimation (>_ 0.57 m) about 65% of  the sand  accumulation  occurs
 below latitude 37°25' and 38% occurs within  the Bay mouth  entrance
 latitudes (37°11' - 36°55').  These results  indicate  that  the  Bay  mouth
 acts as a gateway through which very large quantities of sand  are  advected.
 As well, the accumulation of sand  on the Tangier-Smith sand-shield
 indicates an advection of sand from the Maryland portion of that  feature.
I The sand contributed from shore erosion is then a relatively weak  source.

      The calculation of mass accumulation did not compensate for  shell
 content, thus, the "sand" accumulation is an overestimate.   If we  take a
 liberal estimate of 10% by weight  for shell  fragments (Shideler,  1975; also
 this study, Figures 41 and 42), the results  of this study  indicate that  the
 Bay mouth acts as a source for sand of the order ranging from  16  X 10° to  5
 X  10" m-tons/year distributed as far north as 37°25'.  At  the  intermediate
 level of estimation, we find 12 X  10  m-tons/year.

      The previously postulated sources for silt and clay cannot be readily
 rectified to explain the disparity between the bottom mass-accumulation  and
 the estimated source-strengths.  The bathymetric comparisons are based on  a
 period prior to the sediment influx due to runoff from Hurricane Agnes so
 we cannot appeal to the anomalously high Agnes input  from  the  Susquenna  (31
 X  106 m-tons, a factor of 25 to 30 greater than the "normal" year; Schubel,
 1975).  The results suggest that the major Virginia tributaries act as
 sources for sediment to the Bay.   Both the Rappahannock  and York
 tributaries show clayey-silt stringers entering the Bay.   As well, Ludwick
', (1981) presents evidence that there is deposition of  muds  from the James
[ River estuary in the Thimble Shoals Channel.  The relative strength of
 these potential sources cannot be  determined from available information.

      Mass accumulation rate as a function of depth interval is shown  in
 Figures 52 and 53a, b, c and Tables 17 and 18 for the >_  0.57 m (±) level of
 estimation.  The five latitude slices reflect the principal depositional
 segments dicussed in section VI B  1.  In water depths less than 18 feet
 (5.5 m), the accumulation rate is  relatively low.  Maximum accumulation
 generally occurs between 18 feet (5.5 m) and 42 feet  (12.8 m)  with a
 relative redution in greater depths.  This trend was  noted by  Carron  (1979)
 in a plot of sedimentation rate (deposition  thickness per  unit area y time)
 derived from the same bathymetric  comparisons but with different  smoothing
 procedures.

      Maximum total sediment-mass-accumulation per unit area (0.968
 m-ton/m^/lOO years) occurs in Zone 3.  This  is particularly notable in the
 sand and silt components, each exhibiting maximum in  this  zone.   It  is
 -germane to contrast the sand, silt, and clay components  in Zones  1,2 and  3

                                     124

-------
   37°51'

   37°4I'-

   37°3I'

   37°2I'

   37° II1-
   *f*-'*'+r-'-*~, **
   37°OI
     SAND
   37°5I'

   37°4I'-

   37°3I'-

   37°2I'
   37° 111

   37°OI'
   3705I'
   37°4I'

   37°3I'
   37°2l'

   37° I I'

   37°OI'
ret -.1
                      LEVELS OF ESTIMATION
                          	  £ ±0m
                          	£ ± 0.57m
                          	-  2 ± 1.01 m
                      -v^PER 25,50, and 75%
                        OF   ACCUMULATION
                10     20
                CUMULATIVE
             "'{xlO8 TONS/100 years)
     SILT
                I       2
                CUMULATIVE
              — SMITH  POINT

              — RAPPAHANNOCK  RIVER

              — WOLF TRAP LIGHT
              -*. MOBJACK BAY
              — YORK  RIVER
              — CAPE  CHARLES

              — CAPE  HENRY
             ~4  (xlO8 TONS/100 yeors)
I       2
CUMULATIVE
                              3 (xlO8 TONS/ 100 years)
Figure  51.  Cumulative mass  accumulation as a function of latitude.

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                              ZONE l<  37°54' to 37*36'
              6-12   12-18   18-24 24-30  30-36  36-42   >42
                      ZONE 2=  37°36' to 37°25'
                              ZONE 3- 37°25' to 37°I6'
        0-6   6-12   12-18   18-24 24-30  30-36 36-42   >42
                              ZONE 4= 37°16' to 37°05'
                              ZONE 5^ 37°05' to 36°56'

        0-6    6-12   12-18   18-24  24-30  30-36 36-42   >42
                   DEPTH   INTERVAL  (feet)
 Figure 52.   Total sediment mass accumulation per unit area per century
                             129

-------
 UJ
 >

 O
 O
-X.
CJ
                                ZONE 1= 37°54' to 37°36'
         0-6    6-12   12-18   18-24  24-30  30-36   36-42    >42
                                ZONE 2  37°36' to 37°25
ZONE 3: 37e25'to37°l6l
         0-6    6-12   12-18   18-24  24-30  30-36  36-42   >42
 O
 i
                                ZONE 4: 37°I6'to 37°05'
                                ZONES: 37°05'to36°56'
         0-6    6-12   12-18   18-24  24-30  30-36  36-42   >42
                            DEPTH  INTERVAL (feet)
  Figure 53a.  Sand; mass  accumulation per unit area per century as a
             function of depth interval.
                              130

-------
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 •x
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                              ZONE l« 37°54' to 37°36'
        0-6    6-12   12-18   18-24  24-30  30-36  36-42    >42
                              ZONE 2= 37°36' to 37°25'
                              ZONE 3 37°25' to 37°I6'
        0-6    6-12    12-18   18-24  24-30  30-36  36-42    >42
O
                              ZONE 4= 37°I6' to 37°05'
    0
                              ZONE 5'  37°05' to 36°56'
        0-6   6-12    12-18   18-24  24-30  30-36  36-42   >42
                   DEPTH  INTERVAL (feet)
  Figure 53b.  Silt; mass accumulation per unit  area per century as a

             function of depth interval.

-------
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                              ZONE h 37°54' to 37°36'
        0-6    6-12   12-18   18-24  24-30   30-36  36-42   >42
                          ZONE 2= 37°36' to 37°25'
                              ZONE 3  37°25' to 37°I6'
        0-6    6-12   12-18   18-24  24-30   30-36  36-42    >42
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      h
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                               ZONE 5' 37°05 to 36°564
        0-6    6-12   12-18   18-24  24-30  30-36  36-42   >42
                   DEPTH   INTERVAL  (feet)
   Figure 53c.   Clay; mass accumulation per unit area per century as a
               function of depth interval.

-------
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relative to the earlier discussion of the mapable patterns.  Zones  1 and 3
contain substantial accumulations of sand; the accumulation in Zone 1 is
attributed to southerly advection of sediment from the Tangier-Smith
sand-shield, and the accumulation in Zone 3 is attributed to sources to the
south (including the Bay mouth), and to additional contributing  from the
shallows to the north on the western side of the Bay.  This interpretation
thus views Zone 2 as a relatively inactive area of sand accumulation
between opposing sources.  The contribution from silt to the total  mass
accumulation parallels that of sand:  -the strongest contribution is in Zone
3 followed by Zone 1 with a relatively weak accumulation in Zone 2.  This
may argue for a mixture of sources, particularly since the absolute rate of
mass-accumulation and mass-accumulation rate per unit area follow the same
patterns (Tables 17 and 18) for sand and silt.  As there is little  basis
for arguing that the Maryland portion of the Bay's stem is a principal
source of silt relative to clay, the Bay mouth may serve with  the
"Maryland" Bay-stem, the Potomac, and the Virginia tributaries as secondary
sources along with shore erosion.  Such interpretation is, of  course,
conjectural and is based upon the intuitive notion that clay would  be
expected as the principal component contributed by the tributaries  and by
the "Maryland" Bay-stem whereas the nearshore wave energy could  maintain
silt from the Eastern Shore oceanic shoreline and lagoonal system in
suspension for advection into the Bay where tidal resuspension could  foster
net up-Bay drift.  This argument is tantamount to the claim that silt-sized
particles are carried from the Bay mouth to points throughout  the Virginia
portion of the Bay.

     The zonal distribution of the accumulation of clay-sized  particles
indicates the strongest depositional center occurs in Zone 1 followed by
Zone 3, and a relatively weak contribution in Zone 2 (Table 16).  The
relatively low accumulation of clay (viewed either as mass or  mass  per
area) raises some  interesting questions.  What is the principal  source of
the clay deposited in Zone 3?  What is the fate of the suspended sediment
which escapes the Rappahannock River?  Does the sediment exiting in surface
waters become, after settling, entrained  in up-estuary bottom-flows by
steps in tidal resuspension with ultimate deposition  in Zone  1 where  tidal
energy is relatively small?  Or does the material follow the net down-Bay
drift along the western  side of the Bay?  Resolution  of these  questions
await further research.               .

     The patterns  of deposition and magnitude of  the  accumulations suggest
the following summary interpretation:

     1.)  Appreciable influx of  fine sand occurs  at  the Bay mouth (on the
          order of  10^ m-tons/100 years).  The influx apparently results
          from tidal transport  coupled with  a net up-estuary  bottom-flow
          associated with  estuarine circulation.  The advection  zone  of  the
          sands extends  at  least  as  far  up estuary  as 37°25'  and perhaps  as
          far as  37°41'.

             In addition to  the  sand  accumulating at  the mouth of the
          Bay, there is  significant  quantity  of  sand  moving  from the north
          along  the  fringes  of  the  relict Tangier-Smith  Islands


                                     135

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     sand-shield.  In this case, the transport processes are probably
     dominated traction and suspension driven by wind-waves generated
     during north to westerly wind events coupled with "surface"
     wind-driven and net down-Bay estuarine circulation.

        By comparison to these sources, the sands derived by
     shore erosion are a minor constituent.  Previous work (Schubel
     and Carter, 1976) has assumed shore erosion would be the
     principal source of sand.   >

2.)  Silt-sized particles also are an important component of the
     influx of sediment through the Bay mouth.  Principal centers of
     deposition of silt occur in the central Bay between 37°15' and
     37°45'.  The degrees of partitioning of the total accumulation
     between the oceanic and estuarine sources is not clear, but as
     about fifty percent of the total accumulation occurs south of
     37a25", the Bay mouth likely is a strong source.

3.)  Fifty percent of the total accumulation of clay occurs north of
     Rappahannock River mouth (37°35') which suggests that the
     principal source of clay is the water to the north.  However, as
     the area between 37°40" and 37°55' is a region of relatively low
     tidal-energy relative to the influence of estuarine circulation,
     the region may also represent a trap for sources to the south.
                               136

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                             REFERENCES CITED

Allen, T., 1968, The Coulter Counter:  in_ Particle Size Measurement:
     Chapman & Hall LTD, London, p. 143-153.

Bader, R. G., 1962, Some experimental studies with organic compounds and
     minerals:  Graduate School of Oceanography, Univ. Rhode Island Occas.
     Publ. No. 2, 5 p. (cited in Thomas, 1979).

Behrens, E. W., 1978, Further comparisons of grain size distributions
     determined by electronic particle counting and pipette techniques:
     Jour. Sedimentary Petrology, v. 48, p. 1213-1218.

Belknap, D. F. and J. F. Wehmiller, 1980, Amino acid racemization in
     Quaternary mollusks:  examples from Delaware, Maryland, and Virginia:
     p. 401-414 ^n Hare, P.E., editor, Biogeochemistry of Amino Acids:
     John Wiley & Sons, Inc.

Bennett, R. H. and D. N. Lambert, 1971, Rapid reliable technique for
     determining unit weight and porosity of deep-sea sediments:  Marine
     Geology, v. 11, p. 201-207.

Berner, R. A., 1969, Migration of iron and  sulfur within anaerobic
     sediments during early diagenesis:  Am. Jour. Sci., v. 267, p. 19-42.

	, 1970, Sedimentary pyrite formation:  Am. Jour. Sci., v. 267,
     p. 1-23.

	, 1981, Anew geochemical classification  of sediments:  Jour. Sed.
     Petrology, v. 51, p. 359-365.
                                      !
	, 1982, Burial of organic carbon and  pyrite sulfur in the modern
     ocean:  its geochemical and environmental  significance:  Am. Jour.
     Sci. , v. 282, p. 451-473.

Biggs,  R.  B., 1967, The sediments of  Chesapeake Bay:  p. 235-280 in
     Lauff, G. H., editor, Estuaries, Am. Assoc. Advancement of Science
     Publ. 83, Washington, D.C., 757  p.

Biggs,  R.  B., 1970, Sources and distribuiton of suspended sediments in
      the northern Chesapeake Bay:  Marine Geology, v. 9 p.  187-201.

Brunn,  P.,  1962, Sea leval rise as a  cause  of  shoreline erosion:  Am. Soc,
      Civil Engineer Proc. Waterways  in Harbors  Div. v. 88 p. 117-130.
                                    137

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Byrne, R. J., and G. L. Anderson, 1977, Shoreline Erosion in Tidewater
     Virginia:  Special Report in Applied Marine Science and Ocean
     Engineering No. Ill, Virginia Institute of Marine Science, Gloucester
     Point, Va. 102 p.

Carron, M. J., 1979, The Virginia Chesapeake Bay:  Recent Sedimentation
     and Paleodrainage:  unpublished dissertation, Virginia Institute of
     Marine Science, College of William and Mary, Gloucester Point, Va., 83
     p. plus appendices.

Coulter Electronics, 1975 and revisions, Coulter Counter Model TA or
     Operator's Manual, Coulter Electronics, Inc. Hialeah Fl.

Dunham, K., 1961, Black shale, oil, and sulfide ore:  Advan. Sci., v. 18,
     p. 284-299, (cited in Goldhaber and Kaplan (1974)).

E.P.A. 1979, Quality Assurance for the Chesapeake Bay Program:  U.S.
     E.P.A., EMSL.   Las Vegas, Nevada.

Firek, F., 1975.  Heavy Mineral Distribution in the Lower Chesapeake Bay,
     Virginia:  Thesis Old Dominion University, Norfolk, VA., 147 p.

Firek, F., G. L. Shideler, and P. Fleischer, 1977, Heavy-mineral
     variability in bottom sediments of the Lower Chesapeake Bay, Virginia:
     Marine Geology, v. 23, p. 217-235.

Folger, D. W., 1972, Texture and Organic carbon content of bottom
     sediments in some estuarine of the United States:  p. 391-408 in
     Nelson.  B. W., editor, Environmental framework of Coastal Plain
     Estuaries:  Geol. Soc. Amer. Mem. 133.

Folk, R. L. , 1974,  Petrology of Sedimentary Rocks:  Hemphill Publishing
     Co., Austin, TX  183 p.

Fueillet, J. P. and P. Fleischer 1980, Estuarine Circulation:  Controlling
     factor of clay mineral distribution in James River Estuary Virginia:
     Jour. Sedimentary Petrology v. 50 p. 267-279.

Friedman, G. M. and J. E. Sanders, 1978, Principles of Sedimentology: John
     Wiley & Sons,  792 p.

Galehouse, J. S., 1971, Sedimentation Analysis:  p. 69-94 ^n_ Carver, R.E.,
     editor, Procedures in Sedimentary Petrology:  Wiley Interscience,
     651 p.

Gibbs, R. J., 1974, A settling tube system for sand-size analysis:  Jour.
     Sedimentary Petrology v. 44, p. 583-588.

Gibbs, R. J., M. D. Mathews, and D. A. Link, 1971, The relationship
     between sphere size and settling velocity:  Jour. Sedimentary
     Petrology, v.  41, p. 7-18.
                                    138

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 Goldhaber, M. B. and I. R. Kaplan, 1974, The Sulfur Cycle _in Goldberg,
      E.D., ed., The Sea, v. 5, Marine Chemistry:  John Wil^y" & Sons, New
      York, p. 569-655.

 Granat, M. A., 1976, Dynamics and Sedimentology of Inner Middle Ground
      - Nine Foot Shoal, Chesapeake Bay, Virginia:  Thesis, Old Dominion
      University, Norfolk, Virginia, 150 p.

 Halka, J. P., R. D. Conkwright, R. T. JCerhin, and D. V. Wells, undated.
      Sediment particle size analysis of the Chesapeake Bay Earth Science
      Study:  unpub. MS., Maryland Geological Survey, Baltimore.

 Hallam, A., 1974, A Revolution in Earth Sciences, Continental Drift to
      Plate Tectonics:  Clarendon Press, Oxford, 127 p.

 Harrison, W. R., M. P. Lynch, and A. G. Altschaefel, 1964, Sediments of
      Lower Chesapeake Bay, with emphasis on mass properties:  Jour.
      Sedimentary Petrology, v. 34, p. 727-755.

 Harrison, W. R., J. Malloy, G. A. Rusnak, and J. Terasmae, 1965, Possible
      late - Pleistocene uplift, Chesapeake Bay Entrance:  Jour. Geology v.
      13 p. 201-209.

 Harrison, W. R., J. J. Norcross, N. A. Pore, and E. M. Stanley, 1967,
      Circulation of Shelf Waters Off the Chesapeake Bight, Surface  and
      Bottom Drift of Continental Shelf Waters between Cape Henlopen,
      Delaware,  and Cape Hatteras, North Carolina, June 1963-December 1964:
      ESSA Professional Paper  3, 82 p.

 Hathaway, J. C.  1972, Regional clay mineral facies in estuaries and
      continental margin of the United States east coast,  p. 293-316 in
      Nelson, B. W. editor, Environmental Framework of Coastal Plain
      Estuaries:  Geological Soc. America. Memoir 133.

j Hicks, S. D. and J. F. Crosby, 1974, Trends  and variability of yearly mean
j      sea  level  1893-1972:  NOAA Tech. Memo No.  13, p. 7-8.
I
i
: Holdahl,  S. R.  and N. L. Morrison, 1974, Regional investigations of
      vertical  crustal movements in the U.S., using precise releveling  and
      mareographic data:  Tectonophysics v. 23,  p. 373-390.

 Inter-agency  Committee on Water Resources, 1964, Electronic Sensing of
      Sediments, Report R., Minneapolis, St.  Anthony Falls Hydraulic
      Laboratory, 80  p.

 Jacobs,  Fred,  1978,  Zooplankton distribution, biomass, biochemical
      composition and  seasonal community structure in  Lower Chesapeake  Bay:
      unpub. dissertation, Virginia Institute of Marine Science, Univ.  of
      Virginia,  Gloucester Point,  Va.
                                     139

-------
 Jones, G. B. and M. B. Jordan, 1979, The distribution of organic materials
      and trace metals in sediments form the River Liffey Estuary, Dublin:
      Estuarine and Coastal Marine Science, v. 8 p. 37-47.

 Jordan, R. R., 1974, Pleistocene deposits of Deleware:  in Oaks, R. Q. Jr.
      and J. R. Durban, editors, Post-Miocene Stratigraphy, Central and
      Southern Coastal Plain:  Utah State Univ. Press 275 p.

 Kemp, A. W. L., 1971, Organic carbon and nitrogen:  the surface sediments
      of Lakes Ontario, Erie, and Huron:  Jour. Sedimentary Petrology, v.
      41, p. 537-548.

 Kerhin, R. T., J. P. Halka, and D. V. Wells, 1979, Data Report:  Chesapeake
      Bay Earth Science Study, Sedimentology of Chesapeake Bay:  unpub.
I      report, Maryland Geological Survey, Baltimore.

 Knudsen, M., editors, 1959, Hydrographic Tables:  Tutein and Koch,
      Copenhagen.

 Koch, G. S. J. and R. F. Link, 1970, Statistical Analysis of Geological
      Data:  John Wiley and Sons, Inc.

 Kramer, C. Y., 1972, A first course in Methods of Multivariate Analysis:
      V.P.I, and S.U. Blacksburg, Va.

 LEGO, 1975, Instruction Manual:  Leco Corp. St. Joseph, MI.

 Leventhal, J. S. and V. E. Shaw, 1980, Organic matter in Appalachian
      Devonian black shale:  I. Comparison of techniques to measure organic
      carbon, II. Short range organic carbon content variations:  Jour.
      Sedimentary Petrology, v. 50, p. 77-81.

 Ludwick, J. C., 1981, Bottom sediments and depositional rates near Thimble
      Shoal Channel, Lower Chesapeake Bay, Virginia:  Geological Society
      America Bull. Part 1, v. 92; p. 496-506.

 Manner, H. A., 1949, Sea level changes along the coasts of the United
      States in recent years:  Trans. Amer. Geophysical Union, v. 30, p.
      201-204.

 McManus, D. A., 1982, Phi and sediment size analysis:  discussion:  Jour.
      Sedimentary Petrology, v. 52, p. 1011-1026.

 Meade, R. H., 1969, Landward transport of bottom sediments in estuaries
      of the Atlantic Coastal Plain:  Jour. Sedimentary Petrology v. 39, p.
      222-234.

 Meisburger, E. A., 1972, Geomorphology and sediments of the Chesapeake
      Bay Entrance:  U.S. Army Corps of Engineers, Coastal Engineering
      Research Center, Tech. Memo. 38, 61 p.
                                     140

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Mencher, E., R. A. Copeland, and H. Payson, 1968, Surficial Sediments of
     Boston Harbor, Massachusetts:  Jour. Sedimentary Petrology, v. 38. p.
     79-87.

Nelson, B. W., 1960, Clay minerals of the bottom sediments, Rappahannock
     River, Virginia:  Clays and Clay Minerals, Proc. 7th National Conf.
     p. 135-147.

Newman, W. S. and G. A. Rusnak, 1965, Holocene submergence of the Eastern
     Shore of Virginia:  Science v. 148, p. 1404-1406.

Nichols, N. M., 1972, Sediments of the James River Estuary, Virginia:
     p. 169-212 in Nelson, B. W. editor Environmental Framework of Coastal
     Plain Estuaries:  Geological Society of America Memoir 133.

Nichols, N. M., 1977, Response and recovery of an estuary following a
     river flood:  Jour. Sedimentary Petrology, v. 47, p. 1171-1186.

Nichols, M. M., L.E., Cronin, W. B. , Cronin, M. G., Cross, B. W., Nelson,
 - -  J. W., Pierce, and R. E. Vlanowicz, 1981 Response to freshwater inflow
     in the Rappahannock estuary, Virginia; Operation HIFLO "78";
     Chesapeake Research Consortium, CRC Pub. No. 95, Annapolis Md., 46 pp.

Officer, C. B. and M. M. Nichols, 1980, Box model application to a study
     of suspended sediment distributions and fluxes in partially mixed
     estuaries, in_ Kennedy, V.S. ed., Estuarine Perspectives; New York,
     Academic Press p. 329-340.

Powers, M. C., 1954, Clay diagenesis in the Chesapeake Bay area:  Clays
     and Clay Minerals, National Academy of Science, National Research
     Council.  Publ. 395, p. 430-441.

Rashid, M. A., and G. E. Reinson, 1979, Organic matter in surficial
     sediments of Miramichi Estuary, New Brunswick, Canada:  Estuarine  and
     Coastal Marine Science:  v. 8 p. 23-30.

Rosen, P.  S., 1976, Morphology  and processes of  the Virginia Chesapeake
     Bay Shoreline:  unpublished dissertation, Virginia  Institute of Marine
     Science, College of William  and Mary, Gloucester Point, Va. 313 p.

Ryan,  J. D.,  1953, The sediments  of  Chesapeake Bay:  Maryland Dept. of
     Geology, Mines  and Water Resources  Bull.  12,  120 p.

Sallenger, A. H., Jr., V. Goldsmith, and C. H. Sutton, 1975, Bathymetric
     Comparisons:  A manual  of  methodology, error  criter-ia and  techniques:
     Special  Report  No. 66  in Applied Marine Science  and Engineering,
     Virginia Institute of  Marine Science, Gloucester Point, Va., 34 p.

Sanford, R.  B. and D. J.  P.  Swift,  1971, Comparison of sieving  and
     settling techniques  for size  analysis, using  a Benthos  Rapid Sediment
     Analyzer:   Sedimentology,  v.  17,  p. 257-264.
                                    141

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 SAS Institute, Inc. 1979, SAS Users Guide:  SAS Institute, Inc. Gary, N.C.

 Schlee, J. 1966, A modified Woods Hole Rapid Sediments Analyzer:  Jour.
      Sedimentary Petrology, v. 36, p. 403-413.

 Schubel, J. R., 1975, Suspended sediment in Chesapeake Bay:  Proceedings
      Civil Engineering in The Oceans/Ill, Amer. Soc. Civil Engineers, p.
      245-264.
                                       N
 Schubel, J. R. , and H. H. Carter, 1976, Suspended sediment budget for
      Chesapeake Bay, in Wiley, M. ed., Estuarine Processes, v. II:  New
      York, Academic Press, p. 48-62.

 Schubel, J. R. and C. F. Zabawa, 1972, A Pleistocene Susquehanna River
I      channel connects the lower reaches of the Chester, Miles, and Choptank
      estuaries:  Ches. Biol. Lab. Spec. Report 24.

 Schubel, J. R. and C. F. Zabawa, 1973, Susquehanna River paleochannel
      connects lower reaches of Chester, Miles, and Choptank Estuaries:
      Chesapeake Science, v. 14 p. 58-62.

 Shackleton, N. J. and N. D. Updyke, 1973, Oxygen isotope and paleomagnetic
      stratigraphy of equatorial Pacific core V. 28-238:  Oxygen isotope
      temperatures and ice volumes on a 1(P and 10° year scale:  Quaternary
      Resarch v. 3, p. 39-55.

 Shepard, F. P., 1954, Nomenclature based on sand-silt-clay ratios:  an
      interim report:  Jour. Sedimentary Petrology, v. 24, p. 151-158.

 Shideler, G. L., 1975, Physical parameter distribution patterns in
      bottom sediments of the Lower Chesapeake Bay estuary in Virginia:
      Jour. Sedimentary Petrology, v. 45, p. 728-737.

, Shideler, G. L., 1976, A comparison of electronic particle counting and
I      pipette techniques in routine mud analysis:  Jour. Sedimentary
|      Petrology v. 46, p. 1,017-1,025.

: Swift, D. J. P., J. R. Schubel, and R. W. Sheldon, 1972, Size  analysis
      of fine-grained suspended sediments:  a review:  Jour. Sedimentary
      Petrology, v. 42, p. 122-134.

 Stephenson, L. W., C. W. Cooke, and W. C. Mansfield, 1933, Chesapeake Bay
      region:  International Geol. Cong. XVI Session, Washington, D.C.,
      Guidebook 5, excursion A-5.

 Terzaghi, K. and R. B. Peck, 1948, Soil Mechanics in Engineering Practice:
      John Wiley & Sons, Inc. 566 p.

 Thomas, R. L., 1969, A note on the relationship of grain size, clay
      content, quartz and organic carbon in some Lake Erie and  Lake Ontario
      sediments:  Jour. Sedimentary Petrology, v. 39, p. 803-808.
                                      142

-------
Trask, P. D. ,  1932.  Origin and environment of source sediments of
     petroleum:   Gulf Publishing Co. 323 p. (cited in Folger, 1972).

van Donk, J. 1976, Oxygen - 18 record of the Atlantic Ocean for the entire
     Pleistocene epoch p. 147-163 in Cline and Hages, editors,
     Investigations of Late Quaternary Paleooceanography and
     Paleoclimatology:  Geol.  Soc. Amer. Memoir 145.

Watts, G. M.,  1954, Laboratory and field tests of sounding leads:   Beach
     Erosion Board Tech. Memo. 54, 42 p.

Young, D. K.,  1968, Chemistry of southern Chesapeake Bay sediments:
     Chesapeake Science, v. 9, p. 256-260.

Zeigler, J. M., G. G. Whitney, Jr., and C. R. Hayes, 1960, Woods Hole
     Rapid Sediment Analyzer:   Jour. Sedimentary Petrology, v. 30, p.
     490-495.

Zellmer, L., 1979, Development and Application of a Pleistocene Sea Level
     Curve to the Coastal Plain of Southeastern Virginia:  unpub.  M.S.
     Thesis, Virginia Institute of Marine Science, College of William and
     Mary, Gloucester Point, Va., 85 p.
                                    143

-------
     APPENDIX 1
       LORAN C
BIAS CORRECTION DATA
      144

-------
LORAN-C BIAS CORRECTION DATA
Location
Gwynn Island
Windmill Pt. Light
Smith Pt. Light
Tangier Is. Channel
Saxis Boat Ramp
Onancock Ck. Ent. #1
Onancock Ck. Town Wharf
Occohannock Ck» Ent. #1
Wolf Trap Light
Hungars Ck. Ent., Mkr. 1PA
Swash Channel, York Spit, Mkr. 3
Cape Charles Harbor, 3 M "5" 5A
Tue Marshes Light
York Spit Light
Wise Pt. Channel Mkr • "269"
Back River Ent., Mkr. "4"
Thimble Shoal Light
Fort Wool Pier
James River Bridge
Chesapeake Bay Ent. 2T Bell
Fish Pier, C.B. Bridge Tunnel
Little Ck., BW "LG"
Middle Ground Light
Lynnhaven In. Marina
Lafayette River Ent.
Latitude
37°29.31'
37°35.79'
37°52.88'
37°49. 78'
37°59.18'
37°43.47'
37°42.74'
37°22.55'
37°23.41'
37°23.40'
37°15.73'
37°15.32f
37°14.13'
37°12.57'
37°06.92'
37°06.07'
37°00.87'
36°59.15'
36°58.68'
36°58.45f
36058.05'
36°56.95'
36056.70'
36054.28'
36053.57'
Longitude
76°18.14'
76°14.17'
76°11.04'
75°59.66r
75°43. 89'
75°51.07'
75°45.37'
75°57.86'
76°11.38'
75°59.72'
76°19.97'
76°01.95'
76°23.17'
76°15.27'
75°58.87'
76°15.77'
76°14.42'
76°18.08'
76°28.78'
76°02.28'
76°06.87'
76°10.75'
76°23.55'
76°05.08'
76°19.47'

-------
TO CORRECT FROM THEORETICAL TO REAL
9930-Y
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
_
2
1
1
1
1
1
1
1
1
1
1
2
1
1
1
2
1
1
1
1
1
2
2
2
2
.09
.27
.52
.47
.31
.45
.75
.48
.38
.20
.55
.06
.66
.64
.71
.16
.75
.77
.61
.98
.81
.17
.15
.02 .
.07
9930-Z
+ 1
+ 1
+ 1
+ 1
+ 1
+ 1
+ 1
+ 1
+ 1
+ 1
+ 1
+ 0
+ 1
+ 1
+ 1
+ 1
+ 1
+ 0
+ 1
+ 1
+ 1
+ 1
+ 1
+ 1
+ 1
.31
.31
.32 "
.42
.30
.60
.22
.39
.33
.56
.33
.53
.21
.22
.27
.05
.28
.94
.22
.06
.10
.06
.26
.11
.08
9960-X
- 2
- 2
' - 2
- 2
- 2
- 2
- 2
- 2
- 2
- 2

- 2
- 2
- 2

- 2
- 2
- 2
- 3
- 2
- 2
- 2
- 3
- 2
- 2
.68
.32
.08
.40
.79
.59
.55
.42
.29
.63
-
.22
.97
.59
-
.71
.74
.71
.15
.44
.46
.72
.23
.57
.92
9960-Y
- 0
- 0
- 0
- 0
- 1
- 0
- 0
- 0
- 0
- 1

- 0
- 1
- 0
- 0
- 0
- 0
- 0
- 1
- 0
- 0
- 0
- 0
- 0
.47
.35
.16
.62
.28
.80
.62
.60
.55
.05
-
.20
.06
.55
.77
.17
.67
.52
.09
.15
.25
.29
.67
.31
- 0.35

-------
                  APPENDIX 2
THE MASS OF SEDIMENT ERODED FROM THE SHORELINE
                     149

-------
                MASS OF SEDIMENT ERODED OR ACCRETED




            ALONG THE SHORELINE BY MINUTE OF LONGITUDE




        FOR THE SOUTHERN SHORE OF THE LOWER CHESAPEAKE BAY
Minute of
Longitude
760 oi1
02'
03'
04'
05'
06'
07'
08'
09'
10'
11'
12'
13'
14'
15'
16'
17'

Percent
Gravel
1,073
(1,779)
(20,590)
(21,525)
(12,167)
14,195
14,195
ND
429
4,929
4,983
375
0
0
346
252
182
(15,102)
(0.5)
Sand
2,143,675
157,719
(315,568)
(329,912)
(186,472)
364,329
364,329
ND
8,075
92,864
93,873
150,334
157,133
251,551
172,464
125,782
90,770
3,340,946
100.5
Metric Tons
Silt
0
0
0
0
0
0
0
ND
0
0
0
0
0
0
0
0
0
0

Clay
0
0
0
0
0
0
0
ND
0
0
0
0
0
0
0
0
0
0

Total
2,144,748
155,940
(336,158)
(351,437)
(198,639)
378,524
378,524
ND
8,504
97,793
98,856
150,709
157,133
251,551
172,810
126,034
90,952
3,325,844

NOTES:  ND = No data.




        () = Accretion.
                                150

-------
       MASS OF SEDIMENT ERODED OR ACCRETED




    ALONG THE SHORELINE BY MINUTE OF LATITUDE




FOR THE EASTERN SHORE OF THE LOWER CHESAPEAKE BAY
Minute of
Latitude
370 07'
08'
09'
10'
11'
12'
13'
14'
15'
16'
17'
18'
19'
20'
21'
22'
23'
24'
25'
26'
27'
28'
29'
30'
31'
32'
33'
34'
35'
36'
37'
38'
39'
40'
Gravel
(1,298)
(1,298)
5,390
4,684
7,840
9,904
7,482
(1,568)
(5,153)
ND
(1,344)
(832)
8,043
20,685
ND
ND
ND
0
0
(4,328)
5,413
23,368
35,009
100,006
7,886
0
43
811
55
1,040
469
ND
ND
ND
Metric Tons
Sand Silt
(20,844)
(20,844)
392,413
341,069
707,924
894,219
680,966
(167,725)
(536,944)
ND
(204,702)
153,316
998,288
1,697,597
ND
ND
ND
138,356
159,109
87,059
308,422
996,104
1,643,257
1,133,770
(23,568)
50,059
(68,008)
810,499
20,949
398,025
179,560
ND
ND
ND
(6)
(6)
28,564
24,436
36,561
46,182
37,268
18,224
0
ND
(724)
(236)
1,148
180,230
ND
ND
ND
85,826
98,700
72,942
167
10,807
21,435
132,469
(126,758)
4,789
0
0
49
932
421
ND
ND
ND
Clay
ND
ND
18,708
16,260
23,908
30,199
24,225
11,334
0
ND
0
0
0
82,009
ND
ND
ND
20,292
23,336
17,248
0
43,403
86,807
108,639
-11,416
0
0
0
0
0
0
ND
ND
ND
Total
(22,148)
(22,148)
445,075
386,449
776,233
980,504
749,941
(139,735)
(542,097)
ND
(206,770)
152,248
1,007,479
1,980,521
ND
ND
ND
244,474
281,145
172,921
314,002
1,073,682
1,786,508
1,474,884
(131,024)
54,848
(67,965)
811,310
21,053
399,997
180,450
ND
ND
ND

-------
EASTERN SHORE (cont'd.)
Minute of
Latitude
41'
42'
43'
44'
45'
46'
47'
48'
49'
50'
51'
52'
53'
54'
55'
56'
Gravel
ND
ND
3,949
11,846
5,430
3,620
5,093
4,658
3,025
ND
ND
ND
11,364
106,059
82,824
2,565
Metric Tons
Sand Silt
>
ND
ND
341,841
1,025,522
175,373
116,915
162,419
146,903
94,471
ND
ND
ND
56,057
523,200
505,822
17,771
ND
ND
416
1,247
0
0
0
0
0
ND
ND
ND
224
2,093
3,381
143
Clay
ND
ND
0
0
0
0
0
0
0
ND
ND
ND
272
2,537
815
0
Total
ND
ND
346,206
1,038,615
180,803
120,535
167,512
151,561
97,496
ND
ND
ND
67,917
633,889
592,842
20,479
             462,740     13,914,620     680,924     521,408     15,579,692






Percent         3             89           4           3
NOTES:  ND = No Data.




        () = Accretion.





                               152

-------
       MASS OF SEDIMENT ERODED OR ACCRETED




    ALONG THE SHORELINE BY MINUTE OF LATITUDE




FOR THE WESTERN SHORE OF .THE LOWER CHESAPEAKE BAY
Minute of
Latitude
37° 01'
02'
03'
04'
05'
06'
07'
08'
09'
10'
11'
12'
13'
14'
15'
16'
17'
18'
19'
20'
21'
22'
23'
24'
25'
26'
27'
28'
29'
30'
31'
32 •
33'
34'
35'
Gravel
2,428
4,654
19,410
54,736
167,155
232,563
ND
ND
9,359
15,816
66,518
79,307
ND
ND
ND
ND
627
2,099
(4)
(14)
(1,517)
(3,466)
382
24,045
22,769
49,608
55,269
22,469
52,427
37,448
168
2,878
12,326
ND
ND
Metric Tons
Sand Silt
123,767
237,220
627,943
799,222
1,025,104
1,426,232
ND
ND
602,365
215,154
173,436
194,079
ND
ND
ND
ND
41,807
371,528
8,386
(47,910)
(94,028)
(30,542)
36,748
400,228
379,219
587,676
562,543
586,336
1,368,116
977,226
50,663
307,445
879,936
ND
ND
0
0
33,240
33,240
0
0
ND
ND
2,009
5,735
2,314
2,514
ND
ND
ND
ND
3,802
6,929
30
0
(224)
(329)
(340)
555
525
1,537
1,862
3,694
8,618
6,156
41
301
982
ND
ND
Clay
0
0
56,084
56,084
0
0
ND
ND
5,754
9,584
2,993
3,351
ND
ND
ND
ND
2,963
8,343
0
0
(59)
(249)
9
1,623
1,536
1,690
1,242
3,078
7,182
5,130
0
0
0
ND
ND
Total
126,195
241,874
736,677
943,282
1,192,259
1,658,795
ND
ND
619,487
246,289
245,261
279,251
ND
ND
ND
ND
49,199
388,899
8,412
(47,924)
(95,828)
(34,586)
36,799
426,451
404,049
640,511
620,916
615,577
1,436,343
1,025,960
50,872
310,624
893,244
ND
ND

-------
WESTERN SHORE  (cont'd.)
Minute of
Latitude
36'
37'
38'
39'
40'
41'
42'
43'
44'
45'
46'
47'
48'
49'
50'
51'
52'

Percent
Gravel
3,383
52,430
63,890
17,876
ND
11,576
34,728
14,691
21,803
ND
ND
ND
2,146
32,872
43,843
47,265
30,250
1,306,213
6
Sand
*
110,620
1,714,612
1,887,668
160,385
ND
169,686
509,058
220,521
355,842
ND
ND
ND
244,848
954,752
942,271
1,024,207
655,493
20,759,862
89
Metric Tons
Silt
9,766
151,376
174,567
33,485
ND
145
436
161
114
. ND
ND
: ND
51,162
104,972
61,008
66,313
42,440
809,136
3
Clay
3,395
52,627
71,166
21,782
ND
0
0
0
0
ND
ND
ND
37,081
69,551
34,832
37,860
24,230
518,862
2
Total
127,164
1,971,045
2,197,291
233,528
ND
181,407
544,222
235,373
377,759
ND
ND
ND
335,237
1,162,147
1,081,954
1,175,645
752,413
23,394,073

NOTES:  ND = No Data.




        () = Accretion.
                                154

-------
                MASS OF SEDIMENT ERODED  OR ACCRETED

        ALONG THE SHORELINE BY MINUTE OF LATITUDE/LONGITUDE

           FOR THE EASTERN, WESTERN, AND SOUTHERN SHORES

                    OF THE LOWER CHESAPEAKE BAY

Southern
Shore
Eastern
Shore
Western
Shore
Gravel

(15,102)

462,740

1,306,213
Sand

3,340,946

13,914,620

20,759,862
Metric Tons
Silt

0

680,924

809,136
Clay Total

0 3,325,844

521,408 15,579,692

518,862 23,394,073
Percent     Southern Shore -  8
            Eastern Shore  - 37
            Western Shore  - 55
Total
1,753,851    38,015,428    1,490,060     1,040,270    42,299,609
Percent
                  90
                                155
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-------