VIMS Books and Book Chapters

Printing is not supported at the primary Gallery Thumbnail page. Please first navigate to a specific Image before printing.

Bivalve Molluscs: Barometers of Climate Change in Arctic Marine Systems

Roger Mann, Daphne M. Munroe, Eric N. Powell, Eileen E. Hoffmann, and John M. Klinck

Bivalve mollusks store a complete history of their life in the growth lines in their valves. Through sclerochronology, in combination with isotope signatures, it is possible to reconstruct both post-recruitment growth history at the individual level and commensurate environmental records of temperature and salinity. Growth patterns are integrators of local primary productivity; spatial and temporal changes in growth illustrate commensurate patterns of food availability. Mactrid clams are long-lived, benthic dominant species found on inner continental shelves throughout the Northern Hemisphere where they variously support major fisheries (Spisula solidissima in the Mid-Atlantic Bight, Mactromeris polynyma in eastern Canada, Spisula sachalinensis in Japan) and recreational fisheries (Mactromeris polynyma in Alaska), and serve as dietary items for charismatic species such as bearded seals (Erignathus barbatus) and walrus Odobenus rosmarus divergens). Ongoing studies, employing sophisticated adult growth and larval dispersal models of the response of Spisula solidissima to climate change in the Mid-Atlantic Bight, suggest the general use of mactrids as barometers of climate change over broader geographic footprints. Mactromeris polynyma is a candidate species for shallow arctic marine systems, having a pan-arctic distribution from the Gulf of Maine in the Atlantic to the Bering Sea and Gulf of Alaska in the northern Pacific. The longevity of extant individuals (≤25 years) provides opportunity for detailed reconstruction of the benthic environment and food regimes at the decadal level.
Ecological Role of Blue Catfish in Chesapeake Bay Communities and Implications for Management

Ryan W. Schloesser, Mary C. Fabrizio, Robert J. Latour, Greg C. Garman, Bob Greenlee, Mary Groves, and James Gartland

Rapid increase in abundance and expanded distribution of introduced blue catfish Ictalurus furcatus populations in the Chesapeake Bay watershed have raised regional management concerns. This study uses information from multiple surveys to examine expansion of blue catfish populations and document their role in tidal river communities. Originally stocked in the James, York, and Rappahannock River systems for development of commercial and recreational fisheries, blue catfish have now been documented in adjacent rivers and have expanded their within-river distribution to oligo- and mesohaline environments. Range expansions coincided with periods of peak abundance in 1996 and 2003 and with the concurrent decline in abundance of native white catfish I. catus. Blue catfish in these systems use a diverse prey base; various amphipod species typically dominate the diet of smaller individuals ([FL]), and fishes are common prey for larger blue catfish (>300 mm FL). Recent studies based on stable isotope analyses suggest that adult blue catfish in these systems are apex predators that feed extensively on important fishery resources, including anadromous shads and herrings Alosa spp. and juvenile Atlantic menhaden Brevoortia tyrannus. Minimizing effects on Chesapeake Bay communities by controlling high densities of blue catfish populations is a primary goal of management, but conflicting demands of the commercial and recreational sectors must be resolved. Further, low market demand and human consumption concerns associated with purported accumulation of contaminants in blue catfish pose additional complications for regulating these fisheries.
Six Fish and 600,000 Thirsty Folks—A Fishing Moratorium on American Shad Thwarts a Controversial Municipal Reservoir Project in Virginia, USA

J. E. Olney, D. M. Bilkovic, C. H. Hershner, L. M. Varnell, H. Wang, and R. L. Mann

Moratoria on fishing directly impact fishers, distributors and marketers of product and can have serious socio-economic implications. Moratoria can impact communities but usually populations closely linked to the banned activity. In an unprecedented example, a moratorium on fishing in Virginia has directly impacted a nonfishing citizenry by thwarting plans for a public utility. In May 2003, a panel empowered to regulate marine resources denied permission to withdraw raw water from a pristine freshwater river, the Mattaponi. The controversial action spoiled a multi-million dollar plan to establish the King William Reservoir, a water source considered essential to future growth and development in the region. The facility was designed to serve a projected 600,000 people in 2040 but the Mattaponi Indians, environmentalists, local citizens and commercial fishers opposed the plan. A central issue was conservation of American shad Alosa sapidissima, an anadromous clupeid native to the U.S. east coast. An inriver moratorium on fishing for American shad imposed in 1994 remains in effect. In the reservoir debate, scientists advised the panel that the project would withdraw water in the center of the larval nursery area for this species and in a river that accounted for the highest statewide production of juveniles. Scientists recommended relocating the intake since losses of larvae to withdrawal could be counter to restoration goals of the moratorium. Using quantitative models, municipal authorities argued that only six American shad would be lost annually to impingement or entrainment. The panel rejected this argument and proposals to mitigate losses.
Isabel's Silent Partners: Seasonal and Secular Sea Level Change

J. D. Boon

Tidal conditions fail to explain a paradoxical similarity in water level extremes induced by Hurricane Isabel on 18 September 2003, and the 23 August 1933 storm of record at Hampton Roads, Virginia. Storm surge peaks occurred near astronomical high tide during both storms, but Isabel arrived during neap tides while tides during the 1933 storm were nearer to spring. In addition, Isabel produced a lesser storm surge, yet she yielded a storm tide, or high-water mark, roughly equal to that of the 1933 hurricane. The answer to the paradox lies in observed sea level—water level measured relative to the land—and its movement during the 70 years between these events. Water level analysis shows that the sea level change observed can be divided into three categories at three different time scales: daily (astronomical tides), monthly (seasonal change), and yearly (secular trend in sea level). At Hampton Roads, a secular rise rate of 4.25 mm⋅yr-1 (1.39 ft/century) predicted an increase of 29.8 cm in 70 years; mean sea level for the month of September stood an additional 21.9 cm above the annual mean for 2003. These numbers are comparable to the mean semirange of tide (37.0 cm) at Hampton Roads. Thus seasonal and secular change are both factors of key importance in evaluating storm tide risk at time scales attributable to major hurricanes (100 years). Adoption of a new vertical reference, projected monthly mean sea level, is proposed to facilitate their inclusion in storm tide predictions at decadal time scales.
Physical Response of the York River Estuary to Hurricane Isabel

L. H. Brasseur, A. C. Trembanis, J. M. Brubaker, and C. T. Friedrichs

After making landfall on the North Carolina coast on the morning of 18 September 2003, Category 2 Hurricane Isabel tracked northward parallel to and slightly west of the Chesapeake Bay. At Gloucester Point, near the mouth of the York River estuary, strong onshore winds with speeds in excess of 20 m⋅s-1 persisted for over 12 hours and peak winds reached over 40 m⋅s-1, causing a sustained up-estuary wind stress. Storm surge exceeded 2 m throughout most of the lower Chesapeake Bay. A 600 kHz acoustic Doppler current profiler (ADCP), deployed at a depth of 8.5 m off Gloucester Point, provided high-quality data on waves, storm surge, currents, and acoustic backscatter throughout the water column before, during, and after the storm. Pressure and salinity sensors at three additional sites further up the estuary provided information on water surface slope and saltwater excursion up the estuary. A first-order estimate of three terms of the along-channel momentum equation (barotropic pressure gradient, acceleration, and friction) showed that the pressure gradient appeared to be balanced by the wind stress and the acceleration during the storm. The storm’s path and slow speed were the primary causes of the extremely high storm surge relative to past storms in the area.
Reproductive biology

Christina L. Conrath

Several reproductive specializations are found within the elasmobranchs. All elasmobranchs fertilize internally and produce a relatively small number of large eggs. Elasmobranch fecundity generally ranges from one to two offspring produced a year up to a maximum of 300 in the whale shark (Compagno, 1990; Joung et al., 1996). Elasmobranch reproductive strategies include oviparity, aplacental viviparity and placental viviparity (Wourms, 1977). Oviparous species enclose eggs in an egg case and deposit them into the environment, where embryos develop external to the body of the mother . .Embryos remain in the egg case to develop for a period ranging from less than two months to over one year (Compagno, 1990). Viviparous species retain eggs within the uteri where the embryos develop. The yolk sac of placental viviparous species interdigitates with the uterine wall to form a placenta in which nutrients from the mother are transferred to the embryo. In most species the egg envelope is retained and incorporated into the uteroplacental complex (Hamlett, Wourms and Hudson, 1985). Gestation for viviparous species ranges from less than six months to greater than two years (Compagno, 1990). Viviparous species may have either lecithotrophic or matrotrophic development. Lecithotrophic development occurs when embryos derive their nutrition solely from yolk reserves and occurs in many aplacental viviparous species. Matrotrophic development occurs when embryos supplement the yolk reserves by obtaining maternally derived nutrients during gestation and also occurs in many aplacental species and all placental viviparous species (Wourms and Lombardi, 1992). The advantage of matrotrophy may be the increase in juvenile size at birth and therefore increased survivorship of young. Another important consideration in the evolution of elasmobranch reproductive strategies is the presence or absence of uterine compartments. Uterine compartments are formed in all species with placental development and some species with aplacental development and are believed to be an important step in the evolution of placental viviparity (Otake, 1990).
Tagging methods and associated data analysis

Robert J. Latour

Tagging methods have a long history of use as tools to study animal populations. Although the first attempts to mark an animal occurred sometime between 218 and 201 B.C. (a Roman officer tied a note describing plans for military action to the leg of a swallow and when the bird was released it returned to its nest, which was in close proxiD?ity to the military outpost in need of the information), it is uncertain when fish :"ere first marked (McFarlane, Wydoski and Prince, 1990). An early report published 1? The_ Comp/eat Angler in 1653 by Isaak Walton described how private individuals tied ribbons to the tails of juvenile Atlantic salmon (Salmo salar) and ultimately determined that Atlantic salmon returned from the sea to their natal river (Walton and (otton, ~ 898; McFarlane, Wydoski and Prince, 1990). Since the late 1800s, numerous fish tagging experiments have been conducted with an initial emphasis on salmonids followed soon after by successful attempts at tagging flatfish and cod. Pelagic species, namely Pacific herring (Clupea harengus pallasi) and bluefin tuna (Thrmnus thynnus) Were successfully tagged in the early 1900s, while elasmobranch tagging studies did not commence until the 1930s. Since 1945, large-scale tagging programmes have been initiated all over the world in an effort to study the biology and ecology of fish populations.

Modern tagging studies can be separated into two general categories. Tag-recovery studies are those in which individuals of the target population(s) are tagged, released, and subsequently killed upon recapture, as in a commercial fishery; while capture-recapture studies are designed to systematically tag, release and recapture individuals on multiple sampling occasions
An Unprecedented Scientific Community Response to an Unprecedented Event: Tropical Storm Agnes and the Chesapeake Bay

M. P. Lynch

In June 1972, the remnants of Hurricane Agnes brought destructive floods to the watershed of the Chesapeake Bay basin. Unlike Hurricane Isabel, Agnes did not strike Chesapeake Bay directly, but deposited a record amount of rainfall on the watershed. The evening that the Agnes rainfall began in earnest coincided with a meeting of the Citizens Program for the Chesapeake Bay. The directors of the three largest Chesapeake Bay research institutions, Drs. Donald W. Pritchard, L. Eugene Cronin, and William J. Hargis Jr., were in attendance at this meeting. The potential magnitude of the Agnes rainfall was readily apparent at the meeting as one of the planned evening events had to be moved due to a foot of water in the meeting room. The following morning at breakfast, the three directors committed their institutions to “Operation Agnes,” extensive studies of the biological, chemical, and physical impacts of this event. Hargis, Cronin, and Pritchard were good friends and strong competitors of long standing. Since 1949, Pritchard had been the first full-time director of the Chesapeake Bay Institute (CBI); Cronin had headed the Chesapeake Biological Laboratory (CBL) since 1951; and Hargis had been director of the Virginia Institute of Marine Science (VIMS) (and its predecessor the Virginia Fisheries Laboratory-VFL) since 1959. In 1964, the three directors had set up an informal Chesapeake Bay Research Council (CBRC) to coordinate some of their Chesapeake Bay research activities. They used the CBRC mechanism to coordinate “Operation Agnes,” a commitment that was made without any assurance of financial support for these studies. The gamble taken by the three laboratory directors was successful, eventually resulting in a peer-reviewed book published by The Johns Hopkins University Press entitled The Effects of Tropical Storm Agnes on the Chesapeake Bay Estuarine System. Operation Agnes was the last project undertaken by the CBRC. Reorganization by two of the parent institutions and incorporation of the Chesapeake Research Consortium (CRC) resulted in a realignment of Chesapeake Bay scientific leadership and the leadership of Operation Agnes moved from CBRC to CRC. The scientific community’s response to Tropical Storm Agnes—an unprecedented event— was in itself unprecedented. A number of coincidences came into play: recent (1969) experience with flooding from Hurricane Camille; fortuitous attendance of the leaders of the three largest Chesapeake Bay research institutions at a meeting directly affected by Agnes; and the prior mobilization of the three institutions to conduct extensive hydrographic studies throughout Chesapeake Bay. The most important factor, however, was the strong commitment of three laboratory directors to the understanding of the Chesapeake Bay system.
Effects of Hurricanes on Atlantic Croaker (Micropogonias undulatus) Recruitment to Chesapeake Bay

M. M. Montane and H. M. Austin

Few studies have focused on the effects of climatic perturbations, such as hurricanes, on finfish recruitment and behavior. The Virginia Institute of Marine Science (VIMS) Trawl Survey has sampled continuously throughout the Virginia portion of Chesapeake Bay for 50 years. While hurricanes have impacted Chesapeake Bay during this time, three periods of hurricane activity— September and November 1985 (hurricanes Gloria and Juan), September 1989 (Hurricane Hugo), and September 2003 (Hurricane Isabel)—coincided with the largest spikes in juvenile recruitment of Atlantic croaker (Micropogonias undulatus) for half a century. The fall (October–December) croaker young-of-year indices for 1985, 1989, and 2003 were seven, five, and eight times greater, respectively, than the 50-year average. Typically Atlantic croaker display great interannual variability in Chesapeake Bay, with these fluctuations shown to be weather related. The timing of Atlantic croaker recruitment to Chesapeake Bay is such that late summer/fall hurricanes are most likely to affect them, as opposed to other shelf spawners. Understanding the effects of hurricanes on species, such as croaker, that have enormous ecological, commercial, and recreational importance is essential for prudent fisheries management.
Introduction: management of sharks and their relatives (Elasmobranchii)

John A. Musick

This publication describes the scientific principles and techniques used for resource management of elasrnobranch fisheries with emphasis on the particular context of elasmobranchs. The management characteristics of these fishes are described - their common bycatch character and their biological constraints on productivity (low growth rate, late maturity and Tow fecundity). Stock assessment of elasrnobranchs is described in the context of rnanagement objectives in a wide management context. Special attention is given to accurate species identification given the prevalent aggregating of landings data across species, genera and often families in this group. Techniques and experiences for tagging elasmobranchs for population estimation are described as well as methods of genetic techniques for stock identification. Methods and problems involved in determining ,age, growth, fecundity and mortality rates are described and their use in age-structured models Within the context of the reproductive biology of these fishes. Demographic models to determine the productive of elasmobranch resources are described, Use of surveys to,complement information derived from fisheries is described together with management measures, Last, practices of shark utilization are noted.
Shark Utilization

John A. Musick

Sharks and their relatives provide a multitude of usable products including: meat, fins, liver, skin, cartilage and jaws and teeth. Unfortunately, tens of millions of sharks taken in fisheries each year have their fins removed and their carcasses discarded overboard (Fowler and Musick, 2002). This practice, called finning, represents a considerable waste as the fins on average make up only about 5 % of the total weight of a shark (Vannuccini, 1999). Such waste is contrary to the United Nations Food and Agricultural Organization (FAO) Code of Conduct for Responsible Fisheries (Article 7.2.2 (g)) which stresses the importance of avoiding waste and discards in fisheries. In addition, the FAO International Plan of Action for the Conservation and Management of Sharks (IPOA- Sharks) encourages full use of dead sharks and retention of sharks from which fins have been removed (paragraph 22). Therefore, this Section briefly reviews the wide spectrum of uses that may be afforded by elasmobranchs to encourage their more complete and effective use. For a more comprehensive review see Vannuccini (1999) wherein an entire volume (470 pages) is devoted to the subject. A strong word of caution is necessary here: full utilization of shark carcasses should not be used as a pretext to fish unsustainably (Camhi, 2002). The goal of this manual is to provide information necessary to lead to sustainable elasmobranch fisheries.
Impacts of Tropical Cyclone Isabel on Shallow Water Quality of the York River Estuary

W. G. Reay and K. A. Moore

Water quality impacts from Tropical Cyclone Isabel on the York River estuary were assessed based on long-term, near-continuous, shallowwater monitoring stations along the York River proper (poly- and mesohaline regimes) and its two tidal tributaries—the Mattaponi and Pamunkey rivers (oligohaline and tidal freshwater regimes). Regional rainfall from 18 to 19 September 2003 ranged from 5.8 to 11.7 cm. Peak mean daily stream flow occurred on 21 September 2003 and represented a 20- and 30-fold increase over prestorm conditions on the Mattaponi and Pamunkey rivers, respectively. Isabel produced a storm surge of 1.7 m near the mouth of the estuary and 2.0 m in the upper tidal freshwater regions. The tidal surge resulted in a short-term (12- to 36-hour) pulse of high salinity water (approximately 10 ppt greater than pre-storm conditions) within the oligohaline portion of the estuary. In comparison, salinity levels within the upper tidal fresh water and down-river poly-and mesohaline regions remained relatively unchanged. Following the storm surge, salinity levels within lower portions of the estuary declined 1.5 to 4.5 ppt for an extended period in response to freshwater runoff. Elevated turbidity—in some cases extreme—was in direct response to the storm surge and waves associated with Tropical Cyclone Isabel. With the exception of a single station, maximum storm-associated turbidity levels varied between 192 and >1000 NTUs (nephelometric turbidity units). Turbidity levels returned to prestorm conditions within a 24- to 30-hour period at most stations. Perhaps the most significant environmental impact associated with the passage of Isabel was the persistent low dissolved oxygen (DO) levels (3–4 mg⋅L-1) that occurred at the tidal freshwater stations. Low DO at these stations coincided with increased freshwater inflow to the Mattaponi and Pamunkey rivers, suggesting augmented loadings of readily degradable organic material from the watershed. Mean daily DO levels took approximately two weeks to return to prestorm levels at these sites. Dissolved oxygen levels at the poly- and mesohaline stations within the York River proper remained at or above 5 mg⋅L-1 prior to, during, and after the storm’s passage.
Simulation of Hurricane Isabel Using the Advanced Circulation Model (ADCIRC)

J. Shen, W. Gong, and H. Wang

Hurricane Isabel made landfall near Drum Inlet, about 240 km south of the Chesapeake Bay mouth, on the Outer Banks of North Carolina at 17:00 UTC (GMT 12:00), 18 September 2003. Hurricane Isabel is considered one of the most significant tropical cyclones to affect portions of northeastern North Carolina and east-central Virginia. The ADvanced CIRCulation Model (ADCIRC) model was applied to the Chesapeake Bay to simulate Hurricane Isabel. High-resolution grids were placed inside the Bay and tributaries; coarse grids were placed outside the Bay. The spatial grid resolution in the Bay mainstem is about 200–1000 m and the spatial grid resolution in the tributaries ranges from 50–700 m. A parametric wind model was used to drive the model. The model results show that, with the use of a parametric wind model, the model can predict the peak surge and storm tide histories along the Bay mainstem and tributaries. The model was used to analyze the impact of sea level rise on surge and inundation prediction.
Mortality Estimation

Colin A. Simpfendorfer, Romon Bonfil, and Robert J. Latour

Mortality is an essential parameter in understanding the dynamics of any population and sharks are no exception. Without knowledge of how fast individuals are removed from a population it is impossible to model the population dynamics or estimate sustainable rates of exploitation or other useful management parameters.
What has Been Learned About Storm Surge Dynamics from Hurricane Isabel Model Simulation?

H. Wang, J. Cho, J. Shen, and Y. P. Wang

An unstructured grid hydrodynamic model was used to study storm surge in the Chesapeake Bay during Hurricane Isabel. The model-simulated, storm-induced water level compared reasonably well with the measured data collected around the Bay. Calibrated water level was extracted from the model to further analyze the dynamics of the surge as it formed and propagated along the mainstem Chesapeake. Based on time-series analysis, formation of the surge due to the pumping of coastal waters (hereafter called the primary surge) into the Chesapeake was first identified at the Bay mouth with a peak height of 1.5 m above mean sea level (MSL). Once formed, it propagated northward with gradually diminishing amplitude at a speed of about 5 m⋅sec-1 until reaching Windmill Point, near the mouth of the Rappahannock River in Virginia. Beyond Windmill Point, the surge height increased monotonically toward the northern part of the Chesapeake Bay. Spatial analysis of surge height revealed that a second-stage surge was induced directly by the southerly wind following Hurricane Isabel’s passage inland. The persistent southerly wind induced a setup and a set-down in the upper and lower Chesapeake respectively, with the dividing line near Windmill Point where the water level stayed at approximately 0.5 m above MSL during the event. Space-time analysis provided further evidence that the abnormally high water in the upper Chesapeake Bay was the result of the primary surge wave as well as the second-stage surge caused by the southerly wind-induced setup.
A Global Perspective On The Effects Of Eutrophication And Hypoxia On Aquatic Biota And Water Quality

Robert J. Diaz, Janet Nestlerode, and Minnie L. Diaz

Development associated with human populations has led to the globalization of many environmental problems. In marine systems, the most serious of these problems are directly related to the process of eutrophication. The increased production of organic matter in these marine systems associated with eutrophication is the primary factor impacting species abundance and composition and dissolved oxygen budgets. Oxygen, which is essential to maintaining balance in ecosystem processes through its role in mediating microbial and metazoan activities, has declined to critically low levels in many systems, which has led to the development of hypoxia (<2 ml O2>/l) and anoxia (0 ml O2/l). Currently, most oxygen depletion events are seasonal, but trends toward longer periods that could eventually lead to persistent hypoxic or anoxic conditions are emerging. Over the last 50 years, there has been an increase in the number of systems reporting problems associated with low dissolved oxygen. Currently there are over 100 hypoxic/anoxic areas around the globe, ranging in size from <1 km2 to 70000>km2, that exhibit a graded series of responses to oxygen depletion, ranging from no obvious change to mass mortality of bottom fauna. Ecosystems currently severely stressed by eutrophication induced hypoxia continue to be threatened with the loss of fisheries, loss of biodiversity, alteration of food webs, and simplification of energy flows.
Constraints on Sustainable Marine Fisheries in the United States: A Look at the Record

John A. Musick and Julia K. Ellis

The factors that may either constrain or contribute to sustainable marine fisheries were examined by reviewing and analyzing the history and current status of several U.S. fisheries. Among major factors under consideration are inherent vulnerability (vulnerability in some species is high because of low intrinsic rates of increase and/or naturally infrequent recruitment); environmental degradation (fisheries may collapse because of anthropogenic habitat destruction); availability of data (information necessary co conduce accurate stock assessments may be inadequate for some species); quality of the scientific advice (inappropriate models or scientifically inaccurate assessments may be used); and effectiveness of management decisions (managers may disregard recommendations from scientific committees, and/or implement management measures chat are risk-prone). Fisheries that are examined include the Atlantic Coast striped bass Morone saxatilis fishery, the New England groundfish fishery, the Atlantic shark fishery, the Atlantic and Gulf reef fish fisheries, and the Pacific rockfish fishery. Although many of the factors listed above contributed co declines in these fisheries, the root cause in all cases was harvesting at rates that were much higher than could be sustained by recruitment. Management was largely ineffective because management decisions were risk-prone and motivated by short-term economic considerations rather than long-term sustainability. Only after passage of legislation not only authorizing but specifying mandatory stock rebuilding, has most management been sufficiently precautionary to allow sustainability.
Can We Predict Joint Effects Of Hypoxia And Metals On Fish Survival?

Michael C. Newman

Fish are suddenly exposed to hypoxic conditions during diverse events such as seiche- or turnover-related water movements, bottom water release from reservoirs, ice-over of eutrophic arctic lakes, and rapid shifts in respiration: photosynthesis associated with cultural eutrophication. In each case, chemical equilibria established under hypoxic conditions that result in metal dissolution and accumulation suddenly shift toward chemical equilibria of oxic conditions. Critical changes in speciation include those determining the free ion activity that, as expressed by the Free Ion Activity Model (FIAM), is often the most bioactive form of a dissolved metal. Metal phase can also change rapidly and, in some cases, result in a precipitate on respiratory surfaces. Exposure of fish gills to metal (and integument of larval or small fish) changes O2 exchange dynamics. Changes in mucus quality and production and lamellae morphology decrease the amount of effective gill exchange surface and increase the diffusive layer thickness. These changes exacerbate those associated with the reduced O2 partial pressure gradient. Consequent shifts in blood chemistry (e.g., pH and ion composition) and ventilation also affect metal transport and deposition within fish tissues. Some of these changes have immediate consequences, but others can continue for long periods after the hypoxic conditions pass. Long-term metal effects can influence fish tolerance during future hypoxic episodes.

A joint, similar action model can be applied if the parsimonious assumption is made that asphyxiation constitutes a common mode-of-action for both acute metal effects and hypoxia. Joint action models are applicable based on either conventional dose-effect or survival time approaches. Expansion of such models to a physiologically-based toxicokineticstoxicodynamics framework (e.g., framed around the Fick equation) would be desirable, provided that model parameter requirements remain realistic. Long-term effects may be better addressed with models such as the binary logistic models used by epidemiologists.
Soft Shell Clam Mya arenaria

Patrick K. Baker and Roger Mann

Large populations of soft shell clams persist only in relatively shallow, sandy, mesohaline portions of the Chesapeake Bay. These areas are mostly in Maryland, but also occur in the Rappahannock River, Virginia. In some other portions of the Bay, especially polyhaline portions, low populations of soft shell clams persist subtidally. Restricted populations persist intertidally.

Soft shell clams grow rapidly in the Chesapeake Bay, reaching commercial size in two years or less. They reproduce twice per year, in spring and fall, but probably only fall spawnings are important in maintaining population levels. Major recruitment events do not occur in most years, despite heavy annual sets. Soft shell clams are important food for many predators. Major predators on juveniles include blue crabs, mud crabs, flatworms, mummichogs, and spot. Major predators on adults include blue crabs, eels, and cownose rays. Some other species that may depend heavily on soft shell clams include ducks, geese, swans, muskrats, and raccoons.

Diseases may play an important role in regulating adult populations of soft shell clams; hydrocarbon pollution is linked to increased frequency of disease. Oil pollution does the most widespread and persistent damage to soft shell clams through toxicity, aside from its role in inducing disease. Heavy metals, pesticides, and similar pollutants can be extremely toxic, but the harmful effects to clams do not last if the pollution abates. The main concern with the latter toxicants is bioaccumulation by soft shell clams, with the potential for passing toxic contaminants on to predators or to humans.

Siltation caused by storm events, dredging operations, or erosion, can smother clam populations. Eutrophication, enhanced by nutrient inputs from sewage or agriculture, is not known to have affected soft shell clam populations.
Hard Clam Mercenaria mercenaria

G. Curtis Roegner and Roger Mann

The hard clam is found along the eastern coast of North America from the Gulf of St. Lawrence to Texas. In Chesapeake Bay, the hard clam is restricted to salinities above approximately 12 ppt. An extensive survey of hard clam resources is overdue.

Statements concerning long term trends in populations are not feasible. Hard clams ·grow to a maximum shell length of about 120 mm. There are few documented cases of diseases in wild hard clam populations. Parasitic infestations are also slight. The life cycle of the hard clam includes a pelagic larval phase and a relatively sedentary benthic juvenile and adult phase. In Chesapeake Bay, ripe gametes can be found between May and October, and spawning commences when temperatures rise above 20-23 ·c. The larvae are planktotrophic (feeding). Metamorphosis usually commences at a shell length of 200-210 mm. Predation on new recruits is very high; dense aggregations of hard clams have been found in the absence of predators. Aside from predation and fishing pressure, the natural mortality of larger clams appears very low.

Hard clams are important suspension-feeding infauna, thus they are important in grazing of primary production, transfer of carbon and nitrogen to benthic food chains, and, through excretion, rapid recycling of particulate nitrogen as ammonia. The major food source for hard clams is planktonic microalgae. In Chesapeake Bay, growth occurs in spring and fall, when optimum water temperatures coincide with abundant food.

Clams are capable of living in a variety of sediment types, but higher abundances are found in coarse-grained sediments. Hard clam stocks are susceptible to overfishing. Recruitment rates are poorly understood, as are possible reestablishment periods if areas are depleted through commercial harvesting, and factors influencing larval settlement rates. Hard clam mariculture is well established and could easily be expanded into sites within the Bay. Given the ability of clams to bioaccumulate toxic substances, adequate monitoring should be maintained. The sub lethal effects of toxic material readily found in the lower James River should be examined
Ethical Aspects of Chesapeake Bay Use

Ann Hayward Rooney-Char and Maurice P. Lynch
Kepone® Residues In Chesapeake Bay Biota

M. E. Bender, R. J. Huggett, and W. J. Hargis

Oysters from the James displayed variations in Kepone residue levels related to water temperature and their spawning cycle. Oyster depuralion rates were related to temperature. In summer the "biological half. life" of Kepone in oysters was about one week, while during the winter about 40 days were required for residue levels to decline by 50 per cent. Residues in blue crabs varied as a function of sex, males having considerably higher residues than females. Fin fish levels from the James varied greatly, with residue levels being dependent on species and length of residence for migratory fishes .. Average Kepone residues in freshwater fish species, which are resident their entire Jives, varied from 0.04 to 2.4 μg/g. Long-term resident estuarine fin fish varied less than freshwater species, with mean concentrations between 0.6 and 2.7 μg/g. Short-term resident marine fish species, e.g. American shad and menhaden, exhibited low residues averaging less than 0.1 μg/g, while spot and croaker, which reside in the river for longer periods, bad higher residues averaging 0.81 and 0.75 μg/g respectively.

In the Bay, croaker, spot, trout and flounder all exhibited similar residue patterns showing lower residue levels at stations further up-Bay from the Kepone source in the James River.
Coliform Depuration Of Chesapeake Bay Oysters

Dexter S. Haven, Frank O. Perkins, Reinaldo Morales-Alamo, and Martha W. Rhodes

Oysters contaminated in nature depurated fecal coliforms to levels below 50/100 g in 48 hr over a wide range of environmental conditions typical of the lower Chesapeake Bay region. Temperature was found to be the most crilical environmental factor with conditions below 10-12°C having the potential of inhibiting depuration. Coliform clearance did not appear to be correlated with pumping rate or biodeposition activity of oysters. Oysters infected with the pathogens Dermocystidium marinum and Minchinia nelsoni (MSX) depurated as rapidly as uninfected ones. Meat quality and size of oysters likewise did not affect depuration.

Four commercial-size tanks of different designs were found to yield satisfactory results in 48 hr. Water flow rates over the ranges studied and location of trays within the tanks did not influence depuration.

Biodeposits contained high levels of total and fecal coliforms, but their accumulation in the tanks did not have a detrimental effect under the conditions studied.

Pooling oysters during monitoring of' depuration samples was necessary due lo the variation of coliform levels in individual oysters. Samples of 6-8 pooled oysters appeared to be adequate for estimating coliform levels.

The Medium A-1 test was superior to the elevated temperature coliform plate_ (ETCP) procedure of Cabelli and Heffernan for determination of fecal coliforms in oysters.
The Marine Algae of Virginia

Harold J. Humm

Starting with initial collections near Yorktown back in 1946, Humm over the years gathered information on algae appearing all seasons of the year from bays, marshes, reefs, wrecks and a variety of substrates from the Eastern Shore, Chesapeake Bay and tidewater areas.
Freshwater and Marine Fishes

Robert E. Jenkins

The current list of freshwater fishes known from Virginia stands at 206 species, including 10 that are diadromous and 4 others ranked as freshwater-estuarine. Eight of the freshwater and one of the freshwater-estuarine species were introduced to the state. Several additional strictly freshwater fishes are expected to be discovered. The Virginia freshwater ichthyofauna is relatively rich in species compared with most other states. For example, Maryland and Delaware together have 99 species (Lee et aZ., 1976), West Virginia 151 (Denoncourt et aZ., 1975), Kentucky 201 (Clay, 1975), and North Carolina 195 (Menhinick et aZ., 1974). Some of these totals reflect our adjustments for diadromous and estuarine fishes. The other adjacent state, Tennessee has a much richer freshwater fauna than Virginia. <.....>

Virginia's marine and estuarine fish fauna is characterized by its dynamic nature. Most elements of the fauna are migratory. All are highly mobile. Most are widespread coastally and occur in their preferred habitats in many localities within Virginia and other states. Musick (1972) annotated 208 species of marine and estuarine fishes within Virginia's coastal fish fauna, including 174 marine, 24 estuarine, and 10 diadromous (9 anadromous, 1 catadromous) species. Fourteen (10 diadromous and 4 estuarine) species are shared with the freshwater faunal list.