Mortality of newly metamorphosed eastern oysters (Crassostrea virginica) in mesohaline Chesapeake Bay

 Stocks of eastern oysters, Crassostrea virginica (Gmelin), in mesohaline Chesapeake Bay, USA, exhibit a high degree of inter-annual and spatial variability in recruitment. We found that cumulative oyster spatfall on off-bottom collector plates, measured throughout the summer in 14 years over a span of three decades, was highly positively correlated (r ² = 0.8) with juvenile oyster recruitment on adjacent oyster bars. Total abundances of juvenile oysters on these bars were, however, generally 99.7% lower than predicted from cumulative seasonal larval settlement on collector plates. We propose that although the number of larvae metamorphosing was the key factor in determining the gross annual pattern of recruitment to these mesohaline oyster bars, the actual magnitude of recruitment was governed by post-settlement processes, such as competition for limited resources and predation. We tested the hypothesis that predation may be partly responsible for high post-settlement juvenile oyster mortality. We performed a series of 3-d field investigations over two summers (1989, 1990) at a mesohaline site, employing cages of various mesh sizes (400, 800, 1500 μm) to protect hatchery-reared spat of 0.5 to 4.0 mm shell height. Mortality rates for spat held for 3 d in the estuary (17.8%) were significantly higher (P = 0.0001) for the smallest spat (0.5 to 2.0 mm) compared with those of 2.01 to 4.0 mm (4.2%). In 1990, but not in 1989, enclosure within 400 and 800 μm mesh cages significantly (P = 0.004) increased survival during 3-d deployments (9.4 and 10.1%, respectively) compared with spat unprotected by mesh cages (21.9%). In a series of laboratory predation studies that used the entire community of invertebrates that could penetrate the cages, microscopic juvenile polyclad flatworms, Stylochus ellipticus, were the only organisms that we observed crawling into living oysters and feeding on oyster tissue. Large flatworms (50 to 200 mm²) are known to be important predators on oysters, but this ability of flatworms that were so small (<ca. 5 mm²) and translucent as to be almost invisible without magnification to feed on immediate post-metamorphic oysters has not been documented previously. Our results suggest that the rate of mortality due to predation in mesohaline Chesapeake Bay is much reduced once spat survive for 2 to 3 weeks post-metamorphosis. Thus, it is likely that predation in the 1 to 2 week period immediately after settlement may be a crucial factor in the structuring of eastern oyster populations. Received: 21 December 1998 / Accepted: 2 December 1999     

An exploratory study with the proton microprobe of the ontogenetic distribution of 16 elements in the shell of living oysters (Crassostrea virginica)

Study of the chemical composition of shell of exoskeletonous organisms in the past has required the sacrifice of the organism. Because the beam of the proton microprobe is relatively nondestructive and analyzes the surface layer of the shell, organisms do not have to be killed. The present paper presents results of a preliminary experiment in which distribution of elements (Na to Sr) in shell of living juvenile oysters, Crassostrea virginica (Gmelin), was studied in situ with a proton microprobe at monthly intervals for four months. The relative concentration of 16 elements was measured in the newly deposited prismatic edge of the right valve of three oysters reared in controlled laboratory conditions. Na, Mg, Al, Si, S, Cl, K, Ca, Ti, Cr, Mn, Fe, Cu, Zn, Br, and Sr were detected in concentrations as low as a few parts per million relative to the concentration of standards added to pure CaCO₃. Concentration of elements varied nominally among shells of the three individual oysters and in their successive ontogenetic stages. Fluctuations in concentration of Na, Mg, S, Cl, Ca, Mn, Fe, Cu, and Zn were generally similar in the two normally growing oysters, but differed from those in the oyster that stopped growing. Trends in concentration of Al, Si, and Sr were similar in the three oysters: those of Br were variable. Relative concentrations of Na, Cl, S, Mn, Fe, and Zn increased slightly with age of oysters, that of the other elements stayed relatively constant. Concentration of most elements was higher in shell than in seawater. Variable concentrations, especially of Na, Cl, and Si in valve edges, tend to support the hypothesis of earlier workers that separate mineral phases are present as impurities entrapped within the shell during calcification.     

Growth patterns in oysters, Crassostrea virginica, from different estuaries

We analyzed a data set collected over 15 yr, containing growth data from strains of eastern oysters, Crassostrea virginica (Gmelin, 1791), initiated from parent populations in Long Island Sound, Delaware Bay, and lower Chesapeake Bay. The long-term growth data proved to be a powerful tool for examining patterns of growth differentiation among separated populations of C. virginica. The oyster strains had been grown in a common environment in lower Delaware Bay for up to seven generations. We found that the oyster strains with origins in Long Island Sound were significantly larger over several generations than oyster strains from Delaware Bay and Chesapeake Bay. Chesapeake Bay oyster strains were larger than Delaware Bay oyster strains at 1.5 yr old, but Delaware Bay oysters were larger at 2.5 yr. Year-to-year variation in environmental conditions had a strong significant effect on absolute oyster size and the relative sizes of the oyster strains. Persistent differences between oyster strains from different origins over several generations support a hypothesis that these estuarine populations have experienced long-term genetically-based population differentiation. This result is consistent with hypotheses of population differentiation of oysters based on observations of local reproductive timing. Received: 12 August 1997 / Accepted: 26 May 1998     

Comparative vulnerability to predators,and induced defense responses,of eastern oysters Crassostrea virginica and non-native Crassostrea ariakensis oysters in Chesapeake Bay

Management agencies are considering introducing the Suminoe oyster Crassostrea ariakensis into Chesapeake Bay, USA. It is unknown if the growth of feral populations of this non-native oyster would be regulated by the same predators that once controlled the abundance of the native eastern oyster C. virginica. In laboratory studies, we compared the relative susceptibility of juvenile diploids (shell height < 25 mm) of both oyster species to invertebrate predators of eastern oyster juveniles. Predators included four species of mud crabs [Rhithropanopeus harrisii (carapace width 7–11 mm), Eurypanopeus depressus (6–21 mm), Dyspanopeus sayi (8–20 mm), and Panopeus herbstii (9–29 mm)], the blue crab Callinectes sapidus (35–65 mm), and two sizes of polyclad flatworms (Stylochus ellipticus and possibly Euplana gracilis; planar area ≲5 mm² and ∼14 to 88 mm²). All four species of mud crab and the blue crab preyed significantly (ANOVA, P ≤ 0.05) more on C. ariakensis than on C. virginica, but predation by flatworms of both sizes did not differ significantly between oyster species. The greater susceptibility of C. ariakensis to crab predation was likely due to its shell compression strength being 64% lower than that of C. virginica (P = 0.005). To test for predator-induced enhancement of shell strength, we held oysters of both species for 54 days in the presence of, but protected from, C. sapidus and R. harrisii. Crabs were fed congeneric oysters twice weekly within each aquarium. Compared to controls, shell strength of C. virginica exposed to R. harrisii increased significantly (P < 0.043), as did shell strength of both oyster species exposed to C. sapidus (P < 0.01). Despite the changes in shell strength by both oyster species in the presence of C. sapidus, the shell of C. ariakensis remained 57% weaker than C. virginica. We conclude that, because C. ariakensis exposed to predators continued to have a weaker shell relative to C. virginica, the natural suite of crab and flatworm predators in Chesapeake Bay will likely serve to control the abundance of feral C. ariakensis. We caution that the situation in the natural environment may be sufficiently different in some locations that C. ariakensis may be able to compensate for its greater vulnerability to crab predation and hence become a nuisance species.     

Mitochondrial DNA analysis of native and selectively inbred Chesapeake Bay oysters,Crassostrea virginica

Mitochondrial DNA (mtDNA) genotypes were examined in 1989 in threeCrassostrea virginica (Gmelin) populations native to Chesapeake Bay, USA, and in one population selectively inbred for rapid growth for ten generations. We wished to determine whether this character would be useful as a genetic marker for distinguishing between the inbred line and the native oysters and to determine whether detectable genetic differences exist among present-day native populations ofC. virginica. Thirty mtDNA haplotypes were identified. The average percentage nucleotide difference between native haplotypes was 1.8%. Inbred oysters were characterized by mtDNA haplotypes distinctly different from ancestral native oysters, indicating a high degree of genetic differentiation between the two groups (average percentage mtDNA nucleotide sequence divergence,=21.8%). The common native haplotype was not present in the selectively inbred sample, and six of the seven haplotypes detected in the inbred oysters were not found in the survey of native oysters. Chi-square tests on haplotype frequencies indicated that the native populations were not significantly different from one another. However, the distribution and relatedness of haplotypes suggest that significant change in the oyster gene pool may have occurred over the past few decades.     

Depuration of twelve trace metals in tissues of the oysters Crassostrea gigas and C. virginica

The depuration of 12 trace metals in the mantle, gill, digestive gland, and kidney of Crassostrea gigas and C. virginica was investigated under natural field conditions; oysters from a relatively contaminated environment (Redwood Creek in south San Francisco Bay) were transplanted to a relatively clean environment (Tomales Bay). In the transplanted oysters, the digestive gland and kidney depurated Cd, Cu, Hg, Ag, and Zn more readily than the mantle and gill. Other trace metals As, Fe, Mn, Ni and Se showed varying depuration patterns. The results for Cr and Pb were inconclusive, since initial concentrations were too low to follow any losses. Interspecific differences in trace metal depuration were observed. Biological half-lives for most trace metals were on the order of 23 to 60 d for C. gigas and on the order of 70 to 180 d for C. virginica.     

Metabolism of palmitic,linoleic, and linolenic acids in adult oysters,Crassostrea virginica

This study investigated incorporation and metabolism of saturated [(1-¹⁴C) 16:0] and unsaturated [(1-¹⁴C) 18:26 and (1-¹⁴C) 18:33] fatty acids in adult eastern oysters,Crassostrea virginica Gmelin (spawned from parents obtained in 1986 from Mobjack Bay, Virginia, USA), and the influence of temperature on these processes. InC. virginica, incorporation of injected palmitic (16:0) and linolenic (18:33) acids was increased when oysters which had been grown in warm water (22 to 23°C) were transfered to cold water (5 to 7°C) for 8 to 18 d. Incorporation of linoleic acid (18:26) was unchanged under these conditions. The changes in concentration may have been linked to depression of metabolism in these oysters, in particular that of 16:0, which was reduced by 90%. Oxidation of incorporated fatty acids was much higher in warm than in cold water. Cold-temperature conditioning ofC. virginica altered the distribution of fatty acids among the neutral and polar lipid fractions. Long-term exposure to cold water increased the proportion of fatty acids in the polar fraction, which may be related to maintenance of membrane fluidity. Short-term exposure to cold water had the opposite effect, which may be due to increased energy requirements as the oyster adapts to new conditions. Reutilization of¹⁴C-acyl groups demonstrated de novo synthesis of 16:0 and 18:0 fatty acids. Only limited elongation and no desaturation of the administered fatty acids was observed.     

Levels of intracellular free amino acids used for salinity tolerance by oysters (Crassostrea virginica) are altered by protozoan (Perkinsus marinus) parasitism

Free amino acid (FAA) levels were measured from May through October 1991 in gill tissues of two groups of juvenile oysters (Crassostrea virginica Gmelin), one transferred from a low salinity field site (8) to a field site of high salinity (20) and high Perkinsus marinus (Mackin, Owen, and Collier) prevalence, the other kept at the low salinity field site. Within 24 h, glycine levels in the oysters transferred to high salinity increased 8-fold, taurine concentrations doubled and the total FAA pool rose from 150 mol g^–1 dry wt to 400 mol g^–1 dry wt. Taurine levels reached a plateau within 20 d after transfer to high salinity and remained at that level until P. marinus infections were detected 85 d after transfer. Taurine and glycine levels declined by 40% in the high salinity population as infection intensity increased between 70 and 105 d. Total FAA declined by approximately 33% over this period. The oysters kept at low salinity were not infected and continued to grow while the infected high salinity oysters showed no increase in shell length after Day 85. FAA levels in the low salinity group remained relatively constant throughout the experiment except for an initial rise triggered by an increase in ambient salinity from 8 to 12. The results suggest that salinity tolerance mechanisms in C. virginica may be impaired by P. marinus infection.     

Effects of tidal fluctuations of salinity on pericardial fluid composition of the American oyster Crassostrea virginica

Crassostrea virginica Gmelin were subjected to simulated tidal fluctuations of salinity, and the subsequent effects on osmotic and ionic composition of the pericardial fluid, body water and valve movements were investigated. Ambient salinity fluctuation patterns of 20-10-20, 15-10-15 and 10-5-10 were simulated during 24.8-h periods. An additional 10-5-10 S experiment was performed using a dilution water approximating the ionic composition of Mississippi River water with regard to Mg⁺⁺, Ca⁺⁺ and SO ₄ ⁼ , instead of deionized water. Finally the effects of a 2-week diurnal fluctuation pattern between 20 and 10 S were investigated with respect to pericardial fluid composition. Pericardial fluid osmolality, concentrations of Cl^-, Na⁺, Mg⁺⁺, K⁺, Ca⁺⁺ and ninhydrin-positive substances (NPS) were analyzed periodically throughout all experiments. Pericardial fluid osmolality was slightly hyperosmotic as ambient water salinity decreased during a cycle, and then became slightly hyposmotic as ambient salinity increased. In the 2-week experiment, pericardial fluid osmolality tracked ambient seawater closely through Day 5, but became more intermediate between high and low seawater values as the experiment progressed. Similar patterns during fluctuations of salinity were observed for Na⁺, Cl^-, Mg⁺⁺ and Ca⁺⁺. Pericardial fluid K⁺ levels did not track ambient seawater as closely as did other ions. The ionic composition of dilution water had little effect on the osmotic or ionic response of the oyster's pericardial fluid. Pericardial fluid NPS level varied inversely with salinity during the 20-10-20 cycle. During the longterm fluctuation experiment, NPS values gradually decreased over the 2-week period compared to constant salinity control values. Percent body water also varied inversely with ambient salinity. Solute movement accounted for most of the change in pericardial fluid osmolality during the simulated cycles with water movement responsible for 1 to 11%. Water movement contributed more to the change of pericardial fluid osmolality during the decreasing salinity phase than the increasing phase of a given cycle. During 20-10-20 S cycles, oyster valves remained open 56% of the time (n=23). In contrast, when salinity was abruptly changed from 20 to 10 within 5 min, valve closure occurred in 4.8±0.3 min (n=20). Valves did not reopen for 19.3±1.2 h (n=15).     

Winter quiescence and spring awakening of the Eastern oyster Crassostrea virginica at its northernmost distribution limit

To test the hypothesis that oysters, Crassostrea virginica, from the northernmost part of the species range in the Gulf of St. Lawrence (48°N) open their valves at lower temperatures than those reported for more southern oysters, Hall element sensors were used to monitor their gaping behaviour. These observations were made in a flow-through system and the temperature, salinity and relative fluorescence of unfiltered seawater were monitored. Photoperiod was controlled (15?h dark:9?h light) and light levels were measured but not closely controlled. Gaping behaviour was followed from February to June 2010 (113?days) and from April to May 2011 (34?days) and was classified into three successive phases: quiescent, awakening and active. Although valves were either closed or slightly open during the quiescent phase (maximum gape angle?=?0.49°, SE?=?0.04), they abruptly opened to maximum angles of about 5.88° (SE?=?0.29) during the awakening phase. Moreover, there was noticeable synchrony amongst individuals, since approximately one-half of the monitored population awoke within a 6.6-h period in both study years. Correlative analyses identified temperature as a factor influencing valve movement, and oysters awakened when temperatures were 0.2–4.0?°C (mean?=?2.2, SE?=?0.2). Oysters exerted their maximal gape angle as soon as temperatures reached 2.8–6.6?°C (mean?=?4.8, SE?=?0.2). During the active phase, valves remained open 68.6?% (2010) and 79.7?% (2011) of the time. An unexpected result was the observation of a diurnal rhythm in valve openness whereby the openness was greatest near the end of the afternoon and least in the early morning.     

Crassostrea virginica as an indicator of cadmium pollution

As much as 89, 176 and 292 g Cd g^-1 dry weight were accumulated by adult Crassostrea virginica after treatment for 40 wk with 5, 10 and 15 g Cd kg^-1, respectively, in flowing seawater at ambient salinity and temperature without mortalities. Cadmium accumulation increased with increased concentration of cadmium in seawater; greater amounts were accumulated during the summer months. Uptake patterns measured as cadmium content were similar among the total soft parts, gill, mantle and visceral mass. A continuous increase of cadmium concentration in the visceral mass was observed. This differed from the uptake patterns observed as cadmium concentration in gill, mantle and total soft parts. Although cadmium accumulation in the total soft parts and the tissues was curvilinear over the entire study period, significant linear relations between cadmium concentration and time indicated a general increasing trend. At seawater temperatures below 6°C, when oysters were not actively feeding, cadmium concentrations in the total soft parts varied significantly between treatments, but not within treatments. In the tissues, the rate of uptake expressed as cadmium concentrations was visceral mass>gillmantle. Cadmium concentration in the total soft parts varied inversely with dry weight, whereas cadmium concentration in the total soft parts increased, whereas the content decreased. Cadmium concentration decreased in mantle and gill but increased in the visceral mass during spawning, whereas cadmium content decreased in all tissues. Regression analyses indicated that during spawning dry weight decreased at the same rate in gill and mantle, but they lost less weight and lost it more slowly than visceral mass. Also, during spawning, cadmium content decreased in mantle and gill at the same rate but more slowly than in the visceral mass. In mid-August, Cd concentration decreased despite the continuous addition of cadmium to the seawater; however, Cd content increased, suggesting that organism weight was responsible for fluctuations in cadmium concentrations.     

Crassostrea virginica as an indicator of lead pollution

After treatment with 1.0 and 3.3 g Pb kg^-1 for 20 weeks in flowing seawater at ambient salinity and temperature, Crassostrea virginica accumulated as much as 6.57 and 11.42 g g^-1 dry weight, respectively, and no mortalities were recorded. Lead uptake was curvilinear; however, the general trend was an increase in lead concentration over time. Dry weight of the oyster had no significant relation with tissue lead concentration (g g^-1); however, a significant positive relationship existed between weight and lead content (g). A decrease in lead concentration in the tissues occurred from mid-August to mid-September despite continuous addition of lead to the seawater. Addition of lead to the seawater was terminated after 20 weeks (October), and lead loss was studied for the following 12 weeks. Lead loss was studied well after spawning in an attempt to eliminate any influence this might have on lead concentration in the tissues. After 4 weeks, approximately 54% of the accumulated lead was lost under conditions of a natural temperature decline. The biological half-life of lead in C. virginica tissues was calculated to be 5.5 weeks. In the ensuing 8 weeks, little or no lead loss was observed. Larvae from each treatment developed to the straight-hinged stage within 48 h with no apparent abnormalities. Lead appeared to have no adverse effect on larvae when parents had been treated with 1.0 and 3.3 g kg^-1 seawater for 10 weeks.     

Dietary protein levels and growth of the oyster Crassostrea virginica

The diatom Thalassiosira pseudonana in exponential phase or stationary phase and grown under 3 light regimes was fed to 6 groups of juvenile oysters, Crassostrea virginica Gmelin, for a 10-week period. Oysters fed diets from the stationary phase grew more rapidly and had a higher glycogen content than those fed diets from the exponential phase. The stationary phase, cool white-light diet produced the greatest increase in dry weight, shell height and glycogen content of the 6 diets examined. Oysters grew more rapidly when fed diets richer in carbohydrates than proteins.     

Accumulation and depuration of mercury in the American oyster Crassostrea virginica

To study the kinetics of mercury uptake in oysters, adult Crassostrea virginica (Gmelin) were held in seawater containing 10 g mercury/l (ppb) or 100 g mercury/l (ppb), added in the form of mercuric acetate, for 60 days. Mercury concentration in tissues was determined by analysis of individually homogenized oyster meats, using wet digestion and flameless absorption spectrophotometry. After 45 days, average mercury tissue concentration was 140,000 g mercury/kg tissue (ppb) and 28,000 g mercury/kg tissue (ppb) in the 100 ppb and 10 ppb experimental groups, respectively. After this time, concentrations dropped sharply, probably due to spawning. Clearance of mercury from tissue was studied by exposing treated adults to estuarine water (with no additions) for 30 days (100 ppb group) and 160 days (10 ppb group). Tissue concentrations in the 100 ppb mercury environment group declined from 115,000 to 65,000 ppb, and those of the 10 ppb group declined from 18,000 to 15,000 ppb, in 18 days; there-after, no further decline occurred in either group. Oysters accumulated mercury 1,400 times and 2,800 times above the environmental concentrations of 100 and 10 ppb mercury, respectively. Total self-purification was not achieved over a 6 month cleansing period.     

Selective particle ingestion by oyster larvae (Crassostrea virginica) feeding on natural seston and cultured algae

I investigated selective particle ingestion by oyster larvae (Crassostrea virginica) feeding on natural seston from Chesapeake Bay and laboratory-cultured algae of different sizes or chemical content. In 15 of 16 experiments with complex natural suspensions as food, small(<150 m) and large (>150 m) larvae selected most strongly for small (2 to 4 m) food particles, but in the presence of a large (>10 m)-cell dinoflagellate bloom, large larvae strongly selected much larger (22 to 30 m) food material (presumably dinoflagellates). When fed simplified mixtures of four cultured algal species (Synechococcus bacillaris, Isochrysis sp., Dunaliella tertiolecta, and Prorocentrum minimum) ranging in size from 1 to 11 m, small larvae preferred 1 m algae while large larvae preferred 11 m algae. In experiments with algal mixtures, and with suspensions of natural particles and added algae, large larvae preferred algal species harvested from exponential-phase cultures over other species from stationary-phase cultures. Larval ingestion rates of the cultured alga Thalassiosira pseudonana were about three times higher for cells with a low carbon:nitrogen ratio (7.2:1) than for high C:N ratio (16.2:1) cells when these cells were offered separately in suspensions of equal concentration. As a result, more algal cells, algal C, and algal N was ingested by larvae fed low C:N cells. However, larvae did not show a significant preference for either type of cell when they were offered in a 1:1 cell mixture. Feeding patterns of C. virginica larvae in natural food suspensions can vary with the composition of these complex suspensions, and ingestion seems dependent not only on the size, but on the growth rate and chemical quality of food particles.     

Setting of the American oyster Crassostrea virginica in the James River,Virginia, USA: temporal and spatial distribution

Setting of larvae of the oyster Crassostrea virginica was monitored in the James River, Virginia, USA from 1963 to 1980. Setting patterns were similar in two ways to those described prior to 1960 (before the onset of the oyster pathogen Haplosporidium nelsoni (MSX) in Chesapeake Bay): (1) setting intensity (average number of spat per shell) was greater at stations in the lower than upper estuary, and (2) on the average, 60 to 80% of the total annual set at each station occurred during a 6-week period from mid-August through September. However, annual setting intensity from 1963–1980 was lower than previously recorded, and annual sets occurred as a series of discrete pulses rather than continuously throughout the season. Pulses were each approximately 1 to 2 weeks in duration and separated by a period of diminished or no setting. Cross-correlation analysis of annual setting patterns among stations revealed three zones in the James River: the upper estuary and entire southwest side, the lower estuary, and a mid-estuary transition zone. Setting pulses tended to be synchronous at stations within each zone, but occurred 1 to 2 weeks later at stations in downriver than in upriver zones. The location of zones is related to known aspects of water circulation in the James River estuary. Moreover, pulse setting itself may be related to the absence of strong vertical salinity gradients accompanying the fortnightly stratification-destratification process.Contribution No. 1213 from the Virginia Institute of Marine Science, School of Marine Science, The College of William and Mary     

Interaction of genotype and salinity in larvae of the oyster Crassostrea virginica

Adult Crassostrea virginica were obtained from 4 populations and spawned in the laboratory. The larvae from the within-population crosses and the hybrid crosses were raised at 4 salinities. There were no significant differences in survival of the larvae between the populations. However, one set of hybrids did show overdominance in survival. There were genetic differences between the populations in growth rate, but the expression of the differences depended upon the salinity, i.e, there was significant genotype-environment interaction. There were expressions of nonadditive genetic effects in the hybrid crosses, but the direction and magnitude was dependent upon the salinity. There was as much difference between populations from the same estuary as there was between populations from geographically isolated populations.     

Genetics of larvae and spat growth rate in the oyster Crassostrea virginica

The heritability of oyster (Crassostrea virginica) larval growth rate was estimated to be in the range of 0.25 to 0.50 and a significant part of this genetic variation is of the additive type. Larval growth rate and spat growth rate were found to be highly correlated. These results suggest that a selection program for faster growing larvae and spat would be successful.     

Effects of the dinoflagellates Karlodinium veneficum and Prorocentrum minimum on early life history stages of the eastern oyster (Crassostrea virginica)

The bloom-forming dinoflagellates Prorocentrum minimum and Karlodinium veneficum can have detrimental effects on some marine life, including shellfish, but little is known about their effects on early life history stages of bivalves. In the Chesapeake Bay region, blooms of these dinoflagellates overlap with the spawning season of the eastern oyster, Crassostrea virginica. In laboratory experiments, we compared the effects of P. minimum and K. veneficum on the survival and development of embryos and larvae of the eastern oyster. At 10⁴ cells ml⁻¹, P. minimum did not have a negative effect on embryos and larvae in 2-day exposures. The yield of D-hinge larvae was equal to or greater than in control treatments. At 2 × 10⁴ cells ml⁻¹ (approximately equal biomass to the P. minimum treatment) K. veneficum caused significant mortality to oyster embryos within 1 day and almost no embryos developed into D-hinge larvae. This effect was not alleviated by the provision of an alternate food source (Isochrysis sp.). Significant mortality was observed when larvae were exposed to K. veneficum at concentrations of 10⁴ cells ml⁻¹ (approximately 5 ng ml⁻¹ of karlotoxin). The K. veneficum cultures used in these experiments were relatively low in toxin content, more toxic strains could be expected to cause mortality at lower cell concentrations. Survival and maturation of embryos and larvae may be reduced when spawns of the eastern oyster coincide with high bloom densities of K. veneficum.     

The toxicity of heavy metals to embryos of the American oyster Crassostrea virginica

The acute toxicity of 11 heavy metals to embryos of the American oyster Crassostrea virginica was studied and the concentrations at which 50% of the embryos did not develop were determined. The most toxic metals and their LC₅₀ values were mercury (0.0056 ppm), silver (0.0058 ppm), copper (0.103 ppm) and zinc (0.31 ppm). Those metals that were not as toxic and their LC₅₀ values were nickel (1.18 ppm), lead (2.45 ppm) and cadmium (3.80 ppm). Those metals that were relatively non-toxic and their LC₅₀ values were arsenic (7.5 ppm), chromium (10.3 ppm) and manganese (16.0 ppm). Aluminum was non-toxic at 7.5 ppm, the highest concentration tested.