Showing papers on "Oyster published in 2004"

Habitat complexity disrupts predator–prey interactions but not the trophic cascade on oyster reefs

Abstract: Despite recognition of the significance of both food web interactions and habitat complexity in community dynamics, current ecological theory rarely couples these two processes Experimental manipulations of the abundance of the two predators in an oyster-reef trophic cascade, and the structural complexity provided by reefs of living oysters, demonstrated that enhanced habitat complexity weakened the strengths of trophic interactions The system of tri-trophic interactions included oyster toadfish (Opsanus tau) as the top predator that consumed the mud crab (Panopeus herbstii), which preys upon juvenile oysters (Crassostrea virginica) On reefs of low complexity, toadfish controlled mud crab abundances and indirectly determined the level of mortality of juvenile oysters The indirect effects of toadfish on oysters emerged through their influence on how intensely mud crabs preyed on oysters Augmentation of habitat complexity by substituting vertically oriented, living oysters for the flat shells of dead o

Fishing down the coast: historical expansion and collapse of oyster fisheries along continental margins.

Abstract: Estuarine ecosystems have changed dramatically from centuries of fishing, habitat disturbance, sedimentation, and nutrient loading. Degradation of oyster reefs by destructive fishing practices in particular has had a profound effect on estuarine ecology, yet the timing and magnitude of oyster-reef degradation in estuaries is poorly quantified. Here, I evaluate the expansion and collapse of oyster fisheries in 28 estuaries along three continental margins through the analysis of historical proxies derived from fishery records to infer when oyster reefs were degraded. Exploitation for oysters did not occur randomly along continental margins but followed a predictable pattern. Oyster fisheries expanded and collapsed in a linear sequence along eastern North America (Crassostrea virginica), western North America (Ostreola conchaphila), and eastern Australia (Saccostrea glomerata). Fishery collapse began in the estuaries that were nearest to a developing urban center before exploitation began to spread down the coast. As each successive fishery collapsed, oysters from more distant estuaries were fished and transported to restock exploited estuaries near the original urban center. This moving wave of exploitation traveled along each coastline until the most distant estuary had been reached and overfished.

Comparative Study on Cultivation and Yield Performance of Oyster Mushroom (Pleurotus ostreatus) on Different Substrates (Wheat Straw, Leaves, Saw Dust)

Abstract: The research experiment was carried out to investigate the cultivation of Oyster mushroom on different substrates. Mushroom cultivation is a profitable agribusiness. Incorporation of non conventional crops in existing agricultural system can improve the economic status of the farmer. Mushrooms are the source of protein, vitamins and minerals and are anticancerous, anticholesteral, and antitumorous. Sawdust produced highest yield, biological efficiency and number of fruiting bodies, recommended as a best substrate for Oyster mushroom cultivation.

Cadmium effects on mitochondrial function are enhanced by elevated temperatures in a marine poikilotherm, Crassostrea virginica Gmelin (Bivalvia: Ostreidae).

Abstract: SUMMARY Marine intertidal mollusks, such as oysters, are exposed to multiple stressors in estuaries, including varying environmental temperature and levels of trace metals, which may interactively affect their physiology. In order to understand the combined effects of cadmium and elevated temperature on mitochondrial bioenergetics of marine mollusks, respiration rates and mitochondrial volume changes were studied in response to different cadmium levels (0–1000 μmol l –1 ) and temperatures (15, 25 and 35°C) in isolated mitochondria from the eastern oyster Crassostrea virginica acclimated at 15°C. It was found that both cadmium and temperature significantly affect mitochondrial function in oysters. Elevated temperature had a rate-enhancing effect on state 3 (ADP-stimulated) and states 4 and 4+ (representative of proton leak) respiration, and the rate of temperature-dependent increase was higher for states 4 and 4+ than for state 3 respiration. Exposure of oyster mitochondria to 35°C resulted in a decreased respiratory control and phosphorylation efficiency (P/O ratio) compared to that of the acclimation temperature (15°C), while an intermediate temperature (25°C) had no effect. Cadmium exposure did not lead to a significant volume change in oyster mitochondria in vitro . Low levels of cadmium (1–5 μmol l –1 ) stimulated the rate of proton leak in oyster mitochondria, while not affecting ADP-stimulated state 3 respiration. In contrast, higher cadmium levels (10–50 μmol l –1 ) had little or no effect on proton leak, but significantly inhibited state 3 respiration by 40–80% of the control rates. Elevated temperature increased sensitivity of oyster mitochondria to cadmium leading to an early inhibition of ADP-stimulated respiration and an onset of complete mitochondrial uncoupling at progressively lower cadmium concentrations with increasing temperature. Enhancement of cadmium effects by elevated temperatures suggests that oyster populations subjected to elevated temperatures due to seasonal warming or global climate change may become more susceptible to trace metal pollution, and vice versa .

AFLP-Based Genetic Linkage Maps of the Pacific Oyster Crassostrea gigas Thunberg

Abstract: Amplified fragment length polymorphisms (AFLPs) were used for genome mapping in the Pacific oyster Crassostrea gigas Thunberg. Seventeen selected primer combinations produced 1106 peaks, of which 384 (34.7%) were polymorphic in a backcross family. Among the polymorphic markers, 349 were segregating through either the female or the male parent. Chi-square analysis indicated that 255 (73.1%) of the markers segregated in a Mendelian ratio, and 94 (26.9%) showed significant (P < 0.05) segregation distortion. Separate genetic linkage maps were constructed for the female and male parents. The female framework map consisted of 119 markers in 11 linkage groups, spanning 1030.7 cM, with an average interval of 9.5 cM per marker. The male map contained 96 markers in 10 linkage groups, covering 758.4 cM, with 8.8 cM per marker. The estimated genome length of the Pacific oyster was 1258 cM for the female and 933 cM for the male, and the observed coverage was 82.0% for the female map and 81.3% for the male map. Most distorted markers were deficient for homozygotes and closely linked to each other on the genetic map, suggesting the presence of major recessive deleterious genes in the Pacific oyster.

Recycling waste oyster shells for eutrophication control

Abstract: Oyster shells are a waste product from mariculture that presents a major disposal problem in coastal regions such as southeast Korea. It was found in the present study that pyrolysis of waste oyster shells under defined conditions (750 °C for 1 h under a nitrogen atmosphere) transforms this material into a sustainable reagent for efficient (up to 98%) removal of phosphates from wastewater. In comparison, raw oyster shells removed almost no phosphate from water, whereas oyster shells heated to 750 °C under an air atmosphere removed a moderate proportion (up to 68%) of phosphates from water. X-ray diffraction (XRD) analysis of pyrolyzed oyster shells showed peaks that were characteristic of calcium oxide, whereas analysis of raw oyster shells showed peaks that were characteristic of calcium carbonate. Surface morphology of pyrolyzed oyster shells also differed from that of raw oyster shells. Preliminary economic feasibility analysis indicates that cost of activated oyster shell is competitive with other wastewater treatment chemicals.

Purification and characterization of lysozyme from plasma of the eastern oyster (Crassostrea virginica).

Abstract: Lysozyme was purified from the plasma of eastern oysters (Crassostrea virginica) using a combination of ion exchange and gel filtration chromatographies. The molecular mass of purified lysozyme was estimated at 18.4 kDa by SDS-PAGE, and its isoelectric point was greater than 10. Mass spectrometric analysis of the purified enzyme revealed a high-sequence homology with i-type lysozymes. No similarity was found however between the N-terminal sequence of oyster plasma lysozyme and N-terminal sequences of other i-type lysozymes, suggesting that the N-terminal sequences of the i-type lysozymes may vary to a greater extent between species than reported in earlier studies. The optimal ionic strength, pH, cation concentrations, sea salt concentrations, and temperature for activity of the purified lysozyme were determined, as well as its temperature and pH stability. Purified oyster plasma lysozyme inhibited the growth of Gram-positive bacteria (e.g., Lactococcus garvieae, Enterococcus sp.) and Gram-negative bacteria (e.g., Escherichia coli, Vibrio vulnificus). This is a first report of a lysozyme purified from an oyster species and from the plasma of a bivalve mollusc.

Effects of high pressure treatment on physicochemical characteristics of fresh oysters (Crassostrea gigas)

Abstract: The effects of high pressure (HP) treatment (at 100–800 MPa for 10 min at 20 °C) on physicochemical characteristics of depurated oysters were investigated. HP-treated oysters had higher pH and lightness (Hunter L) values than untreated oysters; the magnitude of changes increased with treatment pressure. HP-induced changes in colour generally imparted a cooked, more voluminous and juicy appearance to the raw oyster tissue. After treatment, oyster muscles became detached from their shells, essentially resulting in shucking. As assessed by sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE), denaturation of oyster adductor muscle proteins occurred as a consequence of HP-treatment. The moisture content of oysters increased while ash and protein contents decreased, relative to untreated oysters, with increasing treatment pressure up to 800 MPa.

Survival of toxoplasma gondii oocysts in eastern oysters (crassostrea virginica)

Abstract: Toxoplasma gondiihas recently been recognized to be widely prevalent in the marine environment. It has previously been determined that Eastern oysters (Crassostrea virginica) can remove sporulated T. gondii oocysts from seawater and that oocysts retain their infectivity for mice. This study examined the long-term survival of T. gondii oocysts in oysters and examined how efficient oysters were at removing oocysts from seawater. Oysters in 76-L aquaria (15 oysters per aquarium) were exposed to 1 3 10 6 oocysts for 24 hr and examined at intervals up to 85 days postexposure (PE). Ninety percent (9 of 10) of these oysters were positive on day 1 PE using mouse bioassay. Tissue cysts were observed in 1 of 2 mice fed tissue from oysters exposed 21 days previously. Toxoplasma gondii antibodies were found in 2 of 3 mice fed oysters that had been exposed 85 days previously. In another study, groups of 10 oysters in 76-L aquaria were exposed to 1 3 10 5 ,5 3 104 ,o r 13 104 sporulated T. gondii oocysts for 24 hr and then processed for bioassay in mice. All oysters exposed to 1 3 10 5 oocysts were infected, and 60% of oysters exposed to 5 3 10 4 oocysts were positive when fed to mice. The studies with exposure to 1 3 104 oocysts were repeated twice, and 10 and 25% of oysters were positive when fed to mice. These studies indicate that T. gondii can survive for several months in oysters and that oysters can readily remove T. gondii oocysts from seawater. Infected filter feeders may serve as a source of T. gondii for marine mammals and possibly humans.

The identification of genes from the oyster Crassostrea gigas that are differentially expressed in progeny exhibiting opposed susceptibility to summer mortality

Abstract: Summer mortality associated with juveniles of the oyster Crassostrea gigas is probably the result of a complex interaction between the host, pathogens and environmental factors. Genetic variability in the host appears to be a major determinant in its sensitivity to summer mortality. Previously, divergent selection criteria based on summer survival have been applied to produce oyster families with resistant and susceptible progeny. In this paper, we describe the use of suppression subtractive hybridization to generate 150 C. gigas clones that were differentially regulated between resistant and susceptible F2 progeny. The nucleotide sequence of these clones was determined. In 28%, the inferred amino sequence was found to match the products of known genes, 14% matched hypothetical proteins and a further 14% appeared to contain open reading frames (ORFs) whose product had no obvious homologue in the nucleotide databases. It has been hypothesized that differences exist in the level of energy generation and immune function between resistant and susceptible progeny. In light of this, clones encoding homologues of cavortin, cyclophilin, isocitrate dehydrogenase, sodium glucose cotransporter, fatty acid binding protein, ATPase H+ transporting lysosomal protein, precerebellin, and scavenger receptor were analyzed by real-time PCR. These transcripts were induced in resistant progeny when compared to their susceptible counterparts. A bacterial challenge of oysters resulted in the suppression of six of these transcripts in only those that were resistant to summer mortality. This study has identified potential candidates for further investigation into the functional basis of resistance and susceptibility to summer mortality.

Pathogenicity testing of shellfish hatchery bacterial isolates on Pacific oyster Crassostrea gigas larvae.

Abstract: Bacterial diseases are a major cause of larval mortality in shellfish hatcheries. Even with proper sanitation measures, bacterial pathogens cannot be eliminated in all cases. The pathogenicity of bacteria isolated from Pacific Northwest shellfish hatcheries to Pacific oyster Crassostrea gigas larvae was investigated. We found 3 highly pathogenic strains and 1 mildly pathogenic strain among 33 isolates tested. These strains appear to be members of the genus Vibrio. Although there have been many studies of bivalve bacterial pathogens, a standard method to assess bacterial pathogenicity in bivalve larvae is needed. Thus, we developed 2 methods using either 15 ml conical tubes or tissue culture plates that were employed for rapidly screening bacterial strains for pathogenicity to Pacific oyster larvae. The tissue culture plates worked well for screening both mildly pathogenic strains and LD50 (lethal dose) assays. This method allowed for non-intrusive and non-destructive observation of the oyster larvae with a dissecting microscope. The LD50 for the 3 highly pathogenic strains ranged between 1.6 and 3.6 x 10(4) colony forming units (CFU) ml(-1) after 24 h and between 3.2 x 102 and 1.9 x 10(3) CFU ml(-1) after 48 h.

Cloning and expression of a pivotal calcium metabolism regulator: calmodulin involved in shell formation from pearl oyster (Pinctada fucata).

Abstract: The shells of bivalves are mainly composed of calcium carbonate, a product of calcium metabolism. In the process of shell formation, the uptake, transport and recruitment of calcium ion are highly regulated and involved in many factors. Among these regulatory factors, calmodulin (CaM), a pivotal multifunction regulator of calcium metabolism in nearly all organisms, is thought to play an important role in the calcium metabolism involved in shell formation. In this study, a full-length CaM cDNA was isolated from the pearl oyster (Pinctada fucata). The oyster calmodulin encodes a 16.8 kDa protein which shares high similarity with vertebrate calmodulin. The oyster CaM mRNA shows the highest level of expression in the gill, a key organ involved in calcium uptake in oyster calcium metabolism. In situ hybridization results revealed that oyster CaM mRNA is expressed at the folds and the outer epithelial cells of the dorsal region of the mantle, suggesting that CaM is involved in regulation of calcium transport and secretion. Oyster CaM also showed a typical Ca2+ dependent electrophoretic shift characterization and calcium binding activity. Taken together, we have identified and characterized a pivotal calcium metabolism regulator of the oyster that may play an important role in regulation of calcium uptake, transport and secretion in the process of shell formation.

Phenoloxidase and QX disease resistance in Sydney rock oysters (Saccostrea glomerata)

Abstract: QX is a fatal disease in Sydney rock oysters (Saccostrea glomerata) that results from infection by the protistan parasite, Marteilia sydneyi. Since 1997, the New South Wales Fisheries Service has bred S. glomerata for resistance to QX disease. The current study shows that the QX resistance breeding program has selected oysters with enhanced phenoloxidase (PO) activities. The third generation of QX-selected oysters was compared to S. glomerata that had never been selected for disease resistance. PO enzyme assays showed that oysters bred for resistance had significantly higher PO activities than the non-selected population. There was no difference between populations in the activities of a variety of other enzymes. Native polyacrylamide gel electrophoresis identified a novel form of PO in QX-selected oysters that contributes to their enhanced PO activities. This novel form of PO may represent a specific QX disease resistance factor.

Modeling the impact of oyster culture on a mudflat food web in Marennes-Oléron Bay (France)

Abstract: We used a carbon-based food web model to investigate the effects of oyster cultivation on the ecosystem of an intertidal mudflat. A previously published food web model of a mudflat in Marennes-Oleron Bay, France, was updated with revised parameters, and a realistic surface area and density of existing oyster cultures on the mudflat. We developed 2 hypothetical scenarios to estimate the impact of oyster cultivation on the food web structure of the ecosystem: one with no oysters, the other with a doubled area devoted to cultivated oysters in the bay. Oysters are direct trophic competitors of other filter feeders, and their presence modifies benthic-pelagic coupling by forcing a shift from pelagic consumers to benthic consumers. Increasing the surface area of cultivated oysters caused secondary production to increase, providing food for top predators (in particular juvenile nekton), reinforcing the nursery role of the mudflat in the ecosystem, and altering the species composition available to the top predators.

Bonamia sp. (Haplosporidia) Found in Nonnative Oysters Crassostrea ariakensis in Bogue Sound, North Carolina

Abstract: The Suminoe oyster Crassostrea ariakensis is being considered for introduction into the middle Atlantic coast region of the United States, where diseases have decimated native stocks of the eastern oyster C. virginica. Triploid C. ariakensis produced at the Virginia Institute of Marine Science (VIMS) and transferred to Bogue Sound, North Carolina, experienced high mortality in the summer of 2003. Histopathological examination of oysters collected 9 d after peak mortality in August revealed the presence of intrahemocytic inclusions, suggesting a Bonamia-like parasite infecting hemocytes in 9.1% (2/22) of the oysters. November sampling of a subsequent October 2003 deployment to Bogue Sound revealed that 47% were infected by Bonamia-like microcells. Diagnosis of a second sample from this group by Bonamia-specific polymerase chain reaction primers revealed 60% prevalence, and subsequent DNA sequence data confirmed that the parasite was a Bonamia. Two samples collected during the peak mortality and ar...