This dissertation investigated ingress of postlarval blue crabs Callinectes sapidus to the Newport River estuary, North Carolina, USA. Data from C. similis, Menippe mercenaria, Pachygrapsus transversus, and Arenaeus cribrarius are included in some chapters for comparison. Changes in tolerance to low salinity were examined by: 1) exposing postlarvae (megalopae) collected in coastal and estuarine areas to a range of salinities and 2) determining the cue that stimulates acclimation of coastal megalopae to low salinities, the time to acclimation, and the decrease in salinity necessary for acclimation. Coastal megalopae were less tolerant to salinities of 5 and 10 than megalopae from the estuary. Coastal megalopae became acclimated to low salinities within 12 h when salinity was reduced from 35 to 31. Spatial patterns in abundance during ingress were investigated simultaneously in coastal and estuarine areas. Coastal distributions were determined using nighttime surface plankton tows at slack water after ebb tide and slack water after flood tide on four nights; two each during spring and neap tides. Estuarine distributions were determined using nightly settlement on 'hog's hair' collectors. C. sapidus megalopae were most abundant at the coast east of Beaufort Inlet, but settlement was restricted to western channels of the estuary. Species-specific patterns in abundance were maintained during two spring/neap cycles, possibly due to interactions between larval behavior and physical forcing. Biophysical mechanisms of estuarine ingress were investigated by comparing nightly abundance in coastal and estuarine areas with environmental variables. Comparisons were made using cross-correlation and cross-fourier analyses. High estuarine abundances were associated with wind-driven estuarine inflow and nighttime flood tides. The seasonal pattern of estuarine ingress was strongly associated with the seasonal pattern of alongshore wind stress, suggesting that inter-annual variations in atmospheric forcing may determine the yearly abundance of megalopae arriving in estuarine nursery habitats. The effect of sampling interval on annual megalopal abundance estimates was determined using an 11-year dataset of nightly settlement. Variability in abundance estimates increased with increasing sampling interval. Switching from a one day to two day sampling interval resulted in a 20 % decrease in the likelihood of detecting a significant correlation between annual abundance and CPUE in the North Carolina blue crab pot fishery. / Dissertation

<p>This dissertation investigated spawning biology of female blue crabs, <italic>Callinectes sapidus</italic>. Females mate following the terminal molt and undertake a spawning migration seaward, producing multiple clutches of larvae. To examine lifetime reproductive potential of female crabs, individual crabs were confined in the field from terminal molt to death. Crabs produced up to 7 clutches over 1-2 spawning seasons and survived up to 394 d after the terminal molt. Time to first clutch and time between clutches were positively correlated with carapace width and best described by degree-days. Size at maturity was negatively correlated with water temperature on the day of the terminal molt. Most measurements of clutch quality and larval fitness were similar for all clutches. The percentage of embryos developing normally decreased 40% from clutch 1 to clutch 4 and clutch volume decreased 50% from clutch 1 to clutch 5. Thus, most of a crab's reproductive output is from the first few clutches. </p><p>Using swimming and abdominal pumping assays, the roles of pheromones in larval release and migratory behavior were investigated. Following delivery of egg extract, bradykinin (a pheromone mimic), and trypsin (an enzyme that generates peptide pheromones), ovigerous crabs responded with increased abdominal pumping, indicating that peptide pheromones stimulate larval release in blue crabs. Ovigerous crabs responded with increased swimming following delivery of egg extract, but not following delivery of a peptide pheromone mimic or an enzyme that produces peptide pheromones. These results suggest that some substance generated from the egg mass stimulates vertical swimming, but that peptides alone do not stimulate swimming. A blend of molecules, possibly including sugars, may be the cue that stimulates swimming behavior. </p><p>Endogenous rhythms in vertical swimming, a mechanism underlying migration in tidal estuaries, were examined in the laboratory under constant conditions in juvenile females, recently-molted females, and females with mature ovaries from Beaufort, NC. Rhythms were variable in each stage, though circatidal rhythms consistent with ebb tide transport were observed in juvenile females and recently-molted females. Crabs with mature ovaries typically swam around the time of high tide. Rhythms were also examined for ovigerous females collected from estuaries with three different tidal regimes: semi-diurnal, diurnal, and non-tidal. Crabs from the tidal estuaries had circatidal or circalunidian swimming rhythms with period lengths corresponding to the tidal period of their home estuary. Swimming occurred primarily on ebb tide. Crabs from the non-tidal estuary had a circadian rhythm of vertical swimming around the time of sunset. Such a rhythm has no obvious migratory significance and migration likely takes place though another mechanism.</p><p>Swimming behavior was also examined in the field in one non-tidal site and three tidal sites. Crabs were tethered in the field and swimming was monitored using archival pressure tags. Crabs tethered in the non-tidal site did not swim, possibly due to the lack of necessary environmental cues. Crabs at the tidal sites swam primarily on ebb tides. Swimming was greatest at the deepest site, which also had the strongest currents. This site is known to be a migratory area for spawning blue crabs. Decreased swimming behavior was observed at the two shallower sites, including one site that is known to be habitat for all stages of blue crabs. These results indicate that swimming behavior is variable among different areas in a single estuary. In areas where swimming is reduced, crabs may continue migrating seaward by walking or may spend additional time in that area to forage. Within each site, peak swimming generally occurred during the time of the most rapid decrease in water level, suggesting that hydrostatic pressure may serve as a cue for swimming. </p><p>Mark-recapture studies were conducted in three rivers (North River, South River, Adams Creek) in eastern North Carolina, and recently-molted female crabs were tagged to ensure a relatively constant time since molting. Most crabs traveled relatively short distances and were recaptured before producing a clutch of eggs. Individuals that moved substantial distances typically moved down-estuary. The Adams Creek canal, connecting Adams Creek with the Newport River estuary, functioned as a migratory corridor, as crabs from both Adams Creek and South River migrated down the canal, presumably using ebb tide transport. Many of the crabs that migrated down the canal into the Newport River were recaptured while ovigerous. Results of this study support the hypothesis that rapid long-distance migratory movements do not begin until production of the first clutch of eggs, though some down-estuary movement takes place by prior to production of the first clutch of eggs.</p><p>Female blue crabs mate following the terminal molt and begin moving seaward soon thereafter by walking and swimming. Once the appropriate salinity (> 22 ppt) is reached, the first clutch of eggs is produced and migration rate rapidly increases. Blue crab spawning biology should be similar throughout the range of the species. After taking latitudinal temperature variation and other local variables into account, results presented here should be applicable not only to blue crabs in North Carolina, but in other areas as well.</p> / Dissertation

Hypoxia or dissolved oxygen concentrations < 2 mg/L is a problem in estuaries worldwide. In Lake Pontchartrain, a 250 km2 de-faunated zone exists as a result of salinity stratification and episodic hypoxia. Mature common rangia clams (Rangia cuneata) are not found within this zone. Blue crabs (Callinectes sapidus) are important estuarine predators and may move in and out of the hypoxic zone to feed on hypoxia-stressed rangia clams. To test the effects of hypoxia on predation, rangia clams were exposed experimentally to severe hypoxic conditions (< 0.75 mg/l) for 72-hours and then presented to blue crabs. One hypoxic and one normoxic clam were added to each aquarium containing a blue crab for each trial, and crab feeding choices were observed and recorded. I found prey choice varied among crabs, but in general, the experimental data demonstrates that crabs chose to feed on hypoxia-stressed clams over clams kept under normoxic conditions.

Many species use color during courtship displays, with the more colorful individuals often selected as potential mates. Female blue crabs, Callinectes sapidus, display prominent red markings on their chelipeds, which is absent in males. I tested the hypothesis that females use this sexual dimorphism as an effective signal to potential mates. Body size was positively correlated with size of the colorful pattern on the crusher dactyl. Digital imaging techniques were used to examine and quantify a pattern of coloration in the female blue crab. Morphometric measurements were made using digital images of the carapace and chelae of crabs collected along the Gulf of Mexico coast in Galveston, Texas. Color complexity was examined on digital images of the chelae using Adobe? Photoshop? and Image J. Specific wavelengths were selected and their presence within the attribute quantified and evaluated. To determine whether male blue crabs prefer more colorful females, males were given a choice between females of different female coloration. Males displayed more often and directed more courtship displays towards the more colorful females. I hypothesize that male blue crabs use cheliped coloration as a visual cue for mate selection.

Uma das marcantes características morfológicas e funcionais dos crustáceos e de outros artrópodes é a presença de um exoesqueleto que cria uma barreira física para o crescimento desses animais. Nos crustáceos, a muda é um evento cíclico, dividido em 5 estágios, e um deles compreende a troca desse exoesqueleto, permitindo o aumento de tamanho. O início, período e a frequência do ciclo de muda dependem da idade e do sexo do animal e de fatores ambientais e fisiológicos. Hormônios como os ecdiesteróides e o hormônio inibidor da muda produzidos e secretados pelos órgãos Y e X, respectivamente, atuam diretamente no ciclo de muda, porém outros hormônios podem regular, de forma positiva ou negativa, este processo. A melatonina é um hormônio encontrado amplamente no reino animal, porém em crustáceos, diferentemente do que ocorre nos vertebrados, a sua síntese e secreção não estão relacionadas com a presença ou ausência de luz, e seu papel na muda tem sido pouco investigado. Os animais foram aclimatados no laboratório à temperatura 22±2 °C e ciclo claro-escuro 12h:12h LD, sendo os experimentos realizados nesta mesma condição. Considerando o acima exposto, os objetivos do presente trabalho foram (1) verificar a produção de melatonina no siri azul Callinectes sapidus, através da investigação da expressão das enzimas AANAT e ASMT no pedúnculo óptico e hepatopâncreas, bem como os níveis hemolinfáticos da indolamina; (2) avaliar se existe um perfil oscilatório diário na expressão gênica dos fatores relacionados com a muda, CasMIH e CasEcR1; (3) verificar se a manipulação com melatonina exógena influencia essa expressão. Para isso, técnicas de imunohistoquímica, citometria de fluxo, ensaio imunoenzimático e PCR quantitativo foram empregadas. Nossos resultados demonstraram uma oscilação dos níveis hemolinfáticos de melatonina em siris em pré-muda, com pico às 8 horas; entretanto, no estágio de intermuda os níveis deste hormônio foram menores e constantes ao longo de 24 horas. Não pudemos comprovar a presença das enzimas da via de síntese da melatonina, uma vez que os anticorpos utilizados não apresentaram homologia às proteínas de C. sapidus. Quanto à expressão gênica, uma oscilação diária semelhante nos transcritos dos genes CasMIH e CasEcR1 ocorreu no hepatopâncreas, independente do estágio de muda. No pedúnculo óptico a oscilação dos genes em questão também foi semelhante, mas apenas na pré-muda; na intermuda houve entre eles uma relação de anti-fase. A administração de melatonina exógena (10-7 mol/siri) levou à inibição da expressão dos genes em relação ao controle: no caso de CasMIH foi de 99,7% no pedúnculo óptico e 100% no hepatopâncreas e o CasEcR1 sofreu inibição de 77% no pedúnculo óptico e 99% no hepatopâncreas. A presença de melatonina na hemolinfa é um forte indício de que o animal a sintetiza e pode estar atuando no ciclo de muda, uma vez que a administração deste hormônio inibiu a transcrição dos genes relacionados ao processo. Diante disso, fica mais clara a relevância de entender a flutuação de hormônios que não estão classicamente envolvidos no ciclo de muda, essencial para o crescimento dos crustáceos, mas que podem apresentar a função de regular este processo, como a melatonina. Ademais, a melatonina poderá ser uma boa ferramenta a ser utilizada no cultivo do siri-azul, como agente indutor da redução do período de intermuda levando à uma ecdise precoce / One of the remarkable morphological and functional features of crustaceans and other arthropods is the presence of an exoskeleton that creates a physical barrier for the animal growth. In crustaceans, molting is a cyclic event usually divided into five stages, one of them comprising the exoskeleton exchange what thus allows the increase in size. The onset, period, and frequency of the molt cycle depend on the animal age and sex, as well as on environmental and physiological factors. Hormones such as ecdysteroids and the molt-inhibiting hormone produced and secreted by the Y- and X- organ, respectively, exert direct effects on the molt cycle. Nevertheless, other hormones are known to positively or negatively regulate this process, such as melatonin. Melatonin is a hormone widely found in the animal kingdom, but in crustaceans, differently from what happens in vertebrates, its synthesis and secretion are not regulated by the presence or absence of light. In fact, its role in the molting process has been poorly investigated. The animals were acclimated in the laboratory at 22±2 °C and light-dark cycle 12h:12h LD, and the experiments were performed under the same condition. Considering the above, the objectives of this study were to: 1) verify the production of melatonin in the blue crab Callinectes sapidus, through the evaluation of the expression of key enzymes involved in the synthesis of melatonin, AANAT and ASMT, in the eyestalk and hepatopancreas, as well as melatonin levels in the hemolymph; 2) evaluate whether there exists a daily oscillatory profile in gene expression of the related molt factors, CasMIH and CasEcR1; (3) whether the exogenous melatonin influences the expression of the latter genes. To achieve these goals, immunohistochemistry, flow cytometry, immunoenzymatic assay, and quantitative PCR techniques were used. Our results demonstrated an oscillation of the hemolymphatic levels of melatonin in premolt crabs, peaking at 8 AM; however, in the intermolt stage, the levels of this hormone were smaller and constant along 24 hours. We were not able to show the presence of the enzymes involved in melatonin synthesis, since the antibodies used had no homology with C. sapidus proteins. We also demonstrated a daily oscillatory profile of CasMIH and CasEcR1 transcripts in hepatopancreas independently of the molt stage. In the eyestalk the oscillatory profile of both genes was also similar, but only in the premolt stage; in intermolt, an antiphase relationship between both genes was found. The exogenous administration of melatonin (10-7 mol/crab) inhibited the expression of CasMIH by 99.7 and 100% in eyestalk and hepatopancreas, respectively, whereas CasEcR1 was inhibited by 77% and 99%, in the eyestalk and hepatopancreas, respectively, compared to saline-treated animals. The presence of melatonin in the hemolymph is a reliable indicator that the animal synthesizes the hormone, and thus melatonin may influence the molt cycle since it inhibited the expression of molt-related genes. Therefore, the relevance of understanding the oscillation of hormones that are not classically involved in the molt cycle - essential for crustacean growth - but which can regulate the process, becomes evident. From an economic standpoint, melatonin may be a useful tool in culturing blue crab, which ultimately can shorten the intermolt stage period leading to an early ecdysis

Uma das marcantes características morfológicas e funcionais dos crustáceos e de outros artrópodes é a presença de um exoesqueleto que cria uma barreira física para o crescimento desses animais. Nos crustáceos, a muda é um evento cíclico, dividido em 5 estágios, e um deles compreende a troca desse exoesqueleto, permitindo o aumento de tamanho. O início, período e a frequência do ciclo de muda dependem da idade e do sexo do animal e de fatores ambientais e fisiológicos. Hormônios como os ecdiesteróides e o hormônio inibidor da muda produzidos e secretados pelos órgãos Y e X, respectivamente, atuam diretamente no ciclo de muda, porém outros hormônios podem regular, de forma positiva ou negativa, este processo. A melatonina é um hormônio encontrado amplamente no reino animal, porém em crustáceos, diferentemente do que ocorre nos vertebrados, a sua síntese e secreção não estão relacionadas com a presença ou ausência de luz, e seu papel na muda tem sido pouco investigado. Os animais foram aclimatados no laboratório à temperatura 22±2 °C e ciclo claro-escuro 12h:12h LD, sendo os experimentos realizados nesta mesma condição. Considerando o acima exposto, os objetivos do presente trabalho foram (1) verificar a produção de melatonina no siri azul Callinectes sapidus, através da investigação da expressão das enzimas AANAT e ASMT no pedúnculo óptico e hepatopâncreas, bem como os níveis hemolinfáticos da indolamina; (2) avaliar se existe um perfil oscilatório diário na expressão gênica dos fatores relacionados com a muda, CasMIH e CasEcR1; (3) verificar se a manipulação com melatonina exógena influencia essa expressão. Para isso, técnicas de imunohistoquímica, citometria de fluxo, ensaio imunoenzimático e PCR quantitativo foram empregadas. Nossos resultados demonstraram uma oscilação dos níveis hemolinfáticos de melatonina em siris em pré-muda, com pico às 8 horas; entretanto, no estágio de intermuda os níveis deste hormônio foram menores e constantes ao longo de 24 horas. Não pudemos comprovar a presença das enzimas da via de síntese da melatonina, uma vez que os anticorpos utilizados não apresentaram homologia às proteínas de C. sapidus. Quanto à expressão gênica, uma oscilação diária semelhante nos transcritos dos genes CasMIH e CasEcR1 ocorreu no hepatopâncreas, independente do estágio de muda. No pedúnculo óptico a oscilação dos genes em questão também foi semelhante, mas apenas na pré-muda; na intermuda houve entre eles uma relação de anti-fase. A administração de melatonina exógena (10-7 mol/siri) levou à inibição da expressão dos genes em relação ao controle: no caso de CasMIH foi de 99,7% no pedúnculo óptico e 100% no hepatopâncreas e o CasEcR1 sofreu inibição de 77% no pedúnculo óptico e 99% no hepatopâncreas. A presença de melatonina na hemolinfa é um forte indício de que o animal a sintetiza e pode estar atuando no ciclo de muda, uma vez que a administração deste hormônio inibiu a transcrição dos genes relacionados ao processo. Diante disso, fica mais clara a relevância de entender a flutuação de hormônios que não estão classicamente envolvidos no ciclo de muda, essencial para o crescimento dos crustáceos, mas que podem apresentar a função de regular este processo, como a melatonina. Ademais, a melatonina poderá ser uma boa ferramenta a ser utilizada no cultivo do siri-azul, como agente indutor da redução do período de intermuda levando à uma ecdise precoce / One of the remarkable morphological and functional features of crustaceans and other arthropods is the presence of an exoskeleton that creates a physical barrier for the animal growth. In crustaceans, molting is a cyclic event usually divided into five stages, one of them comprising the exoskeleton exchange what thus allows the increase in size. The onset, period, and frequency of the molt cycle depend on the animal age and sex, as well as on environmental and physiological factors. Hormones such as ecdysteroids and the molt-inhibiting hormone produced and secreted by the Y- and X- organ, respectively, exert direct effects on the molt cycle. Nevertheless, other hormones are known to positively or negatively regulate this process, such as melatonin. Melatonin is a hormone widely found in the animal kingdom, but in crustaceans, differently from what happens in vertebrates, its synthesis and secretion are not regulated by the presence or absence of light. In fact, its role in the molting process has been poorly investigated. The animals were acclimated in the laboratory at 22±2 °C and light-dark cycle 12h:12h LD, and the experiments were performed under the same condition. Considering the above, the objectives of this study were to: 1) verify the production of melatonin in the blue crab Callinectes sapidus, through the evaluation of the expression of key enzymes involved in the synthesis of melatonin, AANAT and ASMT, in the eyestalk and hepatopancreas, as well as melatonin levels in the hemolymph; 2) evaluate whether there exists a daily oscillatory profile in gene expression of the related molt factors, CasMIH and CasEcR1; (3) whether the exogenous melatonin influences the expression of the latter genes. To achieve these goals, immunohistochemistry, flow cytometry, immunoenzymatic assay, and quantitative PCR techniques were used. Our results demonstrated an oscillation of the hemolymphatic levels of melatonin in premolt crabs, peaking at 8 AM; however, in the intermolt stage, the levels of this hormone were smaller and constant along 24 hours. We were not able to show the presence of the enzymes involved in melatonin synthesis, since the antibodies used had no homology with C. sapidus proteins. We also demonstrated a daily oscillatory profile of CasMIH and CasEcR1 transcripts in hepatopancreas independently of the molt stage. In the eyestalk the oscillatory profile of both genes was also similar, but only in the premolt stage; in intermolt, an antiphase relationship between both genes was found. The exogenous administration of melatonin (10-7 mol/crab) inhibited the expression of CasMIH by 99.7 and 100% in eyestalk and hepatopancreas, respectively, whereas CasEcR1 was inhibited by 77% and 99%, in the eyestalk and hepatopancreas, respectively, compared to saline-treated animals. The presence of melatonin in the hemolymph is a reliable indicator that the animal synthesizes the hormone, and thus melatonin may influence the molt cycle since it inhibited the expression of molt-related genes. Therefore, the relevance of understanding the oscillation of hormones that are not classically involved in the molt cycle - essential for crustacean growth - but which can regulate the process, becomes evident. From an economic standpoint, melatonin may be a useful tool in culturing blue crab, which ultimately can shorten the intermolt stage period leading to an early ecdysis

<p>Reactive oxygen species (ROS) are produced endogenously in all aerobes and are induced by environmental stressors. ROS oxidize and disable essential cellular components such as DNA, proteins, and lipid membranes. Exposure to metals, polycyclic aromatic hydrocarbons (PAHs), and some pesticides can induce oxidative stress in marine invertebrates. All aerobic organisms have a network of antioxidants and enzymes to quench ROS and prevent oxidative damage. This dissertation examines antioxidant and oxidative stress biomarkers in endemic molluscs and crabs from two natural extreme environments: deep-sea hydrothermal vents in the Lau and North Fiji Basin, and cold seeps in the Gulf of Mexico. In addition, the acute toxicity and sub-lethal effects of four insecticides and an herbicide are examined in the estuarine blue crab, <italics>Callinectes sapidus</italics>. Blue crabs are North Carolina's most important fishery species and are frequently found in agricultural drainage ditches, an example of an anthropogenic extreme environment. </p> <p>Total glutathione, catalase, superoxide dismutase, and lipid peroxidation levels were of the same respective order of magnitude in the two vent gastropods, <italics>Alviniconcha</italics> sp. and <italics>Ifremeria nautilei</italics>, and vent mussel, <italics>Bathymodiolus brevior</italics>. These biomarkers activities were similar to those from previous reports on Mid-Atlantic Ridge mussels, except for ~100-fold higher lipid peroxidation levels among Lau molluscs. Principal component analysis (PCA) of mollusc tissue-specific biomarker levels grouped individuals by species rather than by site. </p> <p>Biomarker levels in the seep mussels <italics>Bathymodiolus childressi, B. brooksi</italics>, and <italics>B. heckerae</italics> were similar across species except for elevated foot and gill cytosolic SOD in mussels from MC-640 compared to those from AC-645. PCA of seep mussel biomarker levels differentiated by species with <italics>B. childressi</italics> isolated from <italics>B. brooksi</italics> and <italics>B. heckerae</italics>. The addition of <italics>B. brevior</italics> biomarker data to the PCA showed them grouping around <italics>B. brooksi</italics> and <italics>B. heckerae</italics>. <italics>Bathymodiolus childressi</italics> is ancestral to the other species and contains only methanotrophic endosymbionts. Whether symbionts play a role in alleviating possible toxic conditions remains unknown.</p> <p>Pesticides were acutely toxic to blue crabs in the order of Lambda-cyhalothrin > imidacloprid &#8776; aldicarb > acephate &#8776; Roundup® (glyphosate). Megalopae were almost always more sensitive to pesticides than early stage juveniles. Commercial formations of pesticides generally showed similar toxicity to active ingredients alone. Exposure to LC₂₀ levels of acephate, aldicarb, imidacloprid and Roundup significantly increased the frequency of juvenile mortality after molting. There was no significant change in total glutathione or lipid peroxidation of exposed megalopae. Lambda-cyhalothrin-, imidacloprid-, and aldicarb-based products have the potential to cause acute toxicity and molting-related mortality in shallow creeks and ditches.</p> / Dissertation

The blue crab, Callinectes sapidus, represents an ecologically and economically important component of marine and estuarine ecosystems. In Florida, blue crab landings accounted for $9.6 million dollars during the 2010 fishing season. Accurate stock assessments for this valuable fishery are essential. Age is a critical biological component of accurate stock assessments; however, blue crabs and other crustaceans are especially difficult to age because of the complex nature of discrete growth. Biochemical extraction of an aging pigment, lipofuscin, was developed using blue crab eyestalks. The current study investigated the effects of freezing preservation on lipofuscin extracts and examined whether the extraction methodology, developed by Chesapeake Bay researchers, was useful for aging Tampa Bay blue crabs populations. Significant differences in lipofuscin index were found between samples frozen (2 weeks at -80°C) prior to analysis and those processed and assayed immediately (p < 0.001). Quarterly assays of the cohort of known-age individuals revealed a negative linear trend (y = -0.12x + 0.49, p < 0.001) in lipofuscin index over a 12-month period. This result suggests that extraction of lipofuscin is not appropriate for age determination of Florida blue crabs. Investigations into possible causes of the negative trend in lipofuscin suggest this method deserves further examination and refinement before it is acceptable as a reliable method for age determination in Florida blue crabs. Growth data of the known-age population collected during this study revealed that blue crabs in Tampa Bay can reach exploitable size in under sixth months and female crabs can reach sexual maturity within seven months of hatching. These growth patterns have the potential to enhance future Florida stock assessments.

No description available.

The Food and Drug Administration has recently expressed concern for the safety of seafood and seafood products. One of the concerns is the presence of Bacillus cereus in fresh blue crab meat. Bacillus cereus is a spore-forming pathogen whose spores survive the customary thermal treatments applied during cooking and pasteurization; therefore it could potentially present a health concern to consumers as the microorganism could increase to pathogenic levels. The objectives of this study were to evaluate the effects of a post-processing method i.e. high hydrostatic pressure treatment on the quality of fresh crab meat and to evaluate the effectiveness of high pressures on the inactivation of B. cereus spores. Fresh blue crab meat was pressurized at 300 and 550 MPa at 25° C for 5 min and stored at 4° C for 31 days to determine the pressurization effects on the microbiological, physical, and sensory quality of the meat. A pressure of 300 MPa caused a 1 log reduction in total aerobic plate count and a 3 day lag period, whereas 550 MPa inactivated 2 logs in total aerobic plate count with no evident lag phase. Physical and sensory qualities of pressurized crab meat were not statistically different from the untreated crab meat (P>0.05). A pressure of 300 MPa extended the shelf-life from 17 to over 24 days with the prevalence of Carnobacterium piscicola at the time of spoilage. Crab meat treated with 550 MPa was not rejected by sensory panels at day 31 and Enterococcus spp. was identified as the predominant microorganism. High hydrostatic pressure (550 MPa at 40° C for 15 min) inactivated less than 1 log (0.66 log) of B. cereus spores inoculated in fresh crab meat. The meat essentially had a protective effect on pressure inactivation of the spores. During storage (31 days), surviving B. cereus was suppressed and outgrown by the other pressure resistant microflora at a storage temperature of 12° C. At 4° C, B. cereus could compete with the other pressure-resistant microflora and was isolated even at the end of the storage period (day 31); however, diarrheal toxin was not detected in any stored samples. / Ph. D.