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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 39 (1992), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: . The capacity of the freshwater cryptomonad Chilomonas paramecium to develop a tolerance for seawater in the growth medium was investigated as part of a research program exploring potential microbial food sources for estuarine bivalve mollusks. By gradually increasing the percentage of estuarine seawater included in a freshwater culture medium over the course of 10 years, strains were obtained that tolerate from 16 to 32% seawater (highest salinity 10.5 ppt), achieving equivalent final densities with similar gross biochemical composition. However, after subculture in seawater-containing media for over 20 years, growth rates in more-saline media remained appreciably slower than in low-salinity media. Reduction of C. paramecium growth rate by seawater was found to be exacerbated in media with an initial pH of 3.5 as compared with pH 4.0–5.0, suggesting either a specific H+ effect upon metabolism of the medium carbon source (lactic acid) or a general cation effect upon nutrient uptake or cell metabolism. By contrast, depression of growth rates at high salinity was ameliorated by eliminating sodium-phosphate enrichments in growth media. This suggests that cations in the phosphate salt were contributing to cation-mediated growth inhibition. Results indicate a potential for C. paramecium, cultured in moderately saline media with no phosphate enrichments, to be used as a carbohydrate supplement for laboratory and hatchery feeding of estuarine bivalve mollusks.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 2024-03-15
    Description: This study assessed the energy budget for juvenile Atlantic Sea Scallop, Placopecten magellanicus, during a natural drop in temperature (15.6°C to 5.8°C) over an 8-week time period during the fall at three different enrichment levels of carbon dioxide (CO2). Every 2 weeks, individuals were sampled for ecophysiological measurements of feeding activity, respiration rate (RR) and excretion rate (ER) to enable the calculation of scope for growth (SFG) and atomic oxygen:nitrogen ratios (O:N). In addition, 36 individuals per treatment were removed for shell height, dry tissue weight (DTW) and dry shell weight (DSW). We found a significant decrease in feeding rates as CO2 increased. Those rates also were significantly affected by temperature, with highest feeding at 9.4°C. No significant CO2 effect was observed for catabolic energy processes (RR and ER); however, these rates did increase significantly with temperature. The O:N ratio was not significantly affected by CO2, but was significantly affected by temperature. There was a significant interaction between CO2 and temperature for ER and the O:N ratio, with low CO2 levels resulting in a U-shaped response that was not sustained as CO2 levels increased. This suggests that the independent effects of CO2 and temperature observed at low levels are different once a CO2 threshold is reached. Additionally, there were significant differences in growth estimators (shell height and DSW), with the best growth occurring at the lowest CO2 level. In contrast to temperature variations that induced a trade-off response in energy acquisition and expenditure, results from this research support the hypothesis that sea scallops have a limited ability to alter physiological processes to compensate for increasing CO2.
    Keywords: Alkalinity, total; Ammonia excretion; Animalia; Aragonite saturation state; Assimilated energy; Assimilation efficiency; Assimilation rate; Behaviour; Benthic animals; Benthos; Bicarbonate ion; Biomass/Abundance/Elemental composition; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Cape_Elizabeth; Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Catabolic energy; Cell density; Clearance rate; Coast and continental shelf; Containers and aquaria (20-1000 L or 〈 1 m**2); Date; Day of experiment; Energy, per food mass; EXP; Experiment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Ingestion rate, organic weight; Inorganic matter, particulate; Laboratory experiment; Mollusca; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Organic matter, particulate; Other metabolic rates; Other studied parameter or process; Oxygen/Nitrogen ratio; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; Placopecten magellanicus; Replicate; Respiration; Respiration rate, oxygen; Salinity; Scope for growth; Shell, dry mass; Shell height; Shell thickness; Shell width; Single species; Species, unique identification; Species, unique identification (Semantic URI); Species, unique identification (URI); Suspended matter, total; Temperate; Temperature; Temperature, water; Tissue, dry mass; Treatment; Type
    Type: Dataset
    Format: text/tab-separated-values, 39247 data points
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  • 3
    Publication Date: 2024-03-15
    Keywords: Alkalinity, total; Alkalinity, total, standard error; Animalia; Aragonite saturation state; Benthic animals; Benthos; Bicarbonate ion; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Containers and aquaria (20-1000 L or 〈 1 m**2); Crassostrea virginica; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Hemocytes; Hemocytes, standard error; Infection intensity; Infection intensity, standard error; Laboratory experiment; Laboratory strains; Mollusca; Not applicable; OA-ICC; Ocean Acidification International Coordination Centre; Other; Other studied parameter or process; Oxygen; Oxygen, dissolved; Oxygen, dissolved, standard error; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Partial pressure of carbon dioxide (water) at sea surface temperature (wet air), standard error; pH; pH, standard error; Prevalence; Prevalence, standard error; Reactive oxygen species production; Reactive oxygen species production, standard error; Salinity; Salinity, standard error; Shell height; Shell height, standard error; Single species; Species, unique identification; Species, unique identification (Semantic URI); Species, unique identification (URI); Temperature, water; Temperature, water, standard error; Time point, descriptive; Treatment; Type
    Type: Dataset
    Format: text/tab-separated-values, 1244 data points
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  • 4
    Publication Date: 2024-03-15
    Description: A dynamic energy budget (DEB) model integrating pCO2 was used to describe ocean acidification (OA) effects on Atlantic surfclam, Spisula solidissima, bioenergetics. Effects of elevated pCO2 on ingestion and somatic maintenance costs were simulated, validated, and adapted in the DEB model based upon growth and biological rates acquired during a 12-week laboratory experiment. Temperature and pCO2 were projected for the next 100 years following the intergovernmental panel on climate change representative concentration pathways scenarios (2.6, 6.0, and 8.5) and used as forcing variables to project surfclam growth and reproduction. End-of-century water warming and acidification conditions resulted in simulated faster growth for young surfclams and more energy allocated to reproduction until the beginning of the 22nd century when a reduction in maximum shell length and energy allocated to reproduction was observed for the RCP 8.5 scenario.
    Keywords: Alkalinity, total; Animalia; Aragonite saturation state; Benthic animals; Benthos; Bicarbonate ion; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Coast and continental shelf; Containers and aquaria (20-1000 L or 〈 1 m**2); Experiment day; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Height; Laboratory experiment; Length; Mollusca; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; Replicate; Salinity; Shell, dry mass; Single species; Species, unique identification; Species, unique identification (Semantic URI); Species, unique identification (URI); Spisula solidissima; Temperate; Temperature, water; Tissue, dry mass; Type; Width
    Type: Dataset
    Format: text/tab-separated-values, 15872 data points
    Location Call Number Limitation Availability
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  • 5
    Publication Date: 2024-03-15
    Description: We used flow cytometry to determine if there would be a difference in hematology, selected immune functions, and hemocyte pH (pHi), under two different, future ocean acidification scenarios (pH = 7.50, 7.80) compared to current conditions (pH = 8.09) for Chionoecetes bairdi, Tanner crab. Hemocytes were analyzed after adult Tanner crabs were held for two years under continuous exposure to acidified ocean water. Total counts of hemocytes did not vary among control and experimental treatments; however, there were significantly greater number of dead, circulating hemocytes in crabs held at the lowest pH treatment. Phagocytosis of fluorescent microbeads by hemocytes was greatest at the lowest pH treatment. These results suggest that hemocytes were dying, likely by apoptosis, at a rate faster than upregulated phagocytosis was able to remove moribund cells from circulation at the lowest pH. Crab hemolymph pH (pHe) averaged 8.09 and did not vary among pH treatments. There was no significant difference in internal pH (pHi) within hyalinocytes among pH treatments and the mean pHi (7.26) was lower than the mean pHe. In contrast, there were significant differences among treatments in pHi of the semi-granular+granular cells. Control crabs had the highest mean semi-granular+granular pHi compared to the lowest pH treatment. As physiological hemocyte functions changed from ambient conditions, interactions with the number of eggs in the second clutch, percentage of viable eggs, and calcium concentration in the adult crab shell was observed. This suggested that the energetic costs of responding to ocean acidification and maintaining defense mechanisms in Tanner crab may divert energy from other physiological processes, such as reproduction.
    Keywords: Acid-base regulation; Alkalinity, total; Animalia; Aragonite saturation state; Arthropoda; Benthic animals; Benthos; Bicarbonate ion; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Chiniak_Bay; Chionoecetes bairdi; Coast and continental shelf; Containers and aquaria (20-1000 L or 〈 1 m**2); EXP; Experiment; Fluorescence; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Haemolymph, pH; Hemocyte count; Hemocytes; Immunology/Self-protection; Laboratory experiment; North Pacific; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, intracellular; Salinity; Single species; Species, unique identification; Species, unique identification (Semantic URI); Species, unique identification (URI); Temperate; Temperature, water; Type
    Type: Dataset
    Format: text/tab-separated-values, 690 data points
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