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  • 2010-2014  (3)
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  • 1
    Publication Date: 2024-03-15
    Description: Ocean acidification (OA) can shift the ecological balance between interacting organisms. In this study, we have used a model-system to illustrate the interaction between a calcifying host-organism, the blue mussel Mytilus edulis, and a common bivalve bacterial-pathogen, Vibrio tubiashii, with organisms being exposed to a level of acidification projected to occur by the end of the 21st century. OA exposures of the mussels were carried out in relative long-term (4 months) and short-term (4 days) experiments. We found no effect of OA on the culturability of V. tubiashii, in broth or in seawater. OA inhibited mussel shell growth and impaired crystalline shell structures but did not appear to affect mussel immune parameters (i.e hemocyte counts and phagocytotic capacity). Despite no evident impact on host immunity or growth and virulence of the pathogen, V. tubiashii was clearly more successful in infecting mussels exposed to long-term OA compared to those maintained under ambient conditions. Moreover, OA exposed V. tubiashii increased their viability when exposed to hemocytes of OA treated mussel. Our findings suggest that even though host-organisms may have the capacity to cope with periods of OA, these conditions may alter the out-come of host-pathogen interactions, favoring the success of the latter.
    Keywords: Acid-base regulation; Alkalinity, total; Alkalinity, total, standard deviation; Animalia; Aragonite saturation state; Aragonite saturation state, standard deviation; Bacteria; Bacteria, abundance in colony forming units; Benthic animals; Benthos; Bicarbonate ion; Calcite saturation state; Calcite saturation state, standard deviation; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Category; Coast and continental shelf; Containers and aquaria (20-1000 L or 〈 1 m**2); Density, optical standard deviation; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth; Growth/Morphology; Growth rate, standard error; Haemolymph, pH; Haemolymph, pH, standard error; Hemocytes; Hemocytes, standard error; Heterotrophic prokaryotes; Hsp70 units per protein; Hsp70 units per protein, standard error; Identification; Laboratory experiment; Mollusca; Month; Mortality/Survival; Mytilus edulis; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Optical density; Optical density, standard error; Other studied parameter or process; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; pH, standard deviation; Phagocytotic units; Phagocytotic units, standard error; Potentiometric; Potentiometric titration; Proteobacteria; Registration number of species; Salinity; Salinity, standard error; Species; Species interaction; Survival; Survival rate, standard deviation; Temperate; Temperature, water; Temperature, water, standard deviation; Time in days; Time in hours; Treatment; Type; Uniform resource locator/link to reference; Vibrio tubiashii
    Type: Dataset
    Format: text/tab-separated-values, 1838 data points
    Location Call Number Limitation Availability
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  • 2
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    PANGAEA
    In:  Supplement to: Hernroth, Bodil; Baden, Susanne; Thorndyke, Mike; Dupont, Sam (2011): Immune suppression of the echinoderm Asterias rubens (L.) following long-term ocean acidification. Aquatic Toxicology, 103(3-4), 222-224, https://doi.org/10.1016/j.aquatox.2011.03.001
    Publication Date: 2024-03-15
    Description: We compared effects of exposure to predicted near-future (2100) ocean acidification (OA; pH 7.7) and normal seawater (Control; pH 8.1) on immune and stress responses in the adult sea star Asterias rubens. Analyses were made after one week and after six months of continuous exposure. Following one week exposure to acidified water, the pH of coelomic fluid was significantly reduced. Levels of the chaperon Hsp70 were elevated while key cellular players in immunity, coelomocytes, were reduced by approximately 50%. Following long-term exposure (six months) levels of Hsp70 returned to control values, whereas immunity was further impaired, evidenced by the reduced phagocytic capacity of coelomocytes and inhibited activation of p38 MAP-kinase. Such impacts of reduced seawater pH may have serious consequences for resistance to pathogens in a future acidified ocean.
    Keywords: Alkalinity, total; Animalia; Aragonite saturation state; Asterias rubens; Asterias rubens, 70 kilodalton heat shock protein per protein mass; Asterias rubens, coelomocyte; Asterias rubens, mitogen activated protein kinase p38 per protein mass; Asterias rubens, pH, coelomic fluid; Asterias rubens, phagocytosis; Benthic animals; Benthos; Bicarbonate ion; Calcite saturation state; Calculated; Calculated using CO2SYS; 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); Echinodermata; EPOCA; EUR-OCEANS; European network of excellence for Ocean Ecosystems Analysis; European Project on Ocean Acidification; Experimental treatment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Identification; Immunology/Self-protection; Laboratory experiment; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH meter (Metrohm electrodes); Salinity; see reference(s); Single species; Temperature, water
    Type: Dataset
    Format: text/tab-separated-values, 551 data points
    Location Call Number Limitation Availability
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  • 3
    Publication Date: 2016-09-06
    Description: This paper focuses on the marine foundation eelgrass species, Zostera marina, along a gradient from the northern Baltic Sea to the north-east Atlantic. This vast region supports a minimum of 1480 km2 eelgrass (maximum 〉2100 km2), which corresponds to more than four times the previously quantified area of eelgrass in Western Europe. Eelgrass meadows in the low salinity Baltic Sea support the highest diversity (4–6 spp.) of angiosperms overall, but eelgrass productivity is low (〈2 g dw m-2 d-1) and meadows are isolated and genetically impoverished. Higher salinity areas support monospecific meadows, with higher productivity (3–10 g dw m-2 d-1) and greater genetic connectivity. The salinity gradient further imposes functional differences in biodiversity and food webs, in particular a decline in number, but increase in biomass of mesograzers in the Baltic. Significant declines in eelgrass depth limits and areal cover are documented, particularly in regions experiencing high human pressure. The failure of eelgrass to re-establish itself in affected areas, despite nutrient reductions and improved water quality, signals complex recovery trajectories and calls for much greater conservation effort to protect existing meadows. The knowledge base for Nordic eelgrass meadows is broad and sufficient to establish monitoring objectives across nine national borders. Nevertheless, ensuring awareness of their vulnerability remains challenging. Given the areal extent of Nordic eelgrass systems and the ecosystem services they provide, it is crucial to further develop incentives for protecting them.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
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