ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Abatus cavernosus; Acid-base regulation; Alkalinity, total; Alkalinity, total, standard deviation; Amphipneustes lorioli; Amphipneustes rostratus; Amphipneustes similis; Animalia; Antarctic; Aporocidaris eltaniana; Aragonite saturation state; Aragonite saturation state, standard deviation; Benthic animals; Benthos; Bicarbonate ion; Bicarbonate ion, standard deviation; Bransfield_Strait; Calcite saturation state; Calcite saturation state, standard deviation; Calculated; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Coast and continental shelf; Coelomic fluid, alkalinity; Coelomic fluid, carbon, inorganic, dissolved; Coelomic fluid, pH; Coulometric titration; Ctenocidaris gigantea; DATE/TIME; Difference; Echinodermata; Event label; EXP; Experiment; Field observation; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); LATITUDE; LONGITUDE; Notocidaris gaussensis; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; Polar; Potentiometric; Potentiometric titration; Salinity; Single species; Size; Species; Station label; Sterechinus antarcticus; Sterechinus neumayeri; Temperature, water; Weddell_Sea_OA; δ13C  (1)
  • Acid-base regulation; Alkalinity, total; Ammonium, excretion; Animalia; Aquarium number; Aragonite saturation state; 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; Coast and continental shelf; Coelomic fluid, alkalinity; Coelomic fluid, carbon, inorganic, dissolved; Coelomic fluid, pH; Containers and aquaria (20-1000 L or 〈 1 m**2); Difference; Duration, number of days; Echinodermata; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Holothuria parva; Holothuria scabra; Indian Ocean; Isotope ratio mass spectrometry; Laboratory experiment; OA-ICC; Ocean Acidification International Coordination Centre; Other metabolic rates; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; Potentiometric; Potentiometric titration; Respiration; Respiration rate, oxygen; Salinity; Single species; Species; Temperature, water; Tropical; δ13C; δ13C, Coelomic fluid  (1)
  • Acid-base regulation; Alkalinity, total; Animalia; Aragonite saturation state; Asterias rubens; Benthic animals; Benthos; Bicarbonate ion; Calcite saturation state; Calculated; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Coast and continental shelf; Coelomic fluid, alkalinity; Coelomic fluid, pH; Containers and aquaria (20-1000 L or 〈 1 m**2); Description; Difference; Duration, number of days; Echinaster sepositus; Echinocardium cordatum; Echinodermata; Echinometra mathaei; Eucidaris tribuloides; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Henricia oculata; Holothuria forskali; Holothuria tubulosa; Identification; Laboratory experiment; Not applicable; OA-ICC; Ocean Acidification International Coordination Centre; Other; Paracentrotus lividus; Partial pressure of carbon dioxide (water) at equilibrator temperature (wet air); Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; Phyllacanthus imperialis; Potentiometric; Potentiometric titration; Remaining buffer capacity; Replicates; Salinity; Sample code/label; Single species; Species; Temperate; Temperature, water; Treatment; Tripneustes ventricosus; Tropical  (1)
Collection
Keywords
Publisher
Years
  • 1
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Collard, Marie; De Ridder, Chantal; David, Bruno; Dehairs, Frank; Dubois, Philippe (2014): Could the acid-base status of Antarctic sea urchins indicate a better-than-expected resilience to near-future ocean acidification? Global Change Biology, https://doi.org/10.1111/gcb.12735
    Publication Date: 2024-03-15
    Description: Increasing atmospheric carbon dioxide concentration alters the chemistry of the oceans towards more acidic conditions. Polar oceans are particularly affected due to their low temperature, low carbonate content and mixing patterns, for instance upwellings. Calcifying organisms are expected to be highly impacted by the decrease in the oceans' pH and carbonate ions concentration. In particular, sea urchins, members of the phylum Echinodermata, are hypothesized to be at risk due to their high-magnesium calcite skeleton. However, tolerance to ocean acidification in metazoans is first linked to acid-base regulation capacities of the extracellular fluids. No information on this is available to date for Antarctic echinoderms and inference from temperate and tropical studies needs support. In this study, we investigated the acid-base status of 9 species of sea urchins (3 cidaroids, 2 regular euechinoids and 4 irregular echinoids). It appears that Antarctic regular euechinoids seem equipped with similar acid-base regulation systems as tropical and temperate regular euechinoids but could rely on more passive ion transfer systems, minimizing energy requirements. Cidaroids have an acid-base status similar to that of tropical cidaroids. Therefore Antarctic cidaroids will most probably not be affected by decreasing seawater pH, the pH drop linked to ocean acidification being negligible in comparison of the naturally low pH of the coelomic fluid. Irregular echinoids might not suffer from reduced seawater pH if acidosis of the coelomic fluid pH does not occur but more data on their acid-base regulation are needed. Combining these results with the resilience of Antarctic sea urchin larvae strongly suggests that these organisms might not be the expected victims of ocean acidification. However, data on the impact of other global stressors such as temperature and of the combination of the different stressors needs to be acquired to assess the sensitivity of these organisms to global change.
    Keywords: Abatus cavernosus; Acid-base regulation; Alkalinity, total; Alkalinity, total, standard deviation; Amphipneustes lorioli; Amphipneustes rostratus; Amphipneustes similis; Animalia; Antarctic; Aporocidaris eltaniana; Aragonite saturation state; Aragonite saturation state, standard deviation; Benthic animals; Benthos; Bicarbonate ion; Bicarbonate ion, standard deviation; Bransfield_Strait; Calcite saturation state; Calcite saturation state, standard deviation; Calculated; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Coast and continental shelf; Coelomic fluid, alkalinity; Coelomic fluid, carbon, inorganic, dissolved; Coelomic fluid, pH; Coulometric titration; Ctenocidaris gigantea; DATE/TIME; Difference; Echinodermata; Event label; EXP; Experiment; Field observation; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); LATITUDE; LONGITUDE; Notocidaris gaussensis; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; Polar; Potentiometric; Potentiometric titration; Salinity; Single species; Size; Species; Station label; Sterechinus antarcticus; Sterechinus neumayeri; Temperature, water; Weddell_Sea_OA; δ13C
    Type: Dataset
    Format: text/tab-separated-values, 2540 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Collard, Marie; Laitat, Kim; Moulin, Laure; Catarino, Ana Isabel; Grosjean, Philippe; Dubois, Philippe (2013): Buffer capacity of the coelomic fluid in echinoderms. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 166(1), 199-206, https://doi.org/10.1016/j.cbpa.2013.06.002
    Publication Date: 2024-03-15
    Description: The increase in atmospheric CO2 due to anthropogenic activity results in an acidification of the surface waters of the oceans. The impact of these chemical changes depends on the considered organisms. In particular, it depends on the ability of the organism to control the pH of its inner fluids. Among echinoderms, this ability seems to differ significantly according to species or taxa. In the present paper, we investigated the buffer capacity of the coelomic fluid in different echinoderm taxa as well as factors modifying this capacity. Euechinoidea (sea urchins except Cidaroidea) present a very high buffer capacity of the coelomic fluid (from 0.8 to 1.8 mmol/kg SW above that of seawater), while Cidaroidea (other sea urchins), starfish and holothurians have a significantly lower one (from -0.1 to 0.4 mmol/kg SW compared to seawater). We hypothesize that this is linked to the more efficient gas exchange structures present in the three last taxa, whereas Euechinoidea evolved specific buffer systems to compensate lower gas exchange abilities. The constituents of the buffer capacity and the factors influencing it were investigated in the sea urchin Paracentrotus lividus and the starfish Asterias rubens. Buffer capacity is primarily due to the bicarbonate buffer system of seawater (representing about 63% for sea urchins and 92% for starfish). It is also partly due to coelomocytes present in the coelomic fluid (around 8% for both) and, in P. lividus only, a compound of an apparent size larger than 3 kDa is involved (about 15%). Feeding increased the buffer capacity in P. lividus (to a difference with seawater of about 2.3 mmol/kg SW compared to unfed ones who showed a difference of about 0.5 mmol/kg SW) but not in A. rubens (difference with seawater of about 0.2 for both conditions). In P. lividus, decreased seawater pH induced an increase of the buffer capacity of individuals maintained at pH 7.7 to about twice that of the control individuals and, for those at pH 7.4, about three times. This allowed a partial compensation of the coelomic fluid pH for individuals maintained at pH 7.7 but not for those at pH 7.4.
    Keywords: Acid-base regulation; Alkalinity, total; Animalia; Aragonite saturation state; Asterias rubens; Benthic animals; Benthos; Bicarbonate ion; Calcite saturation state; Calculated; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Coast and continental shelf; Coelomic fluid, alkalinity; Coelomic fluid, pH; Containers and aquaria (20-1000 L or 〈 1 m**2); Description; Difference; Duration, number of days; Echinaster sepositus; Echinocardium cordatum; Echinodermata; Echinometra mathaei; Eucidaris tribuloides; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Henricia oculata; Holothuria forskali; Holothuria tubulosa; Identification; Laboratory experiment; Not applicable; OA-ICC; Ocean Acidification International Coordination Centre; Other; Paracentrotus lividus; Partial pressure of carbon dioxide (water) at equilibrator temperature (wet air); Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; Phyllacanthus imperialis; Potentiometric; Potentiometric titration; Remaining buffer capacity; Replicates; Salinity; Sample code/label; Single species; Species; Temperate; Temperature, water; Treatment; Tripneustes ventricosus; Tropical
    Type: Dataset
    Format: text/tab-separated-values, 6964 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Collard, Marie; Eeckhaut, Igor; Dehairs, Frank; Dubois, Philippe (2014): Acid–base physiology response to ocean acidification of two ecologically and economically important holothuroids from contrasting habitats, Holothuria scabra and Holothuria parva. Environmental Science and Pollution Research, 21(23), 13602-13614, https://doi.org/10.1007/s11356-014-3259-z
    Publication Date: 2024-03-15
    Description: Sea cucumbers are dominant invertebrates in several ecosystems such as coral reefs, seagrass meadows and mangroves. As bioturbators, they have an important ecological role in making available calcium carbonate and nutrients to the rest of the community. However, due to their commercial value, they face overexploitation in the natural environment. On top of that, occurring ocean acidification could impact these organisms, considered sensitive as echinoderms are osmoconformers, high-magnesium calcite producers and have a low metabolism. As a first investigation of the impact of ocean acidification on sea cucumbers, we tested the impact of short-term (6 to 12 days) exposure to ocean acidification (seawater pH 7.7 and 7.4) on two sea cucumbers collected in SW Madagascar, Holothuria scabra, a high commercial value species living in the seagrass meadows, and H. parva, inhabiting the mangroves. The former lives in a habitat with moderate fluctuations of seawater chemistry (driven by day-night differences) while the second lives in a highly variable intertidal environment. In both species, pH of the coelomic fluid was significantly negatively affected by reduced seawater pH, with a pronounced extracellular acidosis in individuals maintained at pH 7.7 and 7.4. This acidosis was due to an increased dissolved inorganic carbon content and pCO2 of the coelomic fluid, indicating a limited diffusion of the CO2 towards the external medium. However, respiration and ammonium excretion rates were not affected. No evidence of accumulation of bicarbonate was observed to buffer the coelomic fluid pH. If this acidosis stays uncompensated for when facing long-term exposure, other processes could be affected in both species, eventually leading to impacts on their ecological role.
    Keywords: Acid-base regulation; Alkalinity, total; Ammonium, excretion; Animalia; Aquarium number; Aragonite saturation state; 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; Coast and continental shelf; Coelomic fluid, alkalinity; Coelomic fluid, carbon, inorganic, dissolved; Coelomic fluid, pH; Containers and aquaria (20-1000 L or 〈 1 m**2); Difference; Duration, number of days; Echinodermata; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Holothuria parva; Holothuria scabra; Indian Ocean; Isotope ratio mass spectrometry; Laboratory experiment; OA-ICC; Ocean Acidification International Coordination Centre; Other metabolic rates; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; Potentiometric; Potentiometric titration; Respiration; Respiration rate, oxygen; Salinity; Single species; Species; Temperature, water; Tropical; δ13C; δ13C, Coelomic fluid
    Type: Dataset
    Format: text/tab-separated-values, 3186 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...