Extracellular acid-base regulation during short-term hypercapnia is effective in a shallow-water crab, but ineffective in a deep-sea crab

By E. F. Pane, J. Barry. 2007

226 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/c9f0f778d71885f4a212fd528464df565a560824

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In Ecology

In Oceanography

Citations in the corpus

Physiological and ecological responses of crustaceans to ocean acidification (2011, unknown): “Two species of crabs, Necora puber and Cancer magister, which are relatively poor iono-regulators, were also able to compensate haemo lymph acid–base disturbances within 24 h when exposed to CO2 at 0.10 to 0.20 kPa (Pane & Barry 2007, Spicer et al. 2007).”
Ecosystem effects of ocean acidification in times of ocean warming: a physiologist’s view (2008, background): “For example, reduced capacity to regulate extracellular pH was recently found in deep-sea versus shallow-water crustaceans (Pane & Barry 2007, see also Spicer et al. 2007) where the slow and hypometabolic mode of life in deep-sea species is reflected in a reduced rate (and thus cost) for acid–base…”
Biological mechanisms supporting adaptation to ocean acidification in coastal ecosystems (2015, unknown): “Buffering hemolymp (HL) or EPF to avoid decreasing pH at calcification sites is an efficient mechanism used, for example, by teleost fish, decapod crustaceans, and cephalopod molluscs (Larsen et al., 1997; Pane and Barry, 2007; Gutowska et al., 2010).”
Physiological basis for high CO2 tolerance in marine ectothermic animals: pre-adaptation through lifestyle and ontogeny? (2009, background): “…Fivelstad et al., 2003, (2) Foss et al., 2003, (3) Melzner et al., 2009, (4) Larsen et al., 1997, (5) Michaelidis et al., 2007, (6) Truchot, 1979, (7) Pane and Barry, 2007, (8) Spicer et al., 2007, (9) Gutowska et al., 2008, (10) Gutowska et al., submitted, 2009, (11) Siikavuopio et al., 2007,…”
Impact of medium-term exposure to CO2 enriched seawater on the physiological functions of the velvet swimming crab Necora puber. (2010, background): “Bicarbonate ions acquired from shell dissolution are thought to be used for the regulation of internal pH in marine invertebrates (see Spicer et al. 1988, Cameron & Iwama 1989, Pörtner et al. 2004, Michaelidis et al. 2005, Pane & Barry 2007) and terrestrial decapod crustaceans (Henry et al. 1981).”
Effects of ocean acidification and warming on the larval development of the spider crab Hyas araneus from different latitudes (54° vs. 79° N) (2010, background): “Studies on adult crustaceans have detected negative effects of CO2 on various physiological processes and performances (Chionoectes tanneri: Pane & Barry 2007, Cancer pagurus: Metzger et al. 2007, Necora puber : Spicer et al. 2007, Palaemon pacificus: Kurihara et al. 2008, Semibalanus balanoides:…”
Cuttlebone calcification increases during exposure to elevated seawater pCO2 in the cephalopod Sepia officinalis (2010, background): “During exposure to hypercapnia of 500‐1000 Pa, crabs nearly compensate extracellular pH and elevate blood [HCO3 - ] to values between 10 and 30 mM (Truchot 1984; Cameron and Iwama 1987; Spicer et al. 2007; Pane and Barry 2007 ).”
Long-term effects of predicted future seawater CO2 conditions on the survival and growth of the marine shrimp Palaemon pacificus (2008, background): “However , the capacity fo r extracellular acid-base regulation in marine crustaceans appears to be species-specific, and also influenced by environmental conditions such as temperature and dissolved oxygen (Pane and Barry , 2007).”
Predicting the impact of ocean acidification on benthic biodiversity: What can animal physiology tell us? (2008, background): “However, in some invertebrates, such as Mytilus edulis (Zange et al., 1990), Callinectes sapidus (Wood and Cameron, 1985), Chionoecetes tanneri (Pane and Barry, 2007), Psammechinus miliaris (Miles et al., 2007) (and including S. nudis) there is only partial, or no, compensation in…”
Elevated pCO2 causes developmental delay in early larval Pacific oysters, Crassostrea gigas (2013, background): “This phenomenon has been observed in Dungeness crabs, Cancer magister (Pane and Barry 2007); blue crabs, Callinectes sapidus (Henry et al.”
Novel microcosm system for investigating the effects of elevated carbon dioxide and temperature on intertidal organisms (2008, methodology): “This particular set-up involved the use of premixed gases; these types of premixed gases have also been used in experiments to bubble into seawater (e.g. Pane & Barry 2007).”
Impact of anthropogenic ocean acidification on thermal tolerance of the spider crab Hyas araneus (2009, unknown): “…on crustaceans were conducted with a different focus and either used concentrations of about 10 000 ppm CO2 (Cameron, 1978, 1985; Wickins, 1984; Cameron and Iwama, 1987; Metzger et al., 2007; Pane and Barry, 2007) or rarely more realistic scenarios (e.g. about 800 ppm used by Spicer et al., 2007).”
Acidification and warming affect both a calcifying predator and prey, but not their interaction (2012, background): “(2) Indirect effects of predators on potential prey organisms may be as strong as direct effects, and prey may be ‘scared to death’ (i.e. respond in an ex - treme and ultimately detrimental way) by the presence of predators (Preisser et al. 2005).”