2002
DOI: 10.1086/340990
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Metabolic Demand, Oxygen Supply, and Critical Temperatures in the Antarctic BivalveLaternula elliptica

Abstract: Oxygen consumption ( ), heartbeat rate and form, and cirMo 2 culating hemolymph oxygen content were measured in relation to temperature in the large Antarctic infaunal bivalve Laternula elliptica. After elevations in temperature from 0Њ to 3Њ, 6Њ, and then 9ЊC, and heartbeat rate rose to new levels, whereaṡ Mo 2 maximum circulating hemolymph oxygen content fell. At 0ЊC, was 19.6 mmol O 2 h Ϫ1 for a standard animal of 2-g tissuė Mo 2 ash-free dry mass, which equates to a 8.95-g tissue dry-mass or 58.4-g tissue … Show more

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Cited by 150 publications
(134 citation statements)
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“…These turbulent and complex oceanographic processes increase heterogeneity in a system that may otherwise be considered highly stenothermal and stable (Barnes et al, 2006;Clarke et al, 2009). Small changes in temperature are known to cause drastic changes in metabolic rates of Antarctic benthic invertebrates in shallow water (Peck et al, 2002;Peck et al, 2004) but to date there is no published work on metabolic rates of deep-sea Antarctic invertebrates.…”
Section: Discussionmentioning
confidence: 99%
“…These turbulent and complex oceanographic processes increase heterogeneity in a system that may otherwise be considered highly stenothermal and stable (Barnes et al, 2006;Clarke et al, 2009). Small changes in temperature are known to cause drastic changes in metabolic rates of Antarctic benthic invertebrates in shallow water (Peck et al, 2002;Peck et al, 2004) but to date there is no published work on metabolic rates of deep-sea Antarctic invertebrates.…”
Section: Discussionmentioning
confidence: 99%
“…Early evidence collected in marine invertebrates (annelids and sipunculids) demonstrated a transition to anaerobic metabolism (including mitochondrial anaerobiosis) at both cold and warm temperature extremes (Zielinski and Pörtner, 1996;Sommer et al, 1997), later on confirmed in crustaceans (Frederich and Pörtner, 2000) and molluscs, i.e. bivalves, gastropods and cephalopods (Pörtner and Zielinski, 1998;Pörtner et al, 1999;Peck et al, 2002;Sokolova and Pörtner, 2003). Studies in a sipunculid (Sipunculus nudus, Zielinski and Pörtner, 1996) and the spider crab (Maja squinado, Frederich and Pörtner, 2000) investigated the pattern of coelomic fluid/haemolymph oxygen tensions in relation to warming and/or cooling and demonstrated development of hypoxia which preceded the onset of anaerobic metabolism towards both cold and warm temperature extremes.…”
Section: Introduction: a Role For Hypoxia In Thermal Limitation?mentioning
confidence: 99%
“…Inclusion of Antarctic marine invertebrates in this picture revealed very narrow windows of thermal tolerance in these organisms, in a temperature range just above freezing. An early transition to "heat" induced anaerobiosis between 2 and 6 • C seen in bivalves reflected the permanently low temperatures of Antarctic seas Peck et al, 2002).…”
Section: Introduction: a Role For Hypoxia In Thermal Limitation?mentioning
confidence: 99%
“…Portner,2 001), however, display a pejus temperature at 4 8C, beyond which a decreased level of aerobic scope limits ecological performance (activity and reproduction) and hence survival of the animals. Aerobic scope is lost and transition to anaerobic metabolism occurs between 6 and 9 8C (Peck et al, 2002). According to Portner (2001), pejus temperatures are more indicative of the limits of geographical distribution of a species, than the temperature extreme an organism can tolerate passively for some time until it dies.…”
Section: Introductionmentioning
confidence: 99%