1990
DOI: 10.2307/1548331
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Respiratory and Cardiovascular Responses of Two Species of Deep-Sea Crabs, Chaceon Fenneri and C. Quinquedens, in Normoxia and Hypoxia

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Cited by 15 publications
(9 citation statements)
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“…Benthic species are better represented by measurements of metabolic enzyme activities that serve as proxies for metabolic capacity. The majority of oxygen consumption and aerobic metabolic enzyme measurements in deep-sea benthic species, including echinoderms (Smith 1983), meiobenthic animals (Shirayama 1992), crabs and shrimp (Childress & Mickel 1985;Henry et al 1990;Walsh & Henry 1990;Childress et al 1990a;Bailey et al 2005), amphipods (Smith & Baldwin 1982;Treude et al 2002), sponges (Witte & Graff 1996) and octopods were at most oneto fivefold lower than shallow-living species after temperature correction and many of these groups show no decline at all (e.g. figures 1c, 2, 3c and 4).…”
Section: Rates Of Metabolism In Relation To Environmental Variablesmentioning
confidence: 99%
“…Benthic species are better represented by measurements of metabolic enzyme activities that serve as proxies for metabolic capacity. The majority of oxygen consumption and aerobic metabolic enzyme measurements in deep-sea benthic species, including echinoderms (Smith 1983), meiobenthic animals (Shirayama 1992), crabs and shrimp (Childress & Mickel 1985;Henry et al 1990;Walsh & Henry 1990;Childress et al 1990a;Bailey et al 2005), amphipods (Smith & Baldwin 1982;Treude et al 2002), sponges (Witte & Graff 1996) and octopods were at most oneto fivefold lower than shallow-living species after temperature correction and many of these groups show no decline at all (e.g. figures 1c, 2, 3c and 4).…”
Section: Rates Of Metabolism In Relation To Environmental Variablesmentioning
confidence: 99%
“…Reduced gill surface area among deep-sea species may, therefore, limit ionexchange capacity. Aside from those adapted for residence in oxygen minimum layers (Childress and Seibel, 1998), the few deep-sea species studied have much lower gill surface areas than their more-active, shallower-living counterparts (Henry et al, 1990;Marshall, 1971;Voss, 1988 Gibbs and Somero (1990) reported greatly reduced capacities for active ion regulation via ATPases in gills of deep-sea fishes relative to shallower species. Although their study focused on Na + /K + -ATPases, their data show that activities of total ATPases declined with increasing depth as well.…”
Section: Ion-exchange Capacitymentioning
confidence: 99%
“…CA catalyzes the reversible hydration/dehydration reaction of CO2 and water (equation 1) and, thus, plays an important role in CO2 excretion and acid-base balance in marine animals by maintaining availability of H + and HCO3 -for transporters (Burnett, 1997;Henry, 1984). Deep-sea species presumably have a much lower requirement for branchial ion transport due to the extreme ionic stability of seawater at depth and their low rates of metabolic and locomotory activity (Henry et al, 1990).…”
Section: Ion-exchange Capacitymentioning
confidence: 99%
“…In response to hypoxia, C.fenneri maintains a relatively constant Mo2 by hyperventilation (i.e., it is oxy-independent), but it ultimately begins to rely on anaerobic metabolism, accumulates lactate and incurs an oxygen debt (Henry et al 1990 a). In contrast, in response to hypoxia (as low as 17 torr) C. quinquedens decreases its rates of oxygen uptake, does not hyperventilate (i.e., it is oxy-independent), and does not accumulate lactate (Henry et al 1990a). Oxygen-minimum zones occur in the habitats of both species, but the frequency of hypoxic encounters is unknown (Henry et al 1990a, b).…”
Section: Introductionmentioning
confidence: 96%