1985
DOI: 10.1016/0300-9629(85)90493-1
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Comparative responses of sea level and montane rufous-collared sparrows, Zonotrichia capensis, to hypoxia and cold

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Cited by 14 publications
(10 citation statements)
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“…Individuals collected at 4500 m a.s.l. have significantly lower critical temperatures (the temperature at which metabolic resources must be used to maintain constant body temperature) than those collected at sea level, consistent with adaptation to cold, high‐altitude habitats (Castro 1983; Castro et al . 1985; Castro & Wunder 1990).…”
Section: Introductionmentioning
confidence: 60%
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“…Individuals collected at 4500 m a.s.l. have significantly lower critical temperatures (the temperature at which metabolic resources must be used to maintain constant body temperature) than those collected at sea level, consistent with adaptation to cold, high‐altitude habitats (Castro 1983; Castro et al . 1985; Castro & Wunder 1990).…”
Section: Introductionmentioning
confidence: 60%
“…This response is often mediated by an increase in metabolic rate, and thermogenic capacity has been shown to be under natural selection in high‐altitude deer mice ( Peromyscus maniculatus ) (Hayes & O’Connor 1999). High‐altitude rufous‐collared sparrows have significantly greater cold tolerance than those from coastal populations (Castro 1983; Castro et al . 1985; Castro & Wunder 1990), suggesting cold adaptation that could be mediated through increased metabolic thermogenic capacity.…”
Section: Discussionmentioning
confidence: 99%
“…The cold, hypoxic conditions of high elevation habitats impose severe physiological stress on endothermic vertebrates, and populations of Z. capensis occurring at different elevations along the Pacific slope in Peru differ in physiological parameters that are likely to be adaptive. Individuals collected at 4500 m asl have significantly higher metabolic rates and reduced lower critical temperatures (the temperature at which metabolic resources must be used to maintain constant body temperature) than those collected at sea level, consistent with local adaptation to cold, high elevation habitats (Castro 1983; Castro et al 1985; Castro and Wunder 1990).…”
mentioning
confidence: 64%
“…The pekin duck also appears to decrease T b in hypoxia (Faraci et al, 1984; Scott et al, 2008), but this has not been consistently observed (Kiley et al, 1985, Bouverot and Hildwein, 1978). In contrast, V̇ o 2 has only been shown to decrease during hypoxia in the Japanese quail (studied at T a = 5°C; Weathers and Snyder, 1974) and, at least in one study, the rufous-collared sparrow (Castro et al, 1985; but see Novoa et al, 1991). Rather, many avian species do not change V̇ o 2 during hypoxia, including the bobwhite quail (Boggs and Kilgore, 1983), burrowing owl (Boggs and Kilgore, 1983; Kilgore et al, 2008) and several small passerines (Novoa et al, 1991) or actually increase V̇ o 2 during hypoxia, including the greylag goose (Scott et al, 2008), bar-headed goose (Black and Tenney, 1980; Scott et al, 2008), house sparrow (Tucker, 1968), and the rosy and house finches (Clemens, 1988).…”
Section: Introductionmentioning
confidence: 96%