1989
DOI: 10.4319/lo.1989.34.2.0324
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Energy budgets of latitudinally separated Scottolana canadensis (Copepoda: Harpacticoida)

Abstract: We tested the hypothesis that evolution in a local population shifts individual metabolic properties to maximize energy budgets under the prevailing temperature regime. We measured scope for growth [ng C (pg dry mass)-' h -'1 in latitudinally separated adult females of Scottolana canadensis (Willey) and used common-rearing techniques to assess the degree of genetic differentiation. Florida (low latitude) females were at an energetic disadvantage at 15"C, but Maine (high latitude) females were not always disadv… Show more

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Cited by 20 publications
(5 citation statements)
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“…The maintenance of relatively high rates of metabolism in summer-acclimatized G. locusta and G. d. duebeni across a range of latitudes may only be possible because of a continued availability of food to fuel the high rates of energy consumption (Lonsdale and Levinton 1989). In the low intertidal G. locusta, high energy turnover may be related to its warm-water ancestry.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…The maintenance of relatively high rates of metabolism in summer-acclimatized G. locusta and G. d. duebeni across a range of latitudes may only be possible because of a continued availability of food to fuel the high rates of energy consumption (Lonsdale and Levinton 1989). In the low intertidal G. locusta, high energy turnover may be related to its warm-water ancestry.…”
Section: Discussionmentioning
confidence: 99%
“…Despite these drawbacks, two general patterns have emerged. Intraspecific comparisons indicate that metabolic compensation can occur between populations, resulting in similar metabolic rates in species spread across latitudes despite differences in habitat temperature (Fox and Wingfield 1937;Vernberg 1962;Mangum 1963;Lonsdale and Levinton 1989;Sommer and Pörtner 2002). In sharp contrast, many antarctic marine invertebrates do not compensate their metabolic rates in the extreme cold and do not conform to the concept of metabolic cold adaptation (Clarke 1991(Clarke , 1993(Clarke , 2003Pörtner et al 2007).…”
Section: Introductionmentioning
confidence: 93%
“…This cold acclimation, or latitudinal compensation hypothesis, has attracted significant research into this singular pattern of metabolic rate and its mechanisms and evolutionary implications (Sommer et al 1997;Dittman 2003). Many different physiological functions can be responsible for temperature-dependent growth rate differentiation, including duration of feeding activity, metabolic rate, digestive efficiency, allocation of resources to growth versus reproduction (Hochachka & Somero 1973;Prosser 1986;Lonsdale & Levinton 1989;Present & Conover 1992). Very few studies have tested the metabolic cold adaptation hypothesis, considering the oxygen consumption of marine invertebrate populations of a widely distributed species in a temperate zone (more than 2000 km) where noticeable environmental gradients exist.…”
Section: Geographic Variation In Metabolismmentioning
confidence: 99%
“…These include duration of feeding activity, digestive efficiency, allocation of resources to growth vs reproduction and others (Hochachka 1973;Prosser 1986;Lonsdale & Levinton 1989;Present & Conover 1992). When testing for genetically based physiological differences between populations it is important to use groups of animals that have been raised in a common environment (Ament 1979;Knaub & Eversole 1988;Garland & Adolph 1991).…”
Section: Introductionmentioning
confidence: 99%