Beyond the ‘3/4‐power law’: variation in the intra‐and interspecific scaling of metabolic rate in animals
By Douglas S. Glazier. Biological Reviews of The Cambridge Philosophical Society, 2005
973 citations recorded by the source corpus.
Subfields: Ecology, Ecology, Evolution, Behavior and Systematics
View Paper: https://www.semanticscholar.org/paper/5ef581234e1e7be8cf904c89aea7d4a8fc64316e
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Citations in the corpus
- Moving on from Metabolic Scaling Theory: hierarchical models of tree growth and asymmetric competition for light (2011, background): “For example, exponent estimates for scaling relationships between metabolic rates and body mass of animals (taken from Glazier 2005) are funnel shaped with respect to sample size, and the 95% confidence intervals get narrower as sample size increases (Fig.”
- Body size in freshwater planktonic crustaceans: an overview of extrinsic determinants and modifying influences of biotic interactions (2011, background): “First, weight-specific metabolic costs are widely perceived to be lower, although this notion is recently contested by Glazier (2005, 2006)—see ‘Respiration’ section.”
- Intraspecific temperature dependence of the scaling of metabolic rate with body mass in fishes and its ecological implications (2012, background): “Glazier (2005) showed that ectothermic vertebrates generally exhibit higher interspecific scaling exponents than endothermic vertebrates and that the effect of temperature on the metabolic scaling may vary among species.”
- Reconsidering the mechanistic basis of the metabolic theory of ecology (2007, neutral): “Glazier (2005), however, documents a variety of intraspecific metabolic allometries: 1) many with allometric exponents differing substantially from 0.75, and 2) many that are poorly described by linear relationships between the logarithms of mass and metabolism.”
- Larval instar as a key element of insect growth schedules (2006, background): “…is a large body of empirical evidence however, which indicate that values of the allometric exponent, relating metabolic activity (and, often also the growth rate) to body mass, are below 1 in most cases and are typically close to 2/3 or 3/4 (West et al. 2001, 2004, Ricklefs 2003, Glazier 2005).”
- Temperature and the metabolic theory of ecology (2006, background): “2006), a comprehensive analysis by Glazier (2005) has revealed considerable heterogeneity in the value of b across a wide range of animal groups, and Makarieva, Gorshkov & Li (2003, 2005) have examined the scaling of metabolic rate from the perspective of a minimum cost for maintaining living tissue”
- Depth‐related trends in metabolism of benthic and benthopelagic deep‐sea fishes (2007, background): “…can be predicted based solely on size and temperature (Gillooly et al. 2001; Brown et al. 2004), more recent analyses demonstrate a wide variation in both the slopes and elevations of the scaling relationships after temperature adjustment (Glazier 2005; Seibel 2007; Seibel and Drazen in press).”
- Bridging the gap between marine biogeochemical and fisheries sciences; configuring the zooplankton link (2014, background): “Furthermore, recent studies suggest that the intraspecific metabolic-scaling exponent may be related to various ecological factors, including zooplankton activity, habitat, and temperature (Glazier, 2005, 2006, 2010).”
- Application of macroecological theory to predict effects of climate change on global fisheries potential (2008, neutral): “Alternative values of the scaling exponent may exist in some taxa (e.g. Clark & Johnston 1999, Glazier 2005, van der Meer 2006, White et al. 2007) or life stages (Pauly 1981).”
- Representing the acquisition and use of energy by individuals in agent‐based models of animal populations (2013, background): “Intraspecific scaling relationships of 218 species are tabulated in the study by Glazier (2005).”