Ecological biogeography of North American mammals: species density and ecological structure in relation to environmental gradients

By C. Badgley, David L. Fox. 2000

206 citations recorded by the source corpus.

Subfields: Ecological Modeling, Ecology, Ecology, Evolution, Behavior and Systematics

View Paper: https://www.semanticscholar.org/paper/c23ac1b91bbd942cfadab7a4bb7ff09702ef580a

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Citations in the corpus

Analysis of determinants of mammalian species richness in South America using spatial autoregressive models (2004, background): “…taxonomy and distribution of mammals are relatively well known, this group frequently has been the subject of studies of patterns of species variability (e.g. Mares and Ojeda 1982, Willig and Selcer 1989, Currie 1991, Pagel et al. 1991, Kerr and Packer 1997, Ruggiero 1999, Badgley and Fox 2000).”
Tectonics, topography, and mammalian diversity (2010, background): “…analyses have focused on environmental properties as predictors of alpha diversity, ecological structure, beta diversity, and for evaluation of null models of species distribution at local to regional scales (Currie 1991, Badgley and Fox 2000, McCain 2005, McKnight et al. 2007, Qian et al. 2009).”
The role of climate in limiting European resident bird populations (2003, unknown): “In addition, Badgley & Fox (2000) showed that after removing the effect of certain climate factors, as we did here, from the distribution of North American species’ number, the remaining residuals did not show any spatial autocorrelation.”
Bergmann's rule and the mammal fauna of northern North America (2004, methodology): “This approach is being increasingly used in analyses of gradients of species richness (Badgley and Fox 2000, Hawkins and Porter 2003, 716 ECOGRAPHY 27:6 (2004) Diniz-Filho et al. 2003, Hawkins et al. 2003) and is appropriate for evaluating almost all macroecological patterns.”
Spatial autocorrelation and red herrings in geographical ecology (2003, methodology): “Another approach is to use multivariate techniques (such as principal components analyses) to reduce the dimensionality and, consequently, the collinearity among the predictors (Vetaas, 1997; Badgley & Fox, 2000).”
Environment–richness relationships for mammals, birds, reptiles, and amphibians at global and regional scales (2010, background): “…amphibians (Buckley and Jetz 2007), and plants (Francis and Currie 2003; Kreft and Jetz 2007), among many others at continental scales or below (e.g., Currie 1991; Kerr and Packer 1997; Badgley and Fox 2000; Hawkins and Porter 2003; Hurlbert and Haskell 2003; Hurlbert 2004; Evans et al. 2006).”
Explaining the global biodiversity gradient: energy, area, history and natural selection (2004, background): “…‘‘relief’’, usually measured as the range of elevation: it has long been known that crinkly areas of the planet have more species (Humboldt in Gould, 2002a; Simpson, 1964; Richerson & Lum, 1980; Badgley & Fox, 2000; O’Brien, Field, & Whittaker, 2000; Hawkins & Porter, 2003a; Hawkins et al., 2003a).”
Water–energy balance and the geographic pattern of species richness of western Palearctic butterflies (2003, background): “…et al., 1998; Kerr et al., 1998; Leathwick et al., 1998; O’Brien et al., 1998, 2000; Kerr & Currie, 1999; Kerr & Packer, 1999; Rutherford et al., 1999; Badgley & Fox, 2000; Boone & Krohn, 2000; Lennon et al., 2000; Balmford et al., 2001; Rahbek & Graves, 2001; van Rensburg et al., 2002; Hawkins…”
Mammalian responses to climate change at the Paleocene-Eocene boundary: Polecat Bench record in the northern Bighorn Basin, Wyoming (2003, background): “Climate plays a large role in structuring living mammalian faunas both geographically and ecologically (Badgley and Fox, 2000).”
The latitudinal gradient of beta diversity in relation to climate and topography for mammals in North America (2009, unknown): “These variables represent important aspects of climate and have high predictive power for species richness of mammals and plants over broad spatial scales (e.g. Currie, 1991; Badgley & Fox, 2000; Qian et al ., 2005; Qian & Ricklefs, 2007).”
Latitudinal variation of diversity in European freshwater animals is not concordant across habitat types (2008, unknown): “Many papers have documented that species richness increases with several surrogates of energy available to the communities of plants or animals (Wright, 1983; Currie, 1991; Badgley & Fox, 2000; Hawkins et al ., 2003).”
Relative influences of current and historical factors on mammal and bird diversity patterns in deglaciated North America (2003, background): “…climatic warming (Pielou, 1991; Graham et al ., 1996), and analyses of diversity gradients on this continent have found that variables reflecting present conditions are able to explain most of the variation in species richness (Currie, 1991; Danell et al ., 1996; Badgley & Fox, 2000).”
Plant species invasions along the latitudinal gradient in the United States (2006, background): “There is growing evidence that diversity peaks at those places with optimal conditions for growth and productivity (Currie 1991, Rosenzweig 1992, Badgley and Fox 2000, Hawkins et al. 2003; but see Huston [1979, 1994]).”
Species Richness and Patterns of Invasion in Plants, Birds, and Fishes in the United States* (2006, background): “This pattern of association suggests that diversity peaks at those places with optimal conditions for growth and productivity (Currie 1991; Rosenzweig 1992; Huston 1979, 1994; Badgley and Fox 2000; Hawkins et al. 2003; what Ricklefs 2004 called ‘local determinism’).”