The life‐history basis of latitudinal diversity gradients: how do species traits vary from the poles to the equator?

By M. Cardillo. 2002

171 citations recorded by the source corpus.

Subfields: Ecological Modeling, Ecology, Evolution, Behavior and Systematics, Nature and Landscape Conservation

View Paper: https://www.semanticscholar.org/paper/f84f3d64afe40190aaff8bbd5d8eb4e33060d2cb

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Citations in the corpus

Species‐energy relationships at the macroecological scale: a review of the mechanisms (2005, background): “In many taxa the number of young per reproductive attempt increases with latitude, i.e. decreases with energy availability : e.g. zooplankton – Poulin (1995), fish – Conover (1992), turtles – Iverson et al. (1993) and birds – Lack (1947, 1948) ; Martin et al. (2000) ; Cardillo (2002).”
Rarity in the tropics: biogeography and macroecology of the primates (2006, background): “However, the tropics might be different in several potentially fundamental ways (Robinson, 1978; Ghalambor & Martin, 2001; Cardillo, 2002; Turner & Hawkins, 2004).”
Niche conservatism in non‐native birds in Europe: niche unfilling rather than niche expansion (2013, methodology): “Following Cardillo (2002), we considered as habitat types saltwater or estuarine, fresh water, forest, woodland and scrub, open habitats, cultivated farmlands and urban areas.”
Global patterns of specialization and coexistence in bird assemblages (2012, background): “…relationship between specialization and species richness (sometimes using latitude as a proxy for richness; Pagel et al., 1991; Eeley & Foley, 1999; Cardillo, 2002; Dyer et al., 2007; Krasnov et al., 2008b; Mason et al., 2008), others have not (Beaver, 1979; Lappalainen & Soininen, 2006; Novotny…”
One-dimensional analyses of Rapoport's rule reviewed through meta-analysis (2007, background): “The same tendency for phylogenetic methods to provide significant evidence in support of the Rapoport effect (in contrast to non-significant latitudinal variation found by crossspecies analysis) was suggested in an independent analysis of global range size patterns in birds (Cardillo, 2002).”
Ecogeographical rules: elements of a synthesis (2008, background): “In other cases the traits are expressed at the level of the species (e.g. geographical range size, population density, global population size; Letcher & Harvey, 1994; Gaston & Blackburn, 1996; Cardillo, 2002a; Reed, 2003; Cruz et al., 2005; Symonds et al., 2006).”
Day length, latitude and behavioural (in)flexibility in baboons (Papio cynocephalus ursinus) (2003, background): “…have examined relationships at a relatively large scale, and have considered factors such as species geographical ranges and Rapoport’s Rule (Cardillo 2002), body size and Bergmann’s Rule (Blackmann and Gaston 1996), life history traits (Cardillo 2002) and species richness (Owens et al.…”
Biogeographical variation in the population density of wild boar (Sus scrofa) in western Eurasia (2006, background): “Comparative studies of species density, demography and life history traits, from the centre to the margins of their range, allow us to explore the responses of species to increasing environmental stress (Cardillo, 2002; Holt & Keitt, 2005).”
Is There a Latitudinal Gradient in the Importance of Biotic Interactions (2009, background): “F or p er so na l u se o nl y. ANRV393-ES40-12 ARI 8 October 2009 8:52 of 69 phylogenetically independent species pairs of birds separated by at least 10◦ of latitude, Cardillo (2002) found no increase in sexual dimorphism or dichromatism at lower latitudes.”
Extrapair Paternity and Sexual Selection in Socially Monogamous Birds: Are Tropical Birds Different? (2008, background): “…determines the degree of sexual dichromatism (Irwin 1994, �urns 1998)�� Moreover, many early studies that reported a latitudinal trend in sexual dichromatism did not control for phylogeny�� Cardillo (2002) analyzed 69 phylogenetically independent pairs of species that differed in breeding…”