2011
DOI: 10.1371/journal.pone.0028942
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Predictable Variation of Range-Sizes across an Extreme Environmental Gradient in a Lizard Adaptive Radiation: Evolutionary and Ecological Inferences

Abstract: Large-scale patterns of current species geographic range-size variation reflect historical dynamics of dispersal and provide insights into future consequences under changing environments. Evidence suggests that climate warming exerts major damage on high latitude and elevation organisms, where changes are more severe and available space to disperse tracking historical niches is more limited. Species with longer generations (slower adaptive responses), such as vertebrates, and with restricted distributions (low… Show more

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Cited by 23 publications
(32 citation statements)
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“…; Pincheira‐Donoso et al. ; Pincheira‐Donoso ; Pincheira‐Donoso et al. ), but to understand this remarkable adaptive radiation, we need to put liolaemid evolution in the context of the rapid development of its geological domain.…”
Section: Discussionmentioning
confidence: 99%
“…; Pincheira‐Donoso et al. ; Pincheira‐Donoso ; Pincheira‐Donoso et al. ), but to understand this remarkable adaptive radiation, we need to put liolaemid evolution in the context of the rapid development of its geological domain.…”
Section: Discussionmentioning
confidence: 99%
“…Indeed, the uplift of the Andes has increasingly been implicated in the proliferation of high biodiversity in other organisms [49][51]. The access to such ecological opportunities appears to have been facilitated by the adaptive potential of Liolaemus to exploit all possible structural and thermal microhabitats [15], [52][55], food resources [56], and to evolve alternative life history strategies to reproduce efficiently across extreme climatic gradients [57], [58]. As a result, Liolaemus species are the dominant (and in extreme elevations and latitudes, sometimes the only) reptiles in most areas of their distribution [14], [15], [59]–[61].…”
Section: Discussionmentioning
confidence: 99%
“…The access to such ecological opportunities appears to have been facilitated by the adaptive potential of Liolaemus to exploit all possible structural and thermal microhabitats [15], [52][55], food resources [56], and to evolve alternative life history strategies to reproduce efficiently across extreme climatic gradients [57], [58]. As a result, Liolaemus species are the dominant (and in extreme elevations and latitudes, sometimes the only) reptiles in most areas of their distribution [14], [15], [59]–[61]. In Liolaemus , the identification of underlying key innovations remains less clear, although multiple independent episodes of evolution of viviparity have apparently opened multiple opportunities to colonize cold climates [24].…”
Section: Discussionmentioning
confidence: 99%
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“…However, this is a questionable statement that may result from her use of a very limited literature (she only cites Jaksic, Núñez & Ojeda, 1980;Mella, 2005) only involving a minor proportion of Liolaemus biodiversity restricted to central Chile. In contrast, broader-scale (in phylogeny, ecology and distribution) studies have consistently shown that these lizards have evolved substantial morphological and ecological diversity, expressed as large variation in body size, body shape, sexual dimorphism, use of microhabitats and of thermal environments, diets, life histories and dispersal potential (Cei, 1986(Cei, , 1993Harmon et al, 2003;Espinoza et al, 2004;Schulte et al, 2004;Cruz et al, 2005;Pincheira-Donoso et al, 2007, 2008b, 2009Pincheira-Donoso, 2011;Pincheira-Donoso & Tregenza, 2011). Therefore, regardless of whether chemical systems of communication have or have not rapidly evolved in Liolaemus, it is difficult to support the view that the evolution of these chemical traits have prevented or limited the evolution of morphological and ecological diversity in these lizards.…”
mentioning
confidence: 99%