2019
DOI: 10.1016/j.jcz.2019.02.003
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Sexual size dimorphism, allometry and fecundity in a lineage of South American viviparous lizards (Liolaemidae: Phymaturus)

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Cited by 10 publications
(9 citation statements)
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“…Consistent with the prediction, our results demonstrated the existence of an isometric relationship between male and female sizes in viviparous species, or even a slope shallower than 1. Valdecantos et al (2019) found a similar pattern (slope ≈ 1) in a clade of viviparous South American lizards (Phymaturus). A similar pattern is apparent in Chinese viviparous lizards (Liang et al 2021), and, at the intraspecific level, in Zootoca vivipara (Roitberg et al 2020).…”
Section: Reproductive Mode Can Influence Life History Traits In Reptilesmentioning
confidence: 53%
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“…Consistent with the prediction, our results demonstrated the existence of an isometric relationship between male and female sizes in viviparous species, or even a slope shallower than 1. Valdecantos et al (2019) found a similar pattern (slope ≈ 1) in a clade of viviparous South American lizards (Phymaturus). A similar pattern is apparent in Chinese viviparous lizards (Liang et al 2021), and, at the intraspecific level, in Zootoca vivipara (Roitberg et al 2020).…”
Section: Reproductive Mode Can Influence Life History Traits In Reptilesmentioning
confidence: 53%
“…In lizards, studies of Rensch's rule have mostly been carried out on closely related species (e.g. at the familyscale; Cox et al 2007;Frýdlová & Frynta 2015;Valdecantos et al 2019;Liang et al 2021) or at the intraspecific level (e.g. Zhao et al 2016;Liang & Shi 2017).…”
Section: Introductionmentioning
confidence: 99%
“…Sexual dimorphism in body size has been reported in several species of whiptails, such as A. tigris (Anderson & Vitt, 1990), A. costatus (Aguilar‐Moreno et al, 2010), A. lineattissimus (Hernández‐Salinas, Ramírez‐Bautista, Pavón, & Rosas Pacheco, 2014) and A. gularis (Pérez‐Almazán, Manríquez‐Morán, Balderas‐Plata, Antonio‐Némiga, & López‐Alcaide, 2017). Sexual dimorphism has commonly been related to sexual selection (Anderson & Vitt, 1990; Olsson, Shine, Wapstra, Ujvari, & Madsen, 2002) and fertility (Aguilar‐Moreno et al, 2010; Olsson et al, 2002; Valdecantos, Lobo, Perotti, Moreno‐Azócar, & Cruz, 2019) in squamates. Snout–vent length seems to be related to sexual selection in Aspidoscelis costatus (Aguilar‐Moreno et al, 2010), while axilla–groin distance has been associated with fecundity in A. gularis and A. costatus (Aguilar‐Moreno et al, 2010; Pérez‐Almazán et al, 2017).…”
Section: Discussionmentioning
confidence: 99%
“…For Thamnophiini, the standard outcome of fecundity selection demonstrates that selection for larger female gapes and larger or longer body sizes translates into increased numbers of offspring (Braña & Brana, 1996;Darwin, 1871;Olsson, Shine, Wapstra, Ujvari, & Madsen, 2002;Valdecantos, Lobo, Perotti, Moreno Azócar, & Cruz, 2019). Likely, sexual dimorphism in Thamnophiini is the result of sexual selection on gape and diet for enhanced energy expenditure needed to increased fecundity and neonate size.…”
Section: Discussionmentioning
confidence: 99%