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Chiropterotriton is a relatively small genus that comprises 15 species with great morphological and ecological diversity. In previous studies, molecular data provided evidence for a considerable number of species that remain undescribed. In this study, we describe one new species, Chiropterotriton chico sp. nov. based on molecular and morphological...

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... phylogenetic analyses were run on the CIPRES Science Gateway (Miller et al. 2010). Finally, we obtained corrected genetic distances (Kimura two- parameter, K2P) using Mesquite v3.04 (Maddison & Maddison 2015), which are shown in Table 2. FIGURE 2. Mitochondrial DNA gene tree of Chiropterotriton from Bayesian analysis of 16S sequences. ...

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... The estimated substitution models were as follows: GTR+G for 12S, tRNA, 16S, the 3rd codon position of COI, K80+G for the 1st codon position of COI, and HKY+1 for the 2 nd codon position of COI. Our concatenated phylogeny has a similar topology as shown in previous studies (Darda 1994;Parra-Olea 2003;García-Castillo et al. 2017), which show two main groups, a northern and southern species groups. (Fig. 2). ...
... , C. multidentatus (mean FW 3.6 in males, 3.5 in females; , and C. priscus (mean FW 3.2 in males, 3.5 in females; . Chiropterotriton aureus has shorter limbs (LI 2.0 in one male, mean 2.3 in females) than C. arboreus (mean LI 0.2 in males, 1.0 in females; García-Castillo et al. 2017), C. cieloensis (mean LI -0.2 in males, 0.1 in females; Rovito and Parra-Olea 2015), C. infernalis (mean LI -0.7 in males, -0.5 in one female; Rovito and Parra-Olea 2015), C. multidentatus (mean LI 0.1 in males, 1.0 in females; , but it has longer limbs than C. dimidiatus (mean LI 3.8 in males, 4.9 in females; García-Castillo et al. 2017), C. miquihuanus (mean LI 4.2 in males, 4.3 in females; , and C. priscus (mean LI 3.2 in males, 3.7 in females; . ...
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Aim The diversity of brood size across animal species exceeds the diversity of most other life‐history traits. In some environments, reproductive success increases with brood size, whereas in others it increases with smaller broods. The dominant hypothesis explaining such diversity predicts that selection on brood size varies along climatic gradients, creating latitudinal fecundity patterns. Another hypothesis predicts that diversity in fecundity arises among species adapted to different microhabitats within assemblages. A more recent hypothesis concerned with the consequences of these evolutionary processes in the era of anthropogenic environmental change predicts that low‐fecundity species might fail to recover from demographic collapses caused by rapid environmental alterations, making them more susceptible to extinctions. These hypotheses have been addressed predominantly in endotherms and only rarely in other taxa. Here, we address all three hypotheses in amphibians globally. Location Global. Time period Present. Major taxa studied Class Amphibia. Methods Using a dataset spanning 2,045 species from all three amphibian orders, we adopt multiple phylogenetic approaches to investigate the association between brood size and climatic, ecological and phenotypic predictors, and according to species conservation status. Results Brood size increases with latitude. This tendency is much stronger in frogs, where temperature seasonality is the dominant driver, whereas salamander fecundity increases towards regions with more constant rainfall. These relationships vary across continents but confirm seasonality as the key driver of fecundity. Ecologically, nesting sites predict brood size in frogs, but not in salamanders. Finally, we show that extinction risk increases consistently with decreasing fecundity across amphibians, whereas body size is a “by‐product” correlate of extinction, given its relationship with fecundity. Main conclusions Climatic seasonality and microhabitats are primary drivers of fecundity evolution. Our finding that low fecundity increases extinction risk reinforces the need to refocus extinction hypotheses based on a suggested role for body size.