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1,047 results for “Salamanders”

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zenodo28/100

FIGURE 2 in A new species of hynobiid salamander (Urodela: Hynobiidae: Pseudohynobius) from Southwestern China

FIGURE 2. Ventral view of the holotype of Pseudohynobius jinfo (CIB 85290).

opennotspecifiedDec 2009View details →
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FIGURE 1 in A new species of hynobiid salamander (Urodela: Hynobiidae: Pseudohynobius) from Southwestern China

FIGURE 1. Dorsal view of the holotype of Pseudohynobius jinfo (CIB 85290).

opennotspecifiedDec 2009View details →
zenodo28/100

FIGURE 2 in A distinctive new species of moss salamander (Caudata: Plethodontidae: Nototriton) from an imperiled Honduran endemism hotspot

FIGURE 2. Dorsal and ventral aspects of the holotype of Nototriton tomamorum sp. nov.

opennotspecifiedDec 2010View details →
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FIGURE 1 in Redescription of an enigmatic salamander, Pseudohynobius puxiongensis (Fei et Ye, 2000) (Urodela: Hynobiidae)

FIGURE 1. Dorsal (A) and ventral (B) views of Pseudohynobius puxiongensis (CIB-XM3364).

opennotspecifiedDec 2011View details →
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FIGURE 4 in Redescription of an enigmatic salamander, Pseudohynobius puxiongensis (Fei et Ye, 2000) (Urodela: Hynobiidae)

FIGURE 4. The karyotype of Pseudohynobius puxiongensis.

opennotspecifiedDec 2011View details →
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FIGURE 2 in Description of a new species of worm salamander (Caudata, Plethodontidae, Oedipina) in the subgenus Oedopinola from the central portion of the Cordillera Nombre de Dios, Honduras

FIGURE 2. Subadult male holotype of Oedipina petiola (USNM 343462; SVL = 42.6 mm) in life.

opennotspecifiedDec 2011View details →
zenodo28/100

FIGURE 2 in Taxonomy and distribution of the salamander genus Bolitoglossa Duméril, Bibron & Duméril, 1854 (Amphibia, Caudata, Plethodontidae) in Brazilian Amazonia

FIGURE 2. Interdigital webbing shapes of right hands and feet of Brazilian Amazonia. Scale 1 mm.

opennotspecifiedDec 2013View details →
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FIGURE 3. A in Description of a New Salamander of the Genus Onychodactylus from Shikoku and Western Honshu, Japan (Amphibia, Caudata, Hynobiidae)

FIGURE 3. A male paratype of O. kinneburi sp. nov. (KUHE 43066) from the type locality in life.

opennotspecifiedDec 2013View details →
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FIGURE 4 in Phylogeography and Genetic Structure in the California Giant Salamander (Dicamptodon ensatus): Impacts of current and historic landscape features

FIGURE 4. Bayesian inference skyline plot of the mtDNA control region of D. ensatus.

opennotspecifiedNov 2021View details →
dryad28/100

Anticipating the potential impacts of Batrachochytrium salamandrivorans on Neotropical salamander diversity

<p>Emergent infectious disease caused by the fungal pathogens <i>Batrachochytrium dendrobatidis</i> (<i>Bd</i>) and <i>B. salamandrivorans</i> (<i>Bsal</i>) represent one of the major causes of biodiversity loss in amphibians. While <i>Bd </i>has affected amphibians worldwide, <i>Bsal </i>remains restricted to Asia and Europe, but also could be a major threat for salamanders in the Western hemisphere, including the 320 bolitoglossine species described. Here we predict the suitable areas for <i>Bsal </i>in the Neotropics and assessed its potential impact on bolitoglossine diversity. For this, we determined the geographic patterns of taxonomic, phylogenetic, and functional diversity for bolitoglossines and modelled the potential distribution of <i>Bsal</i> in the Neotropics. We identified which species and regions could be at risk from an eventual introduction of <i>Bsal </i>in the region, quantified the degree of overlap between regions of high diversity and the suitable conditions for the pathogen, and considered species IUCN Red List status, and geographic range size. We found that regions of high taxonomic, phylogenetic, and functional diversity are concentrated in the Trans-Mexican Volcanic Belt, Sierra Madre Oriental, the southern portion of Sierra Madre del Sur and the mountains of Oaxaca in México, as well as the Chiapan-Guatemalan highlands, and the Cordilleras of Costa Rica and Panama. Alarmingly, the regions of high diversity for bolitoglossines and over 75% of the ranges of the more threatened species could be affected by <i>Bsal</i>. Given the unknown vulnerability of these species, we strongly recommend measures to avoid the introduction of <i>Bsal</i> in the continent.</p>

opencc-zeroNov 2021View details →
dryad28/100

The effect of sampling density and study area size on landscape genetic inferences for the Mississippi slimy salamander (Plethodon mississippi)

<p>In the field of landscape genetics, it is largely unknown how choices regarding population sampling density and study area size impact inferences about which habitat features impede vs. facilitate gene flow. While it is commonly recommended that sampling locations be spaced no further apart than the average individual dispersal distance, for low mobility species, this could lead to a logistically challenging number of sampling locations, or a small and unrepresentative study area. We assessed the effects of sampling density and study area size on landscape genetics inferences for a dispersal-limited amphibian, the Mississippi slimy salamander (<i>Plethodon mississippi</i>), via comparative analysis of nested datasets. Microsatellite-based genetic distances among individuals were divided into three datasets representing either sparse sampling across a large study area, dense sampling across a small study area, or sparse sampling across the same small study area. These datasets were each used as a response variable in maximum likelihood population effects models that assessed the nature and strength of the relationship, if any, between each of five land use classes (i.e., potential predictor variables) and the response variable. Comparative analyses were based on the rank order of effect (i.e., strongest to weakest), sign of effect (i.e., gene flow resistance vs. facilitation), spatial scale of effect, and functional relationship with gene flow. Outcomes were interpreted within the context of five possible combinations of congruence among datasets. We found that each best-fit model associated with the three datasets had the same sign of effect for hardwood forests, manmade structures, and pine forests. However, different sampling densities led to a different inferred functional relationship between agricultural areas and gene flow. Furthermore, study area size appeared to influence the inferred scale of effect of manmade structures and sign of effect of pine forests. Taken together, our findings provided evidence for an influence of sampling density, study area size, and sampling effort upon inferences. Accordingly, in the absence of strong <i>a priori</i> information about spatial-genetic structure and species' life history traits, we recommend iterative subsampling and reanalysis of empirical datasets, coupled with continued investigation into the sensitivities of landscape genetics analyses using simulations or other controlled experimental designs. </p>

opencc-zeroDec 2021View details →
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FIGURE 11 in A nomenclatural and taxonomic review of the salamanders (Urodela) from Holbrook's North American Herpetology

FIGURE 11. Holbrook (1842e)'s illustration by Thomas M. Logan M.D. of Amphiuma means.

opennotspecifiedMay 2022View details →
zenodo28/100

Supplementary material 2 from: Zhang Y, Wang M, Cheng R, Luo Y, Li Y, Liu Z, Chen Q, Shen Y (2022) Mitochondrial characteristics of Pseudohynobius flavomaculatus a protected salamander in China, and biogeographical implications for the family Hynobiidae (Amphibia, Caudata). Zoosystematics and Evolution 98(2): 263-274. https://doi.org/10.3897/zse.98.66578

Figure S2

opencc-zeroJul 2022View details →
zenodo28/100

Supplementary material 1 from: Zhang Y, Wang M, Cheng R, Luo Y, Li Y, Liu Z, Chen Q, Shen Y (2022) Mitochondrial characteristics of Pseudohynobius flavomaculatus a protected salamander in China, and biogeographical implications for the family Hynobiidae (Amphibia, Caudata). Zoosystematics and Evolution 98(2): 263-274. https://doi.org/10.3897/zse.98.66578

Figure S1

opencc-zeroJul 2022View details →
zenodo28/100

Supplementary material 3 from: Zhang Y, Wang M, Cheng R, Luo Y, Li Y, Liu Z, Chen Q, Shen Y (2022) Mitochondrial characteristics of Pseudohynobius flavomaculatus a protected salamander in China, and biogeographical implications for the family Hynobiidae (Amphibia, Caudata). Zoosystematics and Evolution 98(2): 263-274. https://doi.org/10.3897/zse.98.66578

Tables S1, S2

opencc-zeroJul 2022View details →
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FIGURE 7 in Revised taxonomy and distributions of Costa Rican moss salamanders (Caudata: Plethodontidae: Nototriton), with descriptions of new taxa

FIGURE 7. Holotype of Nototriton vereh sp. nov. in life on white background. Photograph by BK.

opennotspecifiedOct 2022View details →
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FIGURE 11 in Revised taxonomy and distributions of Costa Rican moss salamanders (Caudata: Plethodontidae: Nototriton), with descriptions of new taxa

FIGURE 11. Holotype of Nototriton kenorum sp. nov. in life on white background. Photograph by BK.

opennotspecifiedOct 2022View details →
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APPENDIX V in Revised taxonomy and distributions of Costa Rican moss salamanders (Caudata: Plethodontidae: Nototriton), with descriptions of new taxa

APPENDIX V. Morphological measurements taken for the ventral region of the body.

opennotspecifiedOct 2022View details →
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APPENDIX III. Morphological measurements taken for the right side of the head. in Revised taxonomy and distributions of Costa Rican moss salamanders (Caudata: Plethodontidae: Nototriton), with descriptions of new taxa

APPENDIX III. Morphological measurements taken for the right side of the head.

opennotspecifiedOct 2022View details →
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APPENDIX VI in Revised taxonomy and distributions of Costa Rican moss salamanders (Caudata: Plethodontidae: Nototriton), with descriptions of new taxa

APPENDIX VI. Morphological measurements taken for the face.

opennotspecifiedOct 2022View details →

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International Brain Laboratory public data

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OpenNeuro

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Last verified 2026-04-29Open record