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1,047 results for “Salamanders”

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zenodo28/100

Figure 2 in Systematics of dusky salamanders, Desmognathus (Caudata: Plethodontidae), in the mountain and Piedmont regions of Virginia and North Carolina, USA

Figure 2. Estimated natural logarithm of the probability of obtaining the genotypic data across 19 variable loci plotted against the number of designated population clusters. Lines connect median values of –lnP(data|K).

opencc-by-4.0Jan 2008View details →
zenodo28/100

Figure 1 in Systematics of dusky salamanders, Desmognathus (Caudata: Plethodontidae), in the mountain and Piedmont regions of Virginia and North Carolina, USA

Figure 1. Sample localities. The triangle (Population 15) indicates the type locality of Desmognathus planiceps. Solid lines in the lower map indicate approximate boundaries of physiographic provinces.

opencc-by-4.0Jan 2008View details →
zenodo28/100

Figure 5. A in Metamorphosis and evolution of feeding behaviour in salamanders of the family Plethodontidae

Figure 5. A, Kinematic profiles of suction feeding in larval D. quadramaculatus. Gape distance shows a symmetrical profile, with mouth opening and closing taking nearly the same amount of time. Peak hyobranchial depression follows peak gape. Head lifting occurs during mouth opening and head dipping during mouth closing. Note the extremely rapid gape cycle which takes only 28 ms. B, Suction feeding in larval G. porphyriticus. As in A, mouth opening and closing are of nearly the same duration, peak hyobranchial depression follows peak gape, and the gape cycle is extremely rapid at 29 ms.

opencc-by-4.0Apr 2002View details →
zenodo28/100

Figure 6 in A Late Jurassic salamander (Amphibia: Caudata) from the Morrison Formation of North America

Figure 6. Iridotriton hechti gen. et sp. nov., DINO 16453a. Skull region, as exposed. Abbreviations: al.pr, alary process of premaxilla; At, atlas; Crb.2, rib of second vertebra; Cv.2, second vertebra; L.An, left angular; L.D, left dentary; L.Fr, left frontal; L.Mx, left maxilla; L.Oc. left otic capsule; L.P, parietal; L.Pmx, left premaxilla; L.Pra, left prearticular; L.Prf, left prefrontal; L.Pt, left pterygoid; L.Sq, left squamosal; N, possible left nasal; Ps, parasphenoid; R.D, right dentary;?R.Fr, possible right frontal; R.Mx, right maxilla; R.N, right nasal; R.Oc, right otic capsule; R.P, right parietal; R.Pmx, right premaxilla; R.Pt, right pterygoid;?R.Sq, possible right squamosal; St, stapes. Scale bar = 1 mm.

opencc-by-4.0Apr 2005View details →
zenodo28/100

FIGURE 11. A in Two new Salamanders of the genus Onychodactylus from Eastern Honshu, Japan (Amphibia, Caudata, Hynobiidae)

FIGURE 11. A male paratype of O. fuscus sp. nov. (KUHE 48283) in life.

opennotspecifiedDec 2014View details →
zenodo28/100

FIGURE 5 in Two new Salamanders of the genus Onychodactylus from Eastern Honshu, Japan (Amphibia, Caudata, Hynobiidae)

FIGURE 5. Male holotype of O. intermedius sp. nov. (KUHE 47455) in life.

opennotspecifiedDec 2014View details →
dryad28/100

Biological size as a predictor of physiological performance and evolution: Evidence from lungless salamanders

<p>Gross physiological performance in multicellular organisms coordinates processes operating from the cellular to whole-organism level, and thus may be influenced by physical constraints imposed by both cell size and body size. A useful measure of joint cell and body size variation is biological size, defined here as the ratio of body volume to mean cell volume. We surveyed literature data across four vertebrate clades and documented wide variation in two proxies for biological size, even between species of equivalent body size. We evaluated these proxies in a sample of lungless salamanders (Urodela: Plethodontidae) and used linear and evolutionary regressions to compare their power to predict variation in metabolic and water loss physiology to that of body size alone. One proxy (the ratio of body length to the square root of genome size) consistently outperformed mass in predicting water loss rates, and residual variation from evolutionary trends in the other proxy (the ratio of mass to genome size) consistently explained the most variance across all physiological responses. These results suggest that for some traits in some taxa, biological size may be a more functionally relevant predictor of performance than body size alone. Physiological ecology is replete with studies characterizing the effects of body size. We suggest that future studies of size effects additionally consider the role of cell size variation (and genome size variation as one of its determinants) to improve our understanding of when and how biological size influences organismal form and function.</p>

opencc-zeroDec 2022View details →
zenodo28/100

Fig. 4 in Larval Development And Habitat Usage Of Stream-Breeding Fire Salamanders In An Urban Environment

Fig. 4. Principal components analysis of stream substrate composition at 16 stream segments, "Hűvös-ér" stream. PC1 described a gradient from stream segments with a high % cover of fine gravel to segments with a high % cover of concrete. PC2 described a gradient from segments with a high % cover of sand to segments with a high cover of stones

opencc-by-4.0Oct 2022View details →
zenodo28/100

FIGURE 4. The estimated delta K and mean lnL values for each K in Taxonomic reassessment of salamanders (genus Hynobius) from Tsushima Islands Japan, with a resurrection of Hynobius tagoi Dunn, 1923 (Amphibia: Caudata)

FIGURE 4. The estimated delta K and mean lnL values for each K.

opennotspecifiedAug 2023View details →
dryad28/100

Relaxed predation selection on rare morphs of Ensatina salamanders (Caudata: Plethodontidae) promotes a polymorphic population in a novel dune sand habitat

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publicNov 2020View details →
dryad28/100

Data from: Correlations of life-history and distributional-range variation with salamander diversification rates: evidence for species selection

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publicAug 2010View details →
dryad28/100

Data from: Habitat attributes associated with short-term settlement of Ozark hellbender (Cryptobranchus alleganiensis bishopi) salamanders following translocation to the wild

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publicApr 2013View details →
dryad28/100

Data from: LTR retrotransposons contribute to genomic gigantism in plethodontid salamanders

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publicMar 2012View details →
dryad28/100

Data from: The effects of contig length and depth on the estimation of SNP frequencies, and the relative abundance of SNPs in protein-coding and non-coding transcripts of tiger salamanders (Ambystoma tigrinum)

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publicJun 2012View details →
dryad28/100

Vastly underestimated radiation of Amazonian salamanders (Plethodontidae: Bolitoglossa) and implications about plethodontid diversification

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publicApr 2020View details →
dryad28/100

Data from: Preservation-induced morphological change in salamanders and failed DNA extraction from a decades-old museum specimen: implications for Plethodon ainsworthi

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publicFeb 2020View details →
dryad28/100

Data from: Color-biased dispersal inferred by fine-scale genetic spatial autocorrelation in a color polymorphic salamander

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publicApr 2017View details →
dryad28/100

Data from: Molecular phylogenetics of desmognathine salamanders (Caudata: Plethodontidae): a reevaluation of evolution in ecology, life history, and morphology

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publicJul 2009View details →
dryad28/100

Data from: Comparative limb bone loading in the humerus and femur of the tiger salamander: testing the ‘mixed-chain’ hypothesis for skeletal safety factors

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publicJan 2016View details →
dryad28/100

Data from: Bony labyrinth morphometry reveals hidden diversity in lungless salamanders (Family Plethodontidae): structural correlates of ecology, development, and vision in the inner ear

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publicAug 2019View details →

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DANDI Archive for NWB datasets

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dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record