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FIGURE 7 in A new species of fan-throated lizard of the genus Sitana Cuvier, 1829 from coastal Kerala, southern India
FIGURE 7. Maximum-likelihood phylogeny of Draconinae based on 1017bp of mitochondrial Nicotinamide adenine dinucleotide dehydrogenase (NADH) subunit 2 gene. Nodes with high support indicated by black circle (ML? 95, Bayesian PP> 0.99), nodes with support only from Bayesian analyses indicated by grey circles. Species of the genus Sitana have been collapsed for representation purpose. Outgroup, Bufoniceps laungwalaensis has been removed.
FIGURE 5 in A new species of fan-throated lizard of the genus Sitana Cuvier, 1829 from coastal Kerala, southern India
FIGURE 5. Sitana attenboroughii sp. nov. in life, (A) holotype male BNHS 2481, (B) paratype male BNHS 2482.
FIGURE 4 in A new species of fan-throated lizard of the genus Sitana Cuvier, 1829 from coastal Kerala, southern India
FIGURE 4. Sitana attenboroughii sp. nov. hind limb showing arrangement of scales on posterior aspect of thigh. (A–B) holotype male BNHS 2481, (C–D) paratype male BNHS 2482.
FIGURE 1 in A new species of fan-throated lizard of the genus Sitana Cuvier, 1829 from coastal Kerala, southern India
FIGURE 1. Sitana attenboroughii sp. nov. holotype male BNHS 2481, (A) dorsal, (B) ventral. Scale bar 10mm.
FIGURE 2 in A new species of fan-throated lizard of the genus Sitana Cuvier, 1829 from coastal Kerala, southern India
FIGURE 2. Sitana attenboroughii sp. nov. holotype male BNHS 2481 dorsal view of head. Scale bar 10mm.
FIGURE 3 in A new species of fan-throated lizard of the genus Sitana Cuvier, 1829 from coastal Kerala, southern India
FIGURE 3. Sitana attenboroughii sp. nov. holotype male BNHS 2481 latersal view of head. Scale bar 10mm.
FIGURE 7 in A new species of scincid lizard in the genus Oligosoma (Reptilia: Scincidae) from the mid-Canterbury high country, New Zealand
FIGURE 7. Relationship of taxa within Oligosoma Clade 1 of Chapple et al. (2009)—phylogenetic tree of Maximum Likelihood (ML) from five mitochondrial genes (ND2, ND4, Cytb, 16SrRNA, 12SrRNA) and one nuclear gene (Rag-1); ML bootstrap values and Bayesian posterior probabilities for all branches are 100 and 1.0, respectively [after Chapple et al. 2009]. The newly described species Oligosoma hoparatea sp. nov. is highlighted.
FIGURE 6 in A new species of scincid lizard in the genus Oligosoma (Reptilia: Scincidae) from the mid-Canterbury high country, New Zealand
FIGURE 6. Detailed drawings of the holotype of Oligosoma hoparatea sp. nov.—dorsal (upper left), left side (middle left) and ventral (lower left) surfaces of the head showing details of the scalation, and the upper surface of the left front foot (upper right) and lower surface of the left hind foot (lower right). Scale bar = 5 mm and scale is the same for all drawings.
FIGURE 3 in A new species of scincid lizard in the genus Oligosoma (Reptilia: Scincidae) from the mid-Canterbury high country, New Zealand
FIGURE 3. Active greywacke screes at the type locality at 1050 m on the north face Mt Harper showing 'islands' of vegetation amongst large expanses of gravel and boulders that are the habitat of Oligosoma hoparatea sp. nov. [Photograph: Marieke Lettink].
FIGURE 1 in A new species of scincid lizard in the genus Oligosoma (Reptilia: Scincidae) from the mid-Canterbury high country, New Zealand
FIGURE 1. Distribution of Oligosoma hoparatea sp. nov. in the mid-Canterbury high country of the South Island, New Zealand: 1 = type locality on the north face of Mt Harper, 2 = Mt Somers Range (note: the map resolution is insufficient to show all four sites due to the small distance between sites on the same range).
FIGURES 4 & 5 in A new species of scincid lizard in the genus Oligosoma (Reptilia: Scincidae) from the mid-Canterbury high country, New Zealand
FIGURES 4 & 5. Wild Oligosoma hoparatea sp. nov. photographed on screes at the type locality, Mt Harper, January 2010 [Photographs: Marieke Lettink].
FIGURE 2 in A new species of scincid lizard in the genus Oligosoma (Reptilia: Scincidae) from the mid-Canterbury high country, New Zealand
FIGURE 2. North face of Mt Harper viewed from the northern shore of Lake Camp showing the rounded landform with steeply-incised gullies with associated active screes and large outwash fans. Oligosoma hoparatea sp. nov. has been found in screes in the gully at the left (the type locality) and to the left of centre [Photograph: Don Geddes].
Does forest degradation affect lizard assemblage in the Arid Chaco Ecoregion? Dataset
<p>The dataset contains information about vegetation coverage and abundance of three lizard species from two sites with differents degrees of disturbance in the Arid Chaco Ecoregion. Monthly samplings were conducted from November to February during the summer of 2014-2015. Two forested areas were selected for comparison: one section that had experienced high amounts of degradation and one section that had suffered only slight degradation. Observers conducted diurnal visual encounter surveys along seven 200 m long transects in each of the two sites. A total of 14 independent systematically distributed transects were conducted, separated by 50 m parallel intervals. All the surveys were performed under similar weather conditions. We categorized the lizards by sex (male and female) and age (adults and juveniles). The microhabitat ground cover characteristics we assessed were: 1) bare ground, 2) herbs/grass, 3) litter, 4) cacti, and 5) rocks; number of shrubs and trees; and the number of vegetal species. To obtain microhabitat coverage data, pictures were taken where the animals were observed at a distance of 1.5 m above the ground. Using the photographs, we calculated the proportion of each microhabitat coverage characteristic. To calculate the number of trees and shrubs a two meter by two meter cardinally oriented X was superimposed over the exact point where the subjects were found and an observer traced the axis counting the number of trees and shrubs that crossed the line. The total number of vegetal species within each delimited area determined its richness.</p>
Supplementary material 2 from: Nieto-Montes de Oca A, Sánchez-Vega H, Durán-Fuentes I (2018) A new species of knob-scaled lizard (Xenosauridae, Xenosaurus) from the Sierra Madre Oriental of Puebla, Mexico. ZooKeys 737: 141-160. https://doi.org/10.3897/zookeys.737.15095
Variation in selected characters in the genus Xenosaurus : Explanation note: Xenosaurus clades after Nieto-Montes de Oca et al. (2017).
FIGURE 2. Individuals from a in Molecular evidence for conspecificity of two desert Liolaemus lizards (Iguania: Liolaemidae)
FIGURE 2. Individuals from a) near Caspana (MUAP-114), near type locality for Liolaemus audituvelatus; b) Diego de Almagro, type locality of L. manueli; c) and d) Altos Quebrada Agua Colorada; e) and f) Barranquilla (near Caseron). f) is a gravid female. Note that b) male of L. audituvelatus from known distribution and d) male of L. manueli from type locality, are identical and were found 300 km away (in straight line); and, a) and e) are also similar and were found 600 km away (in straight line).
FIGURE 1 in Molecular evidence for conspecificity of two desert Liolaemus lizards (Iguania: Liolaemidae)
FIGURE 1. Distribution maps of Liolaemus audituvelatus and L. manueli based on historical and new records. Type localities of both species are indicated by stars. Historical records of both species gathered from Núñez et al. (1998, 2003, 2012) and GBIF (2016) also are indicated by black circles and squares. New localities of L. audituvelatus are indicated by red circles and red squares for L. manueli. Localities from which DNA samples were obtained for the analyses of this study are indicated with green triangles. The geographic references are in Appendix S2.
FIGURE 5 in Molecular evidence for conspecificity of two desert Liolaemus lizards (Iguania: Liolaemidae)
FIGURE 5. Results of the species delimitation analyses. On the left, the Bayesian consensus topology used for PTP and mPTP analyses is shown. On the right, boxes represent the species delimitations obtained with the three methods, in comparison with the current taxonomy (column nominal taxa).
FIGURE 4 in Molecular evidence for conspecificity of two desert Liolaemus lizards (Iguania: Liolaemidae)
FIGURE 4. Bayesian consensus tree showing the phylogenetic relationships among species of the montanus group and new populations related to L. audituvelatus and L. manueli. Posterior probability is indicated at each node.
FIGURE 3 in Molecular evidence for conspecificity of two desert Liolaemus lizards (Iguania: Liolaemidae)
FIGURE 3. Specimens of Liolaemus audituvelatus collected near Caspana, 65 km north of San Pedro de Atacama, Antofagasta Region (MUAP-113 (LNC135) and MUAP-114 (LNC136)).
FIGURE 2 in A phylogenetic assessment of the meadow lizard Darevskia praticola (Eversmann, 1834) from Iran
FIGURE 2. Phylogenetic tree for ND4 gene, aS BayeSian and ML analySeS Show Similar tree topologieS only the ML tree iS preSented. NumberS on brancheS are bootStrap Support valueS for ML (below) and poSterior probability valueS for BayeSian (above) analySeS. Only valueS greater than 70 and 0.7, reSpectively, are Shown
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.
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.