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3,538 results for “Lizard”

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F in Predatory behaviour of gekkonid lizards, Ptyodactylus spp., towards the scorpion Leiurus quinquestriatus hebraeus, and their tolerance of its venom

F. 1. Scorpions in the stomach contents of a gecko, adult female Ptyodactylus guttatus from Sede Boqer (from the material of Perry, 1979). The contents included 16 termites, three scorpions, three isopodes and two myriapodes (scale, cm and mm).

opennotspecifiedMar 2003View details →
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FIGURE 6 in Rediscovery of the Earless Microteiid Lizard Anotosaura collaris Amaral, 1933 (Squamata: Gymnophthalmidae): A redescription complemented by osteological, hemipenial, molecular, karyological, physiological and ecological data

FIGURE 6. Results of a discriminant analysis on morphometric measurements of male individuals of Anotosaura collaris (blue circles), A. vanzolinia (green circles), Colobosauroides cearensis (orange diamonds) and Dryadosaura nordestina (red squares). Group centroids are represented by a black dot. In parenthesis is the amount of original variation explained by each axis.

opennotspecifiedOct 2013View details →
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FIGURE 3 in Rediscovery of the Earless Microteiid Lizard Anotosaura collaris Amaral, 1933 (Squamata: Gymnophthalmidae): A redescription complemented by osteological, hemipenial, molecular, karyological, physiological and ecological data

FIGURE 3. Individuals of (A) Anotosaura collaris adult, and (B) juvenile, and its congener Anotosaura vanzolinia (C), in life.

opennotspecifiedOct 2013View details →
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FIGURE 4 in Rediscovery of the Earless Microteiid Lizard Anotosaura collaris Amaral, 1933 (Squamata: Gymnophthalmidae): A redescription complemented by osteological, hemipenial, molecular, karyological, physiological and ecological data

FIGURE 4. Sulcate, lateral and asulcate faces of the left hemipenis of (A) Anotosaura collaris (MZUSP 103845) and (B) A. vanzolinia (MZUSP 95328). Scale bars = 1mm.

opennotspecifiedOct 2013View details →
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FIGURE 1 in Rediscovery of the Earless Microteiid Lizard Anotosaura collaris Amaral, 1933 (Squamata: Gymnophthalmidae): A redescription complemented by osteological, hemipenial, molecular, karyological, physiological and ecological data

FIGURE 1. Lateral (A), ventral (B) and dorsal (C) views of the head, and (D) of the entire body, in ventral (above) and dorsal (below) views of the holotype of Anotosaura collaris (MZUSP 788). Scale bar = 1mm.

opennotspecifiedOct 2013View details →
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FIGURE 8. Phylogenetic relationships recovered through a in Rediscovery of the Earless Microteiid Lizard Anotosaura collaris Amaral, 1933 (Squamata: Gymnophthalmidae): A redescription complemented by osteological, hemipenial, molecular, karyological, physiological and ecological data

FIGURE 8. Phylogenetic relationships recovered through a Bayesian (BA) and Maximum Likelihood (ML) analysis of Anotosaura collaris based on mitochondrial (12S, 16S and ND4) and nuclear genes (C-mos and 18S). The value for posterior probabilities (BA), and bootstrap (ML) are show on branches, respectively.

opennotspecifiedOct 2013View details →
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FIGURE 10 in Rediscovery of the Earless Microteiid Lizard Anotosaura collaris Amaral, 1933 (Squamata: Gymnophthalmidae): A redescription complemented by osteological, hemipenial, molecular, karyological, physiological and ecological data

FIGURE 10. Comparison of environmental temperatures at microhabitats used by Anotosaura collaris with its critical thermal limits. CTmax (red) and CTmin (blue) are species means. Dots around the boxplots represent outliers. Whiskers end at the 5th (below) and and the 95th (above) percentiles. Horizontal lines within the box plot represent the 25th, 50th and 75 quartiles. Temperatures measured in December 2012.

opennotspecifiedOct 2013View details →
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FIGURE 2 in Rediscovery of the Earless Microteiid Lizard Anotosaura collaris Amaral, 1933 (Squamata: Gymnophthalmidae): A redescription complemented by osteological, hemipenial, molecular, karyological, physiological and ecological data

FIGURE 2. Lateral (A), ventral (B) and dorsal (C) views of the head, ventral views of right hand (D) and foot (E), and the cloacal region (F) of Anotosaura collaris (MZUSP 103832). Scale bars = 1 mm.

opennotspecifiedOct 2013View details →
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Figure 2 in The Zagros Mountains acting as a natural barrier to gene flow in the Middle East: more evidence from the evolutionary history of spiny-tailed lizards (Uromasticinae: Saara)

Figure 2. The phylogenetic tree of the Uromasticinae subfamily, including the genera Saara and Uromastyx, based two mtDNA (Cytb and 16S) and one nDNA (ACM4) genes. The trees showed the same topologies for both ML and BI trees, and therefore, only the BI tree is presented. The ML bootstrap values and BI posterior probabilities are next to the nodes, respectively.

opennotspecifiedJul 2021View details →
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Figure 5 in The Zagros Mountains acting as a natural barrier to gene flow in the Middle East: more evidence from the evolutionary history of spiny-tailed lizards (Uromasticinae: Saara)

Figure 5. The biogeographic analysis of Saara with S-DIVA (A) and BBM (B) based on Cytb. For these analyses, three regions were considered: (A: blue nodes) the Mesopotamian plain [or western part of Zagros Mountains (WZM); distribution of S. loricata], (B: green nodes) the central Iranian Plateau [or eastern part of Zagros Mountains (EZM); distribution of S. asmussi] and (C: pink nodes) India/Pakistan (IP); distribution of S. hardwickii. The dark blue and dark green circles around nodes show dispersal and vicariance events, respectively.

opennotspecifiedJul 2021View details →
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Figure 1 in The Zagros Mountains acting as a natural barrier to gene flow in the Middle East: more evidence from the evolutionary history of spiny-tailed lizards (Uromasticinae: Saara)

Figure 1. Geographical distribution range of the genus Saara. The grey circles represent distribution points (the points were obtained from valid references e.g. GBIF, reptile database, etc.) and black circles refer to locations of samples that were used in the genetic analyses. Distribution ranges of S. loricata, S. asmussi and S. hardwickii are illustrated with blue, green and pink cross-hatches, respectively.

opennotspecifiedJul 2021View details →
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Figure 3 in The Zagros Mountains acting as a natural barrier to gene flow in the Middle East: more evidence from the evolutionary history of spiny-tailed lizards (Uromasticinae: Saara)

Figure 3. Parsimony haplotype networks of Saara loricata and S. asmussi based on two mtDNA (Cytb and 16S) genes. The haplogroups (A) and (B) refer to S. loricata with Cytb and 16S, respectively. The haplogroups (C) and (D) refer to S. asmussi with Cytb and 16S, respectively.

opennotspecifiedJul 2021View details →
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Figure 8 in Geographic variation and systematic review of the lizard genus Vanzosaura (Squamata, Gymnophthalmidae), with the description of a new species

Figure 8. Vanzosaura savanicola sp. nov. in life, MZUSP 103197 (field number MTR 14675), paratype. A female individual with 28.2 mm snout–vent length (SVL) from Estação Ecológica Serra Geral do Tocantins, municipality of Almas, Tocantins state, Central Brazil.

opennotspecifiedApr 2014View details →
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Figure 4 in Geographic variation and systematic review of the lizard genus Vanzosaura (Squamata, Gymnophthalmidae), with the description of a new species

Figure 4. Regional variation in the scale counts of Vanzosaura populations: DOR, number of dorsal scales; VEN, number of ventral scales, SCA, number of smooth subcaudals; and FPO, number of femoral pores. White bars represent males; grey bars represent females; CAA, Caatinga; ECE, eastern Cerrado; WCE + CHA, western Cerrado + Chaco.

opennotspecifiedApr 2014View details →
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Figure 3 in Geographic variation and systematic review of the lizard genus Vanzosaura (Squamata, Gymnophthalmidae), with the description of a new species

Figure 3. Vanzosaura concatenated mitochondrial maximum-likelihood genealogy based on one individual per locality (N = 40). Trees based on the complete data set (N = 186) and on unique haplotypes (N = 154) are presented in Figures S1–S2. Terminal names show the voucher numbers followed by a short code for the locality (for full details, see Appendix 1). Nodes with boostrap nodal support values ≥ 75 are depicted in the tree. Colours and symbols represent the geographical groups and the species limits proposed here: circles, Vanzosaura multiscutata comb. nov. from Caatinga (CAA); squares, Vanzosaura rubricauda from Chaco and western Cerrado (CHA + WCE); triangles, Vanzosaura savanicola sp. nov. from the Eastern Cerrado (ECE).

opennotspecifiedApr 2014View details →
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Figure 6 in Geographic variation and systematic review of the lizard genus Vanzosaura (Squamata, Gymnophthalmidae), with the description of a new species

Figure 6. Frequencies of colour patterns observed in different populations of Vanzosaura spp. (N> 10 individuals) across the distribution of the genus.

opennotspecifiedApr 2014View details →
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Figure 12 in Geographic variation and systematic review of the lizard genus Vanzosaura (Squamata, Gymnophthalmidae), with the description of a new species

Figure 12. Holotype of Vanzosaura multiscutata (Amaral, 1933) comb. nov., MZUSP 40079, adult male from municipality of Senhor do Bonfim, Bahia, Brazil.

opennotspecifiedApr 2014View details →
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Figure 2 in Geographic variation and systematic review of the lizard genus Vanzosaura (Squamata, Gymnophthalmidae), with the description of a new species

Figure 2. Colour patterns recognized in Vanzosaura spp.: complex (A); intermediate (B); and simple (C). See text for details.

opennotspecifiedApr 2014View details →
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Figure 5 in Geographic variation and systematic review of the lizard genus Vanzosaura (Squamata, Gymnophthalmidae), with the description of a new species

Figure 5. Frequencies of contact (dark grey) and separation (light grey) between the prefrontal scales in the populations from three regional groups of Vanzosaura: CAA, Caatinga; ECE, eastern Cerrado; WCE + CHA, western Cerrado + Chaco.

opennotspecifiedApr 2014View details →
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FIGURE 2 in A critical review and systematic discussion of recent classification proposals for liolaemid lizards

FIGURE 2. Phylogenetic relationships among the major clades of Liolaemus lizards, detailing relationships within the lineomaculatus section, as currently understood (black text) and proposed by Pincheira-Donoso and Núñez (2005; red text). Relationships are those recovered by Espinoza et al. (2004) using morphological and molecular data. Major clade names follow Etheridge (1995) and Schulte et al. (2000). As defined by P-D&N, (1) their subgenus Vilcunia is paraphyletic and nested within Eulaemus; (2) their subgenus Liolaemus is polyphyletic with respect to some members of the lineomaculatus section of the subgenus Eulaemus; and (3) their subgenus Donosolaemus, albeit monophyletic, is nested within the subgenus Eulaemus. See text for details and Fig. 1 for additional comments.

opennotspecifiedJul 2010View details →

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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.

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OpenNeuro

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