Find research datasets worth reusing

opencc-by-4.0Jan 2020View details →

Figure 1 in Age and growth in two populations of Danford's lizard, Anatololacerta danfordi (Günther, 1876), from the eastern Mediterranean

Figure 1. Map showing localities of studied A. danfordi populations. K: Kozan population, S: Saimbeyli population.

opencc-by-4.0Apr 2020View details →

Fig. 2 in Detection and molecular characterization of Cryptosporidium species in wildcaught pet spiny-tailed lizards

Fig. 2. Phylogenetic relationships between Cryptosporidium sp. from the mastigures and other Cryptosporidium spp. The mid-point tree was generated with the neighbor-joining method using Tamura 3-parameter plus Gamma distribution. Nodal values represent boot strap values (> 50%) for neighbor-joining (left) and ML (right). Circle represents the major reptile-associated species. Bar represents the number of nucleotide substitutions per sites.

opencc-by-4.0Apr 2020View details →

Fig. 3 in Detection and molecular characterization of Cryptosporidium species in wildcaught pet spiny-tailed lizards

Fig. 3. Phylogenetic relationships of Cryptosporidium detected from the Arabian blue mastigure and closely-related species/subtypes as inferred by a maximum likelihood analysis of concatenated sequences were constructed from the partial DNA sequences of SSU (left), actin (middle), and HSP70 (right) loci. Numbers represent the boot strap values for NJ (left) and ML (Right). Bar represents the number of nucleotide substitutions per sites. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opencc-by-4.0Apr 2020View details →

Fig. 1 in Detection and molecular characterization of Cryptosporidium species in wildcaught pet spiny-tailed lizards

Fig. 1. Histological findings of the deceased Arabian blue mastigure. (A) jejunoileum showing villous atrophy, muscle layer edema, and degenerated epithelial cells in the lumen. Bar = 500 μm. (B) Cryptosporidium appear as rounded purple structures (arrowheads) on the microvilli of the epithelial cells. HE staining. Bar = 50 μm. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opencc-by-4.0Nov 2021View details →

Fig. 1 in Rapid endangerment of the lizard Podarcis pityusensis by an invasive snake demands an immediate conservation response

Fig. 1. Basic elements of the system. (A) Map showing the location of Ibiza island in relation to the nearest mainland areas in the Iberian Peninsula and northern Africa. (B) The endemic lacertid lizard, Podarcis pityusensis. (C) The invasive colubrid snake, Hemorrhois hippocrepis. Photos by: Javier Pleguezuelos (A), Juan M. Pleguezuelos (B), and Federico Rey (C).

Fig. 6 in A reevaluation of records of Sandveld lizards, Nucras Gray, 1838 (Squamata: Lacertidae), from northern Namibia

Fig. 6. Nucras aff. broadleyi (CAS 214642). (A) Whole body dorsum, (B) lateral view of head, and (C) dorsal view of head. Note the patterning resembling Nucras intertexta and the prominent occipital scale. Photos by M. Murdoch.

Fig. 7 in A reevaluation of records of Sandveld lizards, Nucras Gray, 1838 (Squamata: Lacertidae), from northern Namibia

Fig. 7. Life photo of Nucras aff. broadleyi (CAS 214642) from 48 km west of Kamanjab on the road to Torra Bay (-19.65389, 14.35083), Kunene Region, Namibia. Photo by Randall Babb.

Fig. 5 in A reevaluation of records of Sandveld lizards, Nucras Gray, 1838 (Squamata: Lacertidae), from northern Namibia

Fig. 5. Map of Namibia showing the distribution of Nucras damarana (green circles) and N. cf. broadleyi (blue triangle). Black borders indicate regional boundaries. Regions mentioned in the text are: KU – Kunene, OH – Ohangwena, OM – Omasati, OS – Oshana, OK – Oshikoto, and OT – Otjozondjupa. Map courtesy of Edward L. Stanley.

Fig. 4 in A reevaluation of records of Sandveld lizards, Nucras Gray, 1838 (Squamata: Lacertidae), from northern Namibia

Fig. 4. (A) Life photo of Nucras damarana (MCZ R-190201) from 60 km SE of Ruacana crossroads (-17.48558, 14.86608), Omusati Region, Namibia. (B) Life photo of Nucras holubi from Alldays, Limpopo Province, Republic of South Africa. Note differences in dorsal and lateral patterning. Photos copyright by Johan Marais.

Fig. 3 in A reevaluation of records of Sandveld lizards, Nucras Gray, 1838 (Squamata: Lacertidae), from northern Namibia

Fig. 3. Nucras damarana (MCZ R-190201). (A) Whole body dorsum, (B) lateral view of head, and (C) dorsal view of head. Note the single row of spots and dashes on each flank, and the absence of a discrete occipital scale. Photos by M. Murdoch.

Fig. 2 in A reevaluation of records of Sandveld lizards, Nucras Gray, 1838 (Squamata: Lacertidae), from northern Namibia

Fig. 2. Syntype series of Nucras intertexta damarana Parker, 1936 (NHMUK 1946. 1946.8.6.17–24) from Sissekab (-19.328645, 17.196238), Otjozondjupa Region, Namibia. The image has been modified to provide a uniform background and some extraneous string has been deleted. Photo by A.M. Bauer.

Fig. 1 in A reevaluation of records of Sandveld lizards, Nucras Gray, 1838 (Squamata: Lacertidae), from northern Namibia

Fig. 1. Concatenated mitochondrial RaxML phylogram of the genus Nucras and outgroups used in this study. Bootstrap support (above) and posterior probabilities (below) are shown for the species level and more inclusive nodes. Select nodes containing individuals with identical or minor sequence divergence (less than 2%) from shared localities and from non-focal taxa have been collapsed in order to condense overall tree size; but a full list of the specimens used in this study can be found in Table 1.

Fig. 6 in A new species of the genus Ceratophora Gray, 1835 (Reptilia: Agamidae) from a lowland rainforest in Sri Lanka, with insights on rostral appendage evolution in Sri Lankan agamid lizards

Fig. 6. Ceratophora ukuwelai sp. nov. in life in-situ. (A) Female holotype (NMSL 2020.05.01) in dorsolateral view; (B) male specimen (not collected) in dorsolateral aspect showing rostral appendage; (C) female paratype (NMSL 2020.05.02) in dorsal view. Photos by Suranjan Karunarathna and Sanjaya Kanishka.

Fig. 2 in A new species of the genus Ceratophora Gray, 1835 (Reptilia: Agamidae) from a lowland rainforest in Sri Lanka, with insights on rostral appendage evolution in Sri Lankan agamid lizards

Fig. 2. Bayesian inference tree of Draconinae lizards derived from the analysis of 1,084 bp of ND2 gene sequences. For voucher specimen information and GenBank accession numbers see Table 1. Numbers at tree nodes correspond to BI PP/ML BS support values, respectively; a black circle at a node indicates it is strongly supported (BI PP> 0.95; ML BS> 75%). Colors of clades and locality numbers correspond to those in Fig. 1. Photos by Sanoj Wijayasekara and Sanjaya Kanishka.

Fig. 7 in A new species of the genus Ceratophora Gray, 1835 (Reptilia: Agamidae) from a lowland rainforest in Sri Lanka, with insights on rostral appendage evolution in Sri Lankan agamid lizards

Fig. 7. Habitat of Ceratophora ukuwelai sp. nov. at type locality in Salgala Forest, Kegalle District, Sri Lanka. (A) General view of Salgala Forest; (B) microhabitat of the new species inside the dense forest with good canopy cover and thick leaf litter. Photos by Suranjan Karunarathna.

Fig. 1 in A new species of the genus Ceratophora Gray, 1835 (Reptilia: Agamidae) from a lowland rainforest in Sri Lanka, with insights on rostral appendage evolution in Sri Lankan agamid lizards

Fig. 1. Currently known distribution of Ceratophora ukuwelai sp. nov. and other localities for Ceratophora species examined in the present study. For locality numbers see Table 1. Colors of icons correspond to those in Fig. 2. Star denotes the type locality of the new species (Salgala Forest, Kegalle District, Sri Lanka).

Fig. 3 in A new species of the genus Ceratophora Gray, 1835 (Reptilia: Agamidae) from a lowland rainforest in Sri Lanka, with insights on rostral appendage evolution in Sri Lankan agamid lizards

Fig. 3. Bayesian chronogram for Draconinae resulting from BEAST analysis of 1,084 bp of ND2 gene sequences. Node values correspond to estimated divergence times (in Ma). Blue bars correspond to 95% confidence intervals.

Fig. 4 in A new species of the genus Ceratophora Gray, 1835 (Reptilia: Agamidae) from a lowland rainforest in Sri Lanka, with insights on rostral appendage evolution in Sri Lankan agamid lizards

Fig. 4. Relative rostral appendage (RAL/SVL) evolution among members of the Sri Lankan agamids (genera Ceratophora, Lyriocephalus, and Cophotis). See Table 2 for RAL/SVL data. Colors of branches correspond to average RAL/SVL values in males (A) and females (B); thumbnails show profiles of the respective lizard species (not to scale). Photos by Sanoj Wijayasekara, Sanjaya Kanishka, and Suranjan Karunarathna.

Fig. 5 in A new species of the genus Ceratophora Gray, 1835 (Reptilia: Agamidae) from a lowland rainforest in Sri Lanka, with insights on rostral appendage evolution in Sri Lankan agamid lizards

Fig. 5. Morphology of Ceratophora ukuwelai sp. nov. holotype, adult female (NMSL 2020.05.01). (A) Head in dorsal view; (B) head in ventral view; (C) head in lateral view; (D) heterogeneous scales on dorsal surface of trunk; (E) keeled ventral scales; (F) lateral surfaces of trunk showing heterogeneous scales; (G–H) dorsal and ventral surfaces of femur showing sharp spines; (I) subdigital lamellae on manus; (J) subdigital lamellae on pes; (K) hexagonal-shaped subcaudals. Photos by Suranjan Karunarathna.

Fig. 8 in A new species of the genus Ceratophora Gray, 1835 (Reptilia: Agamidae) from a lowland rainforest in Sri Lanka, with insights on rostral appendage evolution in Sri Lankan agamid lizards

Fig. 8. Syntypes of Ceratophora aspera Günther, 1864 in lateral view: BMNH.1946.30.51 (female, above) and BMNH.1946.30.52 (male, below). Photo by Colin McCarthy (BMNH).