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69 results for “Geoemydidae”

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Fig. 4 in Body Size And Ectoparasitic Infestations In The Mediterranean Pond Turtle, Mauremys Leprosa (Testudines, Geoemydidae), In Majen Belahriti Pond (North-Eastern Algeria)

Fig. 4. Linear regression of body weight (BW) on carapace length (CL) for Mauremys leprosa (N = 43).

opencc-by-4.0Jun 2024View details →
zenodo40/100

Fig. 2 in Geographical and elevational distributions of the Black-breasted Leaf Turtle, Geoemyda spengleri (Gmelin, 1789) (Testudines: Geoemydidae)

Fig. 2. Relationship between elevation and latitude of reliable Geoemyda spengleri occurrences with low positional error (n = 33).

opencc-by-4.0Aug 2022View details →
zenodo40/100

Fig. 1 in Geographical and elevational distributions of the Black-breasted Leaf Turtle, Geoemyda spengleri (Gmelin, 1789) (Testudines: Geoemydidae)

Fig. 1. Geographical distribution of Geoemyda spengleri based on hydrologic unit compartments (Level 10 HUCs). Positions of the reliable occurrences (n = 77) are approximate, as the coordinates were generalized by rounding (see text for details). Multiple symbols may overlap and appear as a single point. Not all localities are shown to protect particularly sensitive populations. Inset: Adult male Geoemyda spengleri from Guangxi Autonomous Region, China. Photo by Jeffrey E. Dawson.

opencc-by-4.0Aug 2022View details →
zenodo40/100

Figure 6 in Phylogenetic relationships and biogeographical history of the genus Rhinoclemmys Fitzinger, 1835 and the monophyly of the turtle family Geoemydidae (Testudines: Testudinoidea)

Figure 6. Time calibration using the program BEAST. The error bar on each node represents the 95% confidence interval calculated by the program. The column on the right shows the time slice of Isthmian closure (3.5–2.5 Mya; Coates & Obando, 1996). Pli + Ple: Pliocene + Pleistocene.

opencc-by-4.0Aug 2008View details →
zenodo40/100

Figure 4 in Phylogenetic relationships and biogeographical history of the genus Rhinoclemmys Fitzinger, 1835 and the monophyly of the turtle family Geoemydidae (Testudines: Testudinoidea)

Figure 4. Strict consensus of three most parsimonious trees produced from 3373 aligned characters (TL = 3337; CI = 0.43; RI = 0.59) using maximum parsimony. Of these, 2315 are constant characters and 798 are potentially parsimony-informative. Numbers above and below branches are bootstrap (> 50%) and Bremer values, respectively.

opencc-by-4.0Aug 2008View details →
zenodo40/100

Figure 3. A, the single most parsimonious tree derived from 2129 in Phylogenetic relationships and biogeographical history of the genus Rhinoclemmys Fitzinger, 1835 and the monophyly of the turtle family Geoemydidae (Testudines: Testudinoidea)

Figure 3. A, the single most parsimonious tree derived from 2129 aligned characters of mitochondrial genes (12S, 16S, cyt-b) (CI = 0.40; TL = 31; RI = 0.58) using maximum parsimony. Of these, 1229 characters are constant and 708 characters are parsimony-informative. Numbers above branches are bootstrap values and below are Bremer values. B, strict consensus of 96 trees generated from 1244 aligned characters of nuclear genes (Rag1 and Cmos) (CI = 0.82; TL = 205; RI = 0.84) using maximum parsimony. Of these, 1086 characters are constant and 90 are parsimonyinformative. Numbers above branches are bootstrap values and below are Bremer values.

opencc-by-4.0Aug 2008View details →
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Figure 2 in Phylogenetic relationships and biogeographical history of the genus Rhinoclemmys Fitzinger, 1835 and the monophyly of the turtle family Geoemydidae (Testudines: Testudinoidea)

Figure 2. Previous hypotheses regarding the position of Rhinoclemmys among geoemydids (upper cladograms) and the relationships among the species of the genus (lower cladograms). †Fossil taxon.

opencc-by-4.0Aug 2008View details →
zenodo36/100

Fig. 3 in Body Size And Ectoparasitic Infestations In The Mediterranean Pond Turtle, Mauremys Leprosa (Testudines, Geoemydidae), In Majen Belahriti Pond (North-Eastern Algeria)

Fig. 3. Size structure of the population of Mauremys leprosa.

opencc-by-4.0Jun 2024View details →
zenodo36/100

Fig. 2 in Body Size And Ectoparasitic Infestations In The Mediterranean Pond Turtle, Mauremys Leprosa (Testudines, Geoemydidae), In Majen Belahriti Pond (North-Eastern Algeria)

Fig. 2. Morphometrical variables of Mauremys leprosa (for abbreviations see table 3).

opencc-by-4.0Jun 2024View details →
zenodo36/100

Figure 1 in Phylogenetic relationships and biogeographical history of the genus Rhinoclemmys Fitzinger, 1835 and the monophyly of the turtle family Geoemydidae (Testudines: Testudinoidea)

Figure 1. Distribution of the family Geoemydidae (data compiled from Iverson, 1992).

opencc-by-4.0Aug 2008View details →
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FIGURE 4 in First description of neonate Batagur trivittata (Testudines: Geoemydidae)

FIGURE 4. Head of neonate Batagur trivittata. Note caruncle (egg-tooth) and eye color. The caruncle is lost during the two months after hatching. (Photographed by Myo Min Win).

opennotspecifiedJul 2020View details →
dryad32/100

Data from: The first complete mitochondrial genome of the Indian Tent Turtle, Pangshura tentoria (Testudines: Geoemydidae): characterization and comparative analysis

Characterization of complete mitogenome is a widely used genomics study for species delineation and evolutionary research. However, the sequences and structural motifs contained within the mitogenome have been rarely examined to understand the phylogeny and evolutionary history among Testudines. Hence, the mitogenomic features of several Testudines taxa are still anonymous to the scientific communities. The present study decodes the first complete mitochondrial genome of the Indian Tent Turtle, Pangshura tentoria (16,657 bp) by using next-generation sequencing. This denovo assembly encodes 37 genes: 13 protein coding genes (PCGs), 22 transfer RNA (tRNAs), two ribosomal RNA (rRNAs), and one control region (CR). The mitogenome contained 19 intergenic spacer and six overlapping regions. Most of the genes were encoded on majority strand, except for one PCG (NADH dehydrogenase subunit 6) and eight tRNAs. Most of the PCGs were started with an ATG initiation codon, except for cytochrome oxidase subunit 1 with 'GTG' and NADH dehydrogenase subunit 5 with 'ATA'. The termination codons, 'TAA' and 'AGA' were observed in NADH dehydrogenase subunit 4l and NADH dehydrogenase subunit 6 respectively. The Relative Synonymous Codon Usage analysis revealed the maximum abundance of Alanine, Isoleucine, Leucine, and Threonine. The non-synonymous/synonymous ratios were <1 in all PCGs, which indicates strong negative selection among all Geoemydid species. The study also found the typical cloverleaf secondary structure in most of the tRNA genes, except for Serine (trnS1) with lack of the conventional DHU arm. The Wobble base pairing was observed in the different stems (DHU, acceptor, and anticodon) of 11 tRNAs. The comparative study of Geoemydid mitogenomes revealed the occurrence of tandem repeats was frequent in the 3´ end of CR. Further, two copies of a unique tandem repeat 'TTCTCTTT' were identified in P. tentoria. The Bayesian and Maximum Likelihood phylogenetic trees using concatenation of 13 PCGs revealed the close relationships of P. tentoria with Batagur trivittata in the studied dataset. All the Geoemydid species showed distinct clustering with high bootstrap support congruent with previous evolutionary hypotheses. We suggest that the generations of more mitogenomes of Geoemydid species, especially for Batagurinae subfamily, are required to improve our understanding their in-depth phylogenetic and evolutionary relationships.

opencc-zeroSep 2020View details →
dryad32/100

Data from: Complex phylogeography in Rhinoclemmys melanosterna: conflicting mitochondrial and nuclear evidence suggests past hybridization (Testudines: Geoemydidae)

We examined differentiation within the Colombian wood turtle Rhinoclemmys melanosterna, and among R. melanosterna and the closely allied species R. diademata, R. funerea and R. punctularia, based on 1060 base pairs of the mitochondrial cyt b gene. We also assessed the phylogenetic relationships among these species using 2050 bp of mtDNA (partial cyt b, 12S and 16S genes) and 3620 bp of nuclear DNA (partial Rag 1, Rag 2, C-mos, R35 and ODC genes). There is considerable phylogeographic structuring within R. melanosterna, with seven distinct clades distributed across the species' range. These clades correspond to some extent with previously described differences in the dorsal pattern of head coloration. Individual and combined analyses of mitochondrial and nuclear DNA indicated contradictory relationships among R. melanosterna, R. diademata, R. funerea and R. punctularia. Mitochondrial DNA sequences revealed R. melanosterna to be non-monophyletic with respect to R. diademata, R. funerea and R. punctularia. In contrast, R. melanosterna constituted a well-supported monophyletic clade using nuclear DNA. This conflict between mitochondrial and nuclear data suggests past gene flow among the allopatrically and parapatrically distributed species R. melanosterna, R. diademata, R. funerea and R. punctularia. Compared to the other Rhinoclemmys species, the taxa under study are weakly differentiated. To assess their taxonomic status, further research is warranted using additional nuclear markers and additional samples of R. diademata, R. funerea and R. punctularia. For the time being, a continued classification of R. melanosterna, R. diademata, R. funerea and R. punctularia as distinct species is justified owing to their allopatric and parapatric distributions, and to conserve the established usage of names that is based on characteristic and distinct phenotypes associated with each species.

opencc-zeroDec 2012View details →
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FIGURE 3 in A new subspecies of Batagur affinis (Cantor, 1847), one of the world's most critically endangered chelonians (Testudines: Geoemydidae)

FIGURE 3. (a) Batagur baska, male, Sundarbans, Bangladesh – photo: S.M.A. Rashid; (b) B. baska, semiadult female (the pointed, upturned snout develops only with increasing age), Sundarbans, Bangladesh – photo: P. Praschag; (c) west coast form of B. affinis, male, Klong La-ngu River, Satun Province, Thailand – photo: B. Horne; (d) west coast form of B. affinis, female, Perak River, Malaysia – photo: E.O. Moll; (e) east coast form of B. affinis, male, Dungun River, Malaysia – photo: E.H. Chan; (f) east coast form of B. affinis, female, Terengganu River, Malaysia – photo: E.O. Moll; (g) Cambodian Batagur male, Sre Ambel River system, Cambodia – photo: R. Holloway; (h) Cambodian Batagur female, Sre Ambel River system, Cambodia – photo: B. Horne. Note differences in head shape, soft part and iris coloration.

opennotspecifiedDec 2009View details →
zenodo32/100

FIGURE 4 in A new subspecies of Batagur affinis (Cantor, 1847), one of the world's most critically endangered chelonians (Testudines: Geoemydidae)

FIGURE 4. Hatchlings of Batagur affinis, (a) west coast form, Perak River, Malaysia; (b) east coast form, Terengganu River, Malaysia – photos: E.O. Moll. Note yellow marginal scutes and silvery blotches in temporal and parietal region in the east coast hatchling.

opennotspecifiedDec 2009View details →
zenodo32/100

FIGURE 2 in A new subspecies of Batagur affinis (Cantor, 1847), one of the world's most critically endangered chelonians (Testudines: Geoemydidae)

FIGURE 2. Parsimony networks for mitochondrial haplotypes of Batagur affinis, B. baska, B. kachuga, and the Cambodian Batagur (connection enforced). Symbol size corresponds to haplotype frequency; missing node haplotypes black. Lines joining haplotypes, one mutational step except otherwise indicated. (a) Network based on a 320-bp-long alignment of cyt b. Haplotypes and their frequencies (see Appendix): B. affinis – A1 (n=9), A2 (n=1); B. baska – B1 (n=5), B2 (n=1), B3 (n=1); B. kachuga – K1 (n=3), K2 (n=1), K3 (n=1); Cambodian Batagur – C (n=7). Haplotypes A1 and B1 include the lectotype of Tetraonyx affinis Cantor, 1847 and topotypic specimens of Emys baska Gray, 1830, respectively (Praschag et al. 2008). Haplotypes K1 and K2 are from topotypic specimens of Emys kachuga Gray, 1831. (b) Network based on a 1067-bp-long alignment of cyt b. Haplotypes and their frequencies: B. affinis – A1 (n=8), A2 (n=1); B. baska – B1 (n=4); B. kachuga – K1 (n=3), K2 (n=1), K3 (n=1); Cambodian Batagur – C (n=7).

opennotspecifiedDec 2009View details →
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FIGURE 5 in A new subspecies of Batagur affinis (Cantor, 1847), one of the world's most critically endangered chelonians (Testudines: Geoemydidae)

FIGURE 5. Historical distribution of Batagur affinis affinis, B. a. edwardmolli, and B. baska (modified from Praschag et al. 2008). Note that the species are extirpated in most of their former ranges.

opennotspecifiedDec 2009View details →
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FIGURE 1 in A new subspecies of Batagur affinis (Cantor, 1847), one of the world's most critically endangered chelonians (Testudines: Geoemydidae)

FIGURE 1. Bayesian reconstruction of the phylogeny of Batagur and allied geoemydid taxa, based on the expanded data set of Le et al. (2007). Numbers above nodes are posterior probabilities (partitioned analysis). Posterior probabilities are identical for unpartitioned analysis, except for the clade comprising B. dhongoka + (B. borneoensis + B. trivittata) and the basal clade of all taxa except Geoemyda and Rhinoclemmys (.97 and.81, respectively). Numbers below nodes, ML and MP bootstrap values. For Pangshura + (Hardella + Batagur) the habitat is coded.

opennotspecifiedDec 2009View details →
zenodo32/100

FIGURE 3 in A new species of the genus Ocadia (Testudines: Geoemydidae) from the middle Miocene of Tanegashima Island, southwestern Japan and its paleogeographic implications

FIGURE 3. Ocadia tanegashimensis (MTE1) from Tanegashima Island. A–C, the carapace in dorsal (A), ventral (B) and anterior (C) views. D, left fifth to seventh costals in ventral view. E–F, the plastron in dorsal (E) and ventral (F) views. Arrows indicate locations of upper ends of the plastral buttresses. Scale bar: 5 cm.

opennotspecifiedDec 2013View details →
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FIGURE 2 in A new species of the genus Ocadia (Testudines: Geoemydidae) from the middle Miocene of Tanegashima Island, southwestern Japan and its paleogeographic implications

FIGURE 2. Picture showing occurrence of Ocadia tanegashimensis (MTE1) from the Kawachi Formation in Kawachi, Minamitane–cho, southern part of Tanegashima Island.

opennotspecifiedDec 2013View details →

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