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160 results for “Cerithioidea”
Figure 5 from: Whelan NV, Johnson PD, Garner JT, Strong EE (2017) On the identity of Leptoxis taeniata – a misapplied name for the threatened Painted Rocksnail (Cerithioidea, Pleuroceridae). ZooKeys 697: 21-36. https://doi.org/10.3897/zookeys.697.14060
Figure 5 - Type and topotypic material of L. picta and its synonym L. taeniata. A, B USNM 12074, Anculosa picta Conrad, 1834 (possible syntypes) C MCZ 294989, Anculosa picta Conrad, 1834 (possible syntype) D NHMUK uncatalogued, Anculosa taeniata Conrad, 1834 (possible paralectotype) E MCZ 294987, Anculosa taeniata Conrad, 1834 (paralectotype) F ANSP 27620, Anculosa taeniata Conrad, 1834 (lectotype) G–I ANSP 413583, Anculosa taeniata Conrad, 1834 (paralectotypes) J, K ANSP 187076, "Leptoxis taeniata", collected by J.H. McLellan, unknown year (topotypic). L–O ANSP 65451, "Leptoxis taeniata", collected by C.W. Johnson, 1894 (topotypic). Scale bar: 5mm.
Figure 4 from: Whelan NV, Johnson PD, Garner JT, Strong EE (2017) On the identity of Leptoxis taeniata – a misapplied name for the threatened Painted Rocksnail (Cerithioidea, Pleuroceridae). ZooKeys 697: 21-36. https://doi.org/10.3897/zookeys.697.14060
Figure 4 - Photographs of live animals. A Painted Rocksnail (L. coosaensis) B Spotted Rocksnail (L. picta)
Figure 2 from: Whelan NV, Johnson PD, Garner JT, Strong EE (2017) On the identity of Leptoxis taeniata – a misapplied name for the threatened Painted Rocksnail (Cerithioidea, Pleuroceridae). ZooKeys 697: 21-36. https://doi.org/10.3897/zookeys.697.14060
Figure 2 - Growth series. A–F Adult (A–C) and juvenile (D–F) shells of the Painted Rocksnail, Leptoxis coosaensis. All individuals grown in captivity. G–L Adult (G–I) and juvenile (J–L) shells of the Spotted Rocksnail, Leptoxis picta. Juveniles grown in captivity. Scale bar: 4 mm.
Figure 1 from: Whelan NV, Johnson PD, Garner JT, Strong EE (2017) On the identity of Leptoxis taeniata – a misapplied name for the threatened Painted Rocksnail (Cerithioidea, Pleuroceridae). ZooKeys 697: 21-36. https://doi.org/10.3897/zookeys.697.14060
Figure 1 - Map showing historical range of the Painted Rocksnail, L. coosaensis, and the Spotted Rocksnail, L. picta.
Figure 3 from: Whelan NV, Johnson PD, Garner JT, Strong EE (2017) On the identity of Leptoxis taeniata – a misapplied name for the threatened Painted Rocksnail (Cerithioidea, Pleuroceridae). ZooKeys 697: 21-36. https://doi.org/10.3897/zookeys.697.14060
Figure 3 - Type material of L. coosaensis and its synonyms and other specimens showing conchological variation seen in L. coosaensis. A USNM 121295, Anculosa coosaensis Lea, 1861 (lectotype) B UMMZ 101139, Anculosa aldrichi Goodrich, 1922 (holotype) C UMMZ 10144, Anculosa brevispira Goodrich, 1922 (holotype) D UMMZ 10145, Anculosa choccoloccoensis, Goodrich, 1922 (holotype) E USNM 1456804, Anculosa coosaensis Lea, 1861 (paralectotype) F–I USNM 121294 Anculosa coosaensis Lea, 1861 (paralectotypes) J USNM 121296 Anculosa coosaensis Lea, 1861 (paralectotype) K, L USNM 504866 "Leptoxis taeniata". N–P USNM 336408 "Leptoxis taeniata". Scale bar: 5 mm.
Figure 8 from: Veeravechsukij N, Krailas D, Namchote S, Wiggering B, Neiber MT, Glaubrecht M (2018) Molecular phylogeography and reproductive biology of the freshwater snail Tarebia granifera in Thailand and Timor (Cerithioidea, Thiaridae): morphological disparity versus genetic diversity. Zoosystematics and Evolution 94(2): 461-493. https://doi.org/10.3897/zse.94.28981
Figure 8 Frequency of ontogenetic stages in the subhemocoelic brood pouches of female Tarebiagranifera (Lamarck, 1816) (morph B) depending on occurrence in Thailand. Blue dots: mitochondrial clade A; pink dots: mitochondrial clade B. Size classes are assigned different colours in the pie charts (see legend) and rivers are coloured according to drainage systems; numbers at the pie charts refer to the total number of dissected specimens and the number of gravid females (in parentheses). The small letters refer to the stations Chiang Mai (a), Ko Samui (b) and Phuket (c) for which meteorological data representing the different climatic regions of Thailand were analysed (see Fig. 12).
Figure 4 from: Veeravechsukij N, Krailas D, Namchote S, Wiggering B, Neiber MT, Glaubrecht M (2018) Molecular phylogeography and reproductive biology of the freshwater snail Tarebia granifera in Thailand and Timor (Cerithioidea, Thiaridae): morphological disparity versus genetic diversity. Zoosystematics and Evolution 94(2): 461-493. https://doi.org/10.3897/zse.94.28981
Figure 4 Bayesiam 50% majority-rule consensus tree showing two major mitochondrial clades in Tarebiagranifera (Lamarck, 1816). Numbers at the nodes correspond to posterior probabilities (left), maximum likelihood (middle) and maximum parsimony (right) bootstrap values. At the tips of the tree voucher numbers (see material list in the main part of the text), country codes (THA: Thailand; TIM: Timor Leste; IDN: Indonesia) and the river where specimens were collected are indicated. The inset map shows the distribution of mitochondrial clades in Thailand (clade A: blue dots; clade B: magenta dots) and major river systems. The letters a–c in the map refer to localities, for which climatic data were available (see also Fig. 12). The inset with box plots shows the altitudinal distribution of mitochondrial caldes A and B, respectively.
Figure 6 from: Veeravechsukij N, Krailas D, Namchote S, Wiggering B, Neiber MT, Glaubrecht M (2018) Molecular phylogeography and reproductive biology of the freshwater snail Tarebia granifera in Thailand and Timor (Cerithioidea, Thiaridae): morphological disparity versus genetic diversity. Zoosystematics and Evolution 94(2): 461-493. https://doi.org/10.3897/zse.94.28981
Figure 6 Results of biometric (a–d) and geometric morphometrics study (e), for four different morphs (A,B,C,Timor) of Tarebiagranifera (Lamarck, 1816). Boxplots of (a) shell height, (b) shell width, (c) height of the last three whorls and (d) index of height of last three whorls agaianst shell width. Significant differences between groups are indicated by bars above the boxplots (e) Relative variance in shell shape along PC1 and PC2. Colour corresponding planes indicate the spread of each morph in the data set.
Figure 2 from: Veeravechsukij N, Krailas D, Namchote S, Wiggering B, Neiber MT, Glaubrecht M (2018) Molecular phylogeography and reproductive biology of the freshwater snail Tarebia granifera in Thailand and Timor (Cerithioidea, Thiaridae): morphological disparity versus genetic diversity. Zoosystematics and Evolution 94(2): 461-493. https://doi.org/10.3897/zse.94.28981
Figure 2 Shells of Tarebiagranifera (Lamarck, 1816) from Timor and Thailand. a. Syntypes (MHNG 1093/72/1-4) from Timor. b–g. Morph A, i.e. specimens from Thailand corresponding to T.granifera (SUT 0514044, SUT 0516123, SUT 0515088, SUT 0515068, SUT 0515059, SUT 0516144). h–m. Morph B, i.e. specimens from Thailand corresponding to named T.lineata (Gray, 1828) (SUT 0515081, SUT 0514046, SUT 0516129, SUT 0515092, SUT 0515095, SUT 0516143). n–s. Morph C from Thailand (SUT 0515079, SUT 0516126, SUT 0515055, SUT 0515091, SUT 0516147, SUT0516142). t–y. Shells of T.granifera from Timor Leste (ZMH 119364, ZMH 119359, ZMH 119357, ZMH 119353, ZMH 119363, ZMH 119361). For locality data, see the material list in the main part of the text. Scale bar: 10 mm.
Figure 12 from: Veeravechsukij N, Krailas D, Namchote S, Wiggering B, Neiber MT, Glaubrecht M (2018) Molecular phylogeography and reproductive biology of the freshwater snail Tarebia granifera in Thailand and Timor (Cerithioidea, Thiaridae): morphological disparity versus genetic diversity. Zoosystematics and Evolution 94(2): 461-493. https://doi.org/10.3897/zse.94.28981
Figure 12 Proportions of gravid vs. non-gravid specimens of Tarebiagranifera (Lamarck, 1816) collected in different months within a given year, plotted on climate charts for localities that are representative for different climatic regimes in Thailand. (a) Chiang Mai for inland locations; (b) Ko Samui for the Gulf of Thailand; (c) Phuket for the Andaman Sea (see also Fig. 8). For colour coding, see the inset legend.
Figure 10 from: Veeravechsukij N, Krailas D, Namchote S, Wiggering B, Neiber MT, Glaubrecht M (2018) Molecular phylogeography and reproductive biology of the freshwater snail Tarebia granifera in Thailand and Timor (Cerithioidea, Thiaridae): morphological disparity versus genetic diversity. Zoosystematics and Evolution 94(2): 461-493. https://doi.org/10.3897/zse.94.28981
Figure 10 Composition of contents of the subhemocoelic brood pouches of female Tarebiagranifera (Lamarck, 1816) (a, c) and proportions of gravid animals, i.e. those with filled brood pouch, versus non-gravid specimens (b, d) from Thailand and Timor Leste. a. Composition of contents of the brood pouches for morph A, B and C from Thailand (THA) and specimens from Timor Leste (see Figs 1, 8 and 9). b. Proportion of gravid vs. non-gravid specimens for morph A, B and C from Thailand and specimens from Timor Leste. c. Composition of contents of the brood pouches for mitochondrial clades A and B, respectively (see also Figs 4, 8, 9). d. Proportion of gravid vs. non-gravid specimens for mitochondrial clades A and B, respectively. For colour coding, see the inset legends.
Figure 1 from: Veeravechsukij N, Krailas D, Namchote S, Wiggering B, Neiber MT, Glaubrecht M (2018) Molecular phylogeography and reproductive biology of the freshwater snail Tarebia granifera in Thailand and Timor (Cerithioidea, Thiaridae): morphological disparity versus genetic diversity. Zoosystematics and Evolution 94(2): 461-493. https://doi.org/10.3897/zse.94.28981
Figure 1 Distribution of the freshwater thiarid snail Tarebiagranifera (Lamarck, 1816) across its range in Southeast Asia, with the focus on occurrences in Thailand, contrasted with type and topotypical material from the island of Timor. Asteriks: type locality of "Melania" granifera Lamarck, 1816, reconstructed to originate from near Kupang in western Timor (see text for more details); black dots: sequenced material used in this study; white dots: shell material from museum collections analysed and literature records; white dots with black dot inside: wet material preserved in ethanol.
Figure 9 from: Veeravechsukij N, Krailas D, Namchote S, Wiggering B, Neiber MT, Glaubrecht M (2018) Molecular phylogeography and reproductive biology of the freshwater snail Tarebia granifera in Thailand and Timor (Cerithioidea, Thiaridae): morphological disparity versus genetic diversity. Zoosystematics and Evolution 94(2): 461-493. https://doi.org/10.3897/zse.94.28981
Figure 9 Frequency of ontogenetic stages in the subhemocoelic brood pouches of female Tarebiagranifera (Lamarck, 1816) depending on occurrence in Thailand and Timor Leste. a. Morph A in Thailand; b. Morph C in Thailand; c. Timor Leste. Blue dots: mitochondrial clade A; pink dots: mitochondrial clade B. Size classes are assigned different colours in the pie charts (see legend) and rivers are coloured according to drainage systems; numbers at the pie charts refer to the total number of dissected specimens and the number of gravid females (in parentheses).
Figure 5 from: Veeravechsukij N, Krailas D, Namchote S, Wiggering B, Neiber MT, Glaubrecht M (2018) Molecular phylogeography and reproductive biology of the freshwater snail Tarebia granifera in Thailand and Timor (Cerithioidea, Thiaridae): morphological disparity versus genetic diversity. Zoosystematics and Evolution 94(2): 461-493. https://doi.org/10.3897/zse.94.28981
Figure 5 Molecular analysis of Tarebia. a–b. Median-joining haplotype networks based on 16S (a) and cox1 (b) sequence data of Tarebiagranifera (Lamarck, 1816). The size of each circle represents the frequency of a haplotype and the colour refers to main mitochondrial clades obtained from the phylogenetic analyses (Fig. 4; blue: clade A, magenta: clade B). Tick marks between circles represent evolutionary steps. c. Results of the bGMYC analysis. Colouration of the matrix cells represents pairwise probabilities of conspecificity. d. Dated molecular tree (only unique haplotypes were included). Numbers at the nodes are node ages in Ma, bars represent 95% highest posterior probabilitiy intervals.
Figure 7 from: Veeravechsukij N, Krailas D, Namchote S, Wiggering B, Neiber MT, Glaubrecht M (2018) Molecular phylogeography and reproductive biology of the freshwater snail Tarebia granifera in Thailand and Timor (Cerithioidea, Thiaridae): morphological disparity versus genetic diversity. Zoosystematics and Evolution 94(2): 461-493. https://doi.org/10.3897/zse.94.28981
Figure 7 Results of biometric (a–d) and geometric morphometrics study (e), for the two mitochondiral clades of Tarebiagranifera (Lamarck, 1816) found in this study. Boxplots of (a) shell height, (b) shell width, (c) height of the last three whorls and (d) index of height of last three whorls agaianst shell width. Significant differences between groups are indicated by bars above the boxplots (e). Relative variance in shell shape along PC1 and PC2. Colour corresponding planes indicate the spread of each morph in the data set.
Figure 3 from: Veeravechsukij N, Krailas D, Namchote S, Wiggering B, Neiber MT, Glaubrecht M (2018) Molecular phylogeography and reproductive biology of the freshwater snail Tarebia granifera in Thailand and Timor (Cerithioidea, Thiaridae): morphological disparity versus genetic diversity. Zoosystematics and Evolution 94(2): 461-493. https://doi.org/10.3897/zse.94.28981
Figure 3 Biometrical parameters (a) and position of landmarks (b). Abbreviations: height of shell (h), width of shell (w), length of aperture (la), width of aperture (wa), height of body whorl (hbw) and height of last three whorls (l3w).
Figure 11 from: Veeravechsukij N, Krailas D, Namchote S, Wiggering B, Neiber MT, Glaubrecht M (2018) Molecular phylogeography and reproductive biology of the freshwater snail Tarebia granifera in Thailand and Timor (Cerithioidea, Thiaridae): morphological disparity versus genetic diversity. Zoosystematics and Evolution 94(2): 461-493. https://doi.org/10.3897/zse.94.28981
Figure 11 Composition of contents of the subhemocoelic brood pouches of female Tarebiagranifera (Lamarck, 1816) (a) and proportions of gravid animals, i.e. those with brood pouch containing juveniles or other stages, and non-gravid specimens (b) from Thailand grouped according to rivers. For colour coding, see the inset legends.
Figure 7 from: Boonmekam D, Krailas D, Gimnich F, Neiber MT, Glaubrecht M (2019) A glimpse in the dark? A first phylogenetic approach in a widespread freshwater snail from tropical Asia and northern Australia (Cerithioidea, Thiaridae). Zoosystematics and Evolution 95(2): 373-390. https://doi.org/10.3897/zse.95.34486
Figure 7 Radulae of "Thiara" aspera (Lesson, 1831) from Thailand. A, B.SUT 0312070, Nakhon Pathom province, pond at Silpakorn University campus; A. Central and lateral teeth; B. Marginal teeth; C, D.SUT 0311020, Samut Sakhon province, Klong Don Ko; C. Central and lateral teeth; D. Marginal teeth. E, F: SUT 0311053, Samut Sakhon Province, Klong Don Ko; E. Central and lateral teeth; F. Marginal teeth. Scale bars: 35 µm (A, E); 5 µm (B, F); 25 µm (C); 10 µm (D).
Figure 4 from: Boonmekam D, Krailas D, Gimnich F, Neiber MT, Glaubrecht M (2019) A glimpse in the dark? A first phylogenetic approach in a widespread freshwater snail from tropical Asia and northern Australia (Cerithioidea, Thiaridae). Zoosystematics and Evolution 95(2): 373-390. https://doi.org/10.3897/zse.95.34486
Figure 4 Results of the analysis of biometric data of "Thiara" aspera (Lesson, 1831) specimens from Australia (yellow), Indonesia (green), Thailand (red) and India/Sri Lanka (blue) and type material of Melaniaaspera Lesson, 1831 (holotype, triangle), Melaniarudis Lea & Lea, 1851 (syntype, square) and Melaniamicrostoma Lea & Lea, 1851 (syntype, diamond). A. Scatter plot of the first two axes of the principal component analysis (PCA) of biometric data. Coloured lines indicate the outline of the convex hull for each geographic group; B, C. Boxplots of PCA 1 (B) and PCA 2 (C); bars above the box plots indicate significant differences of groups resulting from testing with Dunn's test.
Figure 3 from: Boonmekam D, Krailas D, Gimnich F, Neiber MT, Glaubrecht M (2019) A glimpse in the dark? A first phylogenetic approach in a widespread freshwater snail from tropical Asia and northern Australia (Cerithioidea, Thiaridae). Zoosystematics and Evolution 95(2): 373-390. https://doi.org/10.3897/zse.95.34486
Figure 3 Measured shell parameters. A: H – shell height; W – shell width; BW – body whorl height; AL – aperture length; AW – aperture width. B: he – height of embryonic shell; we – width of embryonic shell; de – maximum diameter at one whorl.
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