Find research datasets worth reusing

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.

opencc-by-4.0Mar 2019View details →

Figures 2-11 from: Czaja A, Cardoza-Martínez GF, Meza-Sánchez IG, Estrada-Rodríguez JL, Saenz-Mata J, Becerra-López JL, Romero-Méndez U, Estrada-Arellano JR, Garza-Martínez MA, Paulín JAD (2019) New genus, two new species and new records of subterranean freshwater snails (Caenogastropoda; Cochliopidae and Lithoglyphidae) from Coahuila and Durango, Northern Mexico. Subterranean Biology 29: 89-102. https://doi.org/10.3897/subtbiol.29.34123

Figures 2-11 Shells and opercula of Phreatomascogosgregoi gen. n. et sp. n. 2, 3 holotype, UJMC 400 4, 5 paratype 1, UJMC 401 6, 7 paratype 2, UJMC 401a, shell apex with protoconch 8 umbilicus almost completely covered by a basal keel, UJMC 401b 9 paratype 3, UJMC 401d, conical specimen 10, 11 opercula 11 operculum showing the strongly campanulate shape. Scale bars: 0.5 mm (2–5, 9–11); 0.3 mm (8).

opencc-by-4.0Mar 2019View details →

Figures 12-23 from: Czaja A, Cardoza-Martínez GF, Meza-Sánchez IG, Estrada-Rodríguez JL, Saenz-Mata J, Becerra-López JL, Romero-Méndez U, Estrada-Arellano JR, Garza-Martínez MA, Paulín JAD (2019) New genus, two new species and new records of subterranean freshwater snails (Caenogastropoda; Cochliopidae and Lithoglyphidae) from Coahuila and Durango, Northern Mexico. Subterranean Biology 29: 89-102. https://doi.org/10.3897/subtbiol.29.34123

Figures 12-23 Shells of Balconorbissabinasense sp. n. and Coahuilixparrasense Czaja, Estrada-Rodríguez, Romero-Méndez, Ávila-Rodríguez, Meza-Sánchez & Covich, 2017. 12–14B.sabinasense n. sp., holotype, UJMC 410. 15–18 Paratype 1, UJMC 411. 19–21C.parrasense, UJMC 418, from Nazas River, Durango. 22, 23C.parrasense, fossil specimen from Parras de la Fuente, Coahuila, holotype, UJMC-320, from Czaja et al. 2017c, Fig. 4A, C. Scale bar: 0.5 mm (12–14, 19–23).

opencc-by-4.0Mar 2019View details →

Figure 1 from: Czaja A, Cardoza-Martínez GF, Meza-Sánchez IG, Estrada-Rodríguez JL, Saenz-Mata J, Becerra-López JL, Romero-Méndez U, Estrada-Arellano JR, Garza-Martínez MA, Paulín JAD (2019) New genus, two new species and new records of subterranean freshwater snails (Caenogastropoda; Cochliopidae and Lithoglyphidae) from Coahuila and Durango, Northern Mexico. Subterranean Biology 29: 89-102. https://doi.org/10.3897/subtbiol.29.34123

Figure 1 Map of the study area with localization of the sampling sites along the Álamos and Sabinas River in Coahuila and Nazas River in Durango. Sampling sites as in Table 1.

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.

Figure 2 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 2 Distribution and reproductive strategy of "Thiara" aspera (Lesson, 1831). Stars: type localities of a) Melaniaaspera Lesson, 1831, Monokwari, New Guinea, b) Melaniarudis Lea & Lea, 1851, Amboyna and c) Melaniamicrostoma Lea & Lea, 1851, mountain streams, isle of Negros, Philippines. Pie charts show the percentages of offspring in the brood pouch of female T.aspera in different size classes as defined in Glaubrecht et al. (2009), see inset. The numbers near the pie charts refer to the number of individuals examined per population. Filled circles: material preserved in ethanol; open circles: dry shells.

Figure 6 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 6 Juvenile and embryonic shells of "Thiara" aspera (Lesson, 1831), SUT 0311020, Samut Sakhon Province, Klong Don Ko. A. Lateral view; B. Apical whorls, lateral, C. Apical view. D. Details of the protoconch. Scale bars: 450 µm (A); 250 µm (B); 200 µm (C); 100 µm (D).

Figure 1 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 1 Shells of "Thiara" aspera (Lesson, 1831). A. Holotype of Melaniaaspera Lesson, 1831, MNHN 21098, 'La Nouvelle-Guinée' [more specifically Manokwari on New Guinea Island, West Papua, Indonesia, see Glaubrecht and Podlacha 2010]; B. Syntype of Melaniarudis Lea & Lea, 1851, USNM 119778, Amboyna; C. Syntype of Melaniamicrostoma Lea & Lea, 1851, USNM 119722, mountain streams, isle of Negros, Philippines; D.ZMB 107002, Calcutta, India; E.ZMB 107003, Ceylon, Sri Lanka; F.ZMB 127534, Don Ko Canal, Nakhon Pathom, Thailand; G.ZMB 127535, Don Ko Canal, Nakhon Pathom, Thailand; H.ZMB 127535, Don Ko Canal, Nakhon Pathom, Thailand; I.ZMB 191279, Yehembang River, Bali, Indonesia; J.ZMB 191279, Yehembang River, Bali, Indonesia; K.ZMB 106472, Yehembang, Bali, Indonesia; L. East of Mendaya, stream southwest of Gumicik, Bali, Indonesia; M.ZMB 191278, stream at Tembeeha, road Tirobus-Kendari, Southwest Sulawesi, Indonesia; N.ZMB 107378, Banggai Islands, Peleng Island, West of Peninsula, Tataban river, Central Sulawesi, Indonesia; O.ZMB 107377, Banggai Islands, Peleng Island, West of Peninsula, Tataban river, Central Sulawesi, Indonesia.river; P, Q.ZMB 107617, Wabalarr, Roper River, Northern Territory, Australia; R.ZMB 106599, Berry Springs, Northern Territory, Australia. Scale bar: 1 cm.

Figure 5 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 5 Bayesian 50% majority-rule consensus tree based on partial sequences mitochondrial cytochrome c oxidase subunit 1 (cox1) and 16S rRNA (16S) genes. Support values at nodes refer to Bayesian posterior probabilities (left), Maximum Likelihood (middle) and Maximum Parsimony (right) bootstrap values. AUS: Australia, IDN: Indonesia, THA: Thailand. Numbers at tips refer to DNA vouchers in the collection of the ZMB, see also Table 1.