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Figure 4 from: Davolos D, De Matthaeis E, Latella L, Tarocco M, Özbek M, Vonk R (2018) On the molecular and morphological evolution of continental and insular Cryptorchestia species, with an additional description of C. garbinii (Talitridae). ZooKeys 783: 37-54. https://doi.org/10.3897/zookeys.783.26179
Figure 4 Cryptorchestiagarbinii, male 12 mm, Lake Iznik. A gnathopod I, outside left B gnathopod I, inside right C female 13 mm, Lake Iznik, gnathopod I D gnathopod II.
Figure 7 from: Davolos D, De Matthaeis E, Latella L, Tarocco M, Özbek M, Vonk R (2018) On the molecular and morphological evolution of continental and insular Cryptorchestia species, with an additional description of C. garbinii (Talitridae). ZooKeys 783: 37-54. https://doi.org/10.3897/zookeys.783.26179
Figure 7 Cryptorchestiagarbinii, male 16 mm, Lake Iznik. A gnathopod II, palmar margin and dactylus B gnathopod I C maxilliped D pereopod IV, propodus and dactylus E uropod III F telson.
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 8 from: de Souza Castanheira P, Baptista RLC, Pizzetti DDP, Teixeira RA (2019) Contributions to the taxonomy of the long-jawed orb-weaving spider genus Tetragnatha (Araneae, Tetragnathidae) in the Neotropical region, with comments on the morphology of the chelicerae. Zoosystematics and Evolution 95(2): 465-505. https://doi.org/10.3897/zse.95.36762
Figure 8 Tetragnatha keyserlingi Simon, 1890, male (SMF 1553). A. Dorsal habitus; B. Lateral habitus; C. Ventral habitus; D–G. Left chelicera: D. Upper view; E. Inner view; F. Lower view; G. Outer view; H–J. Left male palp: H. Mesal view; I. Dorsal view; J. Ventral view (paracymbium). Scale bars: 2 mm (A, B, C); 0.5 mm (D, E, F, G); 0.2 mm (H, I, J).
Figure 7 from: de Souza Castanheira P, Baptista RLC, Pizzetti DDP, Teixeira RA (2019) Contributions to the taxonomy of the long-jawed orb-weaving spider genus Tetragnatha (Araneae, Tetragnathidae) in the Neotropical region, with comments on the morphology of the chelicerae. Zoosystematics and Evolution 95(2): 465-505. https://doi.org/10.3897/zse.95.36762
Figure 7 Tetragnatha elongata Walckenaer, 1841, SEM photos. A. Left male chelicera, upper and lower views (MCTP 0229); B. Left female chelicera, upper view (MCTP 43306 ex 0370); C. Left male palp, mesal view (MCTP 0229); D. Left male palp conductor detail and pleats, mesal view (MCTP 0229); E. Tip of conductor detail, dorsal view (MCTP 43306 ex 0370); F. Left male palp paracymbium, ventral view (MCTP 0229); G. Epiandrous field, ventral view (MCTP 43306 ex 0370). Scale bars: 1 mm (A); 0.5 mm (B, C); 0.2 mm (D); 0.01 mm (E); 0.3 mm (F); 0.05 mm (G).
Figure 6 from: de Souza Castanheira P, Baptista RLC, Pizzetti DDP, Teixeira RA (2019) Contributions to the taxonomy of the long-jawed orb-weaving spider genus Tetragnatha (Araneae, Tetragnathidae) in the Neotropical region, with comments on the morphology of the chelicerae. Zoosystematics and Evolution 95(2): 465-505. https://doi.org/10.3897/zse.95.36762
Figure 6 Tetragnatha elongata Walckenaer, 1841, female. A. Dorsal habitus (MCTP 28045); B. Lateral habitus (MCTP 28045); C–F. Left chelicera (MCTP 28045): C. Upper view; D. Inner view; E. Lower view; F. Outer view; G, H. Genital area: G. Genital fold, ventral view (MCTP 28045); H. Internal genitalia, cleared, ventral view (MCTP 28306). Scale bars: 5 mm (A, B); 1 mm (C, D, E, F); 0.5 mm (G); 0.2 mm (H).
Figure 4 from: de Souza Castanheira P, Baptista RLC, Pizzetti DDP, Teixeira RA (2019) Contributions to the taxonomy of the long-jawed orb-weaving spider genus Tetragnatha (Araneae, Tetragnathidae) in the Neotropical region, with comments on the morphology of the chelicerae. Zoosystematics and Evolution 95(2): 465-505. https://doi.org/10.3897/zse.95.36762
Figure 4 Tetragnatha bogotensis Keyserling, 1865 labels. A.T. bogotensis from Taquara, Brazil (NHM); B.T. bogotensis from Bogotá, Colombia (NHM); C.T. ramboi syntype from Rio Grande do Sul, Brazil (MNRJ 42467); D.T. bemalcuei holotype from Paraguay (NMB).
Figure 9 from: de Souza Castanheira P, Baptista RLC, Pizzetti DDP, Teixeira RA (2019) Contributions to the taxonomy of the long-jawed orb-weaving spider genus Tetragnatha (Araneae, Tetragnathidae) in the Neotropical region, with comments on the morphology of the chelicerae. Zoosystematics and Evolution 95(2): 465-505. https://doi.org/10.3897/zse.95.36762
Figure 9 Tetragnatha keyserlingi Simon, 1890, female. A. Dorsal habitus (SMF 1351); B. Lateral habitus (SMF 1351); C. Ventral habitus (SMF 1351); D–G. Left chelicera (MCTP 14749): D. Upper view; E. Inner view; F. Lower view; G. Outer view; H, I. Genital area: H. Genital fold, ventral view (MCTP 14749); I. Internal genitalia, cleared, ventral view (SMF 1504). Scale bars: 2 mm (A, B, C); 1 mm (D, E, F, G); 0.5 mm (H); 0.1 mm (I).
Figure 5 from: de Souza Castanheira P, Baptista RLC, Pizzetti DDP, Teixeira RA (2019) Contributions to the taxonomy of the long-jawed orb-weaving spider genus Tetragnatha (Araneae, Tetragnathidae) in the Neotropical region, with comments on the morphology of the chelicerae. Zoosystematics and Evolution 95(2): 465-505. https://doi.org/10.3897/zse.95.36762
Figure 5 Tetragnatha elongata Walckenaer, 1841, male (MCTP 28045). A. Dorsal habitus; B. Lateral habitus; C. Ventral habitus; D–G. Left chelicera: D. Upper view; E. Inner view; F. Lower view; G. Outer view; H–K. Left male palp: H. Mesal view with tibia; I. Mesal view detail; J. Dorsal view; K. Ventral view (paracymbium). Scale bars: 2 mm (A, B, C); 1 mm (D, E, F, G, H); 0.5 mm (I, J, K).
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.