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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.
Figures 10-13 in Growth and reproductive biology of the amphidromous shrimp Palaemon pandaliformis (Decapoda: Caridea) in a Neotropical river from northeastern Brazil
Figures 10-13. Relationship between fecundity (Fec – number of eggs) and carapace length (10), total length (11), weight (12) and brood pouch volume (13) for Palaemon pandaliformis females collected from Rio Salsa, Canavieiras, Bahia, Brazil.
Figure 8 in Growth and reproductive biology of the amphidromous shrimp Palaemon pandaliformis (Decapoda: Caridea) in a Neotropical river from northeastern Brazil
Figure 8. Von Bertalanffy growth curves for male and female data of Palaemon pandaliformis based on monthly length-frequency distribution from September 2009 and August 2010 in Rio Salsa, Canavieiras, Bahia, Brazil. Center line: mean; dotted lines: confidence intervals (95%); dashed lines: prediction interval (95%). Individual points represent modal carapace length (CL) derived from size-frequency distributions.
Figure 9 in Growth and reproductive biology of the amphidromous shrimp Palaemon pandaliformis (Decapoda: Caridea) in a Neotropical river from northeastern Brazil
Figure 9. Monthly changes in the percentage occurrence of Palaemon pandaliformis female with non-eye (Stage I) and eyed eggs pigmentation (Stage II and III), and precipitation recorded from September 2009 and August 2010 in Rio Salsa, Canavieiras, Bahia, Brazil.
Figure 4 in Growth and reproductive biology of the amphidromous shrimp Palaemon pandaliformis (Decapoda: Caridea) in a Neotropical river from northeastern Brazil
Figure 4. Recruitment pattern of Palaemon pandaliformis and monthly precipitation recorded from September 2009 and August 2010 in Rio Salsa, Canavieiras, Bahia, Brazil.
Figures 2-3 in Growth and reproductive biology of the amphidromous shrimp Palaemon pandaliformis (Decapoda: Caridea) in a Neotropical river from northeastern Brazil
Figures 2-3. Sex ratio (male/total) of Palaemon pandaliformis collected from September 2009 and August 2010 in Rio Salsa, Canavieiras, Bahia, Brazil. (2) Monthly fluctuations. (3) Anomalous probability curve derived from a year sampling collection. * Statistically significant at p ≤ 0.05.
Fig. 1 in Biology and reproductive capacity of Spodoptera eridania (Cramer) (Lepidoptera, Noctuidae) in different soybean cultivars
Fig. 1. Duration (days) and survival (%) of larval instars of Spodoptera eridania fed on different soybean cultivars. Means followed by the same letter differed by Kruskal–Wallis test at 5%. nsNot significant according to Kruskal–Wallis (p> 0.05). *Due to the low number of individuals, it was not possible to apply statistical tests.
Figure 6 in Reproductive biology of the greater lizardfish, Saurida tumbil (Bloch, 1795), in Bushehr coastal waters of Iran
Figure 6. Ovary development in female greater lizardfish (Saurida tumbil, Synodontidae). A) Perinucleolus stage. B) Yolk vesicle stage. C) Yolk globule stage. D) Migratory nucleus stage. E) Mature stage. F) Postovulatory follicles stage. G) Atretic stage. At: Atresia, CA: Cortical alveoli, C: Cytoplasm, F: Follicle layer, Mn: Migratory nucleus, N: Nucleus, Ne: Nucleolus, POF: Postovulatory follicles, Yg: Yolk globule, YV: Yolk vesicle, Z: Zona radiata.
Figure 7 in Reproductive biology of the greater lizardfish, Saurida tumbil (Bloch, 1795), in Bushehr coastal waters of Iran
Figure 7. Testicular development in male greater lizardfish. A) Different stages of sperm development from developing to spawning stages. B) Spermatids. C) Spawning stage with spermatozoa (III). D) Regression stage (IV). SC1: Primary spermatocytes, SC2: Secondary spermatocytes, SD: Spermatids, SG: Spermatogonia, ST: Sertoli cells, SZ: Spermatozoa.
Figure 5 in Reproductive biology of pink cuttlefish Sepia orbignyana in the Aegean Sea (eastern Mediterranean)
Figure 5. Male and female distribution of 50% of the population (ML 50) at the size of maturity of S. orbignyana obtained from the Aegean Sea.
Fig. 9 in Redescription of Chelonarium signatum Dalman, 1824, with Notes on its Reproductive Biology and Occurrence in Paraguay (Coleoptera: Byrrhoidea: Chelonariidae)
Fig. 9. Chelonarium signatum, habitat at Misiones, Paraguay.
FIGURE 3 in A new Werauhia (Tillandsioideae, Bromeliaceae) from Mexico with observations about its reproductive biology
FIGURE 3. Type locality and known distribution of Werauhia maculata in Tabasco, Mexico.
Figure 4 in Reproductive biology of the endangered wattled curassow (Crax globulosa; Galliformes: Cracidae) in the Juruá River Basin, Western Brazilian Amazonia
Figure 4. Chick of Crax globulosa, approximately 10 days old, on 3 September 2016 in Macaco.
Figure 2 in Reproductive biology of the endangered wattled curassow (Crax globulosa; Galliformes: Cracidae) in the Juruá River Basin, Western Brazilian Amazonia
Figure 2. Nest #2 built in the fork, with two eggs.
Figure 1 in Population structure and reproductive biology of the fiddler crab Uca urvillei (Brachyura: Ocypodidae) in Maputo Bay (south Mozambique)
Figure 1. Uca urvillei (H. Milne Edwards, 1852). Size frequency distributions of all individuals sampled during the study period.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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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.