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1,692 results for “Caenogastropoda”
Fig. 1 in Two new species of the genus Pupina (Caenogastropoda: Pupinidae) from Northwestern Vietnam
Fig. 1. Approximate geographic positions of the type localities of Pupina species of Vietnam. The numbers correspond to the species list in Table 1.
Figure 31 in Refining molluscan characters: morphology, character coding and a phylogeny of the Caenogastropoda
Figure 31. Evolution of the foregut. Black hashmarks indicate forward changes, grey hashmarks indicate forward homoplasies (DELTRAN).
Figure 30 in Refining molluscan characters: morphology, character coding and a phylogeny of the Caenogastropoda
Figure 30. Evolution of the nervous system. Black hashmarks indicate forward changes, grey hashmarks indicate forward homoplasies (DELTRAN).
Figure 16 in Refining molluscan characters: morphology, character coding and a phylogeny of the Caenogastropoda
Figure 16. Midgut morphology. White arrows indicate direction of ciliary currents. (A) Neverita duplicata, dorsal view. Scale bar = 1 mm. (B) Cypraea robertsi, dorsal view. Abbreviations: cf, ciliated fold; dgd, digestive gland duct; e, oesophagus; ig, intestinal groove; pyc, pyloric caecum; sa, sorting area; ss, style sac; t1, major typhlosole; t2, minor typhlosole.
Figure 13 in Refining molluscan characters: morphology, character coding and a phylogeny of the Caenogastropoda
Figure 13. Midgut morphology. White arrows indicate direction of ciliary currents. (A) Neocyclotus dysoni ambiguum, dorsal view. (B) Lampanella minima, dorsal view. Scale bar = 1 mm. Abbreviations: cf, ciliated fold; cs, ciliated strip; ctr, ciliary tract; dgd, digestive gland duct; dv, digestive gland vestibule; e, oesophagus; gap, gastric pouch; gp, glandular pad; gs, gastric shield; pyc, pyloric caecum; sa, sorting area; ss, style sac; t1, major typhlosole; t2, minor typhlosole.
Figure 19 in Refining molluscan characters: morphology, character coding and a phylogeny of the Caenogastropoda
Figure 19. Midgut morphology. White arrows indicate direction of ciliary currents. (A) Ilyanassa obsoletus, dorsal view. (B) Urosalpinx cinerea, dorsal view. Scale bar = 1 mm. Abbreviations: ce, caecal extension; dgd, digestive gland duct; e, oesophagus; gp, glandular pad; gs, gastric shield; ig, intestinal groove; int, intestine; po, pouch; sa, sorting area; ss, style sac; t1, major typhlosole; t2, minor typhlosole.
Figure 15 in Refining molluscan characters: morphology, character coding and a phylogeny of the Caenogastropoda
Figure 15. Midgut morphology. White arrows indicate direction of ciliary currents. (A) Bithynia tentaculata, dorsal view. Distal end of gastric chamber obscured in scanning electron micrograph, indicated by dotted line in diagram on right. (B) Littorina littorea, dorsal view. Stippling indicates ciliary tract within gastric chamber extending from oesophageal aperture. Scale bar = 1 mm. Abbreviations: c, caecum; ce, caecal extension; cf, ciliated fold; cs, ciliated strip; ctr, ciliary tract; dgd, digestive gland duct; e, oesophagus; gp, glandular pad; gs, gastric shield; sa, sorting area; ss, style sac; t1, major typhlosole; t2, minor typhlosole.
Figure 6 from: Hofman S, Grego J, Fehér Z, Erőss ZP, Rysiewska A, Osikowski A, Falniowski A (2021) New data on the valvatiform-shelled Hydrobiidae (Caenogastropoda, Truncatelloidea) from southern Greece. ZooKeys 1062: 31-47. https://doi.org/10.3897/zookeys.1062.64746
Figure 6 A shell of lectotype of Valvata hellenica presented by Reischütz and Sattmann (1993)B shell measurements: a – shell height, b – body whorl breadth, c – aperture height, d – spire height, e – aperture breadth, α – apex angle.
Figure 3 from: Hofman S, Grego J, Fehér Z, Erőss ZP, Rysiewska A, Osikowski A, Falniowski A (2021) New data on the valvatiform-shelled Hydrobiidae (Caenogastropoda, Truncatelloidea) from southern Greece. ZooKeys 1062: 31-47. https://doi.org/10.3897/zookeys.1062.64746
Figure 3 Shells of gastropods: D. longipeniaA–D locality 2 (holotype, 2A32, 2B26, 2B27) E locality 1 (2A29); Daphniola hadeiF locality 3 (2A27) G locality 4 (2B19) H locality 5 (2B20) ID. louisi, locality 6 (2A33) J–KGraecoarganiella parnassiana, locality 7 (2A28, 2B23) L–OIsimeropeL locality 8 (2A30) M locality 9 (2A31) N locality 10 (2B21) O locality 11 (2A22) P cf. Islamia sp., locality 12 (2A34). Scale bar: 1 mm.
Figure 2 from: Hofman S, Grego J, Fehér Z, Erőss ZP, Rysiewska A, Osikowski A, Falniowski A (2021) New data on the valvatiform-shelled Hydrobiidae (Caenogastropoda, Truncatelloidea) from southern Greece. ZooKeys 1062: 31-47. https://doi.org/10.3897/zookeys.1062.64746
Figure 2 Type locality of Daphniola longipenia sp. nov. Panagitsa, Arcadia, Peloponnese A spring reservoir B spring head.
Figure 4 from: Hofman S, Grego J, Fehér Z, Erőss ZP, Rysiewska A, Osikowski A, Falniowski A (2021) New data on the valvatiform-shelled Hydrobiidae (Caenogastropoda, Truncatelloidea) from southern Greece. ZooKeys 1062: 31-47. https://doi.org/10.3897/zookeys.1062.64746
Figure 4 Pallial and renal section of female reproductive organs of Daphniola longipenia [bc – bursa copulatrix, cbc – duct of bursa, ga – albuminoid gland, gn – nidamental gland, gp – gonoporus, ov – oviduct, ovl – loop of (renal) oviduct, rs – seminal receptacles (in black) rs1 and rs2 (as defined by Radoman 1973, 1983): rs1 – distal, rs2 – proximal]. Scale bar: 250 μm.
Figure 8 from: Hofman S, Grego J, Fehér Z, Erőss ZP, Rysiewska A, Osikowski A, Falniowski A (2021) New data on the valvatiform-shelled Hydrobiidae (Caenogastropoda, Truncatelloidea) from southern Greece. ZooKeys 1062: 31-47. https://doi.org/10.3897/zookeys.1062.64746
Figure 8 Phylogenetic tree inferred from connected COI and H3 sequences. Bootstrap supports (>60%) and Bayesian probabilities are given.
Figure 7 from: Hofman S, Grego J, Fehér Z, Erőss ZP, Rysiewska A, Osikowski A, Falniowski A (2021) New data on the valvatiform-shelled Hydrobiidae (Caenogastropoda, Truncatelloidea) from southern Greece. ZooKeys 1062: 31-47. https://doi.org/10.3897/zookeys.1062.64746
Figure 7 Phylogenetic tree for COI showing relationships between the studied snails. Bootstrap supports (>60%) and Bayesian probabilities are given.
Figure 8 from: Baur H, Reichenbach F, Neubert E (2012) Sexual dimorphism in shells of Cochlostoma septemspirale (Caenogastropoda, Cyclophoroidea, Diplommatinidae, Cochlostomatinae). ZooKeys 208: 1-16. https://doi.org/10.3897/zookeys.208.2869
Figure 8 - Bar diagrams showing the extent of pigmentation on the lower whorl: classification (missing, interrupted, continuous) of lower (a), median (b), and upper band (c); blue bars females, red bars males. Significance levels of Fisher's exact test: '***' p < 0.001, '**' p < 0.01, '*' p < 0.05, '.' p < 0.1, ' ' p < 1.
Figure 1 from: Baur H, Reichenbach F, Neubert E (2012) Sexual dimorphism in shells of Cochlostoma septemspirale (Caenogastropoda, Cyclophoroidea, Diplommatinidae, Cochlostomatinae). ZooKeys 208: 1-16. https://doi.org/10.3897/zookeys.208.2869
Figure 1 - The 5 distances measured on the shell of Cochlostoma septemspirale: shell height and width, aperture height and width, and whorl width.
Figure 2 from: Baur H, Reichenbach F, Neubert E (2012) Sexual dimorphism in shells of Cochlostoma septemspirale (Caenogastropoda, Cyclophoroidea, Diplommatinidae, Cochlostomatinae). ZooKeys 208: 1-16. https://doi.org/10.3897/zookeys.208.2869
Figure 2 - Scatterplot of first against second principal component in shape space; blue dots females, red triangles males.
Figure 7 from: Baur H, Reichenbach F, Neubert E (2012) Sexual dimorphism in shells of Cochlostoma septemspirale (Caenogastropoda, Cyclophoroidea, Diplommatinidae, Cochlostomatinae). ZooKeys 208: 1-16. https://doi.org/10.3897/zookeys.208.2869
Figure 7 - Boxplots of rip density. Significance levels of Wilcoxon test: '***' p < 0.001, '**' p < 0.01, '*' p < 0.05, '.' p < 0.1, ' ' p < 1.
Figure 5 from: Baur H, Reichenbach F, Neubert E (2012) Sexual dimorphism in shells of Cochlostoma septemspirale (Caenogastropoda, Cyclophoroidea, Diplommatinidae, Cochlostomatinae). ZooKeys 208: 1-16. https://doi.org/10.3897/zookeys.208.2869
Figure 5 - Scatterplots of isosize against first (a) and isosize against second principal component (b) in shape space; blue dots females, red triangles males. Allometry ratio spectrum (c).
Figure 6 from: Baur H, Reichenbach F, Neubert E (2012) Sexual dimorphism in shells of Cochlostoma septemspirale (Caenogastropoda, Cyclophoroidea, Diplommatinidae, Cochlostomatinae). ZooKeys 208: 1-16. https://doi.org/10.3897/zookeys.208.2869
Figure 6 - Scatterplot of best (shell height:shell width) against second best ratio (aperture height:aperture width) for separating females from males; blue dots females, red triangles males.
Figure 4 from: Baur H, Reichenbach F, Neubert E (2012) Sexual dimorphism in shells of Cochlostoma septemspirale (Caenogastropoda, Cyclophoroidea, Diplommatinidae, Cochlostomatinae). ZooKeys 208: 1-16. https://doi.org/10.3897/zookeys.208.2869
Figure 4 - Boxplots of the ratios shell height:aperture height (a) and shell width:aperture width (b), and aperture protrusion (c). Significance levels of Wilcoxon test: '***' p < 0.001, '**' p < 0.01, '*' p < 0.05, '.' p < 0.1, ' ' p < 1.
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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
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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.