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FIGURE 3 in The taxonomic status of the genus Hubertoceras Spath: A new light on sexual dimorphism from the Callovian ammonites of Kutch, India
FIGURE 3. Representatives of Hubertoceras described by Spath (1931) from the Callovian of Kutch. 1-2. Holotype of Hubertoceras omphalodes (Waagen), GSI no. 2030, lateral and ventral views; 'Perisphinctes anceps beds' of Vanda (=middle Callovian anceps beds). 3-4. Holotype of H. dhosaence (Waagen), GSI no. 2035, lateral and apertural views; 'Perisphinctes anceps bed' of Keera (=beds nos. 5-7 of middle Callovian). 5. Holotype of H. hubertus Spath; NHMUK no. C7686, lateral view. 6-7. H. hubertus var. densicostata, GSI no. 16098, lateral and apertural views;?anceps beds of unknown locality. 8. H? sp. nov.; GSI no. 16099, lateral view; athleta beds of Fakirwadi (=athleta beds of upper Callovian). 9. Holotype of H. arcicosta, GSI no. 2099, lateral view; 'Golden Oolite' of Keera (=bed no. 2 of lower Callovian). 10. Holotype of H. mutans; GSI no. 2037, lateral view; 'Katrol group' of North Gudjinsir. Beds are following Jana et al. (2000, 2005). Commencement of body chamber and presence of lappets are indicated by 'x' and arrows respectively. GSI=Geological Survey of India, NHMUK=Natural History Museum, U.K. Scale bar equals 20 mm.
FIGURE 2 in The taxonomic status of the genus Hubertoceras Spath: A new light on sexual dimorphism from the Callovian ammonites of Kutch, India
FIGURE 2. The stratigraphic distribution of the studied antidimorphic pairs under the subfamily Sivajiceratinae of Kutch. Biozonation after Jana et al. (2000, 2005); Bardhan et al. (2012).
FIGURE 1 in The taxonomic status of the genus Hubertoceras Spath: A new light on sexual dimorphism from the Callovian ammonites of Kutch, India
FIGURE 1. Geological map of Kutch showing the major localities (solid squares) from where fossils of the Sivajiceratinae have been collected (modified after Dutta and Bardhan, 2016).
Fig. 2 in Pupal size distribution and sexual dimorphism in wild and laboratory populations of two species of Anastrepha (Diptera: Tephritidae) fruit flies
Fig. 2. Canonical analysis for pupae size parameters of males and females of laboratory and wild populations in Anastrepha ludens. The canonical analysis is represented on the first canonical axis (can 1), where the boxplots indicate the populations (laboratory and wild) and sexes (males and females) (lef). The variables of pupae size: length (mm), width (mm), and weight (mg) are indicated by vectors (right).
Fig. 1 in Pupal size distribution and sexual dimorphism in wild and laboratory populations of two species of Anastrepha (Diptera: Tephritidae) fruit flies
Fig. 1. Size distribution of laboratory and wild Anastrepha ludens and Anastrepha obliqua male and female pupae. The proportion of male and female pupae is shown in 10 pupal size classes (pupal diam mm) on the x-axis.
Fig. 3 in Pupal size distribution and sexual dimorphism in wild and laboratory populations of two species of Anastrepha (Diptera: Tephritidae) fruit flies
Fig. 3. Canonical analysis for pupae size parameters of males and females of laboratory and wild populations in Anastrepha obliqua. The canonical analysis is represented on the first canonical axis (can 1), where the boxplots indicate the populations (laboratory and wild) and sexes (males and females) (lef). The variables of pupae size: length (mm), width (mm), and weight (mg) are indicated by vectors (right).
Figure 1 in Sexual dimorphism in Carinatogecko heteropholis (Minton, Anderson, and Anderson, 1970) (Sauria: Gekkonidae) from Ilam Province, western Iran
Figure 1. Map showing the coordinates of the study site in Karezan region at mountainsides of the Zagros.
Figure 4 in Sexual dimorphism in Carinatogecko heteropholis (Minton, Anderson, and Anderson, 1970) (Sauria: Gekkonidae) from Ilam Province, western Iran
Figure 4. Ordination of the individual males and females of Carinatogecko heteropholis on the first two principal components. Note the relative degree of isolation between males and females, which is mainly attributed to SVL, TL, HL, HW, LFL, LHL, FHL, and VL in the PC1 and SL and IL in the PC2.
Figure 4 in Analysis of sexual dimorphism in the Persian long-tailed desert lizard, Mesalina watsonana (Stoliczka, 1872; Sauria: Lacertidae)
Figure 4. Scatter plots of the head length (HL) against the snout-vent length (SVL) for the Zagros populations (A) Northeastern popUlations (B) Eastern popUlations (C) Male = (▲) and Female = (○). Regression lines are shown whenever the slopes are significantlY different from Zero.
Figure 3 in Analysis of sexual dimorphism in the Persian long-tailed desert lizard, Mesalina watsonana (Stoliczka, 1872; Sauria: Lacertidae)
Figure 3. Ordination of individUal male (▲) and female (○) specimens of the Zagros populations (A) Northeastern populations (B) Eastern popUlations (C) on the first two principal components.
Figure 2 in Analysis of sexual dimorphism in the Persian long-tailed desert lizard, Mesalina watsonana (Stoliczka, 1872; Sauria: Lacertidae)
Figure 2. The mean and standard error (bars) for significantlY different head siZe characters between males and females of Mesalina watsonana, revealed from the analysis of variance (ANOVA). Head length (A), head width (B), head height (C), and snout length (D).
Figure 3 in Sexual dimorphism in Carinatogecko heteropholis (Minton, Anderson, and Anderson, 1970) (Sauria: Gekkonidae) from Ilam Province, western Iran
Figure 3. Presence of swelling in the male of C. heteropholis at base of the tail which accommodate hemipenes (left) and their absence in female (right).
Figure 2 in Sexual dimorphism in Trapelus ruderatus ruderatus (Sauria: Agamidae) with notes on the natural history
Figure 2 (above). Ordination of the individual males and females of Trapelus r. ruderatus on the first two principle components. Note the relative degree of isolation of males and females.
Figure 1 in Analysis of sexual dimorphism in the Persian long-tailed desert lizard, Mesalina watsonana (Stoliczka, 1872; Sauria: Lacertidae)
Figure 1. Geographic distribution of 19 Operational Taxonomic Units (OTU) of Mesalina watsonana used in this study.
Figure 2 in Sexual size dimorphism in Rana (Pelophylax) ridibunda ridibunda Pallas, 1771 from a population in Darre-Shahr Township, Ilam Province, western Iran
Figure 2. The presence of vocal pouches (a) and digital pads (b) in male Rana (Pelophylax) ridibunda ridibunda distinguishes them from females.
Figure 3 in Sexual size dimorphism in Rana (Pelophylax) ridibunda ridibunda Pallas, 1771 from a population in Darre-Shahr Township, Ilam Province, western Iran
Figure 3. Ordination of the individual males and females of Rana (Pelophylax) ridibunda ridibunda on the first two principal components. Note the relative degree of isolation between males and females, which is mainly attributed to SVL, LHL, LFL, HL, and HW in the PC1 and EEL and ELW in the PC2.
Figure 1 in The pupa of Chironomus decorus Johannsen, 1905 - additional description and an unusual sexual dimorphism
Figure 1. Cephalic tubercles and frontal warts of a male pupa of C. decorus from Yankton, South Dakota. The small secondary tubercles, with a small subapical seta, are indicated by arrows.
Figure 2 in Contribution to knowledge of the oribatid mite genus Idiozetes (Acari, Oribatida, Idiozetidae), with description of a new sexually dimorphic species from Vietnam
Figure 2 Idiozetes schusteri sp. n., adult, male (A, B) and female (C) (gnathosoma and legs not shown): A — dorsal view of notogaster; B — right lateral view of notogaster; C — right lateral view. Scale bars 50 μm.
Figure 1 in Contribution to knowledge of the oribatid mite genus Idiozetes (Acari, Oribatida, Idiozetidae), with description of a new sexually dimorphic species from Vietnam
Figure 1 Idiozetes schusteri sp. n., adult, female (gnathosoma and legs not shown): A — dorsal view; B — ventral view. Scale bar 50 μm.
Linked collectors and determiners for: A new Corydoras (Ostariophysi: Siluriformes: Callichthyidae) with an unusual sexual dimorphism from the rio Juruena basin, Brazil.
Natural history specimen data linked to collectors and determiners held within, "A new Corydoras (Ostariophysi: Siluriformes: Callichthyidae) with an unusual sexual dimorphism from the rio Juruena basin, Brazil". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/71f9552c-d7e7-4005-81b5-7e3f99ef447a">https://bionomia.net/dataset/71f9552c-d7e7-4005-81b5-7e3f99ef447a</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/71f9552c-d7e7-4005-81b5-7e3f99ef447a">https://gbif.org/dataset/71f9552c-d7e7-4005-81b5-7e3f99ef447a</a>. Formatted as a Frictionless Data package.
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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.