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8,119 results for “species distribution”
Figs 15–21 in A new species and new data on distribution of the shore bugs of China (Hemiptera: Heteroptera: Saldidae)
Figs 15–21. Rupisalda austrosinica sp. nov.: 15–17 – paramere in various positions, 18 – parandria, 19 – penisfilum, 20 – median endosomal sclerite in ventral view, 21 – spermatheca.
Figs 1–8. 1 in A new species and new data on distribution of the shore bugs of China (Hemiptera: Heteroptera: Saldidae)
Figs 1–8. 1 – Chiloxanthus kozlovi (Kiritshenko, 1912), female (Sichuan). 2–7 – Calacanthia grandis Cobben, 1985; 2 – female (Gansu); 3 – paramere; 4 – parandria; 5–6 – medial endosomal sclerite (5 – lateral view, 6 – ventral view); 7 – female, holotype, forewing (after COBBEN 1985). 8 – Macrosaldula bogdashana Luo & Vinokurov, 2011, female (Xinjiang).
Figs 9–14 in A new species and new data on distribution of the shore bugs of China (Hemiptera: Heteroptera: Saldidae)
Figs 9–14. Rupisalda austrosinica sp. nov.: 9–10 – male (Guangdong); 11 – female (Yunnan); 12 – forewing; 13 – head, frontal view; 14 – female subgenital plate, ventral view. Abbreviations: eg – eversible gland.
Figs 27–29 in Earwigs (Dermaptera) of Socotra Island: checklist, distribution, and description of a new genus and four new species
Figs 27–29. Sketch maps of Socotra Island displaying the known and newly recorded distribution of Dermaptera. Published records are based on HAAS at al. (2004); the occurrence of Labidura riparia (Pallas, 1773) on Samha Island published by these authors is not displayed.
Figs 20–26 in Earwigs (Dermaptera) of Socotra Island: checklist, distribution, and description of a new genus and four new species
Figs 20–26. Guanchia sokotrana (Burr, 1905) comb. nov. (20–23) and Guanchia bituberculata (Brindle, 1966) stat. restit. (24–26). 20 – habitus of male, dorsal view; 21 – male sternal plates, ventral view; 22 – detail of the end of male ultimate tergite; 23 – male genitalia; 24 – habitus of male holotype, 25 – detail of the end of male ultimate tergite; 26 – male genitalia of holotype.
Figs 16–19 in Earwigs (Dermaptera) of Socotra Island: checklist, distribution, and description of a new genus and four new species
Figs 16–19. Anisolabella haasi sp. nov. 16 – habitus of male holotype; 17 – male penultimate sternite, ventral view; 18 – male genitalia; 19 – right paramere of male genitalia.
Figs 11–15 in Earwigs (Dermaptera) of Socotra Island: checklist, distribution, and description of a new genus and four new species
Figs 11–15. Anisolabella planata sp. nov. 11 – habitus of male holotype; 12 – male penultimate sternite, ventral view; 13 – ultimate tergite and forceps of female paratype; 14 – male genitalia; 15 – left paramere of male genitalia.
Figs 6–10 in Earwigs (Dermaptera) of Socotra Island: checklist, distribution, and description of a new genus and four new species
Figs 6–10. Socotralabis bezdeki sp. nov. 6 – habitus of male holotype; 7 – male penultimate sternite, ventral view; 8 – ultimate tergite and forceps of female paratype; 9 – male genitalia; 10 – right paramere of male genitalia.
Figs 1–5 in Earwigs (Dermaptera) of Socotra Island: checklist, distribution, and description of a new genus and four new species
Figs 1–5. Socotralabis hulai sp. nov. 1 – habitus of male holotype; 2 – male penultimate sternite, ventral view; 3 – ultimate tergite and forceps of female paratype; 4 – male genitalia; 5 – right paramere of male genitalia.
Fig. 2 in The Latitudinal Distribution Of Sphingid Species Richness In Continental Southeast Asia: What Causes The Biodiversity 'Hot Spot' In Northern Thailand?
Fig. 2. Estimated local species richness (ACE) from nine quantitative light trapping sites. Fisher's α, an alternative measure of local diversity (not shown), is lowest at the Malaysian sites (α = 7–13) and highest at a montane site in Northwestern Thailand (α = 30), whereas the Vietnam sample and other Thai sites score intermediately (α = 11–21).
Fig. 1. A in The Latitudinal Distribution Of Sphingid Species Richness In Continental Southeast Asia: What Causes The Biodiversity 'Hot Spot' In Northern Thailand?
Fig. 1. A, Estimated species richness (simplified from Beck & Kitching, 2004); B, Sampling intensity (kernels of original distribution records, smoothed; software by Hooge et al., 1999); C, altitudinal zonation (from digital elevation model, http://www.ngdc.noaa.gov/mgg/global/ seltopo.html). Elevation classes are [m]: 0–500 (white), 501–1000, 1001–1500, 1501–2000,>2001 (black); D, Landscape types (simplified from remote sensing data, http://www-gvm.jrc.it/glc2000). Agricultural and highly disturbed areas are printed in light grey, mosaic and bush in dark grey and closed forests in black.
Fig. 3 in The Latitudinal Distribution Of Sphingid Species Richness In Continental Southeast Asia: What Causes The Biodiversity 'Hot Spot' In Northern Thailand?
Fig. 3. Abundance (number of species, y-axis) and the latitudinal mean of their range in four regions. Black bars indicate the approximate latitudinal extend of the regions under investigation.
Figs 34–43. 34–36 in Contribution to the synonymies, distributions, and bionomics of the Old World species of Macrosiagon (Coleoptera: Ripiphoridae)
Figs 34–43. 34–36 – Macrosiagon inferna (Schaufuss, 1872) (34–35 – holotype and labels of Emenadia inferna Schaufuss, 1872; 36 – Macrosiagon longipes Pic, 1929, syntype). 37–38 – Macrosiagon lyauteyi Alluaud, 1902, female from Ihosy. 39–40 – Macrosiagon marcelli Alluaud, 1902 (39 – female from Zimbabwe; 40 – female from Zambia, Serenje, head frontally). 41–43 – Macrosiagon trinotata Pic, 1950 (41 – holotype; 42 – female from Kenya, Tsavo, head frontally; 43 – male from Republic of South Africa, Transwaal).
Figs 8–15. 8–11 in Contribution to the synonymies, distributions, and bionomics of the Old World species of Macrosiagon (Coleoptera: Ripiphoridae)
Figs 8–15. 8–11 – Macrosiagon bequaerti Pic, 1913. (8 – male from Zambia; 9 – male from Guinea; 10–11 – holotype with labels). 12 – Macrosiagon cf. bequaerti Pic, 1913, India. 13–15 – Macrosiagon biguttata (Blanchard, 1846) (13 – syntype label; 14 – male, Australia, Cairns; 15 – female, Australia, Cairns).
Figs 16–24. 16–17 in Contribution to the synonymies, distributions, and bionomics of the Old World species of Macrosiagon (Coleoptera: Ripiphoridae)
Figs 16–24. 16–17 – Ripiphorus dubius, syntypes (syn. of Macrosiagon bimaculata (Fabricius, 1787), photos by Aleksey Gusakov 2008). 18 – Pic's handwritten label with differential diagnosis to Macrosiagon natalense Pic, 1950 (Verbatim: 'diffère de caffrum / par les élytres sans / macule discale / noire le thorax / á bordure rouge / postèrieuere'). 19–24 – Macrosiagon caffra (Fåhraeus, 1870) (19–21 – female syntype with labels; 22–24 – male syntype with labels).
Figs 25–33. 25–27 in Contribution to the synonymies, distributions, and bionomics of the Old World species of Macrosiagon (Coleoptera: Ripiphoridae)
Figs 25–33. 25–27 – Macrosiagon callewaerti Pic, 1950; holotype. (25 – habitus dorsally; 26 – head frontally; 27 – metatarsomeres dorsally). 28–30 – Macrosiagon grombczewskii (Semenov, 1891), holotype (photos M. Engel 2010). 31–33 – Macrosiagon humeralis Pic, 1929. (31 – syntype; 32–33 – male from Tanzania, head frontally and metatarsomeres dorsally).
Figs 1–7. 1–2 in Contribution to the synonymies, distributions, and bionomics of the Old World species of Macrosiagon (Coleoptera: Ripiphoridae)
Figs 1–7. 1–2 – Macrosiagon armata (Waterhouse, 1883), lectotype. 3–7 – M. axillaris (Gerstaecker, 1855) (3–5 – M. axillaris, syntype and labels; 6 – M. maculaticeps Pic, 1913, holotype; 7 – M. elongata Pic, 1950, holotype).
Figs. 20-23 in Contribution to the knowledge of the caddisfly fauna (Trichoptera) of Iran: description of new species and new distributional data
Figs. 20-23. Hydropsyche lundaki sp. nov., male genitalia. 20 – lateral view; 21 – dorsal view; 22 – phallus, ventral view; 23 – right inferior appendage, ventro-caudal view.
Figs. 6-13 in Contribution to the knowledge of the caddisfly fauna (Trichoptera) of Iran: description of new species and new distributional data
Figs. 6-13. Tinodes voriseki sp. nov., male genitalia. 6-11. Holotype from Chuplu. 6 – lateral view; 7 – ventral view; 8 – segment X, dorsal view; 9 – process of basal plate, lateral view; 10 – phallus and paraproctal processes, lateral view; 11 – phallus and paraproctal processes, dorsal view. 12-13. Specimen from Alanje. 12 – process of basal plate, lateral view; 13 – phallus and paraproctal processes, lateral view.
Figs. 14-19 in Contribution to the knowledge of the caddisfly fauna (Trichoptera) of Iran: description of new species and new distributional data
Figs. 14-19. Tinodes hajeki sp. nov., male genitalia. 14 – lateral view; 15 – ventral view; 16 – segment X, dorsal view; 17 – process of basal plate, lateral view; 18 – phallus and paraproctal processes, lateral view; 19 – phallus and paraproctal processes, dorsal view.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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.