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Рис. 2. Arion subfuscus c Камчатки, г. Петропавловск-Камчатский. Фото О.А. ЧернЯгиной (Заметно выделение желтооранжевой слиЗи). in Distribution of an invasive slug, Arion subfuscus (Draparnaud, 1805) in East Asia from Kamchatka to China
Рис. 2. Arion subfuscus c Камчатки, г. Петропавловск-Камчатский. Фото О.А. ЧернЯгиной (Заметно выделение желтооранжевой слиЗи).
Fig. 3 in Distribution of an invasive slug, Arion subfuscus (Draparnaud, 1805) in East Asia from Kamchatka to China
Fig. 3. Findings of Arion subfuscus in East Asia: 1–3 – China, after Wiktor et al. [2000]; 4 – Primorsky Krai near Fokino Town, after Prozorova, Fomenko [2015]; 5, 6 – Kuril Islands, Shikotan and Zelyony isls., after Prozorova [2000, 2002]; 7 – Petropavlovsk-Kamchatsky City.
Data for: Biogeography of oribatid mites (Acari) reflects their ancient origin and points to Southeast Asia as centre of radiation
<p>Understanding the worldwide distribution of species has fascinated scientists at least since Alfred Russel Wallace. Global patterns of belowground biodiversity may fundamentally differ from those of aboveground organisms. Here, we investigated the global distribution of oribatid mites in five biogeographic regions including North America, South America, Eurasia, Africa, and Oceania using a world list on the distribution of ~11,400 described species (including subspecies) at species, genera, and family levels. We found that most “endemic” (i.e., only occurring in one of the regions) species (4297) and also genera (143) occurred in Eurasia indicating that this region was the centre of radiation of oribatid mites. Within Eurasia, oribatid mite diversity was highest in Southeast Asia (1975 species) likely reflecting the long tropical history of this region (at least 200 million years), and also high fluctuations in water levels and island formation on the Sunda Shield. On a family level, oribatid mite diversity did not differ between biogeographic regions indicating that oribatid mites are much older than the tropics and older than the existence of Pangaea supporting the view of their origin in the early Palaeozoic. Finally, among the 55 species that occurred in all biogeographic regions nearly 50 % reproduce by thelytoky and colonize high latitude ecosystems, indicating that compared to sexual species a disproportionally high number of parthenogenetic species are distributed worldwide suggesting that they possess a general-purpose genotype. The other ~50 % sexuals predominantly occur in tropical/subtropical regions across biogeographic regions supporting the view that resource shortage in tropical regions favours sex. Our findings highlight the importance of biogeographical studies of soil animals to better understand their diversity, distribution, and life history strategies. </p>
Fig. 30 in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 30. Coelodontomys asiaticus, new genus and species. A. Occlusal view of right P4–M3 (AMNH 83541). B. Left lower jaw with i2, p4–m3 (AMNH 84344). B1. Occlusal view. B2. Buccal view. B3. Posterior view.
Fig. 29 in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 29. Coelodontomys asiaticus, new genus and species A. Occlusal view of left lower jaw with p4–m3 (AMNH 84344). B. Occlusal view of upper jaw with left and right P4–M3 (AMNH 83541) (in stereo). Scale = 1 cm.
Fig. 26 in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 26. Occlusal view of cheek teeth of Cyclomylus biforatus, new species A. Left P4–M3 (IVPP V 11442, holotype). B. Left m1–3 (IVPP V 11447).
Fig. 27 in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 27. Cheek teeth of Cyclomylus biforatus, new species. A. Left upper molar (IVPP V 11443.1). A1. Occlusal view. A2. Posterior view. A3. Buccal view. B. Buccal view of logitudinal section of right upper molar (IVPP V 11443.2). See figure 10 for abbreviations.
Fig. 24 in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 24. Ventral view of skull of Cyclomylus biforatus, new species (IVPP V 11442, holotype) (in stereo). Scale = 1 cm.
Fig. 20. Right lower jaw with i2, p4–m3 in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 20. Right lower jaw with i2, p4–m3 of Cyclomylus intermedius, new species (IVPP V 823, holotype). A. Occlusal view. B. Buccal view. C. Anterior view showing the relation between i2 and p4.
Fig. 19. Cyclomylus lohensis A in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 19. Cyclomylus lohensis A. Occlusal view of left p4–m3 (IVPP V 11543). B. Left lower jaw with i2, p4–m3 (IVPP V 11456). B1. Occlusal view. B2. Buccal view. B3. Posterior view showing the relation between i2 and m3.
Fig. 16. Cyclomylus lohensis. A in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 16. Cyclomylus lohensis. A. Skull of AMNH 19096 (holotype). A1. Ventral view. A2. Right lateral view. A3. Anterior view. B. Anterior view of transverse section along p4 of right lower jaw (IVPP V 11458) showing the relation between p4 (alveolus) and i2.
Fig. 14 in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 14. Dental measurements of Tsaganomys altaicus specimens. A, B. Histograms of measurements of length of cheek tooth rows. C, D. Histograms of measurements of length of molar rows. E– L. Scatterplot of measurements of length and width of cheek teeth. Solid squares represent the holotype (AMNH 19019), and open circles represent other specimens.
Fig. 9 in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 9. Lower jaws of Tsaganomys altaicus showing the relation between i2 and lower cheek teeth. A. Right lower jaw with i2 and p4–m3 (IVPP V 11417.1). A1. Occlusal view. A2. Buccal view. A3. Ventral view. A4. Anterior view. B. Anterior view of left lower jaw with p4–m2 (AMNH 82273).
Fig. 12 in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 12. Occlusal view of cheek teeth of Tsaganomys altaicus. A. Right p4–m3 of AMNH 83510. B. Right dp4–m3 of IVPP V 11402. C. Right p4 of AMNH 82289.
Fig. 8 in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 8. Left lower jaw of Tsaganomys altaicus (AMNH 19019, holotype). A. Occlusal view (in stereo). B. Lateral view. Scale = 1 cm.
Fig. 31 in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 31. Cheek teeth of Coelodontomys asiaticus, new genus and species. A. Right upper molar (IVPP V 11428). A1. Occlusal view. A2. Anterior view. A3. Buccal view. A4. Posterior view. B. Buccal view of longitudinal section of cheek tooth (IVPP V 11433). Abreviation as in figure 10.
Fig. 11 in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 11. Occlusal view of right lower jaw with p4–m3 of Tsaganomys altaicus (AMNH 83510) (in stereo); Scale = 5 mm.
Fig. 28 in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 28. Coelodontomys asiaticus, new genus and species, showing the relations between incisors and cheek teeth. A. Left upper jaw with I2, P4–M2 (AMNH 85277). A1. Medial view. A2. Anterior view. A3. Buccal view. B. Anterior view of transverse section across p4 of right lower jaw (IVPP V 11434). C. Right lower jaw with i2, p4–m3 (AMNH 83521). C1. Buccal view. C2. Anterior view.
Fig. 6 in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 6. Skull and lower jaw of Tsaganomys altaicus (IVPP V 11390). A. Left lateral view at skull. B. Left lower jaw. B1. Occlusal view. B2. Buccal view.
Fig. 5 in On Tsaganomyidae (Rodentia, Mammalia) of Asia
Fig. 5. Skull and lower jaw of Tsaganomys altaicus (IVPP V 11390). A. Right lateral view of skull. B. Left lower jaw. B1. Occlusal view. B2. Buccal view. Scale = 3 cm.
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
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.