Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
182
datasets available to search
ShareScore release 0.7.1
Dataset results
182 results for “Talpidae”
Distribution. Uotsurijima (Senkaku Is), SW Japan. in Talpidae
Distribution. Uotsurijima (Senkaku Is), SW Japan.
Distribution. Japan, restricted to Echigo Plain in Niigata Prefecture (Honshu). in Talpidae
Distribution. Japan, restricted to Echigo Plain in Niigata Prefecture (Honshu).
Distribution. Sado I in Talpidae
Distribution. Sado I (Japan).
• Holarctic and Indo-Malayan Regions. in Talpidae
• Holarctic and Indo-Malayan Regions.
• 10-25 cm. in Talpidae
• 10-25 cm.
Distribution. Japan (Honshu I). in Talpidae
Distribution. Japan (Honshu I).
Distribution. C in Talpidae
Distribution. C & SW China (Shaanxi, Sichuan, Chongqing, and Yunnan).
Distribution. C in Talpidae
Distribution. C & SW China (Gansu, Shaanxi, Sichuan, and Yunnan).
Distribution. SC China (C Sichuan), restricted to Emei Shan and adjacent area. in Talpidae
Distribution. SC China (C Sichuan), restricted to Emei Shan and adjacent area.
Distribution. SW China (NW Yunnan) and possibly adjacent NE Myanmar (= Burma). in Talpidae
Distribution. SW China (NW Yunnan) and possibly adjacent NE Myanmar (= Burma).
Figure 2 in Complete mitogenome of Chinese shrew mole Uropsilus soricipes (Milne- Edwards, 1871) (Mammalia: Talpidae) and genetic structure of the species in the Jiajin Mountains (China)
Figure 2. Gene content and organization of mitochondrial genome of Uropsilus soricipes.
Figure 11 in Shape variation in the mole dentary (Talpidae: Mammalia)
Figure 11. Horizontal ramus shape showing position of landmarks (numbered coordinates, see Fig. 3) and semilandmarks (un-numbered coordinates) relating to models in Figures 10C–D and 12E–F.
Figure 4 in Shape variation in the mole dentary (Talpidae: Mammalia)
Figure 4. Distribution of talpid coronoid process outline shape in the ES-1 versus ES-2 (A) and ES-2 versus ES-3 (B) shape planes and corresponding outline shape models (C and D). L values = percentage variance accounted for by each axis based on singular values. For symbol shading conventions see text.
Figure 5 in Shape variation in the mole dentary (Talpidae: Mammalia)
Figure 5. Distribution of coronoid process outline shape among fully fossorial moles in the ES-1 versus ES-2 and ES-2 versus ES-3 shape planes for Talpini (A and B, respectively), Scalopini (C and D) and corresponding outline shape models (E and F). Least convex hulls show position within the shape space that each genus occupies. Dotted lines/arrows refer to position of specimens mentioned in the text.
Figure 2 in Shape variation in the mole dentary (Talpidae: Mammalia)
Figure 2. Phylogenetic relationships among the Talpidae proposed by Sánchez-Villagra et al. (2006) based on a maximum-parsimony analysis of 157 morphological characters. Clades indicated (in grey) are discussed in the text (see also Table 1).
Fig. 1 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 1. Two recent phylogenetic hypotheses for the Talpidae, modified to include only extant taxa and to conform to the generic classification of Corbet and Hill (1991). A, Hutchison (1976:13), based on osteology; B, Yates and Moore (1990:15), based on morphology, genetics, and cytogenetics.
Figure 6 in Morphology and phylogeny of scalopine moles (Eulipotyphla: Talpidae: Scalopini) from the eastern Himalayas, with descriptions of a new genus and species
Figure 6. Divergence times estimated using BEAST based on mitochondrial-nuclear concatenated data. Node numbers refer to divergence time in million years (Mya) and Bayesian posterior probabilities (PP).
Figure 4 in Morphology and phylogeny of scalopine moles (Eulipotyphla: Talpidae: Scalopini) from the eastern Himalayas, with descriptions of a new genus and species
Figure 4. Skins (dorsal view, left and ventral views, right) of the holotype of Alpiscaptulus medogensis (KIZ: 037966).
Figure 3 in Morphology and phylogeny of scalopine moles (Eulipotyphla: Talpidae: Scalopini) from the eastern Himalayas, with descriptions of a new genus and species
Figure 3. Occlusal views of the right lower teeth and upper teeth of Alpiscaptulus medogensis (KIZ: 037966; A, B) and Scapanulus oweni (KIZ: 033872; C, D). Scale bar = 5 mm.
FIGURE 2 in A new shrew mole species of the genus Uropsilus (Eulipotyphla: Talpidae) from northwestern Vietnam
FIGURE 2. Lateral view of the body (A), lateral view (B), dorsal view (C), and ventral view (D) of the holotype (IEBR-M- 8101) of Uropsilus fansipanensis sp. nov.
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.