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.
108
datasets available to search
ShareScore release 0.9.0
Dataset results
108 results for “Soricomorpha”
Figure 5 in How common is gigantism in insular fossil shrews? Examining the 'Island Rule' in soricids (Mammalia: Soricomorpha) from Mediterranean Islands using new body mass estimation models
Figure 5. Diagrams comparing the body mass (in g) of extant relatives and fossil species: A, extinct Asoriculus and Nesiotites species and the extant species of the tribe Nectogalini; B, extinct and extant Crocidura species. Lines indicate the body mass range of groups. See the legend for symbols.
Figure 3 in Barcoding, molecular taxonomy, and exploration of the diversity of shrews (Soricomorpha: Soricidae) on Mount Nimba (Guinea)
Figure 3. Histograms of divergence percentage values between all sequences. Black, intraspecific distances; light grey, interspecific distances amongst clade C; dark grey, interspecific distances excluding clade C. All sequences were corrected using the Kimura two-parameter substitution model. Sequences corresponding to nuclear copies of cytochrome b were excluded from the analysis. BRCA, breast cancer gene; COI, cytochrome oxidase I.
Figure 2 in Barcoding, molecular taxonomy, and exploration of the diversity of shrews (Soricomorpha: Soricidae) on Mount Nimba (Guinea)
Figure 2. Neighbour-joining trees built for each marker using PAUP* 4.01b10. Sequences were corrected with the Kimura two-parameter substitution model. Values represented above branches are bootstrap values (1000 replicates). BRCA, breast cancer gene; COI, cytochrome oxidase I.
Figure 1 in Barcoding, molecular taxonomy, and exploration of the diversity of shrews (Soricomorpha: Soricidae) on Mount Nimba (Guinea)
Figure 1. Phylogeny built using Bayesian inference analysis of the concatenated data set of two mitochondrial markers (cytochrome b and 16S) and one nuclear marker (the breast cancer gene, BRCA) (1852 bp). Values represented above and below branches are Bayesian posterior probabilities and bootstrap values (maximum likelihood, 1000 replicates), respectively. The tree was rooted with addition of three Soricinae shrews Neomys fodiens, Soriculus nigrescens, and Nectogale elegans.
Figure 4 in Patterns of morphological variation amongst semifossorial shrews in the highlands of Guatemala, with the description of a new species (Mammalia, Soricomorpha, Soricidae)
Figure 4. Plot of scores on first two axes from principal components analysis of humeri of five species of broad-clawed Cryptotis (see Table 8).
Figure 3 in Patterns of morphological variation amongst semifossorial shrews in the highlands of Guatemala, with the description of a new species (Mammalia, Soricomorpha, Soricidae)
Figure 3. Plot of scores on first two axes from principal components analysis of skulls of the three largest species of broad-clawed Cryptotis (see Table 7).
Figure 1 in Patterns of morphological variation amongst semifossorial shrews in the highlands of Guatemala, with the description of a new species (Mammalia, Soricomorpha, Soricidae)
Figure 1. Anterior aspect of the humerus illustrating variables measured: BS1, breadth of shaft of humerus from superior base of medial epicondyle to superior base of lateral epicondyle; CD, distance from deltoid process to capitulum; DW, width of distal end of humerus; GT, distance from greater tuberosity to teres tubercle; L1, length of humerus from head to capitulum and trochlea; MT, internal distance from medial epicondyle to teres tubercle; PW, width of proximal end of humerus.
Figure 2 in Patterns of morphological variation amongst semifossorial shrews in the highlands of Guatemala, with the description of a new species (Mammalia, Soricomorpha, Soricidae)
Figure 2. Plot of scores on first two axes from principal components analysis of skulls of six species of broad-clawed Cryptotis (see Table 6).
Figure 7 in Patterns of morphological variation amongst semifossorial shrews in the highlands of Guatemala, with the description of a new species (Mammalia, Soricomorpha, Soricidae)
Figure 7. Distance trees resulting from cluster analyses of morphological data sets derived from six species of broad-clawed Cryptotis: A, 21 craniomandibular variables; B, seven humerus variables; C, eight variables from ray I; D, ten variables from ray III; E, ten variables from ray V; F, combined analyses of 28 forefoot variables; G, combined analysis of 59 variables.
Figure 10. X in Patterns of morphological variation amongst semifossorial shrews in the highlands of Guatemala, with the description of a new species (Mammalia, Soricomorpha, Soricidae)
Figure 10. X-ray images of left mani of: A, Cryptotis parvus parvus (USNM 568977); B, Cryptotis mexicanus (USNM 68298); C, Cryptotis griseoventris (USNM 758905); D, Cryptotis mam (USNM 77057); E, Cryptotis oreoryctes (USNM 569854); F, Cryptotis lacertosus (USNM 569442); G, Cryptotis goodwini (USNM 77078).
Figure 9 in Patterns of morphological variation amongst semifossorial shrews in the highlands of Guatemala, with the description of a new species (Mammalia, Soricomorpha, Soricidae)
Figure 9. Anterior aspect of left humeri of A, Cryptotis parvus parvus (USNM 582437); B, Cryptotis mexicanus (USNM 29541); C, Cryptotis mam (USNM 570340); D, Cryptotis goodwini (USNM 275681); E, Cryptotis goodwini (UMMZ 103416); F, Cryptotis oreoryctes (USNM 569877); G, Cryptotis lacertosus (USNM 569503).
Figure 5 in Patterns of morphological variation amongst semifossorial shrews in the highlands of Guatemala, with the description of a new species (Mammalia, Soricomorpha, Soricidae)
Figure 5. Plots of scores on first two axes from principal components analyses of individual rays from five species of broad-clawed Cryptotis: A, six variables from ray I; B, eight variables from ray III; C, six variables from ray V (see Table 9).
Figure 6 in Patterns of morphological variation amongst semifossorial shrews in the highlands of Guatemala, with the description of a new species (Mammalia, Soricomorpha, Soricidae)
Figure 6. Box-and-whisker plot of width of metacarpal of ray III for five species of broad-clawed Cryptotis. Cross within each box represents the mean, shaded box indicates SD, and vertical line shows the range of values for each species.
Figure 8 in Dental polymorphisms in Crocidura (Soricomorpha: Soricidae) and evolutionary diversification of crocidurine shrew dentition
Figure 8. Result of the phylogenetic analysis. A, most parsimonious tree optimized by DELTRAN approach and derived from the weighted 46 characters represented in the data matrix (Supporting Information, Supplementary Material S8: Table 1) highlighting the key character 'A3 (root): second root development' [character 20; retention index (RI) = 0.44]. Tree length = 166; consistency index (CI) = 0.37; RI = 0.50; rescaled consistency index (RC) = 0.18; homoplasy index (HI) = 0.63. B, single-rooted A3, three-dimensional model of Shargainosorex angustirostris Zazhigin & Voyta, 2018 (GIN 959/1069; Mongolian middle Miocene; Crocidosoricinae), transparent medial view. C, single-rooted A3, three-dimensional model of Sorex minutissimus (ZIN 98582), transparent medial view. D, single-rooted A3, three-dimensional model of Crocidura lasiura [ZIN 79019; character (ch.) 20: state (st.) 0], transparent medial view. E, double-rooted A3, three-dimensional model of Crocidura zaitsevi (ZIN 96320; ch. 20: st. 1), transparent medial view. F, double-rooted A3, three-dimensional model of Crocidura phanluongi (ZIN 100307; ch. 20: st. 2), transparent medial view. G, double-rooted A3, three-dimensional model of Crocidura yaldeni (ZMMU S-165343; ch. 20: st. 2), transparent medial view. Abbreviations: 1–2 in yellow circles, the nodes supported by six synapomorphies (synapomorphies 1–3, 39, 43 and 46 indicated by red arrows and filled circles; for character descriptions see Supporting Information, Supplementary Material S8); numbers above the lines are character numbers; numbers below the lines are character-state transformations; blue arrows show supposed 20th character transformation according to the parsimonious analysis: from the plesiomorphic state (0) to the apomorphic states (1 and 2).
Figure 7 in Dental polymorphisms in Crocidura (Soricomorpha: Soricidae) and evolutionary diversification of crocidurine shrew dentition
Figure 7. Results of the analysis of skull shape of the samples of Crocidura based on three-dimensional landmark data. A, principal components (PC) plot for 11 Crocidura species (first vs. fifth axes). B, dorsal view of the shape at the minimum of the first axis corresponds to Crocidura zaitsevi (left shape) with the position of its own landmarks (red balls) and the shape transformation (blue balls) toward the opposite end of the axis; and the shape at the maximum of the axis corresponds to Crocidura yaldeni (right shape; blue landmarks, own; red landmarks, transformation). C, lateral views of the shapes at the minimum and maximum of the first axis, same as B. D, occlusal views of the shapes at the minimum and maximum of the first axis, same as B. For abbreviations and colour key, see legend to Figure 6; also see the Supporting Information (Supplementary Material S6: Figs 1, 3, 4).
Figure 1 in Dental polymorphisms in Crocidura (Soricomorpha: Soricidae) and evolutionary diversification of crocidurine shrew dentition
Figure 1. Crocidura olivieri (ZMMU S-166027) skull and upper tooth row. A, skull, scanned surface in ventral view. B, rostral part of the skull, three-dimensional model, transparent lateral view (cut image). C, upper dentition, threedimensional model, transparent lateral view. D, pulp endocast, three-dimensional model, lateral view. Scale bars: 5 mm in A; 2 mm in B; 1 mm in C, D. Abbreviations: A, antemolar; ABR, anterobuccal root; abrc, radicular (pulpal) canal of ABR; ALR, anterolingual root; alrc, radicular canal of ALR; AMR, antemolar main root; ath, antemolar chamber; HFR, hypoconal flange root; hfrc, radicular canal of HFR; I, incisor; M, molar; MC, metacone; mrc, main radicular canal of antemolars; MSS, mesostyle; MST, metastyle; P, premolar; PBR, posterobuccal root; pbrc, radicular canal of PBR; PC, paracone; PST, parastyle; src, second radicular canal of I1.
Figure 5 in Dental polymorphisms in Crocidura (Soricomorpha: Soricidae) and evolutionary diversification of crocidurine shrew dentition
Figure 5. Crocidura yaldeni (ZMMU S-165342, holotype; A–C), Crocidura lasiura (ZIN 76019; D–F), Crocidura obscurior (MNHN-ZM 2012-1116; G–I), Crocidura olivieri (ZMMU S-166027; J–L) and Crocidura zaitsevi (ZIN 96320; M–O) third
Figure 2 in Dental polymorphisms in Crocidura (Soricomorpha: Soricidae) and evolutionary diversification of crocidurine shrew dentition
Figure 2. Crocidura olivieri (ZMMU S-166027; A–C) and Crocidura yaldeni (ZMMU S-165342, holotype; D–G) upper teeth I1–A3, in medial view. A, D, upper teeth, three-dimensional model. B, E, pulp endocast, three-dimensional model. C, F, upper teeth, three-dimensional model, transparent view. G, magnified part of the incisor root, with fissure between main and second roots. Scale bars: 1 mm. Abbreviations: AAR, antemolar anterior root; AMR, antemolar main root; arc, anterior radicular canal; dg, damaged parts; also see legend to Figure 1.
Figure 4 in Dental polymorphisms in Crocidura (Soricomorpha: Soricidae) and evolutionary diversification of crocidurine shrew dentition
Figure 4. Crocidura obscurior (MNHN-ZM 2012-1116; A, B) and Crocidura phanluongi (ZIN 100307; C, D) third upper antemolar, in medial view. A, C, A3, three-dimensional model. B, D, A3, three-dimensional model, transparent view. Scale bars: 0.5 mm. For abbreviations, see legend to Figure 2.
Figure 3 in Dental polymorphisms in Crocidura (Soricomorpha: Soricidae) and evolutionary diversification of crocidurine shrew dentition
Figure 3. Sylvisorex johnstoni (MNHN-ZM-MO 1991-096; A–D) and Crocidura yaldeni (ZMMU S-165342, holotype; E, F) right half of rostral part and anterior tooth row. A, E, rostral part, three-dimensional model in ventral view with anterior teeth alveoli and explanatory drawing. B, F, rostral part, three-dimensional model in ventral view with anterior teeth. C, upper antemolars, three-dimensional model in buccal view. D, upper antemolars, three-dimensional model in transparent view. Scale bars: 1 mm in A, B, E, F; 0.5 mm in C, D. Abbreviations: (alv), alveolus of single-rooted n-antemolar or I1; (alv*), alveoli of double-rooted A3 (E); see Figure 1.
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.