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.
1,968
datasets available to search
ShareScore release 0.9.0
Dataset results
1,968 results for “morphological taxonomy”
FIGURE 3 in Integrative taxonomy base on morphology and molecular phylogeny with description of a new genus, Progoniogryllus gen. nov. and two new species (Orthoptera: Grylloidea: Gryllidae; Gryllinae)
FIGURE 3. Copulation of P. directus sp. nov. (female above male).
FIGURES 19–22 in Morphology and taxonomy of Psammodiscus Round & Mann (Bacillariophyceae: Rhaphoneidales) with a description of the new species Psammodiscus calceatus
FIGURES 19–22. Psammodicus calceatus sp. nov. (LM. BF); Fig. 20 = holotype. Scale bar = 10 µm.
FIGURES 37–51 in Morphology and taxonomy of Psammodiscus Round & Mann (Bacillariophyceae: Rhaphoneidales) with a description of the new species Psammodiscus calceatus
FIGURES 37–51. Psammodicus calceatus sp. nov., epicingulum.
FIGURE 14 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383
FIGURE 14. Male Boophis obscurus (UADBA uncatalogued) from Ranomafanakely.
FIGURE 2 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383
FIGURE 2. Male holotype of Boophis piperatus sp. nov. (ZSM 377/2004) from Ranomafana.
FIGURE 13 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383
FIGURE 13. Male holotype of Boophis spinophis sp. nov. (ZSM 376/2004) from Ambatolahy.
Fig. 13 in Taxonomy, larval morphology and cytogenetics of Lihelophorus, the Tibetan endemic subgenus of Helophorus (Coleoptera: Hydrophiloidea)
Fig. 13. Head appendages of larvae of Lihelophorus and Helophorus s.str. a–d – mandibles in dorsal view: a – H. (H.) liguricus Angus, 1970 (left mandible); b – H. (Lihelophorus) yangae sp. nov. (left mandible); c–d – H. (Lihelophorus) lamicola Zaitzev, 1908 (c – left mandible; d – right mandible). e–f – left antenna in dorsal view: e – H. (H.) liguricus Angus, 1970; f – H. (Lihelophorus) yangae sp. nov. g–j – labium: g–h – H. (Lihelophorus) yangae sp. nov. (g – ventral; h – dorsal); i–j – H. (Lihelophorus) lamicola Zaitzev, 1908 (i – ventral; j – dorsal). Abbreviations: mp – mandibular penicillus; rt – retinacular tuft.
Fig. 3 in Taxonomy, larval morphology and cytogenetics of Lihelophorus, the Tibetan endemic subgenus of Helophorus (Coleoptera: Hydrophiloidea)
Fig. 3. Habitus of the species of Helophorus (Lihelophorus). a–c – H. lamicola Zaitzev, 1908 (a – Qinghai: Zhaling Hu (lectotype); b–c – Quinghai: Golo). d–g – H. ser Zaitzev, 1908 (d–e – Qinghai: Golo; f – Xizang, Nyainqentanglha Feng; g – Gansu: Xiahe env.). h–k – H. yangae sp. nov. (h – Xizang: 90 km W of Amdo; i – Xizang: 25 km W of Amdo; j – Qinghai: Golo; k – India: Kar Tso (Orchymont coll.)). All specimens to scale.
FIGURE 17 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383
FIGURE 17. Female holotype of Boophis praedictus sp. nov. (ZMA 20131) from Vevembe.
Fig. 44 in Morphology, Phylogenetic Taxonomy, And Systematics Of Ichthyornis And Apatornis (Avialae: Ornithurae)
Fig. 44. An element from YPM 1775 that bears comparison to a pygostyle but which differs markedly from the morphology of that element in YPM 1732 (compare fig. 43).
Fig. 13 in Morphology, Phylogenetic Taxonomy, And Systematics Of Ichthyornis And Apatornis (Avialae: Ornithurae)
Fig. 13. The holotype specimen of Ichthyornis (Guildavis) tener (YPM 1760). The holotype is a partial sacrum comprised of crushed portions of (A) the midsacral series (in dorsal view) and (B) the anterior end (in oblique ventrolateral view).
Fig. 7 in Morphology, Phylogenetic Taxonomy, And Systematics Of Ichthyornis And Apatornis (Avialae: Ornithurae)
Fig. 7. Size and stratigraphic position of individuals referred to Ichthyornis dispar interpreted as variable sampling through time of a constant size range for a single species. Data points represent total humerus length of the indicated specimen(s) in millimeters. The relative size of specimens without data points, those lacking complete humeri, was estimated (i.e., YPM 1738, 1765, SMM 2139, USNM 22820, TMM 42522–1, and Cenomanian specimens, SMNH P2077.67, SMNH P2077.111, SMNH P2077.112, SMNH P2487.5). Shaded region indicates size variation interpreted as constant through time.
FIG. 11 in Phylogenetic Relationships of New World Porcupines (Rodentia, Erethizontidae): Implications for Taxonomy, Morphological Evolution, and Biogeography
FIG. 11. Camera-trap photograph of two Coendou bicolor visiting a mineral lick near the Centro de Investigación Río Los Amigos, Madre de Dios, Peru (courtesy of Dyana LaRosa). In situations like this, porcupines are probably exposed to a greater risk of predation than they would be in the canopy. Coendou prehensilis is the only other Neotropical species known to frequent mineral licks (Montenegro, 2004; Blake et al., 2011).
Figs 3-4 in Notes on the Aphodius (s.str.) fimetarius-complex - morphology, taxonomy, nomenclature and worldwide distribution (with emphasis on the Iberian Peninsula, Austria and Germany) (Scarabaeoidea: Scarabaeidae: Aphodiinae)
Figs 3-4: Parameres in lateral view of (3) Aphodius fimetarius (Oldendorf near Celle, Germany; cHF) and (4) A. cardinalis (neotype; Vejer de la Frontera, Cádiz, Spain; ZSM). Lines a, b and c include angles the values of which are given for several specimens in Fig. 5.
Fig. 10 in Notes on the Aphodius (s.str.) fimetarius-complex - morphology, taxonomy, nomenclature and worldwide distribution (with emphasis on the Iberian Peninsula, Austria and Germany) (Scarabaeoidea: Scarabaeidae: Aphodiinae)
Fig. 10: Distribution of Aphodius fimetarius (red circles) and A. cardinalis (yellow circles) on the Iberian Peninsula; orange circles indicate localities where both species have been found together; larger circles with a dot in the centre indicate localities where specimens with darkened elytra have been found together with normally coloured specimens.
Figure 6 in The phylogeny and taxonomy of Hippopotamidae (Mammalia: Artiodactyla): a review based on morphology and cladistic analysis
Figure 6. Strict consensus tree of the three most parsimonious trees obtained from the cladistic analysis (length = 81, CI = 0.6420, RI = 0.7752). In italic-bold, the bootstrap results are given as an indication of clade robustness.
Figure 3. Cranial character states. A in The phylogeny and taxonomy of Hippopotamidae (Mammalia: Artiodactyla): a review based on morphology and cladistic analysis
Figure 3. Cranial character states. A, lateral view of a Hexaprotodon liberiensis skull. B, Lateral view of a Hippopotamus amphibius skull. C, lateral view of a Hex. mingoz skull. D, three dorsal views of the braincase (from bottom to top: in Hex. harvardi, in Hex. mingoz, in Hip. amphibius). E, four schematic anterior views of the left orbit (from right to left: in Hex. protamphibius, in Hex. harvardi, in Hip. gorgops, in Hex. sivalensis).
Figure 2. External morphologies. A in Taxonomy and description of clionaid sponges (Hadromerida, Clionaidae) from the Pacific Ocean of Mexico
Figure 2. External morphologies. A, Cliona papillae sp. nov., boring into rock and calcareous algae at 5 m depth. B, Detail of the papillae of Cliona papillae sp. nov. The arrow shows the fusion of oscular and ostial papillae. The typical sieve-like ostial papillae are visible to the eye underwater. C, Cliona vallartense sp. nov. growing in beta stage with scattered oscular papillae (arrow) at 4 m depth. D, Cliona vallartense sp. nov. growing in beta stage with numerous oscula (arrow) at 7 m depth. E and F, Cliona raromicrosclera comb. nov. massive orange and beige specimens.
Figure 4 in Morphological and molecular taxonomy of a new Daptonema (Nematoda, Xyalidae) with comments on the systematics of some related taxa
Figure 4. Drawing of Daptonema matrona sp. nov. allotype: A, habitus; B, cephalic region; C, tail.
Fig. 13. A in Phylogenetic relationships based on morphological data and taxonomy of the genus Salvadora Baird & Girard, 1853 (Reptilia, Colubridae)
Fig. 13. A. Longitudinal lines interrupted in the first third of the body. B. Longitudinal lines extending along the body.
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.