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.
15,519
datasets available to search
ShareScore release 0.9.0
Dataset results
15,519 results for “r”
Subspecies and Distribution. . c. canuti Thomas & Wroughton, 1909 — Java (three localities), and Nusa Barong ail'd Bali Is. . c. timorensis R. E. Goodwin, 1979 — Timor I. in Rhinolophidae
Subspecies and Distribution. . c. canuti Thomas & Wroughton, 1909 — Java (three localities), and Nusa Barong ail'd Bali Is. . c. timorensis R. E. Goodwin, 1979 — Timor I.
Subspecies and Distribution. R. c. cognatus K Andersen, 1906 - Andaman Is (South Andaman). R. c. famulus K. Andersen, 1918 - Andaman Is (North, Point, Interview, Baratang, and Narcondam). The species is not known from the Nicobar Is, despite a number of sources listing it from them. in Rhinolophidae
Subspecies and Distribution. R. c. cognatus K Andersen, 1906 - Andaman Is (South Andaman). R. c. famulus K. Andersen, 1918 - Andaman Is (North, Point, Interview, Baratang, and Narcondam). The species is not known from the Nicobar Is, despite a number of sources listing it from them.
Subspecies and Distribution. R p. philippinensis Waterhouse, 1843 - Philippines (Luzon, Polillo, Mindoro, Samar, Negros, Bohol, Siquijor, and Mindanao Is). R p. maros Tate & Archbold, 1939 - N Borneo (Sabah and Sarawak), SW Sulawesi, Kabaena, Buton, Flores, and E Timor Is, and C Papua New Guinea (Mt Karimui and Waro). in Rhinolophidae
Subspecies and Distribution. R p. philippinensis Waterhouse, 1843 - Philippines (Luzon, Polillo, Mindoro, Samar, Negros, Bohol, Siquijor, and Mindanao Is). R p. maros Tate & Archbold, 1939 - N Borneo (Sabah and Sarawak), SW Sulawesi, Kabaena, Buton, Flores, and E Timor Is, and C Papua New Guinea (Mt Karimui and Waro).
Subspecies and Distribution. R c. creaghi Thomas, 1896 - Palawan I (Philippines) and N, W & E Borneo (including Banggi I), although it probably occurs more widely in Borneo. . c. pilosus K. Andersen, 1918 — Lesser Sunda Is (Madura, Nusa Penida, Flores, Semau, and Roti), in Rhinolophidae
Subspecies and Distribution. R c. creaghi Thomas, 1896 - Palawan I (Philippines) and N, W & E Borneo (including Banggi I), although it probably occurs more widely in Borneo. . c. pilosus K. Andersen, 1918 — Lesser Sunda Is (Madura, Nusa Penida, Flores, Semau, and Roti),
Subspecies and Distribution. R. a. afinis Horsfield, 1823 - Malay Peninsula (including Langkawi and Tioman Is), Sumatra, North Pagai I in Mentawai Is, and Java. R. a. hainanusJ. A. Allen, 1906 - Hainan I, China. R. a. himalayanus K Andersen, 1905 — N India (Uttarakhand, Uttar Pradesh, Sikkim, West Bengal, Assam, Meghalaya, Arunachal Pradesh, and Nagaland), Nepal, Bhutan, NE Bangladesh, N Myanmar, and C & S China (Sichuan, Yunnan, Shaanxi, Hubei, Hunan, and Guizhou). R. a. macrurus K. Andersen, 1905 - SE China (Jiangsu, Anhui, Zhejiang, Jiangxi, Fujian, Guangdong, Hong Kong, and Guangxi), S Myanmar, Thailand, Laos, and Vietnam (including Dao Tra Ban and Phu Quoc Is); possibly also Cambodia. R. a. nesites K. Andersen, 1905 - Borneo (including Laut, Sebuku, and Laut Kecil Is) and Anamba and Natuna Is. R. a. princeps K. Andersen, 1905 — Kangean (Kangean and Sepanjang Is), Lombok, Sumbawa, Flores, and Sumba Is. A morphologically distinct subspecies (still unnamed) is known from E Myanmar and N Vietnam. in Rhinolophidae
Subspecies and Distribution. R. a. afinis Horsfield, 1823 - Malay Peninsula (including Langkawi and Tioman Is), Sumatra, North Pagai I in Mentawai Is, and Java. R. a. hainanusJ. A. Allen, 1906 - Hainan I, China. R. a. himalayanus K Andersen, 1905 — N India (Uttarakhand, Uttar Pradesh, Sikkim, West Bengal, Assam, Meghalaya, Arunachal Pradesh, and Nagaland), Nepal, Bhutan, NE Bangladesh, N Myanmar, and C & S China (Sichuan, Yunnan, Shaanxi, Hubei, Hunan, and Guizhou). R. a. macrurus K. Andersen, 1905 - SE China (Jiangsu, Anhui, Zhejiang, Jiangxi, Fujian, Guangdong, Hong Kong, and Guangxi), S Myanmar, Thailand, Laos, and Vietnam (including Dao Tra Ban and Phu Quoc Is); possibly also Cambodia. R. a. nesites K. Andersen, 1905 - Borneo (including Laut, Sebuku, and Laut Kecil Is) and Anamba and Natuna Is. R. a. princeps K. Andersen, 1905 — Kangean (Kangean and Sepanjang Is), Lombok, Sumbawa, Flores, and Sumba Is. A morphologically distinct subspecies (still unnamed) is known from E Myanmar and N Vietnam.
Subspecies and Distribution. A r. robinsoni K. Andersen, 1918 - Malay Peninsula. A r. klossi K. Andersen, 1918 - Tioman, Pemanggil, and Aur Is off SE Malay Peninsula in Rhinolophidae
Subspecies and Distribution. A r. robinsoni K. Andersen, 1918 - Malay Peninsula. A r. klossi K. Andersen, 1918 - Tioman, Pemanggil, and Aur Is off SE Malay Peninsula
Subspecies and Distribution. R.p. pusillus Temminck, 1834 - N Sumatra, N, E & S Borneo (including Banggi I), W Java, and Bali I. R. p. blythi K. Andersen, 1918 - N India (Uttarakhand, Sikkim, West Bengal, Assam, Meghalaya, and Arunachal Pradesh), Nepal, Bhutan, and SE Bangladesh. R.p. calidusG. M. Allen, 1923-SE China (Guizhou, Guangxi, Guangdong, and Fujian, along with a recent record from Beijing area that may represent this subspecies). R. p. gracilis K. Andersen, 1905 - S India (Andhra Pradesh, Karnataka, Kerala, and Tamil Nadu). R.p. lakkhanae Yoshiyuki, 1990 - S China (Yunnan), Thailand, Laos, Vietnam (including Cat Ba I), Cambodia, and Peninsular Malaysia (including Tioman I). R.p. minutillusG. S. Miller, 1906 —Anambas Is (Siantan). R.p. pagi Tate & Archbold, 1939 — Mentawai Is (North Pagai). R.p. parcus G. M. Allen, 1928 - Hainan I, China. R. p. szechwanus K Andersen, 1918 - Myanmar and C China (Sichuan, Guizhou, Hubei, and probably Yunnan). in Rhinolophidae
Subspecies and Distribution. R.p. pusillus Temminck, 1834 - N Sumatra, N, E & S Borneo (including Banggi I), W Java, and Bali I. R. p. blythi K. Andersen, 1918 - N India (Uttarakhand, Sikkim, West Bengal, Assam, Meghalaya, and Arunachal Pradesh), Nepal, Bhutan, and SE Bangladesh. R.p. calidusG. M. Allen, 1923-SE China (Guizhou, Guangxi, Guangdong, and Fujian, along with a recent record from Beijing area that may represent this subspecies). R. p. gracilis K. Andersen, 1905 - S India (Andhra Pradesh, Karnataka, Kerala, and Tamil Nadu). R.p. lakkhanae Yoshiyuki, 1990 - S China (Yunnan), Thailand, Laos, Vietnam (including Cat Ba I), Cambodia, and Peninsular Malaysia (including Tioman I). R.p. minutillusG. S. Miller, 1906 —Anambas Is (Siantan). R.p. pagi Tate & Archbold, 1939 — Mentawai Is (North Pagai). R.p. parcus G. M. Allen, 1928 - Hainan I, China. R. p. szechwanus K Andersen, 1918 - Myanmar and C China (Sichuan, Guizhou, Hubei, and probably Yunnan).
Subspecies and Distribution. R m. mehelyi Matschie, 1901 - S Europe (S Iberian Peninsula, Sardinia, E Sicily, SE Italy, S Albania, E Serbia, S Romania, E North Macedonia, Bulgaria, and Greece), SW Asia (Caucasus, Anatolia, N Iraq, and Zagros Mts in W Iran), and N Africa (N Morocco, N Algeria, and N Tunisia); possibly a record from SE France, and there are apparently records from Afghanistan, although exact localities are uncertain. R m. judaicus K. Andersen & Matschie, 1904 - Levant in Cyprus, N Syria, W Jordan, Israel, NE Egypt (including NW Sinai based on echolocation), and NE Libya. in Rhinolophidae
Subspecies and Distribution. R m. mehelyi Matschie, 1901 - S Europe (S Iberian Peninsula, Sardinia, E Sicily, SE Italy, S Albania, E Serbia, S Romania, E North Macedonia, Bulgaria, and Greece), SW Asia (Caucasus, Anatolia, N Iraq, and Zagros Mts in W Iran), and N Africa (N Morocco, N Algeria, and N Tunisia); possibly a record from SE France, and there are apparently records from Afghanistan, although exact localities are uncertain. R m. judaicus K. Andersen & Matschie, 1904 - Levant in Cyprus, N Syria, W Jordan, Israel, NE Egypt (including NW Sinai based on echolocation), and NE Libya.
R code and raw data
<p>R code and raw data</p>
FIGURES 33‒44 in Rhinusa Stephens: a taxonomic revision of the species belonging to the R. linariae R. herbarum, R. melas, and R. mauritii groups (Coleoptera Curculionidae)
FIGURES 33‒44. Spiculum ventrale of (33) Rhinusa linariae; (34) R. herbarum; (35) R. mateui; (36) R. melas; (37) R. korotyaevi; (38) R. mauritii. Spermatheca of (39) R. linariae; (40) R. herbarum; (41) R. mateui; (42) R. melas; (43) R. korotyaevi; (44) R. mauritii.
FIGURES 23‒32 in Rhinusa Stephens: a taxonomic revision of the species belonging to the R. linariae R. herbarum, R. melas, and R. mauritii groups (Coleoptera Curculionidae)
FIGURES 23‒32. Profemur and protibia of (23) Rhinusa bipustulata, male; (24) R. linariae, male; (25) R. tetra, male; (26) R. tetra, female. Penis in dorsal view of (27) R. linariae; (28) R. herbarum; (29) R. mateui; (30) R. melas; (31) R. korotyaevi; (32) R. mauritii.
F I G U R E 6 in GIFT – A Global Inventory of Floras and Traits for macroecology and biogeography
F I G U R E 6 (a) Total number of trait records per native angiosperm species per region and (b–e) trait coverage per region (number of native angiosperm species with trait information/number of all native angiosperm species) for exemplary traits with characteristic geographic patterns in coverage. Polygons are plotted sequentially in order of decreasing area to show smaller regions on top of larger regions, in the case where they overlap. Regions <25,000 km2 are plotted as points [Colour figure can be viewed at wileyonlinelibrary.com]
F I G U R E 5 in GIFT – A Global Inventory of Floras and Traits for macroecology and biogeography
F I G U R E 5 Taxonomic coverage of distribution data in the Global Inventory of Floras and Traits 1.0 at the family level. Tip color and inner ring color indicate the proportion of species with distribution information relative to all species of a given family, the grey outer ring delimits major clades of vascular plants. The height of bars in the outer ring is proportional to log10 total family species richness. Phylogenetic signal in taxonomic coverage was assessed as Abouheif's Cmean, a measure of phylogenetic autocorrelation based on the sum of the successive squared differences between values of neighbouring tips in the phylogeny (Abouheif, 1999) [Colour figure can be viewed at wileyonlinelibrary.com]
F I G U R E 2 in GIFT – A Global Inventory of Floras and Traits for macroecology and biogeography
F I G U R E 2 Simplified structure of the Global Inventory of Floras and Traits database. Metadata on literature references, species lists and geographic regions builds the backbone of the database (top row). A reference can include several species lists (e.g. for different sub-regions) and a geographic region can be covered by several lists and references. Species lists vary in taxonomic and floristic scope (e.g. all native and naturalized angiosperms) and in the information content (floristic status, functional traits). Primary occurrence information, species names and functional trait data from the literature resources build the main block of original data (yellow). Automated workflows link those to taxonomically standardized working names, to a higher taxonomy and phylogeny of vascular plants and produce derived resources for analyses (blue). Grey bars indicate links among tables in a simplified way (most tables shown here represent several tables in the database) [Colour figure can be viewed at wileyonlinelibrary.com]
F I G U R E 3 in GIFT – A Global Inventory of Floras and Traits for macroecology and biogeography
F I G U R E 3 Trait processing in the Global Inventory of Floras and Traits (GIFT). Original trait records entering GIFT are subjected to three processing steps: (i) Trait values are standardized with respect to language, terminology and measurement unit. (ii) Additional trait values are derived hierarchically for traits that are logically nested (colored rows under "derived traits", see also Figure S1), and taxonomically for species that belong to taxonomic groups that are uniform with respect to a particular trait. (iii) Derived trait values are aggregated at the species level based on the consensus among resources (categorical traits) or summary statistics are computed based on the original values (numerical traits) [Colour figure can be viewed at wileyonlinelibrary.com]
F I G U R E 4 in GIFT – A Global Inventory of Floras and Traits for macroecology and biogeography
F I G U R E 4 Spatial coverage of checklist data stored in the Global Inventory of Floras and Traits 1.0. (a) Regions with checklist data for native vascular plants. Darker green shade indicates overlapping regions. (b–d) Checklist coverage and species richness of major taxonomic groups for regions with theoretically complete inventories. Polygons are plotted sequentially in order of decreasing area to show smaller regions on top of larger regions, in the case where they overlap. Regions <25,000 km2 are plotted as points [Colour figure can be viewed at wileyonlinelibrary.com]
F I G U R E 1 in GIFT – A Global Inventory of Floras and Traits for macroecology and biogeography
F I G U R E 1 Conceptual framework of the Global Inventory of Floras and Traits database (GIFT). The core information in GIFT are species occurrences in geographic regions (islands, political units, protected areas, biogeographical regions) based on Floras and checklist. At the level of the geographical regions, this information is linked to geographic, bioclimatic and socioeconomic properties. At the level of the species, functional traits, taxonomic placement and phylogenetic relationships are linked. This integration of species distribution data in the form of full regional inventories and regional and species characteristics allows for a wide variety of macroecological and biogeographical analyses of taxonomic, phylogenetic and functional diversity as well as for the refinement and validation of other plant distribution and trait datasets [Colour figure can be viewed at wileyonlinelibrary.com]
Supplementary material 3 from: Grunewald K, Schweppe-Kraft B, Syrbe R-U, Meier S, Krüger T, Schorcht M, Walz U (2020) Hierarchical classification system of Germany's ecosystems as basis for an ecosystem accounting – methods and first results. One Ecosystem 5: e50648. https://doi.org/10.3897/oneeco.5.e50648
The area and share of main ecosystem types and sub ecosystem types (ETs, see Tab. 1)) in the German land cover model (LBM-DE) for the time periods 2012, 2015 and 2018. Linear elements such as small scale structures and infrastructures from the topographic-cartographic Information system (ATKIS) were added to the land cover model.
Supplementary material 4 from: Grunewald K, Schweppe-Kraft B, Syrbe R-U, Meier S, Krüger T, Schorcht M, Walz U (2020) Hierarchical classification system of Germany's ecosystems as basis for an ecosystem accounting – methods and first results. One Ecosystem 5: e50648. https://doi.org/10.3897/oneeco.5.e50648
Tab. D: Detailed matrix of pre- and post-use of settlement and transportation areas in Germany in the period 2013-2018 in hectare per day (ha/d). (Data source: IOER)
Supplementary material 1 from: Grunewald K, Schweppe-Kraft B, Syrbe R-U, Meier S, Krüger T, Schorcht M, Walz U (2020) Hierarchical classification system of Germany's ecosystems as basis for an ecosystem accounting – methods and first results. One Ecosystem 5: e50648. https://doi.org/10.3897/oneeco.5.e50648
Proposal of a classification system for ecosystem types (ETs) in Germany, assignment to the European ecosystem types according to EUNIS and to the CLC types of the database LBM-DE
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.