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.
3,630
datasets available to search
ShareScore release 0.9.0
Dataset results
3,630 results for “Forming”
Colour illustrations. Flowers, fruits, leaves and seeds of Musa itinerans (background photo by D.T. Vu); from top to bottom and left to right: colony on PDA after 14 d at 24 °C in darkness (left = obverse,right = reverse), sporodochia formed on CLA, aerial conidiophore, aerial conidiogenous cells, aerial conidia, sporodochial conidia. Scale bars: black = 20 µm, white = 10 µm. in Fusarium chuoi R. Hill, Gaya, D.T. Vu, Sand.-Den. & Crous, R. Hill, Gaya, D.T. Vu, Sand.-Den. & Crous sp. nov.
Colour illustrations. Flowers, fruits, leaves and seeds of Musa itinerans (background photo by D.T. Vu); from top to bottom and left to right: colony on PDA after 14 d at 24 °C in darkness (left = obverse,right = reverse), sporodochia formed on CLA, aerial conidiophore, aerial conidiogenous cells, aerial conidia, sporodochial conidia. Scale bars: black = 20 µm, white = 10 µm.
Data and code from: A review of cisco form diversity and lake depth
<p>Cisco form diversity overlaps with glacial lake coverage in North America. A recent hypothesis proposes that secondary contact among refugial cisco lineages during retreat of the Laurentide Ice Sheet was the basis for the geography of cisco diversity in North American lakes. Glacial lake coverage in North America is also a map of Mysis diluviana distribution, a glacial relic species found in lakes including the Laurentian Great Lakes. The presence of Mysis increases isotopic niche size of cisco, a necessary condition for Mysis to be a key element of cisco clade diversification. We reviewed literature on cisco forms in North American lakes to determine if cisco diversity is related to an ecological opportunity gradient, maximum lake depth with the presence of Mysis. Cisco form diversity increases with lake maximum depth in North America in the presence of Mysis with deeper lakes increasingly likely to hold multiple forms. Lakes without Mysis had only one cisco form and were shallower in general. We hypothesize that Mysis is the basis for the relationship between lake depth and cisco form diversity because of the complex behavior and distribution of Mysis that stems from increasing lake depth. We propose the geography of cisco diversity in North America results from within lake predator–prey processes as a function of lake depth under the Mysis hypothesis vs. secondary contact priming genetic diversity. The two hypotheses are not mutually exclusive. Analysis of a lake set covering both cisco and Mysis ranges points to more lakes having multiple cisco forms.</p>
Integrative biodiversity inventories: characterizing lichen-forming fungal diversity in Glen Canyon National Recreation Area using DNA barcoding and vouchered specimens
<p>The Colorado River and its tributaries on the Colorado Plateau are home to unique desert river ecosystems and changing environmental conditions. Within this region, the Glen Canyon National Recreation Area (GCNRA) is comprised of rugged, high desert terrain and is managed by the United States National Parks Service as both a recreational and conservation area. Despite the ecological and economic importance of GCNRA, significant components of the ecological communities therein remain poorly characterized, including lichens. Accurately characterizing lichen-forming fungal diversity is challenging due to poorly known taxonomic groups, underexplored regions/habitats, and varying interpretations of morphological differences, including the recognition of environmentally modified forms. To better understand lichen diversity in GCNRA, we used an integrative taxonomic approach, incorporating both traditional morphology-based identification and information from the standard fungal DNA barcoding marker, the ITS, to compile a thorough inventory of lichen-forming fungi in Fifty-Mile Canyon. Vouchered lichen specimens were collected in 2019, and from these the ITS marker was sequenced. Candidate species-level lineages were delimited from family-level multiple sequence alignments using the Assemble Species by Automatic Partitioning web server. Specimens comprising DNA-based candidate species were then evaluated using traditional taxonomically diagnostic characters to link these, where possible, to currently described species. For Fifty-Mile Canyon, we document 100 putative species in 15 families, each represented by vouchered specimens, ITS sequence data, and photographic documentation. For comparison, a survey of historic records from GCNRA revealed a total of 124 documented lichen-forming fungal species throughout the NRA and adjacent land. Approximately 50% of the species documented in Fifty-Mile Canyon had not previously been found in GCNRA, and similar proportions of species diversity have been documented in GCNRA but not observed in our survey. We report three species new to North America – <em>Calogaya ferrugineoides</em> (H. Magn.) Arup, Froden & Sochting, <em>Endocarpon deserticola</em> T. Zhang, X. L. Wei & J. C. Wei and <em>Xanthocarpia ferrari</em> (Bagl.) Frödén, Arup & Søchting – verified using ITS sequencing data. In addition, <em>Circinaria squamulosa</em> sp. nov. is formally described here, currently known only from sandstone slabs in Fifty-Mile Canyon. However, the taxonomic identity of many of the candidate species from Fifty-Mile Canyon remained ambiguous at the species level, and some collections likely represent undescribed species-level lineages. Our results revealed unexpected, high species-level diversity of lichen-forming fungi at local scales and that overall lichen diversity across the entire GCNRA is likely vastly undercounted. These data – including DNA barcodes for the vast majority of lichen-forming fungi occurring in this canyon – provide an important resource that can be integrated into subsequent lichen biodiversity research in the southwestern United States and other semi-arid climates.</p>
FIGURE. Distribution in percentages of the vascular flora of Sierra de las Nieves National Park and its surroundings according to the life forms of Raunkiaer (1934). in Vascular flora of the Sierra de las Nieves National Park and its surroundings (Andalusia, Spain)
FIGURE. Distribution in percentages of the vascular flora of Sierra de las Nieves National Park and its surroundings according to the life forms of Raunkiaer (1934).
Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V. v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas). in Canidae
Subspecies and Distribution. V. v. vulpes Linnaeus, 1758 — N Europe (Scandinavia). V. v. abietorum Merriam, 1900 — SW Canada (Alberta & British Columbia). V. v. aegyptiacus Sonnini, 1816 — Egypt, Israel, and Lybia. V. v. alascensis Merriam, 1900 — Alaska and NW Canada (NW Territories & Yukon). V. v. alpheraky: Satunin, 1906 — Kazakhstan. V. v. anatolica Thomas, 1920 — Turkey. V. v. arabica Thomas, 1902 — Arabian peninsula. V. v. atlantica Wagner, 1841 — Algeria (forested Atlas Mts). V. v. bangsi Merriam, 1900 — NE Canada (Labrador). V. v. barbara Shaw, 1800 — NW Africa (Barbary Coast). V. v. beringiana Middendorff, 1875 — NE Siberia (shore of Bering Strait). V. v. cascadensis Merriam, 1900 — NW USA (Cascade Mountains, Oregon & Washington). V. v. caucasica Dinnik, 1914 — SW Russia (Caucasus). V. v. crucigera Bechstein, 1789 — Europe through N & C Russia. V. v. daurica Ognev, 1931 — E Russia (Amur, Siberia & Transbaikalia). V.v. deletrix Bangs, 1898 — NE Canada (Newfoundland). V. v. dolichocrania Ognev, 1926 — SE Siberia (S Ussuri). V. v. flavescens Gray, 1843 — N Iran. V. v. fulva Desmarest, 1820 — E USA. V. v. griffith: Blyth, 1854 — Afghanistan and N Pakistan. V.v. harrimani Merriam, 1900 — Alaska (Kodiak I). V. v. hoole Swinhoe, 1870 — S China (Fujian to Sichuan). V. v. ichnusae G. S. Miller, 1907 — Corsica and Sardinia. V. v. induta G. S. Miller, 1907 — Cyprus. V. v. jakutensis Ognev, 1923 — E Siberia (S of Yakutsk). V. v. japonica Gray, 1868 — Japan. V. v. karagan Erxleben, 1777 — Mongolia, Kazakhstan, and Kirgizstan. V. v. kenaiensis Merriam, 1900 — Alaska (Kenai Peninsula). V. v. kurdistanica Satunin, 1906 — Armenia and NE Turkey. V. v. macroura Baird, 1852 — USA (Mountain States). V. v. montana Pearson, 1836 — Himalayas form China (Yunnan) to C Pakistan. V. v. mecator Merriam, 1900 — SW USA (California & Nevada). V. v. ochroxantha Ognev, 1926 — E Russian Turkestan, Aksai, Kirgizstan, Semirechie. V. v. palaestina Thomas, 1920 —Jordan and Lebanon. V.v. peculiosa Kishida, 1924 — Korea. V. v. pusilla Blyth, 1854 — NW India to Irak. V.v. regalis Merriam, 1900 — N Great Plains of Canada and USA. V. v. rubricosa Bangs, 1898 — E Canada. V.v. schrencki Kishida, 1924 — N Japan (Hokkaido) and NE Russia (Sakhalin). V. v. silacea G. S. Miller, 1907 — Iberian Peninsula. V.v. splendidissima Kishida, 1924 — E Russia (N & C Kurile Is). V. v. stepensis Brauner, 1914 — steppes of S Russia. V. v. tobolica Ognev, 1926 — Russia (lower basin of Ob River) V. v. tschiliensis Matschie, 1907 — NE China. Foxes of European origin were introduced into E USA and Canada in the 17" century, subsequently mixed with local subspecies. Also introduced to Australia in 1800s, and the Falkland Islands (Malvinas).
FIGURE. Floral habit and structure of C. spongifolia. A. Type specimen in situ with open, spathe limb (apex is reflexed out of view), and green spathe tube (ca. 6 cm long). B. Adjacent plant with inflorescences and prophylls. C. Spadix showing from top: sterile appendix, staminate (male) zone, sterile interstice, and green pistillate (female) zone with tapered, conical form. D. Detail of female zone showing a few basal staminodes. E–G. Berries of the preserved type specimen. G. Dissected berry with orthotropous ovules (some outlined) attached by funicles to parietal placentae (arrows). H. Surface of male zone showing closely-packed synandria. I. Synandria separated to show fused anther sacs beneath apical pores (example in center has 8 pores, 8 anthers) J. Mature fruiting head, with single berry removed to show seed packing and 67 seeds extracted (scale bar units: 1 mm) (Bach Ma NP; type 2020; fruit and seeds 2018). Photos: NVD and PJM. in Colocasia spongifolia sp. nov. (Araceae) in southern China and central Vietnam
FIGURE. Floral habit and structure of C. spongifolia. A. Type specimen in situ with open, spathe limb (apex is reflexed out of view), and green spathe tube (ca. 6 cm long). B. Adjacent plant with inflorescences and prophylls. C. Spadix showing from top: sterile appendix, staminate (male) zone, sterile interstice, and green pistillate (female) zone with tapered, conical form. D. Detail of female zone showing a few basal staminodes. E–G. Berries of the preserved type specimen. G. Dissected berry with orthotropous ovules (some outlined) attached by funicles to parietal placentae (arrows). H. Surface of male zone showing closely-packed synandria. I. Synandria separated to show fused anther sacs beneath apical pores (example in center has 8 pores, 8 anthers) J. Mature fruiting head, with single berry removed to show seed packing and 67 seeds extracted (scale bar units: 1 mm) (Bach Ma NP; type 2020; fruit and seeds 2018). Photos: NVD and PJM.
FIGURE. Blades of C. spongifolia. A. Sub-marginal and marginal collective veins, with laminal tissue (2–4 mm) between. B. Marginal collective veins fused below shallow sinus. C. Underside with spongy appearance produced by "false pores"; and thick, rubbery texture indicated by axial wrinkles formed in crease. D. Underside showing primary vein and pinnate lateral veins surrounded by spongy tissue. E. Sub-stomatal cavities revealed by transmitted light (scale unit 0.25 mm), F. Sub-stomatal cavities revealed by removing lower epidermis (A–D: Mengla County, 2018. E–F: Bach Ma NP seedling, ex situ). Photos: PJM. in Colocasia spongifolia sp. nov. (Araceae) in southern China and central Vietnam
FIGURE. Blades of C. spongifolia. A. Sub-marginal and marginal collective veins, with laminal tissue (2–4 mm) between. B. Marginal collective veins fused below shallow sinus. C. Underside with spongy appearance produced by "false pores"; and thick, rubbery texture indicated by axial wrinkles formed in crease. D. Underside showing primary vein and pinnate lateral veins surrounded by spongy tissue. E. Sub-stomatal cavities revealed by transmitted light (scale unit 0.25 mm), F. Sub-stomatal cavities revealed by removing lower epidermis (A–D: Mengla County, 2018. E–F: Bach Ma NP seedling, ex situ). Photos: PJM.
Oil-gas prices and economic activity in selected European countries – evidence form time and frequency domain causality
<p>Data sets related with research: <strong>Oil-gas prices and economic activity in selected European countries – evidence form time and frequency domain causality</strong>. - file name: Data - Time Series - DEU, NOR, POL</p> <p>results of Breitung-Candelon test</p>
Distribution. SE Europe from Albania and Greece (including Crete) N to S Ukraine and S Russia, the Caucasus, Turkey, and N Iran, and through C Asia to W Mongolia, N, E & C China (including Hainan), and the Himalayas; isolated populations in S Croatia and Korea. Specimens collected from SW Syria may representjuvenile Geoffroy's Myotis (M. emarginatus) or a different form, and are not mapped here. in Vespertilionidae
Distribution. SE Europe from Albania and Greece (including Crete) N to S Ukraine and S Russia, the Caucasus, Turkey, and N Iran, and through C Asia to W Mongolia, N, E & C China (including Hainan), and the Himalayas; isolated populations in S Croatia and Korea. Specimens collected from SW Syria may representjuvenile Geoffroy's Myotis (M. emarginatus) or a different form, and are not mapped here.
input files for " Martini bead form factors for nucleic-acids and their application in the refinement of protein/nucleic-acid complexes against SAXS data".
<p>input files for " Martini bead form factors for nucleic-acids and their application in the refinement of protein/nucleic-acid complexes against SAXS data", cf plumed-nest</p>
Data for Embryo-scale epithelial buckling forms a propagating furrow that initiates gastrulation
<p>This is the data and code corresponding to <a href="https://doi.org/10.1038/s41467-022-30493-3">Embryo-scale epithelial buckling forms a propagating furrow that initiates gastrulation</a>, <em>Nature Comms.</em> <strong>13</strong>:3348.</p> <p><strong>Code</strong></p> <p>The file Surface_Evolver_script.txt is ... the Surface Evolver script, use with <a href="http://facstaff.susqu.edu/brakke/evolver/evolver.html">Ken Brakke's Surface Evolver</a></p> <p><strong>Data sources</strong></p> <p>The figure panels are based on the datafiles listed below, visualised either with <a href="http://facstaff.susqu.edu/brakke/evolver/evolver.html">Ken Brakke's Surface Evolver </a>or with <a href="http://www.gnuplot.info/">gnuplot 5</a>. When the datafiles listed do not contain the primary data, they contain a commented last line which is the command line for the software <a href="https://doi.org/10.5281/zenodo.5911337">datamerge</a> to generate it from other datafiles found in the Data_sources subdirectory.</p> <p><strong>Figure 1</strong></p> <p>Fig. 1c : data provided in <code>data_for_Fig_1g.tsv</code></p> <p>Fig. 1f : visualisation from Surface Evolver file <code>Young100dixPoisson000Step013.dmp</code></p> <p>Fig. 1g : <code>myosin_profile_us_only.pdf</code> generated with gnuplot script <code>myosin_profile.plot</code></p> <p><strong>Figure 2</strong></p> <p>Fig. 2a : <code>strain_profile_100_0_time_013.pdf</code> generated with gnuplot script <code>strain_profile.plot</code></p> <p>Fig. 2b : visualisation from Surface Evolver file <code>Young100dixPoisson000Step013.dmp</code></p> <p>Fig. 2c : <code>stress_profile_100_0_time_013.pdf</code> gnuplot script <code>stress_profile.plot</code></p> <p>Fig. 2d : visualisation from Surface Evolver file <code>Young100dixPoisson000Step063.dmp</code></p> <p><strong>Figure 3</strong></p> <p>Fig. 3a : <code>myosin_area.pdf</code> generated with gnuplot script <code>area_AP_DV_paper.plot</code></p> <p>Fig. 3b : <code>area_stripes_t=-1.pdf</code> generated with gnuplot script <code>area_AP_DV_paper.plot</code></p> <p>Fig. 3c : <code>only_AP_stripes_t=-1.pdf</code> generated with gnuplot script <code>area_AP_DV_paper.plot</code></p> <p>Fig. 3d : <code>only_DV_stripes_t=-1.pdf</code> generated with gnuplot script <code>area_AP_DV_paper.plot</code></p> <p>Fig. 3e : visualisation from Surface Evolver file <code>Young100dixPoisson000Step013.dmp Young100dixPoisson000Step063.dmp Young100dixPoisson000Step163.dmp Young100dixPoisson000Step213.dmp</code></p> <p><strong>Figure 4</strong></p> <p>Fig. 4a : visualisation from Surface Evolver file <code>Young100dixPoisson000Step213.dmp</code></p> <p>Fig. 4b : <code>furrow_propagation.pdf</code> generated with gnuplot script <code>furrow_propagation.plot</code></p> <p>Fig. 4c : <code>rate_of_furrowing_t=3.pdf</code> generated with gnuplot script <code>furrow_propagation.plot</code></p> <p>Fig. 4f : <code>curvature.pdf</code> generated with gnuplot script <code>curvature.plot</code></p> <p><strong>Figure 5</strong></p> <p>Fig. 5a : visualisation from Surface Evolver file <code>Young100dixPoisson000Step013.dmp Young100dixPoisson000Step063.dmp Young100dixPoisson000Step113.dmp Young100dixPoisson000Step163.dmp Young100dixPoisson000Step213.dmp</code></p> <p>Fig. 5b : visualisation from Surface Evolver file <code>Young100dixPoisson000Step013.dmp Young100dixPoisson000Step140.dmp</code></p> <p>Fig. 5d : <code>stress_laserablations_profile_100_0_time_063.pdf</code> generated with gnuplot script <code>stress_profile_for_laser_ablations.plot</code></p> <p>Fig. 5e : <code>laser_ablation_recoil.pdf</code> generated with gnuplot script <code>laser_ablation_recoil.plot</code></p> <p><strong>Supp Figure 1</strong></p> <p>Fig. S1a : <code>time_profile_FINI_100_0.pdf</code> generated with gnuplot script <code>time_profile_stress.plot</code></p> <p>Fig. S1b : visualisation from Surface Evolver file <code>Young100dixPoisson000Step013.dmp</code></p> <p>Fig. S1d : visualisation from Surface Evolver file <code>Young100dixPoisson000Step063.dmp</code></p> <p>Fig. S1e : <code>strain_profile_100_0_time_063.pdf</code> gnuplot script <code>strain_profile.plot</code></p> <p>Fig. S1f : <code>stress_profile_100_0_time_063.pdf</code> gnuplot script <code>stress_profile.plot</code></p> <p><strong>Supp Figure 1</strong></p> <p>Fig. S2a : <code>area_stripes_time_evolution.pdf</code> generated with gnuplot script <code>area_AP_DV_paper.plot</code></p> <p>Fig. S2b : <code>area_stripes_time_evolution_SPIM.pdf</code> generated with gnuplot script <code>area_AP_DV_paper.plot</code></p> <p><strong>Supp Figure 3</strong></p> <p>Fig. S3a : visualisation from Surface Evolver file <code>Young100dixPoisson000Step213.dmp</code></p> <p>Fig. S3c : <code>AP_binned_strain.pdf</code> generated with gnuplot script <code>AP_binned_strain.plot</code></p> <p>Fig. S3d : <code>furrow_propagation_experimental.pdf</code> generated with gnuplot script <code>plot_furrow.plot</code></p> <p>Fig. S3e : <code>curvature_DV_indiv.pdf</code> generated with gnuplot script <code>curvature.plot</code></p> <p>Fig. S3f : <code>depth_Gastrulation_ordi_Wild_Type_STITCHED_100_0.pdf</code> generated with gnuplot script <code>depth.plot</code></p>
Distribution. Found in lowland rainforest regions of W & C Africa, including S Nigeria (perhaps one population remaining that may be an intermediate form), S & C Cameroon, S Central African Republic, Equatorial Guinea (extinct on Bioko I), Sao Tomé and Principe Is, Gabon, Republic of the Congo, C & N DR Congo, W & C Angola (two disjunct populations). in Bovidae
Distribution. Found in lowland rainforest regions of W & C Africa, including S Nigeria (perhaps one population remaining that may be an intermediate form), S & C Cameroon, S Central African Republic, Equatorial Guinea (extinct on Bioko I), Sao Tomé and Principe Is, Gabon, Republic of the Congo, C & N DR Congo, W & C Angola (two disjunct populations).
Subspecies and Distribution. B.j.javanicusd'Alton,1823—Java,perhapsBali. B.j.birmanicusLydekker,1898—AsianmainlandincludingMyanmar,SChina(SYunnan,currentpresenceuncertain),Laos,Vietnam,Thailand,Cambodia,andNPeninsularMalaysia. B. j. low: Lydekker, 1912 — Borneo. The domestic form of the Banteng has been introduced, and is now feral, in N Australia, New Guinea, and on various islands of Indonesia (Bali, Sangihe, Sulawesi, Sumbawa, Sumba, and Enggano) and occurs in domestication throughout the islands of SE Asia. in Bovidae
Subspecies and Distribution. B.j.javanicusd'Alton,1823—Java,perhapsBali. B.j.birmanicusLydekker,1898—AsianmainlandincludingMyanmar,SChina(SYunnan,currentpresenceuncertain),Laos,Vietnam,Thailand,Cambodia,andNPeninsularMalaysia. B. j. low: Lydekker, 1912 — Borneo. The domestic form of the Banteng has been introduced, and is now feral, in N Australia, New Guinea, and on various islands of Indonesia (Bali, Sangihe, Sulawesi, Sumbawa, Sumba, and Enggano) and occurs in domestication throughout the islands of SE Asia.
Subspecies and Distribution. M.m.muntjakZimmermann,1780—PeninsularMalaysia,Sumatra,Java,Bali,Borneoandseveralassociatedsmallerislands. M.m.annamensisKloss,1928—SLaos,SVietnam,andCambodia. M.m.aureusC.H.Smith,1826—Pakistan,N&CIndia. M.m.curvostylisGray,1872—Myanmar,Thailand. M.m.malabaricusLydekker,1915—SIndiaandSriLanka. M.m.menglalisWang&Groves,1988—SChina(SYunnan);possiblyalsoinneighboringMyanmar,Laos,andVietnam. M.m.montanusRobinson&Kloss,1918—Sumatranhighlands. M.m.nigripesG.Allen,1930—HainanI. M.m.vaginalisBoddaert,1785—Nepal,Bhutan,NEIndia,andBangladesh. M. m. yunnanensis Ma & Wang, 1988 — S China (from C & N Yunnan and S Sichuan to S Fujian & Guangdong). Forms from mainland Asia have been introduced into the Andaman Is. in Cervidae
Subspecies and Distribution. M.m.muntjakZimmermann,1780—PeninsularMalaysia,Sumatra,Java,Bali,Borneoandseveralassociatedsmallerislands. M.m.annamensisKloss,1928—SLaos,SVietnam,andCambodia. M.m.aureusC.H.Smith,1826—Pakistan,N&CIndia. M.m.curvostylisGray,1872—Myanmar,Thailand. M.m.malabaricusLydekker,1915—SIndiaandSriLanka. M.m.menglalisWang&Groves,1988—SChina(SYunnan);possiblyalsoinneighboringMyanmar,Laos,andVietnam. M.m.montanusRobinson&Kloss,1918—Sumatranhighlands. M.m.nigripesG.Allen,1930—HainanI. M.m.vaginalisBoddaert,1785—Nepal,Bhutan,NEIndia,andBangladesh. M. m. yunnanensis Ma & Wang, 1988 — S China (from C & N Yunnan and S Sichuan to S Fujian & Guangdong). Forms from mainland Asia have been introduced into the Andaman Is.
The dataset of form drag coefficient of ice ridge keel in a two-layer fluid
<p>The LabE measurements and NumS dataset in the research of "Form drag coefficient of ice ridge keel in a two-layer fluid "</p>
Subspecies and Distribution. B.a.acutorostrataLacépede,1804—NAtlanticOcean. B. a. scammoni Demére, 1986 — N Pacific Ocean. An unnamed form is found in the Southern Hemisphere. in Balaenopteridae
Subspecies and Distribution. B.a.acutorostrataLacépede,1804—NAtlanticOcean. B. a. scammoni Demére, 1986 — N Pacific Ocean. An unnamed form is found in the Southern Hemisphere.
Subspecies and Distribution. S.m.murinaWaterhouse,1838—E&SEAustralia,EQueensland(includingFraserI),NewSouthWales,Victoria,andE&SESouthAustralia. S. m. tate: Troughton, 1965 — NE Queensland. The subspecies are probably allopatric, with neither form apparently occurring in mideastern Queensland, a known biogeographical barrier to many terrestrial vertebrates. in Dasyuridae
Subspecies and Distribution. S.m.murinaWaterhouse,1838—E&SEAustralia,EQueensland(includingFraserI),NewSouthWales,Victoria,andE&SESouthAustralia. S. m. tate: Troughton, 1965 — NE Queensland. The subspecies are probably allopatric, with neither form apparently occurring in mideastern Queensland, a known biogeographical barrier to many terrestrial vertebrates.
Subspecies and Distribution. P.p.phocoenaLinnaeus,1758—coastalwatersoftheNAtlanticOcean. P.p.relictaAbel,1905—coastalwatersof theBlackSea,theAzovandMarmaraseas(isolatedpopulation).AfewstragglersfromthispopulationshowupperiodicallyintheAegeanSea,buttheydonotoccurthroughoutmostoftheMediterraneanSea. P.p. vomerina Gill, 1865 — coastal waters of the NE Pacific Ocean. A still unnamed form is present in the coastal waters of the NW Pacific Ocean. in Phocoenidae
Subspecies and Distribution. P.p.phocoenaLinnaeus,1758—coastalwatersoftheNAtlanticOcean. P.p.relictaAbel,1905—coastalwatersof theBlackSea,theAzovandMarmaraseas(isolatedpopulation).AfewstragglersfromthispopulationshowupperiodicallyintheAegeanSea,buttheydonotoccurthroughoutmostoftheMediterraneanSea. P.p. vomerina Gill, 1865 — coastal waters of the NE Pacific Ocean. A still unnamed form is present in the coastal waters of the NW Pacific Ocean.
Subspecies and Distribution. L.o.obscurusGray,1828—coastalwatersofSAfrica(Namibia,SouthAfrica),PrinceEdwardandAmsterdamIs. L. o. fitzroyi Waterhouse, 1838 — coastal waters of S South America as far N as Peru in the Pacific Ocean and N Argentina in the Atlantic Ocean. Dusky Dolphins of a still undescribed form (New Zealand Dusky Dolphins) are present near New Zealand, Campbell, Auckland, and Chatham Is, and an uncertain subspecies has also been observed infrequently off the Falkland Is, Gough I, S Australia, and Tasmania. in Delphinidae
Subspecies and Distribution. L.o.obscurusGray,1828—coastalwatersofSAfrica(Namibia,SouthAfrica),PrinceEdwardandAmsterdamIs. L. o. fitzroyi Waterhouse, 1838 — coastal waters of S South America as far N as Peru in the Pacific Ocean and N Argentina in the Atlantic Ocean. Dusky Dolphins of a still undescribed form (New Zealand Dusky Dolphins) are present near New Zealand, Campbell, Auckland, and Chatham Is, and an uncertain subspecies has also been observed infrequently off the Falkland Is, Gough I, S Australia, and Tasmania.
Subspecies and Distribution. O.c.cuniculusLinnaeus,1758—N,NE&EIberianPeninsula(Spain). O.c.algirusLoche,1858—S,SW&WIberianPeninsula(Spain,Portugal),NMorocco,NAlgeria(includingHabibasI). O.c.brachyotusTrouessart,1917—SFrance. O.c.cnossiusBate,1906—CreteI. O.c.habetensisCabrera,1923—Tanger-Tetouan-AlHoceimaRegion(NMorocco). O. c. huxleyi Haeckel, 1874 — Mediterranean Is (Balearic Is, Corsica, Sardinia, Sicily and Macaronesia (Azores, Madeira, and Canary Is). Original distribution after last Ice Age restricted to Iberian Peninsula, W France, and N Africa. Ancient introductions of the nominate subspecies probably during the Ro- man period have spread it throughout Europe, and now it is present in most of W, C & E Europe and the Mediterranean and Macaronesian Is (these mostly old introductions are also shaded on the map). During the 20" century it has been released into the steppes of the Black Sea in Ukraine and Russia (N Caucasus); introduced into Australia in 1788 and again in 1859 where it is now widespread; it is found on many Pacific Is, islands off the coast of South Africa and Namibia, and in New Zealand; successfully introduced only since 1936 into South America, nowadays with a limited range in Chile, Argentina, and Falkland Is, it is also present in the Caribbean Is (all these modern introductions not shaded in the map). Worldwide as domesticated forms. in Leporidae
Subspecies and Distribution. O.c.cuniculusLinnaeus,1758—N,NE&EIberianPeninsula(Spain). O.c.algirusLoche,1858—S,SW&WIberianPeninsula(Spain,Portugal),NMorocco,NAlgeria(includingHabibasI). O.c.brachyotusTrouessart,1917—SFrance. O.c.cnossiusBate,1906—CreteI. O.c.habetensisCabrera,1923—Tanger-Tetouan-AlHoceimaRegion(NMorocco). O. c. huxleyi Haeckel, 1874 — Mediterranean Is (Balearic Is, Corsica, Sardinia, Sicily and Macaronesia (Azores, Madeira, and Canary Is). Original distribution after last Ice Age restricted to Iberian Peninsula, W France, and N Africa. Ancient introductions of the nominate subspecies probably during the Ro- man period have spread it throughout Europe, and now it is present in most of W, C & E Europe and the Mediterranean and Macaronesian Is (these mostly old introductions are also shaded on the map). During the 20" century it has been released into the steppes of the Black Sea in Ukraine and Russia (N Caucasus); introduced into Australia in 1788 and again in 1859 where it is now widespread; it is found on many Pacific Is, islands off the coast of South Africa and Namibia, and in New Zealand; successfully introduced only since 1936 into South America, nowadays with a limited range in Chile, Argentina, and Falkland Is, it is also present in the Caribbean Is (all these modern introductions not shaded in the map). Worldwide as domesticated forms.
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.