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68 results for “distributional boundary”
Figure 2 from: Murase A, Miki R, Motomura H (2017) Southern limits of distribution of the intertidal gobies Chaenogobius annularis and C. gulosus support the existence of a biogeographic boundary in southern Japan (Teleostei, Perciformes, Gobiidae). ZooKeys 725: 79-95. https://doi.org/10.3897/zookeys.725.19952
Figure 2 Conventional information on the distributional range of the two species of Chaenogobius (sensu Akihito et al. 2013 and Kwun et al. 2017) and a map of mainland Kyushu, southern Japan, showing the position of a long sandy shore on the eastern coast of Kyushu (a bold gray line on left-hand map). The grey-dash and solid lines on the Japanese Archipelago with adjacent areas (right-hand map) indicate the distributional range shared by the two species and that of only C. annularis respectively. Abbreviations for prefecture and island names mentioned in the text are as follows: Ot Oita Prefecture My Miyazaki Prefecture Kg Kagoshima Prefecture TnI Tanega-shima Island YkI Yaku-shima Island.
Micro-Laue diffraction data used in the publication 'Dislocation density distribution at slip band-grain boundary intersections'
<p>The Ti-Bi.xml file is an indexed data set from a differential aperture X-ray micro-Laue diffraction experiment at beamline 34-ID-E, Advanced Photon Source, USA. To obtain strain and rotation field the data need to be feed into LaueGo as specified in <a href="https://www.aps.anl.gov/Science/Scientific-Software/LaueGo">https://www.aps.anl.gov/Science/Scientific-Software/LaueGo</a></p> <p>The GND_data_Zenodo.mat is a Matlab file containing the rotation fields and GND density results. The data structure is explained below:</p> <p>GND_rho_2D and GND_rho_3D are the density of the 33 types of dislocations for all 31 slices of data. Each slice is a 4462x33 matrix where the columns are 33 types of dislocations specified in 'sliplabels'. Each columns has 4462 points giving rise to the 194x23 pixel size image of each slice of data.</p> <p>GND_total_2D and GND_total_3D are the total dislocation density maps in 2D and 3D. Each cell is a slice of the 3D data with 194x23 pixels.</p> <p>For more information, please contact Dr Ben Britton: b.britton@imperial.ac.uk</p>
Subspecies and Distribution. . t. theobaldi Dobson, 1872 - Tenasserim, Myanmar. . t. secatus Thomas, 1915 - Madhya Pradesh, India. Boundaries and complete distribution for subspecies are unknown, but T theobaldi is patchily distributed from C & SW India (Madhya Pradesh, Maharashtra, Karnataka, and Kerala), S China (Yunnan, imprecise locality and therefore not mapped), and SE Asia to Greater Sundas (Borneo, Java) and Sulawesi. Distribution is poorly known in India, and. theobaldi likely is more widespread than presently understood. It presumably will be found on other islands of the Indonesian Archipelago. in Emballonuridae
Subspecies and Distribution. . t. theobaldi Dobson, 1872 - Tenasserim, Myanmar. . t. secatus Thomas, 1915 - Madhya Pradesh, India. Boundaries and complete distribution for subspecies are unknown, but T theobaldi is patchily distributed from C & SW India (Madhya Pradesh, Maharashtra, Karnataka, and Kerala), S China (Yunnan, imprecise locality and therefore not mapped), and SE Asia to Greater Sundas (Borneo, Java) and Sulawesi. Distribution is poorly known in India, and. theobaldi likely is more widespread than presently understood. It presumably will be found on other islands of the Indonesian Archipelago.
Distribution. Widely in tropical Africa, but boundaries of each lineage (presumably separate species) are not known; this species complex occurs almost continuously from Senegal, Gambia, and Guinea E to S Sudan and Ethiopia, and S to Gabon, Republic of the Congo, DR Congo, and Tanzania, with isolated populations in NW Angola, Zambia, Malawi, and N Mozambique; also on Principe and Sâo Tomé Is. in Hipposideridae
Distribution. Widely in tropical Africa, but boundaries of each lineage (presumably separate species) are not known; this species complex occurs almost continuously from Senegal, Gambia, and Guinea E to S Sudan and Ethiopia, and S to Gabon, Republic of the Congo, DR Congo, and Tanzania, with isolated populations in NW Angola, Zambia, Malawi, and N Mozambique; also on Principe and Sâo Tomé Is.
Figure 10 in Species boundaries, geographic distribution and evolutionary history of the Western Palaearctic freshwater mussels Unio (Bivalvia: Unionidae)
Figure 10. Differing shell shapes of Unio pictorum. A, B, Lake Trichonida, Greece. C, Thames River, UK. D, Axios River, Greece. E, Okna River (Danube), Slovakia. F, Axios River, Greece. Scale bar 2 cm.
Subspecies and Distribution. L. t. timidus Linnaeus, 1758 — Scandinavia S to 59° N, N Russia (S to 57° N to 58° N) to E of Ural Mts, Estonia, perhaps Poland, and Altai and Beita Mts in N Xinjiang (China); from Sweden extending in hybrid zones with the subspecies sylvaticus to S coast of Norway and W Latvia. L. t. abet Kuroda, 1938 — Kurile Is (Russia). L. t. ainu Barrett-Hamilton, 1900 — Hokkaido (Japan). L. t. begitschevi Koljuschev, 1936 — Taimyr Peninsula (Russia). L. t. gichiganus J. A. Allen, 1903 — C Yakutia, Kamchatka and Okhotsk Sea coast (Russia). L. t. hibernicus Bell, 1837 — Ireland. L. t. kolymensis Ognev, 1922 — NE Siberia (Russia). L. t. kozhevnikovi Ognev, 1929 — C Russia from 57° to 58°N, whereit intergrades with the nomonotypical timidus S to 53° N. The W boundary is unclear. L. t. lugubris Kastschenko, 1899 — Siberian Altai Mts (Russia). L. t. mordeni Goodwin, 1933 — Russian Far East (Ussuri Valley and lower and middle Amur River) and Heilongjiang (China). L. t. ori Kuroda, 1928 — Sakhalin (Russia). L. t. scoticus Hilzheimer, 1906 — Scotland. L. t. sibiricorumJohansen, 1923 — W & SW Siberia (Russia), N Kazakhstan, and Tacheng Mts in N Xinjiang (China). L. t. sylvaticus Nilsson, 1831 —S Sweden, extending in hybrid zones with nominotypical timidus to S coast of Norway and W Latvia. L. t. transbaikalicus Ognev, 1929 — Trans-Baikal region in E Siberia (Russia) and E Inner Mongolia (= Nei Mongol, China). L. t. varronis Miller, 1901 — at high altitudes in the Alps, C Europe. in Leporidae
Subspecies and Distribution. L. t. timidus Linnaeus, 1758 — Scandinavia S to 59° N, N Russia (S to 57° N to 58° N) to E of Ural Mts, Estonia, perhaps Poland, and Altai and Beita Mts in N Xinjiang (China); from Sweden extending in hybrid zones with the subspecies sylvaticus to S coast of Norway and W Latvia. L. t. abet Kuroda, 1938 — Kurile Is (Russia). L. t. ainu Barrett-Hamilton, 1900 — Hokkaido (Japan). L. t. begitschevi Koljuschev, 1936 — Taimyr Peninsula (Russia). L. t. gichiganus J. A. Allen, 1903 — C Yakutia, Kamchatka and Okhotsk Sea coast (Russia). L. t. hibernicus Bell, 1837 — Ireland. L. t. kolymensis Ognev, 1922 — NE Siberia (Russia). L. t. kozhevnikovi Ognev, 1929 — C Russia from 57° to 58°N, whereit intergrades with the nomonotypical timidus S to 53° N. The W boundary is unclear. L. t. lugubris Kastschenko, 1899 — Siberian Altai Mts (Russia). L. t. mordeni Goodwin, 1933 — Russian Far East (Ussuri Valley and lower and middle Amur River) and Heilongjiang (China). L. t. ori Kuroda, 1928 — Sakhalin (Russia). L. t. scoticus Hilzheimer, 1906 — Scotland. L. t. sibiricorumJohansen, 1923 — W & SW Siberia (Russia), N Kazakhstan, and Tacheng Mts in N Xinjiang (China). L. t. sylvaticus Nilsson, 1831 —S Sweden, extending in hybrid zones with nominotypical timidus to S coast of Norway and W Latvia. L. t. transbaikalicus Ognev, 1929 — Trans-Baikal region in E Siberia (Russia) and E Inner Mongolia (= Nei Mongol, China). L. t. varronis Miller, 1901 — at high altitudes in the Alps, C Europe.
Distribution. NW Madagascar from near Bealalana in the N to the Betsiboka River, S limit is reportedly Ambato Boeni, and E boundary is near Antetemasy (just W of Befandriana Nord). in Indriidae
Distribution. NW Madagascar from near Bealalana in the N to the Betsiboka River, S limit is reportedly Ambato Boeni, and E boundary is near Antetemasy (just W of Befandriana Nord).
Distribution. SW Senegal, Guinea-Bissau, W & SE Guinea, Sierra Leone, Liberia, and W Ivory Coast (E boundary is the Nzo-Sassandra river system). in Cercopithecidae
Distribution. SW Senegal, Guinea-Bissau, W & SE Guinea, Sierra Leone, Liberia, and W Ivory Coast (E boundary is the Nzo-Sassandra river system).
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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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.