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325 results for “Distribution limits”
Distribution. NE DR Congo; distributional limits unknown. in Muridae
Distribution. NE DR Congo; distributional limits unknown.
Figure 5 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 5 Results of quantitative samplings in rockpools at four sites on the eastern coast of Kyushu, southern Japan. Solid bars and plots show mean density (error bars indicating standard error) and occurrence rates of each species of Chaenogobius (upper, C. annularis; lower, C. gulosus) at each site in the two seasons (left, spring; right, autumn) respectively. Abbreviations of the sites on the x-axis are as follows: Ot, Oita; N-My, N-Miyazaki, S-My, S-Miyazaki; TnI, Tanega-shima (these locality names correspond to those used in Fig. 3). Sample sizes, n = 5, except for Tanega-shima in autumn (n = 8).
Figure 4 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 4 Records (circles and a triangle) of Chaenogobius annularis (left) and C. gulosus (right) in south-east Kyushu, southern Japan, based on the examination of museum specimens (qualitative survey). A triangle indicating occurrence of C. gulosus in Tanega-shima Island by possible human-induced transportation.
Figure 3 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 3 Map showing the sampling sites in the present study (squares) and the site of a previous study (triangle, Yaku-shima Island: Murase 2013, 2015) for the quantitative survey in rock pools along the eastern coast of Kyushu, southern Japan.
Figure 1 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 1 Fresh specimens of the two species of Chaenogobius: A Chaenogobius annularis, KPM-NI 42850 (photo number, KPM-NR 179153), 52.7 mm SL, Nobeoka City, Miyazaki Prefecture B Chaenogobius gulosus, KPM-NI 42951 (KPM-NR 179221), 73.0 mm SL, Kadogawa Bay, Miyazaki Prefecture. Photos by A. Murase.
Figure 6 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 6 Images of juveniles of the two species of Chaenogobius on the coasts of Kyushu, southern Japan: A Chaenogobius annularis, fresh specimen, KPM-NI 42964 (photo number KPM-NR 179226), 17.6 mm SL, collected at rockpool environment in Usuki City, Oita Prefecture B Chaenogobius gulosus, fresh specimen, un-catalogued specimen (personal collection number, UMNB-I 3941), 19.2 mm SL, collected with seine net at a small beach in Totoro Port, Nobeoka City, Miyazaki Prefecture, April 2017 C Chaenogobius gulosus, swimming individuals in Tomioka Port, Reihoku Town, Amakusa, Kumamoto Prefecture, May 2017. Photos by A. Murase.
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.
Рис. 2. Схема распространения и мест встречи японского ужа на российском ΔаΛьнем Востоке: 1 — места встречи Αо 1985 г. (по Λитературным Αанным); 2 — места встречи посΛе 1985 г.; 3 — «КΛючевые ΛокаΛитеты» (см. в тексте); 4 — распространение хвойноширокоΛиственных и широкоΛиственных Λесов (по: КоΛесников 1969); 5 — граница распространения манчжурской фауны (по: Куренцов 1965) Fig. 2. Distribution map and finding localities of Hebius vibakari in the Russian Far East: 1 — findings before 1985 (according to the published data); 2 — findings after 1985; 3 — Key localities (see the text of the article); 4 — distribution of coniferous/broad-leaved and broad-leaved forests (see Kolesnikov 1969); 5 — limits of the Manchurian fauna (see Kurentsov 1965) in Особенности Распространения Японского Ужа Hebius Vibakari (H. Boie, 1826) (Colubridae: Natricinae) В Российской Части Ареаλа
Рис. 2. Схема распространения и мест встречи японского ужа на российском ΔаΛьнем Востоке: 1 — места встречи Αо 1985 г. (по Λитературным Αанным); 2 — места встречи посΛе 1985 г.; 3 — «КΛючевые ΛокаΛитеты» (см. в тексте); 4 — распространение хвойноширокоΛиственных и широкоΛиственных Λесов (по: КоΛесников 1969); 5 — граница распространения манчжурской фауны (по: Куренцов 1965) Fig. 2. Distribution map and finding localities of Hebius vibakari in the Russian Far East: 1 — findings before 1985 (according to the published data); 2 — findings after 1985; 3 — Key localities (see the text of the article); 4 — distribution of coniferous/broad-leaved and broad-leaved forests (see Kolesnikov 1969); 5 — limits of the Manchurian fauna (see Kurentsov 1965)
Fig. 2 – a in New records of Tarucus balkanicus at the northern limit of its distribution along the Adriatic coast (Lepidoptera: Papilionoidea, Lycaenidae)
Fig. 2 – a), Rocky habitat of Tarucus balkanicus at the Donje Sitno locality; b), Ruderal habitat at the locality Čavoglave, near the spring of Čikola river; c), T. balkanicus feeding on Satureja sp.
Fig. 3 in Capnodis cariosa (Pallas, 1776) found in a new Romanian location at the northern limit of its distribution range (Coleoptera: Buprestidae)
Fig. 3 – The distribution map of Capnodis cariosa cariosa (Pall.) In Romania (grey dots = old occurrences, red dots = new occurrences).
Fig. 4 in Capnodis cariosa (Pallas, 1776) found in a new Romanian location at the northern limit of its distribution range (Coleoptera: Buprestidae)
Fig. 4 – The entire distribution map of Capnodis cariosa (Pall.) (red dots = GBIF occurrences; blue dot = Romanian new occurrences; grey dot = Romanian old occurrences; "?" = the localities in Iran and Iraq are omitted in GBIF dataset, but the species is present in both countries according to Löbl & Löbl 2016).
considered that it was present. Due to the lack of recent data and the limited information sup- plied by previous authors for Angolan specimens, the presence of L. viridis in Angola is questionable. MAP 74. Distribution of Leptopelis viridis in Angola. in Diversity and Distribution of the Amphibians and Terrestrial Reptiles of Angola Atlas of Historical and Bibliographic Records (1840-2017)
considered that it was present. Due to the lack of recent data and the limited information sup- plied by previous authors for Angolan specimens, the presence of L. viridis in Angola is questionable. MAP 74. Distribution of Leptopelis viridis in Angola.
Data from: Do thermoregulatory costs limit altitude distributions of Andean forest birds?
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Data from: How to assess Drosophila heat tolerance: unifying static and dynamic tolerance assays to predict heat distribution limits
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Data on thermal fertility limits, critical thermal limits and Drosophila distributions
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The environmental factors limiting the distribution of shallow-water terebratulid brachiopods
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Figure 2 in How survival and food intake of tri-spine horseshoe crabsı Tachypleus tridentatus respond to thermal variation: implications for understanding its distribution limit
Figure 2. Effects of (a) different temperature levels for 7 days and (b) the subsequent recovery at 25°C for 3 days on the mean intake rate (%) of juvenile T. tridentatus. Values represent the mean + SD. Mann-Whitney U tests with Bonferroni correction with statistical difference between temperature levels and their recovery (p <0.05) are presented in different lowercase letters.
Distribution. Myanmar, S China (Yunnan), Thailand, Laos, Cambodia, and at least N & C Vietnam; exact distributional limits are uncertain. in Rhinolophidae
Distribution. Myanmar, S China (Yunnan), Thailand, Laos, Cambodia, and at least N & C Vietnam; exact distributional limits are uncertain.
Distribution. Discontinuous and limited to wetland environments from S Republic of the Congo through C DR Congo and SW Tanzania, S to Zambia, Angola, and Botswana. Maps and distributional information here are provisional pending future research. in Bovidae
Distribution. Discontinuous and limited to wetland environments from S Republic of the Congo through C DR Congo and SW Tanzania, S to Zambia, Angola, and Botswana. Maps and distributional information here are provisional pending future research.
Subspecies and Distribution. A. g. guariba Humboldt, 1812 — Brazilian Atlantic Forest from the Rio Sao Francisco (although the Rio Paraguacu is the northernmost known locality) to the Rio Doce; however, based on his studies of morphology and pelage color patterns Gregorin in 2006 indicated that it extends from the Rio Paraguacu in Bahia State, S along the coast across the lower Rio Jequitinhonha extending inland somewhat into Minas Gerais State, S through the Rio Doce valley as far the Rio Paraiba do Sul Basin in Rio de Janeiro. A. g. clamitans Cabrera, 1940 — Brazilian Atlantic Forest S of Rio Doce (but Gregorin has recently identified howlers of the upper Rio Doce, Rio Matip6 and Caratinga, and the middle and upper Rio Jequitinhonha as marking the N limits of this subspecies) through the S of Espirito Santo to Rio de Janeiro, Sao Paulo, Parana, Santa Catarina, and Rio Grande do Sulstates (S limit is Rio Camaqua Basin in Rio Grande do Sul, 31° 10" S, where the Atlantic Forest gives way to the Pampas grasslands), and inland in the forested E of Minas Gerais ("Zona da Mata") and the Brazilian Highlands; also in NE Argentina (E of the Mts in Misiones Province to ¢.28° S). in Atelidae
Subspecies and Distribution. A. g. guariba Humboldt, 1812 — Brazilian Atlantic Forest from the Rio Sao Francisco (although the Rio Paraguacu is the northernmost known locality) to the Rio Doce; however, based on his studies of morphology and pelage color patterns Gregorin in 2006 indicated that it extends from the Rio Paraguacu in Bahia State, S along the coast across the lower Rio Jequitinhonha extending inland somewhat into Minas Gerais State, S through the Rio Doce valley as far the Rio Paraiba do Sul Basin in Rio de Janeiro. A. g. clamitans Cabrera, 1940 — Brazilian Atlantic Forest S of Rio Doce (but Gregorin has recently identified howlers of the upper Rio Doce, Rio Matip6 and Caratinga, and the middle and upper Rio Jequitinhonha as marking the N limits of this subspecies) through the S of Espirito Santo to Rio de Janeiro, Sao Paulo, Parana, Santa Catarina, and Rio Grande do Sulstates (S limit is Rio Camaqua Basin in Rio Grande do Sul, 31° 10" S, where the Atlantic Forest gives way to the Pampas grasslands), and inland in the forested E of Minas Gerais ("Zona da Mata") and the Brazilian Highlands; also in NE Argentina (E of the Mts in Misiones Province to ¢.28° S).
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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)
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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.