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68 results for “distributional boundary”
Distribution. SE Madagascar, from the Mananara River S to the limits of the rainforest near Tolagnaro (= Fort-Dauphin), W limits of the distribution are forests in the Kalambatritra region; the Mananara River serves as a boundary between this species and the White-collared Brown Lemur (FE. cinereiceps), except for isolated populations at Midongy du Sud National Park and Vohipaho, near Vangaindrano. in Lemuridae
Distribution. SE Madagascar, from the Mananara River S to the limits of the rainforest near Tolagnaro (= Fort-Dauphin), W limits of the distribution are forests in the Kalambatritra region; the Mananara River serves as a boundary between this species and the White-collared Brown Lemur (FE. cinereiceps), except for isolated populations at Midongy du Sud National Park and Vohipaho, near Vangaindrano.
Distribution. Restricted and patchy range in NE Madagascar that includes the humid forest belt extending from the Marojejy Massif and the Andapa Basin to Maroantsetra; the Androranga River may be the NE distributional limit in the Tsaratanana Corridor, although further surveys are needed to confirm this, and the Antainambalana River in the Makira Forest protected area is currently regarded as the S boundary. Currently, Marojejy represents the N limit ofits distribution, although historic range maps suggest that it once occurred as far N as the Bemarivo River near Sambava. The NE distributional limit in Makira was only recently established, when a few groups were found in the Antohaka Lava Forest, but informal reports suggest that the unprotected Maherivaratra Forest, outside NE Makira, may also contain Silky Sifakas. in Indriidae
Distribution. Restricted and patchy range in NE Madagascar that includes the humid forest belt extending from the Marojejy Massif and the Andapa Basin to Maroantsetra; the Androranga River may be the NE distributional limit in the Tsaratanana Corridor, although further surveys are needed to confirm this, and the Antainambalana River in the Makira Forest protected area is currently regarded as the S boundary. Currently, Marojejy represents the N limit ofits distribution, although historic range maps suggest that it once occurred as far N as the Bemarivo River near Sambava. The NE distributional limit in Makira was only recently established, when a few groups were found in the Antohaka Lava Forest, but informal reports suggest that the unprotected Maherivaratra Forest, outside NE Makira, may also contain Silky Sifakas.
Distribution. CE Madagascar, the Mangoro and Onive rivers are the N limits of the present range, and the Rienana River in Andringitra National Park is the S boundary. The former distribution probably extended somewhat N and further S to the Manampatrana River, but populations in those regions appear to have been extirpated. in Indriidae
Distribution. CE Madagascar, the Mangoro and Onive rivers are the N limits of the present range, and the Rienana River in Andringitra National Park is the S boundary. The former distribution probably extended somewhat N and further S to the Manampatrana River, but populations in those regions appear to have been extirpated.
Distribution. NW Madgascar, found discontinuously in the coast S of the Manambolo River, from where the distribution swings inland to the uplands before touching the coast again N and E of the Mahavavy River; reports of the Crowned Sifaka as far S as the Sakay River, as far E to Andanotongo, and SE beyond Tsiroanomandidy suggest that its distribution is more complicated than originally believed. Decken's (PF. deckeniz) and Crowned sifakas are often found in the same areas, although the Crowned Sifaka tends to be found further inland than the more coastal Decken's Sifaka. In general, the boundary between these two species is the Mahavavy River, while the Betsiboka River separates the Crowned Sifaka from Coquerel's Sifaka (PF. coquereli). in Indriidae
Distribution. NW Madgascar, found discontinuously in the coast S of the Manambolo River, from where the distribution swings inland to the uplands before touching the coast again N and E of the Mahavavy River; reports of the Crowned Sifaka as far S as the Sakay River, as far E to Andanotongo, and SE beyond Tsiroanomandidy suggest that its distribution is more complicated than originally believed. Decken's (PF. deckeniz) and Crowned sifakas are often found in the same areas, although the Crowned Sifaka tends to be found further inland than the more coastal Decken's Sifaka. In general, the boundary between these two species is the Mahavavy River, while the Betsiboka River separates the Crowned Sifaka from Coquerel's Sifaka (PF. coquereli).
Distribution. Coastal forests of N California from the Klamath Mts of Del Norte County S to Sonoma County. The N border of this species and the S boundary of the Red Tree Vole (A. longicaudus) are poorly defined and this region near Humboldt County, California, warrants further study. in Cricetidae
Distribution. Coastal forests of N California from the Klamath Mts of Del Norte County S to Sonoma County. The N border of this species and the S boundary of the Red Tree Vole (A. longicaudus) are poorly defined and this region near Humboldt County, California, warrants further study.
Subspecies and Distribution. M.b.bobakP.L..S.Muller,1776—EUkraineandacrossSRussiatotheVolgaRiver. M.b.kozloviFokanov,1966—CpartofthedistributionEoftheVolgaRiver,nearUlyanovsk(Russia)withuncertainEboundary. M. b. tschaganensis Bazhanov, 1930 — E part of the distribution in Kazakhstan with uncertain W boundary. Introduced into the Caucasus Mts (Dagestan, Russia). in Sciuridae
Subspecies and Distribution. M.b.bobakP.L..S.Muller,1776—EUkraineandacrossSRussiatotheVolgaRiver. M.b.kozloviFokanov,1966—CpartofthedistributionEoftheVolgaRiver,nearUlyanovsk(Russia)withuncertainEboundary. M. b. tschaganensis Bazhanov, 1930 — E part of the distribution in Kazakhstan with uncertain W boundary. Introduced into the Caucasus Mts (Dagestan, Russia).
Distribution. Widely distributed in South-east Asia (Myanmar, Laos, Thailand, Cambodia, S Vietnam, and Peninsular Malaysia, including offshore islands). Distribution boundary between this species and the Large White-toothed Shrew (C. dracula), especially in Myanmar or whether their distributions overlapped, is not clear. in Soricidae
Distribution. Widely distributed in South-east Asia (Myanmar, Laos, Thailand, Cambodia, S Vietnam, and Peninsular Malaysia, including offshore islands). Distribution boundary between this species and the Large White-toothed Shrew (C. dracula), especially in Myanmar or whether their distributions overlapped, is not clear.
Distribution. Borneo, confined to an area of E Kalimantan, from the Kayan and Sembakung (= Sebuku) rivers in the N, S, and SW to the Mahakam River, the W boundary is not well known but certainly E of the Apau Kayan and the Kayan Mentarang National Park. in Cercopithecidae
Distribution. Borneo, confined to an area of E Kalimantan, from the Kayan and Sembakung (= Sebuku) rivers in the N, S, and SW to the Mahakam River, the W boundary is not well known but certainly E of the Apau Kayan and the Kayan Mentarang National Park.
Supplementary material 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
List of voucher specimens of Chaenogobius annularis from quantitative surveys at rockpools on the eastern coasts of Kyushu : Explanation note: KPM-NI and KPM-NR indicates the number of the specimen and its photograph respectively.
Supplementary material 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
List of voucher specimens of Chaenogobius gulosus from quantitative surveys at rockpools on the eastern coasts of Kyushu : Explanation note: KPM-NI and KPM-NR indicates the number of the specimen and its photograph respectively.
Supplementary material 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
List of voucher specimens of Chaenogobius annularis for distribution records in south-east Kyushu by examination of museum collections : Explanation note: Lots of specimens ordered according to longitude. Number of KPM-NR indicates photographs of fresh specimens deposited in KPM.
Supplementary material 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
List of voucher specimens of Chaenogobius gulosus for distribution records in south-east Kyushu by examination of museum collection : Explanation note: Lots of specimen ordered according to longitude. Number of KPM-NR indicating photographs of fresh specimen deposited in KPM.
Globally Distributed Subducted Materials along the Earth's Core-Mantle Boundary: Implications for Ultra-low Velocity Zones
<p>Supplemental movie files related to the geodynamic models in our manuscript "Globally Distributed Subducted Materials along the Earth’s Core-Mantle Boundary: Implications for Ultra-low Velocity Zones"</p>
Data from: Shaping species with ephemeral boundaries: the distribution and genetic structure of the desert tortoise (Gopherus morafkai) in the Sonoran Desert region
Open the record for dataset details and reuse information.
Fig. 2 in INSUFFICIENT COLD RESISTANCE AND THE EASTERN BOUNDARY OF THE DISTRIBUTION RANGE OF ANT LASIUS FULIGINOSUS (HYMENOPTERA: FORMICIDAE)
Fig. 2 Dynamics of the minimal decade temperatures of 2018–2019 in the nest of the Lasius fuliginosus at the depth 20–30 cm (dotted line) and 50–60 cm (solid line) in vicinity
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.
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