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Distribution. NW Sulawesi (discontinuous range in Central Sulawesi Province), the N form occurs on the Isthmus of Palu from just W of the village of Tomini to the NE (c.120° 30° E), the coastlines of the Isthmus of Palu to the E and to the W,to the villages of Ampibabo and Marantale in the S (c.0° 30" S), the S form occurs in a very small area W to SW of Palu, around the type locality Uwemanje (0° 58' S, 119° 50' E). in Tarsiidae
Distribution. NW Sulawesi (discontinuous range in Central Sulawesi Province), the N form occurs on the Isthmus of Palu from just W of the village of Tomini to the NE (c.120° 30° E), the coastlines of the Isthmus of Palu to the E and to the W,to the villages of Ampibabo and Marantale in the S (c.0° 30" S), the S form occurs in a very small area W to SW of Palu, around the type locality Uwemanje (0° 58' S, 119° 50' E).
Raw data for: Spidroin N-terminal domain forms amyloid-like fibril based hydrogels and provides a protein immobilization platform
<p>Raw data for the article "Spidroin N-terminal domain forms amyloid-like fibril based hydrogels and provides a protein immobilization platform." to be published in Nature communications.</p>
FORM: A Dataset for Driver Monitoring System
<p>The dataset is categorized into four classes (forward, on_phonecall, rotated, mobile_usage,) depending on the driver’s head position.</p>
Distribution. NE Queensland from Mitchell River and near Mt Carbine (where it forms a hybrid zone with Godman's Rock Wallaby, P. godmani) W to Mungana and Undara, S to Burdekin River; W limit uncertain. in Macropodidae
Distribution. NE Queensland from Mitchell River and near Mt Carbine (where it forms a hybrid zone with Godman's Rock Wallaby, P. godmani) W to Mungana and Undara, S to Burdekin River; W limit uncertain.
Distribution. SE Queensland from Fitzroy River S to Nanango (where it forms hybrid zone with the Brush-tailed Rock Wallaby, P. penicillata) and W to beyond Rubyvale and Clermont; W limit uncertain. in Macropodidae
Distribution. SE Queensland from Fitzroy River S to Nanango (where it forms hybrid zone with the Brush-tailed Rock Wallaby, P. penicillata) and W to beyond Rubyvale and Clermont; W limit uncertain.
Distribution. NE Queensland from Mitchell River and near Mt Carbine (where it forms a hybrid zone with the Mareeba Rock Wallaby, P. mareeba) W to "Pinnacles" and N to Bathurst Head; W and N limits uncertain. in Macropodidae
Distribution. NE Queensland from Mitchell River and near Mt Carbine (where it forms a hybrid zone with the Mareeba Rock Wallaby, P. mareeba) W to "Pinnacles" and N to Bathurst Head; W and N limits uncertain.
Subspecies and Distribution. P.c.campbelliThomas,1905—C&EMongoliaandChina(WNingxia,InnerMongolia,andNHebei). P. c. crepidatus Hollister, 1912 — SE Siberia (Altai Mts, Tuva, S Buryatia, and S Zabaykalsky Krai in Russia) and NW Mongolia. A not yet formally described form based on genetic data is present in SW Mongolia. in Cricetidae
Subspecies and Distribution. P.c.campbelliThomas,1905—C&EMongoliaandChina(WNingxia,InnerMongolia,andNHebei). P. c. crepidatus Hollister, 1912 — SE Siberia (Altai Mts, Tuva, S Buryatia, and S Zabaykalsky Krai in Russia) and NW Mongolia. A not yet formally described form based on genetic data is present in SW Mongolia.
FIGURE. Distribution of Dicorynia. Physical map of the Amazonian region with all analyzed specimens of Dicorynia. A large amount of point overlays leading to reduced number of visible points is due to the large percentage of materials being old collections that rely only on the name of the municipality or similar. Source: NASA with modifications. Note that almost all specimens are contained in areas with less than 200 m high and the high elevations of the Guiana shield may represent a form of isolation between the two species. in A Taxonomic Revision of the Amazonian Genus Dicorynia (Fabaceae: Dialioideae)
FIGURE. Distribution of Dicorynia. Physical map of the Amazonian region with all analyzed specimens of Dicorynia. A large amount of point overlays leading to reduced number of visible points is due to the large percentage of materials being old collections that rely only on the name of the municipality or similar. Source: NASA with modifications. Note that almost all specimens are contained in areas with less than 200 m high and the high elevations of the Guiana shield may represent a form of isolation between the two species.
Distribution. Known only form Mt Sagalla and Chawia Forest in the Taita Hills of SE Kenya; possibly also found in NE Tanzania. in Soricidae
Distribution. Known only form Mt Sagalla and Chawia Forest in the Taita Hills of SE Kenya; possibly also found in NE Tanzania.
Plan-form evolution of drainage basins in response to tectonic changes: Insights from experimental and numerical landscapes
<p>The following data contains raw DEMs from the experiment in the simulations referred to in the mentioned manuscript, as well as MATLAB scripts (and legend) used for the analysis of the data.</p> <p>Experiment DEMs are named after the time they were acquired within the experiment, i.e., 4.tif is the DEM of the landscape after a duration of 4 hours of experiment.</p> <p>In MATLAB scripts, the following legend is used:</p> <p>E = Experiment</p> <p>SL = Low concavity simulation</p> <p>SH = High concavity simulation</p> <p>HL = Hack's law analysis</p> <p>A = Asymmetry analysis</p> <p>C = Chi analysis</p> <p>CP = Chi prime analysis</p> <p>ADCP = Across-divide chi prime analysis</p> <p>DAI = Divide asymmetry index analysis</p> <p>CreateStructuredGrid = Function that generates GRIDobj from ASCII files</p> <p>Num_DEM_Load = Script that generates GRIDobj from ASCII files</p>
As currently delineated, this is a complex comprising at least two species, as dem- onstrated by the work of J. M. Lamb and colleagues in 2014 and A. Monadjem and colleagues in 2015. Large gray-bellied specimens attributed to M. triton form two highly divergent molecular and chromosomal clades: on the one hand, from Tanzania, Malawi, and Mozambique (with chromosomal complement of 2n = 20-22, FN = 34); and, on the other, from DR Congo (with 2n = 32, FN = 34. Monotypic. Distribution. Extreme S South Sudan, S Ethiopia (Bale Mts), NE DR Congo, and from Uganda and Kenya SW & S to Angola, Zambia, WC Mozambique, and Malawi. in Muridae
As currently delineated, this is a complex comprising at least two species, as dem- onstrated by the work of J. M. Lamb and colleagues in 2014 and A. Monadjem and colleagues in 2015. Large gray-bellied specimens attributed to M. triton form two highly divergent molecular and chromosomal clades: on the one hand, from Tanzania, Malawi, and Mozambique (with chromosomal complement of 2n = 20-22, FN = 34); and, on the other, from DR Congo (with 2n = 32, FN = 34. Monotypic. Distribution. Extreme S South Sudan, S Ethiopia (Bale Mts), NE DR Congo, and from Uganda and Kenya SW & S to Angola, Zambia, WC Mozambique, and Malawi.
Distribution. SW Zimbabwe, E South Africa, and Swaziland; the range of the form cf. incomtus includes much of C Africa (Gabon, Republic of the Congo, DR Congo, Angola, Zambia, Malawi, and Mozambique). in Muridae
Distribution. SW Zimbabwe, E South Africa, and Swaziland; the range of the form cf. incomtus includes much of C Africa (Gabon, Republic of the Congo, DR Congo, Angola, Zambia, Malawi, and Mozambique).
Distribution. Usambara and Uluguru Mts in Eastern Arc Mts; undescribed form on Nyika Plateau of Malawi and neighboring Zambia. in Muridae
Distribution. Usambara and Uluguru Mts in Eastern Arc Mts; undescribed form on Nyika Plateau of Malawi and neighboring Zambia.
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).
Subspecies and Distribution. L.w.woosnam:Thomas,1906—RwenzoriMts,EDRCongoandSWUganda. L. w. prittiei Thomas, 1911 — highlands of Kigesi, Virunga Mts, and Nyungwe and Kibira forests, SW Uganda, E DR Congo, W Rwanda, and NW Burundi. Woosnam's Brush-furred Rats of a still undescribed form are present W of Lake Kivu in E DR Congo. in Muridae
Subspecies and Distribution. L.w.woosnam:Thomas,1906—RwenzoriMts,EDRCongoandSWUganda. L. w. prittiei Thomas, 1911 — highlands of Kigesi, Virunga Mts, and Nyungwe and Kibira forests, SW Uganda, E DR Congo, W Rwanda, and NW Burundi. Woosnam's Brush-furred Rats of a still undescribed form are present W of Lake Kivu in E DR Congo.
Data from: Climatic niche lability but growth form conservatism in the African woody flora
<p><span>Climatic niche evolution during the diversification of tropical plants has received little attention in Africa. To address this, we characterized the climatic niche of >4000 tropical African woody species, distinguishing two broad bioclimatic groups (forest vs. savanna) and six subgroups. We quantified niche conservatism </span><span>versus</span><span> lability at the genus level and for higher clades, using a molecular phylogeny of >800 genera. Although niche stasis at speciation is prevalent, numerous clades individually cover vast climatic spaces suggesting a general ease in transcending ecological limits, especially across bioclimatic subgroups. </span><span>The forest biome was the main source of diversity, providing many lineages to savanna, but reverse shifts also occurred. </span><span>We identified clades that diversified in savanna after shifts from forest. </span><span>The forest-savanna transition was not consistently associated with a growth form change, though we found evolutionarily labile clades whose presence in forest or savanna is associated respectively with climbing or shrubby species diversification.</span></p>
FIGURES 70‒77. Habitus. 70. Cacopsylla araliae, adult female summer form. 71. Cacopsylla araliae, fifth instar immature. 72 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula
FIGURES 70‒77. Habitus. 70. Cacopsylla araliae, adult female summer form. 71. Cacopsylla araliae, fifth instar immature. 72. Microhabitat of Cacopsylla araliae, interpetiolar space of Aralia elata. 73. Cacopsylla baccatae, teneral adult male. 74. Cacopsylla baccatae, fifth instar immature. 75. Cacopsylla bibari, adult male. 76. Cacopsylla bibari, adult female. 77. Cacopsylla bibari, fifth instar immature. (Photos 70–77 from Cho et al. (2017a))
FIGURES 134‒141. Habitus. 134. Cacopsylla viburnicola, adult female. 135. Cyamophila floribundae, adult female. 136. Cyamophila hexastigma, adult male. 137. Cyamophila hexastigma, adult female. 138. Cyamophila willeti, adult male summer form. 139. Cyamophila willieti, adult female winter form. 140. Cyamophila willieti, fifth instar immature. 141 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula
FIGURES 134‒141. Habitus. 134. Cacopsylla viburnicola, adult female. 135. Cyamophila floribundae, adult female. 136. Cyamophila hexastigma, adult male. 137. Cyamophila hexastigma, adult female. 138. Cyamophila willeti, adult male summer form. 139. Cyamophila willieti, adult female winter form. 140. Cyamophila willieti, fifth instar immature. 141. Psylla alniformosanaesuga, adult male. (Photos 135, 141 from Cho et al. (2017a))
FIGURES 102‒109. Habitus. 102. Cacopsylla lineaticeps, adult female. 103. Cacopsylla maculatili, adult male winter form. 104. Cacopsylla maculatili, adult female winter form. 105. Cacopsylla maculatili, adult male summer form. 106. Cacopsylla maculatili, adult female summer form. 107. Cacopsylla mali, adult male. 108. Cacopsylla mali, adult female. 109 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula
FIGURES 102‒109. Habitus. 102. Cacopsylla lineaticeps, adult female. 103. Cacopsylla maculatili, adult male winter form. 104. Cacopsylla maculatili, adult female winter form. 105. Cacopsylla maculatili, adult male summer form. 106. Cacopsylla maculatili, adult female summer form. 107. Cacopsylla mali, adult male. 108. Cacopsylla mali, adult female. 109. Cacopsylla mali, fifth instar immature. (Photos 103, 105 from Cho et al. (2017b))
FIGURES 94‒101. Habitus. 94. Cacopsylla fulguralis, adult male. 95. Cacopsylla fulguralis, adult female. 96. Cacopsylla hederae, adult male. 97. Cacopsylla hederae, adult female. 98. Cacopsylla jukyungi, adult male winter form. 99. Cacopsylla jukyungi, adult female summer form. 100. Cacopsylla jukyungi, fifth instar immature. 101 in Check list of jumping plant-lice (Hemiptera: Psylloidea) of the Korean Peninsula
FIGURES 94‒101. Habitus. 94. Cacopsylla fulguralis, adult male. 95. Cacopsylla fulguralis, adult female. 96. Cacopsylla hederae, adult male. 97. Cacopsylla hederae, adult female. 98. Cacopsylla jukyungi, adult male winter form. 99. Cacopsylla jukyungi, adult female summer form. 100. Cacopsylla jukyungi, fifth instar immature. 101. Cacopsylla lineaticeps, teneral adult female. (Photos 98–99 from Cho et al. (2017b), 101 from Cho et al. (2017a))
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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)
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.