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FIGURE 1 in First fossil representative of the sawfly subfamily Blennocampinae (Hymenoptera: Tenthredinidae)
FIGURE 1. Eutomostethus karimae sp. nov., holotype UCM-61412. A, Photograph of habitus. B, Detailed photograph of body. C, Detailed photograph of wing. Scale bars = 1 mm.
FIGURE 2 in First fossil representative of the sawfly subfamily Blennocampinae (Hymenoptera: Tenthredinidae)
FIGURE 2. Extant representatives of Eutomostethus and Tomostethus. A, E. longidentus Wei, 2003, male. B, T. fraxini (de Geer, 1775), female. Scale bars = 5mm (A), 2 mm (B).
Dataset and code for : "Representing Vector Geographic Information As a Tensor for Deep Learning Based Map Generalisation"
<p>Dataset and code supporting the experiment about map generation in the article: "Representing Vector Geographic Information As a Tensor for Deep Learning-Based Map Generalisation"</p>
FIGURE. Umbellules within four populations of Sanicula orthacantha, showing the fruits characters and the variation in numbers of staminate flowers (each line represents a plant individual). The ratio of staminate flowers number/ umbellule number is given for each individual. A. China, Hubei, Xuan'en, Qizimei Mountain, H.M. Li, Y.M. Yi & Y.S. Zhang 1077 (NAS). B. China, Jiangxi, Jiujiang, Lushan, H.M. Li, Y.S. Zhang & Y. Xu 1109 (NAS). C. China, Chongqing, Nanchuan, Jinfo Shan, H.M. Li, Y.S. Zhang & X. Zhang 1141 (NAS). D. China, Sichuan, Emei Shan, H.M. Li & Y.S. Zhang 1157 (NAS). All same scale. in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Umbellules within four populations of Sanicula orthacantha, showing the fruits characters and the variation in numbers of staminate flowers (each line represents a plant individual). The ratio of staminate flowers number/ umbellule number is given for each individual. A. China, Hubei, Xuan'en, Qizimei Mountain, H.M. Li, Y.M. Yi & Y.S. Zhang 1077 (NAS). B. China, Jiangxi, Jiujiang, Lushan, H.M. Li, Y.S. Zhang & Y. Xu 1109 (NAS). C. China, Chongqing, Nanchuan, Jinfo Shan, H.M. Li, Y.S. Zhang & X. Zhang 1141 (NAS). D. China, Sichuan, Emei Shan, H.M. Li & Y.S. Zhang 1157 (NAS). All same scale.
FIGURE. Umbellules within two populations of Sanicula orthacantha var. brevispina from China, Sichuan, Emei Shan, showing the fruits characters and the variation in numbers of staminate flowers (each line represents a plant individual). The ratio of staminate flowers number/ umbellule number is given for each individual. A. C.H. Li 1122 (NAS). B. H.M. Li & Y.S. Zhang 1151 (NAS). in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Umbellules within two populations of Sanicula orthacantha var. brevispina from China, Sichuan, Emei Shan, showing the fruits characters and the variation in numbers of staminate flowers (each line represents a plant individual). The ratio of staminate flowers number/ umbellule number is given for each individual. A. C.H. Li 1122 (NAS). B. H.M. Li & Y.S. Zhang 1151 (NAS).
FIGURE. Individuals in two Populations of Sanicula orthacantha var. brevispina from China, Sichuan, Emei Shan, showing the variation in plant size and rhizome character (each line represents a population). A. C.H. Li 1122 (NAS). B. H.M. Li & Y.S. Zhang 1151 (NAS). in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Individuals in two Populations of Sanicula orthacantha var. brevispina from China, Sichuan, Emei Shan, showing the variation in plant size and rhizome character (each line represents a population). A. C.H. Li 1122 (NAS). B. H.M. Li & Y.S. Zhang 1151 (NAS).
FIGURE. Cauline Leaves of Sanicula orthacantha var. brevispina from China, Sichuan, Emei Shan, showing the size and shape of leaves within and between populations (each line represents a plant individual). A. C.H. Li 1122 (NAS). B. H.M. Li & Y.S. Zhang 1151 (NAS). in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Cauline Leaves of Sanicula orthacantha var. brevispina from China, Sichuan, Emei Shan, showing the size and shape of leaves within and between populations (each line represents a plant individual). A. C.H. Li 1122 (NAS). B. H.M. Li & Y.S. Zhang 1151 (NAS).
Distribution. Endemic to subtropical and tropical waters of the Atlantic Ocean in an area ranging from N USA to Brazil and from Ireland to Guinea-Bissau; its distribution may continue as far S as Uruguay in the W, and possibly as far S as Angola in the E. It is occasionally recorded stranding in temperate waters, but these may represent vagrant individuals. in Ziphiidae
Distribution. Endemic to subtropical and tropical waters of the Atlantic Ocean in an area ranging from N USA to Brazil and from Ireland to Guinea-Bissau; its distribution may continue as far S as Uruguay in the W, and possibly as far S as Angola in the E. It is occasionally recorded stranding in temperate waters, but these may represent vagrant individuals.
Distribution. Most records come from either New Zealand or the Atlantic coast of South America, but also recorded in Tasmania, Western Australia, and South Africa; distribution remains unclear due to the small number of confirmed strandings. There are no records of this species between New Zealand and the Pacific coast of South America, but it is unclear whether this represents a break in distribution or a lack of research activity in this region. Earlier records from the Pacific coast of USA have since been reclassified as Perrin's Beaked Whale (M. perrini). in Ziphiidae
Distribution. Most records come from either New Zealand or the Atlantic coast of South America, but also recorded in Tasmania, Western Australia, and South Africa; distribution remains unclear due to the small number of confirmed strandings. There are no records of this species between New Zealand and the Pacific coast of South America, but it is unclear whether this represents a break in distribution or a lack of research activity in this region. Earlier records from the Pacific coast of USA have since been reclassified as Perrin's Beaked Whale (M. perrini).
Distribution. Occurs from the temperate waters of S Atlantic, Indian, and S Pacific oceans to the waters of Antarctica. A record from Burma (= Myanmar) is thought to represent a vagrant individual. in Ziphiidae
Distribution. Occurs from the temperate waters of S Atlantic, Indian, and S Pacific oceans to the waters of Antarctica. A record from Burma (= Myanmar) is thought to represent a vagrant individual.
Distribution. Restricted to the cooler waters of the N Atlantic Ocean from 71° 30" N in the Norwegian Sea, Iceland, and [Labrador (Canada) in the N, to Madeira, Azores, and NE USA to the S; single records from the Gulf of Mexico and E Mediterranean Sea are thought to represent vagrant individuals. In general, this species appears to be more widespread in E Atlantic Ocean than in W Atlantic Ocean, which may be related to preferences for cooler water temperatures. in Ziphiidae
Distribution. Restricted to the cooler waters of the N Atlantic Ocean from 71° 30" N in the Norwegian Sea, Iceland, and [Labrador (Canada) in the N, to Madeira, Azores, and NE USA to the S; single records from the Gulf of Mexico and E Mediterranean Sea are thought to represent vagrant individuals. In general, this species appears to be more widespread in E Atlantic Ocean than in W Atlantic Ocean, which may be related to preferences for cooler water temperatures.
FIGURE. Phylogenetic tree derived from Bayesian analysis, based on nrLSU data. Posterior probability (PP> 0.95) values from the Bayesian analysis are added at the nodes. The scale bar represents the number of nucleotide changes per site. (T) indicates the type specimen for this species. The new species are in bold. in Four new species of Entoloma (Entolomataceae, Agaricomycetes) subgenera Cyanula and Claudopus from Vietnam and their phylogenetic position
FIGURE. Phylogenetic tree derived from Bayesian analysis, based on nrLSU data. Posterior probability (PP> 0.95) values from the Bayesian analysis are added at the nodes. The scale bar represents the number of nucleotide changes per site. (T) indicates the type specimen for this species. The new species are in bold.
Subspecies and Distribution. P.m.maculataGould,1851—EAustralia,NQueensland(CapeYork),SthroughoutEQueenslandtoENewSouthWales(Gosford),alsoinFraserandBribieIs. P.m. sinualis Thomas, 1926 — N Australia, N Western Australia, N Northern Territory (Top End and Groote Eylandt I). Individuals from Barrow I, N Western Australia, are included here but possibly represent a differentstill undescribed species. in Dasyuridae
Subspecies and Distribution. P.m.maculataGould,1851—EAustralia,NQueensland(CapeYork),SthroughoutEQueenslandtoENewSouthWales(Gosford),alsoinFraserandBribieIs. P.m. sinualis Thomas, 1926 — N Australia, N Western Australia, N Northern Territory (Top End and Groote Eylandt I). Individuals from Barrow I, N Western Australia, are included here but possibly represent a differentstill undescribed species.
Distribution. Known from only two isolated localities (Ingwavuma and Ubombo) on E slopes of Lebombo Mts, KwaZulu-Natal Province, E South Africa; owl pellet remains from Weenen, ¢.250 km SW of type locality, appear to represent this species, suggesting that it is more widespread than currently recognized. Possibly extends into SE Swaziland along the Lebombo Mts. in Chrysochloridae
Distribution. Known from only two isolated localities (Ingwavuma and Ubombo) on E slopes of Lebombo Mts, KwaZulu-Natal Province, E South Africa; owl pellet remains from Weenen, ¢.250 km SW of type locality, appear to represent this species, suggesting that it is more widespread than currently recognized. Possibly extends into SE Swaziland along the Lebombo Mts.
Seismic homogenization of poroelastic regions in absence of a representative elementary volume
<p>Data used for figures. Read the list_files.txt to find the corresponding files.</p>
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.
Subspecies and Distribution. D.m.mueller:Schlegel,1866—lowlandsofBird'sHead(=Vogelkop)Peninsula,NWNewGuinea. D. m. lorentziiJentink, 1908 — lowlands of SW New Guinea. D.m.mysoliaeThomas,1913—MisoolI,inWestPapuanIs. D. m. yapeni Groves & Flannery, 1989 — Yapen I, in Cenderawasih (= Geelvink) Bay, NW New Guinea. Population on Salawati I, West Papuan Is, may represent an additional subspecies. in Macropodidae
Subspecies and Distribution. D.m.mueller:Schlegel,1866—lowlandsofBird'sHead(=Vogelkop)Peninsula,NWNewGuinea. D. m. lorentziiJentink, 1908 — lowlands of SW New Guinea. D.m.mysoliaeThomas,1913—MisoolI,inWestPapuanIs. D. m. yapeni Groves & Flannery, 1989 — Yapen I, in Cenderawasih (= Geelvink) Bay, NW New Guinea. Population on Salawati I, West Papuan Is, may represent an additional subspecies.
Distribution. Between the Rio Xingu and the Rio Tocantins in Para and Mato Grosso states, Brazil; two records from Rio Teles Pires, Mato Grosso, might represent an undescribed species. in Cricetidae
Distribution. Between the Rio Xingu and the Rio Tocantins in Para and Mato Grosso states, Brazil; two records from Rio Teles Pires, Mato Grosso, might represent an undescribed species.
Distribution. Restricted to Réunion I; there is an isolated record from S Ethiopia, some several hundred kilometers from the coast. This record represents a vagrant or introduced individual, and the species does not normally occur in Africa. in Molossidae
Distribution. Restricted to Réunion I; there is an isolated record from S Ethiopia, some several hundred kilometers from the coast. This record represents a vagrant or introduced individual, and the species does not normally occur in Africa.
FIGURE. Drosera hirtella: a, specimen Saint-Hilaire B1-1762bis (P00749158), with the designated lectotype highlighted; b, detail of the lectotype, showing the ascending scape and leaves with obovate lamina; c, detail of the individual to the left of the lectotype, representing the "western morphotype", with narrowly obovate lamina. Image extracted from A. de Saint-Hilaire virtual herbarium (2020). in A synopsis of the genus Drosera (Droseraceae) in Brazil
FIGURE. Drosera hirtella: a, specimen Saint-Hilaire B1-1762bis (P00749158), with the designated lectotype highlighted; b, detail of the lectotype, showing the ascending scape and leaves with obovate lamina; c, detail of the individual to the left of the lectotype, representing the "western morphotype", with narrowly obovate lamina. Image extracted from A. de Saint-Hilaire virtual herbarium (2020).
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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.