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FIGURE. The Bayesian tree of the Adaintum pedatum complex based on chloroplast markers and corresponding rhizome type. Support values (Bayesian inference posterior probability (BIPP) (upper) ≥ 0.5, and maximum likelihood bootstrap support (MLBS) (nether) ≥ 50%) are shown above the main branches, the thickened branches indicate MLBS=100 and BIPP=1. Yellow bar means erect rhizome; blue bar means creeping rhizome; gray bar means decumbent or short-creeping rhizome. in Adiantum japonicum, a new species of the Adiantum pedatum complex (Pteridaceae) from Japan
FIGURE. The Bayesian tree of the Adaintum pedatum complex based on chloroplast markers and corresponding rhizome type. Support values (Bayesian inference posterior probability (BIPP) (upper) ≥ 0.5, and maximum likelihood bootstrap support (MLBS) (nether) ≥ 50%) are shown above the main branches, the thickened branches indicate MLBS=100 and BIPP=1. Yellow bar means erect rhizome; blue bar means creeping rhizome; gray bar means decumbent or short-creeping rhizome.
Subspecies and Distribution. T.n.napuF.Cuvier,1822—SMyanmar,Thai/MalayPeninsula,islandsoffWMalayPeninsula(Langkawi&Pangkor),Borneo,SSumatra,BangkaI,islandsoffBorneo(Laut&Serasan). T.n.bangue:Chasen&Kloss,1931—BanggiIandBalembanganI,offNBorneo. T.n.bunguranensisMiller,1901—NatunaIs(=Bunguran),oftWBorneo. T.n.neubronneriSody,1931—NSumatra. T.n.nmiasisLyon,1916—NiasI,offWSumatra. T.n.rufulusMiller,1900—TiomanI,offEMalayPeninsula,RiauandLinggaArchipelagos. T. n. terutus Thomas & Wroughton, 1909 — Terutau I, off W Malay Peninsula. The species was recently reconfirmed for Singapore. Maps that include Vietnam, Cambodia, and Laos in the distribution range are based on the earlier assumption that 7. versicolor was a subspecies of 1. napu. Subsequent studies have indicated that 7. versicolor is a distinct species, and that the range of 1. napu therefore does not extend into Cambodia, Laos, and Vietnam. The northern limit on the Thai-Malay peninsula is not well defined. Specimens of 1. napu have been collected from as far north as Bankachon in southern Myanmar (10° 08" N), but despite fairly intensive camera-trapping in Kui Buri National Park, Thailand (12° N), 7. napu has not been photographed there. At the northern margin ofits range, it is generally rare. It has been reported, for example, that during the flooding of the Chiew Larn Reservoir (Surat Thani Province; about 9° N, 98° 45' E), only six 7. napu were rescued compared with 172 71. kanchil. This area is the transition zone from wetter evergreen forest to drier deciduous types, and it might be that 7° napu is not well adapted to the drier forest types towards the northern limit ofits range. There are unconfirmed reports of the species on Java, where it may have been confused with one of the two color morphs of 7. javanicus. As explained in the Taxonomy section, the subspecific status of the populations of several islands remains unclear. in Tragulidae
Subspecies and Distribution. T.n.napuF.Cuvier,1822—SMyanmar,Thai/MalayPeninsula,islandsoffWMalayPeninsula(Langkawi&Pangkor),Borneo,SSumatra,BangkaI,islandsoffBorneo(Laut&Serasan). T.n.bangue:Chasen&Kloss,1931—BanggiIandBalembanganI,offNBorneo. T.n.bunguranensisMiller,1901—NatunaIs(=Bunguran),oftWBorneo. T.n.neubronneriSody,1931—NSumatra. T.n.nmiasisLyon,1916—NiasI,offWSumatra. T.n.rufulusMiller,1900—TiomanI,offEMalayPeninsula,RiauandLinggaArchipelagos. T. n. terutus Thomas & Wroughton, 1909 — Terutau I, off W Malay Peninsula. The species was recently reconfirmed for Singapore. Maps that include Vietnam, Cambodia, and Laos in the distribution range are based on the earlier assumption that 7. versicolor was a subspecies of 1. napu. Subsequent studies have indicated that 7. versicolor is a distinct species, and that the range of 1. napu therefore does not extend into Cambodia, Laos, and Vietnam. The northern limit on the Thai-Malay peninsula is not well defined. Specimens of 1. napu have been collected from as far north as Bankachon in southern Myanmar (10° 08" N), but despite fairly intensive camera-trapping in Kui Buri National Park, Thailand (12° N), 7. napu has not been photographed there. At the northern margin ofits range, it is generally rare. It has been reported, for example, that during the flooding of the Chiew Larn Reservoir (Surat Thani Province; about 9° N, 98° 45' E), only six 7. napu were rescued compared with 172 71. kanchil. This area is the transition zone from wetter evergreen forest to drier deciduous types, and it might be that 7° napu is not well adapted to the drier forest types towards the northern limit ofits range. There are unconfirmed reports of the species on Java, where it may have been confused with one of the two color morphs of 7. javanicus. As explained in the Taxonomy section, the subspecific status of the populations of several islands remains unclear.
FIGURE 11. Type localities for new species. A. P in Two new species of Pyrgulopsis Call & Pilsbry, 1886 (Mollusca: Caenogastropoda: Hydrobiidae) from springs in the Rio Grande watershed in Texas
FIGURE 11. Type localities for new species. A. P. harrymilleri sp. nov., Vasquez Spring, Presidio Co., TX. Photo by B. Schwartz. B. P. rubra sp. nov., Palo Amarillo Springs, Presidio Co., TX. Photo by K. Perez.
FIGURE 1. Cremastra saprophytica from the type locality. A–C. Flowering plant. D. Flower, dorsal view. E. Flower, lateral view. F in Cremastra saprophytica (Orchidaceae: Epidendroideae), a new leafless autonomously self-pollinating orchid species from Gifu Prefecture, Japan
FIGURE 1. Cremastra saprophytica from the type locality. A–C. Flowering plant. D. Flower, dorsal view. E. Flower, lateral view. F. Flower, front view. Central arrow points to a small smooth callus of lip positioned at the base of midlobe, whereas the other arrows point to the inconspicuous lateral lobes. G. Fruiting plants. H. Fruiting body of Coprinellus disseminates, one of the associated fungi of C. saprophytica.
FIGURE. Euphorbia agatheae in the type locality (Ifaty, north of Toliary). A. habit; B. detail of the bark. Credits: T.Haevermans (A and B). in Taxonomic changes and new species in Malagasy Euphorbia (Euphorbiaceae)
FIGURE. Euphorbia agatheae in the type locality (Ifaty, north of Toliary). A. habit; B. detail of the bark. Credits: T.Haevermans (A and B).
Figure 5 in A new species of Paratrigona Schwarz, 1938 from northeastern Brazil, with notes on the type material of Melipona lineata Lepeletier, 1836 (Hymenoptera: Anthophila: Apidae)
Figure 5. Specimen of Paratrigona lineata (Lepeletier, 1836) from Januária (Minas Gerais State, Brazil), deposited at the BIOSIS, Institute of Biology, Federal University of Bahia, Brazil: (a). Frontal view of head; (b). Lateral view of body; (c). Dorsolateral view of mesosoma; (d). Labels. Arrows indicates presence of setae.
Figure 6 in A new species of Paratrigona Schwarz, 1938 from northeastern Brazil, with notes on the type material of Melipona lineata Lepeletier, 1836 (Hymenoptera: Anthophila: Apidae)
Figure 6. Paratype of Paratrigona lineata glabella Camargo & Moure, 1994, deposited at the Prof. J.M.F. Camargo Collection from the RPSP, University of São Paulo, Ribeirão Preto, Brazil: (a). Frontal view of head; (b). Lateral view of body; (c). Lateral view of mesepisternum; (d). Dorsal view of mesoscutellum; (e). Dorsal view of mesosoma; (f). Labels. Arrows indicate absence or presence of setae. Ownership rights to these images and their copyright belong to RPSP (Coleção Entomológica 'Prof. J.M.F. Camargo'). Photo by E.A.B. Almeida.
Figure 7 in A new species of Paratrigona Schwarz, 1938 from northeastern Brazil, with notes on the type material of Melipona lineata Lepeletier, 1836 (Hymenoptera: Anthophila: Apidae)
Figure 7. Holotype of Paratrigona incerta Camargo & Moure, 1994, deposited at the Prof. J.M.F. Camargo Collection from the RPSP, University of São Paulo, Ribeirão Preto, Brazil: (a). Frontal view of head; (b). Lateral view of body; (c). Lateral view of mesepisternum; (d). Dorsal view of mesosoma; (e). Labels. Arrows indicate presence or absence of setae. Ownership rights to these images and their copyright belong to RPSP (Coleção Entomológica 'Prof. J.M.F. Camargo'). Photo by E.A.B. Almeida.
Figure 3 in A new species of Paratrigona Schwarz, 1938 from northeastern Brazil, with notes on the type material of Melipona lineata Lepeletier, 1836 (Hymenoptera: Anthophila: Apidae)
Figure 3. Lectotype of Melipona lineata Lepeletier, 1836 deposited at the MNHP, Paris, France: (a). Frontal view of head; (b). Lateral view of body; (c, d). Dorsolateral view of mesoscutum and mesoscutellum; (e). Metatibia; (f). Labels of lectotype. Arrows indicate presence of setae.
Figure 4 in A new species of Paratrigona Schwarz, 1938 from northeastern Brazil, with notes on the type material of Melipona lineata Lepeletier, 1836 (Hymenoptera: Anthophila: Apidae)
Figure 4. Paralectotype of Melipona lineata Lepeletier, 1836 deposited at the MNHP, Paris, France: (a). Frontal view of head; (b). Lateral view of head; (c). Lateral view of body; (d). Dorsolateral view of mesosoma; (e). Metatibia; (f). Labels of paralectotype. Arrows indicate absence of setae.
Figure 1 in A new species of Paratrigona Schwarz, 1938 from northeastern Brazil, with notes on the type material of Melipona lineata Lepeletier, 1836 (Hymenoptera: Anthophila: Apidae)
Figure 1. Holotype female (worker) of Paratrigona intermedia Oliveira, Madella-Auricchio & Freitas sp. nov., deposited at the MHNBA, Salvador, Bahia State, Brazil: (a). Frontal view of head; (b). Lateral view of body; (c). Mesepisternum in profile, and iridescence on wing; (d). Dorsolateral view of mesoscutum and mesoscutellum. Arrows indicate presence or absence of setae.
Figure 2 in A new species of Paratrigona Schwarz, 1938 from northeastern Brazil, with notes on the type material of Melipona lineata Lepeletier, 1836 (Hymenoptera: Anthophila: Apidae)
Figure 2. Holotype female of Paratrigona intermedia Oliveira, Madella-Auricchio & Freitas sp. nov., deposited at the MHNBA, Salvador, Bahia State, Brazil: (a). Mesepisternum in profile; (b). Metatibia; (c). Labels. Arrow indicates whitish setae/pilosity.
FIGURE. SEM micrographs of pollen grain of Ephedra aurea (A) from type material (CAT!) and E. nebrodensis (B) from Monte Cuccio, Sicily (CAT!):. Equatorial view (x 2500).. Polar view (x 3000). in Ephedra aurea (Ephedraceae), a new species from Sicily
FIGURE. SEM micrographs of pollen grain of Ephedra aurea (A) from type material (CAT!) and E. nebrodensis (B) from Monte Cuccio, Sicily (CAT!):. Equatorial view (x 2500).. Polar view (x 3000).
FIGURE. SEM micrographs of the seed coats of Ephedra aurea (A) and E. nebrodensis (B):. Seed at low magnification (× 15).. Seed at medium magnification (× 50).. Seed at high magnification (× 300). A. from type material (CAT!) and B. from Sardinia. in Ephedra aurea (Ephedraceae), a new species from Sicily
FIGURE. SEM micrographs of the seed coats of Ephedra aurea (A) and E. nebrodensis (B):. Seed at low magnification (× 15).. Seed at medium magnification (× 50).. Seed at high magnification (× 300). A. from type material (CAT!) and B. from Sardinia.
FIGURE 5 in Type studies on two Paxillus species (Paxillaceae, Boletales) described from China
FIGURE 5. Microscopic features of Tricholompsis yunnanensis (KUN-HKAS 93555). a. Basidiospores; b. Basidia; c. Cheilocystidia; d. Pleurocystidia; e. Pileipellis. Scale bars = 10 μm. Drawings by: Li-Rong Liu.
FIGURE 3 in Type studies on two Paxillus species (Paxillaceae, Boletales) described from China
FIGURE 3. Photos of the collections. a-c. Boletinellus rhytidophyllus (KUN-HKAS 113221, photos by Liu-Kun Jia); d-f. Tricholomopsis yunnanensis (d. KUN-HKAS 80034, photo by Zhu L. Yang; e. KUN-HKAS 48887, photo by Jun-Feng Liang; f. KUN-HKAS 93555, photo by Rui Zhang).
FIGURE 4 in Type studies on two Paxillus species (Paxillaceae, Boletales) described from China
FIGURE 4. Microscopic features of B. rhytidophyllus (KUN-HKAS 113221). a. Basidiospores; b. Basidia and pleurocystidium; c. Cheilocystidia; d. Pleurocystidia; e. Pileipellis. Scale bars = 10 μm. Drawings by: Li-Rong Liu.
FIGURE 2. Maximum likelihood phylogenetic tree generated from a in Type studies on two Paxillus species (Paxillaceae, Boletales) described from China
FIGURE 2. Maximum likelihood phylogenetic tree generated from a three-locus (nrLSU, ITS, and tef1-α) dataset of the Tricholomopsis species. ML bootstrap (BS>50%) are shown above the branches. Voucher specimens and localities where the specimens were collected are provided. The new combination is in bold.
FIGURE 1. Maximum likelihood phylogenetic tree generated from a in Type studies on two Paxillus species (Paxillaceae, Boletales) described from China
FIGURE 1. Maximum likelihood phylogenetic tree generated from a three-locus (nrLSU, ITS, and tef1-α) dataset of the Boletinellus species. ML bootstrap (BS>50 %) are indicated above the branches. Voucher specimens and localities where the specimens were collected are provided. The new combination is in bold.
FIGURES 1–5 in Synopsis of the Japanese species of Aleocharinae (Coleoptera: Staphylinidae), with review of the type specimens II. Genus Myllaena Erichson of tribe Myllaenini with redescription of four Japanese species
FIGURES 1–5 Habitus of Myllaena spp., 1, Lectotype of M. japonica Sharp, 1888; 2, Holotype of M. torrentum Cameron, 1933; 3, Lectotype of M. rufotestacea Cameron, 1933; 4, Lectotype of M. lewisi Cameron, 1933; 5, M. japonica Sharp, 1888 (Shizuoka). Scale bars: 1.0 mm.
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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.