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1,037 results for “newly recorded”
FIGURE 3 in Typification of two newly recorded species of Ampelocissus (Vitaceae) for Thailand
FIGURE 3. Lectotype of Ampelocissus rugosa (Wall. ex Roxb.) Planch. © The Board of Trustees of the Royal Botanic Gardens, Kew. Reproduced with the consent of the Royal Botanic Gardens, Kew.
FIGURE 1 in Typification of two newly recorded species of Ampelocissus (Vitaceae) for Thailand
FIGURE 1. Neotype of Ampelocissus araneosa (Dalz.) Planch. ex Gamble. © The Board of Trustees of the Royal Botanic Gardens, Kew. Reproduced with the consent of the Royal Botanic Gardens, Kew.
FIGURE 2 in Typification of two newly recorded species of Ampelocissus (Vitaceae) for Thailand
FIGURE 2. Distribution map of A. araneosa (black circle) and A. rugosa (black triangle) in Thailand based on specimen data.
FIGURE 4 in Cystoderma carpaticum (Basidiomycota, Agaricales), a rare fungus newly recorded from Croatia
FIGURE 4. Cystoderma carpaticum: A. pileipellis (CNF 1/7034), B–C. basidia (under PhC) (CNF 1/6652), D. basidiospores (under PhC) (CNF 1/6652). Scale bars A = 20 μm, B–C = 5 μm (in C), D = 5 μm. Photos by Z. Tkalčec.
FIGURE 3 in Cystoderma carpaticum (Basidiomycota, Agaricales), a rare fungus newly recorded from Croatia
FIGURE 3. Cystoderma carpaticum. Fresh basidiomes: A = CNF 1/6652, B = CNF 1/7034. Scale bars 10 mm. Photos by M. Čerkez (A), A. Mešić & Z. Tkalčec (B).
FIGURE 2 in Cystoderma carpaticum (Basidiomycota, Agaricales), a rare fungus newly recorded from Croatia
FIGURE 2. Phylogenetic placement of Cystoderma carpaticum based on ITS sequence data and inferred by MP analysis. Bootstrap support ≥70% and the posterior probabilities ≥95% are shown above and below the branches (bs/pp), respectively.
FIGURE 1 in Cystoderma carpaticum (Basidiomycota, Agaricales), a rare fungus newly recorded from Croatia
FIGURE 1. Phylogenetic placement of Cystoderma carpaticum based on LSU sequence data and inferred by MP analysis. Bootstrap support ≥70% and the posterior probabilities ≥95% are shown above and below the branches (bs/pp), respectively.
FIGURE 4 in Impatiens occultans (Balsaminaceae), a newly recorded species from Xizang, China, and its phylogenetic position
FIGURE 4. Bayesian consensus phylogram based on the branch length of the combined data. Numbers above and below branches are Bayesian posterior probabilities (> 0.5) and bootstrap percentages (> 50%), respectively. "-" indicates nodes not supported.
FIGURE 3. Pollen micromorphology under SEM. A–C in Impatiens occultans (Balsaminaceae), a newly recorded species from Xizang, China, and its phylogenetic position
FIGURE 3. Pollen micromorphology under SEM. A–C: Impatiens occultans. A. polar view; B. equatorial view; C. partial view. D–F: I. tuberculata. D. polar view; E. equatorial view; F. partial view. (Voucher specimen of I. occultans, Lai Wei & Jia-Chen Hao 15397, deposited in PE; I. tuberculata, S. X. Yu 4036, deposited in PE).
FIGURE 2. Impatiens occultans A in Impatiens occultans (Balsaminaceae), a newly recorded species from Xizang, China, and its phylogenetic position
FIGURE 2. Impatiens occultans A. flower (front view); B. flower (lateral view); C. habitat; D. habit (photographed by Lai Wei, Jiachen Hao and Yufen Du).
FIGURE 1. Impatiens occultans A in Impatiens occultans (Balsaminaceae), a newly recorded species from Xizang, China, and its phylogenetic position
FIGURE 1. Impatiens occultans A. habit; B. flower (lateral view); C. flower (front view); D. upper lateral sepal; E. lower lateral sepal; F. lower sepal; G. lateral united petals; G1. upper petal; G2. lower petal; H. dorsal petal. (All from Lai wei & Jia-Chen Hao 15397 (PE) and drawn by Yun-Xi Zhu).
FIGURE 4 in Tricholosporum, a newly recorded genus of Agaricomycetes in China
FIGURE 4. Scanning electron microscope illustrations of basidia and basidiospores of Tricholosporum porphyrophyllum. Photos by Zhang Ailing.
FIGURE 2 in Tricholosporum, a newly recorded genus of Agaricomycetes in China
FIGURE 2. The taxonomic position of Tricholosporum porphyrophyllum and other similar genera in the Tricholomataceae based on nlsu rDNA phylogeny by using Bayesian algorithm (BA). (The nlsu sequence fragment of T. porphyrophyllum was submitted to GenBank (accession No. KU954556, KU954558.))
FIGURE 3 in Tricholosporum, a newly recorded genus of Agaricomycetes in China
FIGURE 3. The taxonomic position of Tricholosporum porphyrophyllum and other similar genera in the Tricholomataceae based on rpb2 phylogeny by using Bayesian algorithm (BA). (The rpb2 sequence fragment of T. porphyrophyllum was submitted to GenBank (accession No.KX397356, KX397357))
FIGURE 6 in Tricholosporum, a newly recorded genus of Agaricomycetes in China
FIGURE 6. Features of Tricholosporum porphyrophyllum (A basidiospores, bar=5μm; B basidia, bar =10μm).
FIGURE 1 in Tricholosporum, a newly recorded genus of Agaricomycetes in China
FIGURE 1. The taxonomic position of Tricholosporum porphyrophyllum and other similar genera in the Tricholomataceae based on ITS rDNA phylogeny by using Bayesian algorithm (BA). (The ITS sequence fragment of T. porphyrophyllum was submitted to GenBank (accession No. KU954553, KU954554.))
FIGURE 2 in Stillingia: A newly recorded genus of Euphorbiaceae from China
FIGURE 2. Strict consensus of 72 equally most parsimonious trees based on parsimony analysis of the combined matrix of trnL-F and rbcL sequences. The shortest trees had a length of 441 steps, CI =0.787 and RI =0.665. Numbers above the branches are maximum parsimony bootstrap percentages from a bootstrap test of 1000 runs.
FIGURE 1. Stillingia lineata subsp. pacifica. A in Stillingia: A newly recorded genus of Euphorbiaceae from China
FIGURE 1. Stillingia lineata subsp. pacifica. A, Habitat; B, Male flowers; C, Female flowers; D, Fruits with carpidiophore; E–H, Four different inflorescences (E, Androgynous inflorescence with female flowers on the lower part; F, Male inflorescence; G, Androgynous inflorescence with female flowers on both lower and upper part; H, Female inflorescence); I, Pollen in polar view; J, Pollen in equatorial view; K, Exine ornamentation at mesocolpium in polar view; L, Pollen in equatorial view, showing aperture. Voucher specimens: X.X. Huang 18376 (IBSC). Scale bar = 10 μm (I, J, L), 2 μm (K). Photo credits: A–H by X.X. Huang; I–L by S.C. Li.
FIGURE 5 in Evaluating the occurrence and conservation statuses of Sri Lankan Orchids (Orchidaceae): Observations on newly recorded species and undocumented regions
FIGURE 5. (A). Habenaria pterocarpa (B). Ipsea speciosa (C). Liparis elliptica (D). Liparis brachyglottis (E). Podochilus warnagalensis (F). Zeuxine reginasilvae.
FIGURE 4 in Evaluating the occurrence and conservation statuses of Sri Lankan Orchids (Orchidaceae): Observations on newly recorded species and undocumented regions
FIGURE 4. (A). Acanthephippium bicolor (B). Aerangis hologlottis (C). Anoectochilus regalis (D). Arundina minor (E). Didymoplexis pallens (F). Habenaria dolichostachya.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.