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Figure 2 from: Mazebedi R, Hesselberg T (2020) A preliminary survey of the abundance, diversity and distribution of terrestrial macroinvertebrates of Gcwihaba cave, northwest Botswana. Subterranean Biology 35: 49-63. https://doi.org/10.3897/subtbiol.35.51445
Figure 2 The plan view of Gcwihaba cave (also known as Drotsky's cave) showing its chambers, the approximate position of cave sites surveyed for this study and other internal features (Modified from Dandurand et al. 2019, with permission from Gregory Dandurand).
Supplementary material 2 from: Dai J-H, Zhou Q-J, Zhou R-C, Liu Y (2020) A new species of Bredia (Sonerileae, Melastomataceae) from Sichuan, China. PhytoKeys 152: 1-14. https://doi.org/10.3897/phytokeys.152.53512
Table S2. Summary statistics of sequences used for phylogenetic analyses
Supplementary material 3 from: Dai J-H, Zhou Q-J, Zhou R-C, Liu Y (2020) A new species of Bredia (Sonerileae, Melastomataceae) from Sichuan, China. PhytoKeys 152: 1-14. https://doi.org/10.3897/phytokeys.152.53512
Table S3. Pairwise genetic distances among species of Bredia at the nrITS region
Figure 4 from: Dai J-H, Zhou Q-J, Zhou R-C, Liu Y (2020) A new species of Bredia (Sonerileae, Melastomataceae) from Sichuan, China. PhytoKeys 152: 1-14. https://doi.org/10.3897/phytokeys.152.53512
Figure 4 Three prostrate species of Bredia. AB. guidongensis from Y. Liu 472 (SYS) BB. changii from Y. Liu 548 (SYS) CB. repens Y. Liu 558 (A, PE, SYS).
Figure 3 from: Dai J-H, Zhou Q-J, Zhou R-C, Liu Y (2020) A new species of Bredia (Sonerileae, Melastomataceae) from Sichuan, China. PhytoKeys 152: 1-14. https://doi.org/10.3897/phytokeys.152.53512
Figure 3 Floral details and young fruit of Bredia hispida. A Side view of a flower B top view of a flower C longitudinal section of a flower showing isomorphic stamens and ovary crown D top view of a young fruit E side view of a young fruit showing enlarged ovary crown exserted from hypanthium. Scale bar: 5 mm (C). All from Y. Liu 764 (A, PE, SYS).
Figure 1 from: Dai J-H, Zhou Q-J, Zhou R-C, Liu Y (2020) A new species of Bredia (Sonerileae, Melastomataceae) from Sichuan, China. PhytoKeys 152: 1-14. https://doi.org/10.3897/phytokeys.152.53512
Figure 1 Herbarium specimen of Bredia hispida (A–C) and Phyllagathis deltoidea (D–F). A–C W. B. Ju and H. N. Deng, HGX12702 (CDBI) collected from Shui-wei town, Xuyong County, Sichuan, China, showing the stout long bristles on adaxial surface of the leaf blade and linear-lanceolate calyx lobes, images from National Plant Specimen Resource Center D–F H. H. Su 68119 (IBK, IBSC) collected from Aidian, Ningming County, Guangxi, China, holotype (IBSC) (D, F) and isotype (IBK) (E) of Phyllagathis deltoidea.
Figure 2 from: Dai J-H, Zhou Q-J, Zhou R-C, Liu Y (2020) A new species of Bredia (Sonerileae, Melastomataceae) from Sichuan, China. PhytoKeys 152: 1-14. https://doi.org/10.3897/phytokeys.152.53512
Figure 2 Bredia hispida. A Habitat B a flowering branch, showing the prostrate habit C adaxial leaf surface D abaxial leaf surface E lateral view of leaf, showing the stout long bristles F terminal inflorescence G axillary inflorescences on old branchlets. All from Y. Liu 764 (A, PE, SYS).
Figure 5 from: Dai J-H, Zhou Q-J, Zhou R-C, Liu Y (2020) A new species of Bredia (Sonerileae, Melastomataceae) from Sichuan, China. PhytoKeys 152: 1-14. https://doi.org/10.3897/phytokeys.152.53512
Figure 5 Phylogenetic position of Bredia hispida. Maximum likelihood (ML) phylogenetic tree based on nrITS sequence data. Numbers above branches are bootstrap values obtained from maximum likelihood analyses, and those below branches are Bayesian posterior probabilities (right) and bootstrap values (left) resulting from maximum parsimony analyses. The new species is noted in bold. Asterisk denotes a branch collapsed in Bayesian inference or maximum parsimony analyses.
Supplementary material 1 from: Dai J-H, Zhou Q-J, Zhou R-C, Liu Y (2020) A new species of Bredia (Sonerileae, Melastomataceae) from Sichuan, China. PhytoKeys 152: 1-14. https://doi.org/10.3897/phytokeys.152.53512
Table S1. Source of materials studied and GenBank accession numbers for nrITS
Figure 9 from: Li X, Maria M, Cai R, Barsalote EM, Peneva V, Zheng J (2020) Distribution of trichodorid species in mainland China with description of Trichodorus hangzhouensis sp. nov. (Nematoda, Triplonchida). ZooKeys 945: 163-189. https://doi.org/10.3897/zookeys.945.50424
Figure 9 Phylogenetic relationships of Trichodorus hangzhouensis sp. nov. and other trichodorid nematodes based on ITS2 sequences. The Bayesian tree was inferred under the general time-reversible model of sequence evolution with correction for invariable sites and a gamma-shaped distribution (GTR+I+G). Thoracostoma trachyga served as an outgroup species. Posterior probability values exceeding 70% are given on appropriate clades.
Figure 8 from: Li X, Maria M, Cai R, Barsalote EM, Peneva V, Zheng J (2020) Distribution of trichodorid species in mainland China with description of Trichodorus hangzhouensis sp. nov. (Nematoda, Triplonchida). ZooKeys 945: 163-189. https://doi.org/10.3897/zookeys.945.50424
Figure 8 Phylogenetic relationships of Trichodorus hangzhouensis sp. nov. and other trichodorid species based on D2-D3 28S rRNA gene sequences. The Bayesian tree was inferred under the general time-reversible model of sequence evolution with correction for invariable sites and a gamma-shaped distribution (GTR+I+G). Tripylina tamaki served as an outgroup species. Posterior probability values exceeding 70% are given on appropriate clades.
Figure 6 from: Li X, Maria M, Cai R, Barsalote EM, Peneva V, Zheng J (2020) Distribution of trichodorid species in mainland China with description of Trichodorus hangzhouensis sp. nov. (Nematoda, Triplonchida). ZooKeys 945: 163-189. https://doi.org/10.3897/zookeys.945.50424
Figure 6 Photomicrographs of Trichodorus species, Males A–CT. nanjingensis Liu & Cheng, 1990 D–FT. pakistanensis Siddiqi, 1962 G–IT. cedarus. Scale bars: 20 μm (A–I).
Supplementary material 1 from: Li X, Maria M, Cai R, Barsalote EM, Peneva V, Zheng J (2020) Distribution of trichodorid species in mainland China with description of Trichodorus hangzhouensis sp. nov. (Nematoda, Triplonchida). ZooKeys 945: 163-189. https://doi.org/10.3897/zookeys.945.50424
Table S1. Sequences of nematode species used for the phylogenetic analyses
Figure 5 from: Li X, Maria M, Cai R, Barsalote EM, Peneva V, Zheng J (2020) Distribution of trichodorid species in mainland China with description of Trichodorus hangzhouensis sp. nov. (Nematoda, Triplonchida). ZooKeys 945: 163-189. https://doi.org/10.3897/zookeys.945.50424
Figure 5 Photomicrographs of females of Trichodorus, Paratrichodorus and Nanidorus species A–CT. nanjingensis Liu & Cheng, 1990 D–FT. pakistanensis Siddiqi, 1962 G–IT. cedarus Yokoo, 1964 J–LP. porosusM–ON. renifer Siddiqi, 1974 P–RN. minor (Colbran, 1956). Scale bars: 20 μm (A–R).
Figure 7 from: Li X, Maria M, Cai R, Barsalote EM, Peneva V, Zheng J (2020) Distribution of trichodorid species in mainland China with description of Trichodorus hangzhouensis sp. nov. (Nematoda, Triplonchida). ZooKeys 945: 163-189. https://doi.org/10.3897/zookeys.945.50424
Figure 7 Phylogenetic relationships of Trichodorus hangzhouensis sp. nov. and other trichodorid species based on partial 18S rRNA gene sequences. The Bayesian tree was inferred under the general time-reversible model of sequence evolution with correction for invariable sites and a gamma-shaped distribution (GTR+I+G). Tripyla sp. served as an outgroup species. Posterior probability values exceeding 70% are given on appropriate clades.
Figure 3 from: Li X, Maria M, Cai R, Barsalote EM, Peneva V, Zheng J (2020) Distribution of trichodorid species in mainland China with description of Trichodorus hangzhouensis sp. nov. (Nematoda, Triplonchida). ZooKeys 945: 163-189. https://doi.org/10.3897/zookeys.945.50424
Figure 3 Light photomicrographs of Trichodorus hangzhouensis sp. nov., paratypes A female entire body, arrow points vulva B male entire body C, D anterior region of female E pharyngeal region of male, arrows pointing position of cervical papillae (CP) and excretory pore (exp) F, G vulval region H, I female tail, arrows pointing position of anus (a) J–L male tail, arrows pointing position of male tail supplements (SP). Scale bars: 100 μm (A, B) 20 μm (C–L).
Figure 4 from: Li X, Maria M, Cai R, Barsalote EM, Peneva V, Zheng J (2020) Distribution of trichodorid species in mainland China with description of Trichodorus hangzhouensis sp. nov. (Nematoda, Triplonchida). ZooKeys 945: 163-189. https://doi.org/10.3897/zookeys.945.50424
Figure 4 Distribution map of trichodorid species in China (stars indicate the occurrence of trichodorid taxa).
Supplementary material 4 from: Wu Y-A, Gao J-W, Cheng X-F, Xie M, Yuan X-P, Liu D, Song R (2020) Characterization and comparative analysis of the complete mitochondrial genome of Azygia hwangtsiyui Tsin, 1933 (Digenea), the first for a member of the family Azygiidae. ZooKeys 945: 1-16. https://doi.org/10.3897/zookeys.945.49681
Figure S1
Supplementary material 1 from: Wu Y-A, Gao J-W, Cheng X-F, Xie M, Yuan X-P, Liu D, Song R (2020) Characterization and comparative analysis of the complete mitochondrial genome of Azygia hwangtsiyui Tsin, 1933 (Digenea), the first for a member of the family Azygiidae. ZooKeys 945: 1-16. https://doi.org/10.3897/zookeys.945.49681
Table S1
Figure 2 from: Li X, Maria M, Cai R, Barsalote EM, Peneva V, Zheng J (2020) Distribution of trichodorid species in mainland China with description of Trichodorus hangzhouensis sp. nov. (Nematoda, Triplonchida). ZooKeys 945: 163-189. https://doi.org/10.3897/zookeys.945.50424
Figure 2 Line drawings of Trichodorus hangzhouensis sp. nov., paratypes, Female A entire body B, C pharyngeal region D genital branches E–G vulval region, lateral view H vulva, ventral view I anterior genital branch J copulatory plugs K, L posterior ends. Scale bars: 50 μm.
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)
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.