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zenodo28/100

Figure 1 from: Sgorbati S, D'Antraccoli M, Citterio S, Gentili R, Peruzzi L (2018) Was Charles Darwin right in his explanation of the 'abominable mystery'? Italian Botanist 5: 25-30. https://doi.org/10.3897/italianbotanist.5.24699

Figure 1 - Worldwide maximum concentration of early branching families. Red cells highlight the worldwide highest concentration (15/26, about 60%) of 'Archaeangiospermae' sensu Stuessy (2010). Cells in different tones of green highlight three families ( Amborellaceae , Austrobaileyaceae , Degeneriaceae ) endemic to New Caledonia, NE Australia, and Fiji, respectively. Zealandia continent (yellow dashed line) is drawn according to Mortimer et al. (2017). The distribution of Archaeangiosperm families was obtained from Angiosperm Phylogeny Website (Stevens 2001 onwards), then georeferenced and superimposed through raster analyses in GIS environment, by means of R software (R Core Team 2017).

opencc-by-4.0Mar 2018View details →
zenodo28/100

Figure 8 from: Dai D-Q, Wijayawardene NN, Tang L-Z, Liu C, Han L-H, Chu H-L, Wang H-B, Liao C-F, Yang E-F, Xu R-F, Li Y-M, Hyde KD, Bhat DJ, Cannon PF (2019) Rubroshiraia gen. nov., a second hypocrellin-producing genus in Shiraiaceae (Pleosporales). MycoKeys 58: 1-26. https://doi.org/10.3897/mycokeys.58.36723

Figure 8 Hypocrella bambusae (K(M)52469, isotype, images are accredited to the Royal Botanic Gardens, Kew) A, C fruiting bodies on inflorescence of bamboo B vertical section of stromata showing the perithecia locating D herbarium envelope E filiform ascospores F asci with caps (Staining by cotton blue). Scale bars: 5 mm (A), 200 μm (B), 2 mm (C), 20 μm (E, F).

opencc-by-4.0Oct 2019View details →
zenodo28/100

Figure 7 from: Dai D-Q, Wijayawardene NN, Tang L-Z, Liu C, Han L-H, Chu H-L, Wang H-B, Liao C-F, Yang E-F, Xu R-F, Li Y-M, Hyde KD, Bhat DJ, Cannon PF (2019) Rubroshiraia gen. nov., a second hypocrellin-producing genus in Shiraiaceae (Pleosporales). MycoKeys 58: 1-26. https://doi.org/10.3897/mycokeys.58.36723

Figure 7 Rubroshiraia bambusae (HKAS102255, holotype) A fruiting bodies B, C surface of ascostromata showing the openings of ostiole D vertical section of ascostromata E, F vertical section of locule G peridium of locule H asci and pseudoparaphyses I asci and asci ocular chamber J ascospores K, L immature asci. Scale bars: 1 cm (A), 25 mm (B), 2 mm (C, D), 500 μm (E, F), 200 μm (G), 50 μm (H–L).

opencc-by-4.0Oct 2019View details →
zenodo28/100

Figure 5 from: Dai D-Q, Wijayawardene NN, Tang L-Z, Liu C, Han L-H, Chu H-L, Wang H-B, Liao C-F, Yang E-F, Xu R-F, Li Y-M, Hyde KD, Bhat DJ, Cannon PF (2019) Rubroshiraia gen. nov., a second hypocrellin-producing genus in Shiraiaceae (Pleosporales). MycoKeys 58: 1-26. https://doi.org/10.3897/mycokeys.58.36723

Figure 5 The UV spectrum of the standards and of hypocrellin A and B from the samples (Shiraia bambusicolaHKAS 102253 and Rubroshiraia bambusaeHKAS 102255) were recorded in alcohol at room temperature. HA: hypocrellin A, HB: hypocrellin B.

opencc-by-4.0Oct 2019View details →
zenodo28/100

Figure 6 from: Dai D-Q, Wijayawardene NN, Tang L-Z, Liu C, Han L-H, Chu H-L, Wang H-B, Liao C-F, Yang E-F, Xu R-F, Li Y-M, Hyde KD, Bhat DJ, Cannon PF (2019) Rubroshiraia gen. nov., a second hypocrellin-producing genus in Shiraiaceae (Pleosporales). MycoKeys 58: 1-26. https://doi.org/10.3897/mycokeys.58.36723

Figure 6 Shiraia bambusicolaA–J sexual morph A fruiting bodies (HKAS102253, HKAS102254, HKAS102257, HKAS102261, HKAS102262) B–J photographs from material HKAS102253 B Surface of ascostromata showing the dark openings of ostiole C vertical section of ascostromata D vertical section of locule E pseudoparaphyses F, G asci (G Showing the fissitunicate asci) H–J ascospores K–M asexual morph K vertical section of asexual locules L–M conidia. Scale bars: 2 cm (A), 5 mm (B), 1 mm (C), 100 μm (D, K), 50 μm (F, G), 20 μm (H–J, L, M).

opencc-by-4.0Oct 2019View details →
zenodo28/100

Figure 4 from: Dai D-Q, Wijayawardene NN, Tang L-Z, Liu C, Han L-H, Chu H-L, Wang H-B, Liao C-F, Yang E-F, Xu R-F, Li Y-M, Hyde KD, Bhat DJ, Cannon PF (2019) Rubroshiraia gen. nov., a second hypocrellin-producing genus in Shiraiaceae (Pleosporales). MycoKeys 58: 1-26. https://doi.org/10.3897/mycokeys.58.36723

Figure 4 Hypocrellin A and hypocrellin B HPLC-UV profiles (265 nm) of standards and stromatal HPLC-UV profiles (265 nm) of specimens of Shiraia bambusicola (HKAS 102253) (II) and Rubroshiraia bambusae (HKAS 102255) (III) and DAD spectra of major metabolites.

opencc-by-4.0Oct 2019View details →
zenodo28/100

Figure 3 from: Dai D-Q, Wijayawardene NN, Tang L-Z, Liu C, Han L-H, Chu H-L, Wang H-B, Liao C-F, Yang E-F, Xu R-F, Li Y-M, Hyde KD, Bhat DJ, Cannon PF (2019) Rubroshiraia gen. nov., a second hypocrellin-producing genus in Shiraiaceae (Pleosporales). MycoKeys 58: 1-26. https://doi.org/10.3897/mycokeys.58.36723

Figure 3 Maximum likelihood phylogenetic tree generated from RAxML (GTR+G model), based on combined LSU and ITS sequences data. ML and MP values (MLBP/MPBP) (> 50%), resulting from 1000 bootstrap replicates, are given at the nodes. The original isolate numbers' codes are noted after the species names. The tree is rooted to Pleospora herbarum (CBS 191.86). Ex-type or ex-epitype strains are in bold. Newly generated strains are in red.

opencc-by-4.0Oct 2019View details →
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Figure 2 from: Dai D-Q, Wijayawardene NN, Tang L-Z, Liu C, Han L-H, Chu H-L, Wang H-B, Liao C-F, Yang E-F, Xu R-F, Li Y-M, Hyde KD, Bhat DJ, Cannon PF (2019) Rubroshiraia gen. nov., a second hypocrellin-producing genus in Shiraiaceae (Pleosporales). MycoKeys 58: 1-26. https://doi.org/10.3897/mycokeys.58.36723

Figure 2 Maximum likelihood phylogenetic tree generated from RAxML (GTR+G model), based on combined LSU, SSU, TEF1 and RPB2 sequences data. ML values (MLBP) (> 50%), resulting from 1000 bootstrap replicates and Bayesian posterior probabilities (BYPP) greater than 0.90, are given at the nodes. The original isolate numbers' codes are noted after the species names. The tree is rooted to Dothidea insculpta (CBS 189.58). Ex-type or ex-epitype strains are in bold. Newly generated strains are in red and the new genus is in yellow background.

opencc-by-4.0Oct 2019View details →
zenodo28/100

Figure 1 from: Cao H-F, Ya J-D, Zhang Q-R, Hu X-J, Zhang Z-R, Liu X-H, Zhang Y-C, Zhang A-T, Yu W-B (2019) Gentianella macrosperma, a new species of Gentianella (Gentianaceae) from Xinjiang, China. In: Cai J, Yu W-B, Zhang T, Li D-Z (Eds) Revealing of the plant diversity in China's biodiversity hotspots. PhytoKeys 130: 59-73. https://doi.org/10.3897/phytokeys.130.35476

Figure 1 The major-rule consensus tree of ML analysis based on the total dataset, including ITS and matK. ML bootstrap values and BI posterior probabilities are shown on branches.

opencc-by-4.0Oct 2019View details →
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Figure 3 from: Cao H-F, Ya J-D, Zhang Q-R, Hu X-J, Zhang Z-R, Liu X-H, Zhang Y-C, Zhang A-T, Yu W-B (2019) Gentianella macrosperma, a new species of Gentianella (Gentianaceae) from Xinjiang, China. In: Cai J, Yu W-B, Zhang T, Li D-Z (Eds) Revealing of the plant diversity in China's biodiversity hotspots. PhytoKeys 130: 59-73. https://doi.org/10.3897/phytokeys.130.35476

Figure 3 Gentianella macrosperma, sp. nov. A plant in nature habitat B flowers and inflorescence C flowers, showing pedicels and upper leaves D–E front view and side view of corolla, showing nectaries located close to the throat of the corolla tube F middle cauline leaf, abaxial view, showing veins G plants specimen (from KUN1443554) H opened corolla (5-merous) showing ovary I calyx J seed, front view (left and middle) and side view (right) (from S.L. Chen Tianyi281 (PE00029471)). I, H from the paratype J.D. Ya, Q.R. Zhang & X.J. Hu 17CS16327 (KUN1443565). Scale bars: 5 cm (A, G); 2 cm (B); 2 mm (C–E, I, H); 1 mm (J).

opencc-by-4.0Oct 2019View details →
zenodo28/100

Figure 2 from: Cao H-F, Ya J-D, Zhang Q-R, Hu X-J, Zhang Z-R, Liu X-H, Zhang Y-C, Zhang A-T, Yu W-B (2019) Gentianella macrosperma, a new species of Gentianella (Gentianaceae) from Xinjiang, China. In: Cai J, Yu W-B, Zhang T, Li D-Z (Eds) Revealing of the plant diversity in China's biodiversity hotspots. PhytoKeys 130: 59-73. https://doi.org/10.3897/phytokeys.130.35476

Figure 2 Gentianella macrosperma, sp. nov. A plant B flower, top views C–D show opened corollas, 4- and 5-merous, respectively E flower, showing the length of calyx and corolla subequal F calyx. showing 4-merous G calyx, showing 5-merous H capsule I seeds. Drawn by R.M. Zhang. H and I from the isotype S.L. Chen Tianyi281 (PE00029471), others from the paratype J.D. Ya, Q.R. Zhang & X.J. Hu 17CS16327 (KUN1443565). Scale bars: 2 cm (A); 5 mm (B); 2 mm (C–H); 0.5 mm (I).

opencc-by-4.0Oct 2019View details →
zenodo28/100

Figure 3 from: Fardiansah R, Dupérré N, Widyastuti R, Potapov A, Scheu S, Harms D (2018) Description of three new species of Aposphragisma Thoma, 2014 (Araneae: Oonopidae) from Sumatra, Indonesia. ZooKeys 797: 71-85. https://doi.org/10.3897/zookeys.797.29364

Figure 3 - Aposphragisma globosum sp. n., Male (A, B); Female (C). A, B palp prolateral view C female genitalia dorsal view Scale bar: 0.1mm (A).

opencc-by-4.0Nov 2018View details →
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Figure 8 from: Fardiansah R, Dupérré N, Widyastuti R, Potapov A, Scheu S, Harms D (2018) Description of three new species of Aposphragisma Thoma, 2014 (Araneae: Oonopidae) from Sumatra, Indonesia. ZooKeys 797: 71-85. https://doi.org/10.3897/zookeys.797.29364

Figure 8 - Aposphragisma sumatra sp. n., Male (A, B); Female (C, D). A, C abdomen lateral view B, D abdomen ventral view. Scale bar: 0.1mm (A–D).

opencc-by-4.0Nov 2018View details →
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Figure 5 from: Fardiansah R, Dupérré N, Widyastuti R, Potapov A, Scheu S, Harms D (2018) Description of three new species of Aposphragisma Thoma, 2014 (Araneae: Oonopidae) from Sumatra, Indonesia. ZooKeys 797: 71-85. https://doi.org/10.3897/zookeys.797.29364

Figure 5 - Aposphragisma jambi sp. n., Male (A, B); Female (C, D). A, C abdomen lateral view B, D abdomen ventral view. Scale bar: 0.1mm (A–D).

opencc-by-4.0Nov 2018View details →
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Figure 9 from: Fardiansah R, Dupérré N, Widyastuti R, Potapov A, Scheu S, Harms D (2018) Description of three new species of Aposphragisma Thoma, 2014 (Araneae: Oonopidae) from Sumatra, Indonesia. ZooKeys 797: 71-85. https://doi.org/10.3897/zookeys.797.29364

Figure 9 - Aposphragisma sumatra sp. n., Male (A, B); Female (C). A, B palp prolateral view C female genitalia dorsal view. Scale bar: 0.1mm (A).

opencc-by-4.0Nov 2018View details →
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Figure 4 from: Fardiansah R, Dupérré N, Widyastuti R, Potapov A, Scheu S, Harms D (2018) Description of three new species of Aposphragisma Thoma, 2014 (Araneae: Oonopidae) from Sumatra, Indonesia. ZooKeys 797: 71-85. https://doi.org/10.3897/zookeys.797.29364

Figure 4 - Aposphragisma jambi sp. n., Male (A, B, E, G); Female (C, D, F, H). A, C habitus dorsal view B, D habitus ventral view E, F prosoma ventral view G, H carapace lateral view. Scale bars: 0.5mm (A–D); 0.1mm (E–H).

opencc-by-4.0Nov 2018View details →
zenodo28/100

Figure 1 from: Fardiansah R, Dupérré N, Widyastuti R, Potapov A, Scheu S, Harms D (2018) Description of three new species of Aposphragisma Thoma, 2014 (Araneae: Oonopidae) from Sumatra, Indonesia. ZooKeys 797: 71-85. https://doi.org/10.3897/zookeys.797.29364

Figure 1 - Aposphragisma globosum sp. n., Male (A, B, E, G); Female (C, D, F, H). A, C habitus dorsal view B, D habitus ventral view E, F prosoma ventral view G, H carapace lateral view. Scale bars: 0.5mm (A–D); 0.1mm (E–H).

opencc-by-4.0Nov 2018View details →
zenodo28/100

Figure 5 from: Guerrero-Jiménez G, Vannucchi PE, Silva-Briano M, Adabache-Ortiz A, Rico-Martínez R, Roberts D, Neilson R, Elías-Gutiérrez M (2019) Brachionus paranguensis sp. nov. (Rotifera, Monogononta), a member of the L group of the Brachionus plicatilis complex. ZooKeys 880: 1-23. https://doi.org/10.3897/zookeys.880.28992

Figure 5 Types of eggs in B. paranguensis sp. nov. SEM micrographs of the different types of eggs of B. paranguensis sp. nov. A resting egg from field samples and its special ornamentation and zoom of its membrane, see arrows (A.a, A.b) B parthenogenetic egg and C unfertilized sexual egg, both from cultured samples. Scale bars: 20 µm

opencc-by-4.0Oct 2019View details →
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Figure 6 from: Guerrero-Jiménez G, Vannucchi PE, Silva-Briano M, Adabache-Ortiz A, Rico-Martínez R, Roberts D, Neilson R, Elías-Gutiérrez M (2019) Brachionus paranguensis sp. nov. (Rotifera, Monogononta), a member of the L group of the Brachionus plicatilis complex. ZooKeys 880: 1-23. https://doi.org/10.3897/zookeys.880.28992

Figure 6 Trophi components of B. paranguensis sp. nov. SEM pictures of the trophi components of B. paranguensis sp. nov., collected in June 27, 2015 A ventral view B dorsal view C rami and fulcrum D manubrium E satellites F unco and sub uncus ar: articulation of manubrium, m: membrane; ma: manubrium with posterior claw, see arrow (D); mmc: manubrium middle crest, see arrow (D); rr: reinforced ridge; st: satellites, see arrow (E); su: sub uncus; u: uncus.: b: basifenestras, see arrow (C); f: fulcrum, see arrow (C); mc: manubrium cavities; ra: rami, and projections of the posterior portion of the rami, see arrow (C)). Scale bars: 10 µm.

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Figure 4 from: Guerrero-Jiménez G, Vannucchi PE, Silva-Briano M, Adabache-Ortiz A, Rico-Martínez R, Roberts D, Neilson R, Elías-Gutiérrez M (2019) Brachionus paranguensis sp. nov. (Rotifera, Monogononta), a member of the L group of the Brachionus plicatilis complex. ZooKeys 880: 1-23. https://doi.org/10.3897/zookeys.880.28992

Figure 4 Taxonomic features of B. paranguensis sp. nov. A parthenogenetic female with lateral antennae (LA), gastric glands (gg), an U-shape sinus (us) B anterior dorsal and ventral spines taken by LM and SEMC lorica with an orange peel like surface D foot aperture E lateral antenna (see arrow) FSEM microphotographs of the female, ventral plate and G dorsal plate and H male. Scale bars: 50 µm (A, B, D, F, G, H), 10 µm (C, E). All females from sample collected in June 27, 2015. Males from cultures obtained from females collected in the volcanic maar Rincón de Parangueo.

opencc-by-4.0Oct 2019View details →

ScienceDex guides

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record