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FIGURE 1 in Typification of names in the Sesleria juncifolia species complex (Poaceae)

FIGURE 1. Holotype of the name Sesleria juncifolia Suffren (W0030266). The label on the sheet reporting "Typus….Sesleria tenuifolia Schrader….typificavit L. Pignotti (W) 2011-09-30" is not effective publication (Art. 7.9).

opennotspecifiedDec 2013View details →
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FIGURE 3 in Typification of names in the Sesleria juncifolia species complex (Poaceae)

FIGURE 3. Lectotype of the name Sesleria juncifolia Host (W1885-0002432). The label on the sheet reporting "Typus….Sesleria juncifolia Host….typificavit L. Pignotti (W) 2011-09-30" is not effective publication (Art. 7.9).

opennotspecifiedDec 2013View details →
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FIGURES 1–2. Lectotypes. 1. Ischioceras rugosa Provancher, 1882 in The genus-group names of Mutillidae (Hymenoptera) and their type species, with a new genus, new name, new synonymies, new combinations and lectotypifications

FIGURES 1–2. Lectotypes. 1. Ischioceras rugosa Provancher, 1882 (male, not female). 1a. Specimen and labels. 1b. Previous lectotype labels (not previously published). 2. Mutilla simplicifascia Sichel & Radoszkowski, 1869 (female). 2a. Dorsal view of head and mesosoma. 2b. Dorsal view of metasoma. 2c. Existing labels. (Scales differ.)

opennotspecifiedSep 2008View details →
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FIGURE 3 in Trichopeltinaceae (Dothideomycetes), an earlier name for Brefeldiellaceae, with a new species of Trichopeltina

FIGURE 3. Trichopeltina asiatica (holotype). a–b. Thallus and thyriothecia on surface of host. c. Thyriothecium with central ostiole. d. Cells of thyriothecia when immature. e. Upper wall cells of thallus. f–g. Asci with apical ring. h. Conidium. i. Apical ring. j–k. Ascospores with 3 septa. l. Immature ascospores in 70% lactic acid. Scale bars: c = 50 µm, d–h, j–l = 10 µm, l = 2 µm.

opennotspecifiedAug 2014View details →
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FIGURE 5 in Trichopeltinaceae (Dothideomycetes), an earlier name for Brefeldiellaceae, with a new species of Trichopeltina

FIGURE 5. Pycnoderma bambusinum (syntype). a. Specimen. b. Thyriothecia clustering together on the host surface. c. Cells of upper wall of thyriothecium. d. Arrangement of asci. e. Immature asci. f–g. Mature asci. h–i. Muriform ascospores. Scales bars: c = 50 µm, d = 100 µm, e–h = 20 µm, i = 10 µm.

opennotspecifiedAug 2014View details →
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FIGURE 2 in Trichopeltinaceae (Dothideomycetes), an earlier name for Brefeldiellaceae, with a new species of Trichopeltina

FIGURE 2. Trichopeltina labecula (PC 0084646) a. Specimen. b–c. Thallus on host substrate. d Ascomata and ostiole in 70% lactic acid. e–f. Cells of thallus and ascomata. g. Squash mount of contents of ascoma stained in Melzer's reagent. h. Mature ascus. i. Mature ascus stained in Melzer's reagent. j. Mature ascus stained in cotton blue reagent. k. Immature 1-septate ascospore. l. Immature ascospore stained in cotton blue reagent. m. Ascospore stained in Melzer's reagent. Scale bars: d, e = 100 µm, f, h–j = 20 µm, g, k–m = 10 µm.

opennotspecifiedAug 2014View details →
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FIGURE 1 in Trichopeltinaceae (Dothideomycetes), an earlier name for Brefeldiellaceae, with a new species of Trichopeltina

FIGURE 1. Trichopeltina labecula (lectotype). a. Specimen. b–c. Thallus and thyriothecia a on host substrate. d. Thyriothecia under thallus in 70% lactic acid, showing ostioles. e. Cells of thallus. f. Thyriothecium at maturity composed of darkly pigmented cells. g–h. Asci stained in Melzer's reagent. i. Asci stained in cotton blue reagent. j. Ascospore stained in cotton blue reagent. k. Immature ascospore stained in Melzer's reagent. l. Immature ascospore stained in Melzer's reagent. Scale bars: d, f = 50 µm, e, g–i = 20 µm, j–l = 10 µm.

opennotspecifiedAug 2014View details →
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FIGURE 4. Acrogenotheca pulcherrima. a–b. Specimen. c in Trichopeltinaceae (Dothideomycetes), an earlier name for Brefeldiellaceae, with a new species of Trichopeltina

FIGURE 4. Acrogenotheca pulcherrima. a–b. Specimen. c. Thallus and thyriothecia on surface of host. d. Cells of upper wall of thyriothecia. e. Erect mycelia with branches. f–h. Intercalary or sometimes terminal pycnidia. i–j. Asci. k. Ascus stained in cotton blue reagent. l–o. Ascospores with 2-septa. p–u. Conidia. Scale bars: f–k = 20 µm, l–o = 10 µm, d–e, p–s = 100 µm.

opennotspecifiedAug 2014View details →
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Figure 5 in When names are wrong and colours deceive: unravelling the Pseudoceros bicolor species complex (Turbellaria: Polycladida)

Figure 5. Photomicrograph of histological section of the Pseudoceros aureolineatus hypotype, prepared by Hyman (1939) and deposited at the Yale Peabody Museum, New Haven, CT, USA. The section shows a tubular pharynx (ph), the penis papilla (pp), the prostatic vesicle (pv) and the seminal vesicle (sv). Scale bar, 100 µm.

opennotspecifiedMar 2010View details →
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Figure 4 in When names are wrong and colours deceive: unravelling the Pseudoceros bicolor species complex (Turbellaria: Polycladida)

Figure 4. Colour variations observed in Pseudoceros rawlinsonae (A–I) and Pseudoceros bicolor (J–P). Specimens collected in the US Virgin Islands (A, I), the Bahamas (B), Curaçao (C), Honduras (D), Florida (E, H, L), Belize (F, G, J, K, P), Panama (M), Brazil (N; photo courtesy of V. Padula), and Jamaica (O). Note golden-yellow/orange marginal line surrounding all specimens of P. rawlinsonae, bright yellow/green marginal line around some specimens of P. bicolor (N, O), and interrupted submarginal rust-coloured band of Pseudoceros bicolor marcusorum (P). Size range of specimens, from 7 mm (F) to 28 mm (E).

opennotspecifiedMar 2010View details →
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Figure 3 in When names are wrong and colours deceive: unravelling the Pseudoceros bicolor species complex (Turbellaria: Polycladida)

Figure 3. Bayesian inference tree of 56 specimens. Numbers above nodes indicate Bayesian posterior probabilities, numbers below nodes are maximum likelihood bootstrap values. Asterisk designates holotype of Pseudoceros rawlinsonae.

opennotspecifiedMar 2010View details →
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Figure 2 in When names are wrong and colours deceive: unravelling the Pseudoceros bicolor species complex (Turbellaria: Polycladida)

Figure 2. Photomicrographs of histological sections of reproductive systems. (A) Male and (B) female reproductive system of Pseudoceros bicolor (specimen USFL 026). (C) Reproductive system of Pseudoceros bicolor marcusorum (specimen PAN 035). (D) reproductive system of Pseudoceros rawlinsonae (specimen USVI 058). cg, cement glands; ed, ejaculatory duct; fg, female gonopore; ma, male atrium; mg, male gonopore; mp, male papilla; pv, prostatic vesicle; s, stylet; sv, seminal vesicles; va, vagina. Scale bars, 250 µm.

opennotspecifiedMar 2010View details →
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Figure 1 in When names are wrong and colours deceive: unravelling the Pseudoceros bicolor species complex (Turbellaria: Polycladida)

Figure 1. Holotypes of Pseudoceros bicolor and Pseudoceros aureolineatus. Original drawings by Verrill (1901) of P. bicolor (A) and of P. aureolineatus (B). Photographs of P. bicolor (C) and P. aureolineatus (D) holotypes at the Yale Peabody Museum, New Haven, CT, USA. Note shape of pseudotentacles of P. bicolor compared with the more distinct tentacles of P. aureolineatus.

opennotspecifiedMar 2010View details →
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FIGURE 1 in Comments on 'The valid generic names for the fish species usually placed in Cyclocheilichthys' (KOTTELAT 2013) and a correction of Pasco-viel et al. (2012)

FIGURE 1. Radiograph in lateral view of the anterior part of the postcranial skeleton of Cyclocheilichthys janthochir (BMNH 1866.5.2.145).

opennotspecifiedApr 2013View details →
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Figs. 1– 4 in Resolving a Branching Taxonomy Conundrum—Can One Species be in Two Places at One Time Under the Same Name (Coleoptera: Zopheridae: Colydiinae and Tenebrionidae)?

Figs. 1– 4. Pristoderus species and Notocoxelus angustatus, habitus. 1) Pristoderus flexuosus sensu Germain (FMNH); 2) Pristoderus regularis, holotype (FMNH); 3) Pristoderus collaris, holotype (FMNH); 4) Notocoxelus angustatus sensu Heinze (Snow Entomological Museum Collection). Scale bars = 1 mm.

opennotspecifiedMar 2016View details →
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FIGURE 2 in Alpinia laosensis, the correct name for a species previously misidentified as A. conchigera

FIGURE 2. Alpinia laosensis: (A) Inflorescence, (B) Flowers and A. conchigera: (C) Inflorescence, (D) Flowers. Photos A & B by Ye Xing-Er; based on Y.H. Tong & X.E. Ye 186, Photos C & D by Khang Sinh Nguyen; based on J. Regalado et al. 1979.

opennotspecifiedJun 2021View details →
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FIGURE 1 in Alpinia laosensis, the correct name for a species previously misidentified as A. conchigera

FIGURE 1. Holotype of Alpinia laosensis and A. conchigera. (A) Alpinia laosensis [P032692] (reproduced with permission from: http:// coldb.mnhn.fr/catalognumber/mnhn/p/p032692), (B) A. conchigera [K000292388] (http://specimens.kew.org/herbarium/ K000292388; © copyright of the Board of Trustees of the Royal Botanic Gardens, Kew).

opennotspecifiedJun 2021View details →
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FIGURE 2 in How Kalanchoe marmorata (Crassulaceae subfam. Kalanchooideae), a distinctive central and east African species, received its name, and the later, valid publication of K. macrantha by Maire

FIGURE 2. The bright white flowers of Kalanchoe marmorata, produced during the winter months, are some of the longest in the genus. Photograph: Gideon F. Smith.

opennotspecifiedMay 2021View details →
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FIGURE 1 in How Kalanchoe marmorata (Crassulaceae subfam. Kalanchooideae), a distinctive central and east African species, received its name, and the later, valid publication of K. macrantha by Maire

FIGURE 1. In most forms of Kalanchoe marmorata the leaves are highly mottled with purple blotches on a light dull green background. Photograph: Gideon F. Smith.

opennotspecifiedMay 2021View details →
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FIGURES 46–51 in Description of four new species of Anelaphus Linsley (Coleoptera, Cerambycidae Cerambycinae, Elaphidiini), correction of the spelling of species-group names and description of the female of Anelaphus pilosus Chemsak and Noguera

FIGURES 46–51. Anelaphus nitidipennis Chemsak and Linsley, 1968, female: 46) Dorsal habitus; 47) Ventral habitus; 48) Lateral habitus; 49) Head and pronotum lateral view; 50) Head, frontal view. 51) Prosternum, lateral view.

opennotspecifiedOct 2021View details →

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Allen Brain Atlas

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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.

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behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
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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.

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