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Figure 1 from: Simo-Droissart M, Stévart T, Sonké B, Mayogo S, Kamdem N, Droissart V (2018) New taxonomic and conservation status of Ossiculum (Vandeae, Orchidaceae), a highly threatened and narrow-endemic angraecoid orchid from Central Africa. PhytoKeys 98: 85-97. https://doi.org/10.3897/phytokeys.98.23511
Figure 1 Current distribution of Calyptrochilum aurantiacum in Central Africa (upper map) and in Cameroon (lower map). WS = Wildlife Sanctuary; FR = Forest Reserve; NP = National Park.
Figure 4 from: Simo-Droissart M, Stévart T, Sonké B, Mayogo S, Kamdem N, Droissart V (2018) New taxonomic and conservation status of Ossiculum (Vandeae, Orchidaceae), a highly threatened and narrow-endemic angraecoid orchid from Central Africa. PhytoKeys 98: 85-97. https://doi.org/10.3897/phytokeys.98.23511
Figure 4 Seed banking of Calyptrochilum aurantiacum in Yaoundé (Cameroon). In 2017, an ex situ conservation programme was initiated to support the long term preservation of C. aurantiacum. A Due to the small size of the flowers, manual pollination has been performed under a stereomicroscope. B Fruit development and maturation takes place in a shadehouse established in Yaoundé. C Finally, viable seeds have been harvested and conserved in the freezer (-20°C). Before being preserved at low temperature, seed viability is assessed using the tetrazolium test (red colouration of living embryo). Photographs A and C by V. Droissart, B by Gyslène Kamdem.
Figure 3 from: Simo-Droissart M, Stévart T, Sonké B, Mayogo S, Kamdem N, Droissart V (2018) New taxonomic and conservation status of Ossiculum (Vandeae, Orchidaceae), a highly threatened and narrow-endemic angraecoid orchid from Central Africa. PhytoKeys 98: 85-97. https://doi.org/10.3897/phytokeys.98.23511
Figure 3 Ecology and habit of natural populations of Calyptrochilum aurantiacum. A Flowering individual growing on upper branches of a felled kola tree, along with the angraecoid orchid Diaphananthe plehniana and the fern Microgramma owariensis. B Dense population growing on 1 metre long branches of Duguetia staudtii. C Calyptrochilum aurantiacum and Diaphananthe plehniana growing side by side on Salacia sp. (Celastraceae). Photographs by V. Droissart (June 2017).
FIGURE 1 in Reassessment of the taxonomic status of Craseomys and three controversial species of Myodes and Alticola (Rodentia: Arvicolinae)
FIGURE 1. Collection localities of red-backed voles and mountain voles examined in this work.
Figure 9 from: Sánchez-Vialas A, Calvo-Revuelta M, Castroviejo-Fisher S, De la Riva I (2018) The taxonomic status of Petropedetes newtonii (Amphibia, Anura, Petropedetidae). ZooKeys 765: 59-78. https://doi.org/10.3897/zookeys.765.24764
Figure 9 Ventral view of the right forelimb of Petropedetes newtonii (adult male, MNCN 48728). Arrows point to the dorsal spine on the distal edge of the metacarpal of Finger I and keratinised spicules along the skin surface of the upper arm and labial commissure.
Figure 8 from: Sánchez-Vialas A, Calvo-Revuelta M, Castroviejo-Fisher S, De la Riva I (2018) The taxonomic status of Petropedetes newtonii (Amphibia, Anura, Petropedetidae). ZooKeys 765: 59-78. https://doi.org/10.3897/zookeys.765.24764
Figure 8 Neotype of Petropedetes newtonii (adult male, MNCN 48728). Left: ventral view; right: dorsal view.
Figure 7 from: Sánchez-Vialas A, Calvo-Revuelta M, Castroviejo-Fisher S, De la Riva I (2018) The taxonomic status of Petropedetes newtonii (Amphibia, Anura, Petropedetidae). ZooKeys 765: 59-78. https://doi.org/10.3897/zookeys.765.24764
Figure 7 CT-scan image of the dorsal side of the humerus of Petropedetes johnstoni (A male, ZFMK87709) and P. newtonii (B male, MNCN 48728). Note the differences in the development and extension of the bone crest.
Figure 6 from: Sánchez-Vialas A, Calvo-Revuelta M, Castroviejo-Fisher S, De la Riva I (2018) The taxonomic status of Petropedetes newtonii (Amphibia, Anura, Petropedetidae). ZooKeys 765: 59-78. https://doi.org/10.3897/zookeys.765.24764
Figure 6 CT-scan image of the dorsal side of the hands of Petropedetes johnstoni (A male, ZFMK 87709) and P. newtonii (B male, MNCN 48728). No traces of metacarpal spines are detected in P. johnstoni.
Figure 4 from: Sánchez-Vialas A, Calvo-Revuelta M, Castroviejo-Fisher S, De la Riva I (2018) The taxonomic status of Petropedetes newtonii (Amphibia, Anura, Petropedetidae). ZooKeys 765: 59-78. https://doi.org/10.3897/zookeys.765.24764
Figure 4 Details of the tympanum of Petropedetes johnstoni (A male, ZFMK 87709), P. newtonii (B male, MNCN 48728), and P. vulpiae (C male, non-collected specimen from Río Muni, Equatorial Guinea; photo by Ignacio De la Riva).
Figure 5 from: Sánchez-Vialas A, Calvo-Revuelta M, Castroviejo-Fisher S, De la Riva I (2018) The taxonomic status of Petropedetes newtonii (Amphibia, Anura, Petropedetidae). ZooKeys 765: 59-78. https://doi.org/10.3897/zookeys.765.24764
Figure 5 Thenar tubercle of males of Petropedetes newtonii (A male, MNCN 48728) and P. johnstoni (B male, ZFMK 87709). Note the different shape and size and the presence of a dorsal spine on the distal edge of the metacarpal of Finger I in P. newtonii.
Figure 3 from: Sánchez-Vialas A, Calvo-Revuelta M, Castroviejo-Fisher S, De la Riva I (2018) The taxonomic status of Petropedetes newtonii (Amphibia, Anura, Petropedetidae). ZooKeys 765: 59-78. https://doi.org/10.3897/zookeys.765.24764
Figure 3 Mouth roof region of Petropedetes newtonii (A female, MNCN 48729) and Petropedetes johnstoni (B male, ZFMK 87709).
Figure 2 from: Sánchez-Vialas A, Calvo-Revuelta M, Castroviejo-Fisher S, De la Riva I (2018) The taxonomic status of Petropedetes newtonii (Amphibia, Anura, Petropedetidae). ZooKeys 765: 59-78. https://doi.org/10.3897/zookeys.765.24764
Figure 2 Ventral view of specimens of Petropedetes johnstoni (A male, ZFMK 87709 B female, ZFMK 87710) and P. newtonii (C male, MNCN 48730 D female, MNCN 48729).
Figure 10 from: Sánchez-Vialas A, Calvo-Revuelta M, Castroviejo-Fisher S, De la Riva I (2018) The taxonomic status of Petropedetes newtonii (Amphibia, Anura, Petropedetidae). ZooKeys 765: 59-78. https://doi.org/10.3897/zookeys.765.24764
Figure 10 Distribution map of Petropedetes newtonii based on published records and collection data. 1 Campamento Smith, Luba, Bioko 2 Río Riaco, Caldera de Luba, Bioko 3 Stream Mukokobe, between Belebu and Ureka, Bioko 4 Río Osa, Bioko 5 Río Ole, Bioko 6 Río Sibitá, Bococo, Bioko 7 Musola, Bioko 8 Basilé, Bioko 9 Río Iladyi, Bioko 10 Bakingili, Cameroon 11 Mt. Etinde, Cameroon.
Figure 4 from: de Brito PS, Guimarães EC, Katz AM, Piorski NM, Ottoni FP (2018) Taxonomic status of Aphyocharax avary Fowler, 1913, Aphyocharax pusillus Günther, 1868 and Chirodon alburnus Günther, 1869 (Characiformes, Characidae). Zoosystematics and Evolution 94(2): 393-399. https://doi.org/10.3897/zse.94.28201
Figure 4 Maxillary teeth of: A, Holotype of Aphyocharaxavary: ANSP 39217; B, Syntype of Aphyocharaxpusillus: BMNH1867.6.12.46; C, D; Syntypes of Aphyocharaxpusillus: BMNH 1867.6.13.58-59; E, Lectotype of Chirodonalburnus: BMNH 1869.5.21.10; F, G, two of the three paralectotypes of Chirodonalburnus (head damaged in a third): BMNH 1869.5.21.11-13. A, Photographed by Axel Katz; and B-G, Photographed by Kevin Webb.
Figure 3 from: de Brito PS, Guimarães EC, Katz AM, Piorski NM, Ottoni FP (2018) Taxonomic status of Aphyocharax avary Fowler, 1913, Aphyocharax pusillus Günther, 1868 and Chirodon alburnus Günther, 1869 (Characiformes, Characidae). Zoosystematics and Evolution 94(2): 393-399. https://doi.org/10.3897/zse.94.28201
Figure 3 Recently preserved specimens of Aphyocharaxpusillus: ANSP 178013, 4, 33.1–54.8 mm SL, Peru, Loreto, Rio Napo (Amazon river basin), right bank just upstream from mouth of Mazan river, near town of Mazan (3°29'10"S, 73°6'24''W). Photographed by Mark Sabaj Perez.
Figure 3 from: Zhang L, Wang M, Ma T, Liu J (2018) Taxonomic status of Populus wulianensis and P. ningshanica (Salicaceae). PhytoKeys 108: 117-129. https://doi.org/10.3897/phytokeys.108.25600
Figure 3 The neighbour-joining (NJ) tree of ITS variable sites (A); The neighbour-joining (NJ) tree of four cpDNA variable sites (B).
Figure 2 from: Zhang L, Wang M, Ma T, Liu J (2018) Taxonomic status of Populus wulianensis and P. ningshanica (Salicaceae). PhytoKeys 108: 117-129. https://doi.org/10.3897/phytokeys.108.25600
Figure 2 Principal Coordinates Analysis (PCA) of the 17 populations of 4 species based on genetic distance using SSR data (A); the optimal K value was estimated using (B) the distribution of delta K (K=2) and Bayesian clustering plots for 17 populations of 4 species based on variation at 14 nSSR loci (C).
Figure 1 from: Zhang L, Wang M, Ma T, Liu J (2018) Taxonomic status of Populus wulianensis and P. ningshanica (Salicaceae). PhytoKeys 108: 117-129. https://doi.org/10.3897/phytokeys.108.25600
Figure 1 A Geographical distribution of 17 populations of the four species (Populusadenopoda, Populusdavidiana, Populusningshanica, Populuswulianensis) B The Principal Component Analysis (PCA) plot for the morphological variations of 17 populations of 4 species.
Figure 1 from: Entiauspe-Neto OM, de Sena A, Tiutenko A, Loebmann D (2019) Taxonomic status of Apostolepis barrioi Lema, 1978, with comments on the taxonomic instability of Apostolepis Cope, 1862 (Serpentes, Dipsadidae). ZooKeys 841: 71-78. https://doi.org/10.3897/zookeys.841.33404
Figure 1 Dorsal, lateral and ventral illustrations of previously recognized taxa, Apostolepisdimidiata (A) and A.barrioi (B), according to the diagnoses of Cabral et al. (2017). However, these represent merely phenotypic variations of A.dimidiata and, according to the descriptions of Jan (1862) and Lema (1978), both holotypes of A.barrioi and A.dimidiata present the bottom coloration.
Figure 2 from: Entiauspe-Neto OM, de Sena A, Tiutenko A, Loebmann D (2019) Taxonomic status of Apostolepis barrioi Lema, 1978, with comments on the taxonomic instability of Apostolepis Cope, 1862 (Serpentes, Dipsadidae). ZooKeys 841: 71-78. https://doi.org/10.3897/zookeys.841.33404
Figure 2 The impact of the taxonomic history of Apostolepis Cope, 1862 species. The line refers to the cumulative number of species considered as valid during the time span, suffering either reductions from synonymies or additions from descriptions and revalidations. Inset picture: Apostolepis sp. from Serra do Cachimbo, Pará, Brazil.
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.