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Figure 2 from: Heng L-M, Zheng Y-L, Zhao Y-B, Wang Y-J (2018) Radiation of members of the Soroseris hookeriana complex (Asteraceae) on the Qinghai-Tibetan Plateau and their proposed taxonomic treatment. PhytoKeys 114: 11-25. https://doi.org/10.3897/phytokeys.114.29914
Figure 2 The 50% majority rule consensus tree derived from Bayesian inference of the combined sequences of psbA-trnH and matK. Posterior probabilities and bootstrap percentages are indicated above and below the branches, respectively. The samples named according to FOC (2011) or NCBI, Stebbins (1940) and the present study are listed from left to right.
Figure 1 from: Heng L-M, Zheng Y-L, Zhao Y-B, Wang Y-J (2018) Radiation of members of the Soroseris hookeriana complex (Asteraceae) on the Qinghai-Tibetan Plateau and their proposed taxonomic treatment. PhytoKeys 114: 11-25. https://doi.org/10.3897/phytokeys.114.29914
Figure 1 The 50% majority rule consensus tree derived from Bayesian inference of the nuclear internal transcribed spacer. Posterior probabilities and bootstrap percentages are indicated above and below the branches, respectively. The samples named according to FOC (2011) or NCBI, Stebbins (1940) and the present study are listed from left to right.
Figure 7 from: Rödel M-O, Glos J (2019) Herpetological surveys in two proposed protected areas in Liberia, West Africa. Zoosystematics and Evolution 95(1): 15-35. https://doi.org/10.3897/zse.95.31726
Figure 7 Permutated species accumulation curves (=sample-based rarefaction curve; red line: mean, blue lines: 95% confidence intervalls) of amphibian species richness in a the Krahn-Bassa Proposed Protected Area in eastern Liberia and b the Foya Proposed Protected Area in western Liberia during the March/April 2018 survey. Y-axis: estimated amphibian species richness, x-axis: sample units (each comprising six to 16 man/hour surveys in different localities within the respective areas).
Figure 4 from: Rödel M-O, Glos J (2019) Herpetological surveys in two proposed protected areas in Liberia, West Africa. Zoosystematics and Evolution 95(1): 15-35. https://doi.org/10.3897/zse.95.31726
Figure 4 a, b Dorsal and ventral view of male Hyperoliuszonatus (ZMB 88446) from KBPPA, showing the white gular region with the roundish gland, lacking dilatable skin of a larger vocal sac cH.concolor (ZMB 88542) with juvenile pattern from FPPAd male Phlyctimantisboulengeri (ZMB 88514) from FPPA.
Figure 6 from: Rödel M-O, Glos J (2019) Herpetological surveys in two proposed protected areas in Liberia, West Africa. Zoosystematics and Evolution 95(1): 15-35. https://doi.org/10.3897/zse.95.31726
Figure 6 aCophoscincopussimulans male (ZMB 88507) from FPPAb, cHolaspisguentheri male (ZMB 88471) dHolaspisguentheri female (ZMB 88472) from KBPPAe Juvenile Goniontophisklingi (ZMB 88467) from KBPPA.
Figure 3 from: Rödel M-O, Glos J (2019) Herpetological surveys in two proposed protected areas in Liberia, West Africa. Zoosystematics and Evolution 95(1): 15-35. https://doi.org/10.3897/zse.95.31726
Figure 3 a Juvenile Afrixalusfulvovitattus (ZMB 88539) b Male Hyperoliussoror (ZMB 88540), both from farmbush habitats in FPPA, note fine dark lines in the clear bands of A.fulvovittatus, the closely related A.vittiger is lacking these lines; c–f) dorsal and ventral views of Hyperoliuspicturatusc Female (ZMB 88487) from KBPPA with hourglass pattern, a pattern also often found in combination with dorsolateral line in males d, e Female (ZMB 88464) from KBPPA with common brown back and broad yellow dorsolateral bands and yellow venter f Translucent greenish venter of male (ZMB 88465) from KBPPA.
Figure 2 from: Rödel M-O, Glos J (2019) Herpetological surveys in two proposed protected areas in Liberia, West Africa. Zoosystematics and Evolution 95(1): 15-35. https://doi.org/10.3897/zse.95.31726
Figure 2 aGeotrypetes sp. (ZMB 88492) found dead in the leaf litter in KBPPAbLeptopelismacrotis male (ZMB 88439) from KBPPAc, dConrauaalleni tadpoles (ZMB 88526) from the same puddle in a small stream in FPPA, take note of the differing color, shape and place of insertion of tail fins.
Figure 1 from: Rödel M-O, Glos J (2019) Herpetological surveys in two proposed protected areas in Liberia, West Africa. Zoosystematics and Evolution 95(1): 15-35. https://doi.org/10.3897/zse.95.31726
Figure 1 Natural and disturbed habitats in the Krahn-Bassa (KBPPA) and Foya Proposed Protected Areas (FPPA). a Remaining puddles of a stream in Krahn-Bassa, habitat of Aubriasubsigillata, Amnirana 'albolabris West', Leptopelismacrotis, Hyperoliuschlorosteus and Chiromantisrufescens. b View on a near primary forest patch in FPPA. c Artisanal gold mining area near a small forest stream in FPPA, frogs breeding in these puddles were Xenopustropicalis, Sclerophrysmaculata, Hyperoliuspicturatus, Phlyctimantisboulengeri, Ptychadenalongirostris, P. sp., and Chiromantisrufescens. d Recently slash and burn cleared forest patch in FPPA, prepared for establishing a cacao plantation.
Figure 5 from: Rödel M-O, Glos J (2019) Herpetological surveys in two proposed protected areas in Liberia, West Africa. Zoosystematics and Evolution 95(1): 15-35. https://doi.org/10.3897/zse.95.31726
Figure 5 a Undescribed Phrynobatrachus sp. from KBPPA exhibiting characters of P.gutturosus and P.tokbabPtychadena sp. male (ZMB 88505) from river bank in FPPAc, dPtychadenamascareniensis-complex females with green (c: ZMB 88535) and brown (d: ZMB 88537) vertebral bands from the same rice paddy in FPPAeChiromantisrufescens female (not collected) from KBPPA.
Proposed Guiana Shield Key Biodiversity Areas
<p>Key Biodiversity Areas (KBAs) are identified using globally standard criteria and thresholds to species and sites vulnerability and irreplaceability (Margules and Pressey 2000). KBAs are identified based on the confirmed presence of (1) globally threatened species, (2) restricted-range species, (3) congregations of species that concentrate at particular sites during some stage in their life cycle, and (4) biome-restricted species assemblages. Based on this, species occurrence data were compiled from primary literature, scientific reports and museum records. Only recent data was used (no more than 10 years old) and site location was checked by georeferenced datasets. KBA delineation was based on wilderness patterns, where habitat connectivity is contiguous and most of biological process occur in accordance with biophysical processes. So, the database with occurrence points for species was overlapped with small watershed databases to delineate the KBA limits for the Guiana Shield.</p>
Figure 4 from: Seraphim G, Giupponi APL, Miranda GS (2019) Taxonomy of the thelyphonid genus Typopeltis Pocock, 1894, including homology proposals for the male gonopod structures (Arachnida, Thelyphonida, Typopeltinae). ZooKeys 848: 21-39. https://doi.org/10.3897/zookeys.848.32263
Figure 4 Typopeltisguangxiensis (male). A Carapace B sternum C pedipalps (dorsal) D pedipalps (ventral) E opisthosoma (dorsal) F opisthosoma (ventral) G ommatoids.
Figure 8 from: Seraphim G, Giupponi APL, Miranda GS (2019) Taxonomy of the thelyphonid genus Typopeltis Pocock, 1894, including homology proposals for the male gonopod structures (Arachnida, Thelyphonida, Typopeltinae). ZooKeys 848: 21-39. https://doi.org/10.3897/zookeys.848.32263
Figure 8 Comparison between gonopods of T.laurentianus sp. n. (A, B) and Heterophrynus sp. Pocock, 1894 (C, D). A Male gonopod of T.laurentianus in posterior-dorsal view BSEM of male gonopod of T.laurentianus in posterior-dorsal view CSEM of male gonopod of Heterophrynus sp. in ventral view DSEM of male gonopod of Heterophrynus sp. in dorsal view. Fi = fistula; GO = genital operculum; LaM = lamina medialis; LoD = lobus dorsalis; LoL1 = lobus lateralis primus; LoL2 = lobus lateralis secundus; PI = processus internus; Me = Mensa; Fu = Fulcrum.
Figure 1 from: Seraphim G, Giupponi APL, Miranda GS (2019) Taxonomy of the thelyphonid genus Typopeltis Pocock, 1894, including homology proposals for the male gonopod structures (Arachnida, Thelyphonida, Typopeltinae). ZooKeys 848: 21-39. https://doi.org/10.3897/zookeys.848.32263
Figure 1 Typopeltislaurentianus sp. n., holotype (male). A Carapace B sternum C pedipalps (dorsal) D pedipalps (ventral) E opisthosoma (dorsal) F opisthosoma (ventral) G ommatoid H gonopod.
Figure 3 from: Seraphim G, Giupponi APL, Miranda GS (2019) Taxonomy of the thelyphonid genus Typopeltis Pocock, 1894, including homology proposals for the male gonopod structures (Arachnida, Thelyphonida, Typopeltinae). ZooKeys 848: 21-39. https://doi.org/10.3897/zookeys.848.32263
Figure 3 SEM images of Typopeltislaurentianus sp. n., paratype (male). A Chelicerae (right) B gonopod. Details in dashed rectangles are shown in images C (lower rectangle) and D (upper rectangle). C Fulcrum (Fu) detail D Mensa (Me) detail.
Figure 2 from: Seraphim G, Giupponi APL, Miranda GS (2019) Taxonomy of the thelyphonid genus Typopeltis Pocock, 1894, including homology proposals for the male gonopod structures (Arachnida, Thelyphonida, Typopeltinae). ZooKeys 848: 21-39. https://doi.org/10.3897/zookeys.848.32263
Figure 2 Typopeltislaurentianus sp. n., paratype (female). A Carapace B sternum C pedipalps (dorsal) D pedipalps (ventral) E opisthosoma (dorsal) F opisthosoma (ventral) G ommatoid H gonopod. CCh = circulus chitinosus; ACh = arcus chitinosus.
Figure 7 from: Seraphim G, Giupponi APL, Miranda GS (2019) Taxonomy of the thelyphonid genus Typopeltis Pocock, 1894, including homology proposals for the male gonopod structures (Arachnida, Thelyphonida, Typopeltinae). ZooKeys 848: 21-39. https://doi.org/10.3897/zookeys.848.32263
Figure 7 Distribution map of Typopeltislaurentianus sp. n. (black squares) and T.guangxiensis (black circles).
Figure 6 from: Seraphim G, Giupponi APL, Miranda GS (2019) Taxonomy of the thelyphonid genus Typopeltis Pocock, 1894, including homology proposals for the male gonopod structures (Arachnida, Thelyphonida, Typopeltinae). ZooKeys 848: 21-39. https://doi.org/10.3897/zookeys.848.32263
Figure 6 Typopeltisguangxiensis (female). A Carapace B sternum C pedipalps (dorsal) D pedipalps (ventral) E opisthosoma (dorsal) F opisthosoma (ventral) G ommatoids H gonopod. CCh = circulus chitinosus; ACh = arcus chitinosus.
Figure 5 from: Seraphim G, Giupponi APL, Miranda GS (2019) Taxonomy of the thelyphonid genus Typopeltis Pocock, 1894, including homology proposals for the male gonopod structures (Arachnida, Thelyphonida, Typopeltinae). ZooKeys 848: 21-39. https://doi.org/10.3897/zookeys.848.32263
Figure 5 SEM images of Typopeltisguangxiensis (male). A Chelicerae (right) B gonopod. Details in dashed rectangles are shown in images C (lower rectangle) and D (upper rectangle). C Fulcrum (Fu) detail D Mensa (Me) detail.
Figures 8-12 from: Sinclair BJ (2019) Revision of the southern African genus Stuckenbergomyia Smith, 1971 (Diptera, Empidoidea) and proposal of a new subfamily. African Invertebrates 60(1): 133-145. https://doi.org/10.3897/afrinvertebr.60.35556
Figures 8-12 Stuckenbergomyiasecunda (Smith). 8 Holotype labels (upper label is reverse side of second label) 9 Holotype habitus, lateral view 10 Male habitus, Louwsberg specimen 11 Wing 12 Male foreleg, arrow pointing to fore tibial gland, posterior view. Abbreviations: cua – anterior cubital cell, CuA+CuP – anterior branch of cubital vein + posterior branch of cubital vein, dm – discal medial cell, M1 – first branch of media, M2 – second branch of media, M4 – fourth branch of media, Sc – subcostal vein. Scale bars: 1.0 mm (8–11); 0.5 (12).
Figures 3-7 from: Sinclair BJ (2019) Revision of the southern African genus Stuckenbergomyia Smith, 1971 (Diptera, Empidoidea) and proposal of a new subfamily. African Invertebrates 60(1): 133-145. https://doi.org/10.3897/afrinvertebr.60.35556
Figures 3-7 Stuckenbergomyianamibiensis sp. nov., male and female terminalia. 3 Male, lateral view 4 Male, dorsal view 5 Phallus, dorsal view 6 Female, lateral view 7 Spermatheca, dorsal view. Abbreviations: ej apod – ejaculatory apodeme, epand – epandrium, epiprct – epiproct, hypd – hypandrium, hyprct – hypoproct, pgt – postgonite, ph – phallus, tg – tergite, v apod – ventral apodeme. Scale bars: 0.1 mm.
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.