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Figure 1 from: Huys R, Lee J (2018) Philippiphonte aspidosoma gen. et sp. n., a radically divergent member of the Laophontidae from shell gravel in the East Sea, South Korea, including a review of Folioquinpes Fiers & Rutledge, 1990 (Copepoda, Harpacticoida). ZooKeys 775: 15-46. https://doi.org/10.3897/zookeys.775.26404
Figure 1 Localities in Dokdo island, Korea where Philippiphonte aspidosoma gen. et sp. n. was collected: 1 Gajaebawi (type locality) 2 Mulgol 3 Old harbour.
Figure 4 from: Huys R, Lee J (2018) Philippiphonte aspidosoma gen. et sp. n., a radically divergent member of the Laophontidae from shell gravel in the East Sea, South Korea, including a review of Folioquinpes Fiers & Rutledge, 1990 (Copepoda, Harpacticoida). ZooKeys 775: 15-46. https://doi.org/10.3897/zookeys.775.26404
Figure 4 Philippiphonte aspidosoma gen. et sp. n. (♀): A anal somite and left caudal ramus, dorsal B anal somite and left caudal ramus, ventral C leg 2, anterior D leg 3, anterior.
Figure 3 from: Huys R, Lee J (2018) Philippiphonte aspidosoma gen. et sp. n., a radically divergent member of the Laophontidae from shell gravel in the East Sea, South Korea, including a review of Folioquinpes Fiers & Rutledge, 1990 (Copepoda, Harpacticoida). ZooKeys 775: 15-46. https://doi.org/10.3897/zookeys.775.26404
Figure 3 Philippiphonte aspidosoma gen. et sp. n. (♀): A urosome and right leg 5, ventral B mandible [inset showing gnathobase from different angle] C maxillule, anterior [inset showing small unipinnate element arising from posterior surface] D maxilla E maxilliped F leg 1, anterior [exp-2 and -3 disarticulated].
Figure 7 from: Huys R, Lee J (2018) Philippiphonte aspidosoma gen. et sp. n., a radically divergent member of the Laophontidae from shell gravel in the East Sea, South Korea, including a review of Folioquinpes Fiers & Rutledge, 1990 (Copepoda, Harpacticoida). ZooKeys 775: 15-46. https://doi.org/10.3897/zookeys.775.26404
Figure 7 Harpacticoid copepods exhibiting dorsoventrally flattened body shapes (females only, dorsal view; genital double-somite shaded). A Philippiphonte aspidosoma (Laophontidae) B Porcellidium viride (Philippi, 1840) (Porcellidiidae) C Neopeltopsis pectinipes Hicks, 1976 (Peltidiidae) D Hamondia superba Huys, 1990 (Hamondiidae) E Alteutha oblonga (Goodsir, 1845) (Peltidiidae) F Peltidium purpureum Philippi, 1839 (Peltidiidae) G Zaus abbreviatus Sars, 1904 (Harpacticidae) H Paramenophia platysoma (Thompson & Scott, 1903) (Thalestridae) I Xouthous purpurocinctus (Norman & Scott, 1905) (Pseudotachidiidae) J Xouthous parasimulans (Médioni & Soyer, 1968) (Pseudotachidiidae) K Mucropedia kirstenae Bouck, Thistle & Huys, 1999 (Harpacticidae) L Donsiella phycolimnoriae Hicks, 1990 (Pseudotachidiidae) M Alteuthoides kootare Hicks, 1986 (Peltidiidae) N Peltidiphonte rostrata Gheerardyn & Fiers in Gheerardyn, Fiers, Vincx & De Troch, 2006 (Laophontidae) O Peltobradya bryozoophila Médioni & Soyer, 1968 (Ectinosomatidae) P Scutellidium arthuri Poppe, 1884 (Tisbidae).
Figure 3 from: Leal-Dutra CA, Neves MA, Griffith GW, Reck MA, Clasen LA, Dentinger BTM (2018) Reclassification of Parapterulicium Corner (Pterulaceae, Agaricales), contributions to Lachnocladiaceae and Peniophoraceae (Russulales) and introduction of Baltazaria gen. nov. MycoKeys 37: 39-56. https://doi.org/10.3897/mycokeys.37.26303
Figure 3 Baltazariaoctopodites: a, b basidiomes in the field (INPA280140 and FLOR56460), the detail in a shows the anchorage point in the leaf, the whitish resupinate area in b shows the corticioid portion of the fungus c gloeocystidia d skeletal hyphae, skeletal hyphae inflated in KOH (third from the right) and generative hyphae (first and second from the right) e–hSEM images of papillate skeletal hyphae. Scale bars: a–b = 1 cm; c–d = 10 μm; e–h = 1 μm).
Figure 2 from: Leal-Dutra CA, Neves MA, Griffith GW, Reck MA, Clasen LA, Dentinger BTM (2018) Reclassification of Parapterulicium Corner (Pterulaceae, Agaricales), contributions to Lachnocladiaceae and Peniophoraceae (Russulales) and introduction of Baltazaria gen. nov. MycoKeys 37: 39-56. https://doi.org/10.3897/mycokeys.37.26303
Figure 2 Parapteruliciumsubarbusculum: a–c basidiomes in the field. The detail in c shows the developing corticioid patch d basidiospores e dichophyses f gloeocystidia g, hSEM images of dichophyses; i. SEM images of basidiome surface with abundant dichophyses. Scale bars: a–c = 1 cm; d–f, i = 10 μm; g, h = 5 μm.
Figure 1 from: Leal-Dutra CA, Neves MA, Griffith GW, Reck MA, Clasen LA, Dentinger BTM (2018) Reclassification of Parapterulicium Corner (Pterulaceae, Agaricales), contributions to Lachnocladiaceae and Peniophoraceae (Russulales) and introduction of Baltazaria gen. nov. MycoKeys 37: 39-56. https://doi.org/10.3897/mycokeys.37.26303
Figure 1 Maximum likelihood tree of Russulales on the left with /peniophorales amplified on the right. Support values on the branches are BS (>65) / BPP (>0.95), names in bold represent the newly generated sequences for this study and bold lines show the new genus. Details for the complete tree can be found in Suppl. material 1: SuppFigs 2, 3.
Figure 6 from: Wang C, Zhang M, Li T, Liang X, Shen Y (2018) Additions to tribe Chromosereae (Basidiomycota, Hygrophoraceae) from China, including Sinohygrocybe gen. nov. and a first report of Gloioxanthomyces nitidus. MycoKeys 38: 59-76. https://doi.org/10.3897/mycokeys.38.25427
Figure 6 Line drawings of Gloioxanthomycesnitidus (GDGM41710). a basidiomata b basidiospores c basidia.
Figure 3 from: Wang C, Zhang M, Li T, Liang X, Shen Y (2018) Additions to tribe Chromosereae (Basidiomycota, Hygrophoraceae) from China, including Sinohygrocybe gen. nov. and a first report of Gloioxanthomyces nitidus. MycoKeys 38: 59-76. https://doi.org/10.3897/mycokeys.38.25427
Figure 3 Basidiomata of Sinohygrocybetomentosipes (a–b GDGM43351 c–d GDGM43352 e GDGM43347 f GDGM50075 g–h GDGM50149). Scale bars: 2 cm.
Figure 2 from: Wang C, Zhang M, Li T, Liang X, Shen Y (2018) Additions to tribe Chromosereae (Basidiomycota, Hygrophoraceae) from China, including Sinohygrocybe gen. nov. and a first report of Gloioxanthomyces nitidus. MycoKeys 38: 59-76. https://doi.org/10.3897/mycokeys.38.25427
Figure 2 Phylogenetic overview of the tribe Chromosereae inferred from ITS data using ML method. Two Hygrocybeconica sequences were rooted as outgroups. Bootstrap values (≥50%) are shown around the branches. GenBank accession numbers of downloaded sequences were added after the species name and the collection locations were added at the ends. NA, EA and EU referred to North America, East Asia and Europe, respectively. The newly generated sequences are shown in bold.
Figure 1 from: Wang C, Zhang M, Li T, Liang X, Shen Y (2018) Additions to tribe Chromosereae (Basidiomycota, Hygrophoraceae) from China, including Sinohygrocybe gen. nov. and a first report of Gloioxanthomyces nitidus. MycoKeys 38: 59-76. https://doi.org/10.3897/mycokeys.38.25427
Figure 1 Phylogenetic overview of the family Hygrophoraceae inferred from ITS-LSU-RPB2 data using Maximum Likelihood (ML) method. Typhulaphacorrhiza was selected as outgroup. Bootstrap values (≥50%) were presented around the branches. The newly generated sequences are shown in bold.
Figure 4 from: Wang C, Zhang M, Li T, Liang X, Shen Y (2018) Additions to tribe Chromosereae (Basidiomycota, Hygrophoraceae) from China, including Sinohygrocybe gen. nov. and a first report of Gloioxanthomyces nitidus. MycoKeys 38: 59-76. https://doi.org/10.3897/mycokeys.38.25427
Figure 4 Line drawings of Sinohygrocybetomentosipes. a Basidiomata b Basidiospores c Basidia d Elements of pileipellis cells e Elements of gill trama.
FIGURES 53–58 in A new Afrotropical genus Monocentroptilum gen. n. (Ephemeroptera: Baetidae: Protopatellata)
FIGURES 53–58. Eggs Of Monocentroptilum badium.
Figure 1 from: Wang Zh, Zhao Q, Li W, Che Y, Wang Z (2018) Establishment of a new genus, Brephallus Wang et al., gen. nov. (Blattodea, Blaberidae, Epilamprinae) based on two species from Pseudophoraspis, with details of polymorphism in species of Pseudophoraspis. ZooKeys 785: 117-131. https://doi.org/10.3897/zookeys.785.26565
Figure 1 Maximum likelihood (ML) tree derived from COI gene analysis following GTR GAMMA model with 1000 bootstrap replicates. The bootstrap support are all 100%, in this phylogenetic tree.
Figure 5 from: Wang Zh, Zhao Q, Li W, Che Y, Wang Z (2018) Establishment of a new genus, Brephallus Wang et al., gen. nov. (Blattodea, Blaberidae, Epilamprinae) based on two species from Pseudophoraspis, with details of polymorphism in species of Pseudophoraspis. ZooKeys 785: 117-131. https://doi.org/10.3897/zookeys.785.26565
Figure 5 A female of P.recurvata from Hainan Province. This specimen, collected as a nymph in 8 April 2015, was reared at Southwest University by Lu Qiu and adult emergence occurred in 21 May 2015 B male of P.recurvata from Hainan Province C male of P.clavellata from Yunnan Province D habitat of P.clavellataE male of P.kabakovi from Yunnan Province F female of P.kabakovi from Yunnan Province. A–F Photographed by Lu Qiu G–HBrephallusfruhstorferi (Shelford, 1910) comb. nov. from Hainan Province (Photographed by Xin-Ran Li).
Figure 3 from: Wang Zh, Zhao Q, Li W, Che Y, Wang Z (2018) Establishment of a new genus, Brephallus Wang et al., gen. nov. (Blattodea, Blaberidae, Epilamprinae) based on two species from Pseudophoraspis, with details of polymorphism in species of Pseudophoraspis. ZooKeys 785: 117-131. https://doi.org/10.3897/zookeys.785.26565
Figure 3 A–BP.kabakovi (nymph) scale bars = 5 mm C–DP.clavellata (nymph) E abdomen of female of P.clavellataF–GBrephallusfruhstorferi (Shelford, 1910) comb. nov. (nymph).
Figure 2 from: Wang Zh, Zhao Q, Li W, Che Y, Wang Z (2018) Establishment of a new genus, Brephallus Wang et al., gen. nov. (Blattodea, Blaberidae, Epilamprinae) based on two species from Pseudophoraspis, with details of polymorphism in species of Pseudophoraspis. ZooKeys 785: 117-131. https://doi.org/10.3897/zookeys.785.26565
Figure 2 A–DBrephallusfruhstorferi (Shelford, 1910) comb. nov. (male A–B female C–D) E–FBrephallustramlapensis (Anisyutkin, 1999) comb. nov. (male) G–JP.recurvata (male G–H female I–J) K–NP.clavellata (male K–L female M–N) O–RP.kabakovi (male O–P female Q–R). Scale bars = 10 mm (A–F) Scale bars = 5 mm (G–R).
Figure 4 from: Wang Zh, Zhao Q, Li W, Che Y, Wang Z (2018) Establishment of a new genus, Brephallus Wang et al., gen. nov. (Blattodea, Blaberidae, Epilamprinae) based on two species from Pseudophoraspis, with details of polymorphism in species of Pseudophoraspis. ZooKeys 785: 117-131. https://doi.org/10.3897/zookeys.785.26565
Figure 4 Male genitalia of Pseudophoraspis and Brephallus Wang et al., gen. nov. AP.recurvataBP.clavellataCP.kabakoviDBrephallusfruhstorferi (Shelford, 1910) comb. nov. EBrephallustramlapensis (Anisyutkin, 1999) comb. nov. F supra-anal plate of P.recurvataG supra-anal plate of Brephallustramlapensis (Anisyutkin, 1999) comb. nov. (Scale bars = 1 mm).
FIGURE 1 in Brasilisia n. gen. and Arraia n. gen., two new genera of Ocnerodrilidae (Annelida, Clitellata, Oligochaeta) from Eastern Amazonia, Brazil
FIGURE 1. Sampling location at Alcântara and Rosário counties in Maranhão state, Brazil.
Figure 3 from: Scheffrahn RH, Bourguignon T, Akama PD, Sillam-Dussès D, Šobotník J (2018) Roisinitermes ebogoensis gen. & sp. n., an outstanding drywood termite with snapping soldiers from Cameroon (Isoptera, Kalotermitidae). ZooKeys 787: 91-105. https://doi.org/10.3897/zookeys.787.28195
Figure 3 Brachypterous nymph of Roisinitermesebogoensis gen. & sp. n. Top: Dorsal view of mandibles. Bottom: lateral view of head and thorax.
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.