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Figure 75 from: Schmidt BC (2015) Revision of the Lacinipolia vicina (Grote) complex (Noctuidae, Noctuinae, Eriopygini). In: Schmidt BC, Lafontaine JD (Eds) Contributions to the systematics of New World macro-moths VI. ZooKeys 527: 103-126. https://doi.org/10.3897/zookeys.527.9686
Figure 75 - Neighbour-joining tree of representative mtDNA barcode haplotypes in species of the Lacinipolia vicina group. Sample size and locality are given in brackets, with number of specimens indicated after two-letter state/province abbreviation. Lacinipolia sareta variation is divided into five haplogroups, A–E. Voucher specimen data is given in Suppl. material 1.
Figures 7-13 from: Lee C-F, Bezděk J (2015) Revision of "Phyllobrotica" from Taiwan with description of Jolibrotica gen. n. (Coleoptera, Chrysomelidae, Galerucinae). In: Jolivet P, Santiago-Blay J, Schmitt M (Eds) Research on Chrysomelidae 5. ZooKeys 547: 75-92. https://doi.org/10.3897/zookeys.547.9381
Figures 7-13 - Jolibrotica sauteri. 7 Antenna male 8 Antenna, female 9 Penis, dorsal view 10 Penis, lateral view 11 Gonocoxae 12 Ventrite VIII 13 Spermatheca.
Figures 33-39 from: Lee C-F, Bezděk J (2015) Revision of "Phyllobrotica" from Taiwan with description of Jolibrotica gen. n. (Coleoptera, Chrysomelidae, Galerucinae). In: Jolivet P, Santiago-Blay J, Schmitt M (Eds) Research on Chrysomelidae 5. ZooKeys 547: 75-92. https://doi.org/10.3897/zookeys.547.9381
Figures 33-39 - Haplosomoides shirozui. 33 Antenna male 34 Antenna, female 35 Penis, dorsal view 36 Penis, lateral view 37 Gonocoxae 38 Ventrite VIII 39 Spermatheca.
Figures 1-6 from: Lee C-F, Bezděk J (2015) Revision of "Phyllobrotica" from Taiwan with description of Jolibrotica gen. n. (Coleoptera, Chrysomelidae, Galerucinae). In: Jolivet P, Santiago-Blay J, Schmitt M (Eds) Research on Chrysomelidae 5. ZooKeys 547: 75-92. https://doi.org/10.3897/zookeys.547.9381
Figures 1-6 - Habitus of Jolibrotica sauteri. 1 Male, dorsal view 2 ditto, ventral view 3 ditto, lateral view 4 Female, dorsal view 5 ditto, ventral view 6 ditto, lateral view.
Figures 23-29 from: Lee C-F, Bezděk J (2015) Revision of "Phyllobrotica" from Taiwan with description of Jolibrotica gen. n. (Coleoptera, Chrysomelidae, Galerucinae). In: Jolivet P, Santiago-Blay J, Schmitt M (Eds) Research on Chrysomelidae 5. ZooKeys 547: 75-92. https://doi.org/10.3897/zookeys.547.9381
Figures 23-29 - Jolibrotica chujoi. 23 Antenna male 24 Antenna, female 25 Penis, dorsal view 26 Penis, lateral view 27 Gonocoxae 28 Ventrite VIII 29 Spermatheca.
Figures 30-32 from: Lee C-F, Bezděk J (2015) Revision of "Phyllobrotica" from Taiwan with description of Jolibrotica gen. n. (Coleoptera, Chrysomelidae, Galerucinae). In: Jolivet P, Santiago-Blay J, Schmitt M (Eds) Research on Chrysomelidae 5. ZooKeys 547: 75-92. https://doi.org/10.3897/zookeys.547.9381
Figures 30-32 - Habitus of Haplosomoides shirozui, male. 30 Dorsal view 31 Ventral view 32 Lateral view.
Figure 2 from: Vásquez-Ordóñez AA, Hazzi NA, Escobar-Prieto JD, Paz-Jojoa D, Parsa S (2015) A geographic distribution database of the Neotropical cassava whitefly complex (Hemiptera, Aleyrodidae) and their associated parasitoids and hyperparasitoids (Hymenoptera). ZooKeys 545: 75-87. https://doi.org/10.3897/zookeys.545.6193
Figure 2 - Geographic distributions of Neotropical cassava whitefly species (maps on the left) and their associated parasitoid species (maps on the right) in the CIAT's Arthropod Reference Collection database.
Figure 1 from: Vásquez-Ordóñez AA, Hazzi NA, Escobar-Prieto JD, Paz-Jojoa D, Parsa S (2015) A geographic distribution database of the Neotropical cassava whitefly complex (Hemiptera, Aleyrodidae) and their associated parasitoids and hyperparasitoids (Hymenoptera). ZooKeys 545: 75-87. https://doi.org/10.3897/zookeys.545.6193
Figure 1 - Percentage of occurrence records by Neotropical whitefly species (A), by parasitoids (B) and by country origin (C) in the CIAT's Arthropod Reference Collection database (N=1,311).
Figure 3 from: García-Ruiz I, Valentín-Martínez D, Carrillo-Reyes P, Costea M (2016) Taxonomic and floristic novelties for Echeveria (Crassulaceae) in Central Michoacan, Mexico. PhytoKeys 75: 1-12. https://doi.org/10.3897/phytokeys.75.9198
Figure 3 - Echeveria yalmanantlensis in the new habitat from Michoacan. A General habitat view of young epiphytic plants B–D Leaf rosettes and developing plants E Inflorescence.
Figure 2 from: García-Ruiz I, Valentín-Martínez D, Carrillo-Reyes P, Costea M (2016) Taxonomic and floristic novelties for Echeveria (Crassulaceae) in Central Michoacan, Mexico. PhytoKeys 75: 1-12. https://doi.org/10.3897/phytokeys.75.9198
Figure 2 - Scanning electron microscopy of Echeveria coruana, pollen and seed (García & García 9138). A–C Heteromorphic pollen grains; arrows indicate a few 3-colpate, prolate pollen grains B 4-colpate (left, upper) and 3-colpate pollen (right, down) grains C 3-colpate, prolate pollen grain D–E Seed morphology.
Figure 1 from: García-Ruiz I, Valentín-Martínez D, Carrillo-Reyes P, Costea M (2016) Taxonomic and floristic novelties for Echeveria (Crassulaceae) in Central Michoacan, Mexico. PhytoKeys 75: 1-12. https://doi.org/10.3897/phytokeys.75.9198
Figure 1 - Habitat and general morphology of Echeveria coruana. A Habitat B Leaf rosette of type specimen C Developing plant (in cultivation) D–F Inflorescence D General view E Developing cincinus F Terminal cincinni G–H Flowers of type specimen viewed in the field from different angles I–J Flowers from type specimen fixed in FAA I Dissected flower (removed corolla) to show stamen bases and nectaries. J Conical appendages at the base of antipetalous staminal filaments (indicated with black arrows). Scale bars 1 mm.
Figure 75 from: Moore MR, Jameson ML, Garner BH, Audibert C, Smith ABT, Seidel M (2017) Synopsis of the pelidnotine scarabs (Coleoptera: Scarabaeidae: Rutelinae: Rutelini) and annotated catalog of the species and subspecies. ZooKeys 666: 1-349. https://doi.org/10.3897/zookeys.666.9191
Figure 75 - Pelidnota (Ganonota) matogrossensis Frey (valid name Pelidnota matogrossensis Frey) paratype male from ZMHB. A Dorsal habitus B Lateral habitus C Male genitalia, lateral view D Male parameres, dorsal view.
Figures 5-7 from: Lourenço WR (2016) A preliminary synopsis on amber scorpions with special reference to Burmite species: an extraordinary development of our knowledge in only 20 years. ZooKeys 600: 75-87. https://doi.org/10.3897/zookeys.600.8913
Figures 5-7 - Betaburmesebuthus bellus sp. n. Male holotype. 5 Chelicera, carapace and tergites I-III, dorsal aspect 6 Sternites V-VII showing carinae and spiracles and metasomal segments I-V and telson, ventro-lateral aspect 7 Ventral aspect, showing Coxapophysis, sternum, genital operculum, pectines and sternites with spiracles. Scale bars: 0.5 mm.
Figures 1-4 from: Lourenço WR (2016) A preliminary synopsis on amber scorpions with special reference to Burmite species: an extraordinary development of our knowledge in only 20 years. ZooKeys 600: 75-87. https://doi.org/10.3897/zookeys.600.8913
Figures 1-4 - Betaburmesebuthus bellus sp. n. Male holotype. 1–2 Habitus, dorsal and ventral aspects 3 Ventral aspect in detail, showing sternum, genital operculum and pectines 4 Tergites VI-VII, metasomal segments and telson, dorso-lateral aspect.
Figures 8-9 from: Lourenço WR (2016) A preliminary synopsis on amber scorpions with special reference to Burmite species: an extraordinary development of our knowledge in only 20 years. ZooKeys 600: 75-87. https://doi.org/10.3897/zookeys.600.8913
Figures 8-9 - Betaburmesebuthus bellus sp. n. Male holotype. Righ pedipalp, dorsal and ventral aspects, showing trichobothrial pattern. Dorsal aspect is partially covered by an inclusion. Scale bar: 0.5 mm.
Figure 75 from: Lin Y, Ballarin F, Li S (2016) A survey of the spider family Nesticidae (Arachnida, Araneae) in Asia and Madagascar, with the description of forty-three new species. ZooKeys 627: 1-168. https://doi.org/10.3897/zookeys.627.8629
Figure 75 - Pseudonesticus spinosus sp. n., holotype (male) and paratype (female). A Male habitus, dorsal view B Ditto, ventral view C Female habitus, dorsal view D Ditto, ventral view E Epigyne, ventral view F Ditto, lateral view G Vulva, dorsal view H Vulva, posterior view. Scale bars: A–D = 0.50 mm; E–H = 0.10 mm.
Figure 75 from: Breure ASH, Mogollón Avila V (2016) Synopsis of Central Andean Orthalicoid land snails (Gastropoda, Stylommatophora), excluding Bulimulidae. ZooKeys 588: 1-199. https://doi.org/10.3897/zookeys.588.7906
Figure 75 - Sultana species. A–C Sultana (Metorthalicus) shuttleworthi (Albers, 1854), syntype ZMB 101827 (H = 70.3) D–F Sultana (Metorthalicus) wrzesniowskii (Lubomirski, 1880), holotype MIZW (H = 78.0).
Figure 1 from: Senwanna C, Hyde KD, Phookamsak R, Jones EBG, Cheewangkoon R (2018) Coryneum heveanum sp. nov. (Coryneaceae, Diaporthales) on twigs of Para rubber in Thailand. MycoKeys 43: 75-90. https://doi.org/10.3897/mycokeys.43.29365
Figure 1 Maximum likelihood (RAxML) based on analysis of a combined dataset of LSU, ITS and TEF1 sequence data representing Diaporthales. Bootstrap support values for maximum likelihood (ML, left), maximum parsimony (MP, middle) greater than 70% and Bayesian posterior probabilities (BY, right) equal to or greater than 0.95 are indicated at the nodes. The tree is rooted to Phaeoacremoniumaleophilum (CBS 63194) and P.vibratile (CBS 117115). The newly generated sequences are in blue. The strains from generic type species are in black bold.
Figure 2 from: Senwanna C, Hyde KD, Phookamsak R, Jones EBG, Cheewangkoon R (2018) Coryneum heveanum sp. nov. (Coryneaceae, Diaporthales) on twigs of Para rubber in Thailand. MycoKeys 43: 75-90. https://doi.org/10.3897/mycokeys.43.29365
Figure 2 Coryneumheveanum (MFLU 18-0936). a−d Conidiomata on host surface e−f Acervuli g Conidiogenesis (annellidic; red arrow, proliferation; blue arrow) h−j Conidiophores, conidiogeneous cells with conidia k Conidia l Germinated spores m−p Appressoria q−r Mass of conidia on PDA after 6 months s Mycelium on PDA after 6 months. Scale bars: 5 mm (a), 1000 µm (b), 200 µm (c, d, r), 100 µm (e, f, q), 20 µm (g−k), 50 µm (l, s), 5 µm (m−p).
Figures 75–76 in Reanalysis of the Yunnan population of Scorpiops kubani with a description of a new species, Scorpiops lowei sp. n. (Scorpiones: Scorpiopidae)
Figures 75–76: Scorpiops lowei sp. n., in vivo habitus, under white light. Figure 75. Scorpiops lowei sp. n., male holotype. Figure 76. Scorpiops lowei sp. n., female paratype.
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)
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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.
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.