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952 results for “revised taxonomy”
FIGURE 15 in Haasea Verhoeff, 1895-a genus of tumultuous history and chaotic recordsredefinition, revision of taxonomy and geographic distributions, with descriptions of two new species from Austria and Serbia (Diplopoda, Chordeumatida, Haaseidae)
FIGURE 15. Haasea hungarica (Verhoeff, 1928) from Fruška gora Mt., Serbia. A. Male and female habitus, lateral view. B. Right anterior gonopod, mesal view. C. Right anterior gonopod, lateral view. Scale bars: 1 mm (A), 0.1 mm (B, C).
FIGURE 12 in Haasea Verhoeff, 1895-a genus of tumultuous history and chaotic recordsredefinition, revision of taxonomy and geographic distributions, with descriptions of two new species from Austria and Serbia (Diplopoda, Chordeumatida, Haaseidae)
FIGURE 12. Haasea fonticulorum (Verhoeff, 1910a), male from Tržič, Slovenia. A. Left anterior gonopod, mesal view. B. Left anterior gonopod, lateral view. C. Right posterior gonopod, mesal view. D. Right posterior gonopod, mesal view. E. Right posterior gonopod, posterior view. Abbreviations: a—angiocoxite; ab—anterior branch; asl—anterior sternal lobe; cp—coxal process; dp—distal part; mb—medial branch; mdl—mesodistal lobe; ml—"Opuntia-like" membranous lobe; mp—mesal process; pb—posterior branch; pc—papillated cone; pl—posterior lamella; plp—posterior lateral process; t—telopodite. Scale bars: 0.1 mm.
FIGURE 5 in Haasea Verhoeff, 1895-a genus of tumultuous history and chaotic recordsredefinition, revision of taxonomy and geographic distributions, with descriptions of two new species from Austria and Serbia (Diplopoda, Chordeumatida, Haaseidae)
FIGURE 5. Haasea cyanopida (Attems, 1903), male from Krumau, Kalbling-Sparafeld, Austria, left anterior gonopod. A. Mesal view. B. Lateral view. C. Posterolateral view. D. Postero-distomesal view. E. Distal view. F. Detail of distal part, distal view. G. Detail of distal part, posterolateral view. H. Detail of distal part, lateral view. Abbreviations: a—angiocoxite; alp—anterior lateral process; asl—anterior sternal lobe; dp—distal part; ml—"Opuntia-like" membranous lobe; mp—mesal process; pc—papillated cone; pl—posterior lamella; plp—posterior lateral process; s—sternum; so—seminal opening. Scale bars: 0.1 mm (A–E), 0.02 mm (F, G), 0.05 mm (H).
FIGURE 6 in Haasea Verhoeff, 1895-a genus of tumultuous history and chaotic recordsredefinition, revision of taxonomy and geographic distributions, with descriptions of two new species from Austria and Serbia (Diplopoda, Chordeumatida, Haaseidae)
FIGURE 6. Haasea faucium (Verhoeff, 1931a), lectotype male (ZSM-A20032155). A. Left anterior gonopod, lateral view. B. Right anterior gonopod, mesal view. C. Posterior gonopods. D. Microslide with dissected parts. Abbreviations: a—angiocoxite; ab—anterior branch; cp—coxal process; dp—distal part; mp—mesal process; msp—medial sternal process; pb—posterior branch; pc—papillated cone; pl1, pl1—posterior lamellae; plp—posterior lateral process; t—telopodite. Without scale. Photos credit: A–C. Ulla Biener-Miller, D. Roland Meier.
FIGURES 9–20 in Revision of Hestiasulini Giglio-Tos, 1915 stat. rev. (Insecta: Mantodea: Hymenopodidae) of Borneo, with description of new taxa and comments on the taxonomy of the tribe
FIGURES 9–20. Fore legs of Hestiasulini treated in this paper, anterior view. 9. A. phyllopus, male from the Malay Peninsula (ES). 10. A. phyllopus, male from Brunei, mirrored (CS). 11. A. phyllopus, female from Brunei (CS). 12. A. sarawaca, male from Brunei (CS). 13. P. borneana, holotype (SMNK). 14. H. brunneriana, male from Sri Lanka (CS). 15. H. brunneriana, female from Sri Lanka (CS). 16. A. sarawaca, female from Kalimantan; Photo C. J. Schwarz © RMNH (RMNH). 17. C. moultoni, male from Sarawak (CS). 18. C. moultoni, female from Brunei, mirrored (CS). 19. C. nitida, male from Myanmar (SMNK). 20. C. nitida, male from Sumatra (SMNK) (not to scale).
PLATE 23. Figures 1–6. Flax species, male genitalia. 1 in Revision of the Micronoctuidae (Lepidoptera: Noctuoidea). Part 4, Taxonomy of the subfamilies Tentaxinae and Micronoctuinae
PLATE 23. Figures 1–6. Flax species, male genitalia. 1, Flax lueneborgi, male holotype, slide 2954, Papua New Guinea, Bismarck Isl., Dyaul I.; 2, F. honeyi, male holotype, slide 3526, Solomon I., SE Santa Isabel I., Buala; 3, F. fulturai, male holotype, slide 1043 D.S. Fletcher, Solomon Is., Guadalcanal, Tapenanje; 4, F. fletcheri, male holotype, slide 1728, Solomon Is., Guadalcanal, Ilu Farm; 5, F. solomoni, male holotype, slide 3743, Solomon Is., NW Guadalcanal I., Honiara; 6, F. sanchristobali, male
PLATE 12. Figures 1–8 in Revision of the Micronoctuidae (Lepidoptera: Noctuoidea). Part 4, Taxonomy of the subfamilies Tentaxinae and Micronoctuinae
PLATE 12. Figures 1–8. Micronola, Micronoctua, Tolpia, and Bellulia species, adults. 1, 2, Micronola irani, 1, male holotype, and 2, male paratype, Iran SW, mts. 40 km E [Qasr-e-Shirin] Kasri-Shirin, Sar-e-Mill; 3, 4, 5, Micronoctua karsholti, 3, male holotype, Turkey, Prov. Antalya, 40 km N Alanya, 5 km S Gündogmus, 4, male, Israel, Jerusalem, Kastel, and 5, female Cyprus south, Garyllis river, 20 km north of Limassol; 6, Micronoctua karsholti, forewing and hindwing venation; 7, Tolpia kalimantania,
PLATE 22. Figures 1–6. Flax species, male genitalia. 1 in Revision of the Micronoctuidae (Lepidoptera: Noctuoidea). Part 4, Taxonomy of the subfamilies Tentaxinae and Micronoctuinae
PLATE 22. Figures 1–6. Flax species, male genitalia. 1, Flax kalliesi, male paratype, slide 3731, Australia, NT, Larrakeyah; 2, F. longus, male holotype, slide 5788, Philippines, Luzon, Los Banos; 3, F. semilongus, male holotype, slide 5805, Philippines, Palawan, 14 km W Puerto Princessa; 4, F. micronesia, male holotype, slide 5690, Micronesia, Palau, Babelthuap I.; 5, F. biaki, male holotype, slide 3905, Indonesia, Irian Jaya, Biak Island; 6, F. newirlandi, male holotype, slide 3071, Papua New Guinea,
PLATE 21. Figures 1–6. Flax species, male genitalia. 1 in Revision of the Micronoctuidae (Lepidoptera: Noctuoidea). Part 4, Taxonomy of the subfamilies Tentaxinae and Micronoctuinae
PLATE 21. Figures 1–6. Flax species, male genitalia. 1, Flax tempuensis, male holotype, slide 4538, Indonesia, Sumatra N, 20 km E Sipirok, Mt. Tampu Inanjing; 2, F. neptun, male, holotype, slide 3113, Indonesia, E Bali, Batoeriti; 3, F.brevipennis, male holotype, slide 4545, Indonesia, West Sumatra, 10 km E Rimbo Panti; 4, F. bibrevipennis, male holotype, slide 3737, Indonesia, West Malaysia, Sarawak, Semengoh Forest Reserve; 5, F. serami, male holotype, slide 3206, Indonesia, Seram; 6, F. kuchingi,
PLATE 3. Figures 1–8. Tentax species, adults. 1, 2 in Revision of the Micronoctuidae (Lepidoptera: Noctuoidea). Part 4, Taxonomy of the subfamilies Tentaxinae and Micronoctuinae
PLATE 3. Figures 1–8. Tentax species, adults. 1, 2, Tentax argentescens (Hampson, 1912), 1, male holotype Sri Lanka, Kandy and 2, female, Sri Lanka, Kan. District, Laksapana; 3, T. mini, male holotype, Sri Lanka, Amp. District, Inginiyagala; 4, T. vetus, female holotype, India SW, Nilgiri Hills; 5, 6, T. minima (Hampson, 1926), 5, male holotype, 6, female paratype, Indonesia, Sumbava; 7, T. makasi, male holotype, Indonesia, Sulawesi, Makassar; 8, T. brunnea, male holotype, N Vietnam, Fyan.
PLATE 10. Figures 1–8 in Revision of the Micronoctuidae (Lepidoptera: Noctuoidea) Part 3, Taxonomy of the Tactusinae
PLATE 10. Figures 1–8. Disca, Bellulia, and Duplex species, adults. 1, Disca anser, male paratype, Malaysia W, Selangor; 2. Bellulia kendricki, male holotype, China, Prov. Hainan, Yinggeling,; 3, B. basalia, male holotype, Vietnam N, Suoi Loc stream; 4, B. postea, female paratype, Vietnam N, Ben En Base Camp; 5, Duplex weintraubi, male holotype, East Timor, Cova-Lima District, Tilomar; 6. D. horakae, male holotype, Australia, Northern Territory, Cobourg Peninsula; 7, D. edwardsi, male holotype, Australia, Northern Territory, Mosquito Creak; 8, D. pullata, male paratype, Austra-
PLATE 3. A–D in Tribe Teruliini: new genera and new species of Neotropical leafhoppers with a revised key to genera and species, new records and notes on distribution and taxonomy (Hemiptera: Cicadellidae: Coelidiinae)
PLATE 3. A–D. Teruliini, dorsal habitus. (A) Stalolidia ecuadorensis, sp. nov., holotype; (B) Stalolidia semiovata, sp. nov., holotype; (C) Stalolidia lyrica, sp. nov., holotype; (D) Stalolidia clava, sp. nov., holotype.
PLATE 1. A–I in Tribe Teruliini: new genera and new species of Neotropical leafhoppers with a revised key to genera and species, new records and notes on distribution and taxonomy (Hemiptera: Cicadellidae: Coelidiinae)
PLATE 1. A–I. Teruliini, dorsal habitus. (A) Freytagolidia ligula, sp. nov., holotype; (B) Neodocalidia connectiva sp. nov., holotype; (C) Baluba sharkeyi, sp. nov., holotype; (D) Bolidiana robusta, sp. nov., holotype; (E) Bolidiana trisetacea, sp. nov., holotype; (F) Bolidiana elongata, sp. nov., holotype; (G) Harasupia lyrata, sp. nov., holotype; (H) Hastalidia acinaca, sp. nov., holotype; (I) Jalorpa constricta, sp. nov., holotype.
FIGURE 1 in Revision of the genus Symphytopria Kieffer (Hymenoptera, Diapriidae, Diapriinae) with notes on its taxonomy
FIGURE 1. Holotypes of Symphytopria fulva (A, B, D) and Symphytopria fusciceps (C, E, F): A, E—female in lateral view; C, D—female in dorsal view; B, F—labels. Scale bar: A, D—1 mm; E—0.5 mm.
Figure 2 in Revision of the higher taxonomy of Neotropical freshwater crabs of the family Pseudothelphusidae, based on multigene and morphological analyses
Figure 2. Tree with divergence estimates for nodes of the main groups of the Pseudothelphusoidea (numbers at the nodes represent millions of years before present), with 95% confidence intervals represented by the grey bars. Three fossil crabs were incorporated into the analysis: (1) Hillius youngi Bishop, 1983, from the lower Cretaceous; (2) Tanzanonautes tuerkai Feldmann et al., 2007 in the Potamonautidae, from the Paleogene of Tanzania; and (3) an undetermined Trichodactylidae from the late Middle Paleocene of Peru (Klaus et al., 2017).
Figure 6 in A revised taxonomy and phylogeny of opalinids (Stramenopiles: Opalinata) inferred from the analysis of complete nuclear ribosomal DNA genes
Figure 6. Cladogram showing the evolution of Opalinata* based on the proposed evolution of morphological traits (white circles; Delvinquier and Patterson 1993) and the characteristics of the rRNA genes (green circles). The relationships within Proteromonadida are not clear and are represented as a polytomy. Evolutionary steps are as follows. (1) Uninucleated cells develop cytoplasmic membranes with ridges or folds supported by a cortical cytoskeleton; few flagella* with a transitional helix in its structure; rRNA with secondary structure and GC content similar to that of outgroup taxons (i.e. Blastocystis). (2) Multiple flagella covering the cell surface; marginal falx. (3) Insertions made of short tandem repeats (STRs) in the expansion regions of rRNA; low GC in rRNA insertions and ITS1–ITS2 regions. (4) Binucleated (occasionally four-nucleated) cells. (5) Increase in number and length of rRNA insertions; very low GC content in rRNA insertions and ITS1–ITS2 regions. (6) Axial falx. (7) Multinucleate cells. (8) Partial loss of kineties. The position of Hegneriella* if valid* cannot be determined with available data.
FIGURE 16 in Taxonomy and DNA barcoding of the dark-winged fungus gnat genus Zygoneura Meigen (Diptera: Sciaridae) from China, with revision of the type materials
FIGURE 16. Zygoneura (Zygoneura) sciarina Meigen. A: head, frontal view; B: fourth antennal flagellomere; C: apex of foretibia, prolateral view; D: hypopygium, ventral view; E: wing, dorsal view.
FIGURE 5 in Taxonomy and DNA barcoding of the dark-winged fungus gnat genus Zygoneura Meigen (Diptera: Sciaridae) from China, with revision of the type materials
FIGURE 5. Zygoneura (Pharetratula) disparilis Zhang & Wu. i: slide, front side; ii: slide, flip side; A: habitus, lateral view; B: hypopygium, ventral view; C: fourth antennal flagellomere.
PLATE 15. Figures 1–6 in Revision of the Micronoctuidae (Lepidoptera: Noctuoidea). Part 1, Taxonomy of the Pollexinae
PLATE 15. Figures 1–6. Disca and Pollex subgenus Bilobiana species, male genitalia. 1, D. javai, slide 3907, Indonesia, Jawa W, Djakarta; 2, D. arborita, slide 4516, Indonesia, Sumatra W, Bukittinggi; 3, D. thailandi, slide 4994, Thailand, Mae Hong Son; 4, 5, Pollex (Bilobiana) laosi, slide 3321, 5, P. (B.) laosi, slide 3319, Laos, Prov. Wapi, Wapikhamthong;; 6, P. (B.) flavimacula, slide 5714, Indonesia, Sumatra, Prov. S. Ban.
Figure 1 in Revision shock in Pacific oysters taxonomy: the genus Magallana (formerly Crassostrea in part) is well-founded and necessary
Figure 1. Phylogeny of Ostreidae redrawn from Salvi & Mariottini (2017) derived from (A) mitochondrial DNA sequences (COI + 16S rRNA), (B) nuclear DNA sequences (ITS2 rRNA + 28S rRNA) and (C) combined mitochondrial and nuclear DNA sequences (16S rRNA + COI + ITS2 + 28S rRNAs). Hyotissa hyotis and Neopycnodonte cochlear (Gryphaeidae) were used as outgroup. Maximum likelihood trees are shown, with bootstrap values (≥ 70) reported above the main nodes and Bayesian posterior probabilities (≥ 0.90) reported below the nodes. For methodological details see Salvi & Mariottini (2017).
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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