Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
489
datasets available to search
ShareScore release 0.9.0
Dataset results
489 results for “TE”
Fig. 1. a in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 1. a, Hawksbill turtle (Eretmochelys imbricata) stranded in Alagoas, northeast Brazil. b, Amphipods (Hyachelia lowryi) associated to E. imbricata, arrow indicates H. lowryi specimens. c, Hyachelia lowryi Serejo and Sittrop, 2009 (ZUEC CRU 4385). d, Hyachelia tortugae Barnard, 1967 (ZUEC CRU 4386).
Fig. 6. Male right G1 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 6. Male right G1 from Minuca panema (Coelho, 1972) (A, B: MZUSP 20833) and M. burgersi (Holthuis, 1967) (C, D: UNI 719). a. apical flange, b. "thumb" or palp. Scale bar = 0.5 mm.
Fig. 8 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 8. Molecular phylogeny based on mitochondrial 16S and COI, as well as nuclear 28S for 19 species in the genus Minuca. The outgroups are Leptuca pugilator (Bosc, 1802) and Petruca panamensis (Stimpson, 1859).
Fig. 7 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 7. Female vulva in Minuca panema (Coelho, 1972) (A: MZUSP 20833) and M. burgersi (Holthuis, 1967) (B: UNI 719). Arrow indicates left gonopore. Scale bar = 1.0 mm.
Fig. 5. Male right G1 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 5. Male right G1 tip with setae from Minuca panema (Coelho, 1972) (A, B, C; MZUSP 20833) and M. burgersi (Holthuis, 1967) (D, E, F; UNI 719). A, D, posterior view, B, E, anterior view, C, F, lateral view of tip. a. terminal setae, b. terminal flange. Scale bar = 0.5 mm.
Fig. 4 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 4. Comparison of male major cheliped between Minuca panema (Coelho, 1972) (A, C; MZUSP 20833) and M. burgersi (Holthuis, 1967) (B, D; UNI 719). A, B: outer surface, C, D: inner surface. a. tubercle at distal end of pollex, b. sulcus at pollex-manus junction, c. lateral predactylar tubercle ridge, d. oblique palmar tubercle ridge, e. anterior of carpal cavity, f. tubercle field, g. medial predactylar ridge. Ruler with 1 mm divisions at upper edge of figure 5A, B.
Fig. 3 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 3. Minuca panema (Coelho, 1972) (ZMUSP 20833). A: Dorsal view. B: Lateral carapace view on side of minor cheliped. C: Outer surface of major cheliped. D: Inner surface of major cheliped. E: Second ambulatory leg. F: Oral view of carapace. a. eyebrow, b. postorbital sulcus, c. dental on suborbital margin, d. anterolateral angle, e. posterolateral line, f. posterolateral striae, g. pubescence, h. articulation ridge, i. pre-pollex depression, j. pollex, k. dactyl, l. superior carpal cavity carina, m. apex of oblique ridge, n. pre-dactyl ridge, o. articulation ridge, p. manus-pollex ridge, q. pubescence, r. setae. Scale bar = 10.0 mm.
Fig. 2 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 2. Geographical distribution of Minuca burgersi (Holthuis, 1967) (blue; distributed Bahamas, Curaçao, Barbados), M. aff. burgersi (green; distributed Florida, Virgin Islands, Belize) and M. panema (Coelho, 1972) (red; Atlantic coast of South America: Trinidad Island to Florianópolis, Santa Catarina, Brazil). Modified from Thurman et al. (2021).
Fig. 1. A in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 1. A: Minuca panema (Coelho, 1972) and B: Male Minuca burgersi (Holthuis, 1967). A: From the South Atlantic Ocean – Brazil, São Paulo state, Caraguatatuba, Praia da Enseada (23.726°S, 45.419°W) (ZMUSP 20835). B: From type location, Caribbean – The Netherlands Antilles, Curaçao, Westpunt, Grote Knip, salt pond (12.352°N, 69.15122°W) (UNI 721). Scale bar = 10 mm.
Fig. 4 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 4. Chromosomes of Corinnidae, Trachelidae, and Zodariidae (RTA Clade). Falconina sp. (Corinnidae) (A–E), Orthobula sp. (Trachelidae) (F–H) and Epicratinus sp. (Zodariidae) (I–L): A: Mitotic spermatogonial metaphase, 2nò = 28 telocentric chromosomes. B: Pachytene, 13II+X1X2. Sex chromosomes pair in parallel; they are positively heteropycnotic. C: Spermatocyte I, diplotene. Note 13 autosomal bivalents and two sex chromosome univalents (13II+X1X2). Sex chromosomes pair in parallel on the periphery of the plate. D: Metaphase II, n = 13 telocentric chromosomes. E. Metaphase II, n = 15 (13+X1X2), telocentric chromosomes. Sex chromosomes are associated and positively heteropycnotic. F. Mitotic spermatogonial metaphase, 2nò = 21. G: Mitotic oogonial metaphase, 2nñ = 22 telocentric chromosomes. H: Spermatocyte I, diplotene consisting of 10 autosomal bivalents and a sex chromosome univalent (10II+X). Sex chromosome is positively heteropycnotic. I: Mitotic oogonial metaphase, 2nñ = 44 telocentric chromosomes, except for the subtelocentric X1. J: Spermatocyte I, diplotene composed of 20 autosomal bivalents and two sex chromosome univalents (20II+X1X2). Sex chromosomes are associated in parallel. K: Metaphase II, n = 20 telocentric chromosomes. L. Metaphase II, n = 22 (20+X1X2). Arrowhead = bivalent with two chiasmata. Scale bars = 5 µm.
Fig. 1 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 1. Chromosomes of Oonopidae (Dysderoidea). Cinetomorpha simplex (A–C), Neotrops sp. (D–E) and Neoxyphinus termitophilus (F–G). A. Mitotic spermatogonial metaphase, 2nò = 9. B. Mitotic oogonial metaphase, 2nñ = 10. C. Spermatocyte I, metaphase I showing four autosomal bivalents and a sex chromosome univalent (4II+X). D. Mitotic spermatogonial metaphase, 2nò = 7. E–F. Mitotic oogonial metaphase, 2nñ = 8. G. Spermatocyte I, diplotene consisting of three autosomal bivalents and a sex chromosome univalent (3II+X). Scale bars = 5 µm.
Fig. 3 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 3. Chromosomes of Linyphiidae (A–D), Theridiidae (E–L) and Theridiosomatidae (Araneoidea). Agyneta sp. (A–D), Coleosoma floridanum (E–G), Thymoites sp.1 (H–J), Thymoites sp.2 (K–L) and Naatlo sp. (M-P): A: Mitotic spermatogonial metaphase composed of 24 telocentric chromosomes. B: Mitotic oogonial metaphase with 26 telocentric chromosomes. C: Spermatocyte I (early diplotene) with 11 autosomal bivalents and two positively heteropycnotic sex chromosome univalents arranged in parallel (11II+X1X2). D: Spermatocyte I (metaphase I) with 11 autosomal bivalents and two sex chromosome univalents (11II+X1X2). E, H: Mitotic spermatogonial metaphase, 2nò = 22 telocentric chromosomes. F, I, K: Mitotic oogonial metaphases, 2nñ = 24 telocentric chromosomes. G, J, L: Spermatocyte I, metaphase I (G, J) and early diplotene (L) consisting of 10 autosomal bivalents and two sex chromosome univalents (10II+X1X2). Sex chromosomes are positively heteropycnotic at J and L. While they are associated at G, they pair in parallel in J. Mode of pairing is unclear at L. M: Mitotic spermatogonial metaphase, 2nò = 30. N: Spermatocyte I, metaphase I. Note 14 autosomal bivalents and two sex chromosome univalents (14II+X1X2). O: Metaphase II, n = 14. P: Metaphase II, n = 16 (14+X1X2). Sex chromosomes are positively heteropycnotic. Arrowhead = bivalent with two chiasmata. Scale bars = 5 µm.
Fig. 2 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 2. Mitotic oogonial metaphase of Otiothops birabeni (Palpimanidae), 2nñ = 36. Scale bar = 5 µm.
Fig. 3. Haplotype networks for A. oahuensis. Panels correspond with the 12S in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 3. Haplotype networks for A. oahuensis. Panels correspond with the 12S rDNA gene (Panel A), 16S rDNA gene (Panel B), COI (Panel C), and H3A (Panel D). Colors and locality IDs correspond with those used in all other Figures. Black circles represent unsampled (i.e., missing) haplotypes, with the size of circles proportional to the frequency at which each haplotype was recovered.
Fig. 1 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 1. Map of localities included in this study. M01-Wanead, Yap, Federated States of Micronesia; M02-Las Cabanas Beach, Palawan, Philippines; P01-Baby Beach, Maui, HI, USA; P02-Waiʻānapanapa, Maui, HI, USA; P03-Koki Beach Park, Maui, HI, USA; P04-Hanakaoʻo Park, Maui, HI, USA; P05-Kihei, Maui, HI USA; P06-Kapalaoa Beach, Oʻahu, HI, USA; P07-Pūpūkea Beach Park, Oʻahu, HI, USA; P08-Spencer Beach Park, Hawaiʻi, HI, USA; P09-Nāpoʻopoʻo Park, Hawaiʻi, HI, USA; P10-Blue Pango, Efate, Vanuatu; P11-Pele Island, Vanuatu; P12-Champagne Beach, Espiritu Santo, Vanuatu; P13-Opunohu bay, Moorea, Tahiti, French Polynesia; P14-Upolu, Samoa; P15-The Beachhouse, Viti Levu, Fiji. Colors, shapes, and labels for each locality correspond with other figures and tables. Detailed information for each locality is presented in table 1. Map is edited from a map in the public domain in Wikimedia Commons at https://commons.wikimedia.org/wiki/File:Pacific_Theater_Areas;map1.svg.
Fig. 2 in Tuerkayana latens Ng and Hsi-Te Shih 2023, n. sp.
Fig. 2. Neighbor-Joining trees produced in this study. Panel A represents a Neighbor-Joining tree of A. oahuensis and A. balssi based on COI mitochondrial sequences, while Panel B shows the Neighbor-Joining tree of A. oahuensis based on concatenated dataset including the four genes used in this study. Locality IDs, colors, and shapes correspond with those used in all other Figures, Tables, and Datasets. Bootstrap support values are provided for each major lineage recovered in analyses.
Linked collectors and determiners for: WELT Herbarium at Museum of New Zealand Te Papa Tongarewa.
Natural history specimen data linked to collectors and determiners held within, "WELT Herbarium at Museum of New Zealand Te Papa Tongarewa". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/cafff6a5-1fa4-4a90-a2b3-f3db78b93d02">https://bionomia.net/dataset/cafff6a5-1fa4-4a90-a2b3-f3db78b93d02</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/cafff6a5-1fa4-4a90-a2b3-f3db78b93d02">https://gbif.org/dataset/cafff6a5-1fa4-4a90-a2b3-f3db78b93d02</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: A new species of Naultinus from the Te Paki area, northern New Zealand.
Natural history specimen data linked to collectors and determiners held within, "A new species of Naultinus from the Te Paki area, northern New Zealand". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/9213ee25-a9f3-49f6-bf72-8cb456c14b03">https://bionomia.net/dataset/9213ee25-a9f3-49f6-bf72-8cb456c14b03</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/9213ee25-a9f3-49f6-bf72-8cb456c14b03">https://gbif.org/dataset/9213ee25-a9f3-49f6-bf72-8cb456c14b03</a>. Formatted as a Frictionless Data package.
FIGS. 56–66 in Te Goblin Spider Genus Aprusia Simon, 1893 (Araneae: Oonopidae)
FIGS. 56–66. Morphology of the tarsi of Aprusia spp. 56–61, A. kerala, male, 62, A. kataragama, male; 63, A. kataragama, female; 64, A. vestigator, male; 65, A. vestigator, female; 66, A. veddah, female; 56 = tarsus I, 57 = II, 58, 65 = III, 59–63, 66 = IV. 61 = detail of the clawlike seta. Arrows = clawlike setae. Scale bars: 56–59, 62–66 = 0.05 mm; 60 = 20 µm; 61 = 10 µm.
FIGS. 53–55 in Te Goblin Spider Genus Aprusia Simon, 1893 (Araneae: Oonopidae)
FIGS. 53–55. Aprusia kerala, new species, male holotype (PBI_OON 12360), left palp. 53, prolateral, 54, ventral, 55, detail of the distal part of the bulb. Abbreviations: c = conductor, e = embolus, arrow = conical projection.
ScienceDex guides
Understand access before you commit
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.