Skip to main content
Powered by ShareScore

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.

4,753

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

4,753 results for “SHAPE”

Learn how ShareScore rates datasets ↗
zenodo40/100

Fig. 11 in A New Subfamily of Spiders with Grate-shaped Tapeta from Australia and Papua New Guinea (Araneae: Stiphidiidae: Borralinae)

Fig. 11. Jamberoo actensis. (a,b), male palp (holotype): a, ventral; b, retrolateral. (c–e), epigynum (KS60770): c, ventral; d, lateral; e, dorsal—internal genitalia. Scale lines 0.5 mm: upper, a,b; lower, c–e.

opencc-by-4.0Jun 2008View details →
zenodo40/100

Fig. 19 in A New Subfamily of Spiders with Grate-shaped Tapeta from Australia and Papua New Guinea (Araneae: Stiphidiidae: Borralinae)

Fig. 19. Asmea hayllari. (a,b), male palp (holotype): a, ventral; b, retrolateral. (c–f), epigynum (SAM BS1120): c, ventral; d, lateral; e, posterior; f, dorsal—internal genitalia. Scale lines 0.5 mm: upper, a,b; lower, c–f.

opencc-by-4.0Jun 2008View details →
zenodo40/100

Fig. 6 in A New Subfamily of Spiders with Grate-shaped Tapeta from Australia and Papua New Guinea (Araneae: Stiphidiidae: Borralinae)

Fig. 6. Couranga kioloa. (a,b), male palp (holotype): a, ventral; b, retrolateral. (c,d), epigynum: c, ventral (KS74064); d, dorsal—internal genitalia (KS69664). Scale lines 0.5 mm: upper, a,b; lower, c,d.

opencc-by-4.0Jun 2008View details →
zenodo40/100

Fig. 9 in A New Subfamily of Spiders with Grate-shaped Tapeta from Australia and Papua New Guinea (Araneae: Stiphidiidae: Borralinae)

Fig. 9. Jamberoo johnnoblei. (a,b), male palp: a, ventral (holotype); b, retrolateral (KS46335). (c–g), epigynum: c, ventral, d, lateral (KS84010); e,f, plugged and damaged (KS69656); e, ventral; f, lateral; g, dorsal—internal genitalia (KS69656). Scale lines 0.5 mm: upper lines, a,b; lower line, c–g.

opencc-by-4.0Jun 2008View details →
zenodo40/100

Fig. 16 in A New Subfamily of Spiders with Grate-shaped Tapeta from Australia and Papua New Guinea (Araneae: Stiphidiidae: Borralinae)

Fig. 16. Elleguna major. (a,b), male palp (holotype): a, ventral; b, retrolateral. (c–e), epigynum: c, ventral, fl = flange (KS57656); d, ventral, flanges broken (KS83624); e, dorsal—internal genitalia (KS83624). Scale lines 0.5 mm: upper, a,b; lower, c–e.

opencc-by-4.0Jun 2008View details →
zenodo40/100

Fig. 3. a–i in A New Subfamily of Spiders with Grate-shaped Tapeta from Australia and Papua New Guinea (Araneae: Stiphidiidae: Borralinae)

Fig. 3. a–i, Jamberoo johnnoblei (KS55724, female). (a–f), spinnerets: a, spinneret field and spiracle; b, cribellum; c, ALS (LHS); d, PMS (LHS); e, PLS (RHS); f, PLS, apical (RHS). (g–i), tarsal sensillae: g, hair types, ventral; h, tarsal organ; i, trichobothrium and cuticular sculpturing. (j,k), serrate accessory claw setae, tarsus I (arrows): j, J. johnnoblei (Mogo SF, NSW); k, Stiphidion facetum (KS53620).

opencc-by-4.0Jun 2008View details →
zenodo40/100

Fig. 10 in A New Subfamily of Spiders with Grate-shaped Tapeta from Australia and Papua New Guinea (Araneae: Stiphidiidae: Borralinae)

Fig. 10. Jamberoo boydensis. (a,b), male palp (holotype): a, ventral; b, retrolateral. (c–f), epigynum: c,d, ventral (KS34761, KS34759); e, lateral (KS34759); f, dorsal—internal genitalia (KS10256). Scale lines 0.5 mm: upper, a,b; lower, c–f.

opencc-by-4.0Jun 2008View details →
zenodo40/100

Fig. 4. a–g in A New Subfamily of Spiders with Grate-shaped Tapeta from Australia and Papua New Guinea (Araneae: Stiphidiidae: Borralinae)

Fig. 4. a–g, Jamberoo johnnoblei (Royal National Park, NSW): (a–e), body, subadult male; (f,g), eyes, female. a, carapace; b, sternum and mouthparts; c,d, abdomen, dorsal and ventral; e, spinnerets, ventral; f, eye group, anterior; g, PME tapetum. (h–j), Stiphidion facetum, female: h, eyes, left side; i, PME tapetum (Hornsby, NSW); j, PLE tapetum (Jenolan, NSW).

opencc-by-4.0Jun 2008View details →
zenodo40/100

Fig. 8 in A New Subfamily of Spiders with Grate-shaped Tapeta from Australia and Papua New Guinea (Araneae: Stiphidiidae: Borralinae)

Fig. 8. Distribution records: (a), Jamberoo spp.: J. johnnoblei, d; J. boydensis, h; J. actensis, p; J. australis, s. (b), Couranga spp.: C. kioloa, d; C. diehappy, h. (c), Karriella spp.: K. treenensis, N; K. walpolensis, s. (d), Elleguna spp.: E. major, n; E. minor, d. (e), Asmea spp.: A. akrikensis, p; A. hayllari, s; A. capella, h; A. mullerensis, N.

opencc-by-4.0Jun 2008View details →
zenodo40/100

Fig. 7 in A New Subfamily of Spiders with Grate-shaped Tapeta from Australia and Papua New Guinea (Araneae: Stiphidiidae: Borralinae)

Fig. 7. Couranga diehappy. (a,b), male palp (holotype): a, ventral; b, retrolateral. (c–e), epigynum: c, ventral (KS75360); d, ventral, with plug (KS58105); e, dorsal—internal genitalia (KS75366). Scale line 0.5 mm.

opencc-by-4.0Jun 2008View details →
zenodo40/100

Fig. 2. Male palps. a–d in A New Subfamily of Spiders with Grate-shaped Tapeta from Australia and Papua New Guinea (Araneae: Stiphidiidae: Borralinae)

Fig. 2. Male palps. a–d, Couranga kioloa (KS69663): (a), cymbium and bulb, ventral; (b), distal conductor and embolus (barb on subapical embolus arrowed); (c), tibia, retrolateral; (d), trichobothria on cymbium. (e–g), Karriella treenensis (KS14702): e, tibia, cymbium and bulb, ventral; f, conductor and bipartite median apophysis, proventral; g, RDTA, dorsal. (h,i), Jamberoo johnnoblei (KS8503): h, tibia, cymbium and bulb, ventral; i, bipartite MA processes, retrolateral.

opencc-by-4.0Jun 2008View details →
zenodo40/100

Figs. 9-11. Body shape and colour pattern. 9 in A new species of Cryptarcha (Coleoptera: Nitidulidae) from Madagascar

Figs. 9-11. Body shape and colour pattern. 9 – Cryptarcha jenisi sp. nov.; 10 – C. klugii Reitter, 1876; 11 – C. sicardi Grouvelle, 1906.

opencc-by-4.0Dec 2007View details →
zenodo40/100

Fig. 6 in Areas of endemism in Thailand: has historical partitioning between seasonally dry lowland and aseasonal moist mountain forests shaped biodiversity in Southeast Asia?

Fig. 6. Relationship between elevation and geographical range of Hybos spp. in Thailand. The number of 1° grids in which a species was recorded is plotted against the median elevation of all records. Line fitted by linear regression in PAST (r2=0.1026).

opencc-by-4.0Dec 2014View details →
zenodo40/100

Fig. 5 in Areas of endemism in Thailand: has historical partitioning between seasonally dry lowland and aseasonal moist mountain forests shaped biodiversity in Southeast Asia?

Fig. 5. EZPAE down-weighted against homoplasy, using altitudinally zoned mountain ranges as OGU, 'characters' made additive. Strict consensus tree of two equally parsimonious trees (CI = 0.716, RI = 0.534) produced by maximum parsimony analysis with weighted 'characters' and TBR branch swapping in TNT. Symmetrical resampling support is given under the nodes. Alphabetic codes of termini correspond with mountain ranges as abbreviated in Fig. 3; the suffixes 'low' & 'high' refer to low (<1,250m) and high (>1,250m) elevation sample data.

opencc-by-4.0Dec 2014View details →
zenodo40/100

Fig. 4 in Areas of endemism in Thailand: has historical partitioning between seasonally dry lowland and aseasonal moist mountain forests shaped biodiversity in Southeast Asia?

Fig. 4. EZPAE down-weighted against homoplasy, using altitudinally zoned mountain ranges as OGU, 'characters' made non-additive. Strict consensus tree of four equally parsimonious trees (CI = 0.674, 0.580) produced by maximum parsimony analysis with weighted 'characters' and TBR branch swapping in TNT. Symmetrical resampling support is given under the nodes. Alphabetic codes of termini correspond with mountain ranges as abbreviated in Fig. 3; the suffixes 'low' & 'high' refer to low (<1,250m) and high (>1,250m) sample data.

opencc-by-4.0Dec 2014View details →
zenodo40/100

Fig. 2. PAE using 1 in Areas of endemism in Thailand: has historical partitioning between seasonally dry lowland and aseasonal moist mountain forests shaped biodiversity in Southeast Asia?

Fig. 2. PAE using 1° grids as OGU. Strict consensus tree of 760 equally parsimonious trees (CI = 0.501, RI = 0.557) produced by maximum parsimony analysis with unweighted 'characters' and TBR branch swapping in TNT. Symmetrical resampling support is given under the nodes (see Fig 1A for explanation of alphabetic codes).

opencc-by-4.0Dec 2014View details →
zenodo40/100

Fig. 3 in Areas of endemism in Thailand: has historical partitioning between seasonally dry lowland and aseasonal moist mountain forests shaped biodiversity in Southeast Asia?

Fig. 3. PAE using mountain ranges as OGU. Strict consensus tree of nine equally parsimonious trees (CI = 0.745, RI = 0.722) produced by maximum parsimony analysis with weighted 'characters' and implicit enumeration in TNT. Symmetrical resampling support is given under the nodes. Abbreviations. – CM, Cardamom Mountains; DK, Dong Paya Yen – Khao Yai Forest Complex; DL, Daen Lao Range; LP, Luang Prabang Range; NST, Nakhon Si Thammarat Range; PM, Petchabun Mountains; PR, Phuket Range; PPR, Phu Pan Range; TH, Tenasserim Hills; TT, Thanon Thongchai Range. Grid-B and Grid-L refer to 1° grids (B and L in Fig. 1A) that were not assigned to any mountain range.

opencc-by-4.0Dec 2014View details →
zenodo40/100

Fig. 1 in Areas of endemism in Thailand: has historical partitioning between seasonally dry lowland and aseasonal moist mountain forests shaped biodiversity in Southeast Asia?

Fig. 1. Maps of Thailand showing: A, Grid of 1° of latitude and longitude denoted by single-letters A–W. Mountain ranges are indicated by two- or three letter codes (CD, DK, DL, LP, NST, PM, PPR, PR, TH & TT) and the grids that comprise each range are colour-coded. Grids B and L were not assigned to any mountain range; B, Species richness (number of species) of Hybos present in 1° grids; C, reciprocal weighted endemicity of Hybos spp. calculated for 1° grids.

opencc-by-4.0Dec 2014View details →
zenodo40/100

Text-fig. 54. Scanning electron microscope (SEM; a–e, g, h) and synchrotron x-ray microscopy (SRXTM; f, i) images of unnamed angiosperm fruits and seeds; Torres Vedras locality, Portugal. a) Follicle sp. 1, narrow elongate follicle with sessile and decurrent stigma; b) Follicle sp. 2, broad, dehisced follicle with elongate and transverse fibers lining the locule; c) Angiosperm seed sp. 1 with thin, smooth seed coat; d) Angiosperm seed sp. 2 with verrucate seed coat; e) Angiosperm seed sp. 3 with exotestal and foveolate seed coat; f) Angiosperm seed sp. 4 with smooth seed coat; g, h) Angiosperm seed sp. 5 with raised epidermal cells forming a reticulate pattern; i) Wedge-shaped angiosperm fruit with remains of floral parts near apex. Specimens, TV43-S136726 (a), TV44-S148144 (b), TV43-S170074 (c), TV43-S136747 (d), TV43-S170073 (e), TV38-S174615 (f), TV44-S148003 (g), TV44-S148004 (h), TV43-S174685 (i). Scale bars 300 Μm (a–i). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community

Text-fig. 54. Scanning electron microscope (SEM; a–e, g, h) and synchrotron x-ray microscopy (SRXTM; f, i) images of unnamed angiosperm fruits and seeds; Torres Vedras locality, Portugal. a) Follicle sp. 1, narrow elongate follicle with sessile and decurrent stigma; b) Follicle sp. 2, broad, dehisced follicle with elongate and transverse fibers lining the locule; c) Angiosperm seed sp. 1 with thin, smooth seed coat; d) Angiosperm seed sp. 2 with verrucate seed coat; e) Angiosperm seed sp. 3 with exotestal and foveolate seed coat; f) Angiosperm seed sp. 4 with smooth seed coat; g, h) Angiosperm seed sp. 5 with raised epidermal cells forming a reticulate pattern; i) Wedge-shaped angiosperm fruit with remains of floral parts near apex. Specimens, TV43-S136726 (a), TV44-S148144 (b), TV43-S170074 (c), TV43-S136747 (d), TV43-S170073 (e), TV38-S174615 (f), TV44-S148003 (g), TV44-S148004 (h), TV43-S174685 (i). Scale bars 300 Μm (a–i).

opencc-by-4.0Nov 2019View details →
zenodo40/100

Text-fig. 45. Scanning electron microscope (SEM) images of monocolpate pollen of Dinisia portugallica gen. et sp. nov. from a fragmentary stamen; Torres Vedras locality, Portugal. a) Holotype; stamen fragment showing elongated pollen sacs that yielded the pollen in this Text-figure; b) Two pollen grains showing poorly defined distal aperture (arrowhead) and distinctive vermiform reticulum forming luminae of variable shapes and sizes; note especially the irregularly and incomplete reticulum in the grain on the left; c) Reticulum showing smooth, vermiform muri attached to the smooth surface of the foot layer by long columellae; note that columellae often terminate segments of muri that are not closed; d, e) Pollen grains showing proximal surface (d), poorly defined distal aperture (e, arrowhead) and distinctive vermiform reticulum supported by long columellae; note dense covering of small, spherical orbicules on the inner surface of the anther wall. Specimen, TV44-S148216 (holotype). Scale bars 300 Μm (a), 6 Μm (b, d, e), 3 Μm (c). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community

Text-fig. 45. Scanning electron microscope (SEM) images of monocolpate pollen of Dinisia portugallica gen. et sp. nov. from a fragmentary stamen; Torres Vedras locality, Portugal. a) Holotype; stamen fragment showing elongated pollen sacs that yielded the pollen in this Text-figure; b) Two pollen grains showing poorly defined distal aperture (arrowhead) and distinctive vermiform reticulum forming luminae of variable shapes and sizes; note especially the irregularly and incomplete reticulum in the grain on the left; c) Reticulum showing smooth, vermiform muri attached to the smooth surface of the foot layer by long columellae; note that columellae often terminate segments of muri that are not closed; d, e) Pollen grains showing proximal surface (d), poorly defined distal aperture (e, arrowhead) and distinctive vermiform reticulum supported by long columellae; note dense covering of small, spherical orbicules on the inner surface of the anther wall. Specimen, TV44-S148216 (holotype). Scale bars 300 Μm (a), 6 Μm (b, d, e), 3 Μm (c).

opencc-by-4.0Nov 2019View details →

ScienceDex guides

Understand access before you commit

These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

Compare curated 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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

ScienceDex for faculty

Your academic CV and NIH biosketch

Make your CV in your school's format and your NIH biosketch from it, then download both as Word files.