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.
29,350
datasets available to search
ShareScore release 0.9.0
Dataset results
29,350 results for “new records”
Fig. 5. 3D in A new beaked whale record from the upper Miocene of Menorca, Balearic Islands, based on CT-scan analysis of limestone slabs
Fig. 5. 3D reconstruction resulting from the CT-scan of the ziphiid cetacean Messapicetus cf. longirostris Bianucci, Landini, and Varola, 1992 skull (MDM- 2029) inside two limestone slabs from the Tortonian of Menorca (Balearic Islands, Spain); in ventral view (A1), ventral view without the mandibles (A2).
Fig. 11 in A new beaked whale record from the upper Miocene of Menorca, Balearic Islands, based on CT-scan analysis of limestone slabs
Fig. 11. Geographic distribution of fossil remains of Messapicetus from upper Miocene deposits worldwide (see text for data sources).
Fig. 5 in The first record of the ichthyodectiform fish Cladocyclus from eastern Gondwana: A new species from the Lower Cretaceous of Queensland, Australia
Fig. 5. Ichthyodectiform fish Cladocyclus geddesi sp. nov. (QM F44329) from near Isisford, central-western Queensland, Australia; Lower Cretaceous (upper Albian) strata of the Winton Formation, area of articulation for the lower jaw. Photograph (A) and interpretive drawing (B). Hatched area indicates broken bone.
Fig. 1 in The first record of the ichthyodectiform fish Cladocyclus from eastern Gondwana: A new species from the Lower Cretaceous of Queensland, Australia
Fig. 1. Map showing the discovery site of Cladocyclus geddesi sp. nov. (QM F44329) near the town of Isisford, central-western Queensland, Australia. Gray area indicates the extent of the upper Albian–lower Turonian Winton Formation.
Fig. 6 in The first record of the ichthyodectiform fish Cladocyclus from eastern Gondwana: A new species from the Lower Cretaceous of Queensland, Australia
Fig. 6. Projection of the hyomandibular facet and angle of the parasphenoid in three ichthyodectiform fishes. A. Cladocyclus gardneri Agassiz, 1841 based on AMNH 19129). B. Aidachar pankowskii (Forey and Cavin, 2007) (after Forey and Cavin 2007: fig. 4). C. Ichthyodectes ctenodon Cope, 1871 after Badack 1965: 14). Also, note differences in proportions of the skull in these ichthyodectiforms. QM F44329 (Cladocyclus geddesi sp. nov.) has the same angle of the parasphenoid as Cladocyclus gardneri.
Fig. 4 in The first record of the ichthyodectiform fish Cladocyclus from eastern Gondwana: A new species from the Lower Cretaceous of Queensland, Australia
Fig. 4. Ichthyodectiform fish Cladocyclus geddesi sp. nov. (QM F44329) from near Isisford, central-western Queensland, Australia; Lower Cretaceous upper Albian) strata of the Winton Formation, braincase in dorsolateral view. Photograph (A) and interpretive drawing (B).
Fig. 3 in The first record of the ichthyodectiform fish Cladocyclus from eastern Gondwana: A new species from the Lower Cretaceous of Queensland, Australia
Fig. 3. Ichthyodectiform fish Cladocyclus geddesi sp. nov. (QM F44329) from near Isisford, central-western Queensland, Australia; Lower Cretaceous (upper Albian) strata of the Winton Formation, in lateral view. Photograph (A) and interpretive drawing (B).
Fig. 7 in The first record of the ichthyodectiform fish Cladocyclus from eastern Gondwana: A new species from the Lower Cretaceous of Queensland, Australia
Fig. 7. Outlines of various ichthyodectiform pectoral girdle (cleithrum, coracoid, and scapular) arrangements in lateral external view. A. Allothrissops mesogaster (Agassiz, 1843) (redrawn from Patterson and Rosen 1977: fig. 10). B. Thrissops formosus Agassiz, 1833 (redrawn from Taverne 1977: fig. 5). C. Unamichthys espinosai Alvarado-Ortega, 2004 (IGM 8373). D. Cladocyclus geddesi sp. nov. (QM F44329). E. Cladocyclus gardneri Agassiz, 1841 (AMNH 11877). F. Vallecillichthys multivertebratum Blanco and Cavin, 2003 (redrawn from Blanco-Piñón 2003: fig. 9.2).
Fig. 8 in The first record of the ichthyodectiform fish Cladocyclus from eastern Gondwana: A new species from the Lower Cretaceous of Queensland, Australia
Fig. 8. Phylogenetic relationships of Cladocyclus geddesi sp. nov. (QM F44329). Stratigraphically calibrated strict consensus of 3 most-parsimonious trees (length 223, CI 0.45, RI, 0.67) analysed using T.N.T. 1.1 (Goloboff et al. 2003), with a heuristic search (1000 replicates in "Traditional search" with TBR branch swapping). See Appendix 1 for new character descriptions, taxon-character matrix, and a list of character state transformation for each taxon. Age ranges correspond to those provided in Cavin et al. (2013).
Fig. 8. Sauropod ichnites with well preserved morphologies from the general track record. A–I in New sauropod trackways from the Middle Jurassic of Portugal
Fig. 8. Sauropod ichnites with well preserved morphologies from the general track record. A–I. sauropod manus prints (redrawn from Dalla Vecchia and Tarlao 2000). A. Polyonyx gomesi igen. et isp. nov. from the Middle Jurassic of Portugal. B. Polyonyx isp. from the Middle Jurassic of Portugal. C. left manus print of a quadrupedal dinosaur from the Upper Jurassic of Portugal. D. Unnamed print from the Lower Cretaceous of Italy. E. Titanosaurimanus nana from the Early Cretaceous of Croatia. F. Brontopodus birdi from the Lower Cretaceous of USA. G. Unnamed print from the Upper Cretaceous of Bolivia. H. Breviparopus taghbaloutensis from the Middle Jurassic of Morocco. I. Parabrontopodus mcintoshi from the Upper Jurassic of USA. J–N. Sauropod pes prints. J. Breviparopus taghbaloutensis from the Middle Jurassic of Morocco. K. Polyonyx gomesi igen. et isp. nov. from the Middle Jurassic of Portugal. L. Brontopodus birdi from the Lower Cretaceous of USA. M. Brontopodus aff. B. birdi from the Upper Jurassic of Portugal. N. Unnamed print from the Upper Jurassic of Asturias, Spain. A, B, K, after Santos et al. (1994); C, after Santos et al. (1995), Santos (2003); D, after Dalla Vecchia 1999; E, after Dalla Vecchia and Tarlao 2000; F, L, after Farlow at al. (1989); G, after Lockley et al. (2002); H, J, after Dutuit and Ouazzou (1980), Ishigaki (1989); I, after Lockley et al. 1994a; M, after Meyer et al. 1994, Santos 2003; N, after Lires 2000.
Fig. 9 in New fossil triakid sharks from the early Eocene of Prémontré, France, and comments on fossil record of the family
Fig. 9. Distribution of living triakid genera (areas) and their fossil relatives (geometric symbols) compiled from the literature. The number of symbols (plotting the fossil evidence) is intentionally reduced for western Europe and southeastern USA. Living Mustelus is circumglobal in all temperate and tropical seas and is not figured on the map.
Fig. 1. A in New fossil triakid sharks from the early Eocene of Prémontré, France, and comments on fossil record of the family
Fig. 1. A. Location of the Prémontré Abbey (Aisne, northern France). B. Simplified stratigraphic column of Prémontré with fossiliferous (2–3) and non−fossiliferous (4–12) levels (from Dégrémont et al. 1985: 12).
Fig. 5. Triakid shark Gomphogaleus rodgersi Case, 1994 in New fossil triakid sharks from the early Eocene of Prémontré, France, and comments on fossil record of the family
Fig. 5. Triakid shark Gomphogaleus rodgersi Case, 1994. Prémontré Abbey, late Ypresian. A. UM−PRE 16, anterior tooth, labial face (A1), profile view (A2), and lingual face (A3). B. UM−PRE 17, holotype, antero−lateral tooth, labial face (B1), apical view (B2), and lingual face (B3).
Fig. 7 in New fossil triakid sharks from the early Eocene of Prémontré, France, and comments on fossil record of the family
Fig. 7. Triakid shark Pachygaleus lefevrei (Daimeries, 1891). Prémontré Abbey, late Ypresian. A. UM−PRE 19, anterior tooth, labial face. B. UM−PRE 20, antero−lateral tooth, labial face. C. UM−PRE 21, lateral tooth, labial (C1) and lingual (C2) faces.
Fig. 8 in New fossil triakid sharks from the early Eocene of Prémontré, France, and comments on fossil record of the family
Fig. 8. Fossil record of triakid genera plotted against simplified phylogenetic relationships of extant Triakidae (from Lopez et al. 2006 in part). See text and Appendix 2 for discussion and details.
Fig. 6. Triakid shark Mustelus aff. M. vanderhoefti Herman, 1982 in New fossil triakid sharks from the early Eocene of Prémontré, France, and comments on fossil record of the family
Fig. 6. Triakid shark Mustelus aff. M. vanderhoefti Herman, 1982. Prémontré Abbey, late Ypresian. UM−PRE 18, lateral tooth, lingual face (A), profile view (B), occlusal face (C), and basal face (D).
Fig. 4 in New fossil triakid sharks from the early Eocene of Prémontré, France, and comments on fossil record of the family
Fig. 4. Triakid shark Galeorhinus louisi sp. nov. Prémontré Abbey, late Ypresian. A. UM−PRE 11, holotype, antero−lateral tooth, labial face (A1), apical view (A2), and lingual face (A3). B. UM−PRE 12, antero−lateral tooth, labial face (B1), profile view (B2), and lingual face (B3). C. UM−PRE 13, lateral tooth, labial (C1) and lingual (C2) faces. D. UM−PRE 14, lateral tooth, labial (D1) and lingual (D2) faces. E. UM−PRE 15, more lateral tooth, labial (E1) and lingual (E2) faces.
Fig. 3 in New fossil triakid sharks from the early Eocene of Prémontré, France, and comments on fossil record of the family
Fig. 3. Triakid shark Galeorhinus ypresiensis (Casier, 1946). Forest−lez−Bruxelles, Belgique. A. UM−FLB 1, anterior tooth, lingual face. B. UM−FLB 2, anterior tooth, labial (B1) and lingual (B2) faces. C. UM−FLB 3, anterior tooth, labial (C1) and lingual (C2) faces.
Figure 7 in YELLOW WATER LILIES (NUPHAR, NYMPHAEACEAE) IN GREAT BRITAIN: A NEW HYBRID, A REAPPRAISAL OF RECORDS, AND A REVISED STATUS OF N. ADVENA
Figure 7. Sepals of: A, Nuphar advena from NA1 population, Spottiswoode Loch; B, Nuphar × porphyranthera from NH8 population, Oulten Park (left), and NH2 population, Godstone (right); C, N. lutea (no population code), Norbotten, Sweden. Scale bars are approximate (no measurements of the photographed features were taken). Photographs: R. V. Lansdown.
Figure 6. A in YELLOW WATER LILIES (NUPHAR, NYMPHAEACEAE) IN GREAT BRITAIN: A NEW HYBRID, A REAPPRAISAL OF RECORDS, AND A REVISED STATUS OF N. ADVENA
Figure 6. A, Petiole shape of Nuphar advena from NA1 population, Spottiswoode Loch. B, Petiole shape of Nuphar × porphyranthera from NH8 population, Oulten Park (left); NH6 population, Shropham Ponds (centre); and NH1 population, West Hoathly (right). C, Petiole shape of Nuphar lutea (no population code), Elterwater. Scale bars are approximate (no measurements of the photographed features were taken). Photographs: R. V. Lansdown.
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.