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Text-fig. 3. Occurrence of P1 in maxillae from Deninger bears and cave bears, data after Table 1 (presence = P1 or alveoli observed, absence = no P1 developed, broken = rostral part of maxilla broken). in Anterior Premolar Variability In Pleistocene Cave And Brown Bears And Its Significance In Species Determination
Text-fig. 3. Occurrence of P1 in maxillae from Deninger bears and cave bears, data after Table 1 (presence = P1 or alveoli observed, absence = no P1 developed, broken = rostral part of maxilla broken).
Text-fig. 7. Occurrence of p1 in mandibles from Deninger bears and cave bears, data after Table 3 (presence = p1 or alveoli observed, absence = no p1 developed, broken = diastema fragmented). in Anterior Premolar Variability In Pleistocene Cave And Brown Bears And Its Significance In Species Determination
Text-fig. 7. Occurrence of p1 in mandibles from Deninger bears and cave bears, data after Table 3 (presence = p1 or alveoli observed, absence = no p1 developed, broken = diastema fragmented).
Text-fig. 10. List of Siwalik murine rodents. a) Stratigraphic occurrence of fossil localities of the Potwar Plateau, Pakistan. b) Murine species recovered from the Siwaliks, updated from Kimura et al. (2015). All localities but DP 13 have Y as prefix. in Early Late Miocene Murine Rodents From The Upper Part Of The Nagri Formation, Siwalik Group, Pakistan, With A New Fossil Calibration Point For The Tribe Apodemurini (Apodemus/Tokudaia)
Text-fig. 10. List of Siwalik murine rodents. a) Stratigraphic occurrence of fossil localities of the Potwar Plateau, Pakistan. b) Murine species recovered from the Siwaliks, updated from Kimura et al. (2015). All localities but DP 13 have Y as prefix.
Fig. 6 in Spatio-temporal segregation and size distribution of fish assemblages as related to non-native species occurrence in the middle rio Doce Valley, MG, Brazil
Fig. 6. Least-square means and 95% confidence intervals from ANCOVA of the first three environmental factors from PCA. Different markers represent significantly different means as detected by planned contrasts with 5% significance level, first comparing lakes with any non-native species with those without them, and then comparing the two categories of lakes with non-natives (non-piscivores vs. piscivores).
Fig. 4 in Spatio-temporal segregation and size distribution of fish assemblages as related to non-native species occurrence in the middle rio Doce Valley, MG, Brazil
Fig. 4. Scatterplot of species body size (mean standard length) vs. a relative index of native affinity to lakes containing piscivorous invaders (the proportion of biomass of a given native species in lakes with piscivorous invaders). The estimated regression line is also presented (Y = 0.044*X - 0.279; R2 = 0.443; p = 0.007). Species codes: ast = Astyanax sp.; aus = Australoheros facetus; cyp = Cyphocharax gilbert; cre = Crenicichla lacustris; geo = Geophagus brasiliensis; gym = Gymnotus gr. carapo; hop = Hoplias malabaricus; lep = Leporinus steindachneri; lor = Loricariidae (unidentified species); lyc = Lycengraulis sp.; moe = Moenkhausia doceana; oli = Oligosarcus solitarius; pac = Pachyurus adspersus; pro = Prochilodus vimboides; tra = Trachelyopterus striatulus.
Fig. 5 in Spatio-temporal segregation and size distribution of fish assemblages as related to non-native species occurrence in the middle rio Doce Valley, MG, Brazil
Fig. 5. Least-square means and 95% confidence intervals from ANCOVA of mean individual size and temporal turnover as related to the three lake categories. Different markers represent significantly different means as detected by planned contrasts with 5% significance level, first comparing lakes with any non-native species with those without them, and then comparing the two categories of lakes with non-natives (non-piscivores vs. piscivores).
Fig. 2 in Spatio-temporal segregation and size distribution of fish assemblages as related to non-native species occurrence in the middle rio Doce Valley, MG, Brazil
Fig. 2. Alpha (mean) and beta richness. a) Comparison among the temporal and spatial components of richness. b) Species richness for each lake. The alpha (mean) and beta richness were taken along the temporal component. Lake codes: No = Nova; Ca = Capim; Fe = Ferrugem; Cr = Crentes; Po = Poço Redondo; Ro = Romoalda; Ti = Timburé; Ag = Águas Claras; Pa = Palmeirinha; Ar = Ariranha. "Natives" represents lakes without non-native species; "Non-piscivores" represents lakes with non-piscivorous non-native species; "Piscivores" represents lakes with invasive piscivorous species.
Filtered GBIF dataset of occurrences for food species in the brown bear (Ursus arctos) trophic database
<p>We reviewed 47 studies of brown bear diet in Europe by searching in SCI Journals, master’s and PhD theses, and grey literature. We obtained a list of 276 species in the brown bear diet in Europe and Turkey. We used the R package rgbif to download occurrences of each food species from the Global Biodiversity Information Facility (GBIF). We selected occurrences of food species, with an uncertainty of <1 km2, in Europe, North Africa and the Middle East for the period 1989–2018.</p>
Figure 2 in Revisiting the ideas of trees as templates and the competition paradigm in pairwise analyses of ground-dwelling ant species occurrences in a tropical forest
Figure 2 Presence probabilities of ant species in each tree species only for those one involved in nonrandom pairs for the two sampling techniques and seasons. PR: pitfall,rainy season; PD: pitfall, dry season; WR: Winkler, rainy season; WD: Winkler, dry season. GG= Guarea guidonia; IE= Inga edulis; NM= Nectandra membranacea; PG= Piptadenia gonoachanta.
Figure 6 in A new species and new records of goatfishes of the genus Parupeneus (Mullidae) from the Indian Ocean, with updated occurrence information for P. jansenii in the Western Pacific
Figure 6. – Standard length against four morphometric characters, head length against anal-fin spine height, and total number of gill rakers against caudal-peduncle length in Parupeneus jansenii vs. P. nansen. In P. jansenii the two size groups are distinguished.
Figure 2 in A new species and new records of goatfishes of the genus Parupeneus (Mullidae) from the Indian Ocean, with updated occurrence information for P. jansenii in the Western Pacific
Figure 2. – Standard length against total length in Parupeneus jansenii; greydotted lines: reference lines for TL and the determined SL for the Myanmar specimen; black dashed lines: reference lines for delimitation of small- and large-sized fish
Figure 1 in On the occurrence of the Synodontis eupterus (Mochokidae) in the Adriatic drainage system of Croatia: a case of an introduced aquarium species and suggestions for alien species detection measures
Figure 1. – Synodontis eupterus (from Mala Neretva River) (TL = 193 mm) (catalogue number SE-IOR 8112017).
Arctic migrations shape global meta-communities: Contrasting insights from species occurrence, abundance and biomass
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Environmental controls on butterfly occurrence and species richness in Israel: The importance of temperature over rainfall
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Temporal trends in the spatial bias of species occurrence records
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Data from: Integrated species distribution models to account for sampling biases and improve range wide occurrence predictions
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Costa Rica mosquito community species occurrence and site environmental data, July - August 2017
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SPIKEPIPE: A metagenomic pipeline for the accurate quantification of eukaryotic species occurrences and intraspecific abundance change using DNA barcodes or mitogenomes
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Vertebrate-habitat relationships: Logistic regression models predict probability of occurrence of bird and small mammal species in western Oregon
Logistic regression models predicting probability of occurrence of bird and of small-mammal species were produced using animal-habitat data sets from throughout western Oregon (Garman and Cole 1999 - Vertebrate Habitat Relationships Data Bank (VHRDB), Report to Coastal Landscape Analysis and Modeling Study). Regression coefficients, variables, and metrics related to model predictions are provided here under Entity 1, and in VHRDB as VERTLOGR.
Fig. 3 in A new species of Copionodon representing a relictual occurrence of the Copionodontinae (Siluriformes: Trichomycteridae), with a CT-scan imaging survey of key subfamilial features
Fig. 3. Copionodon exotatos, holotype, MZUSP 120631, 45.0 mm SL. Lateral view of head.
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.