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.
9,882
datasets available to search
ShareScore release 0.9.0
Dataset results
9,882 results for “Scale”
Figure 3 in Dissecting copepod diversity at different spatial scales in southern European groundwater
Figure 3. (A) Multidimensional Scaling plots of centroids of the habitats (region acronyms as in Figure 1; K, karstic aquifers; P, porous aquifers); (B) Magnitude of the different spatial scale contributions to α-diversity and β -diversity variation.
Figure 1 in Dissecting copepod diversity at different spatial scales in southern European groundwater
Figure 1. Map of distribution of the four regions analysed in Southern Europe (CAN, Cantabria; JUR, Jura Massif; LES, Lessinian Massif; KRI, Krim Massif).
Figure 2 in Dissecting copepod diversity at different spatial scales in southern European groundwater
Figure 2. Multidimensional Scaling plots of the local units using presence/absence multivariate data; aggregation at the aquifer type-level and at the regional level is highlighted; labels of units include the region acronyms (as in Figure 1), habitat (Ku, unsaturated karst; Ks, saturated karst; Ph, hyporheic habitat; Ps, saturated porous), and codes of the four replicates (basins A, B, C, D). Each point representing a local unit is the centroid of 12 sampling sites.
Figure 24. Licnobelba latiflabellata, scale bars 50 in Setal losses in the dorsal hysterosoma of Plateremaeoidea (Acari: Oribatida) in the light of ontogenetic studies
Figure 24. Licnobelba latiflabellata, scale bars 50 µm. (A) Anal region of larva; (B) anogenital region of protonymph. Explanation of labels in text.
Figure 16. Licnodamaeus costula, scale bar 50 in Setal losses in the dorsal hysterosoma of Plateremaeoidea (Acari: Oribatida) in the light of ontogenetic studies
Figure 16. Licnodamaeus costula, scale bar 50 µm. (A) Anal region of larva; (B) anogenital region of protonymph. Explanation of labels in text.
Figure 6. Aleurodamaeus setosus, scale bars 50 in Setal losses in the dorsal hysterosoma of Plateremaeoidea (Acari: Oribatida) in the light of ontogenetic studies
Figure 6. Aleurodamaeus setosus, scale bars 50 µm. (A) Anal region of larva; (B) anogenital region of protonymph. Explanation of labels in text.
Figure 2 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)
Figure 2. Non-metric multi-dimensional scaling (MDS) ordination showing hemipteran composition for all sampling periods with selected plant species superimposed.
Figure 5 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)
Figure 5. Annual cyclic pattern of the proportion of the effectively specialized fauna (squares) and singleton species (circles) for the total number of hemipteran species from each sampling period.
Figure 3 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)
Figure 3. Mean number of individuals (from SIMPER analysis) of dominant hemipteran species, during each sampling period, for most plant species.
Figure 1 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)
Figure 1. Interactions between plant species sampled and sampling period for (A) abundance (number of individuals) per plant and (B) species richness per plant (standard error bars are shown).
Figure 6 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)
Figure 6. Relationship between the effectively specialized fauna (squares) and singleton species (circles) for the number of hemipteran species from each sampling period and for the entire collection. An exponential decay equation is fitted for effectively specialized fauna, y = 2.973∗ exp (−0.00575∗ x) + (−1.478), R2 = 0.7598, and for singleton species, y = 22.53∗exp (−0.08466∗x) + 0.2614, R2 = 0.9873.
Figure 5 in Landscape-scale surveys reveal patterns of floral visitation by species of Scarabaeidae (Coleoptera) in the Kruger National Park, South Africa
Figure 5. Adult of Pedinorrhina trivittata (Schaum) on flowers of Peltophorum africanum Sonder (Kruger National Park, South Africa).
Figure 4 in Landscape-scale surveys reveal patterns of floral visitation by species of Scarabaeidae (Coleoptera) in the Kruger National Park, South Africa
Figure 4. Adult of Leucocelis amethystina (MacLeay) on flowers of Grewia bicolor Jussieu (Kruger National Park, South Africa).
Figure 2 in Landscape-scale surveys reveal patterns of floral visitation by species of Scarabaeidae (Coleoptera) in the Kruger National Park, South Africa
Figure 2. Adult of Amazula suavis (Burmeister) on flowers of Terminalia sericea Burchell (Kruger National Park, South Africa).
Figure 3 in Landscape-scale surveys reveal patterns of floral visitation by species of Scarabaeidae (Coleoptera) in the Kruger National Park, South Africa
Figure 3. Adult of Rhabdotis albinigra Burmeister on flowers and foliage of Terminalia prunioides Lawson (Kruger National Park, South Africa).
Figure 1 in Landscape-scale surveys reveal patterns of floral visitation by species of Scarabaeidae (Coleoptera) in the Kruger National Park, South Africa
Figure 1. Map of the Kruger National Park showing specific locations where floral visitors of Terminalia prunioides Lawson and Terminalia sericea Burchell were sampled.
Data for the paper "A new mapping function for spaceborne TEC conversion based on the plasmaspheric scale height"
<p>This dataset works specifically for the paper Wu et al., (2021), "A new mapping function for spaceborne TEC conversion based on the plasmaspheric scale height"</p>
Figure 16. Jacotella neonominata, scale bars 50 in Ontogenetic studies of three species of Gymnodamaeidae (Acari: Oribatida) with a focus on regressions of hysterosomal setae
Figure 16. Jacotella neonominata, scale bars 50 µm. (A) Anal region of larva; (B) anogenital region of tritonymph. Explanation of labels in text.
Figure 4. Arthrodamaeus reticulatus, scale bars 50 in Ontogenetic studies of three species of Gymnodamaeidae (Acari: Oribatida) with a focus on regressions of hysterosomal setae
Figure 4. Arthrodamaeus reticulatus, scale bars 50 µm. (A) Anal region of larva; (B) anogenital region of protonymph. Explanation of labels in text.
Figure 6. Molecular time-scale for decapodiform cephalopods indicating a in A redescription of the fossil coleoid cephalopod genus Palaeololigo Naef, 1921 (Decapodiformes: Palaeololiginidae) and its relationship to Recent squids
Figure 6. Molecular time-scale for decapodiform cephalopods indicating a potential position for the Palaeololiginidae and Chtenopteryx on two alternative decapodiform phylogenies (modified from Strugnell et al. [2006]). The topologies result from two alternative Bayesian analyses using: (A) all three codon positions of three nuclear genes (octopine dehydrogenase, rhodopsin, pax-6) partitioned by codon; and (B) only first and second codon positions of the same three nuclear genes. The divergence dates of Palaeololiginidae from Bathyteuthis and Chtenopteryx and also Chtenopteryx from Bathyteuthis are hypothetical. A simplified possible scenario of morphological character loss is depicted. Notes: Ɨ indicates the presence of suckers on the buccal lappets; • indicates the presence of accessory nidamental glands (which is present in Chtenopteryx, but apparently lost in Bathyteuthis); indicates the presence of fused axons in the giant nerve fibre system; ▲ indicates the "juvenile" characters for Oegopsida detailed by Naef (1923), namely the form of gladius with a long narrow rachis, subterminal position of the fins, and also quadriserial suckers on the arms, which Naef (1923) believed to the ancestral form for all Oegopsida; "open" shapes (O, O, Δ, Z)
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.