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.
733
datasets available to search
ShareScore release 0.7.1
Dataset results
733 results for “predatory”
Fig. 8 in Predatory Mites (Phytoseiidae, Parasitiformes) Of The Fauna Of Ukraine: Redescriptions Of The Species Of Amblyseiella And Chelaseius, With Resurrection Of The Genus Status For Amblyseiulus
Fig. 8. Amblyseiulus ovicinctus (Athias-Henriot, 1961) ♀ (1–7): 1 — dorsal shield; 2 — ventral body surface; 3 — metapodal plates; 4 — posterior part of peritremal schield; 5 — chelicera; 6 — spermatheca; 7 — fragment of leg IV.
Fig. 7 in Predatory Mites (Phytoseiidae, Parasitiformes) Of The Fauna Of Ukraine: Redescriptions Of The Species Of Amblyseiella And Chelaseius, With Resurrection Of The Genus Status For Amblyseiulus
Fig. 7. Amblyseiulus okanagensis (Chant, 1957) ♀ (1–7), Ơ (8, 9): 1 — dorsal shield; 2 — ventral body surface; 3 — metapodal plates; 4 — posterior part of peritremal schield; 5 — chelicera; 6 — spermatheca; 7 — fragment of leg IV; 8 — ventrianal shield; 9 — chelicera with spermatodactyl.
Fig. 8 in Population dynamics and predatory impact of the alien jellyfish Aurelia solida (Cnidaria, Scyphozoa) in the Bizerte Lagoon (southwestern Mediterranean Sea) Abstract
Fig. 8: Path diagram of the interaction between the abiotic (temperature, salinity) and biotic parameter (chlorophyll biomass, mesozooplankton and Aurelia solida) in Bizerte lagoon in 2013 and 2014.
Fig. 6 in Population dynamics and predatory impact of the alien jellyfish Aurelia solida (Cnidaria, Scyphozoa) in the Bizerte Lagoon (southwestern Mediterranean Sea) Abstract
Fig. 6: Prey selectivity of Aurelia solida in Bizerte Lagoon during the present study; Har = Harpacticoids; Biv = bivalve larvae; Gas = gastropods larvae; Lar = larvaceans; Fis = Fish larvae; Cru = crustacean larvae; Cal = Calanoids; Cla = Cladocerans.
Fig. 5 in Population dynamics and predatory impact of the alien jellyfish Aurelia solida (Cnidaria, Scyphozoa) in the Bizerte Lagoon (southwestern Mediterranean Sea) Abstract
Fig. 5: Relation between Aurelia solida bell diameter (cm) and (A) the prey in the gut contents and (B) the prey diversity.
Fig. 4 in Population dynamics and predatory impact of the alien jellyfish Aurelia solida (Cnidaria, Scyphozoa) in the Bizerte Lagoon (southwestern Mediterranean Sea) Abstract
Fig. 4: Variation of the diet composition of Aurelia solida in Bizerte Lagoon in (A) 2013 and (B) 2014; (n) number of analyzed specimens.
Fig. 7 in Population dynamics and predatory impact of the alien jellyfish Aurelia solida (Cnidaria, Scyphozoa) in the Bizerte Lagoon (southwestern Mediterranean Sea) Abstract
Fig. 7: Seasonal variation of Aurelia solida (A-B) feeding rate (prey consumed medusae-1) and (C-D) predation impact (% prey standing stock consumed day-1) in Bizerte Lagoon in 2013-2014.
Fig. 3 in Population dynamics and predatory impact of the alien jellyfish Aurelia solida (Cnidaria, Scyphozoa) in the Bizerte Lagoon (southwestern Mediterranean Sea) Abstract
Fig. 3: Seasonal variation of Aurelia solida (A) abundance and (B) bell diameter in Bizerte lagoon between November 2012 and August 2014; white spots: 0 ind.m-3.
Fig. 1 in Population dynamics and predatory impact of the alien jellyfish Aurelia solida (Cnidaria, Scyphozoa) in the Bizerte Lagoon (southwestern Mediterranean Sea) Abstract
Fig. 1: Map of the Mediterranean Sea showing with locations of the sampling station and the transect in the Bizerte Lagoon between November 2012 and August 2014.
Fig. 12 in A comparison of teeth in Tithonian, Late Jurassic, predatory actinopterygian fishes from Owadów-Brzezinki Lägerstatte and its palaeoecological implications
Fig. 12. Comparison of generalized teeth vertical cross sections of the studied taxa. A. Caturoidea. B. Pachycormidae. Not to scale.
Fig. 8 in A comparison of teeth in Tithonian, Late Jurassic, predatory actinopterygian fishes from Owadów-Brzezinki Lägerstatte and its palaeoecological implications
Fig. 8. SEM overview of tooth of caturoid fish Strobilodus sp. ZPAL P. 16/O-B/2 from Tithonian, Upper Jurassic Kcynia Formation, Corbulomima Limestone (Unit III), Owadów-Brzezinki, Poland. A. Mid-crown section with visible layer of enameloid (en). B. Basal section with exposed orthodentin (ort). C, D. Overview in apical-mid-crown surface. E–H. Changes in enameloid structure from linear through irregular to scale-like in basal direction.
Fig. 5 in A comparison of teeth in Tithonian, Late Jurassic, predatory actinopterygian fishes from Owadów-Brzezinki Lägerstatte and its palaeoecological implications
Fig. 5. Vertical cross-section of tooth of pachycormid fish Orthocormus teyleri Lambers, 1988, NG/PAL/VERT/OB/O1 thin section from ZPAL P. 16/OB/3 from Tithonian, Upper Jurassic Kcynia Formation, Corbulomima Limestone (Unit III), Owadów-Brzezinki, Poland. Basal (A1), mid-crown (A2), and apical (A3) planes, with visible acrodin cap. Internal structure (A4), with visible denteonal canals (white arrows) and inter-denteonal dentin (black arrows).
Fig. 1. A in A comparison of teeth in Tithonian, Late Jurassic, predatory actinopterygian fishes from Owadów-Brzezinki Lägerstatte and its palaeoecological implications
Fig. 1. A. Lithological succession and biostratigraphy of the Owadów-Brzezinki Quarry. The topmost part of the Pałuki Formation and overlying limestone of the Kcynia Formation (Units I–IV). B. Road map with the location of the Owadów-Brzezinki site and its proximity to Tomaszów Mazowiecki in Central Poland. C. General view of the Owadów-Brzezinki section (i.e., Unit III and most fossiliferous Corbulomima Limestone occurring in the middle of the quarry wall).
Fig. 2 in A comparison of teeth in Tithonian, Late Jurassic, predatory actinopterygian fishes from Owadów-Brzezinki Lägerstatte and its palaeoecological implications
Fig. 2. Studied specimens of actinopterygian fishes from Tithonian, Upper Jurassic Kcynia Formation, Corbulomima Limestone (Unit III), OwadówBrzezinki, Poland. A–C. Loose teeth of Caturoidea indet. A. ZPAL P. 16/O-B/FT1. B. ZPAL P. 16/O-B/FT2. C. ZPAL P. 16/O-B/FT3. D. Caturoid Strobilodus sp., ZPAL P. 16/O-B/2, right dentary in lateral view. E. Pachycormid Orthocormus teyleri Lambers, 1988, ZPAL P. 16/O-B/3, left dentary (E1) and right dentary (E2) in lateral view. Dashed white lines indicate thin-sectioning plane; white arrows indicate which teeth were sampled for thin-sectioning (TS), black arrows indicate which samples were chosen for SEM analysis.
Fig. 4 in A comparison of teeth in Tithonian, Late Jurassic, predatory actinopterygian fishes from Owadów-Brzezinki Lägerstatte and its palaeoecological implications
Fig. 4. Cross-sections of teeth caturoidean fishes Strobilodus sp. from Tithonian, Upper Jurassic Kcynia Formation, Corbulomima Limestone (Unit III), Owadów-Brzezinki, Poland. A–C. NG/PAL/VERT/OB/C1–C3, respectively, thin sections from ZPAL P.16./O-B/2, in apical (A1), mid-crown (B1), and basal (C) planes, documenting relative increase in dental pulp cavity diameter in basal direction. Incremental growth lines: irregular (A2) and more regular B2) patterns of growth are documented. Dentin drillings (arrows) present sub-superficially (B3) and superficially (B4).
Fig. 7 in A comparison of teeth in Tithonian, Late Jurassic, predatory actinopterygian fishes from Owadów-Brzezinki Lägerstatte and its palaeoecological implications
Fig. 7. Teeth eruption from alveolar bone of Orthocormus teyleri Lambers, 1988, NG/PAL/VERT/OB/O4 thin section from ZPAL P. 16/O-B/3 from Tithonian, Upper Jurassic Kcynia Formation, Corbulomima Limestone (Unit III), Owadów-Brzezinki, Poland. A1, numerous teeth erupting in posterior tooth row; A2, A3, case of rapid teeth eruption, evidence of odontogenesis of one teeth specimen atop on the another tooth. Arrows indicate the observed phenomenon.
Fig. 3 in A comparison of teeth in Tithonian, Late Jurassic, predatory actinopterygian fishes from Owadów-Brzezinki Lägerstatte and its palaeoecological implications
Fig. 3. Thin sections of teeth of caturoidean fishes Caturoidea indet. (A) and Strobilodus sp. (B, C) from Tithonian, Upper Jurassic Kcynia Formation, Corbulomima Limestone (Unit III), Owadów-Brzezinki, Poland. A. NG/PAL/VERT/OB/C5 thin section from ZPAL P.16./O-B/FT1. A1, general view of vertical thin section with orthodentin histology (ort) and thin enameloid layer (en); A2, close view of apical section, with prominent acrodin cap (ac); A3, A4, crown mid-section with angled orthodentin tubules (highlighted) present. B, C. Horizontal cross section of Strobilodus sp. teeth in apical plane. Arrows indicate phenomena. B. NG/PAL/VERT/OB/C7 thin section from ZPAL P.16./O-B/FT3. B1, overview of teeth structure, with slight mesiodistal compression and mostly solid structure; B2, carinae present as a perturbances in mesial and distal planes of teeth. C. NG/PAL/VERT/OB/C1 thin section from ZPAL P.16./O-B/O2, small central canal surrounded by prominent dental tubules of orthodentin.
Fig. 11 in A comparison of teeth in Tithonian, Late Jurassic, predatory actinopterygian fishes from Owadów-Brzezinki Lägerstatte and its palaeoecological implications
Fig. 11. Microstructure of teeth of pachycormid fish Orthocormus teyleri Lambers, 1988, ZPAL P. 16/O-B/3 from Tithonian, Upper Jurassic Kcynia Formation, Corbulomima Limestone (Unit III), Owadów-Brzezinki, Poland. A, B. General view. C. Enameloid (en) and orthodentin (ort) surface with visible longitudinal ridging (marked by arrows). D. View of singular denteonal canal of orthodentin. E–G. Visible structure of orthodentin layer in vertical view, developed as series of winding, ridged irregular cannals. H. Basal cross section in transverse plane, with visible osteodentin (H1), arrows indicating denteonal canals (H2).
Fig. 6 in A comparison of teeth in Tithonian, Late Jurassic, predatory actinopterygian fishes from Owadów-Brzezinki Lägerstatte and its palaeoecological implications
Fig. 6. Horizontal cross sections of teeth of pachycormid fish Orthocormus teyleri Lambers, 1988. A–C. NG/PAL/VERT/OB/O2–4, respectively, thin sections from ZPAL P. 16/O-B/3 from Tithonian, Upper Jurassic Kcynia Formation, Corbulomima Limestone (Unit III), Owadów-Brzezinki, Poland. A. Apical plane with visible osteodentin (ost), surrounded by orthodentin (ort), and outermost enameloid (en). B. Mid-crown plane. B1, general view; B2, osteodentin layer encircled by marginal capillaries (arrows), which contact with orthodentin; B3, osteodentin densely packed with denteons with central denteonal canals (arrows). C. Basal plane. C1, general view; C2, individual denteons pronounced due to diagenetic processes (arrows).
Fig. 10 in A comparison of teeth in Tithonian, Late Jurassic, predatory actinopterygian fishes from Owadów-Brzezinki Lägerstatte and its palaeoecological implications
Fig. 10. Structure of orthodentin of tooth of caturoid fish Strobilodus sp. ZPAL P. 16/O-B/2 from Tithonian, Upper Jurassic Kcynia Formation, Corbulomima Limestone (Unit III), Owadów-Brzezinki, Poland. A. Boundary between orthodentin (ort) and enameloid (en). B, C. Overview of horizontal surface of orthodentin with dental tubuli (arrows). D. Vertical view of boundary between enameloid and orthodentin, with compact, regular enameloid and (E) irregular, rugose, porous orthodentin surface.
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.