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43 results for “ecological preferences”
Fig. 2 in Ecological fitting: Chemical profiles of plant hosts provide insights on selection cues and preferences for a major buprestid pest
Fig. 2. Ordination (nonmetric multidimensional scaling) plots of volatiles profiles of black ash (BA, Fraxinus nigra), blue ash (Blue, F. quadrangulata), Manchurian ash (MA, F. mandshurica), olive (OL, Olea europaea), and white fringetree (WF, Chionanthus virginicus), five plant hosts of emerald ash borer (Agrilus planipennis). a) Overall plant profiles, b) Green leaf volatile (GLV) profiles, c) monoterpene profiles, d) sesquiterpene profiles, and e) antennally active compounds. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Data from: Ecological opportunity and the evolution of habitat preferences in an arid-zone bird: implications for speciation in a climate-modified landscape
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Data from: Adaptive, but not condition-dependent, body shape differences contribute to assortative mating preferences during ecological speciation
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Data from: Feeding ecology and habitat preferences of top predators from two Miocene carnivore-rich assemblages
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The ecological stage maintains preference differentiation and promotes speciation
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Data from: The ecological stage changes benefits of mate choice and drives preference divergence
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Data from: Testing the role of mating preference in a case of incomplete ecological speciation with gene flow
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Female preference and adverse developmental effects of glyphosate-based herbicides on ecologically relevant traits in Japanese quail
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FIGURES 6-8 in Distribution of Rugilus mixtus (Lohse, 1956) (Coleoptera: Staphylinidae: Paederinae) in Poland with comments of its morphology and ecological preferences
FIGURES 6-8. Forebody of Rugilus erichsoni (6), Rugilus orbiculatus (7), Rugilus mixtus (9).
FIGURE 1 in Distribution of Rugilus mixtus (Lohse, 1956) (Coleoptera: Staphylinidae: Paederinae) in Poland with comments of its morphology and ecological preferences
FIGURE 1. Distribution of Rugilus mixtus in Poland.
Figures 38-43 from: Sarzetti L, Genise J, Sanchez M, Farina J, Molina A (2013) Nesting behavior and ecological preferences of five Diphaglossinae species (Hymenoptera, Apoidea, Colletidae) from Argentina and Chile. Journal of Hymenoptera Research 33: 63-82. https://doi.org/10.3897/jhr.33.5061
Figures 38-43 - Diphaglossa gayi Spinola, 1851. 38 General view of the nesting site beside the Río Negro Bridge, Chile 39 general view of nesting site at Lonconao, Chile 40 tumulus of soil pellets and open entrance 41 main tunnel 42 nest architecture 43 cell, neck with lining, and egg laying on provisions.
Figures 30-37 from: Sarzetti L, Genise J, Sanchez M, Farina J, Molina A (2013) Nesting behavior and ecological preferences of five Diphaglossinae species (Hymenoptera, Apoidea, Colletidae) from Argentina and Chile. Journal of Hymenoptera Research 33: 63-82. https://doi.org/10.3897/jhr.33.5061
Figures 30-37 - Cadeguala albopilosa (Spinola, 1851). 30 General view of the nest site at Bahia Mansa, Parque Nacional Los Alerces (Chubut province) 31 tumulusof unconsolidated soil32 two main tunnels and longitudinal view of the soil containing a thin ash layer 33 a pair of cells with provisions, necks and lateral tunnels, scale line: 1 cm 34 remains of cells of other nest, scale line: 1 cm 35–36 tomography images of one block of soil containing Cadeguala albopilosa nests, arrows indicate cells 37 3D-reconstruction of one nest and isolate cells.
Figures 8-18 from: Sarzetti L, Genise J, Sanchez M, Farina J, Molina A (2013) Nesting behavior and ecological preferences of five Diphaglossinae species (Hymenoptera, Apoidea, Colletidae) from Argentina and Chile. Journal of Hymenoptera Research 33: 63-82. https://doi.org/10.3897/jhr.33.5061
Figures 8-18 - Ptiloglossa tarsata (Friese, 1900). 8 General view of the nesting site at "La Florida" (Salta province), the arrow indicates the location of the nest; 9 Female of Ptiloglossa tarsata foraging in a flower of Solanum sp. 10 Tumulus of unconsolidated soil, scale line: 1 cm 11 General view showing the nest architecture with a cell at the end of the main tunnel 12 Group of scratches probably produced by female´s mandibles. The arrow indicates their location in the main tunne; 13(a) cell with cellophane-like lining and provisions, (b) neck and (c) entrance tunnel, scale line: 1 cm 14 One cell showing the cellophane-like lining on the wall, scale line: 1 cm 15 Spiral closure of one cell, scale line: 0.5 cm 16 Cocoon operculum with holes, scale line: 0.5 cm 17 Scanning electron micrograph of the cocoon operculum showing the fabric of silk threads with small circular holes, scale: 500 µm 18 Onecircular hole surrounded by silk threads, scale: 50 µm.
Figures 24-29 from: Sarzetti L, Genise J, Sanchez M, Farina J, Molina A (2013) Nesting behavior and ecological preferences of five Diphaglossinae species (Hymenoptera, Apoidea, Colletidae) from Argentina and Chile. Journal of Hymenoptera Research 33: 63-82. https://doi.org/10.3897/jhr.33.5061
Figures 24-29 - Ptiloglossa matutina (Schrottky, 1904). 24 General view of the nesting site at Reserva Karadya, Andresito (Misiones province) 25 Nest entrance closed by a plug of soil(arrow), scale line:1 cm 26 Soil with roots, litter, some rocks, and remains of the main tunnel (arrow) 27 Cell showing the larva partially submerged in provisions, cellophane lining, and the wad cotton-like material attached the cell closure, scale line: 0.5 cm 28 Detail of the cell closure with the cotton-like material 29 Cell and neck wall with the lining removed. Note the high curvature.
Figures 19-23 from: Sarzetti L, Genise J, Sanchez M, Farina J, Molina A (2013) Nesting behavior and ecological preferences of five Diphaglossinae species (Hymenoptera, Apoidea, Colletidae) from Argentina and Chile. Journal of Hymenoptera Research 33: 63-82. https://doi.org/10.3897/jhr.33.5061
Figures 19-23 - 19 Nest architecture of Ptiloglossa tarsata (Friese, 1900). 20 Cell with provisions and egg, cell neck, spiral closure, and entrance tunnel of Ptiloglossa tarsata 21 Nest architecture of Ptiloglossa matutina (Schrottky, 1904) 22 Nest architecture of Cadeguala albopilosa (Spinola, 1851) 23 Cell with provisions and egg, cell neck, location of the cell closure and entrance tunnel of Cadeguala albopilosa.
Figures 1-7 from: Sarzetti L, Genise J, Sanchez M, Farina J, Molina A (2013) Nesting behavior and ecological preferences of five Diphaglossinae species (Hymenoptera, Apoidea, Colletidae) from Argentina and Chile. Journal of Hymenoptera Research 33: 63-82. https://doi.org/10.3897/jhr.33.5061
Figures 1-7 - Zikanapis tucumana (Moure, 1945). 1 General view of the nesting site at Vinchina (La Rioja province) before sunrise 2 Female of Zikanapis tucumana during foraging activity 3 Tumulus, turret andopennest entrance 4 Main and lateral tunnel showing one cell at the end (arrow) 5 General view of nest architecture, scale line: 1 cm 6 Remains of a cell with part of the provisions. Note the curvature of neck 7 Nestarchitecture.
Figure 8 in Ecological conditions of Javan langur (Trachypithecus auratus É. Geoffroy Saint-Hilaire, 1812) in Sokokembang Forest (Central Java, Indonesia) through distribution and food preferences
Figure 8. Grooming activities of Javan langurs in Sokokembang forest. Photo by Y.M. Putra.
Figure 5 in Oviposition site preference and reproductive ecology of Teratohyla midas (Anura: Centrolenidae) in the Colombian Amazon
Figure 5. Preference as oviposition site of Teratohyla midas towards leaves of selaginella sp. The observed legend corresponds to the clutches recorded throughout the study area. The legend of expected corresponds to the number of clutches that would be expected to find in relation to the availability of the substrate in the entire study area. The category 'others' refers to other types of leaves present in the area.
Figure 4 in Oviposition site preference and reproductive ecology of Teratohyla midas (Anura: Centrolenidae) in the Colombian Amazon
Figure 4. Clutches of Teratohyla midas deposited on leaves; (a-d) leaves of the fern selaginella sp. with T. midas clutches; (e-f) substrates categorised as other types of leaves. Photographs: Juan C. Diaz-Ricaurte.
Figure 1 in Oviposition site preference and reproductive ecology of Teratohyla midas (Anura: Centrolenidae) in the Colombian Amazon
Figure 1. (a) Study site in the department of Caquetá, Foothill Amazonian of Colombia. (b) Micro-watershed study area of La Perdíz stream tributary of the Hacha River in the Reserva Natural y Comunitaria el Manantial, municipality of Florencia, department of Caquetá, Colombia.
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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)
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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.