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223 results for “Ecology: behavioral”
FIGURE 2 in New Neotropical and Nearctic species of water beetles in the genera Hydraena Kugelann and Ochthebius Leach, a key to North American genera and subgenera of the family, new distribution records, and a synopsis of ecology, behavior and morphology related to aquatic life (Coleoptera: Hydraenidae)
FIGURE 2. Dorsal habitus of Hydraena species.
FIGURE 5 in New Neotropical and Nearctic species of water beetles in the genera Hydraena Kugelann and Ochthebius Leach, a key to North American genera and subgenera of the family, new distribution records, and a synopsis of ecology, behavior and morphology related to aquatic life (Coleoptera: Hydraenidae)
FIGURE 5. Hydraena (Hydraenopsis) belilymba new species, holotype habitus and aedeagus.
FIGURE 24 in New Neotropical and Nearctic species of water beetles in the genera Hydraena Kugelann and Ochthebius Leach, a key to North American genera and subgenera of the family, new distribution records, and a synopsis of ecology, behavior and morphology related to aquatic life (Coleoptera: Hydraenidae)
FIGURE 24. Ochthebius (s. str.) bajaensis, new species, holotype habitus and aedeagus.
FIGURE 25 in New Neotropical and Nearctic species of water beetles in the genera Hydraena Kugelann and Ochthebius Leach, a key to North American genera and subgenera of the family, new distribution records, and a synopsis of ecology, behavior and morphology related to aquatic life (Coleoptera: Hydraenidae)
FIGURE 25. Ochthebius (s. str.) explicitus, new species, holotype habitus and aedeagus.
Supplementary material 2 from: Gauthey Z, Tentelier C, Lepais O, Elosegi A, Royer L, Glise S, Labonne J (2017) With our powers combined: integrating behavioral and genetic data to estimate mating success and sexual selection. Rethinking Ecology 2: 1-26. https://doi.org/10.3897/rethinkingecology.2.14956
JAGS code for the model : Data type: Programming code.
Supplementary material 1 from: Gauthey Z, Tentelier C, Lepais O, Elosegi A, Royer L, Glise S, Labonne J (2017) With our powers combined: integrating behavioral and genetic data to estimate mating success and sexual selection. Rethinking Ecology 2: 1-26. https://doi.org/10.3897/rethinkingecology.2.14956
Data and model outputs : Data type: Body size, behavioural and genetic data, and model output.
Text-fig. 1. Eospondylus primigenius (STÜRTZ) Bundenbach, Eschenbach-Bocksberg quarry, Lower Devonian, Lower Emsian (Zlichovian), Hunsrück Slate, specimens PWL 1996 57LS (NMM) top image (A) x 1.5, and PWL 1996 66LS (NMM) bottom image (B) x 1.7. Specimen with rays bent into strong curves. Such flexibility and attitudes of rays differentiate the behavioral ecology of Eospondylus from all other Hunsrück Slate ophiuroids. Delicateness of the top specimen and robustness of the bottom specimen is perhaps the combined result of real phenotypic differences, differences of preserved detail, and differences of distortion of the rock. [courtesy of Herbert Lutz and Thomas Engel; photos by Alexander Glass]. in Isolated Ossicles Of The Family Eospondylidae Spencer Wright, 1966, In The Lower Devonian Of Bohemia (Czech Republic) And Correction Of The Systematic Position Of Eospondylid Brittlestars (Echinodermata: Ophiuroidea: Oegophiurida)
Text-fig. 1. Eospondylus primigenius (STÜRTZ) Bundenbach, Eschenbach-Bocksberg quarry, Lower Devonian, Lower Emsian (Zlichovian), Hunsrück Slate, specimens PWL 1996 57LS (NMM) top image (A) x 1.5, and PWL 1996 66LS (NMM) bottom image (B) x 1.7. Specimen with rays bent into strong curves. Such flexibility and attitudes of rays differentiate the behavioral ecology of Eospondylus from all other Hunsrück Slate ophiuroids. Delicateness of the top specimen and robustness of the bottom specimen is perhaps the combined result of real phenotypic differences, differences of preserved detail, and differences of distortion of the rock. [courtesy of Herbert Lutz and Thomas Engel; photos by Alexander Glass].
Figure 4 in Notes on the ecology, activity patterns and behavior of the kinkajou (Potos flavus)
Figure 4: Group composition of kinkajous at (A) Pijao and (B) San Juan.
Table ¹: List of fruit species consumed by kinkajous in Pijao and San Juan. in Notes on the ecology, activity patterns and behavior of the kinkajou (Potos flavus)
<p><b>Table ¹:</b> List of fruit species consumed by kinkajous in Pijao and San Juan.</p><table><tbody><tr><th><b>Family</b></th><th><b>Species</b></th><th><b>Locality</b></th></tr></tbody><tbody><tr><th></th><td></td><td><b>Pijao</b></td><td><b>San Įuan</b></td></tr><tr><th>Anacardiaceae</th><td><i>Spondias mombin</i></td><td><b>–</b></td><td>X</td></tr><tr><th>Araliaceae</th><td><i>Dendropanax macrophyllum</i></td><td>X</td><td><b>–</b></td></tr><tr><th>Moraceae</th><td><i>Ficus brevibracteata</i></td><td>X</td><td><b>–</b></td></tr><tr><th></th><td><i>Ficus dendrocida</i></td><td><b>–</b></td><td>X</td></tr><tr><th></th><td><i>Poulsenia armata</i></td><td>X</td><td><b>–</b></td></tr><tr><th>Sapotaceae</th><td><i>Pouteria baehniana</i></td><td><b>–</b></td><td>X</td></tr><tr><th>Ulmaceae</th><td><i>Ampelocera albertiae</i></td><td>X</td><td><b>–</b></td></tr><tr><th>Urticaceae</th><td><i>Cecropia telealba</i></td><td>X</td><td><b>–</b></td></tr><tr><th></th><td><i>Cecropia membanacea</i></td><td><b>–</b></td><td>X</td></tr></tbody></table>
Fig. 3 in A new cave species of Rhamdia (Siluriformes: Heptapteridae) from Serra do Ramalho, northeastern Brazil, with notes on ecology and behavior
Fig. 3. Lateral and dorsal views of large (218.6 mm SL; a and b, respectively; MZUSP 87777) and small (61.2 mm SL; c and d, respectively; LIRP 5643) individuals of R. enfurnada.
Fig. 2 in A new cave species of Rhamdia (Siluriformes: Heptapteridae) from Serra do Ramalho, northeastern Brazil, with notes on ecology and behavior
Fig. 2. Distribution of standard length (mm) classes relative to 121 individuals of R. enfurnada. Data collected in July 2005.
Data from: Post-fledging behavioral ecology of migratory songbirds: How do fledgling activity rates vary across species?
<p>This datsaset contains data for a comparison of fledgling activity rates from 9 songbird species in east-central Illinois, USA, described in the paper: "Jones, TM, and MP Ward. 2021. Post-fledging behavioral ecology of migratory songbirds: how do fledgling activity rates vary across species?"; published in <em>Behavioral Ecology</em>. The dataset contains estimates of fledgling activity rates during the daytime, nighttime, and across the post-fledging period, which were compared to estimates of fledgling morphologies (e.g. mass, tarsus, wing development) and post-fledging survival. Analyses, which can be reproduced with this data, showed that overall rates of post-fledging activity differed by species, but species showed similarities in the development of activity rates across the period. All species exhibited a stead increase in activity rates with age and general patterns mirrored rates of post-fledging mortality, including the presence and absence of post-fledging bottlenecks within each species. Additionally, our findings suggest that fledgling wing development and brood size at fledging contribute to variatio in activity rates within and across species.</p>
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.
Mobile Behavioral Ecological Momentary Assessment and Intervention in Rakai, Uganda
ClinicalTrials.gov study NCT04375423. IPD Sharing: NO. Countries: 0. Publications: 1.
Data from: The origin of snakes: revealing the ecology, behavior, and evolutionary history of early snakes using genomics, phenomics, and the fossil record
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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)
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.