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9,153 results for “behavior”
Figures 3–5 in Asymmetrical male mandibular horns and mating behavior in Agathidium Panzer (Coleoptera: Leiodidae)
Figures 3–5. (3) Expected distribution of body size versus ornament length under nonlinear regression model (dose–response curve) with switch point indicated by dashed line. (4) Expected frequency distribution of body size data in species of Agathidium. (5) Expected frequency distribution of ornament length data in species of Agathidium.
Figures 18–26 in Asymmetrical male mandibular horns and mating behavior in Agathidium Panzer (Coleoptera: Leiodidae)
Figures 18–26. Agathidium species showing variation in horn morphology. (18–20) A. picipes: (18) left lateral; (19) anterior; (20) dorsal. (21–23) A. aristerium: (21) left lateral; (22) anterior; (23) dorsal. (24–26) A. atronitens: (24) left lateral; (25) anterior; (26) dorsal. Scale bars: 0.5 mm.
Figure 4 in Revision of the southern South American endemic genus Anomiopsoides Blackwelder, 1944 (Coleoptera: Scarabaeidae: Scarabaeinae: Eucraniini) and description of its food relocation behavior
Figure 4. Distributional map of Anomiopsoides aurita (Burmeister), A. biloba (Burmeister), and A. catamarcae Martínez.
Figure 3 in Revision of the southern South American endemic genus Anomiopsoides Blackwelder, 1944 (Coleoptera: Scarabaeidae: Scarabaeinae: Eucraniini) and description of its food relocation behavior
Figure 3. Mesotibial apex and external tibial spur of: (a) Anomiopsoides biloba (Burmeister); (b) A. catamarcae Martínez.
Figure 2 in Revision of the southern South American endemic genus Anomiopsoides Blackwelder, 1944 (Coleoptera: Scarabaeidae: Scarabaeinae: Eucraniini) and description of its food relocation behavior
Figure 2. Dorsal view of the head of: (a) Anomiopsoides aurita (Burmeister); (b) A. catamarcae Martínez; (c, d) A. cavifrons (Burmeister), male and female, respectively; (e) A. biloba (Burmeister); (f, g) A. heteroclyta (Bermeister), male and female, respectively.
Neurogenomic divergence during speciation by reinforcement of mating behaviors in chorus frogs (Pseudacris) – De novo reference transcriptome: Assemblerd contigs and gene annotations
<p>Assembled contigs (Trinity) and gene annotations (Trinotate) of a reference transcriptome for the Upland Chorus Frog, <em>Pseudacris feriarum</em>. Data to assemble the contigs were obtained by sequencing four tissue types: Brain, eyes, testis, and somatic (liver/heart/lung/skin/muscle). Raw reads are stored in the NCBI-SRA database (BioProject PRJNA723357).</p>
EEG/LFP/EMG data from freely-behaving rats across the sleep/wake cycle (includes manual identification of behavioral state in 4s epochs)
<p>Open-access data set that contains raw EEG/LFP/EMG data recorded from freely-behaving rats. 40 complete 24-hr recordings across 10 male, Sprague Dawley rats are included. Additionally, manual behavioral state classification is provided for all recordings in 4s epochs. These data form the testing and training set for a recently accepted article (Ellen J.G. and Dash, M.B. <em>An automated neural network for automated behavioral state classification rats</em>, peerJ (<em>in press)</em>) which details an open-source artificial neural network for automated classification of behavioral state. R-code for the automated classifier and detailed instructions for its implementation are freely available at: <a href="https://github.com/jellen44/AutomaticSleepScoringTool"><em> https://github.com/jellen44/AutomaticSleepScoringTool</em></a></p> <p>For additional details about the data set, please see the uploaded readme file.</p> <p> </p>
Figure 2 in Mating behavior of nemerteans: present knowledge and future directions
Figure 2. Schematic representation of compact-headed (primitive) and elongate-headed (modified) sperm of nemerteans. Modified after Stricker and Folsom (1998).
Figure 1 in Mating behavior of nemerteans: present knowledge and future directions
Figure 1. Female Lineus viridis with two males immediately after fertilization and deposition of mucus cocoon. Photo courtesy of K. Reise (Wattenmeerstation List/Sylt, Germany).
Figs. 1–4 in Notes on the feeding behavior of Teratocoris saundersi (Hemiptera: Miridae) in Iceland: phytophagy, zoophagy, and adventitious biting
Figs. 1–4. Teratocoris saundersi Douglas & Scott, 1869 in Iceland: host plant and feeding habits. 1 – Leymus arenarius (Poaceae), a host plant on sandy shore, Reykjavík; 2 – female preying on a chironomid fly on the grass L. arenarius; 3 – male scavenging on a fly on thinstem lady's mantle, Alchemilla filicaulis (Rosaceae); 4 – fifth instar piercing human skin ('adventitious biting').
Behavioral strategies and the spatial pattern formation of nesting
<p>This dataset contains data from a combined field and simulation study regarding spatial pattern formation of nesting, described in the paper: "Batsleer, F., Maes, D., Bonte, D. (2021) Behavioral strategies and the spatial pattern formation of nesting. The American Naturalist".</p> <p>The study investigates the relative importance of environmental and behavioral mechanisms in nest aggregations of the ground-nesting digger wasp <em>Bembix rostrata</em>. A field study was combined with an individual-based model that simulated the possible behaviors of spatial organisation of nesting.</p> <p>In the first analysis, a microhabitat model was built based on the location of the nests from a capture-mark-recapture study (CMR) and environmental variables NDVI (vegetation) and insolation (sun irradiance), derived from detailed remote sensing data from a drone flight.</p> <p>In the second analysis, an IBM was built that combined three possible mechanisms of nest choice to simulate the emerging spatial and network patterns found in the field. This was done by combining an environmental cue (based on the microhabitat model) and two relevant behavioral mechanisms related to local site fidelity and conspecific attraction. Strengths and combinations of the mechanisms could vary. Simulations were compared to the field data to find which combinations and strengths of mechanisms can best explain the emerging spatial and network patterns.</p> <p>The main results are that 1) the observed pattern in nature is best predicted by the simultaneous effect of a weak environmental cue and strong behavioral mechanisms. 2) individuals differ in their combination of mechanisms used and will either use local site fidelity (personal information) or conspecific attraction (inadvertent social information), but not both simultaneously. 3) We demonstrate that the nest pattern formation of a central place foraging insect cannot be considered as the sum of environmental and behavioral mechanisms.</p>
Figs. 27–30 in Oocytes, Larvae, and Cleptoparasitic Behavior of Biastes emarginatus (Hymenoptera: Apidae: Nomadinae: Biastini)
Figs. 27–30. Diagrams of postdefecating larva of Biastes emarginatus. 27. Entire larva, lateral view. 28. Right mandible, outer view. 29, 30. Head, frontal and lateral views respectively. ATP 5 anterior tentorial pit; PTP 5 posterior tentorial pit.
Figs. 23–26 in Oocytes, Larvae, and Cleptoparasitic Behavior of Biastes emarginatus (Hymenoptera: Apidae: Nomadinae: Biastini)
Figs. 23–26. SEM micrographs of first instar of Neopasites cressoni. 23. Head, near frontal view. 24. Close-up of part of left side of head in fig. 23. 25. Head, ventrolateral view. 26. Head, of another specimen, approximate ventrolateral view. ATP 5 anterior tentorial pit.
Figs. 8–15 in Oocytes, Larvae, and Cleptoparasitic Behavior of Biastes emarginatus (Hymenoptera: Apidae: Nomadinae: Biastini)
Figs. 8–15. SEM micrographs of head of first instar Biastes emarginatus. 8. Entire head lateral view. 9. Close-up of top of head showing position of antenna and linear row of sensilla across top. 10. Close-up of antenna with 4 sensilla. 11. Close-up of labrum, approximate lateral view. 12. Ventral view of head from behind showing mandibles and labiomaxillary region. 13. Close-up of labrum, approximate ventral view. 14. Close-up of labiomaxillary region, identified by rectangle in fig. 8, dashed line demarking boundary of sclerotized (above) and membranous (below) areas. 15. Close-up of membranous area of figure 14 identifying palpi and salivary opening. PTP 5 posterior tentorial pit.
Figs. 18, 19 in Oocytes, Larvae, and Cleptoparasitic Behavior of Biastes emarginatus (Hymenoptera: Apidae: Nomadinae: Biastini)
Figs. 18, 19. Microphotographs of cleared head of Biastes emarginatus, lateral (18) and ventral (19) views, respectively. Fig. 20. Microphotographs of cleared head of Neopasites cressoni, lateral view, showing greater curvature to frontal profile. Fig. 21. Microphotograph of side of cleared head of mature larvae of Biastes emarginatus, showing texture of integument associate with rear part of head. Fig. 22. Microphotograph of spiracle of mature larva of Biastes emarginatus, side view. PTP 5 posterior tentorial pit.
Figs. 16, 17 in Oocytes, Larvae, and Cleptoparasitic Behavior of Biastes emarginatus (Hymenoptera: Apidae: Nomadinae: Biastini)
Figs. 16, 17. SEM micrographs of first instar of Biastes emarginatus. 16. Integument of first abdominal segment showing transverse, multidentate spicules. 17. Close-up of area identified by rectangle in fig. 16.
Figs. 3–7 in Oocytes, Larvae, and Cleptoparasitic Behavior of Biastes emarginatus (Hymenoptera: Apidae: Nomadinae: Biastini)
Figs. 3–7. SEM micrographs of mature oocytes of Biastes emarginatus. 3. Entire oocyte, dorsal view, anterior end to the right. 4. Same, approximate ventral view. 5. Close-up of anterior end, near lateral view. 6. Close-up of micropyle and lamellate tubercle from fig. 5. 7. Anterior end of another oocyte, showing variation in shape of lamellate tubercle, anterodorsal view.
Figs. 1, 2 in Oocytes, Larvae, and Cleptoparasitic Behavior of Biastes emarginatus (Hymenoptera: Apidae: Nomadinae: Biastini)
Figs. 1, 2. Microphotographs of Biastes emarginatus. 1. Mature oocyte, lateral view, showing transparent, glassy chorion. 2. First instar apparently attacking another first instar.
Fig. 39 in Hospicidal Behavior of the Cleptoparasitic Wasp Sapyga luteomaculata And Investigation into Ontogenetic Changes in Its Larval Anatomy (Hymenoptera: Vespoidea: Sapygidae)
Fig. 39. Microphotograph of labium of cleared postdefecating fourth instar of Sapyga luteomaculata, showing narrow but pronounced premental sclerite, labial palpi, and articulating arms of stipites.
Figs. 37, 38 in Hospicidal Behavior of the Cleptoparasitic Wasp Sapyga luteomaculata And Investigation into Ontogenetic Changes in Its Larval Anatomy (Hymenoptera: Vespoidea: Sapygidae)
Figs. 37, 38. SEM micrographs of postdefecating fourth instar of Sapyga luteomaculata. 37. Posterior part of abdomen, lateral view, showing dorsal divisions of segments into cephalic and caudal annulets. 38. Spiracle.
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.