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155 results for “Feeding behaviours”
Figure 8 from: Balestra V, Lana E, Vanin S (2022) Observations on the habitat and feeding behaviour of the hypogean genus Eukoenenia (Palpigradi, Eukoeneniidae) in the Western Italian Alps. Subterranean Biology 42: 23-41. https://doi.org/10.3897/subtbiol.42.75784
Figure 8 Approach and bite of Eukoenenia strinatii and two living Collembola (photos by V. Balestra).
Figure 5 from: Balestra V, Lana E, Vanin S (2022) Observations on the habitat and feeding behaviour of the hypogean genus Eukoenenia (Palpigradi, Eukoeneniidae) in the Western Italian Alps. Subterranean Biology 42: 23-41. https://doi.org/10.3897/subtbiol.42.75784
Figure 5 Habitat monitored and different microhabitat where Eukoenenia individuals were observed. A Rimstone dams (gours) in Buranco di Bardineto cave BE. strinatii on wood in Bossea cave CE. strinatii near water in Bossea cave DE. strinatii on Bossea cave ground EE. strinatii on raft of crystalline materials in Bossea cave FE. strinatii on raft of crystalline materials, fungal hyphae and organic remains in Bossea cave. (photos A, C, D, E, F by V. Balestra, B by E. Lana).
Figure 3 from: Balestra V, Lana E, Vanin S (2022) Observations on the habitat and feeding behaviour of the hypogean genus Eukoenenia (Palpigradi, Eukoeneniidae) in the Western Italian Alps. Subterranean Biology 42: 23-41. https://doi.org/10.3897/subtbiol.42.75784
Figure 3 Relation between temperature and relative humidity in the micro-habitat of genus Eukoenenia in the Western Italian Alps. AEukoenenia species BE. strinatii.
Figure 1 from: Balestra V, Lana E, Vanin S (2022) Observations on the habitat and feeding behaviour of the hypogean genus Eukoenenia (Palpigradi, Eukoeneniidae) in the Western Italian Alps. Subterranean Biology 42: 23-41. https://doi.org/10.3897/subtbiol.42.75784
Figure 1 Location of the sampling (maps used for the plate retrieved from https://d-maps.com/carte.php?num_car=2232&lang=en, https://d-maps.com/carte.php?num_car=5894&lang=en, https://d-maps.com/carte.php?num_car=8273&lang=en and modified).
Disparate movement behaviour and feeding ecology in sympatric ecotypes of Atlantic cod
<p>Co-existence of ecotypes, genetically divergent population units, is a widespread phenomenon, potentially affecting ecosystem functioning and local food web stability. In coastal Skagerrak, Atlantic cod (<i>Gadus morhua</i>) occur as two such co-existing ecotypes. We applied a combination of acoustic telemetry, genotyping and stable isotope analysis to 72 individuals to investigate movement ecology and food niche of putative local "Fjord" and putative oceanic "North Sea" ecotypes – thus named based on previous molecular studies. Genotyping and individual origin assignment suggested 41 individuals were Fjord and 31 were North Sea ecotypes. Both ecotypes were found throughout the fjord. Seven percent of Fjord ecotype individuals left the study system during the study while 42 % of North Sea individuals left, potentially homing to natal spawning grounds. Home range sizes were similar for the two ecotypes but highly variable among individuals. Fjord ecotype cod had significantly higher δ<sup>13</sup>C and δ<sup>15</sup>N stable isotope values than North Sea ecotype cod, suggesting they exploited different food niches. The results suggest coexisting ecotypes may possess innate differences in feeding- and movement ecologies and may thus fill different functional roles in marine ecosystems. This highlights the importance of conserving interconnected populations to ensure stable ecosystem functioning and food web structures.</p>
FIGURE 14 in New European Lepidocyrtus Bourlet, 1839 (Collembola, Entomobryidae) with the first description of feeding-related dancing behaviour in Collembola
FIGURE 14. Lepidocyrtus chorus sp. nov., dorsal head chaetotaxy (left side).
Figure 2 in Diet and feeding behaviour of the leaf-litter frog Ischnocnema henselii (Anura: Brachycephalidae) in Araucaria rain forests on the Serra Geral of Rio Grande do Sul, Brazil
Figure 2. Relationship between mouth width and number of ingested animal prey items.
Figure 9 in Feeding behaviour and bite force of sabretoothed predators
Figure 9. Mandibular force profiles of scimitar-toothed machairodonts (Homotherini). Values are presented for the canine, P3P4, and post-M1 interdental gaps. Zx/L-values at the canine are lower than those at post-M1, suggesting a shallow canine bite. No increase in dorsoventral buttressing occurs in the vicinity of the cheek teeth, indicating that the mandibular ramus is adapted for slicing meat exclusively. The Zx/Zycanine values are much higher than those of extant felids, suggesting that prey was restrained prior to the sabre bite.
Figure 5. A in Metamorphosis and evolution of feeding behaviour in salamanders of the family Plethodontidae
Figure 5. A, Kinematic profiles of suction feeding in larval D. quadramaculatus. Gape distance shows a symmetrical profile, with mouth opening and closing taking nearly the same amount of time. Peak hyobranchial depression follows peak gape. Head lifting occurs during mouth opening and head dipping during mouth closing. Note the extremely rapid gape cycle which takes only 28 ms. B, Suction feeding in larval G. porphyriticus. As in A, mouth opening and closing are of nearly the same duration, peak hyobranchial depression follows peak gape, and the gape cycle is extremely rapid at 29 ms.
Disparate movement behaviour and feeding ecology in sympatric ecotypes of Atlantic cod
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Data from: Functional anatomy of the cervical region in the late Miocene amphicyonid Magericyon anceps (Carnivora, Amphicyonidae): implications for its feeding behaviour
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Data from: A three-dimensional computer simulation of feeding behaviour in red and giant pandas relates skull biomechanics with dietary niche partitioning
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Generalised host-plant feeding can hide sterol specialised foraging behaviours in bee-plant interactions
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Data from: Phylogenetic signal, feeding behaviour, and brain volume in Neotropical bats
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Data from: ‘Manipulation’ without the parasite: altered feeding behaviour of mosquitoes is not dependent on infection with malaria parasites
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Data from: Immune response and insulin signalling alter mosquito feeding behaviour to enhance malaria transmission potential
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Integration of Feeding Behaviour by the Liver Circadian Clock Reveals Network Dependency of Metabolic Rhythms [RNA-seq]
GEO Series GSE171183. Mus musculus. 18 samples. Type: Expression profiling by high throughput sequencing.
Interleukin-17 drives sex-dependent weight loss and changes in feeding behaviour during Trypanosoma brucei infection
GEO Series GSE210600. Mus musculus. 16 samples. Type: Expression profiling by high throughput sequencing.
The role of GCN2 kinase in amino acid dependent longevity and feeding behaviour in Drosophila
GEO Series GSE203210. Drosophila melanogaster. 24 samples. Type: Expression profiling by high throughput sequencing.
Movement behaviour and selection for protected areas by the African white-backed vulture, Gyps africanus, in relation to supplementary feeding
<p>This folder contains data that has previously been collected by supervisor, Dr. Adam Kane for the use of this research project which has been presented to the School of Biology and Environmental Science, University College Dublin. The vultures, ID1 and ID2, were tagged and their whereabouts (latitude and longitude) were tracked every four hours over a year and a half long period (May 2015-December 2016). The time and date were recorded for every point and this data was then recorded in a CSV file.</p>
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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.
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DANDI Archive for NWB datasets
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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.