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10 results for “Gallus domesticus”
Fig. 1 in Chewing Lice (Order Mallophaga, Suborders Amblycera And Ichnocera) Fauna Of Domestic Chicken (Gallus Gallus Domesticus) In Ukraine
Fig. 1. Menopon gallinae: ♀: 1 — forehead; 2 — temporal lobe; 3 — antenna; 4 — eyes; 5 — abdomen (×400); ♂: 1 — forehead; 2 — temporal lobe; 3 — antenna; 4 — foot; 5 — bristles; 6 — abdomen posterior (×300).
Fig. 4 in Chewing Lice (Order Mallophaga, Suborders Amblycera And Ichnocera) Fauna Of Domestic Chicken (Gallus Gallus Domesticus) In Ukraine
Fig. 4. Morphology of Goniocotes hologaster: ♀: 1 — forehead; 2 — eyes; 3 — bristles on head; 4 — the rear of the abdomen (×300); ♂: 1 — head; 2 — temporal edges; 3 — overall oval body; 4 — the last segment of the abdomen blade-shaped (×250).
Fig. 3 in Chewing Lice (Order Mallophaga, Suborders Amblycera And Ichnocera) Fauna Of Domestic Chicken (Gallus Gallus Domesticus) In Ukraine
Fig. 3. Morphology of Menacanthus cornutus: ♀: 1 — forehead; 2 — temporal lobe; 3 — sternal plate; 4 — crop; 5 — posterior part of the abdomen with bristles; ♂: 2 — eye; 3 — prothorax with foots; 4 — mesothorax; 5 — metathorax; 6 — abdomenal bristles; 7 — oval shape of the rear of the abdomen; 8 — ejaculatory ducts (×400).
Fig. 2 in Chewing Lice (Order Mallophaga, Suborders Amblycera And Ichnocera) Fauna Of Domestic Chicken (Gallus Gallus Domesticus) In Ukraine
Fig. 2. Morphology Menacanthus stramineus: ♀: 1 — forehead; 2 — temporal lobe; 3 — prothorax; 4 — mesothorax; 5 — metathorax; 6 — tarse; 7 — crop; 8 — the egg chamber; ♂: 1 — prothorax foot; 2 — foot mesothorax; 3 — foot metathorax; 4 — testes; 5 — crop (×400).
Fig. 2. Recent chicken Gallus domesticus Linnaeus, 1758 RAM R1 in Head and neck posture in sauropod dinosaurs inferred from extant animals
Fig. 2. Recent chicken Gallus domesticus Linnaeus, 1758 RAM R1 in right lateral view, illustrating maximally extended pose (A) and ONP (B): last four cervical and first four dorsal vertebrae. Note the strong ventral deflection of the base of the neck in ONP, contrasting with the very strong dorsal deflection illustrated in a live chicken by Vidal et al. (1986: fig. 7).
Open source physiological data and physiological-based kinetic model code for the chicken (Gallus gallus domesticus)
<p>This excel file and mode code (DOI:10.5281/zenodo.3603114) provides:</p> <p>1. Physiological parameters and associated inter-individual variability (sample size, mean, coefficient of variation,) for chicken (<em>Gallus gallus domesticus</em>). These physiological parameters were estimated based on the results of extensive literature searches and specific experimental data described in Lautz et al., (2020).</p> <p>2. An R code for the generic chicken physiologically based model as well as the “soboljansen” code to carry out sensitivity analysis using sobol plots. The code for the generic model allows to run:</p> <p>a. A deterministic PBK model which represents only a single animal.</p> <p>b. A probabilistic PBK model to simulate individual differences in physiological parameters within a population. Sensitivity analyses can be performed to identify which parameters have the most impact on the model’s outputs. Predictions can be compared with experimental data. The model can be used to assess the influence of physiological parameters on the kinetics of chemicals. For PBK modelling purposes, species and chemical specific kinetics (e.g clearance, absorption rate, etc…) should be provided by the user.</p> <p>The full data collection and implementation of the models using case studies are described in (Lautz et al., 2020).</p> <p><strong>The dataset providing the physiological parameters is available in Excel.<br> The R code is presented as meta data to be implemented in R.</strong></p>
Data from: Uninhibited chickens: ranging behavior impacts motor self-regulation in free-range broiler chickens (Gallus gallus domesticus)
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Data from: Sound attenuation in the ear of domestic chickens (Gallus gallus domesticus) as a result of beak opening
Because the quadrate and the eardrum are connected, the hypothesis was tested that birds attenuate the transmission of sound through their ears by opening the bill, which potentially serves as an additional protective mechanism for self-generated vocalizations. In domestic chickens, it was examined if a difference exists between hens and roosters, given the difference in vocalization capacity between the sexes. To test the hypothesis, vibrations of the columellar footplate were measured ex vivo with laser Doppler vibrometry (LDV) for closed and maximally opened beak conditions, with sounds introduced at the ear canal. The average attenuation was 3.5 dB in roosters and only 0.5 dB in hens. To demonstrate the importance of a putative protective mechanism, audio recordings were performed of a crowing rooster. Sound pressures levels of 133.5 dB were recorded near the ears. The frequency content of the vocalizations was in accordance with the range of highest hearing sensitivity in chickens. The results indicate a small but significant difference in sound attenuation between hens and roosters. However, the amount of attenuation as measured in the experiments on both hens and roosters is small and will provide little effective protection in addition to other mechanisms such as stapedius muscle activity.
Data from: Sound attenuation in the ear of domestic chickens (Gallus gallus domesticus) as a result of beak opening
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Microarray analysis of up-regulated genes accompanying filial imprinting in domestic chicks (Gallus gallus domesticus)
GEO Series GSE31055. Gallus gallus. 2 samples. Type: Expression profiling by array.
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Allen Brain Atlas
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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
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