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72 results for “Falco”
Figure 1 in Home range and foraging habitat selection by breeding lesser kestrels (Falco naumanni) in Greece
Figure 1. Minimum convex polygon home ranges (outer: 100%, interior: 95% of locations) of male (A) and female (B) lesser kestrels during the breeding season in central Greece, 2008.
Fig. 3 in Exploratory Analyses Of Foraging Habitat Selection Of The Red-Footed Falcon (Falco Vespertinus)
Fig. 3. Duality diagram of the eigenanalysis of selection ratios of radio-tracked Red-footed Falcons. The top figure shows the habitat loadings () on two factorial axes, while the lower figure shows the habitat preference of individuals (•) in the same factorial space (see also Table 1). The birds can be
Fig. 2 in Exploratory Analyses Of Foraging Habitat Selection Of The Red-Footed Falcon (Falco Vespertinus)
Fig. 2. Global Manly Selection ratios ± Confidence intervals (CI) of the habitat types analysed. The black dots (•) represent the mean selectivity rate of each habitat type considered. A habitat type can be considered as avoided if the global selection ratio is located in the 0–1 interval, while it can be con-
Figure 2 in Histomorphometrical study of the tongue epithelium of the peregrine falcon (Falco peregrinus)
Figure 2. (A) Scanning electron micrograph of the dorsal surface of the lingual apex of the falcon showing that the lingual epithelium is in a carpet shape. (X,550); (B) Scanning electron micrograph of the dorsal surface of the lingual body of the falcon showing the opening of the lingual gland (arrows). (X,300); (C) Scanning electron micrograph of the dorsal surface of the lingual body of the falcon showing the small conical papillae (single arrow) and large conical papillae (double arrows). (X,27).
Figure 1. A in Histomorphometrical study of the tongue epithelium of the peregrine falcon (Falco peregrinus)
Figure 1. A. Photomicrograph of a transverse section of the lingual apex of the falcon showing the dorsal lingual epithelium (E) and lamina propria (LP). (X, 40). B. Photomicrograph of a transverse section of the lingual body of the falcon showing the dorsal lingual epithelium (E) lingual muscles (M) and paraglossum (P). (X, 40). C. Photomicrograph of a transverse section of the lingual body of the falcon showing the dorsal lingual epithelium (E), lingual muscles (M), paraglossum (P) and the lateral epithelium (arrow) (X,40). D. Photomicrograph of a transverse section of the lingual body of the falcon showing the dorsal lingual epithelium (E) lingual muscles (M), lingual glands (G) and opening of the lingual glands (arrow). (X, 40).
Fig. 1 in Characteristics of the hunting behavior of the Red-footed Falcon (Falco vespertinus) in South-Eastern Bulgaria
Fig. 1. Mean duration of the hovering series of Red-footed Falcons in relation to the sex and period of the lifecycle of the birds.
Figure 2 in The Red-footed Falcon Falco vespertinus population in the Danube Delta and its habitat selection for breeding
Figure 2. Relationship between the presence of a breeding population of RfF and explanatory variables selected. The graphics show the relationship between RfF nest presence and (a) the mean temperature of the warmest quarter, (b) the precipitation of the warmest quarter, (c) the number of patches of habitat in 3000 m radius from the nest, (d) the percent of open habitats in 3000 m radius from the nest, (e) the type of nest used (colonial rook nest or solitary magpie and hooded crow nest), (f) the Simpson index.
Figure 1 in The Red-footed Falcon Falco vespertinus population in the Danube Delta and its habitat selection for breeding
Figure 1. Distribution of the occupied nests of Falco vespertinus inside the ROSPA0031 Danube Delta and Razim–Sinoe Complex (and the 3000 m buffer area outside its perimeter) during the breeding season of 2020.
Fig. 3 in Detection of Eumonospora henryae (Apicomplexa: Sarcocystidae) from Falco columbarius (Falconiformes: Aves): Comparison of host-parasite phylogram and comments on the family Sarcocystidae Poche, 1913
Fig. 3. Phylograms of the genus Eumonospora on the left and core land birds modified from McClure et al. (2019) on the right. The boxes under Eumonospora spp. represent detected host species and the shaded boxes encompass the Afroaves. The lines connect parasites and hosts encountered, with the dotted line indicating host switching across order boundaries.
Fig. 1 in Detection of Eumonospora henryae (Apicomplexa: Sarcocystidae) from Falco columbarius (Falconiformes: Aves): Comparison of host-parasite phylogram and comments on the family Sarcocystidae Poche, 1913
Fig. 1. Optical (A, B) and differential interference contrast photomicrographs (C, D) of oocysts and sporocysts of Eumonospora sp. detected from Falco columbarius. Fig. 1A. Sporulated oocyst with stout sporozoites (SZ) inside a sporocyst (SP). Fig. 1B. A collapsed oocyst with a compact sporocyst residuum (SR) within an SP. Fig. 1C. Randomly diffused SR within an SP. Fig. 1D. Eight SZs with diffused SR. Scale bars = 10 μm.
Fig. 2 in Detection of Eumonospora henryae (Apicomplexa: Sarcocystidae) from Falco columbarius (Falconiformes: Aves): Comparison of host-parasite phylogram and comments on the family Sarcocystidae Poche, 1913
Fig. 2. Phylogenetic trees based on three concatenated datasets (A: 18S + cox1, B: 18S + 28S, and C: 28S + cox1). Phylogenetic analyses are performed via Bayesian inference (BI) and maximum likelihood (ML) methods. Nodes are labelled with probability for BI method node support (left) and bootstrap value support for the ML method (right). Similar phylograms are illustrated with both methods in all datasets. Monophyletic clade of Eumonospora spp. branches off earlier than the clade of Besnoitia spp. and the clade comprising genera Hammondia, Heydornia, Neospora, and Toxoplasma. 18S: nuclear small subunit ribosomal DNA; 28S: nuclear large subunit ribosomal DNA; cox1: mitochondrial Cytochrome C oxidase subunit 1; NA: not available.
Sex, body size, and winter weather explain migration strategies in a partial migrant population of American Kestrels (Falco sparverius)
<p>Given increasing evidence that climate change affects the annual cycles of birds, it is important to understand the mechanisms underlying individual migration strategies and population-level patterns in partial migrants. In this study, we found that thermoregulation (body size and winter temperatures) was a key driver of American Kestrel (<em>Falco</em> <em>sparverius</em>) migration decisions. The annual proportion of migrants in the population, however, was not explained by winter weather and may be the result of differential survival. We measured stable hydrogen isotope values (δD) of talon tissues collected from 501 breeding and overwintering birds to distinguish migrant from resident kestrels in a partially migratory population of American Kestrels in southwestern Idaho in 2013–2021. We then evaluated drivers of migration decisions by assessing potential correlates of migration strategies, whether individuals switched migration strategies between years, and whether the proportion of migrants in the population changed over time or was correlated with winter weather. Male kestrels were 1.6 times more likely to migrate than females, and in colder than average winters, smaller birds of both sexes were more likely to migrate than larger birds. Only 27% of 26 recaptured individuals showed evidence of switching their migration strategies on an annual basis. There was no temporal trend in the proportion of migrants in the population, but proportions varied between years. Interestingly, there was no association between winter minimum temperature anomalies and annual migrant proportions in the population, suggesting that differential over-winter survival, or other stochastic processes, may play an important role in population composition. As winters continue to warm, fewer kestrels may migrate and more may remain resident on breeding grounds. However, it is unclear how changes in migration strategies might affect population-level patterns and resilience to climate change.</p>
Sex, body size, and winter weather explain migration strategies in a partial migrant population of American Kestrels (Falco sparverius)
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Data from: Food supplementing peregrine falcon (Falco peregrinus tundrius) nests increases reproductive success without changes in parental mean provisioning rate
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Fiat CR42 " Falco" - Italian Aviation - Free
A personal tribute for our brave pilots during WWII. Song Rights of "Vittorio Daverio" Source: Objaverse 1.0 / Sketchfab
Urban peregrine falcon (Falco peregrinus) breeding season diet in UK, 2020–2022
<p>Diets of urban peregrine falcons in UK were monitored via nest cameras during the breeding season (March-June) from 2020–2022. All prey items were then identified to species level where possible, by Ed Drewitt. This dataset contains the prey items recorded during each year of the study and location of the sites. </p>
Falco peregrinus (Falconidae) - whole organism
Image of Falco peregrinus (Falconidae) - whole organism
FIG. 13. – Falco cuvieri A. Smith,1830,near Banfora 4.XII.2012 in An annotated checklist of the birds of Burkina Faso
FIG. 13. – Falco cuvieri A. Smith,1830,near Banfora 4.XII.2012 (photo G. Boano).
Fig. 1 in Exploratory Analyses Of Foraging Habitat Selection Of The Red-Footed Falcon (Falco Vespertinus)
Fig. 1. Location of the study area within Hungary
Urban peregrine falcon (Falco peregrinus) breeding season diet in UK, 2020–2022
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Allen Brain Atlas
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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.