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297 results for “warbler”
Data from: Examining carry‐over effects of winter habitat on breeding phenology and reproductive success in prairie warblers (Setophaga discolor)
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Evolution of breeding plumages in birds: a multiple-step pathway to seasonal dichromatism in New World Warblers (Aves: Parulidae)
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Evidence of nest material kleptoparasitism in Worm-eating Warblers (Helmitheros vermivorum) in east-central Arkansas, USA
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Implications for evolutionary trends from the pairing frequencies among golden-winged and blue-winged warblers and their hybrids
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Golden-winged Warbler post-fledging movement and stand-scale habitat selection
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Habitat-specific survival of golden-winged warblers (Vermivora chrysoptera) during the non-breeding season in an agricultural landscape
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Wilson Warbler molting and plumage observations
<p>I made observations of a central California population of Wilson's Warbler, <em>Cardellina pusilla, </em>on or after 1 July over ten breeding seasons. I sighted males in definitive prebasic molt as early as 4 July (in 2007) and as late as 1 September (in 1999). I determined that most territorial males at my study site molted on their breeding territories, and individual molt lasted a maximum of 46 days. Following prebasic molt, territorial males engaged in subdued "post-molt singing," which appeared to last no more than seven days in most males, and which I first heard on 13 August (in 1004), and last heard on 6 September (in 1999). I sighted no female in definitive prebasic molt, nor fresh basic plumage, during the study. Of 13 females sighted on or after 21 July, I confirmed that 11 were in late breeding season uniparental brood care, and I could not rule out late brood care for the other two. Most, and possibly all, females not engaged in late season uniparental brood care appear to have vacated their breeding territories before 21 July, as I saw just two possible after that date. This apparent early departure of the majority of resident females from their breeding grounds was much earlier than the departures of resident males, the last of which I sighted on 10 September (in 1999). Early-departing females presumably underwent prebasic molt after 21 July, and at locations not known. Remaining late-nesting females must have molted much later than did resident males, and also likely later than early-departing resident females, and at unknown locations. I last sighted two uniparental brood-tending females, still in worn plumage, on 26 and 29 August respectively, whereas some males had completed prebasic molt as early as 13 August. Two unique findings of this study are a male/female difference in location of prebasic molt, and a likely dichotomy of prebasic molt timing between females which leave their breeding territories relatively early, and those which remain on their territories in uniparental brood care. Another finding, that most, and perhaps all, territorial male Wilson's Warblers engaged in brief post-molt singing following prebasic molt, is a largely unrecognized behavior, but one previously reported in several other passerine species. Post-molt singing may be a reliable indicator that prebasic molt is complete.</p>
Figure 2 in Effect of reed burning and precipitation on the breeding success of Great Reed Warbler, Acrocephalus arundinaceus, on a mining pond
Figure 2. Mean (±SE error bars) clutch size and number of fledglings at Bager Pond, 2008–2011.
Figure 1 in Effect of reed burning and precipitation on the breeding success of Great Reed Warbler, Acrocephalus arundinaceus, on a mining pond
Figure 1. Kaplan–Meier survival curves of GRW nests in breeding seasons 2008–2011.
Wilson Warbler molting and plumage observations
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Data from: Genetic differences between willow warbler migratory phenotypes are few and cluster in large haplotype blocks
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FIGURE 8 in The type of Setophaga ruficoronata (Kaup 1851) is a hybrid: implications for the taxonomy of Myioborus warblers (Passeriformes: Parulidae)
FIGURE 8. The type of Setophaga melanocephalus Tschudi, 1844 (MHNN 92.9187). Dorsal, ventral and side views, with the detail of the face. Currently treated as the nominate subspecies of a polytypic species: Myioborus melanocephalus. Photographs by Maciej Czepiel and Celia Bueno (Musée d'Histoire Naturelle de Neuchâtel).
Fig. 4 Phylogenetic chronogram, a in Mitochondrial evidence for genetic diversity and low phylogeographic differentiation in the Marsh Warbler Acrocephalus palustris (Aves: Acrocephalidae)
Fig. 4 Phylogenetic chronogram, a coalescent analysis implemented in BEAST with lognormal relaxed clock (uniform distribution and 0.01105– 0.02500 substitutions per million years) and population expansion model as priors. Thick horizontal bars represent the 95 % HDP of the age of major nodes and numbers indicate node posterior probability values
Fig. 1 in Mitochondrial evidence for genetic diversity and low phylogeographic differentiation in the Marsh Warbler Acrocephalus palustris (Aves: Acrocephalidae)
Fig. 1 Approximate locations of the sampling sites of A. palustris. Breeding (yellow) and wintering (light blue) distributions (del Hoyo et al. 2006). The names of localities are abbreviated as in Table 1. Germany includes Franconia, Treysa, and Saar
Input data: Can the Hermit Warbler serve as an old-forest indicator species in the Sierra Nevada?
<p>Input data used for occupancy modeling of Hermit Warblers across the Sierra Nevada in 2021.</p>
Input data and R code for "Larger male Yellow Warbler ( Setophaga petechia ) occupy smaller home ranges over winter in natural and agricultural sites in western Mexico"
<p>Data used for modeling Yellow Warbler home ranges in western Mexico from 2012 to 2014.</p> <p> </p> <p> </p>
Metadata for Reed Warbler Age Diet Paper
<p>This dataset comprises metadata which corresponds to a paper prepared for submission entitled "Use of metabarcoding to examine season and ontological variation in prey choice and diet of a generalist songbird, the Eurasian reed warbler".</p> <p>Sample identifiers are given for faecal samples collected from songbirds at Chew Valley Lake in Somerset. Information such as location, date/time of collection, and other environmental data are supplied. Dietary data to be supplied after publication.</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.
Annotated Behaviour and Observability Dataset (ABODe)
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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.