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30 results for “Reed Warbler”
Variation and overlaps in non-breeding regions of three less-studied breeding populations of the Eurasian Reed Warbler: Figures and datasheet
<p>Non-breeding regions of Eurasian Reed Warbler, <em>Acrocephalus scirpaceus</em> breeding in Finland, Jordan, and Kazakhstan as predicted with hydrogen stable isotope analysis.</p> <p>file name corresponds to the following figure titles:</p> <p>"Fig 2": <strong><span>Figure 2:</span></strong><span> The predicted non-breeding regions of Eurasian Reed Warblers breeding in Finland, Jordan, and Kazakhstan.</span></p> <p><span><span>"Fig 3": <strong><span>Figure </span></strong><span>3: Predicted non-breeding regions for Eurasian Reed Warblers sampled at a breeding site in Finland assigned to isotopic clusters A and </span><span><span>B.</span></span></span></span></p> <p><span><span></span></span><span></span><span><span><span>"Fig 4": </span></span></span><strong><span>Figure 4:</span></strong><span> Predicted within population average non-breeding regions for Eurasian Reed Warblers assigned to clusters A-F breeding in Jordan </span><span>(see Table S1 for details).</span></p> <p><span>Also uploaded is a csv file containing the isotopic signature of the birds. The file name is "data_Acrocephalus_scirpaceus"</span></p>
Figure 1 in The effects of weather and reed management on nesting parameters of the Great Reed Warbler, Acrocephalus arundinaceus (Aves: Sylviidae)
Figure 1. The relationship between mean water depth and nest density of the Great Reed Warbler at the Bager Pond for the period 2008-2016.
Figure 2 in The effects of weather and reed management on nesting parameters of the Great Reed Warbler, Acrocephalus arundinaceus (Aves: Sylviidae)
Figure 2. The relationship between the amount of precipitation and nesting success of the Great Reed Warbler at the Bager Pond for the period 2008-2016.
Рис. 2. Типичные местообитания чернобровой камышевки: a — поΛынники в пос. Гайворон; b — тростниковые пΛавни в с. Сосновка Fig. 2. Typical habitats of the black-browed warbler: a — wormwood in the Gaivoron village; b — reed floodplains in the Sosnovka village in in the Ussuri region
Рис. 2. Типичные местообитания чернобровой камышевки: a — поΛынники в пос. Гайворон; b — тростниковые пΛавни в с. Сосновка Fig. 2. Typical habitats of the black-browed warbler: a — wormwood in the Gaivoron village; b — reed floodplains in the Sosnovka village
Figure 3 in Effect of reed burning and precipitation on the breeding success of Great Reed Warbler, Acrocephalus arundinaceus, on a mining pond
Figure 3. Correlation between amount of precipitation and breeding success at Bager Pond, 2008–2011. Data points are Early and Late groups in 4 years.
Figure. The left-hand photo shows the Basra Reed-warbler (Acrocephalus griseldis) caught at Aras River Ornithological Research Station. The right-hand photo compares A. griseldis (left) with a Great Reed-warbler (A. arundinaceus, right). in Endangered Basra Reed-warbler (Acrocephalus griseldis) recorded for the first time in Turkey (Aves: Acrocephalidae)
Figure. The left-hand photo shows the Basra Reed-warbler (Acrocephalus griseldis) caught at Aras River Ornithological Research Station. The right-hand photo compares A. griseldis (left) with a Great Reed-warbler (A. arundinaceus, right).
Videos of Common Cuckoos parasitizing their Reed Warbler hosts in China
<p>Dataset including eight .mp4 videos:</p> <p>Videos 1-3: Egg laying by female cuckoos in host nests.</p> <p>Video 4: The host collected the nest materials for nesting.</p> <p>Videos 5-7: The Common Cuckoo visits the host nest but not egg-laying.</p> <p>Video 8: The calling by a female Oriental Reed Warbler in a nest in the morning.</p>
Data for: Breeding pairs with color aberrations in Oriental reed warblers
<p>One pair of Oriental red warblers was found with color aberrations. Two videos (ESM Video S1 and Video S2) were provided as supplementary material showing Breeding pairs with color aberrations in Oriental reed warblers. Our study shows that the breeding pair breed normally and further egg experiments indicated they can reject foreign eggs as other breeding pairs.</p>
Variation and overlaps in non-breeding regions of the Eurasian Reed Warbler: insight from three breeding populations
<p>Data for Variation and overlaps in non-breeding regions of the Eurasian Reed Warbler: insight from three breeding populations</p>
Videos of Common Cuckoos parasitizing their Reed Warbler hosts in China
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Data for: Breeding pairs with color aberrations in Oriental reed warblers
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Data for: MHC I of the great reed warbler promotes a flat peptide binding mode
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Data on great reed warbler nest activity and song behaviour
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Evolution of population-specific migration routes in the great reed warbler <em>Acrocephalus arundinaceus</em>: Evidence of a novel spring migration strategy
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Dataset on the content of Cu, Ni Cd, Pb, Zn, Ag, Mg, Fe, Co and Ca in the carcass, gastrointestinal tract tissues and the whole body of nestlings of a small passerine bird, the Eurasian Reed Warbler Acrocephalus scirpaceus
<p><span>The data include the description of the age and the </span><span>concentrations of </span><span>Cu, Ni Cd, Pb, Zn, Ag, Mg, Fe, Co and Ca<span> measured in the </span>isolated, emptied gastrointestinal tract, <span>the whole body, and </span>carcass of the each individual nestling of a different age and hence a different stage of <span>post-natal development. The dataset includes also</span> some additional information on the breeding biology of the focal species. </span></p>
Data from: Individual and sex-related patterns of prolonged flights during both day and night by great reed warblers crossing the Mediterranean Sea and Sahara Desert
<p>A wide variety of the barrier crossing strategies exist among migrating songbirds, ranging from strict nocturnal flights to non-stop flights over a few days. We evaluate barrier crossing strategies in a nocturnally migrating songbird crossing the Mediterranean Sea and the Sahara Desert, the great reed warbler, exploring variation between the sexes and within individuals. We used data from 31 year-round light-level geolocators tracks from 26 individuals (13 males and 13 females), with four individuals tracked for 2–3.5 consecutive years. Almost all individuals (25 of 26) prolonged their flights into the day at least on one occasion. The mean duration of these prolonged flights was 19.9 h and did not differ between sexes or seasons. Fifteen birds performed non-stop flights during more than one full day and night (≥ 24 h; mean = 31.9 h; max = 55 h) in autumn and/ or spring, but these flights were generally too short to cross an entire barrier (such as the Sahara Desert) in one non-stop flight. Patterns of prolonged flights showed considerable within-individual variation in females between seasons (autumn versus spring) and in both males and females between years, suggesting high individual flexibility in migration strategy. Significantly more males than females performed prolonged flights during autumn migration, but not spring, possibly reflecting sex-specific carry-over effects. We conclude that great reed warblers have the ability to conduct prolonged continuous flights for up to several nights and days, which potentially would allow them to cross the Sahara Desert in one non-stop flight. However, they typically use a mixed strategy of several nocturnal flights with intermittent stopovers in combination with 1–3 prolonged flights. Prolonged flights covered less than half (44%) of the total flight time across the barriers, and the diurnal parts of the flights covered only 18% of this time.</p>
Contrasting effects of egg size and appearance on egg recognition and rejection response by Oriental reed warblers
<p>Among potential hosts, the rejection of foreign eggs, which is a common and effective strategy to counter brood parasitism, depends on egg recognition. Multi-modal and multi-component recognition cues of brood parasitic eggs, which include both tactile (size, shape, and texture) and visual (size, shape, color, and maculation) cues, are potentially involved in the perception and discrimination of foreign eggs by hosts. An egg rejection experiment on the host with different types of model eggs can help to accurately assess the relative contribution of different components on egg recognition and constraints to rejection, in which videos can help identify the method of host rejection. Here, we assessed egg recognition and rejection responses by Oriental reed warblers (<i>Acrocephalus orientalis</i>), one of the most common hosts of common cuckoos (<i>Cuculus canorus</i>) which breed in eastern China. We designed six groups of model eggs for rejection experiments in which sensory cues included three grades of size and two categories of visual mimicry. Our experiments confirmed that the multi-modal traits, which included variation in size, were significant predictors of egg rejection: we detected significantly higher rejection rates of mimetic spotted model eggs than of non-mimetic blue eggs. However, large model eggs did not yield higher rejection rates and, instead, these were less likely to be rejected and more likely to be deserted compared with smaller eggs. Further video-recording data showed that there was no significant effect of egg size on the egg recognition rate (percentage of nests with evidence of egg-pecking). No evidence that the egg appearance had an effect on the method of egg rejection (ejection or nest desertion) was found. Only visual signals, such as color and maculation, contributed to the recognition of foreign eggs by Oriental reed warblers as recognizable clues, but not the egg size. The egg size had an impact on the type of egg rejection. It was less feasible for the warblers to eject large eggs and that is why they opted more often for desertion as the mean of model egg rejection. The significantly lower egg rejection rate of large eggs suggested that although some of them were recognized as foreign eggs, hosts failed to reject these eggs and finally the eggs were assumed to being accepted by the commonly-used nest-checking methods.</p>
FIGURE 2 in Haemoproteus nucleocondensus n. sp. (Haemosporida, Haemoproteidae) from a Eurasian songbird, the Great Reed Warbler Acrocephalus arundinaceus
FIGURE 2. Bayesian phylogeny of 24 mitochondrial cytochrome b lineages of Haemoproteus spp. and 4 lineages of Plasmodium spp. One lineage of Leucocytozoon is used as outgroup. Codes of lineages and GenBank accession numbers (in parentheses) are given after parasite species names, with the name of new species in bold. Names of parasites with microgametocytes possessing condensed nuclei morphologically similar to the new species are underlined. Posterior probability values>70 are indicated near the nodes.Vertical bars A and B indicate haemoproteid species belonging to the subgenera Haemoproteus and Parahaemoproteus, respectively.
FIGURE 1 in Haemoproteus nucleocondensus n. sp. (Haemosporida, Haemoproteidae) from a Eurasian songbird, the Great Reed Warbler Acrocephalus arundinaceus
FIGURE 1. Gametocytes of Haemoproteus nucleocondensus sp. nov. (a-l) from the blood of Great Reed Warbler, Acrocephalus arundinaceus and Haemoproteus payevskyi (m-t) from the blood of Reed Warbler, Acrocephalus scirpaceus: a, b, i, m, q—young gametocytes; c–h, n–p—macrogametocytes; j–l, r–t—microgametocytes. Long arrows—nuclei of parasites; short arrows—unfilled spaces between gametocyte and envelope of infected erythrocyte; arrow head—pigment granules. Giemsa-stained thin blood films. Bar = 10 µm.
Contrasting effects of egg size and appearance on egg recognition and rejection response by Oriental reed warblers
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