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1,604 results for “Wintering”
Fig. 2 in Circadian activity patterns of the Red fox (Vulpes vulpes) and the Stone marten (Martes foina) in agricultural landscape of Northwestern Bulgaria during autumn-winter period
Fig. 2. Stone marten, Martes foina (left) and Red fox, Vulpes vulpes (right) captured in protected area "Zlatiyata", Northwestern Bulgaria.
Fig. 1 in Is the Kotschy's Gecko Mediodactylus kotschyi (Steindachner, 1870) (Reptilia: Gekkonidae) active during the winter?
Fig. 1. The observed specimens of M. kotschyi rumelicusfrom the building of the University of Food Technologies in Plovdiv (Bulgaria). A – an adult specimen, observed on 09.11.2015; B - an adult specimen, observed on 18.11.2015. Photos: S. Basheva.
Fig. 3 in Evaluation of blood and muscle tissues for molecular detection and characterization of hematozoa infections in northern pintails (Anas acuta) wintering in California
Fig. 3. Phylogenetic assignment of hematozoa mitochondrial DNA cytochrome b sequences originating from northern pintails collected from the Central Valley of California (asterisks). Reference sequences for Leucocytozoon (white circles), Haemoproteus (grey circles), and Plasmodium (black circles) parasites were obtained from the National Center for Biotechnology Information. Bootstrap support values for differentiation of broad taxonomic groups are indicated. Values reported for Haemoproteus and Plasmodium show support for phylogenetic differentiation from the mixed subclade formed by reference sequences a and b.
Fig. 4. Minimum spanning network for hematozoa mitochondrial DNA cytochrome b in Evaluation of blood and muscle tissues for molecular detection and characterization of hematozoa infections in northern pintails (Anas acuta) wintering in California
Fig. 4. Minimum spanning network for hematozoa mitochondrial DNA cytochrome b haplotypes detected in Central Valley northern pintails. Circles are drawn proportional to the frequency at which haplotypes were observed. Shading represents the sample collection from which haplotypes originated: white (2006– 2007 wing muscle), grey (2011–2012 wing muscle), and black (2011–2012 blood). A single mutation separates nodes unless explicitly indicated by number. Lines separating nodes are drawn to scale unless indicated by a break. Parasite taxa have been abbreviated in haplotype names (Leu = Leucocytozoon, Hae = Haemoproteus and Pla = Plasmodium).
Fig. 1 in Evaluation of blood and muscle tissues for molecular detection and characterization of hematozoa infections in northern pintails (Anas acuta) wintering in California
Fig. 1. Locations in the Central Valley of California from which northern pintail tissue samples were collected. Samples (n in 2006–2007, n in 2011–2012) were collected in the Sacramento Valley sub-region at: (A) Sacramento National Wildlife Refuge (NWR; 44,92), (B) Delevan NWR (35,7), (C) Colusa NWR (0,2), (D) Sutter NWR (0,1), (E) Little Dry Creek State Wildlife Area (SWA; 0,5), (F) Howard Slough SWA (0,1), (G) Yolo SWA (0,8) and (H) a private duck hunting club (0,1). Samples were collected in the San Joaquin Valley sub-region at: (I) San Luis NWR (7,0), (J) Kesterson NWR (4,0), (K) Los Banos SWA (14,0), (L) Volta SWA (10,0), (M) a private duck hunting club (2,0), and (N) Mendota SWA (30,40).
Fig. 2 in Evaluation of blood and muscle tissues for molecular detection and characterization of hematozoa infections in northern pintails (Anas acuta) wintering in California
Fig. 2. Estimated prevalence of Leucocytozoon (white bars), Haemoproteus (grey bars), and Plasmodium (black bars) parasites in northern pintails sampled in the Central Valley of California in 2006–2007 and 2011–2012 using occupancy modeling. Error bars represent 95% confidence intervals around point estimates.
Fig. 2 in Apparent fatal winter tick (Dermacentor albipictus) infestation in captive reindeer (Rangifer tarandus)
Fig. 2. Dorsal (A) and ventral view (B) of an adult female Dermacentor albipictus collected from captive reindeer. Inset image shows large goblet cells on the spiracular plate.
Рис. 2. ВоΔопΛавающие и окоΛовоΔные виΔы птиц на берегах Ямуны: 1 — Anas crecca, Himantopus himantopus; 2 — Ardea alba, Egretta garzetta, Ardeola grayii; 3 — Himantopus himantopus; 4 — Himantopus himantopus, Recurvirostra avosetta; 5 — Phalacrocorax niger, Amaurornis phoenicurus; 6 — Platalea leucorodia, Mycteria leucocephala; 7 — Ardea cinerea; 8 — Anas poecilorhyncha Fig. 2. Waterfowl and shorebird species on the Yamuna River: 1 — Anas crecca, Himantopus himantopus; 2 — Ardea alba, Egretta garzetta, Ardeola grayii; 3 — Himantopus himantopus; 4 — Himantopus himantopus, Recurvirostra avosetta; 5 — Phalacrocorax niger, Amaurornis phoenicurus; 6 — Platalea leucorodia, Mycteria leucocephala; 7 — Ardea cinerea; 8 — Anas poecilorhyncha in Aggregation of the wintering birds on the Yamuna River in India
Рис. 2. ВоΔопΛавающие и окоΛовоΔные виΔы птиц на берегах Ямуны: 1 — Anas crecca, Himantopus himantopus; 2 — Ardea alba, Egretta garzetta, Ardeola grayii; 3 — Himantopus himantopus; 4 — Himantopus himantopus, Recurvirostra avosetta; 5 — Phalacrocorax niger, Amaurornis phoenicurus; 6 — Platalea leucorodia, Mycteria leucocephala; 7 — Ardea cinerea; 8 — Anas poecilorhyncha Fig. 2. Waterfowl and shorebird species on the Yamuna River: 1 — Anas crecca, Himantopus himantopus; 2 — Ardea alba, Egretta garzetta, Ardeola grayii; 3 — Himantopus himantopus; 4 — Himantopus himantopus, Recurvirostra avosetta; 5 — Phalacrocorax niger, Amaurornis phoenicurus; 6 — Platalea leucorodia, Mycteria leucocephala; 7 — Ardea cinerea; 8 — Anas poecilorhyncha
Fig. 5 in Avian trichomonosis mortality events in band-tailed pigeons (Patagioenas fasciata) in California during winter 2014-2015
Fig. 5. Haemotoxylin and eosin staining (left) of the oral tissue of a band-tailed pigeon (Patagioenas fasciata monilis) recovered during an avian trichomonosis mortality event showing a diffuse thick layer of necrosis extending through the submucosa and multifocally into the deeper soft tissue layers and skeletal muscle; scale bar is 200 μm. Immunohistochemical staining (right) of trichomonad antigen (red) of the same bird demonstrating large numbers of trichomonads in the oral tissue; scale bar is 50 μm. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2 in Avian trichomonosis mortality events in band-tailed pigeons (Patagioenas fasciata) in California during winter 2014-2015
Fig. 2. Examples of caseonecrotic lesions (white arrowheads) in the oral cavity and upper digestive tracts of band-tailed pigeons (Patagioenas fasciata monolis) collected during an avian trichomonosis mortality event in California, U.S.A., between November 2014 and June 2015. Birds collected from Contra Costa County (A), Marin County (B), and Monterey County (D) in January 2015 and Placer County (E) in February 2015.
Fig. 4 in Avian trichomonosis mortality events in band-tailed pigeons (Patagioenas fasciata) in California during winter 2014-2015
Fig. 4. Body cavity with no adipose (white arrowheads) reserves (A.1) and the caseonecrotic lesions (white arrowheads) in the oral cavity (A.2) of a band-tailed pigeon (Patagioenas fasciata monolis) collected during an avian trichomonosis mortality event in Ventura County, California, U.S.A., in January 2015. Body cavity with abundant adipose (white arrowheads) reserves (B.1) and the caseonecrotic lesions (white arrowheads) in the oral cavity and upper digestive tract (B.2) of a band-tailed pigeon collected during an avian trichomonosis mortality event in Santa Clara County, California, U.S.A., in January 2015.
Fig. 3 in Avian trichomonosis mortality events in band-tailed pigeons (Patagioenas fasciata) in California during winter 2014-2015
Fig. 3. Caseonecrotic lesions (white arrowheads) in the right eye socket (A) and oral cavity (B) of a band-tailed pigeon (Patagioenas fasciata monolis) collected during an avian trichomonosis mortality event in Santa Clara County, California, U.S.A., in January 2015.
Fig. 1 in Avian trichomonosis mortality events in band-tailed pigeons (Patagioenas fasciata) in California during winter 2014-2015
Fig. 1. Number of band-tailed pigeon (Patagioenas fasciata monolis) mortality reports from phone, email, and online form received by county by the California Department of Fish and Wildlife (CDFW; Rancho Cordova, CA) and the California Department of Public Health (Richmond, CA) between November 2014 and June 2015 in California, U.S.A. (A). Number of band-tailed pigeons admitted to wildlife rehabilitation centers in California, U.S.A. and compiled by county between January and December 2015 (B). Number of band-tailed pigeon carcasses collected by county and received by CDFW between November 2014 and June 2015 in California, U.S.A. (C).
Fig. 3 in The first record of the winter stonefly genus Mesyatsia Ricker & Ross, 1975 (Plecoptera: Taeniopterygidae) from Korea
Fig. 3. Habitat of Mesyatsia makartchenkoi Teslenko & Zhiltzova, 1992: South Korea, Odaesan Mts. A. larva, walking on the snow; B. adult, walking on the ice (photograph by Sunghwan Park).
Fig. 2 in The first record of the winter stonefly genus Mesyatsia Ricker & Ross, 1975 (Plecoptera: Taeniopterygidae) from Korea
Fig. 2. Mesyatsia makartchenkoi Teslenko & Zhiltzova, 1992, female. A. terminalia, ventral view; B. terminalia, lateral view. Scale bar = 0.45 mm.
Fig. 4. Neighbor-joining phylogenetic tree reconstructed from a in Isolation and characterization of four unrecorded wild yeasts from the soils of Republic of Korea in winter
Fig. 4. Neighbor-joining phylogenetic tree reconstructed from a comparative analysis of 26S rRNA gene sequences showing the relationships of strain NH33 with closely related species. Bootstrap values (>50%) based on neighbor-joining methods are shown at the branch nodes. Bar, 0.01 substitutions per nucleotide position.
Fig. 1 in Isolation and characterization of four unrecorded wild yeasts from the soils of Republic of Korea in winter
Fig. 1. Morphology of cells from the unrecorded strains incubated at 10℃. The colonies of Leucosporidium scottii NH19 (A), Holtermanniella wattica NH20 (B), Buckleyzyma aurantiaca NH33 (C), and Mrakia aquatica YP416 (D). The budding cells of Leucosporidium scottii NH19 (F), Holtermanniella wattica NH20 (G), Buckleyzyma aurantiaca NH33 (H), and Mrakia aquatica YP416 (I). Bars, 20 μm. All strains were grown after 3 days on YM agar.
Fig. 3. Neighbor-joining phylogenetic tree reconstructed from a in Isolation and characterization of four unrecorded wild yeasts from the soils of Republic of Korea in winter
Fig. 3. Neighbor-joining phylogenetic tree reconstructed from a comparative analysis of 26S rRNA gene sequences showing the relationships of strain NH19 with closely related species. Bootstrap values (>50%) based on neighbor-joining methods are shown at the branch nodes. Bar, 0.01 substitutions per nucleotide position.
Fig. 2. Neighbor-joining phylogenetic tree reconstructed from a in Isolation and characterization of four unrecorded wild yeasts from the soils of Republic of Korea in winter
Fig. 2. Neighbor-joining phylogenetic tree reconstructed from a comparative analysis of 26S rRNA gene sequences showing the relationships of strains NH20 and YP416 with closely related species. Bootstrap values (>50%) based on neighbor-joining methods are shown at the branch nodes. Bar, 0.01 substitutions per nucleotide position.
The TRIple-frequency and Polarimetric radar Experiment for improving process observation of winter precipitation dataset
<p>The combined TRIple-frequency and Polarimetric radar Experiment for improving process observation of winter precipitation (TRIPEx) was a joint field experiment of the University of Cologne, the University of Bonn, the Karlsruhe Institute of Technology (KIT), and the Research Center Jülich. TRIPEx took place at the Jülich Observatory for Cloud Evolution (JOYCE) from 11 November 2015 until 04 January 2016. During this experiment, the X-, Ka- and W-band ground-based Doppler radars were used vertically pointing to observe the clouds. Here we provide the level 2 of the dataset collected during this campaign. Several step processing were applied to minimize the radar offset and attenuation. In addition, we provide the attenuation correction and the quality flags for each processing steps to allow the user to retrieve the data without our correction. The raw and the level 1 of the dataset are available for the users on request from the corresponding author.<br> </p>
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OpenNeuro
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