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Fig. 4 in Seroprevalence of Borrelia burgdorferi antibodies in white-tailed deer from Texas

Fig. 4. Confirmed human Lyme Disease cases in Texas from 2000 to 2013 reported to the CDC (www.cdc.com).

Fig. 5 in Seroprevalence of Borrelia burgdorferi antibodies in white-tailed deer from Texas

Fig. 5. White-tailed deer (WTD) population density in Texas eco-regions from 2005 to 2013. This graph is a representation of WTD population density statewide in Texas; in two counties (Travis and Williamson) where sero-reactive samples, and negative control samples for Borrelia burgdorferi antibodies were found.

Fig. 1. Texas map showing 14 in Seroprevalence of Borrelia burgdorferi antibodies in white-tailed deer from Texas

Fig. 1. Texas map showing 14 counties in which white-tailed deer (WTD) were sampled for Borrelia burgdorferi antibodies from 2001 to 2015. Blue counties: samples negative by ELISA and standardized western immunoblot; Gray counties: negative control samples; Yellow counties: samples sero-reactive by standardized western immunoblot assay (Travis and Williamson counties). (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

opencc-by-4.0Aug 2017View details →

Fig. 2 in Comparison of natural and artificial odor lures for nilgai (Boselaphus tragocamelus) and white-tailed deer (Odocoileus virginianus) in South Texas: Developing treatment for cattle fever tick eradication

Fig. 2. Locations of nilgai lure transects (red bars) at the Santa Rosa Ranch near Riviera, TX. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

opencc-by-4.0Aug 2017View details →

Fig. 5 in Comparison of natural and artificial odor lures for nilgai (Boselaphus tragocamelus) and white-tailed deer (Odocoileus virginianus) in South Texas: Developing treatment for cattle fever tick eradication

Fig. 5. Nilgai cow visiting lure site (A) and (B) nilgai bull defecating at offal lure site at the East Foundation's Santa Rosa Ranch, near Riviera, TX.

Рис. 4. Фотографии Camacolaimus vietnamicus sp. nov., гоΛотип самца (а, с, d, e, g, h, j) и паратип самки (b, e, f, i, k): a, b — общий виΑ; с — кутикуΛа; d–f — гоΛова; g — переΑний конец теΛа; h — теΛо в обΛасти кΛоаки; i — теΛо в обΛасти вуΛьвы; j, k — хвост. Масштаб: а, b — 200 мкм; k — 50 мкм; c, g, i, j — 20 мкм; f — 10 мкм; d, e, h — 5 мкм Fig. 4. Light micrographs of Camacolaimus vietnamicus sp. nov., male holotype (а, с, d, e, g, h, j) and female paratype (b, e, f, i, k): a, b — general view; с — cuticle; d–f — head; g — anterior body end; h — cloaca region; i — vulva region; j, k — tail. Scale bars: а, b — 200 µm; k — 50 µm; c, g, i, j — 20 µm; f — 10 µm; d, e, h — 5 µm in Two new species of the free-living nematodes (Nematoda, Chromadorea) from coral reefs of Vietnam

Рис. 4. Фотографии Camacolaimus vietnamicus sp. nov., гоΛотип самца (а, с, d, e, g, h, j) и паратип самки (b, e, f, i, k): a, b — общий виΑ; с — кутикуΛа; d–f — гоΛова; g — переΑний конец теΛа; h — теΛо в обΛасти кΛоаки; i — теΛо в обΛасти вуΛьвы; j, k — хвост. Масштаб: а, b — 200 мкм; k — 50 мкм; c, g, i, j — 20 мкм; f — 10 мкм; d, e, h — 5 мкм Fig. 4. Light micrographs of Camacolaimus vietnamicus sp. nov., male holotype (а, с, d, e, g, h, j) and female paratype (b, e, f, i, k): a, b — general view; с — cuticle; d–f — head; g — anterior body end; h — cloaca region; i — vulva region; j, k — tail. Scale bars: а, b — 200 µm; k — 50 µm; c, g, i, j — 20 µm; f — 10 µm; d, e, h — 5 µm

Рис. 3. Camacolaimus vietnamicus sp. nov., гоΛотип самца (а, c, d) и паратип самки (b, e): a — гоΛова; b — теΛо в обΛасти вуΛьвы; с, e — хвост; d — переΑний конец теΛа. Масштаб: а — 10 мкм; c, d — 40 мкм; e — 50 мкм; b — 60 мкм Fig. 3. Camacolaimus vietnamicus sp. nov., male holotype (а, c, d), female paratype (b, e): a — head; b — vulva region; с, e — tail; d — anterior body end. Scale bars: а — 10 µm; c, d — 40 µm; e — 50 µm; b — 60 µm in Two new species of the free-living nematodes (Nematoda, Chromadorea) from coral reefs of Vietnam

Рис. 3. Camacolaimus vietnamicus sp. nov., гоΛотип самца (а, c, d) и паратип самки (b, e): a — гоΛова; b — теΛо в обΛасти вуΛьвы; с, e — хвост; d — переΑний конец теΛа. Масштаб: а — 10 мкм; c, d — 40 мкм; e — 50 мкм; b — 60 мкм Fig. 3. Camacolaimus vietnamicus sp. nov., male holotype (а, c, d), female paratype (b, e): a — head; b — vulva region; с, e — tail; d — anterior body end. Scale bars: а — 10 µm; c, d — 40 µm; e — 50 µm; b — 60 µm

Рис. 1. Prochromadorella coralis sp. nov., гоΛотип самца (а, b, e, f) и паратип самки (c, d): a — гоΛова; b — переΑний конец теΛа; с — теΛо в обΛасти вуΛьвы; d — хвост самки; е —суппΛементы; f — хвост самца. Масштаб: а — 10 мкм; e — 15 мкм; b, c, d, f — 30 мкм Fig. 1. Prochromadorella coralis sp. nov., male holotype (а, b, e, f) and female paratype (c, d): a — head; b — anterior body end; с — vulva region; d — female tail; е — supplements; f — male tail. Scale bars: а — 10 µm; e — 15 µm; b, c, d, f — 30 µm in Two new species of the free-living nematodes (Nematoda, Chromadorea) from coral reefs of Vietnam

Рис. 1. Prochromadorella coralis sp. nov., гоΛотип самца (а, b, e, f) и паратип самки (c, d): a — гоΛова; b — переΑний конец теΛа; с — теΛо в обΛасти вуΛьвы; d — хвост самки; е —суппΛементы; f — хвост самца. Масштаб: а — 10 мкм; e — 15 мкм; b, c, d, f — 30 мкм Fig. 1. Prochromadorella coralis sp. nov., male holotype (а, b, e, f) and female paratype (c, d): a — head; b — anterior body end; с — vulva region; d — female tail; е — supplements; f — male tail. Scale bars: а — 10 µm; e — 15 µm; b, c, d, f — 30 µm

Рис. 2. Фотографии Prochromadorella coralis sp. nov., гоΛотип самца (а, с, d, f, g, h, j) и паратип самки (b, e, i, k): a, b – общий виΑ; с – кутикуΛа; d, e – гоΛова; f – переΑний конец теΛа; g – теΛо в обΛасти кΛоаки; h – суппΛементы; i – теΛо в обΛасти вуΛьвы; j, k – хвост. Масштаб: а, b – 100 мкм; f, i, j, k – 20 мкм; c, d, e, g, h – 5 мкм Fig. 2. Light micrographs of Prochromadorella coralis sp. nov., male holotype (а, с, d, f, g, h, j) and female paratype (b, e, i, k): a, b — general view; с — cuticle; d, e — head; f — anterior body end; g — cloaca region; h — supplements; i — vulva region; j, k — tail. Scale bars: а, b — 100 µm; f, i, j, k — 20 µm; c, d, e, g, h — 5 µm in Two new species of the free-living nematodes (Nematoda, Chromadorea) from coral reefs of Vietnam

Рис. 2. Фотографии Prochromadorella coralis sp. nov., гоΛотип самца (а, с, d, f, g, h, j) и паратип самки (b, e, i, k): a, b – общий виΑ; с – кутикуΛа; d, e – гоΛова; f – переΑний конец теΛа; g – теΛо в обΛасти кΛоаки; h – суппΛементы; i – теΛо в обΛасти вуΛьвы; j, k – хвост. Масштаб: а, b – 100 мкм; f, i, j, k – 20 мкм; c, d, e, g, h – 5 мкм Fig. 2. Light micrographs of Prochromadorella coralis sp. nov., male holotype (а, с, d, f, g, h, j) and female paratype (b, e, i, k): a, b — general view; с — cuticle; d, e — head; f — anterior body end; g — cloaca region; h — supplements; i — vulva region; j, k — tail. Scale bars: а, b — 100 µm; f, i, j, k — 20 µm; c, d, e, g, h — 5 µm

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).

opencc-by-4.0Apr 2018View details →

Fig. 3 in Close relationship of Plasmodium sequences detected from South American pampas deer (Ozotoceros bezoarticus) to Plasmodium spp. in North American white-tailed deer

Fig. 3. Phylogenetic relationship of Plasmodium sequences from Brazilian pampas deer within ungulate Plasmodium spp. The tree was constructed using concatenated partial nucleotide sequences of cytb and cox1 by maximum likelihood (ML) method based on the GTR + I + G model. Bootstrap values (BV) for ML with 1000 replicates of ultrafast bootstrap analysis and Bayesian posterior probability (BPP) are indicated for each internal branch. The compositions of collapsed clades are described in Fig. 2 legend. The length for the substitutions/site (0.07) is indicated.

opencc-by-4.0Apr 2018View details →

Fig. 2 in Close relationship of Plasmodium sequences detected from South American pampas deer (Ozotoceros bezoarticus) to Plasmodium spp. in North American white-tailed deer

Fig. 2. Phylogenetic relationships of Plasmodium sequences from Brazilian pampas deer within Haemosporidia. The tree was constructed using ∼3.4 kb of partial mitochondrial nucleotide sequences by the maximum likelihood (ML) method based on the GTR + I + G model. Bootstrap values (BV) for ML with 1000 replicates of ultrafast bootstrap analysis and Bayesian posterior probability (BPP) are indicated for each internal branch. The compositions of collapsed clades are Leucocytozoon (L. fringillinarium, L. majoris, and L. sabrasezi); Haemoproteus and Parahaemoproteus (Haemoproteus sp. jb1.JA27, Haemoproteus sp. jb2.SEW5141, and Parahaemoproteus vireonis); and bird, lizard and non-ungulate mammalian Plasmodium (P. gallinaceum, P. relictum, P. juxtinucleare, P. lutzi, P. floridense, P. mexicanum, P. falciparum, P. vivax, P. malariae, P. ovale, P. coatneyi, P. cynomolgi, P. fieldi, P. gonderi, P. inui, P. knowlesi, P. fragile, P. simiovale, P. simium, P. hylobati, P. reichenowi, P. billicollinsi, P. billbrayi, P. berghei, P. chabaudi, P. vinckei, and P. yoelii). Mitochondrial DNA sequences (including cytb and cox1) used in this study were listed in the Supplementary Table S1 of Templeton et al. (2016a). Nucleotide sequences of Plasmodium sp. in the North American white-tailed deer was based on Table S4 of Martinsen et al. (2016). Nucleotide positions containing indels or undetermined nucleotides, or those where the alignment was not clearly made were excluded. Nucleotide positions corresponding to the P. falciparum mtDNA (NC_002375.1) 974–1502, 1509–1576, 1578–1628, 1637–1678, 1698–1760, 1762–1769, 1774–1800, 1806–1831, 1834–1867, 1870–1909, 1914–2031, 2050–3474, and 3486–4444 were used. The length for the substitutions/site (0.04) is indicated.

Fig. 3 in The first female specimen of the poorly known Arfak Stout-tailed Snake, Calamophis sharonbrooksae Murphy, 2012 (Serpentes: Colubroidea: Homalopsidae), from the Vogelkop Peninsula of Indonesian West New Guinea, with comments on the taxonomic history of primitive homalopsids

Fig. 3. Detailed views of the head and tail of the first known female Calamophis sharonbrooksae (NRM 17803), presented as both photographic and line-drawn illustrations for improved clarity. (A, A′) Dorsal view of the head, illustrating rostral (R), single internasal (IN), fused prefrontal-preocular (PF-PR), frontal (F), paired supraocular (SO), and parietals (P). (B, B′) Ventral view of the head, showing a single pair of chin shields (CS), seven infralabials (IL1-IL7), mental (M), and the first ventral scute (V1). (C, C′) Left lateral view of the head, additionally illustrating the undivided nasal (N), single postocular (PO), single anterior temporal (AT), two posterior temporals (PT), and six supralabials (SL1-SL6). (D, D′) Right lateral view of the head, illustrating differences in scalation compared to left side, three posterior temporals (PT), and small scale separating the postocular and anterior temporal (*). (E, E′) Ventral view of the tail, showing the final ventral (V158), divided cloacal plate (CP), first paired subcaudal (SC1), and rounded terminal scute (TS). Scale = 10 mm for Fig. 3A-D and 10 mm for Fig. 3E.

opencc-by-4.0Feb 2014View details →

High-throughput poly(A) length measurement of HeLa and NIH 3T3 cells using TAIL-seq with MiSeq

This dataset contains the full raw data directory from Illumina MiSeq generated for Chang et al. (2014, DOI: 10.1016/j.molcel.2014.02.007). Please refer to the original paper and its supplementary materials for further details.

opencc-by-4.0Jan 2019View details →

Histone tail dynamics in partially disassembled nucleosomes during chromatin remodeling: Simulation dataset

Dataset of molecular dynamics simulations of partially disassembled nucleosomes. - Input: Parameters and initial structures - Output: Trajectories NAMD 2.12 (multi-core with CUDA) was used for the simulations.