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Fig. 2 in Variations in infection levels and parasite-induced mortality among sympatric cryptic lineages of native amphipods and a congeneric invasive species: Are native hosts always losing?
Fig. 2. Mean parasite prevalences (proportion of infected individuals in %) among amphipod populations/sampling sites and their bootstrapped 95% confidence intervals in the different MOTUs sampled and for the three acanthocephalan species, separately and overall (all three parasites grouped). Overall prevalences in MOTUs assigned different letters are significantly different at the 0.05 level.
Fig. 1 in Variations in infection levels and parasite-induced mortality among sympatric cryptic lineages of native amphipods and a congeneric invasive species: Are native hosts always losing?
Fig. 1. Genetic divergence levels (%) among MOTUs of the G. fossarum/G. pulex species complex found in our sampling sites/rivers. Gammarus roeseli was identified morphologically rather than genetically.
Fig. 3 in Variations in infection levels and parasite-induced mortality among sympatric cryptic lineages of native amphipods and a congeneric invasive species: Are native hosts always losing?
Fig. 3. Mean parasite abundances (mean number of acanthocephalan larvae per individual host) among amphipod populations/sampling sites and their bootstrapped 95% confidence intervals in the different MOTUs sampled and for the three acanthocephalan species, separately and overall (all three parasites grouped). Overall abundances in MOTUs assigned different letters are significantly different at the 0.05 level.
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).
Sempa et al. 2019 - A Retrospective audit of treatment outcomes, side-effect profiles and default and mortality rates of HIV/AIDS patients at the antiretroviral clinic at Pretoria Academic Hospital.
<p>The comprehensive demographic and long-term treatment data of the first, consecutive, 963 patients older than 18 years of age who presented for ART at the Tshwane District Hospital in Gauteng, South Africa during 2004 and 2005 were selected for analysis. All patients started ART after 2004 as part of the South African national HIV treatment plan and were treated according to the National Department of Health HIV guidelines (2004) operative at the time, i.e. eligibility for ART was CD4 <200 cells/µL or WHO stage 4 disease regardless of CD4 count. Treatment was initiated using a standardized triple-drug regimen consisting of two nucleoside reverse transcriptase inhibitors, mostly d4T and 3TC, and one non-nucleoside reverse transcriptase inhibitor, either NVP or EFV. CD4 and HIV-1 VL monitoring was performed at treatment initiation ‘baseline’ and then 6-monthly, according to the national protocol. Demographic, anthropometric, clinical, ART and 5-year longitudinal treatment response data were collected. Excluded all second-line ART visits for all patients who were switched to second-line therapy.</p>
Fig. 2. A in Multiple infestations of gastrointestinal parasites - Probable cause for high mortality of Spot-billed Pelican (Pelecanus philippensis) at Kokrebellur Community Reserve, India
Fig. 2. A. Larvae of Contracaecum sp. in fish, B. Adult Contracaecum sp. worms in the pelican, C. Eggs of Echinostoma sp. in pelican fecal and water samples, D. Eggs of Contracaecum sp. in pelican fecal and water samples and E. Eggs of Opisthorchis viverrini in pelican fecal samples.
Figure. Percent mortality of R. padi treated with crude venom of P. birmanica (CVPB), crude venom of P. sumatrana (CVPS), protein fraction of P. birmanica venom (PFPB), and protein fraction of P. sumatrana venom (PFPS). Bars with the same letters represent nonsignificant differences. in Insect-specific peptides in the venom of wolf spiders (Araneae: Lycosidae)
Figure. Percent mortality of R. padi treated with crude venom of P. birmanica (CVPB), crude venom of P. sumatrana (CVPS), protein fraction of P. birmanica venom (PFPB), and protein fraction of P. sumatrana venom (PFPS). Bars with the same letters represent nonsignificant differences.
Figure 1 in Can wildlife mortality on a local road tell something general? An answer from a protected area in south-western Romania
Figure 1. Study area (blue line–rivers, black line–roads, discontinuous line–Iron Gates Natural Park limits, black dots–localities, red dots–the six studied sectors on the road to Bigăr).
Figure 2. Mortality percentages after feeding the L in Exploring the efficacy of RNAi-mediated gene knock-down via oral delivery of dsRNA in the Colorado potato beetle (Leptinotarsa decemlineata Say)
Figure 2. Mortality percentages after feeding the L. decemlineata larvae dsRNA-treated leaves at different instars. (a) First instar, (b) second instar, (c) third instar, and (d) fourth instar. The percent mortality was compared in the larvae fed potato leaves pretreated with E. coli HT115 (DE3) cells expressing dsV-ATPase compared to the two controls, E. coli HT115 (DE3) cells with empty L4440 plasmid (dsEmp) and E. coli HT115 expressing dsGFP. Different letters on the data points denote significant differences determined by ANOVA followed by the Tukey honest significant difference (HSD) test at a 5% significance level.
Figure 2 in Can wildlife mortality on a local road tell something general? An answer from a protected area in south-western Romania
Figure 2. The studied road in Sector 2 (up left) and Sector 3 (up right), and two road–killed vertebrates identified on the road: Salamandra salamandra (down left) and Talpa sp. (down right).
Fig. 1 in Effect of four multiple nucleopolyhedrovirus isolates on the larval mortality and development of Spodoptera exigua (Lepidoptera: Noctuidae): determination of virus production and mean time to death
Fig. 1. Mean time of death calculated for third-instar larvae of Spodoptera exigua. The numbers above the columns indicate the values calculated for 3 replications. The columns headed by the same letter are not significantly different (Weibull analysis, α = 1.96).
Fig. 1. Cumulative Solenopsis invicta worker ant mortality among Solenopsis invicta virus 3 in Diet with sucrose ameliorates Solenopsis invicta virus 3 (Solinviviridae: Invictavirus) infection in Solenopsis invicta (Hymenoptera: Formicidae) worker ants
Fig. 1. Cumulative Solenopsis invicta worker ant mortality among Solenopsis invicta virus 3-infected and -uninfected colonies provided a diet of crickets (Acheta domesticus) and either supplemented (open symbols) or not supplemented (solid symbols) with a 10% sucrose solution. Analysis of Variance by treatment was conducted for d 21 values and found to be significant (F = 10.0; df = 3,14; P <0.0009). Scheffe's multiple comparison procedure was used to separate the means. Symbols with the same letter are not statistically different.
Fig. 3 in Acute mortality in California tiger salamander (Ambystoma californiense) and Santa Cruz long-toed salamander (Ambystoma macrodactylum croceum) caused by Ribeiroia ondatrae (Class: Trematoda)
Fig. 3. Ribeiroia ondatrae cercaria from Planorbella sp. collected from Ellicott Pond in Ellicott Slough National Wildlife Refuge, Santa Cruz County, California, U.S.A.
Fig. 4 in Acute mortality in California tiger salamander (Ambystoma californiense) and Santa Cruz long-toed salamander (Ambystoma macrodactylum croceum) caused by Ribeiroia ondatrae (Class: Trematoda)
Fig. 4. Molecular phylogenetic analysis by Maximum Likelihood method based on the Hasegawa-Kishino-Yano plus G model with 500 bootstrap replications based on partial 28S rRNA gene sequences of Ribeiroia ondatrae metacercariae from California tiger salamanders (Ambystoma californiense), cercariae from Planorbella sp. and sequences of R. ondatrae publicly available in GenBank with Notocotylus attenuatus as an outgroup. Tree is drawn to scale with branch lengths measure in the number of substitutions per site. The analysis involved 13 nucleotide sequences. All positions with less than 95% site coverage were eliminated. There was a total of 1189 positions in the final dataset.
Fig. 2 in Acute mortality in California tiger salamander (Ambystoma californiense) and Santa Cruz long-toed salamander (Ambystoma macrodactylum croceum) caused by Ribeiroia ondatrae (Class: Trematoda)
Fig. 2. Photomicrograph of California tiger salamanders (Ambystoma californiense) in late-stage metamorphosis from a mortality event in the Ellicott Slough National Wildlife Refuge in Santa Cruz County, California, U.S.A. (A) Cross-section of dorsal tail showing widespread ulcerative dermatitis with superficial serocellular crust formation and intralesional metacercariae (asterisk) (H&E). (B) Metacercariae (asterisk) associated with mixed cellular to granulomatous inflammation widespread in the gills and subcutis (PAS). Inset: Encysted metacercariae are surrounded by mixed-cellular to granulomatous to infiltrate (H&E).
Fig. 1 in Acute mortality in California tiger salamander (Ambystoma californiense) and Santa Cruz long-toed salamander (Ambystoma macrodactylum croceum) caused by Ribeiroia ondatrae (Class: Trematoda)
Fig. 1. Gross photographs of ethanol-fixed salamanders in late-stage metamorphosis from a mortality event in the Ellicott Slough National Wildlife Refuge (ESNWR) in Santa Cruz County, California, U.S.A. showing integumentary lesions. (A) California tiger salamander (Ambystoma californiense) exhibiting an extensive roughening of the skin with multifocal ulceration around the eyes, gular fold, and dorsal tail (arrows). (B) Santa Cruz long-toed salamander (Ambystoma macrodactylum croceum) with ulceration and crust formation on the gular fold and base of the tail (arrow).
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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)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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.