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Fig. 6 in Trypanosomes genetic diversity, polyparasitism and the population decline of the critically endangered Australian marsupial, the brush tailed bettong or woylie (Bettongia penicillata)

Fig. 6. Structures suggestive of amastigotes (arrows) of G2 (Clade A) in heart tissue positive by PCR (H&E stained). Scale bars = (A) 20 µm, (B) 10 µm.

Fig. 5 in Trypanosomes genetic diversity, polyparasitism and the population decline of the critically endangered Australian marsupial, the brush tailed bettong or woylie (Bettongia penicillata)

Fig. 5. Histopathology of two woylies naturally infected with G2 (Clade A) (H&E stained). (A) Multifocal, moderate to severe, chronic, pyogranulomatous myocarditis and (B) endocarditis. (C) Mineralisation of heart tissue. (D) Tongue showing multifocal, moderate, chronic, pyogranulomatous glossitis. (E) Skeletal muscle degeneration. (F) Inflammatory cells around a blood vessel. Scale bars = 20 µm.

opencc-by-4.0Apr 2015View details →

Fig. 4 in Endoparasites in a Norwegian moose (Alces alces) population - Faunal diversity, abundance and body condition

Fig. 4. Counts of abomasal nematodes in moose, hunted during the licensed hunting season, autumn 2013, in Hedmark county, Norway, in relation to slaughter weight, gender (F – females [black]; M – males [grey]) and body condition index (poor – BCI <0 [open circles]; good – BCI> 0 [filled circles]). The lines show model predictions from a quasi-Poisson generalised linear model explaining 72.4% of the deviance. The lines show the model predictions for individuals with BCI equal to 1st and 3rd quartiles.

Fig. 3 in Trypanosomes genetic diversity, polyparasitism and the population decline of the critically endangered Australian marsupial, the brush tailed bettong or woylie (Bettongia penicillata)

Fig. 3. Phylogenetic relationships of the new trypanosome isolates from Western Australian marsupials based on gGAPDH sequences (~810 bp) using Mr Bayes. The tree was rooted with five sequences as outgroups. Bayesian posterior probabilities are shown at nodes. Bar, 0.07 substitutions per site.

Fig. 10 in Trypanosomes genetic diversity, polyparasitism and the population decline of the critically endangered Australian marsupial, the brush tailed bettong or woylie (Bettongia penicillata)

Fig. 10. Scanning electron micrograph of G2 (Clade A) grown in culture with Vero cells. (A) Trypomastigote invading a cell, with the flagella still external to the cell. (B) Dead cell(s) surrounded by amastigotes and trypomastigotes. Scale bars = 2 µm (A), 4 µm (B).

opencc-by-4.0Apr 2015View details →

Fig. 3. A in Endoparasites in a Norwegian moose (Alces alces) population - Faunal diversity, abundance and body condition

Fig. 3. A box–whisker plot showing the prevalence of infection with protostrongylid larvae (dorsal spine larvae) in moose hunted during the licensed hunting season, autumn 2013, in Hedmark county, Norway, in relation to age. The median (solid black line), quartiles (ends of boxes) with the whiskers indicating the variability outside the quartiles, and extreme outliers, individual points, are shown.

opencc-by-4.0Apr 2015View details →

Fig. 1 in Endoparasites in a Norwegian moose (Alces alces) population - Faunal diversity, abundance and body condition

Fig. 1. Histogram of number of parasite groups (parasite diversity) found in individual moose (n = 30) shot during the licensed hunting season, autumn 2013, in Hedmark county, Norway.

Fig. 4 in Trypanosomes genetic diversity, polyparasitism and the population decline of the critically endangered Australian marsupial, the brush tailed bettong or woylie (Bettongia penicillata)

Fig. 4. Prevalence of infection with trypanosomes within the different clades in woylies from the stable and declining populations. 95% confidence intervals (95% CI).

Fig. 2 in Trypanosomes genetic diversity, polyparasitism and the population decline of the critically endangered Australian marsupial, the brush tailed bettong or woylie (Bettongia penicillata)

Fig. 2. Phylogenetic analysis of the relationships between Australian trypanosomes based on 18S rDNA sequences. Phylogenetic trees were constructed by the Bayesian method sequences (~1410 bp). (B) Phylogenetic position of shorter 18S rDNA sequences (786 bp) CHA1, TRY1, TRY2, WYA1, WYA2, BDA1, Q3, Q10, GP63 and GP94. Threes were rooted with from Bayesian posterior probabilities are shown at nodes. In red: trypanosome genotypes found in this study. Bar, 0.2 substitutions per site.

Fig. 2 in What drives population-level effects of parasites? Meta-analysis meets life-history

Fig. 2. Funnel plot of effect size (Hedges' g) by standard error (SE). The white circles represent studies included in the meta-analysis. The black circles represent missing imputed studies. The white diamond represents overall effect size as calculated in the meta-analysis, and the black diamond represents the corrected effect size.

Fig. 1 in What drives population-level effects of parasites? Meta-analysis meets life-history

Fig. 1. Forest plot of effect sizes (rectangles) and confidence intervals (bars) for each study and the effect averaged across all studies (diamond).

Fig. 1 in Trichinella species circulating in wild boar (Sus scrofa) populations in Poland

Fig. 1. Example of electrophoretic patterns obtained from multiplex PCR on Trichinella larvae collected from wild boar. Lane 1 and 8 molecular weight marker (Fermentas 100 bp DNA Ladder); lanes 2 and 4, T. spiralis; lanes 3 and 5, T. britovi; lane 6, T. spiralis and T. britovi mixed infection; lane 7, negative control.

Fig. 3. A in What drives population-level effects of parasites? Meta-analysis meets life-history

Fig. 3. A meta-regression (random effects model) of effect size against host average lifespan using the complete dataset (n = 60). The slope of this regression is significant (p = 0.05).

opencc-by-4.0Dec 2014View details →

Fig. 3 in Gastric nematode diversity between estuarine and inland freshwater populations of the American alligator (Alligator mississippiensis, daudin 1802), and the prediction of intermediate hosts

Fig. 3. Prey content species richness accumulation curves based on 1000 randomizations using Estimate 9.1.0. Data obtained from stomach flushing or necropsy of American alligators from (A) coastal or (B) inland habitats between 2008 and 2011. The black broken line (- -) represents the upper 95% confidence level, and the broken dotted broken line (- · -) represents the lower 95% confidence level of the species accumulation curve. The slow approach to the asymptote in coastal habitats suggests prey contents of sampled alligators did not capture all probable prey. The asymptote of inland alligators slowly begins to plateau, which may suggest our sampling efforts were close to capturing most of the probable prey of alligators.

Fig. 5 in Beyond the disease: Is Toxoplasma gondii infection causing population declines in the eastern quoll (Dasyurus viverrinus)?

Fig. 5. Kaplan Meier survival curves comparing survival trajectories for seronegative (solid line) and seropositive (broken line) eastern quolls. Curves show survival of all quolls first captured at the non-declining site between August 2010 and October 2012.

Fig. 4 in Beyond the disease: Is Toxoplasma gondii infection causing population declines in the eastern quoll (Dasyurus viverrinus)?

Fig. 4. Association between seroprevalence of T. gondii IgG antibodies in eastern quolls at Cradle Mountain and the square-root transformed number of eastern quolls captured 2 months later (y = 2.552–0.022×). Each data point represents a single trapping/sampling session between May 2011 and July 2013.

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Fig. 2 in Gastric nematode diversity between estuarine and inland freshwater populations of the American alligator (Alligator mississippiensis, daudin 1802), and the prediction of intermediate hosts

Fig. 2. Nematode species richness accumulation curve (A) and Coleman rarefaction curve (B) based on 1000 randomizations using Estimate 9.1.0. The black broken line (- -) represents the upper 95% confidence level, and the broken dotted broken line (- · -) represents the lower 95% confidence level of the species accumulation curve (A). Upper and lower Coleman standard deviations are represented by solid black lines (B). Data obtained from stomach flushing or necropsy of American alligators from Florida and Georgia between 2008 and 2011. The rapid approach to the asymptote suggests we captured all possible species of alligator nematodes.

Fig. 3 in Beyond the disease: Is Toxoplasma gondii infection causing population declines in the eastern quoll (Dasyurus viverrinus)?

Fig. 3. Seroprevalence of T. gondii IgG antibodies in juvenile eastern quolls from time of emergence for 2011 cohort ((a) declining sites (Cradoc and Judbury) and (b) nondeclining site (Bruny Island)) and 2012 cohort ((c) declining sites and (d) non-declining site). Declining sites were not surveyed in September 2012, November 2012, March 2013 or September 2013. Vertical axis shows proportion of quolls tested that were seropositive at titres À 64. Error bars represent 95% confidence intervals calculated using the Jeffreys interval estimation for a small sample size with binomial distribution (Brown et al., 2001).

Fig. 2 in Beyond the disease: Is Toxoplasma gondii infection causing population declines in the eastern quoll (Dasyurus viverrinus)?

Fig. 2. Seroprevalence of T. gondii IgG antibodies in adult eastern quolls at (a) declining sites (Cradoc and Judbury) and (b) non-declining site (Bruny Island). Declining sites were not surveyed in September or November 2012 or March 2013. Vertical axis shows proportion of quolls tested that were seropositive at titres À 64. Error bars represent 95% confidence intervals calculated using the Jeffreys interval estimation for a small sample size with binomial distribution (Brown et al., 2001).

Fig. 6 in Beyond the disease: Is Toxoplasma gondii infection causing population declines in the eastern quoll (Dasyurus viverrinus)?

Fig. 6. Comparison of the probability of T. gondii infection with quoll age, by site. Non-declining site = Bruny Island, Cradle Mountain = fluctuating site, Declining sites = pooled data from Cradoc and Judbury sites. Circles represent individual observations of seronegative (probability = 0) and seropositive (probability = 1) quolls at a given age, with darker circles indicating a higher number of quolls with the same combination of age and serological status. Curve illustrates the fitted data, with grey shading representing 95% confidence intervals.