Find research datasets worth reusing

Fig. 6 in Altered parasite community structure in an endangered marsupial following translocation

Fig. 6. Non-metric multidimensional scaling plots showing convergence of parasite community composition in translocated (TYPE T) and resident (TYPE R) woylie groups following translocation. Boxes on the left depict both groups at all time points prior to and including the point of translocation; boxes on the right depict both groups six months after translocation.

Fig. 1 in Ecological and geographical speciation in Lucilia bufonivora: The evolution of amphibian obligate parasitism

Fig. 1. Location of samples for which the COX1 gene was sequenced in this study. Boxes represent the locations of individual samples: red, Lucilia elongata; orange, Lucilia silvarum; green, Lucilia bufonivora.

Fig. 5 in Altered parasite community structure in an endangered marsupial following translocation

Fig. 5. Overall parasite infracommunity richness in (A) translocated and (B) resident woylies over time. TRAN: time of translocation; Error bars represent one standard error.

Fig. 2 in Altered parasite community structure in an endangered marsupial following translocation

Fig. 2. The overall effect of site on mean faecal egg counts (above solid line) and parasite prevalence (below solid horizontal line) for each parasite taxon in (A) translocated and (B) resident woylies. Error bars represent 95% CI.

Fig. 3 in Altered parasite community structure in an endangered marsupial following translocation

Fig. 3. The effect of time since translocation (model coefficients for all sites combined) on mean faecal egg counts (above solid horizontal line) and parasite prevalence (below solid horizontal line) for each parasite taxon in translocated and resident woylies. Left of the dashed vertical line indicates a negative effect, right of the line indicates a positive effect; Error bars represent 95% CI.

Fig. 4 in Altered parasite community structure in an endangered marsupial following translocation

Fig. 4. Significant changes to mean strongyle egg counts (A) and flea prevalence (B) over time. TRAN: time of translocation; Boxplots (A) are delimited by the first (lower) and third (upper) quartile with the median represented by the thick horizontal line; whiskers represent the 1.5 interquartile range; solid black dots represent outliers; Error bars (B) represent 95% CI.

Fig. 1 in Altered parasite community structure in an endangered marsupial following translocation

Fig. 1. Map (from Northover et al., 2019) illustrating the study sites within south-western Australia, including Walcott and Warrup East in relation to Perup Sanctuary (box, right), and Dryandra, situated roughly 250 km north-east of the Upper Warren region.

Fig. 2 in Parasite burden in a short-lived chameleon, Furcifer labordi

Fig. 2. Composition of gastrointestinal parasite taxa in the fecal samples of A) adult F. labordi and B) adult F. cf. nicosiai from January to June and in total.

Fig. 4 in Parasite burden in a short-lived chameleon, Furcifer labordi

Fig. 4. Prevalence of mite infestation in A) F. labordi males and females, B) F. labordi and F. cf. nicosiai.

Fig. 2 in Broad tapeworms (Diphyllobothriidae), parasites of wildlife and humans: Recent progress and future challenges

Fig. 2. Microphotographs of permanent slides of diphyllobothriid tapeworms. A – Dibothriocephalus alasensis from Canis familiaris, Hooper Bay, Alaska, March 18, 1958; fixed after relaxation by R. Rausch (MSBP 17029). B – Dibothriocephalus latus from Homo sapiens, Chile, 19 November 2012; contracted clinical sample fixed with 'cold' fixative by T. Weitzel. C – Dibothriocephalus dalliae from C. familiaris, Alaska, 5 November 1970; fixed after relaxation by R. Rausch (MSBP 26232). D – Diphyllobothrium lanceolatum from Erignathus barbatus, Greenland, 7 October 1987; collected by P. Baagoe (SNM). E – Dibothriocephalus cf. nihonkaiensis from Homo sapiens, Newtok, Alaska, 26 March 1967; fixed after relaxation by R. Rausch (MSBP 26244). F – Diphyllobothrium stemmacephalum from Lagenorhynchus acutus, Wellfleet Bay, Cape Cod, Massachusetts, 1998; collected by J.N. Caira. G – Diphyllobothrium mobile from Ommatophoca rossii, Antarctica, 11 August 1901, Deutsche Südpolar- Expedition; collected by E. Dagobert von Drygalski (ZNB 5188). H – Dibothriocephalus ursi from Ursus arctos middendorfi, Karluk Lake, Kodiak Island, 9 October 1952; fixed after relaxation by R. Rausch; paratype (MSBP 3269). I – Schistocephalus sp. from C. familiaris, Newtok, Alaska, 4 April 1958; fixed after relaxation by R. Rausch (MSBP 17939). Acronyms of museum collections: MSBP – Museum of Southwestern Biology, Division of Parasitology, University of New Mexico, Albuquerque, New Mexico, U.S.A.; SNM – Swedish Museum of Natural History, Stockholm, Sweden; ZNB – Zoologische Museum Berlin, Berlin, Germany.

Fig. 5 in Disentangling Leucocytozoon parasite diversity in the neotropics: Descriptions of two new species and shortcomings of molecular diagnostics for leucocytozoids

Fig. 5. (A) A Bayesian phylogenetic hypothesis of Leucocytozoon species constructed only with partial mitochondrial genomes (5485 bp excluding gaps) and (B) partial cytb gene sequences of leucocytozoids. Branch colors indicate the parasite morphology, with green branches representing parasites in fusiform host cells, and blue branches correspond to a species that develops in roundish host cells. Notice that, since parasite mitochondrial genomes (mtDNA) corresponding to the partial cytb fragments of the MH909275 and MH909276 sequences could not be amplified, they were not included in the phylogenetic hypothesis constructed with mtDNA (Fig. 5A). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 2 in Disentangling Leucocytozoon parasite diversity in the neotropics: Descriptions of two new species and shortcomings of molecular diagnostics for leucocytozoids

Fig. 2. Leucocytozoon neotropicalis sp. nov. from the peripheral blood of its type vertebrate host Greenand-black Fruiteater (Pipreola riefferii) captured at Los Nevados NNP, Colombia. Macrogametocytes (A–E) and microgametocytes (F–I). Black arrows () indicate the deformed host cell nuclei. Parasite nuclei are indicated by white arrow () and nucleoli are shown by double white arrowtips (). Volutin granules are indicated by double black arrowtips () and vacuoles – by white arrowtips (). Uneven cytoplasmic processes may acquire a ribbon-like appearance (asterisk *). Giemsa-stained thin blood films. Scale bar = 10 μm. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1 in Helminths in common eiders (Somateria mollissima): Sex, age, and migration have differential effects on parasite loads

Fig. 1. Distributions of breeding and wintering populations of S. m. borealis, S. m. dresseri, and S. m. sedentaria in North America and Greenland. Populations of S. m. borealis are wintering in two areas in the pictured region; one in Southwest Greenland and one in East Canada (Newfoundland and Labrador). Individuals wintering in Southwest Greenland migrate to breed in West Greenland or Arctic Canada, whereas individuals wintering in East Canada have breeding areas in Arctic Canada (illustrated by the different direction of the red diagonal lines). For S. m. dresseri the breeding and wintering ranges overlap in one area that covers Newfoundland and Labrador as well as the northeastern part of the US, as shown by the grey horizontal lines. The subspecies S. m. sedentaria has its year-round residence in the Hudson Bay area as shown by the blue vertical lines. Dark stars mark the sampling locations of eiders in this study, whereas the white star marks the sampling location of eiders by Tourangeau et al. (2018). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 4 in Molecular prevalence and phylogenetic relationship of Haemoproteus and Plasmodium parasites of owls in Thailand: Data from a rehabilitation centre

Fig. 4. Colour heatmap of pairwise genetic distances estimated from nucleotide sequences of the cytochrome b gene (479 bp) of Haemoproteus spp. based on the Jukes-Canter model. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 3 in Gastrointestinal parasite infestation in the alpine mountain hare (Lepus timidus varronis): Are abiotic environmental factors such as elevation, temperature and precipitation affecting prevalence of parasite species?

Fig. 3. Parasite infestation in faeces and ambient temperature. Correlation between parasite infestation in Alpine mountain hare faeces (n = 52) and average, minimal, and maximal temperature found in Vorarlberg (Austria) during the years 2014 and 2015. Count visualises the number of faecal samples. See text for details on statistics.

Fig. 3 in Molecular prevalence and phylogenetic relationship of Haemoproteus and Plasmodium parasites of owls in Thailand: Data from a rehabilitation centre

Fig. 3. Bayesian phylogeny based on partial cytochrome b gene (479 base pairs) of Haemoproteus species lineages. The lineages reported in this study are given in bold. MalAvi lineage codes and GenBank accession numbers are given after species names. Node values (in percentages) indicate posterior clade probabilities. Vertical bars indicate clades of Haemoproteus subgenus (A), Parahaemoproteus (B). Almost all of the Parahaemoproteus lineages recovered from owls were grouped together (clade B-1, grey box). * indicates lineages infecting Strigiformes.

Fig. 2 in Gastrointestinal parasite infestation in the alpine mountain hare (Lepus timidus varronis): Are abiotic environmental factors such as elevation, temperature and precipitation affecting prevalence of parasite species?

Fig. 2. Number of parasite types per faeces and severity of parasitic infestation. Correlation between number of parasite types per Alpine mountain hare faeces and severity of parasitic infestation (n = 28) found in Vorarlberg (Austria) during the years 2014 and 2015. Count visualises the number of faecal samples. The severity of infestation is indicated by scattered ((+)), low (+), intermediate (++), and high (+++) infestation. See text for details on statistics.

Fig. 3 in Helminths in common eiders (Somateria mollissima): Sex, age, and migration have differential effects on parasite loads

Fig. 3. Prevalences of the cestodes Lateriporus sp. (A) and Microsomacanthus spp. (B), and the acanthocephalan Profilicollis sp. (C) in common eiders. Abbreviations: bor, CD = S. m. borealis, Cape Dorset; bor, GRLD = S. m. borealis, Greenland; bor, NFLD = S. m. borealis, Newfoundland; dre, NFLD = S. m. dresseri, Newfoundland; sed, BI = S. m. sedentaria [data published in Tourangeau et al. (2018)]. n-m = non-migratory, po-m = post-migratory, prm = pre-migratory. Letters describe significant differences between groups: if two groups share a letter, there is no significant difference in their prevalences.

Fig. 2 in Helminths in common eiders (Somateria mollissima): Sex, age, and migration have differential effects on parasite loads

Fig. 2. Examples of gastrointestinal parasites retrieved from common eiders in this study. (A) The trematode Notocotylus sp., (B) the cestode Lateriporus sp., (C) the acanthocephalan, Profilicollis sp. (D) microphallid trematodes, and (E) Microsomacanthus spp. cestodes.

Fig. 5 in Helminths in common eiders (Somateria mollissima): Sex, age, and migration have differential effects on parasite loads

Fig. 5. Cumulative percentages of birds infected with (A) Microsomacanthus spp., (B) Microphallus spp. and (C) Gymnophallus spp. from five different locations. Legend denotes the five infection levels: 0, 1s, 10s, 100s, and 1000s of parasite individuals within a single host. Abbreviations: bor, GRLD = S. m. borealis, Greenland; bor, NFLD = S. m. borealis, Newfoundland; dre, NFLD = S. m. dresseri, Newfoundland; bor, CD = S. m. borealis, Cape Dorset; sed, BI = S. m. sedentaria, Belcher Islands [data published in (Tourangeau et al., 2018)]. nm = non-migratory, po-m = post-migratory, pr-m = pre-migratory.