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opencc-by-4.0Nov 2018View details →

Fig. 1 in First report of Trissolcus japonicus parasitizing Halyomorpha halys in North American agriculture

Fig. 1. White and black circles indicate the locations of 2 sentinel egg masses that were parasitized by Trissolcus japonicus within a heterogeneous landscape at 1 of the field sites in New Jersey. Black lines indicate the nearest tree line, and the inset map of New Jersey indicates with a star where this farm was located.

opencc-by-4.0Jun 2018View details →

Fig. 1 in Parasitism of Plutella xylostella (Lepidoptera: Plutellidae) in southern Pakistan

Fig. 1. Frequency distribution of number of Oomyzus sokolowskii adults emerging from a single Plutella xylostella pupa.

opencc-by-4.0Jun 2018View details →

Fig. 3 in Parasitism of Plutella xylostella (Lepidoptera: Plutellidae) in southern Pakistan

Fig. 3. Relationship between average Plutella xylostella pupal weight and average number of Oomyzus sokolowskii adults emerged per pupa.

opencc-by-4.0Sep 2019View details →

Fig. 1 in Telenomus podisi parasitism on Dichelops melacanthus and Podisus nigrispinus eggs at different temperatures

Fig. 1. Distribution of lifetime parasitism of Telenomus podisi Ashmead (Hymenoptera: Scelionidae) in Dichelops melacanthus eggs (Dallas) (Hemiptera: Pentatomidae) at different temperatures. (A) 15 °C, (B) 20 °C, (C) 25 °C, (D) 30 °C at 80 ± 10% RH and a 14:10 h (L:D) photoperiod. Arrows indicate parasitism of 80%.

opencc-by-4.0Apr 2020View details →

Fig. 2 in Seasonal parasitism of the leaf-cutting ant Atta sexdens Linnaeus (Hymenoptera: Formicidae) by phorid flies (Diptera: Phoridae) in a Brazilian Cerrado-Atlantic Forest ecotone

Fig. 2. Correlation between temperature and the number of leaf-cutting ants Atta sexdens parasitized by Apocephalus attophilus (r = −0.722; df = 9; P <0.05).

opencc-by-4.0Apr 2020View details →

Fig. 1 in Seasonal parasitism of the leaf-cutting ant Atta sexdens Linnaeus (Hymenoptera: Formicidae) by phorid flies (Diptera: Phoridae) in a Brazilian Cerrado-Atlantic Forest ecotone

Fig. 1. Number of leaf-cutting ants Atta sexdens parasitized by Apocephalus attophilus and Eibesfeldtphora tonhascai in a Brazilian Cerrado-Atlantic Forest ecotone. The seasons are as follows: spring (Sep–Nov), summer (Dec–Feb), fall (Mar–May), and winter (Jun–Aug).

opencc-by-4.0Dec 2015View details →

Figure 2 in The parasitic isopod Anilocra physodes, as a novel food source for the lizardfish Synodus saurus (Synodontidae)

Figure 2. - Synodus saurus with an ectoparasite Anilocra physodes still attached to its mouth (arrow). Figure 3. - Several Anilocra physodes found inside a single stomach content of Synodus saurus.

Fig. 2 in An investigation of endoparasites and the determinants of parasite infection in European hedgehogs (Erinaceus europaeus) from Denmark

Fig. 2. Overall parasite prevalence by age. Numbers on the x-axis indicate age in years. Numbers on top of the columns indicate number of individuals, in red for hedgehogs with endoparasites, in blue for hedgehogs without endoparasites. Statistically significant differences in proportions of hedgehogs with endoparasites versus without hedgehogs, were found between juveniles (<1 year) and age classes 1–6 years, and between hedgehogs of one year versus two years of age as shown in the upper right corner of the figure. (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 An investigation of endoparasites and the determinants of parasite infection in European hedgehogs (Erinaceus europaeus) from Denmark

Fig. 4. Overall parasite prevalence by region. Numbers indicate number of individuals, in red for hedgehogs with parasites, in blue without. JNL denotes Jutland north of the Limfjord, and JSL abbreviates Jutland south of the Limfjord. Statistically significant differences in proportions of hedgehogs with endoparasites versus hedgehogs without endoparasites were found between Zealand and Jutland south of the Limfjord (JSL), and Zealand and Falster (p <0.05 in both cases). We removed seven individuals from the analyses (Jutland north of the Limfjord (n = 1), Jutland south of the Limfjord (n = 4), Lolland (n = 1), Bornholm (n = 1)), as they were the only individuals found in April and December, and four were only categorised as collected in "Summer 2016". (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1 in Lack of evidence of vertical transmission of Karyolysus blood parasites in Iberian green lizards (Lacerta schreiberi)

Fig. 1. Karyolysus sp. Trophozoite (a–c) and gamonts (d–f) found in blood smears of L. schreiberi lizards. Scalebar = 10 μm.

Fig. 1. A in An investigation of endoparasites and the determinants of parasite infection in European hedgehogs (Erinaceus europaeus) from Denmark

Fig. 1. A map representing Denmark and the geographical locations of the 299 dead European hedgehogs examined. Colours indicate the different species of endoparasites detected in each individual. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1 in Effect of burrowing cymothoid parasitism on loricariids

Fig. 1. Location of the sampling point for monitoring the ichthyofauna and studying the parasitic interaction of Artystone sp. and loricariids in the Selma stream, which is a tributary of Teles Pires River, Tapajos basin.

Fig. 3 in Effect of burrowing cymothoid parasitism on loricariids

Fig. 3. ANCOVA regression of the length-weight relationship of the hosts Hisonotus chromodontus Britski and Garavello (2007) and Curculionichthys luteofrenatus (Britski and Garavello 2007) with the covariate parasitized (blue points) and not parasitized (red points) by the burrowing cymothoid Artystone sp. in the Selma stream, a tributary of the Teles Pires River, during one year of parasite interaction monitoring. (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 Effect of burrowing cymothoid parasitism on loricariids

Fig. 2. Parasite-host interaction between Hisonotus chromodontus Britski and Garavello (2007) and Artystone sp. in the Selma stream, a tributary of Teles Pires river during monitoring of the interaction (2018–2019): (A) side view of a parasitized specimen photographed before biometrics and biology; (B) dorsal view of a parasitized specimen photographed before biometrics and biology; (C) approximate view of the parasite puncture site with the parasite still lodged in the host's abdomen; (D) parasite removed from the host next to the site it was inserted in the host.

Fig. 2 in An alien parasite affects local fauna-Confirmation of Sinergasilus major (Copepoda: Ergasilidae) switching hosts and infecting native Silurus glanis (Actinopterygii: Siluridae) in Hungary

Fig. 2. Evolutionary history of Sinergasilus based on Bayesian Inference (BI) analysis of 18S rDNA with Ergasilus anchoratus Markewitsch, 1940 designated as outgroup. Support for both maximum likelihood (ML, 1000 bootstrap replicates) and BI (10 million MCMC) indicated at nodes (ML/BI), only nodes with more than 50% support annotated.

Fig. 1 in An alien parasite affects local fauna-Confirmation of Sinergasilus major (Copepoda: Ergasilidae) switching hosts and infecting native Silurus glanis (Actinopterygii: Siluridae) in Hungary

Fig. 1. Micrographs using light microscopy (LM) and scanning electron microscopy (SEM) of Sinergasilus major; (A) Total body (SEM), (B) rostral plate with integumental pores and tactile setules (SEM), (C) thoracic plate with pectinate denticles (SEM), (D) ventral aspect of cephalon (SEM), (E) everted mouth (SEM), (F) inverted mouth (SEM), (G) ventral view of mouth parts (SEM), (H) mouth parts (LM). A1 – antennule 1, A2 – antenna, Ip – integumental pore, Gs – genital somite, Lb – labium, Lr – labrum, M – mouth, Md – mandible, Ml – maxillule, Mx – maxilla, Ps4 – pedigerous somite 4, Pd – pectinate denticles, Tp – thoracic plate, Ts – tactile setules.

Fig. 4 in Hyaloklossia Labb´e, 1896 (Alveolata: Apicomplexa) in frogs: Description of a new species and proposing a new subfamily to accommodate these enigmatic parasites

Fig. 4. Mature sporocysts of Hyaloklossia in the kidney of Pelophylax porosus porosus. (A) Light microscopy of a mature sporocyst in homogenized kidney tissue. (B) Nomarski interference contrast microscopy of a mature sporocyst in squash preparation of renal tubular tissue showing the presence of four spindle-shaped sporozoites. (C) Composite line drawing. Bar = 10 μm. Asterisk: sporocyst residuum.

Fig. 3 in Hyaloklossia Labb´e, 1896 (Alveolata: Apicomplexa) in frogs: Description of a new species and proposing a new subfamily to accommodate these enigmatic parasites

Fig. 3. Light microscopy of hematoxylin and eosin-stained sections of renal tissues of Pelophylax porosus porosus. (A) Mature sporocysts in the renal interstitium. Arrows indicate the transverse section of sporocysts showing four sporozoites with nuclei and a granular sporocyst residuum. (B and C) Immature oocysts. Note the very thin oocyst wall (arrows), sporonts with granular cytoplasm, and nuclei distributed at the cell margin (arrowheads). (D) Immature oocysts with two sporoblasts each and containing two polar nuclei (arrowheads). (E) Mature oocysts in renal epithelial cell showing two sporocysts with elongated sporozoites with circular nuclei (arrowhead) and a granular sporocyst residuum. Arrows indicate the sporocyst wall. Bars = 50 μm (A) and 10 μm (B–E).

Fig. 2 in Hyaloklossia Labb´e, 1896 (Alveolata: Apicomplexa) in frogs: Description of a new species and proposing a new subfamily to accommodate these enigmatic parasites

Fig. 2. Light microscopy of hematoxylin and eosin-stained sections of renal tissue of Pelophylax porosus porosus. Hyaloklossia sporocysts and/or oocysts congregated in a diffused manner in the renal interstitium (circles), and some were found solitarily in renal epithelial cells or in the lumen (arrowheads). Bar = 200 μm. A highresolution version of this slide for use with the Virtual Microscope is available as eSlide: VM06312.

Fig. 5 in Hyaloklossia Labb´e, 1896 (Alveolata: Apicomplexa) in frogs: Description of a new species and proposing a new subfamily to accommodate these enigmatic parasites

Fig. 5. Phylogenetic trees of coccidian parasites belonging to the subfamilies Toxoplasmatinae, Eumonosporinae, and Cystoisosporinae and related taxa using 18S (A), 28S (B), and cox1 (C) sequence data. Sarcocystis rileyi (Sarcocystidae: Sarcocytinae) was used as an outgroup. The nodes are labeled using support from the bootstrap values obtained for neighbor joining (left) and maximum likelihood (right) methods. The unlabeled nodes and hyphens indicate support <50. Scale bars represent the substitutions per site.