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Fig. 4 in Helminth community structure in two species of arctic-breeding waterfowl

Fig. 4. Predicted prevalence (top) and helminth infection intensity (bottom) for the cestode Drepanidotaenia lanceolata enumerated in Pacific black brant (BLBR) and greater whitefronted geese (GWFG) collected in Arctic and Subarctic Alaska (2014). Circles represent predicted means and error bars denote 85% confidence intervals. Predictions are based off the most supported model from AICc selection and all interactions include lower-order effects (see titles).

Fig. 6 in Helminth community structure in two species of arctic-breeding waterfowl

Fig. 6. Predicted prevalence (top) and helminth infection intensity (bottom) for the cestode Tschertkovilepis setigera enumerated in Pacific black brant (BLBR) and greater whitefronted geese (GWFG) collected in Arctic and Subarctic Alaska (2014). Circles represent predicted means and error bars denote 85% confidence intervals. Predictions are based off the most supported model from AICc selection and all interactions include lower-order effects (see titles).

Fig. 2 in Helminth community structure in two species of arctic-breeding waterfowl

Fig. 2. Predicted helminth species richness (SR) for Pacific black brant (BLBR) and greater white-fronted geese (GWFG) collected from Subarctic and Arctic Alaska (2014). Circles represent predicted means and error bars denote 85% confidence intervals. Predictions are based on the most supported model from AICc selection and all interactions include lower-order effects (see title).

Fig. 2 in Temporal and demographic blood parasite dynamics in two free-ranging neotropical primates

Fig. 2. Individual infection status by parasite by year. Strength and thickness of lines are scaled to the number of individuals that took a given infection trajectory from one year to the next. Two diagonal lines span 2012‾2014 because those individuals were not sampled in 2013. The + symbols represent every infection or non-infection found across all individuals in the study.

Fig. 3 in Temporal and demographic blood parasite dynamics in two free-ranging neotropical primates

Fig. 3. Parasite species richness by species, age class and sex. Colors represent females (black) and males (gray).

Fig. 3 in Helminth community structure in two species of arctic-breeding waterfowl

Fig. 3. Predicted prevalence (top) and helminth infection intensity (bottom) for the nematode Trichostrongylus tenuis enumerated in Pacific black brant (BLBR) and greater whitefronted geese (GWFG) collected in Arctic and Subarctic Alaska (2014). Circles represent predicted means and error bars denote 85% confidence intervals. Predictions are based off the most supported model from AICc selection and all interactions include lower-order effects (see titles).

Fig. 4. Syndesmis aonikenki n in Two new species of Syndesmis (Platyhelminthes, Rhabdocoela, Umagillidae) from the sea urchin Pseudechinus magellanicus (Echinodermata, Echinoidea) in the Southwestern Atlantic Ocean

Fig. 4. Syndesmis aonikenki n. sp. A, B, whole mount preparations. C, sagittal section of the body. Abbreviations: ed, ejaculatory duct; eg, egg; f, filament; fg, filament glands; i, intestine; ma, male atrium; ov, ovary; sr, seminal receptacle; st, stylet; u, uterus; va, vagina; vit, vitellaria.

Fig. 3 in Two new species of Syndesmis (Platyhelminthes, Rhabdocoela, Umagillidae) from the sea urchin Pseudechinus magellanicus (Echinodermata, Echinoidea) in the Southwestern Atlantic Ocean

Fig. 3. Schematic reconstruction of Syndesmis aonikenki n. sp. in dorso-ventral view. Abbreviations: eg, egg; f, filament; fg, filament glands; ov, ovary; st, stylet; t, testes; vit, vitellaria.

Fig. 1 in Two new species of Syndesmis (Platyhelminthes, Rhabdocoela, Umagillidae) from the sea urchin Pseudechinus magellanicus (Echinodermata, Echinoidea) in the Southwestern Atlantic Ocean

Fig. 1. Schematic reconstruction of Syndesmis selknami n. sp. in dorso-ventral view. Abbreviations: eg, egg; f, filament; fg, filament glands; ov, ovary; st, stylet; t, testes; vit, vitellaria.

Fig. 2. Syndesmis selknami n in Two new species of Syndesmis (Platyhelminthes, Rhabdocoela, Umagillidae) from the sea urchin Pseudechinus magellanicus (Echinodermata, Echinoidea) in the Southwestern Atlantic Ocean

Fig. 2. Syndesmis selknami n. sp. A, D, whole mount preparations. B, C, E, F, sagittal sections of the body. Abbreviations: b, brain; ed, ejaculatory duct; eg, egg; f, filament; fg, filament glands; i, intestine; ov, ovary; sp, sensory pit; sr, seminal receptacle; t, testes; u, uterus; vc, vacuolar cells; vit, vitellaria. The white arrow heads marks the proximal part of the stylet and black arrow heads mark the distal part.

Fig. 1 in Helminth community structure in two species of arctic-breeding waterfowl

Fig. 1. Study sites in Alaska where Pacific black brant and greater white-fronted geese were collected for helminth examination in 2014; A) Yukon-Kuskokwim Delta (61ǫ N 164ǫ W) in Subarctic western Alaska and B) the Arctic Coastal Plain (70ǫ N 154ǫ) in Arctic Alaska.

Fig. 1 in Temporal and demographic blood parasite dynamics in two free-ranging neotropical primates

Fig. 1. Annual prevalence of single- and co-infections by species. Prevalence indicated for each parasite (dark gray), and each pairwise combination of parasites (light gray). Numbers near the top of each bar show the exact prevalence; black lines indicate 95% confidence intervals; dots indicate expected levels of co-infection (refer to Section 3.2). M-D is co-occurrence of M. mariae and Dipetalonema spp., D-T is Dipetalonema spp. and T. minasense, and M-T is M. mariae and T. minasense.

Fig. 1 in Eosinophilic meningoencephalitis associated with rat lungworm (Angiostrongylus cantonensis) migration in two nine-banded armadillos (Dasypus novemcinctus) and an opossum (Didelphis virginiana) in the southeastern United States

Fig. 1. Caudal end of a male nematode extracted from the brain of Armadillo 1. Arrow indicates bursal rays.

Fig. 2. Maximum parsimony tree inferred from 18S in Novel piroplasmid and Hepatozoon organisms infecting the wildlife of two regions of the Brazilian Amazon

Fig. 2. Maximum parsimony tree inferred from 18S rRNA gene sequences of Hepatozoon spp., with Babesia sp. as outgroup (488 characters; 52 parsimony-informative sites). Numbers at nodes are the support values for the major branches (bootstrap over 500 replicates). The sequences obtained in this study are in bold. Numbers in brackets are GenBank accession numbers.

Fig. 1. Maximum parsimony tree inferred from 18S in Novel piroplasmid and Hepatozoon organisms infecting the wildlife of two regions of the Brazilian Amazon

Fig. 1. Maximum parsimony tree inferred from 18S rRNA gene sequences of piroplasmids (Babesia spp., Theileria spp., Cytauxzoon spp.), with Plasmodium ovale as outgroup (316 characters; 65 parsimony-informative sites). Numbers at nodes are the support values for the major branches (bootstrap over 500 replicates). The sequences obtained in this study are in bold. Numbers in brackets are GenBank accession numbers.

Fig. 2. Neuroparenchyma. Fig. 2a in Eosinophilic meningoencephalitis associated with rat lungworm (Angiostrongylus cantonensis) migration in two nine-banded armadillos (Dasypus novemcinctus) and an opossum (Didelphis virginiana) in the southeastern United States

Fig. 2. Neuroparenchyma. Fig. 2a: Armadillo B. High numbers of eosinophils and lymphocytes expand the perivascular spaces. A focus of hemorrhage, eosinophils, and glial cells interrupts the neuroparenchyma. Photomicrographs are stained with hematoxylin and eosin (H&E). Bar = 200 Mm. Fig. 2b: Armadillo A. Cross section of a nematode larva (200 Mm width) within the thalamus is characterized by a smooth cuticle, coelomyarian musculature, lateral cords, and a distinct pharynx (consistent with a metastrongyle). No inflammatory cells surround the nematode. H&E, Bar = 50 Mm.

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