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Fig. 4 in The Viability of Haemonchus Contortus (Nematoda, Strongylida) and Strongyloides Papillosus (Nematoda, Rhabditida) Larvae Exposed to Various Flavourings and Source Materials Used in Food Production

Fig. 4. The effect of alcohol flavourings and their compounds on the viability of larvae of nematodes of Ruminantia: а — β-Ionone, b — Citronellol, с — Acetoin; for explanations see fig. 1.

Fig. 2 in The Viability of Haemonchus Contortus (Nematoda, Strongylida) and Strongyloides Papillosus (Nematoda, Rhabditida) Larvae Exposed to Various Flavourings and Source Materials Used in Food Production

Fig. 2. The effect of acetate flavourings upon the viability of larvae of nematodes of Ruminantia: а — Ethyl acetate, b — Benzyl acetate; for explanations see fig. 1.

Fig. 3 in The Viability of Haemonchus Contortus (Nematoda, Strongylida) and Strongyloides Papillosus (Nematoda, Rhabditida) Larvae Exposed to Various Flavourings and Source Materials Used in Food Production

Fig. 3. The effect of alcohol flavourings and their compounds on the viability of larvae of nematodes of Ruminantia: а — α-Terpineol, b — Benzyl alcohol, с — Citral, d — L-Linalool; for explanations see fig. 1.

Fig. 1 in The Viability of Haemonchus Contortus (Nematoda, Strongylida) and Strongyloides Papillosus (Nematoda, Rhabditida) Larvae Exposed to Various Flavourings and Source Materials Used in Food Production

Fig. 1. The effect of aldehyde flavourings on the viability of larvae of nematodes of Ruminantia: а — p-Anisaldehyde; b — Benzaldehyde; с — γ-Undecalactone; d — Cinnamaldehyde; the ordinate axis indicates the percentage of living nematode larvae in 24-hour experiment; the abscissa axis indicates the concentration of the active substance (%); (К) control, where the concentration of the active substance is 0 %; (L3) infective larvae of S. papillosusor H. contortus; (L1, L2) non-infective larvae of S. papillosus; small square in the centre corresponds to the median, lower and upper edge of the large rectangle corresponds to first and third quartiles, respectively, the vertical segments, directed upward and downward from the rectangles, correspond to minimum and maximum values (n = 8).

Fig. 5 in The Viability of Haemonchus Contortus (Nematoda, Strongylida) and Strongyloides Papillosus (Nematoda, Rhabditida) Larvae Exposed to Various Flavourings and Source Materials Used in Food Production

Fig. 5. The effect of D-limonene on the viability of larvae of nematodes of Ruminantia: for explanations see fig. 1.

Fig. 9 in Intraspecific Morphological Variation In Free- Living Stages Of Strongyloides Papillosus (Nematoda, Strongyloididae) Parasitizing Various Mammal Species

Fig. 9. Morphometric parameters of free-living females of S. papillosus: а — body length; b — body width; c — length of esophagus; d — length of intestine; e — length of tail; f — distance to vulva; g — number of eggs; on the ordinate axis — length in µm, on the abscissa axis — species of host (Ch — Capra hircus, Oc — Oryctolagus cuniculus, Cp — Cavia porcellus).

Fig. 8 in Intraspecific Morphological Variation In Free- Living Stages Of Strongyloides Papillosus (Nematoda, Strongyloididae) Parasitizing Various Mammal Species

Fig. 8. Morphometric parameters of S. papillosus males: a — body length; b – body width; c — length of esophagus; d — length of intestine; e — length of the tail; f — length of spicules; on the ordinate axis — length in µm, on the abscissa axis — species of host (Ch — Capra hircus, Oc — Oryctolagus cuniculus, Cp — Cavia porcellus).

Fig. 7 in Intraspecific Morphological Variation In Free- Living Stages Of Strongyloides Papillosus (Nematoda, Strongyloididae) Parasitizing Various Mammal Species

Fig. 7. Free-living female of S. papillosus: a — general view; b — anterior part (the arrowheads indicate the bulbs); c — uterus with eggs (the pointer indicates the genital opening); scale bars 100 µm.

Fig. 5 in Intraspecific Morphological Variation In Free- Living Stages Of Strongyloides Papillosus (Nematoda, Strongyloididae) Parasitizing Various Mammal Species

Fig. 5. Morphometric parameters of L3: а — body length; b — body width; c — length of esophagus; d — length of intestine; e — length of the tail end; on the ordinate axis — length in µm, on the abscissa axis — species of host (Ch — Capra hircus, Oc — Oryctolagus cuniculus, Cp — Cavia porcellus).

Fig. 6 in Intraspecific Morphological Variation In Free- Living Stages Of Strongyloides Papillosus (Nematoda, Strongyloididae) Parasitizing Various Mammal Species

Fig. 6. Mature male of S. papillosus: a — general view; b — anterior part (arrowheads indicate bulbs); c — caudal part with spicules in lateral view; d — caudal part with spicules in dorsal view; scale bars 100 µm.

Fig. 3 in Intraspecific Morphological Variation In Free- Living Stages Of Strongyloides Papillosus (Nematoda, Strongyloididae) Parasitizing Various Mammal Species

Fig. 3. Morphometric parameters of L2 of S. papillosus: а — body length; b — body width; c — length of esophagus; d — length of intestine; e — length of the tail; on the ordinate axis — length in µm, on the abscissa axis – species of host (Ch — Capra hircus, Oc — Oryctolagus cuniculus, Cp — Cavia porcellus).

Fig. 2 in Intraspecific Morphological Variation In Free- Living Stages Of Strongyloides Papillosus (Nematoda, Strongyloididae) Parasitizing Various Mammal Species

Fig. 2. Morphometric parameters of L1 of S. papillosus: а — body length; b — body width; c — length of esophagus; d — length of intestine; e — length of tail; on the ordinate axis — length in µm, on the abscissa axis — species of host (Ch — Capra hircus, Oc — Oryctolagus cuniculus, Cp — Cavia porcellus).

Fig. 4 in Intraspecific Morphological Variation In Free- Living Stages Of Strongyloides Papillosus (Nematoda, Strongyloididae) Parasitizing Various Mammal Species

Fig. 4. Third-stage larva of S. papillosus: a — general view; b — anterior part (the pointer indicates the place where the esophagus joins the intestine); c — posterior part; scale bars 100 µm.

Fig. 1 in Intraspecific Morphological Variation In Free- Living Stages Of Strongyloides Papillosus (Nematoda, Strongyloididae) Parasitizing Various Mammal Species

Fig. 1. Rhabditiform larvae of S. papillosus: a — L1 from C. hircus (arrowheads indicate the bulb-like dilatations on the esophagus and the tail); b — L1 from O. hircus (arrowheads indicate bulb-like dilatations on the esophagus and the tail); c — L2 from C. hircus (arrowheads indicate two bulb-like dilatations); scale bars 100 µm.

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Fig. 2. Simplified neighbor-joining tree reconstructed from partial cox1 in Lurking in the dark: Cryptic Strongyloides in a Bornean slow loris

Fig. 2. Simplified neighbor-joining tree reconstructed from partial cox1 gene (716 bp) sequences of Strongyloides spp. S. fuelleborni sequences for Bornean primates cluster within the S. fuelleborni group, together with previously described sequences for the parasite found in African and Japanese primates. The S. stercoralis cluster includes sequences from humans from Laos, Africa and Japan, captive chimpanzees, and dogs. The Strongyloides sp. cluster corresponds to sequences from the slow loris. An alternative hypothesis is presented next to the tree, where instead of representing a different species, Strongyloides sp. would be part of a cryptic assemblage within the S. stercoralis group.

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Fig. 1. Sampling sites within Lots 6 and 7 in Lurking in the dark: Cryptic Strongyloides in a Bornean slow loris

Fig. 1. Sampling sites within Lots 6 and 7 of the Lower Kinabatangan Wildlife Sanctuary, Malaysian Borneo (Nm = Nycticebus menagensis, Pp = Pongo pygmaeus, Mf = Macaca fascicularis, Nl = Nasalis larvatus, Tc = Trachypithecus cristatus, DGFC = Danau Girang Field Centre).

opencc-by-4.0Dec 2019View details →

Fig. 3. Pelodera strongyloides Schneider, 1860. A in First report of five free-living nematode species (Nematoda: Rhabditida) from Korea

Fig. 3. Pelodera strongyloides Schneider, 1860. A. Overall view; B. Anterior part; C. Posterior part of female; D. Posterior part of male; E. Vulval region. Scale bars: A = 50 μm; B-E = 20 μm.

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Fig. 1 in Genetic characterization of Strongyloides fuelleborni infecting free-roaming African vervets (Chlorocebus aethiops sabaeus) on the Caribbean island of St. Kitts

Fig. 1. Schematic of the Strongyloides genotyping scheme referenced here Graphical representation a Strongyloides sp. genotyping scheme after the description of Barratt et al. (Barratt et al., 2019a; Barratt and Sapp, 2020). This scheme was expanded here to include haplotypes XVI and XVII of 18S HVR-I (indicated by a star) identified here from feral vervet monkeys living on the island of St Kitts (GenBank accessions in Table 3). Haplotype names shown in blue belong to S. fuelleborni and those shown in black belong to other Strongyloides species in accordance with this typing scheme. Haplotype sequences are provided in File S1. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

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Fig. 3 in Genetic characterization of Strongyloides fuelleborni infecting free-roaming African vervets (Chlorocebus aethiops sabaeus) on the Caribbean island of St. Kitts

Fig. 3. Neighbor-Joining tree generated from St Kitts S. fuelleborni genotypes and other Strongyloides types This tree was generated by applying the Neighbor-Joining clustering method (Saitou and Nei, 1987) to a pairwise distance matrix computed using Barratt's heuristic from 285 Strongyloides genotypes, including 48 from St. Kitts vervets. Branches are colored according to their cluster membership (A through H) as defined by Ko et al. (2022). We also introduce S. fuelleborni type H (light pink) from St. Kitts vervets, noting that an H-type isolate was found previously in a human from Guinea-Bissau (pink triangle). Divergent S. fuelleborni types described by Ko et al. (2022) were also analyzed (bright green branches without a cluster letter) from Siamang, Douc, and Francois' langur housed in zoological parks in Japan. A version of this same tree with isolate names shown on the branch tips is provided in File S3; Tree B. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)