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Fig. 5 in Infestation and seasonal fluctuation of chigger mites on the Southeast Asian house rat (Rattus brunneusculus) in southern Yunnan Province, China

Fig. 5. Seasonal fluctuation of infestations of the Southeast Asian house rat (R. brunneusculus) with Walchia (W.) turmalis at Jingha, southern Yunnan of China (April 2016–March 2017).

Fig. 1 in Infestation and seasonal fluctuation of chigger mites on the Southeast Asian house rat (Rattus brunneusculus) in southern Yunnan Province, China

Fig. 1. Seasonal fluctuation of overall infestations of the Southeast Asian house rat (R. brunneusculus) with chiggers at Jingha village in southern Yunnan of China (April 2016–March 2017).

Fig. 4 in Infestation and seasonal fluctuation of chigger mites on the Southeast Asian house rat (Rattus brunneusculus) in southern Yunnan Province, China

Fig. 4. Seasonal fluctuation of infestations of the Southeast Asian house rat (R. brunneusculus) with Leptotrombidium (L.) deliense at Jingha, southern Yunnan of China (April 2016–March 2017).

Fig. 6 in Infestation and seasonal fluctuation of chigger mites on the Southeast Asian house rat (Rattus brunneusculus) in southern Yunnan Province, China

Fig. 6. Seasonal fluctuation of infestations of the Southeast Asian house rat (R. brunneusculus) with Leptotrombidium (L.) scutellare at Jingha, southern Yunnan of China (April 2016–March 2017).

Fig. 3 in Infestation and seasonal fluctuation of chigger mites on the Southeast Asian house rat (Rattus brunneusculus) in southern Yunnan Province, China

Fig. 3. Seasonal fluctuation of infestations of the Southeast Asian house rat (R. brunneusculus) with Ascoschoengastia indica at Jingha, southern Yunnan of China (April 2016–March 2017).

opencc-by-4.0Oct 2020View details →

Fig. 1 in Occurrence and infestation rates of Streblidae (Diptera, Hippoboscoidea) on bats (Mammalia, Chiroptera) in a semideciduous seasonal forest fragment in western Paraná, Brazil

Fig. 1. MonthlY average precipitation and temperature in Palotina, PR, Brazil, from 1997 to 2016. Source: SIMEPAR, 2018.

opencc-by-4.0Sep 2010View details →

Fig. 2 in Tubular shell infestations in some Mississippian spirilophous brachiopods

Fig. 2. Diagrammatical reconstruction of the dorsal valve of spiriferide brachiopod Tylothyris laminosa with part of the right spiralium removed to show hypothetical life position of the infester Haplorygma dorsalis ichnogen. et sp. nov. Grey arrow indicates presumable inhalant, open arrows exhalant currents.

Fig. 5 in Blood recovery of wild Mekong snail-eating turtles (Malayemys subtrijuga Schlegel and Müller, 1845) in captivity from leech infestation

Fig. 5. Morphological comparison of Malayemys subtrijuga no. 5 between week 0 (A and B) and week 17 (C and D).

Fig. 4 in Blood recovery of wild Mekong snail-eating turtles (Malayemys subtrijuga Schlegel and Müller, 1845) in captivity from leech infestation

Fig. 4. Symptoms of Placobdelloides siamensis infection on Malayemys subtrijuga: (A) Leech penetration beneath the keratin layer (scute) on plastron from no. 8; (B) Shell holes resulting from leech penetration on plastron from no. 7; (C) Epidermal lesion on the hind foot from no. 6; (D) Keratin mandible jaw with leech consumption from no. 4.

Fig. 3 in Blood recovery of wild Mekong snail-eating turtles (Malayemys subtrijuga Schlegel and Müller, 1845) in captivity from leech infestation

Fig. 3. Trend analysis of red blood cell count (RCC) (left) and white blood cell count (WCC) (right) of Malayemys subtrijuga during captivity recovery from 2 November 2018 (week 0) to 1 March 2019 (week 17). (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 Blood recovery of wild Mekong snail-eating turtles (Malayemys subtrijuga Schlegel and Müller, 1845) in captivity from leech infestation

Fig. 1. Analysis of the mean red blood cell count (RCC) (blue line) and white blood cell count (WCC) (green line) of Malayemys subtrijuga during captivity recovery from 2 November 2018 (week 0) to 1 March 2019 (week 17). (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 Blood recovery of wild Mekong snail-eating turtles (Malayemys subtrijuga Schlegel and Müller, 1845) in captivity from leech infestation

Fig. 2. Analysis of the mean weight of Malayemys subtrijuga during captivity recovery from 2 November 2018 (week 0) to 1 March 2019 (week 17).

opencc-by-4.0Aug 2022View details →

Fig. 1 in Infestation, histology, and molecular confirmation of Sarcoptes scabiei in an Andean porcupine (Coendou quichua) from the Central Andes of Colombia

Fig. 1. Coendou quichua with macroscopic lesions corresponding to hyperkeratosis and alopecia, which extend ventrally from the chest to the inguinal region and base of the tail, hyperkeratosis is also observed in the mandible and the fore and hind limbs up to the carpal and tarsal joints (A, B). Histopathological microphotographs of mangy skin of C. quichua, with the presence of tunnels with (black arrow heads) and without (white arrow heads) mites (Sarcoptes scabiei) in the stratum corneum (C) and skin with predominance of hyperkeratosis (hyp) and acanthosis (ac) (D). Light micrographs of: S. scabiei eggs (E). Dorsal view of a female with the presence of robust dorsal setae (ds), numerous and conspicuous triangular cuticular spines (cs) on its dorsal surface (F). Ventral view of a female with the presence of the legs short, with legs I and II bear a stalked empodium (e) that terminate in a broad pad, and the two hind pairs of legs (III and IV) terminate in long setae or bristles (s) (G). Ventral view of a male with the legs I, II and III bear a stalked empodium (e) that terminate in a broad pad and the last pair (IV) of legs terminate in long setae (s) (H). ch (chelicerae), p (pedipalps).

opencc-by-4.0Aug 2022View details →

Fig. 2 in Infestation, histology, and molecular confirmation of Sarcoptes scabiei in an Andean porcupine (Coendou quichua) from the Central Andes of Colombia

Fig. 2. Histological microphotographs of the development of the mite S. scabiei in the skin of the porcupine C. quichua. Permanent burrows dug by fertilized adult females, with the presence of a developing egg and the shell of another hatched egg (A, B). Burrows with the presence of three eggshells (sh) and feces (fe), where between two and three eggs are laid daily (C). Developing eggs within burrows in the stratum corneum of the skin, which hatch approximately 3–4 days after oviposition (D–F). Developing larvae in the superficial layer of the skin (G, H). Nymph burrowing just below the skin surface to moult into an adult in 3–4 days (I). Side-axial view of an adult female specimen of S. scabiei in a tunnel in the superficial epidermis. The mites have a short and broad gnathosoma (gn), globose idiosoma, short and conical legs I and II, with a delicate chitinous coating (le). Structures associated with the female reproductive system, spermatheca (sp), ovarian nutrient cell (ONC) located inside the ovary (ov), vitellogenic oocyte (oc) in the oviduct (ovd), as well as chorional gland (chg) close to oviporus (op) are visible (J).

opencc-by-4.0Apr 2022View details →

Fig. 2 in Predicting the risk of Alaria alata infestation in wild boar on the basis of environmental factors

Fig. 2. The prevalence of A. alata in wild boar in provinces in Poland calculated from literature values and data from the present study (A) and predicted by percentage of areas covered by WETLANDS (B) (for detailed information, see: Methods). The figure shows prevalence values for a given province and confidence intervals (lower; upper).

opencc-by-4.0Apr 2022View details →

Fig. 2 in Infestation and distribution of chigger mites on Chevrieri's field mouse (Apodemus chevrieri) in Southwest China

Fig. 2. Theoretical curve fitting for the species abundance distribution of chigger mite community on Chevrieri's field mice (Apodemus chevrieri) in southwest China (2001–2019).

opencc-by-4.0Apr 2022View details →

Fig. 1. The 91 in Infestation and distribution of chigger mites on Chevrieri's field mouse (Apodemus chevrieri) in Southwest China

Fig. 1. The 91 investigation sites and the captured sites where Chevrieri's field mice (Apodemus chevrieri) were captured in southwest China (2001–2019).

opencc-by-4.0Apr 2024View details →

Fig. 6 in Flea infestation of rodent and their community structure in frequent and non-frequent plague outbreak areas in Mbulu district, northern Tanzania

Fig. 6. Dendrogram of flea species showing two main groups (AB) of flea community based on farm and forest habitats.

opencc-by-4.0Apr 2024View details →

Fig. 5 in Flea infestation of rodent and their community structure in frequent and non-frequent plague outbreak areas in Mbulu district, northern Tanzania

Fig. 5. Plot showing the predicted effect of locality and season on the probability of flea infestation, based on the final best-fitting generalized linear model with a binomial function. The analysis aimed to identify the factors that strongly influence flea infestation. The strongest predictors of flea infestation were plague persistent localities and short rain seasons. The probability of infestation on these predictors was found to be statistically significant (p <0.05), suggesting a higher likelihood of flea infestation in this locality and season. The bars are 95% confidence interval of the effects.