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Fig. 12 in Habitat and seasonal activity patterns of the terrestrial isopods (Isopoda: Oniscidea) of Belgium

Fig. 12. Corrected number of observations per two-month period for Trichoniscoides albidus (N = 97).

Fig. 10 in Habitat and seasonal activity patterns of the terrestrial isopods (Isopoda: Oniscidea) of Belgium

Fig. 10. Corrected number of observations per two-month period for Metatrichoniscoides leydigii (N = 16).

Fig. 11. a in Habitat and seasonal activity patterns of the terrestrial isopods (Isopoda: Oniscidea) of Belgium

Fig. 11. a, Ligidium hypnorum; b, Androniscus dentiger; c, Haplophthalmus mengii; d, Hyloniscus riparius; e, Metatrichoniscoides leydigii; f, Trichoniscoides albidus; g, Trichoniscoides helveticus; h, Trichoniscus provisorius.

Fig. 8 in Habitat and seasonal activity patterns of the terrestrial isopods (Isopoda: Oniscidea) of Belgium

Fig. 8. Corrected number of observations per two-month period for Haplophthalmus montivagus (N = 157).

Fig. 24 in Habitat and seasonal activity patterns of the terrestrial isopods (Isopoda: Oniscidea) of Belgium

Fig. 24. Corrected number of observations per two-month period for Platyarthrus hoffmannseggii (N = 163).

Fig. 1 in Habitat and seasonal activity patterns of the terrestrial isopods (Isopoda: Oniscidea) of Belgium

Fig. 1. Different habitats in Belgium well suited for terrestrial isopods. a, old forest in Parike, Belgium; b, disused quarry in Reuland, Belgium; c, stream side (dyke) of the Dyle river in Rijmenam, Belgium; d, old cemetery in Rahier, Belgium; e, old stable in a meadow near Saint-Saveur, Belgium.

Fig. 2. a in Habitat and seasonal activity patterns of the terrestrial isopods (Isopoda: Oniscidea) of Belgium

Fig. 2. a, Ligia oceanica; b, Haplophthalmus danicus; c, Miktoniscus patience; d, Trichoniscus pygmaeus; e, Armadillidium pictum; f, Armadillidium vulgare; g, Porcellio dilatatus; h, Porcellio laevis.

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Fig. 1 in Ecological correlates of ectoparasite load in a rodent: Complex roles of seasonality

Fig. 1. Interactive effects of season and body weight (centralized) on tick load in S. dauricus (A); and interactive effects of season and trappability on tick load in S. dauricus (B).

Fig. 7 in Quatrefoil light traps for free-swimming stages of cymothoid parasitic isopods and seasonal variation in their species compositions in the Seto Inland Sea, Japan

Fig. 7. Number of Mothocya parvostis collected at tidal levels: low tide, 1/3 tide, 2/3 tide, and high tide during the three days of sampling.

Fig. 6 in Quatrefoil light traps for free-swimming stages of cymothoid parasitic isopods and seasonal variation in their species compositions in the Seto Inland Sea, Japan

Fig. 6. Temporal variation in water temperature from October 2020 to December 2021. The gap in data is due to faulty logging equipment.

Fig. 8 in Quatrefoil light traps for free-swimming stages of cymothoid parasitic isopods and seasonal variation in their species compositions in the Seto Inland Sea, Japan

Fig. 8. Number of Mothocya parvostis collected on each sampling date (solid line) and tidal levels (broken line) from November 15 (new moon) to December 15 (new moon).

Fig. 5 in Quatrefoil light traps for free-swimming stages of cymothoid parasitic isopods and seasonal variation in their species compositions in the Seto Inland Sea, Japan

Fig. 5. Number of cymothoid juveniles collected in each month from October 2020 to December 2021. Dot bars (red) indicate Mothocya parvostis and diagonal right pattern bars (blue) indicate Ceratothoa verrucosa. (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 Quatrefoil light traps for free-swimming stages of cymothoid parasitic isopods and seasonal variation in their species compositions in the Seto Inland Sea, Japan

Fig. 4. Number of cymothoid mancae collected in each month from October 2020 to December 2021. Dot bars (red) indicate Mothocya parvostis, diagonal right pattern bars (blue) indicate Ceratothoa verrucosa, diagonal left pattern bars (green) indicate Ceratothoa carinata. (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 Quatrefoil light traps for free-swimming stages of cymothoid parasitic isopods and seasonal variation in their species compositions in the Seto Inland Sea, Japan

Fig. 3. Dorsal views of cymothoid free-swimming stages collected by the light trap. (a) and (d): Mothocya parvostis, (b) and (e): Ceratothoa verrucosa, (c): Ceratothoa carinata. (a)–(c): mancae, (d) and (e): juveniles. Scale bars indicate (a)–(c): 1 mm, (d) and (e): 3 mm.

Fig. 2 in Quatrefoil light traps for free-swimming stages of cymothoid parasitic isopods and seasonal variation in their species compositions in the Seto Inland Sea, Japan

Fig. 2. Map showing location of the Seto Inland Sea and sampling site, where light trap sampling was performed.

Fig. 1 in Quatrefoil light traps for free-swimming stages of cymothoid parasitic isopods and seasonal variation in their species compositions in the Seto Inland Sea, Japan

Fig. 1. The quatrefoil light trap using in this study. (a): front view, (b): bottom view without net, (c): Light traps in use underwater. A: 15 W LED fishing light, B: Net to collect organisms in trap (0.5 mm mesh).

Fig. 5 in Influence of seasonality and biological activity on infection by helminths in Cantabrian bear

Fig. 5. Seasonal kinetics of helminths egg-output in Cantabrian brown bears (n = 248) according to their activity periods. (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 Influence of seasonality and biological activity on infection by helminths in Cantabrian bear

Fig. 2. Seasonal variations in the prevalence of helminth infection in feces of brown bears (n = 248) from the western part of the Cantabrian Mountains (Asturias and Le´on provinces, Spain). (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 Influence of seasonality and biological activity on infection by helminths in Cantabrian bear

Fig. 4. Seasonal variations in the prevalence of helminth infection in feces of brown bears (n = 248) from Cantabrian Mountains (Spain) according to their activity periods. (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 Influence of seasonality and biological activity on infection by helminths in Cantabrian bear

Fig. 1. Distribution of the sampling of brown bear feces (n = 248) in the western part of the Cantabrian Mountains (Asturias and Le´on provinces, Spain). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)