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Fig. 3 in Understanding growth relationships of African cymothoid fish parasitic isopods using specimens from museum and field collections

Fig. 3. The relationship between cymothoid size and host size for female and male parasites by parasite species.

Fig. 2 in Understanding growth relationships of African cymothoid fish parasitic isopods using specimens from museum and field collections

Fig. 2. The total number, mean number and standard deviation of parasites collected from the South African Institute for Aquatic Biodiversity and fieldwork, respectively. J = juvenile, M = male, F = female. Attachment type indicated as: B = buccal, T = tongue, P = palate, G = gill.

Fig. 1 in Understanding growth relationships of African cymothoid fish parasitic isopods using specimens from museum and field collections

Fig. 1. Isopods preserved along with their fish hosts from the South African Institute for Aquatic Biodiversity (SAIAB). A. Ceratothoa famosa Hadfield, Bruce & Smit, 2014 in the mouth of Diplodus capensis (Smith, 1844); B. Mothocya affinis Hadfield, Bruce & Smit, 2015 in the gills of Hyporhamphus affinis (Günther, 1866); C. Cymothoa sodwana Hadfield, Bruce & Smit, 2013 in the mouth of Trachinotus botla (Shaw, 1803).

Fig. 4 in Understanding growth relationships of African cymothoid fish parasitic isopods using specimens from museum and field collections

Fig. 4. The relationship between cymothoid size and host size for juvenile parasites by parasite species.

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Fig. 2. Metacirolana shijikiensis, male. A in New record of two cymothoid isopods (Crustacea: Malacostraca: Isopoda) from South Korea

Fig. 2. Metacirolana shijikiensis, male. A, body, dorsal view; B, body, doral view, drawing; C, maxilliped; D, uropod; E, pleotelson. Scale bars: A, B = 1 mm, C, E = 0.1 mm, D = 0.2 mm.

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Fig. 1. Elaphognathia sugashimaensis, male. A in New record of two cymothoid isopods (Crustacea: Malacostraca: Isopoda) from South Korea

Fig. 1. Elaphognathia sugashimaensis, male. A, body, dorsal view; B, body, dorsal view, drawing; C, mandible; D, maxilliped; E, pylopod and enlargement of distal article. Scale bars: A, B = 1 mm, CE = 0.1 mm.

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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.

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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.)

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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. 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).