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Fig. 1 in Global diversity of fish parasitic isopod crustaceans of the family Cymothoidae

Fig. 1. Absolute numbers and cumulative percentage of species of Cymothoidae (373) published per decade since Linnaeus (1758). Data from the World List of Marine, Freshwater and Terrestrial Isopod Crustaceans hosted by the Smithsonian and at the WoRMS database (Schotte et al., 1995 onwards).

opencc-by-4.0Aug 2014View details →
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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.

opencc-by-4.0Apr 2019View details →
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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.

opencc-by-4.0Apr 2019View details →
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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).

opencc-by-4.0Apr 2019View details →
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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.

opencc-by-4.0Apr 2019View details →
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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.

opencc-by-4.0Oct 2016View details →
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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.

opencc-by-4.0Oct 2016View details →
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Fig. 3 Canonical correspondence analysis. Only axes 1 and 2 are shown. Type 2 in Evaluating the correlation between area, environmental heterogeneity, and species richness using terrestrial isopods (Oniscidea) from the Pontine Islands (West Mediterranean)

Fig. 3 Canonical correspondence analysis. Only axes 1 and 2 are shown. Type 2 scaling is shown. A right-angled projection of a point representing a response variable (ecological categories of species) onto an arrow representing an explanatory variable (biotope type)

opencc-by-4.0Oct 2021View details →
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Fig. 2 in Evaluating the correlation between area, environmental heterogeneity, and species richness using terrestrial isopods (Oniscidea) from the Pontine Islands (West Mediterranean)

Fig. 2 Path analysis model. In this model, species richness (S) is the dependent variable. Area (A) and environmental heterogeneity (H) can have a direct effect on S, whereas A can also have an effect on H. The indicators used for A and S are the log-transformed area in square kilometres (LogA) and the number of species (LogS). Different indicators were used for environmental heterogeneity (B, LogB, Shannon, and 1-D, see main text). The symbols bAS, bAH, and bHS indicate the partial standardised regression coefficients

opencc-by-4.0Oct 2021View details →
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Figure 5 in Terrestrial isopods of the genus Protracheoniscus (Isopoda: Oniscidea) in northern Iran with a description of two new species

Figure 5. Protracheoniscus golestanicus sp. nov., male, holotype. A, Pleopod endopodite I; B, pleopod exopodite I; C, pleopod II; D, pleopod exopodite III; E, pleopod exopodite IV; F, pleopod exopodite V. Scales = 0.2 mm.

opencc-by-4.0Jan 2016View details →
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Figure 3 in Terrestrial isopods of the genus Protracheoniscus (Isopoda: Oniscidea) in northern Iran with a description of two new species

Figure 3. Protracheoniscus kiabii sp. nov., male, holotype. A, Pleopod endopodite I; B, pleopod exopodite I; C, pleopod II; D, pleopod exopodite III; E, pleopod exopodite IV; F, pleopod exopodite V. Scales = 0.2 mm.

opencc-by-4.0Jan 2016View details →
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Figure 1 in Terrestrial isopods of the genus Protracheoniscus (Isopoda: Oniscidea) in northern Iran with a description of two new species

Figure 1. Map of Iran with the location of the provinces of Gilan, Mazandaran, and Golestan highlighted; showing the sampling localities of Protracheoniscus kiabii sp. nov. (in black), P. golestanicus sp. nov. (in red), P. ehsani (in blue), and P. major (in green).

opencc-by-4.0Jan 2016View details →
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Figure 2 in Terrestrial isopods of the genus Protracheoniscus (Isopoda: Oniscidea) in northern Iran with a description of two new species

Figure 2. Protracheoniscus kiabii sp. nov., male, holotype. A, Body outline indicating the position of noduli laterales; B, cephalon and first pereonite; C, antenna; D, pereopod I; E, pereopod VII; F, pereopod VII ischium, rostral view; G, telson and uropods. Scale = A and B, 1 mm; C–G, 0.5 mm.

opencc-by-4.0Jan 2016View details →
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Figure 4 in Infestation and effect of parasitic isopod Epipenaeon ingens ingens Nobili, 1906 on commercial shrimp species in the eastern Mediterranean: a case study of the population of brown shrimp Penaeus aztecus Ives, 1891

Figure 4. Data of E. ingens ingens. Expected (pink logistic line) percentage of a female with male, expected (red logistic line) and observed percentage (red circular) of Ov-F, and size structure of female parasite (thick line), female accompanied with male (broken line) and Ov-F (thin line), size at first accompaniment (FAS ) and size at first maturity (FMS ).

opencc-by-4.0Jul 2021View details →
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Figure 2 in Infestation and effect of parasitic isopod Epipenaeon ingens ingens Nobili, 1906 on commercial shrimp species in the eastern Mediterranean: a case study of the population of brown shrimp Penaeus aztecus Ives, 1891

Figure 2. Percentage of infected and uninfected shrimps by carapace length (CL) and by sex of P. aztecus sampled in Antalya Bay (red circular: an observed percentage of the infection, thick line: correlation line).

opencc-by-4.0Jul 2021View details →
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Figure 6 in Infestation and effect of parasitic isopod Epipenaeon ingens ingens Nobili, 1906 on commercial shrimp species in the eastern Mediterranean: a case study of the population of brown shrimp Penaeus aztecus Ives, 1891

Figure 6. Box and Whisker plot representation of the negative effect of E. ingens ingens on the gonadal development of the female host shrimp P. aztecus.

opencc-by-4.0Jul 2021View details →
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Figure 2 in The parasitic isopod Anilocra physodes, as a novel food source for the lizardfish Synodus saurus (Synodontidae)

Figure 2. - Synodus saurus with an ectoparasite Anilocra physodes still attached to its mouth (arrow). Figure 3. - Several Anilocra physodes found inside a single stomach content of Synodus saurus.

opencc-by-4.0Dec 2015View details →
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Fig. 5. Mothocya andoni n in Two new species of branchial fish parasitic isopod of the genus Mothocya Costa, in Hope, 1851 (Isopoda, Cymothoidae) from Nigeria

Fig. 5. Mothocya andoni n. sp. Ƌ (12.0 mm total length, 5.0 mm width) (SAMC–A092738). A, Antennula; B, Antenna; C, Maxilliped; D, Tip of maxillula; E, Mandible palp; F, Maxilla.

opencc-by-4.0Aug 2021View details →
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Fig. 2. Mothocya andoni n in Two new species of branchial fish parasitic isopod of the genus Mothocya Costa, in Hope, 1851 (Isopoda, Cymothoidae) from Nigeria

Fig. 2. Mothocya andoni n. sp. paratype ♀ (non-ovigerous, 18.0 mm total length, 9.0 mm width) (SAMC–A092738). A, Antennula; B, Antenna; C, Mandible; D, Maxillula; E, Maxilla; F, Maxilliped.

opencc-by-4.0Aug 2021View details →
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Fig. 3. Mothocya andoni n in Two new species of branchial fish parasitic isopod of the genus Mothocya Costa, in Hope, 1851 (Isopoda, Cymothoidae) from Nigeria

Fig. 3. Mothocya andoni n. sp. paratype ♀ (non-ovigerous, 18.0 mm total length, 9.0 mm width) (SAMC–A092738). A, Pleopod 1 ventral view; B, Pleopod 2 ventral view; C, Pleopod 3 ventral view; D, Pleopod 4 ventral view; E, Pleopod 5 ventral view; F, Pleopod 1 dorsal view; G, Pleopod 2 dorsal view; H, Pleopod 3 dorsal view; I, Pleopod 4 dorsal view; J, Pleopod 5 dorsal view.

opencc-by-4.0Aug 2021View details →

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