Journal of Parasitology Research

Journal of Parasitology Research / 2019 / Article

Research Article | Open Access

Volume 2019 |Article ID 8176283 |

André M. Alves, Marina G. Leonardo, Geza T. R. Souza, Ricardo M. Takemoto, Flávia S. de Lima, Luiz E. R. Tavares, Cláudia M. Melo, Rubens R. Madi, Verónica L. S. Jeraldo, "Occurrence of Isopods in Two Species of Snappers (Lutjanidae) from Northeast Brazil", Journal of Parasitology Research, vol. 2019, Article ID 8176283, 8 pages, 2019.

Occurrence of Isopods in Two Species of Snappers (Lutjanidae) from Northeast Brazil

Academic Editor: D. S. Lindsay
Received01 Nov 2018
Accepted27 Mar 2019
Published02 May 2019


Parasitic isopod species are poorly known in the northeastern coast of Brazil. In this sense, this study presents novel records of Isopoda of the families Aegidae, Cymothoidae, and Corallanidae. A total 69 specimens of Lutjanus analis and 19 of Lutjanus jocu, of which 46 isopods from 3 different species were collected, i.e. Rocinela signata, Cymothoa excisa, and Excorallana richardsoni. The species R. siganata and E. richardsoni are reported for the first time in L. jocu. A significant relationship between the parasite R. signata and the size of the fish L. jocu was also observed. The isopod C. excisa is considered an incidental finding in L. analis. To the authors’ knowledge, this is the first report of this species in fish from Brazil. The three species of isopods are new occurrences in the State of Sergipe, northeast region of the country. An additional morphological characteristic observed in the dorsal setae of pleotelson in specimens of E. richardsoni was that one end of this structure wws bifid. This information contributes to the current body of knowledge of the morphology of this particular species.

1. Introduction

Lutjanidae is a family of cosmopolitan fish that occur most often in regions of tropical and subtropical seas of Australia, Africa, North America and South America. In Brazil, several species of this family are widely explored by artisanal fishermen. Because of their generalistic carnivorous behavior, they play an important role in the ecological control of other populations in reef environments of coral reefs. On the Brazilian tropical coast, 15 species of fish belonging to Lutjanidae have been reported including the “Cióba” - Lutjanus analis (Cuvier, 1828) - and the “Dentão” - Lutjanus jocu (Bloch & Schneider, 1801). These two species are important fish resources in the State of Sergipe, northeast region of the country [17]. Besides their carnivorous and generalist habits, these fish also have a migratory behavior which may contribute to the occurrence of ectoparasitic infestastions such as crustacean infestation. Crustaceans are the group of ectoparasites with the largest morphological variety and diversity. It is estimated that there are approximately 5.400 species of parasitic crustaceans which include the isopods [8]. To date, more than 9.000 species of isopods have been reported in the literature. They are divided into free-living forms and parasitic forms. Species that have parasitic habits may be fixed in body sites of fish such as the gills, integument, and oral cavity. In South America, several species of isopods have been recorded [914]. However, the fauna of parasitic isopod species is not yet fully known in the northeastern coast of Brazil which warrants studies. In this sense, the present study aimed to report new occurrences for isopods Aegidae, Cymothoidae and Corallanidae and to bring a morphological description of isopods collected from lutjanid from the coast of northeast Brazil.

2. Materials and Methods

For this survey, fish were purchased monthly according to the supply and availability at the Municipal Fishing Terminal of Aracaju, SE, Brazil (10°54′17′′S 37°2′56′′W) between March 2015 and October 2016 directly from artisanal fishermen working along the northeastern coast of Brazil in the Western Atlantic. These fish were shipped to our laboratory and identified at the species level according to the taxonomic keys published by [1]. Parasites from these fish were identified according to the keys provided by Menzies and Kruczynski [15], Brusca and Iverson [16], Thatcher et al. [17], Cardoso et al. [11], and Silva and Souza-Filho [18]. The terminology used was based on Kensley and Schotte [19]. Total length, weight, and parasitological analysis of fish were assessed according to the protocols published by Eiras et al. [20]. Prevalence (p) in percentage and mean intensity (im) were calculated according to guidelines provided by Bush et al. [21]. The correlation coefficient “rs” by Spearman posts was used to determine possible correlations between total host length and parasites abundance. Some specimens of isopods had their appendages removed, mounted on glass slides, and examined under the light microscope. The illustrations of the parasites prepared using a Coleman microscope (model N-120) with a light-coupled camera. Representative specimens were deposited at the Museum of Zoology of the State University of Campinas (ZUEC) - Unicamp, Campinas, SP, Brazil.

3. Results and Discussion

A total of 88 fish, 69 specimens of L. analis, and 19 specimens of L. jocu were analyzed, of which 13.8% were parasitized by at least one species of isopod. We found a total of 46 specimens of parasites which belonged to the families Aegidae, Corallanidae and Cymothoidae. Cymothoa excisa Perty, 1833 (males, females, and juveniles), Rocinela signata Schioedte & Meinert, 1879 and Excorallana richardsoni Lemos de Castro, 1960 were the species of parasites from these three families that were found in the fish examined. R. signata was the species of greater prevalence in both L. analis and L. jocu, followed by E. richardsoni and C. excisa (Table 1).

HostParasitePrevalence(%)Mean Intensity (parasites/fish)Site of infestation

Lutjanus analisC. excisa1.442bc
R. signata2.892bf

Lutjanus jocuE. richarsoni21.058.25bc, bf, bs
R. signata31.571.16bf

The species Cymothoa excisa was found in a juvenile L. analis. There was a positive and significant correlation between the length of L. jocu and the abundance of the parasite R. signata (p = 0.0026). The parasite was found in males and females of two host species: L. analis - 4 isopods in two male specimens and in L. jocu - 6 isopods in 5 male specimens and 1 isopod in 1 female specimen. A male of L. jocu had 2 species of isopods in its gills: R. signata and E. richarsoni.

The following are the morphological characters and taxonomy of the specimens found in the fish examined:

Aegidae Leach, 1815

Rocinela Leach, 1818

Rocinela signata Schioedte & Meinert, 1879 (Figure 1)

Morphological description: Body slightly arched, cephalothorax evident and well-detached, fused to the 1st somite but not inserted to it, and previously triangular. It has two large, prominent, spaced eyes. Pereon with 7 somites, the 5th, 6th, and 7th being the largest and widest ones. Antenna tapering with 15 segments, the 4th being the longest one. In the distal region of this structure, there are 5 large and feathery setae (Figure 1(c)) and a flagellum with 11 segments. Antellunae smaller than the antenna (Figure 1(b)) with 7 segments, the 1st being the most robust and the 3rd the longest one, flagellum with four segments. The inner distal region of the 1st segment has a feathery bristle. In its inner face, near the distal region of the 2nd segment, there are five feathery setae - three larger setae, two smaller setae, and four segmented setae. Pereon with eight pereonites and coxal plates. The pleon has five somites. It has seven pairs of pereopods with single branches which end in scythe, pereopods 1-3 (Figure 1(e)) with a single spine on the posterior margin of the propodium. The telson has an inverted “M” or “W” shape on its dorsal surface which is typically found in this species (Figure 1(a), arrow).

Host: L. analis, L. jocu.

Infestation site: Gills (Gill filaments)

Location: Northeastern Coast, Aracaju, SE, Brazil.

Cymothoidae Leach, 1818

Cymothoa Fabricius, 1793

Cymothoa excisa Perty, 1830 (Figures 2 and 3)

Morphological description: Large and truncated body in the anterior region. Partially convex pereon. Cephalon distinct, not lobed, and deeply immersed in the 1st pereonite, with anterolateral margins surrounding the cefalon. Traces of eyes present and visible, but not prominent (Figure 2(a)). Antenna bases are expanded and well-separated. Antenna has nine segments. Antennula smaller than the antenna, with eight segments. Antero-lateral angles of the 1st sub-acute pereonite. Segments os Pleon (pleonites) to a certain extent are narrower than the pereonites and are deeply immersed in the 7th pereonite. Coxal plates are not strongly expanded, not reaching the edges of the pereonites. Seven pairs of pereopods divided into six segments each, all of which ending as prehensile claws (Figure 3). Male (Figure 2(b)): Body similar to the female’s body, but smaller, having finer structures with few differences compared with those of the female. The juvenile (Figure 2(c)), in the post-mancas stage, morphologically identical to adults, but in smaller size and already presented the last thoracic segment or 7th pereonite and 7th pair of pereopods still absent.

Host: L. analis.

Infestation Site: oral cavity (tongue)

Location: Northeastern Coast, Aracaju, SE, Brazil.

Corallanidae Hansen, 1890

Excorallana Stebbing, 1904

Excorallana richardsoni Lemos de Castro, 1960 (Figures 4 and 5)

Morphological description: Body quite elongated, longer than wide (Figure 4(a)), and slightly arched. Eyes: large, well prominent and contiguous, but do not extend to the anterior margin. Cephalon without tubers. Antenulla (Figure 4(a), highlight of arrow I, Figure 4(b)) smaller than the antenna. Flagellum formed by 6 peduncle segments. Antenna extends and reaches up to pereonite 2 and has 24 peduncle segments forming the flagellum. Six pairs of segmented paws with bristles and spines. The paws end in a scythe as the distal segment. The pleotelson is triangular with a sharply rounded apex, and the anterior region has 4 tubers (Figure 4(a), arrow II). The pleotelson has 2 incisions, one on each side, and there are two small tubers pin front of each incision (Figure 4(a), arrow III). Pleotelson has two setose rows in the dorsal region (Figure 4(a), arrow IV) spaced with bifid setae, with midapical filamentous setae. One end of each setae is bifid (Figure 4(c)). The same bifid setae are present at the apex of the pleotelson and uropods, Uropods with fringes of long feathery setae and slightly longer than the apex of pleotelson,

Host: L. jocu.

Site of Infestation: Buccal cavity, Gills, Body surface.

Location: Northeastern Coast, Aracaju, SE, Brazil.

Lima et al. [22] recorded isopods in Scomberomorus brasiliensis Collette, Russo & Zavala-Camin, 1978 and found R. signata in 31% of parasitized fish. Other authors also reported the presence of the parasite in Lutjanidae (snappers) including Cavalcanti et al. [23] that recorded R. signata in L. synagris with 10% of parasitized fish and a mean intensity of 1.25. The parasite has a distribution from Central America to South America, and has been recorded by Hermida et al. [24] in L. analis, corroborating the registry in the same host of the present study, these authors showed a prevalence of 3.3% and an average intensity of 1.00. Similar results were obtained in the present study, The most recent record of parasitism was published by Cardoso et al. [11] in the coast of Pernambuco, northeast Brazil, in Pseudupeneus maculatus Bloch, 1793 with a prevalence of 8.3%, an average intensity of 1.1, and a variation of 1 or 2 parasites per fish. In the present survey, a lower prevalence of isopods was observed in the fish examined. The gill chamber was the preferred site of infestation for the parasite R. signata. The fish L. jocu is reported here as a new host for R. signata.

Specimens of R. signata had the same number of antenulla segments and antenna flagella as described by Brusca and Iverson [16] with 4 and 11 flagella segments respectively. In addition, this structure had the inverted “W” mark in the telson which is typical of this species. According to Pavanelli et al. [25] and Hermida et al. [24], R. signata is an isopod frequently found in fish in northeast Brazil. As other isopods, R. signata have a negative impact on fish’s health. It induces slow growth and respiratory problems and cause injury to the host especially when large numbers of parasites are observed. In cases of severe parasitic infestation, opportunistic secondary fungal and bacterial infections may occur, which is most observed in confinement situations. However, because they are coastal fish, it was not possible to measure such disturbances, since parasite intensity and host immunity are also a determining factor for the occurrence of infections in aquatic populations.

Cymothoa excisa is a species of isopod that has low specificity, and in the world is already known occurring in several vertebrates, in fishes has been reported in 6 different families of fish including Lutjanidae [26, 27]. In Brazil the only record of this species of isopods in marine fish was made by Thatcher et al. [17] in Micropogonias furnieri (Sciaenidae) (Demarest, 1823). The occurrence of C. excisa in L. analis is in agreement with previous studies published by Weinstein [28] and Bunkley-Williams et al. [29]. These authors found the same parasite in the same species of fish and in the same infestation body site in hosts originated from the Caribbean Coast, Panama, and Bahia Portete, Colombia, respectively. This same isopoda had already been recorded in Lutjanus, in the Yucatan Peninsula, Mexico and Panama, where it was also recorded in three other species of Lutjanidae: Lutjanus synagris, L. mahogoni and Ocyurus chrysurus [19]. However, this parasite had not been found yet in L. analis in Brazil. Although they are protandritic animals, becoming functional males in one part of the cycle and later becoming functional females [19], according to Bonilla-Gómez et al. [26], isopods may be present as solitary parasites or parasites of both sexes may occur in a single host.

Allen [1] states that even L. analis and L. jocu which are both reef fish species, still have some differences regarding habitat: L. analis has preference for sandy bottoms with vegetation, estuaries, and regions near mangroves whereas L. jocu prefers coastal waters, particularly estuaries, and occasionally rivers. C. excisa was found only in L. analis, in this sense, Weinstein [28] explain that the habitat difference between fish species can contribute to the presence of isopoda.

The species E. richardsoni was also found only in male L. jocu. Barriga and Briones [30] reported the occurrence of isopods of the genus Excorallana in the east coast of Mexico; 7 species were identified: E. acuticauda Miers, 1881; E. delaneyi Stone and Heard, 1989; E. oculata Hansen, 1890; E. subtilis Hansen, 1890; E. sexticornis Richardson, 1901; E. tricornis tricornis Hansen, 1890; and Excorallana sp. Luque et al. (2013) reported Excorallana sp. on the body surface of Ageneiosus inermis Linnaeus, 1766, and C. excisa in the buccal cavity of Micropogonias furnieri Desmarest, 1823. To date, these are the only records of these two parasites of fish in Brazil. Koening [31] documented the occurrence of Excorallana oculata along the northeast coast of the country from the State Amapá to the State of Espírito Santo.

In Brazil, E. richardsoni is distributed in the States of Amapá, Pará, Maranhão, Ceará, Rio Grande do Norte, Pernambuco, Alagoas, Espírito Santo, and Rio de Janeiro. The first report of this isopod in the country was published by Koening and Coelho [32] in the State of Ceará. This parasite was found in samples collected during oceanographic expeditions. The author did not specify the host affected. The most recent record of this crustacean in Brazil was made by Silva and Souza-Filho [18] in the States of Amapá, Pará, Ceará, and Pernambuco. The parasite was found in samples from ships and expeditions along the north and northeast coast of Brazil between 1965 and 2000 (Figure 6).

In the present study, the morphological characteristics of E. richardsoni are in agreement with those presented by Silva and Souza-Filho [18]. Menzies and Kruczynski [15] describe that species of the genus Excorallana have bifid setae with mid-apical setae in the dorsal pleotelson region (Figure 4(d)). In our study, all the specimens analized presented the same setae bifid shape with a central midapical seta. However, one of the apical bristles was bifid (Figure 4(d), arrow). This characteristic is not mentioned in previous publications. This additional feature helps in the morphological description and taxonomic classification of these isopod species.

4. Conclusion

In conclusion, low levels of isopod infection were found in the fish species studied. R. signata presented the highest infection rates in L. analis and L. jocu. The presence of E. richardsoni and R. signata in the State of Sergipe, which lies on the northeast Brazil’s Atlantic coast, may have occurred due to the migratory habit of the fish since this ectoparasites has been previously recorded in waters of the State Alagoas, northeastern region of the country, thus increasing its geographical distribution. Although the bifid end of the dorsal setae of the pleotelson is not a definitive morphological character used for the taxonomic identification of E. richardsoni, this particular feature was observed in all specimens examined in this study. The present survey presents the first report of three species of isopods in the state of Sergipe, the first record of Cymothoa excisa in Lutjanus analis in the country. We describe Lutjanus jocu as a novel host for Rocinela signata and Excorallana richardsoni.

Data Availability

No data were used to support this study. The data of the present work comprise a part of the database of a doctoral research that is in progress, being not possible the release of this database of the research.

Conflicts of Interest

The authors declare that there is no conflict of interest regarding the publication of this paper.


We would like to thank the Coordination for the Improvement of Higher Education Personnel (CAPES) for supplying the scholarship from which resources were used to acquire the fish.


We thank the Laboratory of Tropical Biology, Laboratory of Infectious and Parasitic Diseases, Institute of Technology and Research, Universidade Tiradentes, and Laboratory of Parasitology of the Universidade Federal do Mato Grosso do Sul, for providing all necessary structure to carry out this work.


  1. G. R. Allen, “FAO species catalogue,” in Snappers of The World: An Annotated And Illustrated Catalogue of Lutjanid Species Known to Date, FAO Fisheries Synopsis, Rome, Italy, 1985. View at: Google Scholar
  2. T. Frédou and B. P. Ferreira, “Bathymetric trends of northeastern Brazilian snappers (Pisces, Lutjanidae): implications for the reef fishery dynamic,” Brazilian Archives of Biology and Technology, vol. 48, no. 5, pp. 787–800, 2005. View at: Publisher Site | Google Scholar
  3. J. F. Fonseca, Estudo da Dieta do Lutjanus synagris (Linnaeus, 1758) e Ocyurus chrysurus (bloch, 1791), Teleostei: Perciformes: Lutjanidae, no Banco dos Abrolhos, Bahia, Brasil e Pesca das principais espécies de Lutjanídeos e Serranídeos na região [Dissertação], Campos de Rio Claro: Instituto de Biociências da Universidade Estadual Paulista “Júlio de Mesquita Filho”, 2009.
  4. A. Begossi, S. V. Salivonchyk, L. G. Araujo et al., “Ethnobiology of snappers (Lutjanidae): target species and suggestions for management,” Journal of Ethnobiology and Ethnomedicine, vol. 7, no. 1, p. 11, 2011. View at: Publisher Site | Google Scholar
  5. E. G. Sanches, “Criação do vermelho-cioba (Lutjanus analis) submetido a diferentes dietas,” Revista Bioikos, vol. 25, pp. 33–40, 2011. View at: Google Scholar
  6. L. Cavalcante, M. Oliveira, and S. Chellappa, “Aspectos reprodutivos do ariacó, lutjanus synagris nas águas costeiras do rio grande do norte,” Biota Amazônia, vol. 2, no. 1, pp. 45–50, 2012. View at: Publisher Site | Google Scholar
  7. A. Morais, M. Carvalho, L. Cavalcante, M. Oliveira, and S. Chellappa, “Características morfológicas do trato digestório de três espécies de peixes (osteichthyes: lutjanidae) das águas costeiras do rio grande do norte, brasil,” Biota Amazônia, vol. 4, no. 2, pp. 51–54, 2014. View at: Publisher Site | Google Scholar
  8. J. L. Luque, F. M. Vieira, R. M. Takemoto, G. C. Pavanelli, and J. C. Eiras, “Checklist of Crustacea parasitizing fishes from Brazil,” Check List, vol. 9, no. 6, pp. 1449–1470, 2013. View at: Publisher Site | Google Scholar
  9. M. C. Espinosa-Pérez and M. E. Hendrickx, “Checklist isopods (Crustacea: Peracarida: Isopoda) from the Eastern Tropical Pacific,” Belgian Journal of Zoology, vol. 131, no. 1, pp. 43–55, 2001. View at: Google Scholar
  10. J. C. Eiras, R. M. Takemoto, and G. C. Pavanelli, Diversidade de parasitas de peixes de água doce do Brasil, Clichetec, Maringá, Brazil, 2010.
  11. L. Cardoso, M. L. Martins, J. E. Golzio et al., “Rocinela signata (Isopoda: Aegidae) parasitizing the gills of the spotted goatfish Pseudupeneus maculatus (Actinopterygii: Mullidae) in Northeastern Brazil,” Anais da Academia Brasileira de Ciências, vol. 89, pp. 2075–2080, 2017. View at: Publisher Site | Google Scholar
  12. P. Bharadhirajan, S. Murugan, A. Sakthivel, and P. Selvakumar, “Isopods parasites infection on commercial fishes of Parangipettai waters, southeast coast of India,” Asian Pacific Journal of Tropical Disease, vol. 4, no. 1, pp. S268–S272, 2014. View at: Publisher Site | Google Scholar
  13. R. Rajaram, K. Rakesh Kumar, S. Vinothkumar, and E. B. Metillo, “Prevalence of cymothoid isopods (Crustacea, Isopoda) and proximate analysis of parasites and their host fishes, Southeastern India,” Journal of Parasitic Diseases, vol. 42, no. 2, pp. 259–268, 2018. View at: Publisher Site | Google Scholar
  14. G. Rameshkumar and S. Ravichandran, “Problems caused by isopod parasites in commercial fishes,” Journal of Parasitic Diseases, vol. 38, no. 1, pp. 138–141, 2014. View at: Publisher Site | Google Scholar
  15. R. J. Menzies and W. L. Kruczynski, Isopod Crustacea (Exclusive of Epicaridea), Florida Department of Natural Resources, Marine Research Laboratory, (Memoirs of the Hourglass Cruises,VI-I), 1983.
  16. R. C. Brusca and E. W. Iverson, “A guide to the marine isopod crustacea of pacific costa rica,” Revista de Biología Tropical, vol. 33, p. 77, 1985. View at: Google Scholar
  17. V. E. Thatcher, J. d. Silva, G. F. Jost, and J. M. Souza-Conceição, “Comparative morphology of Cymothoa spp.(Isopoda, Cymothoidae) from Brazilian fishes, with the description of Cymothoa catarinensis sp. nov. and redescriptions of C. excisa Perty and C. oestrum (Linnaeus),” Revista Brasileira de Zoologia, vol. 20, no. 3, pp. 541–552, 2003. View at: Publisher Site | Google Scholar
  18. E. d. Silva and J. F. Souza-Filho, “Species of Excorallana (Isopoda, Corallanidae) from northern and northeastern Brazil, with description of a new species, Excorallana lemoscastroi sp. nov,” Nauplius, vol. 25, pp. 2358–2936, 2017. View at: Publisher Site | Google Scholar
  19. B. F. Kensley and M. Schotte, Guide to The Marine Isopod Crustaceans of The Caribbean, Smithsonian Institution Press, Washington, DC, USA, 1989. View at: Publisher Site
  20. J. C. Eiras, R. M. Takemoto, and G. C. Pavanelli, Métodos de estudo e técnicas laboratoriais em parasitologia de peixes, Eduem, Maringá, Brazil, 2006.
  21. A. O. Bush, K. D. Lafferty, J. M. Lotz, and A. W. Shostak, “Parasitology meets ecology on its own terms: margolis et al. revisited,” Journal of Parasitology, vol. 83, no. 4, pp. 575–583, 1997. View at: Publisher Site | Google Scholar
  22. J. T. A. X. Lima, S. Chellappa, and V. E. Thatcher, “Livoneca redmanni Leach (Isopoda, Cymothoidae) e Rocinela signata Schioedte & Meinert (Isopoda, Aegidae), ectoparasitos de Scomberomorus brasiliensis Collette, Russo & Zavala-Camin (Ostheichthyes, Scombridae) no Rio Grande do Norte, Brasil,” Revista Brasileira de Zoologia, vol. 22, no. 4, pp. 1104–1108, 2005. View at: Publisher Site | Google Scholar
  23. E. Cavalcanti, W. Nascimento, R. Takemoto, L. Alves, and S. Chellappa, “Ocorrência de Crustáceos Ectoparasitos no Peixe Ariacó, Lutjanus synagris (Linnaeus, 1758) nas Águas Costeiras do Rio Grande do Norte, Brasil,” Biota Amazônia, vol. 3, no. 1, pp. 94–99, 2013. View at: Publisher Site | Google Scholar
  24. M. Hermida, B. F. Carvalho, C. Cruz, and A. Saraiva, “Parasites of the Mutton Snapper Lutjanus analis (Perciformes: Lutjanidae) in Alagoas, Brazil,” Revista Brasileira de Parasitologia Veterinária, vol. 23, no. 2, pp. 241–243, 2014. View at: Publisher Site | Google Scholar
  25. G. C. Pavanelli, J. C. Eiras, and R. M. Takemoto, Doenças de Peixes: profilaxia, diagnóstico e tratamento, Eduem, Maringá, Brazil, 2008.
  26. J. L. Bonilla-Gómez, A. Ramírez-Rojas, M. Badillo-Alemán, and X. Chiappa-Carrara, “Nuevo registro de Lagodon rhomboides (Pisciformes: Sparidae) como hospedero de Cymothoa excisa (Isopoda: Cymothoidae) en la costa noroeste de la península de Yucatán,” Revista Mexicana de Biodiversidad, vol. 85, no. 2, pp. 633–637, 2014. View at: Publisher Site | Google Scholar
  27. V. L. Leray, L. K. Joca, K. S. Zigler, and R. C. Brusca, “A new host and reproduction at a small size for the “snapper-choking isopod” Cymothoa excisa (Isopoda: Cymothoidae),” Journal of Crustacean Biology, vol. 35, no. 2, pp. 292–294, 2015. View at: Publisher Site | Google Scholar
  28. M. P. Weinstein, “Biology and hostparasite relationships of Cymothoa excisa (Isopoda, Cymothoidae)with three species of snappers (Lutjanidae) on the Caribbean coast of Panama,” Fish Bulletin, vol. 75, pp. 875–877, 1979. View at: Google Scholar
  29. L. Bunkley-Williams, E. H. Williams, and J. Garzon-Ferreira, “Some isopod and copepod parasites (Crustacea) of Colombian marine fishes,” Caribbean Journal of Science, vol. 35, pp. 311–314, 1999. View at: Google Scholar
  30. A. C. Barriga and E. E. Briones, “Isopods of the genus excorallana stebbing, 1904 (crustacea, isopoda, corallanidae) from the east coast of mexico with a supplemental description of E. subtilis,” Gulf Research Reports, vol. 8, pp. 363–374, 1992. View at: Publisher Site | Google Scholar
  31. M. L. KOENING, “Nota sobre a ocorrência de alguns isópodos do Norte e Nordeste do Brasil,” Tropical Oceanography, vol. 13, no. 1, pp. 237–244, 1972. View at: Publisher Site | Google Scholar
  32. M. L. Koening and P. A. Coelho, “A distribuição dos crustáceos pertencentes às ordens Stomatopoda Tanaidacea e Isopoda no Norte e Nordeste do Brasil,” Tropical Oceanography, vol. 13, no. 1, pp. 245–259, 1972. View at: Publisher Site | Google Scholar

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