Cymothoa frontalis Milne Edward, 1840 is a very poorly described cymothoid, notwithstanding the previous redescription of the female. Pertinently, to date, the host of C. frontalis has not been identified with adequate precision. Most of the descriptions of cymothoids carried out hitherto were based primarily on females, but practically ignoring other life cycle stages. The present paper redescribes the female and describes other life cycle stages of the species C. frontalis to get better precision in their identification.
The female phase of C. frontalis is redescribed according to type specimens extant in the NMNH, Paris, and also by the data obtained from live specimens collected during the present study. The general morphology and appendages of various life cycle stages of the species are described. Among 80 fish species from 35 families examined, C. frontalis was recovered only from Strongylura strongylura signifying its oligoxenous host specificity, the prevalence and intensity being 68.65% and 1.9, respectively. Each host fish in more than 85% of the population was infested with a pair of C. frontalis, in three combinations, predominantly with male-female pair (70.9%). C. frontalis exhibited strict site specificity attaching to the buccal cavity of the host fish. The study has also identified three major phases (marsupial, free living and infective) in the life cycle of C. frontalis. The zygotic-staged marsupiumites were developed through five sequential ontogenetic stages. The manca released from the marsupium become infective after a brief period of free swimming life. During the infective phase, C. frontalis completes remaining life cycle stages with successive moulting. Further, six successive stages of the ovigerous females have also been identified.
The present redescription of the female and the description of transitional, male, juvenile and larvae of C. frontalis facilitate precise identification of the species at any stage of the life cycle. Further, the strict host and site specificities of the parasite, as borne out from the present study, and its high degree of prevalence in the host make C. frontalis as an ideal model organism to study the strategies to be adopted for the management of parasites infesting edible fishes.
Cymothoids are ectoparasitic isopods parasitizing teleost fishes inhabiting diverse ecosystems (Trilles 1968, 1994; Brusca 1981; Seng and Seng 1990; Horton and Okamura 2001; Trilles et al. 2011; Hadfield et al. 2013; Aneesh et al. 2014) and have been shown to cause deleterious effects on their hosts (Trilles and Hipea-Jacquotte 2012). For instance, the anemone fish Amphiprion akallopisos, Stolephorus commersonii and Hemiramphus far were severely damaged due to the parasitic infestation by Renocila heterozota, Nerocila phaeopleura and Mothocya plagulophora, respectively (Bowman and Mariscal 1968; Rajkumar et al. 2006; Gopalakrishnan et al. 2010). Five species of Nerocila (N. acuminata, N. phaiopleura, N. loveni, N. depressa and N. longispina) were reported to have induced severe tissue damage in seven fish species such as Gymnothorax eurostus, Thryssa malabarica, Thryssa mystax, Thryssa setirostris, Coilia dussumieri, Opisthopterus tardoore, Escualosa thoracata and Ambassis ambassis (Bowman 1960; Aneesh et al. 2013a). Further, seasonal fluctuations in the population of four Nerocila species were reported from the Malabar Coast of India (Aneesh et al. 2013a). Recent studies conducted in our laboratory have shown profuse infestation of the Indian mackerel Rastrelliger kanagurta and the slender needle fish Strongylura leiura by Norileca indica and Mothocya renardi, respectively (Aneesh et al. 2011, 2013b). Most of the taxonomic descriptions of the cymothoids are based primarily on ovigerous females; the various life cycle stages (excepting perhaps the pre-manca/manca of few Cymothoa sp.) have not received much attention thus far (Richardson 1905; Sartor and Pires 1988; Thatcher et al. 2003, 2007; Trilles and Bariche 2006; Hadfield et al. 2011). Keeping these in view, the present paper addresses the question of precise identification of the cymothoid C. frontalis infesting the belonid fish inhabiting the Malabar Coast.
The genus Cymothoa Fabricius, 1793 comprises about 50 species which usually infest the tongue of the host fish (Trilles 1994; Schotte et al. 2008); some of them are reported to induce atrophy of the host’s tongue (Brusca 1981; Romestand and Trilles 1977; Hadfield et al. 2011, 2013).
Cymothoa frontalis (Milne Edwards, 1840) is a poorly described one, and though the female stage of this species was redescribed by Schioedte and Meinert (1884), their Latin redescription seems inadequate in terms of modern standards. In spite of being a protandric hermaphrodite, only the female stage was subjected to detailed examination thus far; further, its host was not accurately identified even though a single host ‘Cyclopterus’ was doubtfully reported by White (1847). The present study depicts a redescription of the female stage of C. frontalis. It also describes all the other life cycle stages (transitional stage, male, juvenile manca and pre-manca) of this cymothoid using the live samples collected afresh from the Indian spot tail needle fish Strongylura strongylura (Beloniformes, Belonidae). The study also brings out the results of our thorough observation on the host specificity, site specificity, prevalence, intensity and life cycle of the species.
Live marine fishes were collected freshly from the Ayyikkara fish-landing centre (Lat. 11°51′N, Long. 75°22′E; Malabar Coast, India). The various body parts of the fish were examined (immediately after collection) for the presence of cymothoids using a hand lens. The recovered parasites with their host were brought to the laboratory and subjected to detailed examination with the aid of a stereomicroscope (Leica-S6D, Leica Microsystems Ltd., Milton Keynes, UK). The cymothoids thus obtained were preserved in 75% ethanol (after Ramakrishna 1980) and subjected to further taxonomical identification. The survey was conducted twice a week round the year from November 2009 to November 2012. The prevalence (P) and intensity (I) of the recovered C. frontalis were calculated as per the methods described in Margolis et al. (1982) and Bush et al. (1997). The total length of the fish host as well as the parasite (C. frontalis) was measured to the nearest 1 mm. Mouthparts and appendages of the parasite were carefully dissected out using a dissecting needle and a fine pair forceps and observed under the microscope (Leica DM-750). The drawings of the observed mouthparts and appendages were performed using a camera lucida attached to the microscope. The moult stages and the moult-related changes of the parasite were determined through the macroscopical and microscopical observations on the characteristic changes occurring in the carapace and the appendages (after Sudha et al. 2012). The reproductive activity was assessed through microscopic observations of the ovary (after dissecting out) and marsupiumites (after Sudha et al. 2012; Aneesh 2014). Classification of the marsupial stages was carried out taking cues from Bakenhaster et al. (2006). Fish taxonomy and host nomenclature were performed according to FishBase (Froese and Pauly 2012). Voucher specimens were deposited in the collections of the Parasitic Crustacean Museum, Crustacean Biology Research Laboratory, Sree Narayana College, Kannur, Kerala, India.
Cymothoa frontalis - White 1847: 110-?; Dana 1853: 750-751, pl. 49, Figure twelve (a-b); Schioedte and Meinert 1884: 226-228, tab. VI (Cym. XXIV), Figures one and two; Gerstaecker 1901: 261; Nierstrasz 1931: 136; Trilles 1975: 980-981, pl. 1; Avdeev 1978: 282; Avdeev 1979: 53; Avdeev 1990: 32-42; Trilles 1994: 143.
Type material: Ovigerous female (LT. 24 mm) and non-ovigerous female (LT. 18 mm), Mer des Indes, Dussumier, Cymothoa frontalis M. Edw., type (MNHN N° 202).
Non-type material: From S. strongylura, Ayyikkara fish landing centre (Lat. 11°51′N, Long. 75°22′E), Malabar Coast, India; collected by Aneesh, P. T., Helna A. K. and Sudha, K. and deposited in the PCM. Ovigerous female (LT 26 mm) with manca in the brood pouch (PCM N° CF-09), 12 July 2011; non-ovigerous female without brood pouch (LT 28 mm) (PCM N° CF-06), 16 August 2010; ovigerous female with pre-manca in the brood pouch (LT 23 mm) (PCM N° CF-04), 19 May 2010; ovigerous female with eggs in the brood pouch (LT 23 mm) (PCM N° CF-01), 8 December 2009; ovigerous female with eggs in the brood pouch (LT 21 mm) (PCM N° CF-03), 16 January 2010; male (LT 13 mm) (PCM N° CF-02), 8 December 2009; transitional stage (LT 20 mm) (PCM N° CF-08), 25 April 2011; juvenile (LT 8 mm) (PCM N° CF-07), 13 March 2011; 30 manca released by the specimen PCM N° CF-09 (LT 3.2 to 3.4 mm), (PCM N° CF-10), 12 July 2011; 20 pre-manca collected from the brood pouch of the specimen PCM N° CF-04 (LT 2.2 to 2.4 mm) (PCM N° CF-05), 19 May 2010.
Redescription of the ovigerous female
Body about 2.6 times as long as wide, widest at pereonites 5 to 6 (Figures 1D, 2, 3 and 4; Table 1). Cephalon partially immersed in poorly developed amphicephalic process of pereonite 1, as long as wide, anterior margin truncate. Eyes relatively smaller than male, not much developed but moderately distinct. Coxae not visible in dorsal view. Pereonite 1 longest, pereonites 2 to 4 subequal in length; pereonites 5 to 7 decreasing in length progressively, pereonite 7 shortest. The pereonites increase in width from 1 to 6; pereonite 6 widest and slightly wider than pereonite 7. All the pleonites visible, increasing progressively in width posteriorly from 1 to 5; pleonite 5 widest and longest. Pleotelson 1.6 times as wide as long, wider than pleonite 5, posterior margin broadly rounded.
Antennule stouter than antenna, subequal in length to antenna, composed of 8 articles, extending to anterior margin of pereonite 1; articles 1 to 3 slightly wider than others. Antenna with 9 articles, decreasing gradually in width, distal margin of articles 6, 7 and 8 with 3 to 6 setae. Article 9 with 3 to 6 terminal aesthetascs. Mandible palp 3 segmented, without setae in ovigerous female. Maxillule with 4 apical spines slightly recurved. Bi-lobed maxilla with 2 spines on median lobe and 1 spine on lateral lobe. Maxilliped with oostegial lobe with many plumose setae and a palp with 3 small apical and 2 lateral recurved spines on article 3.
Pereopods gradually increase in size from 1 to 7, without spines; basis increasing in width progressively from pereopods 1 to 7. Pleopods not distinctly visible in dorsal view; pleopod 2 without appendix masculina. Endopods of pleopods 4 and 5 moderately and strongly folded, respectively. Uropod rami short, not reaching the distal margin of pleotelson; rami subequal in length, curved and apically rounded.
Brood pouch with 4 pairs of overlapping oostegites arising from the bases of pereopods 2, 3, 4 and 6. Number of eggs or larvae per brood pouch ranges from 320 to 520 according to the size of the female.
Description of the male
Relatively smaller than ovigerous female and transitional stage (Figures 1B, 5 and 6; Table 1). Body 2.67 times as long as wide. Cephalon not immersed in pereonite 1. Eyes small but more prominent than in the female.
Pereonite 1 longest, pereonites 5 and 6 subequal in width and widest. Coxae not visible in dorsal view. All pleonites visible increasing progressively in width posteriorly; pleonite 5 widest and longest. Pleotelson 2 times as wide as long, slightly wider than pleonite 5, posterior margin broadly rounded.
Eight articled antennule stouter and subequal in length to antenna. First 3 articles slightly wider than others. Antennae 9 articled, decreasing gradually in width, distal margin of articles 6, 7 and 8 with 3 to 6 setae; article 9 with 3 terminal aesthetascs. Mandible palp 3 segmented, articles 2 and 3 with several setae on distolateral margin. Maxillule with 4 apical spines slightly recurved; maxilla bi-lobed, with 2 spines on median and lateral lobes. Maxilliped without oostegial lobe and a palp with 3 small apical and 2 lateral recurved spines on article 3.
Pereopods 1 to 7 gradually increasing in size, without spines; basis increasing in width progressively. Penes visible on sternite 7. Pleopods not distinctly visible in dorsal view. Pleopod 2 with appendix masculina. Endopodite of pleopods 4 moderately and 5 strongly folded. Uropod rami, nearly reaching the distal margin of pleotelson; rami subequal in length, curved and apically rounded.
Description of the transitional stage
Body 2.7 times as long as wide (Figures 1C and 7; Table 1); Eyes small and moderately distinct. Cephalon partially immersed in poorly developed amphicephalic process of pereonite 1, as long as wide, anterior margin truncate.
Pereonites, pleonites, antennules, antenna and mandible palp are similar to those of the ovigerous female and maxilla, maxilliped similar to those of the male. Rudimentary penes are visible on sternite 7. Pleotelson 1.8 to 2 times as wide as long, slightly wider than pleonite 5 and uropods similar to those of the ovigerous female. Pereopods and pleopods similar to those of female and male.
Description of the juvenile
Body approximately 3 times as long as wide, relatively narrower and smaller than those of the female, transitional stage and male (Figures 1G, 8, 9 and 10; Table 1). Eyes prominent, ovate and conspicuous in dorsal view; anterior margin of cephalon rounded, not immersed in pereonite 1. Pereonite 1 longest, pereonites 2, 3 and 4 subequal; pereonites 4 and 5 widest and subequal. Pereonites 5 to 7 gradually decreasing in length. Pleonites gradually decreasing in width towards posterior but subequal in length. Pleotelson as long as wide, apical margin rounded with many setae.
Antennule 8 articled, reaching the anterior margin of pereonite 1; articles 5 to 8 with 3 to 5 spinules and article 8 with few terminal aesthetascs. Antenna longer than antennule, 9 articled, extending to anterior margin of pereonite 2; articles 6 to 9 with few spinules, inner margin of articles 3 and 4 with 4 and 5 setae, respectively; distal margin of article 9 with 3 setae; articles 4 and 5 with 1 plumose setae. Article 2 of mandible palp with 4 to 6 marginal setae; third article with 5 to 8 marginal setae and one apical recurved seta. Maxillule, maxilla and maxilliped similar to those of the male stage.
Pereopod 1 without spines, pereopods 2 to 5 with 1 or 2 spines on posterior margin of propodus; pereopods 3 and 5 with 1 spine on the posterior margin of merus and the vestigial pereopod 7 with 3 to 4 spines on carpus and 4 to 6 spines on propodus. Pereopods 1 to 3 dactylus with vestigial teeth; dactylus of pereopods 2 and 3, about 2 times longer than propodus, pereopod 7 with short and blunt dactylus. Penes not developed. The lateral margin of exopodite of all pleopods with small setae, but not on the apical margin. Median margin of protopod with 4/5 retinaculae. Pleopod 2 with thick and vestigial appendix masculina, as long as endopodite. Pleopods 1 and 3 subequal. Endopod of pleopods 4 and 5 moderately folded. Uropod extending beyond the distal margin of pleotelson, inner margin of basis with 3 to 4 plumose setae; rami slightly curved, endopodite relatively large, exopodite with an apical recurved spine. Endopodite margin with 60 to 66 setae. Exopodite with 40 to 44 setae, restricted to the inner margin.
Description of the manca
The manca developed from the pre-manca through moulting shows distinct morphological characters (Figures 1F, 11 and 12; Table 1).
Body elongated and transparent, 3.5 times as long as wide, eyes black, prominent, ovate and conspicuous in dorsal view. Cephalon 1.6 times as wide as long and golden yellow in colour.
Pereonite 1 relatively long; pereonites 2, 3 and 4 subequal in length; longer than pereonites 5 and 6; pereonites 5 and 6 subequal in length; pereonite 7 short and narrow; pereonites 4 and 5 widest. All pleonites visible and subequal in width and length; 4.8 times as wide as long. Pleotelson 1.2 times as wide as long and the apical margin with 18 to 20 plumose setae.
Eight articled antennule extends to anterior margin of pereonite 2; articles 5, 7 and 8 each with 2 setae and article 6 with 1 seta; all the articles with 3 to 4 spinules and article 8 with 4 terminal aesthetascs. Antenna longer than antennule, 11 articled, extending to anterior margin of pereonite 4; all the articles with spinules and article 11 with 4 terminal aesthetascs; inner margin of article 3 with 1 plumose seta. Article 2 of the mandible palp with 1 seta arising from the disto-lateral margin; article 3 with 3 marginal setae and 1 apical recurved seta. Maxillule, maxilla and maxilliped similar to those of the male stage.
Six pereopods; pereopod 1, with 1 spine on merus and carpus. Pereopod 2 with 1 spine on posterior margin of merus; pereopod 3 with 1 spine on the posterior margin of merus and propodus; 1 spine on the posterior margin of propodus of pereopod 4; pereopods 5 and 6 with 1 spine on carpus and 2 to 3 spines on the posterior margin of propodus. Dactyls of pereopods 1 to 3 toothed, 4 to 6 not toothed. Pleopods not distinctly visible in dorsal view. Pleopod 1 with 6 to 8 plumose setae on endopodite and 14 to 18 plumose setae on exopodite. Pleopods 2 to 5, apical margin of exopodite with 14 to 18 plumose setae. Uropod rami subequal, extending strongly beyond the distal margin of pleotelson, apically rounded with 8 to 12 plumose setae. Uropods and pleotelson with many dark chromatophores.
Description of the pre-manca
Body elongated and transparent, 4 times as long as wide, eyes black, prominent, ovate and conspicuous in dorsal view (Figures 1E and 13; Table 1). Cephalon 1.4 times as wide as long, not immersed in pereonite 1. Yolk globules are visible in the pereon, between pereonites 2 and 6. Pereonite 1 slightly long, pereonite 7 short and narrow. Pereonites 4 and 5 widest. All pleonites visible and subequal in width and length; 3.6 times as wide as long. Pleotelson as wide as long, without plumose setae.
Antenna larger than antennule. Eight articled antennule extends to anterior margin of pereonite 2; antenna longer than antennule, 11 articled, extending to anterior margin of pereonite 4; all articles without setae and spinules. Mouthparts are not well developed; mandible palp articles without setae and spines; maxillule, maxilla and maxilliped with poorly developed apical non-recurved spines.
Six pereopods; pereopods 1 to 6 without spines. Distal margin of dactylus of pereopod 1 to 6 slightly indented and then forming a narrow terminal part. Dactylus of pereopod not toothed. Pleopods not distinctly visible in dorsal view. Pleopods 1 to 5 without plumose setae. Uropod rami subequal, extending strongly beyond the distal margin of pleotelson, apically rounded without plumose setae. Uropods and pleotelson with dark chromatophores.
Size: Ovigerous females, 21 to 28 mm; transitional stage, 15 to 23 mm; male, 11 to 13 mm; juvenile, 7 to 9 mm; manca, 3 to 3.4 mm; pre-manca, 2.2 to 2.4 mm.
Host: Present Indian material is from S. strongylura (Van Hasselt 1823). Until now, a single specimen was doubtfully reported by White (1847), from a host belonging to the genus Cyclopterus.
Distribution: Asian Sea (Milne Edwards 1840) and Indian Ocean (White 1847); Singapore (Heller 1868) and Bangkok (Schioedte and Meinert 1884); Malabar Coast, Kerala, India (present study).
Colour: Female and transitional stage - light grey with highly pigmented dorsal surface; male - creamy white with a pigmented lateral and posterior margin of pereonites and pleonites; juvenile - transparent with scattered pigmentation throughout the body. Posterior margin and lateral side of pereonites and pleonites and anterior margin of pleotelson with lining chromatophores, Manca and pre-manca - clear with scattered chromatophores particularly on uropods and pleotelson; cephalon golden yellow in colour.
Occurrence and prevalence of infestation by C. frontalis on S. strongylura
Eighty species of fishes belonging to 35 families were examined from November 2009 to November 2012 for the presence of C. frontalis; however, this cymothoid was recovered only from the belonid fish S. strongylura, signifying its oligoxenous host specificity (Table 2).
Among 134 members of host fish (S. strongylura) examined, 92 were infested by C. frontalis, the prevalence being 68.65%. A total of 171 C. frontalis including 67 ovigerous females, 14 transitional stages, 68 males and 22 juveniles were recovered; the mean intensity being equal to 1.9 (Table 3) (Figure 1B,C,D,E,F,G). Out of 92 infested members of S. strongylura, 79 were found with two members of C. frontalis appearing like a pair, but in three combinations such as male-female, male-transitional and juvenile-juvenile, with the male-female pair being predominant (56 out of 79); the large ovigerous female was attached on the floor of the buccal cavity, their cephalon facing towards the opening of the host mouth; male settled just behind the female on the gill arch (Figure 1A,G,H,I). In the case of the male-transitional pair (12 out of 79), both were found attached on the tongue of the host. The juvenile pair (11 out of 79) prefers the mucous membrane of the lower beak of the fish (Figure 1G). Unpaired females or transitional stages were also observed in 11 and 2 instances, respectively.
Life cycle of C. frontalis
The present study identified three major phases (such as marsupial, free living and infective) in the life cycle of C. frontalis. The details of each phase are represented in Table 4 and Figures 14 and 15. The marsupial phase encompasses one zygotic, three embryonic (ES I, ES II and ES III) and two larval (pre-manca and manca) stages, and each stage is found to be distinct from one another by their precise morphological characteristics (Figure 14). Round zygotic-staged eggs appear in light florescent yellow colour, the size being 1.2 to 1.3 mm. Early-staged tissue differentiation seems to occur during ES I, and the embryo at this stage attains subspherical or ovoid shape without changing the colour from the preceding stage. The ES II-staged marsupiumite is characterized by the development of cephalic lobe, early limb bud and pigmented eye spot, and at this stage, the embryo becomes elongated. Marsupiumite at ES III appears as curved and segmented with thoracic and abdominal limb buds. By this stage (ES III), the embryonic development seems to be completed, and the egg gets ready to hatch out the larva called pre-manca; within the marsupium, it moults and transforms into the manca. Significantly, within the marsupium, the development of marsupiumites of C. frontalis is synchronous evidenced by the presence of only one of the aforesaid developmental stages at a time. After a brief period of residence in the marsupium, the manca is seen released into the surrounding water where it leads a free swimming life. (During the present study, the free swimming manca was successfully reared for a maximum of 8 days in our laboratory.) Subsequently, manca enters into the infectious stage, quite likely as a single pair by parasitizing its host fish (S. strongylura). Through moulting, the paired manca becomes the juveniles which are usually found attached to the mucous membrane of the lower beak of the host (Figure 1G). Both members of the juvenile pair would undergo moulting (sequential?) which in turn induces remarkable morphological changes, leading to their transformation into functional paired males which settle within the host’s buccal cavity. Within the buccal cavity, both males undergo moulting. However, by this process one of the (male) members becomes transitional but retains some of the male characters (Figure 7C,D,E). The transitional further undergoes two sequential moults; interestingly, by the culmination of the second moult (also referred to as ‘oostegition moult’), it transforms into an ovigerous female with brood pouch or marsupium (a cavity formed by the overlapped, plate-like oostegites developed from the endopodites of the second, third, fourth and sixth pereopods). The female life is continued further by engaging itself in reproduction and also in parental care, by keeping the eggs and larvae in their brood pouch, until they are released. The brood pouch is formed and removed in an alternative manner through oostegition and de-oostegition moults, respectively; oostegition moult occurs before the oviposition (spawning), followed by marsupial life and larval (manca) release, after which de-oostegition moult ensues. Based on the presence or absence of the brood pouch and/or marsupiumites, six consecutive stages of the ovigerous female (Fs 1 through Fs 6) were identified (Figure 15 and Table 4). The Fs 1-staged female that developed right from the transitional through the first oostegition moult is characterized by the presence of a growing ovary and a well-developed marsupium, but without marsupiumites; oviposition ensues and the eggs are deposited in the marsupium and this brooded ovigerous female is designated to be at Fs 2. Upon completion of the marsupial life, manca are released and the female with the old empty marsupium is referred to be at Fs 3 stage. The females at Fs 3 stage undergo de-oostegition moult (to remove the old marsupium) and enter Fs 4 stage, during which time it undergoes oostegition moult and transforms into Fs 5 stage with newly formed second marsupium and growing ovary. Excepting the meagre size difference and for the presence of a well-developed oostegial lobe of the maxilliped, the females at Fs 5 stage morphologically resemble the females at Fs 1 stage. Subsequent to oviposition, the females at Fs 5 would be transformed into Fs 6 stage, characterized by the presence of a second set of marsupiumites. Except the size differences, the females at Fs 6 stage would resemble those at Fs 2 stage.
With the redescription of the females of C. frontalis and the description (of the transitional stage, the male, the juvenile and the larvae) as depicted in the present paper, we update the diagnosis of the species (C. frontalis) carried out by Milne Edwards (1840) and Schioedte and Meinert (1884); to our knowledge, this report appears to be the first of its kind, wherein the cymothoid crustacean is being described by collating the data from all the stages in its life cycle.
The presence of transitional stage, as observed in the life cycle of C. frontalis (present study), is an indication of the protandrous sex reversal, akin to what has been reported in other cymothoids (Bowman 1960; Williams and Williams 1985; Tsai and Dai 1999). Significantly, at this (transitional) stage, C. frontalis is found to retain some of the male characteristics including the appendix masculina and two spines on the median and lateral lobes of the maxilla; the penes, however, become rudimentary at this stage. After its transformation into the ovigerous female, the spines on the lateral lobe of maxilla are reduced to one and the appendix masculina and penes are seen to have completely disappeared.
Apart from the intense body tanning, the presence of plumose setae on the oostegial lobe of the maxilliped (Figure 2H) during the female phase makes C. frontalis distinct from those of other cymothoids described so far. On the other hand, C. frontalis resembles another cymothoid such as Cymothoa spinipalpa (described by Thatcher et al. 2007) in the possession of folded endopodite of the fourth and fifth pleopod.
The pre-manca and manca of C. frontalis possess appendages in all pereonites except the seventh one. In pre-manca, pereopods lack spines and there are no setae on pleopods, uropod and pleotelson. Manca, on the other hand, possesses six pairs of spiny pereopods, and their pleopods, uropod rami, pleotelson are with plumose setae facilitating the free swimming life. The toothed dactylus on the first three pairs of pereopods would help the larva (manca) to cling on to the host fish during the infective stage. Contrary to this, in the manca of Agarna malayi and N. indica, the dactyli of all pereopods are devoid of teeth; teeth are, however, present on the propodus of the first three pereopods (Aneesh et al., unpublished). In pre-manca and manca of C. frontalis, the uropod basis and subequal rami are extremely extended beyond the distal margin of the pleotelson. Such an extension is not prominent in the case of the cymothoid M. renardi (Aneesh et al., unpublished). In the juvenile stage of C. frontalis, pleopodal setae and pareopodal spines and teeth are found to be more or less in a reduced state. By the onset of the adult male stage, all these structures completely disappeared and the limbs become short; the carapace gets gradually calcified and arched with intense tanning. In the female stage, the telson is kept in an upright position enabling the pleopods under constant vibration to aerate the marsupiumites.
Notwithstanding the fact that a single host ‘Cyclopterus’ was doubtfully reported by White (1847), until now, the host fish of C. frontalis was not accurately identified. Out of the 80 fish species examined during the present study, C. frontalis was recovered only from the belonid fish S. strongylura, showing its oligoxenous host specificity. Rarely though, oligoxenous host specificity has also been reported in other cymothoid species such as N. indica, M. renardi and N. longispina parasitizing R. kanagurta, S. leiura and A. ambassis, respectively (Aneesh et al. 2011, 2013a, b).
In C. frontalis, broods are held in the female marsupium. This observation agrees with the previous reports on other cymothoids Elthusa vulgaris (Brusca 1978), Anilocra pomacentri (Adlard and Lester 1995) and Glossobius hemiramphi (Bakenhaster et al. 2006). The life cycle of C. frontalis passes through marsupial, free living and infective phases. During the marsupial phase, six sequential and morphologically distinct stages including one zygotic, three embryonic (ES I-III) and two larval stages (pre-manca and manca) are completed. Marsupiumites of cymothoids E. vulgaris, A. pomacentri and G. hemiramphi have also been reported to have five distinct ontogenic stages (Brusca 1978; Adlard and Lester 1995; Bakenhaster et al. 2006). The synchronized pattern of marsupial development as observed in C. frontalis (present study) looks comparable with what was reported in G. hemiramphi (Bakenhaster et al. 2006). However, in C. frontalis, the exact duration of the successive development of each marsupial stage from their preceding stage is not clear. The final marsupial stage (manca) of C. frontalis showed close resemblance to that of A. pomacentri (Adlard and Lester 1995) and C. spinipalpa (Thatcher et al. 2007). In A. pomacentri, the manca is released within 2 days after they appeared in the marsupium (Adlard and Lester 1995). In the present study, it is observed that after a brief period of marsupial residence, the manca of C. frontalis is released into the water and lead a free swimming life until it infests the host fish (S. strongylura). Deviating from this pattern, the manca of G. hemiramphi have been shown to infest other species of fish temporarily, before settling on its specific host Hemiramphus brasiliensis (Bakenhaster et al. 2006). The exact mechanism that helps manca to find its specific host is unclear. The physical characteristics of this larval form are suggested to facilitate precise attachment to the specific host (Bakenhaster et al. 2006). Evidences are not available to suggest if the environmental cues or host-derived factors are likely to influence the host-specific attachment. The success rate of the larvae for host attachment is also not available.
From the manca stage of C. frontalis, the transformation to successive stages (juveniles, male, transitional and female stages) is accomplished by the intervening moult. The present report on the existence of six successive stages (Fs 1 to Fs 6) of the ovigerous females of C. frontalis could be considered first of its kind due to a paucity of any such attempt on other cymothoid species.
Admittedly, the duration of the life cycle of C. frontalis could not be assessed during the present study. Previous reports suggest that the average duration to complete the life cycle of cymothoids is nearly 1 year; the entire life cycle of G. hemiramphi on its fish host (H. brasiliensis) is completed within 1 year (Bakenhaster et al. 2006). In A. pomacentri, the female without dislodging from the host or host death was shown to have an average life span of 13.5 months (Adlard and Lester 1995).
Not only would the present redescription of the female and description of the remaining stages in the life cycle of C. frontalis provide us with added information on its biology, but the study would also help us identify the cymothoid parasite very precisely. Further, the observations made through the present study could give us valuable cues for identification of other (parasitic) cymothoids as well. The occurrence of ovigerous females of C. frontalis at different reproductive phases throughout the study period indicates its high fecundity rate which could be a parasitic adaptation. Further, very pertinently, the features such as strict host specificity, site specificity, high rate of prevalence, characteristic life cycle stages, protandric hermaphroditism, the existence of different classes of ovigerous females and occurrence of fecund females all the way through different moult stages make C. frontalis an ideal model organism to study the physiological basis of parasitism and hermaphroditism which in turn would be helpful to study the strategies to be adopted for the management of parasites infesting edible fishes.
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The authors gratefully acknowledge University Grant Commission, New Delhi (F.No: 38-218/2009 (SR); dated: 24/12/2009) and Kerala State Council for Science Technology and Environment, Government of Kerala (No. (T) 093/SRS/2011/CSTE; dated: 25/06/2011) for financial support to carry out this work.
Authors and Affiliations
Post Graduate Department of Zoology and Research Centre, Sree Narayana College, Kannur, 670 007, India
The authors declare that they have no competing interests.
APT is the main worker on the topic and prepared the draft of the manuscript. SK is the mentor who critically followed the work with timely discussion, interpreted the results and corrected the manuscript. HAK helped the main worker for observation and identification, helped in the drawing and is involved in the interpretation of results. AG critically reviewed the manuscript and made significant comments for the improvement of the paper. TJP helped to describe and redescribe the specimen and compared with the type material, reviewed the article and made necessary corrections/modifications. All authors read and approved the final manuscript.
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Thamban, A.P., Kappalli, S., Kottarathil, H.A. et al.Cymothoa frontalis, a cymothoid isopod parasitizing the belonid fish Strongylura strongylura from the Malabar Coast (Kerala, India): redescription, description, prevalence and life cycle.
Zool. Stud.54, 42 (2015). https://doi.org/10.1186/s40555-015-0118-7