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Elthusa epinepheli n. sp. (Crustacea, Isopoda, Cymothoidae) a branchial parasite of the grouper Epinephelus howlandi (Serranidae, Epinephelinae) off New Caledonia.

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The cymothoid isopod Elthusa epinepheli sp. nov., a branchial parasite of the blacksaddle grouper Epinephelus howlandi (Serranidae, Epinephelinae) from the coral reef of New Caledonia (Southwestern Pacific), is described and figured.Within the genus, E. epinepheli shows some similarity with E. raynaudii and E. myripristae. The ovigerous female of E. epinepheli can be distinguished from E. raynaudii by a less ovate body; cephalon deeply immersed in pereonite 1; eyes almost concealed by the amphicephalic processes; pereonites 3–7 distinctly decreasing in size (width and length); pleonites 1–5 distinctly increasing in width; and pleotelson larger. E. epinepheli can be distinguished from E. myripristae by the anterior margin of the cephalon being rounded in dorsal view and all pleonites being visible. E. epinepheli is the first species of Elthusa reported from the host genus Epinephelus. Elthusa epinepheli sp. nov. (Isopoda, Cymothoidae), parasite branchial du mérou Epinephelus howlandi du récif corallien de Nouvelle-Calédonie, est décrit et représenté. A l’intérieur du genre, E. epinepheli est morphologiquement proche des deux espèces E. raynaudii et E. myripristae. Par rapport à E. raynaudii, la femelle ovigère de E. epinepheli est caractérisée par un corps moins ovale, un céphalon profondément inclus dans le péréonite 1, des yeux presque entièrement dissimulés par les processus amphicéphaliques, des péréonites dont la taille (largeur et longueur) diminue nettement du troisième au septième, des pléonites dont la largeur augmente nettement du premier au cinquième et un pléotelson plus grand. Le bord antérieur arrondi de son céphalon et le fait que tous les pléonites soient visibles permet de distinguer E. epinepheli de E. myripristae. E. epinepheli est le premier Elthusa signalé sur des poissons du genre Epinephelus. Keywords: Isopoda - Cymothoidae - Elthusa epinepheli sp. nov. - Epinephelus howlandi - New Caledonia
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DOI: 10.2478/s11686-010-0020-8
© W. Stefan´ski Institute of Parasitology, PAS
Acta Parasitologica, 2010, 55(2), 177–187; ISSN 1230-2821
Elthusa epinepheli sp. nov. (Crustacea, Isopoda, Cymothoidae)
a branchial parasite of the grouper Epinephelus howlandi
(Serranidae, Epinephelinae) from off New Caledonia
Jean-Paul Trilles1*and Jean-Lou Justine2,3
1Équipe Adaptation écophysiologique et Ontogenèse, UMR 5119 (CNRS-UM2-IFREMER), CC. 092, Université de Montpellier 2,
Place E. Bataillon, F-34095 Montpellier Cedex 05, France; 2UMR 7138 Systématique, Adaptation, Evolution, Muséum National d'Histoire
Naturelle, Case postale 52, 57, rue Cuvier, 75231 Paris cedex 05, France; 3Aquarium des Lagons, B.P. 8185, 98807 Nouméa, Nouvelle-Calédonie
Abstract
The cymothoid isopod Elthusa epinepheli sp. nov., a branchial parasite of the blacksaddle grouper Epinephelus howlandi (Ser-
ranidae, Epinephelinae) from the coral reef of New Caledonia (Southwestern Pacific), is described and figured. Within the genus,
E. epinepheli shows some similarity with E. raynaudii and E. myripristae. The ovigerous female of E. epinepheli can be dis-
tinguished from E. raynaudii by a less ovate body; cephalon deeply immersed in pereonite 1; eyes almost concealed by the
amphicephalic processes; pereonites 3–7 distinctly decreasing in size (width and length); pleonites 1–5 distinctly increasing
in width; and pleotelson larger. E. epinepheli can be distinguished from E. myripristae by the anterior margin of the cephalon
being rounded in dorsal view and all pleonites being visible. E. epinepheli is the first species of Elthusa reported from the host
genus Epinephelus.
Résumé
Elthusa epinepheli sp. nov. (Isopoda, Cymothoidae), parasite branchial du mérou Epinephelus howlandi du récif corallien de
Nouvelle-Calédonie, est décrit et représenté. A l’intérieur du genre, E. epinepheli est morphologiquement proche des deux espèces
E. raynaudii et E. myripristae. Par rapport à E. raynaudii, la femelle ovigère de E. epinepheli est caractérisée par un corps moins
ovale, un céphalon profondément inclus dans le péréonite 1, des yeux presque entièrement dissimulés par les processus am-
phicéphaliques, des péréonites dont la taille (largeur et longueur) diminue nettement du troisième au septième, des pléonites
dont la largeur augmente nettement du premier au cinquième et un pléotelson plus grand. Le bord antérieur arrondi de son cé-
phalon et le fait que tous les pléonites soient visibles permet de distinguer E. epinepheli de E. myripristae. E. epinepheli est le
premier Elthusa signalé sur des poissons du genre Epinephelus.
Keywords
Isopoda, Cymothoidae, Elthusa epinepheli sp. nov., Epinephelus howlandi, New Caledonia
Introduction
The genus Elthusa Schioedte et Meinert, 1884 was established
for the single species Elthusa emarginata (Bleeker 1857), type
species by monotypy, but the Latin diagnosis given by the
Danish authors did not allow an accurate definition of this
genus, nor its separation from other related genera. Elthusa has
most recently been redefined and revised, at least provisionally,
by Bruce (1990) and 28 nominal species are recognized (Trilles
and Justine 2006). Several species remain incompletely de-
scribed, and the hosts for many species are still unknown
(Trilles 1994, Trilles and Justine 2006). Most species are known
from the Pacific or from the Indo-Pacific area (Kensley et al.
2004, Trilles and Justine 2006), including E. parabothi Trilles
et Justine, 2004 and E. arnoglossi Trilles et Justine, 2006 from
New Caledonia. Only four species have been reported from the
Atlantic Ocean, including the recently described E. alvara-
doensis Rocha-Ramírez, Chávez-López et Bruce, 2005, from
the coast of Central Veracruz, Mexico. There are no records
from the Mediterranean (Trilles and Justine 2006).
*Corresponding author: jean-paul.trilles@univ-montp2.fr
Jean-Paul Trilles and Jean-Lou Justine
178
Cymothoid isopods have rarely been reported from
groupers (Teleostei, Serranidae, Epinephelinae). Three species
were collected attached to the body walls, Anilocra dimidiata
Bleeker, 1857 from Epinephelus sp. (Monod 1934), A. gigan-
tea (Herklots 1870) from Epinephelus sp. (Bruce and Harrison-
Nelson 1988) and A. laticauda Milne Edwards, 1840 from
Fig. 1. Elthusa epinepheli sp. nov. Aand B. Ovigerous female, holotype.A– dorsal view, B– lateral view. Cand D. Male. C– dorsal view,
D– lateral view. E– manca larva 2, dorsal view. Scale bars = 5 mm (A, B), 4.5 mm (C, D), 0.5 mm (E)
Elthusa epinepheli sp. nov. from New Caledonia 179
Fig. 2. Elthusa epinepheli sp. nov. Ovigerous female. A– cephalon and first pereonite; B– frons, ventral view; C– antennule; D– antenna;
E– mandible; F– maxillule; G– maxilla; H maxilliped; I– maxilliped article 3 apex; J– brood pouch; K– sternite 7 (a, fleshy lobe;
b, remainder of penes); M– uropod
Jean-Paul Trilles and Jean-Lou Justine
180
Fig. 3. Elthusa epinepheli sp. nov. Ovigerous female. A-F– left pereopods 1–6 respectively, lateral view; G-H– left pereopod 7 (G, lateral
view; H, medial view)
Upeneus martinicus (Richardson 1905), Epinephelus guttatus
(Hochberg and Ellis 1972) and Cephalopholis fulva (Trilles
and Vala 1975). Nerocila arres Bowman et Tareen, 1983 was
reported from the caudal fin of Epinephelus tauvina (Bowman
and Tareen 1983) and Cymothoa borbonica Schioedte et Mein-
ert, 1884 from the mouth of the same fish species. This record
of Elthusa epinepheli is the first record of a gill-attaching cy-
mothoid from groupers.
While examining groupers from New Caledonia (South-
western Pacific) for metazoan parasites during 2003–2008, we
collected a new species of Elthusa from a grouper of the genus
Epinephelus, E. howlandi (Günther). In this article, we describe
all stages (ovigerous female, male and manca larva 2) of the
new species.
Materials and methods
More than 400 groupers belonging to 28 species, including 23
specimens of Epinephelus howlandi, have been examined for
gill parasites over a 7-year period in New Caledonia (Justine et
al., submitted). The parasitized fish (308 mm in fork length, 496
g in weight) was collected by line on 27 June 2006 (off
Nouméa, in the centre of Récif Toombo, 22°26΄10˝S,
166°33΄00˝E). Isopods were removed alive from the right gill
chamber of the fish and measured for total length (TL) and max-
imum width (W). All measurements are in millimetres. Parasites
were preserved in 70% ethanol. Mouthparts and appendages
were carefully dissected and figures were drawn using a cam-
era lucida. Specimens are deposited in the collections of the
Muséum National d’Histoire Naturelle, Paris (MNHN). Fish
taxonomy is according to Froese and Pauly (2009).
Results
Family Cymothoidae Leach, 1814
Genus Elthusa Schioedte et Meinert, 1884
Elthusa Schioedte et Meinert, 1884: 337; Nierstrasz, 1915: 96;
Nierstrasz, 1931: 128; Bruce, 1990: 254; Trilles, 1994: 164.
Livoneca Bleeker, 1857: 21.
Lironeca Miers, 1880: 465.
Type species: The type species is Livoneca emarginata
Bleeker, 1857, by monotypy (Schioedte and Meinert 1884).
One of Bleeker’s type specimens, reported and figured by
Schioedte and Meinert, held in the collections of the Rijksmu-
seum von Natuurlijke Historie, Leiden, is now apparently lost
and not available (Trilles 1979). One female syntype extant in
this museum is too fragile for dissection (Bruce 1990). Another
is held in the collection of the MNHN, Paris, under registra-
tion No. 241 (Trilles 1976). Several additional specimens
were recently collected by Trilles and Randall from two species
of Parupeneus (Teleostei, Mullidae) and the species is being
redescribed.
Elthusa epinepheli sp. nov. (Figs 1–7)
Description
Ovigerous female. Body about 2 times as long as wide,
widest at pereonite 3, very weakly twisted to the right side.
Dorsum weakly vaulted at the level of pereon and pleon
(Fig. 1A, B).
Cephalon about 1.3 times as wide as long, sub-triangular,
deeply immersed in pereonite 1, anterior margin rounded in
dorsal view and ventrally flexed, forming lobe between bases
of antennae, posterior margin rounded. Eyes small, about 0.2
times width of cephalon, black, set close to the margin of
cephalon (Fig. 2A, B).
Pereon broad, about 0.9 as wide as long. Pereonite 1
longest, 2–7 progressively decreasing in length. Posterior mar-
gin of pereonite 7 slightly rounded. Coxal plates of pereonites
2–7 conspicuous in dorsal view.
Pleon about 3.5 times as wide as long; all pleonites visible
but pleonite 1 narrower than others and partially concealed by
pereonite 7, pleonites 1–5 progressively widest towards pos-
terior, 2–4 entirely conspicuous in dorsal view and subequal in
length, 5 slightly longest with posterior margin very broadly
rounded, nearly straight. Pleotelson hemispherical, slightly
asymmetrical, about 1.35 times as wide as long, 2.3 times
longer than pleon, posterior margin rounded.
Brood pouch very prominent in lateral view, made up of
five pairs of alternatively overlapping oostegites arising from
sternites 1 to 4 and 6 (Fig. 2J); anterior pair partly overlapping
mouth parts (Fig. 2B); sternite 7 with 2 distal submedian
fleshy lobes and remainder of penes (Fig. 2K).
Antennule with 8 articles, not extending to posterior of
cephalon but extending to posterior of eyes, basal article not
contiguous. Antenna, slightly longer than antennule, com-
posed of 10 articles, nearly reaching posterior margin of
cephalon, with bases wide apart (Fig. 2C, D).
Mandible without setae and spines, prominent molar, in-
cisor acute but reduced, palpal article 1 slender and longest,
palpal article 3 longer than 2. Maxillule with 3 terminal spines.
Maxilla medial and lateral lobes each with 2 spines. Maxilliped
article 3 with 2 blunted spines and oostegial lobe bearing
some plumose setae (Fig. 2E-I).
Pereopods almost similar with anterolateral carina on ba-
sis increasing in size from pereopod 1 to 7, distinctly dilated
merus, propodus short and dactyli short extending to middle
of carpus (Fig. 3A-H).
Pleopods with all rami lamellar, decreasing progressively
in size, exopod larger than endopod; all pleopods without
coupling hooks on medial margin of peduncle; pleopod 2
without appendix masculina; endopods 2–5 with small, simple
proximomedial lobe, increasing in size from pleopod 2 to 5
(Fig. 4A-F).
Uropods short, right and left uropods differing in size,
rami unequal, exopod shorter than endopod, apices blunted
pointed (Fig. 2M).
Elthusa epinepheli sp. nov. from New Caledonia 181
Jean-Paul Trilles and Jean-Lou Justine
182
Fig. 4. Elthusa epinepheli sp. nov. Ovigerous female. A-D– left pleopods 1–4 respectively, posterior view; E-F– left pleopod 5 (E, poste-
rior view; F, anterior view; c, proximomedial lobe). Male. G– antennule, H– antenna, I– mandible palp, J– maxillule, K– maxilla apex,
L– maxilliped, M– maxilliped article 3 apex, N– sternite 7 (a, penes; b, pleopod 1), O– uropod
Elthusa epinepheli sp. nov. from New Caledonia 183
Male. Smaller than female; body bilaterally symmetrical,
about 2.5 times as long as wide, lateral margins straight; dor-
sum weakly vaulted (Fig. 1C, D).
Cephalon about 1.8 times as wide as long, distinctly im-
mersed in pereonite 1, anterior margin forming broad sub-
truncate rostrum, posterior margin rounded.
Pereon 0.4 times as wide as long. Pereonite, 3–7 subequal
in length; posterior margin of pereonite 7 slightly rounded.
Coxal plates 2–7 conspicuous in dorsal view.
Pleon about 3.2 times as wide as long, posterior margin of
pleonite 5 weakly bisinuate. Pleotelson about 0.6 times as
long as wide, posteriorly broadly rounded. Elongate paired
penes on posterior margin of sternite 7 (Fig. 4N).
Antennule and antenna similar to female, without setae, but
antenna proportionally longer than in female and composed of
11 articles (Fig. 4G, H).
Mandible palp, articles decreasing in size from 1 to 3, article
3 slender and shortest. Maxilla with 2 large curved spines each
on medial and lateral lobe. Maxilliped article 3 with 2 or 3 (ac-
cording to the right or left body side) recurved spines (Fig. 4I-M).
All pereopods similar to those of female with anterolateral
carina on basis increasing in size from 1 to 7 but merus pro-
portionally less dilated than in female (Fig. 5A-H).
Pleopod rami lamellar, exopod larger than endopod,
without coupling hooks on peduncle. Pleopod 2 with appen-
dix masculina about 0.6 times as long as endopod. Simple
Fig. 5. Elthusa epinepheli sp. nov. Male. A-F– right pereopods 1–6, respectively (A-C, lateral view; D-F, medial view); G-H– right
pereopod 7 medial and lateral view, respectively
Jean-Paul Trilles and Jean-Lou Justine
184
Fig. 6. Elthusa epinepheli sp. nov. Male. A-E– left pleopods 1–5 respectively, posterior view (a, proximomedial lobe). Manca larva 2.
F– antennule, G– antenna, H– mandible palp, I– maxillule, J– maxilla, K– maxilliped
Elthusa epinepheli sp. nov. from New Caledonia 185
Fig. 7. Elthusa epinepheli sp. nov. Manca larva 2. A-F– pereopods 1–6 respectively, lateral view; G– pleonites 4–5, pleotelson, uropods;
H-K– left pleopods 1, 2, 4, 5 respectively, posterior view
Jean-Paul Trilles and Jean-Lou Justine
186
proximomedial lobe particularly conspicuous in pleopods
4–5 (Fig. 6A-E).
Uropods about 0.6 times as long as pleotelson, rami weakly
unequal, bluntly rounded, exopod slightly longer than endopod
(Fig. 4O).
Manca larva 2 (pullus 2). The specimen illustrated in Fig-
ure 1E is at the intramarsupial stage 2 (manca larva 2 or pul-
lus 2), just before spawning. It shows 7 pereonites but only 6
pereopods, an enlarged semi-circular cephalon, ovate pereon
and narrowed pleon with pleonites 1–5 decreasing progres-
sively in width towards posterior. Posterior margin of pleotel-
son rounded, with sparse plumose setae (Fig. 7G).
Antennule composed of 6 articles extending to the middle
of pereonite 1, with simple spiny short seta on antero-distal
margin of article 4, large seta on the postero-distal margin of
article 5 and four similar setae on article 6. Antenna slightly
longer than antennule, composed of 10 articles, with plumose
seta on antero-distal margin of articles 4–5, two spiny setae on
the antero-distal margin of article 5, spiny seta on the antero-
distal margin of article 9 and tuft of four fine setae on distal
margin of article 10 (Fig. 6F, G).
Mandible palp with small seta on lateral margin of article
2 and palpal article 3 with 4 setae increasing gradually in
length along disto-lateral margin. Maxillule with 3 terminal
spines and maxilla with 3 spines on medial lobe. Maxilliped
article 3 with 2 recurved spines (Fig. 6H-K).
All pereopods similar with acute dactyli, increase slightly
in length from pereopod 1 to 6, with spines or setae on pereo-
pods 2–6: pereopod 2, 2 small setae on posterior margin of
propodus; pereopod 3, 1 spine on ischium and 2 on propodus;
pereopod 4, 1 spine on ischium, 4 on merus, 2 on carpus and
3 on propodus; pereopod 5, 1 spine on ischium, 4 on merus, 3
on carpus and 3 on propodus; pereopod 6, 2 spines on ischium,
2 spines and 1 seta on merus, 3 spines and 1 seta on carpus and
3 spines on propodus (Fig. 7A-F).
Pleopods 1–4 have peduncles with coupling hooks and
lamellar rami with long plumose setae. Pleopod 5 with only
1 short seta on peduncle and rami without setae (Fig. 7H-K).
Uropod rami extending beyond posterior of pleotelson;
both rami subequal in length; apices of both rami rounded, with
plumose setae on posterior margin (Fig. 7G).
Type-host: Epinephelus howlandi (Günther) (Serranidae).
Type-locality: Off Nouméa, New Caledonia.
Site: Branchial cavity.
Type-material: Female holotype (ovigerous with many
manca larvae 2 in the brood pouch; TL = 37 mm), Muséum
National d’Histoire Naturelle, Paris, MNHN-IS 6257, male
(TL = 20 mm), MNHN-IS 6258, off Nouméa, in the centre of
Récif Toombo, 22°26΄10˝S, 166°33΄00˝E, New Caledonia, 27
June 2006. Parasitological number MNHN JNC 1886.
Etymology: Epithet taken from the host genus.
Remarks
Bruce (1990) recognised 25 species of Elthusa Schioedte et
Meinert, 1884, most of which had been previously accommo-
dated in Livoneca Leach, 1818. With the description of Elthusa
epinepheli sp. nov., 29 species are now recognised. Most (25)
are known from the Pacific or Indo-Pacific area and only four
species are reported from the Atlantic Ocean (Trilles and Jus-
tine 2006).
Elthusa epinepheli is the third species of Elthusa reported
from New Caledonia (the others are E. parabothi Trilles et Jus-
tine, 2004 and E. arnoglossi Trilles et Justine, 2006) and the
first collected from gills of groupers of the genus Epinephelus
(Serranidae, Epinephelinae).
Elthusa epinepheli can be considered uncommon. Epi-
nephelus howlandi in New Caledonia had a surprisingly low
diversity of gill parasites, with only two species of monoge-
neans and apparently – an exceptional fact – no copepod
(Hinsinger and Justine 2006a, b). Absence of copepods and
presence of this isopod suggests that some unknown biogeo-
graphical or biological feature differentiates E. howlandi from
the other groupers in this locality.
The new species can be easily distinguished from the fol-
lowing five species, Elthusa arnoglossi Trilles et Justine,
2006, E. nanoides (Stebbing, 1905), E. propinqua (Richardson,
1904), E. samariscii (Shiino, 1951) and E. sigani Bruce, 1990,
all of which are distinctly asymmetrical. The remaining species
have a bilaterally symmetrical body or are only weakly asym-
metrical. Of these, only two species, Elthusa myripristae
Bruce, 1990 and E. raynaudii (Milne Edwards, 1840) show
some similarity to E. epinepheli. E. myripristae can be easily
separated by the cephalon, which has a distinct medial rostral
point and pleonite 1, which is totally concealed by pereonite
7, and therefore is not visible in dorsal view. E. epinepheli can
be separated from E. raynaudii by a number of characters, in-
cluding: female body slightly more twisted to one side, more
elongated and less ovate, pereonites 3 to 7 decreasing distinctly
in width and length, pleonites increasing distinctly in width
from 1 to 5, pleotelson bigger (width and length) and slightly
asymmetrical, cephalon more deeply immersed in pereonite 1
and eyes almost concealed by the amphicephalic processes, an-
tenna composed of 10 articles (11 in E. raynaudii), mandible
palp without setae (5 and 2 setae on disto-lateral margin of ar-
ticles 2 and 3 respectively in E. raynaudii), maxillule with 3
spines (4 in E. raynaudii), pereopods 5–7 with carina most pro-
nounced forming a more prominent boss, dactyli smaller, all
pleopods without coupling hooks on medial peduncle margin
and endopods 3–5 with proximomedial lobe (with coupling
hooks and without proximomedial lobe in E. raynaudii); male
body with cephalon more deeply embedded in pereonite 1,
pleon proportionally shorter and wider than in E. raynaudii,
pleonite 1 more concealed by pereonite 7 and pleotelson larger
and distinctly dissimilar in shape, antenna with 11 articles in-
stead of 13, mandible palp without setae and maxillule with
only 3 spines instead of 6.
Acknowledgements. Lenaïg Hemery and Géraldine Colli, students,
participated in the fishing operations and parasitological survey.
Napoléon Colombani (IRD) provided safe navigation and excellent
Elthusa epinepheli sp. nov. from New Caledonia 187
fishing skills on board R/V Coris. Angelo di Matteo provided tech-
nical help. Ian Beveridge kindly edited the English.
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... Bruce, (1990) gave a new provisional diagnosis to the genus, transferring 20 species from Livoneca Leach, 1818 into Elthusa along with the description of two new species, Elthusa myripristae Bruce, 1990 and Elthusa sigani Bruce, 1990. A further six species have since been described from New Caledonia, Mexico, Japan, and Hawaii (Trilles & Justine, 2004, 2006, 2010Rocha-Ramírez et al., 2005;Saito & Yamauchi, 2016;Hadfield et al., 2017, respectively). Hadfield et al., (2016a) transferred Ceratothoa parva Richardson, 1910 to the genus Elthusa and an Elthusa homonym was corrected (Hadfield et al., 2016b). ...
... Elthusa has a wide distribution, with species reported from all oceans except the Antarctic Ocean and northern Polar waters (Bruce, 1990;Trilles & Justine, 2004, 2006, 2010Rocha-Ramírez et al., 2005;Saito & Yamauchi, 2016;Hadfield et al., 2017;Öktener et al., 2018;Van der Wal et al., 2019). Among the described species, only two species, Elthusa raynaudii (Milne Edwards, 1840) from Travancore (currently part of Kerala state) by Pillai, (1954) and Elthusa samariscii (Shiino, 1951), from Kerala, southwest coast of India by Kumar & Bruce, (1997), have been reported from India. ...
... Species included (sensu stricto): Elthusa acutinasa van der Wal et al., 2019, Elthusa atlantniroi (Kononenko, 1988), Elthusa caudata (Schioedte & Meinert, 1884), Elthusa emarginata (Bleeker, 1857), Elthusa foveolata (Hansen, 1897), Elthusa frontalis (Richardson, 1910), Elthusa menziesi (Brusca, 1981), Elthusa methepia (Schioedte & Meinert, 1884), Elthusa nanoides (Stebbing, 1905), Elthusa nierstraszi Hadfield et al., 2016a, b, Elthusa ochotensis (Kussakin, 1979, Elthusa philippinensis (Richardson, 1910), Elthusa poutassouiensis (Penso, 1939), Elthusa raynaudii (Milne Edwards, 1840), Elthusa rotunda van der Wal et al. 2019, Elthusa samoensis (Schioedte & Meinert, 1884), Elthusa sigani Bruce, 1990, Elthusa sinuata (Koelbel, 1879, Elthusa splendida (Sadowsky & Moreira, 1981), Elthusa tropicalis (Menzies & Kruczynski, 1983), Elthusa vulgaris (Stimpson, 1857) Bruce, 1990, Elthusa parva (Richardson, 1910), Elthusa propinqua (Richardson, 1904), Elthusa sacciger (Richardson, 1909), Elthusa epinepheli Trilles & Justine, 2010, Elthusa moritakii Saito & Yamauchi, 2016, Elthusa neocytta (Avdeev, 1975, E l t h u s a p a r a b o t h i T r i l l e s & J u s t i n e , 2 0 0 4 , Elthusa samariscii (Shiino, 1951), and Elthusa turgidula (Hale, 1926). ...
Article
The genus Elthusa Schioedte & Meinert, 1884 from Indian waters is reviewed and three new species are described from India. A revised generic diagnosis is provided based on the type species and 13 species of Elthusa are regarded as Elthusa incertae sedis. Female stages of Elthusa fistularia sp. nov. collected from Fistularia petimba Lacepède,1803 and Elthusa pseudorhombus sp. nov. from Pseudorhombus dupliciocellatus Regan, 1905 are described based on the female. Elthusa uranoscopus sp. nov. from Uranoscopus guttatus Cuvier, 1829 described from female and male. The female and male stages of Elthusa samariscii (Shiino, 1951) are redescribed and the transitional and larval (premanca and manca) stages are described. All the species were collected from the southwest coast of India. Elthusa fistularia sp. nov. is distinguished by cephalon 1.20 times wider than long; pleotelson broadly rounded, 1.70 times as wide as long, lateral margin convex; widest pleon 0.80 width of widest pereon; uropod rami subequal; and antenna 9-segmented, antennular bases moderately wide set. Elthusa pseudorhombus sp. nov. is characterized by cephalon 1.70 times wider than long; widest pleon 0.75 width of widest pereon; pleotelson 1.50 times as wide as long, evenly rounded; antenna with 10 articles, antennal bases widely separated; and uropod endopod shorter than exopod. Elthusa uranoscopus sp. nov. can be identified by cephalon 1.60 times wider than long, moderately immersed in the pereonite 1; widest pleon 0.84 width of widest pereon; pleotelson 1.80 times as wide as long posterior margin rounded, lateral margins convex; antenna 11 articled, slightly longer than antennula, greatly wider antennal bases; and uropod rami, endopod longer than exopod.
... Concerning the gnathiid prevalence (58.33%) and intensity (8-22 parasites⁄infested fish), approximately the same results were obtained by Jones and Grutter [9], and the attributed the change of parasite prevalence and intensity to host type and seasons (temperature). With regard to the damage (mucus, gill erosion and multifocal hemorrhagic spots) caused by gnathiids, allow us to conclude that the result of a double parasitic action; mechanical damage on the skin, gills and pharyngeal mucosa [19][20][21]. Additionally, the gnathiids are blood sucking parasite, so it has a well developed and strong mouth parts where, the mouthparts of the parasite penetrate the epidermis and cause hemorrhage from vessels in the dermis [21][22][23]. ...
... With regard to the damage (mucus, gill erosion and multifocal hemorrhagic spots) caused by gnathiids, allow us to conclude that the result of a double parasitic action; mechanical damage on the skin, gills and pharyngeal mucosa [19][20][21]. Additionally, the gnathiids are blood sucking parasite, so it has a well developed and strong mouth parts where, the mouthparts of the parasite penetrate the epidermis and cause hemorrhage from vessels in the dermis [21][22][23]. The feeding times for the three praniza stages of G. africana are approximately 2, 3 and 10 h [17,18]. ...
... Brucethoa epinepheli (Trilles & Justine, 2010) comb nov. ...
Article
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Brucethoa isro n. sp., a new species of deep-sea cymothoid is described and illustrated from the host fish Spinyjaw greeneye, Chlorophthalmus corniger Alcock, 1894, at depths of 265 to 458 metres from the southwest coast of India. Brucethoa isro n. sp. is recovered from the base of the gill cavity, facing the head towards the anterior, and the dorsal body closely adpressed against the gill, while the ventral brood presses against the inner wall of the operculum. Brucethoa isro n. sp., the second species of the genus, is characterized by: head weakly immersed in pereonite 1, very elongated body (3.15 times as long as wide); body dorsum not vaulted, almost flat; all coxae short, 0.5 times as the length of corresponding pereonites; sternite 7 with prominent posterior lobes. All adult life stages of the new species are described [including females (ovigerous and non-ovigerous), males, transitional, and juvenile. The species is currently known from the southwest coast of India and is the type locality. Additionally, this research provides valuable ecological insights into Brucethoa isro n. sp. and its habitat. As part of the taxonomic contributions, two species, Brucethoa alvaradoensis (Rocha-Ramírez, Chávez-López & Bruce, 2005) comb. n. and Brucethoa epinepheli (Trilles & Justine, 2010) comb. n., are transferred from the Elthusa genus to the Brucethoa genus.
... Cymothoidae (Crustacea, Isopoda) is among the most diverse parasitic isopods infesting various fish hosts. They are attached to the host body surface, buccal, or gill cavities (Mahmoud et al. 2014a, b;Trilles and Justine 2010) and occasionally burrowing in the musculature of their hosts, causing sever tissue damage and fish mortalities (Rhode 2005;Smit et al. 2014). In Egypt, interest on the Mediterranean isopods has increased in the last decade; it was reported as the main source of isopod infestation problems occurred in marine fish farms and the inland lakes. ...
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With the opening of the Suez Canal in 1869, many changes have occurred in the Mediterranean Sea ecosystem so became a home to many invasive Lessepsian marine species that have migrated from the Red Sea. About 500 marine species including pufferfish have immigrated and rapidly established a population in the Mediterranean Sea causing significant impact on its ecosystem and fisheries sector. The parasitic fauna of these pufferfish has scarcely been studied in the Mediterranean Sea and also in their native habitat. During this surveillance study on the invasive pufferfish species from the Egyptian Mediterranean coast, the female cymothoid isopod Elthusa raynaudii was detected from the branchial cavity and also in the buccal cavity of 23.9% of the examined Lagocephalus sceleratus. The isolated isopod species was firstly identified and described through electron microscopy and molecular phylogeny based on the sequences of mitochondrial 16S rRNA gene. Additionally, the description of eggs, embryonic stage, and manca of E. raynaudii was firstly provided. The pathological impact on the infested fish tissues was investigated and revealed curling and loss of secondary gill lamellae in addition to mucous exudates in between the gill filaments and granuloma formation in the gill arch. The study provided the first report of L. sceleratus as a new host for the isopod E. raynaudii collected from the Egyptian Mediterranean coast as a new locality record. The role of the Lessepsian invasive pufferfish in transmitting parasites to the native fish species was discussed. Graphical Abstract
... The misidentification also results from the lack of any attempt to relate the specimens to the generic and species taxonomy for extant Cirolanidae. It is true that in some families, notably Sphaeromatidae Latreille, 1802 and Cymothoidae, Leach, 1818 that some taxa show very different ontogenetic stages as well as strong sexual dimorphism, and there are many publications that illustrate these male and female stages (e.g., Bruce, 1997;Hadfield & Smit, 2020;Harrison & Holdich, 1982, 1984Trilles et al., 1999;Trilles & Justine, 2010). It is also true that it may not be possible to identify manca (i.e. ...
... Martin et al. (2013Martin et al. ( , 2014aMartin et al. ( , b, 2015a has revised the Australian buccal-attaching genera. Trilles & Justine (2006, 2010 provided further data on gill-attaching species from New Caledonia. Bruce (2004) reviewed the freshwater isopods of Malaysia and Singapore; no Cymothoidae are known from purely freshwater habitats, though some genera do have freshwater species (e.g., see Tsai & Dai, 1999;Yamano et al., 2011). ...
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Cymothoa rhina Schioedte & Meinert, 1884 is redescribed from specimens collected in Singapore, the female of which is designated as neotype. Adult female Cymothoa rhina can be identified by the acute anterior margin of the cephalon, anterolateral projections on pereonite 1 extending anteriorly along half the length of the cephalon, pleotelson posterior margin subtruncate (rounded in the male), and pereopod 7 ischium inferior margin with a bulbous protrusion and the basis with a distinct carina (weak in the male). Cymothoa rhina is known only from the Philippines, Guam and now Singapore, from Lutjanidae hosts.
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The branchial-attaching cymothoid genus, Elthusa Schioedte & Meinert, 1884 is a genus with a worldwide distribution of 36 species, including the three species described here. Elthusa raynaudii (Milne Ed-wards, 1840) is the only species that has been described from southern Africa. All South African material held at the National Museum of Natural History, Paris, France (MNHN) and the Iziko South African Museum, Cape Town (SAMC) identified as, or appearing to belong to, Elthusa was examined. Four species were identified, Elthusa raynaudii and three species that proved to be undescribed. Elthusa xena sp. n. can be distinguished by an evenly rounded pereonite 1 anterior margin, a roughly rectangular pleotelson, and narrowly rounded uropod apices that extend to more than half the length of the pleotelson. Elthusa acutinasa sp. n. is identified by the produced and narrowly rounded cephalon anterior margin, acute uro-pods that are shorter than half the length of the pleotelson, and pereonite 1 anterior margin with medial projection. Elthusa rotunda sp. n. is characterised by the round body shape, broadly rounded uropod apices, and protrusions on the proximal and lateral margins of the merus and carpus of pereopod 7. A key to the South African Elthusa species is provided, together with a table summarising the hosts and localities of the 33 previously known species of Elthusa. A peer-reviewed open-access journal Serita van der Wal et al. / ZooKeys 841: 1-37 (2019) 2
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The parasite was obtained on the gill cavity of the blue whiting, Micromesistius poutassou (Risso), from the Aegean Sea Coast, Turkey. This cymothoid is a typical parasite of the blue whiting, but it is poorly known. It was reported from the same host as Meinertia (Ceratothoa) potassoniensis and Meinertia poutassouiensis with an inadequate description. The specimens examined in this study show the diagnostic characters of Elthusa Schioedte & Meinert, 1884. The previous two species are proposed to be transferred to the genus Elthusa. The ovigerous female, non-ovigerous female and male species are redescribed by drawings for the first time. The Mediterranean Sea is a new geographical record for the genus Elthusa.
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Livoneca sinuata Koelbel, 1879 (Isopoda, Cymothoidae) is known from the Mediterranean Sea. In this study, this species is redescribed and transferred to the genus Elthusa according to the current status of this: body weakly twisted, antennula shorter than antenna, posterior margin of cephalon not trilobed, pleonite 1 slightly narrower than pleonite 2, maxilliped with oostegital lobe and pleopods all lamellar, without lobes or folds. This species was collected on the red bandfish, Cepola macrophthalma, and reported for the first time in the Sea of Marmara, Turkey. The species is also photographed for the first time on the host.
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The new cymothoid species, Elthusa winstoni sp. n., a branchial parasite of fishes from the family Acan-thuridae Bonaparte, 1835 in Hawaii, is described and figured. The female adults can be distinguished by the strongly vaulted body and compacted body shape; rostrum with a small median point; short antennae which are close together (only 6 articles in both antennula and antenna); short and wide uropods extending to half the length of the pleotelson; short dactyli on pereopod 7; and large recurved robust setae on the maxilla. This is the first record of an Elthusa Schioedte & Meinert, 1884 species from the Hawaiian Islands and only the fifth cymothoid described from this region.
Article
Nine species of the Cymothoid Isopoda parasitic in the buccal or abdominal cavity of Japanese fishes are described in this report. They are Codonophilus trigonocephalus (Leach), Rhexanella verrucosa (Schi ?? dte & Meinert), Indusa minabensis n. sp., Cymothoa pulchra Lanchester, C. eremita Brünnich, Livoneca sacciger Richardson, L. samariscii u. sp., Irona melanosticta Schi ?? dte & Meinert, and Ichthyoxenus japonensis Richardson, and are parasitic in due order on Caranx (Longirostrum) delicatissimus (Döderlein), Pagrosomus major(Temminck & Schlegel), Chaunax fimbriatus (Hilgendorf), Diodon holacanthus Linné, Aulopus japonicus (Günther), Synaphobranchus pinnatus (Gronow), Samariscus japonicus Kamohara, Hyporhamphus sajori (Temminck & Schlegel), and Acheilognathus sp. All of them except Ichthyoxenus japonensis, which lives in the abdominal cavity, are discovered from the buccal or branchial cavity of the host. Cymothoa pulchra is recorded for the first time from Japan. The two new species are defined as follows: Indusa minabensis n. sp.: Female 23mm×13mm, nearly symmetrical and highly convex above. Head triangular, with distinct eyes. Antennae comparatively long and slender; those of the lst pair contiguous at the base, 8-jointed, and the 2nd pair longer being composed of 11-12 joints. Thorax oval in outline; antero-lateral angle of the lst segment not produced, but angular. Lateral parts of all thoracic segments slightly expanded having round post-lateral angle. Epimerae in the 2nd to 7th segments, narrow and linear. Basis of pereiopoda without carina. Abdomen one third as long as body; anterior segments covered by the 7th thoracic segment in lateral regions. Pleotelson more or less circular. Peduncle of uropod somewhat acuminate at inner distal angle; exopodite longer than endopodite. Male 10.5mm×5.0mm, relatively narrower than the female, symmetrical and slightly convex above. Head triangular, with distinct eyes. Both pairs of antennae comparatively longer than in the female, but composed of the same number of joints. Thorax oblong, with narrow epimerae. The lst abdominal segment not covered by the thorax. Pleotelson with margin round but more or less notched. Livoneca samariscii n. sp.: Represented only by a female. 10.1mm×5.9mm. Body only slightly convex above, asymmetrical having one side more expanded than the other, and with mar-supium vaulted but empty. Head triangular, very little immersed in the thorax, and with dis-tinct eyes. Antennae slender and long; those of the lst pair separated at the base, 8-jointed; the 2nd pair longer and 10-jointed. The lst thoracic segment sinuated in front, having anteriorly curved lateral parts and with angular antero-lateral corner. Other segments directed more or less obliquely backwards in lateral region and with anteriorly arched posterior borders. Epi-merae very narrow, linear, and shorter than lateral margins of segments. Pereiopoda without ca-rina on the basis. Abdomen nearly one third as long as body. The first 5 segments curved anteri-orly; lateral parts of anterior segments covered by the thorax on one side. Pleotelson semicircu-lar, two thirds as long as wide. Basis of uropod angular at inner distal corner; exopodite longer than endopodite. Lamellar maxilliped has anterior margin bearing a few short plumose setae and a palp tipped by 2 hooks.
Article
Die Isopoden-Sammlung im Naturhistorischen Reichs-Museum zu Leiden, obwohl nicht sehr gross, ist dennoch von hohem Interesse und grossem Wert. Sie enthält eine grosse Zahl von Formen, welche von Bleeker vor 60 Jahren in Ost-Indien gefangen und von Schiödte und Meinert in ihrer grossen Arbeit (25, 26) beschrieben worden sind. Überdies wurden während der letzten Jahren dem Museum zahlreiche Tiere geschenkt, welche ebenso vom Indischen Archipel stammen und von Herrn P. J. Buitendijk erbeutet worden sind. In dieser und den folgenden Publikationen habe ich die Absicht die verschiedenen Gruppen der Isopoden der Reihe nach zu behandeln; aus praktischen Gründen fange ich mit den Cymothoiden an. Wie ich schon bei einer früheren Gelegenheit (17, p. 1) auseinander gesetzt habe, herrscht eine grosse Verwirrung bezüglich Angabe und Anwendung von Namen, welche morphologisch vielfach ganz unrichtig sind. Der Morphologie wird von den Systematikern oft gar keine Rechnung getragen, ein Umstand, dem jene Verwirrung zuzuschreiben ist. Daher werde ich mich immer streng an folgende Nomenklatur halten. Prosoma: Kopf mit: Antennulae. Antennae. Mandibulae. Maxillae I. Maxillae II. Thoracomer I mit Thoracopodien I = Maxillipeden. Mesosoma = Thorax = Pereion mit den Thoracomeren II— VIII, welche die Thoracopodien II—VIII (Pereiopodien I—VII)
Article
Dans un premier travail (Trilles, 1977), nous avons pu étudier une partie des spécimens indéterminés de Cymothoadiens du Rijksmuseum van Natuurlijke Historie de Leiden: tous proviennent de la Méditerranée et de l'Atlantique Nord-oriental. Toujours grâce à l'extrême obligeance de la Direction de cet établissement et du Professeur L. B. Holthuis, nous avons pu poursuivre l'étude de cette importante collection de Cymothoidae en examinant les échantillons Africains, Américains et Indo-ouest-Pacifiques. Ainsi 135 tubes ont été inventoriés; 18 ne renferment que des espèces libres (50 et 51, 78 à 91, 115 et 121), 7 contiennent à la fois Isopodes libres et des Cymothoidae (26, 42, 45, 47, 53, 63 et 120), les autres ne renferment que des parasites. Nous avons effectivement reconnu: Anilocridae. — Anilocra Leach, 1818; Nerocila Leach, 1818; Rosca Schioedte et Meinert, 1881; Braga Schioedte et Meinert, 1881; Renocila Miers, 1880. Cymothoidae — Ceratothoinae. — Glossobius Schioedte et Meinert, 1883; Ceratothoa Dana, 1852. — Cymothoinae. — Cymothoa Fabricius, 1787; Ichthyoxenus Herklots, 1870; Telotha Schioedte et Meinert, 1884; Enispa Schioedte et Meinert, 1884. — Lironecinae. — Lironeca Leach, 1818; Irona Schioedte et Meinert, 1884; Cterissa Schioedte et Meinert, 1884. Ils renferment au total 33 espèces distinctes (4 d'Afrique, 7 d'Amérique et 22 Indo-ouest-Pacifique). En plus de cela, ont été inventoriés: 3 échantillons que nous rapportons pour l'instant au genre Aegathoa Dana, 1852 (Indo-ouest-Pacifique); 9 échantillons encore indéterminés, qui correspondent à des espèces certainement nouvelles (1 d'Afrique, 2 d'Amérique et 6 Indo-ouest-Pacifique) ;