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      Nematode parasites of four species of Carangoides (Osteichthyes: Carangidae) in New Caledonian waters, with a description of Philometra dispar n. sp. (Philometridae) Translated title: Nématodes parasites de quatre espèces de Carangoides (Osteichthyes: Carangidae) des eaux de Nouvelle-Calédonie, avec description de Philometra dispar n. sp. (Philometridae)

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      Parasite
      EDP Sciences
      Parasitic nematode, New species, Marine fish, New Caledonia, South Pacific

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          Abstract

          Parasitological examination of marine perciform fishes belonging to four species of Carangoides, i.e. C. chrysophrys, C. dinema, C. fulvoguttatus and C. hedlandensis (Carangidae), from off New Caledonia revealed the presence of nematodes. The identification of carangids was confirmed by barcoding of the COI gene. The eight nematode species found were: Capillariidae gen. sp. (females), Cucullanus bulbosus (Lane, 1916) (male and females), Hysterothylacium sp. third-stage larvae, Raphidascaris ( Ichthyascaris) sp. (female and larvae), Terranova sp. third-stage larvae, Philometra dispar n. sp. (male), Camallanus carangis Olsen, 1954 (females) and Johnstonmawsonia sp. (female). The new species P. dispar from the abdominal cavity of C. dinema is mainly characterised by the body length (5.14 mm), the lengths of markedly unequal spicules (163 and 96 μm) and gubernaculum (102 μm long) provided with a dorsal protuberance and a small, reflexed dorsal barb on its posterior portion. The finding of C. bulbosus represents the first record of this parasite a century after its discovery; the first study of this species by scanning electron microscopy (SEM) enabled detailed redescription. The finding of Johnstonmawsonia sp. in C. fulvoguttatus is the first record of a rhabdochonid nematode from a host belonging to the Carangidae family. Johnstonmawsonia africana Moravec & Puylaert, 1970 and J. campanae Puylaert, 1973 are transferred to Prosungulonema Roytman, 1963 as P. africanum (Moravec & Puylaert, 1970) comb. n. and P. campanae (Puylaert, 1973) n. comb.

          Translated abstract

          L’examen parasitologique de poissons perciformes marins appartenant à quatre espèces de Carangoides, C. chrysophrys, C. dinema, C. fulvoguttatus et C. hedlandensis (Carangidae) de Nouvelle-Calédonie a révélé la présence de nématodes. L’identification des carangidés a été confirmée par barcoding du gène COI. Les huit espèces de nématodes trouvées étaient: Capillariidae gen. sp. (femelles), Cucullanus bulbosus (Lane, 1916) (mâles et femelles), Hysterothylacium sp. (larves de troisième stade), Raphidascaris (Ichthyascaris) sp. (femelles et larves), Terranova sp. (larves de troisième stade), Philometra dispar n. sp. (mâle), Camallanus carangis Olsen, 1954 (femelles) et Johnstonmawsonia sp. (femelle). La nouvelle espèce P. dispar, de la cavité abdominale de C. dinema, se caractérise principalement par la longueur du corps (5.14 mm), les longueurs des spicules sensiblement inégales (163 et 96 μm) et un gubernaculum (102 μm de long) montrant une protubérance dorsale et un petit ardillon dorsal orienté vers l’arrière sur sa partie postérieure. La trouvaille de C. bulbosus représente la première mention de ce parasite, un siècle après sa découverte; la première étude de cette espèce par MEB a permis une redescription détaillée de l’espèce. La découverte de Johnstonmawsonia sp. chez C. fulvoguttatus est la première mention d’un nématode Rhabdochonidae chez un hôte appartenant à la famille Carangidae. Johnstonmawsonia africana Moravec & Puylaert, 1970 et J. campanae Puylaert, 1973 sont transférés vers Prosungulonema Roytman, 1963 comme P. africanum (Moravec & Puylaert, 1970) n. comb. et P. campanae (Puylaert, 1973) n. comb.

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          A quick and simple method, usable in the field, for collecting parasites in suitable condition for both morphological and molecular studies.

          Many methods have been proposed for collecting and fixing parasites, but most were written before the molecular age, and were intended to be practised by experienced parasitologists in well-equipped laboratories. We describe here a very simple method, illustrated by photographs, for collecting helminths from the digestive tract of vertebrates. It only requires a few plastic vials, some ethanol and a means to heat water. Basically, the method consists of: (a) the extraction of all organs from the abdominal cavity; (b) opening the digestive system longitudinally; (c) agitate gut and contents in a saline solution (i.e. ca. 9% NaCl or 1/4 sea water in tap water); (d) decant in saline as many times as needed to clean contents; (e) immediately fix parasites in near-boiling saline; (f) discard saline and keep specimens in 95% ethanol. Additional information is given for collecting parasites from fish gills with a similar process. The method will collect most helminths (digeneans, larval cestodes, nematodes, acanthocephalans) from the digestive tract, and monogeneans and isopod and copepod crustaceans from fish gills. The specimens will be suitable for both morphological study and DNA sequencing. The method is simple, fast, inexpensive and can be used by untrained personnel, even in the field without electricity and without a binocular microscope. It can also be used by trained parasitologists who need to expedite treatment of abundant samples.
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            An annotated list of parasites (Isopoda, Copepoda, Monogenea, Digenea, Cestoda and Nematoda) collected in groupers (Serranidae, Epinephelinae) in New Caledonia emphasizes parasite biodiversity in coral reef fish.

            Abstract: Over a 7-year period, parasites have been collected from 28 species of groupers (Serranidae, Epinephelinae) in the waters off New Caledonia. Host-parasite and parasite-host lists are provided, with a total of 337 host-parasite combinations, including 146 parasite identifications at the species level. Results are included for isopods (5 species), copepods (19), monogeneans (56), digeneans (28), cestodes (12), and nematodes (12). When results are restricted to those 14 fish species for which more than five specimens were examined and to parasites identified at the species level, 109 host-parasite combinations were recorded, with 63 different species, of which monogeneans account for half (32 species), and an average of 4.5 parasite species per fish species. Digenean records were compared for 16 fish species shared with the study of Cribb et al. (2002); based on a total of 90 parasite records identified at the species level, New Caledonia has 17 new records and only seven species were already known from other locations. We hypothesize that the present results represent only a small part of the actual biodiversity, and we predict a biodiversity of 10 different parasite species and 30 host-parasite combinations per serranid. A comparison with a study on Heron Island (Queensland, Australia) by Lester and Sewell (1989) was attempted: of the four species of fish in common and in a total of 91 host-parasite combinations, only six parasites identified at the species level were shared. This suggests strongly that insufficient sampling impairs proper biogeographical or ecological comparisons. Probably only 3% of the parasite species of coral reef fish are already known in New Caledonia.
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              An annotated list of fish parasites (Isopoda, Copepoda, Monogenea, Digenea, Cestoda, Nematoda) collected from Snappers and Bream (Lutjanidae, Nemipteridae, Caesionidae) in New Caledonia confirms high parasite biodiversity on coral reef fish

              Background Coral reefs are areas of maximum biodiversity, but the parasites of coral reef fishes, and especially their species richness, are not well known. Over an 8-year period, parasites were collected from 24 species of Lutjanidae, Nemipteridae and Caesionidae off New Caledonia, South Pacific. Results Host-parasite and parasite-host lists are provided, with a total of 207 host-parasite combinations and 58 parasite species identified at the species level, with 27 new host records. Results are presented for isopods, copepods, monogeneans, digeneans, cestodes and nematodes. When results are restricted to well-sampled reef fish species (sample size > 30), the number of host-parasite combinations is 20–25 per fish species, and the number of parasites identified at the species level is 9–13 per fish species. Lutjanids include reef-associated fish and deeper sea fish from the outer slopes of the coral reef: fish from both milieus were compared. Surprisingly, parasite biodiversity was higher in deeper sea fish than in reef fish (host-parasite combinations: 12.50 vs 10.13, number of species per fish 3.75 vs 3.00); however, we identified four biases which diminish the validity of this comparison. Finally, these results and previously published results allow us to propose a generalization of parasite biodiversity for four major families of reef-associated fishes (Lutjanidae, Nemipteridae, Serranidae and Lethrinidae): well-sampled fish have a mean of 20 host-parasite combinations per fish species, and the number of parasites identified at the species level is 10 per fish species. Conclusions Since all precautions have been taken to minimize taxon numbers, it is safe to affirm than the number of fish parasites is at least ten times the number of fish species in coral reefs, for species of similar size or larger than the species in the four families studied; this is a major improvement to our estimate of biodiversity in coral reefs. Our results suggest that extinction of a coral reef fish species would eventually result in the coextinction of at least ten species of parasites.
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                Author and article information

                Journal
                Parasite
                Parasite
                parasite
                Parasite
                EDP Sciences
                1252-607X
                1776-1042
                2016
                12 September 2016
                : 23
                : ( publisher-idID: parasite/2016/01 )
                : 40
                Affiliations
                [1 ] Institute of Parasitology, Biology Centre of the Czech Academy of Sciences Branišovská 31 370 05 České Budějovice Czech Republic
                [2 ] Service de Systématique moléculaire, UMS 2700 CNRS, Muséum National d’Histoire Naturelle, Sorbonne Universités CP 26 43 rue Cuvier 75231 Paris cedex 05 France
                [3 ] ISYEB, Institut Systématique, Évolution, Biodiversité, UMR7205 CNRS, EPHE, MNHN, UPMC, Muséum National d’Histoire Naturelle, Sorbonne Universités CP51 57 rue Cuvier 75231 Paris cedex 05 France
                Author notes
                Article
                parasite160062 10.1051/parasite/2016049
                10.1051/parasite/2016049
                5018933
                27615321
                63573fc3-bfec-4ee1-a9e2-031107a4e890
                © F. Moravec et al., published by EDP Sciences, 2016

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 10 August 2016
                : 28 August 2016
                Page count
                Figures: 8, Tables: 1, Equations: 0, References: 72, Pages: 18
                Categories
                Research Article

                parasitic nematode,new species,marine fish,new caledonia,south pacific

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