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An Unique Association Between Argulus Alosae (Branchiura) and Mysis Stenolepis (Mysidacea)

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An Unique Association Between Argulus Alosae (Branchiura) and Mysis Stenolepis (Mysidacea)

Auteurs : Cathy J. Jackson ; David J. Marcogliese

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DOI: 10.1163/156854095X01051

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<p>910 males examined had the supposed specific character of rod-like or foliaceous endopods on the pleopods of the second abdominal segment. Eleven had no endopods and four had additional endopods on the pleopods of the third, fourth and fifth. One of these (74.2 mm) had endopods on pleopods 3-5 in a bifid condition similar to that seen on juvenile females. Four males representing these various conditions are lodged in the Western Australian Museum (WAM 323-94). It should be noted that P. japonicus is the only species of Panulirus that may have tiny to small, simple or bifid endopods on the pleopods of the male and when present they may be on one abdominal segment (second) or all (second to fifth). The taxonomic character of the uninterrupted transverse abdominal grooves of the second, third and fourth segments not joining the corresponding pleural groove was confirmed for all the specimens of P. japonicus in the sample studied (males 23, females 2). REFERENCES GEORGE, R. W. & L. B. HOLTHUIS, 1965. A revision of the Indo-West Pacific spiny lobsters of the P. japonicus group. Zool. Verh., Leiden, 72: 1-36. AN UNIQUE ASSOCIATION BETWEEN ARGULUS ALOSAE (BRANCHIURA) AND MYSIS STENOLEPIS (MYSIDACEA) BY CATHY J. JACKSON Department of Biology, University of New Brunswick, Fredericton, New Brunswick, Canada E3B 6E1 and DAVID J. MARCOGLIESE Department of Fisheries and Oceans, Maurice Lamontagne Institute, P.O. Box 1000, Mont-Joli, Quebec, Canada G5H 3Z4 (to whom correspondence) INTRODUCTION Branchiurans are typically crustacean parasites of fishes, although larvae have been known to infect amphibians (Overstreet et al., 1992). In the course of a survey of mysids for parasites, we observed ectoparasites on animals collected in Passamaquoddy Bay, New Brunswick, Canada. These ectoparasites were identified as Argulus alosae Gould, 1841. This is the first report known to us of a phoretic association between fish lice and invertebrates.</p>
<p>911 MATERIALS AND METHODS A total of 637 mysids (Mysis stenolepis S. I. Smith, 1873) were collected by towing a plankton net close to the bottom in 8-10 m of water near the mouth of the Magaguadavic River in Passamaquoddy Bay, New Brunswick (45°07'N 66°55'W) in August 1991. Mysids were sorted and fixed in 70% ethanol. Individual mysids were dissected and examined for parasites using a stereo- microscope. Branchiurans were removed and stored in AFA. Abundance is defined as the mean number of parasites per mysid, including infected and uninfected animals. Voucher specimens were deposited in the collection of the Canadian Museum of Nature, Ottawa, Canada, under Acc. No. (NMCC 1995-0015). RESULTS AND DISCUSSION A total of 30 fish lice were found associated with mysids, giving an abun- dance of 0.05. All fish lice were identified as Argulus alosae. Mean length (and length range) was 3.03 ± 0.97 (0.64-5.4) mm; mean width (and width range) was 1.49 ± 0.5 (0.42-2.78) mm. The sex of these animals could not be deter- mined, and it is presumed that they are juveniles. Adult females reach 12 mm, and males 6 mm in length (Kabata, 1988). The lice were located ventrally in the marsupium near the juncture of the cephalothorax and abdomen of the mysids. The preoral stylet had not pierced the mysids' bodies. Thus, it is presumed that this association is phoretic, and not parasitic. Most branchiurans are not very host specific (Kabata, 1988). In eastern Canada, A. alosae has been found on blackspotted stickleback, Gasterosteus zvheatlandi Putnam, 1866; Atlantic tomcod Microqadus tomcod (Walbaum, 1792); shortnose sturgeon Acipenser brevirostrum Lesueur, 1818; and brook charr Salvelinusfontinalis (Mitchill, 1815) (cf. Frimeth, 1987; Kabata, 1988). Argulus alosae is considered a marine and brackish species (Kabata, 1988), and all the fish above are marine or anadromous and can be found inshore in brackish waters (Scott & Scott, 1988). Branchiurans mate while free-swimming and lay their eggs on submerged objects (Kabata, 1988). They are capable of swimming from fish to fish (Kabata, 1988) and can be collected free in the water column (Overstreet et al., 1992). Thus, it is conceivable that they could become associated with potential carrier hosts such as mysids. Because mysids are active swimmers (Mauchline, 1980) and undergo migrations (Amaratunga & Corey, 1975), these associations may serve to further increase the branchiurans dispersal capability. Unusual associations such as the one described herein may also provide insight into evolutionary origins or modifications of parasitism (Williams & Bunkley-Will- iams, 1944).</p>
<p>912 ACKNOWLEDGEMENT We thank Bill Hogans, Atlantic Reference Centre, for collecting the mysids. LITERATURE CITED AMARATUNGA, T. & S. COREY, 1975. Life history of Mysis stenolepis Smith (Crustacea, Mysidacea). Canadian Journ. Zool., 53: 942-952. FRIMETH, J., 1987. Potential use of certain parasites of brook charr (Salvelinus fontinalis) as biological indicators in the Tabusintac River, New Brunswick, Canada. Canadian Journ. Zool., 65: 1989-1995. KABATA, Z., 1988. Copepoda and Branchiura. In: L. MARGOLIS & Z. KABATA (eds.), Guide to the parasites of fishes of Canada. Part II. Crustacea. Canadian spec. Publ. Fish. aquat. Sci., 101: 3-127. MAUCHLINE, J., 1980. The biology of mysids and euphausiids. Adv. mar. Biol., 18: 1-681. OVERSTREET, R. M., I. DYKOVÁ & W. E. HAWKINS, 1992. Branchiura. In: Microscopic anatomy of invertebrates. Crustacea, 9: 385-413. (Wiley-Liss, Inc.). SCOTT, W. B. & M. G. SCOTT, 1988. Atlantic fishes of Canada. Canadian Bull. Fish. aquat. Sci., 219: 1-731. WILLIAMS, E. H., Jr., & L. BUNKLEY-WILLIAMS, 1994. Four cases of unusual crustacean-fish associations and comments on parasitic processes. Journ. aquat. Anim. Health, 6: 202-208. EVIDENCE FOR THE DISPLACEMENT OF GAMMARUS DUEBENII BY GAMMARUS PULEX (AMPHIPODA) IN A FRESHWATER SITE IN BRITTANY, FRANCE BY ALISON M. DUNN Department of Pure and Applied Biology, University of Leeds, Leeds LS2 9JT, U.K. Populations of Gammarus duebenii Liljeborg, 1852 have been reported from fresh water in a number of sites in Britain and Western France (Hynes, 1954; Pinkster et al., 1970). However, G. duebenii is rarely present in sympatry with Gammarus pulex (Linnaeus, 1758) and it has been suggested that G. duebenii is displaced by G. pulex in fresh water localities. It has been proposed that G. duebenii is displaced due to competition with G. pulex for resources (Kinne, 1959; Pinkster et al., 1970) and the superior reproductive rate of G. pulex (cf. Hynes, 1955); and that G. duebenii is driven extinct due to predation by G. pulex upon recently moulted congeners (Dick et al., 1993). Here I present evidence that G. duebenii has been displaced by G. pulex in a freshwater site in Brittany. Pinkster et al. (1970) studied the distribution of G. duebenii and G. pulex in 364 sites in Brittany and found that G. duebenii was predominant in Western Brit- tany, but that G. pulex predominated further East. A narrow zone of overlap was recorded. In this zone G. duebenii had been forced back by G. pulex and was confined to the upper reaches of the streams. In only four ( 1 %) sites were both G. duebenii and G. pulex found in sympatry. In two of these sites only G. duebenii</p>
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