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This study investigated the spatial distribution of Tetramicra brevifilum spores in the musculature of infected turbot Scophthalmus maximus, with the aim of identifying the most appropriate body locations for diagnostic assays. A PCR protocol optimized for the detection of T. brevifilum spores in turbot muscle is also described. In fish showing low- and moderate-intensity infection, the spatial distribution of spores was best fitted by a negative binomial distribution, indicating a clumped spatial pattern; the negative binomial coefficient k was lower for fish with low-intensity infection, indicating a more markedly clumped pattern in these fish. In fish with high-intensity infection, the spatial distribution of spores was best fitted by the Poisson distribution, indicating a random pattern. In both low- and moderate-intensity infection, spores were present at highest density in the musculature adjoining the dorsal fins. Samples for PCR were therefore obtained from this location. PCR amplification was of the small subunit ribosomal DNA (SSUrDNA), using a pair of species-specific primers that amplify the 1250 bp product. The PCR protocol developed showed better sensitivity than microscopical techniques (detection rate by microscopy 25%, versus 42% by PCR), suggesting that it may be useful for routine screening for Tetramicra brevifilum infection in cultured turbot.

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A parasitological study of rays captured on the Atlantic continental shelf off the estuary Muros-Noia in NW Spain (42°35' to 42°41' N, 9°2' to 9°10' W; mean capture depth 11.6 ± 4.1 m) was performed. A total of 128 rays were examined: 52 specimens of Raja microocellata, 60 of R. brachyura, 6 of R. montagui, 3 of R. undulata and 7 of an unidentified Raja species, known locally as 'fancheca'. A total of 23 macroparasite species were detected: 5 monogeneans (Acanthocotyle sp., Calicotyle kroyeri, Empruthotrema raiae, Merizocotyle undulata, Rajonchocotyle emarginata), 11 cestodes (Acanthobothrium sp., Crossobothrium sp., Echeneibothrium sp., Echinobothrium brachysoma, Grillotia erinaceus, Grillotia sp., Lecanicephalum sp., Nybelinia lingualis, Onchobothrium uncinatum, Phyllobothrium lactuca, Tritaphros retzii), 6 nematodes (Anisakis simplex, Hysterothylacium sp., Histodytes microocellatus, Piscicapillaria freemani, Proleptus sp., Pseudanisakis baylisi) and a copepod (Holobomolochus sp.). All parasite species were present in several ray species, except for Acanthocotyle sp. and G. erinaceus (detected only in R. brachyura), H. microocellatus (detected only in R. microocellata) and T. retzii (detected only in R. montagui). Three species (C. kroyeri, M. undulata, E. brachysoma) have not been reported previously from Spain. The host with the highest parasite species richness was R. brachyura (18 species), followed by R. microocellata (17) and the unidentified Raja species (14). The parasite with the highest prevalence in R. microocellata was M. undulata, followed by R. emarginata, Acanthobothrium sp. and Echeneibothrium sp. The species with the highest prevalence in R. brachyura was R. emarginata, followed by C. kroyeri and P. baylisi. Some differences in parasite prevalence were detected between sexes and among size classes in both R. brachyura and R. microocellata.KEY WORDS: Raja spp. · Monogenea · Cestoda · Nematoda · Copepoda · Galicia (NW Spain) Resale or republication not permitted without written consent of the publisherDis Aquat Org 70: [93][94][95][96][97][98][99][100] 2006 MATERIALS AND METHODSWe examined 52 specimens of Raja microocellata, 60 of R. brachyura, 6 of R. montagui, 3 of R. undulata and 7 of an unidentified Raja species called 'fancheca' by local fishermen. At least 10 specimens were captured and examined per month between March 1999 and March 2000. All captures were from the Atlantic continental shelf off the mouth of the estuary of MurosNoia, in an area situated at 42°35' to 42°41' N, 9°2' to 9°10' W. Mean capture depth was 11.6 ± 4.1 m. All specimens were captured with a traditional local fishing apparatus called a 'trasmallo ' or 'miño' (Rivas Lago 1996). Fish were transferred to the laboratory in refrigerated containers, and examined after storage at 4°C for 2 nights or less.Before dissection, rays were measured and weighed. The following organs and tissues were examined under a stereomicroscope for helminths and crustacean parasites: skin, nasal fossae, gills, heart, digestive ...

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