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        316                              C. Brugnano et al. / Journal of Marine Systems 81 (2010) 312–322
















































        Fig. 4. Principal component analysis performed on log-transformed and normalised chemical–physical parameter data set (temperature, salinity, chlorophyll a and dissolved
        oxygen).

        Clausocalanus arcuicornis (6.9%), Corycaeus typicus (6.3%), and  40–150 m, H. longicornis in the layer 100–200 m, and P. gracilis in the
        Ctenocalanus vanus (5.6%). Group III included mostly intermediate  layer 150–300 m (Fig. 8B, C, D).
        species with abundance maxima recorded in the pelagic system; eight  All the other species, not belonging to the above-said groups,
        species accounted for 64.9% of similarity in this group: Corycaeus  generally, occurred in deeper waters with scarce abundances with re-
        furcifer (12.4%), Lucicutia flavicornis (11.4%), Pleuromamma gracilis  spect to the others, such as S. dentata, Neocalanus gracilis, P. abdominalis,
        (10.7%), Haloptilus longicornis (6.0%), Oncaea mediterranea (6.0%),  Lucicutia longicornis, Clausocalanus paululus, Clausocalanus pergens,
        Oithona atlantica (5.7%), C. vanus (5.4%) and C. typicus (5.4%). In group  Eucalanus crassus, Lubbockia squillimana, Corycaeus flaccus, Lucicutia
        IV, seven species accounted for 63.61% of similarity: P. gracilis (16.3%),  clausi. Their mean abundances in these layers are shown in Table 3.
        C. furcifer (12.5%), L. flavicornis (9.9%), P. abdominalis (8.0%), Oncaea
        conifera (6.5%), Scolecithricella dentata (6.5%) and O. atlantica (3.9%).  4. Discussion
          Four main copepod assemblages were identified by cluster
        analysis at 46% of similarity level (Fig. 7): group A included Acartia  The θ–S profiles show that the hydrological status of the area
        clausi, with a wider horizontal distribution range extended from  around the Egadi Archipelago can be seen as a crossroad of eastern
        coastal to pelagic surface areas, than Acartia adriatica and Isias clavipes  and western waters in the Mediterranean. According to Sparnocchia
        occurring only along the coastal area in front of Sicily; group B, in  et al. (1999), at the entrance of the Western Mediterranean Basin, just
        which there are the dominant species, C. furcatus, A. negligens,  after crossing the section Sicily–Tunisia, the eastern outflow of LIW
        T. stylifera, that showed decreasing abundances from inshore to  presents a core salinity of 38.77–38.78. This signature was found from
        offshore stations, and O. plumifera, more or less uniformly widespread  300 m depth to the bottom in stations 10 and 12. Two branches of
        in coastal neritic and pelagic surface waters (Table 2); group C,  MAW flow at the surface towards the eastern Mediterranean and
        constituted by C. typicus, C. arcuicornis, C. jobei, N. minor and  cross the Sicily–Tunisia section (Astraldi et al., 1999), where the
        Calocalanus pavo, occurring mostly in neritic and pelagic subsurface  presence of MAW is characterized by a high seasonal variability. In
        waters (Table 3; Fig. 8A, E); group D, mostly composed of those  late summer, the smaller stream along the southern Sicilian shelf
        species that had a broad vertical distribution, ranging from the surface  presents a subsurface core characterized by a minimum of salinity of
        to great depth. Among these, Heterorhabdus papilliger, O. atlantica  37.3 located at about 40 m depth (Sorgente et al., 2003). Our findings
        and O. conifera were generally more abundant in the layer between  are in agreement with this feature and put in evidence a more pelagic
        40 and 80 m, L. flavicornis, C. furcifer and O. mediterranea in the layer  character of the stations on the western side of Marettimo (DCM
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