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C. Bracciali et al. / Marine Environmental Research 113 (2016) 116e123  117
          sensu Rosenweig and Lomolino, 1997; Lefebvre et al., 1997)by  was a sheltered site exposed to the north-east and characterized by
          which they are able to live along a gradient of different environ-  a gently sloping bottom and a maximum depth of 20 m. In contrast,
          mental conditions (Losos et al., 2004). Here, we used a classical  Punta Basana was situated on the southern coast, where study site
          morphometric analysis (Cheverud et al., 1983) to test whether two  is exposed to the main current of the open sea Sicilian Strait, and
          different hydrodynamics conditions elicited different expressions  characterized by a steeply sloped bottom and a maximum depth of
          in functional trait patterns in a zooplanktivorous model fish,  40 m. The hypothesis of different hydrodynamics was generated
          Chromis chromis. (Actinopterygii: Perciformes: Pomacentridae;  from the observation made at the beginning of 2007 that two sites
          Fasola et al., 1997; Guidetti, 2000), at small spatial scale (few kms).  had different water current velocities when a Valeport current
            Damselfish is an useful model for this purpose as it is a strictly  meter was kept in situ in both sites for four days in three occasions
          territorial non-migratory species (the home range is thought to be  (January, March and June 2007). This field dataset was later used to
          only few hundreds of meters from where they build their nests;  validate seasonal hydrodynamics patterns as downloaded from
          Picciulin et al., 2004) that abundantly inhabits Mediterranean  MyOcean  daily  database  (http://marine.copernicus.eu).  Field
          subtidal habitats from few meters to more than 35 m (Aguzzi et al.,  observed and satellite derived hydrodynamics data were highly
          2013). It reproduces in summer up early autumn in Southern  confident and two sites resulted to have water current velocity on
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          Mediterranean, diurnally relies on zooplankton, spends most day-  average 10.1 ± 4.9 cm s  1  and 17.2 ± 5.2 cm s , respectively in
          time for food searching at the middle column (Pinnegar et al., 2007;  Cammello Bay (hereafter LOW-HYDRO) and Punta Basana (here-
          Bracciali et al., 2012, 2014). As most zooplanktivorous fish,  after HIGH-HYDRO) (Table 1). Contextually, to test the hypothesis
          C. chromis has limited energetic reserves and need to feed contin-  that different hydrodynamics would have been able to generate
          uously (Boddeke, 1963; Charnov et al., 1976) during both larval/  different trophic conditions affecting functional and life history
          juvenile (Macpherson and Raventos, 2005) and adult (Dulcic and  traits in damselfish, experimental trophic conditions were set by
          Kraljevic, 1995) stages. Thus, local oceanographic conditions  measuring some water column variables. Water samples were
          affecting food availability may emerge as primary factors indirectly  collected through a Niskin bottle at middle water column (~10 m) to
          influencing life history of this species (Macpherson and Raventos,  measure suspended chlorophyll-a, total (TSM), inorganic (ISM) and
          2005). Here, we hypothesized that hydrodynamics at small  organic matter (POM). Once brought back to the laboratory, water
          spatial scale (at the scale of km) plays a role of effector in deter-  samples were filtered on Whatman GF-F 0.45 mm fiberglass filters
          mining both individual growth (via food encountering-energetic  and stored at  20 C. POM was estimated by ignition loss and

          costs ratio) and body shape e by affecting swimming perfor-  chlorophyll-a through the classical acetone extractive method, ac-
          mance and water column position in our Mediterranean  cording to details reported in many companion studies (e.g. Sar  a
          damselfish.                                           et al., 1999, 2003; 2011). Unfortunately, we did not collect
                                                               zooplankton at the time of this study, and then the chosen water
                                                               column variables indirectly described the amount of suspended
          2. Materials and methods                             food available for zooplanktivorous species as damselfish. Thus, we
                                                               did some assumptions to support our experimental hypothesis, as
          2.1. Study area and a-priori oceanographic contextualization  follows (i) chlorophyll-a concentration, a proxy of the phyto-
                                                               plankton biomass, can be in turn used as a proxy of trophic sub-
            The study was conducted in the Egadi Marine Protected Area, on  strates for zooplankton (e.g. ciliates; Stromberg et al., 2009) and (ii)
          the Island of Marettimo (Egadi Archipelago, western Sicily) in two  some zooplankton species, such as cladocerans and copepods being
          areas with different hydrodynamic conditions located less than  the main feeding resource to C. chromis, have similar fatty acids
          5.0 km from one another (Fig. 1). Cammello Bay on the north coast
































               Fig. 1. Location of the Island of Marettimo. The map shows the position of the LOW-HYDRO site of Cammello Bay and the HIGH-HYDRO site of Punta Bassana.
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