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76                                               Gianmarco Ingrosso et al.


          and Cladocora caespitosa (Linnaeus, 1767), live in shallow water and are
          obligatorily or facultative zooxanthellate, i.e., they may harbour microalgal
          endosymbionts that are known to enhance coral calcification (Schuhmacher,
          1984 and references therein).
             The bioconstructions of C. caespitosa are the best known (Fig. 3B). This
          species, endemic to the Mediterranean Sea, exhibits growth rates that may
                          1
          exceed 5mmyear    (Peirano et al., 1999) and calcification rates that average
          1.1–1.7kg CaCO 3 m  2  year  1  (Rodolfo-Metalpa et al., 1999), which is com-
          parable to values of many tropical reef corals (Peirano et al., 2001). The col-
          onies of C. caespitosa, obligatorily zooxanthellate, are common throughout
          the Mediterranean on rocks and pebbles about 3–30m depth, often in turbid
          water (Bianchi, 2009). When abundant, C. caespitosa may typically occur in
          two distinct formations: beds and banks (Morri et al., 2000b). Beds are com-
          posed by numerous small (10–30cm in diameter) subspherical colonies in
          dense populations. Banks are made up of large colonies, reaching several dec-
          imetres in height and covering areas of several square metres. Banks originate
          from beds under conditions of undisturbed accretion by means of three mech-
          anisms: (i) fusion of adjacent colonies; (ii) “pouring” of the build-up due to
          gravity; and (iii) inclusion of satellite colonies (Peiranoetal.,1998). Mixed
          distributions of beds and banks can also be found, while a third formation
          has been recently described: free-living coral nodules or coralliths (Kersting
          et al., 2017a,b).
             Banks are the most important bioconstructions of C. caespitosa and may
          deserve to be called reefs. They harbour a rich associated biota comprising
          several phyla (Antoniadou and Chintiroglou, 2010; Koukouras et al., 1998;
          Lumare, 1966), but no species seems exclusive to this habitat (Bianchi,
          2009). In the Gulf of Trieste (North Adriatic Sea), Pitacco et al. (2014) esti-
          mated 89 infauna taxa associated with C. caespitosa and the most abundant
          were molluscs (50%), followed by polychaetes (20%) and crustaceans
          (7%). Along the Italian coast (Fig. 3D), banks have been described in the
          Gulf of Manfredonia (Colantoni and Gallignani, 1975), the Ionian Sea
          (Lumare, 1966), the Ligurian Sea (Morri et al., 1994b) and the Gulf of
          Trieste (Pitacco et al., 2014; Zunino et al., 2018).

          2.2.5 Vermetid Reefs
          Vermetids are sessile and gregarious prosobranch gastropods of the family
          Vermetidae, widely distributed in the warm southern waters of the Medi-
          terranean Sea (Keen, 1961), where their reefs or platforms are built up by
          a complex of four cryptic species, all previously named Dendropoma petraeum
          (Monterosato, 1884) (Fig. 4A). Templado et al. (2016) split the old taxon
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