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Mediterranean Bioconstructions Along the Italian Coast        87


              leading to a quick growth of these bioherms. However, the accumulation rates
                                            1
              appeared low (0.006–0.83mmyear ), oscillating greatly with different depths
              and time periods (Ballesteros, 2006; Garrabou and Ballesteros, 2000; Sartoretto
                                                                            1
              et al., 1996; Teixido ´ et al., 2011). The highest rates (0.20–0.83mmyear )
              were recorded between 8000 and 5000 years BP. In more recent times, appre-
              ciable radiocarbon accumulation rates of 0.11–0.42mmyear  1  have been
              recorded only for bioherms growing in relatively shallow waters (10–35m
              depth) (Bertolino et al., 2013), while an average growth rate of about
                          1
              0.15mmyear   was measured on coralligenous pillars from the Ionian Sea
              (Bertolino et al., 2017b), a rate comparable with that recorded by Di
                                                              1
              Geronimo et al. (2002) for similar pillars (0.27mmyear ) in the southern
              Ionian Sea. Radiocarbon dating in bioherms from different localities of the
              Ligurian Sea indicated average growth rates ranging from of 0.03 to
              0.05mmyear  1  over 3000 years (Bertolino et al., 2013). In some cases, the
              growth of the bioherms showed an incoherent and chaotic temporal growth
              pattern (Bertolinoetal.,2017a), with older layers overlapping younger ones.
              This phenomenon could be related to favourable periods for carbonate
              deposition, alternating with partial destruction phases due, for example, to
              intense mud deposition after episodes of intense floods (Fig. 8).
                 In the northern Adriatic continental shelf, biogenic frameworks are
              generally superimposed on hard bottoms of still debated origin. Marine
              sediments may be consolidated by methane-related calcium carbonate
              cementation, thanks to seepage of CH 4 -rich fluids, observable near many
              offshore reefs (Gordini et al., 2012). Meandering-shaped morphologies
              and the distributions of many reefs, especially those off Chioggia, suggest
              the importance of Pleistocenic rivers, Holocene tidal channels and beach
              bars which are initial substrate for current coralligenous build-ups. The
              lithification of these sandy palaeochannels is estimated to have started from
              7000 years BP, likely due to the interaction between marine and less saline
              fluids related to onshore freshwater discharge at sea through a sealed water
              table (Tosi et al., 2017).
                 Sabellaria bioconstructions, which are formed from tubes made by sand
              grains, are mostly ephemeral. They strictly depend on the balance between
              bottom sediment features and water movement, supplying sand and particles
              for tube building and growth. Sabellaria larvae show preferential settlement
              either onto living bioconstructions or onto their ruins, so ensuring reef
              persistence and recovery. Hence, the age of these bioconstruction greatly
              exceeds the age of the living worms, since the reef may repeatedly
              follow a cyclical progression of settlement, growth and destruction phases
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