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Proceedings of the Second Mediterranean Symposium on Marine

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PROCEEDINGS OF THE SECOND MEDITERRANEAN SYMPOSIUM ON MARINE VEGETATION (ATHENS, 12-13 DECEMBER 2003)<br />

194<br />

Six samplings were carried out between<br />

summer 1998 and spring 2002 (August 98,<br />

March 99, June 99, June 01, September 01 and<br />

March 02) in order to m<strong>on</strong>itor <str<strong>on</strong>g>the</str<strong>on</strong>g> marine<br />

benthic vegetati<strong>on</strong> characteristics. The sampling<br />

was destructive (1 random sample from a<br />

permanent stati<strong>on</strong>-square 5 x 5 m per sampling<br />

period) <strong>on</strong> a quadrate 20cm x 20cm, which is<br />

c<strong>on</strong>sidered to be <str<strong>on</strong>g>the</str<strong>on</strong>g> minimal sampling area in<br />

<str<strong>on</strong>g>the</str<strong>on</strong>g> case <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> <str<strong>on</strong>g>Mediterranean</str<strong>on</strong>g> infralittoral<br />

communities.<br />

Phytobenthos community structure was<br />

analyzed in terms <str<strong>on</strong>g>of</str<strong>on</strong>g> species number, total<br />

coverage, Shann<strong>on</strong>-Weaver diversity (H’, log2<br />

basis) and Pielou evenness (J’) indices.<br />

Fig. 1: The study area<br />

The Ecological Evaluati<strong>on</strong> Index (EEI) was calculated according to Orfanidis et al. (2001),<br />

described also <strong>on</strong> <str<strong>on</strong>g>the</str<strong>on</strong>g> site: www.fishri.gr (Laboratories / <strong>Marine</strong> Ecology / Water quality).<br />

The EEI is an original metric for <str<strong>on</strong>g>the</str<strong>on</strong>g> ecological status evaluati<strong>on</strong> based <strong>on</strong> <str<strong>on</strong>g>the</str<strong>on</strong>g> c<strong>on</strong>cept <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

morphological and functi<strong>on</strong>al groups (Littler and Littler 1980; 1984). The species were<br />

divided in two Ecological State Groups (ESG):<br />

In <str<strong>on</strong>g>the</str<strong>on</strong>g> ESG I were grouped <str<strong>on</strong>g>the</str<strong>on</strong>g> thick lea<str<strong>on</strong>g>the</str<strong>on</strong>g>ry, <str<strong>on</strong>g>the</str<strong>on</strong>g> articulate upright calcareous and <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

crustose calcareous species. Most <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g>m are k-selected species. In <str<strong>on</strong>g>the</str<strong>on</strong>g> ESG II were<br />

grouped <str<strong>on</strong>g>the</str<strong>on</strong>g> foliose, <str<strong>on</strong>g>the</str<strong>on</strong>g> filamentous and <str<strong>on</strong>g>the</str<strong>on</strong>g> coarsely branched upright species. Most <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

<str<strong>on</strong>g>the</str<strong>on</strong>g>m are r-selected species.<br />

Each sampling stati<strong>on</strong> was classified in <strong>on</strong>e <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> five classes <str<strong>on</strong>g>of</str<strong>on</strong>g> ES after a simple crosscomparis<strong>on</strong><br />

<str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> coverage value <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

ESG I and <str<strong>on</strong>g>the</str<strong>on</strong>g> ESG II <strong>on</strong> a matrix (Fig. 2). The<br />

numerical scoring system was used to<br />

express <str<strong>on</strong>g>the</str<strong>on</strong>g> category <str<strong>on</strong>g>of</str<strong>on</strong>g> ecological status as<br />

a number (Bad=2, Low=4, Moderate=6,<br />

Good=8 and High=10).<br />

RESULTS<br />

In total 60 taxa were identified (12<br />

Chlorophyceae, 16 Phaeophyceae and 32<br />

Rhodophyceae). At all <str<strong>on</strong>g>the</str<strong>on</strong>g> studied stati<strong>on</strong>s<br />

<str<strong>on</strong>g>the</str<strong>on</strong>g> Rhodophyceae were qualitatively<br />

Fig. 2: Matrix for <str<strong>on</strong>g>the</str<strong>on</strong>g> evaluati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> ESC<br />

dominant and <str<strong>on</strong>g>the</str<strong>on</strong>g> Phaeophyceae were<br />

quantitatively dominant (Table 1).<br />

The canopy layer <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> vegetati<strong>on</strong> was well developed at Stati<strong>on</strong>s 1, 4, 5 and 6, mainly<br />

due to <str<strong>on</strong>g>the</str<strong>on</strong>g> presence <str<strong>on</strong>g>of</str<strong>on</strong>g> Cystoseira species. O<str<strong>on</strong>g>the</str<strong>on</strong>g>r species, e.g. Dictyopteris<br />

membranacea, formed a pseudo-canopy layer when <str<strong>on</strong>g>the</str<strong>on</strong>g>y were massively present. A<br />

well-developed bushy layer, composed mainly by Jania rubens, Laurencia optusa,

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