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EMPAFISH Booklet no. 1 Ecological <strong>effects</strong> <strong>of</strong> Atlanto-Mediterranean MPAs in the EU<br />

mortality <strong>of</strong> P. lividus, the high intensity <strong>of</strong> fishing in un<strong>protected</strong> <strong>areas</strong> would<br />

explain the patterns observed. Additionally, Sala & Zabala (1996) showed that<br />

the population structure <strong>of</strong> this species is determined by fish predation within<br />

the <strong>protected</strong> area <strong>of</strong> the MIMR, while recruitment success determines the<br />

population structure in un<strong>protected</strong> <strong>areas</strong>.<br />

� Fish movement (including spillover)<br />

As in the other MPAs selected as case studies within the CE <strong>project</strong> BIOMEX<br />

(http://biomex.univ-perp.fr), studies have been undertaken to test the<br />

hypothesis that spillover from MPAs to neighbouring <strong>areas</strong> should have as a<br />

consequence the observation <strong>of</strong> gradients <strong>of</strong> fish biomass across boundaries.<br />

In Medes, this hypothesis is going to be tested by using UVC, baited video,<br />

and collection <strong>of</strong> fish eggs and larvae by plankton nets as sampling<br />

techniques, following a sampling design including several sites inside the MPA<br />

plus other sites outside the MPA (to the North). Results <strong>of</strong> these studies are<br />

being analysed at present.<br />

� Other biological (e.g. density-dependent) <strong>effects</strong><br />

Natural mortality (M) rates were determined for five common species (Coris<br />

julis, Diplodus annularis, Diplodus sargus, Serranus cabrilla and Symphodus<br />

roissali) by UVC in the MIMR (Macpherson et al. 2000). This study showed low<br />

variability <strong>of</strong> M at seasonal and interannual scales. The mortality rates were<br />

not affected by a “reserve effect”, i.e. they were not significantly different<br />

between the <strong>protected</strong> and un<strong>protected</strong> study sites <strong>of</strong> the MIMR. This finding<br />

was explained by the higher abundance <strong>of</strong> piscivorous predators in the<br />

<strong>protected</strong> <strong>areas</strong>, which are the main cause <strong>of</strong> natural mortality in fishes.<br />

Macpherson et al. (1997) evidenced a density-dependent effect on mortality<br />

from settlement to recruitment to the adult population in three species <strong>of</strong><br />

sparid fishes, Diplodus puntazzo, D. sargus and D. vulgaris. This densitydependent<br />

effect on mortality <strong>of</strong> settlers explained the low variability in yearclass<br />

strength for the three species studies. Additionally, this study showed<br />

that mortality rates did not differ significantly in <strong>protected</strong> and un<strong>protected</strong><br />

<strong>areas</strong> <strong>of</strong> the MIMR, suggesting that <strong>marine</strong> reserves are not necessarily a sink<br />

for post-settlement fishes.<br />

The MIMR has also allowed for interesting studies on the reproduction and<br />

territoriality <strong>of</strong> the dusky grouper Epinephelus marginatus, scarce elsewhere<br />

in the Mediterranean (Zabala et al. 1997a, b). These authors reported the first<br />

observations on reproductive behaviour in this species by scuba diving<br />

surveys in 1996. This study also showed that Oblada melanura preys strongly<br />

on recently spawned eggs, suggesting that high densities <strong>of</strong> this sparid fish<br />

may undermine the reproductive success <strong>of</strong> the dusky grouper in the MIMR.<br />

� Effects on habitat (including impact <strong>of</strong> divers)<br />

MIMR receives ca. 60,000 divers per year, concentrated between April and<br />

September. Most divers visit the same diving places where buoys are located<br />

and maintained by the Park Service. The diving spots represent ca. 10% <strong>of</strong><br />

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