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Tomasello, Di Maida, Calvo, Pirrotta, Borra & Procaccini Seagrass meadows at the extreme of environmental tolerance
Stagnone inner waters, surely plays an additional role in their help in the laboratory. Thanks to Elio Biffali, Elvira
determining stressful environmental conditions. Mauriello and the Molecular Biology Service of SZN for
their assistance during the microsatellite analysis. We
How can the high genetic and genotypic diversity found thank Wiebe Kooistra for the constructive comments.
within the lagoon be explained considering the genetic Finally, we would like to thank the anonymous reviewers
isolation and the absence of recent reproductive events in who significantly contributed to improve the manuscript.
the innermost area of the lagoon? First, the genetic diver-
sity of P. oceanica meadows is generally high in the whole References
geographic area where the Stagnone is located (i.e. South-
ern Tyrrhenian Sea and Sicily Strait). Values recorded in Agnesi V., Macaluso T., Orru` P., Ulzega A. (1993) Paleogeog-
our study are comparable to previous results from mead- rafia dell’arcipelago delle Egadi (Sicilia) nel Pleistocene
ows along the southern Sicilian and Tunisian coasts sup.-olocene. Naturalista Siciliano, S. IV, XVII(1-2), 3–22.
(Arnaud-Haond et al. 2007b), where flowering and seeds
washed ashore have been observed more frequently than Alberto F., Mata L., Santos R. (2001) Genetic homogeneity in
in the rest of the basin (Calvo et al. 2006). The presence the seagrass Cymodocea nodosa at its Northern Atlantic limit
of multiple genotypes in each of the atolls and the rela- revealed through RAPD. Marine Ecology Progress Series, 221,
tively high genetic diversity in the Atolls area could result 299–301.
from a high ancestral diversity in the lagoon. Influx of
genotypes into the lagoon, which may have been frequent Alberto F., Correia L., Arnaud-Haond S., Billot C., Duarte
in the past, has diminished to almost nothing in recent C.M., Serra˜o E. (2003) New microsatellite markers for the
times, due to an almost complete closure of the northern endemic Mediterranean seagrass Posidonia oceanica. Molecu-
entrance (Agnesi et al. 1993). This hypothesis is also sup- lar Ecology Notes, 3, 253–255.
ported by recent findings of banquette formed by fruits of
P. oceanica, which were probably able to enter the lagoon Arnaud-Haond S., Belkhir K. (2007) GENCLONE 1.0: a new
in the past from outside its northern opening (Calvo et al. program to analyse genetics data on clonal organisms.
1995). Reduction in gene flow between the lagoon and the Molecular Ecology Notes, 7, 15–17.
open sea may have led to genetic drift. The harsher envi-
ronmental conditions may have also favored the selection Arnaud-Haond S., Alberto F., Teixeira S., Procaccini G., Serra˜o
of a reduced number of genotypes which were able to E., Duarte C.M. (2005) Assessing genetic diversity in clonal
cope with the extreme temperature and salinity conditions organisms: low diversity or low resolution? Combining
of this area. The excess of heterozygosity present in this power and cost efficiency in selecting markers. Journal of
area could support the existence of selection, through the Heredity, 96, 434–440.
advantage of heterozygous genotypes, although replicated
genotypes did not have a larger number of heterozygous Arnaud-Haond S., Duarte C.M., Alberto F., Serra˜o E. (2007a)
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In light of these results, we can conclude that the
P. oceanica atoll-like structures within the Stagnone di Arnaud-Haond S., Migliaccio M., Diaz-Almela E., Teixeira S.,
Marsala lagoon are composed of multiple genotypes. Vliet M., Alberto F., Procaccini G., Duarte C.M., Serra˜o E.
Although the worst scenario would have been if atolls (2007b) Vicariance patterns in the Mediterranean Sea: east–
were composed of a single genotype, the genetic isolation, west cleavage and low dispersal in the endemic seagrass Posi-
lack of flowering and low growth performances are a cause donia oceanica. Journal of Biogeography, 34(6), 963–976.
for concern, threatening the survival of the species in this
area. The P. oceanica population living in the northern Ashton P.J., Mitchell D.S. (1989) Aquatic plants: patterns and
basin of the lagoon under extreme environmental condi- modes of invasion, attributes of invading species and assess-
tions could serve as an experimental model for what might ment of control programs. In: Drake J.A., Mooney H.A., Di
happen under predicted environmental changes in the Castri F., Groves R.H., Kruger F.J., Rejma`nek M., William-
whole of the Mediterranean as a result of global warming. son M.H. (Eds), Biological Invasions: A Global Perspective.
John Wiley & Sons Ltd, London, UK: 111–154.
Acknowledgements
Belkhir K., Borsa P., Chikhi L., Raufaste N., Bonhomme F.
We thank Luciano Fici, Filippo Luzzu, Alessandro Todaro (1996–2002) GENETIX, Logiciel Sous WindowsÔ Pour la
and Antonino Scannavino for their support in field activi- Genetique des Populations. Laboratoire Ge´nome et Popula-
ties, Carmelina Bellavia, Cesare Costantini, Ivan Blanch, tions, CNRS UPR 9060. Universite´ de Montpellier II, Mont-
Emauela Dattolo, Marianna Migliaccio and Ilia Serra for pellier (France).
Billingham M.R., Thorsten B.H.R., Alberto F., Serra˜o E.A.
(2003) Is asexual reproduction more important at geograph-
ical limits? A genetic study of the Seagrass Zostera marina in
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Se´diments actuels et Holoce`nes. La mer Pe´lagienne, ´etude
Marine Ecology 30 (2009) 288–300 ª 2009 Blackwell Verlag GmbH 297