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254                        CALOGERO MUSCARELLA & ALESSANDRO BARAGONA




                 by relating the number of endemic species with the  due to the sea depth in this coastal area), so that
                 area of the islands (Linear function model data: y  even the colonization of scarcely vagile insects, as
                 =0.1608x + 8.9845; R = 0.3209; Pearson correlation  the Tenebrionids, was made easier in these periods
                 index r = 0.54, see figure 8).               (Fattorini, 2001). This way, species belonging to
                   Also,  no  relations  seem  to  exist  between  the  groups with a high tendency to speciation have had
                 number of endemic species and the geological struc-  the  possibility  to  reach  the Aeolian  islands  and
                 ture of the islands (volcanic or sedimentary). Alicudi  rapidly differentiate (Fattorini, 2011). This might
                 and Favignana, for instance, show the same number  be the case of the disderid spiders, present in Lipari
                 of endemic taxa (6) but they are characterised by a  with  two  endemic  taxa  -  Harpactea  aeoliensis
                 profoundly different lithology (see figure 6).  Alicata, 1973 and Dysdera flagellifera aeoliensis
                   The complex paleogeographic history (see fur-  Alicata, 1973 (Alicata, 1973); of the Curculionid
                 ther on) of the circum-sicilian islands, together with  Beetles Otiorhynchus (Arammichnus) meligunensis
                 the dispersive features typical of every taxa, seem  Magnano, 1992 and Pseudomeira aeolica Bellò,
                 to have been the most incisive factors determining  Pesarini et Pierotti, 1997; of the Blattaria, present
                 the endemic population, and it does not seem pos-  with three exclusive species (Ectobius aeoliensis
                 sible to hypothesize a unique colonisation and spe-  Failla et Messina, 1974, E. filicensis Failla et Mess-
                 ciation model. Quite certainly, the different islands  ina, 1974 ed E. parvosacculatus Failla et Messina,
                 (or at least the different archipelagoes), have had  1974) or of the gastropods of the Oxychilus type
                 different population means, whose vicariantist and  Fitzinger, 1833, O. (Hyalocornea) alicurensis (Ben-
                 dispersalist models overlap.                 oit, 1857) of Alicudi and O. (Oxychilus) lagrecai
                                                              Giusti, 1973 of Filicudi. A likely hypothesis to ex-
                 Considerations on the endemic populations    plain the genesis of some endemic species recon-
                 and  paleogeography  of  the  circum-sicilian  nects to the high degree of environmental instability
                 islands                                      typical of the Aeolian islands: continuous eruptions
                                                              allegedly determined the nullification of the present
                 Aeolian Archipelago                          fauna, repeatedly causing “bottleneck” effects, trig-
                                                              gering and quickening the birth of many of the en-
                   The  Aeolian  Islands  are  of  relatively  recent  demic species present on these islands (Lo Cascio
                 formation:  the  most  reliable  radiometric  dating  & Navarra, 2003; Fattorini, 2009; Lo Cascio &
                 estimate that the archipelago formed approximately  Sparacio, 2010). This might as well be the origin of
                 1.3 million years ago (in reference to the disap-  some taxa such as Anoxia (Mesanoxia) matutinalis
                 peared apparatuses), while the most ancient rocks  moltonii Sabatinelli, 1976, exclusive of Vulcano but
                 above sea level, present in Filicudi, date back to  present with the nominal subspecies in the nearby
                 about 600,000 years ago (De Rosa et al., 2004;  Lipari and Salina, Anthaxia (Haplantaxia) flaviae
                 Lucchi et al., 2013). They are separate from Sicily  Lo Cascio et Sparacio, 2010 known for Panarea,
                 by a sea area which is up to 2000 m. deep and have  Salina and Lipari but sympatric in the latter with the
                 always been isolated, even during the marine re-  akin A. (Haplantaxia) scutellaris Genè, 1839 prob-
                 gressions in Pleistocene. Considering the relatively  ably for a process of “double invasion” (Lo Cascio
                 young age of the archipelago, the high number of  & Sparacio, 2010) and especially the Lacertid Podar-
                 endemic species found today (30) and its relative  cis raffoneae (Mertens, 1952) and its subspecies. In
                 faunistic richness are surprising (cf. Lo Cascio &  particular, for P. raffoneae, it would be otherwise
                 Navarra, 2003). Based on this interpretative model,  difficult to explain the supposed “antiquity”, con-
                 the entire Aeolian fauna should be of recent ac-  sidering that the molecular clocks that have been
                 quisition as entirely formed by propagules of high  used for the datations confer it an age between 2
                 vagility species which rapidly differentiated on the  and 13 million years, well before the formation of
                 spot thanks to the well known phenomena of the  the “present” Aeolian islands (see Lo Cascio &
                 “bottleneck” and the “founder effect”. We should  Navarra, 2003). Its current distribution, limited to
                 as well consider that during the phases of marine  a few peripheral islets and Vulcano, is interpreted
                 regression the distance between Sicily and these is-  as relictual in the field of an original area which
                 lands was undoubtedly shorter (though not annulled  probably involved the whole archipelago; the most
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