The phylogenies of all eight European species of Philaenus were estimated from cytochrome oxidase subunit I, cytochrome B and internal transcribed spacer 2 (ITS2) fragments of DNA using phylogenetic reconstruction methods: maximum parsimony (MP), maximum likelihood (ML) and Bayesian inference (BI) analyses. Based on the topologies of all obtained phylogenetic trees, the monophyly of Philaenus is well supported, being congruent with morphological, ecological and chromosomal data. Three phylogenetic lineages were distinguished in the mitochondrial and combined (mtDNA with ITS2) trees. The first lineage is represented by only one species, Philaenus maghresignus, which inhabits Maghreb and southern Spain. Clade A includes three species: P. tarifa (Southern Iberia), P. italosignus (Sicily and Southern Italy) and P. signatus (the Balkans and Middle East). In clade B two subclades were recognized: B1 represented by P. loukasi (Southern Balkans) and P. arslani (Middle East), and B2 comprising P. spumarus (the most widespread Palaearctic species) and P. tesselatus (from Southern Iberia and Maghreb). These clades were also retrieved in trees reconstructed from nuclear sequences. However, four species (P. maghresignus, P. tarifa, P. italosignus and P. signatus) showed unresolved polytomy at the base of the nuclear tree. Clade A together with P. maghresignus clustered with the 'signatus' group defined from morphology, and clade B with the 'spumarius' group; these might be considered separate subgenera. Genetic distances in mitochondrial DNA between ingroup species ranged from 14.0% between P. signatus and P. spumarius to 2.4% between P. tesselatus and P. spumarius. By contrast, genetic divergence of ITS2 between ingroup species was very low, at most 2.1%. The divergence of Philaenus species is estimated to have occcurred between 7.9 and 0.6 Ma. Possibly three main speciation events occurred: the first at the Miocene/Pliocene boundary (c. 5.5 Ma) for deeper splits; the second between 4.2 and 2.5 Ma in the Pliocene, when pairs of more closely related species diverged; and the most recent during the Pleistocene glaciations, when the separation of P. tesselatus and P. spumarius took place. The species status of all Philaenus species is confirmed except for P. tesselatus.
Abstract. Cicada orni L. is one of the most abundant and common species of cicada in Greece. However, this species was not found during recent field work on the Greek islands of Samos and Ikaria. Instead, the very closely related C. mordoganensis Boulard was found practically everywhere on these islands. C. orni and C. mordoganensis are very closely related species which are morphologi cally very similar (sibling species), even the male genitalia, and the acoustic signals produced by males during courtship and pair formation have the same general pattern. In order to describe the acoustic signals produced by these sibling species, temporal and spectral analyses were made of the calling songs of the males and certain acoustic variables were measured. Based on the duration of echemes, the number of pulse units they contain, the intervals between echemes and the number of echemes per second, the song of C. mordoganensis is distinct from that of C. orni. Cluster analysis of the acoustic characteristics of C. mordoganensis from Samos and Ikaria and of C. orni from the Greek mainland (Dionysos, north of Athens) gave a clear and distinct separation of these species.Moreover, as there has been very little divergence between these two species at the protein electrophoretic level, the acoustic divergence has evolved independently of allozyme divergence. This may imply that in these cicadas acoustic divergence, and there fore premating isolation, may have evolved rapidly and resulted in rapid speciation at low levels of general genetic differentiation.
Populations of the Tenus Philaenus were collected during the last 12 years at several places in Greece ranging in altitude from sea level to 2000 m. Within some of these populations the species P. spumarius (Linnaeus, 1758), which is widely distributed in Greece, and the Mediterranean species P. signatus (Melichar, 1896) occurred together. These two species can be easily distinguished by the size of the adults, and more precisely by internal genital structures. Surprisingly, some mountainous populations of P. spumarius also contained a new species. Externally the new species closely resembled P. spumarius, hut careful examination of the male genitalia provided clear identification characteristics. Thv new species comprised one bisexual common colour morph similar to populi of P. spumarius and P. signalus and two rare unisexual morphs which are lacking both in P. spumarius and P. signatus. The new species occurred only at altitudes above 1200 m on Eryngium spp.
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