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The Mediterranean coastline is a dynamic and complex system which owes its complexity to its past and present vicissitudes, e.g. complex tectonic history, climatic fluctuations, and prolonged coexistence with human activities. A plant species that is widespread in this habitat is the sea daffodil, Pancratium maritimum (Amaryllidaceae), which is a perennial clonal geophyte of the coastal sands of the Mediterranean and neighbouring areas, well adapted to the stressful conditions of sand dune environments. In this study, an integrated approach was used, combining genetic and environmental data with a niche modelling approach, aimed to investigate: (1) the effect of climate change on the geographic range of this species at different times {past (last inter-glacial, LIG; and last glacial maximum, LGM), present (CURR), near-future (FUT)} and (2) the possible influence of environmental variables on the genetic structure of this species in the current period. The genetic results show that 48 sea daffodil populations (867 specimens) display a good genetic diversity in which the marginal populations (i.e. Atlantic Sea populations) present lower values. Recent genetic signature of bottleneck was detected in few populations (8%). The molecular variation was higher within the populations (77%) and two genetic pools were well represented. Comparing the different climatic simulations in time, the global range of this plant increased, and a further extension is foreseen in the near future thanks to projections on the climate of areas currently—more temperate, where our model suggested a forecast for a climate more similar to the Mediterranean coast. A significant positive correlation was observed between the genetic distance and Precipitation of Coldest Quarter variable in current periods. Our analyses support the hypothesis that geomorphology of the Mediterranean coasts, sea currents, and climate have played significant roles in shaping the current genetic structure of the sea daffodil especially during LGM because of strong variation in coastline caused by glaciations.

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Our investigation aims to understand the genetic structure and evolutionary history of Petagnaea gussonei, an ancient and endangered species belonging to the Saniculoideae subfamily (Apiaceae). It is paleoendemic to Sicily, with a small number of populations in the Nebrodi Mountains. A\ud total of seven chloroplast microsatellite repeat loci and 12 AFLP primer combinations were used to screen 115 individuals\ud corresponding to 17 populations. The ratio of seed to pollen flow was also calculated using the modified Ennos equation. A relatively high level of genetic diversity was detected with AFLPs (e.g., 0.045\H\0.278), and a moderate variation was also found using cpSSRs (0\Hk\0.667). Two different haplotypes (B and W) were\ud identified, with five populations being monomorphic for haplotype B. There was no genetic differentiation on the basis\ud of haplotypic frequency (GST) and similarity (RST), and no phylogeographic structure was detected among the populations. AFLP values also confirmed that the populations are\ud not very genetically differentiated. The principal component analysis based on pairwise genetic differences showed three\ud groupings without a geographical correlation. The AMOVA analysis indicates that theamount of variation is higher within\ud populations (82 %) than among populations (18 %). Results of the pollen flow/seed flow ratio indicated positive values for\ud each population, indicating that gene flow by seed is not more efficient than by pollen. Instead, the total pollen/seed flow for all population presents a negative value, suggesting that pollen dispersal does not appear to be more effective over the\ud long range for gene flow than seed dispersal. This differentiation level supports the hypothesis that the fragmentation and isolation of the residual populations is in progress. This\ud phenomenon is due not only to post-ice age climate changes, but also to direct and indirect anthropic actions

In this paper, we studied the relationships of the only surviving Italian population of Ipomoea imperati (Convolvulaceae), a pantropical sandy coastal species, in Sicily and other populations in the Mediterranean region. Herbarium samples which are representative of extinct populations growing  in Campania (Italy) were also investigated together with populations from various Atlantic and Mediterranean localities. Chloroplast DNA microsatellites (cp-SSR) and nuclear ribosomal Internal Transcribed Spacer (ITS) sequences  were jointly employed, in order to detect relationships among populations. Our aims were several-fold: (1) to clarify if the species is autochthonous in the Mediterranean basin or a post-Columbian introduction; (2) to investigate phylogeographic patterns in the species and (3) to establish the possible role of dispersal in explaining the patterns observed. Chloroplast microsatellite variation indicates that extinct Italian mainland populations of I. imperati from Campania are not closely related to the extant Sicilian one, as they do not share haplotypes. Chloroplast DNA microsatellite variation is largely between populations, and the within populations component accounts for only approximately 10%. CpDNA data is consistent with a single Mediterranean entry point hypothesis or with the notion that some populations display plesiomorphic variability. ITS data is congruent with the possibility that the presence of I. imperati in the Mediterranean is the result of transatlantic dispersal. The population from Sicily and extinct populations from Campania share an ITS type. A Bayesian analysis employing clock calibration data on an expanded ITS dataset with appropriate outgroups indicates that dates of transoceanic distribution are probably earlier than historical times.

In this study, we used several molecular techniques to develop a fast and reliable protocol (DNA Verity Test, DVT) for the characterization and confirmation of the species or taxa present in herbal infusions. As a model plant for this protocol, Camellia sinensis, a traditional tea plant, was selected due to the following reasons: its historical popularity as a (healthy) beverage, its high selling value, the importation of barely recognizable raw product (i.e., crushed), and the scarcity of studies concerning adulterants or contamination. The DNA Verity Test includes both the sequencing of DNA barcoding markers and genotyping of labeled-PCR DNA barcoding fragments for each sample analyzed. This protocol (DVT) was successively applied to verify the authenticity of 32 commercial teas (simple or admixture), and the main results can be summarized as follows: (1) the DVT protocol is suitable to detect adulteration in tea matrices (contaminations or absence of certified ingredients), and the method can be exported for the study of other similar systems; (2) based on the BLAST analysis of the sequences of rbcL+matK±rps7-trnV(GAC) chloroplast markers, C. sinensis can be taxonomically characterized; (3) rps7-trnV(GAC) can be employed to discriminate C. sinensis from C. pubicosta; (4) ITS2 is not an ideal DNA barcode for tea samples, reflecting potential incomplete lineage sorting and hybridization/introgression phenomena in C. sinensis taxa; (5) the genotyping approach is an easy, inexpensive and rapid pre-screening method to detect anomalies in the tea templates using the trnH(GUG)-psbA barcoding marker; (6) two herbal companies provided no authentic products with a contaminant or without some of the listed ingredients; and (7) the leaf matrices present in some teabags could be constituted using an admixture of different C. sinensis haplotypes and/or allied species (C. pubicosta).