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ISRAEL JOURNAL OF PLANT SCIENCES  49

             deliberately omitted from it the morphologically unfit-  Table 1. Source of sampled populations (taxonomy following
                                                                Domina et al. 2016).
             ting C. parlatoris. The complex in that cladogram
                                                                                   Elevation (m  Coordinates (WGS84,
             appears as sister to a clade of three taxa: C. aeolica  Taxon and populations  a.s.l.)  decimal degrees)
             Lojac. subsp. aeolica (Eolian Islands), C. aeolica subsp.  Centaurea busambarensis
                                                                 1. Busambra          1300   37.854759 N, 13.415954 E


             pandataria (Fiori & B eg.) Anzal. (Ventotene, Pontian


                                                                 2. Kumeta            930    37.970513 N, 13.256235 E

             Islands of Latium), and C. papposa (Cape Bon in Tuni-  3. Pizzuta        1030   37.997086 N, 13.246412 E

                                                                 4. Isnello, al castello  570  37.945732 N, 14.005906 E


             sia). Together, these two clades are nested within C.
             cineraria L. (coasts of Latium and Basilicata, peninsular  C. erycina
                                                                 5. Erice             720    38.035189 N, 12.591671 E


             Italy).
               However, the recent survey of the “Centaurea      C. panormitana subsp.
                                                                  panormitana
             group” (C. sect. Centaurea)byHilpold et al.(2014),  6. Punta Mastrangelo  850   38.064298 N, 13.243363 E



                                                                 7. Pizzolungo        40     38.063512 N, 12.570256 E

             based on DNA sequence data and a much extended


                                                                 8. Monte Pellegrino, S  150  38.153465 N, 13.360442 E
             sampling of taxa from other areas, resulted in a poorly  slope


                                                                 9. Monte Pecoraro    750    38.162269 N, 13.123313 E
             resolved tree that partly contradicts the earlier phylo-  10. Favignana, Monte  100  37.920730 N, 12.307299 E


             genetic hypothesis. At present, relationships within C.  Santa Caterina
             sect. Centaurea are better considered as poorly under-  C. panormitana subsp.
             stood. The molecular data, while supporting the      umbrosa
                                                                 11. Monte Gallo      500    38.218151 N, 13.311306 E


             assumption of widespread hybridization, correlate bet-  12. Monte Pellegrino, N  200  38.187822 N, 13.335711 E


             ter with geographical distribution patterns than with  slope

                                                                 13. Monte Grifone    250    38.071647 N, 13.370249 E

             morphology. These findings support our approach of
                                                                 C. panormitana subsp.
             considering, in the first place, diversity and diversifica-
                                                                  todaroi
             tion within geographically defined boundaries.       14. Mongerbino       30     38.110688 N, 13.538341 E



                                                                 15. Monte Catalfano  100    38.114900 N, 13.513798 E

               The Centaurea busambarensis complex on the
             whole shows pronounced character variation, both    C. panormitana subsp.
                                                                  seguenzae
             within and between populations, so that the delimita-  16. Capo Tindari  20     38.137394 N, 15.052898 E


             tion of its constituent taxa is often uncertain (Giardina
                                                                 C. saccensis
             et al. 2007). We therefore undertook to complement  17. Gole della Tardara  130  37.614346 N, 13.052547 E


             the studies done up to now (Raimondo & Bancheva
             2004; Raimondo et al. 2004; Palla et al. 2005; Bancheva  conditions, to observe intra-populational variability and
             et al. 2006; Geraci et al. 2007) by sampling wild popu-  interactions between morphology and environment.
             lations and using statistical methods to analyze their  Eleven populations of taxa attributed to the four
             morphological variation patterns, so as to clarify their  subspecies of Centaurea panormitana were compared
             taxonomic status. In the process, we paid particular  with six populations of the other taxa of the C. busam-
             attention to plants from the island of Favignana (Egadi  barensis complex (see Table 1 and Figure 1).
             Archipelago, W Sicily), which show pronounced mor-   As recommended by Guarino and Rampone (2006),
             phological differences when compared with popula-  we used the original descriptions of the taxa involved
             tions of the other taxa described and named so far.  to draw up a list of characters of potential diagnostic
                                                                usefulness. A total of 26 characters were used: 19 con-
             Material and methods                               tinuous quantitative, four discrete quantitative and
                                                                three qualitative.
             The specimens used for statistical analysis were newly
             collected throughout the geographical range of the
                                                                Nineteen continuous quantitative characters (mm)
             Centaurea busambarensis complex. For each popula-
             tion, 10 measurements were taken for each quantita-  1. Whole plant, height
             tive character from each of at least 10 different plants  2. Rosette leaves, length
             (see Electronic Supplement 1, supplemental material).  3. Rosette leaves, width
             Voucher specimens were deposited in PAL and FI. Her-  4. Lower stem leaves, length
             barium studies were complemented with observation  5. Lower stem leaves, width
             in the field and cultivation in uniform environmental  6. Upper stem leaves, length
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