Page 6 - Palombo_Ferretti _2005
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ARTICLE IN PRESS
          112                   M.R. Palombo, M.P. Ferretti / Quaternary International 126–128 (2005) 107–136

          difference between the Italian fossil form and the extant  Azzaroli (in Ambrosetti et al., 1972) erected this new
          Asian elephants and attributed the Upper Valdarno    taxon on an almost complete skeleton from Madonna
          specimens to ‘‘E.’’ primigenius, described a few years  della Strada near Scoppito (L’Aquila, Abruzzi; Mac-
          earlier by Blumenbach (1799). In 1825, however, after  cagno, 1962a; CLA). He then assigned to this subspecies
          the discovery of some complete skulls from the Upper  also specimens collected in sandy deposits near Farneta
          Valdarno, Nesti was able to prove that the fossil    (Chiana Valley, Tuscany). The material from Farneta
          elephant occurring in the Upper Valdarno sediments   (IGF) includes two fragmented skulls, isolated molars,
          was, actually, different from the species described by  post-cranials and a partial skeleton belonging to an old
          Blumenbach. Given its more southern distribution with  individual. According to Azzaroli (1977a), derived
          respect to the then known range of the woolly        characters possessed by M. m. vestinus are:a larger
          mammoth, Nesti (1825) named the new Italian species  overall size (the shoulder height of the type specimen
          ‘‘E.’’ meridionalis. The M. meridionalis sample from the  from Scoppito is 3750 mm) compared with M. meridio-
          Upper Valdarno includes some skeletons, several skulls  nalis from Upper Valdarno (the shoulder height of a
          and mandibles and hundreds of isolated molars and    male skeleton from Upper Valdarno is 3350 mm), and a
          post-cranials (IGF, MPM, MPB, NHMB). Thorough        more advanced cranial morphology (Fig. 4). The skull is
          descriptions of this material are provided by Weithofer  shorter and deeper, with very long tusk sheaths. The
          (1893), Azzaroli (1966, 1977a), and Ferretti (1998,  cranium is higher with its vertex more caudally
          1999).                                               displaced. The forehead is extremely concave. The tusks
            The type material of M. meridionalis pertains to the  are larger, but similar in shape to those of M.
          second lacustrine sequence (Montevarchi) of the Upper  meridionalis from Upper Valdarno. A recent revision
          Valdarno Plio-Pleistocene succession (Albianelli et al.,  of the material ascribed to this subspecies demonstrated,
          1995; Magi et al., 1992). Fossil vertebrates have been  on the other hand, that M. m. vestinus does not differ
          retrieved from various levels along the Montevarchi  from the type form from Upper Valdarno in its dental
          sequence, and have been grouped into two distinct    characters (Ferretti, 1999). This makes discrimination
          faunal assemblages, based on faunal turnover (see    between the two taxa very difficult, if skulls are not
          below):the older Matassino Fauna and the Tasso       available. Indeed, given the low number of complete and
          Fauna (Azzaroli, 1977a, b; Azzaroli et al., 1988; Gliozzi  undeformed late Villafranchian M. meridionalis skulls at
          et al,. 1997). Most of the M. meridionalis specimens from  hand, and considering the variability of extant ele-
          Upper Valdarno belong to old museum collections, and  phants’ skull morphology (Beden, 1979; Deraniyagala,
          no precise stratigraphic data are known. Nevertheless,  1955), the validity of vestinus, as a separate sub-species
          the material as a whole is quite homogeneous. Indeed, a  from typical M. meridionalis, should be considered with
          statistical analysis of two selected samples that included  caution.
          specimens with known provenance failed to reveal any   At Pietrafitta, Perugia, a locality broadly coeval with
          significant metric differences between the Matassino and  Scoppito and Farneta (Ambrosetti et al., 1987, 1992),
          Tasso mammoth material (Ferretti, 1998). Descriptive  numerous complete skeletons of M. meridionalis have
          statistics for upper and lower second and third molars  been retrieved (CET). Unfortunately, skulls are crushed
          (M2–m2; M3–m3) of M. meridionalis from Upper         and deformed. The molars from Pietrafitta do not show
          Valdarno (Matassino and Tasso faunas pooled sample)  any clear advancement with respect to the Upper
          are given in Table 3.                                Valdarno sample (Figs. 3c and d; Table 4). Isolated
            Following Azzaroli (1977a), late Italian populations  mammoth teeth from other Italian localities referable to
          of southern mammoth, approximately dated between     the same time interval, such as Mugello (Tuscany;
          1.5 and 0.8 Ma, are generally considered as more derived  Abbazzi et al., 1995; IGF), Redicicoli (Rome; MPR),
          than the typical form from Upper Valdarno and        Torrente Crostolo (Reggio Emilia; Ambrosetti and
          included into a separate subspecies, M. m. vestinus.  Cremaschi, 1976; MSNRE), and Leffe lower level



          Table 3
          Summary statistics of dental variables of second and third molars of M. meridionalis from Upper Valdarno (‘Matassino’ and Tasso faunas), Italy
          Tooth Length     Width (W)   Height (H)  Plates a    Enamel thickness  Lamellar frequency b  Hypsodonty index (H/W)
               N Mean Range  N Mean Range N Mean Range  N Mean Range N  Mean  Range  N  Mean  Range  N  Mean  Range
          M2   13 212  175–243 15 89  80–103 11 120  103–148 17 9  8–10  17  2.7  2.2–3.4  6  5.0  4.5–6.0  11  1.40  1.00–1.60
          m2   2  204  200–209 3  83  82–86  2  103  102–104 3  9  9–10  3  2.8  2.7–2.9  3  5.5  5.5–6.5  3  1.30  1.00–1.60
          M3   21 269  226–343 29 101  83–123 27 131  101–160 33 13  11–14 33  3.2  2.6–3.9  36  5.0  4.0–6.0  13  1.30  1.10–1.60
          m3   16 282  236–350 12 91  81–113 12 112  91–140  19 13  12–14 19  3.0  2.4–3.7  10  5.0  4.5–6.0  6  1.30  1.20–1.30
            a
            Excluding talons.
            b
            According to Maglio (1973).
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