“…Although the evolutionary hypotheses on the ovary position in Melastomataceae are scarce (see Soltis et al, 2003), the ontogenetic model presented here for the origin and variation of the gynoecial hypanthium gives support to explain the existence of disparate conditions, even between close groups. For example, we can mention the predominance of superior ovaries in Merianieae (Michelangeli et al, 2015) and Microlicieae (except Lavoisiera ; Almeda and Martins, 2001; Fritsch et al, 2004), which are sister groups of clades that predominantly have inferior ovaries, Miconieae (Mendoza and Ramírez, 2006) and Rhexieae (Eyde and Teeri, 1967), respectively. This same development model could be taken as a starting point to investigate similar variations in other Myrtales, which also exhibit lability in the ovary position (Dahlgren and Thorne, 1984), such as Crypteroniaceae (Renner, 2007), Lythraceae (Graham and Graham, 2014), Myrtaceae (Schmid, 1980; Wilson, 2011), and Penaeaceae (Schönenberger and Conti, 2003).…”