Aw. Meerow et al., Systematics of Amaryllidaceae based on cladistic analysis of plastid rbcL and trnL-F sequence data, AM J BOTANY, 86(9), 1999, pp. 1325-1345
Cladistic analyses of plastid DNA sequences rDcL and trnL-F are presented s
eparately and combined for 48 genera of Amaryllidaceae and 29 genera of rel
ated asparagalean families. The combined analysis is the most highly resolv
ed of the three and provides good support for the monophyly of Amaryllidace
ae and indicates Agapanthaceae as its sister family. Alliaceae are in turn
sister to the Amaryllidaceae/Agapanthaceae clade. The origins of the family
appear to be western Gondwanaland (Africa), and infrafamilial relationship
s are resolved along biogeographic lines. Tribe Amaryllideae, primarily Sou
th African, is sister to the rest of Amaryllidaceae; this tribe is supporte
d by numerous morphological synapomorphies as well. The remaining two Afric
an tribes of the family, Haemantheae and Cyrtantheae, are well supported, b
ut their position relative to the Australasian Calostemmateae and a large c
lade comprising the Eurasian and American genera, is not yet clear The Eura
sian and American elements of the family are each monophyletic sister clade
s. Internal resolution of the Eurasian clade only partially supports curren
tly accepted tribal concepts, and few conclusions can be drawn on the relat
ionships of the genera based on these data. A monophyletic Lycorideae (Cent
ral and East Asian) is weakly supported. Galanthus and Leucojum (Galantheae
pro parte) are supported as sister genera by the bootstrap. The American c
lade shows a higher degree of internal resolution. Hippeastreae (minus Grif
finia and Worsleya) are well supported, and Zephyranthinae are resolved as
a distinct subtribe. An Andean clade marked by a chromosome number of 2n =
46 (and derivatives thereof) is resolved with weak support. The plastid DNA
phylogenies are discussed in the context of biogeography and character evo
lution in the family.