Phylogenetics of the hamamelidae and their allies:: Parsimony analyses of nucleotide sequences of the plastid gene rbcL

被引:75
作者
Qiu, YL
Chase, MW
Hoot, SB
Conti, E
Crane, PR
Sytsma, KJ
Parks, CR
机构
[1] Univ N Carolina, Dept Biol, Chapel Hill, NC 27599 USA
[2] Field Museum, Dept Geol, Chicago, IL 60605 USA
[3] Univ Wisconsin, Dept Bot, Madison, WI 53706 USA
关键词
D O I
10.1086/297611
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Over the past decade it has become increasingly clear that the angiosperm subclass Hamamelidae is polyphyletic. To examine phylogenetic affinities of various lineages in the complex and to evaluate the positions of lower hamamelids in angiosperm phylogeny, we performed a parsimony analysis using nucleotide sequences of the plastid gene rbcL from 134 species, including representatives of 25 families that have traditionally been placed in the Hamamelidae; most rosid families; and selected members of the caryophyllids, asterids, monocots, and magnoliids. Platanaceae, Eupteleaceae, Tetracentraceae, Trochodendraceae, Buxaceae, Didymeleaceae, and Myrothamnaceae occupy basal positions in the eudicots, together with Ranunculales-Papaverales, Nelumbonaceae, Proteaceae, and Gunneraceae. Cercidiphyllaceae, Daphniphyllaceae, and Hamamelidaceae are placed among basal rosids, being closely related to Paeonia and Saxifragaceae s.s. and their allies. Nothofagaceae, Fagaceae, Juglandaceae, Ticodendraceae, Myricaceae, Betulaceae, and Casuarinacae form a monophyletic group, which in some trees is embedded in a large rosid clade that includes many nitrogen-fixing species. Ulmaceae, Moraceae, Cannabaceae, Urticaceae, Cecropiaceae, and Barbeyaceae are also part of this "nitrogen-fixing clade," and they are related to Rhamnus, Elaeagnus, Dirachma, and Rosaceae. Leitneriaceae are clearly a member of Sapindales. Eucommiaceae form a clade with Aucuba and Garrya among the asterids.
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收藏
页码:891 / 905
页数:15
相关论文
共 130 条
[51]   EVOLUTIONARY TREES FROM DNA-SEQUENCES - A MAXIMUM-LIKELIHOOD APPROACH [J].
FELSENSTEIN, J .
JOURNAL OF MOLECULAR EVOLUTION, 1981, 17 (06) :368-376
[52]  
FELSENSTEIN J, 1985, EVOLUTION, V39, P783, DOI 10.1111/j.1558-5646.1985.tb00420.x
[53]   TOWARD DEFINING COURSE OF EVOLUTION - MINIMUM CHANGE FOR A SPECIFIC TREE TOPOLOGY [J].
FITCH, WM .
SYSTEMATIC ZOOLOGY, 1971, 20 (04) :406-&
[54]  
FRIIS EM, 1994, PL SYST EVOL S, V8, P31
[55]  
FRIIS EM, 1991, POLLEN SPORES, P169
[56]  
FRIIS EM, 1988, BIOL SKR DAN VID SEL, V31, P1
[57]   Sapindales: Molecular delimitation and infraordinal groups [J].
Gadek, PA ;
Fernando, ES ;
Quinn, CJ ;
Hoot, SB ;
Terrazas, T ;
Sheahan, MC ;
Chase, MW .
AMERICAN JOURNAL OF BOTANY, 1996, 83 (06) :802-811
[58]   TRICHOMES AND STOMATA, AND THEIR TAXONOMIC SIGNIFICANCE IN URTICALES [J].
GANGADHARA, M ;
INAMDAR, JA .
PLANT SYSTEMATICS AND EVOLUTION, 1977, 127 (2-3) :121-137
[59]   PHYTOCHEMICAL ASPECTS OF PHYLOGENY IN HAMAMELIDAE [J].
GIANNASI, DE .
ANNALS OF THE MISSOURI BOTANICAL GARDEN, 1986, 73 (02) :417-437
[60]   SYSTEMATIC RELATIONSHIPS OF THE SAXIFRAGALES REVEALED BY SEROLOGICAL CHARACTERISTICS OF SEED PROTEINS [J].
GRUND, C ;
JENSEN, U .
PLANT SYSTEMATICS AND EVOLUTION, 1981, 137 (1-2) :1-22