Am. J. Bot. Visit Plant Cell Online
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow An erratum has been published
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (41)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Clausing, G.
Right arrow Articles by Renner, S. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Clausing, G.
Right arrow Articles by Renner, S. S.
Agricola
Right arrow Articles by Clausing, G.
Right arrow Articles by Renner, S. S.
(American Journal of Botany. 2001;88:486-498.)
© 2001 Botanical Society of America, Inc.

Molecular phylogenetics of Melastomataceae and Memecylaceae: implications for character evolution1

G. Clausing 2, 4 and S. S. Renner 3, 4

2Institut für Spezielle Botanik, Universität Mainz, D-55099 Mainz, Germany; 3Department of Biology, University of Missouri-St. Louis, 8001 Natural Bridge Rd., St. Louis, Missouri 63121 USA; and The Missouri Botanical Garden, St. Louis, Missouri 63166 USA

Melastomataceae are among the most abundant and diversified groups of plants throughout the tropics, but their intrafamily relationships and morphological evolution are poorly understood. Here we report the results of parsimony and maximum likelihood (ML) analyses of cpDNA sequences from the rbcL and ndhF genes and the rpl16 intron, generated for eight outgroups (Crypteroniaceae, Alzateaceae, Rhynchocalycaceae, Oliniaceae, Penaeaceae, Myrtaceae, and Onagraceae) and 54 species of melastomes. The sample represents 42 of the family's currently recognized ~150 genera, the 13 traditional tribes, and the three subfamilies, Astronioideae, Melastomatoideae, and Memecyloideae (= Memecylaceae DC.). Parsimony and ML yield congruent topologies that place Memecylaceae as sister to Melastomataceae. Pternandra, a Southeast Asian genus of 15 species of which five were sampled, is the first- branching Melastomataceae. This placement has low bootstrap support (72%), but agrees with morphological treatments that placed Pternandra in Melastomatacaeae because of its acrodromal leaf venation, usually ranked as a tribe or subfamily. The interxylary phloem islands found in Memecylaceae and Pternandra, but not most other Melastomataceae, likely evolved in parallel because Pternandra resembles Melastomataceae in its other wood characters. A newly discovered plesiomorphic character in Pternandra, also present in Memecylaceae, is a fibrous anther endothecium. Higher Melastomataceae lack an endothecium as do the closest relatives of Melastomataceae and Memecylaceae. The next deepest split is between Astronieae, with anthers opening by slits, and all remaining Melastomataceae, which have anthers opening by pores. Within the latter, several generic groups, corresponding to traditional tribes, receive solid statistical support, but relationships among them, with one exception, are different from anything predicted on the basis of morphological data. Thus, Miconieae and Merianieae are sister groups, and both are sister to a trichotomy of Bertolonieae, Microlicieae + Melastomeae, and Dissochaeteae + Blakeeae. Sonerileae/Oxysporeae are nested within Dissochaeteae, Rhexieae within Melastomeae, and African and Asian Melastomeae within neotropical Melastomeae. These findings have profound implications for our understanding of melastome morphological evolution (and biogeography), implying, for example, that berries evolved from capsules minimally four times, stamen connectives went from dorsally enlarged to basal/ventrally enlarged, and loss of an endothecium preceded poricidal dehiscence.

Key Words: endothecium • Melastomataceae • Memecylaceae • Myrtales • ndhF • phylogeny • rbcLrpl16




This article has been cited by other articles:


Home page
ANN BOT (LOND)Home page
T. ABE
Threatened Pollination Systems in Native Flora of the Ogasawara (Bonin) Islands
Ann. Bot., August 1, 2006; 98(2): 317 - 334.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
C. Lohne and T. Borsch
Molecular Evolution and Phylogenetic Utility of the petD Group II Intron: A Case Study in Basal Angiosperms
Mol. Biol. Evol., February 1, 2005; 22(2): 317 - 332.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Bot.Home page
S. S. Renner
Bayesian analysis of combined chloroplast loci, using multiple calibrations, supports the recent arrival of Melastomataceae in Africa and Madagascar
Am. J. Botany, September 1, 2004; 91(9): 1427 - 1435.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Bot.Home page
W. S. Judd and R. G. Olmstead
A survey of tricolpate (eudicot) phylogenetic relationships
Am. J. Botany, September 1, 2004; 91(10): 1627 - 1644.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Bot.Home page
P. W. Fritsch, F. Almeda, S. S. Renner, A. B. Martins, and B. C. Cruz
Phylogeny and circumscription of the near-endemic Brazilian tribe Microlicieae (Melastomataceae)
Am. J. Botany, July 1, 2004; 91(7): 1105 - 1114.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Bot.Home page
J. Schonenberger and E. Conti
Molecular phylogeny and floral evolution of Penaeaceae, Oliniaceae, Rhynchocalycaceae, and Alzateaceae (Myrtales)
Am. J. Botany, February 1, 2003; 90(2): 293 - 309.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Bot.Home page
J. C. Hall, K. J. Sytsma, and H. H. Iltis
Phylogeny of Capparaceae and Brassicaceae based on chloroplast sequence data
Am. J. Botany, November 1, 2002; 89(11): 1826 - 1842.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Bot.Home page
S. A. Kelchner
Group II introns as phylogenetic tools: structure, function, and evolutionary constraints
Am. J. Botany, October 1, 2002; 89(10): 1651 - 1669.
[Abstract] [Full Text] [PDF]


Home page
ANN BOT (LOND)Home page
S. JANSEN, T. WATANABE, and E. SMETS
Aluminium Accumulation in Leaves of 127 Species in Melastomataceae, with Comments on the Order Myrtales
Ann. Bot., July 1, 2002; 90(1): 53 - 64.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Bot.Home page
S. S. Renner, G. Clausing, and K. Meyer
Historical biogeography of Melastomataceae: the roles of Tertiary migration and long-distance dispersal
Am. J. Botany, July 1, 2001; 88(7): 1290 - 1300.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2001 by the Botanical Society of America, Inc.