Skip Navigation

Systematic Biology 2004 53(2):309-326; doi:10.1080/10635150490423737
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
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 Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (45)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Danforth, B. N.
Right arrow Articles by Pearson, A.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Danforth, B. N.
Right arrow Articles by Pearson, A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 2004 Society of Systematic Biologists

Single-Copy Nuclear Genes Recover Cretaceous-Age Divergences in Bees

Bryan N. Danforth, Seán G. Brady1, Sedonia D. Sipes2 and Adam Pearson

Department of Entomology, Comstock Hall, Cornell University Ithaca New York 14853, USA; E-mail: bnd1{at}cornell.edu (B.N.D.)

Edited by Ted Schultz: Associate Editor


   Abstract

We analyzed the higher level phylogeny of the bee family Halictidae based on the coding regions of three single-copy nuclear genes (long-wavelength [LW] opsin, wingless, and elongation factor 1-{alpha} [EF-1{alpha}]). Our combined data set consisted of 2,234 aligned nucleotide sites (702 base pairs [bp] for LW opsin, 405 bp for wingless, and 1,127 bp for EF-1{alpha}) and 779 parsimony-informative sites. We included 58 species of halictid bees from 33 genera, representing all subfamilies and tribes, and rooted the trees using seven outgroups from other bee families: Colletidae, Andrenidae, Melittidae, and Apidae. We analyzed the separate and combined data sets by a variety of methods, including equal weights parsimony, maximum likelihood, and Bayesian methods. Analysis of the combined data set produced a strong phylogenetic signal with high bootstrap and Bremer support and high posterior probability well into the base of the tree. The phylogeny recovered the monophyly of the Halictidae and of all four subfamilies and both tribes, recovered relationships among the subfamilies and tribes congruent with morphology, and provided robust support for the relationships among the numerous genera in the tribe Halictini, sensu Michener (2000). Using our combined nucleotide data set, several recently described halictid fossils from the Oligocene and Eocene, and recently developed Bayesian methods, we estimated the antiquity of major clades within the family. Our results indicate that each of the four subfamilies arose well before the Cretaceous–Tertiary boundary and suggest that the early radiation of halictid bees involved substantial African–South American interchange roughly coincident with the separation of these two continents in the late Cretaceous. This combination of single-copy nuclear genes is capable of recovering Cretaceous-age divergences in bees with high levels of support. We propose that LW opsin, wingless, and EF-1{alpha} (F2 copy) may be useful in resolving relationships among bee families and other Cretaceous-age insect lineages.

Keywords: Bayesian methods; biogeography; molecular evolution; phylogeny

Received June 17, 2003; Revised August 31, 2003; Accepted November 4, 2003


1 Present address: Department of Entomology, National Museum of Natural History, Smithsonian Institution Washington, D.C. 20560, USA; E-mail: sbrady{at}lab.si.edu

2 Present address: Department of Plant Biology, Southern Illinois University Carbondale, Illinois 62901–6509, USA; E-mail: ssipes{at}plant.siu.edu


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
ScienceHome page
A. L. Toth, K. Varala, T. C. Newman, F. E. Miguez, S. K. Hutchison, D. A. Willoughby, J. F. Simons, M. Egholm, J. H. Hunt, M. E. Hudson, et al.
Wasp Gene Expression Supports an Evolutionary Link Between Maternal Behavior and Eusociality
Science, October 19, 2007; 318(5849): 441 - 444.
[Abstract] [Full Text] [PDF]


Home page
Syst BiolHome page
J. Hughes, M. Kennedy, K. P. Johnson, R. L. Palma, and R. D. M. Page
Multiple Cophylogenetic Analyses Reveal Frequent Cospeciation between Pelecaniform Birds and Pectinopygus Lice
Syst Biol, April 1, 2007; 56(2): 232 - 251.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
B. N. Danforth, S. Sipes, J. Fang, and S. G. Brady
The history of early bee diversification based on five genes plus morphology
PNAS, October 10, 2006; 103(41): 15118 - 15123.
[Abstract] [Full Text] [PDF]


Home page
Proc R Soc BHome page
S. G Brady, S. Sipes, A. Pearson, and B. N Danforth
Recent and simultaneous origins of eusociality in halictid bees
Proc R Soc B, July 7, 2006; 273(1594): 1643 - 1649.
[Abstract] [Full Text] [PDF]


Home page
Syst BiolHome page
M. P. Schwarz, S. Fuller, S. M. Tierney, and S. J. B. Cooper
Molecular Phylogenetics of the Exoneurine Allodapine Bees Reveal an Ancient and Puzzling Dispersal from Africa to Australia
Syst Biol, February 1, 2006; 55(1): 31 - 45.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.