Host range evolution in a selected group of osmiine bees (Hymenoptera: Megachilidae): the Boraginaceae-Fabaceae paradox
Version of Record online: 25 OCT 2012
© 2012 The Linnean Society of London
Biological Journal of the Linnean Society
Volume 108, Issue 1, pages 35–54, January 2013
How to Cite
Sedivy, C., Dorn, S., Widmer, A. and Müller, A. (2013), Host range evolution in a selected group of osmiine bees (Hymenoptera: Megachilidae): the Boraginaceae-Fabaceae paradox. Biological Journal of the Linnean Society, 108: 35–54. doi: 10.1111/j.1095-8312.2012.02013.x
- Issue online: 17 DEC 2012
- Version of Record online: 25 OCT 2012
- Manuscript Revised: 9 JUL 2012
- Manuscript Accepted: 9 JUL 2012
- Manuscript Received: 31 MAY 2012
Additional Supporting Information may be found in the online version of this article:
Figure S1. Phylogeny of bee species of the Annosmia-Hoplitis group. Parsimony bootstrap consensus tree with bootstrap values.
Figure S2. Phylogeny of bee species of the Annosmia-Hoplitis group. Maximum likelihood tree with bootstrap values. All nodes with bootstrap values of less than 50% were collapsed.
Table S1. Collection localities, voucher numbers and GenBank accession numbers of the bee species of the Annosmia-Hoplitis group included in the phylogeny. The names of the authors of the study are given by initials. Voucher specimens are deposited in the Entomological Collection of the ETH Zurich. ALG, Algeria; CYP, Cyprus; FRA, France; GRE, Greece; ITA, Italy; IRI, Iran; ISR, Israel and Palestine; JOR, Jordan; MAR, Morocco; OMA, Oman; POR, Portugal; SUI, Switzerland; SYR, Syria; TUN, Tunisia; TUR, Turkey; UEA, United Arab Emirates; USA, United States of America.
Table S2. Primers used and reaction conditions applied for the five genetic markers used in this study.
Please note: Wiley Blackwell is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.