Am. J. Bot. Join the BSA
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 Supplemental Data
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 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 (12)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Collin, C. L.
Right arrow Articles by Shykoff, J. A.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Collin, C. L.
Right arrow Articles by Shykoff, J. A.
Agricola
Right arrow Articles by Collin, C. L.
Right arrow Articles by Shykoff, J. A.
(American Journal of Botany. 2003;90:579-585.)
© 2003 Botanical Society of America, Inc.


Reproductive Biology

Outcrossing rates in the gynomonoecious-gynodioecious species Dianthus sylvestris (Caryophyllaceae)1

Carine L. Collin2 and Jacqui A. Shykoff

Laboratoire d'Écologie, Systématique et Évolution, CNRS UPRESA 8079, Université de Paris-Sud (XI), Bâtiment 360, F-91405 Orsay Cedex, France

Some species described as gynodioecious are truly gynomonoecious-gynodioecious. Three distinct phenotypes may be found in their natural populations—female and hermaphrodite pure-sexed plants bearing either only pistillate or perfect flowers, respectively, and mixed plants bearing both types of flowers. In one such species, Dianthus sylvestris, we investigated mating system parameters using allozyme data. Outcrossing rates and correlations of outcrossed paternity were calculated for the three types of plants and separately for pistillate and perfect flowers on mixed plants. The mean outcrossing rate for the population was tm ± SD = 0.885 ± 0.032. Females were more outcrossed than hermaphrodites (0.987 ± 0.112 and 0.790 ± 0.076, respectively), whereas mixed plants were not significantly more or less outcrossed than hermaphrodites (0.840 ± 0.060). Within mixed plants, perfect flowers showed an intermediate outcrossing rate (0.898 ± 0.057), whereas pistillate flowers were as selfed as perfect flowers on hermaphrodite plants (0.782 ± 0.111). Family estimates of outcrossing rates were highly variable. Globally, no biparental inbreeding was detected in this species, and there was a mean of 61.5 ± 19.9% of full-sibs within families. Floral dimorphism between small pistillate and large perfect flowers together with pollinator preference for larger flowers could explain the observed patterns for both mating parameters. The advantages of gynomonoecy-gynodioecy are discussed. We conclude that mixed plants do not reduce selfing for all flowers on a plant, but perfect flowers on these plants seem to have an outcrossing advantage.

Key Words: biparental inbreeding • correlations of outcrossed paternity • geitonogamy • gynomonoecy-gynodioecy • selfing




This article has been cited by other articles:


Home page
ANN BOT (LOND)Home page
T. R. Meagher
Linking the Evolution of Gender Variation to Floral Development
Ann. Bot., August 1, 2007; 100(2): 165 - 176.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Bot.Home page
S.-M. Chang
Gender-specific inbreeding depression in a gynodioecious plant, Geranium maculatum (Geraniaceae)
Am. J. Botany, July 1, 2007; 94(7): 1193 - 1204.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2003 by the Botanical Society of America, Inc.