Am. J. Bot. Tips for Better Browsing
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
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 (22)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Doligez, A.
Right arrow Articles by Joly, H. I.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Doligez, A.
Right arrow Articles by Joly, H. I.
Agricola
Right arrow Articles by Doligez, A.
Right arrow Articles by Joly, H. I.

American Journal of Botany, Vol 84, 461, Copyright © 1997 by Botanical Society of America, Inc.


REPRODUCTIVE BIOLOGY

Mating system of Carapa procera (Meliaceae) in the french guiana tropical forest

A Doligez and HI Joly

The mating system of the tropical rainforest tree Carapa procera was studied for a population located within a sylvicultural trial in French Guiana. We used the mixed-mating model with the genotypes of 47 open-pollinated progenies at ten polymorphic loci, obtained through isozyme analysis. Seeds were collected on both logged and unlogged (control) plots, which were interspersed. A high multilocus outcrossing rate (0.78) was found for the global population. and there was indirect evidence for nonrandom mating for outcrosses. It is argued that this may be due to some kind of positive assortative mating, probably biparental inbreeding. Correlation of selfing between sibs was not significantly different from zero. and the proportion of full-sibs among outcrossed sib-pairs was significant but low (0.16). We found significant differences between outcrossing rates when computing separate estimates for the 14 trees located on logged plots (tm = 0.63) and the 33 trees located on undisturbed plots (tm = 0.85). It is argued that the decrease in density is probably not the only cause of the decrease in outcrossing rate on logged plots. Lastly, several points concerning the reliability of the estimation are outlined. In particular. the downward bias due to ignoring null alleles during genetic interpretations of zymograms is quantified in a few cases by simulating artificial populations.


This article has been cited by other articles:


Home page
J HeredHome page
J. F. Fernandez-M. and V. L. Sork
Mating Patterns of a Subdivided Population of the Andean Oak (Quercus humboldtii Bonpl., Fagaceae)
J. Hered., November 1, 2005; 96(6): 635 - 643.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Bot.Home page
S.-L. Lee, K. K.-S. Ng, L.-G. Saw, A. Norwati, M. H. S. Salwana, C.-T. Lee, and M. Norwati
Population genetics of Intsia palembanica (Leguminosae) and genetic conservation of Virgin Jungle Reserves in Peninsular Malaysia
Am. J. Botany, March 1, 2002; 89(3): 447 - 459.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Bot.Home page
O. J. Rocha and G. Aguilar
Variation in the breeding behavior of the dry forest tree Enterolobium cyclocarpum (guanacaste) in Costa Rica
Am. J. Botany, September 1, 2001; 88(9): 1600 - 1606.
[Abstract] [Full Text]


Home page
GeneticsHome page
R. G. Shaw, D. L. Byers, and F. H. Shaw
Genetic Components of Variation in Nemophila menziesii Undergoing Inbreeding: Morphology and Flowering Time
Genetics, December 1, 1998; 150(4): 1649 - 1661.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1997 by the Botanical Society of America, Inc.