Skip Navigation

This Article
Right arrow Full Text (PDF)
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 Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by McDonald, D. B.
Right arrow Search for Related Content
PubMed
Right arrow Articles by McDonald, D. B.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 1993 International Society for Behavioral Ecology

research-article

Demographic consequences of sexual selection in the long-tailed manakin

David B. McDonald

Archbold Biological Station,PO Box 2057,Lake Placid, FL 33852, USA

ABSTRACT

Demographic divergence between the sexes is a major consequence of sexual selection. Matrix-based demographic measures, including the sensitivity and elasticity of {lambda} (population growth rate, fitness) to survival and fertility rates are powerful indexes of intersexual divergence. Many morphological, behavioral, and ecological differences distinguish males and females in lekking long-tailed manakins (Chiroxiphia linearis), and none is more dramatic than the demographic divergence. Only 16 of 142 (8%) banded males copulated during an 8-year period. The mean estimated age of male copulators was 10.1 years (SD = 2.2), and only 5 of 166 copulations were by males less double equals8 years old. Females probably begin reproduction at age 1 or 2. The reproductive value curve reached a peak of 15.0 for 12th-year males, versus 2.7 for sixth-year females. The matrix-based elasticity of X to survival rates was greater in males (91% of total elasticity) than in females (80% of total). In a literature-based, interspecific comparison, the difference in elasticity to survival between the male and female manakins (91–80=11; ranks 2 and 9 of 16 species/sex combinations) was greater than that between the sexes in northern elephant seals (90–84=6; ranks 3 and 8), which have the highest variance of male mating success documented for mammals; red deer (88–87=1; ranks 4 and 5); Galapagos cactus finches (79–74=5; ranks 10 and 12); and acorn woodpeckers (76–74=2; ranks 11 and 13). In the face of continuing debate over appropriate measures of sexual selection, matrix-based demographic techniques facilitate quantitative, comparative analyses of the life-history consequences of sexual selection. Measures of intersexual demographic divergence may provide insights into heretofore puzzling instances of sexual selection in species with little dimorphism in size or ornament.

Key words: age structure, comparative demography, delayed production, elasticity, life history, mankin, Pipridae, re-productivevalue, sensitive analysis, sexual selection[Behav Ecol 4:297–309 (1993)].


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
Behav EcolHome page
J. M. Trainer, D. B. McDonald, and W. A. Learn
The development of coordinated singing in cooperatively displaying long-tailed manakins
Behav. Ecol., January 1, 2002; 13(1): 65 - 69.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
D. McDonald and W. Potts
Cooperative display and relatedness among males in a lek-mating bird
Science, November 11, 1994; 266(5187): 1030 - 1032.
[Abstract] [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.