Demographic consequences of sexual selection in the long-tailed manakin

Demographic divergence between the sexes is a major consequence of sexual selection. Matrix-based demographic measures, including the sensitivity and elasticity of λ (population growth rate, fitness) to survival and fertility rates are powerful indexes of intersexual divergence. Many morphological,...

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Published in:Behavioral Ecology
Main Author: McDonald, David B.
Format: Text
Language:English
Published: Oxford University Press 1993
Subjects:
Online Access:http://beheco.oxfordjournals.org/cgi/content/short/4/4/297
https://doi.org/10.1093/beheco/4.4.297
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spelling fthighwire:oai:open-archive.highwire.org:beheco:4/4/297 2023-05-15T16:05:44+02:00 Demographic consequences of sexual selection in the long-tailed manakin McDonald, David B. 1993-01-01 00:00:00.0 text/html http://beheco.oxfordjournals.org/cgi/content/short/4/4/297 https://doi.org/10.1093/beheco/4.4.297 en eng Oxford University Press http://beheco.oxfordjournals.org/cgi/content/short/4/4/297 http://dx.doi.org/10.1093/beheco/4.4.297 Copyright (C) 1993, International Society for Behavioral Ecology Articles TEXT 1993 fthighwire https://doi.org/10.1093/beheco/4.4.297 2007-06-25T07:45:06Z Demographic divergence between the sexes is a major consequence of sexual selection. Matrix-based demographic measures, including the sensitivity and elasticity of λ (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 ≦8 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. Text Elephant Seals HighWire Press (Stanford University) Galapagos Behavioral Ecology 4 4 297 309
institution Open Polar
collection HighWire Press (Stanford University)
op_collection_id fthighwire
language English
topic Articles
spellingShingle Articles
McDonald, David B.
Demographic consequences of sexual selection in the long-tailed manakin
topic_facet Articles
description Demographic divergence between the sexes is a major consequence of sexual selection. Matrix-based demographic measures, including the sensitivity and elasticity of λ (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 ≦8 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.
format Text
author McDonald, David B.
author_facet McDonald, David B.
author_sort McDonald, David B.
title Demographic consequences of sexual selection in the long-tailed manakin
title_short Demographic consequences of sexual selection in the long-tailed manakin
title_full Demographic consequences of sexual selection in the long-tailed manakin
title_fullStr Demographic consequences of sexual selection in the long-tailed manakin
title_full_unstemmed Demographic consequences of sexual selection in the long-tailed manakin
title_sort demographic consequences of sexual selection in the long-tailed manakin
publisher Oxford University Press
publishDate 1993
url http://beheco.oxfordjournals.org/cgi/content/short/4/4/297
https://doi.org/10.1093/beheco/4.4.297
geographic Galapagos
geographic_facet Galapagos
genre Elephant Seals
genre_facet Elephant Seals
op_relation http://beheco.oxfordjournals.org/cgi/content/short/4/4/297
http://dx.doi.org/10.1093/beheco/4.4.297
op_rights Copyright (C) 1993, International Society for Behavioral Ecology
op_doi https://doi.org/10.1093/beheco/4.4.297
container_title Behavioral Ecology
container_volume 4
container_issue 4
container_start_page 297
op_container_end_page 309
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