Effects of spontaneous mutation accumulation on sex ratio traits in a parasitoid wasp.

Sex allocation theory has proved extremely successful at predicting when individuals should adjust the sex of their offspring in response to environmental conditions. However, we know rather little about the underlying genetics of sex ratio or how genetic architecture might constrain adaptive sex-ra...

Olles dieđut

Bibliográfalaš dieđut
Váldodahkkit: Pannebakker, B, Halligan, D, Reynolds, K, Ballantyne, G, Shuker, D, Barton, N, West, SA
Materiálatiipa: Journal article
Giella:English
Almmustuhtton: 2008
_version_ 1826278770327158784
author Pannebakker, B
Halligan, D
Reynolds, K
Ballantyne, G
Shuker, D
Barton, N
West, SA
author_facet Pannebakker, B
Halligan, D
Reynolds, K
Ballantyne, G
Shuker, D
Barton, N
West, SA
author_sort Pannebakker, B
collection OXFORD
description Sex allocation theory has proved extremely successful at predicting when individuals should adjust the sex of their offspring in response to environmental conditions. However, we know rather little about the underlying genetics of sex ratio or how genetic architecture might constrain adaptive sex-ratio behavior. We examined how mutation influenced genetic variation in the sex ratios produced by the parasitoid wasp Nasonia vitripennis. In a mutation accumulation experiment, we determined the mutability of sex ratio, and compared this with the amount of genetic variation observed in natural populations. We found that the mutability (h(2)(m)) ranges from 0.001 to 0.002, similar to estimates for life-history traits in other organisms. These estimates suggest one mutation every 5-60 generations, which shift the sex ratio by approximately 0.01 (proportion males). In this and other studies, the genetic variation in N. vitripennis sex ratio ranged from 0.02 to 0.17 (broad-sense heritability, H(2)). If sex ratio is maintained by mutation-selection balance, a higher genetic variance would be expected given our mutational parameters. Instead, the observed genetic variance perhaps suggests additional selection against sex-ratio mutations with deleterious effects on other fitness traits as well as sex ratio (i.e., pleiotropy), as has been argued to be the case more generally.
first_indexed 2024-03-06T23:48:55Z
format Journal article
id oxford-uuid:71eccc93-48de-48d2-8a4c-ec3d0dccd6ab
institution University of Oxford
language English
last_indexed 2024-03-06T23:48:55Z
publishDate 2008
record_format dspace
spelling oxford-uuid:71eccc93-48de-48d2-8a4c-ec3d0dccd6ab2022-03-26T19:46:46ZEffects of spontaneous mutation accumulation on sex ratio traits in a parasitoid wasp.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:71eccc93-48de-48d2-8a4c-ec3d0dccd6abEnglishSymplectic Elements at Oxford2008Pannebakker, BHalligan, DReynolds, KBallantyne, GShuker, DBarton, NWest, SASex allocation theory has proved extremely successful at predicting when individuals should adjust the sex of their offspring in response to environmental conditions. However, we know rather little about the underlying genetics of sex ratio or how genetic architecture might constrain adaptive sex-ratio behavior. We examined how mutation influenced genetic variation in the sex ratios produced by the parasitoid wasp Nasonia vitripennis. In a mutation accumulation experiment, we determined the mutability of sex ratio, and compared this with the amount of genetic variation observed in natural populations. We found that the mutability (h(2)(m)) ranges from 0.001 to 0.002, similar to estimates for life-history traits in other organisms. These estimates suggest one mutation every 5-60 generations, which shift the sex ratio by approximately 0.01 (proportion males). In this and other studies, the genetic variation in N. vitripennis sex ratio ranged from 0.02 to 0.17 (broad-sense heritability, H(2)). If sex ratio is maintained by mutation-selection balance, a higher genetic variance would be expected given our mutational parameters. Instead, the observed genetic variance perhaps suggests additional selection against sex-ratio mutations with deleterious effects on other fitness traits as well as sex ratio (i.e., pleiotropy), as has been argued to be the case more generally.
spellingShingle Pannebakker, B
Halligan, D
Reynolds, K
Ballantyne, G
Shuker, D
Barton, N
West, SA
Effects of spontaneous mutation accumulation on sex ratio traits in a parasitoid wasp.
title Effects of spontaneous mutation accumulation on sex ratio traits in a parasitoid wasp.
title_full Effects of spontaneous mutation accumulation on sex ratio traits in a parasitoid wasp.
title_fullStr Effects of spontaneous mutation accumulation on sex ratio traits in a parasitoid wasp.
title_full_unstemmed Effects of spontaneous mutation accumulation on sex ratio traits in a parasitoid wasp.
title_short Effects of spontaneous mutation accumulation on sex ratio traits in a parasitoid wasp.
title_sort effects of spontaneous mutation accumulation on sex ratio traits in a parasitoid wasp
work_keys_str_mv AT pannebakkerb effectsofspontaneousmutationaccumulationonsexratiotraitsinaparasitoidwasp
AT halligand effectsofspontaneousmutationaccumulationonsexratiotraitsinaparasitoidwasp
AT reynoldsk effectsofspontaneousmutationaccumulationonsexratiotraitsinaparasitoidwasp
AT ballantyneg effectsofspontaneousmutationaccumulationonsexratiotraitsinaparasitoidwasp
AT shukerd effectsofspontaneousmutationaccumulationonsexratiotraitsinaparasitoidwasp
AT bartonn effectsofspontaneousmutationaccumulationonsexratiotraitsinaparasitoidwasp
AT westsa effectsofspontaneousmutationaccumulationonsexratiotraitsinaparasitoidwasp