Phenotypic plasticity in opsin expression in a butterfly compound eye complements sex role reversal

<p>Abstract</p> <p>Background</p> <p>Animals often display phenotypic plasticity in morphologies and behaviors that result in distinct adaptations to fluctuating seasonal environments. The butterfly <it>Bicyclus anynana</it> has two seasonal forms, wet and d...

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Main Authors: Everett Andrew, Tong Xiaoling, Briscoe Adriana D, Monteiro Antónia
Format: Article
Language:English
Published: BMC 2012-11-01
Series:BMC Evolutionary Biology
Subjects:
Online Access:http://www.biomedcentral.com/1471-2148/12/232
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spelling doaj-f23257d482e54442bfcfd48eddd999432021-09-02T04:44:40ZengBMCBMC Evolutionary Biology1471-21482012-11-0112123210.1186/1471-2148-12-232Phenotypic plasticity in opsin expression in a butterfly compound eye complements sex role reversalEverett AndrewTong XiaolingBriscoe Adriana DMonteiro Antónia<p>Abstract</p> <p>Background</p> <p>Animals often display phenotypic plasticity in morphologies and behaviors that result in distinct adaptations to fluctuating seasonal environments. The butterfly <it>Bicyclus anynana</it> has two seasonal forms, wet and dry, that vary in wing ornament brightness and in the identity of the sex that performs the most courting and choosing. Rearing temperature is the cue for producing these alternative seasonal forms. We hypothesized that, barring any developmental constraints, vision should be enhanced in the choosy individuals but diminished in the non-choosy individuals due to physiological costs. As a proxy of visual performance we measured eye size, facet lens size, and sensitivity to light, e.g., the expression levels of all opsins, in males and females of both seasonal forms.</p> <p>Results</p> <p>We found that <it>B. anynana</it> eyes displayed significant sexual dimorphism and phenotypic plasticity for both morphology and opsin expression levels, but not all results conformed to our prediction. Males had larger eyes than females across rearing temperatures, and increases in temperature produced larger eyes in both sexes, mostly via increases in facet number. Ommatidia were larger in the choosy dry season (DS) males and transcript levels for all three opsins were significantly lower in the less choosy DS females.</p> <p>Conclusions</p> <p>Opsin level plasticity in females, and ommatidia size plasticity in males supported our visual plasticity hypothesis but males appear to maintain high visual function across both seasons. We discuss our results in the context of distinct sexual and natural selection pressures that may be facing each sex in the wild in each season.</p> http://www.biomedcentral.com/1471-2148/12/232<it>Bicyclus anynana</it>Reaction normOmmatidiaOpsinSexual dimorphismTemperature-size rulePhenotypic plasticityBody sizeAllometryVisionOptics
collection DOAJ
language English
format Article
sources DOAJ
author Everett Andrew
Tong Xiaoling
Briscoe Adriana D
Monteiro Antónia
spellingShingle Everett Andrew
Tong Xiaoling
Briscoe Adriana D
Monteiro Antónia
Phenotypic plasticity in opsin expression in a butterfly compound eye complements sex role reversal
BMC Evolutionary Biology
<it>Bicyclus anynana</it>
Reaction norm
Ommatidia
Opsin
Sexual dimorphism
Temperature-size rule
Phenotypic plasticity
Body size
Allometry
Vision
Optics
author_facet Everett Andrew
Tong Xiaoling
Briscoe Adriana D
Monteiro Antónia
author_sort Everett Andrew
title Phenotypic plasticity in opsin expression in a butterfly compound eye complements sex role reversal
title_short Phenotypic plasticity in opsin expression in a butterfly compound eye complements sex role reversal
title_full Phenotypic plasticity in opsin expression in a butterfly compound eye complements sex role reversal
title_fullStr Phenotypic plasticity in opsin expression in a butterfly compound eye complements sex role reversal
title_full_unstemmed Phenotypic plasticity in opsin expression in a butterfly compound eye complements sex role reversal
title_sort phenotypic plasticity in opsin expression in a butterfly compound eye complements sex role reversal
publisher BMC
series BMC Evolutionary Biology
issn 1471-2148
publishDate 2012-11-01
description <p>Abstract</p> <p>Background</p> <p>Animals often display phenotypic plasticity in morphologies and behaviors that result in distinct adaptations to fluctuating seasonal environments. The butterfly <it>Bicyclus anynana</it> has two seasonal forms, wet and dry, that vary in wing ornament brightness and in the identity of the sex that performs the most courting and choosing. Rearing temperature is the cue for producing these alternative seasonal forms. We hypothesized that, barring any developmental constraints, vision should be enhanced in the choosy individuals but diminished in the non-choosy individuals due to physiological costs. As a proxy of visual performance we measured eye size, facet lens size, and sensitivity to light, e.g., the expression levels of all opsins, in males and females of both seasonal forms.</p> <p>Results</p> <p>We found that <it>B. anynana</it> eyes displayed significant sexual dimorphism and phenotypic plasticity for both morphology and opsin expression levels, but not all results conformed to our prediction. Males had larger eyes than females across rearing temperatures, and increases in temperature produced larger eyes in both sexes, mostly via increases in facet number. Ommatidia were larger in the choosy dry season (DS) males and transcript levels for all three opsins were significantly lower in the less choosy DS females.</p> <p>Conclusions</p> <p>Opsin level plasticity in females, and ommatidia size plasticity in males supported our visual plasticity hypothesis but males appear to maintain high visual function across both seasons. We discuss our results in the context of distinct sexual and natural selection pressures that may be facing each sex in the wild in each season.</p>
topic <it>Bicyclus anynana</it>
Reaction norm
Ommatidia
Opsin
Sexual dimorphism
Temperature-size rule
Phenotypic plasticity
Body size
Allometry
Vision
Optics
url http://www.biomedcentral.com/1471-2148/12/232
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AT tongxiaoling phenotypicplasticityinopsinexpressioninabutterflycompoundeyecomplementssexrolereversal
AT briscoeadrianad phenotypicplasticityinopsinexpressioninabutterflycompoundeyecomplementssexrolereversal
AT monteiroantonia phenotypicplasticityinopsinexpressioninabutterflycompoundeyecomplementssexrolereversal
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