Co-gradient variation in growth rate and development time of a broadly distributed butterfly.

Widespread species often show geographic variation in thermally-sensitive traits, providing insight into how species respond to shifts in temperature through time. Such patterns may arise from phenotypic plasticity, genetic adaptation, or their interaction. In some cases, the effects of genotype and...

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Main Authors: Madeleine Barton, Paul Sunnucks, Melanie Norgate, Neil Murray, Michael Kearney
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3990641?pdf=render
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spelling doaj-01a2c42f3a2d4e61a42bfe17b420420e2020-11-25T02:05:45ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0194e9525810.1371/journal.pone.0095258Co-gradient variation in growth rate and development time of a broadly distributed butterfly.Madeleine BartonPaul SunnucksMelanie NorgateNeil MurrayMichael KearneyWidespread species often show geographic variation in thermally-sensitive traits, providing insight into how species respond to shifts in temperature through time. Such patterns may arise from phenotypic plasticity, genetic adaptation, or their interaction. In some cases, the effects of genotype and temperature may act together to reduce, or to exacerbate, phenotypic variation in fitness-related traits across varying thermal environments. We find evidence for such interactions in life-history traits of Heteronympha merope, a butterfly distributed across a broad latitudinal gradient in south-eastern Australia. We show that body size in this butterfly is negatively related to developmental temperature in the laboratory, in accordance with the temperature-size rule, but not in the field, despite very strong temperature gradients. A common garden experiment on larval thermal responses, spanning the environmental extremes of H. merope's distribution, revealed that butterflies from low latitude (warmer climate) populations have relatively fast intrinsic growth and development rates compared to those from cooler climates. These synergistic effects of genotype and temperature across the landscape (co-gradient variation) are likely to accentuate phenotypic variation in these traits, and this interaction must be accounted for when predicting how H. merope will respond to temperature change through time. These results highlight the importance of understanding how variation in life-history traits may arise in response to environmental change. Without this knowledge, we may fail to detect whether organisms are tracking environmental change, and if they are, whether it is by plasticity, adaptation or both.http://europepmc.org/articles/PMC3990641?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Madeleine Barton
Paul Sunnucks
Melanie Norgate
Neil Murray
Michael Kearney
spellingShingle Madeleine Barton
Paul Sunnucks
Melanie Norgate
Neil Murray
Michael Kearney
Co-gradient variation in growth rate and development time of a broadly distributed butterfly.
PLoS ONE
author_facet Madeleine Barton
Paul Sunnucks
Melanie Norgate
Neil Murray
Michael Kearney
author_sort Madeleine Barton
title Co-gradient variation in growth rate and development time of a broadly distributed butterfly.
title_short Co-gradient variation in growth rate and development time of a broadly distributed butterfly.
title_full Co-gradient variation in growth rate and development time of a broadly distributed butterfly.
title_fullStr Co-gradient variation in growth rate and development time of a broadly distributed butterfly.
title_full_unstemmed Co-gradient variation in growth rate and development time of a broadly distributed butterfly.
title_sort co-gradient variation in growth rate and development time of a broadly distributed butterfly.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Widespread species often show geographic variation in thermally-sensitive traits, providing insight into how species respond to shifts in temperature through time. Such patterns may arise from phenotypic plasticity, genetic adaptation, or their interaction. In some cases, the effects of genotype and temperature may act together to reduce, or to exacerbate, phenotypic variation in fitness-related traits across varying thermal environments. We find evidence for such interactions in life-history traits of Heteronympha merope, a butterfly distributed across a broad latitudinal gradient in south-eastern Australia. We show that body size in this butterfly is negatively related to developmental temperature in the laboratory, in accordance with the temperature-size rule, but not in the field, despite very strong temperature gradients. A common garden experiment on larval thermal responses, spanning the environmental extremes of H. merope's distribution, revealed that butterflies from low latitude (warmer climate) populations have relatively fast intrinsic growth and development rates compared to those from cooler climates. These synergistic effects of genotype and temperature across the landscape (co-gradient variation) are likely to accentuate phenotypic variation in these traits, and this interaction must be accounted for when predicting how H. merope will respond to temperature change through time. These results highlight the importance of understanding how variation in life-history traits may arise in response to environmental change. Without this knowledge, we may fail to detect whether organisms are tracking environmental change, and if they are, whether it is by plasticity, adaptation or both.
url http://europepmc.org/articles/PMC3990641?pdf=render
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