Different modes of evolution in males and females generate dichromatism in fairy‐wrens (Maluridae)
Sexual dichromatism in birds is often attributed to selection for elaboration in males. However, evolutionary changes in either sex can result in plumage differences between them, and such changes can result in either gains or losses of dimorphism. We reconstructed the evolution of plumage colors in...
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| Published in | Ecology and evolution Vol. 3; no. 9; pp. 3030 - 3046 |
|---|---|
| Main Authors | , , |
| Format | Journal Article |
| Language | English |
| Published |
England
John Wiley & Sons, Inc
01.09.2013
Blackwell Publishing Ltd |
| Subjects | |
| Online Access | Get full text |
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| Abstract | Sexual dichromatism in birds is often attributed to selection for elaboration in males. However, evolutionary changes in either sex can result in plumage differences between them, and such changes can result in either gains or losses of dimorphism. We reconstructed the evolution of plumage colors in both males and females of species in Maluridae, a family comprising the fairy‐wrens (Malurus, Clytomias, Sipodotus), emu‐wrens (Stipiturus), and grasswrens (Amytornis). Our results show that, across species, males and females differ in their patterns of color evolution. Male plumage has diverged at relatively steady rates, whereas female coloration has changed dramatically in some lineages and little in others. Accordingly, in comparisons against evolutionary models, plumage changes in males best fit a Brownian motion (BM) model, whereas plumage changes in females fit an Ornstein Uhlenbeck (OU) multioptimum model, with different adaptive peaks corresponding to distributions in either Australia or New Guinea. Levels of dichromatism were significantly associated with latitude, with greater dichromatism in more southerly taxa. Our results suggest that current patterns of plumage diversity in fairy‐wrens are a product of evolutionary changes in both sexes, driven in part by environmental differences across the distribution of the family.
Illustration of both males and females of five species representative of the Maluridae family showing the range of plumage dimorphism present in the family: (A) Wallace's fairy‐wren (Sipodotus wallacii), (B) Southern emu‐wren (Stipiturus malachurus), (C) splendid fairy‐wren (Malurus splendens), (D) lovely fairy‐wren (Malurus amabilis), and (E) white‐shouldered fairy‐wren (Malurus alboscapulatus). Males are illustrated above females in each species pair. |
|---|---|
| AbstractList | Abstract
Sexual dichromatism in birds is often attributed to selection for elaboration in males. However, evolutionary changes in either sex can result in plumage differences between them, and such changes can result in either gains or losses of dimorphism. We reconstructed the evolution of plumage colors in both males and females of species in
M
aluridae, a family comprising the fairy‐wrens (
M
alurus
,
C
lytomias
,
S
ipodotus
), emu‐wrens (
S
tipiturus
), and grasswrens (
A
mytornis
). Our results show that, across species, males and females differ in their patterns of color evolution. Male plumage has diverged at relatively steady rates, whereas female coloration has changed dramatically in some lineages and little in others. Accordingly, in comparisons against evolutionary models, plumage changes in males best fit a
B
rownian motion (
BM
) model, whereas plumage changes in females fit an
O
rnstein
U
hlenbeck (
OU
) multioptimum model, with different adaptive peaks corresponding to distributions in either
A
ustralia or
N
ew
G
uinea. Levels of dichromatism were significantly associated with latitude, with greater dichromatism in more southerly taxa. Our results suggest that current patterns of plumage diversity in fairy‐wrens are a product of evolutionary changes in both sexes, driven in part by environmental differences across the distribution of the family. Sexual dichromatism in birds is often attributed to selection for elaboration in males. However, evolutionary changes in either sex can result in plumage differences between them, and such changes can result in either gains or losses of dimorphism. We reconstructed the evolution of plumage colors in both males and females of species in Maluridae, a family comprising the fairy‐wrens (Malurus, Clytomias, Sipodotus), emu‐wrens (Stipiturus), and grasswrens (Amytornis). Our results show that, across species, males and females differ in their patterns of color evolution. Male plumage has diverged at relatively steady rates, whereas female coloration has changed dramatically in some lineages and little in others. Accordingly, in comparisons against evolutionary models, plumage changes in males best fit a Brownian motion (BM) model, whereas plumage changes in females fit an Ornstein Uhlenbeck (OU) multioptimum model, with different adaptive peaks corresponding to distributions in either Australia or New Guinea. Levels of dichromatism were significantly associated with latitude, with greater dichromatism in more southerly taxa. Our results suggest that current patterns of plumage diversity in fairy‐wrens are a product of evolutionary changes in both sexes, driven in part by environmental differences across the distribution of the family. Illustration of both males and females of five species representative of the Maluridae family showing the range of plumage dimorphism present in the family: (A) Wallace's fairy‐wren (Sipodotus wallacii), (B) Southern emu‐wren (Stipiturus malachurus), (C) splendid fairy‐wren (Malurus splendens), (D) lovely fairy‐wren (Malurus amabilis), and (E) white‐shouldered fairy‐wren (Malurus alboscapulatus). Males are illustrated above females in each species pair. Sexual dichromatism in birds is often attributed to selection for elaboration in males. However, evolutionary changes in either sex can result in plumage differences between them, and such changes can result in either gains or losses of dimorphism. We reconstructed the evolution of plumage colors in both males and females of species in Maluridae, a family comprising the fairy-wrens (Malurus, Clytomias, Sipodotus), emu-wrens (Stipiturus), and grasswrens (Amytornis). Our results show that, across species, males and females differ in their patterns of color evolution. Male plumage has diverged at relatively steady rates, whereas female coloration has changed dramatically in some lineages and little in others. Accordingly, in comparisons against evolutionary models, plumage changes in males best fit a Brownian motion (BM) model, whereas plumage changes in females fit an Ornstein Uhlenbeck (OU) multioptimum model, with different adaptive peaks corresponding to distributions in either Australia or New Guinea. Levels of dichromatism were significantly associated with latitude, with greater dichromatism in more southerly taxa. Our results suggest that current patterns of plumage diversity in fairy-wrens are a product of evolutionary changes in both sexes, driven in part by environmental differences across the distribution of the family. Illustration of both males and females of five species representative of the Maluridae family showing the range of plumage dimorphism present in the family: (A) Wallace's fairy-wren (Sipodotus wallacii), (B) Southern emu-wren (Stipiturus malachurus), (C) splendid fairy-wren (Malurus splendens), (D) lovely fairy-wren (Malurus amabilis), and (E) white-shouldered fairy-wren (Malurus alboscapulatus). Males are illustrated above females in each species pair. Sexual dichromatism in birds is often attributed to selection for elaboration in males. However, evolutionary changes in either sex can result in plumage differences between them, and such changes can result in either gains or losses of dimorphism. We reconstructed the evolution of plumage colors in both males and females of species in Maluridae, a family comprising the fairy-wrens (Malurus, Clytomias, Sipodotus), emu-wrens (Stipiturus), and grasswrens (Amytornis). Our results show that, across species, males and females differ in their patterns of color evolution. Male plumage has diverged at relatively steady rates, whereas female coloration has changed dramatically in some lineages and little in others. Accordingly, in comparisons against evolutionary models, plumage changes in males best fit a Brownian motion (BM) model, whereas plumage changes in females fit an Ornstein Uhlenbeck (OU) multioptimum model, with different adaptive peaks corresponding to distributions in either Australia or New Guinea. Levels of dichromatism were significantly associated with latitude, with greater dichromatism in more southerly taxa. Our results suggest that current patterns of plumage diversity in fairy-wrens are a product of evolutionary changes in both sexes, driven in part by environmental differences across the distribution of the family. Sexual dichromatism in birds is often attributed to selection for elaboration in males. However, evolutionary changes in either sex can result in plumage differences between them, and such changes can result in either gains or losses of dimorphism. We reconstructed the evolution of plumage colors in both males and females of species in Maluridae, a family comprising the fairy-wrens ( Malurus , Clytomias , Sipodotus ), emu-wrens ( Stipiturus ), and grasswrens ( Amytornis ). Our results show that, across species, males and females differ in their patterns of color evolution. Male plumage has diverged at relatively steady rates, whereas female coloration has changed dramatically in some lineages and little in others. Accordingly, in comparisons against evolutionary models, plumage changes in males best fit a Brownian motion (BM) model, whereas plumage changes in females fit an Ornstein Uhlenbeck (OU) multioptimum model, with different adaptive peaks corresponding to distributions in either Australia or New Guinea. Levels of dichromatism were significantly associated with latitude, with greater dichromatism in more southerly taxa. Our results suggest that current patterns of plumage diversity in fairy-wrens are a product of evolutionary changes in both sexes, driven in part by environmental differences across the distribution of the family. |
| Author | Pruett‐Jones, Stephen Jordan Price, J. Johnson, Allison E. |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24101992$$D View this record in MEDLINE/PubMed |
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| Copyright | 2013 The Authors. published by John Wiley & Sons Ltd. 2013. This work is published under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2013 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd 2013 |
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| Issue | 9 |
| Keywords | Maluridae selection Fairy-wrens sexual dimorphism plumage evolution |
| Language | English |
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| Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Funding Information A. E. Johnson was supported by the Dubner Family Fellowship at University of Chicago and S. Pruett-Jones was supported, in part, by a grant from the Women's Board at University of Chicago. |
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| Snippet | Sexual dichromatism in birds is often attributed to selection for elaboration in males. However, evolutionary changes in either sex can result in plumage... Abstract Sexual dichromatism in birds is often attributed to selection for elaboration in males. However, evolutionary changes in either sex can result in... |
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| SubjectTerms | Birds Brownian motion Carotenoids Coloration Dimorphism Ecology Endangered & extinct species Evolution Evolution & development Fairy‐wrens Females Macroevolution Males Maluridae Malurus splendens Monogamy Original Research Phylogenetics Plumage plumage evolution selection Sexual dimorphism Sperm Veganism |
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| Title | Different modes of evolution in males and females generate dichromatism in fairy‐wrens (Maluridae) |
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