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C(4) anatomy can evolve via a single developmental change

C(4) photosynthesis is a complex trait that boosts productivity in warm environments. Paradoxically, it evolved independently in numerous plant lineages, despite requiring specialised leaf anatomy. The anatomical modifications underlying C(4) evolution have previously been evaluated through interspe...

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Detalles Bibliográficos
Autores principales: Lundgren, Marjorie R., Dunning, Luke T., Olofsson, Jill K., Moreno‐Villena, Jose J., Bouvier, Jacques W., Sage, Tammy L., Khoshravesh, Roxana, Sultmanis, Stefanie, Stata, Matt, Ripley, Brad S., Vorontsova, Maria S., Besnard, Guillaume, Adams, Claire, Cuff, Nicholas, Mapaura, Anthony, Bianconi, Matheus E., Long, Christine M., Christin, Pascal‐Antoine, Osborne, Colin P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849723/
https://www.ncbi.nlm.nih.gov/pubmed/30557904
http://dx.doi.org/10.1111/ele.13191
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author Lundgren, Marjorie R.
Dunning, Luke T.
Olofsson, Jill K.
Moreno‐Villena, Jose J.
Bouvier, Jacques W.
Sage, Tammy L.
Khoshravesh, Roxana
Sultmanis, Stefanie
Stata, Matt
Ripley, Brad S.
Vorontsova, Maria S.
Besnard, Guillaume
Adams, Claire
Cuff, Nicholas
Mapaura, Anthony
Bianconi, Matheus E.
Long, Christine M.
Christin, Pascal‐Antoine
Osborne, Colin P.
author_facet Lundgren, Marjorie R.
Dunning, Luke T.
Olofsson, Jill K.
Moreno‐Villena, Jose J.
Bouvier, Jacques W.
Sage, Tammy L.
Khoshravesh, Roxana
Sultmanis, Stefanie
Stata, Matt
Ripley, Brad S.
Vorontsova, Maria S.
Besnard, Guillaume
Adams, Claire
Cuff, Nicholas
Mapaura, Anthony
Bianconi, Matheus E.
Long, Christine M.
Christin, Pascal‐Antoine
Osborne, Colin P.
author_sort Lundgren, Marjorie R.
collection PubMed
description C(4) photosynthesis is a complex trait that boosts productivity in warm environments. Paradoxically, it evolved independently in numerous plant lineages, despite requiring specialised leaf anatomy. The anatomical modifications underlying C(4) evolution have previously been evaluated through interspecific comparisons, which capture numerous changes besides those needed for C(4) functionality. Here, we quantify the anatomical changes accompanying the transition between non‐C(4) and C(4) phenotypes by sampling widely across the continuum of leaf anatomical traits in the grass Alloteropsis semialata. Within this species, the only trait that is shared among and specific to C(4) individuals is an increase in vein density, driven specifically by minor vein development that yields multiple secondary effects facilitating C(4) function. For species with the necessary anatomical preconditions, developmental proliferation of veins can therefore be sufficient to produce a functional C(4) leaf anatomy, creating an evolutionary entry point to complex C(4) syndromes that can become more specialised.
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spelling pubmed-68497232019-11-15 C(4) anatomy can evolve via a single developmental change Lundgren, Marjorie R. Dunning, Luke T. Olofsson, Jill K. Moreno‐Villena, Jose J. Bouvier, Jacques W. Sage, Tammy L. Khoshravesh, Roxana Sultmanis, Stefanie Stata, Matt Ripley, Brad S. Vorontsova, Maria S. Besnard, Guillaume Adams, Claire Cuff, Nicholas Mapaura, Anthony Bianconi, Matheus E. Long, Christine M. Christin, Pascal‐Antoine Osborne, Colin P. Ecol Lett Letters C(4) photosynthesis is a complex trait that boosts productivity in warm environments. Paradoxically, it evolved independently in numerous plant lineages, despite requiring specialised leaf anatomy. The anatomical modifications underlying C(4) evolution have previously been evaluated through interspecific comparisons, which capture numerous changes besides those needed for C(4) functionality. Here, we quantify the anatomical changes accompanying the transition between non‐C(4) and C(4) phenotypes by sampling widely across the continuum of leaf anatomical traits in the grass Alloteropsis semialata. Within this species, the only trait that is shared among and specific to C(4) individuals is an increase in vein density, driven specifically by minor vein development that yields multiple secondary effects facilitating C(4) function. For species with the necessary anatomical preconditions, developmental proliferation of veins can therefore be sufficient to produce a functional C(4) leaf anatomy, creating an evolutionary entry point to complex C(4) syndromes that can become more specialised. John Wiley and Sons Inc. 2018-12-17 2019-02 /pmc/articles/PMC6849723/ /pubmed/30557904 http://dx.doi.org/10.1111/ele.13191 Text en © 2018 The Authors Ecology Letters published by CNRS and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letters
Lundgren, Marjorie R.
Dunning, Luke T.
Olofsson, Jill K.
Moreno‐Villena, Jose J.
Bouvier, Jacques W.
Sage, Tammy L.
Khoshravesh, Roxana
Sultmanis, Stefanie
Stata, Matt
Ripley, Brad S.
Vorontsova, Maria S.
Besnard, Guillaume
Adams, Claire
Cuff, Nicholas
Mapaura, Anthony
Bianconi, Matheus E.
Long, Christine M.
Christin, Pascal‐Antoine
Osborne, Colin P.
C(4) anatomy can evolve via a single developmental change
title C(4) anatomy can evolve via a single developmental change
title_full C(4) anatomy can evolve via a single developmental change
title_fullStr C(4) anatomy can evolve via a single developmental change
title_full_unstemmed C(4) anatomy can evolve via a single developmental change
title_short C(4) anatomy can evolve via a single developmental change
title_sort c(4) anatomy can evolve via a single developmental change
topic Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849723/
https://www.ncbi.nlm.nih.gov/pubmed/30557904
http://dx.doi.org/10.1111/ele.13191
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