Extreme functional specialization of fertile leaves in a widespread fern species and its implications on the evolution of reproductive dimorphism

Abstract Resource allocation theory posits that organisms distribute limited resources across functions to maximize their overall fitness. In plants, the allocation of resources among maintenance, reproduction, and growth influences short‐term economics and long‐term evolutionary processes, especial...

Full description

Saved in:
Bibliographic Details
Main Authors: Jacob S. Suissa, Noah Barkoff, James E. Watkins
Format: Article
Language:English
Published: Wiley 2024-07-01
Series:Ecology and Evolution
Subjects:
Online Access:https://doi.org/10.1002/ece3.11552
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849422802827870208
author Jacob S. Suissa
Noah Barkoff
James E. Watkins
author_facet Jacob S. Suissa
Noah Barkoff
James E. Watkins
author_sort Jacob S. Suissa
collection DOAJ
description Abstract Resource allocation theory posits that organisms distribute limited resources across functions to maximize their overall fitness. In plants, the allocation of resources among maintenance, reproduction, and growth influences short‐term economics and long‐term evolutionary processes, especially during resource scarcity. The evolution of specialized structures to divide labor between reproduction and growth can create a feedback loop where selection can act on individual organs, further increasing specializaton and  resource allocation. Ferns exhibit diverse reproductive strategies, including dimorphism, where leaves can either be sterile (only for photosynthesis) or fertile (for spore dispersal). This dimorphism is similar to processes in seed plants (e.g., the production of fertile flowers and sterile leaves), and presents an opportunity to investigate divergent resource allocation between reproductive and vegetative functions in specialized organs. Here, we conducted anatomical and hydraulic analyses on Onoclea sensibilis L., a widespread dimorphic fern species, to reveal significant structural and hydraulic divergences between fertile and sterile leaves. Fertile fronds invest less in hydraulic architecture, with nearly 1.5 times fewer water‐conducting cells and a nearly 0.5 times less drought‐resistant xylem compared to sterile fronds. This comes at the increased relative investment in structural support, which may help facilitate spore dispersal. These findings suggest that specialization in ferns—in the form of reproductive dimorphism—can enable independent selection pressures on each leaf type, potentially optimizing spore dispersal in fertile fronds and photosynthetic efficiency in sterile fronds. Overall, our study sheds light on the evolutionary implications of functional specialization and highlights the importance of reproductive strategies in shaping plant fitness and evolution.
format Article
id doaj-art-c2b98804435a4791afec9ec8b489b22d
institution Kabale University
issn 2045-7758
language English
publishDate 2024-07-01
publisher Wiley
record_format Article
series Ecology and Evolution
spelling doaj-art-c2b98804435a4791afec9ec8b489b22d2025-08-20T03:30:55ZengWileyEcology and Evolution2045-77582024-07-01147n/an/a10.1002/ece3.11552Extreme functional specialization of fertile leaves in a widespread fern species and its implications on the evolution of reproductive dimorphismJacob S. Suissa0Noah Barkoff1James E. Watkins2Department of Ecology and Evolutionary Biology University of Tennessee Knoxville Knoxville Tennessee USADepartment of Biological Sciences University of Notre Dame Notre Dame Indiana USADepartment of Biology Colgate University Hamilton New York USAAbstract Resource allocation theory posits that organisms distribute limited resources across functions to maximize their overall fitness. In plants, the allocation of resources among maintenance, reproduction, and growth influences short‐term economics and long‐term evolutionary processes, especially during resource scarcity. The evolution of specialized structures to divide labor between reproduction and growth can create a feedback loop where selection can act on individual organs, further increasing specializaton and  resource allocation. Ferns exhibit diverse reproductive strategies, including dimorphism, where leaves can either be sterile (only for photosynthesis) or fertile (for spore dispersal). This dimorphism is similar to processes in seed plants (e.g., the production of fertile flowers and sterile leaves), and presents an opportunity to investigate divergent resource allocation between reproductive and vegetative functions in specialized organs. Here, we conducted anatomical and hydraulic analyses on Onoclea sensibilis L., a widespread dimorphic fern species, to reveal significant structural and hydraulic divergences between fertile and sterile leaves. Fertile fronds invest less in hydraulic architecture, with nearly 1.5 times fewer water‐conducting cells and a nearly 0.5 times less drought‐resistant xylem compared to sterile fronds. This comes at the increased relative investment in structural support, which may help facilitate spore dispersal. These findings suggest that specialization in ferns—in the form of reproductive dimorphism—can enable independent selection pressures on each leaf type, potentially optimizing spore dispersal in fertile fronds and photosynthetic efficiency in sterile fronds. Overall, our study sheds light on the evolutionary implications of functional specialization and highlights the importance of reproductive strategies in shaping plant fitness and evolution.https://doi.org/10.1002/ece3.11552cavitationdimorphismembolismhydraulicsreproductionresource allocation
spellingShingle Jacob S. Suissa
Noah Barkoff
James E. Watkins
Extreme functional specialization of fertile leaves in a widespread fern species and its implications on the evolution of reproductive dimorphism
Ecology and Evolution
cavitation
dimorphism
embolism
hydraulics
reproduction
resource allocation
title Extreme functional specialization of fertile leaves in a widespread fern species and its implications on the evolution of reproductive dimorphism
title_full Extreme functional specialization of fertile leaves in a widespread fern species and its implications on the evolution of reproductive dimorphism
title_fullStr Extreme functional specialization of fertile leaves in a widespread fern species and its implications on the evolution of reproductive dimorphism
title_full_unstemmed Extreme functional specialization of fertile leaves in a widespread fern species and its implications on the evolution of reproductive dimorphism
title_short Extreme functional specialization of fertile leaves in a widespread fern species and its implications on the evolution of reproductive dimorphism
title_sort extreme functional specialization of fertile leaves in a widespread fern species and its implications on the evolution of reproductive dimorphism
topic cavitation
dimorphism
embolism
hydraulics
reproduction
resource allocation
url https://doi.org/10.1002/ece3.11552
work_keys_str_mv AT jacobssuissa extremefunctionalspecializationoffertileleavesinawidespreadfernspeciesanditsimplicationsontheevolutionofreproductivedimorphism
AT noahbarkoff extremefunctionalspecializationoffertileleavesinawidespreadfernspeciesanditsimplicationsontheevolutionofreproductivedimorphism
AT jamesewatkins extremefunctionalspecializationoffertileleavesinawidespreadfernspeciesanditsimplicationsontheevolutionofreproductivedimorphism