Diverse mangroves deviate from other angiosperms in their genome size, leaf cell size and cell packing density relationships.

Environmental factors cell size genome size stomata stomatal density vein density

Journal

Annals of botany
ISSN: 1095-8290
Titre abrégé: Ann Bot
Pays: England
ID NLM: 0372347

Informations de publication

Date de publication:
08 03 2023
Historique:
received: 11 08 2022
accepted: 12 12 2022
pmc-release: 14 12 2023
pubmed: 15 12 2022
medline: 10 3 2023
entrez: 14 12 2022
Statut: ppublish

Résumé

While genome size limits the minimum sizes and maximum numbers of cells that can be packed into a given leaf volume, mature cell sizes can be substantially larger than their meristematic precursors and vary in response to abiotic conditions. Mangroves are iconic examples of how abiotic conditions can influence the evolution of plant phenotypes. Here, we examined the coordination between genome size, leaf cell sizes, cell packing densities and leaf size in 13 mangrove species across four sites in China. Four of these species occurred at more than one site, allowing us to test the effect of climate on leaf anatomy. We found that genome sizes of mangroves were very small compared to other angiosperms, but, like other angiosperms, mangrove cells were always larger than the minimum size defined by genome size. Increasing mean annual temperature of a growth site led to higher packing densities of veins (Dv) and stomata (Ds) and smaller epidermal cells but had no effect on stomatal size. In contrast to other angiosperms, mangroves exhibited (1) a negative relationship between guard cell size and genome size; (2) epidermal cells that were smaller than stomata; and (3) coordination between Dv and Ds that was not mediated by epidermal cell size. Furthermore, mangrove epidermal cell sizes and packing densities covaried with leaf size. While mangroves exhibited coordination between veins and stomata and attained a maximum theoretical stomatal conductance similar to that of other angiosperms, the tissue-level tradeoffs underlying these similar relationships across species and environments were markedly different, perhaps indicative of the unique structural and physiological adaptations of mangroves to their stressful environments.

Sections du résumé

BACKGROUND AND AIMS
While genome size limits the minimum sizes and maximum numbers of cells that can be packed into a given leaf volume, mature cell sizes can be substantially larger than their meristematic precursors and vary in response to abiotic conditions. Mangroves are iconic examples of how abiotic conditions can influence the evolution of plant phenotypes.
METHODS
Here, we examined the coordination between genome size, leaf cell sizes, cell packing densities and leaf size in 13 mangrove species across four sites in China. Four of these species occurred at more than one site, allowing us to test the effect of climate on leaf anatomy.
RESULTS
We found that genome sizes of mangroves were very small compared to other angiosperms, but, like other angiosperms, mangrove cells were always larger than the minimum size defined by genome size. Increasing mean annual temperature of a growth site led to higher packing densities of veins (Dv) and stomata (Ds) and smaller epidermal cells but had no effect on stomatal size. In contrast to other angiosperms, mangroves exhibited (1) a negative relationship between guard cell size and genome size; (2) epidermal cells that were smaller than stomata; and (3) coordination between Dv and Ds that was not mediated by epidermal cell size. Furthermore, mangrove epidermal cell sizes and packing densities covaried with leaf size.
CONCLUSIONS
While mangroves exhibited coordination between veins and stomata and attained a maximum theoretical stomatal conductance similar to that of other angiosperms, the tissue-level tradeoffs underlying these similar relationships across species and environments were markedly different, perhaps indicative of the unique structural and physiological adaptations of mangroves to their stressful environments.

Identifiants

pubmed: 36516425
pii: 6902007
doi: 10.1093/aob/mcac151
pmc: PMC9992938
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

347-360

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Auteurs

Guo-Feng Jiang (GF)

Guangxi Key Laboratory of Forest Ecology and Conservation, and State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, College of Forestry, Guangxi University, Daxuedonglu 100, Nanning, Guangxi 530004, PR China.

Su-Yuan Li (SY)

Guangxi Key Laboratory of Forest Ecology and Conservation, and State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, College of Forestry, Guangxi University, Daxuedonglu 100, Nanning, Guangxi 530004, PR China.

Russell Dinnage (R)

Institute of Environment, Department of Biological Sciences, Florida International University, Miami, FL 33199USA.

Kun-Fang Cao (KF)

Guangxi Key Laboratory of Forest Ecology and Conservation, and State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, College of Forestry, Guangxi University, Daxuedonglu 100, Nanning, Guangxi 530004, PR China.

Kevin A Simonin (KA)

Department of Biology, San Francisco State University, San Francisco, CA 94132USA.

Adam B Roddy (AB)

Institute of Environment, Department of Biological Sciences, Florida International University, Miami, FL 33199USA.

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Classifications MeSH