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Extreme heat increases stomatal conductance and drought‐induced mortality risk in vulnerable plant species
Tree mortality during global‐change‐type drought is usually attributed to xylem dysfunction, but as climate change increases the frequency of extreme heat events, it is necessary to better understand the interactive role of heat stress. We hypothesized that some drought‐stressed plants paradoxically...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299030/ https://www.ncbi.nlm.nih.gov/pubmed/34741566 http://dx.doi.org/10.1111/gcb.15976 |
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author | Marchin, Renée M. Backes, Diana Ossola, Alessandro Leishman, Michelle R. Tjoelker, Mark G. Ellsworth, David S. |
author_facet | Marchin, Renée M. Backes, Diana Ossola, Alessandro Leishman, Michelle R. Tjoelker, Mark G. Ellsworth, David S. |
author_sort | Marchin, Renée M. |
collection | PubMed |
description | Tree mortality during global‐change‐type drought is usually attributed to xylem dysfunction, but as climate change increases the frequency of extreme heat events, it is necessary to better understand the interactive role of heat stress. We hypothesized that some drought‐stressed plants paradoxically open stomata in heatwaves to prevent leaves from critically overheating. We experimentally imposed heat (>40°C) and drought stress onto 20 broadleaf evergreen tree/shrub species in a glasshouse study. Most well‐watered plants avoided lethal overheating, but drought exacerbated thermal damage during heatwaves. Thermal safety margins (TSM) quantifying the difference between leaf surface temperature and leaf critical temperature, where photosynthesis is disrupted, identified species vulnerability to heatwaves. Several mechanisms contributed to high heat tolerance and avoidance of damaging leaf temperatures—small leaf size, low leaf osmotic potential, high leaf mass per area (i.e., thick, dense leaves), high transpirational capacity, and access to water. Water‐stressed plants had smaller TSM, greater crown dieback, and a fundamentally different stomatal heatwave response relative to well‐watered plants. On average, well‐watered plants closed stomata and decreased stomatal conductance (g (s)) during the heatwave, but droughted plants did not. Plant species with low g (s), either due to isohydric stomatal behavior under water deficit or inherently low transpirational capacity, opened stomata and increased g (s) under high temperatures. The current paradigm maintains that stomata close before hydraulic thresholds are surpassed, but our results suggest that isohydric species may dramatically increase g (s) (over sixfold increases) even past their leaf turgor loss point. By actively increasing water loss at high temperatures, plants can be driven toward mortality thresholds more rapidly than has been previously recognized. The inclusion of TSM and responses to heat stress could improve our ability to predict the vulnerability of different tree species to future droughts. |
format | Online Article Text |
id | pubmed-9299030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92990302022-07-21 Extreme heat increases stomatal conductance and drought‐induced mortality risk in vulnerable plant species Marchin, Renée M. Backes, Diana Ossola, Alessandro Leishman, Michelle R. Tjoelker, Mark G. Ellsworth, David S. Glob Chang Biol Primary Research Articles Tree mortality during global‐change‐type drought is usually attributed to xylem dysfunction, but as climate change increases the frequency of extreme heat events, it is necessary to better understand the interactive role of heat stress. We hypothesized that some drought‐stressed plants paradoxically open stomata in heatwaves to prevent leaves from critically overheating. We experimentally imposed heat (>40°C) and drought stress onto 20 broadleaf evergreen tree/shrub species in a glasshouse study. Most well‐watered plants avoided lethal overheating, but drought exacerbated thermal damage during heatwaves. Thermal safety margins (TSM) quantifying the difference between leaf surface temperature and leaf critical temperature, where photosynthesis is disrupted, identified species vulnerability to heatwaves. Several mechanisms contributed to high heat tolerance and avoidance of damaging leaf temperatures—small leaf size, low leaf osmotic potential, high leaf mass per area (i.e., thick, dense leaves), high transpirational capacity, and access to water. Water‐stressed plants had smaller TSM, greater crown dieback, and a fundamentally different stomatal heatwave response relative to well‐watered plants. On average, well‐watered plants closed stomata and decreased stomatal conductance (g (s)) during the heatwave, but droughted plants did not. Plant species with low g (s), either due to isohydric stomatal behavior under water deficit or inherently low transpirational capacity, opened stomata and increased g (s) under high temperatures. The current paradigm maintains that stomata close before hydraulic thresholds are surpassed, but our results suggest that isohydric species may dramatically increase g (s) (over sixfold increases) even past their leaf turgor loss point. By actively increasing water loss at high temperatures, plants can be driven toward mortality thresholds more rapidly than has been previously recognized. The inclusion of TSM and responses to heat stress could improve our ability to predict the vulnerability of different tree species to future droughts. John Wiley and Sons Inc. 2021-11-20 2022-02 /pmc/articles/PMC9299030/ /pubmed/34741566 http://dx.doi.org/10.1111/gcb.15976 Text en © 2021 The Authors. Global Change Biology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Primary Research Articles Marchin, Renée M. Backes, Diana Ossola, Alessandro Leishman, Michelle R. Tjoelker, Mark G. Ellsworth, David S. Extreme heat increases stomatal conductance and drought‐induced mortality risk in vulnerable plant species |
title | Extreme heat increases stomatal conductance and drought‐induced mortality risk in vulnerable plant species |
title_full | Extreme heat increases stomatal conductance and drought‐induced mortality risk in vulnerable plant species |
title_fullStr | Extreme heat increases stomatal conductance and drought‐induced mortality risk in vulnerable plant species |
title_full_unstemmed | Extreme heat increases stomatal conductance and drought‐induced mortality risk in vulnerable plant species |
title_short | Extreme heat increases stomatal conductance and drought‐induced mortality risk in vulnerable plant species |
title_sort | extreme heat increases stomatal conductance and drought‐induced mortality risk in vulnerable plant species |
topic | Primary Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299030/ https://www.ncbi.nlm.nih.gov/pubmed/34741566 http://dx.doi.org/10.1111/gcb.15976 |
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