<p>Significant effort has been put into understanding the role of abscisic acid (ABA) on stomatal response to water stress. However, the parametrization of ABA controls in current models of stomatal conductance (<InlineEquation ID="IEq1"> <EquationSource Format="TEX">\(g_s\)</EquationSource> </InlineEquation>) remains challenging. Here, we synthesized current literature that quantifies ABA relation with <InlineEquation ID="IEq2"> <EquationSource Format="TEX">\(g_s\)</EquationSource> </InlineEquation>, water potential (<InlineEquation ID="IEq3"> <EquationSource Format="TEX">\(\Psi\)</EquationSource> </InlineEquation>), or both, across various experimental settings. We compiled a total of 242 datasets covering 60 plant species, with 193 observation sets linking <InlineEquation ID="IEq4"> <EquationSource Format="TEX">\(g_s\)</EquationSource> </InlineEquation> and ABA and 138 observation sets linking <InlineEquation ID="IEq5"> <EquationSource Format="TEX">\(\Psi\)</EquationSource> </InlineEquation> and ABA. <InlineEquation ID="IEq6"> <EquationSource Format="TEX">\(\Psi\)</EquationSource> </InlineEquation> was measured in either the leaf, stem, or root, as reported in the corresponding studies. We examined different fitting functions to approximate the relation between <InlineEquation ID="IEq7"> <EquationSource Format="TEX">\(\Psi\)</EquationSource> </InlineEquation> and ABA, and <InlineEquation ID="IEq8"> <EquationSource Format="TEX">\(g_s\)</EquationSource> </InlineEquation> and ABA. Statistical correlations were used to determine the best fit of <InlineEquation ID="IEq9"> <EquationSource Format="TEX">\(g_s\)</EquationSource> </InlineEquation> vs ABA and <InlineEquation ID="IEq10"> <EquationSource Format="TEX">\(\Psi\)</EquationSource> </InlineEquation> vs ABA relationships, and to exclude datasets with poor correlations. No statistically significant differences were found between stomatal sensitivity to ABA (<InlineEquation ID="IEq11"> <EquationSource Format="TEX">\(\beta\)</EquationSource> </InlineEquation>, unitless) and biome type or the source of ABA (Kruskal-Wallis, P &gt; 0.05). Statistical differences were found between <InlineEquation ID="IEq12"> <EquationSource Format="TEX">\(\beta\)</EquationSource> </InlineEquation> and experimental conditions (Kruskal-Wallis, P &lt; 0.05), likely due to observational uncertainties. The overall distribution of <InlineEquation ID="IEq13"> <EquationSource Format="TEX">\(\beta\)</EquationSource> </InlineEquation> in all classifications suggests a typical sensitivity range (<InlineEquation ID="IEq14"> <EquationSource Format="TEX">\(\beta\)</EquationSource> </InlineEquation>) of 0.21 - 21.59 (median 1.87). These findings can be used to guide the development and evaluation of mechanistic models of <InlineEquation ID="IEq15"> <EquationSource Format="TEX">\(g_s\)</EquationSource> </InlineEquation>, providing realistic parameterizations of the links between ABA and stomatal closure.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

A synthesis of stomatal sensitivity to ABA across species and experiments

  • A. Chaput,
  • C. Pappas,
  • S. Fatichi

摘要

Significant effort has been put into understanding the role of abscisic acid (ABA) on stomatal response to water stress. However, the parametrization of ABA controls in current models of stomatal conductance ( \(g_s\) ) remains challenging. Here, we synthesized current literature that quantifies ABA relation with \(g_s\) , water potential ( \(\Psi\) ), or both, across various experimental settings. We compiled a total of 242 datasets covering 60 plant species, with 193 observation sets linking \(g_s\) and ABA and 138 observation sets linking \(\Psi\) and ABA. \(\Psi\) was measured in either the leaf, stem, or root, as reported in the corresponding studies. We examined different fitting functions to approximate the relation between \(\Psi\) and ABA, and \(g_s\) and ABA. Statistical correlations were used to determine the best fit of \(g_s\) vs ABA and \(\Psi\) vs ABA relationships, and to exclude datasets with poor correlations. No statistically significant differences were found between stomatal sensitivity to ABA ( \(\beta\) , unitless) and biome type or the source of ABA (Kruskal-Wallis, P > 0.05). Statistical differences were found between \(\beta\) and experimental conditions (Kruskal-Wallis, P < 0.05), likely due to observational uncertainties. The overall distribution of \(\beta\) in all classifications suggests a typical sensitivity range ( \(\beta\) ) of 0.21 - 21.59 (median 1.87). These findings can be used to guide the development and evaluation of mechanistic models of \(g_s\) , providing realistic parameterizations of the links between ABA and stomatal closure.