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高光谱叶片反射率可检测对树木表型的基因与环境交互作用,助力气候变化下的大规模监测与恢复规划。

Hyperspectral Leaf Reflectance Detects Interactive Genetic and Environmental Effects on Tree Phenotypes, Enabling Large-Scale Monitoring and Restoration Planning Under Climate Change.

作者信息

Corbin Jaclyn P M, Best Rebecca J, Garthwaite Iris J, Cooper Hillary F, Doughty Christopher E, Gehring Catherine A, Hultine Kevin R, Allan Gerard J, Whitham Thomas G

机构信息

Department of Biological Sciences, Northern Arizona University, Flagstaff, Arizona, USA.

School of Earth and Sustainability, Northern Arizona University, Flagstaff, Arizona, USA.

出版信息

Plant Cell Environ. 2025 Mar;48(3):1842-1857. doi: 10.1111/pce.15263. Epub 2024 Nov 4.

DOI:10.1111/pce.15263
PMID:39497286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11788971/
Abstract

Plants respond to rapid environmental change in ways that depend on both their genetic identity and their phenotypic plasticity, impacting their survival as well as associated ecosystems. However, genetic and environmental effects on phenotype are difficult to quantify across large spatial scales and through time. Leaf hyperspectral reflectance offers a potentially robust approach to map these effects from local to landscape levels. Using a handheld field spectrometer, we analyzed leaf-level hyperspectral reflectance of the foundation tree species Populus fremontii in wild populations and in three 6-year-old experimental common gardens spanning a steep climatic gradient. First, we show that genetic variation among populations and among clonal genotypes is detectable with leaf spectra, using both multivariate and univariate approaches. Spectra predicted population identity with 100% accuracy among trees in the wild, 87%-98% accuracy within a common garden, and 86% accuracy across different environments. Multiple spectral indices of plant health had significant heritability, with genotype accounting for 10%-23% of spectral variation within populations and 14%-48% of the variation across all populations. Second, we found gene by environment interactions leading to population-specific shifts in the spectral phenotype across common garden environments. Spectral indices indicate that genetically divergent populations made unique adjustments to their chlorophyll and water content in response to the same environmental stresses, so that detecting genetic identity is critical to predicting tree response to change. Third, spectral indicators of greenness and photosynthetic efficiency decreased when populations were transferred to growing environments with higher mean annual maximum temperatures relative to home conditions. This result suggests altered physiological strategies further from the conditions to which plants are locally adapted. Transfers to cooler environments had fewer negative effects, demonstrating that plant spectra show directionality in plant performance adjustments. Thus, leaf reflectance data can detect both local adaptation and plastic shifts in plant physiology, informing strategic restoration and conservation decisions by enabling high resolution tracking of genetic and phenotypic changes in response to climate change.

摘要

植物对快速环境变化的响应方式取决于其遗传特性和表型可塑性,这会影响它们的生存以及相关生态系统。然而,在大空间尺度和长时间范围内,遗传和环境对表型的影响难以量化。叶片高光谱反射率提供了一种从局部到景观尺度绘制这些影响的潜在有力方法。我们使用手持式野外光谱仪,分析了野生种群以及跨越陡峭气候梯度的三个6年生实验性公共花园中基础树种弗氏杨的叶片水平高光谱反射率。首先,我们表明,使用多变量和单变量方法,通过叶片光谱可以检测种群间和克隆基因型间的遗传变异。光谱在野生树木中以100%的准确率预测种群身份,在公共花园内准确率为87%-98%,在不同环境间准确率为86%。多种植物健康光谱指数具有显著的遗传力,基因型占种群内光谱变异的10%-23%,占所有种群间变异的14%-48%。其次,我们发现基因与环境的相互作用导致公共花园环境中光谱表型出现种群特异性变化。光谱指数表明,遗传上不同的种群在面对相同环境压力时,对其叶绿素和水分含量进行了独特的调整,因此检测遗传身份对于预测树木对变化的响应至关重要。第三,当种群被转移到相对于原生环境年平均最高温度更高的生长环境时,绿色度和光合效率的光谱指标下降。这一结果表明,远离植物本地适应条件时,生理策略发生了改变。转移到较凉爽环境的负面影响较小,表明植物光谱在植物性能调整方面具有方向性。因此,叶片反射率数据可以检测植物生理中的局部适应和可塑性变化,通过对响应气候变化的遗传和表型变化进行高分辨率跟踪,为战略恢复和保护决策提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a85/11788971/0f77da50117e/PCE-48-1842-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a85/11788971/6ff16cee8a40/PCE-48-1842-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a85/11788971/d6cf96eff1e1/PCE-48-1842-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a85/11788971/a1720ac74454/PCE-48-1842-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a85/11788971/2e3ca5da9a51/PCE-48-1842-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a85/11788971/0f77da50117e/PCE-48-1842-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a85/11788971/6ff16cee8a40/PCE-48-1842-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a85/11788971/d6cf96eff1e1/PCE-48-1842-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a85/11788971/a1720ac74454/PCE-48-1842-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a85/11788971/d082a56a2a99/PCE-48-1842-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a85/11788971/2e3ca5da9a51/PCE-48-1842-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a85/11788971/0f77da50117e/PCE-48-1842-g006.jpg

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