Abstract

Spectroscopy is becoming an increasingly powerful tool to alleviate the challenges of traditional measurements of key plant traits at the leaf, canopy, and ecosystem scales. Spectroscopic methods often rely on statistical approaches to reduce data redundancy and enhance useful prediction of physiological traits. Given the mechanistic uncertainty of spectroscopic techniques, genetic modification of plant biochemical pathways may affect reflectance spectra causing predictive models to lose power. The objectives of this research were to assess over two separate years, whether a predictive model can represent natural and imposed variation in leaf photosynthetic potential for different crop cultivars and genetically modified plants, to assess the interannual capabilities of a partial least square regression (PLSR) model, and to determine whether leaf N is a dominant driver of photosynthesis in PLSR models. In 2016, a PLSR analysis of reflectance spectra coupled with gas exchange data was used to build predictive models for photosynthetic parameters including maximum carboxylation rate of Rubisco (Vc,max), maximum electron transport rate (Jmax) and percentage leaf nitrogen ([N]). The model was developed for wild type and genetically modified plants that represent a wide range of photosynthetic capacities. Results show that hyperspectral reflectance accurately predicted Vc,max, Jmax and [N] for all plants measured in 2016. Applying these PLSR models to plants grown in 2017 resulted in a strong predictive ability relative to gas exchange measurements for Vc,max, but not for Jmax, and not for genotypes unique to 2017. Building a new model including data collected in 2017 resulted in more robust predictions, with R2 increases of 17% for Vc,max. and 13% Jmax. Plants generally have a positive correlation between leaf nitrogen and photosynthesis, however, tobacco with reduced Rubisco (SSuD) had significantly higher [N] despite much lower Vc,max. The PLSR model was able to accurately predict both lower Vc,max and higher leaf [N] for this genotype suggesting that the spectral based estimates of Vc,max and leaf nitrogen [N] are independent. These results suggest that the PLSR model can be applied across years, but only to genotypes used to build the model and that the actual mechanism measured with the PLSR technique is not directly related to leaf [N]. The success of the leaf-scale analysis suggests that similar approaches may be successful at the canopy and ecosystem scales but to use these methods across years and between genotypes at any scale, application of accurately populated physical based models based on radiative transfer principles may be required.

Highlights

  • Projected population increases, rising global affluence, and mounting pressures from a changing global climate necessitate improvements to global food supply (Tilman et al, 2009; Foley et al, 2011)

  • Measurements for the Model Set 1 made over the 2016 growing season (Fig. 1) represented a wide range of meteorological conditions (Fig. S1), which coupled with the different cultivars and genetic modifications, yielded a wide range of values for Vc,max (14.7–279.8 μmol CO2 m−2 s−1) and Jmax (92.8–323.2 μmol CO2 m−2 s−1)

  • In model set 1, six latent variables (LVs)'s were used for the Vc,max build, while nine latent variables (LV's) were used for Jmax and [N]

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Summary

Introduction

Projected population increases, rising global affluence, and mounting pressures from a changing global climate necessitate improvements to global food supply (Tilman et al, 2009; Foley et al, 2011). Despite being one of nature's most conserved processes, photosynthesis has a staggering number of component inefficiencies (Long et al, 2006; Evans, 2013). These inefficiencies inspire current research efforts to improve crop yields through manipulating photosynthetic pathways (Ort et al, 2015; Andralojc et al, 2018) and exploiting natural variation in photosynthetic rates (Lawson et al, 2012; Meacham et al, 2016). Regardless of the means of improvement, the ability to non-destructively sample phenotypic variation in photosynthetic capacity among tens to hundreds of thousands of plants representing genotypic variation within a reasonable time presents a significant phenotyping challenge (Furbank and Tester, 2011)

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