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      Hyperspectral Reflectance-Derived Relationship Matrices for Genomic Prediction of Grain Yield in Wheat

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          Abstract

          Hyperspectral reflectance phenotyping and genomic selection are two emerging technologies that have the potential to increase plant breeding efficiency by improving prediction accuracy for grain yield. Hyperspectral cameras quantify canopy reflectance across a wide range of wavelengths that are associated with numerous biophysical and biochemical processes in plants. Genomic selection models utilize genome-wide marker or pedigree information to predict the genetic values of breeding lines. In this study, we propose a multi-kernel GBLUP approach to genomic selection that uses genomic marker-, pedigree-, and hyperspectral reflectance-derived relationship matrices to model the genetic main effects and genotype × environment ( G ×  E) interactions across environments within a bread wheat ( Triticum aestivum L.) breeding program. We utilized an airplane equipped with a hyperspectral camera to phenotype five differentially managed treatments of the yield trials conducted by the Bread Wheat Improvement Program of the International Maize and Wheat Improvement Center (CIMMYT) at Ciudad Obregón, México over four breeding cycles. We observed that single-kernel models using hyperspectral reflectance-derived relationship matrices performed similarly or superior to marker- and pedigree-based genomic selection models when predicting within and across environments. Multi-kernel models combining marker/pedigree information with hyperspectral reflectance phentoypes had the highest prediction accuracies; however, improvements in accuracy over marker- and pedigree-based models were marginal when correcting for days to heading. Our results demonstrate the potential of using hyperspectral imaging to predict grain yield within a multi-environment context and also support further studies on the integration of hyperspectral reflectance phenotyping into breeding programs.

          Most cited references25

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          Monitoring vegetation phenology using MODIS

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            Genomic Selection in Wheat Breeding using Genotyping-by-Sequencing

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              REGULATION OF LIGHT HARVESTING IN GREEN PLANTS.

              When plants are exposed to light intensities in excess of those that can be utilized in photosynthetic electron transport, nonphotochemical dissipation of excitation energy is induced as a mechanism for photoprotection of photosystem II. The features of this process are reviewed, particularly with respect to the molecular mechanisms involved. It is shown how the dynamic properties of the proteins and pigments of the chlorophyll a/b light-harvesting complexes of photosystem II first enable the level of excitation energy to be sensed via the thylakoid proton gradient and subsequently allow excess energy to be dissipated as heat by formation of a nonphotochemical quencher. The nature of this quencher is discussed, together with a consideration of how the variation in capacity for energy dissipation depends on specific features of the composition of the light-harvesting system. Finally, the prospects for future progress in understanding the regulation of light harvesting are assessed.
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                Author and article information

                Journal
                G3 (Bethesda)
                Genetics
                G3: Genes, Genomes, Genetics
                G3: Genes, Genomes, Genetics
                G3: Genes, Genomes, Genetics
                G3: Genes|Genomes|Genetics
                Genetics Society of America
                2160-1836
                22 February 2019
                April 2019
                : 9
                : 4
                : 1231-1247
                Affiliations
                [* ]Plant Breeding and Genetics Section, School of Integrative Plant Science, Cornell University, Ithaca, New York, 14853
                []Global Wheat Program, International Maize and Wheat Improvement Center (CIMMYT), Ciudad de México, 06600, México
                []Colegio de Postgraduados, CP 56230, Montecillos, Edo. de México, Mexico,
                [§ ]Facultad de Telemática, Universidad de Colima, Colima, Colima, 28040, México
                [** ]Department of Plant Pathology, Kansas State University, Manhattan, Kansas, 66506
                [†† ]International Rice Research Institute (IRRI), DAPO Box 7777, Metro Manila, 1301, Philippines
                Author notes
                [1 ]Corresponding Author: International Maize and Wheat Improvement Center, CIMMYT Km45 Carretera Mex-Veracruz, El Batán, Texcoco, México. C.P 56237, E-mail: S.Mondal@ 123456cgiar.org
                Author information
                http://orcid.org/0000-0003-1154-337X
                http://orcid.org/0000-0002-5840-0803
                http://orcid.org/0000-0001-9429-5855
                http://orcid.org/0000-0002-4676-5071
                http://orcid.org/0000-0002-7856-1399
                http://orcid.org/0000-0001-6896-8024
                http://orcid.org/0000-0002-8582-8899
                Article
                GGG_200856
                10.1534/g3.118.200856
                6469421
                30796086
                86a2652a-9b2f-4381-a10a-98d3f5003206
                Copyright © 2019 Krause et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 22 November 2018
                : 15 February 2019
                Page count
                Figures: 8, Tables: 3, Equations: 7, References: 49, Pages: 17
                Categories
                Genomic Prediction

                Genetics
                hyperspectral reflectance,genomic prediction,high throughput phenotyping,wheat breeding,genotype-by-environment interaction,gblup,genpred,shared data resources

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