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Determination of seed oil content and fatty acid composition in sunflower through the analysis of intact seeds, husked seeds, meal and oil by near‐infrared reflectance spectroscopy
Author(s) -
PérezVich B.,
Velasco L.,
FernándezMartínez J. M.
Publication year - 1998
Publication title -
journal of the american oil chemists' society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.512
H-Index - 117
eISSN - 1558-9331
pISSN - 0003-021X
DOI - 10.1007/s11746-998-0064-1
Subject(s) - sunflower , near infrared reflectance spectroscopy , meal , sunflower oil , fatty acid , composition (language) , sunflower seed , helianthus annuus , chemistry , food science , chromatography , near infrared spectroscopy , horticulture , biology , biochemistry , linguistics , philosophy , neuroscience
A methodological study was conducted to test the potential of near‐infrared reflectance spectroscopy (NIRS) to estimate the oil content and fatty acid composition of sunflower seeds. A set of 387 intact‐seed samples, each from a single plant, were scanned by NIRS, and 120 of them were selected and further scanned as husked seed, meal, and oil. All samples were analyzed for oil content (nuclear magnetic resonance) and fatty acid composition (gas chromatography), and calibration equations for oil content and individual fatty acids (C 16:0 , C 16:1 , C 18:0 , C 18:1 , and C 18:2 ) were developed for intact seed, husked seed, meal, and oil. For intact seed, the performance of the calibration equations was evaluated through both cross‐ and external validation, while cross‐validation was used in the rest. The results showed that NIRS is a reliable and accurate technique to estimate these traits in sunflower oil (validation r 2 ranged from 0.97 to 0.99), meal ( r 2 from 0.92 to 0.98), and husked seeds ( r 2 from 0.90 to 0.97). According to these results, there is no need to grind the seeds to scan the meal; similarly accurate results are obtained by analyzing husked seeds. The analysis of intact seeds was less accurate ( r 2 from 0.76 to 0.85), although it is reliable enough to use for pre‐screening purposes to identify variants with significantly different fatty acid compositions from standard phenotypes. Screening of intact sunflower seeds by NIRS represents a rapid, simple, and cost‐effective alternative that may be of great utility for users who need to analyze a large number of samples.