The possibility of using near-infrared spectroscopy (NIRS) for the authentication of wild European sea bass (Dicentrarchus labrax) was investigated in this study. Three different chemometric techniques to process the NIR spectra were developed, and their ability to discriminate between wild and farmed sea bass samples was evaluated. One approach used spectral information to directly build the discrimination model in a latent variable space; the second approach first used wavelets to transform the spectral information and subsequently derived the discrimination model using the transformed spectra; in the third approach a cascaded arrangement was proposed whereby very limited chemical information was first estimated from spectra using a regression model, and this estimated information was then used to build the discrimination model in a latent variable space. All techniques showed that NIRS can be used to reliably discriminate between wild and farmed sea bass, achieving the same classification performance as classification methods that use chemical properties and morphometric traits. However, compared to methods based on chemical analysis, NIRS-based classification methods do not require reagents and are simpler, faster, more economical, and environmentally safer. All proposed techniques indicated that the most predictive spectral regions were those related to the absorbance of groups CH, CH2, CH3, and H2O, which are related to fat, fatty acids, and water content.

Ottavian, M.; Facco, P.; Fasolato, L.; Novelli, E.; Mirisola, M.; Perini, M.; Barolo, M. (2012). Use of Near-Infrared Spectroscopy for fast fraud detection in seafood: application to the authentication of wild European sea bass (Dicentrarchus labrax). JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 60 (2): 639-648. doi: 10.1021/jf203385e handle: http://hdl.handle.net/10449/20729

Use of Near-Infrared Spectroscopy for fast fraud detection in seafood: application to the authentication of wild European sea bass (Dicentrarchus labrax)

Perini, Matteo;
2012-01-01

Abstract

The possibility of using near-infrared spectroscopy (NIRS) for the authentication of wild European sea bass (Dicentrarchus labrax) was investigated in this study. Three different chemometric techniques to process the NIR spectra were developed, and their ability to discriminate between wild and farmed sea bass samples was evaluated. One approach used spectral information to directly build the discrimination model in a latent variable space; the second approach first used wavelets to transform the spectral information and subsequently derived the discrimination model using the transformed spectra; in the third approach a cascaded arrangement was proposed whereby very limited chemical information was first estimated from spectra using a regression model, and this estimated information was then used to build the discrimination model in a latent variable space. All techniques showed that NIRS can be used to reliably discriminate between wild and farmed sea bass, achieving the same classification performance as classification methods that use chemical properties and morphometric traits. However, compared to methods based on chemical analysis, NIRS-based classification methods do not require reagents and are simpler, faster, more economical, and environmentally safer. All proposed techniques indicated that the most predictive spectral regions were those related to the absorbance of groups CH, CH2, CH3, and H2O, which are related to fat, fatty acids, and water content.
European sea bass
PLS-DA
Wavelet analysis
Authentication
Near-infrared spectroscopy
Fraud detection
2012
Ottavian, M.; Facco, P.; Fasolato, L.; Novelli, E.; Mirisola, M.; Perini, M.; Barolo, M. (2012). Use of Near-Infrared Spectroscopy for fast fraud detection in seafood: application to the authentication of wild European sea bass (Dicentrarchus labrax). JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 60 (2): 639-648. doi: 10.1021/jf203385e handle: http://hdl.handle.net/10449/20729
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10449/20729
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