Spectral Variable Selection for Partial Least Squares Calibration Applied to Authentication and Quantification of Extra Virgin Olive Oils Using Fourier Transform Raman Spectroscopy

2005 ◽  
Vol 59 (10) ◽  
pp. 1286-1294 ◽  
Author(s):  
H. Michael Heise ◽  
Uwe Damm ◽  
Peter Lampen ◽  
Antony N. Davies ◽  
Peter S. McIntyre

The limits of quantitative multivariate assays for the analysis of extra virgin olive oil samples from various Greek sites adulterated by sunflower oil have been evaluated based on their Fourier transform (FT) Raman spectra. Different strategies for wavelength selection were tested for calculating optimal partial least squares (PLS) models. Compared to the full spectrum methods previously applied, the optimum standard error of prediction (SEP) for the sunflower oil concentrations in spiked olive oil samples could be significantly reduced. One efficient approach (PMMS, pair-wise minima and maxima selection) used a special variable selection strategy based on a pair-wise consideration of significant respective minima and maxima of PLS regression vectors, calculated for broad spectral intervals and a low number of PLS factors. PMMS provided robust calibration models with a small number of variables. On the other hand, the Tabu search strategy recently published (search process guided by restrictions leading to Tabu list) achieved lower SEP values but at the cost of extensive computing time when searching for a global minimum and less robust calibration models. Robustness was tested by using packages of ten and twenty randomly selected samples within cross-validation for calculating independent prediction values. The best SEP values for a one year's harvest with a total number of 66 Cretian samples were obtained by such spectral variable optimized PLS calibration models using leave-20-out cross-validation (values between 0.5 and 0.7% by weight). For the more complex population of olive oil samples from all over Greece (total number of 92 samples), results were between 0.7 and 0.9% by weight with a cross-validation sample package size of 20. Notably, the calibration method with Tabu variable selection has been shown to be a valid chemometric approach by which a single model can be applied with a low SEP of 1.4% for olive oil samples across three different harvest years.

2014 ◽  
Vol 70 (5) ◽  
Author(s):  
Nor Fazila Rasaruddin ◽  
Mas Ezatul Nadia Mohd Ruah ◽  
Mohamed Noor Hasan ◽  
Mohd Zuli Jaafar

This paper shows the determination of iodine value (IV) of pure and frying palm oils using Partial Least Squares (PLS) regression with application of variable selection. A total of 28 samples consisting of pure and frying palm oils which acquired from markets. Seven of them were considered as high-priced palm oils while the remaining was low-priced. PLS regression models were developed for the determination of IV using Fourier Transform Infrared (FTIR) spectra data in absorbance mode in the range from 650 cm-1 to 4000 cm-1. Savitzky Golay derivative was applied before developing the prediction models. The models were constructed using wavelength selected in the FTIR region by adopting selectivity ratio (SR) plot and correlation coefficient to the IV parameter. Each model was validated through Root Mean Square Error Cross Validation, RMSECV and cross validation correlation coefficient, R2cv. The best model using SR plot was the model with mean centring for pure sample and model with a combination of row scaling and standardization of frying sample. The best model with the application of the correlation coefficient variable selection was the model with a combination of row scaling and standardization of pure sample and model with mean centering data pre-processing for frying sample. It is not necessary to row scaled the variables to develop the model since the effect of row scaling on model quality is insignificant.


1995 ◽  
Vol 49 (12) ◽  
pp. 1766-1771 ◽  
Author(s):  
Christopher J. de Bakker ◽  
Peter M. Fredericks

The petroleum products unleaded gasoline and reformate have been analyzed by Fourier transform (FT) Raman spectrometry with the use of a fiber optic cable that allows a measurement to be carried out remotely from the spectrometer. Samples were contained in glass cuvettes, and collection of high-quality spectra was simple. Fuel properties such as research octane number (RON), motor octane number (MON), density, benzene content, and flexible volatility index (FVI) were determined by application of the partial least-squares multivariate statistical approach. Analytically useful calibrations ( R2 > 0.97) were obtained for all of the significant fuel properties studied. Cross-validation results were, as expected, worse than the calibration results but still indicated the usefulness of the method. Standard errors of prediction with the use of cross validation for models that contained 14–28 samples include: MON = 0.12, RON = 0.16, benzene % = 0.09, and density = 0.0018. These results demonstrate that it is feasible to undertake on-line analyses of petroleum fuels by fiber-optic FT-Raman spectrometry.


2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
Jie Yu Chen ◽  
Han Zhang ◽  
Jinkui Ma ◽  
Tomohiro Tuchiya ◽  
Yelian Miao

This rapid method for determining the degree of degradation of frying rapeseed oils uses Fourier-transform infrared (FTIR) spectroscopy combined with partial least-squares (PLS) regression. One hundred and fifty-six frying oil samples that degraded to different degrees by frying potatoes were scanned by an FTIR spectrometer using attenuated total reflectance (ATR). PLS regression with full cross validation was used for the prediction of acid value (AV) and total polar compounds (TPC) based on raw, first, and second derivative FTIR spectra (4000–650 cm−1). The precise calibration model based on the second derivative FTIR spectra shows that the coefficients of determination for calibration(R2)and standard errors of cross validation (SECV) were 0.99 and 0.16 mg KOH/g and 0.98 and 1.17% for AV and TPC, respectively. The accuracy of the calibration model, tested using the validation set, yielded standard errors of prediction (SEP) of 0.16 mg KOH/g and 1.10% for AV and TPC, respectively. Therefore, the degradation of frying oils can be accurately measured using FTIR spectroscopy combined with PLS regression.


Agronomy ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 666
Author(s):  
Rafael Font ◽  
Mercedes del Río-Celestino ◽  
Diego Luna ◽  
Juan Gil ◽  
Antonio de Haro-Bailón

The near-infrared spectroscopy (NIRS) combined with modified partial least squares (modified PLS) regression was used for determining the neutral detergent fiber (NDF) and the acid detergent fiber (ADF) fractions of the chickpea (Cicer arietinum L.) seed. Fifty chickpea accessions (24 desi and 26 kabuli types) and fifty recombinant inbred lines F5:6 derived from a kabuli × desi cross were evaluated for NDF and ADF, and scanned by NIRS. NDF and ADF values were regressed against different spectral transformations by modified partial least squares regression. The coefficients of determination in the cross-validation and the standard deviation from the standard error of cross-validation ratio were, for NDF, 0.91 and 3.37, and for ADF, 0.98 and 6.73, respectively, showing the high potential of NIRS to assess these components in chickpea for screening (NDF) or quality control (ADF) purposes. The spectral information provided by different chromophores existing in the chickpea seed highly correlated with the NDF and ADF composition of the seed, and, thus, those electronic transitions are highly influenced on model fitting for fiber.


2002 ◽  
Vol 56 (3) ◽  
pp. 337-345 ◽  
Author(s):  
S. Kamaledin Setarehdan ◽  
John J. Soraghan ◽  
David Littlejohn ◽  
Daran A. Sadler

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