Investigation of the Effects of Virgin Olive Oil Cleaning Systems on the Secoiridoid Aglycone Content Using High Performance Liquid Chromatography–Mass Spectrometry

Phenolic compounds are useful markers to control olive oil technological processes, including the virgin olive oil (VOO)/water separation after olive oil extraction. In this investigation, VOO extracted from olives of cv. Coratina using a mild oil/water separator called the hydrocyclone sedimentation system (Hydroil) was compared with VOO obtained using a conventional vertical centrifuge separator (Cenoil), which is mostly used in the modern olive oil industry. Secoiridoid aglycones were selected, among phenolic compounds, as markers and analyzed using reversed‐phase liquid chromatography coupled to linear quadrupole ion‐trap mass spectrometry with electrospray ionization in the negative mode. VOO samples obtained using the Hydroil system were found to contain significantly higher levels of secoiridoid aglycones, compared to the Cenoyl‐type samples. In particular, the total content of the aglycones of decarboxymethyl oleuropein, decarboxymethyl ligstroside, ligstroside, and oleuropein, expressed in terms of oleuropein, was estimated as 35.40 ± 0.80 mg kg^?1, compared to 8.06 ± 0.41 mg kg^?1 in the Cenoil samples (n = 3). Since no significant difference in residual water (P < 0.05) was found between the two types of VOO samples, the higher amount of secoiridoids obtained for Hydroil‐type ones was explained by the lower extent of oxidation occurring during the mild oil/water separation achieved using the Hydroil system.     

Determination of the SiH content of hydrogen silicone oil by a combination of the fourier transform near infrared,attenuated total reflectance–fourier transform infrared,and partial least squares regression models

To verify the feasibility of the determination of the Si?H content (HC) of hydrogen silicone oil (HS‐oil) with Fourier transform near infrared (FT‐NIR) spectroscopy and attenuated total reflectance (ATR)–Fourier transform infrared (FTIR) spectroscopy combined with the partial least squares regression (PLS‐R) model, HS‐oil samples were synthesized from concentrated hydrosilicone oil (HC = 1.4 wt %), octamethylcyclotetrasiloxane, and hexamethyldisiloxane or prepared by the dilution of concentrated hydrosilicone oil with octamethylcyclotetrasiloxane. The FT‐NIR PLS‐R model (8695–4000 cm^?1, two principal components) was developed from the FT‐NIR spectral data, and the coefficient of determination for cross‐validation (R²) and the coefficient of determination for external validation (r²) were 0.992 and 0.995, respectively. The ATR–FTIR PLS‐R model (2302–2040 cm^?1, one principal component) was developed from the ATR–FTIR spectral data; it produced an R² of 0.995 and an r² of 0.996. This study demonstrated that the combination of FT‐NIR and ATR–FTIR spectroscopy with the PLS‐R model were successfully used to determine the HC of the HS‐oil. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40694.     

Determination of the Si?H content of hydrogen silicone oil by a combination of the fourier transform near infrared,attenuated total reflectance–fourier transform infrared,and partial least squares regression models

To verify the feasibility of the determination of the Si? H content (HC) of hydrogen silicone oil (HS‐oil) with Fourier transform near infrared (FT‐NIR) spectroscopy and attenuated total reflectance (ATR)–Fourier transform infrared (FTIR) spectroscopy combined with the partial least squares regression (PLS‐R) model, HS‐oil samples were synthesized from concentrated hydrosilicone oil (HC = 1.4 wt %), octamethylcyclotetrasiloxane, and hexamethyldisiloxane or prepared by the dilution of concentrated hydrosilicone oil with octamethylcyclotetrasiloxane. The FT‐NIR PLS‐R model (8695–4000 cm^?1, two principal components) was developed from the FT‐NIR spectral data, and the coefficient of determination for cross‐validation (R²) and the coefficient of determination for external validation (r²) were 0.992 and 0.995, respectively. The ATR–FTIR PLS‐R model (2302–2040 cm^?1, one principal component) was developed from the ATR–FTIR spectral data; it produced an R² of 0.995 and an r² of 0.996. This study demonstrated that the combination of FT‐NIR and ATR–FTIR spectroscopy with the PLS‐R model were successfully used to determine the HC of the HS‐oil. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40694.     

Composition and Physical Stability of the Colloidal Dispersion in Veiled Virgin Olive Oil

Veiled virgin olive oil (VOO) samples of nine different olive cultivars are chosen to have a wide range of physicochemical and biological properties of colloidal dispersions. The contents of proteins and phospholipids range from 40 to 190 mg kg⁻¹ and from 70 to 200 mg kg⁻¹, respectively. The effect of lab-scale centrifugation on cloudy appearance is studied measuring the decrease of turbidity grade values. The time to obtain unveiled oils (20 NTU) is modeled by a logistic equation, and a clear relationship between the initial water content and the above time is observed with a different trend between two groups of the VOO samples. Four VOO samples are selected to study the aggregation phenomena of microdroplets of water, pulp particles, and olive stone fragments via optical microscopy and dynamic light scattering during lab-scale gravity sedimentation. All VOOs are unstable with the cloudiness disappearing within the 230 days of investigation due to an overall diameter increase of cloudy components which is modeled by a power-law equation. The VOO samples, characterized by both small diameter values of dispersed components (150–250 nm) and high values of water content, show the fastest aggregation kinetics, but they have the longest time of cloudiness stability. Practical Applications: Water content and size distribution of VOO cloudy components can be key factors to control the colloidal stability. If removal of cloudy appearance is required, centrifugation can be applied to obtain a fast oil clarification which shows a power law relationship of water content with time. Instead, if physical stability of the colloidal dispersion is required, the aggregation phenomena should be slow down through VOO processing to obtain small diameters of the cloudy components. Tuning both the water content and dispersed phase diameter in the VOO can be the first step towards the control of phenomena related to the colloidal dispersion for every olive oil processing organization, above and beyond the simple removal of cloudy appearance by filtration.     

Application of FTIR Spectroscopy for the Determination of Virgin Coconut Oil in Binary Mixtures with Olive Oil and Palm Oil

Rapid Fourier transform infrared (FTIR) spectroscopy combined with attenuated total reflectance (ATR) was applied for quantitative analysis of virgin coconut oil (VCO) in binary mixtures with olive oil (OO) and palm oil (PO). The spectral bands correlated with VCO, OO, PO; blends of VCO and OO; VCO and PO were scanned, interpreted, and identified. Two multivariate calibration methods, partial least square (PLS) and principal component regression (PCR), were used to construct the calibration models that correlate between actual and FTIR-predicted values of VCO contents in the mixtures at the FTIR spectral frequencies of 1,120–1,105 and 965–960 cm⁻¹. The calibration models obtained were cross validated using the “leave one out” method. PLS at these frequencies showed the best calibration model, in terms of the highest coefficient of determination (R ²) and the lowest of root mean standard error of calibration (RMSEC) with R ² = 0.9992 and RMSEC = 0.756, respectively, for VCO in mixture with OO. Meanwhile, the R ² and RMSEC values obtained for VCO in mixture with PO were 0.9996 and 0.494, respectively. In general, FTIR spectroscopy serves as a suitable technique for determination of VCO in mixture with the other oils.     

Thai Tea Seed Oil and Virgin Olive Oil Similarly Reduce Plasma Lipids: A Pilot Study within a Healthy Adult Male Population

The potential cardiovascular benefit of virgin olive oil (VOO) is widely recognized. However, the use of VOO at very high cooking temperatures makes these oils poorly suited for many Asian dishes. The use of tea seed oil (TSO) is increasing in Thailand, with TSO having a higher smoke point than VOO. The current study examines the effects of daily TSO intake in healthy adults. In a randomized, single-blind crossover design, 12 men consumed for 3 weeks 40 g day⁻¹ of food prepared with either TSO or VOO as a cooking oil. Plasma lipids, thiobarbituric acid reactive substances (TBARS), and oxidant defense enzyme activities are measured before and after each 3-week intervention period. Gas chromatography analysis of TSO and VOO demonstrates that both oils are equally high in monounsaturated fatty acid. The dietary incorporation of TSO and VOO for three weeks reduces low-density lipoprotein cholesterol (LDL-C) concentrations by 15% and 13%, respectively; with total cholesterol (TC) levels lowered by 10% in both groups. No significant changes in TBARS or antioxidant enzyme activity is observed. These results support the concept that Thai TSO can be utilized as a suitable and healthy alternative oil for high-temperature cooking in many Thai and Asian diets. Practical Applications: Tea seed oil from Camellia oleifera grown in Thailand has been recently reported to favorably lower lipid profiles in hamsters fed a high-fat diet in a manner similar to feeding refined olive oil or grapeseed oil. A pilot crossover trial is conducted to compare the effects of three weeks of daily intake of either TSO or VOO in healthy human adults. Consumption of both oils produced significant reductions in TC and LDL-C. Thai TSO leads to favorable lipid profiles and is a reasonable choice for many Thai and Asian food recipes.     

Influence of the extraction process on dissolved oxygen in olive oil

The influence of the olive oil processing steps [paste malaxation (PM), decanter centrifugation (DC), and vertical centrifugation (VC)] on the dissolved oxygen (DO) concentration in virgin olive oil (VOO) right after production was investigated at industrial plant scale for two successive years. The influence of this parameter on quality decay during shelf life, assessed by peroxide value (PV) analysis, was also monitored. The VC step showed the higher oxygenation effect (50% increase in comparison to the control), and a good linear regression (r² = 0.83) was found between the initial DO concentration and the PV after 2 days. An 18‐months shelf life test, performed on VOO sampled before and after the VC, indicated the slowest decay kinetics in the oils with the lower initial DO concentration, i.e. the non‐centrifuged oils.     

Effect of Greek sage and summer savory extracts on vegetable oil thermal stability

The effect of ethanol and acetone extracts obtained from Greek sage (Salvia fruticosa) and summer savory (Satureja hortensis L.) on the thermal stability of vegetable oils heated at frying temperature (180 °C) was studied. Virgin olive oil (VOO), refined olive oil (ROO), sunflower oil (SO), and a commercial oil blend suitable for frying (BL), enriched with each extract obtained from the two plant materials at a concentration of 3 g/kg oil, were heated at 180 °C for 10 h. Changes during heating were assessed by quantification of total polar materials and determination of p‐anisidine values. The acetone extract obtained from Greek sage showed a better inhibitory effect against thermal oxidation of heated refined oils (BL, ROO, SO) than the respective ethanol extract, although the latter was found to have a relatively higher total phenol content. Both summer savory extracts effectively retarded the thermal oxidation reactions during oil heating, showing a more pronounced effect than the Greek sage acetone extract. The activity of the acetone extract obtained from summer savory was stronger (SO, BL) or similar (ROO, VOO) to that of the summer savory ethanol extract, although the latter was found to have a higher total phenol content.     

Pure lycopene from tomato preserves extra virgin olive oil from natural oxidative events during storage

In this study, changes in an extra virgin olive oil treated with lycopene during storage were analyzed. Pure lycopene (0.5 and 1.0 mg) obtained from tomato was added to two separate bottles, each containing 100 mL of extra virgin olive oil, while another bottle containing the same oil was stored without any treatment. Samples enriched with pure lycopene showed PV remarkably lower than the sample without lycopene, and the total phenol contents were higher in treated oil samples than in the reference sample. In addition, a good correlation (r ²=0.969) between total phenol content and antioxidant power calculated as Trolox Equivalent Antioxidant Capacity (TEAC) was observed. The concentration of added lycopene decreased very slowly; after about 8 mon its residual value was over 60% with respect to the initial concentration.     

Dietary Virgin Olive Oil Reduces Oxidative Stress and Cellular Damage in Rat Brain Slices Subjected to Hypoxia–Reoxygenation

We investigated how virgin olive oil (VOO) affected platelet and hypoxic brain damage in rats. Rats were given VOO orally for 30 days at 0.25 or 0.5 mL kg⁻¹ per day (doses A and B, respectively). Platelet aggregation, thromboxane B₂, 6-keto-PGF_1α, and nitrites + nitrates were measured, and hypoxic damage was evaluated in a hypoxia–reoxygenation assay with fresh brain slices. Oxidative stress, prostaglandin E ₂, nitric oxide pathway activity and lactate dehydrogenase (LDH) activity were also measured. Dose A inhibited platelet aggregation by 36% and thromboxane B₂ by 19%; inhibition by dose B was 47 and 23%, respectively. Virgin olive oil inhibited the reoxygenation-induced increase in lipid peroxidation (57% in control rats vs. 2.5% (P < 0.05) in treated rats), and reduced the decrease in glutathione concentration from 67 to 24% (dose A) and 41% (dose B). Brain prostaglandin E ₂ after reoxygenation was 306% higher in control animals, but the increases in treated rats were only 53% (dose A) and 45% (dose B). The increases in nitric oxide production (213% in controls) and activity of the inducible isoform of nitric oxide synthase (175% in controls) were both smaller in animals given VOO (dose A 84%; dose B 12%). Lactate dehydrogenase activity was reduced by 17% (dose A) and 42% (dose B). In conclusion, VOO modified processes related to thrombogenesis and brain ischemia. It reduced oxidative stress and modulated the inducible isoform of nitric oxide synthase, diminishing platelet aggregation and protecting the brain from the effects of hypoxia–reoxygenation. This study was partially supported by a grant from the Ministerio de Ciencia y Tecnología, Spain (AGL−04-7935-C03-02).     

Stability and radical‐scavenging activity of heated olive oil and other vegetable oils

The effect of heating at 180 °C on the antioxidant activity of virgin olive oil (VOO), refined olive oil (ROO) and other vegetable oil samples (sunflower, soybean, cottonseed oils, and a commercial blend specially produced for frying) was determined by measuring the radical‐scavenging activity (RSA) toward 1,1‐diphenyl‐2‐picrylhydrazyl radical (DPPH^?). The RSA of the soluble (polar) and insoluble (non‐polar) in methanol/water fractions of olive oil samples was also measured. The stability of heated oils was assessed by determining their total polar compound (TPC) content. VOO was the most thermostable oil. Total polar phenol content and the RSA of VOO heated for 2.5 h decreased by up to 70 and 78%, respectively, of their initial values; an up to 84% reduction in RSA of VOO polar and non‐polar fractions also occurred. Similar changes were observed in the RSA of ROO and its non‐polar fraction after 2.5 h of heating. The other oils retained their RSA to a relatively high extent (up to 40%) after 10 h of heating, but in the meantime they reached the rejection point (25–27% TPC). The results demonstrate that VOO has a remarkable thermal stability, but when a healthful effect is expected from the presence of phenolic compounds, heating has to be restricted as much as possible.     

Application of a spectroscopic method to estimate the olive oil oxidative status

A rapid Fourier transformed infrared (FTIR) attenuated total reflectance (ATR) spectroscopic method coupled with partial least squares (PLS), was developed to estimate the oxidation degree of extra virgin olive oil (EVOO). The reference values of EVOO oxidation for the FTIR calibration were obtained by the specific absorptions at 232 and 270 nm, due to the presence of conjugated diene (CD) and conjugated triene (CT) groups, as monitored by the UV spectrophotometric determination. Specific washing procedures were applied to the EVOO to obtain EVOOP and EVOOTP samples, without phenolic compounds and without tocopherols and phenols, respectively. To obtain different oxidation degrees covering wide CD and CT ranges, EVOO, EVOOP, and EVOOTP samples were subjected to a forced oxidation at 60°C for 20 days and aliquots of the oils were daily analyzed. Regression of the FTIR/PLS‐predicted CD and CT of individual oxidized oils EVOO, EVOOP, EVOOTP, and all combined oils (EVOOALL) against UV–Visible reference values demonstrated the good quality of the models in terms of R² and RMSECV values. The results of the study indicated that a strong correlation existed between FTIR and UV–Visible peak intensities. Practical applications: The FTIR‐ATR method coupled with PLS elaboration was developed and applied to predict the oxidation degree of EVOO samples with considerable advantages in terms of simplicity, analysis time, and solvent consumption as compared to the standard method. Moreover, suitable adjustments of the equipment could permit a rapid control at‐line in oil sector.     

Comparative study of olive oil quality from Chemlali Sfax versus Arbequina cultivated in Tunisia

The effects of the geographical region on the behavior of the Arbequina olive cultivar (cv) cultivated in the south of Tunisia (in the arid zone of Sfax) was compared to an autochthonous cultivar (Chemlali Sfax). Various olive parameters were analyzed, such as ripening index, pulp/stone ratio, oil contents, and sensory profiles. Most of the quality indices and fatty acid composition showed significant variations among olive cultivars. Arbequina cv is characterized by high oil yield with a less total phenols and pigments content than Chemlali Sfax cv. Cielab spectrophotometer coordinate L*, b*, and a* values show a great difference in olive oil colors. In spite of their low oleic acid contents, autochthonous cultivar presented a higher induction time (6.82 and 2.68 h for Chemlali and Arbequina, respectively) and high contents of phenolic compounds (158.28 and 110.27 mg/kg for Chemlali Sfax and Arbequina, respectively). The most important compounds identified were oleuropein aglycon (45.50 mg/kg), hydroxytyrosol (3.68 mg/kg), 1‐acetoxypinoresinol (6.23 mg/kg) in Chemlali Sfax oil and hydroxytyrosol glucoside (25.15 mg/kg), tyrosol (12.51 mg/kg), and oleuropein aglycon (30.60 mg/kg) in Arbequina oil. Chemlali Sfax also possessed a very bitter taste, whereas the Arbequina had a sweet taste amongst its attributes. The principal component analysis of the results indicated that the geographical region has significantly affected the olive oil quality.     

Profile of enzyme in drupe of oueslati's cv. olives during ripening phases: A support method implementation in the production of extra virgin olive oil

Quality of virgin olive oil (VOO) depends on phenolic molecules content, which depends on the biochemical characteristics of olive fruits, namely endogenous enzymes. In order to ascertain the influence of olive fruit ripening degree on the phenol content, enzyme activities in olive fruits, and the quality of the corresponding oils were studied during Oueslati olive ripening. In fact, three enzymes were studied: peroxidase (POX) in olive seeds, polyphenoloxidase (PPO), and β-glucosidase (β-GL) in olive fruits mesocarp. Each enzyme showed specific trend: POX activity increased gradually until reaching a maximum (17.061 ± 0.101 U g⁻¹ FW) at ripening index (RI) 3.6 and then decreased slowly at advanced ripening stage. However, the maximum of PPO activity (240.421 ± 0.949 U g⁻¹ FW) was observed earlier at RI of 0.7. Concerning β-glucosidase activity, its maximal was 60.857 ± 1.105 U g⁻¹ FW at RI 2.8, then, it decreased sharply to reach 17.096 ± 0.865 U g⁻¹ FW at RI 3.9. A significant increase of total phenol content as well as the antioxidant activity were observed during Oueslati olive ripening. Moreover, phenolic profile indicated that appropriate harvesting date of Oueslati olives coincided with RI 3.9 given that highest content of most important individuals phenolic compounds responsible for the main VOO biological properties achieved on this date. Furthermore, phenols amount of Oueslati VOO was principally due to PPO enzyme activity as the increase in total phenols coincides with the decrease in PPO activity.     

Impact of frying on key fatty acid ratios of canola oil

The study was carried out to investigate the changes in saturated (SFA), monoene (MUFA), trans (TFA), and polyunsaturated (PUFA) fatty acids and the key fatty acid ratios (SFA/UFA, cis PUFA/SFA, C18:2/C16:0 and C18:3/C16:0) during potato chips frying in canola oil using single bounce attenuated total reflectance FTIR (SB‐ATR‐FTIR) spectroscopy. The data obtained from GC‐FID were used as reference. The calibration of main fat groups and their key fatty acid ratios were developed by partial least square (PLS) regression coefficients using 4000 to 650 cm^?1 spectral range. FTIR PLS regression for the predicted SFA, MUFA, TFA, and PUFA were found 0.999, 0.998, 0.998, and 0.999, respectively, whereas for SFA/UFA, cis PUFA/SFA, C18:2/C16:0 and C18:3/C16:0 the regression coefficients were 0.991, 0.997, 0.996, and 0.994, respectively. We conclude that FTIR‐PLS could be used for rapid and accurate assessment of changes in the main fat groups and their key fatty acid ratios ratio during the frying process. Practical applications: FTIR‐ATR method is very simple, rapid, and environmentally friendly. No sample preparation is required and one drop of oil is enough for FTIR analysis. The proposed method could be applied for quick determination of key fatty acid ratios in the food processing industry.     

Changes in Total Polar Compounds,Peroxide Value,Total Phenols and Antioxidant Activity of Various Oils Used in Deep Fat Frying

In this study, the effect of deep fat frying on oil degradation, total phenols (TP) and total antioxidant activity (TAA) of hazelnut, corn, soybean and olive oils were investigated. Oil degradation and oxidation were monitored by measuring the total polar compounds (TPC) and the peroxide value (PV). The amount of TPC in corn, soybean and olive oils increased significantly with the time increment (p < 0.05). The PV of the oils did not exceed the maximum acceptable limit of 10 mequiv O₂/kg after 125 min frying except for hazelnut oil (10.64 mequiv O₂/kg). Deep-fat frying did not cause any significant change in the TP of corn oil, soybean oil and olive oil (p < 0.05). A significant decrease in the antioxidant activity was observed after 50 min frying using hazelnut oil and corn oil (p < 0.05). However, the antioxidant activity of soybean oil and olive oil significantly decreased after 75 and 25 min frying, respectively.     

Synthesis of two modified carotenoids and their behavior during light exposure

Two modified carotenoids, β‐6‐hydroxy‐2, 5, 7, 8‐tetramethyl‐chromane carboxylic acid β‐apo‐8'‐carotenoate (Caro‐Trolox) and 3, 5‐di‐tert‐butyl‐4‐hydroxy benzoic acid β‐apo‐8'‐carotenoate (Caro‐BHT) were synthesized by esterification of β‐apo‐8'‐carotenol with Trolox and with 3, 5‐di‐tert‐butyl‐4‐hydroxy benzoic acid, respectively. Their activity under light exposure was examined comparatively to that of Trolox, α‐tocopherol, β‐carotene, β‐apo‐8'‐carotenoic acid (CA} and ethyl β‐apo‐8'‐carotenoate. The substrate used was purified sunflower oil. In the absence of a photosensitizer (240 W/m² , 25 °C) Caro‐Trolox (200 mg/kg) behaved as an antioxidant and was quite stable (1/5 of the initial amount remained after 2‐wk storage). Caro‐BHT (200 mg/kg) showed no antioxidant activity and was quite unstable (it was destroyed within 7 d). In the presence of 5 mg/kg chlorophyll α (12000 lx, 25 °C) similar observations were made. The activity of Caro‐Trolox was concentration‐dependent. At a 100‐mg/kg level of addition its activity was similar to that of the mixture of α‐t_copherol (100 mg/kg) and β‐carotene (10 mg/kg). Its performance at the 10‐mg/kg level was slightly better than that of the other carotenoids. The antioxidant behavior of the modified carotenoids was attributed to the presence of the phenolic moiety as supported by the results of the 1, 1‐diphenyl‐2‐picrylhydrazyl test (e.g. EC₅₀ after 15 min: 26.2, Caro‐Trolox; 35.8, Caro‐BHT; 122, CA; 22.3, Trolox).     

Proposed parameters for monitoring quality of virgin olive oil (Koroneiki cv)

The overall quality of virgin olive oil (VOO) is closely related to its oxidative stability that is usually evaluated through the stability index measured by the Rancimat apparatus. Quality characteristics and also pro‐oxidant and antioxidant content for 52 Greek VOO samples (Koroneiki cv) were used to build up a model capable of predicting stability. Collinearity diagnostics, variable selection, and regression analysis were applied to the experimental data to locate the contribution of each parameter to the keeping quality of the samples. The predictive ability of the model was confirmed for a second VOO ample set of the same cultivar. It was found that except for the peroxide value, which negatively influences the stability, other important parameters were α‐tocopherol, total polar phenol and total chlorophyll content. It is concluded that the colorimetric determination of total polar phenols, the spectrometric determination of total chlorophylls and the high‐performance liquid chromatography analysis of α‐tocopherol, not presently included in the established methods of official analysis, can be used for a better evaluation of VOO quality. These parameters, which can be easily adopted as routine methods by the industry, seem to be of utmost importance for shelf life prediction and expiration dating if applied for the promotion of the most competitive products in the international olive oil market.     

Bioactive Compounds in Virgin Olive Oil of the PDO Montoro-Adamuz

Virgin olive oil (VOO) is generally recognized as a healthy fat because of its fatty acid composition and content in minor compounds but a wide range of these substances can be found in commercial oils. The concentration of compounds with attributed health benefits were analyzed in VOO of the PDO Montoro‐Adamuz. Oleic acid represented around 79 % of the total fatty acids, and the mean squalene and tocopherols concentrations were 5800 and 247 mg/kg respectively. Despite the changes found in polyphenols concentration in the oils analyzed for six consecutive crops, these substances accounted for more than 700 mg/kg. Moreover, the effect of irrigation regime and sun radiation on the content in bioactive substances of these oils was also assessed. No significant differences were detected between oils from trees irrigated ad libitum or rain‐feed. In contrast, the level of tree radiation exerted a great effect on the concentration of bioactive substances in oils. Oils from trees cultivated in a sunny area (south orientation) had a higher percentage of oleic acid and concentration in phenolic compounds than those from shady areas (north orientation). The opposite was detected for tocopherols and squalene which were more concentrated in oils from olives of the shady area. The results obtained in this study point out VOO of the PDO Montoro‐Adamuz as a very healthy fat due to their composition in bioactive substances, in particular their richness in phenolic compounds.     

Characterization and chemometric study of crude and refined oils from table olive by‐products

Table olive processing produces defective fruits and the conditioning operations give rise to solid by‐products which are processed to obtain oil. In this study, the most relevant characteristics of crude oils extracted from table olive by‐products were high average acidity values (4.5%, green olives; 8.1%, ripe olives), ECN42 values of 0.34 (green olives) and 0.10 (ripe olives), while 2‐mono‐palmitin averaged 0.92%. The overall content of sterols was 2257 mg/kg (green olives) and 1746 mg/kg (ripe olives), while the concentration of cholesterol was 36 mg/kg (green olives) and 19 mg/kg (ripe olives). The effect of refining was mainly reflected by a decrease in acidity and sterols. Although most characteristics were in agreement with the established regulation for olive oil, the overall trans fatty acid content, the low apparent β‐sitosterol content, and the relatively high cholesterol content prevented their inclusion into classes of crude or refined lampante or pomace olive oils, not even into the vegetable oil category. Therefore, the oils analyzed should be considered for non‐edible purposes. The physicochemical characteristics used for chemometric discrimination permitted discrimination among types of oils (crude, 100%; physically refined, 90%; chemically refined, 100%), elaboration styles (green and ripe olives, 100%) and cultivars (Gordal, Manzanilla, Hojiblanca and Cacereña, 100%), with the sterol composition being the most useful parameter for discrimination.