GYA Grasas y Aceites 0017-3495 Consejo Superior de Investigaciones Cientificas GYA201344_e043-0351141 10.3989/gya.0351141 Articles Chemical properties of virgin olive oil from Iranian cultivars grown in the Fadak and Gilvan regions Propiedades químicas de aceites de oliva virgen de cultivares iraníes de las regiones de Fadak y Gilvan Chemical properties of virgin olive oil from Iranian cultivars grown in the Fadak and Gilvan regions Homapour M. 1 Ghavami M. 1 * Piravi-Vanak Z. 2 Hosseini S.E. 1 Food Science and Technology Department, College of Food Science and Technology, Science and Research Branch, Islamic Azad University, Tehran, Iran Institute of Standards and Industrial Research of Iran Karaj, Iran Corresponding author: mehrdad_ghavami@yahoo.com 31 12 2014 2014 65 4 10.3989/gya.0351141 24 03 2014 02 06 2014 © 2014 CSIC 2014 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial (by-nc) Spain 3.0 License. SUMMARY

The aim of this study is to evaluate the chemical compositions (total phenol, fatty acid, sterolic compounds) of Iranian virgin olive oil (Zard, Rowghani, Mari) cultivated in the Gilvan (Zanjan Province) and Fadak (Qom Province) regions. Total phenols were determined using the Folin-Ciocalteu assay. Fatty acid and sterol profiles were also analyzed using gas chromatography. In most cases, significant effects (P<0.05) of cultivars and locations were detected by the chemical composition of the oil samples. The fatty acid analysis indicated that the Mari variety from Gilvan had high oleic/low linoleic acid content; therefore it is a highly resistant olive oil against oxidation. Furthermore, the high mean values of total sterols were also obtained for the Mari variety. The oil of the Zard variety from Gilvan had the maximum amount of phenols as a positive quality index. Therefore, the Mari variety, especially from Gilvan has been suggested as a superior cultivar compared to the Zard and Rowghani varieties.

 RESUMEN

Propiedades químicas de aceites de oliva virgen de cultivares iraníes de las regiones de Fadak y Gilvan. El objetivo de este estudio fue evaluar la composición química (fenoles totales, ácidos grasos, y esteroles) de aceites de oliva virgen iranies (Zard, Rowghani, Mari) cultivados en las regions de Gilvan (provincia de Zanjan) y Fadak (provincia de Qom). Los fenoles totales se determinaron utilizando el método de Folin-Ciocalteu. Los perfiles de ácidos grasos y de esteroles se determinaron mediante cromatografía de gases. En la mayoría de los casos, existen diferencias significativos de los cultivares y los lugares detectados por la composición química (P<0,05). El análisis de ácidos grasos indicó que la variedad Mari de Gilvan presenta una relación alta oleico/linoleico; por lo tanto, es un aceite de alta resistencia contra la oxidación. Por otra parte, los valores medios altos de esteroles totales también fueron obtenidos para la variedad Mari. El aceite de la variedad Zard de Gilvan presentó la mayor cantidad de fenoles, considerado este valor como un índice de calidad positivo. La variedad Mari especialmente en Gilvan se sugeriere como un cultivar superior en comparación con las variedades Zard y Rowghani.

 KEYWORDS Chemical composition Iranian cultivar Virgin olive oil PALABRAS CLAVE Aceite de olive virgin Composición química Cultivares iranies 1. INTRODUCTION

The olive tree (Olea europaea Linn.) is one of the oldest known agricultural trees in the world, and originated in upper Mesopotamia, the maritime parts of Asia Minor and part of northern Iran at the southern coast of the Caspian Sea (Kiralan et al., 2009). Irainan olive oil has received more attention recently as a major component of the Mediterranean diet (Piravi-Vanak et al., 2009). The majority of olive cultivars are located in the north of Iran (Gilan, Golestan and Zanjan) and to a smaller extent in the Khozestan, Qom and Fars regions. The traditional olive varieties grown in Iran include Zard, Rowghani, Mari, Gelooleh, Shengeh, Khormazeitoon, Khara, Dakal, Dezful, and Phishomi. Foreign cultivars namely Koroneiki and Arbequina are also cultivated and harvested in Iran (IOOC, 2012).

Virgin olive oil is acknowledged for its pleasant aroma and flavor, oxidative stability, nutritional and health effects due to its chemical compositions. Fatty acids are the most predominant components in olive oil. The beneficial health-promoting effects of virgin olive oil have been attributed to its high monounsaturated fatty acids (MUFAs) and other natural compounds such as vitamins, polyphenols and other radical scavenging components (AL-Maaitah et al., 2009; Pinelli et al., 2003). Furthermore, it has been reported that the high content of oleic acid might reduce the risk of breast cancer and decrease low density lipoprotein (LDL) cholesterol and triglycerides, hence decreasing blood pressure and cardiovascular disease (Pinelli et al., 2003; Covas et al., 2007). Fatty acid composition also affects the oxidative stability of edible oils; consequently the high resistance of virgin olive oil to oxidation is mainly due to its high oleic acid content (Cinquantaa et al., 2001). This leads to an important commercial benefit of olive oil.

Plant-derived sterols (phytosterols) are the most important portion of the unsaponifiable fraction of lipids present in all plant-based food (Casas et al., 2004). As reported in previous studies, every plant oil has a distinctive sterol profile which is a useful criterion for the classification of virgin olive oils based on their fruit variety (Ben Temime et al., 2008). Additionally, it has been suggested that sterols possess numerous biological characteristics such as cholesterol-lowering, anti-inflammatory and immune regulatory effects (Carr et al., 2010), antihypertensive and antioxidant activity (Yoshida et al., 2003) as well as antimicrobial features; therefore, they are considered as ingredients of functional foods (Ben Temime et al., 2008). Furthermore, the quantitative and qualitative analyses of fatty acids and sterolic composition can be helpful for the detection of authenticity and olive oil adulteration (Al-Ismail et al., 2010).

Virgin olive oil is an important source of phenolic compounds as natural antioxidants (Saitta et al., 2009). Antioxidants can lead to a delay or slow propagation of undesirable changes in shelf life and nutritional properties and they are related to olive oil stability (Boskou, 2006). Furthermore, the antioxidant activity can lead to reduce the risk of oxidative stress and associated diseases such as Alzheimer, cancer, diabetes, rheumatoid, arthritis, inflammatory and cardiovascular diseases (Boskou, 2006; Saitta et al., 2009; Prakash and Kumar, 2011).

The chemical compounds, fatty acid profiles and sterol composition of olive fruits are influenced by several factors. The effects of the nature of the cultivar, crop year (Allalout et al., 2009; Boskou, 2006), geographical region, climate (Piravi et al., 2012), irrigation and water-stress situations (Stefanoudaki et al., 2001), degree of fruit ripeness, processing methods (Morello et al., 2004; Boskou, 2006) and storage conditions (Ben Temime et al., 2008), have been previously reported. Therefore, the diversity of these parameters influences the quality and composition of virgin olive oil in each location. However, there is little scientific evidence about the chemical properties of Iranian virgin olive oils in the Fadak and Gilvan regions. Fadak is considered the most important organic olive farm and Gilvan is the most significant olive cultvation region in Iran. Therefore, the aim of this study is to evaluate the composition of three common Iranian monovarieties (Zard, Rowghani and Mari) in these two top olive harvesting regions. Hence, the effects of environmental conditions and the nature of the olive cultivar on various parameters such as total phenols, fatty acid composition and sterol profiles of olive oils are investigated.

 2. MATERIALS AND METHODS 2.1. Sample collection

Olive fruits (Olea europaea) of three Iranian monovarieties, Mari, Zard and Rowghani were collected from the Fadak farm (Qom Province) and Gilvan (Zanjan Province) in Iran. Sampling was conducted from the 10th of October to the 15th of November in the year 2012. The fresh and undamaged fruits (∼5 kg sample) were randomly hand-picked from ∼35 trees at each region of the farm. The maturity index (MI) of olive fruits was approximately 5, which has been determined according to the following formula (Boskou, 2006): MI = ( a × 0 ) + ( b × 1 ) + ( c × 2 ) + ( d × 3 ) + ( e × 4 ) + ( f × 5 ) + ( g × 6 ) + ( h × 7 ) / 100

Where a, b, …, h are the number of olives in each of the seven color classes from dark green to dark black. After harvesting, the samples were transported to the Olive Research Station of Roudbar (Gilan, Iran) within 24 h for oil extraction.

 2.2. Oil extraction

Oil extraction was performed using the laboratory oil mill. The olive fruits were crushed in a hammer mill and kneaded for 20 min at 25 °C. The collected olive pulp was centrifuged at 3000 rpm for 5 min and transferred into dark brown glass bottles and stored at –20 °C until experimental studies.

 2.3. Analytical methods 2.3.1. Materials

Silica gel 60 F254 Aluminium sheets, n-hexane, KOH, hexane/diethylether (65: 35, v/v), chloroform, methanol and sodium carbonate were purchased from Merck Darmstadt, Germany, gallic acid, Folin-Ciocalteu reagent was obtained from Sigma-Aldrich. All chemical agents were analytical grade.

 2.3.2. Determination of total phenols

The total phenols of olive oil samples were measured using the Folin-Ciocalteu reagent by spectrophotometer (Shimadzu, model UV-3100, Kyoto, Japan) at 765 nm as described by Montedoro et al. (1992). The concentration of total phenols was determined using gallic acid for the calibration curve (R2 = 0.998). The analyses were repeated in triplicates for each sample.

 2.3.3. Analysis of sterolic compounds

Sterols were determined both qualitatively and quantitatively using the IOOC (COI/T.20/Doc. no. 10/Rev. 1, 2001) standard method. The olive oil samples were saponified with an ethanolic potassium hydroxide solution followed by the extraction of the unsaponifiable matter. The sterol fraction was then separated onto a 20 × 20 cm thin layer chromatography (TLC) sheet made of silica gel 60 F254. The streols were analyzed by gas chromatography (YL6100GC, Young-Lin Inc., Korea) coupled with an FID detector. The chromatograph was equipped with a TYM5 capillary column ((95%) dimethyl-(5%) diphenylpolysiloxane with a cross linked phase of poly (dimethyldiphenyl) siloxane) of 30 m in length and an internal diameter of 0.25 mm and with a uniform thickness between 0.10 to 0.30 µm. The operating conditions were as follows: column temperature: 260 °C, injector temperature: 280 °C and detector temperature: 300 °C. The velocity of the carrier gas (Hydrogen) was 10 to 30 cm·s−1. The amount of injected sample was 2 µL with the flow rate of 1 mL·min−1. The quantification was performed by α-cholestanol (0.2% w/v, in chloroform) as internal standard.

 2.3.4. Analysis of fatty acids

The fatty acid analysis was carried out based on the global method IOOC (COI/T.20/Doc. no. 25, 2006). The fatty acid methyl esters were prepared according to IOOC method (COI/T.20/Doc. no. 24, 2002). Methylated fatty acids were analyzed using gas chromatography (YL6500GC, Young-Lin Inc., Korea) equipped with a capillary column CP-Sil 18 (60 m × 0.25 mm; particle size) and flame ionization detector (FID). Hydrogen was used as the carrier gas and the injection quantity was 1.2 µL with a flow rate of 4 mL·min−1. The temperature conditions of chromatograph were as follows: injector 250 °C, oven 175 °C (isothermal condition) and detector 300 °C. The results were expressed as the relative percentage of each fatty acid.

Iodine Values (IV) were determined according to the percentages of fatty acids using following formula (Haghighat Kharazi et al., 2012): IV = ( C 16 : 1 % ) × 0.95 + ( C18 : 1 % ) × 0.86 + ( C18 : 2 % ) × 1.732 + ( C18 : 3 % ) × 2.616

The Cox Value (oxidizability) of all olive oil samples was calculated based on the following relation as described by Fatemi and Hammond (1980): Cox Value = [ 1 ( 18 : 1 % ) + 10.3 ( 18 :M 2 % ) + 21.6 ( 18 : 3 % ) ] / 100

2.4. Statistical analysis

One-way analysis of variance (ANOVA; P<0.05) was used to compare the data using SPSS 12.0 software (SPSS INC., Chicago, IL, USA, 2002). Significant treatment means were calculated by Duncan's New Multiple Range Test (Haquea et al., 2009). The data are shown as mean values plus standard errors of means.

 3. RESULTS AND DISCUSSION 3.1. Total phenolic compounds

The total phenolic content as the natural antioxidants and quality index of the olive oil was determined using Folin–Ciocalteu by the spectrophotometric assay (Gallina-Toschi et al., 2005; Haghighat Kharazi et al., 2012). As shown in Fig. 1, the significantly (P<0.05) highest concentration of total phenols was detected in the Zard variety of Gilvan (180 ± 3.00 mg of gallic acid·kg−1 of oil) while the significantly (P<0.05) lowest concentrations were found in the Rowghani (104.00 ± 4.00 mg of gallic acid·kg−1 of oil) and Mari (113.00 ± 3.00 mg of gallic acid·kg−1 of oil) cultivars of Fadak. Consequently, this might cause improvements in the oxidative stability of virgin olive oil in the Zard variety of Gilvan. However, other components such as fatty acid composition, tocopherols and the presence of sterolic compounds might also be important factors for these characteristics (Gallina-Toschi et al., 2005). These obtained values were consistent with those reported that the amount of total phenolic compounds in olive oil is variable among different varieties and regions (Haghighat Kharazi et al., 2012).

Total phenols of the virgin olive oils from the Fadak and Gilvan regions. Different small letters show significant differences at P<0.05.

 3.2. Total sterols

The sterol fraction in olive oil might be regarded as a major component for detecting adulteration and checking authenticity of all cultivars (Table 1). In all varieties, the predominant components of the total sterol fraction were β-sitosterol, Δ5-avenasterol and campesterol. The other sterols in trace amounts include cholesterol, brassicasterol, stigmasterol, chlerosterol, stigmastadienol, stigmastenol and Δ7-avenasterol (Phillips et al., 2002; Cunha et al., 2006).

The percentages of sterol composition (mean values ± SE) of virgin olive oil of Iranian cultivars in the Gilvan and Fadak regions

Sterols
Olive oils Cholesterol Brassicasterol Campesterol Stigmasterol Clerosterol β-Sitosterol Δ5-Avenasterol Δ5, 24- Stigma stadienol Stigmastenol Δ7-Avenasterol Apparent β-Sitosterol Campesterol/ Stigmasterol
ZF 0.10 ± 0.00b 0.00 ± 0.00c 3.11 ± 0.01c 0.48 ± 0.00d 0.84 ± 0.00b 88.39 ± 0.18c 6.39 ± 0.16a 0.23 ± 0.00d 0.09 ± 0.00d 0.34 ± 0.00c 95.46 ± 0.01a 6.40 ± 0.04b
RF 0.13 ± 0.00b 0.03 ± 0.00c 5.49 ± 0.01a 0.40 ± 0.04d 1.05 ± 0.01a 87.11 ± 0.22d 3.34 ± 0.12b 0.62 ± 0.01a 0.62 ± 0.00b 1.16 ± 0.15a 92.88 ± 0.05d 13.86 ± 1.61a
MF 0.00 ± 0.00c 0.00 ± 0.00c 3.81 ± 0.15b 0.76 ± 0.05c 0.96 ± 0.04a 92.08 ± 0.28a 1.78 ± 0.09e 0.34 ± 0.04c 0.02 ± 0.02d 0.24 ± 0.02c 94.47 ± 0.16b 5.01 ± 0.55b
ZG 0.24 ± 0.04a 0.23 ± 0.01a 3.48 ± 0.22bc 3.00 ± 0.11a 0.57 ± 0.03c 88.55 ± 0.32c 2.88 ± 0.07c 0.47 ± 0.04b 0.20 ± 0.01c 0.38 ± 0.04c 92.50 ± 0.33d 1.15 ± 0.03c
RG 0.01 ± 0.01c 0.19 ± 0.01a 2.98 ± 0.03a 2.65 ± 0.14c 0.99 ± 0.02a 88.07 ± 0.25c 2.45 ± 0.10d 0.30 ± 0.00cd 1.02 ± 0.05a 0.69 ± 0.02b 92.56 ± 0.10d 1.09 ± 0.06c
MG 0.01 ± 0.01c 0.12 ± 0.03b 3.26 ± 0.07c 2.19 ± 0.02b 0.61 ± 0.02c 91.05 ± 0.07b 1.43 ± 0.02e 0.01 ± 0.00e 0.66 ± 0.02b 0.65 ± 0.03b 93.81 ± 0.09c 1.48 ± 0.05c

ZF, Zard variety of Fadak; RF, Rowghani variety of Fadak; MF, Mari variety of Fadak; ZG, Zard variety of Gilvan; RG, Rowghani variety of Gilvan; MG, Mari variety of Gilvan. Values with different small letters in a column are significantly different at P<0.05

Total sterols of the virgin olive oils from the Fadak and Gilvan regions. Different small letters show significant differences at P<0.05.

The data showed that β-sitosterol is the most abundant sterol in olive oil. The highest β-sitosterol content was found in the Mari variety of the Fadak region (92.08%) and the lowest concentration was in the Rowghani variety of Fadak (87.11%). In previous studies, it has also been reported that β-sitosterol accounts for more than 75% of total sterols (Boskou, 2006; Ben Temime et al., 2008). The obtained data is similar to those published by some authors for virgin olive oil (Phillips et al., 2002; Ben Temime et al., 2008). The health-promoting effects of β-sitosterol such as lowering plasma cholesterol, preventing different types of cancers (colon, prostate, and breast) has been previously mentioned by Awad et al. (2000), Whiting (2007) and Ben Temime et al. (2008). Regarding the fact that all olive fruits were harvested at the same maturity index (Salvador et al., 2001), the observed differences might be due to cultivar and geographical parameters such as climate and soil type (Cunha et al., 2006).

The levels of Δ5-avenasterol in olive oil samples were relatively lower than the values reported previously by Ben Temime et al. (2008); Rivera del Alamo et al. (2004) and they are in the range of 1.43% (Mari cultivar of Gilvan) to 6.39% (Zard cultivar of Fadak), although they are in agreement with the results obtained by Itoh et al. (1981).The Δ5-avenasterol content of the Zard variety of Fadak (6.39%) was significantly (P <0.05) higher than the other cultivars and the Mari variety of Fadak (1.78%) and Gilvan (1.43%) were significantly (P <0.05) the lowest ones. Wang et al. (2002) reported that Δ5-avenasterol at elevated temperatures exhibited antioxidant activity and improved oxidative stability in olive oil under frying condition.

As shown in Table 1, the campesterol content of olive oils range from 2.65% (Rowghani cultivar in Gilvan region) to 5.49% (Rowghani cultivar of Fadak). According to the Codex Alimentarius and IOOC standard, the maximum concentration of campesterol should be lower than 4% of the total sterols (Codex, 2003; IOOC, 2011). The mean values for all cultivars (2.65% to 3.81%) except the Rowghani olive oil of Fadak (5.49%) was in agreement with the standards. Similar values were reported by Ben Temime et al. (2008). Higher values of some virgin olive oil exceeded the upper limit of the international standards such as the Rowghani variety of Fadak in this study, which has also been previously determined by Rivera del Alamo et al. (2004).

Table 1 shows that the values of stigmasterol for the Zard (0.48%) and Rowghani (0.40%) varieties of Fadak. The acceptable level of stigmasterol according to the Codex Alimentarius and IOOC standard must be less than that of campesterol (Codex, 2003; IOOC, 2011). Our findings indicated a similar result. The data showed that stigmasterol was significantly (P<0.05) affected by the geographical location. Similar findings were previously obtained by Ben Temime et al. (2008) and Salvador et al. (2001). Organoleptic defects and high acidity levels due to high contents of stigmasterol have been given attention in previous studies (Ben Temime et al., 2008). The ratio of campesterol to stigmasterol as the quality index has also been evaluated as shown in Table 1.

The apparent β-sitosterol (sum of chlerosterol, β-sitosterol, Δ5-avenasterol, stigmastadienols and sitostanol) according to the authenticity index must exceed 93% of total sterols based on the Codex Alimentarius and International Olive Oil Council (IOOC) Standard (Codex, 2003; IOOC, 2011). The obtained data was consistent with the standard values and those reported by Ben Temime et al. (2008).

According to Codex Alimentarius standard, the minimum concentration for total sterols of olive oil is 1000 mg·kg−1 (Codex, 2003). Total sterol concentrations in the varieties examined were found to be greataer than the standard limit and the lowest level was 1123 mg·kg−1 for the Zard variety of Gilvan while the Mari oil of Fadak had a higher quantity of this class compound (1925 mg·kg−1). The antioxidant activity and health-promoting effects of total sterols of olive oil have been already mentioned (Yoshida et al., 2003; Carr et al., 2010); therefore, the Mari oil was evaluated as a good variety, regarding sterols. The findings in this work were in agreement with those reported by Ben Temime et al. (2008) who found that values varied between 1017 mg·kg−1 and 1522 mg·kg−1, but our results were low compared with Alves et al. (2005) who found the total content of sterol to range from 2003 to 2682 mg·kg−1.

 3.3. Fatty acid composition

Table 2 presents the fatty acid composition of olive oil cultivars in both regions. The predominant fatty acid of all cultivars is oleic acid followed by lower concentrations of linoleic, palmitic, stearic and palmitoleic acids with traces of linolenic and arachidic acids. The obtained results are consistent with previously published literature (Aguilera et al., 2005; Hashempour et al., 2010; Haghighat Kharazi et al., 2012).

Fatty acid percentage (mean values ± SE) of virgin olive oils in the Fadak and Gilvan regions

Fadak Gilvan
ZF RF MF ZG RG MG
C16:0 12.85 ± 0.95b 18.10 ± 0.00a 13.00 ± 0.60b 13.10 ± 0.30b 16.75 ± 0.15a 11.4 ± 0.10b
C16:1t 0.05 ± 0.05a 0.10 ± 0.00a 0.10 ± 0.00 a 0.05 ± 0.05 a 0.05 ± 0.05 a 0.01 ± 0.00a
C16:1c 1.10 ± 0.10b 1.40 ± 0.00a 1.15 ± 0.05b 1.15 ± 0.05b 1.40 ± 0.10a 0.95 ± 0.05b
C17:0 – – – – – –
C17:1 – 0.10 ± 0.00a 0.10 ± 0.00a 0.10 ± 0.00a – 0.01 ± 0.00a
C18:0 3.05 ± 0.15a 2.80 ± 0.00b 2.30 ± 0.00d 2.75 ± 0.05bc 2.90 ± 0.00ab 2.55 ± 0.05c
C18:1 66.25 ± 0.85d 57.00 ± 0.00e 74.75 ± 0.45b 69.05 ± 0.25c 58.25 ± 0.05e 76.90 ± 0.1a
C18:2 15.40 ± 0.2c 18.70 ± 0.00b 7.10 ± 0.00e 12.55 ± 0.05d 19.05 ± 0.05a 6.70 ± 0.00g
C18:3 0.40 ± 0.00 a 0.40 ± 0.00 a 0.35 ± 0.00 a 0.40 ± 0.00 a 0.40 ± 0.00 a 0.40 ± 0.00a
C20:0 0.25 ± 0.05a 0.20 ± 0.00 a 0.20 ± 0.00 a 0.20 ± 0.00 a 0.20 ± 0.00 a 0.25 ± 0.05a
C20:1 0.60 ± 0.00bc 0.90 ± 0.00a 0.65 ± 0.05b 0.55 ± 0.05bc 0.60 ± 0.00bc 0.50 ± 0.00c
C22:0 0.05 ± 0.05a 0.10 ± 0.00a 0.10 ± 0.00a 0.10 ± 0.00 a 0.05 ± 0.05a 0.15 ± 0.05a
C22:1 – 0.30 ± 0.00 a – – 0.35 ± 0.00 a –
SFA 16.20 ± 1.10b 21.20 ± 0.00a 15.60 ± 0.60b 16.10 ± 0.35b 19.90 ± 0.10a 14.35 ± 0.05b
UFA 83.8 ± 1.10b 78.90 ± 0.00c 84.2 ± 0.40ab 83.8 ± 0.35b 80.10 ± 0.10c 85.6 ± 0.05a
MUFA 68.00 ± 0.90d 59.80 ± 0.00e 76.75 ± 0.35b 70.90 ± 0.3c 60.65 ± 0.15e 78.55 ± 0.05a
PUFA 15.80 ± 0.20c 19.10 ± 0.00b 7.45 ± 0.05e 12.95 ± 0.05d 19.45 ± 0.05a 7.10 ± 0.00g
SFA/UFA 0.19 ± 0.15b 0.27 ± 0.00a 0.19 ± 0.01b 0.19 ± 0.01b 0.284 ± 0.00a 0.167 ± 0.00b
MUFA/PUFA 4.30 ± 0.00d 3.13 ± 0.00e 10.3 ± 0.02b 5.47 ± 0.00c 3.11 ± 0.02e 11.06 ± 0.01a
Oleic/Linoleic 4.30 ± 0.00d 3.04 ± 0.00e 10.52 ± 0.06b 5.50 ± 0.00c 3.05 ± 0.01e 11.47 ± 0.02a
Cox Value 2.33 ± 0.03c 2.58 ± 0.00b 1.55 ± 0.02e 2.06 ± 0.01d 2.63 ± 0.01a 1.54 ± 0.00e
IV 85.73 ± 1.17a 83.78 ± 0.00bc 78.59 ± 0.47d 83.26 ± 0.25c 85.74 ± 0.22ab 79.69 ± 0.39d

ZF, Zard variety of Fadak; RF, Rowghani variety of Fadak; MF, Mari variety of Fadak; ZG, Zard variety of Gilvan; RG, Rowghani variety of Gilvan; MG, Mari variety of Gilvan.

SFA, Saturated fatty acid; UFA, Unsaturated fatty acid; MUFA, Monounsaturated fatty acid; PUFA, Polyunsaturated fatty acid; IV, Iodine Value.

Values with different small letters in a same row are significantly different at P<0.05.

The amount of palmitic acid, the major saturated fatty acid, is found in the range of 11.4% to 18.1%, which is in accordance with the IOOC and Codex standard (7.5–20%). As shown in Table 2, the least mean palmitic acid content was determined in the Mari variety of Gilvan as the low mean annual temperature. Ranalli et al. (1999) and Kiralan et al. (2009) noted that fatty acid composition is temperature dependent and as the temperature decreases the saturated fatty acid contents increase.

The mean values of oleic acid as the predominant fatty acid were in the range of 57% to 76% (Table 2) according to olive oil Codex standard (Codex, 2003) and IOOC regulations (IOOC, 2011). In the previous studies, the amounts of oleic acid of Iranian cultivars were also aligned with the international regulations (Hashempour et al., 2010; Haghighat Kharazi et al., 2012). Besides, changes in oleic acid contents were observed in different varieties of olive oil, which might be due to the diversity of cultivars and environment conditions. The Mari variety of Gilvan (76.90 ± 0.10) achieved the highest mean value (P<0.05). The data indicated that the oleic acid content of each variety in Gilvan with a higher annual mean temperature is significantly (P<0.05) higher than that obtained from the Fadak region. This is in agreement with previous studies which also reported that the increase in environmental temperature leads to a decrease in the oleic acid content (Rondanini et al., 2011). High oleic acid content leads to an increase in oxidative stability and antihypertensive activity and LDL cholesterol lowering effects have been shown (Psaltopoulou et al., 2004).

Based on the obtained data, the percentage of linoleic acid (6.7% to 19.05%) was in agreement with the Codex standard and IOOC regulation (3.5 to 21%). The Mari variety of Gilvan contains the significantly lowest linoleic acid content (P<0.05) among all other olive samples. Rondanini et al. (2011) stated that there is a negative correlation between oleic acid and linoleic acid contents of olive oils which is in accordance with our findings. The ratio of oleic to linoleic acid was also in the range of 3.04% to 11.47% and the Mari variety of Gilvan showed the highest mean value. Consequently, the variation in oleic and linoleic compositions may be explained by different enzyme activities during triacylglycerol biosynthesis for each cultivar (Hashempour et al., 2010).

There were no significant differences (P≥0.05) between cultivars regarding linolenic acid contents. Moreover, linolenic acid contents of the all cultivars were in accordance with the standards (Codex: <1.5 and IOOC: ≤1). In the current study, the cultivars with low levels of linoleic and palmitic acids showed concurrently high oleic acid contents such as the Mari variety of Gilvan, which has been also published by other researchers (Rondanini et al., 2011).

The level of palmitoleic acid as a minor fatty acid in olive oil ranged from 0.95% to 1.40%. The Rowghani variety of Gilvan and Fadak had significantly the highest concentrations among all cultivars (P<0.05). The average content of palmitoleic acid was consistent with those established by the Codex standard and IOOC regulation (0.3–3.5%).

As shown in Table 2 the stearic acid content was 0.35% to 3.05%, which is in the range of the criteria established in the IOOC and Codex (0.5–5%). The results also showed that the Mari variety of Fadak (2.30 ± 0.00) had the lowest stearic acid content while the Zard variety of Fadak (3.05 ± 0.15) contained the highest amount (P<0.05). In general, the ratio of saturated to unsaturated (S/US) fatty acids was 0.167% to 0.284% and the Mari variety of Gilvan had the lowest mean value due to the lower content of palmitic and stearic acids.

Based on our findings, the Iodine Values ranged from 78 for the Mari variety of Fadak to 85 for the Zard variety of Fadak and were in agreement with the Codex standard (75–94). Significant differences (P <0.05) were observed among all cultivars and locations (except for the Mari cultivar). The lowest mean for Iodine Values was obtained for the Mari varieties of Fadak and Gilvan (Table 2), however the unsaturated fatty acids of this cultivar were at the highest concentrations. This might be attributed to the ratio of oleic to linoleic acid, which is higher than other olive oils in the current study; therefore, it means that the percentage of monounsaturated fatty acid is greater than polyunsaturated fatty acid in this variety. As a result, the above-mentioned olive oils are more resistant to oxidation. The Cox Value as a determinant factor in oil stability also confirmed the obtained results. On the other hand, the Mari cultivars of Gilvan (1.54) and Fadak (1.55) which had the lowest value are more stable than other olive oil samples. In contrast, the highest Cox Value was observed in the Rowghani oil of Gilvan (2.63) due to its high content of polyunsaturated fatty acid, especially linoleic acid. Haghighat Kharazi et al. (2012) also found that the oil of the Mari cultivar is more stable against oxidation than the Zard and Phishomi oils.

 4. CONCLUSIONS

A study on Iranian virgin olive oil (Zard, Rowghani and Mari) in Gilvan (Zanjan Province) and Fadak (Qom Province) revealed that the total phenols, fatty acid profile and sterol composition of olive oils correspond with the standards of Codex Alimentaurious except for the Rowghani olive oil of Fadak regarding to campesterol. The results suggested that not only olive cultivars, but also the climate of the growing region of olive fruits plays important roles in the chemical composition of fruit and consequently the extracted oil. The fatty acid analysis, Iodine and Cox Value showed that Mari oil is superior to Zard and Rowghani oils regarding oxidative stability, especially at the Gilvan location. In the current study, the Mari variety of Fadak showed significantly the highest total content of sterols (P<0.05) as compared to other samples. Therefore, the Mari cultivar was recommended as a superior cultivar compared to Zard and Rowghani, especially in Gilvan. Further study is required to obtain data on the characteristics of these Iranian cultivars (Zard, Rowghani and Mari) and also foreign cultivars grown in other regions of Iran. Additionally, it has been suggested that the evaluation of other chemical compositions of Iranian olive oils such as pigments, tocopherol concentrations and organoleptic qualities of oils is necessary.

 ACKNOWLEDGMENTS

The support of Islamic Azad University, Science and Research Branch of Tehran and Institute of Standards and Industrial Research of Iran are gratefully acknowledged.

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