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Plant Breed. Biotech. : Plant Breeding and Biotechnology

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Research Article

Effect of Genotype, Growing Year and Planting Date on Agronomic Traits and Chemical Composition in Sunflower (Helianthus annuus L.) Germplasm

Plant Breeding and Biotechnology 2014;2(1):35-47.
Published online: March 31, 2014

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*Corresponding author: Hong Sig Kim, hongsigk@chungbuk.ac.kr, Tel: +82-43-261-2513, Fax: +82-43-261-2513
• Received: March 26, 2014   • Revised: March 28, 2014   • Accepted: March 29, 2014

Copyright © 2014 The Korean Society of Breeding Science

This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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  • Sunflower is one of the most widely cultivated oil crops. It produces seeds which have abundant health benefits. The objective of this research was to determine the effects of two growing years and five planting dates on agronomic traits and chemical compositions in sunflower accessions. In this study, genotype by year interaction was significant for days to flowering, weight of seeds per plant, oil, palmitic acid, stearic acid, oleic acid, linoleic acid, all tocopherol and phytosterol components. The major source of variation in most agronomic traits and chemical compositions in sunflower was attributed by variation among genotypes. Days to flowering, head length, and weight of seeds per plant decreased when planting date was delayed. Oil content, stearic acid, oleic acid, α-tocopherol, total tocopherol, β-sitosterol, and total sterol contents decreased but linoleic acid increased when planting date was delayed. From this study, valuable information will be provided for sunflower breeders and growers in developing and producing functional food resources and products.
Sunflower (Helianthus annuus L.) is one of the most widely cultivated oil crops in the world, which has also been considered as an important crop for biodiesel production (Duane 2007). Sunflower seeds have abundant health benefits, which include reduction of blood cholesterol, anti-inflammatory properties, artery cleansing properties, etc (Ologunde et al. 2008). The various health benefits of sunflower seeds can be attributed to the high levels of polyunsaturated and monounsaturated fats, phytosterols, tocopherols, protein, copper, folates, iron, zinc, and vitamin B (Roche et al. 2010). Sunflower oil contains four commercially important fatty acids: palmitic (16:0, 3.1 ~ 7.6%), stearic (18:0, 1.3 ~ 4.1%), oleic (18:1, 18.1 ~ 75.5%), and linoleic (18:2, 18.1 ~ 74.1%) (Lee et al. 2010; Izquierdo et al. 2002; Baydar and Erbas 2005). Although seed oil of standard cultivated sunflower is considered to be of good quality for edible purposes, the development of cultivars with high oleic acid has been an important breeding objective for this crop. One advantage of oils with high oleic acid is its higher degree of oxidative stability than oils low in oleic acid, which is desirable for seed storage (Dehmer and Friedt 1998; Delplanque 2000a; Flagella et al. 2002). From the nutritional point of view, a diet rich in monounsaturated fatty acids has been suggested to reduce cholesterol in blood plasma, in that it lowers low density lipoprotein but not high density lipoprotein, thus lower the risk of coronary heart disease (bDelpanque 2000b; Izquierdo and Aguirrezabal 2008).
Agronomic and yield traits such as plant height (Ahmad and Hassan 2000), number of seeds per head (Kaleem et al. 2009), and 100-seed weight (Hassan et al. 2003) in sunflower are significantly influenced by the temperature and growth durations which are particular traits of seasonal changes (Qadir et al. 2007). Genotypes and environmental factors such as temperature during the period of seed development and maturation may have effects on oil content in sunflower seed (Ahmad and Hassan 2000). The fatty acid composition of sunflower seed is known to be different among cultivars and environmental conditions (Flagella et al. 2002). Ahmad and Hassan (2000) depicted that lower temperature and lesser growing days favor the high stearic acid accumulation. Flagella et al. (2002) reported that sunflower maturation under different environmental conditions would accumulate different concentration of oleic acid. Similarly, significant variations in linoleic acid content have also been observed among locations, planting dates and sunflower hybrids by Ahmad et al. (2001). The tocopherol content of vegetable oils depends on seed’s genealogy, harvesting season, climatic conditions, and the refining procedures (Bauernfeind 1977). Fernandez-Cuesta et al. (2012) reported that variation of tocopherol content in sunflower kernel was mainly explained by the effect of genotypes and the interaction of genotype × environment while variation of phytosterol content in kernel was mainly attributable to the effect of the environment and the interaction of genotype × environment. Sunflower yield tends to decrease when sowing date was delay, and grain oil percentage showed a slight decrease associated with delayed sowing (Gustavo et al. 2007). Flagella et al. (2002) reported that the prolongation of the grain filling phase in a cooler period by adjusting sowing date resulted in lower oil content both in 1996 and 1997 seasons. Oil content of sunflower seed has been reported to decrease with lateness of planting date (Robertson 1981). Jones (1984), Unger (1986), and Cilardi et al. (1990) observed a decrease in oleic acid concentration and conversely an increase in linoleic acid in sunflower genotypes as seeding dates were delayed.
Valuable genetic resources and information of their interactions with environments are indispensable in breeding high quality sunflower cultivars. In order to obtain valuable genetic resources, this study was performed to determine the effects of growing years and planting dates on agronomic traits and chemical compositions in sunflower. From this study, valuable information will be provided for sunflower cultivations and help in developing functional food resources.
Effects of growing years on agronomic traits and seed chemical composition

Field test

Sixteen accessions with superior agronomic traits and high phytochemical composition contents were collected from the National Agro-biodiversity Center in Suwon, Republic of Korea (Table 1). All of 16 accessions were planted on 27 May 2010 and on 28 May 2011 on the same field at Chungbuk National University in Cheongju (latitude 37°45′ N, longitude 128°40′ E, altitude 297 m). Experiment was laid out in randomized complete block design with three replications. A plot was consisted of four rows, each in 4 m length. Plant spacing was 60 cm between rows and 30 cm between plants. N-P205-K2O fertilizers were applied at a ratio of 0.12-0.09-0.09 t ha−1 as basal application. Seeds were harvested from August to October, and were dried with hot air-dryer at 35°C for 7 days.

Evaluation of agronomic traits

Days to flowering, days from flowering to maturity, days to maturity, stem length, head length, and seed weight per plant were measured as agronomic traits. Stem length was measured (in centimeters) at the completion of flowering. Five plants were selected at random from each plot and their heights were measured from the soil surface to top of flower. Five heads were taken randomly from each plot and diameter of each head was measured using measuring tape.

Sample preparation and chemicals

Sunflower seeds were ground in a cyclone sample mill fitted with a 30 mesh screen into particles of 0.5 mm diameter or less, and stored at −20°C prior to extraction. Three samples were taken from each germplasm. Fatty acid methyl esters (FAME), phytosterols (β-sitosterol, campesterol and stigmasterol) and tocopherols (α-, β-, γ-, δ-tocopherol) standards were purchased from Sigma-Aldrich (Sigma Chemical Co., St. Louis, MO, USA). The trimethyl silyl ether (TMS) derivatives of all sterols were prepared using N,O-bis-[Trimethylsiyl] trifluoroacetamide (BSTFA) reagent from Supelco (Supelco Co., Bellefonate, PA, USA).

Oil extraction

Sunflower oil was extracted from three gram of ground seed with ether for eight hours in a Soxhlet type extractor according to AOCS method (AOCS 1993). The oil extract was evaporated by distillation at reduced pressure in a rotary evaporator at 50°C until the solvent was totally removed. Crude extract was then weighed.

Analysis of fatty acids

Seventy microliter of sunflower oil was transferred to a screw-cap vial with 2 ml mixture of methanol, heptane, benzene, 2,2-dimethoxypropane, and H2SO4 (37:36:20:5:2 V/V) and held at 80°C for 20 min for methylation of the oil fatty acid. The fatty acid composition of sunflower oil was determined using a gas chromatography system (Agilent 6850) equipped with a flame ionization detector. Samples were separated by Agilent Innowax column (30 m × 0.25 mm × 0.25 μm). Splitless (1:50) injection was used and the carrier gas was nitrogen at a flow-rate of 0.8 ml min−1. Nitrogen (30 ml min−1), hydrogen (30 ml min−1), and dry air (300 ml min−1) were used as auxiliary gases. Injector and detector temperature was 250°C and 280°C, respectively. The oven temperature was held at 150°C for 5 min and then increased by 5°C min−1 to 230°C.

Analysis of tocopherol and phytosterol

A half gram of ground sunflower seed was accurately weighted into a 50 ml screw-cap test tube, and then 1 ml 5α-cholestane (500 ppm in hexane) was added as an internal standard. The sample was saponified by adding 10 ml pyrogallol (3%) and 2 ml KOH (60%). The solution was vortexed for 1 min and heated at 80°C water bath for 20 min. Unsaponifiable fraction was recovered by extraction with hexane. The recovered fraction was pipetted into glass vials and dried under nitrogen at room temperature. TMS derivatives were prepared by dissolving the unsaponifiable material into 150 μl of BSTFA reagent. Silylation was achieved after heating the mixture for 1 h at 60°C. Samples were stored at 4°C prior to analysis.
Chromatographic analysis was carried out on a GC-FID (Agilent 6850). HP-5 column with 0.25 μm film thickness (30 m × 0.25 mm I.D., USA) was used for separation. Splitless (1:10) injection was used and the carrier gas was nitrogen at a flow-rate of 1 ml min−1. Nitrogen (30 ml min−1), hydrogen (30 ml min−1), and dry air (300 ml min−1) were used as auxiliary gases for the flame ionization detector. The injector and detector temperatures were 300°C. The oven temperature was held at 200°C for 1 min and then increased by 10°C min−1 to 245°C, the temperature was maintained for 10 min, finally increased by 8°C min−1 to 280°C and then held for 25 min. Individual sterols and tocopherols were mainly identified by the retention time of corresponding standards and their contents were determined from the ratio of each peak area compared to the internal standards.
Statistical analysis
ANOVA was carried out to test any significant differences among genotypes and growing years on agronomic traits and chemical compositions with SAS software version 9.2 using the following model:
Yijk=μ+ei+r(e)ij+gk+geik+ɛijk
where Yijk was observation of genotype k in year i in jth replication; μ was the grand mean; ei and gk were the effects of year i and genotype k, respectively; r(e)ij was jth replication nested within year i; geik was the genotype by year interaction of genotype k in year i and ɛijk was the residual of genotype k, year i in replication j. Replication and residual effect were considered as random variables.
Effects of planting dates on agronomic traits and chemical compositions

Field test

IT031831, a USA germplasm with high oil and oleic acid contents, was planted on five dates at 10 day intervals in Chungbuk National University, Cheongju (latitude 37°45′ N, longitude 128°40′E, altitude 297 m) in 2010: May 7, May 17, May 27, June 7, and June 17. Experimental design was a randomized block design with three replications.

Statistical analysis

Duncan’s multiple range test was used to test any significant difference among planting dates by the SAS program (Software version 9.1, SAS Institute Inc.).
Effects of growing years on agronomic traits and chemical compositions

Weather conditions during 2010 and 2011 growing seasons

The mean temperature of the day from flowering to maturity was slightly higher in 2011 than in 2010 season (from July to October). More frequent rainfall was observed in 2010 from May to July, compared to the cropping season (August to October) in 2011 (Fig. 1).
In this study, all agronomic traits except days from flowering to maturity between two years were found to be significantly different. Days to flowering, days from flowering to maturity, days to maturity, and seed weight per plant were found to be significantly different among sixteen genotypes. However, genotype × year interaction only significantly affected the days to flowering and seed weight per plant (Table 2). The mean value of days to flowering was observed to be slightly longer in 2011 (79) than in 2010 (75) growing season. Days to flowering of most accessions were found to be longer in 2011 than in 2010. However, days to flowering of some accessions such as IT032111 and IT031678 were longer in 2010 than in 2011 (Table 3). This could be due to the fact that the interaction between genotype and year significantly affected the days to flowering (Table 2). Early maturity was found in IT031967, while late maturity was observed in IT032103 and IT032111 both during 2010 and 2011 seasons. Stem length and weight of seeds per plant were found to be higher in 2010 than in 2011 in all sixteen genotypes. IT032017 was observed to be the shortest genotype both in 2010 (184.7 cm) and in 2011 (157.1 cm), while CSF352 was the tallest. Head length was found to be longest in IT031753 (AVG. = 17.5 mm), while shortest in IT032012 (AVG. = 12.8 mm) in both years. Seed weight per plant of IT032014 was observed to be the highest both in 2010 (70.8 g) and in 2011 (58.9 g), while IT032111 was the lowest in 2010 (20.4g) and 2011 (19.8g) (Table 3).
Genotype × year interactions significantly affected oil, stearic acid, oleic acid, and linoleic acid contents. Oil content, stearic acid, oleic acid, linoleic acid, and unsaturated fatty acid composition between two years were found to be significantly different. Oil, stearic acid, oleic acid, and linoleic acid contents were found to be significantly different among sixteen genotypes (Table 4). In general, variety effect was a major factor for observed variation in oil and fatty acids except stearic which was predominantly influenced by the interaction of genotype × year (36.2%). In particular, genotype effect dominantly occupied very high proportion of total sums of squares in oil content (80.4%), oleic acid (80.4%), and linoleic acid (77.7%) (Fig. 2).
Oil contents of most genotypes were higher in 2010 than in 2011. However, oil contents of some genotypes such as IT032012 and IT032014 were higher in 2011 than in 2010. These results could be due to the interaction effect of genotypes and years which significantly affected oil content in sunflower seed. Same pattern was also found in stearic, oleic and linoleic acid contents. The mean values of stearic and oleic acid contents were slightly higher in 2011 (4.1% and 51.0%) than in 2010 (3.4% and 46.4%). However, the average of linoleic acid content was slightly higher in 2010 (44.8%) than in 2011 (39.1%). IT031967, IT031965 and IT032017 showed high oil level (over 40%) both during 2010 and 2011 seasons. It could be possible that genotypes had significant influence on the oil content synthesis. High oleic acid content was found in IT031699 by the average of 69.8% between two years, while high linoleic acid level was found in CSF352 (AVG. = 70.7%) (Table 5).
Genotype × year interaction significantly affected all tocopherol and phytosterol components. All tocopherol and phytosterol components except γ-tocopherol showed significant differences between two years. All tocopherol and phytosterol components showed significant differences among sixteen genotypes (Table 6). Genotype effect had the highest percentage of sum of squares for α-tocopherol (53%), total tocopherol (47%), stigmasterol (38%), β-sitostrol (45%), and total sterol (39%) contents. For campesterol, variation was mainly explained by genotype × year interaction (45% of sum of squares). For β-tocopherol and γ-tocopherol, there were similar percentage of sum of squares for genotype (23% and 29%) and genotype × year interaction (25% and 30%) (Fig. 3). The mean values of α-T, β-T, γ-T, total tocopherol, campesterol, stigmasterol, β-sitosterol, and total sterol contents were all observed to be higher in 2011 than in 2010 growing season (Table 7). As mentioned earlier, the mean temperature was slightly higher but the precipitation was lower in 2011 than in 2010 during sunflower maturity period (from August to October) (Fig. 1). Whether these two factors had an influence on the observed difference in tocopherol and phytosterol components in the two growing years brings an attention for further research in sunflower. IT031965, IT031913 and IT032014 showed highest α-tocopherol and total tocopherol levels both in 2010 and 2011 seasons. CSF352 showed highest β-sitosterol and total sterol contents by the mean of two years (2633.9 μg g−1 and 2934.8 μg g−1, respectively) (Table 7).
Effects of planting dates on agronomic traits and chemical compositions

Weather conditions in 2010 growing season

The mean temperature increased from sowing period (May) to flowering period (August), while it decreased during maturity period (from August to October). Similar pattern was also observed for rainfall in 2010 growing season (Fig. 4).

Agronomic traits

Days to flowering of sunflower sown in May 7 (64) and May 17 (61) were found to be longest followed by May 27 (56), June 7 (52), and June 17 (51). Days from flowering to maturity of sunflower sown in May 7 (43), May 27 (40), and June 7 (41) were significantly longer (P<0.05) than in May 17 (31) and June 7 (34). There was no significant difference in days to maturity among May 7 (97), May 17 (92), May 27 (96), and June 7 (93) planting dates. However, June 17 (85) was significantly the shortest (P<0.05). Stem length in June 7 planting (297 cm) was the longest, followed by May 27 (286 cm), June 17 (265 cm), May 17 (246 cm), and May 7 (238 cm) planting. Head length in May 7 planting (21.2 cm) was longest, followed by June 7 (20.0 cm), May 27 (19.9 cm), and May 17 (19.7 cm), while June 17 (17.8 cm) planting was shortest. Seed weight per plant was found to be highest in May 7 (81.6 g) and May 17 (76.4 g) sowing, while June 17 planting was the lowest (36.1 g). In general, days to flowering became shorter when planting date was delayed. Similar patterns were also found in head length and weight of seeds per plant. When planting date was delayed head length and weight of seeds per plant decreased (Table 8).

Oil and fatty acid contents

Oil content of the seeds sown in May 7 (35.6%) was the highest among five different planting dates, and there was no significant difference among May 17 (31.5%), May 27 (31.1%), and June 7 (30.5%) planting, while June 17 planting showed the lowest oil level (27.4%). Same patterns were also observed in stearic and oleic acid contents, where a decrease in content value was observed when planting date was delayed. On the contrary, linoleic acid content increased when planting date was delayed. Palmitic, saturated fatty acid and unsaturated fatty acid contents showed no significant differences among five different planting dates (Table 9).

Tocopherol and phytosterol contents

The α-tocopherol content of sunflower seeds sown in May 7 (202.6 μg g−1), May 17 (199.2 μg g−1), May 27 (196.8 μg g−1), and June 7 (165.8 μg g−1) were significantly higher (P<0.05) than in June 17 (151.6 μg g−1). The total tocopherol content of sunflower seeds sown in May 7 (209.7 μg g−1), May 17 (206.7 μg g−1), and May 27 (203.9 μg g−1) were significantly higher (P<0.05) than in June 7 (171.9 μg g−1) and June 17 (156.9 μg g−1). β-tocopherol and γ-tocopherol contents showed no significant differences among five different planting dates. Campesterol content of sunflower seeds sown in May 7 (141.2 μg g−1), May 17 (179.8 μg g−1), May 27 (150.8 μg g−1), and June 7 (142.9 μg g−1) were significantly higher (P<0.05) than in June 17 (107.5 μg g−1). Stigmasterol contents of sunflower seeds sown in May 7 (240.3 μg g−1), May 17 (250.5 μg g−1), and May 27 (237.5 μg g−1) were significantly higher (P<0.05) than in June 7 (205.8 μg g−1), while June 17 (152.3 μg g−1) had the lowest stigmasterol level. The β-sitosterol content of sunflower seeds sown in May 7 (1995.8 μg g−1), May 17 (1869.2 μg g−1), May 27 (1863.5 μg g−1), and June 7 (1847.2 μg g−1) were significantly higher (P<0.05) than in June 17 (1488.3 μg g−1). The total phytosterol content of sunflower seeds sown in May 7 (2377.3 μg g−1), May 17 (2269.4 μg g−1), May 27 (2251.8 μg g−1), and June 7 (2195.8 μg g−1) were significantly higher (P<0.05) than in June 17 (1748.0 μg g−1) (Table 10). In general, α-tocopherol, total tocopherol, β-sitosterol and total phytosterol contents decreased when planting date was delayed.
Agronomic traits such as plant height (Ahmad and Hassan 2000), number of seeds per head (Kaleem et al. 2009), and 100-seed weight (Hassan et al. 2003) in sunflower are significantly influenced by the temperature and growth durations which are particular traits of seasonal changes (Qadir et al. 2007). Similar results were found in our study. All agronomic traits except days from flowering to maturity between two years were found to be significantly different. Days to flowering, days from flowering to maturity, days to maturity, and seed weight per plant were found to be significantly different among sixteen genotypes. However, genotype × year interaction only significantly affected the days to flowering and seed weight per plant. This indicated that variations in the agronomic traits due to environment and genotype effects are higher than by the interaction of both factors.
In our study, variety effect was a major factor for observed variation in oil and fatty acids except stearic which was predominantly influenced by the interaction of genotype × year. This indicated that there could be significant changes in oil content and fatty acid composition in sunflower seed produced from different genotypes in different environment. These results were in conformity with other finding in which the genotypes and environmental factors such as temperature during the period of seed development and maturation might have affected oil content in sunflower seed (Ahmad and Hassan 2000). The mean value of oil content was observed to be slightly higher in 2011 (35.1%) than in 2010 (32.0%). The mean temperature in 2011 growing season was generally higher than in 2010 during sunflower maturity period (from August to October) (Fig. 1). It could be considered that high temperature during the period of seed maturation is attributable to higher oil content. Similar results were obtained in previous studies which found the oil content of sunflowers to be maximum when matured at high temperature but to be progressively decreased as it matured at low temperature (Ahmad et al. 2001; Vega et al. 2002). The mean values of stearic and oleic acid contents were slightly higher in 2011 than in 2010. However, the average of linoleic acid content was slightly higher in 2010 than in 2011. Similar results were also found in the previous research that environmental factors affected oil contents and fatty acid composition of sunflower seed and therefore, seeds varied in their oil content and fatty acid composition depending on their environment of growth (Fick et al. 1974). Baydar and Erbas (2005) reported that the most important health benefit of sunflower seeds is imparted by the polyunsaturated (linoleic acid) and monounsaturated (oleic acid) fatty acids that it contains. These components protect the heart against various heart diseases like blockage of arteries, by lowering cholesterol and eliminating bad cholesterol or low density lipoprotein. More than 90% of the fat in sunflower seeds is unsaturated fatty acids which help maintain high density lipoprotein (Izquierdo and Aguirrezabal 2008). In this study, the highest unsaturated fatty acid content was found in IT031753 with 91.9% among sixteen sunflower accessions (Table 5).
Fernandez-Cuesta et al. (2012) reported that variation of tocopherol content in sunflower kernel was mainly explained by the effect of genotypes and the interaction of genotype × environment, and variation in kernel phytosterol content was mainly attributable to the effect of the location and the interaction of genotype × environment. In our study, genotype × year interaction significantly affected all tocopherol and phytosterol components. All tocopherol and phytosterol components except γ-tocopherol showed significant differences between two years. All tocopherol and phytosterol components showed significant differences among sixteen genotypes. These results indicate less effect of environment on tocopherol and phytosterol contents as compared to the effect of genotypes. It may require a greater effort for sunflower breeders that new breeding materials should be evaluated for their target environments prior to main breeding activities for agronomic traits and chemical compositions due to ubiquitous of genotype by environment interaction.
Effects of planting dates on agronomic traits and chemical compositions
Planting date is one of the most important cultivation practices to be considered in sunflower production, as it is in all crops. In this study, when planting date was delayed days to flowering, head length and weight of seeds per plant decreased. Previous study also reported that sunflower seed weights per plant tended to decrease when planting date was delayed (Gustavo et al. 2007). Oil content of sunflower seed has been reported to decrease with delay of planting date (Robertson 1981). Ahmad and Hassan (2000) depicted that lower temperature and lesser growing days favor the high stearic acid accumulation. Jones (1984), Unger (1986), and Cilardi et al. (1990) observed a decrease in oleic acid concentration and, conversely, an increase in linoleic acid in sunflower genotypes as seeding dates are delayed. Fatty acid composition of sunflower is influenced by temperature, mainly regulating the ratio of oleic and linoleic acid (Garces et al. 1989). Similar results were observed in our study, when planting date was delayed, oil, stearic acid and oleic acid contents decreased but linoleic acid content increased. In our study, when planting date was delayed, days to flowering, head length, weight of seeds per plant, oil, stearic acid, oleic acid, α-tocopherol, total tocopherol, β-sitosterol and total sterol contents decreased but linoleic acid content increased. Similar results were also reported by other researchers (Moore and Guy 1997; Ozer 2003), who noted that late planting not only reduced seed yield, but also decreased oil levels in oilseed crop. The result of this study will provide valuable information for sunflower breeders and growers in developing and producing functional food resources and products.
This work was supported by research grant of Chungbuk National University in 2012.
Fig. 1
Mean temperature and rainfall during 2010 and 2011 growing seasons.
pbb-02-35f1.jpg
Fig. 2
Sums of squares in percentage for oil and fatty acids detected.
pbb-02-35f2.jpg
Fig. 3
Sums of squares in percentage for tocopherol and phytosterol contents detected.
pbb-02-35f3.jpg
Fig. 4
Mean temperature and rainfall during 2010 growing season.
pbb-02-35f4.jpg
Table 1
Origin of sixteen sunflower accessions investigated in this study.
Table 1
No. IT No. Origin
1 IT031967 USA
2 IT031965 USA
3 IT032017 Canada
4 IT031831 USA
5 IT031699 USA
6 IT031938 USA
7 IT032111 Korea
8 IT031725 USA
9 IT032103 Korea
10 IT031913 USA
11 IT031687 Canada
12 IT032012 USA
13 CSF352 Korea
14 IT031848 USA
15 IT031753 USA
16 IT032014 Canada
Table 2
Analysis of variance in agronomic traits of sixteen sunflower germplasm in two growing years. Data show sums of squares with F-test results.
Table 2
Source of variation df Days to flowering DFFTMz Days to maturity Stem length (cm) Head length (cm) SWPPy (g)
Year (Y) 1 247.0** 0.58ns 270.0* 170329.7** 203.2** 12524.2**
Replication (year) 4 113.9 93.2 99.3 3957.7 41.2 793.0
Genotype (G) 15 23723.0** 7840.4** 23064.6** 28944.4ns 104.8ns 7262.2**
G X Y 15 1008.6** 773.1ns 435.5ns 29663.5ns 162.5ns 4500.6*
Error 60 1126.7 1732.0 2688.6 89126.3 421.4 7135.5

Total 95 26219.3 10439.2 26588.2 322021.7 933.1 32215.6

*Significant at 0.05 level,

**Significant at 0.01 level,

nsnot significant

zdays from flowering to maturity,

yseed weight per plant

Table 3
Agronomic traits of sixteen sunflower germplasm in 2010 and 2011.
Table 3
No. Genotype Days to flowering DFFTM Days to maturity Stem length (cm) Head length (cm) SWPP (g)

2010 2011 2010 2011 2010 2011 2010 2011 2010 2011 2010 2011
1 IT031967 60 66 31 28 91 94 208 189 17.2 15.0 60.8 44.0
2 IT031965 60 67 32 28 92 95 193 169 18.1 13.0 62.5 47.8
3 IT032017 66 68 26 21 92 89 184 157 17.0 15.5 61.2 54.1
4 IT031831 68 69 25 26 93 95 225 193 15.6 15.3 49.0 38.0
5 IT031699 74 91 18 12 92 103 243 192 21.5 12.4 56.3 36.7
6 IT031938 70 74 23 20 93 94 281 180 18.8 14.9 53.7 34.9
7 IT032111 104 91 25 44 129 135 269 197 15.2 15.3 20.4 19.8
8 IT031725 65 69 48 46 113 115 228 197 15.3 11.9 63.4 31.2
9 IT032103 104 110 26 23 130 133 277 227 16.0 11.2 47.8 45.4
10 IT031913 74 79 44 40 118 119 256 203 18.4 9.2 44.7 39.1
11 IT031687 85 83 37 40 122 123 255 210 17.4 12.5 54.7 47.2
12 IT032012 69 69 23 28 92 97 250 192 11.6 14.0 43.3 33.7
13 CSF352 108 121 11 12 119 133 262 226 15.9 14.9 23.5 26.9
14 IT031848 68 66 24 23 92 89 251 195 15.1 12.6 38.4 26.0
15 IT031753 65 66 27 29 92 95 234 199 18.7 16.1 59.3 53.4
16 IT032014 64 69 28 28 92 97 246 203 17.2 15.4 70.8 58.9

Mean 75 79 28 28 103 107 241 195 16.9 14.0 50.6 39.8

SD 16 17 9 10 15 17 28 17 2.2 1.9 14.0 11.0

LSD (0.05) 10.1 2.6 11.7 8.8 14.8 9.1 21.8 35.6 2.5 1.7 9.8 6.9
Table 4
Analysis of variance in oil and fatty acid contents of sixteen sunflower germplasm in two growing years. Data show sums of squares with F-test results.
Table 4
Source of variation df Oil Palmitic Stearic Oleic Linoleic SFAz USFAy
Year (Y) 1 144.8** 3.0** 7.8** 431.5** 635.9** 19.7** 5.2ns
Replication (year) 4 31.1 4.3 2.6 175.9 140.6 8.6 17.95
Genotype (G) 15 2672.4** 30.7** 12.2** 13424.5** 13067.2** 50.9ns 123.0ns
G X Y 15 422.6** 15.9** 19.9** 2523.3** 2648.5** 56.7ns 172.1ns
Error 60 53.6 46.8 12.4 149.5 298.7 74.2 258.2

Total 95 3324.6 100.6 55.0 16704.7 16827.0 210.1 576.5

*Significant at 0.05 level,

**Significant at 0.01 level,

nsnot significant

zsaturated fatty acid (palmitic acid + stearic acid),

yunsaturated fatty acid (oleic acid + linoleic acid)

Table 5
Oil and fatty acid contents of sixteen sunflower germplasm in 2010 and 2011. (%)
Table 5
No. Genotype Oil Palmitic Stearic Oleic Linoleic SFA USFA

2010 2011 2010 2011 2010 2011 2010 2011 2010 2011 2010 2011 2010 2011
1 IT031967 44.1 45.1 5.3 5.5 3.8 5.3 49.8 62.2 41.1 27.0 9.0 10.8 91.0 89.2
2 IT031965 42.6 42.2 5.4 5.2 3.2 3.8 43.2 55.7 48.2 35.3 8.6 9.0 91.4 91.0
3 IT032017 42.1 42.2 4.8 5.2 3.3 3.5 57.0 51.3 34.9 40.0 8.1 8.7 91.9 91.3
4 IT031831 29.1 39.0 4.7 6.1 4.0 3.1 60.8 63.1 30.5 27.7 8.7 9.2 91.3 90.8
5 IT031699 23.2 29.9 4.7 6.2 3.2 4.5 69.2 70.3 22.9 19.0 7.9 10.7 92.1 89.3
6 IT031938 28.9 29.0 5.3 5.0 4.1 4.4 23.0 44.8 67.6 45.8 9.4 9.3 90.6 90.7
7 IT032111 33.1 38.1 6.9 6.9 2.6 4.2 22.2 25.4 68.3 63.5 9.5 11.1 90.5 88.9
8 IT031725 28.3 25.9 5.7 9.0 3.2 6.7 50.8 64.7 40.3 19.6 8.9 15.8 91.1 84.2
9 IT032103 33.5 37.1 5.7 6.0 3.0 4.2 24.1 25.1 67.2 64.7 8.6 10.2 91.4 89.8
10 IT031913 26.7 30.4 5.2 5.6 3.5 3.9 50.8 48.1 40.5 42.4 8.8 9.5 91.2 90.5
11 IT031687 25.0 25.9 4.8 5.3 4.1 3.5 51.4 62.6 39.7 28.6 8.9 8.8 81.1 91.2
12 IT032012 33.8 30.3 5.5 5.1 3.2 3.9 51.5 54.3 39.8 36.7 8.7 9.0 91.3 91.0
13 CSF352 29.1 38.4 6.7 6.7 3.0 3.1 23.2 16.0 67.1 74.2 9.7 9.8 90.3 90.2
14 IT031848 24.5 38.1 5.7 5.2 3.8 3.3 57.2 46.7 33.3 44.8 9.5 8.5 90.5 91.5
15 IT031753 26.0 32.0 5.1 4.6 3.2 3.3 54.9 65.5 36.8 26.6 8.3 7.9 91.7 92.1
16 IT032014 41.6 37.7 5.4 5.3 3.1 4.5 52.9 60.8 38.6 29.4 8.5 9.8 91.5 90.2

Mean 32.0 35.1 5.4 5.8 3.4 4.1 46.4 51.0 44.8 39.1 8.8 9.9 90.5 90.1

SD 7.1 6.0 0.6 1.1 0.4 0.9 14.9 16.2 14.6 16.4 0.5 1.8 2.6 1.8

LSD (0.05) 0.9 1.4 0.6 1.3 0.4 0.9 1.5 1.7 2.7 2.1 0.5 1.6 2.1 1.6
Table 6
Analysis of variance in tocopherol and phytosterol contents of sixteen sunflower germplasm in two growing years. Data show sums of squares with F-test results.
Table 6
Source of variation df Tocopherol Phytosterol


α β γ Total Campez Stigmay β-sitox Total
Year (Y) 1 7401.2** 45.2** 2.7ns 11897.0** 7760.5** 51200.2** 2585981.8** 3696188.4**
Replication (year) 4 3356.9 32.2 4.7 4427.8 2131.7 4877.0 362177.5 508763.7
Genotype (G) 15 67900.0** 84.9** 31.7** 64287.6** 16608.2** 68376.4** 4501284.9** 4811998.3**
G X Y 15 45913.9** 93.0** 33.3** 50972.3** 23697.0** 52858.3** 2332641.8** 2985940.3**
Error 60 3163.4 120.3 38.8 4775.0 2227.2 3635.7 247937.2 320860.7


Total 95 127735.4 375.6 111.3 136359.8 52424.6 180947.5 10030023.0 12323752.0

zcampesterol,

ystigmasterol,

xβ-sitosterol

*Significant at 0.05 level,

**Significant at 0.01 level,

nsnot significant

Table 7
The tocopherol and phytosterol contents of sixteen sunflower germplasm in 2010 and 2011. (μg g−1)
Table 7
No. Genotype α-tocopherol β-tocopherol γ-tocopherol Total Tocopherol Campesterol Stigmasterol β-sitosterol Total sterol

2010 2011 2010 2011 2010 2011 2010 2011 2010 2011 2010 2011 2010 2011 2010 2011
1 IT031967 240.2 209.2 7.3 8.1 0.4 0.7 247.8 218.0 92.2 153.2 285.4 302.2 1801.2 2152.5 2178.8 2607.9
2 IT031965 259.2 295.9 7.1 7.7 0.4 0.0 266.7 303.6 133.7 107.8 250.4 330.4 1892.3 1917.4 2276.4 2355.5
3 IT032017 274.6 193.8 8.4 6.8 0.0 0.2 282.9 200.2 93.7 147.0 226.6 253.0 1787.1 2142.2 2107.3 2542.2
4 IT031831 177.0 219.6 8.9 8.5 2.1 1.3 188.0 228.4 108.8 110.6 191.1 237.5 1632.8 2174.7 1932.8 2522.8
5 IT031699 146.4 169.8 4.6 8.8 0.0 0.9 151.0 181.5 92.8 105.8 233.5 248.4 1414.3 1792.0 1740.7 2146.2
6 IT031938 170.9 212.4 4.8 7.9 1.0 0.3 176.7 220.6 126.9 113.2 215.9 242.0 1657.6 1719.7 2000.4 2074.9
7 IT032111 163.5 216.1 4.5 7.9 0.9 2.2 168.9 226.2 109.6 144.8 219.0 198.7 2205.7 2488.0 2534.3 2831.5
8 IT031725 218.7 202.3 8.6 6.4 0.3 0.2 227.7 208.8 121.4 139.9 193.1 270.9 1699.2 2095.6 2013.7 2506.4
9 IT032103 174.5 231.8 4.7 9.4 1.4 2.5 180.6 243.7 108.1 171.7 168.0 226.5 1780.3 2742.8 2156.5 3141.0
10 IT031913 219.2 262.6 5.0 8.2 0.0 0.4 224.2 271.2 118.2 128.0 227.2 342.8 2065.5 2177.8 2410.9 2648.6
11 IT031687 209.8 144.6 6.8 6.4 0.7 0.0 217.4 150.9 162.3 103.7 280.9 247.5 2429.1 2068.7 2872.3 2419.9
12 IT032012 186.0 197.9 4.5 7.7 0.0 1.2 190.5 207.8 134.8 139.4 225.1 267.6 2075.5 2365.1 2435.5 2772.2
13 CSF352 154.0 212.4 4.6 6.3 1.0 1.9 159.6 220.6 97.3 126.5 194.5 253.6 2379.8 2888.0 2571.6 3298.0
14 IT031848 158.8 238.5 6.7 8.3 1.7 1.3 167.2 247.1 125.3 176.4 209.3 232.4 1914.6 2271.8 2249.2 2680.5
15 IT031753 186.2 250.2 8.5 9.9 0.0 0.4 194.6 260.6 123.5 117.0 218.3 213.3 1883.8 1862.1 2225.6 2192.4
16 IT032014 239.9 230.1 7.8 8.7 0.2 0.0 247.8 238.8 99.7 107.6 206.3 260.7 1758.3 2209.0 2064.3 2677.3

Mean 198.7 218.0 6.4 7.9 0.6 0.8 205.7 226.7 115.5 130.8 221.5 258.0 1898.6 2191.7 2235.6 2588.6

SD 39.6 35.5 1.7 1.1 0.7 0.8 40.2 35.8 19.1 23.4 31.0 38.9 273.9 317.1 280.1 330.1

LSD (0.05) 8.1 6.8 0.9 1.4 0.5 0.7 8.7 9.2 6.8 5.0 8.9 8.9 77.6 58.6 91.9 67.6
Table 8
Agronomic traits of IT031831 at five different planting dates.
Table 8
Planting date Days to flowering DFFTMz Days to maturity Stem length (cm) Head length (cm) WSPPy (g)
May 7 64ax 43a 97a 238e 21.2a 81.6a
May 17 61a 31c 92a 246d 19.7b 76.4a
May 27 56b 40a 96a 286b 19.9b 59.1b
June 7 52c 41a 93a 297a 20.0b 64.5b
June 17 51c 34b 85b 265c 17.8c 36.1c

zdays from flowering to maturity

yweight of seeds per plant

xsame letters in each column are not significantly different by duncan’s multiple range test, p<0.05

Table 9
Oil and fatty acid contents of IT031831 at five different planting dates. (%)
Table 9
Planting date Oil Palmitic Stearic Oleic Linoleic SFAz USFAy
May 7 35.6±1.37ax 4.9±0.3a 3.8±0.2a 70.3±3.3a 20.9±2.9d 8.8±0.6a 91.2±0.6a
May 17 31.5±0.7ab 4.6±0.2a 3.8±0.6a 69.7±3.1a 21.9±3.5cd 8.5±0.5a 91.5±0.5a
May 27 31.1±4.2ab 4.5±0.2a 3.5±0.2b 66.0±1.4ab 25.9±1.5c 8.1±0.3a 91.9±0.3a
June 7 30.5±1.5ab 4.6±0.3a 3.2±0.7b 61.4±1.6b 30.9±0.9b 7.8±0.8a 92.2±0.8a
June 17 27.4±4.4b 4.8±0.4a 2.9±0.3b 55.7±3.2c 36.6±3.0a 7.8±0.6a 92.2±0.6a

zsaturated fatty acid (palmitic acid + stearic acid)

yunsaturated fatty acid (oleic acid + linoleic acid)

xsame letter in each column are not significantly different by duncan’s multiple range test, p<0.05

Table 10
Tocopherol and phytosterol contents of IT031831 at five different planting dates. (μg g−1)
Table 10
Planting date Tocopherol Phytosterol

α β γ Total Campesterol Stigmasterol β-sitosterol Total
May 7 202.6±8.5az 7.1±1.7a 0.13±0.2 209.7±9.6a 141.2±2.3a 240.3±15.2a 1995.8±115.7a 2377.3±113.2a
May 17 199.2±15.4a 7.5±1.9a - 206.7±16.8a 179.8±1.4a 250.5±10.9a 1869.2±137.9a 2269.4±156.3a
May 27 196.8±8.3a 7.0±0.7a - 203.9±8.3a 150.8±5.2a 237.5±8.1a 1863.5±73.2a 2251.8±66.2a
June 7 165.8±9.5a 5.9±1.2a 0.3±0.2 171.9±9.0ab 142.9±9.0a 205.8±1.9b 1847.2±23.3a 2195.8±25.6a
June 17 151.6±43.3b 5.1±0.8a 0.3±0.3 156.9±43.6b 107.5±4.6b 152.3±15.2c 1488.3±113.3b 1748.0±110.8b

zsame letter in each column are not significantly different by duncan’s multiple range test, p<0.05

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Effect of Genotype, Growing Year and Planting Date on Agronomic Traits and Chemical Composition in Sunflower (Helianthus annuus L.) Germplasm
Plant Breed. Biotech.. 2014;2(1):35-47.   Published online March 31, 2014
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Effect of Genotype, Growing Year and Planting Date on Agronomic Traits and Chemical Composition in Sunflower (Helianthus annuus L.) Germplasm
Plant Breed. Biotech.. 2014;2(1):35-47.   Published online March 31, 2014
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Effect of Genotype, Growing Year and Planting Date on Agronomic Traits and Chemical Composition in Sunflower (Helianthus annuus L.) Germplasm
Image Image Image Image
Fig. 1 Mean temperature and rainfall during 2010 and 2011 growing seasons.
Fig. 2 Sums of squares in percentage for oil and fatty acids detected.
Fig. 3 Sums of squares in percentage for tocopherol and phytosterol contents detected.
Fig. 4 Mean temperature and rainfall during 2010 growing season.
Effect of Genotype, Growing Year and Planting Date on Agronomic Traits and Chemical Composition in Sunflower (Helianthus annuus L.) Germplasm

Origin of sixteen sunflower accessions investigated in this study.

No. IT No. Origin
1 IT031967 USA
2 IT031965 USA
3 IT032017 Canada
4 IT031831 USA
5 IT031699 USA
6 IT031938 USA
7 IT032111 Korea
8 IT031725 USA
9 IT032103 Korea
10 IT031913 USA
11 IT031687 Canada
12 IT032012 USA
13 CSF352 Korea
14 IT031848 USA
15 IT031753 USA
16 IT032014 Canada

Analysis of variance in agronomic traits of sixteen sunflower germplasm in two growing years. Data show sums of squares with F-test results.

Source of variation df Days to flowering DFFTMz Days to maturity Stem length (cm) Head length (cm) SWPPy (g)
Year (Y) 1 247.0** 0.58ns 270.0* 170329.7** 203.2** 12524.2**
Replication (year) 4 113.9 93.2 99.3 3957.7 41.2 793.0
Genotype (G) 15 23723.0** 7840.4** 23064.6** 28944.4ns 104.8ns 7262.2**
G X Y 15 1008.6** 773.1ns 435.5ns 29663.5ns 162.5ns 4500.6*
Error 60 1126.7 1732.0 2688.6 89126.3 421.4 7135.5

Total 95 26219.3 10439.2 26588.2 322021.7 933.1 32215.6

*Significant at 0.05 level,

**Significant at 0.01 level,

nsnot significant

zdays from flowering to maturity,

yseed weight per plant

Agronomic traits of sixteen sunflower germplasm in 2010 and 2011.

No. Genotype Days to flowering DFFTM Days to maturity Stem length (cm) Head length (cm) SWPP (g)

2010 2011 2010 2011 2010 2011 2010 2011 2010 2011 2010 2011
1 IT031967 60 66 31 28 91 94 208 189 17.2 15.0 60.8 44.0
2 IT031965 60 67 32 28 92 95 193 169 18.1 13.0 62.5 47.8
3 IT032017 66 68 26 21 92 89 184 157 17.0 15.5 61.2 54.1
4 IT031831 68 69 25 26 93 95 225 193 15.6 15.3 49.0 38.0
5 IT031699 74 91 18 12 92 103 243 192 21.5 12.4 56.3 36.7
6 IT031938 70 74 23 20 93 94 281 180 18.8 14.9 53.7 34.9
7 IT032111 104 91 25 44 129 135 269 197 15.2 15.3 20.4 19.8
8 IT031725 65 69 48 46 113 115 228 197 15.3 11.9 63.4 31.2
9 IT032103 104 110 26 23 130 133 277 227 16.0 11.2 47.8 45.4
10 IT031913 74 79 44 40 118 119 256 203 18.4 9.2 44.7 39.1
11 IT031687 85 83 37 40 122 123 255 210 17.4 12.5 54.7 47.2
12 IT032012 69 69 23 28 92 97 250 192 11.6 14.0 43.3 33.7
13 CSF352 108 121 11 12 119 133 262 226 15.9 14.9 23.5 26.9
14 IT031848 68 66 24 23 92 89 251 195 15.1 12.6 38.4 26.0
15 IT031753 65 66 27 29 92 95 234 199 18.7 16.1 59.3 53.4
16 IT032014 64 69 28 28 92 97 246 203 17.2 15.4 70.8 58.9

Mean 75 79 28 28 103 107 241 195 16.9 14.0 50.6 39.8

SD 16 17 9 10 15 17 28 17 2.2 1.9 14.0 11.0

LSD (0.05) 10.1 2.6 11.7 8.8 14.8 9.1 21.8 35.6 2.5 1.7 9.8 6.9

Analysis of variance in oil and fatty acid contents of sixteen sunflower germplasm in two growing years. Data show sums of squares with F-test results.

Source of variation df Oil Palmitic Stearic Oleic Linoleic SFAz USFAy
Year (Y) 1 144.8** 3.0** 7.8** 431.5** 635.9** 19.7** 5.2ns
Replication (year) 4 31.1 4.3 2.6 175.9 140.6 8.6 17.95
Genotype (G) 15 2672.4** 30.7** 12.2** 13424.5** 13067.2** 50.9ns 123.0ns
G X Y 15 422.6** 15.9** 19.9** 2523.3** 2648.5** 56.7ns 172.1ns
Error 60 53.6 46.8 12.4 149.5 298.7 74.2 258.2

Total 95 3324.6 100.6 55.0 16704.7 16827.0 210.1 576.5

*Significant at 0.05 level,

**Significant at 0.01 level,

nsnot significant

zsaturated fatty acid (palmitic acid + stearic acid),

yunsaturated fatty acid (oleic acid + linoleic acid)

Oil and fatty acid contents of sixteen sunflower germplasm in 2010 and 2011. (%)

No. Genotype Oil Palmitic Stearic Oleic Linoleic SFA USFA

2010 2011 2010 2011 2010 2011 2010 2011 2010 2011 2010 2011 2010 2011
1 IT031967 44.1 45.1 5.3 5.5 3.8 5.3 49.8 62.2 41.1 27.0 9.0 10.8 91.0 89.2
2 IT031965 42.6 42.2 5.4 5.2 3.2 3.8 43.2 55.7 48.2 35.3 8.6 9.0 91.4 91.0
3 IT032017 42.1 42.2 4.8 5.2 3.3 3.5 57.0 51.3 34.9 40.0 8.1 8.7 91.9 91.3
4 IT031831 29.1 39.0 4.7 6.1 4.0 3.1 60.8 63.1 30.5 27.7 8.7 9.2 91.3 90.8
5 IT031699 23.2 29.9 4.7 6.2 3.2 4.5 69.2 70.3 22.9 19.0 7.9 10.7 92.1 89.3
6 IT031938 28.9 29.0 5.3 5.0 4.1 4.4 23.0 44.8 67.6 45.8 9.4 9.3 90.6 90.7
7 IT032111 33.1 38.1 6.9 6.9 2.6 4.2 22.2 25.4 68.3 63.5 9.5 11.1 90.5 88.9
8 IT031725 28.3 25.9 5.7 9.0 3.2 6.7 50.8 64.7 40.3 19.6 8.9 15.8 91.1 84.2
9 IT032103 33.5 37.1 5.7 6.0 3.0 4.2 24.1 25.1 67.2 64.7 8.6 10.2 91.4 89.8
10 IT031913 26.7 30.4 5.2 5.6 3.5 3.9 50.8 48.1 40.5 42.4 8.8 9.5 91.2 90.5
11 IT031687 25.0 25.9 4.8 5.3 4.1 3.5 51.4 62.6 39.7 28.6 8.9 8.8 81.1 91.2
12 IT032012 33.8 30.3 5.5 5.1 3.2 3.9 51.5 54.3 39.8 36.7 8.7 9.0 91.3 91.0
13 CSF352 29.1 38.4 6.7 6.7 3.0 3.1 23.2 16.0 67.1 74.2 9.7 9.8 90.3 90.2
14 IT031848 24.5 38.1 5.7 5.2 3.8 3.3 57.2 46.7 33.3 44.8 9.5 8.5 90.5 91.5
15 IT031753 26.0 32.0 5.1 4.6 3.2 3.3 54.9 65.5 36.8 26.6 8.3 7.9 91.7 92.1
16 IT032014 41.6 37.7 5.4 5.3 3.1 4.5 52.9 60.8 38.6 29.4 8.5 9.8 91.5 90.2

Mean 32.0 35.1 5.4 5.8 3.4 4.1 46.4 51.0 44.8 39.1 8.8 9.9 90.5 90.1

SD 7.1 6.0 0.6 1.1 0.4 0.9 14.9 16.2 14.6 16.4 0.5 1.8 2.6 1.8

LSD (0.05) 0.9 1.4 0.6 1.3 0.4 0.9 1.5 1.7 2.7 2.1 0.5 1.6 2.1 1.6

Analysis of variance in tocopherol and phytosterol contents of sixteen sunflower germplasm in two growing years. Data show sums of squares with F-test results.

Source of variation df Tocopherol Phytosterol


α β γ Total Campez Stigmay β-sitox Total
Year (Y) 1 7401.2** 45.2** 2.7ns 11897.0** 7760.5** 51200.2** 2585981.8** 3696188.4**
Replication (year) 4 3356.9 32.2 4.7 4427.8 2131.7 4877.0 362177.5 508763.7
Genotype (G) 15 67900.0** 84.9** 31.7** 64287.6** 16608.2** 68376.4** 4501284.9** 4811998.3**
G X Y 15 45913.9** 93.0** 33.3** 50972.3** 23697.0** 52858.3** 2332641.8** 2985940.3**
Error 60 3163.4 120.3 38.8 4775.0 2227.2 3635.7 247937.2 320860.7


Total 95 127735.4 375.6 111.3 136359.8 52424.6 180947.5 10030023.0 12323752.0

zcampesterol,

ystigmasterol,

xβ-sitosterol

*Significant at 0.05 level,

**Significant at 0.01 level,

nsnot significant

The tocopherol and phytosterol contents of sixteen sunflower germplasm in 2010 and 2011. (μg g−1)

No. Genotype α-tocopherol β-tocopherol γ-tocopherol Total Tocopherol Campesterol Stigmasterol β-sitosterol Total sterol

2010 2011 2010 2011 2010 2011 2010 2011 2010 2011 2010 2011 2010 2011 2010 2011
1 IT031967 240.2 209.2 7.3 8.1 0.4 0.7 247.8 218.0 92.2 153.2 285.4 302.2 1801.2 2152.5 2178.8 2607.9
2 IT031965 259.2 295.9 7.1 7.7 0.4 0.0 266.7 303.6 133.7 107.8 250.4 330.4 1892.3 1917.4 2276.4 2355.5
3 IT032017 274.6 193.8 8.4 6.8 0.0 0.2 282.9 200.2 93.7 147.0 226.6 253.0 1787.1 2142.2 2107.3 2542.2
4 IT031831 177.0 219.6 8.9 8.5 2.1 1.3 188.0 228.4 108.8 110.6 191.1 237.5 1632.8 2174.7 1932.8 2522.8
5 IT031699 146.4 169.8 4.6 8.8 0.0 0.9 151.0 181.5 92.8 105.8 233.5 248.4 1414.3 1792.0 1740.7 2146.2
6 IT031938 170.9 212.4 4.8 7.9 1.0 0.3 176.7 220.6 126.9 113.2 215.9 242.0 1657.6 1719.7 2000.4 2074.9
7 IT032111 163.5 216.1 4.5 7.9 0.9 2.2 168.9 226.2 109.6 144.8 219.0 198.7 2205.7 2488.0 2534.3 2831.5
8 IT031725 218.7 202.3 8.6 6.4 0.3 0.2 227.7 208.8 121.4 139.9 193.1 270.9 1699.2 2095.6 2013.7 2506.4
9 IT032103 174.5 231.8 4.7 9.4 1.4 2.5 180.6 243.7 108.1 171.7 168.0 226.5 1780.3 2742.8 2156.5 3141.0
10 IT031913 219.2 262.6 5.0 8.2 0.0 0.4 224.2 271.2 118.2 128.0 227.2 342.8 2065.5 2177.8 2410.9 2648.6
11 IT031687 209.8 144.6 6.8 6.4 0.7 0.0 217.4 150.9 162.3 103.7 280.9 247.5 2429.1 2068.7 2872.3 2419.9
12 IT032012 186.0 197.9 4.5 7.7 0.0 1.2 190.5 207.8 134.8 139.4 225.1 267.6 2075.5 2365.1 2435.5 2772.2
13 CSF352 154.0 212.4 4.6 6.3 1.0 1.9 159.6 220.6 97.3 126.5 194.5 253.6 2379.8 2888.0 2571.6 3298.0
14 IT031848 158.8 238.5 6.7 8.3 1.7 1.3 167.2 247.1 125.3 176.4 209.3 232.4 1914.6 2271.8 2249.2 2680.5
15 IT031753 186.2 250.2 8.5 9.9 0.0 0.4 194.6 260.6 123.5 117.0 218.3 213.3 1883.8 1862.1 2225.6 2192.4
16 IT032014 239.9 230.1 7.8 8.7 0.2 0.0 247.8 238.8 99.7 107.6 206.3 260.7 1758.3 2209.0 2064.3 2677.3

Mean 198.7 218.0 6.4 7.9 0.6 0.8 205.7 226.7 115.5 130.8 221.5 258.0 1898.6 2191.7 2235.6 2588.6

SD 39.6 35.5 1.7 1.1 0.7 0.8 40.2 35.8 19.1 23.4 31.0 38.9 273.9 317.1 280.1 330.1

LSD (0.05) 8.1 6.8 0.9 1.4 0.5 0.7 8.7 9.2 6.8 5.0 8.9 8.9 77.6 58.6 91.9 67.6

Agronomic traits of IT031831 at five different planting dates.

Planting date Days to flowering DFFTMz Days to maturity Stem length (cm) Head length (cm) WSPPy (g)
May 7 64ax 43a 97a 238e 21.2a 81.6a
May 17 61a 31c 92a 246d 19.7b 76.4a
May 27 56b 40a 96a 286b 19.9b 59.1b
June 7 52c 41a 93a 297a 20.0b 64.5b
June 17 51c 34b 85b 265c 17.8c 36.1c

zdays from flowering to maturity

yweight of seeds per plant

xsame letters in each column are not significantly different by duncan’s multiple range test, p<0.05

Oil and fatty acid contents of IT031831 at five different planting dates. (%)

Planting date Oil Palmitic Stearic Oleic Linoleic SFAz USFAy
May 7 35.6±1.37ax 4.9±0.3a 3.8±0.2a 70.3±3.3a 20.9±2.9d 8.8±0.6a 91.2±0.6a
May 17 31.5±0.7ab 4.6±0.2a 3.8±0.6a 69.7±3.1a 21.9±3.5cd 8.5±0.5a 91.5±0.5a
May 27 31.1±4.2ab 4.5±0.2a 3.5±0.2b 66.0±1.4ab 25.9±1.5c 8.1±0.3a 91.9±0.3a
June 7 30.5±1.5ab 4.6±0.3a 3.2±0.7b 61.4±1.6b 30.9±0.9b 7.8±0.8a 92.2±0.8a
June 17 27.4±4.4b 4.8±0.4a 2.9±0.3b 55.7±3.2c 36.6±3.0a 7.8±0.6a 92.2±0.6a

zsaturated fatty acid (palmitic acid + stearic acid)

yunsaturated fatty acid (oleic acid + linoleic acid)

xsame letter in each column are not significantly different by duncan’s multiple range test, p<0.05

Tocopherol and phytosterol contents of IT031831 at five different planting dates. (μg g−1)

Planting date Tocopherol Phytosterol

α β γ Total Campesterol Stigmasterol β-sitosterol Total
May 7 202.6±8.5az 7.1±1.7a 0.13±0.2 209.7±9.6a 141.2±2.3a 240.3±15.2a 1995.8±115.7a 2377.3±113.2a
May 17 199.2±15.4a 7.5±1.9a - 206.7±16.8a 179.8±1.4a 250.5±10.9a 1869.2±137.9a 2269.4±156.3a
May 27 196.8±8.3a 7.0±0.7a - 203.9±8.3a 150.8±5.2a 237.5±8.1a 1863.5±73.2a 2251.8±66.2a
June 7 165.8±9.5a 5.9±1.2a 0.3±0.2 171.9±9.0ab 142.9±9.0a 205.8±1.9b 1847.2±23.3a 2195.8±25.6a
June 17 151.6±43.3b 5.1±0.8a 0.3±0.3 156.9±43.6b 107.5±4.6b 152.3±15.2c 1488.3±113.3b 1748.0±110.8b

zsame letter in each column are not significantly different by duncan’s multiple range test, p<0.05

Table 1 Origin of sixteen sunflower accessions investigated in this study.
Table 2 Analysis of variance in agronomic traits of sixteen sunflower germplasm in two growing years. Data show sums of squares with F-test results.

Significant at 0.05 level,

Significant at 0.01 level,

not significant

days from flowering to maturity,

seed weight per plant

Table 3 Agronomic traits of sixteen sunflower germplasm in 2010 and 2011.
Table 4 Analysis of variance in oil and fatty acid contents of sixteen sunflower germplasm in two growing years. Data show sums of squares with F-test results.

Significant at 0.05 level,

Significant at 0.01 level,

not significant

saturated fatty acid (palmitic acid + stearic acid),

unsaturated fatty acid (oleic acid + linoleic acid)

Table 5 Oil and fatty acid contents of sixteen sunflower germplasm in 2010 and 2011. (%)
Table 6 Analysis of variance in tocopherol and phytosterol contents of sixteen sunflower germplasm in two growing years. Data show sums of squares with F-test results.

campesterol,

stigmasterol,

β-sitosterol

Significant at 0.05 level,

Significant at 0.01 level,

not significant

Table 7 The tocopherol and phytosterol contents of sixteen sunflower germplasm in 2010 and 2011. (μg g−1)
Table 8 Agronomic traits of IT031831 at five different planting dates.

days from flowering to maturity

weight of seeds per plant

same letters in each column are not significantly different by duncan’s multiple range test, p<0.05

Table 9 Oil and fatty acid contents of IT031831 at five different planting dates. (%)

saturated fatty acid (palmitic acid + stearic acid)

unsaturated fatty acid (oleic acid + linoleic acid)

same letter in each column are not significantly different by duncan’s multiple range test, p<0.05

Table 10 Tocopherol and phytosterol contents of IT031831 at five different planting dates. (μg g−1)

same letter in each column are not significantly different by duncan’s multiple range test, p<0.05