Journal of Asian Scientific Research, 2015, 5(9): 465-472
Journal of Asian Scientific Research
ISSN(e): 2223-1331/ISSN(p): 2226-5724
URL: www.aessweb.com
EVALUATION OF TRAITS RELATED TO DROUGHT STRESS IN
SESAME (SESAMUM INDICUM L.) GENOTYPES
1†
Masoud Golestani --- Hassan Pakniyat
2
1
Department of Agriculture, Payame Noor University (PNU), Tehran, Iran
Department of Crop Production and Plant Breeding, College of Agriculture Shiraz University, Shiraz, Iran
2
ABSTRACT
In order to evaluate traits related to drought stress in eight sesame (sesamum indicum L.)
genotypes, two experiments were carried out in randomized complete design with three
replications in the field of the Research Station of College of Agriculture, Shiraz University, Iran.
The two experiments differed with respect to their irrigation regimes. Yield related traits (number
of days to maturation, NDM; number of capsules per plant, NCP; 1000 seed weight, TSW; harvest
index, HI; biological yield, BY and grain yield, GY) and physiological traits(canopy temperature,
TC, leaf water potential, LWP; leaf osmotic potential, LOP; initial water content, IWC and rate of
water loss, RWL) were evaluated under both conditions. The results showed that drought
decreased all yield related traits except HI, significantly. LWP and LOP decreased under drought
stress, while RWL increased, significantly. TC and IWC did not show significant changes under
drought stress. Based on the results, it is reasonable to assume that high yield of sesame plants
under drought conditions could be obtained by selecting breeding materials with lowest reduction
in NDM, NCP, TSW, BY, GY, LWP and LOP and the highest reduction in RWL. Under non-stress
condition LOP in both stages was the best traits. Under drought condition LWP, LOP at both
stages and RWL at grain filling stage were the most suitable traits.
© 2015 AESS Publications. All Rights Reserved.
Keywords: Drought stress, Physiological traits, Sesame genotypes, Yield related traits, Irrigation regimes.
Contribution/ Originality
This study is one of very few studies which have investigated the effects of drought stress on
physiological and yield related traits of sesame genotypes.
1. INTRODUCTION
Sesame (Sesamum indicum L.) is a one of the oldest oil seed crops, growing widely in tropical
and subtropical areas [1]. Sesame seeds contain oil (44-58%), protein (18-25%), carbohydrate
† Corresponding author
DOI: 10.18488/journal.2/2015.5.9/2.9.465.472
ISSN(e): 2223-1331/ISSN(p): 2226-5724
© 2015 AESS Publications. All Rights Reserved.
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Journal of Asian Scientific Research, 2015, 5(9):465-472
(~13.5%) [2] and also two unique substances: sesamin and sesamolin known to have a cholesterol
lowering effect in humans [3]. Drought is one of the most important abiotic stresses which affect
almost every aspect of plant growth [4]. The arid and semi-arid regions where sesame is grown are
specified by high temperatures, high evaporation demand and occurrence of unpredictable drought
[5]. This plant is relatively drought tolerant [6]. Resistance to water stress in sesame is important in
many country with low rainfall. Traits correlated with drought tolerance such as yield components
and physiological traits are suitable indicators for selection of drought tolerant genotypes in
breeding programs to reduce the impact of water deficit on crop yield [7]. Understanding of
physiological mechanisms that enable plants to adapt to water deficit and maintain growth and
productivity during stress period could help in screening and selection of tolerant genotypes and
using these traits in breeding programs [8]. Therefore, the use of physiological traits as an indirect
selection would be important in augmenting yield-based selection procedures. In the present study,
the effects of drought stress on traits such as yield related traits (NDM, NCP, TSW and HI) and
physiological traits (TC, LWP, LOP, IWC and RWL) was studied. Efforts have been made to
enhance the efficiency of selection for drought tolerant genotypes based on yield and specific
physiological traits [9]. TC has already been considered to be effective for drought resistance
screening in pearl millet (Pennisetum glaucum) [10] safflower (Carthamus tinctorius L.) [11] and
sunflower (Helianthus annuus L.) [12]. LWP and LOP are other criterion used by several
researchers in safflower [11] wheat [13] and sunflower [14]. Several researchers have used IWC
and RWL from excised leaves as screening criteria in drought resistance breeding programs [5, 11,
15]. The objectives of this study were to investigate the effects of drought stress on yield related
traits and physiological traits under drought stress of 8 sesame genotypes and identify the efficient
traits for screening drought tolerant genotypes.
2. MATERIAL AND METHODS
Field experiments. The field experiments were conducted in the Research Station of the
Agriculture College of Shiraz University, Iran (29° 50´ N and 52° 46´ E, 1810 m altitude) during
2003. The soil texture was clay loam (fine, mixed, mesic and calcixerollic xerochrepts). Eight
sesame genotypes (Table 1) were provided from Agricultural and Natural Resources Research
Center of Fars, Iran. These genotypes were evaluated in a randomized complete block design with
three replications in two separate experiments under drought stress and non-stress conditions. Nonstress experiment was irrigated by 100% of calculated crop water requirement (CWR) [16] while
drought stress experiment was irrigated by 60% of calculated CWR. Each plot consisted of six 4-m
long rows spaced 50 cm apart with a 10 cm plant distance in the rows. The four middle rows were
used for sampling.
Fertilizer was applied at the rate of 120 Kg/ha N and 50 Kg/ha P2O5. Crops received one half
of N in urea form and total amount of P 2O5 at planting, while the remaining N was applied at
tillering stage. Planting time was in 9th June in 2003.
Determination of yield related traits. Before harvesting, 10 plants were selected from two
middle rows and then their NCP and TSW were measured. The plants were harvested from an area
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Journal of Asian Scientific Research, 2015, 5(9):465-472
of 3 m2 in October when they almost turned yellow but the capsules were not split yet.
Table-1. Names and origin of 8 sesame lines
Entry
1
2
3
4
5
6
7
8
Lines
TN 240
TN 239
TN 238
Progeny of the landrace of Dezfoul
Sesame landrace of Dezfoul
Darab 14
Line 1 from progeny of the landrace of Darab
Line 2 from progeny of the landrace of Darab l
Origin
Seed and Plant Improvement Institute
Seed and Plant Improvement Institute
Seed and Plant Improvement Institute
Dezfoul
Dezfoul
Darab
Darab
Darab
Source: Agricultural and Natural Resources Research Center of Fars, Iran
Then BY and GY (kg/ha) were determined. The Harvest Index (HI) was calculated as the ratio
between GY and BY.
Determination of physiological traits. The canopy temperature (T C) of each plot was measured
at the flowering and grain filling stages at 15:30 hour in both experiments using an infrared
thermometer (Kane-May Model Infratrace 800). The instrument was pointed down at three random
points in each plot and held at an oblique angle to the canopy surface to minimize the influence of
soil exposure [15]. The leaf water potential (LWP) was measured at the flowering and grain filling
stages using a pressure chamber (PMS Model) technique [11]. The leaf osmotic potential (LOP)
was measured at the flowering and grain filling stages, after sap extraction using the Cryoscopy
method and a digital thermometer ETI-2001 Model. LOP [15] was determined as:
LOP = [(T/1.86) × 2.27]
Where, T= freezing point of sap
The rate of water loss (RWL) from excised leaves and initial water content (IWC) were
measured at the flowering and grain filling stages [17] by following equations:
RWL = {[(W0 −W2)
+ (W2 −W4) + (W4 −W6)]/[3 ×Wd×(T2 – T1)])
IWC = [(W0 −Wd)/Wd]
Where, T2-T1= time interval between two subsequent measurements (2 h), W 0= fresh weight,
(W2, W4 and W6) = weight after 2, 4 and 6 hours in a controlled chamber at 25°C, and W d= ovendry at 50°C for 24 hours.
Statistical analysis. The data were statistically analyzed by software SAS [18]. Differences
among yield related traits and physiological traits were analyzed using t-test and Duncan test at 5%
level. The correlation between drought indices and physiological traits were analyzed using SAS
[18].
3. RESULT AND DISCUSSION
The mean of GY and some related traits for both experiments are shown in Table 2. Analysis
of variance revealed that genotypes differed significantly for the most traits under drought stress
and non-stress conditions. There were significant differences between genotypes in NCP, TSW, HI,
BY and GY in both conditions while in NDM only in drought stress conditions. Drought stress
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Journal of Asian Scientific Research, 2015, 5(9):465-472
reduced significantly the NDM, NCP, TSW, BY and GY of genotypes while it did not reduced HI
significantly. NDM showed a significant reduction of 7.41 percent under drought stress. Drought
stress accelerated all growth stages, reduced the normal growth and development periods, dry
matter production and final yield. These results were consistent with the results of Pouresmaiel, et
al. [19]. There was significant decrease in the flowering period in all genotypes under stress
condition but physiological maturity period was the lowest as compared with flowering period.
NCP and TSW suffered a significant reduction of 53.71 and 23.21, respectively. The significant
decrease in TSW showed that irrigation at reproductive growth and seed development was very
important. Decrease in TSW observed under water stress was in accordance with the findings of
Razi and Assad [20] in sunflower and Pouresmaiel, et al. [19] in sesame. GY in non-stress
conditions varied from 1090 to 1757.6 kg/ha, and under drought condition they varied from 580 to
1120 kg/ha. BY and GY reduction occurred to the extent of 36.82 and 37.34 percent under drought
condition, significantly. GY suffered a maximum reduction of 52.05 percent. GY was greater in
non-stress conditions than stress conditions, a consequence of more NDM, NCP and TSW.
Genotypes did not differ significantly in respect to HI under drought stress compared with nonstress conditions and this could emphasize that the range of reduction in GY was similar to the rate
of biomass under drought stress.
Mean of water-related traits in sesame genotypes at the flowering and grain filling stages
under non-stress and stress conditions are shown in Table 3. Genotypes differ significantly in
respect to LWP at the flowering stage while did not differ at grain filling stage under non-stress
conditions (p<0.05). There were significant differences between LWP of genotypes in both stages
under drought conditions (p<0.05). LWP decreased in all genotypes under stress conditions at both
stages, significantly. This result is consistent with that of Golestani and Assad [15] who observed
decrease in the LWP under drought condition in wheat. Genotypes were significantly different with
regard to LOP in both stages under both conditions (p<0.05). The trend of LOP reduction at both
stages was similar to LWP under stress conditions. Other investigators [21-23] also reported that
drought resistant cultivars had lower ψs values as compared with susceptible wheat cultivars.
Sesame genotypes did not differ significantly in respect to RWL under non-stress conditions in
both stages while differ significantly under drought conditions in both stages. RWL increased
significantly (P<0.01) under drought stress condition as compared with non-stress conditions. The
changes in IWC of genotypes were significant in both stages under both conditions (p<0.05). The
results showed that IWC increased in the majority of genotypes except one genotype at flowering
stage and two genotypes at grain filling stage under drought stress conditions. The differences in
the TC of genotypes were not significant in both stages under both conditions (p<0.05). Pinter, et al.
[24] and Golestani and Assad [15] reported that (Ta - Tc) is a valuable technique in screening
drought resistant genotypes while in this study T C could not apply in discriminating between
genotypes.
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Journal of Asian Scientific Research, 2015, 5(9):465-472
Table-2. Mean of number of days to maturation (NDM), number of capsules per plant (NCP), 1000 seed weight (TSW) ,
harvest index (HI), biological yield (BY) and grain yield (GY) in sesame lines under non-stress and stress conditions.
Means within each row (column) followed by same capital (small) letters are not significantly different at DMRT (t test) (probability level
5%).
Table-3. Mean of physiological traits including canopy temperature (TC), leaf water potential (LWP), leaf osmotic potential
(LOP), initial water content (IWC) and rate of water loss (RWL) in sesame lines at the flowering (F) and grain filling (G)
stages under non-stress and stress conditions.
Means within each row (column) followed by same capital (small) letters are not significantly different at DMRT (t test) (probability level
5%).
Correlation between suitable drought resistance indices in these sesame lines including mean
productivity (MP), geometric mean productivity (GMP), harmonic mean (HM) and stress tolerance
index (STI) [25] with physiological traits (table 4) was used to determine the suitable physiological
traits in screening resistant sesame lines. Under non-stress condition LOP in both stages were the
best traits because of significant correlation between these traits with drought resistance indices.
Under drought condition LWP, LOP at both stages and RWL at grain filling stage were the most
suitable physiological traits.
Leaf water potential (LWP) at both stages under non-stress condition were not suitable traits in
spite of significant correlation between these traits with drought resistance indices because of nonsignificant differences between genotypes for these traits. Initial water content (IWC) at grain
filling under drought condition could not discriminate between lines as well as drought resistance
indices in spite of significant correlation between these traits with drought resistance indices.
Canopy temperature (TC) at both stages and both conditions could not discriminate between lines
because of non-significant difference between genotypes.
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Journal of Asian Scientific Research, 2015, 5(9):465-472
Table-4. Significant pearson correlation coefficient (r) between suitable drought indices including mean productivity (MP),
geometric mean productivity (GMP), harmonic mean (HM) and stress tolerance index (STI) with physiological traits
including leaf water potential (LWP), leaf osmotic potential (LOP), rate of water loss (RWL) and initial water content
(IWC) in sesame genotypes at the flowering (F) and grain filling (G) stages under non-stress and stress conditions.
Drought indices
Stages
Conditions
MP
F
Non-stress
Stress
Non-stress
Stress
Non-stress
Stress
Non-stress
Stress
Non-stress
Stress
Non-stress
Stress
Non-stress
Stress
Non-stress
Stress
G
GMP
F
G
HM
F
G
STI
F
G
Physiological traits
LWP
LOP
-0.450*
-0.757**
-0.780*
-0.807**
-0.433*
-0.893**
-0.797*
-0.928**
-0.471*
-0.767**
-0.785**
-0.801**
-0.445*
-0.893**
-0.791**
-0.925**
-0.488*
-0.773**
-0.786**
-0.790**
-0.453*
-0.887**
-0.782**
-0.916**
-0.460*
-0.767**
-0.792**
-0.830**
-0.444*
-0.887**
-0.803**
-0.937**
RWL
-0.880**
-0.879**
-0.873**
-0.890**
IWC
-0.889**
-0.886**
-0.877**
-0.896**
*, ** significant at 0.05 and 0.01, respectively
4. CONCLUSIONS
It is concluded from the results of this study that sesame genotypes respond differentially to
drought stress. Under drought stress condition, NDM, NCP, TSW, BY, GY, LWP and LOP
significantly (P < 0.01) decreased while RWL increased significantly (P < 0.05). Based on the
results, it is reasonable to assume that high yield of sesame plants under drought conditions could
be obtained by selecting breeding materials with the lowest reduction in NDM, NCP, TSW, BY,
GY, LWP and LOP and the highest reduction in RWL. Under non-stress condition LOP in both
stages was the best traits. Under drought condition LWP, LOP at both stages and RWL at grain
filling stage were the most suitable physiological traits.
REFERENCES
[1]
D. Bedigian, "Evolution of sesame revisited: Domestication, diversity and prospects," Genetic
Resources and Crop Evolution, vol. 50, pp. 779 – 787, 2003.
[2]
C. Borchani, S. Besbes, C. H. Blecker, and H. Attia, "Chemical characteristics and oxidative
stability of sesame seed, sesame paste, and olive oils," J. Agric. Sci. and Technol., vol. 12, pp. 585596, 2010.
[3]
A. Pal, "Nutritional, medicinal and industrial uses of sesame (Sesamum Indicum L.) seeds," An
Overview.Agriculture Conspectus Scientifics, vol. 75, pp. 159-168, 2010.
[4]
M. Golbashy, M. Ebrahimi, K. S. Khavari, and R. Choukan, "Evaluation of drought tolerance of
some corn (Zea Mays L.) hybrids in Iran," Afr. J. Agric. Res., vol. 5, pp. 2714-2719, 2010.
© 2015 AESS Publications. All Rights Reserved.
470
Journal of Asian Scientific Research, 2015, 5(9):465-472
[5]
J. R. Witcombe, P. A. Hollington, C. J. Howarth, S. Reader, and K. A. Steele, "Breeding for abiotic
stresses for sustainable agriculture," Phil. Trans. R. Soc. B, vol. 363, pp. 703-716, 2007.
[6]
S. Boureima, M. Eylettes, M. Diouf, T. A. Diop, and P. Van Damme, "Sensitivity of seed
germination and seedling radicle growth to drought stress in sesame sesamum indicum L," Res. J.
Environ. Sci., vol. 5, pp. 557-564, 2011.
[7]
S. M. Almeida, D. S. J. A. Gonçalves, J. Enciso, V. Sharma, and J. Jifon, "Yield components as
indicators of drought tolerance of sugarcane," Sci. Agric., vol. 65, pp. 620-627, 2008.
[8]
M. Zaharieva, E. Gaulin, M. Havaux, E. Acevedo, and P. Monnevaux, "Drought and heat responses
in the wild wheat relative aegilops geniculata roth," Crop Science, vol. 41, pp. 1321-1329, 2001.
[9]
G. C. Wright and N. C. Rachaputi, Drought and drought resistance. In: R. M. Goodman (Ed).
Encyclopedia of plant and crop science. New York: Marcel Dekker, Inc, 2004.
[10]
P. Singh and E. T. Kanemasu, "Leaf and canopy temperature of pearl millet genotypes under
irrigated and nonirrigated conditions," Agronomy Journal, vol. 75, pp. 497-501, 1983.
[11]
J. Ashkani, H. Pakniyat, Y. Emam, M. T. Assad, and M. J. Bahrani, "The evaluation and
relationships of some physiological traits in spring safflower (Carthamus Tinctorius L.) under stress
and non-stress water regimes," J. Agric. Sci. Technol., vol. 9, pp. 267-277, 2007.
[12]
Alza and M. Fernandez-Martinez, "Genetic analysis of yield and related traits in sunflower
(Helianthus Annuus L.) in dry land and irrigated environments," Euphytica, vol. 95, pp. 243-251,
1997.
[13]
R. B. David and J. M. Duniway, "Effects of mycorrhizal infection on drought tolerance and recovery
in safflower and wheat," Plant Soil, vol. 197, pp. 95-103, 1997.
[14]
A. J. Karamanos and A. Y. Papatheohari, "Assessment of drought resistance of crop genotypes by
means of water potential," Crop Science, vol. 39, pp. 1792-1797, 1999.
[15]
A. S. Golestani and M. T. Assad, "Evaluation of four screening technique for drought resistance and
their relationship to yield reduction ration in wheat," Euphytica, vol. 13, pp. 293-299, 1998.
[16]
A. Alizadeh, Soil, water and plant relationship, 4th ed. Iran: Emam Reza University Press, 2004.
[17]
J. M. Clarke and T. N. McCaig, "Excised-leaf water retention capability as an indicator of drought
resistance of triticum genotypes," Canadian Journal of Plant Science, vol. 62, pp. 571-578, 1982.
[18]
SAS, Statistical analysis software, version 8. USA: SAS Institute, 2000.
[19]
H. Pouresmaiel, M. H. Saberi, and H. Fanaei, "Evaluation of terminal drought stress tolerance of
sesamum indicum L. genotypes under the Sistan region conditions," International Journal of
Science and Engineering Investigations, vol. 2, pp. 58-61, 2013.
[20]
H. Razi and M. T. Assad, "Comparison of selection criteria in normal and limited irrigation in
sunflower," Euphytica, vol. 105, pp. 83-90, 1999.
[21]
R. Grumet, R. S. Albrechtensen, and A. D. Hanson, "Growth and yield of barley isopopulations
differing in solute potential," Crop Science, vol. 27, pp. 991-995, 1987.
[22]
A. Blum, "Osmotic adjustment and growth of barley genotypes under drought stress," Crop Science,
vol. 29, pp. 230-233, 1989.
[23]
J. T. Musick, O. R. Jones, B. A. Stewart, and D. A. Dusek, "Water-yield relationships for irrigated
and dryland wheat in the U.S Southern plains," Agronomy Journal, vol. 86, pp. 980-986, 1994.
© 2015 AESS Publications. All Rights Reserved.
471
Journal of Asian Scientific Research, 2015, 5(9):465-472
[24]
J. P. S. Pinter, G. Zipoli, R. J. Reginato, R. D. Jackson, S. B. Idso, and J. P. Hopman, "Canopy
temperature as an indicator of differential water use and yield performance among wheat cultivars,"
Agricultural Water management, vol. 18, pp. 35-48, 1990.
[25]
M. Golestani and H. Pakniyat, "Evaluation of drought tolerance indices in sesame lines," J. Sci.
Technol. Agric. Natur. Resour., vol. 11, pp. 141-150, 2007.
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