Printer Friendly

Effect of Drought and Salt Stresses on Germination and Early Seedling Growth of Different Color-seeds of Sesame (Sesamum indicum).

Byline: M. El Harfi, H. Hanine, H. Rizki, H. Latrache and A. Nabloussi


High salinity and drought are common environmental problems affecting seed germination and plant growth especially in arid and semi-arid regions. Sesame (Sesamum indicum L.) is an oilseed crop rated moderately salt and drought tolerant but it is sensitive at germination and seedling stages. The effect of salt stress (NaCl) and water stress (PEG-6000), using the same osmotic potential (0 to -1.4 MPa), on germination and early seedling growth of sesame genotypes with different color seeds was studied. Germination percentage (GP), germination rate (GR), mean germination time (MGT), root length (RL) and shoot length (SL) were investigated. Drought and salt stresses, seed color and interaction of each stress with seed color had a significant effect on all studied parameters (P < 0.01).

Yellow and brown seeds exhibited higher GP and GR and lower MGT than white and black seeds in absence and presence of both stresses. Germination was reduced and delayed by both stresses. However, it continued at all concentrations of NaCl, while it ceased at -1.0 MPa of PEG. Reduction in GP and GR was gradual for yellow and brown seeds and drastic for white and black ones, already from -0.2 MPa of PEG and NaCl. At equivalent osmotic potential, salt stress had a lower inhibitory effect on germination and seedling growth than drought stress. For Moroccan cultivars, having yellow and brown seeds, seedling growth was more affected by both stresses than seed germination, thus RL and SL could be taken as selection criteria for drought and salt tolerance at early growth stages. Sesame cultivars having intermediate seed colors (brown and yellow) could be recommended for moderate saline soils.

Keywords: Sesame; Seed color; Germination; Salinity stress; Drought; Seedling growth


Drought and salinity are two major abiotic stresses due to their wide occurrence and high magnitude of their impact (Bartels and Sunkar, 2005). Severe drought and high salinity could promote land desertification and salinization, processes which are rapidly increasing on a global scale. More than 10% of arable land has become desertified or salinized, and average yields of major crops have been reduced by more than 50% (Wu et al., 2011). Salinity and drought stresses are physiologically related because both induce osmotic stress and most of the metabolic responses of stressed plants are similar (Kumar et al., 2011). Water stress effects on plant growth and seed yield are genotype- dependent (Bannayan et al., 2008) and also depend on the timing, duration and magnitude of the water deficit (Pandey et al., 2001). Salt stress adversely affects the growth of plants during all development stages (Jamil et al., 2006).

Seed germination is the beginning of plants life cycle and it is usually the most critical stage in seedling establishment, determining successful crop production (Almansouri et al., 2001). Germination and seedling growth declined with many abiotic factors such as salt and drought stresses which are two of the most important abiotic stresses that limit number of seedling and seedling growth (Almansouri et al., 2001; Farooq et al., 2009, 2015). Salinity has also been identified as the major factor influencing seedbed establishment in arid and semi-arid regions (Almansouri et al., 2001). Increasing salinity can influence seed germination either by toxic effects of specific ions, such as Na, Cl and SO4, or by creating osmotic pressure which impedes seed water uptake (Kaya et al., 2006; Shaikh et al., 2007). Soil salinity and water deficit decrease the soil water potential that leads to late and inadequate germination associated with failure of stand establishment.

As a result, the crop productivity is adversely affected (Willenborg et al., 2005). Sesame (Sesamum indicum L.) is well known as one of the oldest oil crops used by humans for thousands of years for edible oil, paste, cake and confectionary purposes (Weiss, 2000). The chemical composition of sesame seed shows that it is an important source of oil (50-60%), protein (18-25%), carbohydrate and ash (Elleuch et al., 2007; El Khier et al., 2008). Seed oil is highly unsaturated edible oil, rich in essential fatty acids such as linoleic acid. Sesame seed oil contains almost equal levels of oleic (35 to 54%) and linoleic (39 to 59%), 10% of palmitic acid and 5% of stearic acid (Hall, 2003). It is also rich in various bioactive compounds including phytosterols, tocopherols and lignans such as sesamin, sesamolin and sesaminol, which are known to play an important role in providing stability against oxidation of oil and contribute to antioxidative activity (Al- Yemeni et al., 2000).

Compared to other crops, sesame has better drought tolerance; however, it remains particularly sensitive to drought occurring during germination and seedling stages (Orruno and Morgan, 2007; Boureima et al., 2011). In fact, germination and seedling growth are reduced under drought; however magnitude of decrease varied according to the drought level and the cultivar (Heikal et al., 1982; Mensah et al., 2006; Hassanzadeh et al., 2009; Boureima et al., 2011; Bahrami et al., 2012). Sesame is often grown under irrigation conditions in arid and semi-arid areas, which are characterized by high temperatures, high levels of solar radiation, high evaporative demand and unpredictable occurrence of drought (Witcombe et al., 2008; Hassanzadeh et al., 2009). All these combined factors cause an increasing soil salinity which is a serious constraint limiting the production of this crop. However, just few studies have been carried out on the effect of salt stress on sesame seed germination.

These showed that germination and early seedling growth parameters were negatively affected and the effect severity varied according to the salt stress level and the cultivar (Purohit el al., 2005; Ramirez et al., 2005; Bahrami and Razmjoo, 2012). No previous research achieved in regard to sesame germination under drought and salt stress conditions has considered the seed color effect. Furthermore, no comparative study on the effect of drought and salt stress on germination and early seedling growth parameters has been conducted. This study was, therefore, carried out to evaluate and compare the effect of salt stress (NaCl) with that of water stress (PEG) on sesame germination and early seedling growth, and various cultivars characterized by different seed colors.

Materials and Methods

The experiment was conducted in the laboratory of Bioprocess and BioInterfaces, Faculty of Science and Technology of Beni-Mellal, Morocco. The used plant material consisted of four sesame genotypes: Two Moroccan cultivars and two American accessions. Moroccan cultivars, characterized by yellow and brown seeds, were collected through a survey conducted in Tadla- Azilal region, the most important area of sesame cultivation in Morocco. American accessions, characterized by black and white seeds, were provided by Dr. Bradley Morris from ARS-USDA (Griffin, GA). Seeds of these materials were increased and samples of the new obtained seeds were experimented in this study.

Drought stress was induced by polyethylene glycol (PEG-6000) treatment. Seven levels, with different osmotic potentials of -0.2, -0.4, -0.6, -0.8, -1, -1.2 and -1.4 MPa, were prepared and used as described by Michel and Kaufmann (1973). Salt stress, with the same osmotic potentials (from -0.2 to -1.4 MPa), was adjusted using NaCl, according to Coons et al. (1990). Distilled water served as a control.

The experiment was conducted in a double factorial completely randomized design, with three replications. The first factor was the seed color (genotype), with four levels, and the second was the stress solution (NaCl or PEG), with eight levels.

For each treatment, 100 seeds of each genotype cultivar were allowed to germinate in a Petri dish on filter paper moistened with 10 mL of appropriate levels of NaCl and PEG-6000. The Petri dishes were covered to prevent moisture loss by evaporation. The experiment was conducted at 25degC in an incubator for seven days and 2 mL of each solution was added to Petri dish every 24 h. When the radicle reached up 2 mm length, the seed was considered germinated (ISTA, 1985). Germinated seeds were counted at regular intervals every day until the end of the experiment period (seven days). Germination percentage (GP), determined on the seventh day, and germination rate (GR) were calculated as follows (Farooq et al., 2005):

GP = (N7/100) x100

GR = S [(Gi - Gi-1)/i].

N7 = number of seed germinated on the 7th day

Gi = number of seed germinated on day i

Gi-1 = number of seed germinated on day i-1

Mean germination time (MGT), expressed in d, is the inverse of GR (MGT = 1/GR). Root length and shoot length, expressed in cm, were measured on the seventh day after end of experiment (Bray, 1963). Shoot length was measured from the cotyledons to the collar, and the root length was measured from the collar to the root tip.

Analysis of variance (ANOVA) to determine statistically significant differences among seed colors, salinity or drought levels and the interactions seed color by salinity and seed color by drought was performed. Duncan's new multiple range test was applied to compare treatment means. The used statistical program was SAS 9.1.3 for windows.


Effects of Water and Salt Stresses and Seed Color on Seed Germination

Both water stress and salt stress had a significant effect on germination percentage (GP), germination rate (GR) and mean germination time (MGT) of all sesame seed types (colors) (P < 0.01). However, inhibition of germination was more pronounced in case of water stress, using PEG (Fig. 1). There were significant differences between seed types for these parameters. In absence of any stress, GP was around 40% for black seed, 56% for white seed and 100% for yellow and brown seeds (Fig. 1), while GR was 19, 26, 99 and 98%, respectively (Fig. 2). The corresponding MGT was 0.054 d for black seed, 0.040 d for white seed and 0.010 d for yellow and brown seed (Fig. 3). There was a significant effect of seed color x drought and seed color x salinity interactions on those parameters (P < 0.01), indicating that the seed types reacted differently to the level of both stresses. Yellow and brown seeds continued to germinate until -1.4 MPa of NaCl and -1 MPa of PEG.

There was a gradual reduction in GP with increase in the level of water and salt stress i.e., decreasing the osmotic potential from -0.6 to -1.2 MPa of NaCl solutions and from -0.4 to -1 MPa of PEG solutions (Fig. 1). Under salt stress, drastic reduction of GP (Fig. 1) and GR (Fig. 2) and the drastic delay of MGT (Fig. 3) occurred at -1.4 MPa, whilst under water stress, they occurred at -1.0 MPa. Below this osmotic potential, no germination was recorded (Fig. 1). For white and black seeds, there was a drastic decrease of GP (Fig. 1) and GR (Fig. 2) and a consequent delay of MGT (Fig. 3) already from -0.2 MPa of PEG and NaCl solutions, indicating the sensitivity of such seeds to low level of water and salt stresses. White seed stopped to germinate at or below -1 MPa of PEG and at -1.4 MPa of NaCl, while black seed stopped to germinate at or below -0.8 MPa of PEG and at -1.4 MPa of NaCl (Fig. 1).

Thus, yellow or brown seeds of the Moroccan cultivars exhibited higher GP and GR and lower MGT than white and black seeds of American accessions, in absence of stress and under different levels of drought and salt stress. Besides, for all seed types, both stresses affected and delayed seed germination. However, at equivalent level of stress (same osmotic potential), NaCl had lower inhibitory effect than PEG.

Effects of Water and Salt Stresses and Seed Color on Early Seedling Growth

Drought and salt stress had a significant effect on root length (RL) and shoot length (SL) of all seed types (P<0.01). However, for both root length (Fig. 4) and shoot length (Fig. 5), inhibition of elongation was more pronounced in case of water stress using PEG, compared to salt stress using NaCl. Also, there were significant differences between seed types (colors) for root and shoot length. In absence of any stress, RL was 5.50 cm for black seed, 5.44 cm for brown seed, 5.05 cm for yellow seed and 4.60 cm for white seed (Fig. 4), while SL was 5.57, 4.10, 4.60 and 5.02 cm, respectively (Fig. 5). Under drought stress (PEG) and salt stress (NaCl), RL and SL decreased for all seed types by increasing level of these stresses i.e., decreasing the osmotic potential. However, the decrease was, in general, greater for PEG than NaCl (Fig. 4 and 5).

At the same osmotic potential, and for all seed types, PEG had higher inhibitory effect on RL and SL than NaCl. Similarly to seed germination parameters, there was significant interaction seed color x drought and seed color x salinity on early seedling growth parameters (P<0.01). For both RL and SL, seed types reacted differently to the level of both stresses. Under intermediate salt stress (-0.6 MPa of NaCl), RL was reduced by 58% for white seed, 40% for black seed, 22% for brown seed and 16% for yellow seed (Fig. 4), while SL was reduced by 54, 48, 32 and 59%, respectively (Fig. 5). In case of severe salt stress (-1.2 MPa of NaCl), RL was decreased, respectively, by 88, 86, 91 and 90% (Fig. 4), and SL was decreased, respectively, by 88, 87, 88 and 84% for these four seed types (Fig. 5). These results indicate that, for early seedling growth, yellow and brown seeds were globally the least affected by intermediate and severe salt stress.

Under intermediate water stress (-0.4 MPa of PEG), RL was reduced by 58% for black seed, 55% for brown seed, 48% for white seed and 45% for yellow seed (Fig. 4), while SL was reduced by 46, 71, 38 and 64%, respectively (Fig. 5). This indicates that, surprisingly, early seedling growth of black and white seeds would be less affected than that of yellow and brown seeds under intermediate drought. Under relatively severe water stress (- 0.8 MPa of PEG), there was no germination for black seeds (Fig. 1), while RL was decreased by 74, 88 and 96% for brown, yellow and white seeds, respectively (Fig. 4). SL was reduced by 81, 86 and 97%, respectively for these three seed types (Fig. 5). Thus, regarding early seedling growth, brown seed was the most tolerant to relatively severe drought, followed by yellow seed. White seed was the most sensitive.


All the seed germination parameters measured, GP, GR and MGT, were affected by both water and salt stresses. GP and GR were decreased, while MGT increased with increase in stress levels. However, yellow and brown seeds of the local Moroccan cultivars were less affected than white and black seeds of the American accessions, indicating that Moroccan genotypes were more tolerant to both stresses than American ones. Also, regarding seedling growth parameters, RL and SL have been affected by water and salt stress. They decreased with increased stress levels. Nevertheless, brown and yellow seeds were less affected than white and black seeds for these parameters. Thus, Moroccan genotypes were more tolerant to both stresses than American ones.

Previous studies on sesame had also evidenced the effect of genotype and drought level (Boureima et al., 2011; Bahrami et al., 2012; Keshavarzi, 2012) and the effect of genotype and salt stress level (Bahrami and Razmjoo, 2012; Tabatabaei and Naghibalghora, 2014) on seed germination and seedling growth parameters. Reduction in germination parameters may be attributed to lower infusibility of water through the seed coat and initial water uptake of the seed under stress condition (Khayatnezhad and Gholamin, 2011; Bahrami, et al., 2012). Natural color of sesame seeds varies from black, intermediate colors (e.g., brown, golden, yellow) to white (Zhang et al., 2013). Differences in the behavior of such seeds during germination can be observed. Because of color pigment in seed coat, seed color influences water uptake, gas diffusion, seed dormancy, seed quality, germination and seedling emergence in some crops (Atis et al., 2011).

Our findings are in agreement with those of Suma and Srimathi (2014) who had reported that sesame seeds with dark brown color recorded better germination percentage in comparison with black and creamed sesame seed due to their better stamina in physical, physiological and biochemical phenomenon. Also, Yao et al. (2010) concluded that brown seeds of Chenopodium album were salt tolerant and could germinate rapidly to a high percentage in a wide range of environments; while black seeds were salt sensitive, indicating that the seeds with different colors react differently to germination conditions. To germinate, yellow and brown seeds could tolerate till -1 MPa of PEG, and from -1.2 MPa, no germination was recorded. Similarly, for sunflower, none of the seeds could germinate at -1.2 MPa (Kaya et al., 2006).

However, in a recent study on safflower, it was shown that seeds ceased to germinate already from -0.25 MPa (Zraibi et al., 2011), indicating that sesame is more tolerant than safflower to drought stress during germination stage. To germinate, yellow and brown seeds could tolerate till -1.2 MPa of NaCl. However, a drastic decline in germination features was observed fro m -1.2 to -1.4 MPa. This could be explained by the fact that the osmotic potential -1.2 MPa is the critical salinity tolerance level or threshold. It seems that at osmotic potential -1.4 MPa and below, water potential inside the germinating seed became higher than that outside, i.e. in NaCl substrate and consequently there is no more water uptake through the seed coat, which causes germination failure. Additionally, it is assumed that extreme salinity might be toxic to the seed embryo and thus germination is severely inhibited.

This is in accordance with findings of Bahrami and Razmjoo (2012) who had reported, for some sesame cultivars, a sharp decline in germination, from 50-56% to 0-5%, when salinity level was increased, respectively from 14.65 to 18.45 dS m-1. Also, drastic reduction was also observed in rapeseed germination, from 80% at -0.9 MPa to 0% at -1.2 MPa (Pace and Benincasa, 2010).

For all seed types (colors), NaCl and PEG adversely affected the germination and early seedling growth of sesame. This is may be due to alteration of enzymes and hormones found in the seed (Botia et al., 1998) or to the metabolic disorders induced by stress and generation of Reactive Oxygen Species (Almas et al., 2013). It could also be a deficit of hydration of the seeds due to high osmotic potential causing inhibition of the mechanisms leading to the output of the radicle out of the coat and therefore a seed germination delay (Gill et al., 2001; 2003).

However, higher germination percentage under NaCl stress compared to that of PEG, at the same water potential, indicated that adverse effect of PEG on the germination was due to osmotic effect rather than specific ion accumulation (Zhang et al., 2010). These findings are in accordance with those of other studies on various species, such as barley (Zhang et al., 2010), safflower (Zraibi et al., 2011), sunflower (Kaya et al., 2006), soybean (Khajeh-Hosseini et al., 2003), durum wheat (Sayar et al., 2010), pea (Okcu et al., 2005) and cowpea (Murillo-Amador et al., 2002). This demonstrates that for the same water potential, water stress is more severe than salt stress. For NaCl treated seeds, not considering extreme salt concentrations, ion (Na+ and/or Cl-) uptake makes seeds and seedlings osmotic potential more negative than that of external substrate.

In other words, the accumulation of ion by the imbibing seed embryo leads to create a water potential gradient between the embryo and substrate, and thus maintain water uptake during seed germination (Dodd and Donovan, 1999; Zhang et al., 2010; Shitole and Dhumal, 2012). PEG molecules do not enter in the seed and once water potential of the seed and its surrounding environment are in equilibrium, the seed will not continue to imbibe (Michel, 1983; Mehra et al., 2003). Also, MGT in NaCl solution was lower than MGT in PEG solution for the same water potential. This could be explained, as mentioned above, by more rapid water uptake in NaCl solutions. Similar findings were reported by Zhang et al. (2010) in barley, Khajeh-Hosseini et al. (2003) in soybean and Zraibi et al. (2011) in safflower.

On the other hand, by comparing the effect of PEG and NaCl on germination percentage and root and shoot length, water and salt stresses, regardless of their level, had lesser inhibitory effect on seed germination than seedling growth, for yellow and brown seeds characterizing the local Moroccan cultivars. This result agrees with that of Zraibi et al. (2011) having evaluated different safflower varieties under drought and salt stress. Contrarily, these stresses had less inhibitory effect on seedling growth than seed germination, for white and black seeds characterizing the American accessions. A similar finding was reported for sunflower (Kaya et al., 2006). Thus, it could be suggested that, in sesame, early selection for drought and salt tolerance should be based on germination percentage for white and black seed types and on root and shoot length for yellow and brown seed types.

In fact, it was reported that root and shoot length were the most important parameters in salt stress sensitivity evaluation, providing a relevant index to the response of plants to this stress (Jamil and Rha, 2004; Jamil et al., 2006). This would indicate that, under high salinity environmental conditions, high root length and high shoot length at early seedling growth stage could be pertinent selection criteria for sesame salt tolerance breeding program.


Drought stress had more pronounced inhibitory effect on sesame seed germination and early seedling growth than salt stress. During germination and early seedling growth, Moroccan genotypes characterized by yellow and brown seeds were more tolerant to both stresses than American genotypes characterized by white and black seeds. This indicates that, contrarily to American cultivars, the Moroccan ones might be selected under drought and salt stresses conditions. Seedling growth was more affected by both stresses than seed germination for Moroccan cultivars, and thus root length and/or shoot length could be relevant selection criteria in sesame breeding program for drought and salt tolerance at early growth stages. Our findings may have agronomic and ecological implications, allowing intermediate seed colors (brown, yellow) sesame cultivars to grow in moderate saline soils.

However, these cultivars should be further investigated at later growth stages to confirm their tolerance, evaluating the effects of both stresses on other morphological, physiological and agronomic attributes.


The authors would like to thank Dr. Bradley Morris from ARS-USDA (Griffin, GA) for providing the American accessions used in this study.


Almansouri, M., M. Kinet and S. Lutts, 2001. Effect of salt and osmotic stresses on germination in durum wheat (Triticum durum Desf.). Plant Soil, 231: 243-254

Almas, D.E., S. Bagherikia and K.M. Mashaki, 2013. Effects of salt and water stresses on germination and seedling growth of Artemisia vulgaris L. Int. J. Agric. Crop Sci., 56: 762-765

Al-Yemeni, M.N., M.A. Hussain and A.Y. Basahy, 2000. Mineral composition of some sesame seeds (Sesamum indicum L.) grown in the Gizan area of Saudi Arabia. Phyton, 67: 121-125

Atis, I., M. Atak, E. Can and K. Mavi, 2011. Seed coat color effects on seed quality and salt tolerance of red clover (Trifolium pratense). Int. J. Agric. Biol., 13: 363-368

Bannayan, M., F. Nadjafi, M. Azizi, L. Tabrizi and M. Rastgoo, 2008. Yield and seed quality of Plantago ovata and Nigella sativa under different irrigation treatments. Ind. Crop Prod., 27: 11-16

Bahrami, H., J. Razmjoo and A. Ostadi Jafari, 2012. Effect of drought stress on germination and seedling growth of sesame cultivars (Sesamum indicum L.). Int. J. Agric. Sci., 2: 423-428

Bahrami, H. and J. Razmjoo, 2012. Effect of salinity stress on germination and early seedling growth of ten sesame cultivars (Sesamum indicum L.). Int. J. Agric. Sci., 2: 529-537

Bartels, D. and R. Sunkar, 2005. Drought and salt tolerance in plants. Crit. Rev. Plant Sci., 24: 23-58

Botia, P., M. Carvajal, A. Cerda and V. Martinez, 1998. Response of eight Cucumis melo cultivars to salinity during germination and early vegetative growth. Agronomy, 18: 503-513

Boureima, S., M. Eyletters, M. Diouf, T.A. Diop and P. Van Damme, 2011. Sensitivity of seed germination and seedling radicle growth to drought stress in sesame (Sesamum indicum L.). Res. J. Environ Sci., 5: 557-564

Bray, J.R., 1963. Root production and the estimation of net productivity. Can. J. Bot., 41: 65-72

Coons, M.J., R.O. Kuehl and N.R. Simons, 1990. Tolerance of ten lettuce cultivars to high temperature combined with NaCl during germination. J. Amer. Soc. Hortic. Sci., 115: 1004-1007

Dodd, G.L. and L.A. Donovan, 1999. Water potential and ionic effects on germination and seedling growth of two cold desert shrubs. Amer. J. Bot., 86: 1146-1153

El Khier, M.K.S., K.E.A. Ishag and A.E.A. Yagoub, 2008. Chemical composition and oil characteristics of sesame seed cultivars grown in Sudan. Res. J. Agric. Biol. Sci., 4: 761-766

Elleuch, M., S. Besbes, O. Roiseux, C. Blecker and H. Attia, 2007. Quality characteristics of sesame seeds and by-products. Food Chem., 103: 641-650

Farooq, M., A. Wahid, N. Kobayashi, D. Fujita and S.M.A. Basra, 2009. Plant drought stress: effects, mechanisms and management. Agron. Sustain. Dev., 29: 185-212.

Farooq, M., M. Hussain, A. Wakeel and K.H.M. Siddique, 2015. Salt stress in maize: effects, resistance mechanisms and management. A review. Agron. Sustain. Dev., 35:461-481

Farooq, M., S.M.A. Basra, K. Hafeez and N. Ahmad, 2005. Thermal hardening: a new seed vigor enhancement tool in rice. J. Integr. Plant Biol., 47: 187-193

Gill, P.K., A.D. Sharma, P. Singh and S.S. Bhullar, 2001. Effect of various abiotic stresses on the growth, soluble sugars and water relations of sorghum seedlings grown in light and darkness. Bulg. J. Plant Physiol., 27: 72-84

Gill, P.K., A.D. Sharma, P. Singh and S.S. Bhullar, 2003. Changes in germination, growth and soluble sugar contents of Sorghum bicolor (L.) Moench seeds under various abiotic stresses. Plant Growth Regul., 40: 157-162

Hall, III, C., 2003. Sesame seed oil. In: Lipids for Functional Foods and Nutraceuticals, 1 edition, pp: 83-90. F.D. Gunstone (ed.). The Oily Press, Bridgewater, United Kingdom

Hassanzadeh, M., A. Asghari, S. Jamaati-e-Somarin, M. Saeidi, R. Zabihi-e- Mahmoodabad and S. Hokmalipour, 2009. Effects of water deficit on drought tolerance indices of sesame (Sesamum indicum L.) genotypes in moghan region. Res. J. Environ. Sci., 3: 116121

Heikal, M.M., M.A. Shaddad and A.M. Ahmed, 1982. Effect of water stress and gibberellic acid on germination of flax, sesame and onion seeds. Biol. Plant., 24: 124-129

ISTA, 1985. International rules for seed testing, rules 1985. Seed Sci. Technol., 13: 299-355

Jamil, M. and E.S. Rha, 2004. The effect of salinity (NaCl) on the germination and seedling of sugar beet (Beta vulgaris L.) and cabbage (Brassica oleracea L.). Kor. J. Plant Res., 7: 226-232

Jamil, M., D.B. Lee, K.Y. Jung, M. Ashraf, S.C. Lee and E.S. Rha, 2006. Effect of salt (NaCl) stress on germination and early seedling growth of four vegetables species. J. Cent. Eur. Agric., 7: 273-282

Kaya, M.D., G. Okcu, M. Atak, Y. Cikiliand O. Kolsarici, 2006. Seed treatments to overcome salt and drought stress during germination in sunflower (Helianthus annuus L.). Eur. J. Agron., 24: 291-295

Keshavarzi, M.H.B., 2012. The effect of drought stress on germination and early growth of Sesamum indicum seedlings under laboratory conditions. Int. J. Agric. Manage. Dev., 2:271-275

Khajeh-Hosseini, M., A.A. Powell and I.J. Bingham, 2003. The interaction between salinity stress and seed vigor during germination of soybean seeds. Seed Sci. Technol., 31: 15-725

Khayatnezhad, M. and R. Gholamin, 2011. Effects of water and salt stresses on germination and seedling growth in two durum wheat (Triticum durum Desf.) genotypes. Sci. Res. Essays, 6: 4597-4603

Kumar, S.G., A.M. Reddy and C. Sudhakar, 2003. NaCl effects on proline metabolism in two high yielding genotypes of mulberry (Morus alba L.) with contrasting salt tolerance. Plant Sci., 165: 1245-1251

Mehra, V., J. Tripathi and A.A. Powell, 2003. Aerated hydration treatment improves the response of Brassica juncea and Brassica campestris seeds to stress during germination. Seed Sci. Technol., 31: 57-70

Mensah, J.K., B.O. Obadoni, P.G. Eroutor and F. Onome-Irieguna, 2006. Simulated flooding and drought effects on germination, growth, and yield parameters of sesame (Sesamum indicum L.). Afr. J. Biotechnol., 5: 1249-1253

Michel, B.E. and M.R. Kaufmann, 1973. The osmotic potential of polyethylene glycol 6000. Plant Physiol., 51: 914-916

Michel, B.E., 1983. Evaluation of the water potentials of solutions of polyethylene glycol 8000 both in the absence and presence of other solutes. Plant Physiol., 72: 66-70

Murillo-Amador, B., R. Lopez-Aguilar, C. Kaya, J. Larrinaga-Mayoraland A. Flores Hernandez, 2002. Comparative effects of NaCl and polyethylene glycol on germination, emergence and seedling growth of cowpea. J. Agron. Crop Sci., 188: 235-247

Okcu, G., M.D. Kaya and M. Atak, 2005. Effects of salt and drought stresses on germination and seedling growth of pea (Pisum sativum L.). Turk. J. Agric. For., 29: 237-242

Orruno, E. and M.R.A. Morgan, 2007. Purification and characterization of the 7S globulin storage protein from sesame (Sesamum indicun L.). Food Chem., 100: 926-934

Pace, R. and P. Benincasa, 2010. Effect of salinity and low osmotic potential on the germination and seedling growth of rapeseed cultivars with different stress tolerance. Ital. J. Agron./Riv. Agron., 5: 69-77

Pandey, R.K., J.W. Maranville and A. Admou, 2001. Tropical wheat response to irrigation and nitrogen in a Sahelian environment. I. Grain yield, yield components and water use efficiency. Eur. J. Agron., 15: 93-105

Purohit, A., H.S. Gehlot, P. Khurana and P. Agarwal, 2005. An evaluation of early seedling growth characteristics of sesame cultivars under salt stress. Plant Arch., 5: 249-256

Ramirez, R., D. Gutierrez, R. Villafana and J.I. Lizaso, 2005. Salt tolerance of sesame genotypes at germination, vegetative and maturity stages. Commun. Soil Sci. Plant Anal., 36: 2405-2419

Sayar, R., H. Bchini, M. Mosbahi and M. Ezzine, 2010. Effects of salt and drought stresses on germination, emergence and seedling growth of durum wheat (Triticum durum Desf.). J. Agric. Res., 5: 2008-2016

Shaikh, F., B. Gul, W.Q. Li, X.J. Liu and M.A. Khan, 2007. Effect of calcium and light on the germination of Urochondra setulosa under different salts. J. Zhejiang Univ. Sci. B, 8: 20-26

Shitole, S.M. and K.N. Dhumal, 2012. Effect of water Stress by polyethylene glycol 6000 and sodium chloride on seed germination and seedling growth of Cassia angustifolia. Int. J. Pharm. Sci. Res., 3: 528-531

Suma, N. and P. Srimathi, 2014. Influence of Color Grading on seed and seedling quality characters of Sesamum indicum. J. Agric. Vet. Sci., 7: 25-27

Tabatabaei, S.A. and S.M. Naghibalghora, 2014. The effect of salinity stress on germination characteristics and biochemical changes of sesame seeds. Agric. Res. Moldova, 2: 61-68

Weiss, E.A., 2000. Sesame. In: Oilseed Crops, 2nd edition, pp: 131-164. Blackwell Science Ltd., London, UK

Willenborg, C.J., J.C. Wildeman, A.K. Miller, B.G. Rossnagel and S.J. Shirtliffe, 2005. Oat germination characteristics differ among genotypes, seed sizes and osmotic potential. Crop Sci., 45: 2023-2029

Witcombe, J.R., P.A. Hollington, C.J. Howarth, S. Reader and K.A Steele, 2008. Breeding for abiotic stresses for sustainable agriculture. Phil. Trans. R. Soc. B, 363: 703-716

Wu, C., Q. Wang, B. Xie, Z. Wang, J. Cui and T. Hu, 2011. Effects of drought and salt stress on seed germination of three leguminous species. Afr. J. Biotechnol., 10: 17954-17961

Yao, S., H. Lan and F. Zhang, 2010. Variation of seed heteromorphism in: Chenopodium album and the effect of salinity stress on the descendants. Ann. Bot., 105: 1015-1025

Zhang, H., L.J. Irving, C. McGill, C. Matthew, D. Zhou and P. Kemp, 2010. The effects of salinity and osmotic stress on barley germination rate: Sodium as an osmotic regulator. Ann. Bot., 106: 1027-1035

Zhang, H., M. Hongmei, L. Wei, C. Li, R. Zhao and C. Wang, 2013. Genetic analysis and QTL mapping of seed coat color in sesame (Sesamum indicum L.). PLoS One, 8: e63898

Zraibi, L., A. Nabloussi, M. Kajeiou, A. El Amrani, A. Khalid and H. Serghini Caid, 2011. Comparative germination and seedling growth response to drought and salt stresses in a set of safflower (Carthamus tinctorius) varieties. Seed Technol., 33: 39-52
COPYRIGHT 2016 Asianet-Pakistan
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2016 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Author:El Harfi, M.; Hanine, H.; Rizki, H.; Latrache, H.; Nabloussi, A.
Publication:International Journal of Agriculture and Biology
Article Type:Report
Date:Dec 31, 2016
Previous Article:Production, Optimization and Partial Characterization of Thermostable and Alkaline Amylase from Bacillus licheniformis KSU-6.
Next Article:Evaluation of Nutritive Value and Identification of Fungi in Silage from New Kenaf (Hibiscus cannabinus) Cultivars.

Terms of use | Privacy policy | Copyright © 2019 Farlex, Inc. | Feedback | For webmasters