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Article

Seed Priming Enhances Seed Germination and Morphological Traits of Lactuca sativa L. under Salt Stress

by
Bikash Adhikari
,
Omolayo J. Olorunwa
and
T. Casey Barickman
*
Department of Plant and Soil Sciences, Mississippi State University, North Mississippi Research and Extension Center, Verona, MS 38879, USA
*
Author to whom correspondence should be addressed.
Seeds 2022, 1(2), 74-86; https://doi.org/10.3390/seeds1020007
Submission received: 2 March 2022 / Revised: 24 March 2022 / Accepted: 29 March 2022 / Published: 1 April 2022
(This article belongs to the Special Issue Seed Priming Approaches That Achieve Environmental Stress Tolerance)

Abstract

:
Seed germination is the stage in which plants are most sensitive to abiotic stress, including salt stress (SS). SS affects plant growth and performance through ion toxicity, decreasing seed germination percentage and increasing the germination time. Several priming treatments were used to enhance germination under SS. The objectives of this study were (1) to identify priming treatments to shorten the emergence period, (2) to evaluate priming treatments against the SS, and (3) to induce synchronized seed germination. Salt-sensitive ‘Burpee Bibb’ lettuce seeds were treated with 0.05% potassium nitrate, 3 mM gibberellic acid, and distilled water. All the primed and non-primed seeds were subjected to 100 mM sodium chloride (NaCl) or 0 mM NaCl (control). The seven-day experiment, arranged in a complete randomized block design with four replications, was conducted in a growth chamber maintained with 16/8 h photoperiod (light/dark), 60% relative humidity, and a day/night temperature of 22/18 °C. The result indicated that hydro-primed (HP) seeds were better synchronized under SS. Similarly, fresh mass (FM) and dry mass (DM) of cotyledon, hypocotyl, and radicle were the highest in HP lettuce regardless of SS. Electrolyte leakage was the lowest in the HP lettuce, while other priming methods under SS increased membrane permeability, leading to osmotic stress and tissue damage. Overall, hydro-priming can be a good priming method for synchronizing germination and increasing FM and DM by creating the least osmotic stress and ion toxicity in lettuce under SS.

1. Introduction

Salt stress (SS) is destructive abiotic stress that affects crop production in arid and semiarid areas [1]. For this reason, it poses a severe threat to food security. At least 20% of crop cultivation land has been damaged by salt accumulation worldwide [2]. It is estimated that around 4000 hectares of land are affected daily and 50% of the arable land is affected by the salt in the soil [3,4]. It is speculated that more than 50% of the cultivable land will turn into non-arable land by the mid-21st century [5]. SS, especially under sodium chloride (NaCl), affects plant growth and performance through ion toxicity and osmotic stress in leaves and roots. Several reports on the relation between SS and seed germination state that SS also suppresses seed germination percentage and increases the germination time [6,7,8]. Most crops are reported to be sensitive to SS even as low as 3 dSm−1 electrical conductivity [9]. The suppression is due to the adverse physiological and biochemical changes in germinating seeds exposed to SS [1]. Specifically, Na+ and Cl impair the seed growth and development through osmotic and ion-specific toxic effects [5,10,11]. Na+, on the one hand, can replace the K+ cation and promote ion toxicity, while Cl controls the vegetative growth [12].
Seeds are supposed to turn into healthy and vigorous plants with proper metabolisms and physiological performances. To achieve that outcome, seeds maintain low moisture content during their physiological maturity [13]. Lettuce seeds with moisture levels less than 5% can be stored for a long period [14]. However, the extended seed storage period can deteriorate the germination and viability of the seed [15]. Seeds stored for an extended period when subjected to SS can result in even poorer germination and seedling growth. Seed germination and seedling growth are critical stages for crop establishment and are considered the stages in which plants are the most sensitive to abiotic stresses [16,17]. The ‘two-phase growth response to SS’ concept by Lauchi and Grattan [18] stated that the germination rate is directly correlated with the level of salt treatments applied.
Several seed priming treatments, including hydro- (HP), potassium nitrate- (KNO3), and gibberellic acid-priming (GA3), were used to enhance germination and performance under SS [19,20]. The purpose of these priming treatments was to shorten the emergence period and protect the seeds from biotic and abiotic factors during the crucial phase of seedling establishment, synchronizing emergence and leading to a uniform stand and improved yields. Priming is a rehydrating approach that uses different biochemical agents to allow regulated seed rehydration, stimulating metabolic processes that are ordinarily active during the early stages of germination, while preventing the seed from progressing to complete germination [21]. Plant species/genotype and physiology, environmental conditions exposed to the seed lot and vigor, and the priming method used all play roles in the success of seed priming [22]. Priming treatments have some beneficial effects, such as germination enhancement, emergence synchronization, early seedling growth, and minimizing the deleterious effect of abiotic and biotic stress. This has been demonstrated in many crops, such as wheat (Triticum aestivum) [23], chickpea (Cicer arietinum) [24], sunflower (Helianthus pp.) [25], and cotton (Gossypium spp.). [26]. Additionally, several other reports on maize (Zea mays), broccoli (Brassica oleracea var. italica), cauliflower (Brassica oleracea var. botrytis), and other leafy vegetables stated that priming reduced the mean germination time (MGT) and increased the mean germination rate (MGR) and synchronization index (Z) [27,28]. MGT is a measure of the time spread of the germination while MGR is the reciprocal of MGT [29,30]. Similarly, Z is a degree of homogeneity of germination over time [31], which indicates the highest synchronized germination when the Z value is the lowest [32]. These parameters are the measures of germination, seed vigor, and response to abiotic and biotic stress, which help to improve understanding of the roles of different priming methods used under different environmental conditions and on different crops [33,34].
Several studies have been conducted to investigate the influence of different priming methods on different C3 plants. However, there has been very little information on the interactive effect of various priming methods and salt levels on the germination synchronization, germination parameters, or morphological and biochemical traits in lettuce. Hence, the objectives of this study are (1) to distinguish the priming treatments that can effectively shorten the emergence period, (2) to evaluate the responses of priming treatments under SS, and (3) to induce synchronized seed germination in lettuce. Overall, the goal of this study is to examine priming approaches to overcoming the negative effects of SS on lettuce germination.

2. Materials and Methods

2.1. Planting Materials and Priming Treatment

The salt-susceptible Lactuca sativa (cv. ‘Burpee Bibb’) (BB) seeds were purchased from Burpee (Warminster, PA, USA). The susceptibility of BB was determined from a study by Adhikari et al. [35]. Before sowing, 200 lettuce seeds were treated with three different priming treatments: (1) 0.5% KNO3, (2) 3 mM GA3, and (3) hydro-priming. These priming agents were prepared using distilled water. A set of non-primed (NP) seeds were also included for comparison with primed seeds. Seeds were immersed in different priming treatments for different numbers of hours (KNO3 = 2 h 30 min; GA3 = 12 h 45 min; and hydro-priming = 2 h 30 min), as described by Mahmoudi et al. [36], with few modifications. Soon after the priming, seeds were rinsed four times with distilled water and were left to dry at room temperature until they regained their original moisture content, which took approximately 2 days (maximum).

2.2. Salt Treatment and Germination

All the primed and non-primed seeds were subjected to either 0 mM NaCl (control) or 100 mM NaCl concentration. The NaCl solution was prepared using distilled water. Before sowing, seeds were soaked in 200 mL of either control or 100 mM NaCl for around 2 h and left to dry for 2 more hours to regain their original moisture content at room temperature. The germination was carried out by placing 25 seeds per treatment per replication in a 10 cm Petri dish with a double-layer filter paper in the growth chamber. The 0 mM NaCl treatment was considered as a control. The growth chamber was maintained with 16/8 h photoperiod (light/dark), 330 µmol/m2/s of photosynthetic photon flux density (PPFD), 50–60% relative humidity, and a day/night temperature of 22/18 °C. Treatments were arranged in a complete randomized block design with four replications each.

2.3. Germination Parameters and Morphological Traits

2.3.1. Germination Parameters

Seed germination was recorded every 24 h for 5 days. Seeds were considered germinated when the radicle protruded through the seed coat and had a length of at least 2 mm. The mean germination time (MGT), mean germination rate (MGR), germination index (GI), and synchronization index (Z) were measured using the following equations:
MGT =   i = 1 k n i   × t i i = 1 k n i [37]
where
niti = seeds germinated at ith interval with the corresponding time interval
ni = number of seeds germinated in the ith time
ti = time taken for seeds to germinate at ith count
MGR = 1 M G T [29]
GI = i = 1 k n i t i   [38]
Z = i = 1 k C n i , 2 C   n i , 2   [31]
where
Cni,2 = ni (ni − 1)/2

2.3.2. Seeds’ Morphological Traits

Five days after sowing, seeds were divided into cotyledon, hypocotyl, and radicle for the determination of growth parameters. Fresh mass (FM), dry mass (DM), and length of all parts of the seeds were recorded.

2.4. Electrolyte Leakage

Electrolyte leakage (EL) was determined using the method described by Quartacci et al. [39]. The cotyledon and the hypocotyl parts of the lettuce plant were cut into 3–4 mm pieces and placed in a 50 mL tube containing 23–30 mL of double-distilled water. The initial electrical conductivity (EC1) was recorded after two hours using the digital EC meter (FisherbrandTM accumet AP85 portable waterproof pH/Conductivity meter, Thermo Fisher Scientific, Waltham, MA, USA). The samples were then immersed in liquid nitrogen for 2–3 min and placed back in the same 50 mL tube for an additional 2 h, with continuous shaking. The final electrical conductivity (EC2) was then recorded. EL was calculated using the following equation:
E L   ( % ) = E C 1 E C 2

2.5. Data Analysis

Statistical analysis of the data was performed using SAS (version 9.4; SAS Institute, Cary, NC, USA). Data were analyzed using PROC GLM analysis of variance (ANOVA), followed by mean separation. The standard errors were based on the pooled error term from the ANOVA table. Tukey’s test (p ≤ 0.05) was used to differentiate between genotype classifications and treatment.

3. Results

The effects of different priming methods on lettuce seeds subjected to salt stress (SS) were studied through various germination indicators, such as mean germination time (MGT), mean germination rate (MGR), germination index (GI), and synchronization index (Z). These parameters help to achieve a better understanding of seed germination and growth in primed lettuce seeds subjected to SS. Additionally, the electrolyte leakage in germinated seed parts and the morphological traits of cotyledon, hypocotyl, and radicle, including fresh mass (FM), dry mass (DM), and length, were recorded.

3.1. Germination Parameters

None of the priming methods affected MGT, MGR, and GI values in lettuce subjected to SS (Table 1). There was no interaction effect observed between different priming and salt treatments, except for Z (p < 0.05). The Z value was recorded as the lowest in HP lettuce under both salt treatment levels. The Z values of other priming methods (GA3 and KNO3) were recorded highest; however, they were not significantly different when compared with the NP control.

3.2. Morphological Traits

3.2.1. Fresh Mass

The FM data (Figure 1) indicated a significant (priming × salt treatment) interaction effect on FM of all morphological parameters (hypocotyl, cotyledon, and radicle). Figure 1A demonstrates that hydro-priming resulted in higher cotyledon FM compared to other priming methods (GA3 and KNO3). Although there was no significant difference in the hypocotyl FM compared to its control, the hypocotyl FM was recorded highest (Figure 1B) compared to other priming methods, irrespective of the salt treatments. There was no significant effect of GA3- and KNO3-priming on hypocotyl FM when treated with salt, compared to the control. Additionally, the cotyledon and radicle FMs of GA3- and KNO3- primed lettuce were not significantly different from non-primed (NP) lettuce under both salt treatment levels. Similarly, there was no significant difference in radicle FM of HP salt-treated lettuce compared to the control (Figure 1C). However, the highest radicle FM was observed for HP lettuce.

3.2.2. Dry Mass

The dry mass (DM) of lettuce responded differently to different priming methods when subjected to two salt treatments, as presented in Figure 2. Priming under different salt treatment levels had a significant interaction effect on cotyledon, hypocotyl, and radicle DMs. Cotyledon DM in HP lettuce was significantly higher compared to other priming methods (GA3 and KNO3). Interestingly, there was no significant difference in the cotyledon DM of HP lettuce subjected to SS compared to the control (Figure 2A). It is also worth noting that DM due to hydro-priming increased by almost 100% compared to GA3-, KNO3- and NP in both salt treatment levels.
The DM of hypocotyl was found to be significantly different (p < 0.05) in different priming methods studied under different salt treatment levels (Figure 2B). Although no salt treatment effect was observed within the priming methods, a significant interaction effect showed that hypocotyl DM was measured the highest in HP lettuce and the lowest in GA3-primed lettuce. As in cotyledon DM, priming and salt treatment were significantly affected in the radicle DM. DM of the radicle was recorded highest in the HP lettuce, followed by the NP lettuce (Figure 2C).

3.2.3. Hypocotyl and Radicle Lengths

The priming methods and salt treatment interacted to significantly affect the hypocotyl and radicle lengths (Figure 3). There was a significant decrease (p < 0.05) in hypocotyl length by 42%, 49%, and 44% in GA3-primed, KNO3-primed, and NP lettuce, respectively, when subjected to SS, as compared to the control (Figure 3A). However, the HP lettuce remained unaffected by the salt treatment compared to the control. The hypocotyl length was recorded highest in the HP lettuce. As in hypocotyl length, a significant decrease in radicle length by 58%, 59%, and 72% was observed in GA3-primed, KNO3-primed, and NP lettuce, respectively, under SS as compared to the control (Figure 3B). However, there was no significant decrease (14%) in radicle length recorded in HP and salt-treated lettuce compared to the control. Overall, the length parameters revealed the non-significant suppression in the hypocotyl and radicle length of HP lettuce subjected to 100 mM NaCl.

3.3. Electrolyte Leakage

The membrane injury (EL) was noticeably increased in lettuce primed with GA3, KNO3, and NP subjected to 100 mM NaCl compared to the control, except for HP lettuce (Figure 4). The increase in EL by 38%, 25%, and 60% was recorded in GA3, KNO3, and NP lettuce, respectively, under SS compared to the control. However, there was no significant membrane damage caused in HP lettuce. Salt-treated HP lettuce reflected the lowest EL compared to other salt-treated primed lettuce.

4. Discussion

Seed germination and seedling growth are two important stages for crop establishment [17]. These stages are critically sensitive to any abiotic stress, including SS, resulting in poor or delayed germination [7,16]. Lettuce is a moderately salt-tolerant crop (electrical conductivity threshold of 1.3–2.0 dS/m), and can be affected by the osmotic effect of salt in the first phase of salt absorption (osmotic stress phase), followed by the second phase of inhibition of potassium (K+) ions, the third phase (salt-specific effect phase) of inability to prevent salt ions from accumulating to toxic levels, and the final phase of oxidative stress and cell death [40,41,42]. During the first phase, the water potential is affected, leading to decreased water uptake by plants, while the second and third phases disturb the ion homeostasis of the cell, leading to membrane disorganization and inhibition of photosynthesis in plants [42]. This four-phase effect of SS was reported in several crops, such as tomato (Solanum lycopersicum) [43], wheat (Triticum aestivum) [44], sugar beet (Beta vulgaris) [45], beans (Phaseolus vulgaris) [46], and several other C3 crops [42]. Under normal conditions, the cytosol in plants contains 100 mM of K+ and less than 10 mM Na+ [47]. However, under SS, the cytosolic Na+ and Cl can increase up to 100 mM, becoming cytotoxic [47]. A cytotoxic situation leads to protein denaturation, membrane damage, and destabilization, ultimately causing electrolyte leakage and cell death [47]. The current study demonstrated that 100 mM NaCl treatment increases the mean germination time (MGT) and reduces the mean germination rate (MGR). Supporting these results, several reports on SS stated that concentration beyond the crop threshold could decrease the germination rate and increase germination time [6,7,16]. This situation could be caused by the plant’s quick response to the high osmotic pressure created by SS, leading to the inhibition of cellular and biosynthetic processes [47]. While the SS caused seed growth inhibition in crops and leafy vegetables with moderate to low salt tolerance, seed priming, in contrast, was reported to improve the overall physiological and morphological performance of those crops [21]. For example, calcium chloride, used on wheat (Triticum aestivum) and sorghum (Sorghum bicolor); potassium chloride, used on wheat; deionized or distilled water, used on maize (Zea mays), barley (Hordeum vulgare), and Chinese cabbage (Brassica rapa subsp. Pekinensis); Gibberellic acid, used on pea (Pisum sativum), maize (Zea mays), rice (Oryza sativa), and alfalfa (Medicago sativa); glycine betaine, used on safflower (Carthamus tinctorius); potassium nitrate, used on sunflower (Helianthus spp.); and potassium chloride, used on broccoli (Brassica oleracea var. italica), were reported effective in SS amelioration through improved seed germination rate and improved yield [23,48,49,50,51,52,53,54,55,56]. Priming methods are crop-specific, and a recent study was conducted to demonstrate the difference in the efficacy levels of different priming methods based on several reports in C3 and C4 plants.
Previously, it has been reported that synchronized seed growth is also enhanced by the crop-specific seed priming method [11]. In our study, HP seeds had more synchronized seed growth, with the lowest synchronization index (Z), which aligned with the earlier report by Khajeh-Hosseini et al. [11,32]. The current study also demonstrated that hydro-priming inhibited the negative effects of SS on seed germination, while there was a minimal response to KNO3 and GA3 of lettuce seeds under SS. Previous research by Mahmoudi et al. [36] found that HP lettuce seedlings could alleviate the NaCl effects on lettuce seedlings better than KNO3 and GA3. The NaCl-inhibiting ability of hydro-priming could be due to the ambient or high-water potential (Ψ = 0 MPa) environment created by hydro-priming during the early germination period [47]. Moreover, the decline in synchronization in KNO3- and GA3-primed lettuce could be due to a reduction in water potential and cell dehydration caused by SS, leading to a decrease in metabolic activities and protein destabilization during the germination period [47]. Thus, it is worth noting that HP lettuce maintained seed germination and growth in a synchronized pattern even under SS better than the rest of the priming treatments under SS, which agrees with the results reported by Mahmoudi et al. [36].
The salt treatment severely impacted the overall morphological parameters. The use of different priming methods reflected the significantly different growth responses compared to the SS created by 100 mM NaCl. Under SS, FM and DM in KNO3- and GA3-treated lettuce were found to be indifferent to those in non-primed (NP) lettuce, and were also reduced significantly, as reported earlier in melon (Cucumis melo) [57] and chickpea (Cicer arietinum) [58]. The germination and seedling improvement with KNO3 and GA3 have previously been documented in ‘Vista’ lettuce [59] and cabbage (Brassica oleracea var. capitata) [60]. However, the effectiveness of KNO3 and GA3 on salt-stressed BB lettuce was limited in the current study. The previous report documented that poor performance of priming agents can be due to amorphous tissue in the seed coat, which controls the permeability of seeds, disrupting the endogenous osmotic equilibrium [21,61]. The disparity can result in nutritional imbalance and poor seedling growth [62]. Although KNO3 was reported to be effective in improving the seedling growth and establishment in sunflower (Helianthus spp.) and GA3 was reported to be effective in onion (Allium cepa) and sesame (Sesamum indicum), the poor performances of KNO3 and GA3 suggested that the effects of priming under SS can be crop-specific [63]. On the contrary, the FM and DM of lettuce primed with distilled water (HP) increased significantly, irrespective of the salt treatments. The positive response of hydro-priming even under SS can be due to the stimulatory effect of priming on the mediation of cell division in germinating seeds in the early germination stage [64]. The better performance of HP lettuce in terms of water absorption can also be due to the early commencement of metabolic activity in the seeds before the start of radicle emergence [65]. Additionally, improved water-use efficiency has been documented with hydro-priming [66]. The improved water-use efficiency could be due to the efficient breakdown of stored food reserves in the seed during the second phase (lag phase of seed germination), which initiates the onset of cell wall loosening and expansion for the third phase (post-germination phase) [47]. Hydro-priming was reported to improve seed germination, seedling emergence, and productivity in many field crops [8,24,26,63]. The current study also aligned with a study conducted in romaine lettuce by Mahmoudi et al. [36], which demonstrated that HP seeds exhibited higher adaptive potential under SS compared to KNO3- and GA3-primed lettuce seeds. Thus, the use of hydro-priming for lettuce under SS could be an effective priming method to improve the FMs and DMs of different morphological traits in germinated seeds.
Abiotic stress is the major source of reactive oxygen species production (ROS), which deteriorates the growth and performance of plants. Since seed degradation is linked to a loss of structural and metabolic integrity and biochemical aberrations, assessing changes in oxidative stress biomarkers, such as electrolyte leakage (EL), is a good method for figuring out which factors promote seed synchronization [67,68]. EL is prevalent in a range of species, tissues, and cell types, and can be caused by a variety of stresses, including salt stress [69,70]. In the current study, an increase in EL leakage was significantly different in salt-treated lettuce, causing membrane injury, unlike in the control. The most prominent EL was observed in the KNO3-, GA3-, and non-primed lettuce subjected to SS. Chiu et al. [71] reported that improvement in germination by any priming might be due to enhanced repair of the membrane. However, KNO3- and GA3-priming failed to suppress the ROS induced by SS, leading to significant membrane injury. On the contrary, HP lettuce maintained the suppression of ROS even under SS, thus inhibiting the EL and maintaining the seed germination, as reported by Chiu et al. [71] and Mahmoudi et al. [36]. The outcome of the current study establishes that the positive effect of hydro-priming on EL in lettuce could be related to the higher FM and DM reduction, as well as the lowest synchronization index in the presence of SS, thus sparing few electrons for the production of reactive oxygen species [72]. In this study, the FMs and DMs of seed parts were statistically similar in KNO3- and GA3-primed seeds, while HP lettuce was significantly different and highest compared to the NP control. This suggests that BB lettuce can ensure better seed growth and germination with HP seeds even under SS, but not with KNO3- or GA3-primed seeds. In addition, the lowest seed synchronization index and electrolyte damage due to hydro-priming provides enough evidence to validate the positive impact of hydro-priming in seed germination and synchronization with minimal cell damage. Overall, this research suggests that hydro-priming has a mitigating impact on membrane injury in plants exposed to SS.

5. Conclusions

This study investigated the effects of different priming methods on salt-sensitive BB lettuce cultivars subjected to SS. Seed priming has the potential to improve seed germination and establishment by initiating germination metabolism without radicle protrusion. Thus, the current report shows the benefits of seed priming in the improvement of productivity in several field crops [73]. In addition, seed priming is cost- and resource-effective [73]. To validate the response of several priming methods in lettuce, this research was conducted to demonstrate that HP seeds showed better synchronization under both salt treatment levels than any other primed seeds. Similarly, the FMs and DMs of cotyledons, hypocotyls, and radicles were recorded the highest in HP lettuce, irrespective of salt treatments. It is important to note that low electrolyte leakage could be attributed to the better seed synchronization and higher FM and DM in HP lettuce under SS. After analyzing the overall morphological, biochemical, and germination traits, it is concluded that HP lettuce performed better under SS compared to lettuce primed with KNO3 and GA3. Based on these results, using hydro-priming for lettuce subjected to SS can be a suitable priming method to ameliorate the deleterious effect of SS and enhance the synchronized seed germination. In addition, hydro-priming can also be beneficial in stimulating various signaling cascades during the early growth phase, producing faster and more efficient defense responses in lettuce. Thus, suggesting hydro-priming as an effective priming technique in lettuce tends to benefit a grower in terms of better growth synchronization and higher FM and DM.

Author Contributions

B.A.: conceptualization, methodology, validation, formal analysis, investigation, writing—original draft, writing—review and editing, visualization, methodology, validation, investigation. O.J.O.: methodology, validation, formal analysis, investigation. T.C.B.: conceptualization, methodology, validation, formal analysis, investigation, resources, data curation, writing review and editing, visualization, supervision, project administration, funding acquisition. All authors have read and agreed to the published version of the manuscript.

Funding

The project funding is based on work that is supported by the USDA-NIFA Hatch Project under accession number 149210.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

We thank Thomas Horgan and Skyler Brazel at the Vegetable Physiology Laboratory for their technical assistance for their help during data collection.

Conflicts of Interest

The authors declare that they have no known competing financial interest or personal relationships that could have appeared to influence the work reported in this paper.

References

  1. Ibrahim, E.A. Seed priming to alleviate salinity stress in germinating seeds. J. Plant Physiol. 2016, 192, 38–46. [Google Scholar] [CrossRef] [PubMed]
  2. Hussain, M.; Ahmad, S.; Hussain, S.; Lal, R.; Ul-Allah, S.; Nawaz, A. Rice in saline soils: Physiology, biochemistry, genetics, and management. In Advances in Agronomy; Sparks, D.L., Ed.; Academic Press: Cambridge, MA, USA, 2018; Volume 148, pp. 231–287. [Google Scholar]
  3. Zaman, M.; Shahid, S.A.; Pharis, R.P. Salinity a Serious Threat to Food Security—Where Do We Stand? Int. At. Energy Agency Bull. 2016, 39, 9–10. [Google Scholar]
  4. Park, H.J.; Kim, W.Y.; Yun, D.J. A New Insight of Salt Stress Signaling in Plant. Mol. Cells 2016, 39, 447–459. [Google Scholar] [CrossRef] [PubMed]
  5. WMO. State of the Global Climate 2020: Provisional Report; WMO: Geneva, Switzerland, 2021; ISBN 4146702018922. [Google Scholar]
  6. Rouhi, H.R.; Aboutalebian, M.A.; Sharif-Zadeh, F. Effects of hydro and osmopriming on drought stress tolerance during germination in four grass species. Int. J. AgriScience 2011, 1, 107–114. [Google Scholar]
  7. Jamil, M.; Lee, C.C.; Rehman, S.U.; Lee, D.B.; Ashraf, M.; Rha, E.S. Salinity (NaCl) tolerance of Brassica species at germination and early seedling growth. Electron. J. Environ. Agric. Food Chem. 2005, 4, 970–976. [Google Scholar]
  8. Omid, A.; Farzad, S.-Z. Osmo and hydro priming improvement germination characteristics and enzyme activity of Mountain Rye (Secale montanum) seeds under drought stress. J. Stress Physiol. Biochem. 2012, 8, 253–261. [Google Scholar]
  9. Francois, L.E.; Maas, E.V. Crop response and management of salt-affected soils. In Handbook of Plant and Crop Stress; Marcel Dekker Press Inc.: New York, NY, USA, 1999; pp. 169–201. [Google Scholar]
  10. Mahmoudi, H.; Kaddour, R.; Huang, J.; Nasri, N.; Olfa, B.; M’Rah, S.; Hannoufa, A.; Lachaâl, M.; Ouerghi, Z. Varied tolerance to NaCl salinity is related to biochemical changes in two contrasting lettuce genotypes. Acta Physiol. Plant. 2011, 33, 1613–1622. [Google Scholar] [CrossRef]
  11. Khajeh-Hosseini, M.; Powell, A.A.; Bingham, I.J. The interaction between salinity stress and seed vigour during germination of soyabean seeds. Seed Sci. Technol. 2003, 31, 715–725. [Google Scholar] [CrossRef]
  12. Jenks, M.A.; Hasegawa, P.M.; Jain, S.M. Advances in Molecular Breeding toward Drought and Salt Tolerant Crops; Springer: Dordrecht, The Netherlands, 2007; ISBN 1402055773. [Google Scholar]
  13. Tekrony, D.M.; Egli, D.B. Accumulation of seed vigour during development and maturation. In Basic and Applied Aspects of Seed Biology; Springer: Berlin/Heidelberg, Germany, 1997; pp. 369–384. [Google Scholar]
  14. Walters, C.; Towill, L.; Collins, C.O. Seeds and pollen. In Commercial Storage Fruits, Vegetables, and Florist and Nursery Stocks; United States Department of Agriculture: Washington, DC, USA, 2004; p. 735. [Google Scholar]
  15. Shaban, M. Review on physiological aspects of seed deterioration. Int. J. Agric. Crop Sci. 2013, 6, 627–631. [Google Scholar]
  16. Yadav, P.V.; Maya, K.; Zakwan, A. Seed priming mediated germination improvement and tolerance to subsequent exposure to cold and salt stress in capsicum. Res. J. Seed Sci. 2011, 4, 125–136. [Google Scholar] [CrossRef] [Green Version]
  17. Hubbard, M.; Germida, J.; Vujanovic, V. Fungal endophytes improve wheat seed germination under heat and drought stress. Botany 2012, 90, 137–149. [Google Scholar] [CrossRef]
  18. Läuchli, A.; Grattan, S.R. Plant growth and development under salinity stress. In Advances in Molecular Breeding toward Drought and Salt Tolerant Crops; Springer: Dordrecht, The Netherlands, 2007; pp. 1–32. [Google Scholar]
  19. Taylor, A.G.; Harman, G.E. Concepts and technologies of selected seed treatments. Annu. Rev. Phytopathol. 1990, 28, 321–339. [Google Scholar] [CrossRef]
  20. Afzal, I.; Basra, S.M.A.; Farooq, M.; Nawaz, A. Alleviation of salinity stress in spring wheat by hormonal priming with ABA, salicylic acid and ascorbic acid. Int. J. Agric. Biol. 2006, 8, 23–28. [Google Scholar]
  21. Paparella, S.; Araújo, S.S.; Rossi, G.; Wijayasinghe, M.; Carbonera, D.; Balestrazzi, A. Seed priming: State of the art and new perspectives. Plant Cell Rep. 2015, 34, 1281–1293. [Google Scholar] [CrossRef]
  22. Parera, C.A.; Cantliffe, D.J. Presowing seed priming. Hortic. Rev. 1994, 16, 109–141. [Google Scholar]
  23. Iqbal, M.; Ashraf, M.; Jamil, A.; Ur-Rehman, S. Does seed priming induce changes in the levels of some endogenous plant hormones in hexaploid wheat plants under salt stress? J. Integr. Plant Biol. 2006, 48, 181–189. [Google Scholar] [CrossRef]
  24. Kaur, S.; Gupta, A.K.; Kaur, N. Effect of osmo-and hydropriming of chickpea seeds on seedling growth and carbohydrate metabolism under water deficit stress. Plant Growth Regul. 2002, 37, 17–22. [Google Scholar] [CrossRef]
  25. Kaya, M.D.; Okçu, G.; Atak, M.; Cıkılı, Y.; Kolsarıcı, Ö. Seed treatments to overcome salt and drought stress during germination in sunflower (Helianthus annuus L.). Eur. J. Agron. 2006, 24, 291–295. [Google Scholar] [CrossRef]
  26. Casenave, E.C.; Toselli, M.E. Hydropriming as a pre-treatment for cotton germination under thermal and water stress conditions. Seed Sci. Technol. 2007, 35, 88–98. [Google Scholar] [CrossRef]
  27. Wu, L.; Huo, W.; Yao, D.; Li, M. Effects of solid matrix priming (SMP) and salt stress on broccoli and cauliflower seed germination and early seedling growth. Sci. Hortic. 2019, 255, 161–168. [Google Scholar] [CrossRef]
  28. Singh, H.; Jassal, R.K.; Kang, J.S.; Sandhu, S.S.; Kang, H.; Grewal, K. Seed priming techniques in field crops—A review. Agric. Rev. 2015, 36, 251–264. [Google Scholar] [CrossRef] [Green Version]
  29. Ranal, M.A.; de Santana, D.G.; Ferreira, W.R.; Mendes-Rodrigues, C. Calculating germination measurements and organizing spreadsheets. Braz. J. Bot. 2009, 32, 849–855. [Google Scholar] [CrossRef] [Green Version]
  30. Soltani, E.; Ghaderi-Far, F.; Baskin, C.C.; Baskin, J.M. Problems with using mean germination time to calculate rate of seed germination. Aust. J. Bot. 2015, 63, 631–635. [Google Scholar] [CrossRef]
  31. Labouriau, L.G. On the frequency of isothermal germination in seeds of Dolichos biflorus L. Plant Cell Physiol. 1978, 19, 507–512. [Google Scholar] [CrossRef]
  32. Ranal, M.A.; Santana, D.G. How and why to measure the germination process? Braz. J. Bot. 2006, 29, 1–11. [Google Scholar] [CrossRef] [Green Version]
  33. Mavi, K.; Demir, I.; Matthews, S. Mean germination time estimates the relative emergence of seed lots of three cucurbit crops under stress conditions. Seed Sci. Technol. 2010, 38, 14–25. [Google Scholar] [CrossRef]
  34. Damalas, C.A.; Koutroubas, S.D.; Fotiadis, S. Hydro-priming effects on seed germination and field performance of faba bean in spring sowing. Agriculture 2019, 9, 201. [Google Scholar] [CrossRef] [Green Version]
  35. Adhikari, B.; Olorunwa, O.J.; Wilson, J.C.; Barickman, T.C. Morphological and Physiological Response of Different Lettuce Genotypes to Salt Stress. Stresses 2021, 1, 285–304. [Google Scholar] [CrossRef]
  36. Mahmoudi, H.; Massoud, R.B.; Baatour, O.; Tarchoune, I.; Salah, I.B.; Nasri, N.; Abidi, W.; Kaddour, R.; Hannoufa, A.; Lachaâl, M. Influence of different seed priming methods for improving salt stress tolerance in lettuce plants. J. Plant Nutr. 2012, 35, 1910–1922. [Google Scholar] [CrossRef]
  37. Ellis, R.H.; Roberts, E.H. The quantification of ageing and survival in orthodox seeds. Seed Sci. Technol. 1981, 9, 373–409. [Google Scholar]
  38. AOSA (Association of Official Seed Analysts). SCST (Society of Commercial Seed Technologists). Rules for testing seeds. J. Seed Technol. 1993, 16, 1–113. [Google Scholar]
  39. Quartacci, M.F.; Glišić, O.; Stevanović, B.; Navari-Izzo, F. Plasma membrane lipids in the resurrection plant Ramonda serbica following dehydration and rehydration. J. Exp. Bot. 2002, 53, 2159–2166. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  40. Munns, R.; James, R.A.; Läuchli, A. Approaches to increasing the salt tolerance of wheat and other cereals. J. Exp. Bot. 2006, 57, 1025–1043. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  41. Jamil, A.; Riaz, S.; Ashraf, M.; Foolad, M.R. Gene expression profiling of plants under salt stress. Crit. Rev. Plant Sci. 2011, 30, 435–458. [Google Scholar] [CrossRef]
  42. Ahmad, P.; Azooz, M.M.; Prasad, M.N.V. Salt Stress in Plants; Springer: Berlin/Heidelberg, Germany, 2013. [Google Scholar]
  43. Szepesi, Á. Role of salicylic acid pre-treatment on the acclimation of tomato plants to salt-and osmotic stress. Acta Biol. Szeged. 2005, 49, 123–125. [Google Scholar]
  44. James, R.A.; Von Caemmerer, S.; Condon, A.G.T.; Zwart, A.B.; Munns, R. Genetic variation in tolerance to the osmotic stress componentof salinity stress in durum wheat. Funct. Plant Biol. 2008, 35, 111–123. [Google Scholar] [CrossRef]
  45. Gzik, A. Accumulation of proline and pattern of α-amino acids in sugar beet plants in response to osmotic, water and salt stress. Environ. Exp. Bot. 1996, 36, 29–38. [Google Scholar] [CrossRef]
  46. Gadallah, M.A.A. Effects of proline and glycinebetaine on Vicia faba responses to salt stress. Biol. Plant. 1999, 42, 249–257. [Google Scholar] [CrossRef]
  47. Taiz, L.; Zeiger, E.; Møller, I.M.; Murphy, A. Plant Physiology and Development; Sinauer Associates Incorporated: Sunderland, MA, USA, 2015; ISBN 1605353531. [Google Scholar]
  48. Alasvandyari, F.; Mahdavi, B.; Hosseini, S.M. Glycine betaine affects the antioxidant system and ion accumulation and reduces salinity-induced damage in safflower seedlings. Arch. Biol. Sci. 2017, 69, 139–147. [Google Scholar] [CrossRef]
  49. Tabassum, T.; Farooq, M.; Ahmad, R.; Zohaib, A.; Wahid, A. Seed priming and transgenerational drought memory improves tolerance against salt stress in bread wheat. Plant Physiol. Biochem. 2017, 118, 362–369. [Google Scholar] [CrossRef]
  50. Tsegay, B.A.; Andargie, M. Seed priming with gibberellic acid (GA3) alleviates salinity induced inhibition of germination and seedling growth of Zea mays L., Pisum sativum var. abyssinicum A. Braun and Lathyrus sativus L. J. Crop Sci. Biotechnol. 2018, 21, 261–267. [Google Scholar] [CrossRef]
  51. Imran, M.; Boelt, B.; Mühling, K. Zinc seed priming improves salt resistance in maize. J. Agron. Crop Sci. 2018, 204, 390–399. [Google Scholar] [CrossRef]
  52. Tahira, T.; Riaz, A.; Muhammad, F.; Basra, S.M.A. Improving salt tolerance in barley by osmopriming and biopriming. Int. J. Agric. Biol. 2018, 20, 2455–2464. [Google Scholar]
  53. Kim, I.-J.L.; Yun, B.-W.; Jamil, M. GA mediated OsZAT-12 expression improves salt resistance of rice. Int. J. Agric. Biol 2016, 18, 330–336. [Google Scholar]
  54. Bajehbaj, A.A. The effects of NaCl priming on salt tolerance in sunflower germination and seedling grown under salinity conditions. Afr. J. Biotechnol. 2010, 9, 1764–1770. [Google Scholar]
  55. Younesi, O.; Moradi, A. Effect of priming of seeds of Medicago sativa ‘bami’with gibberellic acid on germination, seedlings growth and antioxidant enzymes activity under salinity stress. J. Hortic. Res. 2014, 22, 167–174. [Google Scholar] [CrossRef] [Green Version]
  56. Hassini, I.; Martinez-Ballesta, M.C.; Boughanmi, N.; Moreno, D.A.; Carvajal, M. Improvement of broccoli sprouts (Brassica oleracea L. var. italica) growth and quality by KCl seed priming and methyl jasmonate under salinity stress. Sci. Hortic. 2017, 226, 141–151. [Google Scholar] [CrossRef]
  57. Farooq, M.; Basra, S.M.A.; Rehman, H.; Ahmad, N.; Saleem, B.A. Osmopriming improves the germination and early seedling growth of melons (Cucumis melo L.). Pak. J. Agric. Sci. 2007, 44, 529–536. [Google Scholar]
  58. Sarwar, N.; Yousaf, S.; Jamil, F.F. Induction of salt tolerance in chickpea by using simple and safe chemicals. Pak. J. Bot. 2006, 38, 325. [Google Scholar]
  59. Nasri, N.; Kaddour, R.; Mahmoudi, H.; Baatour, O.; Bouraoui, N.; Lachaâl, M. The effect of osmopriming on germination, seedling growth and phosphatase activities of lettuce under saline condition. Afr. J. Biotechnol. 2011, 10, 14366–14372. [Google Scholar]
  60. Jamil, M.; Ashraf, M.; Rha, E. Alleviation of salt stress using gibberellic acid in Chinese cabbage. Acta Agron. Hung. 2012, 60, 345–355. [Google Scholar] [CrossRef] [Green Version]
  61. Zhou, J.; Wang, Y.; Jahufer, Z. Location and chemical composition of semi-permeable layer of forage seeds. Bangladesh J. Bot. 2013, 42, 23–30. [Google Scholar] [CrossRef] [Green Version]
  62. Bradford, K.J. A water relations analysis of seed germination rates. Plant Physiol. 1990, 94, 840–849. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  63. Sahoo, S.; Borgohain, P.; Saha, B.; Moulick, D.; Tanti, B.; Panda, S.K. Seed priming and seedling pre-treatment induced tolerance to drought and salt stress: Recent advances. In Priming and Pretreatment of Seeds and Seedlings; Springer: Singapore, 2019; pp. 253–263. [Google Scholar]
  64. Sivritepe, N.; Sivritepe, H.O.; Eris, A. The effects of NaCl priming on salt tolerance in melon seedlings grown under saline conditions. Sci. Hortic. 2003, 97, 229–237. [Google Scholar] [CrossRef]
  65. Aschermann-Koch, C.; Hofmann, P.; Steiner, A.M. Presowing treatment for improving seed quality in cereals. Germination and vigour. Seed Sci. Technol. 1992, 20, 435–440. [Google Scholar]
  66. McDonald, M.B. Seed priming. In Seed Technology and Its Biological Basis; Sheffild Academic Press: Sheffild, UK, 2000; pp. 287–325. [Google Scholar]
  67. Adetunji, A.E.; Varghese, B.; Pammenter, N.W. Effects of inorganic salt solutions on vigour, viability, oxidative metabolism and germination enzymes in aged cabbage and lettuce seeds. Plants 2020, 9, 1164. [Google Scholar] [CrossRef]
  68. Al-Maskri, A.; Khan, M.M.; Al-Manther, O.; Al-Habsi, K. Effect of accelerated aging on lipid peroxidation, leakage and seedling vigor (RGR) in cucumber (Cucumis sativus L.) seeds. Pak. J. Agric. Sci. 2002, 39, 330–337. [Google Scholar]
  69. Shabala, S.; Demidchik, V.; Shabala, L.; Cuin, T.A.; Smith, S.J.; Miller, A.J.; Davies, J.M.; Newman, I.A. Extracellular Ca2+ ameliorates NaCl-induced K+ loss from Arabidopsis root and leaf cells by controlling plasma membrane K+-permeable channels. Plant Physiol. 2006, 141, 1653–1665. [Google Scholar] [CrossRef] [Green Version]
  70. Demidchik, V.; Maathuis, F. Ion Channels and Plant Stress Responses; Springer: Berlin/Heidelberg, Germany, 2010; ISBN 3642104940. [Google Scholar]
  71. Chiu, K.Y.; Wang, C.S.; Sung, J.M. Lipid peroxidation and peroxide-scavenging enzymes associated with accelerated aging and hydration of watermelon seeds differing in ploidy. Physiol. Plant. 1995, 94, 441–446. [Google Scholar] [CrossRef]
  72. Khan, M.N.; Zhang, J.; Luo, T.; Liu, J.; Rizwan, M.; Fahad, S.; Xu, Z.; Hu, L. Seed priming with melatonin coping drought stress in rapeseed by regulating reactive oxygen species detoxification: Antioxidant defense system, osmotic adjustment, stomatal traits and chloroplast ultrastructure perseveration. Ind. Crops Prod. 2019, 140, 111597. [Google Scholar] [CrossRef]
  73. Hasanuzzaman, M.; Fotopoulos, V. Priming and Pretreatment of Seeds and Seedlings: Implication in Plant Stress Tolerance and Enhancing Productivity in Crop Plants; Springer: Singapore, 2019; ISBN 9789811386244. [Google Scholar]
Figure 1. Fresh Mass (FM) of the: (A) cotyledon; (B) hypocotyl; and (C) radicle, (mean ± SE, n = 4), of BB lettuce, non-primed and seed-primed with GA3, KNO3, and hydro-priming, and further subjected to 100 mM of NaCl salt stress. 0 mM NaCl was considered as a control. Bars marked with different lowercase letters indicate statistically significant difference using Tukey’s honestly difference test at α = 0.05.
Figure 1. Fresh Mass (FM) of the: (A) cotyledon; (B) hypocotyl; and (C) radicle, (mean ± SE, n = 4), of BB lettuce, non-primed and seed-primed with GA3, KNO3, and hydro-priming, and further subjected to 100 mM of NaCl salt stress. 0 mM NaCl was considered as a control. Bars marked with different lowercase letters indicate statistically significant difference using Tukey’s honestly difference test at α = 0.05.
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Figure 2. Dry Mass (DM) of the: (A) cotyledon; (B) hypocotyl; and (C) radicle (mean ± SE, n = 4) of BB lettuce, non-primed and seed-primed with GA3, KNO3, and hydro-priming, and further subjected to 100 mM of NaCl salt stress. 0 mM NaCl was considered as a control. Bars marked with different lowercase letters indicate statistically significant difference using Tukey’s honestly difference test at α = 0.05.
Figure 2. Dry Mass (DM) of the: (A) cotyledon; (B) hypocotyl; and (C) radicle (mean ± SE, n = 4) of BB lettuce, non-primed and seed-primed with GA3, KNO3, and hydro-priming, and further subjected to 100 mM of NaCl salt stress. 0 mM NaCl was considered as a control. Bars marked with different lowercase letters indicate statistically significant difference using Tukey’s honestly difference test at α = 0.05.
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Figure 3. Length of: (A) hypocotyl; and (B) radicle, (mean ± SE, n = 4) of BB lettuce, non-primed and seed-primed with GA3, KNO3, and hydro-priming, and further subjected to 100 mM of NaCl salt stress. 0 mM NaCl was considered as a control. Bars marked with different lowercase letters indicate statistically significant difference using Tukey’s honestly difference test at α = 0.05.
Figure 3. Length of: (A) hypocotyl; and (B) radicle, (mean ± SE, n = 4) of BB lettuce, non-primed and seed-primed with GA3, KNO3, and hydro-priming, and further subjected to 100 mM of NaCl salt stress. 0 mM NaCl was considered as a control. Bars marked with different lowercase letters indicate statistically significant difference using Tukey’s honestly difference test at α = 0.05.
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Figure 4. Electrolyte leakage (mean ± SE, n = 4) in BB lettuce, non-primed and seed-primed with GA3, KNO3, and hydro-priming, and further subjected to 100 mM of NaCl salt stress. 0 mM NaCl was considered as a control. Bars marked with different lowercase letters indicate statistically significant difference using Tukey’s honestly difference test at α = 0.05.
Figure 4. Electrolyte leakage (mean ± SE, n = 4) in BB lettuce, non-primed and seed-primed with GA3, KNO3, and hydro-priming, and further subjected to 100 mM of NaCl salt stress. 0 mM NaCl was considered as a control. Bars marked with different lowercase letters indicate statistically significant difference using Tukey’s honestly difference test at α = 0.05.
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Table 1. Mean responses of various germination parameters of lettuce seeds for evaluation of the effects of different priming methods (GA3, hydro-priming, KNO3, and NP) and two salt treatment levels (control and 100 mM NaCl).
Table 1. Mean responses of various germination parameters of lettuce seeds for evaluation of the effects of different priming methods (GA3, hydro-priming, KNO3, and NP) and two salt treatment levels (control and 100 mM NaCl).
PrimingTreatmentMGT 3MGRZGI
GA3Control2.16 ± 0.03a 1,20.5 ± 0.01a0.72 ± 0.05a11.8 ± 0.14a
NaCl2.23 ± 0.11a0.4 ± 0.02a0.65 ± 0.11ab11.5 ± 0.12a
HydroControl2.01 ± 0.02a0.5 ± 0.03a0.32 ± 0.08c12.5 ± 0.01a
NaCl2.04 ± 0.01a0.4 ± 0.08a0.42 ± 0.03c12.3 ± 0.02a
KNO3Control2.17 ± 0.04a0.5 ± 0.01a0.71 ± 0.09a11.8 ± 0.16a
NaCl2.37 ± 0.18a0.4 ± 0.03a0.55 ± 0.13b11.2 ± 0.18a
Non-primingControl2.17 ± 0.02a0.5 ± 0.01a0.71 ± 0.03a11.8 ± 0.08a
NaCl2.32 ± 0.11a0.4 ± 0.02a0.56 ± 0.18ab11.2 ± 0.43a
Priming************
Salt**********
Priming × Salt treatmentNSNS**NS
1 Values represent the mean ± SE, n = 25. 2 Different lowercase letters indicate significant differences in parameters (p < 0.05) as assessed by Tukey’s test. NS represents nonsignificant p > 0.05; **, *** represent significance levels at p ≤ 0.01 and p ≤ 0.001, respectively. 3 MGT = mean germination time (day); MGR = mean germination rate (day−1); GI = germination index (unitless); and Z = synchronization index (unitless).
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Adhikari, B.; Olorunwa, O.J.; Barickman, T.C. Seed Priming Enhances Seed Germination and Morphological Traits of Lactuca sativa L. under Salt Stress. Seeds 2022, 1, 74-86. https://doi.org/10.3390/seeds1020007

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Adhikari B, Olorunwa OJ, Barickman TC. Seed Priming Enhances Seed Germination and Morphological Traits of Lactuca sativa L. under Salt Stress. Seeds. 2022; 1(2):74-86. https://doi.org/10.3390/seeds1020007

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Adhikari, Bikash, Omolayo J. Olorunwa, and T. Casey Barickman. 2022. "Seed Priming Enhances Seed Germination and Morphological Traits of Lactuca sativa L. under Salt Stress" Seeds 1, no. 2: 74-86. https://doi.org/10.3390/seeds1020007

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