Journal of Stress Physiology & Biochemistry, Vol. 21, No. 1, 2025, pp. 77-85 ISSN 1997-0838 Original Text Copyright © 2024 by Alhoshan and Hammoud
ORIGINAL ARTICLE
OPEN /¿"l ACCESS
Effect of Different Levels of Glycine on Growth and Yield of Two Potato Cultivars under Field Conditions
Mouhamad Alhoshan*, and Nizar Hammoud
1 Department of Horticulture, General Commission for Scientific Agriculture Research, GCSAR, Damascus, Syria
*E-Mail: [email protected] ORCID: 0000-0002-8064-8610
Received September 5, 2024
This field investigate was conducted in 2021 and 2023 to evaluate the response of two potato cultivars to different levels of glycine in terms of plant dry mass (PDM), yield, total sold solutions (TSS), and some miniral elements analysis from aerial parts of potato plants. Two potato cultivars namely, Spunta and Larissa were exposed to three levels of glycine (0.0, 1.5 and 3.0 mM). Trial pieces were conducted as a factorial based on a randomized complete block design with three replications. glycine treatments led to significant effects on most characters, i.e., PDM and yield of two potato cultivars were significantly increased in all concentrations of glycine as compared to the control. As well, P content was increased by foliar application of glycine in all levels. but, K and Fe content in aerial parts were decreased. Also, a positive correlations were found among N and K, or/and K and Fe elements. Moreover, the results of this research revealed that increasing levels of glycine have positive effects on growth, biomass and yield of potato cultivars.
Key words: Potato. Glycine. Plant dry mass. Yield
Abbreviations: PDM plant dry mass, TSS total sold solutions, N nitrogen, P phosphorus, K potassium, Na sodium, Zn zinc, Fe iron.
A potato yield losses in the world, as a result of climate alteration is expected to range between 18 and 32% during the first three decades of this century (Hijmans, 2003; Monneveux et al., 2014). Drought, salinity, low and high temperatures are the most important limiting factors among different environmental constraints which induce plant stress and reduce crop productivity in many parts of the world (Lawlor, 2002). Generally, a great challenge in the future, rises demand for nutrition products and for fresh water resources because of increasing a predicted world population of 9 billion by 2050 and altered food behaviors (Costa et al., 1997; Araus et al., 2008; Singh and Kaur, 2009; Levy et al., 2013; Lobell et al., 2008), also, growing crisis in many parts of the world i.e., COVID-19 and wars.
However, potato (solanum tuberosum L.) is presented in the fourth greatest main food crop after wheat, maize and rice (Singh and Kaur, 2009). In agriculture there are many procedures that have been proposed and used widely to inhance mineral nutrition of plants under regular or stress conditions (Pérez-Jiménez et al., 2015; Sánchez et al., 2005), i.e., inorganic fertilizers have an inevitable role in food production of agricultural crops (Souri and Hatamian, 2019). Furthermore, nitrogen is an essential macroelement for plant growth and development. As well, plants are required it in the largest quantities for their metabolisms and represents up to 2% of plant dry mass (Masclaux-Daubresse et al., 2010). In addition, because of the main source of N for plants are nitrate, they absorb it from agricultural soil in the form of nitrate and ammonium, while organic N such as amino acids, can also be taken up by plants (Nasholm et al., 2009). Moreover, organic nitrogen must be converted into nitrate or ammonium prior to become biologically available (Gonzalez-Perez et al., 2015), and which represents 96-99% of total nitrogen in soil, could be directly absorbed by plants and significantly influence plant physiology and nutritional quality (Paungfoo-Lonhienne et al., 2008).
In the other hand, amino acids characterize a main part of the low-molecular weight organic N that is dissolved in the soil. The existence and concentrations
of different amino acids vary significantly from one ecosystem to another. In general, these compounds are found at low concentrations in the soil, =0.01 to 10 mM (Jones et al., 2005). Plus, amino acids have various important biological functions in plant cells including detoxification of toxins and heavy metals (Hussain et al., 2018; Rizwan et al., 2017; Bashir et al., 2018), optimizing the nutrient uptake, translocation and metabolism, vitamin biosynthesis, growth biostimulation, contribute in the tolerance of plants to environmental stresses such as drought, salinity, high and low temperatures, other than in the synthesis and production of aminochelate fertilizers (Jeppsen, 1991; Sharma and Dietz, 2006; Souri and Hatamian, 2019). Furthermore, amino acids have been shown to improve plant growth, yield, and nutrient uptake (Garcia et al., 2011). In these patches, glutamic acid, serine, glycine, alanine, and aspartic acid are the most abundant amino acids (Lipson and Nasholm, 2001). Conversely, the simple amino acid (glycine has a single hydrogen atom as its side chain with the chemical formula NH2-CH2-COOH is regarded as a proof of life), was the original nutrient form for organisms (Xu et al., 2017) and is one of the most plentiful free amino acids in agricultural soil. Also, the glycine concentration of soil ranges from 1.14 to 2.39 |g N/g, corresponding to more than 30% of total free amino acids (Wang et al., 2013; Gonzalez-Perez et al., 2015). However, this research was conducted to study the response of growth and yield of two potato cultivars to different levels of glycine under field conditions.
MATERIALS AND METHODS
Plant material, growing conditions and experimental design
In this investigate, a field experiment was conducted as a factorial based on a randomized complete block design with three replications and carried out from the Februry to April 2021 and 2023 for two years at Algotta research station of general commission for scientific agriculture research, located in Damascus, Syria (33° 24.64' N, 36° 30.87' E and 616 m above the mean sea level) to examine the effects of application of three levels of amino acid 'glycine' (0.0, 1.5, and 3.0 mM) on two potato cultivars (Spunta and Larissa). Tubers (about
50-70 gr) were kept at room temperature of 25°C for two weeks to germinate and then cultivated in the soil with deminshes 25 cm between plants and 75 cm between rows. Before planting, some samples of the medium culture were prepared for analyzying (table 1). All plants were irrigated normally. Therefore, glycine treatments were applied at the stage of beginning flowers. At the end of the experiment (i.e., 110 days) all parts of potato plants were collected for analyzying.
Plant dry mass
At the end of this research, aerial parts of potato plants (shoots and stems) of each cultivar and in each block and replicate were dried to specify a fixed dry weight.
Yield
The harvest of tuber yield of potato cultivars and calculations (t/h) were done alone in each block and replicate.
Total soluble solids (TSS)
Tubers samples of potato cultivars were collected randomly and the TSS measurements were done by using a field device (Refractometer).
Analysis of ions
Shoots of plants were dehydrated and digested in an acid mixture consisting of sulfuric, nitric and per-chloric acids in the ratio of 1:8:1 (v/v). The aliquot was filtered and used for determination of K, Na and with Flame photometer (Allen et al., 1986). Nitrogen was measured using micro Keldahl method (Jackson, 1958) and the P concentration of plant samples was determined, by colorimetrically after nitric perchloric digestion method (Hanson, 1950).
Oven dried grinding 0.5 g sample was taken into 50 ml conical flask and 5 ml HNO3+ HCO4 was added into it. After that, it was transferred into digestion chamber for 2.5 hours. Then it was cooled down. Again, 20 ml of distilled water was added and heated with digestion chamber at 280 °C for 30 minutes. The solution was then transferred into 100 ml volumetric flask with filter paper and made the volume 100 ml (stock solution). 5 ml extract solution in addition with 20 ml distilled water was taken into 50 ml volumetric flask. Then, At last, 1 ml LnCl2 was added and the volume was made 50 ml with distilled water. Finally, reading of Na+ and K+ was taken
by atomic absorption spectrophotometer (Bar-Tal et al., 1991). By atomic absorption spectrometry (Perkin Elmer, Waltham, MA model 5000 spectrophotometer), the concentrations of Zn and Fe were determined (Allen et al, 1986).
Data analysis
To determine the difference among treatments and between cultivars, the mean data of two years were tested and subjected to analysis of variance (ANOVA) by using SAS and MSTATC programs, and conducted as a factorial based on a randomized complete block design with three replications. Comparison of means was achieved by using LSD test (p < 0.05) and the correlation coefficients between the characters were done by using PROC CORR of SAS program.
RESULTS
Analysis of variance for plant dry mass (PDM), potassium (K) and iron (Fe) of potato cultivars revealed statistical significance (p < 0.01) between cultivars. As well as, these statistical significances (p < 0.01) between treatments were shown for PDM, yield, phosphorus (P) and Fe. As well, analysis of variance for total soluble solids (TSS) was not significant in the studied cultivars, treatments and between interactions treatments and cultivars (table 2).
Plant dry mass and yield
The interaction effects of cultivars and glycine levels were significant (p < 0.01) on plant dry mass (PDM) and (p < 0.05) on yield of potato cultivars (table 2). Under regular conditions of irrigation, the maximum and minimum values of PDM were attained in Spunta (93.3 g/plant) and Larissa (80.0 g/plant), and yield were achieved in Larissa (38.99 t/h) and Spunta (31.3 t/h). On the other hand, under glycine treatments (1.5 and 3.0 mM), the maximum and minimum values of PDM were obtained in Spunta (153.3 g/plant) and Larissa (116.7 g/plant) in the treatment 3.0 mM, likewise, yield in Larissa (52.52 and 40.96 t/h) in the treatment 3.0 and 1.5 mM, respectivily (table 5). PDM and yield were significantly increased in the tested cultivars at 1.5 and 3.0 mM of glycine treatments compared to the conrtol under normal conditions. Maximum increasing were observed at 3.0 mM of glycine treatment (55.71 % and 44.0 %) for PDM and yield as compared to the normal
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Table 1 Physical and chemical properties of the experimental soil.
pH
EC (dSm1)
CaCo3 (%)
Available K
(mg kg1)
Available P
(mg kg1)
Total
N %
Tissue of soil
Organic content
%
Mechanical analysis %
Sand Silt
Clay
8.4 0.92
50.2
453
336
0.14
clay
2.68
20
23
57
Table 2 Analysis of variance for plant dry mass (PDM), yield, total sold solutions (TSS), nitrogen (N), phosphorus (P), potassium {K): sodium (Na), zinc (Zn), iron (Fe), cultivar (Cult), treatment (Treat) and replication (Rep) of potato cultivars evaluated at three levels of glycine.
Source of variation Mean square
df PDM (g) Yield m TSS N (%) P (%) K (%) Na (mg/kg) Na/K Zn (mg/kg) Fe (mg/kg)
Cult 1 1440" 14.87 "s 0.056ns 1.78* 0.0004ns 2.52" 0.0005 14.75 " 255.53 " 3578169 "
Treat 2 4128" 361.16" 0.39 ns 0.72n£ 0.008 " 0.036 " 0.0002 1.55 " 26.11 831060 "
Rep 2 17.39 49.97 0.187 0.447 0.0003 0.0004 0.0005 0.015 35.82 8448
Treat*Cult 2 431.7" 74.59' 0.271ns 0.6481,5 0.001nE 0.013 * 0.00004ni 1.49 " 89.55115 1003115 "
Error 10 20.9 17.3 0.42 0.26 0.0004 0.002 0.001 0.026 51.44 22967
C.V - 3.9 9.6 11.84 19.84 19.85 8.75 8.05 12.97 8.20 10.76
** Significant at P < 0.01, * Significant at P < 0.05, non-significant, respectively.
Table 3 Analysis of variance for plant dry mass (PDM), yield, phosphorus (P), potassium (K), and iron (Fe) of potato cultivars evaluated at three levels of glycine.
Treatment PDM (g) Yield (t/h) P {%) K {%) Na/K Fe (mg/kg)
0.0 niM 86.67c 35.15c 0.06 b 0.660 a 0.685 = 1627a
1.5 mM 128.5b 43.97b 0.122a 0.532 b 1.41b 1619fl
3.0 mM 135.0 a 50.62a 0.132a 0.520 h 1.66 a 978"
+44.75 +25.1 +103.3 -19.4 +105.8 -0.5
+55.71 +44.0 +120 -21.21 +142.3 -40.0
LSD % 5.8 5.35 0.027 0.064 0.21 195
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.Mean followed by the same letter in each column are not significant different according LSD test (probability level of 5 %)
Elements analysis of the aerial parts of potato plants
The interaction effects of cultivars and glycine levels
were significant (p < 0.05, p < 0.01) on K and Fe contents, respectivily (table 2). Under normal conditions of irrigation, the highest and lowest values of K were
attained in Spunta (0.98 %) and Larissa (0.34 %), and Fe were achieved in Spunta (2437 mg/kg) and Larissa (818 mg/kg). On the other hand, under glycine treatments (1.5 and 3.0 mM), the maximum and minimum values of K were obtained in Spunta and Larissa at the treatments 1.5 and 3.0 mM of glycine. likewise, Fe (1622 mg/kg) in Spunta at the treatment 1.5 mM and Larissa (454 mg/kg) at the treatment 3.0 mM of glycine (table 5). K and Fe were significantly decreased in the tested cultivars by increasing levels of glycine compared to the normal conditions. But, regarding to the P element, our results revealed increasing values by increasing levels of glycine as compared to the control (table 3). Then again, the higher values of N, K and Fe were found in Spunta as compared to Larissa cultivar. But, the opposite results were found in Zn element (table 4).
Relationship between the traits
Correlation coefficients between of different traits and cultivars were calculated and are presented in table 6. Our results revealed that PDM was highly and positively correlated with yield and phosphorus. Also, a positive correlation was found between potassium and nitrogen, as well, between potassium and iron (table 6).
DISCUSSION
Amino acids such as, glycine and glycine betaine were discovered in a wide varieties of microorganisms and higher plants (Rhodes and Hanson, 1993). As well, they are considered as an organic osmolites that clearly gathers in many plant species and they found to be plentiful in chloroplasts, which plays a main role in regulating, protecting the thylakoid membrane and consequently maintaining the amount of photosynthesis (Genard et al., 1991).
However, similar to the findings Noroozlo et al.,
(2019) on Lettuce and sweet basil, and Shooshtari et al.,
(2020) on cucumber, our results indicated that PDM and yield of two potato cultivars were increased by increasing levels of glycine. The maximum increaseing of PDM was observed in Spunta cultivar by 39% and 28% at the treatments of glycine 3 and 1.5 mM respectivily, and Larissa by 58% at the treatment 1.5 mM as compared to their controls (table 5). On the other
hand, yield was increased in Spunta cultivar by 56% and Larissa by 35% at the treatment 3 mM as compared to their controls (table 5). Similarly, our results showed highly and positively correlated between plant dry mass and yield (table 6). In fact, glycine is one of the main amino acids that is essential for protein biosynthesis in plant cells (Ma et al., 2017). As well, many studies indicated that foliar application of glycine can increase chlorophyll biosynthesis and photosynthetic rates resulting in improved plant growth (Garcia et al., 2011). Also, other investigations showed that amino acids could affect not only plant nitrogen metabolism, but also carbon metabolism due to their strong interactions (Nunes-Nesi et al., 2010) and in the result, plant growth and yield of crops could be improved (Zhang et al., 2015).
Conversely, in this research, we obsearved increasing in P by about 120% in potato plants at the treatment 3 mM as compared to the control (table 3). Moreover, our results indicated that K and Fe were decreased by increasing levels of glycine in all treatments, accept Fe values in the culivar Larissa at the treatment 1.5 mM (table 3 and 5). The maximum decreasing of K and Fe were 21 and 40% at the treatment 3 mM as compared to the controls (table 3). As well, the positive corrolation between K and Fe indicats that increasing levels of K leads to increasing levels of Fe conversely (table 6). However, results of Shooshtari et al., (2020) on cucumber plants revealed that there is no significant effect on the leaves content of K and Fe elements between the treatments of foliar application of glycine and control. Nevertheless, study of Noroozlo et al., (2019) on lettuce displayed significant increasing of Fe percent at the treatment 1000 mg/L of glycine, while its percent in the other concentrations of glycine was decreased and they noticed that there is no significant effect as compared to the control.
On the other hand, P is an essential macro-nutrient for growth and development in all living organisms. It serves various basic biological functions as a structural element, in energy metabolism, in the activation of metabolic intermediates, in signal transduction and in the regulation of enzymes. Likewise, K does an activator of many enzymes, share in synthesis of amino acids and
proteins, opening and closing of stomata. As well, Fe intervenes in chlorophyll synthesis, cytochromes and nitrogenase (Vreugdenhil et al., 2007). Then again, at
the end of potato plants cycle, K is playing a main role in transporting nutrition materials from the aerial parts to the tubers. In fact, amino acids such as glycine improve chlorophyll biosynthesis and photosynthesis rates and enhance protein biosynthesis and in the result, they are improving growth and development of plants (Khan et al., 2012; Souri and Hatamian, 2019).
CONCLUSION
In the present study, we have been able to gather evidence that foliar application of glycine in all levels increased plant dry mass and yield of potato plants. As well, concentration of glycine, 3 mM was more effective as compared to the other levels. However, our outcomes recommend that amino acids: Case of glycine, are effective to improve plant growth and yield of potato cultivars.
ACKNOWLEDGMENT
This work was supported by the General Commission for Scientific Agriculture Research, and Department of Horticulture Science. Damascus- Syria. CONFLICTS OF INTEREST
The authors declare that they have no potential conflicts of interest.
REFERENCES
Allen S.E., Grimshaw H.M. and Rowland A.P. (1986) Chemical analysis. In Methods of plant ecology, ed. By P.D. Moore and S. B. Chapman. Blackwell: Oxford.
Araus J.L., Slafer G.A., Royo C. and Serret M.D. (2008) Breeding for yield potential and stress adaptation in cereals. Critical Rev. Plant Sci., 27,377-412. Bar-Tal A., Fergenbaun S. and Sparks D.L. (1991) Potassium-salinity interaction in irrigated corn. Irrig. Sci, 12, 27-35. Costa L.D., Vedove G.D., Gianquintoi G., Giovanardi R. and Peressotti A. (1997) Yield, water use efficiency and nitrogen uptake in potato: influence of drought stress. Potato Res., 40,19-34. Garcia A.L., Madrid R., Gimeno V., Rodriguez-Ortega W.M., Nicolas N. and Garcia-Sanchez F. (2011) the
effects of amino acids fertilization incorporated to the nutrient solution on mineral composition and growth in tomato seedlings. Spanish J. Agric. Res., 9,852861.
Genard H., Saos J.L.E., Hillard J., Tremolieres A. and Boucaud J. (1991) Effect of salinity on lipid composition, glycine betaine content and photosynthetic activity in chloroplasts of suaeda maritima. Plant Physiol. Biochem., 29,421-427.
Gonzalez-Perez P., Zhang R., Wang X., Ye J., and Huang D. (2015) Characterization of the amino acid composition of soils under organic and conventional management after addition of different fertilizers. J. Soil. Sediment, 15, 890-901. doi: 10.1007/s11368-014-1049-3
Hanson W.C. (1950) The photometric determination of phosphorus in fertilizers using the phosphovanadomolybdate complex. J. Sci. of Food and Agri., 1 , 172-173.
Hijmans R.J. (2003) The effect of climate change on global potato production. Amer. J. Potato Res., 80,271-279.
Hussain A., Ali S., Rizwan M., Ziaur Rehman M.Z., Hameed A., Hafeez F., Alamri S.A., Alyemeni M.N. and Wijaya L. (2018) Role of zinc-lysine on growth and chromium uptake in rice plants under Cr stress. J. Plant Growth Regul., 37, 1413-1422.
Jackson M.L. (1958) Soil chemical analysis. New Jersey: Prentice-Hall Inc. Englewood Cliffs.
Jeppsen R.B. (1991) Mineral supplementation in plants via amino acid chelation. Amer. Chem. Soc., 25, 320-331.
Jones D.L., Healey J.R., Willett V.B., Farrar J.F. and Hodge A. (2005) Dissolved organic nitrogen uptake by plants an important N uptake pathway? Soil Biol. Biochem., 37,413-423.
Khan A.S., Ahmad B., Jaskani M.J., Ahmad R. and Malik A.U. (2012) Foliar application of mixture of amino acids and seaweed (Ascophylum nodosum) extract improve growth and physicochemical properties of grapes. Inter. J. Agric. Biol., 14, 383388.
Lawlor D.W. (2002) Limitation to photosynthesis in water-deficited leaves: stomata vs. metabolism and the role of ATP. Ann. Bot, 89,871-885.
Levy D., Coleman W.K. and Veilleux R.E. (2013) Adaptation of potato to water shortage: irrigation management and enhancement of tolerance to drought and salinity. Amer. J. Potato Res., 90,186206.
Lipson D. and Nasholm T. (2001) The unexpected versatility of plants: Organic nitrogen use and availability in terrestrial ecosystems. Oecologia, 128,305-316.
Lobell D.B., Burke M.B., Tebaldi C., Mastrandrea M.D., Falcon W.P. and Naylor R.L. (2008) Prioritizing climate change adaptation needs for food security in 2030. Sci., 319,607-610.
Ma Q., Cao X., Xie Y., Xiao H., Tan X. and Wu L. (2017) Ehects of glucose on the uptake and metabolism of glycine in pakchoi (Brassica chinensis L.) exposed to various nitrogen sources. BMC Plant Biol., 17:58.
Masclaux-Daubresse C., Daniel-Vedele F., Dechorgnat J., Chardon F., Gaufichon L. and Suzuki A. (2010) Nitrogen uptake, assimilation and remobilization in plants: Challenges for sustainable and productive agriculture. Ann. Bot., 105,1141-1157.
Monneveux P., Ramirez D.A., Awais-Khan M., Raymundo R.M., Loayza H. and Quiroz R. (2014) Drought and heat tolerance evaluation in potato (Solanum tuberosum L.). Potato Res., 57,225-247.
Nasholm T., Kielland K. and Ganeteg, U. (2009) Uptake of organic nitrogen by plants. New Phytol., 182, 3148.
NoroozloY.A., Souri M.K. and Delshad M. (2019) Effects of foliar application of glycine and glutamine amino acids on growth and quality of sweet basil. Adv. Hort. Sci, 33,495501.
Noroozlo Y.A., Souri M.K. and Delshad M. (2019) Stimulation effects of foliar applied glycine and glutamine amino acids on lettuce growth. Open Agric, 4,164-172.
Nunes-Nesi A., Fernie A.R. and Stitt M. (2010) Metabolic and signaling aspects underpinning the regulation of plant carbon nitrogen interactions. Mol. Plant., 3,973-996.
Paungfoo-Lonhienne C., Lonhienne T.G., Rentsch D., Robinson N., Christie M., Webb R.I., et al. (2008) Plants can use protein as a nitrogen source without
assistance from other organisms. Proc. Natl. Acad. Sci, 105, 4524-4529.
Pérez-Jiménez M., Pazos-Navarro M., López-Marín J., Gálvez A., Varó P. and del Amor F.M. (2015) Foliar application of plant growth regulators changes the nutrient composition of sweet pepper (Capsicum annuum L.). Scientia Hortic., 194,188-93.
Rhodes D. and Hanson A. (1993) Quaternary ammonium and tertiary sulfonium compounds in higher plants. Ann. Rev. Plant Physiol. Plant Mol. Biol., 44,357-384.
Rizwan M., Ali S., Hussain A., Ali Q., Shakoor M.B., Ziaur-Rehman M., Farid M. and Asma M. (2017) Effect of zinc-lysine on growth, yield and cadmium uptake in wheat (Triticum aestivum L.) and health risk assessment. Chemosphere, 187, 35-42.
Sánchez A.S., Juárez M., Sánchez-Andreu J., Jordá J. and Bermúdez D. (2005) Use of humic substances and amino acids to enhance iron availability for tomato plants from applications of the chelate FeEDDHA. J. Plant Nutr, 28,1877-1886.
Shooshtari F.Z., Souri M.K., Hasandokht M.R. and Jari S.K. (2020) Glycine mitigates fertilizer requirements of agricultural crops: case study with cucumber as a high fertilizer demanding crop. Chem. Biol. Technol. Agric., 7:19.
Singh J. and Kaur L. (2009) Advances in potato chemistry and technology. In Bradshaw J.E. and Ramsay G. (Eds.), potato origin and Production. 67, pp. 1 -26. Academic Press is an imprint of Elsevier. USA.
Souri M.K. and Hatamian M. (2019) Aminochelates in plant nutrition: a review. J. of Plant Nutr., 42, 67-78.
Vreugdenhil D., Bradshaw J., Gebhardt C., Govers F., Mackerron D.K.L., Taylor M. and Ross H. (2007) Potato biology and biotechnology. In Kirkman M.A. (Eds.) Global Markets for Processed Potato Products. 2, Amsterdam, United Kingdom.
Wang X.L., Ye J., Gonzalez Perez P., Tang D.M. and Huang D.F. (2013) The impact of organic farming on the soluble organic nitrogen pool in horticultural soil under open field and greenhouse conditions: a case study. Soil Sci. Plant Nutr, 59, 237-248.
Xu W.Q., Zhu Q. and Hu C.H. (2017) The Structure of glycine dihydrate: implications for the crystallization of glycine from solution and its structure in outer space. Angew. Chem. Int. Edit., 56, 2030-2034.
Zhang L., Garneau M.G., Majumdar R., Grant J.,
Tegeder M. (2015) Improvement of pea biomass and seed productivity by simultaneous increase of phloem and embryo loading with amino acids. Plant J, 81,134-146.