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Evidence of nitrogen and potassium losses in soil columns cultivated with maize under salt stress

Evidências de perdas de nitrogênio e potássio em colunas de solo cultivadas com milho sob estresse salino

ABSTRACT

The aim of this study was to evaluate the accumulation of salts in the soil from irrigation water and of N and K from fertilization. The experiment was conducted in PVC columns (20 cm in diameter and 100 cm in height), filled with non-saline soil, and cultivated with maize. A completely randomized block design in a 4 x 4 factorial was used, with four levels of salinity (0.5, 2.5, 5.0 and 7.5 dS m-1), four N rates, and five replicates. Nitrogen was applied as urea and potassium nitrate at the following rates: N1: N recommendation for maize (2.6 g column-1); N2: 0.3 times (0.78 g column-1) the recommended N1 dose; N3 and N4 with N based on N1 and N2 doses, respectively, reduced proportionally based on the evapotranspiration reduction caused by salinity. After 74 days from sowing, root and soil samples were collected at different soil depths. The electrical conductivity of the saturated extract (ECe) and the concentration of ions (Ca2+, Na+, and Cl-) increased as a function of salinity and soil depth. The opposite was observed for the root system. The increase in salinity also resulted in K+ and NO3- accumulation in the soil column, mainly in treatments with higher N rates (N1 and N3). At the end of the experiment, 88% of the NO3- applied at the highest salinity treatment (7.5 dS m-1) and the highest N rate (N1) was below 20 cm soil depth, evidencing a N loss process caused by leaching.

Key words:
salinity; nitrate; nutrients leaching

RESUMO

Objetivou-se com o trabalho avaliar o acúmulo no solo de sais provenientes da água de irrigação e de N e K provenientes da adubação. O experimento foi conduzido em colunas de PVC (20 cm de diâmetro e 100 cm de altura), preenchidas com solo arenoso, não salino, cultivado com milho. Utilizou-se delineamento em blocos inteiramente casualizados em arrajamento fatorial 4 x 4, composto por quatro níveis de salinidade (0,5, 2,5, 5,0 e 7,5 dS m-1) e quatro doses de N, com cinco repetições. As quatro doses de N, aplicadas como ureia e nitrato de potássio, foram as seguintes: N1: seguindo a recomendação de N para o milho (2,6 g coluna-1); N2: 0,3 vezes N1 (0,78 g coluna-1); N3 e N4: Taxa reduzida de N1 e N2, respectivamente, com base na redução da evapotranspiração causada pela salinidade. Aos 74 dias após o plantio foram coletadas as raízes e amostras de diferentes camadas do solo. A condutividade elétrica do extrato saturado (CEes) e as concentrações de íons (Ca, Na e Cl) aumentaram em função da salinidade e da profundidade. O contrário foi observado no sistema radicular. O aumento da salinidade provocou o acúmulo de K e NO3- nas colunas de solo, principalmente nas maiores doses de N (N1 e N3). Para o tratamento de maior salinidade (7,5 dS m-1) e maior dose de N (N1) verificou-se que 88% do NO3- encontrava-se abaixo de 20 cm do solo ao final do experimento, mostrando perda por lixiviação.

Palavras-chave:
salinidade; nitrato; lixiviação de nutrientes

Introduction

Salt-stress effects on plant development are mainly due to osmotic and toxic components, which cause reduction in stomatal opening, photosynthetic activity, nutrient uptake and balance, transpiration, and plant growth (Azevedo Neto & Tabosa, 2000Azevedo Neto, A. D. de; Tabosa, J. N. Estresse salino em plântulas de milho: Parte II - Distribuição dos macronutrientes catiônicos e suas relações com sódio. Revista Brasileira de Engenharia Agrícola e Ambiental, v.4, p.165-171, 2000. https://doi.org/10.1590/S1415-43662000000200006
https://doi.org/10.1590/S1415-4366200000...
; Munns & Tester, 2008Munns, R.; Tester, M. Mechanisms of salinity tolerance. Annual Review of Plant Biology, v.59, p.651-668, 2008. https://doi.org/10.1146/annurev.arplant.59.032607.092911
https://doi.org/10.1146/annurev.arplant....
; Willadino & Camara, 2010Willadino, L.; Camara, T. R. Tolerância das plantas à salinidade: Aspectos fisiológicos e bioquímicos. Enciclopédia Biosfera, v.6, p.1-23, 2010.; Prisco et al., 2016Prisco, J. T.; Gomes Filho, E.; Miranda, R. de S. Physiology and biochemistry of plants growing under salt stress. In: Gheyi, H. R.; Dias, N. da S.; Lacerda, C. F. de; Gomes Filho, E. Manejo da salinidade na agricultura: Estudo básico e aplicados. 2.ed. Fortaleza: INCTSal, 2016. Cap.12, p.163-180.; Tagliaferre et al., 2016Tagliaferre, C.; Guimarães, D. U. G.; Gonçalves, L. J.; Amorim, C. H. F.; Campos, W. V.; Rocha, F. A. Absorption of nutrients by cowpea irrigated with saline water under different leaching fractions. Revista Brasileira de Engenharia Agrícola e Ambiental, v.20, p.1067-1071, 2016. https://doi.org/10.1590/1807-1929/agriambi.v20n12p1067-1071
https://doi.org/10.1590/1807-1929/agriam...
). The reduction in water uptake and plant (root and shoot) growth caused by salinity culminates with the reduced capacity of the plant to extract nutrients from the soil, especially those required in larger quantities by plants (Shenker et al., 2003Shenker, M.; Ben-Gal, A.; Shani, U. Sweet maize response to combined nitrogen and salinity environmental stresses. Plant Soil, v.256, p.139-147, 2003. https://doi.org/10.1023/A:1026274015858
https://doi.org/10.1023/A:1026274015858...
; Ramos et al., 2012Ramos, T. B.; Simunek, J.; Gonçalves, M. C.; Martins, J. C.; Prazeres, A.; Pereira, L. S. Two-dimensional modeling of water and nitrogen fate from sweet sorghum irrigated with fresh and blended saline waters. Agricultural Water Management, v.111, p.87-104, 2012. https://doi.org/10.1016/j.agwat.2012.05.007
https://doi.org/10.1016/j.agwat.2012.05....
; Lacerda et al., 2016bLacerda, C. F. de; Ferreira, J. F. S.; Liu, X.; Suarez, D. L. Evapotranspiration as a criterion to estimate nitrogen requirement of maize under salt stress. Journal of Agronomy and Crop Science, v.202, p.192-202, 2016b. https://doi.org/10.1111/jac.12145
https://doi.org/10.1111/jac.12145...
).

Although positive responses to nutrient supplementation have been observed in plants under salt-stress (Hu & Schmidhalter, 2005Hu, Y.; Schmidhalter, U. Drought and salinity: A comparison of their effects on mineral nutrition of plants. Journal of Plant Nutrition and Soil Science, v.168, p.541-549, 2005. https://doi.org/10.1002/jpln.200420516
https://doi.org/10.1002/jpln.200420516...
), especially under conditions of low soil fertility (Grattan & Grieve, 1999Grattan, S. R.; Grieve, C. M. Salinity-mineral nutrient relations in horticultural crops. Scientia Horticulturae, v.78, p.127-157, 1999. https://doi.org/10.1016/S0304-4238(98)00192-7
https://doi.org/10.1016/S0304-4238(98)00...
), these responses are not present at the same intensity as found in non-saline conditions (Irshad et al., 2008Irshad, M.; Eneji, A. E.; Yasuda, H. Comparative effect of nitrogen sources on maize under saline and non-saline conditions. Journal of Agronomy and Crop Science, v.194, p.256-261, 2008. https://doi.org/10.1111/j.1439-037X.2008.00310.x
https://doi.org/10.1111/j.1439-037X.2008...
; Lacerda et al., 2016aLacerda, C. F. de; Costa, R. N. T.; Bezerra, M. A.; Neves, A. L. R.; Sousa, G. G. de; Gheyi, H. R. Estratégias de manejo para uso de água salina na agricultura. In: Gheyi, H. R.; Dias, N. da S.; Lacerda, C. F. de; Gomes Filho, E. Manejo da salinidade na agricultura: Estudo básico e aplicados. 2.ed. Fortaleza: INCTSal, 2016a. Cap.21, p.337-352.,bLacerda, C. F. de; Ferreira, J. F. S.; Liu, X.; Suarez, D. L. Evapotranspiration as a criterion to estimate nitrogen requirement of maize under salt stress. Journal of Agronomy and Crop Science, v.202, p.192-202, 2016b. https://doi.org/10.1111/jac.12145
https://doi.org/10.1111/jac.12145...
), resulting in nutrient losses and reduced N use efficiency. As a consequence, a large percentage of the nutrients applied to the soil can be lost mainly by leaching, causing economic losses and contamination of ground water (Shenker et al., 2003Shenker, M.; Ben-Gal, A.; Shani, U. Sweet maize response to combined nitrogen and salinity environmental stresses. Plant Soil, v.256, p.139-147, 2003. https://doi.org/10.1023/A:1026274015858
https://doi.org/10.1023/A:1026274015858...
; Segal et al., 2010Segal, E.; Shouse, P.; Poss, J. A.; Crohn, D. M.; Bradford, S. A. Recommendations for nutrient management plans in a semi-arid environment. Agriculture Ecosystems & Environment, v.137, p.317-328, 2010. https://doi.org/10.1016/j.agee.2010.03.002
https://doi.org/10.1016/j.agee.2010.03.0...
; Ramos et al., 2012Ramos, T. B.; Simunek, J.; Gonçalves, M. C.; Martins, J. C.; Prazeres, A.; Pereira, L. S. Two-dimensional modeling of water and nitrogen fate from sweet sorghum irrigated with fresh and blended saline waters. Agricultural Water Management, v.111, p.87-104, 2012. https://doi.org/10.1016/j.agwat.2012.05.007
https://doi.org/10.1016/j.agwat.2012.05....
; Mendes et al., 2016Mendes, W. da C.; Alves Júnior, J.; Cunha, P. C. R. da; Silva, A. R. da; Evangelista, A. W. P.; Casaroli, D. Potassium leaching in different soils as a function of irrigation depths. Revista Brasileira de Engenharia Agrícola e Ambiental, v.20, p.972-977, 2016. https://doi.org/10.1590/1807-1929/agriambi.v20n11p972-977
https://doi.org/10.1590/1807-1929/agriam...
). This problem is aggravated in the case of nutrients with high soil mobility, such as nitrate. The objective of this study was thus to measure and quantify the losses of N and K from soil cultivated with maize under salt-stress using soil columns.

Material and Methods

The experiment was conducted at the US Salinity Laboratory (ARS - USDA), Riverside, CA (33o 59’ N; 117o 21’ W), from September 13th to November 26th, 2013. During the experiment the average maximum, minimum, and average air temperature were 26.7, 12.8 and 20 ºC, respectively. Maize plants were grown in columns of polyvinyl chloride (PVC) with 20 cm in diameter and 100 cm in length. Columns were filled with sieved (5-mm mesh) non-saline (ECe of 1.6 dS m-1) sandy loam soil with pH 6.8, collected from a site near to the experimental area. A nylon mesh and a cap adapted with a drainage pipe were attached to the bottom of each PVC tube to retain the soil, but allow the drainage water to pass and to be collected into 1-L glass bottles with wide mouths set below the drainage pipes (Lacerda et al., 2016bLacerda, C. F. de; Ferreira, J. F. S.; Liu, X.; Suarez, D. L. Evapotranspiration as a criterion to estimate nitrogen requirement of maize under salt stress. Journal of Agronomy and Crop Science, v.202, p.192-202, 2016b. https://doi.org/10.1111/jac.12145
https://doi.org/10.1111/jac.12145...
).

The experiment was conducted in a completely randomized block design following a 4 x 4 factorial arrangement, composed of four levels of salinity (S1 = 0.5; S2 = 2.5; S3 = 5.0; and S4 = 7.5 dS m-1) and four N rates, with five replications. Saline treatments were obtained by adding NaCl, CaCl2.2H2O, and MgCl2.6.H2O salts in a 7:2:1 molar charge ratio (Mc), according to the approximate relationship between ECw and concentration (mmolc L-1 = ECw x 10). Irrigation was performed every other day. During the experiment, two rain events occurred (13 and 25 mm). The average leaching fraction for treatments S1, S2, S3 and S4 were respectively, 0.16, 0.17, 0.19, and 0.23, considering both irrigation and rainfall quantities.

The four N rates, applied as urea and potassium nitrate, were as follows: N1: N recommendation for maize in California (206 kg ha-1); N2: 0.3 times the N recommendation for maize in California (62 kg ha-1), N3, reduction based on N1 considering the decrease in evapotranspiration caused by salinity in the previous stage; N4, reduction based on N2 considering the decrease in evapotranspiration caused by salinity in the previous stage. The proportions of N for all treatments were described by Lacerda et al. (2016b)Lacerda, C. F. de; Ferreira, J. F. S.; Liu, X.; Suarez, D. L. Evapotranspiration as a criterion to estimate nitrogen requirement of maize under salt stress. Journal of Agronomy and Crop Science, v.202, p.192-202, 2016b. https://doi.org/10.1111/jac.12145
https://doi.org/10.1111/jac.12145...
.

The N and K application (120 kg ha-1 of K2O) in each treatment was distributed during the vegetative growth stage as follows: 15% at sowing; 25%-20 days after sowing (DAS); 30%-35 DAS, and 30%-50 DAS. The other nutrients were applied following technical recommendations for maize in California (Lacerda et al., 2016bLacerda, C. F. de; Ferreira, J. F. S.; Liu, X.; Suarez, D. L. Evapotranspiration as a criterion to estimate nitrogen requirement of maize under salt stress. Journal of Agronomy and Crop Science, v.202, p.192-202, 2016b. https://doi.org/10.1111/jac.12145
https://doi.org/10.1111/jac.12145...
).

Five seeds of maize (Zea mays L.) cv. Nothstine Dent OG Lot # 41629 (Johnny’s Selected Seeds, Winslow, ME, USA) were sown per column. Thinning was done seven DAS, leaving only one plant per column. The treatments with saline waters were initiated eight DAS.

Four soil samples per column, at different depths (0-20, 20-40, 40-60, and 60-80 cm), were collected at the end of the experiment (74 DAS). The electrical conductivity of the soil saturation extract (ECe) was determined according to Richards (1954)Richards, L. A. Diagnosis and improvement of saline and alkali soils. Washington: United States Salinity Laboratory, 1954. 160p.. The concentrations of nitrate, K, Na, Ca and Cl were also determined in the saturation extract. Concentrations of K, Na and Ca were obtained by plasma optical emission spectrometry (AOAC, 1990AOAC - Association of Official Agricultural Chemists. Official methods of analysis. 15.ed. Washington: AOAC, 1990. 1289p.), Cl by the methodology given by Gaines et al. (1984)Gaines, T. P.; Paker, M. B.; Gascho, G. J. Automated determination of chorides in soil and plant tissue by sodium nitrate extration. Agronomy Journal, v.76, p.371-374, 1984. https://doi.org/10.2134/agronj1984.00021962007600030005x
https://doi.org/10.2134/agronj1984.00021...
and the nitrate concentration according to the salicylic acid method (Cataldo et al., 1975Cataldo, D. A.; Haroon, M.; Schrader, L. E.; Youngs, V. L. Rapid colorimetric determination of nitrate in plant tissue by nitration of salicylic acid. Communications in Soil Science and Plant Analysis, v.6, p.71-80, 1975. https://doi.org/10.1080/00103627509366547
https://doi.org/10.1080/0010362750936654...
). The root biomass of each soil column was also measured at the end of the experiment.

The differences among salt treatments, N application, and the interaction between salt and N were tested using a twoway analysis of variance (F test). The regression analysis and Tukey’s test were used to evaluate the effects of salinity and N application, respectively.

Results and Discussion

The results of the analysis of variance related to the effects of salinity (S) of the irrigation water, nitrogen rates (N), and the interactions between S x N, and between S and N with soil depth layers (L) are given in Table 1.

Table 1
Summary of the analysis of variances of the data for root dry mass (RDM), saturation extract electrical conductivity (ECe), sodium (Na), calcium (Ca), magnesium (Mg), chloride (Cl), potassium (K), and nitrate (NO3), in soil cultivated with maize as related to different levels of salinity, nitrogen rates, and soil layers

There was a statistically significant interaction at a 1% probability level (F test) between the salinity of the irrigation water and the soil layers for all parameters evaluated (ECe, salt, and mineral nutrients). Salinity of the irrigation water is one of the main factors that contributes to lesser utilization of nutrients by plants, thus increasing their accumulation in the soil. In turn, development of the root system is compromised due to the increased concentration of salts in the soil (Willadino & Camara, 2010Willadino, L.; Camara, T. R. Tolerância das plantas à salinidade: Aspectos fisiológicos e bioquímicos. Enciclopédia Biosfera, v.6, p.1-23, 2010.; Prisco et al., 2016Prisco, J. T.; Gomes Filho, E.; Miranda, R. de S. Physiology and biochemistry of plants growing under salt stress. In: Gheyi, H. R.; Dias, N. da S.; Lacerda, C. F. de; Gomes Filho, E. Manejo da salinidade na agricultura: Estudo básico e aplicados. 2.ed. Fortaleza: INCTSal, 2016. Cap.12, p.163-180.; Santos et al., 2016Santos, R. V.; Cavalcante, L. F.; Vital, A. F. M.; Lacerda, C. F. de; Souza, E. R. de; Lima, G, S. de. Interações salinidade-fertilidade do solo. In: Gheyi, H. R.; Dias, N. da S.; Lacerda, C. F. de; Gomes Filho, E. Manejo da salinidade na agricultura: Estudo básico e aplicados. 2.ed. Fortaleza: INCTSal, 2016. Cap.18, p.277-294.; Tagliaferre et al., 2016Tagliaferre, C.; Guimarães, D. U. G.; Gonçalves, L. J.; Amorim, C. H. F.; Campos, W. V.; Rocha, F. A. Absorption of nutrients by cowpea irrigated with saline water under different leaching fractions. Revista Brasileira de Engenharia Agrícola e Ambiental, v.20, p.1067-1071, 2016. https://doi.org/10.1590/1807-1929/agriambi.v20n12p1067-1071
https://doi.org/10.1590/1807-1929/agriam...
).

The root dry mass (RDM) decreased with increasing soil depth and with the increased salinity of the applied water (Figure 1).

Figure 1
Effect of salinity of irrigation water (0.5, 2.5, 5 and 7.5 dS m-1) and soil depth on root dry mass per plant

The data agree with previous observations that the plant root system, especially for grasses, is concentrated in the top 30 cm of soil, decreasing with depth from the surface. However, the decrease in root dry mass was accentuated by the increase in the salt concentration in the irrigation water, as verified by the statistically significant interaction S x L (Table 1). This effect became more evident in the first 10 cm of the soil, where the plants that received low-salt irrigation water (0.5 dS m-1) had 4.5 g of roots while the treatment with the highest concentration of salts had a mean of 1.2 g.

Salinity is one of the main factors that reduce crop productivity. Inhibition of plant growth (root and shoot) due to salt-stress may be caused by the reduction of osmotic potential and/or excessive accumulation of ions, which may induce ionic toxicity, nutritional imbalance or both (Munns & Tester, 2008Munns, R.; Tester, M. Mechanisms of salinity tolerance. Annual Review of Plant Biology, v.59, p.651-668, 2008. https://doi.org/10.1146/annurev.arplant.59.032607.092911
https://doi.org/10.1146/annurev.arplant....
; Lacerda et al., 2016bLacerda, C. F. de; Ferreira, J. F. S.; Liu, X.; Suarez, D. L. Evapotranspiration as a criterion to estimate nitrogen requirement of maize under salt stress. Journal of Agronomy and Crop Science, v.202, p.192-202, 2016b. https://doi.org/10.1111/jac.12145
https://doi.org/10.1111/jac.12145...
). Salinity effects (osmotic, toxic and nutritional) reduce the net assimilation of CO2, accelerate the senescence of mature leaves, and inhibit leaf expansion, thus reducing the area destined to the photosynthetic process (Lacerda et al., 2003Lacerda, C. F. de; Cambraia, J.; Oliva, M. A.; Ruiz, H. A.; Prisco, J. T. Solute accumulation and distribution during shoot and leaf development in two sorghum genotypes under salt stress. Environmental and Experimental Botany, v.49, p.107-120, 2003. https://doi.org/10.1016/S0098-8472(02)00064-3
https://doi.org/10.1016/S0098-8472(02)00...
; Munns & Tester, 2008Munns, R.; Tester, M. Mechanisms of salinity tolerance. Annual Review of Plant Biology, v.59, p.651-668, 2008. https://doi.org/10.1146/annurev.arplant.59.032607.092911
https://doi.org/10.1146/annurev.arplant....
).

The soil chemical characteristics were affected by the treatments, as evidenced by the increase in the electrical conductivity of the soil-saturated extract as a function of salinity of irrigation water (Figure 2A). As expected, the highest ECe values were observed in the treatment with the highest salt concentration (S4 = 7.5 dS m-1), while the lowest values occurred in the treatments with lower salt concentrations, respectively, S1 (0.5 dS m-1) and S2 (2.5 dS m-1). It was also verified that the increase in ECe in deeper soil layers was caused mainly by the downwards flow of the irrigation water causing the leaching of salts and increase in ECe with depth (Figure 2A).

Figure 2
Electrical conductivity (A), soluble Na (B), soluble Ca (C), soluble Cl (D), soluble Mg (E) and soluble K (F) in saturation extract of soil in different depths as a function of irrigation water salinity (S1 - 0.5; S2 - 2.5; S3 - 5.0 and S4 - 7.5 dS m-1)

Water entering the soil is able to solubilize the chemical elements (mainly the chlorides and sulphates) in the upper part of the profile and translocate them to deeper layers (Brady & Weil, 2013Brady, N. C.; Weil, R. R. Elementos da natureza e propriedades dos solos. 3.ed. Porto Alegre: Bookman, 2013. 704p.; Mendes et al., 2016Mendes, W. da C.; Alves Júnior, J.; Cunha, P. C. R. da; Silva, A. R. da; Evangelista, A. W. P.; Casaroli, D. Potassium leaching in different soils as a function of irrigation depths. Revista Brasileira de Engenharia Agrícola e Ambiental, v.20, p.972-977, 2016. https://doi.org/10.1590/1807-1929/agriambi.v20n11p972-977
https://doi.org/10.1590/1807-1929/agriam...
). Irrigation water itself (saline or brackish water) contributes to the increase in salt concentration and, consequently, to the increase in soil electrical conductivity (Ayers & Westcot, 1999Ayers, R. S.; Westcot, D. W. A qualidade de água na agricultura. 2.ed. Campina Grande: UFPB, 1999. 153p.).

An increase was observed in the concentration of soluble sodium, calcium, magnesium and chloride in the soil with increasing irrigation water salinity (Figures 2B, C, D and E). This trend is due to the chemical composition of the saline waters used for irrigation. According to Medeiros et al. (2016)Medeiros, J.F.; Gheyi, H.R.; Costa, A.R.F.C.; Tomaz, H.V.C. Manejo do solo-água-planta em áreas afetadas por sais. In: Gheyi, H. R.; Dias, N. da S.; Lacerda, C. F. de; Gomes Filho, E. Manejo da salinidade na agricultura: Estudo básico e aplicados. 2.ed. Fortaleza: INCTSal, 2016. Cap.20, p.319-335., the main elements present in saline water are the cations Na+, Ca2+ and Mg2+ and the anions Cl-, SO42- and HCO3-. Thus, the accumulation of Ca2+, Mg2+, Cl- and, especially Na+ in soils irrigated with saline waters is to be expected, and the higher the concentration of these elements in the irrigation water, the greater the accumulation of these constituents in the soil (Ayers & Westcot, 1999Ayers, R. S.; Westcot, D. W. A qualidade de água na agricultura. 2.ed. Campina Grande: UFPB, 1999. 153p.).

All treatments received the same amount of potassium, but the potassium distribution in the soil was similar to that of other cations, that is, more accentuated in the treatments with higher concentration of salts (Figure 2F) and higher nitrogen rates (Figure 3).

Figure 3
Mean values of potassium concentration in the soil saturation extracts in response to the combination of four levels (S1 to S4) of salinity (0.5, 2.5, 5.0 and 7.5 dS m-1), and four rates of N (N1 - N recommendation for maize (2.6 g column-1); N2 - 0.3 times of recommendation N1 (0.78 g column-1); N3 and N4 - Reduced rate of N1 and N2, respectively, based on the reduction in evapotranspiration caused by salinity. Each bar represents the average value of the four layers of soil

The largest K concentrations occurred in the treatment with the highest N and salt in the irrigation water (Figure 3). The concentration of K in the soil extracts of the S4N1 treatment was approximately 153% greater than found in the treatments with lower N levels and lower salt concentration (S1N2 and S1N4). Root growth under salt-stress was restricted by both the osmotic and toxic effects of the salt ions (Figure 1), which resulted in lower nutrient uptake by plants and inhibited translocation of mineral nutrients, especially K (Figures 2F and Figure 3). Shabala & Cuin (2008)Shabala, S.; Cuin, T. A. Potassium transport and plant salt tolerance. Physiologia Plantarum, v.133, p.651-669, 2008. https://doi.org/10.1111/j.1399-3054.2007.01008.x
https://doi.org/10.1111/j.1399-3054.2007...
attributed the low potassium use efficiency in plants under salt stress to the physicochemical similarities between Na+ and K+. According to the authors, sodium competes with potassium inside the plant for ionic transport sites and metabolic processes.

Low nitrate accumulation (NO3-) in the soil was recorded in treatments with different N rates and irrigation using fresh water (S1N1, S1N2, S1N3 and S1N4) (Figure 4A), especially in treatments with reduced amounts of N (S1N2 and S1N4).

Figure 4
Soil nitrate accumulation caused by irrigation water salinity and four rates of nitrogen (N1 to N4). A - 0.5 (S1); B - 2.5 (S2); C - 5.0 (S3); D - 7.5 dS m-1 (S4)

Nitrate was the only evaluated parameter that presented a significant interaction (salinity x soil layer x N rate), as shown in Table 1. In treatments with higher levels of nitrogen (N1 and N3), NO3- accumulation was observed in the deeper regions of the soil. This effect became more evident when higher salt concentrations were used (starting at 2.5 dS m-1), according to Figures 4B, C and D. In the treatment with saline water (7.5 dS m-1) and 100% of N recommendation for maize crop (S4N1), 88% of nitrate was below 20 cm of soil depth.

The soil extract results showed a high loss of N due to the leaching of NO3-, as well as to the low N utilization by the crop under saline irrigation. Under salt-stress conditions, the processes of absorption and assimilation of nutrients by plants are affected, mainly nitrate, which is the main source of nitrogen in agricultural soils and, most frequently, limits the growth of plants (Meloni et al., 2004Meloni, D. A.; Gulotta, M. R.; Martínez, C. A.; Olivia, M. A. The effects of salt stress on growth, nitrate reduction and proline and glycinebetaine accumulation in Prosopis alba. Brazilian Journal Plant Physiology, v.16, p.39-46, 2004. https://doi.org/10.1590/S1677-04202004000100006
https://doi.org/10.1590/S1677-0420200400...
). The marked reduction in root growth in treatments with elevated salinity (Figure 1) reduces the potential of utilization of N and others nutrients (Shenker et al., 2003Shenker, M.; Ben-Gal, A.; Shani, U. Sweet maize response to combined nitrogen and salinity environmental stresses. Plant Soil, v.256, p.139-147, 2003. https://doi.org/10.1023/A:1026274015858
https://doi.org/10.1023/A:1026274015858...
; Segal et al., 2010Segal, E.; Shouse, P.; Poss, J. A.; Crohn, D. M.; Bradford, S. A. Recommendations for nutrient management plans in a semi-arid environment. Agriculture Ecosystems & Environment, v.137, p.317-328, 2010. https://doi.org/10.1016/j.agee.2010.03.002
https://doi.org/10.1016/j.agee.2010.03.0...
; Ramos et al., 2012Ramos, T. B.; Simunek, J.; Gonçalves, M. C.; Martins, J. C.; Prazeres, A.; Pereira, L. S. Two-dimensional modeling of water and nitrogen fate from sweet sorghum irrigated with fresh and blended saline waters. Agricultural Water Management, v.111, p.87-104, 2012. https://doi.org/10.1016/j.agwat.2012.05.007
https://doi.org/10.1016/j.agwat.2012.05....
). Moreover, the increase in electrical conductivity can affect the movement of nutrients in the soil because it reduces its displacement by mass flow, mainly restricting nitrogen and potassium uptake (Santos et al., 2016Santos, R. V.; Cavalcante, L. F.; Vital, A. F. M.; Lacerda, C. F. de; Souza, E. R. de; Lima, G, S. de. Interações salinidade-fertilidade do solo. In: Gheyi, H. R.; Dias, N. da S.; Lacerda, C. F. de; Gomes Filho, E. Manejo da salinidade na agricultura: Estudo básico e aplicados. 2.ed. Fortaleza: INCTSal, 2016. Cap.18, p.277-294.).

Nutrients losses by leaching below the root zone may be more significant in systems where plants are subject to saline stress. In this situation, plants tend to decrease growth and water use, mainly due to the osmotic effects and salinity toxicity of sodium and chloride (Lacerda et al., 2003Lacerda, C. F. de; Cambraia, J.; Oliva, M. A.; Ruiz, H. A.; Prisco, J. T. Solute accumulation and distribution during shoot and leaf development in two sorghum genotypes under salt stress. Environmental and Experimental Botany, v.49, p.107-120, 2003. https://doi.org/10.1016/S0098-8472(02)00064-3
https://doi.org/10.1016/S0098-8472(02)00...
; Munns & Tester, 2008Munns, R.; Tester, M. Mechanisms of salinity tolerance. Annual Review of Plant Biology, v.59, p.651-668, 2008. https://doi.org/10.1146/annurev.arplant.59.032607.092911
https://doi.org/10.1146/annurev.arplant....
; Lacerda et al., 2016bLacerda, C. F. de; Ferreira, J. F. S.; Liu, X.; Suarez, D. L. Evapotranspiration as a criterion to estimate nitrogen requirement of maize under salt stress. Journal of Agronomy and Crop Science, v.202, p.192-202, 2016b. https://doi.org/10.1111/jac.12145
https://doi.org/10.1111/jac.12145...
). Furthermore, leaching losses had the most significance for nutrients needed in higher concentrations by the plant (such as N) and fertilizers highly soluble in water, such as containing nitrate.

Conclusions

  1. Nitrate and potassium accumulation, especially in the soil layers below 20 cm depth, was observed in the treatments with high salinity, evidence of losses of these elements by leaching below the rootzone.

  2. The increase in electrical conductivity of irrigation water caused a significant reduction in maize root biomass, especially in the upper 20 cm of soil.

Acknowledgments

Authors acknowledge the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Instituto Nacional de Ciência e Tecnologia em Salinidade (INCTSal), and Universidade Federal do Ceará, Brazil, for financial support provided to the senior author. Additional support, such as technical assistance and consumables, was provided by US Salinity Laboratory (ARS/USDA).

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Publication Dates

  • Publication in this collection
    Aug 2018

History

  • Received
    10 Oct 2017
  • Accepted
    12 Apr 2018
  • Published
    30 June 2018
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