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Revista Brasileira de Ciência do Solo

On-line version ISSN 1806-9657

Rev. Bras. Ciênc. Solo vol.38 no.6 Viçosa Nov./Dec. 2014

http://dx.doi.org/10.1590/S0100-06832014000600018 

DIVISÃO 3 - USO E MANEJO DO SOLO
COMISSÃO 3.1 - FERTILIDADE DO SOLO E NUTRIÇÃO DE PLANTAS

 

Effect of potassium sources on the antioxidant activity of eggplant1

 

Fontes potássicas alterando a atividade de antioxidante da berinjela

 

 

Douglas José MarquesI; Fernando BroettoII; Mozart Martins FerreiraIII; Allan Klynger da Silva LobatoIV; Fabricio William de ÁvilaV; Fabricio José PereiraVI

IProfessor, Universidade José do Rosário Vellano - UNIFENAS. Campus Rod. MG, 179, km 0. CEP 37130-000 Alfenas (MG), Brasil. E-mail: douglasjmarques81@yahoo.com.br
IIProfessor, Universidade Estadual Paulista, Campus de Botucatu. Distrito de Rubião Júnior, s/n. CEP 18618-970 Botucatu (SP), Brasil. E-mail: broetto@ibb.unesp.br
IIIProfessor, Departamento de Ciência do Solo, Universidade Federal de Lavras - UFLA. Caixa Postal 3037. CEP 37200-000 Lavras (MG), Brasil. E-mail: mozartmf@ufla.br
IVProfessor, Universidade Federal Rural da Amazônia. Av. Presidente Tancredo Neves, 2501, Bairro Montese. CEP 66077-901 Paragominas (PA), Brasil. E-mail: allanllobato@yahoo.com.br
VProfessor, Universidade Estadual do Centro-Oeste-UNICENTRO. Rua Simeão Camargo Varela de Sá, 03, Vila Carli. CEP 85040-080 Guarapuava (PR), Brasil. E-mail: fabriciowilliamavila@yahoo.com.br
VIProfessor, Departamento de Biologia, UFLA. E-mail: fabriciopereira@dbi.ufla.br

 

 


ABSTRACT

Potassium participates in the essential processes in plant physiology, however, the effects of K sources on plant metabolism have been little studied. Also, in certain cases, K sources and concentrations may cause undesirable effects, e.g., soil salinization. The objective was to evaluate the effect of K sources and levels on the enzyme activity of the antioxidant system and protein content in eggplant (Solanum melongena L.) leaves and to determine the most suitable K sources for these physiological characteristics. The experiment was conducted in randomized blocks, in a 2 × 4 factorial design, consisting of two K sources (KCl and K2SO4) and rates (250, 500, 750, and 1000 kg ha-1 K2O), with four replications. The following variables were evaluated: plant height, number of leaves per plant, superoxide dismutase (SOD), catalase (CAT), and leaf protein content. There was an increase in CAT activity with increasing K levels until 30 days after transplanting (DAT), when K2SO4 was applied and until 60 DAT, when KCl was used; after this period, the enzyme activity decreased under both sources. The activity of SOD increased in the presence of KCl, but was reduced with the application of K2SO4. For both K sources, increasing rates reduced the protein content and number of leaves per plant, and this reduction was greater under KCl application. Thus it was concluded that KCl tends more strongly to salinize the soil than K2SO4. Both for KCl and for K2SO4, the increasing rates adversely affected the activities of CAT and SOD and the levels of leaf protein in eggplant. The potential of KCl to reduce the enzyme activity of SOD and CAT, leaf protein content and plant growth of eggplant was stronger than that of K2SO4.

Index terms: Solanum melongena L., potassium, superoxide dismutase, catalase, protein


RESUMO

O potássio participa dos processos essenciais na fisiologia da planta; contudo, os efeitos de fontes potássicas no metabolismo das plantas têm sido pouco estudados. Além disso, diferentes fontes e concentrações de K podem levar a efeitos indesejados como a salinização do solo. Dessa forma, objetivou-se avaliar o efeito de fontes e doses de K sobre a atividade de enzimas do sistema antioxidante e o teor de proteínas em folhas de berinjela, bem como qual das fontes de K pode ser mais adequada em razão dessas características fisiológicas (Solanum melongena L.). O experimento foi conduzido em blocos casualizados e esquema fatorial 2 × 4, sendo os fatores duas fontes (KCl e K2SO4) e doses de K (250, 500, 750 e 1000 kg ha-1 de K2O), com quatro repetições. As variáveis avaliadas foram: altura das plantas, número de folhas por planta, atividade da superóxido dismutase (SOD), catalase (CAT) e teor foliar de proteína. Observou-se aumento na atividade da CAT com a elevação das doses de K até os 30 dias após o transplante (DAT) para K2SO4 e até 60 DAT para KCl; após esse período a atividade da enzima reduziu em ambas as fontes. A atividade da SOD aumentou na presença do KCl, mas reduziu com a aplicação do K2SO4. Para ambas as fontes de K, o aumento das doses promoveu redução no teor de proteínas e no número de folhas das plantas, sendo essa redução maior com a utilização do KCl. Dessa forma, concluiu-se que o KCl apresentou maior poder de salinização do solo em comparação ao K2SO4. Tanto para KCl quanto para K2SO4, a elevação das doses influenciou negativamente as atividades da CAT e SOD e os teores de proteína foliares em berinjela. O KCl apresentou maior potencial de redução das atividades das enzimas SOD e CAT dos teores foliares de proteínas e do desenvolvimento das plantas de berinjela.

Termos de indexação: Solanum melongena L., potássio, superóxido dismutase, catalase, proteina


 

 

INTRODUCTION

Plants have a high requirement for K and one of the reasons is the need to maintain a high K content in the cytoplasm, mainly to ensure enzyme activity (Malavolta, 2006). Another reason is that K in cytosol and chloroplast stroma is required at high concentrations to maintain anion neutralization and an appropriate pH level for cell functioning (Marschner, 1995). Also, K can participate in the control of stomatal opening and closing which is essential for photosynthesis (Steineck & Haeder, 1978). Despite its importance, excess K reduces the soil osmotic potential, making the soil saline, resulting in a modified soil in which the growth of most species is prejudiced by the presence of high concentrations of soluble salts, exchangeable Na, or both in the rhizosphere (SSSA, 2008).

Among the potash mineral fertilizers available on the Brazilian market, potassium chloride (KCl) is the most popular, due to the abundant supply and best value for money. Aside from KCl, potassium sulfate (K2SO4) and potash and magnesium sulphate (K2SO4.2MgSO4), other K sources are widely used in different agricultural segments in Brazil (Ernani et al., 2007). These K sources induce different salinity levels in the soil; for example, KCl has a higher salt content than K2SO4 (Kamburova & Kirilov, 2008). However, there are no studies that prove the higher efficiency of this source for eggplant. In the case of some vegetables, e.g., potato and eggplant, KCl application has resulted in lower yields compared to potassium sulfate (Wuzhong, 2002).

Salinity can restrict the absorption of water and nutrients, reduce photosynthetic processes and increase respiration, inducing a reduction in plant growth (Khadri et al., 2006). In the case of water deficit, the activity of the enzyme system and the production of compounds related to the antioxidant system of plants are altered (Chaves et al., 2002). This plant response occurs due to excessive accumulation of reactive oxygen species (ROS) in plant cells, in particular of superoxide, hydroxyl radical and hydrogen peroxide (Moller et al., 2007). Salinity can promote an intense ROS production that can lead to the degradation of proteins and membranes, reducing photosynthesis and plant growth (Bose et al., 2014). Among the enzymatic mechanisms involved in detoxification of ROS, there are the isoforms of the enzyme superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX), and peroxidase phenols (POX). Superoxide dismutase acts by converting O2- into H2O2 and is localized mainly in the mitochondria and chloroplasts. These organelles generate most of the ROS in plant cells (Apel & Hirt, 2004). Peroxidades and catalases convert H2O2 into water and molecular oxygen, which are harmless to plants (Moller et al., 2007). Although the salinization leads to the production of ROS, at certain concentrations, K has an effect of reducing the harmful effects of salinization and ROS, mitigating stress effects (Abbasi et al., 2014). This effect has been widely investigated in view of the need to understand its relationship with salinity and stress tolerance better.

Thus, this study aimed to evaluate the effect of K sources and levels on the development, enzyme activity of the antioxidant system and the protein content of eggplants.

 

MATERIAL AND METHODS

The experiment was carried out at the Faculty of Agricultural Sciences of the São Paulo State University, Botucatu, SP (lat 22º 51' S, long 48º 26' W; 815 m asl). The climate was classified as Cwa, according to the international classification of Köppen (Cunha & Martins, 2009), which is a warm temperate climate with rainy summers and dry winters, at an average temperature below 17 ºC in the coldest month and above 23 ºC in the hottest month. We used eggplant cultivar Embu. The experiment was arranged in a randomized block factorial design with two K sources (KCl and K2SO4) × four K2O rates (250, 500, 750, and 1000 kg ha-1 K2O), with four replications. The K2O levels were defined according to recommendations of Raij et al. (1996) for treatments and equivalent K values per pot for eggplant (Table 1). Equivalent K2O contents per pot were calculated, considering 58 % for KCl and 44 % for K2SO4. The soil was classified as a medium-textured Latossolo Vermelho distroférrico (Oxisol) (Embrapa, 1997), containing 615 g kg-1 sand, 45 g kg-1 silt and 340 g kg-1 clay in the 0-20 cm layer. The soil was sieved (5 mm), resulting in a total volume of 32 L, and distributed in plastic pots. The soil chemical characteristics at the beginning of the experiment were the following: pH (4.1), organic matter (17 g dm-3), Presin (2 mg dm-3), K (0.2 mmolc dm-3), Ca (2 mmolc dm-3), and Mg (1 mmolc dm-3). The calculations for liming and N and P base fertilization were based on recommendations of Raij et al. (1996) for eggplant. To increase saturation to 80 %, the application of 96 g dolomitic limestone (PRNT = 91 %) per pot was required for acidity correction. Nitrogen (3.2 g per pot) was applied in the form of ammonium sulfate and P (28.2 g per pot) as thermophosphate. Half the recommended amount was supplied in form of organic fertilization by adding 160 g of cattle-manure compost per pot, corresponding to 10 t ha-1. Eggplant seedlings were grown in trays with 128 cells, 6.0 to 6.2 cm high, containing substrate composed of inert and pathogen-free material. The seedlings were planted when they had 3-4 true leaves, about 35 days after sowing.

 

 

Topdressing fertilization was initiated 15 days after transplanting (DAT), and repeated fortnightly. The N source used as topdressing was calcium nitrate of which a total rate of 22.82 g per pot was split into 14 applications. The pots were arranged in a spacing of 0.63 m between plants and 1.0 m between rows. Tensiometers were installed at a depth of 0.20 m and 0.15 m away from the plant stem. Irrigation was applied by hand to raise the soil moisture to field capacity, corresponding to a matric potential of approximately -30 kPa. During the experiment, aliquots of the soil solution were collected every seven days. The solution was collected with an extractor installed at a depth of 0.15 m, 0.10 m away from the plant stem. A digital conductivity meter was used to determine electrical conductivity (EC) and the EC readings were corrected based on soil moisture.

The plant height and number of leaves per plant were determined, and plant leaves were collected to assess the enzymatic activity 30, 60, 90, and 110 DAT. Leaves for enzyme analyses were sampled in triplicate, always at 8:00 AM, in standardized collections in the mid- region of the canopy. The leaf samples were frozen in liquid N and maintained in an ultrafreezer (-80 ºC) until enzymatic analyses. Subsequently, the samples were ground in liquid N and prepared to obtain extracts for analysis of the activities of superoxide dismutase (SOD), catalase (CAT) and the protein content. Superoxide dismutase (EC 1.15.1.1) was extracted from 300 mg of plant material ground in 3 mL potassium phosphate buffer at a concentration of 100 mmol L-1 (TFK, pH 6.8); 0.1 mmol L-1 EDTA; 0.1 % (v/v) 2-mercaptoethanol; 0.1 % (v/v) Triton X-100; 30 mg polyvinylpyrrolidone (PVP) and 20 mmol L-1 ascorbate. After centrifugation at 15,000g for 15 min at 4 ºC, the supernatant was collected for further analysis.

The SOD activity was determined as described by Giannopolitis & Ries (1977). The reaction medium consisted of 52.5 mmol L-1 TFK (pH 7.8); 0.1 mmol L-1 EDTA; 13 mmol L-1 methionine (pH 7.8); 2 mmol L-1 riboflavin; 0.075 mmol L-1 nitroblue tetrazolium (NBT) and an 10 µL aliquot of enzyme extract. The production of blue formazan from NBT reduction in the presence of light was monitored by a spectrophotometer at 560 mmol L-1. Results were expressed in units of SOD mg-1 protein, assuming that 1 unit of SOD is the amount of enzyme required to reduce the production of blue formazan by 50 %. Catalase (EC 1.11.1.6) was extracted from 300 mg of plant material ground in liquid N in 3 mL of a solution consisting of: 100 mmol L-1 trifluoromethyl ketone (pH 7.0); plus 2 mmol L-1 EDTA; 0.1 % (v/v) Triton X-100; 0.1 % (v/v) 2-mercaptoethanol; 20 mmol L-1 ascorbate; 30 mg PVPP. An aliquot of 20 L of supernatant obtained by centrifugation of the homogenate at 15,000g for 15 min at 4 ºC was used to assess enzyme activity.

The reaction medium (3 mL) contained 50 mmol L-1 TFK (pH 7.0) and 12.5 mmol L-1 H2O2 and the reaction was initiated by adding 20 µL extract. The CAT activity was determined by monitoring the drop in absorbance of hydrogen peroxide in the spectrophotometer at 280 nm (Peixoto et al., 1999). The enzymatic activity was calculated from a molar extinction coefficient of H2O2 (e = 39.4 mmol L-1 cm-1) and the specific CAT activity (mKat). The protein concentration was used to calculate the enzymatic activities of SOD and CAT. The leaf protein content was assessed by the Bradford (1976) method. For the preparation, 100 mg of the dye Coomassie Brilliant Blue G-250 was dissolved in 50 mL 95 % ethanol; 100 mL of 85 % phosphoric acid was added and this diluted in 1 L of distilled water. To prepare bovine serum albumin (BSA), 0.88 g NaCl in 100 mL of distilled H2O was used to obtain a 0.15 molar saline solution and 100 mL albumin. Three 100 mL aliquots of the extract and 5 mL Bradford reagent were used, readings were taken on a spectrophotometer at 595 nm absorbance, and a standard curve prepared to calculate the protein with bovine serum albumin.

The results were subjected to analysis of variance (ANOVA) and means compared by the Scott-Knott or Student's t-test at p<0.05 (Steel et al., 2006). Standard deviations were calculated and the estimators of regression and Pearson correlation applied using software SISVAR (Ferreira, 2011).

 

RESULTS AND DISCUSSION

The electrical conductivity increased linearly proportional to increasing K2O rates, regardless of the source (Figure 1). However, electrical conductivity values were significantly higher when KCl was used, indicating salinity of the soil in comparison with K2SO4. This result proves the greater effect of soil salinization of KCl than K2SO4. The saline index of K2SO4 per unit K2O is equivalent to half the rate of potassium chloride (Kamburova & Kirilov, 2008). Although the demand for KCl fertilizer in agriculture is great for being cheaper than other K sources, our data corroborate those described in the literature confirming the major effect of KCl in the salinization of the environment and the indication of K2SO4 as source with a lower saline index (Nogueira et al., 2001).

 

 

The activity of CAT (Figure 2) and SOD (Figure 3) evaluated in eggplant leaves showed different patterns according to the K sources in the four evaluations. When the K source was KCl, there was a positive quadratic relationship (R2 = 0.74 and 0.94) of CAT activity with K2O rates 30 and 60 DAT. The maximum activities were 12 mmol L-1 H2O2 min mg fresh weight at 30 DAT and 9 at 60 DAT, respectively, at 500 and 750 kg ha-1 K2O (Figure 2a). The assessment 90 and 110 DAT showed a decrease in CAT activity with increasing K2O rates.

 

 

 

 

For K2SO4 as K source, there was a positive quadratic response of CAT enzyme activity with K2O rates only in the evaluation 30 DAT (Figure 2b). Similarly to KCl at 60 and 90 DAT, the CAT activity decreased with increasing K rates 60, 90 and 110 DAT. Figure 2(a,b) also show a positive response of CAT activity to K2O rates up to approximately 500 kg ha-1.

These results show responses in CAT activities according to the plant age, suggesting some considerations. The first is that, whatever the source, at rates above 500 kg ha-1 K2O, the eggplants may be affected by salt excess in the plant cells, reducing enzyme activity. The other is that, after 90 DAT, topdressing with K sources (KCl and K2SO4) is not recommendable because the plant would respond negatively to fertilization, which in addition to the financial loss could cause soil salinization. These results, indicating increased CAT activity 30 and 60 DAT, may be related to the phenological stage of the crop, with maximum growth activity in this period. In the phenological stages 90 and 110 DAT, a drop in activity was noted since the plants already entered senescence. The presence of salt in the soil has two major effects on plant growth. The first is that the high concentration in the soil solution reduces the ability of the plant to absorb water, delaying growth. This is known as the osmotic effect caused by drought or salinity. The second is that the salt may enter the transpiration stream and eventually damage the leaf cells, reducing further growth and causing a major physiological disorder (Mahajan & Tuteja, 2005). Marques et al. (2011) demonstrated the negative effect of the sources KCl and K2SO4 on leaves of eggplants grown at different K2O concentrations.

The responses of SOD activity to K rates and sources are shown in figure 3(a,b). At 30 and 110 DAT using KCl (Figure 3a), there was a quadratic response with reduction in SOD activity up to a rate of 750 kg ha-1 K2O, above which there was an increase in enzyme activity. For K2SO4 (Figure 3b), the SOD activity increased linearly with increasing K2O concentrations. According to Alscher et al. (2002), within the cell, SODs are the first line of defense against AOS. These proteins belong to the metallo-enzymes that protect cells from superoxide radicals by catalyzing the dismutation of O2- in O2 and H2O2 (van Breusegem et al., 2001). Several studies have demonstrated the role of enzymatic antioxidant mechanisms in the protection against secondary oxidative stress induced by salinity (Rubio et al., 2009).

Regardless of the K sources, the protein content assessed in eggplant leaves decreased quadratically with increasing rates (Figure 4a,b). The results found in this study agree with those reported by Piza et al. (2003) for the cultivation of pineapple [Ananas comosus (L.) Merrill] in saline, where the levels of total soluble proteins decreased at all values of salinity applied. Proteolysis also provides amino acids required for cell maintenance and growth and protein degradation is also accelerated during nutritional disorders that may be caused by salinity, in order to keep the level of amino acids that would result in greater control of osmotic capacity, for amino acids are known as osmotically active compounds (Viestra, 1993).

 

 

Table 2 presents the mean values of number of leaves per plant in relation to the K2O rates, for KCl and K2SO4. The interaction for sources and rates was significant. When the K source was K2SO4, leaf production was significantly higher at 500 and 750 kg ha-1. With the use of KCl however the differences in number of leaves were significant, according to the rate. These results indicate that despite the change in enzyme activity (SOD and CAT) and decreased protein content in eggplant leaves, the plants did not paralyze leaf production, indicating that eggplant can be grown in environments with soil salinity problems. Environmental stresses such as high temperatures, excess light, drought, and salinity are worldwide limiting to crop yields (Mittler, 2006). These conditions negatively influence plant survival and production and accumulation of biomass and grain yield of the economically most important crops (Grover et al., 2001). Significant differences were observed 30 and 60 DAT in the interaction of sources (KCl and K2SO4) × K2O rates (250, 500, 750 and 1000 kg ha-1 K2O) (Table 3), noting that plant height was higher for source K2SO4. Although the sources (KCl and K2SO4) affected the SOD and CAT activity, protein content and plant growth of eggplant (Tables 2 and 3), it was observed that plant death was not increased at the sources and concentrations tested. The negative effects may have been mitigated by the plant architecture in bush form with various bifurcations, facilitating salt dilution in the plant tissues.

 

 

 

CONCLUSIONS

1. The potential of KCl to salinize soils is higher than that of K2SO4.

2. High rates of KCl as well as of K2SO4 adversely affected the enzyme activities of catalase (CAT) and superoxide dismutase (SOD) as well as leaf protein contents in eggplant.

3. The potential of KCl to reduce the enzyme activities of SOD and CAT, leaf protein content and the development of eggplants is higher than that of K2SO4.

 

ACKNOWLEDGEMENT

The first author wishes to thank the Brazilian Federal Agency for Support and Evaluation of Graduate Education (CAPES) for a postgraduate scholarship.

 

LITERATURE CITED

ABBASI, G.H.; AKHTAR, J.; ANWAR-UL-HAQ, M.; ALI, S.; CHEN, Z. & MALIK, W. Exogenous potassium differentially mitigates salt stress in tolerant and sensitive maize hybrids. Pakistan J. Bot., 46:135-146, 2014.         [ Links ]

ALSCHER, R.G.; ERTURK, N. & HEALT, L.S. Role of superoxide dismutase (SODs) in controlling oxidative stress in plants. J. Exp. Bot., 53:1331-1341, 2002.         [ Links ]

APEL, K. & HIRT, H. Reactive oxygen species: Metabolism, oxidative stress, and signal transduction. Ann. Rev. Plant Biol., 55:373-399, 2004.         [ Links ]

BOSE, J.; RODRIGO-MORENO, A. & SHABALA, S. ROS homeostasis in halophytes in the context of salinity stress tolerance. J. Exp. Bot., 65:1241-1257, 2014.         [ Links ]

BRADFORD, M.M. A rapid and sensitive method for quantitation of microgram quantities of protein utilizing the principle of protein-dyebinding. Anal. Biochem., 72:248-254, 1976.         [ Links ]

CHAVES, M.M.; PEREIRA, J.S.; MAROCO, J.; RODRIGUES, M.L.; RICARDO, C.P.P.; OSORIO, M.L.; CARVALHO, I.; FARIA, T. & PINHEIRO, C. How plants cope with water stress in the field. Photosynthesis and growth. Ann. Bot., 89:907-916, 2002.         [ Links ]

CUNHA, A.R. & MARTINS, D. Classificação climática para os municípios de Botucatu e São Manoel, SP. Irriga, 14:1-11, 2009.         [ Links ]

EMPRESA BRASILEIRA DE PESQUISA AGROPECUÁRIA - EMBRAPA. Centro Nacional de Pesquisa de Solos. Manual de métodos de análises de solo. Rio de Janeiro, 1997. 212p.         [ Links ]

ERNANI, P.R.; ALMEIDA, J.A. & SANTOS, F.C. Potássio. In: NOVAIS, R. F.; ALVAREZ V, V. H.; BARROS, N.F.B.; FONTES, R.L.F.; CANTARUTTI, R.B. & NEVES, J.C.L., eds. Fertilidade do solo. Viçosa, MG, SBCS, 2007. p.551-594.         [ Links ]

FERREIRA, D. SISVAR: A computer statistical analysis system. Ci. Agrotec., 35:1039-1042, 2011.         [ Links ]

GIANNOPOLITIS, C.N. & RIES, S.K. Superoxide dismutases. I: Occurrence in higher plants. Plant Physiol., 59:309-314, 1977.         [ Links ]

GROVER, A.; KAPOOR, A.; LAKSHMI, O.S.; AGARWAL, S.; SAHI, C.; KATIYAR-AGARWAL, S.; AGARWAL, M. & DUBEY, H. Understanding molecular alphabets of the plant abiotic stress responses. Curr. Sci., 80:206-216, 2001.         [ Links ]

KAMBUROVA, K. & KIRILOV, P.L. Calculating the salt index of pK and NPK liquid fertilizers from potassium phosphates. J. Chem. Technol. Metal., 43:227-230, 2008.         [ Links ]

KHADRI, M.; TEJERA, N.A. & LLUCH, C. Sodium chloride-ABA interaction in two common bean (Phaseolus vulgaris ) cultivars differing in salinity tolerance. Environ. Exp. Bot., 60:211-218, 2006.         [ Links ]

MAHAJAN, S. & TUTEJA, N. Cold, salinity and drought stresses: An overview. Arch. Biochem. Biophys., 444:139-158, 2005.         [ Links ]

MALAVOLTA, E. Manual de nutrição mineral de plantas. São Paulo, Agronômica Ceres, 2006. 638p.         [ Links ]

MARSCHNER, H. Mineral nutrition of higher plants. San Diego, Academic Press, 1995. 889p.         [ Links ]

MARQUES, D.J.; BROETTO, F.; SILVA, E.C.; FREITAS, J.M.N.; LOBATO, A.K.S. & ALVES, G.A.R.A. Changes in leaf proline and fruit production induced by potassium stress in eggplant. J. Food Agric. Environ., 9:91-194, 2011.         [ Links ]

MITTLER, R. Abiotic stress, the field environment and stress combination. Trends Plant Sci., 11:15-19. 2006.         [ Links ]

MOLLER, I.M.; JENSEN, P.E. & HANSSON, A. Oxidative modifications to cellular components in plants. Ann. Rev. Plant Biol., 58:459-481, 2007.         [ Links ]

NOGUEIRA, F.D.; SILVA, E.B.E. & GUIMARÃES, P.T.G. Adubação potássica do cafeeiro: Sulfato de potássio. Washington, SOPIB, 2001. 81p.         [ Links ]

PEIXOTO, P.H.P.; CAMBRAIA, J.; SANT'ANNA, R.; MOSQUIM, P.R. & MOREIRA, M.A. Aluminum effects on lipid peroxidation and the activities of enzymes of oxidative metabolism in sorghum. R. Bras. Fisiol. Veg., 11:137-143, 1999.         [ Links ]

PIZA, I.M.T.; LIMA, G.P.P. & BRASIL, O.G. Atividade de peroxidase e níveis de proteínas em plantas de abacaxizeiro micropropagadas em meio salino. R. Bras. Agroci., 9:361-366, 2003.         [ Links ]

RAIJ, B.van; CANTARELLA, H.; QUAGGIO, J.A. & FURLANI, A.M.C., eds. Recomendações de adubação e calagem para o estado de São Paulo. Campinas, Instituto Agronômico de Campinas, 1996. 285p. (Boletim Técnico, 100)        [ Links ]

RUBIA, M.C.; BUSTOS-SANMAMED, P.; CLEMENTE, M.R. & BECANA, M. Effects of salt stress on the expression of antioxidant genes and proteins in the model legume Lotus japonicus . New Phytol., 181:851-859, 2009.         [ Links ]

STEINECK, O. & HAEDER, H.E. The effect of potassium on growth and yield components of plants. In: CONGRESS INTERNATIONAL OF THE POTASH INSTITUTE, 11., Bern, 1978. Proceedings... Bern, IPI, 1978. p.165-187.         [ Links ]

STEEL, R.G.D.; TORRIE, J.H. & DICKEY, D.A. Principles and procedures of statistics: A biometrical approach. 3.ed. Moorpack, CA, Academic Internet Publishers, 2006. 666p.         [ Links ]

SOIL SCIENCE SOCIETY OF AMERICA - SSSA. Glossary of soil science terms. Madison, 2008. 88p.         [ Links ]

VAN BREUSEGEM, F.; VRANOVA, E.; DAT, J.F. & INZE, D. The role active oxygen species in plant signal transduction. Plant Sci., 161:405-414, 2001.         [ Links ]

VIESTRA, R.D. Protein degradation in plants. Ann. Rev. Plant Physiol., 44:385-410, 1993.         [ Links ]

WUZHONG, N. Yield and quality of fruits of solanaceous crops as affected by potassium fertilization. Better Crops, 13:6-8, 2002        [ Links ]

 

 

Received for publication on October 2, 2013 and approved on July 25, 2014

 

 

1 Part of the Master's thesis of the first author.

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