Kinetics of K release from soils of Brazilian coffee regions: effect of organic acids

Cinética de liberação do potássio em solos de regiões cafeeiras: efeito de ácidos orgânicos

SEÇÃO II - QUÍMICA E MINERALOGIA DO SOLO

Kinetics of K release from soils of Brazilian coffee regions: effect of organic acids¹

Cinética de liberação do potássio em solos de regiões cafeeiras: efeito de ácidos orgânicos

Vladimir Antônio Silva^I; Giuliano Marchi^II; Luiz Roberto Guimarães Guilherme^III; José Maria de Lima^III; Francisco Dias Nogueira^IV; Paulo Tácito Gontijo Guimarães^IV

^IInstituto Nacional de Colonização e Reforma Agrária – INCRA. Rua Olhos D'água 829, Bairro Candolas, CEP 38900-000 Bambuí (MG). E-mail: [e-mail]

^IIEmbrapa Cerrados. Rod. BR 020, km 18, Caixa Postal 08223, CEP 73310-970 Planaltina (DF). E-mail: [e-mail]

^IIIAssociate Professor, Departamento de Ciência do Solo, Universidade Federal de Lavras – DCS/UFLA. Caixa Postal 3037, CEP 37200-000 Lavras (MG), E-mail: [e-mail]; [e-mail]

^IVEmpresa de Pesquisa Agropecuária de Minas Gerais – EPAMIG. CEP 37200-000 Lavras (MG). E-mail: [e-mail]; [e-mail]

SUMMARY

Kinetic studies on soil potassium release can contribute to a better understanding of K availability to plants. This study was conducted to evaluate K release rates from the whole soil, clay, silt, and sand fractions of B-horizon samples of a basalt-derived Oxisol and a sienite-derived Ultisol, both representative soils from coffee regions of Minas Gerais State, Brazil. Potassium was extracted from each fraction after eight different shaking time periods (0–665 h) with either 0.001 mol L^-1 citrate or oxalate at a 1:10 solid:solution ratio. First-order, Elovich, zero-order, and parabolic diffusion equations were used to parameterize the time dependence of K release. For the Oxisol, the first-order equation fitted best to the experimental data of K release, with similar rates for all fractions and independent of the presence of citrate or oxalate in the extractant solution. For all studied Ultisol fractions, in which K release rates increased when extractions were performed with citrate solution, the Elovich model described K release kinetics most adequately. The highest potassium release rate of the Ultisol silt fraction was probably due to the transference of "non-exchangeable" K to the extractant solution, whereas in the Oxisol exchangeable potassium represented the main K source in all studied fractions.

Index terms: successive extractions, first order, zero order, parabolic diffusion, Elovich.

RESUMO

Estudos de cinética de liberação de K podem contribuir para avaliação da disponibilidade deste nutriente no solo para as plantas. Este trabalho teve como objetivos investigar a cinética de liberação do potássio nas frações terra fina, areia, silte e argila de dois solos do Estado de Minas Gerais, Brasil, originalmente cultivados com cafeeiro e comparar quatro equações para descrevê-la. As frações foram submetidas a oito extrações sucessivas (0 a 665 h) com citrato e oxalato 1 mmol L^-1, sendo os resultados de K liberado somados e plotados em função do tempo. Foram comparadas as equações de ordem zero, primeira ordem, Elovich e parabólica de difusão, a fim de verificar qual delas melhor descreve a cinética. Na condução do experimento utilizaram-se amostras do horizonte B de um Latossolo Vermelho distroférrico originado de basalto e de um Nitossolo originado de sienito nefelínico. Para cada equação foram calculados o coeficiente de correlação (r) e o erro-padrão da estimativa (EP). A equação de primeira ordem descreveu melhor os resultados do Latossolo e a equação de Elovich se ajustou melhor aos resultados do Nitossolo. As velocidades de liberação do K para o Latossolo foram semelhantes em todas as frações estudadas, não sendo observado efeito dos ácidos orgânicos na velocidade de liberação do K, porque a maior parte do K liberado foi proveniente da forma trocável. No Nitossolo, o citrato acelerou a liberação do K em todas as frações estudadas, e a fração silte foi a que apresentou maior velocidade, pois possivelmente a maior parte do K proveniente desta fração estava na forma não-trocável.

Termos de indexação: extrações sucessivas, primeira ordem, ordem zero, Elovich, parabólica de difusão.

INTRODUCTION

The low natural K reserves in most tropical soils (Melo et al., 2000; Wood et al., 2000) and the dependence of Brazilian agriculture on imported K justify research efforts on the rational use of K fertilization in Brazil. The prediction of yield response to K fertilizer applications based on soil tests for exchangeable K is sometimes of limited accuracy (Pal et al., 2001), particularly for perennial crops such as coffee. The K uptake from nonexchangeable forms by plants has been described (Fitzpatrick & Guillard, 2004) and several mineralogical studies confirmed great differences among soils concerning the K-supply potential.

Studies on the mineralogy and distribution of K among different soil compartments can contribute to a better understanding of K dynamics. However, these studies provide little information on soil K behavior when the exchangeable pool is depleted. K release and its availability can be estimated in successively cultivated soils, requiring long-term experiments (Benipal & Pasricha, 2002).

Successive extractions of K from soils by chemical extractants can simulate the absorption of available K by plants, providing short-term results, which allow the evaluation of K release from soil compartments, e.g., from different granulometric fractions, and complement studies on K mineralogy or even on successive crop cultivation. Nevertheless, mineral weathering rates in the rhizosphere may be higher than in the bulk soil (Ochs et al., 1993). In this context, the use of low molecular weight organic acids as extractants is recommended to mimic the plant environment.

Organic ligands such as citrate and oxalate are involved in K release reactions in the soil and have been used as extractants in successive extraction experiments in Brazil (Meurer & Castilhos, 2001) and elsewhere (Srinivasarao et al., 2006). The great affinity of Brazilian Oxisols for citrate and oxalate (Marchi et al., 2006b) and the influence of these organic acids on exchangeable Al (Li et al., 2005) as well as on the surface charge (Marchi et al., 2006a) of variable-charge soils also calls for a better understanding of their effect on other soil properties, e.g., on plant nutrient availability.

The most commonly used mathematical equations to investigate the kinetics of soil K release are zero order, first order, Elovich, and parabolic diffusion (Martin & Sparks, 1983; Lopez-Pineiro & Navarro, 1997; Mengel et al., 1998; Singh et al., 2002, Srinivasarao et al., 2006). Once the best fitting model is found, K release rates for each soil material can be compared.

The kinetics of K released by oxalic acid was studied by Meurer & Castilhos (2001) in paddy soils in southern Brazil, but no studies have been carried out in Brazilian upland soils. The purpose of this work was: (a) to evaluate the kinetics of K release by citrate and oxalate from different granulometric fractions (whole soil, sand, silt, and clay) of an Oxisol and an Ultisol in Minas Gerais State under coffee; and (b) to find the best fitting mathematical model to describe K release kinetics in each studied soil fraction.

MATERIAL AND METHODS

Samples were collected from the B horizon of a basalt-derived Oxisol from São Sebastião do Paraíso (80–120 cm depth), and of a sienite-derived Ultisol from Poços de Caldas (65–85 cm depth), both representative soils of coffee regions in Minas Gerais State, Brazil (Table 1).

The samples were air-dried, sieved (2 mm mesh) and dispersed with 0.1 mol L^-1 NaOH. The suspension was submitted to ultrasonic dispersion for 10 min (Misonix, XL2020; 20 kHz) and then fractionated into sand (> 50 µm) - by sieving - silt (2–50 µm), and clay (< 2 µm) - by centrifugation (Jackson, 1975).

For K extractions by citrate and oxalate solutions (concentration = 0.001 mol L^-1 in 0.03 mol L^-1 NaCl; pH = 5.5; Table 2), 4 g of each fraction and 40 mL of the extractant solution were filled into 100 mL centrifuge tubes. These tubes were shaken constantly for 1.0, 2.72, 4.48, 12.18, 33.11, 90.02, 244.69, and 665.14 h using an end-over shaker, and after each extraction period, the tubes were centrifuged at 2.800 g for 15 min. Three replications were performed. After every extraction, the supernatant was discarded and a new extractant solution added. K in the supernatant was analyzed by flame photometry.

Zero-order, first-order, Elovich, and parabolic diffusion models were tested statistically to determine which one fitted best to the data on K kinetics release for each soil and soil fraction.

The zero-order equation was calculated as:

where K¥ denotes the accumulated amount of K released over all extractions (mg kg^-1); K_t denotes the accumulated amount of K released in the time period t (mg kg^-1); k denotes the zero-order rate constant (mg kg^-1 h^-1), and t denotes the time (h).

The first-order equation was calculated as (Martin & Sparks, 1983):

where k' denotes the release rate constant for the first order reaction (h^-1), and the elements of the equation are as described for equation 1.

The simplified parabolic diffusion equation was as follows (Melo et al., 2005; Galadima & Silvertooth, 1998):

where a denotes the initial rate constant and refers to the Kt intercept of the straight line plot of lnKt vs. lnt; k" denotes the slope of the fitted line for the K diffusion rate, and the other elements of the equation are as described for equation 1.

The Elovich equation was as follows (Galadima & Silvertooth, 1998; Bedrossian & Singh, 2004):

all terms as previously described.

The best-fitting equation was identified based on the coefficient of determination of the linearized equations (R²) and the standard error of estimate (SEE) defined by: SEE = [S (Kt–Kt*)² / (n–2)]^½, where Kt and Kt* are the respective experimental and model-estimated K released amounts and n is the number of observations (Jardine & Sparks, 1984).

RESULTS AND DISCUSSION

The first order and the Elovich models were the equations that best fitted the experimental data, in agreement with results reported elsewhere (Lopez-Pineiro & Navarro, 1997; Mengel et al., 1998; Srinivasarao et al., 2006). For the Oxisol, the first-order equation best described K release to the extractant solution, whereas the zero order and parabolic diffusion equations did not fit the experimental data (Table 3). The results for K extraction by citrate and oxalate were similar to those found by Zhu & Luo (1993) for 12 soils from China and by Song & Huang (1988), which used the same extractants for K extraction from biotite, muscovite, microcline, and orthoclase.

The K release rates (k')¹ estimated by the first-order equation for all fractions of the studied Oxisol were similar for the citrate and oxalate extractant solutions (Table 4).

The greatest differences in K-release rates (first-order constants, k') were verified for the clay fraction, where the K extraction rate by citrate solution (0.01139 h^-1) was by 7.4 and 5.5 % higher than for control and oxalate, respectively.

Great part of the extracted K from the Oxisol came from the exchangeable form (Mehlich-1, Table 1). The use of organic acids increased the K release from silt and sand fractions, which shows that these two fractions represent the main K reserve of this soil (Figure 1).

For the Ultisol, the Elovich equation fitted the experimental results best (Table 5), indicating that K release from this soil is a diffusion-controlled process (Cox & Joern, 1997).

The k" from the Elovich equation can be used to compare different materials in relation to the K release rates (Martin & Sparks, 1983; Cox & Joern, 1997). Citrate extractant caused higher k" values than oxalate, except for the silt fraction (Table 6). The oxalate extractant was very similar to the control.

The k" values extracted by citrate from the Ultisol whole soil fraction were 89 and 108 % higher than for the control and oxalate, respectively. This difference is due to the K released from the nonexchangeable pool, as the cumulative values for K extraction kinetics were almost twice as high as those of exchangeable K (Mehlich-1, Table 1).

The citrate extraction also increased the amount of K extracted from the sand fraction, where the amount of released K was greater by 81 and 37 % when extracted with citrate than with control and oxalate, respectively. The k" value was smaller in the sand, indicating that nonexchangeable-K release is a slow process in this fraction.

For the Ultisol silt fraction, the k" coefficients were similar, probably because almost all K was released from exchangeable K. The k" coefficient for the clay fraction was 46 and 39 % greater in citrate extracts than in control and oxalate, respectively.

Most K from the Ultisol silt fraction was more rapidly released than from the clay and sand fractions of this soil (Figure 2). For all granulometric fractions of this soil, extractions by citrate were faster than by the control and oxalate extractant. The higher K extraction capacity of citrate compared with oxalate might be related to the higher value of the stability constant (K_s) for the formation of K-citrate when compared with K-oxalate complexes (Martell & Smith, 2003; Table 2).

The most important fraction in terms of K release from the Ultisol was silt, in which the k" value was highest in all treatments. In this case, the higher k" values were due to greater amounts of K released from the nonexchangeable pool. Similar results were reported by Mengel et al. (1998) in loess-derived soils and by Castilhos et al. (2002) and Villa et al. (2004) in lowland soils.

The smaller difference in terms of extraction capability between citrate and oxalate in the Oxisol compared with the Ultisol might be related to the surface charge of each soil. Since the cation exchange capacity of the Oxisol is about 4 times lower than of the Ultisol (Table 1), a greater anion adsorption is expected in the first (an oxidic soil) than in the second (Marchi et al., 2006b). Citrate is therefore less adsorbed in the Ultisol and since it has a higher charge and higher K_s (Martell & Smith, 2003) then oxalate (Table 2), it would be able to extract more K via formation of a K-organic acid complex.

Despite the higher exchangeable K in the Oxisol than in the Ultisol, the long-term K release was greater in the Ultisol, as the total cumulative K release at the end of kinetics shows (Figures 1 and 2). This shows that much of the K from the Ultisol can come from the non exchangeable fraction and that organic acids play an important role in this process, since the cumulative K release was higher for organic acids compared with the control. Also, the importance of the soil surface charge must be taken into account when evaluating the effect of organic acids on K extraction, e.g., a more weathered soil, such as an Oxisol will adsorb more organic anions than an Ultisol (Marchi et al., 2006b), thus reducing the capability of the organic acids to work as effective soil potassium extractants.

Studies on K uptake by plants in these soils are necessary to validate the K-release kinetics and to define the best mathematical modeling and the coefficients to be used as ancillary indexes to evaluate K availability to plants most adequately. This should be evaluated in future research.

CONCLUSIONS

1. The kinetics of K release differed between soils and among their granulometric fractions.

2. The K release was fast during the initial extractions, followed by a slow release after 300 hours.

3. The first-order equation fitted to the K release in the Oxisol was most adequate, whereas in the Ultisol the process was better described by the Elovich model.

4. The organic acid effects on the slope of K release were greater for the Ultisol than for the Oxisol.

5. The citrate extractant increased the rate of K release in the Ultisol.

LITERATURE CITED

Received for publication in november of 2006 and approved in october of 2007.

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1

Part of the Thesis submitted by the first author for the degree of Master of Soil Science and Plant Nutrition at Universidade Federal de Lavras – UFLA.

Publication Dates

• Publication in this collection
  30 June 2008
• Date of issue
  Apr 2008

History

• Accepted
  Oct 2007
• Received
  Nov 2006