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Assessment of Electrical Conductivity of Saturated Soil Paste from 1:5 Soil‐Water Extracts for Reclaimed Tideland Soils in South‐Western Coastal Area of Korea

Abstract

BACKGROUND: Measurement of electrical conductivity of saturated soil paste (ECe) for assessment of soil salinity is time‐consuming, and thus conversion of EC of 1:5 soilwater extract (EC1:5) to ECe using a dilution factor may be of help to monitor salinity of huge number of soil samples. This study was conducted to evaluate the dilution factor for reclaimed tideland (RTL) soils of South Korea. METHODS AND RESULTS: Soil samples (n=40) were collected from four RTLs, and analyzed for EC1:5, ECe, and cation compositions of 1:5 soil‐water extract. The dilution factor (8.70) was estimated by regression analysis between EC1:5 and ECe, and the obtained dilution factor was validated by applying to an independent data set (n=96) of EC1:5 and ECe. The ECe measured and predicted was strongly correlated (r2=0.74, P<0.001), but ECe was overestimated by 16% particularly for the soils with high clay content and low sodium adsorption ratio (SAR). CONCLUSION: This study suggests that using the dilution factor to convert EC1:5 to ECe is feasible method to monitor changes in the soil salinity of the study RTL. However, overestimation of ECe should be cautioned for the soils with high clay content and low SAR.

Keywords: Dilution factor Salt affected soils Sodium adsorption ratio Soil extract Soil salinity

Introduction

Reclaimed tideland (RTL) accounts for 8.3% of total arable land in South Korea (MOAF, 2017). Due to high salinity of the RTL soils, rice (Oryza sativa L.) is highly recommended as a pioneer crop over other salinity‐tolerant crops after reclamation of salt‐affected soils although rice is not tolerant to salinity as excessive salts leach down below rooting zone in lowland rice culture system by irrigation of less saline water (Abrol et al., 1988). However, due to surplus production of rice over consumption, there is social pressure on decreasing rice production by converting land‐use of RTL from rice to upland crops cultivation (Lee et al., 2003a). High soil salinity is a major constraint for the growth of upland crops in RTL, however, due to disruption of plant physiology caused by osmotic stress and specific ion toxicity (Castillo et al., 2007) as well as poor soil physical conditions such as destruction of soil aggregates by sodium (Na+) (Rengasamy and Olsson, 1991). Therefore, careful measurement and monitoring of soil salinity and ion concentrations is strongly required for assessment the suitability for upland crop cultivation in RTL soils.

Soil salinity is conventionally assessed with electrical conductivity (EC) of saturated soil paste extracts (ECe) as ECe is the best indicator of the salinity experienced by plant roots, and thus ECe is regarded as a standard method for determination of soil salinity (US Salinity Laboratory Staff, 1954; Rhoades et al., 1989; Herrero and Pérez‐Coveta, 2005). However, as saturated paste extraction is time-consuming and requires more skills for determining the correct standard point of saturation (Al‐Busaidi et al., 2006), measurement of ECe is inconvenient and costly method to determine soil salinity when the number of sample is huge or frequent monitoring is required (Aboukila and Norton, 2017). For these reasons, soil‐water extract at varying ratio such as 1:1 (EC1:1), 1:2 (EC1:2), and 1:5 (EC1:5) of soil:water mass ratio has been commonly used; the 1:5 ratio is preferred in Australia, China, Central Asia and South Korea (Rayment and Higginson, 1992; Shirokova et al., 2000; Lee et al., 2003b), whereas the 1:1 ratio in the United States and Canada (Hogg and Henry, 1984; He et al., 2013; Zhang et al., 2005). However, it is necessary to convert the EC measure with soil-water extract to ECe for field implication as the suitability of a crop for soil salinity is established based on ECe (US Salinity Laboratory Staff, 1954).

Salinity measured with soil‐water extract is lower than ECe due to dilution with water, and thus dilution factor needs to be adopted to convert EC of soil‐water extract to ECe (Zhang et al., 2005; He et al., 2013; Aboukila and Abdelaty, 2017). Many studies reported statistically significant correlation between ECe and EC of soil‐water extract; e.g., for EC1:5, dilution factors of 5.48‒7.98 have been reported (Sonmez et al., 2008; Khorsandi and Yazdi, 2011; Aboukila and Abdelaty, 2017; Aboukila and Norton, 2017). In South Korea, a wide range (5.49‒9.94) of dilution factor for EC1:5 has been reported for nine RTL soils including Namyang, Daeho, Seokmun, Seosan, Nampo, Busa, Gyehwa, Sopo, and Bojeon RTLs (Lee et al., 2003b). However, most of the RTLs were constructed in 1970‒1990 and no relevant study has been conducted for new RTLs constructed since 2000s, highlighting the necessity of development of a dilution factor to convert EC1:5 to ECe for the new RTLs that might save time, cost, and labor for salinity monitoring. This study was conducted to find a dilution factor to estimate ECe from EC1:5 using the relationship between EC1:5 and ECe for the new RTL soils.

Materials and Methods

Soil Sampling

Soil samples (n=40) were collected from 0‐20 cm soil depth of four RTLs, Goheung (GH, n=9), Gunnae (GN, n=7), Samsan (SS, n=7), and Youngsangang (YS, n=17) in April 2018 (Table 1). The number of samples and sampling sites for each RTL was determined by considering the area of RTL and spatial distribution of the sampling locations. The soil samples were air-dried and passed through 2‐mm sieve.

Soil Analysis

The soil samples were analyzed for particle size distribution using the pipette method (Gee and Bauder, 1986). For the measurement of EC1:5 and soluble cations, soil suspension was obtained by adding 50 mL of deionized water to 10 g soils in 100‐mL polyethylene bottles. The suspension was shaken at 150 rev min‐1 for 30 min and the suspension was filtered through No. 2 Whatman filter paper into 100‐mL polyethylene bottles. The solution was analyzed for EC with a conductivity meter (Orion 3 STAR, Thermo Fisher Scientific Korea, Seoul, Korea) and cations (Na+, K+, Ca2+, and Mg2+) concentrations using an Atomic Absorption Spectrometer (Analyst 800, Perkin Elmer, Waltahm, USA). Sodium adsorption ratio (SAR) was calculated using the cation concentrations.

Saturated pastes were prepared by adding deionized water to approximately 500 g of soil samples in a plastic container until it reached a condition of complete saturation as described in the USDA Handbook 60 (USDA, 1954). The extracts of saturated pastes were obtained under vacuum using a vacuum extractor (SampleTek 24VE, MAVCO INDUSTREIS, Inc., Kentucky, USA), and EC was measured using the conductivity meter.

Calculation and Statistical Analysis

Prior to statistical analysis, the data set was tested for normality of distribution with Kolmogorov‐Smirnov test and homogeneity of variance with Levene’s test. The data set was normally distributed and homogenous. The linearity of EC1:5 with cation concentration was assessed by the relationship between EC1:5 and cation concentration (Na+, K+, Ca2+, and Mg2+). In addition, EC1:5 was compared with the EC (ECc) calculated using the concentration of cations following the equation (APHA‐AWWA‐WPCF, 1992):

figure

where, k is electrical conductivity of infinitely diluted solution consisting of the cations and A is monovalent ionic coefficient. The k was calculated as follows:

figure

where, Zi is the absolute value of the charge, λi is the equivalence conductance (S cm‐1, 1 S cm‐1= 1000 dS m‐1), and Ci is the concentration (mM) of ith cation. The λ of Na+, K+, Ca2+, and Mg2+ are 50.1, 73.5, 59.5, and 53.1 S cm‐1, respectively. The A was calculated using the Davies equation for the solution with ionic strength (IS ) < 0.5 M as follows:

figure

where, IS was calculated as (Σ(Ci)(Zi)2)/2000.

To find the dilution factor for conversion of EC1:5 to ECe, simple linear regression model was fit for the data of EC1:5 (x variable) and ECe (y variable). The y intercept of the regression equation was forced to 0 as ECe should be 0 when EC1:5 is 0. Dilution factor was obtained from the slope of the regression equation. To validate the dilution factor, ECe was predicted using an independent data set (n=96) of GH RTL obtained from the Korea Rural Community Corporation (2016). The significance of the difference (ECdiff) between ECe predicted and measured was assessed with paired t-test. The relationship between ECdiff and soil variables such as clay content and SAR was explored to investigate the effect of soil properties on ECdiff.

Results and Discussion

Soil texture, EC1:5, ECe, and Cation Composition of 1:5 Extract

Particle of the soils (n=40) was widely distributed; 0.6‒65.5% for sand, 13.6‒75.6% for silt, and 6.0‒43.9% for clay (Fig. 1a). Across the samples (n=40), EC1:5 ranged from 0.41 to 3.37 dS m‐1 (mean: 1.14±0.08 dS m‐1) and ECe ranged from 3.09 to 37.0 dS m‐1 (mean: 9.62±0.88 dS m‐1) (Table 2). The ECe in the present study was within the range (1‒30 dS m‐1) reported for other RTL soils in South Korea (Lee et al., 2003b). Among cations in the 1:5 extract, Na+ was dominant cation (4.94±0.23 mM) followed by Mg2+ (1.37±0.13 mM), Ca2+ (0.61±0.11 mM), and K+ (0.37±0.13 mM). Sodium adsorption ratio ranged from 1.46 to 9.96 (Fig. 1b). The cation concentration was correlated with EC1:5 in a positive manner (Fig. 2), reflecting the role of cations in increasing EC (APHA‐AWWA‐WPCF, 1992).

The regression equation between EC1:5 measured and calculated using the equations 1‒3 suggests that the contribution of the measured cations to EC1:5 was 34.9% (Fig. 3). The remainder should be attributed to counterbalancing anions such as NO3, PO43‐, and SO42‐ as well as undetermined cations including H+, Al species (Al3+ and Al(OH)nm), and trace cations.

Relationship between EC1:5 and ECe

There was a linear relationship between EC1:5 and ECe and the dilution factor for conversion of EC1:5 to ECe was estimated to be 8.70 from the slope of the regression equation (Fig. 4). A wide range of dilution factor for EC1:5 has been reported; 5.37 and 5.48 (Khorsandi and Yazdi, 2011), 5.79 (Aboukila and Norton, 2017), 7.89 (Aboukila and Abdelaty, 2017), 7.98 (Sonmez et al., 2008), and 5.49‒9.94 (Lee et al., 2003b).

The differences in the dilution factor should be ascribed to the difference in the ionic compositions (Tolgyessy, 1993), silt content (Lee et al., 2003b), type of clay (Sonmez et al., 2008), type of salts present (Richard and Gouny, 1965), gypsum content (Khorsandi and Yazdi, 2007, 2011), equilibration times and methods (He et al., 2013), and the ECe range of soil samples used to develop the conversion equations (Lee et al., 2003b; Aboukila and Norton, 2017). Soil texture might also affect the dilution factor (Monteleone et al., 2016) though a narrow range (0.05‒0.86) of difference in the dilution factor among different texture group has been reported (Hogg and Henry, 1984; Sonmez et al., 2008). Such a wide range of dilution factors suggests that it is not straightforward to apply a dilution factor of one study to soils from different area as such variables that might affect the dilution factor should differ with sites.

Validation of the Dilution Factor

There was a significant difference between ECe measured and predicted by applying the dilution factor (8.70) to EC1:5 of the independent data set from GH RTL (Table 3). However, the ECe predicted and measured was linearly correlated, and the regression equation (ECe predicted =1.16×ECe measured) indicated that the dilution factor overestimate ECe by 16% on average (Fig. 5). Ideally, if the predicted values of ECe were exactly the same as the measured EC values, the slope would be 1.0, r2 would equal 1.0, and the y intercept would equal 0. However, when monitoring of the relative changes in ECe rather than determination of the exact ECe is interested, the dilution factor could be successfully adopted.

The ECdiff between ECe predicted and measured was positively correlated with clay content and negatively with SAR (Fig. 6). The positive correlation between ECdiff with clay indicates that ECe predicted is likely to be overestimated with increasing clay content. Clay content may affect the relationship between ECe and EC1:5 as saturation percentage of soils, which is defined as the ratio of the amount of water added to saturate dry soil samples, differs with soil texture; i.e., saturation percentage tends to increase with clay content (Aali et al., 2009). Slavich and Petterson (1993) reported that the dilution factor for the conversion of EC1:5 to ECe decreases with increasing saturation percentage, indicating that soil with a high clay content and thus a high saturation percentage might have a lower dilution factor compared to soil with a low clay content and thus a low saturation percentage. Therefore, in the present study, the increased magnitude of the overestimation of ECe predicted with clay content indicates that a real dilution factor for the soils decreases with increasing clay content. This result suggests that the application of dilution factor to the soils with high clay content should be cautioned.

The negative correlation between ECdiff and SAR suggests that ionic composition also affects dilution factor due to difference in solubility of the cation-anion pairs, particularly the presence of gypsum (CaSO4) (Khorsandi and Yazdi, 2007). Though the pattern of dilution factor as affected by gypsum content is not uncovered yet, it is widely reported that the presence of gypsum abates the relationship between EC1:5 and ECe, leading to loss of linearity of the regression (Visconti et al., 2010; He et al., 2013). Considering the low solubility of salts consisted of divalent cations (e.g., Ca2+ and Mg2+) than those of monovalent (e.g., Na+), we postulate that the dilution factor is more applicable the soils with high SAR (i.e., containing more Na+ compared to Ca2+ and Mg2+) due to high solubility of the Na‐based salts in the soils. Considering the potential effect of clay content and SAR on the ECdiff, the strong relationship between EC1:5 and ECe could be attributed to the narrow range (1.46 to 9.96) of SAR of the soils used for development of the dilution factor rather than clay content as clay content varied widely (6.0‒43.9%) (Fig. 1), suggesting that SAR may be more influential than clay content in the variations in the dilution factor among soils.

Conclusions

This study shows that the dilution factor to convert EC1:5 to ECe in the study RTL soils is 8.70. Though the ECe predicted by using the dilution factor overestimated ECe by 16% when compared to the measured ECe, the linear relationship between ECe predicted and measured suggested that the dilution factor can be used in monitoring of the changes in soil ECe of the study RTLs. Using the dilution factor is expected to save time and cost when huge number of soil samples are monitored. However, the relationship between ECdiff and soil variables indicated cautions are required for the soils with high clay content and low SAR. Further study is necessary to investigate the effect of clay content and SAR on the relationship between EC1:5 and ECe and thus on the dilution factor.

Note

The authors declare no conflict of interest.

ACKNOWLEDGEMENT

This work was carried out with the support of ”Cooperative Research Program for Agriculture Science and Technology Development (Project No. PJ013873042019)”, Rural Development Administration, Republic of Korea.

Tables & Figures

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Table 1. Brief information of reclaimed tideland (RTL) investigated in this study

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Fig. 1. Selected characteristics of the soils: (a) particle distribution and (b) sodium adsorption ratio (SAR).

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Table 2. Summary of electrical conductivity (EC1:5) of 1:5 soil‐water extract and electrical conductivity (ECe) of saturated soil paste (n=40)

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Fig. 2. Relationship between cation concentration and EC of 1:5 soil‐water extract. For Na+ and K+, the data was best fitted with an exponential model. For K+, to obtain a general trend, four outliers of which K+ concentration was greater than 0.4 mM were not used for the regression analysis.

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Fig. 3. Relationship between EC1:5 measured and calculated using the equations 1‒3. The broken line is 1:1 line. The slope of the regression equation indicates that the contribution of measured cations to EC1:5 measured was 34.9%.

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Fig. 4. Relationship between EC1:5 and ECe. The slope of the regression equation indicates that the dilution factor to convert EC1:5 to ECe is 8.70.

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Table 3. Statistics summary for the paired t‐test (n=24) between ECe measured (ECe_measured) and predicted (ECe‐pridicted) by applying the dilution factor (8.70) obtained in the present study to another data set (n=96) of Goheung RTL

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Fig. 5. Relationship between ECe measured and predicted using the dilution factor (8.70) for independent data set (n=96) of Goheung RTL.

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Fig. 6. Relationship of the difference in ECe predicted and measured with soil variables: (a) clay content and (b) sodium adsorption ratio (SAR). The ECe was predicted by applying the dilution factor (8.70) obtained in the present study (shown in Fig. 4) to independent data set (n=96) of Goheung RTL (shown in Fig. 5).

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Korean Journal of Environmental Agriculture

Assessment of Electrical Conductivity of Saturated Soil Paste from 1:5 Soil‐Water Extracts for Reclaimed Tideland Soils in South‐Western Coastal Area of Korea

@article{HGNHB8_2019_v38n2_69,
author={Hyun‐Jin. Park and Hye In. Yang and Se‐In. Park and Bo‐Seong. Seo and Dong‐Hwan. Lee and Han‐Yong. Kim and Woo‐Jung. Choi},
title={Assessment of Electrical Conductivity of Saturated Soil Paste from 1:5 Soil‐Water Extracts for Reclaimed Tideland Soils in South‐Western Coastal Area of Korea},
journal={Korean Journal of Environmental Agriculture},
issn={1225-3537},
year={2019},
volume={38},
number={2},
pages={69-75},
doi={10.5338/KJEA.2019.38.2.15},
url={https://doi.org/10.5338/KJEA.2019.38.2.15}