1. Introduction
Soil salinity is undoubtedly a basic factor which determines in a large extent soil suitability for the agricultural productivity. The problem of soil salinity makes its early presence in arid and semi-arid regions. Around 995 million hectares world-wise are estimated to suffer from salinity problems [
1]. Soil salinity assessment is based on measurements of the electrical conductivity of the saturated paste extract (EC
e), which has been established as the standard method [
2]. EC
e is considered as the most appropriate index for the estimation of the crop response to salinity. Unfortunately, this method is tedious, time consuming and requires skills and expertise to reach at saturation percentage (SP) especially in clay soils. In cases where salinity monitoring involves repeated soil sampling during the growing season and in different parts of the field, producing a large number of soil samples for the EC
e to be measured, it appears to be a difficult and laborious method [
3].
For these reasons, instead of measuring EC
e a number of researchers find it easier to measure the EC of various soil over water mass ratios, (soil:water), such as 1:1, 1:2, 1:2.5, 1:5, which are more easily attainable. It is to be noted that the soil over water mass ratios are very little correlated with the actual soil conditions. These methods can be practically very useful when one is not interested in the determination of the absolute EC values or the absolute soil salt concentration, but on the relative changes of these. A serious disadvantage of the methods measuring EC of the various soil over water mass ratios, is the effect associated with the larger water quantities on the solubility of the less soluble salts such as gypsum or lime. For the case of gypsum, for as long as the dilution increases, the concentration of all ions decreases, except those of calcium cations and the SO
4 anions which remain relatively constant. In this respect, as the degree of dilution increases for the cases of soils containing gypsum or lime, there appears a large change in the ion concentration in relation to the natural soil solution due to the presence of less soluble salts [
3,
4]. The most widely used soil over water mass ratios, (soil:water), are the 1:1 and the 1:5.
Although a strong linear relationship between EC
e and EC
1:1 or EC
1:5, has been reported, the coefficients entering this relationship are not unique but they vary according to the area of interest. The range of their differences and the causes leading to this are not yet clear. In
Table 1 and
Table 2 the respective equations EC
e =
f(EC
1:1) and EC
e =
f(EC
1:5) together with the appropriate references are shown. As for the relationship EC
e =
f(EC
1:1) proposed by [
2] this had the form EC
e = 3(EC
1:1). In this case the effect of soil particle composition or the organic content presence were not investigated [
5]. Sonmez et al. [
4], Franzen [
5], and Hogg and Henry [
6] studied the above relationship in three different soil types and they proposed three different equations corresponding to each separate soil type.
The possibility of the EC
e prediction from measurements of the EC
1:5 has been investigated in a number of regions world-wise [
3,
4,
7,
8,
9,
10]. In
Table 2 these EC
e =
f(EC
1:5) expressions together with the appropriate references are given. It is to be noted that in these expressions the effect of soil particle composition or the specific kind of salts and the organic content presence were taken into consideration. Less examined was the subject of EC
1:5 measurement in relation to the methodology followed for the acquisition of the soil over water mass ratio [
9].
Slavich and Petterson [
10] gave an expression for the multiblicative
f factor in the EC
e =
fEC
1:5 relationship according to the Equation (1) below, where
θSP denotes the saturation percentage.
Moreover, they presented the range and the mean values of f as a function of the clay content. From Equation (1) the increase of θSP leads to a decrease of f.
Visconti et al. [
11] presented EC
e =
f(EC
1:5) relationships for soils with gypsum mass percentage between 0.2–1.5% and >1.5%. For the case where gypsum mass percentage is less than 0.2% the EC
e =
f(EC
1:5) is strongly linear.
Khorsandi and Yazdi [
3] from the comparison between measured EC
e and EC
1:5 in soils from Iran reached to the conclusion that, it seems that gypsum concentration has greater impact by far on the accuracy of models in predicting EC
e than texture.
He et al. [
9,
12] tested other different methods for the determination of the EC
1:5 and concluded that the way of preparing the 1:5 soil over water mass ratio, regarding shaking the mixture and the time for equilibrium could end up in different EC
1:5 values. More specifically the time for equilibrium depends on the value of EC
e. In this respect for EC
e < 4 dS m
−1 the required time for equilibrium is larger than that for the case where EC
e > 4 dS m
−1. He et al. [
12] presented EC
e =
f(EC
1:5) models for each different method of acquiring values of EC
1:5. The ln-transformed model was shown to be better than the non-transformed and the exponential one for the whole lot of soil samples. Moreover, very good results were obtained from the curvilinear model for the range of EC
e < 4 dS m
−1. Present work aims at investigating the relationship EC
e =
f(EC
1:1) or EC
e =
f(EC
1:5) in soil samples collected from five areas of Greece and to compare those values with EC
e values derived from models developed for other regions in the world.
2. Materials and Methods
Soil samples were collected from five areas over Greece and more specifically from the Prefectures of Evia (49 samples), Lakonia (12 samples), Preveza (7 samples), Argolida (90 samples) and from the island of Kos (40 samples) at the depths of 0 to 15 cm (
Figure 1). The soils were under different crop cultivations or non-cultivated and represent soils of different soil salinity levels. Also considered to be representative of irrigated soils.
After the collection, soil samples were taken to the Agricultural Hydraulics Laboratory where they were left for air-drying. After this, samples were ground and sieved in 2 mm sieves. For the preparation of the saturated pastes, the standard method was followed [
13]. According to this, 350 g of air dried soil were used. The soil paste was left 24 h for the equilibration. Subsequently, using Buchner funnel and applying suction to the saturated paste, the saturated paste extract was collected and its electrical conductivity EC
e was measured by a conductivity meter. For the SP determination, a small portion of the paste was oven dried at 104 °C for 24 h and the standard gravimetric procedure was applied.
For the 1:1 soil over water ratio in a 100 g of soil, a 100 g distilled water were added and the mixture was shaken for 1 min by hand 4 times at 30 min-intervals, left afterwards to reach equilibrium for 4 h and soon after the extract was obtained [
13]. For the 1:5 soil over water ratio in a 50 g of soil, a 250 g distilled water were added and the same process described above was followed.
3. Results and Discussion
In
Table 3 a general classification of the values EC
e, EC
1:1 and EC
1:5 of the 198 soil samples in three classes 0–2, 2–4 και >4 dS m
−1 together with their percentage in each class are shown. The soil samples electrical conductivity varies between 0.47 and 37.5 dS m
−1 for the saturation extract, from 0.16 to 20.1 dS m
−1 for the 1:1 extract and from 0.1 to 5.08 for the 1:5 extract. From these findings it is obvious that a quite large range of EC values are examined when the SP method e.g., EC
e is compared to the EC
1:1 and the EC
1:5.
The mean EC value for the saturation extract is about two times larger than the value of EC for the 1:1 extract and 6.5 times larger than for the 1:5 extract. Our expression for the relationship EC
e =
f(EC
1:1) are almost identical to those of Sonmez et al. [
4] and of Zhang et al. [
14] who reported approximately twofold dilution when they compared the SP result with 1:1 soil/water extract. For the relationship EC
e =
f(EC
1:5) our results are almost the same with those of Aboukila and Norton [
7] who reported that mean EC
e value was 5.7 times larger than EC
1:5 while Sonmez et al. [
4] reported that mean EC
e value was 8 times larger.
According to the measured SP it seems that 30 samples (15.1%) have SP values between 20–45% and 168 samples (84.9%) have SP > 45%. From these findings it is shown that the large majority of the soil samples corresponds to fine soil texture [
8].
In
Figure 2 the linear relationship between EC
e and EC
1:1,
, for the whole lot of soil samples is presented (R
2 = 0.972).
These results are similar with the findings of other researchers in the sense that they too found a strong linear relationship between EC
e and EC
1:1. The slope (1.83) is close to what it was found by Hogg and Henry [
6], (1.56) and by Zhang et al. [
14], (1.79) as well as by Sonmez et al. [
4], (2.03) for the fine texture soils. Nonetheless our findings differ much from the findings of [
5] who found a value for the slope 2.96, or from those of the [
2] who found a value for the slope 3. Also, the values of their slopes do not change if the curve fitting linear correlation is with an intercept equal to zero, in other words if the line is forced to pass from the origin. More specifically the slope has a value equal to 1.847 and the R
2 = 0.97.
If our soil samples are separated according to their SP values, for the EC
e =
f(EC
1:1) linear curve fitting prediction, then one can see that the slope for SP values lying in the range 20–45% is larger than for the SP values larger than 45% (
Figure 3). More specifically the slope for the first case is 2.11 while for the second case is 1.79. This fact indicates that EC
e versus EC
1:1 relationship is affected from the soil mechanical analysis, since the saturation percentage SP depends strongly on the clay content, as well as, the type of the clay. When the soil texture is changing from coarse to fine, a decreasing trend in the slopes are observed both in our results and the results of [
4,
5].
In
Figure 4 the results of the comparison between EC
e and EC
1:5 are shown. The EC
e =
f(EC
1:5) relationship is given by the expression
. Also shown is R
2 = 0.931, indicating a strong linearity. The value of the slope when it is imposed the line to pass from the origin is practically unaffected, becoming
. These findings are similar to the findings of other researchers [
3,
4,
7,
8,
15] who also found strong linearity for the relationship EC
e =
f(EC
1:5). It is to be mentioned that our results do not match exactly with the other researchers’ findings but lie in between them. To be more specific the slope is less than the one found by [
4] but it is larger than the one obtained by [
3] or [
7].
These differences may be attributed to the clay content and the clay type of the soils examined, but most seriously to the methodologies applied for the EC
1:5 measurements. The last factor seems to play the most serious role in the relationship between EC
e and EC
1:5 [
12]. This could be supported because in this present work there is no gypsum in the soils examined and the soils were fine-textured as those in the works used for comparison. In this respect the methodology applied for the acquisition of the EC
1:5 values appears to be the basic different factor considering present work and the work of other scientists. Apart from this factor, concerning the acquisition of EC
1:5, another probable factor could be the range of the EC
e values from which the EC
e =
f(EC
1:5) relationship in this work, in relation to the other similar works, was estimated. We consider that these two factors were responsible for the fact that our findings gave values of the slope in the EC
e =
f(EC
1:5) expression close but not identical to similar findings of other scientists presented in the literature.
In
Figure 5 the comparison is shown between the predicted EC
e values, as these were obtained by an ln-transformed model (ln(EC
e) =
f(ln(EC
1:5)) and the predicted EC
e values, as these were obtained by the linear model (EC
e =
f(EC
1:5), against the actually measured EC
e values. From
Figure 5 it is shown that the predicted EC
e values, as these were obtained by an ln-transformed model are very close to the 1:1 line and give better results than those obtained by the linear model. It is to be noted that a strong linearity was obtained in the ln-transformed model, as this was also reported by He et al. [
12] for each one out of the four examined cases of equilibrium, concerning EC
1:5 determination (data not shown). It is to be reminded that in their work the majority of their soil samples (67%) had SP values in the range 20–45% while in the present work in this range only the 15.1% were included. Therefore, the ln-transformed model seems to have a general validity for all soil types and in this sense, it is a reliable methodology for the estimation of EC
e from the EC
1:5 measurements.
It is to be noted again that if, soil samples are separated according to their SP values, for the determination of the ECe = f( EC1:5 ) relationship, then one can see that the slope, for SP values lying in the range 20–45%, is larger than for the SP values larger than 45%