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To cite this article: Yishak Beyene, Fanuel Laekemariam, Alemayehu Kiflu, Gifole Gidago, Lakew
Getaneh & Alemu Andualem (2022): Phosphorus Sorption Characteristics of Acidic Luvisols and
Nitisols under Varying Lime Rates, and Response Validation Using Wheat, Communications in Soil
Science and Plant Analysis, DOI: 10.1080/00103624.2022.2070637
Introduction
Soil acidity is a critical issue requiring urgent attention because of its impact on crop production and
productivity (Fanuel and Kibebew 2021; Melese and Yli-Halla 2016; Tessema, Argaw, and Adgo 2012).
In acid soils, phosphorus (P) is highly fixed due to intensive weathering and the leaching of basic
cations attributed to high rainfall conditions (Fanuel and Kibebew 2021; Habtamu 2015). Acidity is
also associated with aluminum (Al), iron (Fe), hydrogen (H), manganese (Mn) toxicities to plant roots
in the soil solutions and also cause corresponding deficiencies of the available phosphorus (av. P),
calcium (Ca), magnesium (Mg) and potassium (K)(Kisinyo et al. 2014). Significant P fixation and its
precipitation as iron and aluminum phosphates are widespread in acidic soils (Shen et al. 2001) This
situation is very common in Luvisols and Nitisols.
Nitisols and Luvisols are soils with deep, well-drained, red tropical soil having high clay content
(IUSS 2014). In red soils with high clay content, there could be P fixation (Birru, Heluf, and Gupta
2003; Brady and Well 2008) and there is a need to study sorption characteristics. In acidic soils,
CONTACT Fanuel Laekemariam maedotmeklit@gmail.com College of Agriculture, Wolaita Sodo University, P.O.Box 138,
Wolaita Sodo, Ethiopia
Supplemental data for this article can be accessed online at https://doi.org/10.1080/00103624.2022.2070637
© 2022 Taylor & Francis Group, LLC
2 Y. BEYENE ET AL.
Figure 1. Location map of study areas, SNNPRS in Ethiopia and Dawro and Wolaita Zone in SNNPRS (a), Location of study areas in
Dawro and Wolaita Zone (b), Kechi (c) and Farawocha (d) sites.
Crop type
The dominant crops grown in Farawocha area include avocado (Persea americana), banana (Musa
balbisiana), cassava (Manihot esculenta), ginger (Zingiber officinale), maize (Zea mays), taro (Colocasia
esculenta), and teff (Eragrostis abyssinica). In Kechi, the crops grown include avocado (Persea
americanaMill.), barley (Hordeum vulgare), beans (Phaseolus vulgaris), banana (Musa acuminate
Colla), enset (Ensete ventricosum), coffee (Coffea arabica), mango (Mangifera indica). pea (Pisum
sativum), potato (Solanum tuberosum) and wheat (Triticum aestivum).
Climate
For the Farawocha site, the 10 years (2010–2019) monthly temperature ranges from 13°C to 25°
C with annual rainfall ranging from 1184 to 1854 mm (Figure 2) whereas, at Kechi, the monthly
temperature ranges from 14°C to 24°C and an annual rainfall of the area varies from 1443 to
2535 mm (Figure 3) (PDAV, 2020).
Temperature (OC)
25
RF (mm)
150 20
100 15
10
50
5
0 0
Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec
Months
Temperature (OC)
35
200
RF (mm)
30
150 25
20
100 15
10
50
5
0 0
Months
Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec
peroxide and dispersing the soils with sodium hexametaphosphate. The pH of the soils was measured
in water suspension in a 1:2.5 (soil: liquid ratio) potentiometrically using a glass-calomel combined
electrode (Van Reeuwijk 1992). The Walkley and Black (1934) wet digestion method was used to
determine soil organic carbon content. The total nitrogen (TN) was determined by the Kjeldahl
method (Bremner 1960).
Available phosphorous (av. P), calcium (Ca2+), potassium (K+), magnesium (Mg2+), sodium (Na+),
sulfur (S), copper (Cu), iron (Fe), manganese (Mn), zinc (Zn) and boron (B) were extracted according
to the procedure of Mehlich-3 (Mehlich 1984). The concentration of elements in the supernatant was
measured using an inductively coupled plasma (ICP) spectrometer. The exchangeable acidity (Al3+
and H+) was measured by displacement with 1 M KCl and titration with 0.05 M sodium hydroxide
(NaOH) (Sahlemedhin and Taye 2000). Cation Exchange Capacity (CEC) of soils was determined by
the ammonium acetate method (Sahlemedhin and Taye 2000).
Phosphorous sorption
After 30 days of incubation, the soils were air-dried at ambient temperature (20–25°C), sieved
through a 2 mm sieve, and were used to study P sorption characteristics. Phosphorus sorption
characteristics were determined by the batch equilibrium method in which soil samples were
agitated with known concentrations of P solutions (Graetz and Nair 2008). Phosphorus as KH2
PO4 was dissolved in a 0.01 M solution of CaCl2 (calcium chloride) in distilled water. The CaCl2
solution is used as the aqueous solvent phase to improve centrifugation and minimize cation
exchange (Fuhrman et al. 2004).
To study the P sorption, a 2 g air-dried incubated soil sample was placed in a 100 ml plastic bottle of
30 ml 0.01 M CaCl2 (Fernandes and Coutinho 1994). The sample was mixed continuously with
a constant agitation speed of 350 rpm for better mass transfer with a high interfacial area of contact.
Afterward, the calculated amount of stock solution of P for each rate was added. The concentrations of
the stock solution were 0, 10, 20, 30, 40 and 50 mgPL−1 (KH2PO4). Each sorption set for P was
replicated three times. The mixture was shaken at 25°C on a reciprocal shaker for 24 hr (Graetz and
Nair 2008). After equilibration time, the suspension was filtered through Whatman paper No. 42 filter
paper and the concentration of P in the clear extract was determined by the ascorbic acid method.
A blank was run for each soil with the same amount of soil and total volume of 30 ml 0.01 M CaCl2
solution (without P) and it was subjected to the same procedure. This serves as a background control
during the analysis to detect interfering compounds or contaminated soils. The P sorption data for the
soils were fitted into the following equation such as Langmuir and Freundlich.
Langmuir equations (Kleinman and Sharpley 2002)
C 1 C
¼ þ (3)
X Xmk Xm
6 Y. BEYENE ET AL.
Field experiment
The field experiment consisted of six rates of P (0, 8.2, 16.4,24.6,32.9 and 41.1 kg P applied in the form
of NPSB fertilizer (19% N, 16.4 P, 7% S and 0.1% B) and three rates of lime (0, 650, and 1300 kgha−1).
NPSB fertilizer rates was equivalent to 0, 50, 100,150,200, and 250 kgha−1. The experiment was laid out
in factorial combination in randomized complete block design with three replications. In addition, 50
kgha−1 KCl (60% K2O), and 100 kg urea (46% N) were used as supplements. Bread wheat variety
Alidoro which was developed and released by Kulumsa Agricultural Research Center (KARC) in 2007
was used as a test crop. The plot size was 2 m x 2 m (4 m2) which consisted of eight rows. The plant
COMMUNICATIONS IN SOIL SCIENCE AND PLANT ANALYSIS 7
spacing was 25 cm between rows with a seeding rate of 125 kg ha−1. All NPSB and KCl fertilizer were
applied at the time of sowing and urea were applied by split application of which 25% was at the
sowing and 75% at tillering stage.
The field lime requirement was estimated based on exchangeable acidity as follows
g
kg of soil�0:20m�10 m2�B:D:ðcm3Þ�1000�1:5
CmolEA 4
Lime requirement ¼ 2000 and PAS
Where, 0.20 m is the plow depth; 104 m2 is an area for 1 ha of land; EA is exchangeable acidity; B.D is
soil bulk density of the soil multiplied by 1000 to convert g cm−3 to kg m−3 and a 1.5 multiplication factor
was adopted based on a recommendation by Birhanu et al. (2016). For the assumption that the permissible
acid saturation percentage (PAS) level for wheat is 10% (Fanuel and Kibebew 2021). Lime was applied one
month before planting to all plots at once in broadcast and incorporated into the soil by using a hoe.
At full maturity, the crop was harvested, then threshed, and converted to kg ha−1. The yield was
adjusted to 12.5% moisture to ensure uniform treatment comparison.
ð100 MCÞ
Adjusted grain yield ¼ Grain yield obtainedðkg per haÞx
ð100 12:5Þ
Where MC- is the moisture content of bread wheat grains at the time of measurement and 12.5 is the
standard moisture content of bread wheat in percent. Finally, yield per plot was converted to kg ha−1
Table 1. Surface soil characteristics of Farawocha (Nitisols) and Kechi (Luvisols) sites before liming.
Parameter Unit Farawocha site Kechi site
Soil Particle size distribution
Sand % 24 20
Silt % 24 38
Clay % 52 42
Soil texture Clay Clay
Bulk Density g/cm3 1.2 1
pH 4.5 5.3
Exchangeable Acidity cmol(+)kg−1 4.18 1.47
Exchangeable Hydrogen cmol(+)kg−1 0.33 0.75
Exchangeable Aluminum cmol(+)kg−1 3.84 0.72
% OC % 2.44 3.97
% TN % 0.17 0.44
Available P mgkg−1 3.2 2.74
Sulfur mgkg−1 29.54 8.24
Boron mgkg−1 0.39 0.02
Iron mgkg−1 178.69 415.63
Manganese mgkg−1 198.78 311.27
Copper mgkg−1 0.66 0.72
Zinc mgkg−1 4.04 4.27
Calcium cmol(+)kg−1 2.44 4.33
Magnesium cmol(+)kg−1 0.33 0.75
Available Potassium cmol(+)kg−1 0.67 0.24
Sodium cmol(+)kg−1 0.17 0.07
Calcium Saturation Percentage % 16.7 11.5
Magnesium Saturation Percentage % 2.24 1.99
Exchangeable Sodium % 1.2 0.52
Cation Exchanging Capacity cmol(+)kg−1 14.6 37.72
2015; Nand, Baligar, and Jones 2011). Furthermore, Abreha (2013) associated the low S content with
acidic soil reaction, as it aggravates the adsorption of the sulfate ion (SO42-) with Al and Fe
compounds.
In the Nitisol, the exchange site was occupied in the order of Ca > K > Mg> Na whereas it was Ca >
Mg > K > Na in Luvisols. The soil Ca and Mg saturation percentage were rated under a very low
category according to Ethiopian Soil Information System (2014). This might be due to the leaching of
Ca and Mg that led to the dominance of Al in the exchanging sites. This is consistent with the
observation of Miller 20166), and Neina (2019) who reported that leaching and acidity are the main
influencing factors on soils with very low Ca and Mg saturation percentages. The CEC values qualify
under medium and very high levels in Farawocha site and Kechi sites, respectively (Hazelton and
Murphy 2007).
The concentration of micronutrients were found to be in sequence of Mn > Fe >Zn > Cu >B (N)
and Fe>Mn >Zn > Cu >B (Kechi). High concentration Fe could lead to toxicity for most of the crop
species (Jones 2003). The B content at both research farms soils was rated under very low (<
0.5mgkg−1) according to the EthioSIS(2014).
Adsorped P (mgKg-1)
350
300
250
200
150
100
50
0
0 10 20 30 40 50 60
Equilibruim Con. P (mgL-1)
Figure 4. Phosphate adsorption isotherm of Nitisols.
300
250
200
150
100
50
0
0 10 20 30 40 50 60
Equilibrium Conc. of P (mgL-1)
Figure 5. Phosphate adsorption isotherm of Luvisols.
0 − 100, 100–400 and > 400 mg P kg−1 are classified as low, moderate and high respectively. Therefore,
Nitisols without lime was found to be a high P sorping soils and changed to moderate P sorpition with
lime, and all the P sorpition values at Luvisols were found under moderate P sorption levels. An earlier
study by Kisinyo et al. (2013) revealed that the application of lime decreases the amount of
10 Y. BEYENE ET AL.
P adsorption maximum under maize growing acid soils of Kenya. Abdenna et al. (2020), reported that
lime treatment probably increased the availability of P through decreased sorption; and Sato (2003)
also indicated decreased P sorption with increased pH. He reported decreased P adsorption by 21% as
pH increased from 4.7 to 5.9 and by 34% as pH increased further to 7.0 through liming
0.14
0.12
0.1
0.08
0.06
0.04
0.02
0
0 10 20 30 40 50 60
Equilibrium Conc. of P (mgL-1)
Figure 6. Langmuir adsorption isotherms of Nitisols.
COMMUNICATIONS IN SOIL SCIENCE AND PLANT ANALYSIS 11
0.35
0.3
0.25
0.2
0.15
0.1
0.05
0
0 10 20 30 40 50 60
0% Limed 50% Limed 100% Limed 150 Limed
2
1.5
1
0.5
0
0 0.5 1 1.5 2
Log Ce mgL-1
Figure 8. Freundlich adsorption isotherms of Nitisols.
1.5
0.5
0
0 0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 1.8
LogCe mgL-1
Figure 9. Freundlich adsorption isotherms of Luvisols.
relatively smaller Xm values of the present soils could be due to the application of lime and which have
also a significant increase in soil pH and available P with liming could be attributed to the presence of Ca2
+
ions contained in the lime. The Ca2+ ions displace H+ and Al3+ ions from the soil adsorption sites which
are relatively low P fixing soils than other soil types (Kisinyo 2016; Muindi et al. 2015; The et al. 2006).
The Langmuir binding energy (k) values of 0.51–9.3 L mg−1 with the mean value of 3.23 Lmg−1
(Nitisols) and 0.19–0.25 Lmg−1 with the mean value of 0.22 L mg−1 (Luvisols). The values of k for the
soils were greater than 0.07 L mg−1 suggesting that there is no risk of loss of P into the water (Mcdowell
12 Y. BEYENE ET AL.
Table 3. P-sorption indices of soils at Farawocha (Nitisols) and Kechi (Luvisols) sites derived from Langmuir and Freundlich equations.
Langmuir equation P sorption Indices Freundlich equation P sorption Indices
2
Soil type Lime Xm K MBC EPRl R N Kf EPRf R2 P
mgkg−1 Lmg−1 Lkg−1 mgkg−1 Lkg−1 mgkg−1 mgkg−1 Kgha−1
Nitisols 0% 1000a 0.51c 510.07a 92.23a 0.82b 3.10b 101.2b 59.38a 0.85c 142.5a
50% 667b 0.52c 346.84b 62.12b 0.66d 4.21a 212.3a 55.4b 0.96a 132.96b
100% 125c 2.65b 331.25c 43.3c 0.81c 2.56c 100.63b 52.2c 0.90b 125.28c
150% 37d 9.21a 340.77d 23.98d 0.86a 2.25d 45.30c 21.8d 0.91b 52.32d
LSD 0.05 3.01 0.22 0.068 0.096 0.001 0.26 1.19 0.98 0.001 2.31
CV% 0.23 2.5 0.01 0.09 0.12 3.04 0.37 0.88 0.38 0.09
Luvisols 0% 251a 0.19c 47.69a 39.20a 0.83b 2.45d 120.41d 52.42a 0.96b 104.48a
50% 142c 0.25a 35.5d 15.7b 0.68d 1.56b 78.57b 28.00b 0.97a 56.20b
100% 166b 0.23b 38.18c 11.30c 0.71c 1.01a 112.5a 22.86c 0.95c 45.72c
150% 166b 0.25a 41.5b 7.90d 0.90a 2.035c 16.3c 12.97d 0.94d 25.94d
LSD 0.05 1.97 0.01 0.056 0.04 0.001 0.10 1.15 0.098 0.0001 1.54
CV% 0.34 1.74 0.07 0.11 0.39 1.78 0.78 0.16 0.06 0.05
Xm = Langmuir sorption maximum, k = bonding energy of the Langmuir, MPBC = maximum P buffering capacity EPRl = External
P requirement of Langmuir, EPRf = External P requirement of Freundlich, Kf = Freundlich surface coverage and n = sorption energy
of the Freundlich. Numbers in each column for a particular soil type followed by the same letter are not significantly different
(P > 0.05)
and Sharpley 2002). The value of Freundlich sorption energy (n) was highest (4.21 L kg−1) in 50%
limed and lowest (2.25 L kg−1) at 150% limed soil for the Nitisols whereas Luvisols the value of n was
highest (2.41 L kg−1) 0% limed and lowest (1.05 L kg−1) at 100% limed (Table 3).
The Freundlich adsorption capacity (Kf), which is a measure of the reactive surface area (relative
adsorption capacity) of the soil, is presented in (Table 3). In Nitisols, Kf values ranged from 45.03 mg
kg−1 (150% limed) to 212.3 mg kg−1 (50% limed) whereas in the Luvisols it ranged from 16.3 mg kg−1
(150% limed) to 120.41 mg kg−1 (0% limed). Overall, the lowest Kf values in both soil types were
recorded at 150% limed. According to Sarafaz, Abid, and Mehdi (2009), a larger Kf value implies
a larger adsorbing capacity. For practical purposes, the Kf may be used to differentiate soils having
different P adsorption capacities. Thus, the soils limed at 150% had a lower sorption capacity relative
to the others. The variation observed in P sorption capacities (Kf) among soils in the different sites
might be ascribed to differences in oxides of Al and Fe and clay content in soils (Obura 2008). The
Freundlich parameter Kf was found to be a practically useful parameter in summarizing the adsorp
tion properties of soil over a wide range of equilibrium concentrations.
The maximum value of Xm, EPR, and kg P ha−1 was recorded in both soils without liming. In both
soil types, Xm, EPR, and kg P ha−1 decreased following the order of 0% < 50% <100% < 150% limed.
Application of lime decreased soil EPR, Xm and kg P ha−1 probably due to the reduction of soil
P sorption thus making both the native and the applied P available for plants uptake. Similar studies in
tropical acid soils indicated that lime application increased soil av. P (Kisinyo et al. 2014; Muindi et al.
2015).
Phosphate fertilizer increased soil P content due to the release of phosphate ions into the soil
solution during its dissolution. Increased soil av. P in acid soils due to phosphorus fertilizer application
has been reported elsewhere (Opala et al. 2014). Langmuir adsorption maximum (Xm) was strongly
and positively correlated with soil properties at the Nitisols i.e., (r = 0.99, ex. Fe3+); (r = 0.84, ex. Al3+)
and Xm was strongly and negatively correlated with soil properties of Ca, Mg and av. P i.e., (r = −0.98,
Ca); (r = −0.98, Mg); (r = −0.90, av. P) while Luvisols (r = 0.99, ex. Fe3+); (r = 0.97, ex. Al3+) and Xm
were strongly and negatively correlated with soil properties of Ca, Mg and av. P i.e., (r = −0.84, Ca);
(r = −0.95, Mg); (r = −0.93, av. P). This is in agreement with the observation by Zhang et al. (2005) and
Asmare (2014), who reported a positive correlation between Xm and Al. Similarly, Zinabu, Wassie,
and Dhyna (2015) found a strong and positive correlation between Al and Xm and the adsorption
COMMUNICATIONS IN SOIL SCIENCE AND PLANT ANALYSIS 13
parameters were positively and strongly correlated with an ex. Fe3+ and Al3+ indicate the presence of
reactive and strong P adsorption sites on Fe and Al oxides (Chunye et al. 2009; Thomas, Omueti, and
Ikhane 2018).
Luvisols were demanding the application of P fertilizer at a rate of 238 kg ha−1 TSP (48 kg P ha−1) and
200 kg ha−1 TSP (40 kg P ha−1), respectively, across all soils which is equivalent to 20 mg P kg−1 of soil
(Daba et al. 2002).
Accordingly, these values are greater than the blanket recommendation of 94.5 kg P ha−1 and
64.48 kg P ha−1 in Nitisols and Luvisols, respectively, concerning 0% limed. The application of
P fertilizers based on the blanket recommendation in the study area may result in a substantial yield
deficit, i.e. yield remaining much below the maximum, owing to P deficiency. Therefore, a strong
emphasis should be given on the ways to minimize P fixation and to increase P use efficiency,
especially for soils with relatively high P fixing capacity.
Therefore, the use of soil test P fertilizer recommendation based on the adsorption curves together
with plant response for the applied P for different crop varieties should be done for the soils of the
study area rather than using the usual conventional practice which could underestimate or over
estimate the amount P fertilizer to be applied. Since the EPRf of the soils calculated from the
Freundlich equation (Table 3) is an estimate of P sorption potential (Wang et al. 2000) and an
adequate EPR for most crops (Abdenna et al. 2020; Asmare 2014; Ayenew et al. 2018; Fekadu,
Wassie, and Gashaw 2017; Zinabu, Wassie, and Dhyna 2015), diverse crop varieties in the study
area could require a different amount of P fertilizer.
Thus, it could be inferred that the external and internal P requirement of a crop, as well as
the variety, has to be investigated to find a reasonable amount of fertilizer to be applied to
a particular soil concerning crops and sites. External P requirement (EPRf) were strongly and
positively correlated with adsorption parameters and soil properties at Farawocha site i.e.,
(r = 0.80, Xm); (r = 0.99, ex. Al3+); (r = 0.99, ex. acidity); (r = 0.85, ex. Fe3+) and EPRf were
strongly and negatively correlated with soil properties of Ca, Mg and av. P i.e., (Ca, r = −0.79);
(Mg, r = −0.81); (av. P, r = −0.57) whereas Kechi site (Xm, r = 0.83,); (ex. Al3+, r = 0.77) and
(ex. acidity, r = 0.78) (ex. Fe3+, r = 0.85) and EPRf were strongly and negatively correlated with
soil properties of Ca, Mg and av. P i.e., (Ca, r = −0.54); (Mg, r = −0.73); (av. P, r = −0.65). The
adsorption parameters were positively and strongly correlated with Fe3+ and Al3+ indicating the
presence of reactive and strong P adsorption sites on Fe and Al oxides (Chunye et al. 2009;
Thomas, Omueti, and Ikhane 2018).
Table 4. Effects of LR on soil pH, ex. acidity, ex.Al3+ and ex. H+ at Nitisols and Luvisols.
ex. acidity ex. Al 3+ ex. H +
Soil type LR(%) pH (cmol(+)kg−1) (cmol(+)kg−1) (cmol(+)kg−1)
Nitisols 0 4.55d 4.18a 3.84a 0.33a
50 5.38c 0.73b 0.34b 0.39a
100 6.09b 0.23c 0.01c 0.23b
150 6.60a 0.23c 0.01c 0.22b
LSD 0.05 0.094 0.10 0.15 0.14
CV% 0.57 4.10 4.91 16.61
Luvisols 0 5.33c 1.47a 0.72a 0.75a
50 5.78bc 0.17b 0.04b 0.13b
100 6.27c 0.15b 0.07b 0.08c
150 6.51a 0.17b 0.05b 0.12b
LSD 0.05 0.092 0.04 0.03 0.035
CV% 0.42 3.29 6.95 6.85
Means within a column for a particular soil type followed by the same letter(s) are not significantly different from each other
at (p = 0.05)
ions into the soil solution and likely displacement of Al3+, H+ and Fe3+ ions by Ca2+ ions it contains.
This led to the observed reduction in P sorption at both soil types (Caires et al. 2008; Kisinyo et al.
2013; Buni 2014; Opala 2017). Similar studies have reported increased soil pH, available P, reduction
in Al levels and P sorption in acid soils due to lime application (Kisinyo 2016; Sabine, Dorothea, and
Schmidhalter 2018; Temesgen et al. 2017). Liming acid soils increased soil pH, ex. Ca and decreased Al
and acid saturation. Ex. Al decreased with increased pH and was fully precipitated at low pH (Abdenna
et al. 2020).
Lime had significant effects (P ≤ .05) on soil nutrients of av. K, Ca and Mg. In Nitisols the soil
nutrients like av. P, av. K, Ca and Mg were found to be lowest for 0% limed soil with 3.2 Ppm,
261.8 mg kg−1, 488.2 mg kg−1 and 39.20 mg kg−1 respectively. The highest value was recorded for av.
P = 6.32 Ppm by 150%, av. K = 319.3 mg kg−1 by 50%, Mg = 86.63 mg kg−1 by 150%, and
Ca = 3659.9 mg kg−1 by 150% limed. whereas Luvisols av. P, av. K, Ca and Mg were found to be
lowest for 0% limed soil with 2.74 Ppm, 95.27 mg kg−1, 89.9 mg kg−1 and 866.7 mg kg−1 respectively.
The highest value was recorded for av. P = 8.72 Ppm by 150%, av. K = 319 mg kg−1 by 50%,
Mg = 606 mg kg−1 by 150%, and Ca = 8851.2 mg kg−1 by 150% limed. With increase lime rate the
increase of available P was recorded which could be due to reduction in Al levels and P sorption in
acid soils due to lime application as reported by many researchers (Abdenna et al. 2020; Kisinyo
et al. 2013; The et al. 2006) and application of lime improved av.K, Ca and Mg in soil (Achalu et al.,
2012; Tariq and Mott 2006). Table 5 shows the effect of liming on soil OC and TN of Nitisols and
Luvisols. Lime had significant effects (P ≤ .05) on soil OC. The soil nutrients of Nitisols OC and TN
were lowest (2.38% and 0.17%), respectively, for 0% limed and the highest value (OC = 2.14% by
150%, TN = 0.17% by all lime rate).
Whereas Luvisols site the soil nutrients of OC and TN lowest value (4.08% and 0.47%), respectively,
were recorded by 150% limed and the highest value (OC = 4.48% at 100% and TN = 0.47% 100 and
150% limed). Lime did not influence TN at the Nitisols. Similar findings were recorded by Jefar and
Gebresilassie (2017), who found that the application of lime for acid soil amelioration and better
soybean performance in southwestern Ethiopia.
The increase in extractable S content in soil due to liming may be attributed to increased
soil pH. An increase in Zn content may be related to the replacement of Zn by Mg from
specific sites on soil exchange complex which in turn increased the extractable Zn in soil
(Barman, Lalit, and Raj Kumar 2014; Srivastava and Gupta 1996). Liming also increases the
solubility of B in the soils of the Nitisols and Luvisols. Barman, Lalit, and Raj Kumar (2014),
also found liming, increased the B retention capacity of soil due to the formation of insoluble
metaborate.
16 Y. BEYENE ET AL.
Table 5. Shows the effects of LR on the exchangeable bases (av. P, av.K, Ca and Mg),OC and TN at Nitisols and Luvisols.
av. K Ca Na Mg OC av. P TN
Soil type LR (%) mgkg−1 mgkg−1 mgkg−1 mgkg−1 % mgkg−1 %
Nitisols 0 261.81c 488.2d 38.78 39.20a 2.44a 3.2d 0.17a
50 319.30a 1588.6c 39.82 56.87b 2.41b 4.53c 0.17a
100 309.00b 2752.6b 40.50 73.93c 2.39c 5.36b 0.17a
150 316.2a 3659.9a 35.65 86.63 d 2.31d 6.32a 0.17a
LSD 0.05 3.73 7.34 3.91 4.31 0.14 0.18 0.05
CV% 0.44 0.12 3.58 2.38 2.16 1.96 1.56
Luvisols 0 95.27d 866.7d 15.2b 89.9d 4.48ab 2.74c 0.44b
50 319.00a 5961.1c 37.4b 557.6c 4.29b 8.00b 0.48a
100 277.95c 7267.3b 38.71a 581.4b 4.08c 7.41b 0.47a
150 310.65b 8851.2a 37.23b 606.4a 4.40ab 8.72a 0.47 a
LSD 0.05 7.49 7.15 1.29 2.60 0.33 0.82 0.05
CV% 1.06 0.04 1.42 0.20 2.74 6.79 1.56
Means within a column for a particular soil type followed by the same letter(s) are not significantly different from each other at
(p = 0.05).
Lime had significant effects (P ≤ .05) on soil micronutrients of Fe3+ and Mn (Table 6). In the Nitisols,
the lowest values of Fe and Mn (130 mg kg−1 and 150 mg kg−1), respectively, occurred in the 150% limed
whilst the highest values (178 mg kg−1 and 198.40 mg kg−1) occurred in the unlimed (0%) soil. Similarly,
in Luvisols the lowest values of Fe3+ and Mn (173.24 mg kg−1 and 104.04 mg kg−1), respectively, occurred
in the 50% limed and the highest values (415.63 mg kg−1 and 311.2 mg kg−1), respectively, occurred in the
unlimed soil. Liming reduces the levels of Fe and Mn in acid soils. This is possible as a result of
precipitation of Fe and Mn as carbonates, oxides or hydroxides resulting from an increase in pH
(Adane 2014; The et al. 2006).
Lime had significant effects (P ≤ .05) on soil CEC (Table 6). The lowest CEC values in Nitisols and
Luvisols were recorded by 0% limed whereas liming at 150% in both soil types resulted in the highest
CEC value, which could be attributed to the change in pH (Adane 2014).
Table 6. Effects of Liming Rates (LR) on soil micronutrients, Sulfur (S), and cation exchange capacity (CEC) at Nitisols and Luvisols.
B Cu Zn S CEC Mn Fe
Soil type LR(%) mgkg−1 mgkg−1 mgkg−1 mgkg−1 cmol(+)kg−1 (mgkg−1) (mgkg−1)
Nitisols 0 0.39c 0.66c 4.04a 29.54d 14.58b 198.40a 178.69a
50 0.47b 0.79b 4.30c 34.1c 16.09ab 167.17b 156.61b
100 0.51a 0.88a 4.60b 39.06b 14.73b 159.60c 129.82c
150 0.51a 0.90a 4.57b 44.04a 17.99a 150.1d 130.60c
LSD 0.05 0.014 0.03 0.14 1.63 2.68 4.71 4.24
CV% 1.06 1.47 1.08 1.57 5.99 0.99 1.01
Luvisols 0 0.02b 0.72d 4.27c 8.24c 37.73b 311.27a 415.63d
50 1.34a 4.36c 60.81a 54.46b 40.15ab 294.38b 403.19b
100 1.28ab 4.55b 56.17b 70.23a 40.50ab 285.21c 378.21a
150 1.22b 5.01a 57.9ab 72.12a 42.73a 104.04d 173.21c
LSD 0.05 0.19 0.45 3.24 1.37 4.0 1.94 1.94
CV% 7.16 4.41 2.56 0.95 3.49 0.23 0.28
Means within a column for a particular soil type followed by the same letter(s) are not significantly different from each other at
(p = 0.05).
COMMUNICATIONS IN SOIL SCIENCE AND PLANT ANALYSIS 17
Table 7. Grain yield (kg/ha) of wheat as affected by the interaction effect of lime and NPSB fertilizer rate in the luvisols.
NPSB
P (Kg/ha) (kg/ha) Lime rate
0 50%(650 kg) 100% (1300 kg) Mean
0 0 791.3k 1611.6ij 1532 j 1311.6
8.2 50 1857.4hij 2222 h 2934ef 2337.8
16.4 100 2256gh 2769.5fg 3444.1bcde 2823.2
24.6 150 2133.1hi 3149.7def 3935.9ab 3072.9
32.9 200 2948ef 3601.1bcd 4345.2a 3532.6
41.1 250 3286.9cdef 3913.6ab 3735.3bc 3644.96
Mean 1856.6 2877.92 3321.08 -
LSD (5%) 534.16
CV(%) 11.48
LSD = Least Significant Difference at 5% level; CV (%) = Coefficient of Variation; Means in columns followed by the same
letter(s) are not significantly different at 5% level of significance
P rate is efficiently utilized by crops and subsequently resulted in better crop growth and yield. The
result further suggests that liming, or increasing the rate of P alone cannot serve to achieve the
maximum potential of acid soil.
Conclusion
In acidic Nitisols and Luvisols where P was deficient, the Freundlich was found the best-fitted model in
describing the soil P-sorption isotherms. Meanwhile, liming significantly reduced the exchangeable
acidity, Fe3+, and P required from external sources. Divergently liming was also found to be positively
and significantly correlated with soil pH, available P, Ca2+, Mg2+, K, S, and micronutrients (B, Cu, and
Zn). Both soils in the absence of lime would demand external P (kg/ha) between 104.48 kg/ha (Luvisols)
and 142.5 kg/ha (Nitisols) but the amount of P at the increasing rate of lime was reduced by 63.3% in the
Nitisols, and by 79.3% in Luvisols. Furthermore, field validation of external P requirement on the
Luvisols indicated the substantial yield increments using 32.9 kg P ha−1 X 1300 kg lime ha−1, yet
P under real test exceeds the model estimation by 26.8%. Based on the model and field test, it was
concluded that blanket P fertilizer recommendation leads to under-application. Generally, owing to the
strongly acidic soil reaction of both soil types, the result signifies a huge variation in P sorption capacity.
Therefore, to ensure optimum P supply of acid soils, examining soils’ P sorption capacity, and exploring
possible reclamation measures along with validation of EPR using different crops is suggested.
Acknowledgments
We are very grateful Wolaita Sodo University for funding this research.
Disclosure statement
No potential conflict of interest was reported by the author(s).
Funding
This work was funded by the Wolaita Sodo University.
ORCID
Fanuel Laekemariam http://orcid.org/0000-0001-6913-5171
Alemayehu Kiflu http://orcid.org/0000-0002-9227-3289
Lakew Getaneh http://orcid.org/0000-0002-5318-2974
18 Y. BEYENE ET AL.
Data availability
Data presented in this manuscript can be made available as per the policy of the journal.
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