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Low soybean yields in western Kenya have been attributed to low soil fertility despite much work done on nitrogen (N) and phosphorus (P) nutrition leading to suspicion of other nutrient limitations. To investigate this, a nutrient omission trial was set up in the greenhouse at the University of Eldoret-Kenya to diagnose the nutrients limiting soybean production in Acrisols from Masaba central and Butere sub-Counties, and Ferralsols from Kakamega (Shikhulu and Khwisero sub-locations) and Butula sub-Counties and to assess the effect of liming on soil pH and soybean growth. The experiment was laid out in a completely randomized design with ten treatments viz; positive control (complete), negative control (distilled water), complete with lime, complete with N, minus macronutrients P, potassium (K), calcium (Ca), magnesium (Mg) and sulphur (S) and with, micro-nutrients boron (B), molybdenum (Mo), manganese (Mn), copper (Cu) and zinc (Zn) omitted. Visual deficiency symptoms observed included interveinal leaf yellowing in Mg omission and N addition and dark green leaves in P omission. Nutrients omission resulted in their significantly low concentration in plant tissues than the complete treatment. Significantly (P 0.05) lower shoot dry weights (SDWs) than the complete treatment were obtained in different treatments; omission of K and Mg in Masaba and Shikhulu, Mg in Khwisero, K in Butere and, P, Mg and K in Butula. Nitrogen significantly improved SDWs in soils from Kakamega and Butula. Liming significantly raised soil pH by 9, 13 and 11% from 4.65, 4.91 and 4.99 in soils from Masaba, Butere and Butula respectively and soybean SDWs in soils from Butere. The results show that, poor soybean growth was due to K, Mg and P limitation and low pH in some soils. The results also signify necessity of application of small quantities of N for initial soybean use.
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RESEARCH ARTICLE
Nutrients Limiting Soybean (glycine max l)
Growth in Acrisols and Ferralsols of Western
Kenya
Ludy Keino
1
*, Frederick Baijukya
2
, Wilson Ngetich
1
, Abigael N. Otinga
1
, John
R. Okalebo
1
, Ruth Njoroge
1
, John Mukalama
3
1Department of Soil Science, University of Eldoret, Eldoret, Kenya, 2International Institute of Tropical
Agriculture (IITA), Dar es Salaam, Tanzania, 3International Centre for Tropical Agriculture, Nairobi, Kenya
*ludykeino@yahoo.com
Abstract
Low soybean yields in western Kenya have been attributed to low soil fertility despite much
work done on nitrogen (N) and phosphorus (P) nutrition leading to suspicion of other nutrient
limitations. To investigate this, a nutrient omission trial was set up in the greenhouse at the
University of Eldoret-Kenya to diagnose the nutrients limiting soybean production in Acrisols
from Masaba central and Butere sub-Counties, and Ferralsols from Kakamega (Shikhulu
and Khwisero sub-locations) and Butula sub-Counties and to assess the effect of liming on
soil pH and soybean growth. The experiment was laid out in a completely randomized
design with ten treatments viz; positive control (complete), negative control (distilled water),
complete with lime, complete with N, minus macronutrients P, potassium (K), calcium (Ca),
magnesium (Mg) and sulphur (S) and with, micro-nutrients boron (B), molybdenum (Mo),
manganese (Mn), copper (Cu) and zinc (Zn) omitted. Visual deficiency symptoms observed
included interveinal leaf yellowing in Mg omission and N addition and dark green leaves in P
omission. Nutrients omission resulted in their significantly low concentration in plant tissues
than the complete treatment. Significantly (P0.05) lower shoot dry weights (SDWs) than
the complete treatment were obtained in different treatments; omission of K and Mg in
Masaba and Shikhulu, Mg in Khwisero, K in Butere and, P, Mg and K in Butula. Nitrogen sig-
nificantly improved SDWs in soils from Kakamega and Butula. Liming significantly raised
soil pH by 9, 13 and 11% from 4.65, 4.91 and 4.99 in soils from Masaba, Butere and Butula
respectively and soybean SDWs in soils from Butere. The results show that, poor soybean
growth was due to K, Mg and P limitation and low pH in some soils. The results also signify
necessity of application of small quantities of N for initial soybean use.
Introduction
Soybean stands out as the most popular grain legume in the world. Its popularity is attributed
to a number of factors related to its composition and productivity. Soybean is a source of the
most consumed edible oil and protein source for livestock feeds[1]. Many other soybean
PLOS ONE | DOI:10.1371/journal.pone.0145202 December 30, 2015 1/20
OPEN ACCESS
Citation: Keino L, Baijukya F, Ngetich W, Otinga AN,
Okalebo JR, Njoroge R, et al. (2015) Nutrients
Limiting Soybean (glycine max l) Growth in Acrisols
and Ferralsols of Western Kenya. PLoS ONE 10(12):
e0145202. doi:10.1371/journal.pone.0145202
Editor: David A Lightfoot, College of Agricultural
Sciences, UNITED STATES
Received: April 9, 2015
Accepted: December 1, 2015
Published: December 30, 2015
Copyright: © 2015 Keino et al. This is an open
access article distributed under the terms of the
Creative Commons Attribution License, which permits
unrestricted use, distribution, and reproduction in any
medium, provided the original author and source are
credited.
Data Availability Statement: The data is fully
available in the manuscript.
Funding: This study was funded by N2Africa, grant
number OPP1020032(13-1947) (http://www.N2Africa.
org).
Competing Interests: The authors have declared
that no competing interests exist.
products are directly used for human consumption including soymilk, soya sauce, protein
extracts and concentrates. Apart from nutritional qualities, soybean yield is higher than other
common grain legumes, has relatively few field and storage pests and diseases and has a high
nitrogen fixing ability[2]. Cultivation of soybean is gaining interest in Africa following high
demand from the booming livestock feed industry (which consumes about 7080% of soybean
produced per year) and need to improve N uptake by the crops which is obtained frombiological
nitrogen fixation[3,4,5]. Kenya is not an exception with substantial demand of approximately
150,000 mt yr
-1
[6]. Despite this huge demand, soybean production in Kenya is estimated at 8,000
mtyr
-1
, with 80% of the volume produced in western Kenya. Yield gap in western Kenya remains
wide with average yields of 600 kg ha
-1
against the potential yield of 3,000 kg ha
-1
[5,7].
Low soybean yields in western Kenya are largely attributed to declining soil fertility[7,8].
Adaptive research campaigns initiated across western Kenya by the N2Africa project team to
assess the responses of soybean to the application of P and K fertilizers and their combination
with inoculants recorded yield increase on only 60% of the sites[9]. An increase in soybean
grain yields upon the application of commercial rhizobial inoculants (legume fix) with P fertil-
izers has also been reported [8]. The yields obtained were however lower (620 kgha
-1
) than the
potential yield (yields obtained when the farmers use well adapted, high yielding varieties and
better management practices)[5]. In these studies low yields mainly coincided with poor nodu-
lation and a lack of response to P and K fertilizers and inoculants and may indicate that other
nutrients may be limiting [9]. The soils not responding to P and K application were grouped as
non-responsive. These non-responsive soils include the highly weathered-nutrient-depleted
soils (Acrisols and Ferralsols); the majority of which are on land owned by poor farmers.
The low crop yields experienced in these Acrisols and Ferralsols could be attributed to
chemical, physical and biological factors. The biological factors involve plants genetic variabil-
ity for nodulation and nitrogen fixation [10]also on the presence of the compatible rhizobial
inoculants [11]. Soil physical properties which are of importance in crop production are soil
bulk density, water holding capacity, aeration, soil texture and structure[12]. The chemical fac-
tors include nutrient limitations which can be caused by intensive cultivation with minimal fer-
tilizer use, nutrient removal via crop harvests, soil erosion, and leaching during heavy rainfall
and soil acidity[13]. The minimal fertilizer use in this region can be attributed to lack of money
by the farmers to purchase fertilizer and their low expertise on how to use the fertilizers effec-
tively among others. Nutrient deficiencies such as P, Ca, Mg, Mo and K can also be associated
with soil acidity. A decrease in soil pH increases the concentration of Fe and Al ions among
other cations such as Mn
4+
,H
+
and Cu
2+
in soil solution[13,14]. These ions cause P sorption
through their reaction with phosphate ions to form insoluble compounds[14]. When acidifica-
tion processes occur in the soil, the hydrogen ion concentration is increased. The hydrogen ion
displaces the cations which becomes susceptible to leaching especially during heavy rainfall.
[15,16]. This can be the case in western Kenya since most of the soils (about 0.9 million hect-
ares of land) have pH values less than 5.50[17]. Liming, which has been documented as a con-
ventional way of amending acidic soils can benefit these soybean farmers[18]. Given the over
aching need to close the yield gap in smallholder farms in western Kenya, there is need to shift
the focus to nutrients other than N, P and K which have received the most attention without
much increase in yield[19]. This has been linked to the results from the sites where previous
experiments had been carried out by an N2Africa research team through International Centre
of Tropical Agriculture (CIAT), to test the effects of P and K fertilizers applied together with
the inoculants on soybean yields. These resulted to lower grain yields of soybean compared to
the potential yields. This study therefore aimed at investigating the factors causing this non-
responsiveness by establishing other nutrients limiting soybean production and also to assess
the effects of liming on soil pH and soybean performance.
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
PLOS ONE | DOI:10.1371/journal.pone.0145202 December 30, 2015 2/20
Materials and Methods
Study soils, sampling and analysis
The soils that were used in the experiment were collected from five distinct locations representing
major soybean growing areas in western Kenya (Table 1). The fields in which these soils were
obtained were privately owned. The permission to collect the soils from these lands was granted
by the farmers who owned them. These sites were identified with the help of a research scientist
from International Centre for Tropical Agriculture(CIAT) Maseno -Kenya. Field experiments
had been carried out in these sites by an N2Africa research team through CIAT to test the effects
of P and K fertilizers with inoculants on soybean where they showed very little response. The soil
types in these sites were sourced from the farm management handbook of western Kenya [20].
The soil types were classified according to the international FAO soil classification system. The
soils from Masaba central were classified as chromic Acrisols. These soils are well drained, deep
to very deep, red to dark brown, friable, sandy to clay. The soil type from Kakamega (Khwisero
and Shikhulu sub-location) is Ferralo-humic Acrisols. These soils are well drained, deep to very
deep, yellowish red to dark reddish brown, friable to firm, sandy clay, with an acid or thick acid
humic top soil. The soils from Butula were classified as Rhodic Ferralsols and their characteristics
are; well drained, moderately deep to deep, dark reddish brown to strong brown, friable sandy,
clay loam to clay. From each site approximately 60 kg of soil were collected by taking the top soil
(020 cm) at 20 points in a zig zag manner using a hand hoe. The 20 soil portions from one site
were mixed to come up with a composite representative sample. The soils were then air-dried
and sieved to pass a 5 mm. From the remaining soils of each location, a sub-sample of about 250
g was taken for chemical and physical characterization at the Crop Nutrition Laboratory in Nai-
robi-Kenya for pH, total N, extractable P, organic carbon, exchangeable cations (Ca, K, Mg) and
particle size following methods described in [21]. These characteristics are shown in Table 2.Soils
from all the sites were strongly acidic (4.50 to 5.00) except for the soils from Kakamega (Khwisero
sub-location) which were moderately acidic (5.08)[17]. Percentage nitrogen levels were moderate
for all the soils (0.12 to 0.25)[21]. The levels of extractable P were below the critical level (<10
mg/kg) in all the soils while the exchangeable cations were of low to moderate levels[21].
Nutrient treatments
The composition of the nutrient solutions were based on Hoagland half strength solution[22],
according to specific requirements of soybean. The ion concentrations were in milli-moles per
Table 1. Location and characteristics of the sites where experimental soils were sampled from.
Site Sub-
location
District Latitude Longitude Altitude
(m asl)
Soil type Average Rainfall and
temperature (per annum)
Masaba
Central
Masaba Butere 034
0
27
38.2E
00
0
1159.9N 1331 Chromic Acrisols 16851882 mm, 13.930.2°C
Kakamega Khwisero Kakamega
south
034
0
40
20.4E
00
0
1226.0N 1488 Ferralo-humic
Acrisols
17301929 mm, 14.127.1°C
Kakamega Shikhulu Kakamega
South
034
0
40
05.4E
00
0
1214.6N 1508 Ferralo-humic
Acrisols
17301929 mm, 14.127.1°C
Butere Emutsatsa Butere 034
0
27
56.9E
00
0
1151.35N 1344 Chromic Acrisols 16851882 mm, 13.930.2°C
Butula Bukhalalire Butula 034
0
16
48.9E
00
0
1911.8N 1219 Rhodic
Ferrasols
17902016 mm, 15.828.6°C
All the sites were under the humid lower midland zones Source:[20]
doi:10.1371/journal.pone.0145202.t001
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
PLOS ONE | DOI:10.1371/journal.pone.0145202 December 30, 2015 3/20
litre (mmol/l) for the macro-nutrients and micro-moles per litre (μmol/l) for the micro-nutri-
ents. The macro-nutrients tested were P, K, Mg, Ca, S, and micronutrients (B, Mo, Mn, Cu and
Zn) (Table 3). The treatments included one positive control (complete nutrient solution), nega-
tive control (only distilled water), 5 treatments where one element was omitted from the nutri-
ent solution, one treatment where the micro-nutrient mixture was omitted from the nutrient
solution, one treatment with an additional nitrogen source in the nutrient solution and one
treatment with lime addition to the soils (Table 4). The purpose of the complete plus N treat-
ment was to assess whether the poor performances of plants with omitted elements was due to
Table 2. Physico- chemical properties of the soils used in the experiment.
Parameters Masaba Kakamega (Khwisero) Kakamega (Shikhulu) Butere Butula
pH (water) 4.65 5.08 4.99 4.91 4.99
Total N (%)
a
0.13 0.24 0.20 0.13 0.15
Available P (mg/kg)
b
4.43 7.27 4.58 2.11 6.18
Organic C
a
1.50 3.13 2.59 1.25 1.58
C:N ratio 11.53 13.04 12.95 9.62 10.53
CEC
c
K (cmol
c
/kg) 0.16 0.18 0.17 0.10 0.16
Ca (cmol
c
/kg) 1.10 4.34 3.22 1.03 2.49
Mg (cmol
c
/kg) 0.51 1.70 0.93 0.39 0.98
TEXTURE
d
Sand (%) 54 48 52 60 58
Clay (%) 30 32 32 18 24
Silt (%) 16 20 16 22 14
Textural class Sandy clay loam Sandy clay loam Sandy clay loam Sandy loam Sandy clay loam
a
Vario max CN[47]
b
Fox and Kamprath[48]
c
ICP-OES (Perkin Elmer, Inc.)
d
Based on Stokes law
doi:10.1371/journal.pone.0145202.t002
Table 3. Nutrient salts and rates used to prepare nutrient solutions.
Element Salt Rate of application
Macro-nutrients (millimols/l)
N and Ca Ca(NO
3
)
2
.4H
2
O/NH
4
NO
3
/ CaCl
2
.2H
2
O N = 7.5
Ca = 2.5
PH
3
PO
4
P = 0.5
Mg, S and K MgSO
4
/K
2
SO
4
Mg = 1
SO
4-
=1
K=3
Micro-nutrients (Micromoles/l)
BH
3
BO
3
7.13
Mo Na
2
MoO
4
-2H
2
O 0.01
Zn ZnSO
4
0.96
Cu CuSO
4
1.04
Mn MnCl
2
7.4
Source:[49]; modied from Hoagland solution[22].
doi:10.1371/journal.pone.0145202.t003
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
PLOS ONE | DOI:10.1371/journal.pone.0145202 December 30, 2015 4/20
the element in question alone or to nitrogen limitation. In literature e.g.[11,23], it was docu-
mented that poor performance of soybean plants in nutrient omission trials was also due to
nitrogen deficiencies. The inclusion of the lime treatment stemmed from the fact that all the
experimental soils were acidic. Lime and plus nitrogen treatments were added only to the com-
plete treatment. The lime requirements of the soils were determined using the procedure
described by[24], with the target pH of 6.2. This method relies on the initial soil pH and soil
texture of the test soil. This is followed by referring to the appropriate tables based on the target
pH and crop to be grown. From these tables, the calcium carbonate equivalency and the actual
amount to be applied are obtained[24]. The liming material that was used is Koru lime with
the following composition; CaOburnt lime (20.8%), MgO (1.06%), Fe
2
O
3
(0.29%), Al
2
O
3
(1.2%) and SiO
2
(0.42%).
Set up of the experiment
Assessment of limiting nutrients was carried out in the greenhouse at the University of Eldoret
located at 0° 34' N and 35° 18' E. The experiment adopted the so called double pot technique
[25]. This method offers an easy and rapid means of identifying the nutrients that are in short
supply in the soils. In this technique, two pots are used whereby the upper pot (pot 1, Fig 1) has
a gauze fitted at the bottom and is filled with soil. The lower pot (pot 2, Fig 1) is filled with
nutrient solution and has a lid to support the upper pot. A space of approximately 1 cm is left
between the bottom of the upper pot and the nutrient solution to allow oxygen supply to the
plant roots. The plant is therefore provided with two sources of nutrients (test soil and nutrient
solution) for its simultaneous uptake. It is during the initial stage of growth (germination) that
the plant obtains nutrients from the soil alone. Seeds or seedlings are planted in the soil and as
the plants grow the roots pass through the gauze and reach the nutrient solution in the lower
pot. When a nutrient is omitted from the nutrient solution, the plant can take it up from the
soil only. The absence of an element can be seen from the deficiency symptoms developed such
as limited growth and leaf chlorosis. The symptoms can be visible in the early growth stages
and thus can be used to draw conclusions for fertilizer recommendations. The technique
ensures those nutrients applied such as P and K are not fixed by the soil as it would be the case
if soil alone (single pot) is used. In this experiment, the upper pots were provided by parts of a
common sewage pipe with 9 cm diameter. A mesh was cut into small pieces and tied to their
Table 4. Treatments used in the experiment.
No. Treatments Macro-nutrients Micro-nutrients Lime
NPKMgCaS
1Complete - + + + + + + -
2Complete plus lime - + + + + + + +
3Control - - - - - - - -
4P omitted - - + + + + + -
5Complete plus N + + + + + + + -
6K omitted - + - + + + + -
7Mg omitted - + + - + + + -
8Ca omitted - + + + - + + -
9S omitted - + + + + - + -
10 Micro-nutrients omitted - + + + + + - -
KEY: + (Nutrient included in the nutrient solution)(Nutrient omitted from nutrient solution)
doi:10.1371/journal.pone.0145202.t004
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
PLOS ONE | DOI:10.1371/journal.pone.0145202 December 30, 2015 5/20
bottom, to prevent the soil from falling into the solution, but providing passage for the roots.
Small plastic pots of 2 l volume served as the bottom pots.
Experimental design
The experiment was laid out in a completely randomized design (CRD) whereby the treat-
ments were replicated four times. The set up was repeated three times to allow for the destruc-
tive sampling at three time intervals. There were 120 pots per soil (10 treatments x 4
replications x 3 pots per replication) giving a total of 600 pots for the five soils. The treatments
were randomly allocated to the pots (experimental units). The experimental factors were the
soils and the nutrient treatments. The pots were rotated two times a week to be able to elimi-
nate any biasness from one side of the greenhouse
Management of experiment
Soybean cultivar TGX 1740-2F (SB19) was planted in the experiment (3
rd
May to 2
nd
June
2013) with the temperatures in the greenhouse ranging from a minimum of 18.3 to a maximum
of 35.8°C. This cultivar was chosen because it is commonly grown in western Kenya due to its
early maturity and promiscuity in nitrogen fixation. From previous experiments this cultivar
has also had low yields after application of inoculants and P and K fertilizers. The seeds were
obtained from CIAT Maseno-Kenya. They were inoculated using the commercial Biofix inocu-
lant containing Bradyrhizobium japonicum strain USDA 110 which was acquired from MEA
Fertilizers Ltd-Kenya. Three seeds were sown per pot and were thinned to single uniform
plants per pot 7 days after emergence. The thinned plants were left in the specific pots and the
soils in the pots were covered with gravel to reduce evaporation. Prior to establishing the exper-
iment, the field capacity of each of the soils was established by saturating the soils with water
and covering them using perforated polythene papers. They were then weighed and then left
for 48 hours in the greenhouse. The difference between the weight of the container plus
Fig 1. Illustration of the set up of the double pot experiment.
doi:10.1371/journal.pone.0145202.g001
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
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saturated soil and that of the container plus soil after 48 hours represented the field capacity.
During the experiment the pots were watered daily with distilled water and the soils main-
tained at field capacity. The nutrient solution was renewed at 3 weeks after planting by pouring
out the old solution and adding a new solution into the container. One molar HCl was used to
regulate the pH of the alkaline nutrient solutions while 0.1 molar NaOH was used to regulate
the pH of the acidic nutrient solution (-K). The target pH was 6.3 to 6.5.
Data collection
Data were collected on stem length and shoot dry weight.These measurements were taken 14,
21 and 28 days after emergence (DAE). The destructive sampling was done at the three time
intervals to help in determination of the relative growth rate and nutrient sufficiency quotients.
The plants were oven dried at 65°C for 48 hrs to determine shoot dry weight. After drying, the
plant samples at the final harvest were ground. The four samples from each replicate represent-
ing one treatment were aggregated. They were then sent to the Crop Nutrition Laboratory Ser-
vices Ltd, Nairobi-Kenya for elemental analysis using inductively coupled plasma optical
emission spectrometry (ICP-OES, Perkin Elmer Inc). The extraction solution used was Meh-
lich 3 Extractant: (0.2 N CH
3
COOH + 0.25 N NH
4
NO
3
+ 0.015 N NH
4
F + 0.013 N HNO
3
+
0.001 M EDTA).The analysis carried out established, N, P, K, Ca, Mg, Mn, B, Zn and Cu con-
centrations in the plant tissue samples within the soil types. Analysis for S and Mo was not car-
ried out because during the time of analysis, machines for analysis were broken down. Visual
observations for any deficiency symptoms were recorded daily from 8 days after emergence to
the end of the experimental period.
Determination of relative growth rate and nutrient sufficiency quotients
(SQs)
The relative growth rate based on shoot dry weight was calculated between two time intervals
1421 DAE and 2128 DAE as shown in Eq 1. This reflected the net growth of the plants grow-
ing on different nutrient solutions. The relative growth rates obtained were then used to calcu-
late the nutrient sufficiency quotients, to show the relationship between nutrient treatments
and the complete treatment. This was done as shown in Eq 2 i.e. dividing the relative growth
rate of the element in question to that of the complete treatment. The SQs were then multi-
plied by 100 to reflect the percentage growth of a given treatment compared to the complete
treatment. The nutrient treatments with SQs less than 50% were considered to be more limit-
ing, those more than 50% were considered to be less limiting[11,23].The formulas used in cal-
culation of relative growth rate and finally the nutrient sufficiency quotients were; [25].
Rs ¼lnS2lnS1
t2t1Rs 1
Where; Rs = Relative growth rate, S = shoot dry weights in g, t = time in days and
ln = natural logarithm
The following formula was used to calculate SQs; [23,26].
SQx ¼Rsx
RsC
SQ 2
Where; SQ
x
= Sufciency quotient for x, where x is the nutrient element in question, (RS)-
x = Relative growth rate of plants growing in nutrient solutions with x (nutrient element in
question) omission and RS(C) = Relative growth rate of plants growing on complete nutrient
solution.
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
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Statistical analysis
Analysis of variance was done to compare the effects of the different treatments on growth and per-
formance of soybean using Genstat 12
th
edition. The effects of the different treatments were com-
pared by computing the least square means and theirstandarderrorsofthedifference(SED).All
the single nutrient treatments were compared to the complete treatments[25] using the least signifi-
cant differences to establish their extent of limitation. If a treatment was significantly lower than the
complete treatment, then it was considered to be limiting in the soils. Significance of the difference
was evaluated at P0.05 significant level. Each soil was analyzed separately to be able to identify
limiting nutrients specific to each soil. Data analysis for shoot nutrient concentration was done irre-
spective of the soil types (across the soils) whereby the soils served as replicates.
Results
Visual observations
The most common deficiency symptom observed was that of Mg where there was interveinal
leaf yellowing especially in treatments of plus nitrogen and a few of Mg omitted treatments
across the soils (Fig 2A). Deficiencies of K were also noted mainly on older leaves of K omitted
Fig 2. Nutrient deficiency symptoms noted during plant growth. (A) Mg deficiency in plus nitrogen
treatment in Ferralsols from Kakamega (Shikhulu Sub-location), (B) K deficiency in minus K treatments in
Ferralsols from Kakamega (Shikhulu sub-location), (C) P deficiency in minus magnesium treatmentsin
Ferralsols from Butula, (D) Micro-nutrient deficiencies in minus micro-nutrient treatmentsin Acrisols from
Masaba Central.
doi:10.1371/journal.pone.0145202.g002
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
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treatments and also on several other treatments. These were characterized by leaf yellowing
with tissue necrosis along the leaf margins (Fig 2B). Early leaf drop was observed in plants
growing in the treatments with both Mg and K deficient treatments, and this led to low shoot
dry weights being recorded by the same treatments, especially at the final harvest. Plants grow-
ing in the control (only distilled water) and in the treatments where P and Ca were omitted
maintained green leaf colour to the end of the experimental period. Other treatments (com-
plete, minus sulphur, minus micro-nutrients and complete plus lime) had pale yellow leaves at
the time of harvesting (Fig 3G) indicating possible deficiencies of nitrogen.
There were well-developed rooting systems in all the treatments (Fig 3E) except in calcium
omitted treatments and also in some of the plus nitrogen treatments (Fig 3F). Addition of
nitrogen to the nutrient solution had a variable response across the soils. Ferralsols from Kaka-
mega and Butula produced very leafy green plants (Fig 3G) while in the Acrisols from Masaba
Fig 3. Soybean plants at the time of harvest. (E) Plants growing on complete nutrient solution on different soils, (F) Plants growing on minus calcium
nutrient solution on different soils, (G) Plants growing on different nutrient treatments in Ferralsols from Kakamega (Shikhulu sub-location). Complcomplete
treatment, MN- minus micro-nutrients.
doi:10.1371/journal.pone.0145202.g003
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
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central and Butere, the foliage was less and there was a scorching characteristic at the tips and
edges of the leaves (Fig 4).
Trends of shoot nutrient concentration as influenced by the treatments in
different soils
Table 5 shows the shoot nutrient concentration in the soybean plants across the soils. Omission
of P, Mg, K, and Ca resulted to their significantly (P 0.05) low concentration than the
Fig 4. Scorching and necrosis of leaves in nitrogen added treatments in Acrisols from Masaba
central.
doi:10.1371/journal.pone.0145202.g004
Table 5. Effects of the different treatments on shoot nutrient concentrations across the different soils.
Treatments %P %N %Mg %K %Ca B (ppm) Cu (ppm) Mn(ppm) Zn (ppm)
Control 0.15
a
2.51
ab
0.34
b
0.83
a
0.68
b
24.90
a
3.32
ab
428
a
49.40
cd
Minus Ca 0.30
ab
2.30
ab
0.38
b
1.99
b
0.39
a
26.52
a
1.88
a
410
a
31.56
a
Minus K 1.42
e
2.96
b
0.59
c
1.18
a
1.68
e
42.56
e
5.52
d
545
a
64.5
e
Minus Mg 1.40
e
2.95
b
0.24
a
2.99
d
1.56
de
50.30
f
4.95
bcd
459
a
59.84
de
Minus micro-nutrients 0.83
d
2.04
ab
0.39
b
2.49
bcd
1.40
d
28.84
ab
3.16
ab
409
a
32.68
a
Minus P 0.21
a
2.78
ab
0.36
b
2.01
b
0.93
c
32.46
bcd
3.14
ab
476
a
43.58
abc
Minus S 0.66
cd
1.98
a
0.38
b
2.26
bc
1.40
d
33.94
bcd
3.44
abc
430
a
34.98
ab
Plus nitrogen 0.52
bc
4.06
c
0.35
b
2.60
cd
1.04
c
30.54
abc
5.25
cd
436
a
40.62
abc
Complete 0.79
d
2.15
ab
0.40
b
2.46
bc
1.45
d
34.92
cd
4.33
bcd
387
a
46.86
bc
Complete plus lime 0.74
cd
2.22
ab
0.36
b
2.27
bc
1.58
de
37.32
de
3.58
abc
156
a
35.70
ab
Grand mean 0.703 2.6 0.3772 2.107 1.211 34.23 3.86 414 44
S.E.D 0.1293 0.468 0.0378 0.252 0.0934 2.836 0.951 172.9 6.24
F.Probability<.001 0.002 <.001 <.001 <.001 <.001 0.011 NS <.001
C.V. 29.1 28.5 15.8 18.9 12.2 13.1 39 66.1 22.5
Similar letters in each column shows non-signicant difference to shers protected LSD (P 0.05). conc.concentration.
doi:10.1371/journal.pone.0145202.t005
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
PLOS ONE | DOI:10.1371/journal.pone.0145202 December 30, 2015 10 / 20
complete treatment. Omission of micro-nutrients from the nutrient solution resulted into sig-
nificantly lower B and Zn in the plant tissues than the complete treatment across the soils.
Application of N to the nutrient solution led to its significantly higher concentration in the
plant tissues than the complete treatment across the soils. It also led to significantly low con-
centration of P and Ca than the complete treatment. Lime application to the soils did not differ
significantly (P 0.05) from the complete treatment in all the treatments analyzed. The con-
trol treatment had significantly lower P, K, Ca and B concentration in their plant tissues than
the complete treatment.
Elimination of Ca from the nutrient solution led to significantly lower accumulation of P,
Ca, B, Cu and Zn in the shoots compared to the complete treatment across all the soils. Omis-
sion of Mgand Kfrom the nutrient solution led to significantly (P0.05) higher concentration
of P, K, B Zn and P, Mg, Ca, B and Zn respectively compared to the complete treatment across
all the soils (Table 5).
Effects of treatments on root dry weights at final harvest
The treatments differed significantly (P 0.001) from each other in terms of root dry weight
in soils from all the sites (Table 6). The control treatment had significantly lower root dry
weights than the complete treatment in soils from all the sites. In soils from Masaba central,
omission of Ca, K, Mg and addition of N in the nutrient solution resulted in significantly lower
root dry weights than the complete treatment. Omission of Mg, K, Ca, and addition of N to the
nutrient solution in Kakamega (Khwisero Sub-location) had significantly lower root dry
weights than the complete treatment. In Kakamega (Shikhulu Sub-location) omission of Ca, K
and Mg significantly reduced the root dry weights than the complete treatment while in Butere,
this occurred with the omission of K and addition of N to the nutrient solution. Omission of K,
Mg, addition of N to the nutrient solution and addition of lime to the soils significantly reduced
the root dry weights than the complete treatment in soils from Butula. Application of lime in
Acrisols from Masaba and Butere significantly increased root dry weights than the complete
treatment (Table 6).
Table 6. Root dry weights (g/plant) for the different treatments in soils from different sites.
Treatments Masaba Kakamega 1 Kakamega 2 Butere Butula Across soils
Control 0.11
a
0.16
b
0.14
bc
0.09
b
0.14
bc
0.13
bc
Minus Ca 0.11
a
0.15
ab
0.15
bc
0.14
cd
0.18
cd
0.15
c
Minus K 0.08
a
0.15
ab
0.08
a
0.04
a
0.06
a
0.08
a
Minus Mg 0.10
a
0.11
a
0.10
ab
0.14
cd
0.09
ab
0.11
b
Minus MN 0.18
b
0.23
d
0.18
cd
0.21
e
0.17
cd
0.19
de
Minus P 0.18
b
0.21
cd
0.24
e
0.12
bcd
0.18
cd
0.18
d
Minus S 0.20
b
0.22
cd
0.19
cde
0.21
e
0.18
cd
0.20
de
Plus N 0.08
a
0.18
bc
0.23
e
0.11
bc
0.16
c
0.15
c
Complete 0.19
b
0.24
d
0.23
de
0.16
d
0.23
d
0.21
e
Complete+Lime 0.25
c
0.21
cd
0.19
cde
0.26
f
0.16
c
0.21
e
F.Probability <.001 <.001 <.001 <.001 <.001 <.001
S.E.D 0.0286 0.02201 0.02769 0.217 0.0295 0.0128
% CV 27.2 16.9 22.8 21.1 26.9 25.2
Similar letters in each column shows non-signicant difference to shers protected LSD (P 0.05). Means are compared between the different
treatments within the same soil (along the column). MNmicronutrients. Kakamega1 (Khwisero sub-location), Kakamega2 (Shikhulu sub-location)
doi:10.1371/journal.pone.0145202.t006
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
PLOS ONE | DOI:10.1371/journal.pone.0145202 December 30, 2015 11 / 20
Effects of treatments on shoot biomass accumulation at final harvest
The treatments differed significantly (P 0.001) in the soils from all the sites with respect to
the shoot dry weights. The control treatments had significantly lower shoot dry weights com-
pared to the complete treatment in all the soils except those from Kakamega (Khwisero Sub-
location) (Table 7). In Acrisols from Masaba central, omission of K, Mg, and, Ca resulted in
significantly lower shoot dry weights compared to the complete nutrient treatment. Shoot dry
weight of the S, P, micro-nutrients omitted treatments, plus lime and nitrogen added treat-
ments were not significantly different from the shoot dry weight of the complete nutrient treat-
ment. When Mg was excluded from the nutrient solution in Ferralsols from Kakamega
(Khwisero sub-location), there was significantly lower shoot dry weights compared to that of
the complete treatment. There was no significant difference in shoot dry weights between the
complete treatment and when K, Ca, P, S and micro-nutrients were omitted from the nutrient
solutions. Addition of Nitrogen to the nutrient solution increased the shoot dry weights signifi-
cantly than the complete treatment. Lime addition to the soils on the other hand did not differ
significantly than the complete treatment (Table 7).
In Ferralsols from Kakamega (Shikhulu sub-location), omission of K, and Mg resulted in
significantly lower shoot dry weights compared to the complete treatment (Table 7). There
were no significant differences from the complete treatment when Ca, P, S and micro-nutrients
were omitted from the nutrient solution. Addition of nitrogen to the nutrient solution signifi-
cantly increased the shoot dry weights compared to the complete treatment while lime addition
to the soils did not differ significantly from the complete treatments (Table 7). In Acrisols from
Butere, significantly lower shoot dry weights were obtained when K was omitted from the
nutrient solution. Omission of Ca resulted in significantly higher shoot dry weights than the
complete treatment (Table 7). Omission of S, micro-nutrients and P resulted in shoot dry
weights that were not significantly different from the complete treatment. The shoot dry
weights of the nitrogen added nutrient solutions did not differ significantly from the complete
treatment while lime addition to the soils significantly increased the shoot dry weights than the
complete treatment (Table 7). When K, P and Mg were omitted from the nutrient solution in
Ferralsols from Butula, there was significantly lower shoot dry weights compared to the
Table 7. Shoot dry weights (g/plant) for the different treatments in soils from the different sites.
Treatments Masaba Kakamega 1 Kakamega 2 Butere Butula Across soils
Control 0.28
b
0.38
ab
0.41
ab
0.22
a
0.38
bc
0.33
bc
Minus Ca 0.37
bc
0.68
cd
0.57
cd
0.56
de
0.64
f
0.56
ef
Minus K 0.16
a
0.49
abc
0.28
a
0.15
a
0.20
a
0.25
a
Minus Mg 0.29
b
0.33
a
0.29
a
0.25
ab
0.29
ab
0.29
ab
Minus MN 0.41
cd
0.70
d
0.48
bc
0.49
cd
0.43
bcd
0.50
de
Minus P 0.41
cd
0.40
ab
0.45
bc
0.28
ab
0.38
bc
0.38
c
Minus S 0.43
cd
0.62
cd
0.48
bc
0.48
cd
0.48
cde
0.50
d
Plus N 0.42
cd
1.01
e
1.06
e
0.37
bc
0.86
g
0.74
g
Complete 0.52
de
0.57
bcd
0.59
cd
0.37
bc
0.57
def
0.52
de
Complete+Lime 0.61
e
0.54
bcd
0.64
d
0.63
e
0.61
ef
0.61
f
F.Probability <.001 <.001 <.001 <.001 <.001 <.001
S.E.D 0.0577 0.0981 0.0695 0.0685 0.0702 0.0330
% CV 20.9 24.3 18.7 25.5 20.5 22.2
Similar letters in each column shows non-signicant difference to shers protected LSD (P 0.05). Means are compared between the different
treatments within the same soil (along the column). MNmicronutrients. Kakamega1 (Khwisero sub-location), Kakamega2 (Shikhulu sub-location)
doi:10.1371/journal.pone.0145202.t007
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
PLOS ONE | DOI:10.1371/journal.pone.0145202 December 30, 2015 12 / 20
complete treatment. Omission of Ca, micro-nutrients and S resulted in shoot dry weights that
were not significantly different from that of the complete treatment. The shoot dry weights of
the nitrogen added nutrient solutions were significantly higher than those of the complete
treatment while those of lime application did not differ significantly (Table 7).
Omission of K resulted in significantly lower shoot dry weights than the control (distilled
water only) treatment in Acrisols from Masaba central. It was not significantly different from
the control treatment in Acrisols from Butere and Ferralsols from Kakamega (Khwisero and
Shikhulu sub-location). Omission of Mg did not differ significantly from the control treatment
in terms of shoot dry weights in the soils from all the sites (Table 7).
Nutrient sufficiency quotients
The sufficiency quotients were multiplied by 100 to show the percentage growth of a nutrient
treatment compared to the complete treatment. From this experiment, omission of Ca from
the nutrient solution in Ferralsols from Kakamega (Shikhulu sub-location), micro-nutrients in
Ferralsols from Kakamega (Khwisero sub-location) and Acrisols from Butere and S omission
from the nutrient solution in the Ferralsols from Kakamega (Khwisero sub-location) and
Butula had sufficiency quotients greater than 100% (Table 8). Omission of Mg and K from the
nutrient solution led to lowest sufficiency quotients in all the Acrisols and Ferralsols. The suffi-
ciency quotients of minus K were negative in Ferralsols from Butula while those of minus Mg
were negative in Ferralsols from Kakamega (Shikhulu sub-location) (Table 8). The control
treatment had low sufficiency quotients in Acrisols from Masaba central and Butere but these
values were high than those of minus Mg and minus K. In other soils, they had high sufficiency
quotients, even greater than P omitted treatments in Ferralsols from Kakamega (Khwisero and
Shikhulu sub-locations) and in Butula. They were greater than minus Ca and minus micro-
nutrients in Ferralsols from Butula (Table 8).
Lime addition to the soils led to higher nutrient sufficiency quotients than the complete
treatment in Acrisols from Butere and Ferralsols from Butula. In Acrisols from Masaba central
and Ferralsols from Kakamega (Khwisero and Shikhulu Sub-locations) the sufficiency quo-
tients of the limed treatments were lower than those of the complete treatments. Nitrogen
application to the nutrient solution increased the nutrient sufficiency quotients compared
withthe complete treatment in all the soils except in those from Masaba central (Table 8).
Table 8. Percent nutrient sufficiency quotients for different treatments and site combination based on shoot dry weights.
Kakamega
SITE/TREATMENT Masaba Khwisero Shikhulu Butere Butula
Control 42 85 74 42 96
Minus Ca 85 97 113 79 94
Minus K 18 64 48 1 -4
Minus Mg 35 28 -1 50 30
Minus MN 69 126 77 124 92
Minus P 68 68 71 49 82
Minus S 78 122 91 86 106
Plus N 61 178 145 115 110
Complete 100 100 100 100 100
Complete plus lime 83 82 84 129 112
Kakamega1 (Khwisero sub-location), Kakamega2 (Shikhulu sub-location)
doi:10.1371/journal.pone.0145202.t008
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
PLOS ONE | DOI:10.1371/journal.pone.0145202 December 30, 2015 13 / 20
Effects of the lime application on soil pH
The treatments differed significantly (P 0.05) in terms of soil pH in all the soils except in Fer-
ralsols from Kakamega (Khwisero and Shikhulu sub-locations). Application of lime to the
Acrisols from Masaba central and Butere and Ferralsols from Butula raised the soil pH signifi-
cantly (P 0.05) compared to the other treatments except minus Mg in Ferralsols from Butula
(Table 9).
Discussion
Visual observations and plant tissue nutrient concentrations in different
soils
Hydroponic systems have been frequently used to study the effects of mineral nutrient defi-
ciencies on plant growth and physiology. This is because they are important in identification of
the visual symptoms for diagnostic purposes[27]. In the current study, several deficiency symp-
toms were noted in the double pot experiment which was used to mimic the hydroponic sys-
tems and thus helped in identifying the nutrients limiting in the test soils.The interveinal
yellowing of the leaves can be attributed to magnesium deficiency[28]. This can be related to
the low Mg concentration in plant tissues growing in magnesium omitted treatments. These
values were below the sufficiency ranges (0.3 to 0.6%) for soybean plant at early growth stages
[29]. This indicated that the magnesium levels in the soils were low (as shown by the initial soil
analysis). Since the element was not provided by the nutrient solution, there was insufficient
amount for plant uptake. This treatment also accumulated significantly higher amounts of
other nutrients such as, P, K, B and Zn than most of the treatments (Table 5). The low accumu-
lation of Mg in plant tissues growing in Mg-omitted treatments and high accumulation of
other elements may suggest that the poor performance of the plants indicates that this nutrient
is limiting in the soils.
The plants grown on K-omitted nutrient solution had their older leaves turning yellow with
tissue necrosis along the leaf margins, a factor that could be attributed to K deficiency[30]. The
concentration of K in the shoot tissues of the plants growing in K-omitted treatments were
Table 9. Effects of the different treatments on soil pH of the soils from different sites.
Treatments Masaba Kakamega1 Kakamega2 Butere Butula Across soils
Control 4.55
a
5.12
a
5.16
a
4.81
a
5.13
b
4.95
bc
Minus Ca 4.56
a
5.25
a
5.14
a
5.12
b
5.03
b
5.02
c
Minus K 4.60
a
5.12
a
5.09
a
4.80
a
5.05
b
4.93
bc
Minus Mg 4.67
a
5.19
a
5.06
a
4.85
a
5.20
bc
4.99
c
Minus MN 4.68
a
5.05
a
4.75
a
4.91
ab
4.98
b
4.87
b
Minus P 4.70
a
5.13
a
4.91
a
4.97
ab
4.91
ab
4.92
bc
Minus S 4.66
a
5.06
a
5.13
a
4.84
a
4.96
ab
4.93
bc
Plus N 4.54
a
5.02
a
4.81
a
4.78
a
4.63
a
4.75
a
Complete 4.64
a
5.14
a
5.18
a
4.89
a
4.91
ab
4.95
bc
Plus lime 5.07
b
5.30
a
5.24
a
5.41
c
5.53
c
5.31
d
S.E.D 0.0882 0.1081 0.1728 0.0974 0.1543 0.0576
F. Probability 0.005 NS NS 0.002 0.013 <.001
C.V. 1.9 2.1 3.4 2 3.1 2.6
Statistical analysis and treatment comparisons done per soil (along the column). Means followed by the same letter are not signicantly different (LSD,
P0.05) MNmicronutrients. Kakamega1 (Khwisero sub-location), Kakamega2 (Shikhulu sub-location)
doi:10.1371/journal.pone.0145202.t009
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
PLOS ONE | DOI:10.1371/journal.pone.0145202 December 30, 2015 14 / 20
lower compared to the other nutrients. These concentrations were below the sufficiency ranges
(1.7 to 2.5%) for soybean plant tissues at early growth stages[29]. The same plants also had sig-
nificantly high concentration of other elements such as P, Mg, Ca, Band Zn (Table 5). This
shows that K may be limiting in the soils because of high concentration of other nutrients and
thus growth is limited by low K.Low K uptake can also be attributed to low concentration of K
in the soils. Similar results were found out when working with non-responsive soils in Zimba-
bwe using a double pot experiment[11]. The presence of other elements in high concentrations
in K omitted treatments can be attributed to K competitive ability especially for Ca and Mg
[31]. This competition occurs because there are a limited number of ion carrier sites on the
root plasma membrane and thus the ions of the same ion strength can out compete each other
for the sites[32].
Apart from the dark green leaves and stunted plants grown in minus P treatments, some
plants exhibited interveinal reddening which is associated with P deficiency in soybean plants
in some instances[33]. This can be evidenced by lower P concentrations in plant tissues grow-
ing in P omitted treatments. These concentrations were below the sufficiency ranges (0.3 to
0.6%) required for soybean at early growth stages[29]. The P deficiency symptoms in P omitted
treatments can be attributed to the minimal amounts of P available for plant uptake in all the
soils which can be seen from the results of initial soil analysis. The poor root development in
Ca omitted treatments can be associated with roles of calcium in root growth. Calcium is
involved in cell growth, both at the plant terminal and the root tips. Absence of Ca leads to
browning and dying of the root tips and thus leading to poorly developed root systems.
Although all the growing tips are sensitive to Ca deficiency, those of the roots are affected more
severely[34]. The significantly low concentration of other elements such as; P, B, Cu and Zn
(Table 5) in Ca omitted treatments than the complete treatment can be attributed to the nutri-
entslow uptake resulting from a poorly developed rooting system.
Nitrogen application to the nutrient solution was to help identify whether the poor perfor-
mance in the various nutrient-omitted treatments was due to the nutrient in question or nitro-
gen deficiency. Addition of nitrogen to the nutrient solution led to the nitrogen concentrations
in the plant tissues to fall within the required sufficiency ranges (3.55.5%)[29]. Although
there were no to few nodules in most of the treatments, nitrogen added treatments did not
have nodules in all the soils. This could be attributed to the ability of nitrogen to inhibit nodu-
lation when supplied in large amounts [35]. Field experiments have shown a reduction in the
nodule number when nitrogen was applied to soybean [35]and also in common bean, lima
bean, green gram and lab lab [36]. It was also found out that addition of N (>2.5 mM) inhib-
ited nodulation in cowpea and soybean [37] under hydroponic solutions. There was low nodu-
lation in most of the treatments despite the low N content. This could be attributed to the low
pH of most of the soils which are not favourable for soybean nodulation and nitrogen fixation
and thus nitrogen deficiencies could be noted.The low N concentration (below the sufficiency
ranges3.5 to 5.5) in all the treatments except the plus N treatment (Table 5) can be attributed
to the moderate initial N contents in soils and poor nodulation. This could also be attributed to
the fact that maximum nitrogen fixation occurs at R3 to R5 stages of soybean growth [3]yet the
plants in this study were harvested at V3 stage.
The insignificant difference between the lime applied treatment and the complete treatment
in terms of shoot nutrient concentration may be due to the good supply of the nutrients from
the nutrient solution in the lower pot that was not influenced by lime application.This may
also be due to its ability to improve the pHof the soil which may have contributed to improved
soil nutrient availability. Manganese concentrations in lime-added treatments were lower than
all the other treatments. Lime reduces manganese concentration through mass action when
applied to the soils by raising the soil pH. It was found out that liming reduced Mn
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
PLOS ONE | DOI:10.1371/journal.pone.0145202 December 30, 2015 15 / 20
concentrations in the soil, but the concentration in the leaves was sufficient but decreased with
subsequent seasons under liming[38].
Effects of the nutrient treatments on shoot dry weights
All the treatments were compared against the complete treatment in terms of shoot and root
dry weights to determine their extent of limitation. This is because theoretically it is expected
that the complete treatment should have the best performance because of the optimal nutrient
conditions for growth. If the treatment had significantly lower SDWs than the complete treat-
ment, it meant that the element was limiting[25].The poor performance of plants (in terms of
shoot dry weights) growing in magnesium-omitted treatments may be attributed to the impor-
tant roles played by magnesium in the plants. Magnesium is an important component of chlo-
rophyll which helps in capturing energy from the sun for growth and development; Mg also
plays an important role in activation of a number of enzymes important in protein synthesis
and P reactions[39]. Magnesium deficiencies are widely reported and have resulted in ailments
such as grass tetany in ruminant animals feeding on grasses with Mg deficiency[17]. Most field
Mg deficiencies are induced by competing cations such as, K
+
,NH
4+
,Ca
2+
and Mn
2+
[40].
Magnesium deficiency symptoms have also been reported in the field trials. These are more
pronounced in cases where K fertilizers were used when there was little Mg available in the soil
[41].The poor performance of plants growing in minus K treatments in terms of the shoot dry
weights indicated that K is limiting in these soils. It has been reported that relatively large
amounts of K are required by high yielding soybean varieties[34]. This is because the dry mat-
ter yield, nodule parameters and the total nitrogen accumulation increases with increasing K
supply. This can be associated with the improvement of nitrogenase activity and thus enhanc-
ing biological nitrogen fixation (BNF)[34,42].The low shoot dry weights could be attributed to
the premature leaf fall.
The poor performance of plants growing in P omitted treatments in terms of shoot dry
weights in all the soils except in Acrisols from Butere indicates that P is limiting in these soils.
This agrees with many findings that P is one of the most limiting elements affecting soybean
production in soils of western Kenya and this can be attributed to the widespread occurrence
of soils with high P fixation capacity [2]. This can be the case in this study since the Acrisols
and Ferralsols used were all acidic, suggesting the presence of iron and aluminum ions respon-
sible for P fixation.Despite the poor root development in Ca-omitted treatments as explained
earlier, the plants growing in this treatment were not significantly different from the complete
treatment in terms of shoot dry weight in Ferralsols from Kakamega (Khwisero and Shikhulu
Sub-locations). This can be attributed to the soil Ca status (moderate) especially for the Ferral-
sols from Kakamega (Khwisero and Shikhulu sub-locations) and Butula.
Potassium, Ca and Mg are the cations which are more prone to leaching from the soils. This
occurs more in areas with heavy rainfall. Organic and sandy soils are prone to K leaching. Reg-
ular application of the fertilizers with these cations should be carried out to replenish the soils
[34]. Extensive weathering of the Acrisols and Ferralsols has also led to the leaching of these
cations over time[36].
Omission of S from the nutrient solution was not significantly different from the complete
treatment in terms of shoot dry weights. Sulphur deficiency in plants is mainly indicated by
chlorosis of young leaves. Sulphur is widely known for its functions in protein synthesis
because it is a component of amino acids cysteine and methionine. Its availability therefore is
mainly assessed by the analysis of the grains to establish their contents[40]. Micro-nutrients
are very important in soybean nutrition. For instance, maximum production in leguminous
plants can be obtained through effective nodulation and molybdenum application and this is
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
PLOS ONE | DOI:10.1371/journal.pone.0145202 December 30, 2015 16 / 20
well expressed in terms of yield and nitrogen concentration in the plant tissues[43]. This can
be seen in the low (below the sufficiency ranges) accumulation of nitrogen in minus micro-
nutrients treatments
Addition of nitrogen led to variable responses of soybean in the different soils. There was
high foliage production in plants growing in nitrogen-added treatments in Ferralsols from
Kakamega (Khwisero and Shikhulu sub-locations) and in Butula and thus led to significantly
higher shoot dry weights compared to the complete treatment. From initial soil analysis, soils
from Kakamega (Khwisero and Shikulu sub-locations) and Butula had higher nitrogen levels
than those of Butere and Masaba Central although they were all at moderate levels (0.12 to
0.25). These low N levels might have led to the difference in plant performance. These can also
be attributed to the moderate carbon levels in the soils from Butula and Kakamega. Nitrogen
supply to plants increases leaf area and canopies. In dicots, impact of nitrogen supply in hydro-
ponic systems on leaf growth is due to increased cell growth as observed by other earlier stud-
ies[39]. Results from field experiments have shown an increase in soybeans and other grain
legumes dry matter and grain yields despite the reduction in nodulation upon the application
of nitrogenous fertilizers [3,35,36]. This shows that nitrogen applied soybean plants can out-
compete those grown on inoculation, unless management of the inoculated plants is improved.
Those plants growing in Acrisols from Butere and Masaba central had less foliage and thus the
shoot dry weights were not significantly different from those of the complete treatment. This
can be attributed to the necrosis and scorching of the leaf tips and edges in these plants. This
might be due to nickel deficiency thus leading to accumulation of urea in the leaves of N-added
nutrient solution in these soils. High concentration of urea in plant leaves causes death of cells
leading to necrotic lesions at leaf tips. Nickel which is a constituent of urease enzyme helps in
hydrolysis of urea thus preventing its accumulation in plant leaves[44].
The significant increase of soybean shoot dry weights in response to lime application in
Acrisols from Butere (Table 7) can be attributed to the ability of lime to significantly raise the
soil pH in these soils (Table 9). It raises soil pH by replacing the H
+
on the cation exchange
complex with Ca
2+
. The H
+
then combines with the hydroxyl ions (OH
-
) to form water. Cal-
cium ions in the liming material also replaces the aluminum and manganese ions from the
exchange sites thus increasing the cation saturation in the soil solution[45]. The rise in soil pH
upon lime application might have contributed to the better performance of plants by increasing
the availability of plant nutrients. Research in western Kenya has shown the positive influence
of using lime in addressing the problem of soil acidity and therefore enhancing soil fertility
[18]. Application of quick lime (CaO 21%) resulted in increase in soil pH and improved avail-
able P content in the soils of western Kenya[46]
Effects of the nutrient treatments on Nutrient Sufficiency Quotients
The nutrient SQ is an index that can be used to assess the nutrient availability. It tells the ability
of a soil to supply plant nutrients and thus can be used for fertilizer recommendations[23,47].
Sufficiency quotient which is the ratio of the relative growth rate between time points helps in
indicating those nutrients which are present in insufficient amounts. The sufficiency quotients
were therefore obtained by dividing the relative growth rates of the different treatments by the
complete treatments. In the current study, all the treatments apart from the complete treatment
should therefore have a sufficiency quotient of below 100%. This is because the complete treat-
ment is provided with all the nutrients[25]. From the study, those nutrients with SQs less than
50% were considered to be more limiting. These included K and Magnesium in soils from
Masaba, Shikhulu, Butere and Butula and P in soils from Butere, those more than 50% were
considered to be less limiting and included Ca, micro-nutrients, P and S in Masaba, Ca, K and
Nutrient Limitations in Acrisols and Ferralsols of Western Kenya
PLOS ONE | DOI:10.1371/journal.pone.0145202 December 30, 2015 17 / 20
P in soils from Khwisero, micro-nutrients, P and S in soils from Shikhulu, Ca and S in soils
from Butere and Ca, micro-nutrients and P in soils from Butula. Those above 100 were consid-
ered not limiting; micro-nutrients and S in Khwisero, Ca in soils from Shikhulu, micro-nutri-
ents in soils from Butere and S in soils from Butula. The low SQs in K and Mg omitted
treatments can be attributed to their premature leaf fall which led to their low shoot dry
weights.
Conclusions
The most limiting nutrients in Acrisols and Ferralsols studied for soybean production are K,
Mg, and P. Magnesium and P were found to be the most limiting nutrients in both the Acrisols
and Ferralsols; K was limiting in the Acrisols from Masaba central and Butere and Ferralsols
from Kakamega (Shikhulu sub-location) and Butula. Lime application improved soil pH in all
the soils and improved shoot dry weights over the complete treatment in all the Acrisols and
Ferralsols from Kakamega (Shikhulu Sub-location) and in Butula. Addition of N to the nutrient
solution significantly raised SDWs in soils from Kakamega (Khwisero and Shikhulu sub-loca-
tion) and Butula and improved the shoot nitrogen concentration to the required sufficiency
levels across the soils. This signifies the necessity of application of small quantities of N for ini-
tial soybean use. To increase soybean yields in Acrisols and Ferralsols of western Kenya, fertil-
izer formulations containing Mg, K, P, and Ca (complete fertilizer) and liming in combination
with the inoculants in low pH soils are recommended. Further work should focus on establish-
ing the response of soybean to combined application of limiting nutrients, formulating new fer-
tilizer blends for legumes including establishing detailed economic viability of nutrient use for
soybean production in these soils.
Acknowledgments
We thank the farmers for allowing us to collect the soils used in the experiment from their
farms. We also thank the laboratory technicians at the University of Eldoret and Crop Nutri-
tion laboratory in Nairobi-Kenya for their assistance in analyses of soil and plant samples.
Author Contributions
Conceived and designed the experiments: LK FB WN JO. Performed the experiments: LK.
Analyzed the data: LK. Contributed reagents/materials/analysis tools: FB WN JO. Wrote the
paper: LK AO RN JM FB WN. Identified the research sites: JM.
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... In this case, the symptoms of deficiency can be observed on the plant, such as colour disappearance, growth retardation, death of parts of the plant or the death of the plant completely, knowledge and identification of the condition can be achieved better through the analysis of plant tissues, the plants in which such a deficiency occurs are low Production is often of poor quality [6]. ...
... This type of deficiency occurs when nutrients are insufficient, and this deficiency may occur for two main reasons, the first is when the soil begins to form, its nutrient content is very low or it may not contain these elements, because it was formed in lands free of primary mineral substances or it has undergone long periods washing processes The second reason is that the soil may contain sufficient nutrients to meet the plant's need, but the plant is unable to absorb them to meet its need despite their abundance, and this may be due to several factors, the prevailing composition of that soil or high salinity, moisture stress or certain diseases such as Disease of Root nodes While the likelihood of identifying this severe deficiency through soil analysis is low, there is a chance that the actual deficiency in the plant will reveal it [6]. The mentioned cases can be explained as follows: Factors impact how ready plants are for nutrients. ...
...  Soil reaction (PH): the PH ( pH value) of the environment in which the plant grows has a direct impact on the readiness of some nutrients, as it was found that plants get nutrients, especially micro ones, more in the case that the environment in which plants grow tends to acidic, and their readiness gradually decreases as the PH value rises There are some elements, such as molybdenum, that are better prepared for plants in neutral reactive soils and processing decreases with a decrease in the pH value PH( soils that tend towards acidic), so fertilizers whose final reaction in the soil is acidic have a better effect and it is preferable to add them to calcareous soils because the latter can fix nutrients, especially when their reaction tends towards-basicity [6].  Contrast (conflict ) and fixation: by contrast, it means the presence of a nutrient element in the soil that may help to provide another nutrient element or vice versa, so adding a nutrient element in the form of a chemical fertilizer may change the balance of the soil solution, followed by the provision of nutrients or vice versa, for example, as the results of some studies indicated that Fertilizing with phosphate fertilizers has led to an increase in the yield of yellow corn and at the same time to reduce the readiness of the element zinc in poor lands with this element, in addition, phosphates when added to the soil, they may be with iron, zinc and manganese insoluble compounds, which leads to the appearance of signs of deficiency of these elements on the plant [6]. ...
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... Studies show that most arable lands in SSA are deficient in important plant nutrients including N, P and K (Youssef and Eissa 2014;Keino et al. 2015). As a result, potato farming in these countries is heavily dependent on synthetic fertilizers (FAO 2008). ...
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An understanding of the mineral nutrition of plants is of fundamental importance in both basic and applied plant sciences. The Second Edition of this book retains the aim of the first in presenting the principles of mineral nutrition in the light of current advances. This volume retains the structure of the first edition, being divided into two parts: Nutritional Physiology and Soil-Plant Relationships. In Part I, more emphasis has been placed on root-shoot interactions, stress physiology, water relations, and functions of micronutrients. In view of the worldwide increasing interest in plant-soil interactions, Part II has been considerably altered and extended, particularly on the effects of external and interal factors on root growth and chapter 15 on the root-soil interface. The second edition will be invaluable to both advanced students and researchers.