Investigation of industrial wastewater effects on wheat yield, growth, nutrients germination and lead bio-accumulation
A Conceptual Research Paper (Environmental Sciences)
Author: Aiman Afzal
laureatefolks@gmail.com
ABSTRACT:
Due
to the scarcity of freshwater several farmers have started using contaminated water
for the purpose of irrigation. The current study investigated the effect of lead
bioaccumulation in a wheat cultivar named Cv. Shafaq-2006. The experimental
analysis has consisted of 7 lead treatments for example 0 to1000mg lead/kilogram.
It was revealed in results that Pb negatively impacted the parts of crop and severely
decreases the fresh weight of seedling (− 74%), germination (−30%), dry weight of
seedling (−77%), tolerance index (− 84%), root fresh weight (− 50%), plant
height (− 33%), vigour index (− 89%), leaves number (− 41%), shoot dry weight (−
71%), fresh weight of shoot (− 62%), dry
weight of root (− 63%), and length of root (− 45%). The physiological attributes
also showed negative impacts such as transpiration rate (− 72%), stomatal
conductance (− 82%) and rate of photosynthesis (− 74%). Correspondingly,
biochemical parameters such as total chlorophyll, chlorophyll b, chlorophyll a and
carotenoids also respond negatively like − 43, − 42, − 53 and −41 respectively.
In T6 the attributes of yield like seed weight/plant, seed number/plant, the harvest
index and 1,000 seed weight were decreased by 88%, 90%, 61% and 44% respectively.
Besides, in the highest concentration of lead (T6) the contents of protein (−
81%), potassium (− 55%) and phosphorous (− 60%) were highly effected. In
comparison to the control plant the accumulation of Lead was extremely higher
(119%) in seeds. The bioaccumulation of Lead in parts of crop above threshold
concentrations is a serious concern for human health.
1. INTRODUCTION:
In
developing countries such as Pakistan the scarcity of freshwater is a major problem
for agriculture. Presently, farmers have started using contaminated industrial
wastewater to meet the requirements of water (Rezapour, et al., 2019). The wastewater
discharged from industries contains large amount of toxic heavy metals for
instance lead (Pb), cadmium (Cd), nickle (Ni), zinc(Zn), iron(Fe) and maganese(Mn)
etc. These heavy metals (HM) bioaccumulate in different parts of crop and lead
to several severe health concerns to ecosystem and human (Wang, et al., 2017). There are also several resources for the
entry of heavy metals in the ecosystem such as industrial effluents, activities
of mining, sludge use as manure and agronomic practices (Zhang, et al., 2018).Globally the contamination of heavy metals(HMs)
causes a sharpe rise in problems of environmental and human health. The
cultivation of crops near such polluted areas lead to the poor growth of crops
and bioaccumulation of heavy metals(HMs) in crops. Howerever,the ingestion of
these acccumulated HMs pose high risk to the health of livestock &humans (Khan, et al., 2013).
Zajac
in their study investigated one hundred and ninety five toxic Site
Identification Program sites in thirty three middle and low income countries
and stated that almost 820,000 childbearing age women living at these areas have
significant risk of lead exposure (Zajac, et al., 2020).
Lead (Pb) is a significant persistent pollutant in the environment that has 150
to 1500 years retention time and ability to pose several negative impacts on
human (Vergara, et al., 2020). Lead accumulates
in plants through several means such as air, water and soil. The detrimental
impacts of lead includes reduction in germination, interference in uptake of
nutrients (Tiwari, et al., 2013), reduction in
photosynthesis, mitosis inhibition in tip, disturbed respiration, (Rizwan, et al., 2017)delay in growth of plant (Shekar, et al., 2011), alternations in enzymatic activities, changes
in metabolism, alternation in morphology of roots (Bergqvist, et
al., 2014), inflamed vacuoles, injured thylakoid, expended
plasmolysis and deformed nucleolus (Rafaqat, et al., 2015).
HMs significantly affected the parts of crop by causing the formation of malondialdehyde
and reactive oxygen species in excessive amount predominantly in mitochondria
and chloroplast of root, leaves, and shoots (Basharat, et al.,
2014). It is reported in the study by Rafaqat at el that the chromium
toxicity in Brassica napus L. damages
the ultra-structures of its roots. Besides, they are also responsible for
altering the plant’s natural antioxidant enzymes (Gill, et al.,
2014). The ROS (reactive oxygen species) are capable for attacking
biomolecules and may cause death of cells. Therefore, the contamination of lead
is a major problem for agriculture. In Pakistan wheat, rice, sugarcane and
cotton are most significant cash crops that account 75% of total output. (Yang, et al., 2013) The main food crop of Pakistan is wheat. Farmers
are utilizing industrial polluted water for irrigation due to the scarcity of
water farmers for irrigation. Several chronic health impacts are caused by the
presence of lead in food chain (Vaiserman,
et al., 2016). The tolerance
of metal in crops is improved by the utilization of plant growth regulator such
as 5-aminolevulinic acid (Ali,
et al., 2015). So, this study
was executed and designed to examine the effects or impacts of lead on yield, growth
of seedling, germination, mineral contents, biochemical and physiological
parameters.
2. MATERIAL AND METHODS
2.1.Germination
experiment:
Shafaq
2006 is a wheat cultivar that was chosen as test crop specie. This experiment was
done in the growth room in 90mm petri dishes. Firstly proper washing and
sterilization of petri dishes were done. Blotting paper was placed in all petri
dishes and then after surface sterilization of twenty five seeds they were also
placed in all petri dishes. Seven lead treatments named as T1, T2, T3, T4, T5,
T6, T7 were prepared for irrigation by utilizing lead nitrate. Lead treatments
have 0, 100, 200, 400, 600, 800 and 1,000mg Pb/L respectively.
|
Specie of Crop |
Pb treatments |
Seeds/petri dish |
Replicates |
|
1 |
7 |
25 |
4 |
Completely
randomized design was used to place all these petri dishes and in each
respective petri dish 2ml of lead treatment was added daily. As radical started
emergence the readings of germination were noted. Data was collected for estimating
length of plumule, percentage of germination, length of radical, fresh biomass
and length of seedling. The estimation of both Tolerance index and Seedling
vigor index were done by multiplying the length of seedling with percentage of germination.
The Tolerance Index of metals is a diagnostic measurement that is used for
identification of high degree metal tolerant organisms samples.
2.2.Pot
experiment
The
setup of this experiment was placed in ambient condition in Botanical Garden of
GCU, Lahore. No extra instruments were utilized to regulate any abiotic factor
such as temp, light and humidity. All 12 inch earthen pots were properly washed
then dried and lined with polythene bag. Each pot was filled with 5.5kg soil mix
with the 1:6 ratios of humus and garden soil respectively. Different
concentrations of lead nitrate were added in the soil. Seven lead treatments
named as To, T1, T2, T3, T4, T5, T6 were prepared have 0, 100, 200, 400, 600,
800 and 1,000mg of lead/kg respectively.
The position of pot was consistently altered on a weekly basis to keep uniform
climatic condition. All
All
lead treatments comprised of constant agronomic practices. The measurement of all
parameters was carried out at the time of harvest. All plants were properly
rinsed after the harvesting. Later they were dried and polythene zipper bags were
used to store them. Measuring rod & electric balance were used to measure
the length, fresh biomass and dry biomass of root, shoot. The estimation of dry
weight were carried out by drying the samples of crop were at 70°C temperature for
a whole day. The attributes of yield were determined by the Zadoks protocols.
2.3.Biochemical
and Physiological attributes
For
the measurement of stomatal conductance, rate of photosynthesis and
transpiration LCA4 Model Infra-Red Gas Analyzer was used. Leaves of tree were
selected from each pot. At every 75th and 130th day readings were noted. Arnon
protocols were followed to measure the contents of chlorophyll. Carotenoid was
extracted in dim light in which one gram of fresh leaves were chosen
arbitrarily and then crushed in (CH3)2CO. Then filtration
of homogenate was carried out and the final volume was raised upto 50ml by
adding more (CH3)2CO. Spectrophotometer was used for the
estimation of carotenoids at the 440.5 nm wavelength.
“Carotenoids
contents = [V × 383 × (As − Ab)] / (100 × W)”
Where:
"V" is volume utilized for investigation; “383” is carotenoids extinction
coefficient; “As” is sample absorbance; “Ab” is error in cuvette; “W” is sample
weight in grams.
2.4.
Mineral
contents and quality attributes
Flame
photometer was used to estimate Potassium. The quantification of phosphorous was
carried out by drying one gram of sample of plant that later crushed. Then
sample was placed in the furnace at
Percentage
of contents of Nitrogen = (A − B) × Normality of acid × 14.01 × 10 × 100/ Volume of sample
Where
‘A’ is used hydrochloric acid, B is hydrochloric acid utilized for blank; 14.01
is N atomic mass. whereas, the estimation of protein was carried out by
multiplying 6.25 with percentage of nitrogen contents.
2.5. Accumulation of Lead
Chandra
protocol is followed for the determination of lead accumulation in plants
shoots, roots & leaves. The sample of crop was firstly rinsed with double
distilled water then with 10mm solution of CaCl2. Later dried and at
450°C samples were turned into ashes. Then 2% nitric acid is used for the digestion
of ashes. After digestion of ashes it was filtered by using glass fiber filter.
|
Treatments |
Dry
weight of Seedling in grams |
Fresh
weight of Seedling in grams |
Percentage
Germination |
Tolerance
index |
Seedling
vigor Index |
|
To |
0.064±0.006 a |
0.125±0.013 a |
100±0.01 a |
99.99±3.45 a |
2916.67±100.66 a |
|
T1 |
0.052±0.010 b |
0.111±0.012 a |
100±0.01 a |
76.33±1.43 b |
2226.67±41.63 b |
|
T2 |
0.043±0.002 c |
0.084±0.006 b |
98±0.01 b |
57.14±1.93 c |
1638.87±39.40 c |
|
T3 |
0.030±0.002 d |
0.062±0.016 c |
96±0.01 c |
47.59±2.59 d |
1272.40±73.74 d |
|
T4 |
0.024±0.003 de |
0.025±0.010 c |
87±0.01 d |
35.08±2.79 e |
893.87±73.60 e |
|
T5 |
0.021±0.002 de |
0.043±0.003 cd |
80±0.01 e |
23.43±1.10 f |
546.67±25.72 f |
|
T6 |
0.017±0.001 e |
0.033±0.006 d |
70±0.01 f |
15.08±1.91 g |
308.00±38.97 g |
|
F ratio |
38.9816 |
35.0304 |
1.0868 |
539.2539 |
693.2351 |
|
LSD |
0.0085 |
1.01698 |
343.9316 |
3.9219 |
107.5930 |
Table 1: Impact of
Lead on parameters of wheat germination
|
|
|
|
|
|
|
|
Figure 1: Toxicity of Lead (Pb) during germination of wheat
Data analysis:
ANOVA
test and Duncan Multiple Range
Test
(DMRT) were used for the evaluation of Results.
3. RESULTS AND DISCUSSION
The
present study shown several important outcomes concerning to the toxicity of lead
in the wheat germination, biochemical, physiological, growth and attributes of
yield. Information related to the features of germination shown that lead
treatments had severely affected the percentage of germination, length of plumule,
dry weight of crop, length of radical, fresh weight of the wheat and length of seedling
as depicted in Fig. 1 & Table 1. The gradual Intensification of
lead leads towards detrimental effects in wheat crop. In germination highest decrease
was noted for example thirty percent. In comparison to the control in T6
(1000mg lead/L) the length of radical,
seedlings fresh weight, seedlings dry weight, seedling vigor index & tolerance index was
reduced by 45%, 74%, 77%, 89% and 74% respectively as depicted in Figure 1
& Table 1 also. It was observed
by the Chun that during the process of germination at 0mg Pb/kg to 0.5 mg lead/kilogram
concentration there is insignificant harmful effect of lead on index of
germination and required energy. Likewise, at low concentration of lead
contamination there is non-significant impact of lead contamination on rate of growth
of shoots & roots (Alghobar
and Suresha,
2017). But the concentration
of lead above 4.5mg/kg in soil is harmful for the plant because it leads to
reduction in germination (Yourtchi
and Bayat, 2013). Lead toxicity majorly affects the roots of plants in
comparison to other parts of plant (Barberon and Geldner, 2014).
Excessive
contamination of lead caused the reactive oxygen species (ROS) formation in chloroplast,
mitochondria & cellular compartments (Shahid, et al., 2014).
The results obtained from this study about growth of seedlings corroborates with the
study conducted by Yadav who stated that with increasing concentration of lead
the attributes of growth were significantly affected (Yadav, et al., 2018).
|
Treatments |
Root length (cm) |
Plant height (cm) |
Number of leaves |
Fresh weight (g) |
Dry weight (g) |
||
|
Root |
Shoot |
Root |
Shoot |
||||
|
T0 |
25.0 ± 0.15 a |
68.7 ± 0.25 |
26.33 ± 0.58 |
1.26 ± 0.05 |
7.02 ± 0.09 |
0.92 ± 0.04 |
5.62 ± 0.01 |
|
T1 |
22.5 ± 0.26 |
66.1 ± 0.29 |
25.67 ± 0.57 |
1.19 ± 0.03 |
5.77 ± 0.04 |
0.83 ± 0.04 |
4.45 ± 0.06 |
|
T2 |
20.9 ± 0.25 |
64.7 ± 0.38 |
23.99 ± 0.16 |
1.10 ± 0.09 |
5.09 ± 0.08 |
0.72 ± 0.05 |
3.79 ± 0.09 |
|
T3 |
18.1 ± 0.38 |
62.0 ± 0.23 |
24.43 ± 0.23 |
0.95 ± 0.03 |
4.18 ± 0.07 |
0.63 ± 0.04 |
3.25 ± 0.02 |
|
T4 |
16.0 ± 0.52 |
61.2 ± 0.31 |
22.97 ± 0.20 |
0.86 ± 0.01 |
3.85 ± 0.05 |
0.52 ± 0.06 |
2.89 ± 0.03 |
|
T5 |
14.7 ± 0.26 |
60.2 ± 0.25 |
22.03 ± 0.04 |
0.76 ± 0.02 |
3.59 ± 0.06 |
0.40 ± 0.02 |
2.38 ± 0.07 |
|
T6 |
13.5 ± 0.24 |
58.2 ± 0.32 |
20.96 ± 0.07 |
0.62 ± 0.04 |
2.53 ± 0.04 |
0.34 ± 0.05 |
1.61 ± 0.02 |
|
F-ratio |
561.35 |
437.63 |
31.05 |
59.59 |
1596.57 |
76.79 |
2052.58 |
|
LSD |
0.5479 |
0.5295 |
0.8978 |
0.0872 |
0.1140 |
0.07463 |
0.0899 |
Table 2: Effect of different Lead concentrations on growth attributes
of wheat
|
Treatments |
Rate of Transpiration (mmol m−2
s−1) |
rate of Photosynthetic (µmolCO2) |
Stomatal conductance (mmolH2O/m2s) |
|
T0 |
0.99 ± 0.020 |
8.088 ± 0.162 |
0.398 ± 0.008 |
|
T1 |
0.734 ± 0.016 |
7.087 ± 0.156 |
0.289 ± 0.006 |
|
T2 |
0.689 ± 0.013 |
6.787 ± 0.129 |
0.281 ± 0.005 |
|
T3 |
0.654 ± 0.014 |
5.987 ± 0.132 |
0.141 ± 0.003 |
|
T4 |
0.572 ± 0.011 |
4.203 ± 0.084 |
0.127 ± 0.003 |
|
T5 |
0.352 ± 0.006 |
3.502 ± 0.063 |
0.093 ± 0.002 |
|
T6 |
0.263 ± 0.004 |
2.115 ± 0.036 |
0.069 ± 0.0001 |
|
F-ratio |
1,830.3037 |
4,962.6695 |
1,338.3403 |
|
LSD |
0.0173 |
0.09328 |
0.0110 |
Table 3: Effect of lead toxicity on
wheat’s physiological attributes
The
co-cropping of soybean and T. minuta has increased the accumulation of lead in the later
crops but no impact on health was caused by the consumption of grains of soybean (Vergara, et al., 2020). Data related to the attributes of growth
revealed that the concentration of lead ranging from 0.01 to 0.05 significantly
impact the growth of crop as depicted in Table 2 also. In T6 length of
root (13.5±0.24 cm), the height of plant (58.2±0.32 cm) and leaves a number
(21.67±0.05) were noticed minimum. At higher concentration of lead both fresh &
dry weight was significantly reduced. In T6 fresh weight of shoot (2.53 ± 0.04),
roots (0.66 ± 0.05) and dry weight of shoot (0.34±0.04), roots (1.61 ± 0.02) were
also noticed minimum and also depicted in Table 2.
Gopal
& Rizvi study also corroborates with this observation that with the
increase in lead concentration decreases the weight and length of shoot and root.
The detrimental effects of lead were not apparent in the life of plants at their early
stage but as the level of maturity of the plant increases its adverse effects also
increased (Gopal &
Rizvi, 2008). The uptake of metal, bioaccumulation and translocation is
proportional to the age attribute. It is also reported by Antoniadis study that when
lead was present in an excessive amount the development of root was poor (Antoniadis, et al., 2017). The key reason behind the decrease in plant
biomass is the reduced photosynthetic rate and metabolism of nitrogen (Hamid, et al., 2010). It was reported that the fresh weight of
brassica was significantly affected by lead (Pb) concentration (Osma, et al., 2012).
|
|
|
|
|
|
|
Treatments |
Contents Of Potassium |
Phosphorous contents (ppm) |
Protein contents (%) |
Nitrogen contents (%) |
|
T0 |
409.20 ± 0.10 a |
18.87 ± 0.08 |
9.63 ± 0.06 |
1.54 ± 0.01 |
|
T1 |
350.37 ± 0.15 b |
16.85 ± 0.08 |
7.90 ± 0.08 |
1.24 ± 0.02 |
|
T2 |
349.60 ± 0.30 c |
15.10 ± 0.22 |
5.68 ± 0.10 |
0.90 ± 0.01 |
|
T3 |
339.33 ± 0.21 d |
12. 86 ± 0.15 |
5.01 ± 0.01 |
0.79 ± 0.01 |
|
T4 |
311.96 ± 0.12 e |
10. 09 ± 0.06 |
3.44 ± 0.09 |
0.60 ± 0.00 |
|
T5 |
291.33 ± 0.21 f |
8.51 ± 0.12 |
2.55 ± 0.09 |
0.39 ± 0.02 |
|
T6 |
269.57 ± 0.31 g |
7.39 ± 0.14 |
1.75 ± 0.01 |
0.26 ± 0.02 |
|
F-ratio |
139,098.1018 |
2,947.2309 |
4,585.5065 |
3,851.3114 |
|
LSD |
0.3729 |
0.2395 |
0.1283 |
0.0224 |
Table 4: Effect
of different Pb concentrations on wheat’s quality attributes and mineral
content
The results of this study corroborate with the Zeng study who applied lead acetate
at 6 different levels i.e. 0 to 900 mg/kg in his experimental analysis. This
might be expected that lead poses a non-harmful effect at low concentration. With
the increase in the concentration of lead, all biochemical & physiological features
of the wheat crop were decreased that might be because of the toxicity of lead
as it decreases the synthesis of chlorophyll, damages the structure of
chloroplast, reduces the activities of carotenoids and restricted activities of
enzymes. Lead toxicity also causes carbon dioxide deficiency (due to stomatal
closure), obstructions in ETC (electron transport chain) and alternation in the thylakoid
membrane (Zeng et al., 2006). It was reported
that the presence of metal decreases the chlorophyllase that leads to low content
of chlorophyll. And it was revealed by the studies that contents of chlorophyll
a are less disturbed than chlorophyll b contents. Rafaqat in their research
observed that elevated chromium stress decreases the Brassica napus L photosynthesis rate (Gill, et al., 2017).
The
quality and minerals content attributes of wheat decreased significantly by all
lead treatments (p≤0.01; 0.05) (Table 4). In T6 the content of Phosphorous,
nitrogen, potassium and protein decreased from 11 to 58%, 38 to 82%, 14 to 34% and
18 to 81% respectively in comparison to the control. The attributes of yield
were ranges as follows, K contents (409.20–269.57 ppm), contents of P
(17.75–6.79 ppm), contents of protein (9.63–1.75%) and N contents
(1.54–0.28%). The lead treatment significantly changed the results of the Pot
experiment (Table 5). Yield decreases at higher concentrations. In T6 minimum
weight of seed/plant (0.85 ± 0.09 g), seeds number/plant (16.33 ± 0.58), harvest
index (263.39±11.52%), the weight of straw /plant (2.62±0.12 g) and weight of 1000
seeds (29.99±0.74 g) was noticed (Table 5). The attributes of all
yields were decreased by the increasing concentrations of lead so to meet the growing
feed requirement of the population farmers are intended to grow such crop varieties
that produce more yields.
|
Treatments |
Seed weight/plant (g) |
Number of seed/plant |
Straw weight/plant (g) |
1,000 seed weight (g) |
Harvest index (%) |
|
T0 |
7.57 ± 1.10 a |
158.68 ± 28.04 a |
6.98 ± 0.13 a |
54.60 ± 0.79 a |
700.29 ± 12.99 a |
|
T1 |
4.54 ± 1.22 b |
84.33 ± 18.01 a |
5.13 ± 0.08 b |
46.39 ± 0.48 b |
515.41 ± 8.04 b |
|
T2 |
3.01 ± 1.07 c |
55.67 ± 19.86 ab |
4.48 ± 0.05 c |
43.63 ± 0.33 c |
449.56 ± 5.50 c |
|
T3 |
2.28 ± 0.98 cd |
37.00 ± 16.52 b |
4.07 ± 0.06 d |
42.79 ± 0.14 c |
408.39 ± 6.10 d |
|
T4 |
1.49 ± 0.06 cd |
21.00 ± 1.00 b |
3.69 ± 0.15 e |
41.48 ± 0.19 d |
370.65 ± 14.94 e |
|
T5 |
1.34 ± 0.03 d |
19.00 ± 1.00 b |
3.32 ± 0.08 f |
39.11 ± 0.79 e |
333.84 ± 8.63 f |
|
T6 |
0.85 ± 0.09 d |
16.33 ± 0.58 b |
2.62 ± 0.12 g |
30.03 ± 0.63 f |
263.48 ± 10.61 |
|
F-ratio |
24.2617 |
3.3286 |
577.7730 |
557.7549 |
684.2652 |
|
LSD |
1.4529 |
104.6137 |
0.17924 |
0.9465 |
39.2345 |
Table
5: Effect of
various concentrations of lead on yield attributes of wheat
|
Treatments |
Concentration of Pb in roots
(μg/g) |
Concentration of Pb in shoots
(μg/g) |
Concentration of Pb in seeds
(μg/g) |
|
T0 |
4.7 ± 0.05 |
0.9 ± 0.09 |
0.194 ± 0.01 a |
|
T1 |
39.3 ± 0.03 |
15.6 ± 0.04 |
0.213 ± 0.06 b |
|
T2 |
53.9 ± 0.08 |
22.4 ± 0.08 |
0.271 ± 0.09 c |
|
T3 |
79.2 ± 0.04 |
37.3 ± 0.07 |
0.304 ± 0.02 d |
|
T4 |
94.6 ± 0.02 |
49.1 ± 0.05 |
0.356 ± 0.03 e |
|
T5 |
180.3 ± 0.05 |
60.7 ± 0.06 |
0.383 ± 0.07 f |
|
T6 |
221.2 ± 0.02 |
87.3 ± 0.04 |
0.422 ± 0.02 g |
|
F-ratio |
24.2617 |
259,169.857 1 |
22,153.4285 |
|
LSD |
1.4529 |
0.17512 |
0.00175 |
Table 6: Accumulation of lead in roots, shoots and seeds of the wheat plant
The current focus of scientists is to develop more yield producing improved and new
crop varieties with the help of genetic engineering. The present research
investigates the detrimental impacts of lead on the yield of wheat crops. It is
reported in a study by Xiong that vegetable crops such as spinach and cabbage
which were grown near smelter contain concentrations of heavy metals such as Pb,
Zn and Cd in them. Lead restricts enzymatic activities by interfering with the enzyme’s
active sites that results in low yield (Xiong, et al., 2014).
It is reported in a study that the yield of corn mint affected by 16% from a
400m away lead source through the air. Similarly, it was observed that air
pollution is responsible for the reduction in essential oils yield by 14%. Gill
et al. stated that chromium
toxicity in cultivars of oilseed rape caused an increase in the number and size of grains
of starch (Gill, et al., 2014).
Elite
molecular transporters genes were revealed by the presence of heavy metals. MTs
tend to perform the activity of transmembrane transportation of water (Gill, et al., 2017). The depictions of outcomes by the accumulation of
lead in parts of wheat crop such as shoot, root & seed was shown in Table no.
6. The drastic alternations in the treatment means were also revealed. In
comparison to control treatments, the degree of increase in the amount of lead was relatively
alarming. For example, in T6 roots, seeds and shoots showed 4600%, 118% and
9800% increase in the quantity of lead respectively. The concentration of Pb declines
majorly in roots then shoot and then in seeds of the wheat plant. In comparison to
control the concentration of lead was significantly increased in T6 as depicted
in Table 6 also. The amount of lead is directly related to the uptake
of lead by roots. Different variables which contribute towards the adsorption of
lead are microbial activity, fertilizer type, pH of the soil, extractable lead
concentration in soil, fertilizer amount, precipitates of phosphate and carbonate
(Gupta, et al., 2019). It was reported by Antoniadis that translocation of lead was significantly
decreased by the movement of metal towards aerial parts, which indicated that
accumulation of Pb was more in roots than shoots and seeds (Antoniadis, et al., 2017).
Several studies revealed that there was a high amount of lead accumulation in roots such as Kenaf root tend to retain up to 85% of total lead, Tlaspi praecox up to 80% of total lead and Brassica junce tends to hold up to 95% of
total lead.
It
is concluded by Zhang that cultivars of rice have several factors for translocation
and uptake of metal. Translocation and absorption of lead to leaves of plants
rely upon different factors that vary from one crop to another crop (Zhang, et al., 2010). Accumulators in shoots tend to store more
lead in plant shoots while accumulators in roots tend to hold more lead in
plants roots and permit transportation of only a minute concentrations of Pb to
aerial crop parts. Similarly, it is revealed in another study that the surface area
of roots determines the uptake of Pb by plants (Shahid, et al., 2016). Heavy metal significantly impacts the
tip cells of the root as disruption of the cell membrane, enlarged vacuole, injuries in
thylakoid of mitochondria and plasmolysis was most noticeable in cells of root (Gill, et al., 2014). The
difference in the rate of translocation was caused by the existence of significant
lead concentration in plants. It was concluded by Sharma that lower molecular
complexes and ions are more moveable forms than other forms. Roots might accumulate
more concentration of (Pb) lead in such plants but high molecular complexes &
weight constrain distribution & translocation of lead to above-ground parts
of the crop. Basharat et al. conducted an experimental analysis and observed
that lead is responsible for the decrease in.
macronutrients concentration in shoot, decline in biomass, increase in MDA &
reactive oxygen species (Khan,
et al., 2013). It is revealed
in a study that the application of plant growth regulators can counter the detrimental
impacts of such heavy metals in wheat and other crops (Ali, et al.,
2015).
4. CONCLUSION:
This study revealed that lead causes several adverse impacts on wheat yield, germination,
biochemical, physiological, mineral, growth and quality feature. Results
revealed that all negative effects of Pb (lead) were mainly caused by a reduced
rate of photosynthesis and associated phenomena such as reduced conductance of
stomata and reduced rate of transpiration. It was also observed that the rate
of accumulation of lead in parts of wheat crop such as seeds, shoots & roots
was above the permissible/threshold level. In Pakistan wheat is an essential
food therefore the contamination of Pb in wheat is alarming. The gradual accumulation
of lead (Pb) eventually causes serious illness & disorders. So certain
remedial practices ought to be taken on to limit the entry of lead into wheat
from contaminated soils. So, currently, it is the need of an hour to maintain the supply of lead-free wheat.
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