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DEVELOPMENT OF MATHEMATICAL
MODEL TO PREDICT THE TRANSPORT OF
E.COLI IN A NATURAL POND
Eluozo, S. N
Subaka Nigeria Limited, Port Harcourt, Rivers State of Nigeria
F.E.Ezeilo
Department of Civil Engineering,
Rivers State University of Science and Technology,
Port Harcourt, Rivers State, Nigeria
ABSTRACT
Development of mathematical model to predict the rate of microbial
depositions (E.coli) in a natural pond has been carried out. The models were
developed to monitor the rate of concentration at different periods, with
respect to the length of the pond at various sample station. Results of the
theoretical values were compared with the experimental analysis. The analysis
was thoroughly done to determine the physiochemical parameters of the pond.
Microbial traces were found from the experimental analysis at different
periods up to hundred days. The developed model compared favourably well
with the experimental values. The values explain the rate of microbial growth
and level of lag phase condition. The growth rate of the microbes were found
to be higher because there is high deposition of substrate for growth and
energy, while at some periods it degrades showing that the substrates have
reduced in concentration including the inhibition from the pH. In some cases
when the microbes developed lag phase condition it may be as a result of
other environmental factors. Finally, the growth rates are between fifty and
hundred days, showing that there is constant regeneration of the microbes
including other environmental factors. This condition calls for regulation of
waste dump at the study location. This will reduce the concentration of the
microbes. The pollution that deposited at the pond should be remediated to
prevent the death rate of aquatic habitat that may not favour some marine
habitats. The pollution will reduce the surface water pH and cause more harm
to the marine habitats.
Key words: Mathematical Model E.Coli and Natural Pond
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1. INTRODUCTION
Pond is known to be man-made or natural water body which is between 1 m2 and 2 ha
(~5 acres or 20,000 m2) in area, this types holds water for four months of the year or
more (Biggs et al., 2005). The superiority of water usually means the constituent
which must be present for finest growth of aquatic organisms. The determinant of
high-quality growth in water body includes dissolved oxygen, hardness, turbidity,
alkalinity, nutrients, temperature, etc. Conversely, other parameters like biological
oxygen demand, and chemical oxygen demand indicate contamination stage of a
given water body. In most water bodies, a variety of chemical parameters, these occur
in low concentrations. This concentration level increases due to human behavior, and
lack of environmental instruction (Mishra, 1991). The fish ponds in several areas
experience lots of biodegradations, pollutions are generated from different activities
of man, consequently, it begins to reduce the constituent of the water bodies that
affect the marine habitats, and some published data reflect adverse effects at
concentrations higher than acceptable limit (GESAMP, 1985). The productivity
depends on physiochemical characteristics of the water body (Huct, 1986). There is
dearth of information on the fish ponds. The purpose of this present investigation was
to determine the values of the major physiochemical parameters of fish ponds and its
environ. Furthermore, to determine if there is any build up of toxic substances which
could lead to bio-accumulation and magnification leading to health implications.
(Ehiagbonare and Ogunrinde 2010) Majority of water obtainable on the earth is saline
in nature; only small amount is fresh water. Freshwater has become a panic product
due to over exploitation and pollution (Ghose and Basu 1968; Gupta and Shukle;
2006; Patil and Tijare, 2001; Singh and Mathur, 2005). contamination is caused when
a vary in the physical, substance or biological situation in the environment
destructively affect quality of human life as well as other animals life and plant
(Lowel and Thompson, 1992; Okoye et al., 2002). Industrial, sewage, metropolitan
wastes are been continuously added to water bodies hence influence the
physiochemical quality of water making them unfit for use of domestic animals and
other organisms (Dwivedi and Pandey, 2002). Uncontrolled domestic waste water
release into pond as resulted in eutrophication of ponds as confirmation by
considerable algal bloom, dissolve oxygen reduction in the subsurface water leads to
large fish kill and other oxygen requiring organism (Pandey, 2003) Effluent is release
into environment with improved concentration of nutrient, sediment and toxic
substances may have a severe negative collision on the value and life forms of the
getting water body when discharge untreated or partially treated (Forenshell, 2001;
Miller and Siemmens 2003; Schulz and Howe, 2003). Water pollution by overflow
has become a question of substantial public and scientific worry in the light of
evidence of their extreme toxicity to human health and to biological ecosystems
(Katsuro et al., 2004). The incidence of heavy of metals in industrial and municipal
sewage effluents constitute a major source of the heavy metals entering aquatic
media. Hence there should be regular evaluation of these sewage effluents to ensure
that adequate measures are taken to reduce pollution level to the minimum.
Worldwide water bodies are primary means for disposal of waste, especially the
effluents from industrial, municipal sewage and agricultural practices that are near
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them. This effluent can alter the physical, chemical, and biological nature of receiving
water body (Sandoyin, 1991). The initial effect of waste is to degrade physical quality
of the water. Later biological degradation becomes evident in terms of number,
variety and organization of the living organism in the water (Gray, 1989).
3. REQUIRED
1. Sterile filtration unit for holding 47mm diameter membrane filters with suction
device (wagteck international)
2. Sterile grid membrane filters of 47mm diameter with a pore size of 0.45um (oxide).
3. Sterile 47mm diameter cellulose pads (both culture medium to be added just before
use).
4. Sterile Petri dishes 50-60mm diameter
5. Sterile membrane lauryl sulphate broth (lactose sodium lauryl sulphate broth)
6. Autoclaving unit, blunt ended forceps, sterile bottles, grease pencil, incubator at 44 oc,
Bunsen burner, Petri-dish holders and oblique light source.
4. PROCEDURE
1. Assembling the Filtration Unit: The sterile broth is aseptically added to the
cellulose pad in a Petri-dish. The membrane filter is aseptically removed from the
sterile pack using a flame sterilized blunt forceps and placed on the filter base with
the grid-side uppermost and centrally. Next, the filter lid was screwed into place.
2. Suction Filtration of water sample: 100ml of the different water samples were
thoroughly mixed by inverting the bottles several times and gently poured into the
assembled filtration unit.
The water was drawn into the filter membrane by suction using the hand held
pressure pump.
A blunt-ended forceps was sterilized by naked Bunsen flame, cooled and the
membranes were aseptically removed from the filtration unit after unscrewing the lid
of the filtration unit.
The membranes were placed, grid-side uppermost, on the culture medium pads in the
Petri-dishes, ensuring there were no air bubbles trapped under the membranes.
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The Petri-dishes were closed and the top of the lids were labeled with the code
numbers of the water samples and volumes of water used using a grease pencil.
3. Incubation of Samples: The Petri-dishes were packed in a Petri dish holder with lids
uppermost and placed inside the incubator at 44 oc for 12 16 hours. Examination,
count and calculation of E.coli colonies:
Following incubation and using oblique lighting, the membranes were examined one
after the other for yellow lactose fermenting colonies, 1-3mm in diameter. The
number of colonies if any was counted. Any plink and small colonies less than 1mm
in diameter were ignored. Number of colonies too numerous to count were reported
as too numerous to count (indicative of gross contamination).
To calculate the presumptive E. coli count/100ml water sample, the number of
colonies counted per membrane was multiplied by 1
V
V
V ( x)
to
ln C ( x) K ln t
ln
C( x )
C( x )
C( x )
C( x )o
C( x )
C( x )o
C( x )
C( x ) o
( x)
V( x )
V
ln
t
t
(5)
(6)
t
V
t
ln K x
to
V
to
t KVx
V
to
(7)
(8)
K ln t t Vx V
o
(9)
K ln 1t Vx V
C( x)
(10)
K ln 1t
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(11)
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Where
C( x)
K ln 1t
(12)
C ( x)Vx tv C ( x) Vx tv
(13)
Co
Vo
C(o)
S
V
V(o) S
V
C (o) V (o)
(14)
+ S C (o) V =
C (o) V (o)
+ S C (o) V -
V 0
(15)
=>
C( x )
But
C( x )
VC( x)
V
Sv S 2 4
2
V 2 ( x)
4
V2
2
1
=>
=>
(16)
VC( x)
C( x )
Sv S 2V 2 4
2v
C( x )
C( x ) A
(17)
V 2x
4
V2
2
1 4
2
(18)
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1 4
2
(19)
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B=1
C( x )
But
Cx
1 1 4
t
t
1 4
1 1
2
1 4
1 1
2
(20)
L
V
1 1 4
(21)
Theoretical values
1.40E-03
3.00E-03
4.76E-03
6.78E-03
8.93E-03
1.10E-02
1.30E-02
1.60E-02
1.90E-02
2.00E-02
Experimental values
1.80E-03
3.26E-03
4.42E-03
6.75E-03
8.36E-03
1.19E-02
1.37E-02
1.58E-02
1.85E-02
2.02E-02
Theoretical values
10
20
30
40
50
60
70
80
90
100
1.40E-03
3.00E-03
4.76E-03
6.78E-03
8.93E-03
1.10E-02
1.30E-02
1.60E-02
1.90E-02
2.00E-02
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Experimental
values
1.80E-03
3.26E-03
4.42E-03
6.75E-03
8.36E-03
1.19E-02
1.37E-02
1.58E-02
1.85E-02
2.02E-02
editor@iaeme.com
Theoretical values
(different velocity
2.13E-04
4.43E-04
3.40E-05
4.89E-05
3.00E-05
4.31E-05
6.10E-03
1.60E-02
2.30E-02
2.10E-02
Experimental values
2.80E-04
4.26E-04
3.42E-04
4.75E-04
3.36E-04
1.19E-04
6.37E-03
1.58E-02
2.85E-02
2.02E-02
Experimental values
10
20
30
40
50
60
70
80
90
100
2.13E-04
4.43E-04
3.40E-05
4.89E-05
3.00E-05
4.31E-05
6.10E-03
1.60E-02
2.30E-02
2.10E-02
2.80E-04
4.26E-04
3.42E-04
4.75E-04
3.36E-04
1.19E-04
6.37E-03
1.58E-02
2.85E-02
2.02E-02
Theoretical values at
different velocity
5.68E-04
9.17E-04
1.24E-03
1.37E-03
1.24E-03
9.41E-04
9.26E-04
9.23E-04
8.02E-04
1.20E-01
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Experimental values
4.88E-05
3.23E-05
2.66E-03
3.45E-03
2.66E-03
9.51E-04
9.51E-05
1.31E-04
8.12E-03
1.17E-01
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Distance
1.5
3
4.5
6
7.5
9
10.5
12
13.5
15
Experimental values
4.88E-05
3.23E-05
2.66E-03
3.45E-03
2.66E-03
9.51E-04
9.51E-05
1.31E-04
8.12E-03
1.17E-01
2.50E-02
y = -6E-06x3 + 0.0002x2 + 0.0001x + 0.0014
R = 0.9976
Concentration Mg/l
2.00E-02
1.50E-02
Theoretical values
Experimental values
1.00E-02
5.00E-03
0.00E+00
0
10
15
20
Distance (MM)
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Concentration Mg/l
2.00E-02
1.50E-02
Theoretical values
Experimental values
1.00E-02
0.00E+00
0
20
40
60
80
100
120
3.50E-02
y = -1E-05x4 + 0.0005x3 - 0.0047x2 + 0.0172x 0.0176
R = 0.9437
3.00E-02
Concentration Mg/l
2.50E-02
2.00E-02
1.50E-02
Experimental values
1.00E-02
5.00E-03
0.00E+00
0
-5.00E-03
10
15
20
Distance (mm)
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3.50E-02
y = -7E-09x4 + 2E-06x3 - 0.0001x2 + 0.0026x 0.0176
R = 0.9437
3.00E-02
Concentration Mg/l
2.50E-02
2.00E-02
1.50E-02
Experimental values
1.00E-02
5.00E-03
0.00E+00
0
20
40
-5.00E-03
60
80
100
120
1.40E-01
y = 0.0003x3 - 0.006x2 + 0.0346x - 0.0486
R = 0.8454
1.20E-01
Concentration Mg/l
1.00E-01
8.00E-02
Theoretical values at
different velocity
6.00E-02
Experimental values
4.00E-02
2.00E-02
0.00E+00
0
-2.00E-02
10
15
20
Distance (m)
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1.20E-01
Concentration Mg/l
1.00E-01
8.00E-02
Theoretical values at
different velocity
6.00E-02
Experimental values
Poly. (Experimental values)
4.00E-02
2.00E-02
0.00E+00
0
-2.00E-02
10
15
20
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contribute to the rate of growth if it cannot inhibit the microbes at that time. The
analytical model compared favourably well with the experimental values this proof
the authenticity of the predictive model simulated.
7. CONCLUSION
Development of mathematical model to predict the rate of microbial depositions
(E.coli) in a natural pond has been carried out. The behaviour of the microbes in the
pond was thoroughly explained from the results. High concentrations were found
between 9 to 13.5 metres at the period of 20 - 90 days, while the lag phase occurred
between 1.5 metres to 9 metres. The condition can be attributed to the rate of substrate
deposition in the pond while the figure with respect to time the lag was found between
10 to 50 days. The theoretical and experimental values compared favourably well.
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