Journal Pre-proof A comprehensive assessment of groundwater quality for drinking purpose in a Nigerian rural Niger delta community H.I. Owamah PII:
S2352-801X(18)30304-7
DOI:
https://doi.org/10.1016/j.gsd.2019.100286
Reference:
GSD 100286
To appear in:
Groundwater for Sustainable Development
Received Date: 26 December 2018 Revised Date:
13 July 2019
Accepted Date: 6 October 2019
Please cite this article as: Owamah, H.I., A comprehensive assessment of groundwater quality for drinking purpose in a Nigerian rural Niger delta community, Groundwater for Sustainable Development (2019), doi: https://doi.org/10.1016/j.gsd.2019.100286. This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. © 2019 Published by Elsevier B.V.
A comprehensive assessment of groundwater quality for drinking purpose in a Nigerian rural Niger Delta community a*
H. I. a*Owamah Department of Civil Engineering, Faculty of Engineering, Delta State University, PMB1, Abraka, Oleh Campus, Delta State, Nigeria *Email:
[email protected];
[email protected] *Tel: +2348035705814
Abstract This study gives a first time comprehensive report on the quality of groundwater in Emevor community in the Niger Delta region of Nigeria, for dry and wet season monitoring. Water samples were collected from ten (10) bore-holes (BHs) and 10 hand-dug wells (HDWs), on monthly basis, for eight (8) consecutive months spanning from May to August, 2016 (wet season) and October 2016 to January 2017 (dry season). Following standard procedures, thirtythree (33) water quality parameters were analyzed. But for pH being less and Ba higher than the prescribed values of the WHO and SON, all other physicochemical parameters were within the WHO and SON standards. While the low pH value was linked to mineral dissolution, the high Ba value was attributed to oil exploration activities in the area. The main mineral classes in the aquifer (Calcium-Iron, Sodium-Magnesium and Zinc-Potassium) were found to be the determinants of the groundwater chemical composition and ionic exchanges. ANOVA showed a significant difference in the concentration of parameters that exceeded regulatory limits for BHs and HDWs. Microorganisms isolated from the water samples obtained from BHs and HDWs are Enterobacter aerogenes and E. coli. The higher organic pollution recorded for the HDWs corroborated the higher values of E. coli obtained. By implication, this study shows that BHs were safer drinking water sources in the community. Regular monitoring of groundwater in Emevor and neighboring communities is recommended given the increase in anthropogenic activities in the area of study. Keywords: Groundwater, quality parameters, public health, pollution, Niger-Delta
1
A comprehensive assessment of groundwater quality for drinking purpose in a Nigerian
2
rural Niger Delta community
3 4
Abstract
5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21
This study gives a first time comprehensive report on the quality of groundwater in Emevor community in the Niger Delta region of Nigeria, for dry and wet season monitoring. Water samples were collected from ten (10) bore-holes (BHs) and 10 hand-dug wells (HDWs), on monthly basis, for eight (8) consecutive months spanning from May to August, 2016 (wet season) and October 2016 to January 2017 (dry season). Following standard procedures, thirty-three (33) water quality parameters were analyzed. But for pH being less and Ba higher than the prescribed values of the WHO and SON, all other physicochemical parameters were within the WHO and SON standards. While the low pH value was linked to mineral dissolution, the high Ba value was attributed to oil exploration activities in the area. The main mineral classes in the aquifer (Calcium-Iron, Sodium-Magnesium and Zinc-Potassium) were found to be the determinants of the groundwater chemical composition and ionic exchanges. ANOVA showed a significant difference in the concentration of parameters that exceeded regulatory limits for BHs and HDWs. Microorganisms isolated from the water samples obtained from BHs and HDWs are Enterobacter aerogenes and E. coli. The higher organic pollution recorded for the HDWs corroborated the higher values of E. coli obtained. By implication, this study shows that BHs were safer drinking water sources in the community. Regular monitoring of groundwater in Emevor and neighboring communities is recommended given the increase in anthropogenic activities in the area of study.
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Keywords: Groundwater, quality parameters, public health, pollution, Niger-Delta
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Introduction
25
One of the essential requirements for the sustenance of life and good health is water (Abubakar,
26
2018a). Within the last two decades, the world has recorded some achievements in the area of
27
improvement of access to improved drinking water (IDW) and hygiene in line with the Sustainable
28
Development Goals (SDGs) (WHO/UNICEF JMP Report, 2015; Abubakar, 2016, Kulinkina et al.,
29
2017). IDW source could be described as a source well protected from external contamination, in
30
particular, faecal matter (Abubakar, 2018b). Report has shown that globally, more than 2.6 billion
31
people gained access to IDW sources since the 1990s (Mkwate et al., 2017). This achievement
32
notwithstanding, access to IDW is still a problem as about 663 million people in the world are yet
33
to have access to IDW sources (Mkwate et al., 2017). This has made many people depend heavily
34
on untreated water from private boreholes, unprotected shallow wells, streams, rivers etc.
35
(WHO/UNICEF JMP, 2015).
1
36
While with a population of 319 million people, as at 2015, only 24% of the people in Sub-Saharan
37
Africa had access to improved drinking water (IDW). Latin America and Caribbean, West Asia
38
and North Africa, East Asia and South-east Asia had theirs as 65%, 90% and 94% respectively
39
(UNICEF/WHO, 2017, p. 3; Abubakar, 2018). It is also worthy to note that 70% of the global
40
population that depends on surface water for drinking reside in sub-Saharan bet (UNICEF/WHO,
41
2015 p. 11). While 723 million new users of piped water were recorded in the Eastern part of Asia
42
between 1990 and 2015, a decline from 43% to 33% was obtained in the sub-Saharan African
43
(UNICEF/WHO, 2015, p. 9). In Nigeria, 67% of the population were reported in 2015 to have had
44
access to improved drinking water sources. This was however still short of meeting with the 77%
45
MDG goal and much less than the global mean of 91% (UNICEF/WHO, 2015, p. 9). The Nigeria
46
Demographic and Health Surveys of 2013 showed that 50.8% (rural) and 14.4% (urban) of
47
Nigerian households used unimproved drinking water sources (Abubakar, 2019).
48 49
Drinking of contaminated water alongside inadequate hygiene and poor sanitation has been
50
indicted of being directly or indirectly, the cause of over a million annual global deaths (WHO,
51
2012). It has also been reported that not less than eighty percent (80%) of all water-borne diseases
52
in developing nations are traceable to drinking of contaminated water, poor hygiene, and open
53
defecation (Abubakar, 2018). About 50% and one fifth of these people without access to improved
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drinking water sources in the world reside in Sub-Saharan Africa (SSA) and Southern Asia
55
respectively (Mkwate et al., 2017). Recently, countries in SSA were reported to have recorded
56
some achievements, as forty-three percent of their population now have access to potable water.
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This is however, through private boreholes that are mostly not tested for quality (WHO/UNICEF
58
JMP, 2015). Nigeria, with it a 2017 estimated population of more than 190 million people, is a
59
notable nation in the Sub-Saharan Africa (NPC, 2017). She however, still
60
challenges in the in the area of provision of IDW, given the near absence of treated public water
61
supply scheme, especially in the rural areas and small towns. This has thus, made a lot of people
62
resident in Nigerian depend on groundwater for drinking (Dahunsi et al., 2014). Though some
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groundwater drinking water quality studies have been carried out on mostly, urban cities of
64
Nigeria, with findings showing that many of the wells were contaminated with faecal bacteria and
65
in some cases, other pollutants (Owamah et al., 2013; Dahunsi et al., 2014; Sojobi, 2016), such
66
extensive drinking water quality studies cannot be said of rural communities that are even more 2
has enormous
67
prone to anthropogenic activities that create water contaminants such as open defecation, careless
68
disposal of waste materials on the soil, open dumps, unsanitary systems of sewage disposal, siting
69
of water wells near pit latrines and septic tanks etc. (Sojobi, 2016).
70
Furthermore, Nigeria in the last 20 years, has witnessed an unprecedented growth in the number of
71
individual boreholes but drinking water from these, especially the ones in rural communities, are
72
rarely checked for quality compliance (Owamah et al., 2013). Detailed scientific information on
73
the quality of groundwater used as source of drinking water is crucial for the formulation of
74
policies relating to water supply and public health. It is however noteworthy to state that only little
75
or none of such about Emevor community in the Niger-Delta region of Nigeria is available in
76
scientific literature. This research was therefore carried out to critically assess the quality status of
77
groundwater in the study area to serve as baseline water quality data for the community and other
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Isoko neighboring communities with similar geological formation and anthropogenic activities.
79
2. Materials and methods
80
2.1.Study Area
81
Emevor is one of the popular communities in the Isoko North Local Government Area
82
(INLGA), Delta State, Nigeria. The siting of the National Open University of Nigeria study
83
center in Emevor has increased both her population and pressure on resources such as water.
84
Fig. 1a shows that the INLGA lies between 50 − 20′ and 50 − 37′ north latitudes and 6 0 − 12′
85
and 6 0 − 13′ east longitudes. The map of Nigeria showing Delta State is also shown in Fig. 1b.
86
The INLGA is made up of eight clans and a total of 43 communities with two unique climatic
87
seasons. The wet season (WS) runs from March through August while the dry season (DS)
88
begins from September to end in February (Agbogidi et al. 2007). The INLGA with
89
predominantly rainforest vegetation, has a mean annual precipitation of 2800 mm, monthly
90
temperature of 310C and relative humidity range of 76- 90%
91
INLGA with a population of about 140,000 persons as at 2006 is well known as a major crude
92
oil producing LGA in Nigeria (Owamah et al., 2013).
93 94
2.2. Sampling and analysis
3
(Owamah et al., 2013). The
95
Following standard methods, water samples were obtained in triplicate from randomly selected
96
sites (APHA, 2012). Because Emevor community has ten (10) small distinct villages, water
97
samples were collected from ten (10) bore-holes [BHs] (wells with electric pump) and 10
98
hand-dug wells[HDWs] (artificial pumpless wells), on monthly basis, for eight (8) consecutive
99
months spanning from May to August, 2016 (wet season) and October 2016 to January 2017
100
(dry season) as shown in Fig. 1a. (Sojobi, 2016). Collection of samples was done in a manner
101
that ensured that each of the ten small villages that make up the community had two wells (BH
102
and HDW) sampled. New polyethylene bottles, washed three times on site with the same water
103
to be sampled, were used for samples collection. Preservation of samples was done in line with
104
standard protocol (APHA, 2012).
105
Samples for physico-chemical and microbial investigations were placed in an ice-containing
106
box before being transported to Dukoria Laboratories, Nigeria for water quality analyses.
107
Concentrated HNO3 was used for the preservation of water samples meant for metal analysis.
108
Thirty BH and HDW water samples were respectively obtained monthly to give 240 samples
109
each of BHs and HDWs (120 per climatic season). Samples were stored at 40C, using a
110
refrigerator, to ensure that contents remained intact prior to laboratory analyses.
111
2.3.
Analytical procedures
112
Adopting standard protocol, samples were analyzed for numerous physicochemical parameters
113
(Emenike et al., 2018). Turbidity was measured in-situ with a movable 2100P turbidimeter
114
(HACH). pH, total dissolved solids (TDS) and electrical conductivity (EC) were determined
115
with a movable multimeter (Hanna Instruments, Model HI 9812). The concentrations of the
116
other physicochemical parameters (Na, Ca, Mg, K, NO3-, Cl-, NO3-, HCO3-, SO42-, Fe, Ba, Cu,
117
Pb, Ca etc.) were determined in the laboratory. Following APHA (2012) and Owamah (2013),
118
anions were measured with an ultraviolet (UV) spectrophotometer (DR 2800, HACH, USA)
119
through the (UV) spectrophotometer screening method.
120
The analysis of the concentration of metals was done using an atomic absorption
121
spectrophotometer (AAS) (Sens AA 3000, GBC, Australia) in accordance with procedures
122
outlined in APHA (2012). The estimation of the faecal coliforms (FC) bacteria was through the
123
use of the membrane filtration technique (APHA, 2012). Standard plate count method was
124
adopted to count the bacterial colonies that are visible in “colony forming units” (CFU) /100
125
mL. The other physiochemical parameters were measured in accordance with standard 4
126
methods outlined in APHA (2012) and Khan et al. (2013). The mean of data gotten for the
127
various physicochemical and biological parameters were compared with the drinking water
128
standard of the WHO and SON. The correlational relationships among the parameters tested
129
were also investigated. For reproducibility sake, blank, pre-analyzed and standard samples
130
were analyzed after every ten (10) samples (Owamah et al., 2013).
131
2.4. Statistical analysis
132
In-situ and laboratory data obtained were analyzed with Microsoft Excel (2010 version) to
133
compute mean, standard deviation (SD) and correlation coefficient (CC) (Sojobi, 2016). The
134
mean groups of variables were compared using the Analysis of Variance (ANOVA) at 95%
135
confidence level. Patterns among the result variables were shown in graphs and tables
136
(Emenike et al., 2018).
137
3. Results and Discussion
138
3.1.
Physicochemical and microbiological parameters
139
The statistics of the experimental data obtained from this study are displayed in Tables 1 and 2
140
for wet and dry seasons respectively. pH values ranged from 4.92 to 6.28 and 6.50 to 4.82 for
141
the wet and dry seasons respectively. Average values were 5.63 (wet) and 5.55(dry) to give a
142
seasonal mean variation of 0.08. Greater values were recorded in the peak of the WS. This
143
could be attributed to dilution effect as water level rose, thereby making the pH move from
144
slightly acidic toward neutral. In both seasons, while the BH water samples were generally
145
more acidic than those of the HDWs, the most acidic values were obtained from BH samples of
146
DS (Fig. 2a.). The highest pH value (6.50) was obtained in a sample collected from a HDW in
147
November. These pH values corroborate information in literature on the groundwater quality of
148
communities in the Niger Delta region of Nigeria (Owamah et al., 2013).
149
Since the stipulated pH range of the WHO and SON goes from 6.50 – 8.50 (Table 3), it shows
150
that groundwater in the community is generally acidic and needs to be given some chemical
151
treatment to bring it to normal. pH of less than 6.5 could cause gastrointestinal irritation in
152
humans and would therefore require alkaline treatment for improvement to the required range
153
of 6.5–8.5 (Sojobi, 2016). The acidic nature of groundwater in the area of study could be
154
linked to the geological formation of the area (Owamah et al., 2013; Egboh and Emeshie,
5
155
2008). Sojobi (2016), and Akinyemi and Souley (2014) had earlier reported acidic pH values
156
(<6.5) for the groundwater of Omu-Aran, Kwara State and Ogun State of Nigeria, respectively.
157
The TDS of the study area groundwater showed average values of 41.93 mg/L (WS) and 40.65
158
mg/L (DS). Seasonal mean variation value of 1.28 mg/L (wet-dry) was also obtained. Actual
159
values ranged from (33.00-53.70) mg/L in the WS and (32.80-49.00) mg/L in the dry season.
160
The highest WS and DS values were respectively recorded in October and December. BH
161
water samples, generally, had higher TDS values than those of HDWs; showing that it is more
162
of natural than anthropogenic cause.
163
The WHO and SON prescribed maximum TDS value of 250 mg/L (Table 3) is well above the
164
values obtained in the study. Since the mean TDS values for the BH and HDW water samples
165
for both seasons are less than 1gL−1, it shows that groundwater in Emevor is freshwater
166
(Sojobi, 2016; Emenike et al., 2018). Though the SON and WHO stipulated limit is 5.00 NTU,
167
turbidity was not detected in any of the samples. This could be very deceptive, if used by the
168
residents to consider their groundwater water clean and safe (Akhtar et al., 2014). Electrical
169
conductivity (EC) being a function of dissolved mineral matter, has a direct relationship with
170
TDS. For the wet and dry seasons, the average EC values obtained were 77.21µS/cm and 78.92
171
µS/cm respectively and had -1.71µS/cm as the seasonal mean variation. As shown in Fig. 2c,
172
the highest conductivity value of 98.55 µS/cm was found in a BH water sample of DS in the
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month of December. This value is within the WHO prescribed limit of 1,000 µS/cm. The
174
mean EC values of 77.21µS/cm and 78.92µS/cm further show that the groundwater is
175
freshwater since both mean values are less than 1500 µS/cm (Mondal et al., 2008; Sojobi,
176
2016). Conductivity is a function of the total ionic composition of water and thus shows its
177
level of chemical richness. It is usually boosted by sodium, magnesium, calcium, other
178
minerals and the geology of the soil. The electrical conductivity of natural waters is mainly due
179
to dissolved mineral matter (Ademoroti, 1996). Tables 1 and 2 show that Emevor groundwater
180
is not saline as salinity was not detected in all of the samples for both wet and dry seasons. The
181
maximum acceptable limit is however 200‰ (Table 3).
182
While the mean value of TSS in the WS is 0.38 mg/L, it was not detected in the DS for all
183
samples. Only few samples showed results for TSS and this corroborates the finding in this
184
study that turbidity was not detected in all of the water samples. The presence of suspended
185
solids in water affects the clarity of the water and makes it unaesthetic. Though there is no 6
186
guideline limit stipulated for TSS by the WHO and SON, previous studies showed that TSS of
187
1000mg/L is acceptable (Sojobi, 2016). The alkalinity values of the groundwater were found to
188
be on the average of 8.50 mg/L and 6.73mg/L in the WS and DS respectively to give a mean
189
seasonal variation of 1.77 mg/L. Similar values were earlier obtained by Egboh and Emeshie
190
(2008) for groundwater in the neighbouring Ndokwa East Local Government Area. Alkalinity
191
was only not detected in samples with low pH values, there was no distinct pattern of seasonal
192
variation as the presence of alkalinity depends on pH of solution. However, the overall values
193
were relatively higher in the HDW samples of the WS as shown in Tables 1 and 2. Although
194
there are no regulatory guideline values for alkalinity by the WHO and SON, values obtained
195
in this study lie within the safe limits in literature (Dahunsi et al., 2014). Chemical oxygen
196
demand (COD) is a measure of the required oxygen for complete oxidation of carbon (IV)
197
oxide and organic matter present in a sample of water. Tables 1 and 2 show that COD was only
198
slightly detected. The seasonal mean values were 1.62mg/L (WS) and 2.28mg/L (DS). This
199
resulted in a negative seasonal mean variation of -0.66 mg/L, indicative of higher COD values
200
in the dry season. These mean values are less than the maximum desired value of 5 mg/L by
201
the WHO and hence, in order.
202
For the case of ammonia-nitrogen, though no value was detected in the wet season, some
203
samples in the DS had variable values. The seasonal mean value calculated for the DS was
204
2.41mg/L. The major sources of ammonia in groundwater could be excessive availability of
205
nitrogen in the soil following indiscriminate disposal of nitrogen reach organic substances on
206
the soil. The desired level of NH3-N in drinking water is 0.5mg/L (SON, 2007). Water with
207
higher values need to be treated chemically to acceptable limit. The measurement of colour and
208
appearance are important indices in ascertaining the aesthetic acceptability of potable water.
209
Pure water is usually colourless and insipid. Colour was not detected in all the samples. While
210
total organic carbon (TOC) was not detected in many of the WS water samples, values
211
obtained in the DS ranged from 0.01 to 0.80%. The DS mean value is 0.28%. In the same vein,
212
total hydrocarbon was not detected in most of the samples for both seasons. The DS however
213
had a mean value of 0.01mg/L.
214
Odour, calculated as threshold odour intensity number (TON) was not detected in any of the
215
samples analyzed. Ideally, drinking water should not have any detectable odour. Odour in
216
drinking water usually shows that pollution had occurred in the water source. Total hardness, 7
217
defined in terms of the total concentration of calcium and magnesium ions expressed as
218
calcium carbonate showed seasonal mean values of 15.63mg/L (wet) and 10.75mg/L (dry) with
219
a variation of 4.88 mg/L. The peak and least values of 25.00 mg/L and 8.00 mg/L were
220
obtained from HDWs in the months of August and February, respectively.
221
obtained are far lower than the WHO and SON guideline values (Table 3). Furthermore, since
222
the mean values are less than 50.00 mg/L, the groundwater is classified as soft water (Owamah
223
et al., 2013; Abd El Salam and Abu-Zuid, 2015). Ejoh et al. (2018) also found water from
224
Egini and Ubogo rivers, in the Niger Delta region of Nigeria to be soft. Water hardness poses
225
no real health threat but may result in soap wastage.
The values
226 227
There were no values of total phosphorous in the WS unlike the DS that had considerably low
228
values from few samples collected from the HDWs. The DS mean value calculated is
229
0.02mg/L. Phosphorous compounds occur in natural water, effluent and sludge almost entirely
230
in phosphate forms (Ademoroti, 1996). Phosphate in drinking water of ≤75mg/L has been
231
reported to pose no health risk in drinking water (Owamah et al., 2013). The obtained values in
232
this study therefore show that phosphorous has no health-related impact on the groundwater of
233
the study area. The detection of phosphorous at an insignificant level unlike the nitrogen
234
related contaminants shows that wastewater effluent and other solid waste from the community
235
could be mainly nitrogenous. Sojobi et al. (2016) obtained mean phosphate values of 14.27
236
mg/L and 15.6 mg/L respectively for BHs and HDWs of Omu-Aran, Kwara State, Nigeria.
237
Values of 27.5 ± 0.9 mg/L and 6.8–18.8 mg/L were obtained for boreholes in different cities of
238
Northeastern Nigeria and were linked to domestic effluent, fertilizer and open defecation
239
(Ishaku et al., 2011). HCO3- was not detected in many samples of the wet season. The seasonal
240
mean values are 10.37mg/L (wet) and 3.30mg/L (dry) with a seasonal mean variation of 7.07
241
mg/L. The values of the SD show that the variation pattern for rainy and dry seasons were
242
random and suggestive of being caused by anthropogenic activities (Sojobi, 2016). The
243
seasonal mean values obtained for chloride are 5.50mg/L and 13.63mg/L for dry and wet
244
seasons respectively. The highest was obtained in the WS, from a HDW water sample, in the
245
month of October.
246
Egboh and Emeshie (2008) also found greater levels of chloride in the WS for communities in
247
the neighbouring Ndokwa East Local Government Area of Delta State. Similar values were 8
248
also reported for several neighbouring communities by Owamah et al. (2013). The presence of
249
large concentration of chloride in water could be as a result of natural processes like the
250
passage of water through salty hydrogeological formations or pollution from sea water
251
intrusion. The values obtained as shown in Tables 1 and 2 are below the maximum guideline
252
value of 200.00 mg/L stipulated by the SON. The mean nitrate (NO3-) values obtained in this
253
study are 2.88 mg/L and 3.03 mg/L for BH and HDW water samples, respectively. A higher
254
nitrate (0.02–42.45 mg/L) was obtained by Devic et al. (2014) and they attributed it to the
255
activities of the residents. Ingestion of NO3- above permissible limits could cause
256
methemoglobinemia in kids (Emenike et al., 2018) and in some cases cancer (Sojobi, 2016).
257
Values of nitrate concentration recorded for the study area are below the SON permissible
258
limit of 50 mg/L and WHO limit of 10 mg/L for both seasons and water wells and therefore
259
portends no health risk to residents of the community. Sulphate (SO42-) obtained in the
260
groundwater samples ranged from 1.50 mg/L to 5.00 mg/L in the WS and 2.00 mg/L to 12.00
261
mg/L in the DS. The seasonal mean values are 3.24 mg/L (WS) and 6.63mg/L (DS) with a
262
variation of -3.39 mg/L. Higher values were obtained in the DS from BH water samples.
263
Sulphate is one of the least toxic ions but cathartic problems could be experienced by people
264
when ingested at concentration of 600.00 mg/L and above. Taking in of excess sulphate has
265
also been reported to have caused dehydration (WHO, 1996). The values of SO42- obtained in
266
this study are below the maximum permissible values of 500 and 100.00 mg/L stipulated by
267
WHO and SON respectively. For DO, seasonal mean values obtained are 10.38mg/L (wet) and
268
10.00mg/L (dry) with a mean seasonal variation of 0.38 mg/L. Actual values obtained ranged
269
from 8.00 – 12.00mg/L in both seasons. Borehole and HDW water samples had mean DO
270
values of 9.8 mg/L and DO (9.1 mg/L) respectively. These are all above the minimum SON
271
and WHO recommendations of 7.5 mg/L and 4 mg/L, respectively, and hence in order.
272
The BOD5 values ranged from 4.00 – 6.80 mg/L in the WS and 3.00 – 6.00 mg/L in the DS.
273
Seasonal average values are 4.83mg/L (WS) and 4.78 mg/L (DS) with a seasonal mean
274
variation of 0.05 mg/L. According to Owamah et al. (2013), the highest allowable BOD5 value
275
is 6.00 mg/L. Greater values indicate organic pollution. The HDW water samples were found
276
to have higher mean BOD5 of 5.22 mg/L in comparison with mean value of 4.60 mg/L from
277
BH water samples. This indicates the occurrence of higher organic pollution in HDWs than
278
BHs. The observed higher organic pollution of the HDW water samples could be attributed to 9
279
nearness to septic tanks, and poor design and construction of the HDWs (unsealed wells and
280
wells without caps etc.) in the community. The later could contaminate groundwater as it
281
enables polluted surface water to reach the groundwater without filtration by the soil.
282 283 284
3.2. Microbial contamination
285
The higher organic pollution obtained from the HDW water samples as noticed by its higher
286
BOD5 values corroborates the values of E. coli obtained from water samples of the boreholes
287
and HDWs. Samples from the HDWs had higher mean E. coli value of 228.44 cfu/ml than
288
BHs’ with mean value of 180.56 cfu/ml. HDW water samples also had a mean total coliform
289
count of 2.65 cfu/ml, which is again, greater than the mean value of 0.94 cfu/ml obtained from
290
BH water samples. The values recorded for total coliform count/100ml sample revealed
291
seasonal mean values of 0.38 cfu/ml (WS) and 3.30 cfu/ml (DS). The actual values ranged
292
from 0.00 cfu/ml to 1.80 cfu/ml in the WS and 1.00 cfu/ml to 5.76 cfu/ml in the DS. While
293
greater values were gotten from the HDW samples of dry season, the BH water samples had
294
the least count. The highest value of 5.76 cfu/ml was found in a HDW water sample in the DS
295
of January. The WHO standard is zero count per 100ml and therefore implies that groundwater
296
of the study area is slightly contaminated with fecal matter and need to be treated chemically or
297
by simple boiling. Microorganisms isolated from the water samples obtained from BHs and
298
HDWs are Enterobacter aerogenes and E. coli.
299
The presence of these microorganisms in the water samples, whether pathogenic or non-
300
pathogenic, provides a warning signal that the water should be treated before being used
301
(Abubakar, 2018; Ugochukwu and Ojike (2019). These organisms are typically found in the
302
intestinal tract of animals and humans, grains, plant surfaces and feces (Thakur et al., 2012;
303
Sojobi, 2016). The detection of these organisms in the sampled BH and HDW water samples
304
shows that the groundwater would have had contact with the feces of man and or animals
305
(Mackie, et al. 2006). Agbabiaka and Sule (2010) found E. aerogenes in the borehole water
306
samples of Ilorin metropolis, Kwara State and attributed it to unsanitary surroundings of the
307
water wells, animal litter and fowl droppings. Sojobi (2016) recorded similar finding in his
308
study of groundwater in Omu-Aran, Kwara State. The study attributed the bacterial
309
contamination to droppings from sheep and goat litter in the community, and the closeness of
10
310
septic tanks to water wells. This is also the situation in Emevor community where goat and
311
poultry litters is easily seen. Poorly constructed water wells are in some cases sited close to
312
poorly constructed septic tanks. Majority of the BHs are also shallow. Okiki and Ivbijaro
313
(2013) and Thakur et al. (2012) had earlier reported the presence of E. aerogenes in the water
314
samples of HDWs and boreholes in Imota, Lagos, Nigeria and Sloan, Pradesh. Jacinta and
315
Adebayo (2015) found E. coli and E. aerogenes in the boreholes and HDWs of Gwagwalada
316
area of Abuja, Nigeria.
317
Though Mackie et al. (2006) reported that E. aerogenes do not cause diseases in healthy
318
persons, Sojobi (2016) revealed that they are of considerable health risks to man given their
319
resistance to common antibiotics. Furthermore, Olufemi and Oluwole (2012) had noted that E.
320
coli and E. aerogenes caused the last cholera outbreak in Ibadan, Nigeria. While there was no
321
detection of fungi in all the water samples of HDWs and BHs, spore-forming yeasts were
322
detected. Yeast contamination of groundwater resource had been reported in Umudike, Benin
323
City, Calabar, and Jos (Sojobi, 2016).
324
It is advisable for residents of Emevor community to treat their groundwater before
325
consumption in order to prevent the outbreak of water-borne diseases in the community as the
326
presence of these microorganisms in the water samples is a warning signal Uzochukwu and
327
Chibike (2018).
328
Though ANOVA test revealed no significant difference (P<0.05) between the physico-
329
chemical parameters of BH and HDW water samples, it indicated that there was a significant
330
difference between the microbial parameters. There was also, no significant difference
331
(P<0.05) in the seasonal variation of the physical and chemical factors obtained. It can
332
therefore be said that though the geological formation in the community is similar, the aquifers
333
through different anthropogenic activities now have different microbiological properties. This
334
is evidenced by the fact that the BH and HDWs were found to have different levels of bacterial
335
contamination even when some were located close to each other.
336 337
3.3.Metals
338
The major cations studied in this research are sodium (Na), potassium (K), magnesium (Mg)
339
and calcium (Ca). Results obtained show that the most abundant of the cations is sodium with
340
the highest concentration value of 18.99 mg/L followed by calcium with the value of 18.00 11
341
mg/L, magnesium (7.80 mg/L) and potassium (13.01mg/L) as found in the water samples
342
collected from BHs in the wet season. The seasonal mean values of the cations (wet – dry) are
343
14.49mg/L –13.92mg/L, 6.89mg/L–6.52mg/L, 10.50mg/L–5.76mg/L and 11.62mg/L–
344
5.30mg/L for sodium, potassium, magnesium and calcium respectively. This showed that the
345
distribution of cations concentration decreased from WS to DS. The observed values are within
346
acceptable WHO/SON limits except for potassium which exceeded the threshold limit value of
347
2 mg/L. K is usually not a serious health related parameter in drinking water quality studies.
348
The other metals studied in this research include Lead (Pb), Cadmium (Cd), Zinc (Zn), Copper
349
(Cu), Iron (Fe) and Barium (Ba).
350
Tables 1 and 2 contain the mean, standard deviation and range of the metals concentrations.
351
The BHs in the WS had a relative abundance for cations (Na>Ca>Mg>K> Ba>Zn>Cu>Fe) and
352
anions (Cl->SO42->NO3-> HCO3-). The HDWs however, had a relative abundance of
353
Na>Ca>Mg>K>Ba>Zn>Cu>Fe for cations and HCO3->Cl->SO42->NO3- for anions. For the dry
354
season, the boreholes had a relative abundance of Na>K>Mg>Ca>Zn>Ba>Cu>Fe for cations
355
and
356
Na>Ca>Mg>K>Ba>Cu>Fe>Zn and Cl-> HCO3-> SO42-> NO3- for cations and anions,
357
respectively. This finding is unlike the relative cations and anions abundance obtained by
358
Devic et al. (2014) which were Ca>Mg>Na>K and HCO3−, SO42− >Cl−> NO3−, respectively.
359
Sojobi (2016) also obtained different cations and anions relative abundance of Na > k > Ca
360
>Mg> Zn > Pb and Cl− >PO42− > SO42− > NO3– respectively, in the BHs, and cations
361
(Ca>Na>K>Mg>Pb) and anions (NO3−> PO42− > SO4
362
Aran groundwater, Kwara State, Nigeria.
363
Mean Na concentration of 12.67 mg/L (boreholes) and 13.82 mg/L (HDWs) obtained, are less
364
tha the SON and WHO stipulated maximum value of 200 mg/L. Todd (1980) reported that
365
sodium could cause corrosion and formation of scale in boilers. High sodium concentration in
366
water can be suggestive of strong water-aquifer interaction due to exchange of cations and or
367
anthropogenic activities like wastewater disposal (Sojobi, 2016). For Mg, the mean
368
concentration values are 10.25mg/L for BHs and 5.12 mg/L for HDWs. Though these mean
369
values exceeded the SON prescribed maximum value of 0.2 mg/L, they are below the WHO
370
maximum limit of 200 mg/L. The relative high Mg value can be associated with the presence
371
of basalts, kaolinite, and hematite in the geological formation of the study area (Owamah et al.,
Cl->SO42->NO3->
HCO3-
for
anions.
12
The
2−
HDWs
however,
had
it
as
> Cl−) in the shallow wells of Omu-
372
2013; Trostle et al., 2014). Values obtained in this study corroborate the finding of
373
Nwankwoala et al. (2014) of mean Mg value of 0.89 mg/L for boreholes in Yenagoa, in the
374
same Niger-Delta Region of Nigeria like the study area. Nwankwoala et al. (2014) linked the
375
presence of the high Mg to dissolution of minerals like feldspar and mica. Anthony et al.
376
(2008) had reported of extreme high concentrations of 68–173 mg/L for groundwater in
377
Manali, India. High magnesium concentration in the groundwater of Serbia was attributed to
378
domestic effluents, chemical fertilizers and minerals (Devic et al., 2014).
379
Though mean Ca values of 8.65 mg/L (BHs) and 12.82 mg/L (HDWs) were less than the 49.3
380
mg/L of Viswanath et al. (2015), they are higher than the 2.97 mg/L for neighboring Yenagoa,
381
Bayesa State, Nigeria as obtained by Nwankwoala et al. (2014) . This suggests that coastal
382
areas may be prone to having lower calcium values in their groundwater, possibly due to the
383
effects of dilution.
384
Since the WHO permissible limit is 200 mg/L, the mean Ca concentration values obtained in
385
this study for both BHs and HDWs are compliant. The presence of Ca in the groundwater of
386
communities in the Niger-Delta Region of Nigeria had been attributed by Nwankwoala et al.
387
(2014) to feldspars and micas dissolution in the groundwater. Kim et al. (2015) however,
388
reported that Ca in groundwater could be as a result of the release of carbonate minerals in the
389
course of the dissolution of silicate compounds. The mean K values in the HDW and borehole
390
water samples are 6.82 mg/L and 5.52 mg/L, respectively, and are above the mean values of
391
4.9 mg/L and 0.91 mg/L recorded respectively by Ishaku et al. (2011) and Trostle et al. (2014).
392
For the other metals studied, as displayed in Tables 1 and 2, the highest concentration of 1.90
393
mg/L was recorded for barium in the month of October in a sample collected from a HDW.
394
Lead and cadmium had the least concentration. Pb was only slightly detected with a value of
395
0.01mg/L in just one sample of the wet season. It was neither detected in the BH or HDW
396
water samples of the dry season, nor had measurable overall seasonal mean values for wet and
397
dry seasons. Lead is therefore not of health concern in the groundwater of the community. Oni
398
and Hassan (2013) found elevated Pb concentration in groundwater samples of wells close to a
399
landfill and reported that Pb in groundwater could be linked to improper disposal of Pb-
400
containing domestic waste substances within the surrounding of water wells especially when
401
there is absence of industrial activities. Pb can lead to subencelophalopathic disorders (Sojobi,
402
2016). Cadmium was not detected in the WS and DS for the BH and HDW samples. Zinc 13
403
concentrations ranged from 0.01 to 1.00mg/L in the WS and from <0.001 to 0.12mg/L in the
404
DS. The overall seasonal mean values are 0.16mg/L in the WS and 0.04mg/L in the DS. For
405
copper, the concentrations ranged from <0.001 to 0.09mg/L in the WS and from <0.001 to
406
0.20mg/L in the DS with seasonal mean values of 0.14mg/L and 0.05mg/L respectively. Iron
407
concentration values ranged from <0.001 to 0.06mg/L in the WS and from <0.001 to 0.05mg/L
408
in the DS with seasonal mean values of 0.03mg/L and 0.03mg/L for wet and dry seasons
409
respectively. Lastly, Barium had values ranging from 0.88 to 1.90mg/L in the WS and from
410
<0.001 to 1.88mg/L in the DS. The overall seasonal mean values for barium are 1.16mg/L for
411
the WS and 0.58mg/L for the DS. Apart from barium, the other metals tested had seasonal
412
mean values that complied with the WHO/SON limit for potable water (Table 3). As shown in
413
Fig. 2b, Ba was higher in the WS for both BHs and HDWs. This could be attributable to
414
greater dissolution of barium containing minerals during the rains.
415
4. Correlation analysis of the physicochemical parameters studied
416
In accordance with the work of Sojobi (2016), the correlation classes adopted for the study are:
417
perfect (R2 = 1), very strong (±0.9 ≤ R2 <1), strong (±0.7 ≤ R2 < ±0.9), moderate (±0.5 ≤ R2 < ±0.7),
418
and weak (R2 < ±0.5). From Table 4, by correlation coefficients (CC), the main cations influencing
419
the presence and concentration of TDS in the groundwater were identified as Ca (0.99), Mg (0.99),
420
Ba (0.99), Fe (-0.98), Na (0.95), and K (0.85). TDS was also, very strongly correlated with BOD5
421
(0.89), NO3- (-0.84), TSS (0.86) and perfectly with dissolved oxygen (DO) (0.97). These results are
422
in accordance with the findings of Emenike et al. (2018); Sojobi (2016) and Viswanath et al. (2015)
423
in which Ca was reported to be an influential factor for the estimation of TDS in groundwater. Table
424
4 also shows that the notable mineral classes influencing the TDS and EC in the study area
425
groundwater are Mg-Ca (0.98), Ca-Fe class (-0.98), Na-K (0.97) and Na-Mg class (0.96). NO3- was
426
associated with Mg-Ca group with CC (-0.91- (0.85) respectively. Mg and Ca were found to have no
427
correlation with Cl-. Following the finding of Skrzypek et al. (2013), the presence of Mg2+ and Ca2+
428
in the groundwater may be associated with other anions. The strong CC of (0.98) between
429
Magnesium and Calcium reflects huge mutual dependence and same anthropogenic sources (Devic
430
et al., 2014; Emenike et al., 2018). NO3- has perfect CC with Cd (0.98) and Mg (-0.91) and very
431
strong CC with Ba (-0.84) showing that it could have come from anthropogenic activities such as the
432
release of domestic wastewater on the environment.
14
433
Table 4 reveals that affinity reactions and ionic exchanges were occurring in the hydrogeological
434
formation of the area of study (Sojobi, 2016; Emenike 2018). While Cl- and SO42- had strong
435
preferential affinity for the anions and cations, NO3- was perfectly correlated with Mg (-0.91) and Cd
436
(0.98).
437
notwithstanding, majority of the anions that make up the aquifer minerals may not prefer the
438
dissolved Mg and hence may be the cause of the high mg concentration in the BH and HDW
439
samples (Sojobi, 2016). Emenike et al. (2018) reported that groundwater chemistry is mainly
440
affected by the dissolution of minerals and the activities of man. pH and EC were respectively found
441
to be, perfectly (0.96) and very strongly (-0.90) correlated with SO42-. Electrical conductivity
442
correlated weakly with DO, Iron, NO3−, Ca and BOD5 showing that the mentioned physicochemical
443
factors may not be appropriate for the estimation of EC in the study area groundwater. This is
444
however, different from the report of Sojobi (2016) for Omu-Aran groundwater, in Kwara State
445
Nigeria.
When an aquifer is rich in magnesium, it will allow its dissolution into it. This
446 447
Table 5 gives a brief of the different groundwater contaminants and their related health effects. It
448
also shows that ground water pollutants vary from location to location as a result of differences in
449
geological formations and anthropogenic activities. Table 6 however compares the results obtained
450
from different previous authors about groundwater quality in different locations of the world with
451
the findings of this study. It can be seen from Table 6, that quality of groundwater in the study area
452
is relatively safer and cleaner than lots of other groundwater studied in the past. However, in line
453
with the SDG 6.1 goal of achieving universal and equitable access to safe and affordable drinking
454
water for all by 2030, the study area needs urgent attention as bacterial and barium contamination
455
found, could have adverse health effects on the community dwellers especially on children and the
456
aged.
457 458
5. Conclusion
459
A detailed evaluation of the quality of groundwater in Emevor community of the Niger-Delta
460
region of Nigeria was carried out. The groundwater was found to be mainly contaminated with
461
coliform bacteria and slightly with Ba. Entero bacteriaceae and Escherichia coli species were
462
also found in the water samples, most especially, the HDWs. The presence of coliform bacteria
463
in the groundwater samples was linked to the nearness of HDWs and BHs to pit-latrines,
15
464
poorly constructed septic tanks and presence of many open dumps in the community. The Ba
465
contamination was linked to oil explorations and processing activities in the region, geological
466
formation and careless disposal of electronic wastes.
467
The study recommends the development of modern sanitary systems in the community and
468
public awareness by the supervising ministry and relevant non-governmental organizations.
469
Though huge priorities should be given to the provision of improved water to the people by
470
government; in the interim, improvement of water quality at household level, through
471
chlorination, addition of alum, filtration, solar disinfection and boiling is advised. This study
472
has been able to generate a broad water quality database for the study area, which could help
473
engineer future water project development in the region.
474 475
Acknowledgement
476
The financial support of the Academic Research and Entrepreneurship Development Initiative, Asaba,
477
Nigeria and the technical support of its Vice-President (consultant Chemist), Mr Samuel Ilabor are
478
highly appreciated.
479 480 481 482 483 484 485 486 487
References Abd El-Salam, M. M. A., & Abu-Zuid, G. I. (2015). Impact of landfill leachate on the groundwater quality: a case study in Egypt. Journal of Advanced Research, 6, 579–586.
488 489
Abubakar, I.R. (2018b). Strategies for coping with inadequate domestic water supply in Abuja, Nigeria, Water International, DOI: 10.1080/02508060.2018.1490862.
490
Abubakar, I.R. (2016). Quality dimensions of public water services in Abuja, Nigeria.
491
Utilities Policy, 38, 43-51.
492
Ademoroti, C.M.A. 1996. Environmental Chemistry and Toxicology. Ibadan: Foludex Press Ltd.
493 494 495 496 497 498 499
Agbabiaka, T. O.,& Sule, I. O. (2010). Bacteriological assessment of selected borehole water samples in Ilorin Metropolis. IJABR, 2(2), 31–37. Agbogidi, O.M., P.G. Eruotor, S.O. Akparobi and G.U Nnaji, 2007. Heavy metal contents of maize (Zea mays L.) grown in soil contaminated with crude oil. International Journal of Botany 3(4):385-389. Akhtar, M. M., Tang, Z., & Mohamadi, B. (2014). Contamination potential assessment of potable groundwater in Lahore. Polish Journal of Environmental Studies, 23(6), 1095–1916. Akinyemi, J. O.,& Souley, S. O. (2014). Monitoring the quality of some sources of irrigation water
Abubakar, I.R. (2019). Factors influencing household access to drinking water in Nigeria. Utilities Policy, 58, 40-51 Abubakar, I.R. (2018a). Exploring the determinants of open defecation in Nigeria using demographic and health survey data, Science of the Total Environment, 637–638, 1455–1465.
16
500 501 502 503 504 505 506 507 508 509 510 511 512
in different parts of Ogun State, Nigeria. IERI Proceedings, 9, 123–128. Al-ahmadi, M. E., & El-Fiky, A. A. (2009). Hydrogeochemical evaluation of shallow alluvial aquifer of Wadi Marwani, western Saudi Arabia. Journal of King Saudi University, 21, 179–190 American Public Health Association (APHA) 2012. “Standard Methods for Examination of Water and Waste-water”; 22nd Edition, Washington DC: American Public Health Association.
513 514 515 516 517 518 519 520 521 522
Dahunsi, S. O., Owamah, H. I., Ayandiran, T. A., Oranusi, U. S., & (2014). Drinking water quality and public health of selected communities in South Western Nigeria. Water Quality, Exposure and Health, 6, 143–153. Devic, G., Djordjevic, D., & Sakan, S. (2014). Natural and anthropogenic factors affecting the groundwater in Serbia. Science of the Total Environment, 468–46, 933–942. Egboh, S.H.O and E.M. Emeshili, 2008. The fluoride content of drinking water samples from Ndokwa Area, South-South Nigeria. Journal of Chemical Society of Nigeria 33(2): 54-61. Ejoh A.S, Unuakpa, B.A. Ibadin, F.H. Edeki, S.O. (2018). Dataset on the assessment of water quality and water quality index of Ubogo and Egini rivers, Udu LGA, Delta State Nigeria , Data in Brief 19, 1716–1726.
523 524
Emenike, P. C., Nnaji, C.C & Tenebe, I.T. (2018). Assessment of geospatial and hydrochemical interactions of groundwater quality, southwestern Nigeria, Environ Monit Assess. 190: 440
525 526 527 528 529 530 531 532 533 534 535 536 537 538 539 540 541 542 543 544
https://doi.org/10.1007/s10661-018-6799-8.
Ayanbimpe, G. M., Abbah, V. E., & Ior, C. A. (2012). Yeasts and yeast-like fungal contaminants of water used for domestic purposes in Jos, Nigeria. Microbiology Research, 3(e24), 99–102. Bacquart, T., Frisbie, S., Mitchell, E., Grigg, L., Cole, C., Small, C., & Sakar, B. (2015). Multiple inorganic toxic substances contaminating the groundwater of Myingyan Township, Myanmar: Arsenic, manganese, fluoride, iron, and uranium. Science of the Total Environment, 517, 232–245
Gerlach, R. F., Cury, J. A., Krug, F. J.,& Kine, S. R. (2002). Effect of lead on dental enamel formation. Toxicology, 175, 27–34. Ishaku, J. M., Kaigama, U., & Onyeka, N. R. (2011). Assessment of groundwater quality using factor analysis in Mararaba-mubi area, Northeastern Nigeria. Journal of Earth Sciences and GeotechnicalEngineering, 1(1), 9–33. Jacinta, A. N., & Adebayo, I. A. (2015). Determination of coliforms in different sources of drinking water in Gwagwalada Abuja. Report and Opinion, 7(1), 1–6. Khan, S., Shahnaz, M., Jehai, N., Rehman, S., Shah, M. T.,& Din, S. (2013). Drinking water quality and human health risk in Charsadda district, Pakistan. Journal of Cleaner Production, 60, 93–101. Kulinkina A. V., Plummer, J. D., Chuic, K.H.K., Kosinski, C.K., Adomako-Adjei, T., Egorov, A.I., Nwankwoala, H. O., Amadi, A. N., Oborie, E., & Ushie, F. A. (2014). Hydrochemical factors and correlation analysis in groundwater quality in Yenagoa, Bayelsa State, Nigeria. Applied Ecology and Environmental Sciences, 2(4), 100–105. Machdar, E., N.P. van der Steen, L. Rashid- Sally and P.N.L. Lens, 2013. Application of quantitative microbial risk assessment to analyze the public health risk from poor drinking water quality in a low income area in Accra, Ghana. Science of the Total Environment 449: 134-142. 17
545 546 547 548 549 550 551 552 553
Mackie, R. I., Koike, S., Krapac, I., Chee-Sanford, J.,Maxwell, S., & Aminov, R. I. (2006). Tetracycline residues and tetracycline resistance genes in groundwater impacted by swine production facilities. Animal Biotechnology, 17, 157–176. Melles, Z. M., & Kiss, S. A. (1992). Influence of the magnesium content of drinking water and of magnesium therapy on the occurrence of preeclampsia. Magnesium Research, 5, 277– 279. Mkwate , R.C, Chidya, R.C.G ,Wanda, E.M.M. (2017). Assessment of drinking water quality and rural household water treatment in Balaka District, Malawi. Physics and Chemistry of the Earth 100, 353-362.
554 555 556 557 558 559 560 561 562 563 564 565 566 567 568 569 570 571 572 573 574 575 576 577 578 579 580 581 582 583 584 585 586 587 588 589 590
Mondal, N. C., Singh,V. S., Saxena, V.K.,&Prasad, R. K. (2008). Improvement of groundwater quality due to fresh water ingress in Potharlanka Island, Krishna delta, India. Environmental Geology, 55(3), 595–603. National Population Commission of Nigeria (NPC). http://www.informationng.com/tag/nationalpopulation- commission. Accessed on the 25th of December , 2018 at 14.22 Nigerian time. Okiki, P., & Ivbijaro, J. O. (2013). Bacteriological and physicochemical qualities of well water in Imota-Lagos, Nigeria and health effects associated with its usage. Advances in Life Science and Technology, 13, 18–25. Olufemi, F., & Oluwole, M. F. (2012). Microbiological examination of sachet water due to a cholera outbreak in Ibadan, Nigeria. Open Journal of Medical Microbiology, 2, 115–120. Oni, A. A., & Hassan, A. T. (2013). Groundwater quality in the vicinity of Aba-Eku dumpsite, Ibadan, Southwest, Nigeria. A detailed report. Ethiopian Journal of Environmental Studies and Management, 6(6), 589–600. Owamah, I.H., Asiagwu, A.K.,. Egboh, S.H.O & Phil-Usiayo, S. (2013). Drinking water quality at Isoko North communities of the Niger Delta Region, Nigeria Toxicological & Environmental Chemistry, Vol. 95, No. 7, 1116–1128. Oyelami, A. C., Aladejana, J. A., & Agbede, O. O. (2013). Assessment of the impact of open waste dumpsites on groundwater quality: a case study of the Onibu-Eja dumpsite, Southwestern Nigeria. Procedia Earth and Planetary Science, 7, 648–651. Porowska, D. (2014). Assessment of groundwater contamination around reclaimed municipal landfill-Otwock area, Poland. Journal of Ecological Engineering, 15(4), 69–81 Rao, N. S. (2014). Spatial control of groundwater contamination using principal component analysis. Journal of Earth System Science, 123(4), 715–728. Saeedi, R., Naddafi, K., Alimohammadi, M., & Nazmara, S. (2012). Denitrification of drinking water using a hybrid heterophic/autotrophic/BAC bioreactor. Desalination Water Treatment, 45, 1–10. Shu,W. U., Yue-heng, H. U., & Dan, Z. U. O. (2011). Discussion on parameter choice for managing water quality of the drinking water source. Procedia Environmental Sciences, 11, 1465– 1468. Sojobi, S.O (2016). Evaluation of groundwater quality in a rural community in North Central of Nigeria. Environ Monit Assess (2016) 188:192. SON, 2007. Standrad Organization of Nigeria (SON). Nigerian Standard for Drinking Water Quality, Nigeria, NIS 554: 2007. Srinivas, Y., Muthuraj, D., Oliver, D. H., Raj, A. S., & Chandrasekar, N. (2013). Environmental applications of geophysical methods to map groundwater quality at Tuticorin, Tamilnadu, India. Environmental Earth Science, 70, 2143–2152. 18
591 592 593 594 595 596 597 598 599 600 601 602 603 604 605 606 607 608 609 610 611 612 613 614 615 616 617 618 619 620 621 622 623 624 625 626 627 628 629 630 631 632 633
Thakur, M., Negi, S., Kumar, A., Patil, S., Kumar, A., & Sharma, N. (2012). Prevalence and characterization of water contamination indicator bacteria with special reference to coliforms from drinking water supply in Sloan City of Himachal Pradesh. Biological Forum-An International Journal, 4(1), 85–89. Todd, D. L. (1980). Groundwater hydrology (pp. 267–315). New York: John Wiley and Sons. Trostle, K., Derry, L., Vigier, N., & Chadwick, O. (2014). Magnesium isotope fractionation during arid pedogenesis on the Island of Hawaii (USA). Procedia Earth and Planetary Science, 10, 243–248. Ugochukwu, U.C. and Ojike, C. (2019). Assessment of the groundwater quality of a highly populated district in Enugu State of Nigeria, Environment, Development and Sustainability https://doi.org/10.1007/s10668-019-00315-6,
Vasanthaviger, M., Srinivasamoorthy, K., & Prasanna, M. V. (2013). Identification of groundwater contamination zones and its sources by using multivariate statistical approach in hirumanimuthar sub-basin, Tamil Nadu, India. Environmental Earth Science, 68, 1783– 1795. Verd, V. S., Domingues S. J., Gonzales, Q. M., Vidal, M. M., Mariano, S. A. C., de Roque, C. C., & Sevilla, M. J. M. (1992). Association between calcium content of drinking water and fractures in children (in Spanish). Anales Españoles de Pediatría, 37, 461–465. Viswanath, N. C., Kumar, P. G. D., & Ammad, K. K. (2015). Statistical analysis of quality of water in various water shed for Kozhikode City, Kerala, India. Aquatic Procedia, 4, 1078–1085. Wanke, H., Nwakfila, A., Hamutoko, J. T., Lohe, C., Nembo, F., Petrus, I., David, A., Beukes, H., Masule, N., & Quinger, M. (2015). Hand dug wells in Namibia: an underestimated water source or a threat to human health? Journal of Physical Chemistry. doi:10.1016/j.pce.2015.01.004. WHO 2003. “Emerging issues in water and infectious disease”. Geneva: World Health Organization. WHO, 2011. World Health Organization (WHO). Guidelines for Drinking-water Quality, fourth ed. WHO Press, Geneva, Switzerland. ISBN 978 92 4 154815 1. WHO, 2012. World Health Organization (WHO). Global Burden of Disease. WHO Press, Geneva, Switzerland. WHO/UNICEF, 2015. World Health Organization (WHO) and United Nations Children's Fund (UNECEF), Progress on Sanitation and Drinking Water e 2015 Update and MDG Assessment, WHO, Switzerland, 2015. Available. http://www. unicef.org/publications/index_82419.html. Yang, C. Y., & Chiu, H. F. (1999). Calcium and magnesium in drinking water and risk of death from rectal hypertension. American Journal of Hypertension, 12, 894–899. Yang, C. Y., Chiu, H. F., Chang, C., Wu, T. N., & Sung, F. C. (2002). Association of very low birth weight with calcium levels in drinking water. Environmental Research Section A, 89, 189–194. List of Tables
634
Table 1: Summary statistics of groundwater quality for wet (rainy) season
635
Table 2: Summary statistics of groundwater quality for dry season 19
636
Table 3. Drinking water quality guidelines
637
Table 4: Correlation Analysis
638
Table 5: Review of water-related diseases and causative contaminants
639
Table 6: Comparison of groundwater monitoring results of previous studies and this study
640 641
List of Figures
642
Fig. 1a: Map of Isoko North showing Study Area
643
Fig. 1b. Map of Nigeria showing Delta State
644
Fig 2a. Average value of pH in boreholes and HDWs for wet and dry seasons
645
Fig 2b. Average concentrations of barium in boreholes and HDWs for wet and dry seasons
646
Fig 2c. Average concentrations of electrical conductivities in boreholes and HDWs for wet and dry
647
seasons
648 649 650 651 652 653 654 655
20
Table 1: Summary statistics of groundwater quality for wet (rainy) season Parameters
Borehole
No. of Data
Handdug Well
Temp.0C pH EC( µS/cm) Salinity (‰)
120 120 120 120
Max. Value 27.00 5.49 88.70 ND
Min. Value
Mean
STD
No. of Data
Max. Value
Min. Value
Mean
SD
25.40 4.92 80.55 ND
26.20 5.14 84.51 ND
0.75 0.24 2.91 ND
120 120 120 120
28.90 6.28 76.00 ND
25.90 5.94 63.00 ND
27.05 6.12 69.91 ND
1.17 0.16 5.17 ND
TDS (mg/L) TSS (mg/L) Turbidity(NTU) Alkalinity (mg/L) DO (mg/L) BOD5 (mg/L) COD (mg/L) NH3-N (mg/L) Colour (pt-co) NO3-N (mg/L) TOC (%) THC (mg/L) Odour (TON) Total Hardness (mg/L) Total Phosphorous (mg/L) HCO3 (mg/L) Cl (mg/L) SO4 (mg/L) TCC (Count/100ml) Na (mg/L) K (mg/L) Mg (mg/L) Ca (mg/L) Pb (mg/L) Cd (mg/L) Zn (mg/L) Cu (mg/L) Fe (mg/L) Ba (mg/L)
120 120 120 120 120 120 120 120 120 120 120 120 120 120
53.70 1.00 ND ND 12.00 5.00 2.70 ND ND 0.05 0.01 0.01 ND 15.00
38.40 ND ND ND 8.00 4.00 ND ND ND ND ND ND ND 1ND
44.53 0.25 ND ND 9.75 4.25 1.33 ND ND 0.01 ND ND ND 11.50
5.68 0.43 ND ND 1.48 0.43 1.33 ND ND 0.02 ND ND ND 2.06
120 120 120 120 120 120 120 120 120 120 120 120 120 120
51.70 2.00 ND 23.00 12.00 6.80 2.00 ND ND ND ND 0.01 ND 25.00
33.00 ND ND 1ND 1ND 4.00 1.80 ND ND ND ND ND ND 15.00
39.33 0.50 ND 17.00 11.00 5.40 1.90 ND ND ND ND ND ND 19.75
7.37 0.87 ND 6.04 1.00 1.08 0.07 ND ND ND ND ND ND 3.96
120
ND
ND
ND
ND
120
ND
ND
ND
ND
120 120 120 120
ND 3.00 2.80 1.20
ND ND 1.50 ND
ND 3.00 1.98 0.30
ND ND 0.51 0.52
120 120 120 120
28.06 1ND 5.00 1.80
12.20 6.00 4.00 ND
20.74 8.00 4.50 0.45
7.37 1.41 1.00 0.80
120 120 120 120 120 120 120 120 120 120
18.99 13.01 17.80 18.00 0.01 ND 0.07 0.07 0.06 1.22
3.03 1.52 1.30 8.00 ND ND 0.02 0.01 ND 1.04
14.32 6.86 10.75 11.23 ND ND 0.04 0.03 0.02 1.10
6.55 4.08 6.91 6.48 ND ND 0.02 0.02 0.03 0.61
120 120 120 120 120 120 120 120 120 120
15.76 9.45 15.00 15.32 ND ND 1.00 0.09 0.05 1.90
13.70 5.34 5.00 8.00 ND ND 0.01 ND ND 0.88
14.65 6.92 10.25 12.00 ND ND 0.27 0.25 0.03 1.22
0.74 1.67 3.70 2.83 ND ND 0.42 0.14 0.03 0.50
Note: ND=Not detected
Table 2: Summary statistics of groundwater quality for dry season
Parameters
Boreholes
Hand-dug Wells
No. of Data
Max. Value
Mean
STD
27.90 4.95 98.55 ND
Min. Value 25.30 4.82 87.10 ND
Max. Value 26.50 6.50 71.30 ND
Min. Value
Mean
SD
1.00 0.06 4.23 -
No. of Data 120 120 120 120
Temp.0C pH EC( µS/cm) Salinity (‰).
120 120 120 120
26.53 4.90 92.74 -
26.00 5.99 6ND ND
26.30 6.20 65.10 ND
0.19 0.26 4.10 ND
TSS (mg/L) Turbidity(NTU) Alkalinity (mg/L) DO (mg/L) BOD5 (mg/L) COD (mg/L) NH3-N (mg/L) Colour (pt-co) NO3-N (mg/L) TOC (%) THC (mg/L) ODOUR (TON) Total Hardness (mg/L) Total Phosphorous (mg/L) HCO3 (mg/L) Cl (mg/L) SO4 (mg/L) TCC (Count/100ml) Na (mg/L) K (mg/L) Mg (mg/L) Ca (mg/L) Pb (mg/L) Cd (mg/L) Zn (mg/L) Cu (mg/L) Fe (mg/L)
120 120 120 120 120 120 120 120 120 120 120 120 120
ND ND ND 12.00 6.00 3.00 4.00 ND 5.00 0.80 ND ND 13.00
ND ND ND ND 3.00 ND 2.70 ND ND 0.01 ND ND 9.00
ND ND ND 1ND 4.80 1.73 2.63 ND 2.38 0.40 ND ND 11.25
ND ND ND 2.00 1.30 1.31 1.59 ND 1.85 0.32 ND ND 1.48
120 120 120 120 120 120 120 120 120 120 120 120 120
ND ND 22.70 1ND 5.00 4.00 3.40 ND 5.00 0.30 0.02 ND 15.00
ND ND 8.00 ND 4.00 0.40 ND ND ND 0.02 ND ND 8.00
ND ND 13.45 1ND 4.75 2.83 2.18 ND 3.03 0.16 0.01 ND 10.25
ND ND 5.82 ND 0.43 1.47 1.31 ND 1.84 0.11 0.01 ND 2.77
120
0.01
ND
0.01
ND
120
0.02
ND
0.02
ND
120 120 120 120
ND 2ND 12.00 3.60
ND 13.00 2.00 1.00
ND 18.25 8.50 2.35
ND 3.03 4.09 0.92
120 120 120 120
26.40 9.00 5.00 5.76
ND ND 4.00 1.80
6.60 9.00 4.75 4.24
10.44 ND 0.43 1.48
120 120 120 120 120 120 120 120 120
18.52 11.00 8.00 8.00 ND ND 0.12 0.09 0.03
12.00 7.30 4.00 2.00 ND ND ND ND <0.001
15.94 8.26 6.25 4.79 ND ND 0.06 0.04 0.02
2.59 1.04 1.48 2.17 ND ND 0.14 0.03 0.01
120 120 120 120 120 120 120 120 120
15.00 5.50 6.70 9.00 ND ND 0.05 0.20 0.05
9.68 3.00 2.20 2.00 ND ND <0.001 <0.001 0.02
11.90 4.77 5.27 5.81 ND ND 0.02 0.05 0.04
2.01 1.03 1.79 2.57 ND ND 0.03 0.09 0.01
Ba (mg/L)
120
1.08
<0.001
0.50
0.50
120
1.88
<0.001
Note: ND=Not detected
Table 3. Drinking water quality guidelines S/N 1 2 3 4 5 6 7 8 9 10 111 12
Parameter Ph Cadmium (Cd) Chloride (Cl-) Chromium (Cr) Copper (Cu) Iron ( Fe) Lead (Pb) Zinc (Zn) Nickel (Ni) Barium (Ba) Nitrate (NO3-) Nitrite (NO2)
13
Sulphate (SO42-) Total coliform (TC) E. coli count Electrical Conductivity (EC) (µS/cm ) Total Suspended Solid (TSS) Total Solid (TS) Total Dissolved Solid (TDS) Salinity (%) Turbidity Magnesium (Mg) Calcium (Ca) Sodium (Na) Potassium (K) Dissolved Oxygen (DO) BOD5 Total Alkalinity (mg/L CaCO3) Hardness ((mg/L CaCO3) Colour apparent (Hz)
14 15 16 17 18 19 20 22 22 23 24 25 26 27 28 29 30
WHO (2006) 6.5–8.5 0.003 0.050 2.00 0.30 ND1 0.020
SON (2007) 6.5-8.5 0.003 250 0.050 1.00 0.30 0.01 3.00 0.02
10 1.0
50.0 0.2
500
100
0x102 0x102 1000
10 1000
500 1 200 200 200 30 4 500 15 -apparent (Hz)
500 5 0.2 200 7.5 6 150 15 (TCU)
Note: Beside pH, EC, Salinity and Colour apparent; other parameters were reported in mg/L. Sources: Adapted from Kulinkina et al. (2017) and Sojobi (2016) following minor updating
0.66
0.77
Table 4: Correlation Analysis
EC( µS/cm)
pH pH
TDS (mg/l)
TSS (mg/L)
ALKAL. (mg/l)
DO (mg/l)
BOD5 (mg/l)
NO3N (mg/l)
TH (mg/l)
HCO3 (mg/l)
Cl (mg/l)
SO4 (mg/l)
Na (ppm)
K (ppm)
Mg (ppm)
Ca (ppm)
EC( µS/cm)
-0.99
1
0.02
-0.04
1
TSS (mg/L)
0.32
-0.27
0.86
1
ALKAL,(mg/l)
0.59
-0.45
-0.21
0.32
1
DO (mg/l)
0.16
-0.14
0.97
0.96
0.03
1
BOD5 (mg/l)
0.46
-0.45
0.89
0.95
0.18
0.95
1
NO3-N (mg/l)
-0.48
0.53
-0.84
-0.76
0.11
-0.83
-0.92
1
TH(mg/l)
0.28
-0.24
0.90
0.99
0.23
0.98
-0.79
1
HCO3 (mg/l)
0.21
-0.05
-0.28
0.21
0.91
-0.05
0.96 0.032
0.38
0.13
1
-0.02
0.17
-0.31
0.12
0.80
-0.12
-0.16
0.52
0.04
0.98
1
0.96
-0.90
-0.10
0.33
0.80
0.10
0.38
-0,30
0.26
0.48
0.28
1
Na (ppm)
-0.15
0.17
0.95
0.87
-0.09
0.95
0.80
-0.65
0.90
-0.05
-0.04
-0.18
1
K (ppm)
-0.34
0.38
0.85
0.78
-0.08
0.85
0.64
-0.44
0.81
0.07
0.12
-0.31
0.97
1
0.99
0.86
-0.19
0.97
0.92
-0.91
0.90
-0.311
-0.38
0.00
0.90
0.77
1
0.99
0.93
-0.85
0.95
-0.16
-0.21
0.013
0.96
0.85
0.98
1
SO4 (mg/l)
Zn (ppm)
Cu (ppm)
Fe (ppm)
Ba (ppm)
1
TDS (mg/l)
Cl (mg/l)
Cd (ppm)
Mg (ppm)
0.14
-0.17
Ca (ppm)
0.10
-0.10
0.99
0.92
-0.08
Cd (ppm)
-0.60
0.66
-0.72
-0.66
0.09
-0.71
-0.86
0.98
-0.68
0.42
0.58
-0.39
-0.49
-0.26
-0.81
-0.73
1
Zn (ppm)
0.57
-0.46
0.49
0.87
0.75
0.68
0.76
-0.49
0.81
0.62
0.48
0.67
0.55
0.49
0.50
0.60
-0.43
0.550
0.48
0.52
0.61
-0.47
0.99
1
-0.98
0.58
-0.53
-0.54
1
0.99
-0.73
0.62
0.63
-0.98
Cu (ppm)
0.59
-0.49
0.50
0.87
0.74
0.70
0.789
-0.53
0.82
0.59
0.45
0.68
Fe (ppm)
0.10
-0.11
-0.98
-0.88
0.13
-0.97
-0.84
0.73
-0.91
0.13
0.15
-0.99
-0.94
-0.94
Ba (ppm)
0.11
-0.11
0.99
0.93
-0.05
0.99
0.94
-0.84
0.96
-0.1
0.14 0.189
0.03
0.95
0.85
0.98
1
1
Table 5: Water Quality Parameters Ph Sulphate Nitrite and Nitrate
Review of water-related diseases and causative contaminants Causes Related Health Condition(s)
Author(s)
Nature of geological formation and minerals Fertilizer contamination Excessive application of fertilizer, sewage disposal, manure application, wastewater, leakage, landfill leachate, municipal runoff
Gastrointestinal irritation Laxative action Methemoglobinemia in infants
Emenike et al. (2018), Kulinkina et al. (2017), WHO (2003), Khan et al. (2013) Mkwate (2017); Khan et al. (2013), Owamah et al. (2013) Saeedi et al. (2012)
Subencephalopathic, neurological, and effects
WHO (2003)
Acute toxicity
Tiredness, abdominal discomfort, irritability and anemia
Gerlach et al. (2002)
High levels of Pb in children
Khan et al. (2013); Dahunsi et al.(2014)
Moderate levels of Pb
Convulsion, neurological damage, organ failure, coma, and death Hearing loss, inhibit growth, learning disabilities
Khan et al. (2013)
Accumulative toxicity
Lead poisoning
Mkwate (2017), Shu et al. (2011)
Cadmium
High toxicity
Kidney disease, anaemia, albuminuria, and osteomalacia
Dahunsi et al. (2014), Shu et al. (2011)
Mercury
Accumulative toxicity
nervous system breakdown, heart, kidney, stomach troubles Harm liver, cardiovascular diseases
Shu et al. (2011)
Lead
Copper Mangnese Zinc Chromium Arsenic
High concentration
Calcium Magnesium
Deficiency Deficiency
Water low in Mg
Arthroncus, soft bone, Manganese-poisoning and pneumosclerosis Retard intelligence development and cardiosvascular, sickness, vomiting Contact dermatitis and respiratory cancer Stomach ache, diarrhea, bowel disease, edema, hernolytic anemia, jaundice, death Osteoporosis and hypertension Cardiovascular diseases atherosclerotic vascular disease, acute myocardial infarction, preeclampsia in pregnant women, diabetes, osteoporosis, Increase in morbidity and mortality, cardiovascular problems, pregnancy disorders, neurodegenerative disease, cancer
Source: Sojobi (2016) after slight updates
Table 6: Comparison of groundwater monitoring results of previous studies and this study
Owamah et al. (2013), Shu et al. (2011) Shu et al. (2011) Shu et al. (2011) Shu et al. (2011) Mkwate (2017), Shu et al. (2011) Khan et al. (2013), Yang and Chiu (1999) Melles and Kiss (1992); Yang et al. (2002); Sojobi (2016)
Sojobi (2016), Verd et al. (1992)
Author(s)
Contaminants present
Ugochukwu and Ojike (2019) Emenike et al. (2018)
Area covered in the Study/Country Enugu Metropolis, Enugu State/Nigeria Abeokuta South/Nigeria
Pb, Coliform Bacteria
No. of Groundwater Sources/Samples 14 Nos. hand-dug wells (HDWs)
Acidity; Na2+, Mg2+, Fe2+, and EC
21 Nos. groundwater samples
Kulinkina et al. (2017)
Rural communities/Ghana
pH, turbidity, manganese, chloride and iron. Concentrations of total dissolved solids (TDS) EC, turbidity , FC , and FS
94 and 68 Nos. boreholes in the dry season and wet season respectively
Mkwate et al. (2017)
Balaka District/Malawi
Sojobi (2016)
Omu-Aran/Nigeria
NO3 −, Mg, TH, pH and Mg, Pb, TH, pH and DO
10 Nos. bore-holes and 3 Nos. hand-dug wells
Wanke et al. (2015)
Omusati/Oshama, Okongo/Ohangwena, Omatjete/Omaruno, Okanguati/kutnene/Namibia Myingyan and Tha Pyay Thar/Asia Sagamu, Mosimi, Ogijo and Odogunyan/Nigeria
F, NO3, SO4, TDS, E-coli
15 Nos. deep wells (up to 30m) and 44 Nos. shallow wells (1-3m)
As, Mn, U, F, Fe
20 Nos. wells
TSS and TS Pb, Ni, Cr, and Cd, Coliform Bacteria
72 Nos. samples
Rao (2014)
Andhra Pradesh/India
30 Nos. samples
Akhtar et al. (2014)
Lahore/Pakistan
EC, Na+, Cl-, SO42-, Mg2+, Ca2+ TDS, Turbidity
Akinyemi & Souley (2014)
Abeokuta North, Ifo, Obafemi, Obafemi Owode, Odeda/Nigeria
Porowska (2014)
Owamah et al. (2013)
Bacquart et al. (2015) Dahunsi et al. (2014)
Srinivas et al. (2013)
Total of 11 boreholes and shallow wells
Recommendation(s) Treatment of HDW water of the study area before use Regular monitoring of groundwater Treating water in locally sustainable ways
Large scale adoption of house hold water treatment and continued monitoring of the water sources Provision of proper sanitary system , restriction of domesticated animals from boreholes and wells and household treatment Regular monitoring and relevant treatment
Regular monitoring and testing of drinking water Public outreaches/workshops, properly design and construction of wells There is need for remediation
340 Nos. wells
Regular monitoring and protection of aquifer against contamination
pH, Mg
1 No. spring, 1 No. well, 1 No. borehole
To be treated prior to drinking and irrigation.
Otwock/Poland
HCO3−, Cl−, Ca2+, Mg2+, Na, K, Fe, DOC
32 Nos. samples (1–2.7 m)
Provision of engineered landfill
Isoko North Local Government Area, Delta State/Nigeria Tuticorin/India
pH, Coliform Bacteria, Pb and Cd
144 Nos. samples
EC, pH, TDS, Ca, Mg, Na, K, TH, Cl TDS, EC, Na+, Cl−, HCO3− K+, F−, pH, SO42−, , Br−
21Nos. wells (10-m depth)
Public workshops. Proper design and construction of wells Groundwater unsuitable for irrigation
Vasanthaviger et al. (2013)
Thirumanimuthar/India
Oyelami et al. (2013)
Ido –Osun/Nigeria
Cl-, Na, Mn
20 Nos. wells
Oni & Hassan (2013)
Aba-Eku (Ibadan)/Nigeria
Pb, Cd, Fe
2 Nos. wells
194 Nos. samples
Groundwater has hydrogeochemical regimes Regular monitoring & better domestic waste management required Landfill to be provided plus adoption proper
Al-ahmadi & El-Fiky (2009) This study
Wadi Marwani/Saudi-Arabia Emevor/Nigeria
pH, TDS, Mg, Na, SO42-, Cl-, NO32pH, Ba, total coliform
16 Nos. wells (5–15.3 m) 10 Nos. each of boreholes and hand-dug wells
waste management practice None as groundwater was safe for drinking Regular monitoring and testing of drinking water, public workshops, proper design and construction of wells
Source: Adapted from Sojobi (2016) after slight updates
6009’E
6023’E 5037’N Aniocha Oshimilli North North Ika South Ika North East Aniocha South Oshimilli South
Abia shaka
Ethiope West Warri North
Sapel e Okpe
Warri SouthWest
Warri South
Ndokwa West
Ethiope East
Uvwie
Ndokwa East
Ellu
N
Owhelogbo
Isoko Ughelli North North Isoko South
BomadiUghelli South
Otibio Otor-Owhe
Patani
0
Idoni
Lake Ora
Udu
Burutu
Aradhe
Ukwuani
25Km
Study Area
Lake Okparo Ozoro
Ofagbe
Ivrogbo Oruovo Akiewe
Orie
Emevor Owevwe
Okpe Oghara Ivede Ogheneore Iyede Ivorogbe
N KEY Towns Study Area Town Boundary Main Road River
0
25Km
5020’N
Fig. 1a: Map of Isoko North showing Study Area Source: Ministry of Lands, Surveys & Urban Development, Asaba, (2013)
6009’E
6023’E
Fig. 1b: Map of Nigeria showing Delta State
7 6 5
pH
4 3 2 1 0 Series1
BH Wet
BH Dry
HDW Wet
HDW Dry
5.12
4.9
6.12
6.2
Well Type and Season
Fig 2a. Average value of pH in boreholes and hand-dug wells for wet and dry seasons
1.4 1.2
Ba (Mg/L)
1 0.8 0.6 0.4 0.2 0 Series1
BH Wet
BH Dry
HDW Wet
HDW Dry
1.1
0.5
1.22
0.66
Well Type and Season
Fig 2b. Average concentrations of barium in boreholes and hand-dug wells for wet and dry seasons
120 100
EC(µS/cm)
80 60 40 20 0 Series1
BH Wet
BH Dry
HDW Wet
HDW Dry
84.51
92.74
69.91
65.1
Well Type and Season
Fig 2c. Average concentrations of electrical conductivities in boreholes and hand-dug wells for wet and dry seasons
• • • • •
Baseline information on the quality of groundwater of rural Nigerian communities is scarce. This study provides a first time comprehensive report on the quality status of groundwater in Emevor. The groundwater was found acidic with elevated concentration of Ba, and coliform bacteria. ANOVA (p<0.05) showed a significant difference in the concentration of parameters that exceeded regulatory limits Correlation analysis showed that the main cations influencing the groundwater TDS were Ca, Mg, Ba, Fe, Na and K.