By Onu, B (2024).
Greener Journal of Environment Management and
Public Safety ISSN: 2354-2276 Vol. 12(1), pp. 1-9, 2024 Copyright ©2024, Creative Commons
Attribution 4.0 International. |
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Analysis of Heavy Metals in Chrysichthys nigrodigitatus, Micropogonias undulatus and Mugil cephalus Fish Species Caught in
Brass River
Federal University Otuoke,
Faculty of Science, Biology Department.
ARTICLE INFO |
ABSTRACT |
Article No.: 031924037 Type: Research Full Text: PDF, PHP, HTML, EPUB, MP3 |
This research analyses
heavy metals presence in Chrysichthys nigrodigitatus, Micropogonias
undulatus and Mugil Cephalus fish species found in Brass River. This study focuses on the
concentrations of major heavy metals (Pb, Cd, Cr, Hg and As) in the three
fishes named above. The fish samples
were collected from fishermen from the Brass River during the months of
September and October 2023. The heavy metal concentration in the fish samples
were analysed through the Atomic Absorption Spectrophotometer in order to
estimate the presence of heavy metals pollution in fish species of the river.
The result show that the concentration of Pb (0.204 µg/ml), Cd (0.022 µg/ml)
and Cr (0.004 µg/ml) were the highest in the Chrysichthys
nigrodigitatus with a high relative standard deviation. While Hg and
As have negative values. In Micropogonias undulatus, the concentration
of Pb (0.241µg/ml), Cd (0.020µg/ml) and Cr (0.018µg/ml) were the highest with
a relative standard deviation of 8.28%, 19.94% and 15.55% respectively. Hg
and As have negative values. While in Mugil
cephalus, the concentration of Pb (0.337µg/ml) and Cr
(0.007µg/ml) were the highest with a relative standard deviation of 9.53% and
3.56% respectively. Cd, Hg and As have negative values. The level of these
heavy metals in fishes of the river were found below the permissible limit.
Thus, the study revealed that the heavy metals concentration in fish in Brass
River is low. However, the heavy metals analysed in
this research are known to be very toxic even at low concentrations. Hence,
adequate attention should be given to ensure that there is no further
pollution of heavy metals in the river in order to avoid future deleterious
health effects to humans. |
Accepted: 22/03/2024 Published:
05/04/2024 |
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*Corresponding Author Dr. Benefit Onu E-mail: benefitonu28@ gmail.com |
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Keywords:
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INTRODUCTION
Environmental
pollution through heavy metals has become a universal problem in aquatic
network due to their toxicity, accumulation and bio-magnification (Afshan et
al., 2014). Trace metals in contrast to most pollutants, are not bio
degradable, and they undergo a global ecological cycle in which natural water
are the main pathways. Heavy metals can be concentrated along the food chain,
producing their toxic effect at points far from the source of pollution (Tilzer
and Khondker, 1993). The pollution of aquatic network is a growing threat to
the environment due to agricultural, domestic and industrial contaminants.
Metals make up an important fraction of environmentally hazardous substances.
Nigerian rivers, streams and ponds have received high levels of heavy metals as
a result of the development of industries and anthropogenic activities around
these water bodies (Ahmed et al., 2003; MacFarlane and Burchette 2000; Amisah
et al., 2009).
Heavy metal is any metallic chemical element
that has a relatively high density and is toxic or poisonous at low
concentrations (Ngumbu et al., 2017). Some metals, including chromium
(Cr), lead (Pb), cadmium (Cd), arsenic (As) and mercury (Hg) are known to be very toxic even at low concentrations
(Nguyen et al., 2005), Others, such as copper (Cu), iron (Fe), zinc
(Zn), manganese (Mn) and cobalt (Co) are known to be essential elements which
play important roles in biological metabolism at very low concentrations (Ajmal
et al., 1988; Subotić et al., 2013). However, an excess or
dearth of any of these metals can disrupt biochemical functions in both humans
and animals, at higher concentrations they can lead to poisoning (Lenntech,
2014). The metal which has a relatively high density and toxic at low quantity
is referred as heavy metal, arsenic (As), lead (Pb), mercury (Hg), cadmium
(Cd), chromium (Cr), thallium (TI), etc. fall in this group
Some trace elements are also known as heavy
metals, e.g., copper (Cu), selenium (Se) and zinc (Zn). They are essential to
maintaining the body metabolism, but they are toxic at higher concentrations.
These heavy metals can get to our bodies through food, drinking water and air
(Lenntech, 2014).
These metals are discharged into the
environment through several anthropogenic sources such as the burning of fossil
fuels, transportation, industrial effluent discharge and indiscriminate waste
dumping and are often washed into receiving bodies such as sediment, soil and
water bodies by rain run-off therefore, the aquatic ecosystem receives the bulk
of contaminants from anthropogenic sources (Eletta et al., 2003). These
metals are of particular concern due to their toxic effect at certain levels of
exposure and ability in bio-accumulate in an ecosystem, body tissues and organs
(Babalola, 2010; Eletta et al., 2003).
The occurrence of toxic metals in pond,
stream and river water affects the lives of humans and animals that depend upon
these water sources for their daily life (Khan. 2000). The consumption of
aquatic resources containing toxic metals may cause serious health hazards
through food chain magnification (Khan. 2000; Akan et
al., 2012). Heavy metal intake by fish in polluted aquatic environments
vary and depend on ecological requirements, metabolism and other factors such
as salinity, water pollution level, food and sediment (Adeniyi, 2007; Ajeagah et
al., 2013; Milenković et al., 2005; Vuković et al.,
2014).
The results of many researches show
bioaccumulation of metal pollutants from the water in various tissues of
aquatic organisms (Has-Schön et al., 2006; Monroy et al., 2014;
Zhuang et al., 2013). Various species of fish can be bioindicators of
contamination with heavy metals and others pollutants (Dural et al.,
2007; Huang, 2003, USEPA. 2009: Molina, 2011; FAO, 2012). Feeding habits have a
great influence on pollutants accumulation, especially regarding heavy metals
in different fish species (Amundsen et al.,
1997; Merciai et al., 2014; Abubakar et al., 2015). Many studies
have been done on the levels of heavy metals in fish samples in Africa, Nigeria
and elsewhere (Voegborlo and Akagi, 2007; Voegborlo and
adimado, 2010 and Kwaansa-Ansah, 2012).
In Brass Local Government Area (LGA), limited
research on heavy metals in fish have been
reported. Although, Brass local Government Area is not a heavily industrialize
area, but with the presence of the crude oil exploration companies, it has its
share of pollutants within her environment. Anthropogenic activities such as
crude oil spillage and other chemical waste, domestic wastewater and petrol
from fishing and transport boats have increased over the years, and have led to
very serious environmental pollution within and along the Brass River.
Study area
Brass
is a Local Government Area in Bayelsa State, southern Nigeria. Its headquarter
is in the town of Twon-Brass on Brass Island along the coast, it has a
coastline of approximately 90 km on the Bight of Bonny. It has an area of 1,404
km2 and a population of 185,049 at the 2006 census. It is a traditional town of
the Ijo people, it became a slave-trading port in the early 19th century. It
was ruled by African merchant “houses,” which were encouraged by the European
traders (Gertzel, 1962).
Brass has enormous deposits of crude oil and
natural gas and because of the rich natural resources has the presence of
several national and international oil mining companies. The activities of
these oil mining companies have contributed to the most of the economic development
of the Brass area. In Brass people another economic activity that sustain
livelihood in the area is Fishing and the making of fishing nets, construction
of canoes also is another key economic feature of the Brass people.
The study area is characterized by an
equatorial climate, with a wet season (April to October) and a dry season
(November to March), and with rather constant ambient temperatures (27-34°C)
year-round.
Sample collection
The
three fish samples were randomly collected through the assistance of fisherman
using traps and set nets around the Brass River in Brass Local Government Area
and were immediately transported to the laboratory for analysis. Before the
analysis of the heavy metals’ concentration, the fishes were properly rinsed in
distilled water to remove dirts and debris from the skin and gills
Digestion of Fish
Samples
10g
of each fish were weighed and dried in the hot air oven at 105oC. The
samples were digested with a mixture of HNO3, HClO3 and H2SO4.
These chemicals were mixed in a ratio of 10:4:1. The heavy metals Lead (Pb),
Cadmium (Cd), Chromium (Cr), Hg and As concentrations in the samples were
evaluated using Varian Spectra A100 Atomic Absorption Spectroscopy (AAS) using
prepared standard solution.
Silver Catfish, Chrysichthys
nigrodigitatus
The
silver catfish, Chrysichthys nigrodigitatus (Lacépède,
1803) is among the dominant African commercial fishes of high economic
value and widely serves as food for human consumption in West Africa (Leveque, 1997, Adite and van
Thielen, 1995). This catfish belongs to the genus Chrysichthys,
family Claroteidae, Siluriformes order and Ostariophysi super
order. Synonimies are Pimelodus nigrodigitaus, Arius
acutivelus, Chrysichthys furcatus, Chrysichthys buettikoferi
and Chrysichthys cameronensis (Leveque et
al., 1992). In
general, the species showed grew silvery colour with a white belly and a black
adipose. Chrysichthys nigrodigitatus exhibited a pointed snout slightly
longer than or equal to the width of the mouth and the pre-maxyllary tooth
plate width made 20-30% of the head length (Leveque et al., 1992; Laleye et al., 1995). In the tropical estuary
of Nigeria, Asuquo et al., (1999) the species
as foraging on a variety of benthic food resources. The specie also habits in
salt and fresh water areas in Nigeria.
Croaker (Micropogonias undulatus)
The
croaker (Micropogonias undulatus) is a
species of marine ray-finned fish belonging to the family Sciaenidae and
is closely related to the black drum (Pogonias cromis), the silver perch
(Bairdiella chrysoura), the spot croaker (Leiostomus xanthurus),
the red drum (Sciaenops ocellatus), the spotted seatrout (Cynoscion
nebulosus), and the weakfish (Cynoscion regalis). It is commonly
found in estuaries from Massachusetts to the Gulf of Mexico (Sperry and Thomas, 1999). The name croaker is descriptive
of the noise the fish makes by vibrating strong muscles against its swim
bladder, which acts as a resonating chamber much like a ball. The Atlantic
croaker is the loudest of the drum family (Sperry and
Thomas, 1999). When full-grown at 2 to 3 years old, croakers reach between
18 and 20 inches in length and 4 to 5 pounds, but on average are 1/2-2 pounds.
The fish's lifespan can reach up to 8 years (Froese and
Pauly, 2017).
Mullet (Mugil
cephalus)
Adult
mullets grow to a length of 9 to 19.5 inches (35 to 50 cm). Immature mullet are
3 to 8 inches (7.6 to 17.8 cm) long. Distinguishing characteristics include an
irregularly round, silvery body, dark bluish green back and dark longitudinal
stripes on the sides, and a small mouth. The mullet's diet includes
zooplankton, benthic (bottom-dwelling) organisms and detritus (dead plants and
animals), and small invertebrates (Arthur et al., 1997; FAO, 1995;
Harrison and Senou, 1999). Larger fish, turtles, water snakes, and wading
birds’ prey on mullet. They reach sexual maturity in three years. Mating season
lasts from late October to December. Mature adults leave the bays, collect in
large schools, and migrate offshore to mate. During spawning season, females
scatter one to seven million round eggs on the bottom. Eggs are not guarded by
adults. After an incubation period of 36 to 50 hours, depending on water
temperature, the young mullet hatch. Of millions of eggs spawned in offshore
waters, most are eaten by other species. Juveniles return to coastal locations
to mature after they have reached 15 to 32 mm long. Their lifespan is seven
years for males and eight years for females, with a probable average lifespan
of five years (Oren, 1981; Badran, 1994; Plumb, 1999; Chen et al., 2002).
Statistical Analyses
Data
were given as mean ± RSD for each of the measured variables. All
statistical analyzes were performed using SPSS version 21.0. All the
concentration values for five heavy metals in the tissues of fish species were
normally distributed at the 95% confidence level. The data were presented in
tabular and graphical form.
RESULT AND DISCUSSION
Table 1:
Sample A: Chrysichthys nigrodigitatus (Silver catfish)
Parameter |
Concentration (µg/ml) |
% Relative standard Deviation (RSD) |
Mean Absorbance |
Cd |
0.022 |
HIGH |
0.0034 |
Cr |
0.004 |
HIGH |
0.0163 |
Hg |
-0.132 |
0.36 |
-0.0198 |
Pb |
0.204 |
HIGH |
0.0103 |
As |
-0.108 |
18.21 |
-0.0370 |
Figure 4: Graph showing the concentration of
heavy metals in Chrysichthys nigrodigitatus (Silver catfish)
In figure 4, the
result show that the concentration of Pb (0.204 µg/ml), Cd (0.022 µg/ml) and Cr (0.004 µg/ml) were the highest in the Chrysichthys
nigrodigitatus with a high Relative Standard Deviation. While Hg and As
have negative values.
Table
2: Sample B: Croaker (Micropogonias undulatus)
Parameter |
Concentration (µg/ml) |
% Relative standard Deviation (RSD) |
Mean Absorbance |
Cd |
0.020 |
19.94 |
0.0031 |
Cr |
0.018 |
15.55 |
0.0228 |
Hg |
-0.116 |
1.56 |
-0.0174 |
Pb |
0.241 |
8.28 |
0.0122 |
As |
-0.367 |
HIGH |
-0.0150 |
In figure 5, the
result show that the concentration of Pb (0.241µg/ml), Cd (0.020µg/ml) and Cr
(0.018µg/ml) were the highest in Micropogonias undulatus with a relative
standard deviation of 8.28%, 19.94% and 15.55% respectively. Hg and As have
negative values.
Figure 5: Graph
showing the concentration of heavy metals in Croaker (Micropogonias
undulatus)
Table 3:
Sample C: Mullet (Mugil cephalus)
Parameter |
Concentration (µg/ml) |
% Relative standard Deviation (RSD) |
Mean Absorbance |
Cd |
-0.012 |
HIGH |
-0.0019 |
Cr |
0.007 |
3.56 |
0.0187 |
Hg |
-0.144 |
0.35 |
-0.0218 |
Pb |
0.337 |
9.53 |
0.0170 |
As |
-0.367 |
HIGH |
-0.0150 |
Figure 6: Graph showing the concentration of
heavy metals in Mullet (Mugil cephalus)
In figure 6, the
result show that the concentration of Pb (0.337µg/ml) and Cr (0.007µg/ml) were
the highest in the Mugil Cephalus with a relative standard deviation of
9.53% and 3.56% respectively. Cd, Hg and As have negative values.
DISCUSSION
The
result show that the concentration of Pb (0.204 µg/ml), Cd (0.022 µg/ml) and Cr
(0.004 µg/ml) were the highest in the Chrysichthys nigrodigitatus with a
high Relative Standard Deviation. While Hg and As have negative values. In
Micropogonias undulatus, the concentration of Pb (0.241µg/ml), Cd
(0.020µg/ml) and Cr (0.018µg/ml) were the highest with a relative standard deviation
of 8.28%, 19.94% and 15.55% respectively. Hg and As have negative values. In Mugil
Cephalus, the concentration of Pb (0.337µg/ml) and Cr (0.007µg/ml) were the
highest with a relative standard deviation of 9.53% and 3.56% respectively. Cd,
Hg and As have negative values. The level of these heavy metals in fishes of
the river were found below the permissible limit.
The heavy metals concentrations were
variously distributed in the fish tissues. The Pb content in three fish muscle
was the highest heavy metal observed in this study. However, the values were
lower than the WHO required concentration in fish (Zrnčić
et al., 2013). The three fish
species, Chrysichthys nigrodigitatus, Micropogonias undulatus and
Mugil cephalus feed on plankton and algae and it can be one of the reasons
for their higher lead bioaccumulation. The variation of accumulation of heavy
metals in different fish species is attributed to several feeding habits.
Significant concentrations of Cd are present in the three fish tissues, The
accumulation of Cd in fish tissues is shown in several studies (Has-Schön et al., 2006; Jarić et al.,
2011; Castro-Gonzalez
et al., 2008). Mercury is one of the very toxic metals with a
tendency to bind to the sulfide group of proteins and deposits in muscles (Castro-Gonzalez et al., 2008) in this study,
Mercury concentration in the fish tissues were found to be negative. But these
values of heavy metal contents are also below the maximum permitted
concentrations of these pollutants according to the Commission of the European
Communities (EC), hence the three fish can be acceptable for human consumption.
However, the heavy metals analysed in this research are known to be very toxic
even at low concentrations (Tešić et al.,
2014). Considering all these results, it is necessary to monitor the
presence of heavy metals as environmental pollutants in the future, thus
ensuring a good ecological status of the Brass River, as well as providing
healthy and safe fresh fish.
CONCLUSION
The
research work reveals the presence of heavy metal concentrations level in the
selected fish species collected from the Brass River. Overall, the heavy metal
concentration level in the fish species were below the standard acceptable
limits which may not pose threat on human health. However, the heavy metals
analysed in this research are known to be very toxic even at low
concentrations. The Brass River should be protected to save the aquatic biota
of the river and more sustainable measures should be taken to ensure better
fish quality and aquatic life of the Brass River. Adequate attention should be
given to ensure that there is no any further pollution of heavy metals in the
river in order to avoid future deleterious health issues to humans.
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Cite this Article: Onu, B (2024). Analysis of Heavy
Metals in Chrysichthys nigrodigitatus,
Micropogonias undulatus and Mugil
cephalus Fish Species Caught in Brass River. Greener Journal of Environmental Management and Public Safety,
12(1): 1-9. |