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Animal Research International (2013) 10(3): 1792 1798 1792

BIOACCUMULATION AND TOXIC EFFECTS OF SOME HEAVY METALS IN


FRESHWATER FISHES

IBEMENUGA, Keziah Nwamaka


Department of Biological Sciences, Anambra State University, Uli, Anambra State, Nigeria.
Email: jesusvesselofhonour@yahoo.com Phone: +234 8126421299

ABSTRACT

The contamination of the aquatic systems with heavy metals from natural anthropogenic
sources has become a global problem which poses threats to ecosystems and natural
communities. Hence this study reviews the effects of heavy metals in freshwater fishes.
Fishes bioaccumulate heavy metals (including cadmium, zinc, lead and copper) through
various organs such as gills, liver, stomach and intestine. The effects of these heavy
metals are highlighted.

Keywords: Bioaccumulation, Toxicity, Heavy metals, Cadmium, Zinc, Lead, Copper, Freshwater fish

INTRODUCTION leaching or seepage (Ezemonye and Kadiri,


2000). Heavy metals and organic compounds
Heavy metal according to Dianne and William can bioaccumulate in aquatic biota (USEPA,
(1999) embraces any metal exposure to which 1991) and biomagnify in food chains.
is clinically undesirable and which constitute a Bioaccumulation is the net build-up of
potential hazard. The presence of heavy metals substances from water in an aquatic organism
in the aquatic environment is a major concern as a result of enhanced uptake and slow
because of their toxicity and threat to plant and elimination of such substance (Bhattacharya et
animal life, thus disturbing the natural ecological al., 2009). Heavy metals are conservative
balance (Bhattacharya et al., 2008). The rate at pollutants in that they are broken down over
which heavy metals gain entry into the aquatic such a long time scale that they effectively
systems is alarming. The occurrence of heavy become permanent additions to the aquatic
metals in aquatic ecosystems in excess of environment (Mason, 1996). Since heavy metals
natural loads has become a wide spread bioaccumulate and have deleterious effects on
problem and a matter of concern over the last the aquatic ecosystems (Roux, 1994; Ezemonye
few decades (Voegborlo et al., 1999; Canli et et al., 2006) bioaccumulation measurements are
al., 1998; Dirilgen, 2001; Vutukuru, 2005). The necessary. Bioaccumulation measurements refer
sources of toxic heavy metals in aquatic to studies on methods of monitoring the uptake
environment could be traced to both natural and and retention of pollutants like metals or
anthropogenic sources for changes arising from pesticides in organs or tissues of organisms
anthropogenic activities have taken place in such as fish (Roux, 1994). Hence Olaifa et al.
aquatic ecosystem affecting the aquatic habitat (2004) and Vinodhini and Narayanan (2008)
(Olomukoro and Ezemonye, 2011) and fish, the reported that among aquatic animal species,
major component of the food chain leading to fishes cannot escape from the detrimental
humans (Mason, 1996). Through human effects of these pollutants. Thus fish health,
activities such as industrialization, urbanization growth, development and survival is affected.
and agriculture, effluents are discharged into The characteristic feature of heavy metals is
water systems either directly or through run-of, their strong attraction to biological tissues and

ISSN: 1597 3115 ARI 2013 10(3): 1792 1798


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Ibemenuga 1793

in general their slow elimination from biological Cadmium, a heavy metal commonly
systems (Nwani et al., 2009). The uptake of used in environmental studies, is highly toxic
heavy metals in fish was found to occur through and widely distributed in the environment
absorption across the gill surface or through the (Ghiasi et al., 2010). Cadmium is highly toxic to
gut wall tract (Obasohan, 2007; Nwani et al., some aquatic life (Mason, 1996) particularly
2009). Diffusion facilitated transport or fishes (Suresh et al., 1993). Fish bioaccumulate
absorption in gills and surface mucus are the heavy metals including cadmium through
mechanisms of uptake from water (Oguzie, various gateways. Fish accumulation of
2003). Bioaccumulation of metals reflects the chemicals especially those with poor water
amount ingested by the organisms, the way in solubility occurs because of the very intimate
which the metals were distributed among the contact with the medium that carries the
different tissues and the extent to which the chemicals in solution or suspension and also
metals is retained in each tissue type (Murugan, because fish have to extract oxygen from the
et al., 2008). In light of the above this study medium by passing enormous volumes of water
seeks to address issues pertaining to the over the gills (Akan et al., 2009). The gills, skin
bioaccumulation of some heavy metals in fish. and digestive tract are potential sites of
absorption of water borne chemicals (Vinodhini
MATERIALS AND METHODS and Narayanan, 2008; Akan et al., 2009). The
chemicals once absorbed are transported by the
A comprehensive literature search was made blood to either a storage point such as bone, or
from the internet and serial materials of to the liver for transportation (Akan et al.,
University of Nigeria, Nsukka. Different journal 2009). Cadmium has deleterious effects on fish
articles, proceedings of learned societies of (Table 1).
fisheries and hydrobiology and textbooks were
consulted in relation to heavy metals and their Zinc: Zinc, an essential element is one of the
effects on freshwater fishes. most common heavy metal pollutants (Kori-
Siakpere et al., 2008). Zinc is an essential
RESULTS AND DISCUSSION element acting as structural component and
having properties indispensable for life (Bengari
Cadmium: Cadmium, the most toxic and non- and Patil, 1986; Murugan et al., 2008). The
essential heavy metal has wide distribution in sources of zinc and other heavy metals in
the earths crust and aquatic environments natural waters may be from geological rock
(Muthukumaravel et al., 2007). Cadmium occurs weathering or from human activities such as
naturally in some phosphate rock and this may industrial and domestic waste water discharges
account for the high concentration of cadmium and animals where it forms constituent
in some phosphate fertilizers (Geisy, 1978; functions in maintaining cytoplasmic integrity
Oronsaye, 2001) such as super phosphate (Weatherly et al., 1980; Kori-Siakpere et al.,
fertilizer. With increased urbanization and 2008). Since zinc is an unnatural substance, it
industrialization (Akan et al., 2009) there has may persist for years without decomposition.
been rapid and persistent increase in the Zinc is toxic to fish and macroinvertebrates at
manufacture and utilization of cadmium over sublethal concentration (Folorunsho and
the years. It is to be expected that run off from Oronsaye, 1990; Ajiwe et al., 2000; Nsofor et
agricultural land treated with cadmium bearing al., 2007). Although zinc is an essential element
fertilizers can enrich the aquatic environment (Dimari et al., 2008) it is a potential toxicant to
with the metal (Oronsaye, 2001). Cadmium has fish (Everall et al., 1989; Murugan et al., 2008)
many industrial applications and measurable with adverse effects (Table 2). Liver and kidney
amounts of the metal may be discharged as are the primary sites of zinc accumulation
effluents to surface water (Onuoha et al., 1996; (Murugan et al., 2008).
Oronsaye, 2001).

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Bioaccumulation and toxic effects of some heavy metals in freshwater fishes 1794

Table 1: Effects of cadmium on freshwater fish


Fish Effects Sources
Gasterosteus aculeatus Formation of vacuoles, and sloughing of the Eller (1971)
epithelial layer from the secondary lamellae
and the enlarged subepithelial spaces reduce Oronsaye (1997)
the amount of oxygen diffusing into fish by
increasing the water to blood distance;
severe constriction of the blood spaces and Oronsaye and Brafield (1984)
the enlarged red blood spaces and the
enlarged red blood cells reduce blood flow
and make oxygen transport less efficient.
Many of the chloride cells degenerate.

Fundulus heteroclutus Increase in the number of chloride cells Gardner and Yevich (1970)
Oronsaye (1997)

Oreochromis mossambicus Reduction of proteins due to the impact on Muthukumaravel et al. (2007)
the protein synthetic pathway.

Cyprinus carpio Enhance susceptibility to disease due to Ghiasi et al. (2010)


decrease in innate immune response.

Table 2: Effects of zinc on freshwater fish


Fish Effects Sources
Heteroclarias sp. Affects tissue respiration leading to death by Kori-Siakpere et al. (2008)
hypoxia, induce changes in vein and heart
physiology, and causes a significant decrease
in haemoglobin and haematocrit. Decreases
plasma protein.

Oreochromis niloticus Result in several dysfunctions in fish. Exerts Tuurala and Soivio (1982)
adverse effects by accruing structural damage
Salmo gaidneri which affects the growth, development and Kori-Siakpere et al. (2008)
survival.

Clarias ischeriensis Decrease in plasma protein attributed to renal Kori-Siakpere et al. (1995)
excretion or impaired protein synthesis or due Kori-Siakpere et al. (2008)
to liver disorder.

Salmo gardnerii Cause toxic changes in ventilatory and heart Hughes and Tort (1975)
physiology Kori-Siakpere et al. (2008)

Clarias gariepinus Sublethal levels adversely affect hatchability, Cardeihac et al. (1981)
survival and haematological parameters of Kori-Siakpere et al., (2008)
fish

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Ibemenuga 1795

Table 3: Effects of lead on freshwater fish


Fish Effects Sources
Tilapia galillilaeus Delay embryonic development, suppress Al-kahtani (2009)
reproduction, and inhibit growth, increase mucus
Clarias lazera formation, neurological problem, enzyme inhalation
and kidney dysfunction.

Clarias gariepinus Lamella shrinkage, degeneracy of epithelium, Olojo et al. (2005)


branchial arterial rupture and ischemia, reduction in
growth rate and loss in body weight, degenerates
liver cells synctial arrangement.

Salmo gardnerii and Inhibits egg hatching, excessive mucus secretion, Weber e al. (1997)
Salvelinus namaycush hypertrophy and deformation of gill.

Poecilia latipinna Filaments and hyperplasila of epithelial cells hence Mobarak et al. (2010)
lamellae fuses and gill lamellae curls at the tips,
increases secretion of mucus from gills and skin,
dilation of bile canaliculi and liver sinusoids,
extravasation of blood and necrosis/pyknosis cell
nuclei in liver.

Auratus auratus Genotoxic and cytotoxic damage in both gill and fin Cavas (2007)
epithelia cells.

Lead: Lead residues according to Mason Conclusion: Heavy metals are diffuse and
(1996) are rich in heavy metals resulting in conservative pollutants that bioaccumulate and
considerable contamination of freshwater biomagnify along the food chain with
systems. Lead is released into the environment deleterious effects on the aquatic ecosystems.
mainly through exhaust pipes of automobiles as Although cadmium, zinc, lead and copper are
a result of its presence in gasoline (Nsofor et vital in metabolic processes, efforts should be
al., 2007). Fishes bioaccumulate lead through made to ensure that they and other heavy
various organs including gills, stomach, liver and metals do not exceed the prescribed world
intestine. The biological effects of sublethal Health Organization (WHO) and Federal
concentrations of lead on fish are presented Environmental Protection Agency (FEPA)
(Table 3). acceptable limits. All environmental policy
should be enhanced and campaigns carried out
Copper: Copper is among the heavy metals to educate the public on the importance to
enrichment of Lagos lagoon reported by Okoye protect and preserve aquatic systems and their
(1991) in which he implicated inland based resident biota.
urban and industrial wastes. The gill is an
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