Subscribe Now Subscribe Today
Research Article

Cadmium, Copper, Lead and Zinc Tissue Levels in Bonga Shad(Ethmalosa fimbriata) and Tilapia (Tilapia guineensis)Caught from Imo River, Nigeria

Monday U. Etesin and Nsikak U. Benson
Facebook Twitter Digg Reddit Linkedin StumbleUpon E-mail

An investigation of the muscle-liver tissue concentrations of heavy metals (Cd, Cu, Pb and Zn) in two commercially important fish species (Ethmalosa fimbriata-Bonga shad and Tilapia guineensis-Tilapia) caught from three stations within Imo River was carried out in 2004. Heavy metal contents varied significantly (p>0.05) depending on the fish species and on the type of tissues. The concentrations of the essential elements (Zn, Cu) were relatively higher in the muscle and liver tissues than the non-essential metals (Pb, Cd). The trends in tissue elemental concentrations in both species of fish was Zn>Cu>Pb>Cd. Heavy metal levels in liver tissues of both fish species were comparatively higher than levels obtained from muscle tissue. In general, T. guineensis showed higher levels of metal concentrations than E. fimbriata. The concentrations of Cu, Cd, Pb and Zn in both fish species were within tolerance limits that are safe for human consumption.

Related Articles in ASCI
Similar Articles in this Journal
Search in Google Scholar
View Citation
Report Citation

  How to cite this article:

Monday U. Etesin and Nsikak U. Benson, 2007. Cadmium, Copper, Lead and Zinc Tissue Levels in Bonga Shad(Ethmalosa fimbriata) and Tilapia (Tilapia guineensis)Caught from Imo River, Nigeria. American Journal of Food Technology, 2: 48-54.

DOI: 10.3923/ajft.2007.48.54



In recent times, human mediated activities have led to the introduction of many potentially hazardous inorganic compounds, heavy metals into our environment particularly as a result of industrial attributable point sources (Udosen, 1998). Heavy metals are natural trace components of aquatic ecosystems (Fernandez-Leborans and Olalla-Herrero, 2000; Yilmaz, 2005) and may be available at much lower concentrations in waters compared to major cations and anions (Radojevic and Bashkin, 1999). Aside natural sources of heavy metals in aquatic environments, human-mediated/ anthropogenic sources include industrial wastes arising from manufacturing, mining, agricultural and metal finishing plants. Other anthropogenic sources are domestic wastewaters, non-point and atmospheric precipitation (Langston et al., 1999; Van den Broek et al., 2002). However, there has been a growing concern as a result of enhanced elemental levels in aquatic ecosystems as well as in tissues of aquatic organisms especially fishes (Kalay and Canli, 2000; Riba et al., 2003; Akueshi et al., 2003).

Although many heavy metals are considered as essential macro- and micro-elements especially at non-adverse-effect-levels (Borovik, 1990; Hossain and Khan, 2001), they can exert toxic effects at concentrations encountered in polluted environment. Additionally, metals unlike many organic pollutants are known to biopersist in the environment (Radojevic and Bashkin, 1999) and can become bioconcentrated in the food chain (Eja et al., 2003), so that levels in the upper members of the chain are elevated than concentrations in the overlying water column. Within recent years, there has been an increasing interest in the utilization of fishes as bioindicators of the integrity of aquatic environmental systems (Fausch et al., 1990; Whitefield, 1996; Wildianarko et al., 2000; Akueshi et al., 2003). Several studies have indicated enhanced levels of both non-essential and essential heavy metal load in muscle and liver tissues of fishes (Ekpo and Ibok, 1999; Zyadah, 1999; Flessas et al., 2000; Hossain and Khan, 2001).

The coastal aquatic ecosystems of the Niger Delta region of Nigeria has of recent received much attention because of the considerable man-mediated perturbations these fragile environments have been subjected to, through accidental or deliberate oil spill, untreated industrial wastewater and sewage discharges and agricultural runoffs. Imo River is one of the numerous lowland rivers found in the Niger Delta, located within latitude 4o25'-4o45' N and longitude 7o19'-7o45' E. It extends along the coast from the River Niger in the north and discharges into the Atlantic Ocean in the south at the Bight of Bonny. Along the banks of the river, semi-urban settlements are sited. Also, located down the lower reaches of the river is Aluminium Smelting Plant (ALSCON) at Ikot Abasi, Akwa Ibom State. Oil exploitation activities are prevalent in the upper reaches of this coastal water system. In view of the industrial, agricultural and oil drilling activities, Imo River receives large amount of untreated wastewater and sewage, domestic wastes and icthyocides, used by local fish-farmers. Moreover, it is a multi-use resource for artisanal and commercial fishing and transportation. It is important to note however, that the degradation of the hydrological integrity of the ecosystem constitute a concern considering the health statuses of its flora and fauna and the health implications the consumption of its products could have on the people of the region.

The present study investigated the cadmium, copper, lead and zinc concentrations in two commercially important species of fishes- Bonga shad (E. fimbriata) and Tilapia (Tilapia guineensis) caught within the Imo River system. These species differ in feeding habits and habitat. Bonga shad is a highly commercial species and occurs in inshore waters, lagoons, brackish and marine environments. It feeds by filtering phytoplankton, chiefly diatoms (Whitehead, 1985). On the other hand, T. guineensis are benthopelagic, usually occurring in freshwater and brackish systems. It is a commercial species and feeds on shrimps, plankton, bivalves and detritus (Teugels and Thys van den Audenaerde, 1991). In general, these two species of fish are very important in commercial/artisanal fishery in Imo River system and adjourning waters. They are marketed fresh, smoked and dried.

Materials and Methods

Bonga shad (Ethmalosa fimbriata) and Tilapia (Tilapia guineensis) were caught using gill nets from three locations representing the upper, middle and lower reaches of the river. The first station (OBG) is located on 4o29' N,7o8' E, upstream of Imo River (Rivers State) where a number of small-scale industrial activities are sited. The second station (IAS) is located in Ikot Abasi (Akwa Ibom State), where the Aluminium Smelting plant is sited. Moreover, domestic wastewaters are channeled into the water body within this area. The third station (DRN) representing the downstream region of the river was chosen far from any industrial activities. The fishes collected at each station were labeled with an identification number, the date and place of collection, before they were taken to the laboratory for analysis in ice-packed coolers, until being placed into a freezer at 4°C.

Pretreatment of Samples Collected
Samples of fishes from each location were taken to the laboratory on the same day and later dissected to remove the liver and epixial muscle on the dorsal surface of each species of fish. The livers and pieces of edible muscle tissues (8.0 g) were dried at 105°C until they reached a constant weight. Each dried sample was ground, using porcelain mortar and pestle and 0.5 g of the powdered form was separately digested using perchloric and nitric acids in a silica beaker and later evaporated to dryness on a hot plate. The white residue of each digest was dissolved in 10 mL of 20% nitric acid. The solutions were filtered into acid-washed volumetric flasks and diluted to 50 mL prior to elemental analysis. Replicates, three blanks and standards were treated similarly. Concentrations of cadmium, copper, lead and zinc were then determined using an inductively coupled plasma spectrometer (Optima 3000-Perkin Elmer).

Results and Discussion

The investigated metal levels in liver and muscle tissues were measured as mg kg-1 on a dry weight basis. Importantly, considerations will be made on the tissue elemental contents and the bioconcentrated ratio in muscle with respect to liver. However, more emphasis will be on the heavy metal concentration in the muscle because of its dietary significance. The mean concentrations recorded for copper (Cu), cadmium (Cd), lead (Pb) and zinc (Zn) in muscle and liver tissues of E. fimbriata- Bonga shad and Tilapia guineensis-Tilapia are presented in Fig. 1 and 2, respectively. As indicated in Fig. 1, zinc levels were relatively higher in both the muscle and liver tissues of E. fimbriata than other elements considered. Zinc concentrations in muscle tissues were 7.78±5.40, 11.48±0.20 and 14.00±3.12 mg kg-1 dry weight at IAS, DRN and OBG stations, respectively. On the other hand, Zn levels in the liver tissues of E. fimbriata indicated higher values with DRN, OBG and IAS stations recording concentration of 39.26±1.00, 33.00±2.41 and 26.41±3.53 mg kg-1dry weight, respectively.

Fig. 1: Tissue elemental concentration in Ethmalosa fimbriata caught from Imo river ecosystem

Fig. 2: Tissue elemental concentrations in Tilapia guineensis caught from Imo river ecosystem

The average concentrations of copper obtained at OBG, IAS and DRN stations for liver and muscle tissues of the fish species were 6.03±1.00, 4.29±1.16, 2.62±0.10 and 0.47±0.24, 0.21±0.40, 1.93 mg kg-1 dry weight, respectively. The variation of Pb and Cd levels in E. fimbriata followed the trend as Zn and Cu, which recorded higher concentrations in the liver than muscle tissue. The concentrations of Pb (0.56±0.28, 0.19±0.36, 0.09±0.24 mg kg-1 dry wt.) and Cd (0.09±0.01, 0.1±0.01, 0.02±0.01 mg kg-1 dry wt.) found in the muscle tissues at OBG, IAS and DRN stations, respectively were however lower than values obtained from the liver tissues, which were Pb: 1.06±0.02, 0.55±1.20, 1.32±0.10 mg kg-1 and Cd: 0.28±0.03, 0.40±0.01, 0.03±0.01 mg kg-1 dry wt. In general, the trend in elemental bioaccumulation in E. fimbriata in both muscle and liver tissues was Zn>Cu>Pb>Cd.

All the metals considered were detected in the target organ (liver) of Tilapia guineensis albeit at different levels and their respective mean levels at the three stations in the liver and muscle tissues were: Cd (0.26±0.24 and 0.02±0.01 mg kg-1); Zn (45.91±18.17 and 10.96±2.07 mg kg-1); Pb (0.47±0.39 and 0.59±0.19 mg kg-1) and Cu (12.30±8.93 and 1.10±0.84 mg kg-1). The concentrations of all these metals in liver tissues of Tilapia species were comparatively higher than levels obtained from the muscle tissues, with Zn displaying the highest tissue load (Fig. 2). This observation presupposes the low metal absorption potential in the muscle and moreover confirms earlier reports that target organs such as liver, gonads and gills of aquatic organisms have inherent potential to bioaccumulate heavy metals at enhanced levels compared to the muscle tissue (Abdel-Moniem et al., 1994; Arellano et al., 1999; Huang, 2003; Yilmaz, 2005). In general, muscle tissues of aquatic biota are not considered as excellent bioaccumulator of heavy metals (Kargin and Erdem, 1991; Shoham-Frider et al., 2002; Yilmaz, 2005).

However, the liver is the preferred organ for metal accumulation as could be deduced from the present study (Karadede and Unlu, 1998; Shoham-Frider et al., 2002). In both the Tilapia and Bonga shad, relatively high concentrations of Zn and Cu were found in the liver. Similar reports of preferential bioaccumulation of Zn and Cu in liver to muscle tissues of biota are available (Amundsen et al., 1997; Roditi-Elasar, 1999; Al-Yousuf et al., 2000; Yilmaz, 2003). Several researchers have documented the anomalous concentrations of essential elements especially Zn and Cu than other heavy metals in tissues of fishes (Farkas et al., 2000; Wong et al., 2001; Chou et al., 2003). Moreover, in aquatic organisms, the liver plays a prime role in the sequestration of adsorbed metal through detoxification by cysteine-rich metal binding proteins (metallothioneins), synthesized in response to changes in heavy metal balance (Langston et al., 1999).

The degree to which a metal is concentrated by a species, expressed in this study as the muscle to liver ratio (MLR) of metal concentrations was relatively higher for Pb (0.34) than Cd (0.26), Zn (0.29) and Cu (0.28) in E. fimbriata. Thus, the order of metal MLR in E. fimbriata is Pb>Zn>Cu>Cd. However, a different order was found in T. guineensis species: Cd>Pb>Zn>Cu. The MLR was higher for Cd (0.42) than Pb (0.38), Zn (0.20) and Cu (0.09). This presupposes that the rate of homeostasis of essential elements was relatively higher in E. fimbriata than T. guineensis (Chen and Chen, 2001). This is expected and the observation is supported by the higher concentration of the non-essential element, Cd in E. fimbriata which could have induced the metallothioneins to displace the essential metals (Zn, Cu) from pre-existing MTs (Riba et al., 2003). Cadmium levels in T. guineensis were lower in both muscle and liver tissues (Fig. 2).

Tissue elemental load in aquatic organisms is variable and species dependent, as well as being a function of the biota’s environment (Eja et al., 2003; Canli and Atli, 2003). However, the affiance of metal uptake from an impacted ecosystem through direct or indirect ingestion or absorption through biomembranes in food and water could differ in relation to metabolism, physiology, ecological requirements, pollution gradients of pelagic column, sediment and food as well as the prevailing temperature and salinity (Romeo et al.,1999). T. guineensis are benthopelagic species with sedentary habits. Therefore, the relatively higher tissue elemental concentrations observed when compared to E. fimbriata may be attributed to its feeding habits and the contamination gradients of the pelagic column of Imo River with respect to its sediment compartment. Benthopelagic fishes have been reported as having high levels of heavy metals derived primarily from residual toxic levels in water and sediment (Huang, 2003). More so, taking the species factor into consideration, the heavy metal difference were significant (p>0.05). In general, this study revealed that the muscle tissues of E. fimbriata indicated higher preference for the bioaccumulation of non-essential elements (Pb, Cd) than Zn and Cu. This was however in contrast to the muscle metal bioaccumulation preference indicated by T. guineensis for essential elements.


Since there are many environmental factors which have been claimed by various researchers to influence the bioaccumulation of heavy metals to toxic levels in organisms, it would be unreasonable to attribute the levels of these metals in E. fimbriata and T. guineensis to any specific factor(s). It is perhaps more rational to posit that these elemental tissue load might have been largely influenced by their feeding habits as well as the contamination gradients of the Imo River surface water and sediment. From the results, the concentrations of heavy metals in liver and muscle tissues of both species investigated did not exceed the acceptable levels proposed for human consumption (USEPA, 1995). However, the levels of Cd and Pb in the species call for serious concern because they could bioaccumulate and biopersist in their tissues over time. This study therefore highlights this potential danger (Cd- and Pb-poisoning), which could occur owing to long-term consumption of these species. Thus, precautions need to be taken in order to forestall future heavy metal pollution in the river as well as in the biota. This research is however a precursor to the holistic approach needed to fully assess the elemental contents of sediments, water and several other biota of the Imo River ecosystem.

1:  Abdel-Moniem, M., A. Khaled and M. Iskander, 1994. A study on levels of some heavy metals in El-Mex wes Alexandria, Egypt. Proceedings of the 4th Conference on Environmental Protection is a Must, May 12-15, 1994, Alexandria, Egypt, pp: 155-174.

2:  Akueshi, E.U., E. Oriegie, N. Ocheakiti and S. Okunsebor, 2003. Levels of some heavy metals in fish from mining lakes on the Jos Plateau, Nigeria. Afr. J. Nat. Sci., 6: 82-86.

3:  Al-Yousuf, M.H., M.S. El-Shahawi and S.M. Al-Ghais, 2000. Trace metals in liver, skin and muscle of Lethrinus lentjan fish species in relation to body length and sex. Sci. Total Environ., 256: 87-94.
CrossRef  |  Direct Link  |  

4:  Amundsen, P.A., F.J. Staldvik, A.A. Lukin, N.A. Kashulin, O.A. Popova and Y.S. Reshetnikov, 1997. Heavy metal contamination in freshwater fish from the border region between Norway and Russia. Sci. Total Environ., 201: 211-224.
CrossRef  |  Direct Link  |  

5:  Arellano, J.M., J.B. Ortiz, D.S. Capeta and M.L.G. Canales et al., 1999. Levels of copper, zinc, manganese and iron in two fish species from salt marshes of Cadiz Bay (Southwest Iberian Peninsula). Bol. Inst. Esp. Oceanogr., 15: 485-488.
Direct Link  |  

6:  Borovik, A.S., 1990. Characterization of Metal ions in Biological Systems. In: Heavy Metal Tolerance in Plants, Shaw, A.J. (Ed.), Evolutionary Aspects, CRC Press Inc., Florida.

7:  Canli, M. and G. Atli, 2003. The relationship between heavy metal (Cd, Cr, Cu, Fe, Pb and Zn) levels and size of six Mediterranean fish species. Environ. Poll., 121: 129-136.
PubMed  |  

8:  Chen, Y.C. and M.H. Chen, 2001. Heavy metals in nine species of fish caught in coastal waters off Ann-Ping, SW Taiwan. J. Food Drug Anal., 9: 107-114.
Direct Link  |  

9:  Chou, C., L.A. Paon, J.D. Moffat and B. Zwicker, 2003. Bioaccumulation and interrelationship of manganese and zinc in horse mussel, M. modiolus from Eastern Canada. Fish. Sci., 69: 369-374.
CrossRef  |  Direct Link  |  

10:  Eja, M.E., O.R. Ogri and G.E. Arikpo, 2003. Bioconcentration of heavy metals in surface sediments from the great Kwa river estuary, Calabar, Southeastern Nigeria. J. Nig. Environ. Soc., 1: 247-256.

11:  Ekpo, B.O. and U.J. Ibok, 1999. Temporal variation and distribution of trace metals in freshwater and fish from Calabar River, S.E. Nigeria. Environ. Geochem. Health, 21: 51-66.
CrossRef  |  Direct Link  |  

12:  Farkas, A., J. Salanki and I. Varanka, 2000. Heavy metal concentrations in fish of Lake Balaton, lakes and reservoirs. Res. Manage., 5: 271-279.
CrossRef  |  Direct Link  |  

13:  Fausch, K.D., J. Lyons, J.R. Karr and P.L. Angermeier, 1990. Fish communities as indicators of environmental degradation. Am. Fish. Symposium, 8: 123-144.

14:  Fernandez-Leborans, G. and Y. Olalla-Herrero, 2000. Toxicity and bioaccumulation of lead and cadmium in marine protozoan communities. Ecotoxicol. Environ. Saf., 49: 266-276.
CrossRef  |  Direct Link  |  

15:  Flessas, C., Y. Coulillard, B. Pinel-Alloul, L. St-Cur and P.G.C. Campbell, 2000. Metal concentrations in two freshwater gastropods (Mollusca) in the St. Lawrence River and relationship with environmental contamination. Can. J. Fish. Aquatic Sci., 57: 126-137.
CrossRef  |  Direct Link  |  

16:  Huang, W., 2003. Heavy metal contaminations in common benthic fishes caught from the coastal waters of eastern Taiwan. J. Food Drug Anal., 11: 324-330.

17:  Hossain, M.S. and Y.S.A. Khan, 2001. Trace metals in penaeid shrimp and spiny lobster from the bay of Bengal. Sci. Asia, 27: 165-168.

18:  Kalay, M. and M. Canli, 2000. Elimination of essential (Cu, Zn) and non-essential (Cd, Pb) metals fromtissues of a freshwater fish Tilapia zilli. Turk. J. Zool., 24: 429-436.
Direct Link  |  

19:  Karadede, H. and E. Unlu, 1998. Investigations of the heavy metal accumulations in Cyprinion macrostomus (Heckel, 1843) (Cyprindae) from the Ataturk Dam Lake. Proceedings of the 15th Turkish Biology Congress, September 7-14, 1998, Turkey, pp: 181-189.

20:  Kargin, F. and C. Erdem, 1991. Accumulation of copper in liver, spleen, stomach, intestine, gill and muscle of Cyprinus carpio. Doga Turk. J. Zool., 15: 305-314.

21:  Langston, W.J., G.R. Burt and N.D. Pope, 1999. Bioavailability of metals in sediments of the Dogger Bank (Central North Sea): A mesocosm study. Estuarine, Coastal Shelf Sci., 48: 519-540.
CrossRef  |  Direct Link  |  

22:  Radojevic, M. and V.N. Bashkin, 1999. Practical Environmental Analysis. 1st Edn., The Royal Society of Chemistry, UK., ISBN-13: 9780854045945, Pages: 466.

23:  Riba, I., E. Garcia-Lugue, J. Blasco and T.A. DelValls, 2003. Bioavailability of heavy metals bound to estuarine sediments as a function of pH and salinity values. Chem. Speciation Bioavailability, 15: 101-114.
CrossRef  |  Direct Link  |  

24:  Roditi-Elasar, M., 1999. Marine pollution as a morbidity factor in dolphins: Evidence from heavy metal concentrations in tissues and bones of modern dolphins found along the Mediterranean Coast of Israel and in bones of dolphins from Ancient times Israel.

25:  Romeo, M., Y. Siau, Z. Sidoumou and M. Gnassia-Barellia, 1999. Heavy metal distribution in different fish species from the Mauritania coast. Sci. Total Environ., 232: 169-175.
CrossRef  |  Direct Link  |  

26:  Shoham-Frider, E., A. Amiel, M. Roditi-Elasar and N. Kress, 2002. Risso‚Äôs dolphin (Grampus griseus) stranding on the coast of Isreal (eastern Mediterranean). Autopsy results and trace metal concentrations. Sci. Total Environ., 295: 157-166.
Direct Link  |  

27:  Teugels, G.G. and D.F.E. Thys van den Audenaerde, 1991. Tilapia. In: Checklist of the Freshwater Fishes of Africa (CLOFFA), Daget, J., J.P. Gosse, G.G. Teugels and D.F.E. Thys van den Audenaerde (Eds.). Vol. 4, ISNB, Brussels; MRAC, Tervuren, ORSTOM, Paris, pp: 482-508.

28:  Udosen, E.D., 1998. Trace metal levels in Anthropteris orientalis from battery industry environment. Global J. Pure Applied Sci., 4: 35-42.

29:  US EPA, US Environmental Protection Agency, 1995. Integrated Risk Information System. Environmental Protection Agency, Washington, DC.

30:  Van den Broek, J.L., K.S. Gledhill and D.G. Morgan, 2002. Heavy metal concentrations in the mosquito fish, Gambusia holbrooki, in the manly lagoon catchment. UTS Freshwater Ecology Report, Department of Environmental Sciences, University of Technology, Sydney, Australia, pp: 25.

31:  Whitehead, P.J.P., 1985. FAO special catalogue. Vol. 7. Clupeoid fishes of the world. FAO Fish. Synop., 125: 1-303.

32:  Whitfield, A.K., 1996. Fishes and the environmental status of South African estuaries. Fish. Manage. Ecol., 3: 45-57.
CrossRef  |  Direct Link  |  

33:  Widianarko, B., C.A.M. VanGestel, R.A. Vrerweij and N.M.V. Straaalen, 2000. Associations between trace metals in sediment, water and guppy, Poecilia reticulata (Peters), from urban streams of Semarang, Idonesia. Ecotoxicol. Environ. Saf., 45: 15-34.

34:  Wong, C.K., P.P.K. Wong and L.M. Chu, 2001. Heavy metal concentrations in marine fish collected from culture sites in Hong Kong. Arch. Environ. Contami. Toxicol., 40: 60-69.
CrossRef  |  Direct Link  |  

35:  Yilmaz, A.B., 2003. Levels of heavy metals (Fe, Cu, Ni, Cr, Pb and Zn) in tissue of Mugil cephalus and Trachurus mediterraneus form Iskenderun Bay, Turkey. Environ. Res., 92: 277-281.
Direct Link  |  

36:  Yilmaz, A.B., 2005. Comparison of heavy metal levels of grey mullet (Mugil cephalus L.) and sea bream (Sparus aurata L.) caught in Iskenderun Bay (Turkey). Turk. J. Vet. Anim. Sci., 29: 257-262.
Direct Link  |  

37:  Zyadah, M.A., 1999. Accumulation of some heavy metals in Tilapia zilli organs from lake Manzalah, Egypt. Turk. J. Zool., 23: 365-372.
Direct Link  |  

©  2021 Science Alert. All Rights Reserved