Subscribe Now Subscribe Today
Research Article
 

Mercury Concentration of Four Dominant Species in the Bebar Peat Swampy Forest River, Malaysia



B.Y. Kamaruzzaman, M.C. Ong and A.H. Khali
 
Facebook Twitter Digg Reddit Linkedin StumbleUpon E-mail
ABSTRACT

Muscle, stomach and gill from four dominant fish species, Mytus nemurus, Pristolepis fasciata, Ompok bimaculatus and Osteochilus hasseltii, caught from Bebar peat swamp forest river were analyzed for mercury (Hg). The concentration of Hg was measured with a fast and sensitive Flow Injector Mercury Spectrometer (FIMS). The average Hg concentration of all species caught was 0.169 μg g-1 dry weights, lower than a limit for human consumption recommended by the World Health Organization, 0.5 μg g-1 dry weights. The mean concentration of Hg was relatively high in stomach (0.28x0.12 μg g-1 dry weights) followed by gill (0.17x0.06 μg g-1 dry weights) and lowest in muscle (0.05x0.02 μg g-1 dry weights). The positive relationship of Hg with fish length and weight suggesting that the accumulation of Hg were formed in the fish.

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

 
  How to cite this article:

B.Y. Kamaruzzaman, M.C. Ong and A.H. Khali, 2007. Mercury Concentration of Four Dominant Species in the Bebar Peat Swampy Forest River, Malaysia. Pakistan Journal of Biological Sciences, 10: 1103-1107.

DOI: 10.3923/pjbs.2007.1103.1107

URL: https://scialert.net/abstract/?doi=pjbs.2007.1103.1107

INTRODUCTION

In undeveloped areas, elevated mercury concentrations in piscivorous fish have been associated with a broad combination of physical, chemical and biological features of the lakes and watersheds. Physical factors which have been shown to be linked to higher mercury concentrations in fish include wetland areas, small lake size and warmer water temperature (Miskimmin et al., 1992; Bodaly et al., 1993), while important chemical factors include high background concentrations of mercury, low p humic-stained waters and moderately high Dissolved Organic Carbon (DOC) concentrations (Lange et al., 1993; Shilts and Coker, 1995; Wescott and Kalff, 1996). Higher mercury concentrations in fish also are associated with various biological properties of the fish. Mercury, because it bioaccumulates, generally increases in concentration with fish length and age (MacCrimmon et al., 1983). It also biomagnifies and generally increases in concentration with increasing food chain length (Vander Zanden and Rasmussen, 1996).

Human activities, such as deforestation and agriculture, along with geochemistry, are associated with natural-Hg release from soil, Hg atmospheric transport and redistribution, as well as Hg methylation potential of ecosystems (Roulet et al., 1999). Mercury acquisition, accumulationand biomagnification in fish are associated with both Hg chemical form and fish feeding-behavior (Hoyle and Handy, 2005; Klinck et al., 2005). Due to its reactivity with sulfur containing amino acids, Hg is stored in fish protein matrices, rather than in fatty tissues (Harris et al., 2003). Carnivorous fish at the top of the food chain acquire large amounts of monomethylmercury that are bioaccumulated as a function of fish size (Barbosa et al., 2003).

In freshwater ecosystems, fish play a key role in the distribution of mercury between the different biotic compartments. They represent a wide variety of trophic levels, from strictly herbivorous species to carnivorous species of the third or fourth orderand occupy virtually all ecological niches (demersal, benthopelagic and pelagic species). Mercury biomagnification along the food webs, principally based on cumulative transfers of the methylated form of the metal monomethylmercury, can lead to extremely high concentrations in piscivorous species at the top of the trophic networks (Boudou and Ribeyre, 1996; Morel et al., 1998; Wiener et al., 2003) and to considerable mercury burdens in the whole fish biomass.

MATERIALS AND METHODS

Study area background: The study was located within the South East Pahang Peat Swamp Forest which situated in Pekan district area (Fig. 1). A limited extent of freshwater

Fig. 1: The study area and sampling locations at Bebar River (5 stations) and Serai River (2 stations)

The lower reaches of rivers are brackish; the swamp forest contains freshwater, presumably acidic.

Sampling: Sampling was carefully planned so that the number fish caught are sufficient and representative. In this study, 5 stations are located along Sungai Bebar and 2 stations along Sungai Serai (Fig. 1). The fish were caught with a beam trawl at 7 locations which were accessed by boat. The fish were sampled at each station over 24 h until a sufficient number of individuals, at least 5-10 fishes, were caught. The fish samples were transported to the laboratory and stored at -20°C prior to analysis. Fish samples were thawed at room temperatureand their length and weight were recorded using the callipers and 3 decimal points of measuring weight, respectively. They were dissected using stainless steel scalpels and Teflon forceps using a laminar flow bench. Biological samples such as fish, craband mollusk were separated from the body and transferred into polypropylene vials. Before acid digestion, a porcelain mortar was employed to grind and to homogenise the dry tissue samples.

Hg analysis: The fish samples were digested according to the methods (Hirokatsu et al., 2000) with some modifications. A Flow Injector Mercury Spectrometer (FIMS) was used for the quick and precise determinations of Hg in the digested samples. Briefly, the digestion method involved the heating of 50 mg of sample in a sealed teflon vessel with mixed concentrated acids of HNO3 and HClO4 H2SO4 and H2O2. The teflon vessels were kept at 90°C for 45 min. After cooling, a mixed solution of SnCl2 was added. The content of the vessel was thoroughly transferred into a 10 mL polypropylene test tube and was diluted to 10 mL with deionized water. A clear solution with no residue should be obtained at this stage. The precision assessed by replicate analyses was within 3%.

RESULTS AND DISCUSSION

A total of 20 fishes were analyzed for Hg concentration with a mean size from 94 to 383 mm. Two species dominantly caught were two-spotted glass catfish (Ompok bimaculatus) and long whisker catfish (Mytus nemurus). Other species caught were banded leaf (Pristolepis fasciata) and hard-lipped barp (Osteochilus hasseltii). The biggest fish caught was the Mytus nemurus (383 mm) and the smallest fish was Pristolepis fasciata (94 mm).

Table 1 shows the concentration of Hg in fish at Bebar peat swamp forest river. In this study, a bigger fish like Mytus nemurus and Ompok bimaculatus had higher concentrations of Hg, compared to smaller fishes such as Pristolepis fasciata and Osteochilus hasseltii. Average concentration of Hg in Mytus nemurus was 0.28x0.02 μg g-1 dry weights, ranged from 0.26 to 0.29 μg g-1 dry weights and Ompok bimaculatus ranging from 0.08 to 0.27 μg g-1 dry weights with average 0.18x0.06 μg g-1 dry weights. For small fishes, Pristolepis fasciata, the average concentration was 0.09x0.02 μg g-1 dry weights, ranged from 0.07 to 0.11 μg g-1 dry weights and Osteochilus hasseltii has Hg concentration of 0.07 μg g-1 dry weights. Averaging across species, the mean Hg concentration in the study area was comparable to the concentration obtained in other studies elsewhere in Malaysia (Table 2).

The mean concentration of Hg was relatively high in fish stomach (0.28x0.13 μg g-1 dry weights, ranged from 0.01 to 0.17 μg g-1 dry weights) followed by gill (0.17x0.10 μg g-1 dry weights, ranged from 0.05 to 0.42 μg g-1 dry weights) and lowest in muscle (0.05x0.05 μg g-1 dry weights, ranged from 0.09 to 0.52 μg g-1 dry weights).

Table 1: Concentration of Hg in fish at Bebar peat swamp forest river

Table 2: The comparison of previous study to the current study in Bebar river

In this study, it is interesting to note that the mean Hg concentrations in all fish species behave in a similar way in the examined tissues. It appears that the mean concentrations were high in stomach followed by gill and muscle tissue. The higher Hg concentration in fish is due to their dietary habits, where species like Ompok bimaculatus and Mytus nemurus, represented by bottom sediments and predatory behaviour. Hg is known to be easily accumulated in aquatic organisms of marine, fluvial and lacustral ecosystem (Porcela et al., 1995).

The well relationship formed between the Hg concentration and the fish size suggesting that Hg bioaccumulation has occurred and many results for different species in other studies indicating the occurrence of bioaccumulation (Marcovecchio et al., 1986). In this study, a statistically significant correlation was also observed between metal concentrations in fish with the length of the fish (Fig. 2).

Fig. 2: Relationship of Hg concentrations in muscle, gill and stomach versus length of fish caught in the study area

In the fish muscle, the correlation between length and Hg concentration in gill was not significant (r = 0.1629), probably of the low Hg concentration found in gill. But on contrary, the correlation of the Hg concentration in muscle and stomach were fairly significantly with r = 0.5775 and r = 0.4149, respectively.

Health Canada’s guideline for total methyl Hg content in most fishes both marine and freshwater fish that can be consume be human is 0.5 μg g-1 dry weights. However in many other countries like United States and the ASEAN countries, the limits set for total Hg content is slightly higher of about 1.0 μg g-1 dry weights. In this study, this observation suggests that the average methyl Hg content 0.17x0.07 μg g-1 dry weights (ranged 0.07 to 0.29 μg g-1 dry weights) in most fish in the peat swamp forest river are lower compared to the limit for human consumption recommended by the World Health Organization, 0.5 μg g-1 dry weights (WHO, 1972).

ACKNOWLEDGMENTS

This research was conducted with joint funding from the Research Fundamental funding and UNDP/GEF Funded Grant. The authors wish to express their gratitude to Pahang Forestry Department staff and KUSTEM Netloft teams for their invaluable assistance and hospitality throughout the sampling period.

REFERENCES
1:  Agusa, T., T. Kunito, G. Yasunaga, H. Iwata, A. Subramaniam, A. Ismail and S. Tanabe, 2005. Concentration of trace elements in marine fish and its risk assessment in Malaysia. Mar. Poll. Bull., 51: 896-911.
Direct Link  |  

2:  Barbosa, A.C., J. Souza, J.G. Dorea, W.F. Jardim and P.S. Fadini, 2003. . Mercury biomagnification in a tropical black water, Rio Negro, Brazil. Arch. Environ. Contam. Toxicol., 45: 235-246.
Direct Link  |  

3:  Bodaly, R.A., J.W.M. Rudd, R.J.P. Fudge and C.A. Kelly, 1993. Mercury concentrations in fish related to size of remote Canadian Shield lakes. Can. J. Fish Aqua. Sci., 50: 980-987.
Direct Link  |  

4:  Boudou, A. and F. Ribeyre, 1996. Mercury in the Food Webs: Accumulation and Transfer Mechanisms. In: Mercury and its Effects on Environment and Biology, Sigel, H. and A. Sigel, (Eds.). Marcel Dekker, New York, pp: 289-319.

5:  Harris, H.H., I.J. Pickering and G.N. George, 2003. The chemical form of mercury in fish. Science, 301: 1203-1203.
Direct Link  |  

6:  Hirokatsu, A., E.S. Castillo, N. Cortes-Maramba, A.T. Francisco-Rivera and D.T. Teresa, 2000. Health assessment for mercury exposure among schoolchildren residing near a gold processing and refining plant in Apokon, Tagum, Davao del Norte, Philippines. Sci. Total Environ., 259: 31-43.
Direct Link  |  

7:  Hoyle, I. and R.D. Handy, 2005. Dose-dependent inorganic mercury absorption by isolated perfused intestine of rainbow trout, Oncorhynchus mykiss, involves both amiloride-sensitive and energy-dependent pathways. Aqua. Toxicol., 72: 147-159.
Direct Link  |  

8:  Klinck, J., M. Dunbar, S. Brown, J. Nichols, A. Winter, C. Hughes and R.C. Playle, 2005. Influence of water chemistry and natural organic matter on active and passive uptake of inorganic mercury by gills of rainbow trout (Oncorhynchus mykiss). Aqua. Toxicol., 72: 161-175.
Direct Link  |  

9:  Lange, T.R., H.E. Royals and L.L Connor, 1993. Influence of water chemistry on mercury concentration in large mouth bass from Florida lakes. Trans. Am. Fish Soc., 122: 74-84.
Direct Link  |  

10:  MacCrimmon, H.R., C.D. Wren and B.L. Gots, 1983. Mercury update by lake trout, Salvelinus namaycush, relative to age, growth and diet in Tadenac Lake with comparative data from other Precambrian Shield lakes. Can. J. Fish Aqua. Sci., 40: 114-120.

11:  Marcovecchio, J.E., V.J. Moreno and A. Perez, 1986. . Bio-magnification of total mercury in Bahia Blanca estuary shark. Mar. Pollut. Bull., 17: 276-278.

12:  Miskimmin, B.M., J.W.M. Rudd and C.A. Kelly, 1992. Influence of dissolved organic carbon, pH and microbial respiration rates on mercury methylation and demethylation in lake water. Can. J. Fish Aqua. Sci., 49: 17-22.
Direct Link  |  

13:  Morel, F.M.M., A.M.L. Kraepiel and M. Amyot, 1998. The chemical cycle and bioaccumulation of mercury. Annu. Rev. Ecol. Sys., 29: 543-566.
Direct Link  |  

14:  Porcela, D.B., J.W. Huckabee and B. Wheatly, 1995. Mercury as a Global Pollutant. Kluwer Academic Publishers, Dordrecht, The Netherlands.

15:  Roulet, M., M. Lucotte, N. Farella, G. Serique and H. Coelho et al., 1999. Effects of recent human colonization on the presence of mercury in Amazonian ecosystems. Water Air Soil Pollut., 112: 297-313.
Direct Link  |  

16:  Shilts, W.W. and W.B. Coker, 1995. Mercury anomalies in lake water and in commercially harvested fish, Kaminak Lake area, district of Keewatin, Canada. Water Air Soil Pollut., 80: 881-884.
Direct Link  |  

17:  Vander-Zanden, M.J. and J.B. Rasmussen, 1996. A trophic position model of pelagic food webs: Impact on contaminant bioaccumulation in lake trout. Ecol. Monograph, 66: 451-477.
Direct Link  |  

18:  Wescott, K.A. and J. Kalff, 1996. Environmental factors affecting methyl mercury accumulation in zooplankton. Can. J. Fish Aquatic Sci., 53: 2221-2228.
Direct Link  |  

19:  WHO, 1972. Mercury: Environmental Health Criteria. World Health Organization, Geneva.

20:  Wiener, J., D. Krabbenhoft, G. Heinz and A. Scheuhammer, 2003. Ecotoxicology of Mercury. In: Handbook of Ecotoxicology, Hoffman, D.J., B.A. Rattner, G.A. Jr. Burton and J. Jr. Cairns (Eds.). Lewis Publishers, Boca Raton, FL., USA., pp: 409-463.

©  2021 Science Alert. All Rights Reserved