1. Introduction
Aquatic organisms have the ability to accumulate heavy metals from water column, suspended and bed sediments. Therefore, accumulation of heavy metals in aquatic organisms can pose a long lasting effect on biogeochemical cycling in the river ecosystem [1,2]. The accumulation of toxic heavy metals in the tissues of aquatic biota to hazardous levels has becomes a problem of increasing public health concern to both animals and humans. Excessive metal concentration in surface water could lead to health hazards in man, either through drinking of water and/or consumption of fish [3-6].
Among aquatic animals, fishes are widely used to evaluate the health of aquatic ecosystems because pollutants build up in the food chain and are responsible for adverse effects and consequent death [7,8]. In this study, the concentration of metals in fish (Catla catla and Labeo rohita) organs (liver gill and muscle) were used to calculate Bioaccumulation Factor (BAF).
2. Methodology
2.1. Study Area
In the present investigation river Cauvery of Karnataka stretch was chosen as study area (Figure 1). Cauvery is one of the principal river systems in Southern India, takes birth at Talacauvery (Kodagu) and ends by merges with Bangala kolli in Tamilnadu after traversing of around 800 km.
2.2. Monitoring Stations
Eight numbers of Monitoring stations, three from upstream and five from downstream to Krishnarajasagara dam were selected based on human interference, availability of fish and human consumption. The sampling stations (Figure 1) are described as fallows.
Monitoring station 1 (V1): This station is situated in Kushalnagara, 18 km from Mercara city of Coorg district. This place attracts lakhs of tourists during summer because of prevailing cold climate. The Tibatian refugee colony is located 7 km away from this station nearby place called Bayalukuppe. The river receives perceptible amount of domestic sewage at this point.
Monitoring station 2 (V2): This point is located near Rameshwara temple of Ramanathapura town, where the State Fisheries department is rearing around 18 varieties of fishes. Besides domestic activities, ash dropping is a part of ritual practice in this station.
Monitoring station 3 (V3): This station is located near railway bridge of Hampapura village. Here water is
abstracted to Krishnaraja Nagar and Krishna raja pete of Mysore district for drinking purpose. The flow rate is almost nil because of back flow triggered by Krishnaraja Sagar dam.
Monitoring station 4 (V4): It is situated 2 km down from Nimishambha temple of Srirangapatna known as Melapura in Mandya district, where the tributary Lokapavani merges with Cauvery. Srirangapatna, city of historic, religious, and cultural hub located around 13 km from Mysore. Here river is extensively used for bathing, washing, Boating and fishing. Immersion of ash is regularly witnessed.
Monitoring station 5 (V5): This point is located at Bannur bridge of Mysore District. The agricultural land, grazing field and cremation ground contribute considerable sum of pollutants into river Cauvery.
Monitoring station 6 (V6): This station is situated 1 km down from Cauvery—Kabini Sangama near Tirumakundalu Narasipura of Mysore district. Kabini River carries industrial wastes from Nanjangud industrial area to the Cauvery. Intensive sand dredging activity is in practice especially during summer. Low flow rate and nutriaent rich sediment allow luxuriant growth macrophytes.
Monitoring station 7 (V7): It is situated at Harle village, 3km from Kollegala town. Upstream to this point tributary Suvarnavathy joins Cauvery. Extensive sand mining is practiced almost throughout the year, besides agriculture and fishing activities. Water abstraction and Sewage intrusion from town are two other major anthropogenic interferences practiced with river at greater extent.
Monitoring station 8 (V8): It is located at Kanakapura Sangama nearly about 36 km from Kanakapura town, Ramanagara district, Arkavathi river confluence Cauvery at this point. Among the tributaries of river Cauvery, Arkavathi is richly contaminated with industrial and domestic sewages but the flow is restricted in summer. It is a recreational and weekend picnic spot for Bangaloreans.
2.3. Sampling, Preservation and Preparation
Fish: Fish samples of two different species (Catla catla and Labeo rohita) weighing around 750 ± 100 g were captured during March, April and May of 2010 dry season. The samples at frozen condition were transported to the laboratory on the same day and stored until dissecttion.
Prior to sample preparation fishes were thoroughly rinsed with distilled water to remove excess mucus coating, adhered particles and other adsorbed metals. Fishes were dissected to separate organs viz. liver gill and muscle according to FAO method [9]. After dissection, all the tissue samples were separately oven-dried at 105˚C ± 20˚C and cooled to constant weight in room temperature.
Water: water samples were collected separately in 100 ml polythene bottles prewashed with acidified water, deionised water and 2 ml of nitric acid was added as preservative. All the water samples were stored in insulated cooler containing ice and brought on the same day to the laboratory and maintained at 4˚C ± 2˚C until processing and analysis was over as suggested in [10].
2.4. Microwave Digestion
Fish: 1 g dry weight of the discrete regions (organ) of sample were introduced in to Teflon reaction vessel and 5 mL of 65% Nitric acid was added, the vessel was inserted into microwave chamber and subjected for digestion program as follows Step-I: 5 minute at 20% power (240 W); 1 minute at 30% power (360 W); 5 minutes at 25 % power (300 W), cooled and the digester was reopened.
Step-II: 1mL of 30% Hydrogen peroxide was added and set to 25% power 3 minutes, 50% power (600 W) for 3minutes, cooled and the digester was reopened.
Step-III: 1mL of (20%) Perchloric acid was added and power set to 50% (600 W) for 2 minutes, cooled and the digester was reopened.
The resulted sample was cooled and diluted to 100ml using deionised water.
After dilution Fe, Pb, Zn, Mn, Ni, Cu, Cr, Co and Cd contents of the tissues were measured on a Shimatzu AAS-6300, atomic absorption spectrophotometer. The sample whose metal concentration was below the detection limit in flame furnace (in ppm) was subjected to graphite furnace (in ppb) analysis.
Water: 10 ml of water samples were added to Teflon tubes/ reference vessel fallowed by 1 ml of Conc. HNO3, the vessel was closed with valve and tightened. They were inserted into a single safety shield carousel and, into the microwave chamber. The system was pre-programmed using the Ethos D control terminal (equipped with software) for 5 min of microwave digestion at 250 W power and left for automatic ventilation for 2 min. The digested solution was cooled and made up to 100 mL with Milli-Q distilled water and stored in special containers ready for analysis.
3. Results and Discussion
The metal concentration in river water, fish and bioaccumulation factor for fish tissues are given in Table 1.
Table 1. The heavy metal concentrations in fish (µg∙g−1 dry wt.), river water (µg∙l−1) with standard error and their bioaccumulation factor (BAF).
The concentration of metals in water column between eight sampling sites not differs significantly and showed higher concentration in comparison with fish tissues.
The concentration of all the analyzed metals in both the species of fish tissues were observed to be high in downstream stations. It could be due to dumped agricultural and industrial wastes to downstream region of the river through streams and tributaries at significant level. In addition to this Sand dredging activities makes metal to available for fish and other aquatic life consumption.
The liver tissue of both the species contained higher accumulation fallowed by gills and muscle tissues. The higher levels of metals in liver relative to gills and muscle may be attributed to the affinity or strong coordination of metallothionein protein with the metals [11,12].
The concentrations of metals in fish samples indicated that Catla catla seemed to be good accumulator fish species than Labeo rohita. These observations are might be due to different fish feeding habit and habitat. These results agree with that obtained by Karadede-Akin, et al. [13] and Rauf, et al. [14] in the river Tigris and Ravi respectively.
Among the analysed essential metals (Fe, Zn, Mn, Ni, Cu and Cr) Fe was found highest and Cr was least. Liver tissue of Catla catla of downstream stations were exhibited very negligible concentrations of non essential metals (Pb and Cd) and BDL was noticed in muscle. In other hand Labio rohita has not showed Pb and Cd accumulation.
The bioaccumulation factor (BAF) (Table 1) of heavy metals in different samples revealed increase trend from upstream to downstream, which can be explained on the basis of inflow of anthropogenic pollutants to the Cauvery in the downstream stretch. Also, the BAF values showed elevated trend in case of essential trace metals than nonessential metals.
BAF for fishes is in the sequence of Ni > Zn > Cu > Mn > Fe > Cr > Pb > Cd. The BAF values for different heavy metals from water to fishes or sediment to fishes are a key component of human exposure to the metal through food chain. The lowest BAF value in this study is for Cd; one of the likely reasons is being that it is more mobile in the natural environment than the other metals.
4. Conclusion
From the present study, it concluded that the metal concentrations were lower in fish tissues of both the species than water column. Fish samples of downstream stations have combatively accumulated more metals than upstream stations as metals concentration varies in water of the river stretch. This suggested that metal accumulation in fish bodies appears as site specific, corresponding with the metallic toxicity of the two aquatic components, viz., water sediment and planktons.