Journal of Earth and Environmental Sciences

Bioaccumulation of Heavy Metals in Fish Species from the Meiliang Bay, Taihu Lake, China

Xiaoyu Li1*, Sivakumar Rajeshkumar2, Bangjun Zhang3, Chune Zhou4

1Department of Limnology, College of Life Science, Henan Normal University, Henan, China

2Department of Molecular Biology and Biochemistry, College of Life Science, Henan Normal University, Henan, China

3Department of Toxicology and Ecology, College of Life Science, Henan Normal University, Henan, China

4Department of Biopolymers College of Life Sciences, Henan Normal University, Henan, China

*Corresponding author: Xiaoyu Li, College of Life Science, Henan Normal University, Henan, China. Tel: +863733329390; Email: lixiaoyu65@263.net

Received Date: 09 July, 2017; Accepted Date: 24 August, 2017; Published Date: 04 September, 2017

Citation: Li X, Rajeshkumar S, Zhang B, Zhou C (2017) Bioaccumulation of Heavy Metals in Fish Species from the Meiliang Bay, Taihu Lake, China. J Earth Environ Sci: JEES-124. DOI: 10.29011/2577-0640.100024


 1.      Abstract

The bioaccumulation of Cr, Cu, Cd, Pb contents were determined in Cyprinus carpio Linnaeus and Pelteobagrus fluvidraco, which were caught from the Meiliang Bay, Taihu Lake, a large, shallow and eutrophic lake of China. The results showed that the Cr, Cu, Cd and Pb contents in the edible parts of the two-fish species were much lower than Chinese Food Health Criterion [1]. The results showed marked differences in the four analyzed metal contents between the two species and organs as well as significant variations. Pb contents were the highest in the liver of fish, Cd contents were almost the same in all organs of fish, Cr contents mainly enriched in the kidney and liver, Cu contents were the highest in gills, the total metal bioaccumulation was the greatest in the liver and gills and the lowest in the muscle. Although the total accumulation was the highest in P. fluvidraco. This investigation indicated that fish products in Taihu Lake were still safe for human consumption, but the amount consumed should be controlled under the Chinese Food Health Criterion to avoid excessive intake of Pb.

2.      Keywords: Bioaccumulation; Cyprinus carpio; Heavy metal; Pelteobagrus fluvidraco; Taihu Lake


    Introduction

In the recent years, world consumption of fish has increased simultaneously with the growing concern of their nutritional and therapeutic benefits. In addition to its important source of protein, fish typically have rich contents of essential minerals, vitamins and unsaturated fatty acids [2]. The American Heart Association recommended eating fish at least twice per week in order to reach the daily intake of omega-3 fatty acids [3].

The concentrations of heavy metals in fish have been extensively studied over the past several decades. Research has shown that extent of accumulation of heavy metals in fish is dependent on the metal types, fish species, and the tissues respectively [4,5]. Water chemistry [6] directly affects the accumulation of heavy metal in fish. Sediment is also know to an important factor heavy metal accumulation in fish, as it is considered as the major source of contaminants for bottom dwelling and bottom feeding aquatic organisms [7], which in turn represents the concentrated source of metals in the diet of fish.

Fish is an important part of the human diet because of its high nutritional quality [8]. However, nonessential trace elements in the edible tissues of fish have been detected due to be bioaccumulation in organism and the highly persistent and non-biodegradable properties [9,10]. However, fish are relatively situated at the top of the aquatic food chain; therefore, they normally can accumulate heavy metals from food, water and sediments [11,12]. The content of toxic heavy metals in fish can counteract their beneficial effects; several adverse effects of heavy metals to human health have been known for long time [13]. This may include serious threats like renal failure, liver damage, cardiovascular diseases and even death [14,15]. Therefore, many international monitoring programs have been established in order to assess the quality of fish for human consumption and to monitor the health of the aquatic ecosystem [16]. According to the literatures, metal bioaccumulation by fish and subsequent distribution in organs is greatly inter-specific. In addition, many factors can influence metal uptake like sex, age, size, reproductive cycle, swimming patterns, feeding behavior and living environment (i.e., geographical location) [12,17,18]. Hence, fishes are considered as one of the best indicator of heavy metal contamination in coastal environment [19,20].

Taihu Lake is the third largest freshwater lake China, is located in the Yangtze delta plain on the border of the Jiangsu and Zhejiang provinces of eastern China. It plays an important role in flood control, water supply, and fisheries [21]. Rapid industrial and economic development has occurred around the lake since the 1980s. Yuan et al [22] reported that Taihu Lake was moderately polluted by heavy elements based on their study of sediments whereas increased nutrient inputs related to population and economic growth have led to eutrophication. Most pollutants come from rivers discharging into Meiliang Bay and other parts of the Taihu Lake [23]. The northern and western parts of Taihu Lake are often covered by algae blooms in summer, autumn and even spring [24]. A lot of researches have been carried on the pollution of Taihu Lake and its catchment [25-31], but most of them consider the issue of sediment pollution. J Zhong et al. [32] observed that denitrification in the sediment of Meiliang Bay, Taihu Lake. However, earlier studies in Taihu Lake            recorded on the levels of contamination of heavy metal concentrations, especially chromium, copper and lead [32-35].

The average concentration of chromium in water samples during summer was 0.35μg/L and in winter was 2.84μg/L. Copper concentration in water samples was 0.71μg/L in both the seasons. The average concentration of lead in sediments during summer was 0.58μg/g and in winter it was 8.53μg/g. Since, the study area is being considered as an important source for fishery, the presence of toxic heavy metals in water and sediments would be the primary source for the biomagnifications of metals in fish, invertebrates and other aquatic plants animals and cause ill effects to those who consume the contaminated fish [34,36]. The primary goal of this study was to determine the bioaccumulation and seasonal variation of four heavy metals, including Cr, Cd, Cu and Pb in the fish species Cyprinus carpio Linnaeus and Pelteobagrus fluvidraco collected from Meiliang Bay, Lake Taihu. We choose Meiliang Bay as research object, this could help us understand enrichment behavior of heavy metals in shallow lake ecosystems and emphasize the need to discard the most polluted tissues of the fish.

4.      Materials and Methods

4.1.  Site description

We selected seven sampling sites within Meiliang Bay located in northern and western parts of Taihu Lake (Figure 1). The Lake Taihu is the third largest fresh water lake in China and located between 30º 05՜-32º 08՜ N and between 119º 08՜ - 121º 55՜ E, downstream of the Yangtze River. It is 68.5 km long and 56 km wide, with an average depth of 2.0 m and an area of 2388 km2 [37,38]. The drainage basin of the lake is about 36500 km2, and more than 200 brooks, canals and rivers are connected with the lake [39].

The industry and agriculture in the Taihu Basin provide 14 % of China’s gross domestic product [40]. In the northern region as well as in several river mouths (at Xia Jiang), another agricultural wastewater capacity of 100 Million Liters Per Day (MLD). Tourist activities and fishing by local fishermen are significant part of the economy for the local coastal inhabitants, Xihui park, a world-famous tourist spot located in the west of Wuxi, attracts tourists not only from China but also from different parts of the globe adds its own stress on the ecosystem. Inputs from the river mouth to the lake are the routes of urban waste to this coastal environment.

4.2.  Field sampling

We conducted ten samples of each fish (C. carpio and P. fluvidraco) the size of fish we selected was 17-21 cm for all species were collected at each sampling sites during two seasons summer (June) and winter (December) by professional fishermen using a multifilament, nylongill net and trawl from inside the Meiliang Bay, Taihu Lake during 2016, according to the National field Manual for the Specification for Freshwater Monitoring in China. Samples were washed with clean water at the point of collection, separated by species, placed on ice, brought to the laboratory on the same day and then frozen at -20 ºC until dissection.

4.3.  Biot

Frozen fish samples were thawed at room temperature and dissected using stainless steel scalpels. One gram of accurately weighed epaxial muscle on the dorsal surface of the fish, the entire liver, kidney and intestine and two gill racers from each sample were dissected for analysis. Dissected samples were transferred to Teflon beaker were performed in an acid digestion to prepare the sample for heavy metal analysis (Kenstar closed vessel microwave were digested with 5 mL of nitric acid (65%) and after complete digestion the samples were cooled to room temperature and diluted to 25 mL with double distilled water. All the digested samples were analyzed three times for metals such as Cd, Cr, Cu and Pb using Atomic Absorption Spectrophotometer (AAS ZEEnit-700P) and the instrument was calibrated with standard solutions prepared from commercially available chemicals Merck, Germany [41].

4.4.  Statistical analysis

In the present study, Correlation analysis data were generated separately for two fish species (C. carpio and P. fluvidraco). The correlation of this different elements are calculated using the different values (p<0.05) for different organs for two fish samples. All the statistical analysis has done using SPSS software (version 20).

5.      Result and Discussion

The heavy metal concentration in fish is important both with respect   to nature management and human consumption. The present study documents bioaccumulation heavy metals in two fish species from Meiliang Bay, Lake Taihu. However, the concentrations may be raised in coastal ecosystems due to the release of industrial waste agricultural and mining activities. As a result, aquatic organisms were exposed to elevated levels of heavy metals [42]. The aquatic organisms exposed to heavy metals from the run-off water tend to accumulated it in their body but fishes are more commonly affected than other species [43,44].

Copper are recognized as essential elements, required by a wide variety of enzymes and other cell components having vital functions in all living things. But excessive Cu intake will damage human health. Excessive Cu intake will cause poisoning, nausea, acute stomach pains, diarrhea and fever, etc. The National Research Council has listed the estimated safe and adequate daily intake of Cu for adults as 1.5-3.0 mg. Pb is a neurotoxin that causes behavioral deficits in vertebrates, decreases in survival and growth rates, causes learning disabilities, and metabolism.

The World Health Organization has recommended that dietary Pb should not exceed 0.3 μg/g (wet weight basis), and with a recommended limit of 450 μg of Pb per day for adults. Cd is not an essential element, and the World Health Organization/Food and Agricultural Organization (WHO/FAO) has determined a maximum tolerable daily intake of 55 μg/(person d). The estimated safe and adequate daily dietary intake of Cr is set at 50-200 μg/d.

In the present study, the level of the Cd, Cr, Cu and Pb bioaccumulation in kidney, liver, gill, intestine and muscle of C. carpio and P. fluvidraco was determined during summer and winter seasons and summarized in (Table 1). In general, the bioaccumulation of heavy metals in different organs shows difference with respect to their capacity. In C. carpio, mean Cd (0.173       μg/g),      Cr            (0.118 μg/g), Cu                          (0.336     μg/g)       and         Pb           (0.636    μg/g)       concentrations appeared considerably higher in gills than in other tissues during summer. During winter, mean concentration of Cd (0.22 μg/g), Cu (0.144 μg/g), Pb (0.496 μg/g) and Cr (0.112 μg/g), was higher in kidney and gills of C. carpio. Whereas, in Pfluvidraco mean Cd (0.053 μg/g), Cr (0.316 μg/g), Cu (0.093 μg/g) and Pb (0.76 μg/g) concentrations were higher in liver and kidney during summer. During winter, the mean concentration of Cd (0.23 μg/g), Cr (0.216 μg/g), Cu (0.06 μg/g) and Pb (0.502 μg/g) concentrations appear considerably higher in gills and liver than in other tissues. Based on the mean concentration of heavy metals analyzed during summer season in various organs of C. carpio the sequence seems to be as follows: liver, Pb>Cu>Cr>Cd; kidney,      Pb>Cu>Cd>Cr;    gill,          Pb>Cr>Cu>Cd; intestine, Pb>Cu>Cr>Cd and muscle Pb>Cu>Cr>Cd respectively. Mean concentration of metals in the liver, kidney, gill, intestine and muscle of     C. carpio during winter       indicates                the                                following sequence              Pb>Cu>Cd>Cr; Pb>Cu>Cr>Cd; Pb>Cr>Cu>Cd;Pb>Cu>Cd>Cr and Pb>Cu> Cd>Cr respectively. The distribution of Pb, Cu and Cr in C. carpio during summer and winter is of the following order gill> kidney> intestine>liver>muscle, while the concentration of Cd indicates the sequence of kidney>gill>muscle>liver>intestine during summer and kidney>gill>intestine>liver>muscle during winter seasons. The Mean concentration in the liver, kidney, gill, intestine and muscle of P. fluvidraco is of the following sequence Pb>Cr>Cu>Cd; Pb>Cr>Cd>Cu; Pb>Cr>Cu>Cd; Pb>Cr>Cd>Cu and Pb>Cr>Cu>Cd during summer. However, during winter the sequence of mean concentration in liver was Pb>Cr>Cu>Cd, Pb>Cr>Cu>Cd in kidney, Pb>Cr>Cu>Cd in gill, intestine and Pb>Cr> Cu>Cd in muscle. The distribution of metals in P. fluvidraco during summer is in the following order: liver>kidney>gill> intestine> muscle for Cu and Pb, and liver>kidney>gill> intestine>muscle for Cr and Cd. However, during winter the sequence of distribution of metals was liver>kidney >gill>muscle>intestine for Cd and for Cr, Cu and Pb the sequence was liver>kidney>gill> intestine>muscle. In general, the concentration of heavy metals was lower in the muscle tissues compared to other organs (liver, kidney, gill and intestine) of both P. fluvidraco and C. carpio. Similar results have been reported in Cyprinus carpio and Acanthobrama marmid species [35,45,46].

Chromium is an essential heavy metal because metal amount of trivalent Cr (III) plays an essential role of Cu and Cr may have toxic effects for humans. Lead is an environmental contaminant that can cause serious damage to human health. It competes with calcium (Ca2+) at enzymatic locations in organisms. The mail exposure route of non-occupationally exposed individuals is food consumption [47]. Like Pb, Cd is also a non-essential element that competes with calcium (Ca2+) at enzymatic locations in organisms. Excessive Cd exposure may give rise to renal-, pulmonary-, hepatic-, skeletal-, and reproductive toxicity effects and cancer. However, the metal concentration in muscle tissue is important because it is the chief edible part of the fish. The mean concentration of heavy metals levels in two fish samples found in our study were lower than the maximum permitted concentrations proposed by Chinese Food Health Criterion [1].

The high concentration of metals in the gills of P. fluvidraco and C. carpio is due to the metals complication with the mucus, which is difficult to be removed completely from the tissue before the analysis. The concentration of metals in the gill reflects the level of the metals in the waters where the fish live, whereas the concentration in liver and kidney represents storage of metals [48,49]. Thus, the gills in fish are more often recommended as environmental indicator organs of water pollution than any other fish organs. Differences in the levels of heavy metal concentrations were observed between the P. fluvidraco and C. carpio indicating higher concentration of heavy metals in all organs of P. fluvidraco (except in the liver and kidney of C. carpio). In liver, higher concentrations of Pb were recorded in P. fluvidraco (0.76 μg/g) than in C. carpio (0.63 μg/g). The increased metal bioaccumulation (Cu, Cr, Cd and Pb) in the different tissue of two fish significantly different for during summer and winter season and it is shown in (Figure 2). The variation in the level of heavy metals among different species depends upon its feeding habit, age, size and length of the fish and their habitats [50,51].

The levels of heavy metal in fish also vary with respect to species and different aquatic environments [52]. Moreover, the affinity for metal absorption from contaminated water and food may differ in relation to ecological needs, metabolism and the contamination gradients of water, food and sediment, as well as other factors such as salinity, temperature and interacting agents [48]. The results of the present study illustrate the accumulation patterns of heavy metals in different parts of C. carpio and P. fluvidraco in Taihu Lake. Person’s Correlation (PC) matrix for analyzed to compare the total heavy metal accumulation levels in two fish tissues results are presented in (Table 2). The heavy metals in P.

fluvidraco muscle, Cu and Pb concentrations were higher than those observed in C. carpio. Cd, Cr and Cu concentrations were higher in gill and kidney of P. fluvidraco respectively than the C. carpio. A large number of studies [53,54] have shown that the bioaccumulation of heavy metal in fish muscle is significantly correlated with fish species. The results observed in this study were in good agreement with the above consensus.

Bioaccumulation was prone to be strongest in carnivorous species (P. fulvidraco), followed by omnivorous (C. carpio) species, and it tended to be stronger in bottom-living fish than that in pelagic fish.

In conclusion, significant differences were identified among muscle, gill, liver, kidney, and intestine of the fish (P. fluvidraco and C. carpio) in view of the bioaccumulation of the selected heavy metals from Taihu Lake. The concentration of metals like Cu, Cr, Cd and Pb were found to be higher during summer than the winter season. The seasonal variation of metals in the fish species might be due to physicochemical and biotic factors of the lake, which influences the bioavailability of metals. The heavy metals concentration found in edible parts of two commonly available fish are not heavily burdened with metals. The concentrations are below the limited value prescribed by Chinese Food Health Criterion [1] and also compared with other ecosystems shown in (Table 3). However, high level of heavy metals was found in liver, kidney and gill and even though fish livers and gill are seldom consumed, it may represent good bio- monitor of metals present in the surrounding environment. The results of this study demonstrate that the remediation efforts to reduce metal contamination of Taihu Lake have reduced the bioaccumulation of heavy metals in fish species this lake and also the potential health hazards associated with their consumption.

6.      Acknowledgments 

The study is supported by the National Natural Science Foundation of China (No. 31472285), the Innovation Scientists and Technicians Troop Construction Projects of Henan Province, China (No. 164200510001), and the Key Subjects of Biology in Henan Province, China.


Figure 1: Categories of sampling sites based on pollution sources from different land use types in the Meiliang Bay, Taihu Lake, China.



Figure 2: Concentrations of toxic metals (Cu, Cr, Cd and Pb) in Cyprinus carpio and Pelteobagrus fluvidraco during summer and winter seasons. Hypothesis testing method including one-way Analysis of Variance (ANOVA) followed by Least Different (LSD). Values are statistically significant at p<0.05. Values that do not share the same superscript letter (a-d) are significantly different. 

 

Sampling sites

Land use type

S1 - Tuo shan

North outer bay were believed to be affected by intense levels of anthropogenic activity.

S2 - Mei liang hu

Were located in the central area of the lake and the reservoirs

S3- Sha zhu nan

Drinking water resource area free of nearby factories and other pollution sources.

S4- Xiao wan li

North of bay (former drinking water resource, now stop).

S5- Ma shan shui chang

West of bay (former drinking water resource, now stop).

S6- Long tou zhu

North of bay usually suffer heavy blooms in summer.

S7- Wu tang men

North of bay where there is less anthropogenic pollution coming from the surrounding land.

   
 

 

Summer

 

Winter

 

Cd

Cu

Cr

Pb

Cd

Cu

Cr

Pb

C. carpio

               

Muscle

0.042 ±0.001

0.037±0.002

0.083±0.001

0.087±0.003

0.023±0.001

0.097±0.002

0.092±0.001

0.066 ±0.003

Gill

0.173±0.041

0.338±0.000

0.118±0.003

0.636±0.038

0.123±0.004

0.144±0.001

0.112±0.003

0.496 ±0.038

Liver

0.031±0.004

0.06±0.001

0.037±0.001

0.067±0.002

0.023±0.004

0.028±0.001

0.046±0.001

0.042 ±0.002

Kidney

0.24±0.016

0.076±0.00

0.042±0.001

0.4±0.023

0.22±0.016

0.51±0.001

0.033±0.001

0.23±0.023

Intestine

0.035±0.002

0.078±0.015

0.085±0.002

0.048±0.007

0.026±0.001

0.058±0.015

0.028±0.002

0.028 ±0.003

P.

fulvidraco

               

Muscle

0.028±0.001

0.034±0.001

0.048±0.001

0.052±0.002

0.023±0.00

0.036±0.005

0.032±0.002

0.036 ±0.032

Gill

0.022±0.001

0.028±0.002

0.168±0.002

0.182±0.021

0.012±0.001

0.017±0.041

0.157±0.026

0.138 ±0.005

Liver

0.025±0.014

0.093±0.001

0.316±0.002

0.706±0.056

0.23±0.003

0.055±0.001

0.216±0.001

0.502 ±0.003

Kidney

0.053±0.016

0.09±0.001

0.253±0.002

0.76±0.056

0.023±0.003

0.06±0.001

0.212±0.028

0.21 ±0.023

Intestine

0.06±0.012

0.01±0.015

0.133±0.002

0.483±0.037

0.05±0.012

0.03±0.019

0.113±0.012

0.323 ±0.037

Data are presented as the mean (average of ten samples) value ±SD in wet weight.

 

Table1: Contents (µg/g) of heavy metals in different organs of fish during summer and winter seasons.

 

 

 

Cd

Cr

Cu

Pb

Muscle (n = 20) (p <0.05)

 

 

 

Cd

1

 

 

 

Cr

0.17

1

 

 

Cu

-0.07ns

0.78

1

 

Pb

-0.04ns

0.51

0.62

1

Gill (n = 20) (p <0.05)

 

 

 

Cd

1

 

 

 

Cr

-0.11ns

1

 

 

Cu

-0.11ns

0.95

1

 

Pb

-0.61ns

0.06

0.23

1

Liver (n = 20) (p <0.05)

 

 

 

Cd

1

 

 

 

Cr

0.52

1

 

 

Cu

0.44

0.42

1

 

Pb

0.99

0.56

0.52

1

Kidney (n = 20) (p <0.05)

 

 

 

Cd

1

 

 

 

Cr

0.87

1

 

 

Cu

0.62

0.65

1

 

Pb

0.99

0.84

0.61

1

Intestine (n = 20) (p <0.05)

 

 

 

Cd

1

 

 

 

Cr

0.69

1

 

 

Cu

0.57

0.93

1

 

Pb

0.96

0.52

0.36

1

p < 0.05; ns: not significant at significance level 0.05 (2-tailed).

 

                                       

Table 2: Correlation between Contents in tissues of two fish heavy metals from Taihu Lake, China.

 

 

 

Sample

 

Description

 

Cu

Cd

Cr

Pb

Reference

 

 

1

Taihu Lake fish samples

Muscle

0.21

0.12

0.34

0.61

Present study

 

 

Gill

0.24

0.12

0.16

0.49

Present study

 

 

Liver

1.45

0.12

0.35

0.6

Present study

 

 

Kidney

0.36

0.15

0.07

0.52

Present study

 

 

Intestine

0.44

0.14

0.15

0.45

Present study

 

 

2

Shahpura Lake, Bhopal

Muscle

-

BDL

0.33 mg/kg

6 mg/kg

[55]

 

 

3

Kolleru Lake, Kerala

Muscle

-

0.11

11

1.84

[56]

 

 

Liver

-

0.22

19

2.98

[56]

 

 

Gill

-

0.37

30

3.77

[56]

 

 

4

Pulicat Lake, India

Muscle

-

0.02

0.02

0.6

[57]

 

 

Gill

-

0.5

0.2

1.1

[57]

 

 

Liver

-

0.5

0.3

1.6

[57]

 

 

Kidney

-

-

-

-

[57]

 

 

Intestine

-

0.4

0.2

0.9

[57]

 

 

5

Dhanmondi Lake, Bangladesh

Muscle

-

-

-

2.08

[58]

 

 

6

Bedirkale Tokat, Turkey

Total

-

-

1.3

1.1

[59]

 

 

7

Akin Tokat, Turkey

Total

-

-

0.85

1.95

[59]

 

 

Kidney

 

 

 

 

 

 

 

 

Intestine

 

 

 

 

 

 

 

8

Taihu Lake, China

(total 4 fish

 

0.003-

ND-0.387

0.177-0.287

[33]

 

 

species)

 

0.021

 

 

9

Taihu Lake, China

(total 8 fish

 

0.01-0.07

0.06-0.18

0.08-0.43

[34]

 

 

species)

 

 

 

 

 

 

 

 

Permissible limit in fishes

 

 

 

 

 

 

 

 

 

FAO (1983)1

 

-

2

1

01-Jun

 

 

 

 

WHO (1985)2

 

3

-

0.15

2

 

 

 

 

EU (2001) 3

 

1

-

1

-

 

 

 

 

FEPA (2003)4

 

1.3

-

0.15

2

 

 

 

 

 

 

 

 

 

 

 

 

 

 

EU (2008) 3

 

0.5-1

0.5-1

0.5

-

 

 

 

 

CFH (1994) 5

 

 50 mg/kg

0.1 mg/kg

2.0 mg/kg

0.5 mg/kg

Criterion

 

1. Food and Agriculture Organization of the United Nations [60]

3. European Union [61,62].

2. World Health Organization

 

4. Federal Environmental Protection

Agency [63]

5. Chinese Food Health Criterion [1]

 

Table 3: Comparison of metal content in fish samples (µg/g) observed by different authors and other toxicology values.

 

 

1.       Chinese Food Health Griteria 1994. GB 15201-94 for Cd, GB 15199-94 for Cu, GB 14935-94 for Pb and GB 13106-91 for Zn[S]. Minstry of Health of People’s Republic of China.

2.       Medeiros RJ, dos Santos LM, Freire AS, Santelli RE, Braga AMCB, et al. (2012) Determination of inorganic trace elements in edible marine fish from Rio de Janeiro State Brazil. Food Chemistry 23: 535-541.

3.       Kris-Etherton P, Harris W, Appel L (2002) Fish consumption, fish oil, omega-3 fatty acids, and cardiovascular disease. Circulation 106: 2747-2757.

4.       Korkmaz Gorur F, Keser R, Akcay N, Dizman S (2012) Radioactivity and heavy metal concentrations of some commercial fish species consumed in the Black Sea Region of Turkey. Chemosphere 87: 356-361.

5.       Petrovic Z, Teodrorovic V, Dimitrijevic M, Borozan S, Beukovic M, et al. (2013 Environmental Cd and Zn concentration in liver and kidney of erupean hare from different Serbian region: age and tissue difference. Bull. Environ Contamin Toxicol 90: 203-207.

6.       Driscoll CT, Yan C, Schofield CL, Munson R, Holsapple J (1994) The mercury cycle and fish in the Adirondack Lake. Environ Sci Technol 28: 136-143.

  1. Farag AM, Woodward DF, Goldstein JN, Brumbaugh W, Meyer JS (1998) Concentration of metals associated with mining waste in sediments, biofilm, benthic macro invertebrates, and fish from the Coeur d’Alene River Basin, Idaho. Arch Environ Contam Toxicol 34: 119-127.

8.       Sioen I, De Henauw S, Verdonck F, Van Thuyne N, Van Camp J (2007) Development of a nutrient database and distributions for use in a probabilistic risk-benefit analysis of human seafood consumption. J Food Compost Anal 20: 662-670.

9.       Burger J, Gochfeld M (2005) Heavy metals in commercial fish in New Jersey. Environ Res 99: 403-412.

10.   Zhang W, Wang WX (2012) Large-scale spatial and interspecies differences in trace elements and stable isotopes in marine wild fish from Chinese waters. J Hazard Mater 215: 65-74.

11.   Yilmaz F, Ozdemir N, Demirak A, Tuna AL (2007) Heavy metal levels in two fish species Leuciscus cephalus and Lepomis gibbosus. Food Chemistry 100: 830-835.

12.   Zhao S, Feng C, Quan W, Chen X, Niu J, Shen Z (2012) Role of living environments in the accumulation characteristics of heavy metals in fishes and crabs in the Yangtze River Estuary, China. Mar Pollut Bull 64: 1163-1171.

13.   Castro-Gonzalez MI, Mendez-Armenta M (2008) Heavy metals: implications associated to fish consumption. Environ Toxicol Pharmacol 26: 263-271.

14.   Al-Busaidi M, Yesudhason P, Al-Mughairi S, Al-Rahbi WAK, Al-Harthy KS, et al. (2011) Toxic metals in commercial marine fish in Oman with reference to national and international standards. 85: 67-73.

15.   Rahman MS, Molla AH, Saha N, Rahman A (2012) Study on heavy metals levels and its risk assessment in some edible fishes from Bangshi River, Savar, Dhaka, Bangladesh. Food Chemistry 134: 1847-1854.

16.   Meche A, Martins MC, Lofrano BESN, Hardaway CJ, Merchant M, et al. (2010) Determination of heavy metals by inductively coupled plasma-optical emission spectrometry in fish from the Piracicaba River in Southern Brazil. Micro J 94: 171-174.

17.   Mustafa C, Guluzar A (2003) The relationships between heavy metal (Cd, Cr, Cu, Fe, Pb, Zn) levels and the size of six Mediterranean fish species. Environ. Pollut 121: 129-136.

18.   Yilmaz AB (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 Animal Sci 29: 257-262.

19.   Evans DW, Dodoo DK, Hanson DJ (1993) Trace elements concentrations in fish livers Implications of variations with fish size in pollution monitoring. Mar Pollut Bull 26: 329-334.

20.   Rashed MN (2001) Monitoring of environmental heavy metals in fish from Nasser Lake. Environ Int 27: 27-33.

21.   Yunkai L, Chen Y, Song B, Olson D, Yu N, et al. (2009) Ecosystem structure and functioning of Lake Taihu (China) and the impacts of fishing. Fish Res 95: 309-324.

22.   Yuan HZ, Shen J, Liu EF, Wang JJ, Meng XH (2011) Assessment of nutrients and heavy metals enrichment in surface sediments from Taihu Lake, a eutrophic shallow lake in China. Environ Geochem Health 33: 67-81.

23.   Huang Y (2000) The water quality of Lake Taihu and its protection. In: Research on Lake Sciences. Nanjing Institute of Geography and Limnology, Chinese Academy of Sciences Nanjing. 239-246.

24.   Hu W, Zhai S, Zhu Z, Han H (2008) Impacts of the Yangtze River water transfer on the phosphorus release of the sediments from different tropic areas in Taihu Lake, China. Environ Pollut 130: 288-295.

25.   Zhang YP, Qu WC (2001) Determination of heavy metal contents in the sediments from Taihu Lake and its environmental significance. Rock and Mineral Analysis 20: 34-36.

26.   Dai XL, Sun C (2001) The characteristics of heavy metals distribution and pollution in sediment from Lake Taihu. Sbanghai Environ Sci 20: 71-74.

27.   Fan CX, Zhu YX, Ji ZJ. et al., (2002) Characteristics of the pollution of heavy metals in the sediment of Yilihe River, Taihu Basin. J Lake Sci 14: 235-241.

28.   Wang H, Wang CX, Wang ZJ (2002) Speciations of heavy metals in surface sediment of Taihu Lake. Environ. Chemistry 21: 430-435.

29.   Yuan XY, Chen J, Ji JF, et al. (2002) Characteristics and environmental changes of pollution elements in Taihu sediments and soil near the lake. Acta Sedimntologica Sinica 20: 427-434.

30.   Liu EF, Shen J, Zhu YX, Weila X, Guangwei Zhu, et al. (2004) Source analysis of heavy metals in surface sediments of Lake Taihu. J Lake Sci 16: 113-119.

31.   Yan HT, Zhu YX, Hu SY (2004) Magnetic studies on heavy metal pollution and multivariate analysis in West Tiaoxi Basin. China Environ Sci 24: 385-389

32.   Zhong J, Fan C, Liu G, Zhang L, Shang J, et al. (2010) Seasonal variation of potential denitrification rates of surface sediment from Meiliang Bay, Taihu Lake, China. J Environ Sci 22: 961-967.

33.   Chi QQ, Zhu GW, Alan L (2007) Bioaccumulation of heavy metals in fishes from Taihu Lake, China. J Environ Sci 19: 1500-1504.

34.   Tao Yu, Yuan Z, Xiaona H, Wei M (2012) Distribution and bioaccumulation of heavy metals in aquatic organisms of different trophic levels and potential health risk assessment from Taihu Lake, China. Ecotoxicol Environ Saf 81: 55-64.

35.   Li Pengfei, Zhang Jian, Xie H, Liu C, Liang S, et al. (2015) Heavy Metal Bioaccumulation and Health Hazard Assessment for Three Fish Species from Nansi Lake, China. Bull Environ Contam Toxicol 94: 431- 436.

36.   Bao L, Wang D, Li T, Li Y, Zhang G, et al. (2015) Accumulation and risk assessment of heavy meals in water sediment, and aquatic organisms in rural rivers in the Taihu Lake region. China Environ Sci Pollut Res 22: 6721-6731.

37.   Chen YW, Fan CX, Teubner K, Dokulil M (2003) Changes of nutrients and phytoplankton chlorophyll-a in a large shallow lake, Taihu, China: An 8-year investigation. Hydrobiologia 506: 273-279.

38.   Qin BQ, Xu PZ, Wu QL, Luo LC, Zhang YL (2007) Environmental issues of Lake Taihu, China. Hydrobiologia 194: 3-14.

39.   Li W, Yang Q, Liu G (1994) Algal bloom in Lake Taihu and its control. In: Sund H, Yu X, Stabel H, Yuan K, Geller W, She F (Eds.), Environmental Protection and Lake Ecosystem, China. Science and Technology Press Beijing 243-261.

40.   Wang C, Bi J, Ambrose B, Jr A (2015) Development and application of mathematical model to support total maximum daily load for the Taihu Lakes on fluent rivers, China, Ecol. Eng 83: 258-267.

41.   Kingston HM, Jassie LB (1988) Introduction to microwave sample preparation. Washington, DC: American Chemical Society.

42.   Sankar TV, Zynudheen AA, Anandan R, Viswanathanair PG (2006) Distribution of organochlorine pesticides and heavy metal residues in fish and shellfish from Calicut redion, Kerala, India. Chemosphere 65: 583-590.

43.   Guven K, Zbay C, Unlu E, Satar A (1999) Acute lethal toxicity and accumulation of copper in Gammarus pulex (L.) (Amphipoda). Turk. J Biol 23: 513-521.

44.   Henry F, Amara R, Courcot L, Lacouture D, Bertho M L (2004) Heavy metals in four fish species from the French coast of the eastern English Channel and southern bight of the North Sea. Environ Int 30: 675-683.

45.   Kargin F, Erdem C (1991) Accumulation of copper in liver, spleen, stomach, intestine, gill and muscle of Cyprinus carpio. Turk. J Zoology 15: 306-314.

46.   Unlu E, Sevim-Pakdemir S, Akba O (1994) Investigation of some heavy metal accumulation in muscle tissue organs of Acanthobrama marmid (Heckel, 1843) in the Tigris River 327-334.

47.   Liu P, Wang CN, Song XY, Wu YN (2010) Dietary intake of lead and cadmium by children and adults-result calculated from dietary recall and available lead/cadmium level in food in comparison to result from food duplicate diet method. Int J Hyg Environ Health 213: 450-457.

48.   Romeoa M, Siaub Y, Sidoumou Z, Gnassia-Barelli M (1999) Heavy metals distribution in different fish species from the Mauritania coast. Sci Total Environ 232: 169-175.

49.   Rao LM, Padmaja G (2000) Bioaccumulation of heavy metals in M. cyprinoids from the harbor waters of Visakhapatnam. Bull Pure Applied Sci 19: 77-85.

50.   Amundsen PA, Staldvik FJ, Lukin AA, Kashulin NA, Popova OA, et al. (1997) Heavy metal contamination in freshwater fish from the border region between Norway and Russia. Sci Total Environ 201: 211-224.

51.   Wantanabe KH, Desimone FW, Thiyagarajah A, Hartley WR, Hindrichs AE (2003) Fish tissue quality in the lower Mississippi River and health risks from fish consumption. Sci Total Environ 302: 109-126.

52.   Kalay M, Ay O, Canil M (1999) Heavy metal concentrations in fish tissues from the Northeast Mediterranean Sea. Bull Environ Contam Toxicol 63: 673-681.

53.   Yu T, Zhang Y, Meng W, Hu X (2012) Characterization of heavy metals in water and sediments in Taihu Lake, China. Environ Monit Assess 184: 4367-4382.

54.   Jayaprakash M, SenthilKumar R, Giridharan L, Sujitha SB, Sarkar SK, et al. (2015) Bioaccumulation of metals in fish species from water and sediments in macrotidal Ennore creek, Chennai, SE coast of India: A metropolitan city effect. Ecotoxicol Environ Saf 120: 243-255.

55.   Shrivastava P, Saxena A, Swarup A (2003) Heavy metal pollution in a sewage-fed lake of Bhopal, (M. P) India. Lakes and Reservoirs Res Manag 8: 1-4.

56.   Sekar CK, Chary NS, Kamala TC, Raj DSS, Rao AS (2003) Fractionation studies and bioaccumulation of sediment-bound heavy metals in Kolleru Lake by edible fish. Environ Int 29: 1001-1008.

57.   Prabhu Dass Batvari B, Kamala-Kannan S, Shanthi K, Krishnamoorthy R, Lee KJ, et al. (2008) Heavy metals in two fish species (Carangoidel malabaricus and Belone stronglurus) from Pulicat Lake, North of Chennai, and Southeast Coast of India. Environ Monit Assess 145: 167-175.

58.   Begum A, Amin MN, Kaneco S, Ohta K (2005) Selected elemental composition of the muscle tissue of three species of fish, Tilapia nilotica, Cirrhina mrigala and Clarius batrachus, from the fresh water Dhanmondi Lake in Bangladesh. Food Chemistry 99: 439-443.

59.   Mendil D, Uluozlu OD (2007) Determination of trace metal levels in sediment and five fish species from lakes in Tokat, Turkey. Food Chemistry 101: 739-745.

60.   Food and Agriculture Organization (FAO) (1983) Compilation of legal limits for hazardous substances in fish and fishery products. FAO Fishery Circular No: 463: 5-100.

61.   European Union (EU) (2008) Commission Regulation (EC) No: 629/2008. Setting maximum levels for certain contaminants in food stuffs. Official Journal of the European Union L.

62.   European Union (EU) (2001) Commission Regulation as Regards Heavy Metals, Di- rective, 2001/22/EC, No: 466.

63.   Federal Environmental Protection Agency (FEPA) (2003) Guidelines and Standards for Environmental Pollution Control in Nigeria. 238.

 

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