Publisher: Taylor & Francis Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH, UK Toxicological & Environmental Chemistry Publication details, including instructions for authors and subscription information: http://www.tandfonline.com/loi/gtec20 Acute toxicity of the synthetic pyrethroid pesticide fenvalerate to some air breathing fishes Madhuban Datta (Bhattacharya) a & Anilava Kaviraj a a Department of Zoology, University of Kalyani, Kalyani-741235, West Bengal, India Available online: 30 Sep 2011 To cite this article: Madhuban Datta (Bhattacharya) & Anilava Kaviraj (2011): Acute toxicity of the synthetic pyrethroid pesticide fenvalerate to some air breathing fishes, Toxicological & Environmental Chemistry, 93:10, 2034-2039 To link to this article: http://dx.doi.org/10.1080/02772248.2011.626416 PLEASE SCROLL DOWN FOR ARTICLE Full terms and conditions of use: http://www.tandfonline.com/page/terms-and- conditions This article may be used for research, teaching, and private study purposes. Any substantial or systematic reproduction, redistribution, reselling, loan, sub-licensing, systematic supply, or distribution in any form to anyone is expressly forbidden. The publisher does not give any warranty express or implied or make any representation that the contents will be complete or accurate or up to date. The accuracy of any instructions, formulae, and drug doses should be independently verified with primary sources. The publisher shall not be liable for any loss, actions, claims, proceedings, demand, or costs or damages whatsoever or howsoever caused arising directly or indirectly in connection with or arising out of the use of this material. Toxicological & Environmental Chemistry Vol. 93, No. 10, December 2011, 20342039 Acute toxicity of the synthetic pyrethroid pesticide fenvalerate to some air breathing fishes Madhuban Datta (Bhattacharya) * y and Anilava Kaviraj Department of Zoology, University of Kalyani, Kalyani-741235, West Bengal, India (Received 6 February 2011; final version received 16 September 2011) Lethal concentrations (LC 50 ) of a synthetic pyrethroid pesticide, fenvalerate, for three species of air breathing fish Clarias batrachus, Channa punctatus and Heteropneustes fossilis were determined under water and acetone soluble condition in the laboratory using the static bioassay procedure of the American Public Health Association (APHA,1995). Acetone soluble fenvalerate was found more toxic than the water-soluble fenvalerate irrespective of species and exposure periods. The LC 50 value upon 96 days exposure to acetone soluble fenvalerate for C. batrachus, Channa C. punctatus and Heteropneustes H. fossilis were 1.35, 1.0 and 0.65 mg L 1 , respectively. It is concluded from the present study that fenvalerate is highly toxic even to the hardy air breathing fishes and the pesticide, when dissolved in water, remains photostable and active to render toxicity for long duration. Keywords: pyrethroid; fenvalerate; LC 50 ; air breathing fish; solvent Introduction Toxicity of synthetic pyrethroid pesticide depends upon their structure, stereochemistry and formulations (Polat et al. 2002; Datta and Kaviraj 2003; Saha and Kaviraj 2008). Fenvalerate is a cyanophenoxybenzyl non-cyclopropanoid pyrethroid. The Environmental Protection Agency of the United States classifies fenvalerate products as toxicity class II (I most toxic, IVleast toxic). In India, fenvalerate is registered for use on a wide array of crops including cotton, tobacco plants, soybeans, corn, vegetables, apples, peaches, pears and nuts, as termiticide and insect repellent (Madan et al. 2000). Fenvalerate enters freshwater aquatic environments as runoff from agricultural plots, as drift from forest- spray activities, and from direct spraying of water bodies. The pesticide has been found to be highly toxic to fish and aquatic invertebrates (Tilak et al. 2001; Tandon et al. 2005). The objective of this study was to evaluate the acute toxicity of fenvalerate to three air breathing fish species, namely Clarias batrachus, Channa punctatus and Heteropneustes fossilis. These fish possess air breathing organs; they inhabit areas like ditches, swamps, marshes and small ponds that in turn act as the accumulation sites of pesticides applied in agricultural fields. Therefore, these fish are considered to be hardy and resistant to adverse ecological conditions. Since fenvalerate is used as both acetone and aqueous solution, *Corresponding author. Email: madhuban@indiatimes.com; madhubanb@gmail.com yPresent address: Nabadwip Vidyasagar College, Nabadwip, Nadia, W.B., India. ISSN 02772248 print/ISSN 10290486 online 2011 Taylor & Francis http://dx.doi.org/10.1080/02772248.2011.626416 http://www.tandfonline.com D o w n l o a d e d
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bioassays were made with both water soluble from of fenvalerate and acetone soluble form of fenvalerate. Materials and methods Adult specimens of C. batrachus (mean weight 7.1 g 1.2; mean length 8.1 0.5), C. punctatus (mean weight 5.3 g 0.8; mean length 8.2 0.4) and H. fossilis (mean weight 5.7 g 0.9; mean length 5.6 0.9) were procured from local hatcheries and were stocked in 30 L glass aquaria. The fish were acclimatized to this condition in laboratory for 96192 h before use. The fish were fed a diet prepared from rice bran, wheat flour, mustard oil cake, fishmeal and vitamin-mineral mixture (92% dry matter and 8% moisture with the principal nutrients such as crude protein and crude lipid being 30.5% and 5.1% of dry matter, respectively) ad libitum during acclimatization. Emulsified concentrate of fenvalerate ((RS)-alpha-cyano-3-phenoxybenzyl (RS)-2 -(4-chlorophenyl)-3-methyl-buty- rate) with 20% active ingredient was procured from Rallis India Ltd, Mumbai (TATAfen 20 E). Two different stock solutions of fenvalerate were prepared for the bioassay, one by dissolving the product in water and another in acetone. Different concentrations used for both solutions of fenvalerate are given in Table 1. Two sets of control were used in the bioassays, one with dilution water as the medium and another with 0.5 mL acetone/L water as the medium, to match water and acetone soluble fenvalerate, respectively. Static bioassays, following the method of APHA (1995), were conducted in 15 L glass aquaria each containing 3 L of nonchlorinated tap water (pH: 8.00 0.04, free CO 2 : 6.0 0.3 mg L 1 , dissolved oxygen: 6.2 0.2 mg L 1 , alkalinity: 75.2 3.8 mg L 1 as CaCO 3 , hardness: 260 11 mg L 1 as CaCO 3 ) and three fish. The aquaria were arranged Table 1. Concentrations of fenvalerate used under different solvent conditions. Concentration of fenvalerate (mg L 1 ) Solvents C. batrachus C. punctatus H. fossilis Water 0.0 (WC) 0.0 (WC) 0.0 (WC) 2.0 2.0 0.7 2.5 2.5 1.0 3.0 3.0 2.0 4.0 4.0 3.0 5.0 5.0 4.0 5.5 6.0 5.0 6.0 6.5 6.0 Acetone 0.0 (SC) 0.0 (SC) 0.0 (SC) 0.6 0.5 0.5 0.8 0.8 0.6 1.2 1.0 0.7 1.5 1.5 0.9 2.0 2.0 1.0 2.5 3.0 1.2 3.0 3.5 1.4 4.0 4.0 Note: WCWater control; SCSolvent control (0.5 mL acetone/L). Toxicological & Environmental Chemistry 2035 D o w n l o a d e d
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in randomized block design so that there were three replicates for each of the concentration and control tested. A temperature of 29.5 0.4
C was maintained in the
test medium during the experiments. Mortality and the behavioural changes of the test animals were recorded every 24 h, and dead animals, if any were removed. No food was provided during the bioassay to avoid interference of excretory products of fish with the test chemical. The median lethal concentration (LC 50 ) with 95% confidence limit for fenvalerate was estimated for 24, 48, 72 and 96 h by probit analysis (Finney 1971). Duncans multiple range test was employed for comparing mean mortality values, after estimating the residual variance by repeated measures of ANOVA (Winner 1971) for arc sine transformed mortality data (dead individuals/initial number of individuals). Time of exposure was the repeated measure factor while treatment (concentrations and controls) was the second factor. In addition, LC 50 values were compared by the method of APHA (1995). Results and discussion LC 50 values of water-soluble and acetone-soluble fenvalerate for the test fishes have been summarized in Tables 2 and 3, respectively. H. fossilis was found to be the most susceptible species followed by C. punctatus and C. batrachus under both solubility conditions. The results indicated that acetone soluble fenvalerate, irrespective of species and exposure period, was more toxic than the water soluble one. The LC 50 value of water-soluble fenvalerate did not show any significant difference between hours of exposure. But, the LC 50 values of acetone soluble fenvalerate varied significantly between the exposure periods. For C. batrachus and C. punctatus the 24 h LC 50 value of acetone-soluble fenvalerate did not vary significantly from 48 h; however, it varied significantly from that of 72 h and 96 h. Between other exposure periods the LC 50 value of acetone soluble fenvalerate did not show any significant variation. For H. fossilis there was no significant difference of the LC 50 value of acetone-soluble fenvalerate between any exposure period except between 24 and 96 h. Duncans multiple range test carried to compare mean mortality between concentrations of fenvalerate showed that minimum effective concen- tration that produced significant mortality from control was 2.5 and 1.2 mg L 1 (C. batrachus); 1.0 and 0.7 mg L 1 (H. fossilis); 2.5 and 0.87 mg L 1 (C. punctatus) for water-soluble and acetone-soluble fenvalerate respectively. The behavioural changes of the fish exposed to lethal concentrations of fenvalerate (both water and acetone soluble) were more or less similar irrespective of the species. These included rapid and erratic swimming, Table 2. LC 50 values (mg L 1 ) with 95% confidence limits (in parentheses) of fenvalerate dissolved in water. Exposure time (h) C. batrachus C. punctatus H. fossilis 24 3.88 3.50 2.86 (3.34.4) (3.144.21) (2.143.84) 48 3.42 3.33 2.23 (2.93.9) (2.83.9) (1.692.94) 72 3.30 3.12 1.78 (2.83.8) (2.723.57) (1.222.59) 96 3.19 2.93 1.78 (2.73.6) (2.453.49) (1.222.59) 2036 M. Datta and A. Kaviraj D o w n l o a d e d
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tremors, partial or complete loss of equilibrium, gulping respiration and increased surfacing initially. Responses became more acute with increasing concentrations of fenvalerate. The fishes became lethargic before death. LC 50 values of fenvalerate determined in the present study (1.78 to 3.88 mg L 1 for the aqueous solution and 0.65 to 2.39 for the acetone solution) indicate that the pesticide is highly toxic even to the air breathing fishes. Fenvalerate has already been marked as supertoxic to fish (Scott et al. 1987) because of its low LC 50 value (510 mg L 1 ) for most of the species tested so far. The 2496 h LC 50 values of C. batrachus and C. punctatus found in the present investigation are comparable to the 48 and 96 h LC 50 values of fathead minnow (Bradbury et al. 1987; Bradbury and Coats 1989); 96 h LC 50 value of African catfish, Mystus vittatus (Verma et al. 1981) and 96 h LC 50 value of Gulf toad fish (Mayer 1987), while the LC 50 values for H. fossilis found in the present investigation are comparable to the 48 h LC 50 value of Lepomis macrochirus (Dyer et al. 1989) and 96 h LC 50 value of Mugil cephalus (Mayer 1987). 96 h LC 50 value of fenvalerate for the carp Catla catla (6 mg L 1 ) observed by Tandon et al. (2005) is higher than any of the LC 50 values determined for the air breathing fishes in the present investigation. The present results further indicate that fenvalerate may become more toxic to fish in the exposed field if it is used as acetone solution in the sources. The general mode of action of fenvalerate is presumed to bring out changes in sodium ion permeability and depolarization of the nerve membrane (Eisler 1992). Toxicity is probably due to effects on both peripheral and central nervous system caused by interference with sodium ion permeability in stimulated nerve membranes and depolarization of nerve membranes. It probably accounts for the erratic movements and convulsions shown by the fish exposed to lethal concentrations of fenvalerate. Fenvalerate also acts as a potent inhibitor of ATPases (Clark 1982). But exact mechanism of toxicity for the species under study is not yet known. Although synthetic pyrethroids have been structurally modified to make their active principle photostable, ambient environmental conditions still profoundly influence toxicity of these pesticides to fish and other aquatic organisms. Cypermethrin have been found to become practically non-toxic to air breathing fish H. fossilis after 7 h of light exposure (Saha and Kaviraj 2009). The LC 50 value of the same pyrethroids did not change beyond 48 h exposure to common carp, tadpole larva and the crustacean zooplankton (Saha and Kaviraj 2008). Most of them become inactive after 24 h of exposure to light rendering LC 50 values unchanged beyond 24 h of exposure. The results of the this revealed that the LC 50 value of fenvalerate also did not change significantly beyond 24 h of Table 3. LC 50 (mg L 1 ) values with 95% confidence limits (in parentheses) of fenvalerate dissolved in acetone. Exposure time (h) C. batrachus C. punctatus H. fossilis 24 2.39 1.81 0.89 (2.052.79) (1.472.2) (0.791.01) 48 1.76 1.33 0.81 (1.452.12) (1.061.68) (0.720.92) 72 1.53 1.23 0.76 (1.261.85) (0.961.59) (0.660.86) 96 1.35 1.02 0.65 (1.091.67) (0.731.41) (0.550.77) Toxicological & Environmental Chemistry 2037 D o w n l o a d e d
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exposure when dissolved in water. But the LC 50 value changed up to 72 h for C. batrachus and C. punctatus and up to 96 h for H. fossilis when dissolved in acetone indicating that the acetone solution of fenvalerate remain active, photostable and toxic for long duration. From this study it is concluded that the dosing solutions with only 20% active ingredient fenvalerate is quite toxic to the air breathing fish studied, and further careful studies with the technical grade fenvalerate are required to assess its full toxic potentiality. Acknowledgements We thank the Head, Department of Zoology, University of Kalyani for providing necessary facilities for this research. References APHA (American Public Health Association). 1995. Standard methods for the examination of water and wastewater. Washington DC, USA: American Public Health Association, American Water Works Association and Water Pollution Control Federation. Bradbury, S.P., and J.R. Coats. 1989. Toxicokinetics and toxicodynamics of pyrethroid insecticides in fish. Environmental Toxicology and Chemistry 8: 37380. Bradbury, S.P., D.M. Symonik, J.R. Coats, and G.J. Atchison. 1987. Toxicity of fenvalerate and its constituent isomers to the fathead minnow, Pimephales promelas and bluegill, Lepomis macrochirus. Bulletin of Environmental Contamination and Toxicology 38: 72735. Clark, J.M., and F. Matsumura. 1982. Two different types of inhibitory effects of Pyrethroids on nerve Ca
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