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    This article was downloaded by: [Anilava Kaviraj]On: 05 November 2011, At: 09:23Publisher: Taylor & FrancisInforma Ltd Registered in England and Wales Registered Number: 1072954 Registeredoffice: Mortimer House, 37-41 Mortimer Street, London W1T 3JH, UK

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    Acute toxicity of the synthetic

    pyrethroid pesticide fenvalerate to

    some air breathing fishesMadhuban Datta (Bhattacharya) a& Anilava Kaviraj a

    aDepartment 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

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    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 (LC50) of a synthetic pyrethroid pesticide, fenvalerate, forthree species of air breathing fish Clarias batrachus, Channa punctatus andHeteropneustes fossilis were determined under water and acetone solublecondition in the laboratory using the static bioassay procedure of the AmericanPublic Health Association (APHA,1995). Acetone soluble fenvalerate was foundmore toxic than the water-soluble fenvalerate irrespective of species and exposureperiods. The LC50 value upon 96 days exposure to acetone soluble fenvaleratefor C. batrachus, Channa C. punctatus and Heteropneustes H. fossilis were 1.35,1.0 and 0.65mg L1, respectively. It is concluded from the present study thatfenvalerate is highly toxic even to the hardy air breathing fishes and the pesticide,when dissolved in water, remains photostable and active to render toxicity forlong duration.

    Keywords: pyrethroid; fenvalerate; LC50; 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

    (Imost toxic, IV least 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: [email protected]; [email protected] 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

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    bioassays were made with both water soluble from of fenvalerate and acetone soluble form

    of fenvalerate.

    Materials and methodsAdult 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) andH. fossilis (mean weight

    5.7g 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 (TATAfen20 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 CO2:

    6.0 0.3mgL1, dissolved oxygen: 6.2 0.2mgL1, alkalinity: 75.2 3.8mgL1 as

    CaCO3, hardness: 260 11mgL1 as CaCO3) and three fish. The aquaria were arranged

    Table 1. Concentrations of fenvalerate used under different solventconditions.

    Concentration of fenvalerate (mg L1)

    Solvents C. batrachus C. punctatus H. fossilis

    Water 0.0 (WC) 0.0 (WC) 0.0 (WC)2.0 2.0 0.72.5 2.5 1.03.0 3.0 2.04.0 4.0 3.05.0 5.0 4.05.5 6.0 5.06.0 6.5 6.0

    Acetone 0.0 (SC) 0.0 (SC) 0.0 (SC)0.6 0.5 0.50.8 0.8 0.61.2 1.0 0.71.5 1.5 0.92.0 2.0 1.02.5 3.0 1.2

    3.0 3.5 1.44.0 4.0

    Note: WCWater control; SCSolvent control (0.5 mL acetone/L).

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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 0.4C 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 (LC50) with 95% confidence limit forfenvalerate 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, LC50 values were compared by the method of APHA

    (1995).

    Results and discussion

    LC50 values of water-soluble and acetone-soluble fenvalerate for the test fishes have been

    summarized in Tables 2 and 3, respectively. H. fossiliswas 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 LC50 value of water-soluble

    fenvalerate did not show any significant difference between hours of exposure. But, the

    LC50 values of acetone soluble fenvalerate varied significantly between the exposure

    periods. For C. batrachus and C. punctatus the 24 h LC50 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 LC50 value of acetone solublefenvalerate did not show any significant variation. For H. fossilis there was no significant

    difference of the LC50 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 L1

    (C. batrachus); 1.0 and 0.7 mg L1 (H. fossilis); 2.5 and 0.87mg L1 (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. LC50values (mg L1) 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)

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    tremors, partial or complete loss of equilibrium, gulping respiration and increased

    surfacing initially. Responses became more acute with increasing concentrations offenvalerate. The fishes became lethargic before death.

    LC50 values of fenvalerate determined in the present study (1.78 to 3.88 mg L1 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 LC50 value (510mg L1) for most

    of the species tested so far.

    The 2496 h LC50 values of C. batrachus and C. punctatus found in the present

    investigation are comparable to the 48 and 96 h LC50values of fathead minnow (Bradbury

    et al. 1987; Bradbury and Coats 1989); 96 h LC50value of African catfish, Mystus vittatus

    (Verma et al. 1981) and 96 h LC50 value of Gulf toad fish (Mayer 1987), while the LC50values for H. fossilis found in the present investigation are comparable to the 48 h LC50value of Lepomis macrochirus (Dyer et al. 1989) and 96 h LC50 value of Mugil cephalus

    (Mayer 1987). 96 h LC50 value of fenvalerate for the carp Catla catla (6 mg L1) observed

    by Tandon et al. (2005) is higher than any of the LC50 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 LC50value 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 lightrendering LC50values unchanged beyond 24 h of exposure. The results of the this revealed

    that the LC50 value of fenvalerate also did not change significantly beyond 24 h of

    Table 3. LC50(mg L1) 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)

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    exposure when dissolved in water. But the LC50value changed up to 72 h forC. batrachus

    andC. punctatusand up to 96 h forH. fossiliswhen 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 facilitiesfor this research.

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