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Neotropical Entomology

versão impressa ISSN 1519-566Xversão On-line ISSN 1678-8052

Neotrop. Entomol. v.33 n.2 Londrina mar./abr. 2004

https://doi.org/10.1590/S1519-566X2004000200017 

CROP PROTECTION

 

Developmental stress by diflubenzuron in Haematobia irritans (L.) (Diptera: Muscidae)

 

Estresse por diflubenzurom no desenvolvimento de Haematobia irritans (L.) (Diptera: Muscidae)

 

 

Juliana J. da SilvaI; Júlio MendesI; Cecília LomônacoII

ILab. Parasitologia
IILab.Ecologia Evolutiva. Instituto de Biologia, Universidade Federal de Uberlândia, C. postal 593, 38400-902, Uberlândia, MG

 

 


ABSTRACT

This study aimed to assess the effect of sub-lethal concentrations of the insect growth regulator (IGR), diflubenzuron, on the body size of the horn fly Haematobia irritans (L.) and on its developmental stability, by fluctuating asymmetry (FA) analysis. Breeding media with different sub-lethal diflubenzuron concentrations and a control medium, were prepared to obtain morphometric measures on adult individuals. Principal component analysis was used to generate an index of general body size, using the correlation matrix of the original characters. Levels of FA and the multivariate index of size were compared among treatments. Contrary to the expectations, the exposure to diflubenzuron did not result in a significant and concomitant increase in the level of FA across treatments or in the number of individuals showing developmental instability. Nevertheless, a significant reduction of size due to the diflubenzuron may reflect the ability of H. irritans to perform physiological and morphological adjustments allowing phenotype compensation, at least to some extent, for stressful environmental conditions. On the other hand, the IGR may be selecting more symmetrical and resistant individuals. From the pest control point of view, the reduction of size may be a positive effect of the IGR since size is usually directly related to fitness.

Key words: Insecta, pest control, horn fly, insect growth regulator, fluctuating asymmetry


RESUMO

Este trabalho teve como objetivo verificar o efeito de concentrações sub-letais do regulador de desenvolvimento de insetos (IGR), diflubenzurom, no tamanho e na estabilidade do desenvolvimento da mosca-dos-chifres, Haematobia irritans (L.), por meio da análise de assimetria flutuante (AF). Adultos criados em substratos com diferentes concentrações sub-letais de diflubenzurom e em meios-controle foram submetidos a medidas morfométricas. Utilizou-se a análise de componentes principais para se obter um índice multivariado de tamanho, a partir de uma matriz de correlação dos caracteres originais. Os níveis de AF e o índice multivariado de tamanho foram comparados entre os tratamentos. Contrariamente ao esperado, a exposição ao diflubenzurom não resultou em aumento significativo e proporcional às concentrações utilizadas nos níveis de AF entre os tratamentos. Entretanto, a redução no tamanho devido ao efeito deste IGR pode estar refletindo a capacidade de H. irritans de realizar ajustes fisiológicos e morfológicos, de modo que os fenótipos compensem, pelo menos até certo ponto, as condições ambientais de estresse. Há ainda a possibilidade de o IGR estar selecionando indivíduos mais simétricos e resistentes. Do ponto de vista do controle de pragas, a redução no tamanho de indivíduos submetidos a concentrações sub-letais deste IGR pode ser vantajosa, uma vez que tamanho está usualmente diretamente relacionado à aptidão do indivíduo.

Palavras - chave: Insecta, controle de pragas, mosca-dos-chifres, regulador de crescimento, assimetria flutuante


 

 

Fluctuating asymmetry (FA) is defined as random differences between the scores for morphological bilateral traits on the two sides of individuals in a population (Van Valen 1962). The degree of FA provides a measure of developmental instability, which can be influenced by genetic or environmental stress as well as by the ability of the genome to maintain the organized development under conditions of stress (Parsons 1990, Palmer & Strobeck 1996, Møller & Swaddle 1997). Much empirical and theoretical evidences suggest that other kinds of asymmetry, including antisymmetry and directional symmetry may be important markers of developmental instability (Møller & Thornhill 1997). Antisymmetry occurs when a significant difference exists between sides and the larger side is randomly distributed within a sample, and directional asymmetry occurs when there is a consistent bias in a character toward greater development on one side (Palmer & Strobeck 1986).

FA has been attracting the attention of biologists because of reports that it may be negatively correlated with fitness components such as fecundity, growth rate or adult longevity (Mitton & Grant 1984, Leary & Allendorf 1989, Ueno 1994). Fly populations exposed to conventional insecticides may experiment an increase in their FA index (Mckenzie & Clarke 1988, Clarke & Ridsdill-Smith 1990). Nevertheless, because of the capacity of species to show plasticity, an environmental stress may not be sufficiently severe to significantly increase FA levels of the target population (Parson 1992), but may cause reduction in its growth rate which may be also related to decrease in insect fitness (David et al. 1994, Santos 2001).

Diflubenzuron is an insect growth regulator (IGR), which causes physiological and morphological changes during insect development, due to its interference with cuticle deposition (Chamberlain 1975, Grosscurt 1978, Graf 1993). Some studies have demonstrated the susceptibility of the horn fly, Haematobia irritans (L.) to diflubenzuron (Hopkins & Chamberlain 1976, Kunz & Bay 1977, Silva & Mendes 2002). If this IGR affects horn fly survivorship, concomitant changes in horn fly FA levels and/or on body size may occur. This hypothesis was tested on the present investigation where the effect of sub lethal concentrations of diflubenzuron on the body size of horn fly and on its developmental stability, inferred by FA analysis, were assessed.

 

Materials and Methods

Collecting Horn Flies and Preparing the Breeding Media. Horn flies were collected using an entomological net, from February 2000 to January 2001 at the farm Douradinho near Uberlândia city, MG, Brazil (18o55'23''S and 48o17'19''W). The flies were transferred to entomological cages (30 x 40 x 33 cm) and taken to the laboratory where a moistened filter paper was placed inside the cage as an egg-laying substratum. Eggs were removed from the filter paper and transferred to flasks containing breeding media. To prepare the medium, diflubenzuron, (95.34%) (Champion Farmoquímico Ltda., Brazil) was diluted in acetone (Merk) and mixed with previously homogenized fresh cattle manure in order to obtain the sub-lethal concentrations of 30 ppb; 25 ppb and 20 ppb (i.e. giving concentrations which are not lethal for at least 30 of the exposed individuals). Equivalent quantities of acetone used to prepare the tested media were added to 1000 g of cattle manure to be used as control. Thereafter, 100 g of treated and control media were transferred separately to the flasks (15 cm x 12 cm) containing a layer of approximately 2 cm of previously sterilized soil. Four replicates of each concentration and respective controls were used. Subsequently, 50 eggs were placed on the surface of the breeding media in each of the containers, which were then maintained in a growth chamber at 25.0 ±± 0.5oC and 12:12 h of photoperiod. Flasks were monitored daily checking the number of emerged adults up to 20 days, by which time all adults had emerged. Emerged flies were preserved in ethanol 70% until be examined. Details of methods and aspects of horn fly susceptibility to this IGR are given in Silva & Mendes (2002).

Obtaining Morphometric Measures. The wings and legs from around 28 flies (14 females and 14 males) from each of these media concentrations were dry mounted on microscope slides with a cover slip applied. Slides were scanned and images were amplified x 3.0. The measurements were obtained using the computer program CorelDraw, version 5.0 (CorelDraw 1994). The following characters were measured: distance between distal extremity of the vein R2+3 and the interception point of dm-cu-M1 (wing measure A); distance between the interception points of dm-cu-M1 and R1-C (wing measure B) (Fig. 1); hind tibia and hind femur length. These characters were chosen because they are essentially plane structures. Each one of these body parts was measured three times. The wing veins provide many well-defined morphological landmarks and are commonly used in morphological analysis (Klingenberg & McIntyre 1998). Measurements of bilateral traits were obtained for both sides in order to evaluate FA for each treatment and control. FA was calculated as the mean difference between the right and left side, i.e. [(å | R-L | ) / n] , the most common index of FA, according to Palmer & Strobeck (1986).

 

 

Statistical Analysis. A two factor analysis of variance (ANOVA) was used to determine whether the between sides variation was significantly larger than the measurement error (Woods et al. 1998, Perfectti & Camacho 1999). According to Palmer & Strobeck (1986, 1992) it is necessary to distinguish AF from other kinds of asymmetry. A t-test was performed to verify whether the means of the signed right minus left distribution were not significantly different from zero in order to discard the occurrence of directional asymmetry. Antisymmetry was tested by departures of the right-left frequency distribution from normality using Kolmogorov-Smirnov test. Size dependence of FA was tested for each sample by regressing the unsigned absolute difference of the right minus left measurements on trait size. The controls were pooled in only one group since they did not differ statistically in relation to the amount of FA among the tested characters (Zar 1984). Also, no significant differences between male and female levels of FA were detected. Consequently, a single ANOVA was performed to test for differences in the levels of FA among treatments and control (Palmer & Strobeck, 1986, Preziosi et al. 1999). The power of this analysis was also obtained accordingly to Zar (1984).

A PCA multivariate analysis was used to verify the nature and magnitude of variation in morphological characters. An index of general body size (in a multivariate sense) was then estimated using a correlation matrix of the original characters (Manly 1994). The characters used to obtain the scores of the first component were those significantly correlated (wing measure A, femur and tibia, all obtained from the left side). Only 10 males and 10 females were considered in this analysis since some individuals, from which it was not possible to obtain all the measured characters, were discarded. The normality and homoscedasticity of the index of size distribution were verified using respectively the Kolmogorov-Smirnov test and procedures suggested by Zar (1984). Once again, the controls were pooled to form a single group since no differences in size were detected among them (H = 2.86, P = 0.413). Differences between treatments and control were checked using Kruskal-Wallis test and a Tukey-type test for multiple comparisons with equal sample sizes (Zar 1984). All statistical procedures were performed using computer software package Systat for Windows, version 9.0 (Systat 2000).

 

Results

All distributions were normal (i.e. no evidence of antisymmetry was found) and no correlation between size and FA were observed (Table 1). The asymmetry in the femur as well as in the tibia fluctuated around a mean zero, whereas the FA distributions for the wing measurements were both found to be skewed (Table 1). Since the wing traits do not fulfill the criteria for FA, they were omitted from further parametric analysis. For other variables there was a significant level of FA relative to measurement error, indicated by the highly significant sides x individuals effect (F = 10.462, P < 0.001 for tibia and F = 12.582, P < 0.001 for femur), which means that the measurement error was negligible. The ANOVA indicated no differences in femur and tibia FA levels among treatments (Table 2). The power of the ANOVA for both characters was estimated to be 0.87, indicating a 13% chance of having committed a Type II error in this analysis.

 

 

 

 

In the PCA, the first component, which is related to the axes that exhibit greatest variance among individuals, explained 57,7% of the total variance (Table 3). In morphological analysis this first component is interpreted as a size representation (Manly 1994). The scores of the size were normally distributed but the treatments showed unequal variances. The nonparametric Kruskal-Wallis analysis indicated differences of size among treatments (H = 13.26, P = 0.004). Individuals emerged from the 25 ppb and 30 ppb treatment were significant smaller than those emerged from 20 ppb treatment as well as from the control group (Fig. 2).

 

 

 

 

Discussion

Although some studies have reported FA as an indicator of developmental stress in response to insecticide exposure (McKenzie & Clarke 1988, Clarke & Redsdill-Smith 1990), the exposure to diflubenzuron, independent of its concentration, did not result in a significant and concomitant increase in the level of FA. These results are at odds with the prediction that asymmetrical individuals should be more frequent after exposure to diflubenzuron.

Several factors may be influencing the observed results. On the one hand, Parsons (1992) pointed out that in some cases a relatively severe environmental stress was necessary to induce significant FA alterations. In our experiment, the low levels of FA in horn flies after exposure to Diflubenzuron might be due to the peculiar mode of action of this substance, which is very different to that of conventional insecticides (Grosscurt 1978, Graf 1993). On the other hand, the sub-lethal concentrations may be selecting less asymmetric individuals that are also more resistant to diflubenzuron. In these case, severe effects of the IGR were buffered by the individuals ability to cope with it, resulting in a decrease of developmental instability. Other studies show that the absence of correlation between fitness and levels of FA may be the result of choosing characters not affected by developmental instability. In fact, there is no concordance of FA for multiple characters among individuals within populations, suggesting a lack of general buffering capacity at the individual level during developmental processes (Eggert & Sakaluk 1994, Evans & Marshall 1996).

Bjorksten et al. (2000) verified through an extensive literature review that FA is not only related to a particular trait but it is also stress-specific. Environmental causes of stress, other than toxins, include temperature, parasites and food availability. In addition, genetic causes of developmental instability may be due to mutation or disruption of co-adapted gene complexes produced by inbreeding or hybridization (Scheiner et al. 1991, Graham 1992, Møller 1995).

The significant reduction of size due to the effect of diflubenzuron in our populations may reflect the ability of H. irritans to perform physiological and morphological adjustments, so that phenotypes compensate, at least to some extent, for stressful environment conditions. According to Cullum et al. (2001), biomass or fitness reduction is, in part, explained by the increased metabolic expenditure required to sustain life. Lomônaco & Germanos (2001) have already reported that the levels of FA of the wing of Musca domestica L. (Diptera Muscidae) were minimized by the considerable plastic potential for body size reduction and this same pattern of variation was reported by Bubli et al. (1998) for Drosophila melanogaster Meigen (Diptera: Drosophilidae), both studies dealing with sources of stress other than insecticides.

Developmental instability due to exposure to insecticides may result in genetic selection for resistance, which may be morphologically expressed by an increase in FA levels (Mckenzie & Clarke 1988), or by a reduction in body size (Bjorksten et al. 2000). Given that the exposure of an insect population to sub-lethal concentrations results in development of individuals with smaller size, and since size is usually directly related to fitness (David et al. 1994), one can predict that the surviving population will present low fitness. If it is not a starting-point in the selection for a resistant population, this result might be positive from the pest control point of view.

 

Acknowledgments

Our thanks to Dr. Peter E. Gibbs for improving the English text, and for helpful comments on the manuscript.

 

Literature Cited

Bjorksten, T.A., K. Fowler & A. Pomiankowski. 2000. What does sexual trait FA tell us about stress? Trends Ecol. Evol. 15: 163-166.         [ Links ]

Bubli, O.A., A.G. Imasheva & V. Loeschcke. 1998. Selection for knockdown resistance to heat in Drosophila melanogaster at high and low larval densities. Evolution 52: 619-625.         [ Links ]

Chamberlain, W.F. 1975. Insect growth regulating agents for control of arthropods of medical and veterinary importance. J. Med. Entomol. 12: 395-400.         [ Links ]

Clarke, G.M & T.J. Ridsdill-Smith. 1990. The effect of avermectin B1 on developmental stability in the bush fly, Musca vetustissima, as measured by fluctuating asymmetry. Entomol. Exp. Appl. 54: 265-269.         [ Links ]

CorelDraw. 1994. version 5.0. Corel Corporation Ltd., Dublin.

Cullum, A.J., A.F. Bennett & R.E. Lenski. 2001. Evolutionary adaptation to temperature. IX. preadaptation to novel stressful environments of Escherichia coli adapted to high temperature. Evolution 55: 2194-2202.         [ Links ]

David, J.R.B., B. Moreteau, J.P. Gauthier, G. Petavy, A. Stockel & A.G. Imasheva. 1994. Reaction norms of size characters in relation to growth temperature in Drosophila melanogaster: An isofemale line analysis. Evolution 26: 177-298.         [ Links ]

Eggert, A.K. & S.K. Sakaluk. 1994. Fluctuating asymmetry and variation in the size of courtships food gifts in decorated crickets. Amer. Nat. 144: 708-716.         [ Links ]

Evans, A.S. & M. Marshall. 1996. Developmental instability in Brassica campestris (Cruciferae): fluctuating asymmetry of foliar and floral traits. J. Evol. Biol. 9: 717-736.        [ Links ]

Graf, J.F. 1993. The role of insect growth regulators in arthropod control. Parasitol. Today 9: 471-474.         [ Links ]

Graham, J.H. 1992. Genomic coadaptation and developmental stability in hybrid zones. Acta Zool. Fenn. 191: 121-131.         [ Links ]

Grosscurt, A.C. 1978. Diflubenzuron: some aspects of its ovicidal and larvicidal mode of action and an evaluation of its practical possibilities. Pestic. Sci. 9: 373-386.         [ Links ]

Hopkins, D.E. & W.F. Chamberlain. 1976. Diflubenzuron: relationship between age of exposure immature horn flies and inhibition of maturation. Souwthwest. Entomol. 1: 114-117.         [ Links ]

Klingenberg, C.P. & G.S. MacIntyre. 1998. Geometric morphometrics of developmental instability: Analyzing patterns of fluctuating asymmetry with procrustes methods. Evolution 52: 1363-1375.         [ Links ]

Kunz, S.E. & D.E. Bay. 1977. Diflubenzuron: Effects on the fecundity, production and longevity of the horn fly. Souwthwest. Entomol. 2:27-31.         [ Links ]

Leary, R.F. & F.W. Allendorf. 1989. Fluctuating asymmetry as an indicator of stress: implications for conservation biology. Tree 4: 214-216.         [ Links ]

Lomônaco, C. & E. Germanos. 2001. Variações fenotípicas em Musca domestica L. (Diptera: Muscidae) em resposta à competição larval por alimento. Neotrop. Entomol. 30: 223-231.         [ Links ]

Manly, B.F.J. 1994. Multivariate statistical methods, 2nd ed., London, Chapman & Hall, 215p.         [ Links ]

McKenzie, J.A. & G.M. Clarke. 1988. Diazinon resistence, fluctuating asymmetry and fitness in the Australian Sheep Blowfly, Lucilia cuprina. Genetics 120: 213-220.         [ Links ]

Mitton, J.B. & M.C. Grant. 1984. Associations among protein heterozygosity, growth rate and developmental homeostasis. Annu. Rev. Ecol. Syst. 15: 479-499.         [ Links ]

Møller, A.P. 1995. Leaf-mining insects and fluctuating asymmetry in elm Ulmus glabra leaves. J. Anim. Ecol. 64: 697-707.         [ Links ]

Møller, A.P. & J.P. Swaddle. 1997. asymmetry, development stability, and evolution. Oxford, Oxford University Press, 302p.         [ Links ]

Møller, A.P. & R. Thornhill. 1997. Developmental instability is heritable. J. Evol. Biol. 10: 69-76.         [ Links ]

Palmer, R.A. & C. Strobeck. 1986. Fluctuating asymmetry: measurement analysis, patterns. Ann. Rev. Ecol. 17: 391-421.         [ Links ]

Parsons, P.A. 1990. Fluctuating asymmetry: An epigenetic measure of stress. Biol. Rev. 65: 131-145.         [ Links ]

Parsons, P.A. 1992. Fluctuating asymmetry: A biological monitor of environmental and genomic stress. Heredity 68: 361-364.         [ Links ]

Perfectti, F. & J.P. Camacho. 1999. Analysis of genotypic differences in developmental stability in Annona cherimola. Evolution 53: 1396-1405.         [ Links ]

Preziosi, R.F., W.E. Snyder, C.P. Grill & A.J. Moore. 1999. The fitness of manipulating phenotypes: Implications for studies of fluctuating asymmetry and multivariate selection. Evolution 53: 1312-1318.         [ Links ]

Santos, M. 2001. Fluctuating asymmetry is non-genetically related to mating success in Drosophila buzzatii. Evolution 55: 2248-2256.         [ Links ]

Scheiner, S.M., R.L. Caplan & R.F. Lyman. 1991. The genetics of phenotypic plasticity III genetic correlations an fluctuating asymmetries. J. Evol. Biol. 4: 51-68.         [ Links ]

Silva, J.J. & J. Mendes. 2002. Effect of diflubenzuron on immature stages of Haematobia irritans (L.) (Diptera: Muscidae) in Uberlândia, State of Minas Gerais, Brazil. Mem. Inst. Oswaldo Cruz 97: 679-682.         [ Links ]

Systat. 2000. version 9.0. SPSS Inc., Chicago.

Ueno, H. 1994. Fluctuating asymmetry in relation to two fitness components, adult longevity and male mating success in a ladybird beetle, Harmonia axyridis (Coleoptera: Coccinellidae). J. Ecol. Entomol. 19: 87-88.         [ Links ]

Van Valen, L. 1962. A study of FA. Evolution 16: 125-142.         [ Links ]

Woods R.E., M.J. Hercus & A.A. Hoffmann. 1998. Estimating the heritability of fluctuating asymmetry in field Drosophila. Evolution 52: 816-824.         [ Links ]

Zar, J.H. 1984. Biostatistical analysis, New Jersey, Prentice Hall, 718p.         [ Links ]

 

 

Received 18/10/02.
Accepted 15/02/04.

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