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CHEMICAL COMPOSITION AND TOXICITY OF CITRUS ESSENTIAL OILS ON Dysmicoccus brevipes (HEMIPTERA: PSEUDOCOCCIDAE) 1 1 Paper extracted from the master's dissertation of the first author.

CARACTERIZAÇÃO QUÍMICA E TOXICIDADE DE ÓLEOS ESSENCIAIS CÍTRICOS SOBRE Dysmicoccus brevipes (HEMIPTERA: PSEUDOCOCCIDAE)

ABSTRACT

The insect Dysmicoccus brevipes (Hemiptera: Pseudococcidae) has been reported as an important pest for several crops, especially coffee. The citrus essential oils can be obtained as by-products of the citrus-processing industry and have been tested as an alternative to control different insect groups. Therefore, the objective of this work was to determine the chemical composition and evaluate the toxicity of commercial sweet orange (Citrus sinensis), bitter orange (Citrus aurantium) and Sicilian lemon (Citrus limon) essential oils and pure monoterpene D-limonene on D. brevipes. The essential oils were analyzed by gas chromatography. Two bioassays were conducted; the first assessing the insect mortality in all oils and the second assessing the lethal concentrations (LC50 and LC95) of the most effective oils. The main components of the oils were D-limonene (83.33%) and Linalool (8.91%) (sweet orange); D-limonene (78.53%) and γ-terpinene (12.65%) (bitter orange); D-limonene (59.78%), beta-pinene (14.71%) and γ-terpinene (10.19%) (Sicilian lemon) and the compound D-limonene had 97% of purity. The highest mortalities were found with the use of the Sicilian lemon (98.68%) and sweet orange (94.11%)oils. The sweet orange oil presented lethal concentrations at 2.21% (LC50) and 3.55% (LC95), and the Sicilian lemon oil at 0.72% (LC50) and 2.91% (LC95). The main component of the sweet orange and Sicilian lemon essential oils was the D-limonene, and the Sicilian lemon oil was most effective oil to control D. brevipes.

Keywords:
Cochineal; Mortality; Natural products.

RESUMO

O inseto Dysmicoccus brevipes (Hemiptera: Pseudococcidae) tem sido relatado como uma praga de importância para diversas culturas, em especial a cafeicultura. Os óleos essenciais cítricos podem ser obtidos como subprodutos da indústria de sucos e vem sendo testados como alternativa no controle de diferentes grupos de insetos. Logo, objetivou-se neste trabalho determinar a composição química e avaliar a toxicidade de óleos essenciais comerciais de laranja doce (Citrus sinensis), laranja amarga (Citrus aurantium), limão Siciliano (Citrus limon) e do monoterpeno D-limoneno sobre a D. brevipes. Os óleos essenciais foram analisados por cromatografia gasosa. Foram realizados dois bioensaios. O primeiro para avaliar a mortalidade em todos os óleos e o segundo para avaliar as concentrações letais (CL50 e CL95) dos óleos mais efetivos. Os constituintes majoritários do óleo de laranja doce foram o D-limoneno (83,33%); linalol (8,91%), do óleo de laranja amarga foram o D-limoneno (78,53%); γ-terpineno (12,65%), do óleo de limão Siciliano foram o D-limoneno (59,78%); beta-pineno (14,71%); γ-terpineno (10,19%) e o composto D-limoneno (97% de pureza). O óleo de limão Siciliano e laranja doce foram os que apresentaram maior percentual de mortalidade, sendo 98,68%, 94,11%.As CL50 e CL95, para o óleo de laranja doce foram de 2,21% e 3,55% e para o óleo de limão Siciliano foram de 0,72% e 2,91%, respectivamente. Portanto, o composto majoritário presente na composição química do óleo essencial de laranja doce e do limão Siciliano foi o D-limoneno e o mais efetivo sobre D. brevipes foio óleo de limão Siciliano.

Palavras-chave:
Cochonilha-branca; Mortalidade; Produtos naturais.

INTRODUCTION

Cochineals (Hemiptera: Coccoidea) constitute one of the main groups of insect pests in various production systems, and may infest cultivated and wild plants (SANTA-CECÍLIA, 2005SANTA-CECÍLIA, L. V. C.; SOUZA, B. Controle biológico de cochonilhas-farinhenta sem cultivos protegidos. Informe Agropecuário Belo Horizonte: EPAMIG , 2005. v. 26, n. 225, p. 24-30 .). The species Dysmicoccus brevipes (Hemiptera: Pseudococcidae) has been found attacking economically important crops such as coffee and pineapple (SANTA-CECÍLIA et al., 2007; CULIK, 2008CULIK, M. P. et al. Diaspididae (Hemiptera: Coccoidea) of Espírito Santo, Brazil. Journal of Insect Science, Tucson, v. 8, n. 17, p. 1-6, 2008.). This cochineal is a polyphagous species that infests roots, leaves and fruits of different cultures (SANTA-CECÍLIA et al., 2007).

In coffee crops, the cochineals have been causing yield losses due to injuries to the plant rosettes from flowering to harvest (SANTA-CECÍLIA et al., 2007SANTA-CECÍLIA, L. V. C. et al. Cochonilhas - farinhentas em cafeeiros: bioecologia, danos e métodos de controle. Belo Horizonte: EPAMIG, 2007. 48 p. (Boletim Técnico, 79).). Infestation of coffee crops by cochineal in the State of Espírito Santo (ES), Brazil, have caused fruit dehydration and consequently yield reductions (MATIELLO; COSTA, 2010MATIELLO, J. B.; COSTA, F. F. Coró das pastagens “ataca” em cafezais: surto de cochonilha da roseta do cafeeiro no Espírito Santo. Revista Brasileira de Tecnologia Cafeeira, Varginha, v. 6, n. 17, p. 30-32, 2010.).

The method used to control insect-pests in Brazil has been predominantly the use of conventional insecticides, which can cause several problems related to their toxicity to humans, contamination of the environment and remaining residues in foods (THOMAZINI; VENDRAMIM; LOPES, 2000THOMAZINI, A. P. B. W.; VENDRAMIM, J. D.; LOPES, M. T. R. Extratos aquosos de Trichilia pallida e a traça-do-tomateiro. Scientia Agrícola, São Paulo, v. 57, n. 1, p. 13-17, 2000.). Therefore, studies on alternatives to mitigate such problems are needed, such as the use of essential oils.

Essential oils are complex compounds that consist of several components, however, they are often characterized by their components of higher concentrations (BAKKALI; AVERBECK; AVERBECK, 2008BAKKALI, F.; AVERBECK, S.; AVERBECK, D. Biological effectis of essential oils. Food and Chemical Toxilology, Oxford, v. 46, n. 2, p.446-475, 2008.). The insecticidal activity of natural products has been studied, since several plants have the potential to affect the insect behavior and metabolism, either by toxicity or repellency (SOUSA et al., 2005SOUSA, A. H. et al. Bioactivity of vegetal powders against Callosobruchus maculatus (Coleoptera: Bruchidae) in caupi bean and seed physiological analysis. Revista de Biologia e Ciências da Terra, Campina Grande, v. 5, n. 2, p. 1-6, 2005.; BRITO; OLIVEIRA; BORTOLI, 2006BRITO, J. P.; OLIVEIRA, J. E. M.; BORTOLI, S. A. Toxicidade de óleos essenciais de Eucalyptus spp. Sobre Callosobruchus maculatus (Fabr. 1775) (Coleoptera: Bruchidae). Revista de Biologia e Ciência da Terra, São Cristóvão, v. 6, n. 1, p.96-103, 2006.).

Essential oils from plants of the genus Citrus are obtained as by-products of the citrus-processing industry. Their major component is the D-limonene, whose content vary from one species to another (BIZZO; HOVELL; REZENDE, 2009BIZZO, H. R.; HOVELL, A. M.; REZENDE, C. M. Óleos essenciais no Brasil: aspectos gerais, desenvolvimento e perspectivas. Química Nova, São Paulo, v. 32, n. 3, p. 588-594, 2009.). Some researchers tested these oils as potential insecticides to control Spodoptera litura (Lepidoptera: Noctuidae), Myzuspersicae (Hemiptera: Aphididae) (ISMAN, 2000ISMAN, M. B. Plant essential oils for pest and disease management. Crop Protection, Guildford, v.19, n. 1, p. 603-608, 2000.), Aedes albopictus (Diptera: Culicidae) and Musca domestica (Diptera: Muscidae) (GIATROPOULOS et al., 2012GIATROPOULOS, A. et al. Evaluation of bioefficacy of three Citrus essential oils against the dengue vector Aedes albopictus (Diptera: Culicidae) in correlation to their components enantiomeric distribution. Parasitology Research, Berlin, v. 111, n. 6, p. 2253-2263, 2012.; KUMAR et al., 2012KUMAR, P. et al. Insecticidal evaluation of essential oils of Citrus sinensis L. (Myrtales: Myrtaceae) against housefly, Muscadomestica L. (Diptera: Muscidae). Parasitology research, Berlin, v. 110, n.5, p. 1929-1936, 2012.).

Therefore, the objective of this work was to determine the chemical composition and evaluate the toxicity of commercial sweet orange (Citrus sinensis), bitter orange (Citrus aurantium) and Sicilian lemon (Citrus limon) essential oils and pure monoterpene D-limonene on D. brevipes.

MATERIAL AND METHODS

The experiments were conducted in the laboratories of the Center for Agricultural Sciences of the Espírito Santo Federal University (CCA-UFES). The chemical composition of the oils was assessed at the Analytical Center and their toxicity was evaluated through bioassays at the Center for Scientific and Technological Development on Phytosanitary Management of Pests and Diseases.

Origin and chemical analysis of the essential oils

Commercial essential oils from sweet orange, bitter orange and Sicilian lemon were obtained from the citrus-processing (fruit peel) and provided by the industry Ferquima Indústria e Comércio LTDA, and the pure D-limonene (97% purity) was provided by the company Sigma Aldrich.

The essential oils were analyzed through gas chromatography coupled to mass spectrometry (GC-MS, QP-PLUS-2010, Shimadzu), using a fused-silica capillary chromatographic column (30 m long and 0.25 mm of internal diameter), with stationary phase Rtx-5MS, helium as the carrier gas and temperatures of 220ºC (injector) and 300ºC (detector). The initial temperature of the column was 60°C, increasing by 3°C every minute until reaching the maximum temperature of 240°C (COSTA et al., 2013COSTA, A. V. et al. Cymbopogon citratus (Poaceae) essential oil on Frankliniella schultzei (Thysanoptera: Thripidae) AND Myzus persicae (Hemiptera: Aphididae). Bioscience Journal, Uberlândia, v. 29, n. 6, p. 1840-1847, 2013.).

The chemical composition of the essential oils was analyzed by gas chromatography in a GC-2010-Plus (Shimadzu) equipped with flame ionization detector (GC-FID), using a capillary column (30 m long and 0.25 mm of internal diameter) with stationary phase Rtx-5MS, nitrogen as the carrier gas and temperatures of 240ºC (injector) and 250°C (detector). The temperature of the column was the same used in the GC-MS analyzes. Samples of the oils (10 mg) was diluted in 1 mL of dichloromethane, and 1 μL of this solution was injected for evaluation (COSTA et al., 2013COSTA, A. V. et al. Cymbopogon citratus (Poaceae) essential oil on Frankliniella schultzei (Thysanoptera: Thripidae) AND Myzus persicae (Hemiptera: Aphididae). Bioscience Journal, Uberlândia, v. 29, n. 6, p. 1840-1847, 2013.).

The components of the oils were identified by comparing the mass spectra obtained with those in the Willey 330,000 spectrographic database, and by the Kovats index (KI) calculated for each component (ADAMS, 2007ADAMS, R. P. Identification of essential oil components by gas chromatography mass spectroscopy. 4. ed. Carol Stream: Allured Publishing Corp, 2007. 804 p.).

The relative percentage of each compound was calculated by the ratio between the integral area of their respective peaks and the total area of all constituents of the sample, whose data were obtained by the gas chromatograph with flame ionization detector.

Culture of D. brevipes (Cockerell, 1893) (Hemiptera: Pseudococcidae)

The insects used in the bioassays were collected from coffee plants (Coffea canephora) in Alegre ES (20°47'09"S; 41°31'28"W) and cultivated in laboratory. The culture was maintained in the Laboratory of Entomology of the CCA-UFES in an air-conditioned room at 25 ± 1ºC, relative humidity of 70 ± 10% and 12-hour photophase, on Japanese pumpkins (Tetsukabuto), which served as food substrate, following the methodology described by Sanches and Carvalho (2010SANCHES, N. F.; CARVALHO, R. S. Procedimentos para manejo da criação e multiplicação do predador exótico Cryptolaemus montrouzieri. Cruz das Almas: Embrapa Mandioca e Fruticultura, 2010. p. 1-5. (Circular Técnica, 99).).

Bioassays

The mortality (toxicity) of insects in the bioassays was evaluated following the methodology described by Santa-Cecília et al. (2010), using 4.5-cm-diameter leaf discs of conil on coffee leaves, arranged in 9-cm-diameter Petri dishes with 5-mm-deep layer of a 3% agar-water solution. Each leaf disc was infested with 15 second-instar nymphs of D. brevipes, and each treatment had 3 replications.

The bioassays were conducted in an air-conditioned chamber (25 ± 1°C, relative humidity of 70 ± 10% and photophase of 12h). Evaluations were carried out at 24, 48 and 72 hours after applying the treatments to the leaf discs, by counting the dead individuals, which are characterized by a change to darker colors compared with those at the beginning of the experiment, and absence of movements.

In Bioassay I, the sweet orange, bitter orange, Sicilian lemon and pure D-limonene solutions were used at concentrations of 10% (v v-1) to identify the most toxic products. The sweet orange and Sicilian lemon essential oils promoted the highest mortality rates (above 90%), thus, they were subjected to concentration-mortality curves (LC50 and CL95) in Bioassay II. The essential oil concentrations were 1.4, 1.9, 2.7, 3.7 and 5.2% (v v-1) (sweet orange), and 1.4, 1.9, 3.7, 5.2 and 7.2% (v v-1) (Sicilian lemon). The essential oil solutions were solubilized in Tween® 80 (0.05% v v-1) and distilled water.

The control treatment consisted of water, using the Tween® 80 (0.05% v v-1) as solvent. The Bioassay II was evaluatedat three periods, in order to analyze the effect of the products on different generations of the insects.

Data analysis

The Bioassay I was arranged in a completely randomized design, with means compared by the Tukey's test (p≤0.05) and mortality values corrected using the Abbott’s formula (1925ABBOTT, W. S. A method for computing the effectiveness of an insecticide. Journal of Economic Entomology, Oxford, v. 18, n. 1, p. 265-267, 1925.) in the program R Development Core Team (2009). The mortality data (number of dead insects) in Bioassay II were analyzed using the Probit regression (FINNEY, 1952FINNEY, D. J. Probit Analysis: a statistical treatment of the sigmoid response curve. 2. ed. New York-London: Cambridge University Press, 1952.318 p.), estimating the lethal concentrations LC50 and CL95. The program POLO-PC was used for the analysis, which determined the lethal concentration with a confidence interval of 95% (LEORA SOFTWORE, 1987). The curves were compared (between generations in the same oil and between oils) through confidence intervals (ROBERTSON et al., 2007ROBERTSON, J. L. et al. Bioassays with Arthropods. 2. ed. Boca Raton: CRC Press, 2007.199 p.).

RESULTS AND DISCUSSION

The main components of the oils were D-limonene (83.33%) and Linalool (8.91%) (sweet orange); D-limonene (78.53%) and γ-terpinene (12.65%) (bitter orange); D-limonene (59.78%), beta-pinene (14.71%) and γ-terpinene (10.19%) (Sicilian lemon) (Table 1).

These results were similar, with some numerical differences, to the works of Assunção (2013ASSUNÇÃO, G. V. Caracterização química e avaliação da atividade larvicida frente ao Aedes aegypti do óleo essencial da espécie Citrus sinensis L. Osbeck (laranja doce). 2013. 93 f. Dissertação (Mestrado em Química: Área de Concentração em Química de Produtos Naturais e Alimentos) - Universidade Federal do Maranhão, São Luís, 2013.) and Koketsu et al. (1983KOKETSU, M. et al. Óleos Essenciais de Frutos Cítricos Cultivados no Brasil. Rio de Janeiro: Embrapa, 1983. v. 7, 21 p. (Boletim de Pesquisa).). These variations probably occur due to factors related to the oil extraction method, genetic characteristics of the species and environmental conditions in which they were grown (ASSUNÇÃO, 2013ASSUNÇÃO, G. V. Caracterização química e avaliação da atividade larvicida frente ao Aedes aegypti do óleo essencial da espécie Citrus sinensis L. Osbeck (laranja doce). 2013. 93 f. Dissertação (Mestrado em Química: Área de Concentração em Química de Produtos Naturais e Alimentos) - Universidade Federal do Maranhão, São Luís, 2013.).

According to the preliminary tests in Bioassay I, using the products at concentration of 10% (v v-1), the Sicilian lemon (98.68%) and sweet orange (94.11%) essential oils and the pure D-limonene (69.03%) presented the highest percentages of mortality. The bitter orange essential oil presented the lowest mortality rate, which did not differ from the pure D-limonene (Table 2).

Based on the results of the Bioassay I, the sweet orange and Sicilian lemon essential oils presented mortality above 90% at the concentration of 10% (v v-1), thus, they were selected for the Bioassay II, in which the LC50 and CL95 were estimated.

The inclination of the LC50 and LC95 curves of the sweet orange and Sicilian lemon essential oils on D. brevipes, with their respective confidence intervals are described in Table 3. No significant differences were found between the generations, regardless of the essential oil used.

The inclination of the curve indicates the variability among individuals in the population (KERNS; GAYLOR, 1992KERNS, D. L.; GAYLOR, M. J. Insecticide resistance in field populations of the cotton aphid (Hemiptera: Aphididae). Journal of Economic Entomology , Oxford, v. 85, n. 1, p. 1-8, 1992.). Curves with lower inclination indicate greater genetic variability, suggesting the presence of more than one genotype in the population, i.e., a greater heterogeneity of response to the applied treatment, resulting in resistance of the population to the product used (SIQUEIRA; GUEDES; PICANÇO, 2000SIQUEIRA, H. A. A.; GUEDES, R. N. C.; PICANÇO, M. C. Insecticide resistance in populations of Tuta absoluta (Lepdoptera: Gelechiidae). Agricultural and Forest Entomology, St Albans, v. 2, n. 2, p. 147-153, 2000.). The inclination of the mortality curve was higher for sweet orange oil, indicating higher mortality in small doses, compared with the curve for Sicilian lemon oil.

Table 1
Chemical composition of bitter orange (BO), sweet orange (SO) and Sicilian lemon (SL) essential oils.

Table 2
Mean mortality rate of Dysmicoccus brevipes treated with different citrus essential oils at 10% concentration (v v-1) (temperature of 25 ± 1°C, relative humidity of 70 ± 10% and photophase of 12h).

The treatment with Sicilian lemon essential oil presented a more heterogeneous D. brevipes population compared with the treatment with sweet orange essential oil. This variability among individuals of the same population is denoted by the inclination of the concentration-mortality curve (KERNS; GAYLOR, 1992KERNS, D. L.; GAYLOR, M. J. Insecticide resistance in field populations of the cotton aphid (Hemiptera: Aphididae). Journal of Economic Entomology , Oxford, v. 85, n. 1, p. 1-8, 1992.). This result indicates an intra-populational genetic diversity or different selective pressures on the individuals, which contribute to the development of insect resistance in the case of continuous use of these oils, and may explain the variability obtained in these results.

Table 3
Inclination of curves of lethal concentrations (LC50 and LC95) of sweet orange and Sicilian lemon essential oils to Dysmicoccus brevipes(Temperature 25 ± 1°C, relative humidity of 70 ± 10% and photophase of 12h).

The Sicilian lemon oil was more toxic to D. brevipes than the sweet orange oil because its lower lethal concentration (LC50 of 0.72% and LC90 of 2.91%). Most of the insecticidal capacity of citrus essential oils are due to the substances D-limonene and Linalool, which have contact (degrade exoskeleton cuticle lipids) and fumigant actions against insects (BUSS; PARK-BROWN, 2002BUSS, E. A.; PARK-BROWN, S. G. Natural products for insect pest management. Gainesville: UF/IFAS, 2002. Disponível em: <Disponível em: http:// edis.ifas.ufl.edu/IN197 >. Acesso em: 06 ago. 2015.
http:// edis.ifas.ufl.edu/IN197...
; ROZMAN; KALINOVIC; KORUNIC, 2007ROZMAN, V.; KALINOVIC, I.; KORUNIC, Z. Toxicity of naturally occurring compounds of Lamiaceae and Lauraceae to three stored-products insects. Journal of Stored Products Research, Oxford, v. 43, n. 1, p. 349-355, 2007.).

The insecticidal activityof the pure D-limonene (at 10% of the solution) was evaluated because it is the most common compound in the essential oils tested, however, when applied singly, it caused mortalities below 90%, denoting that the bioactivity of the essential oils is usually due to the major constituents.

However, the bioactivity may also be affected by minor constituents, which may promote a synergism with the major constituents, thus increasing mortality (JIANG et al., 2009JIANG, Z. et al. Comparative toxicity of essential oils of Litseapungens and Litseacubeba and blends of their major constituents against the cabbage looper, Trichoplusiani. Journal of Agricultural and Food Chemistry, Washington, v. 57, n. 1, p.4833-4837, 2009.). The interactions between major and minor constituents are complex and may affect the characteristics of the essential oil, as well as the deleterious effects on insects.

The greater insecticidal activity of the Sicilian lemon and sweet orange essential oils, compared with the pure D-limonene, was probably due to the synergy of their compounds. Moreover, the complexinteractions between components of essential oils can change the physiology of insects (KHALFI et al., 2008KHALFI, O. et al. Chemical composition and insecticidal properties of Origanumglandulosum (Desf.) essential oil from Algeria. Journal Science of Food and Agriculture, New York, v. 88, n. 1, p.1562-1566, 2008.; RATTAN, 2010RATTAN, R. S. Mechanism of action of insecticidal secondary matabolites of plant origin. Crop Protection , New York, v. 29, n. 9, p. 913-920, 2010.).

Therefore, the Sicilian lemon (Citrus limon) and sweet orange (Citrus sinensis) essential oils showed insecticidal activity on D. brevipes, which can be attributed to interactions between major and minor constituents, since the chemical compounds are very important for the insecticidal activity, regardless of their concentration in the essential oil.

CONCLUSION

The major compound present in the chemical composition of the sweet orange (Citrus sinensis), bitter orange (Citrus aurantium) and Sicilian lemon (Citrus limon) essential oils was the D-limonene. The Sicilian lemon essential oil promoted the highest mortality rates of D. brevipes with a lower lethal concentration and thus, it was the most effective for controlling this insect.

ACKNOWLEDGMENTS

The authors thank to the institutions NUDEMAFI, CAPES and FAPES for technical and financial support.

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  • 1
    Paper extracted from the master's dissertation of the first author.

Publication Dates

  • Publication in this collection
    Jul-Sep 2017

History

  • Received
    04 May 2016
  • Accepted
    05 Dec 2016
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