Subscribe Now Subscribe Today
Fulltext PDF
Research Article
Toxicity of Croton urucurana Against the Subterranean Termite Heterotermes sulcatus (Isoptera: Rhinotermitidae)

Mayra Layra dos Santos Almeida, Angelica Silva Oliveira, Gabriel dos Santos Carvalho, Leonardo Santana da Silva, Luciana Barboza Silva, Eliane Carneiro Bueno dos Santos and Fabiana Elaine Casarin

The chemical insecticides used in soil against the subterranean termites result in polluting of soil ecosystems and become causes of human health hazards because of such risks, there is a need of developing ecofriendly baits for the control of these termites. With this objective, a study was carried out to evaluate the termiticide potential of ethanol extract of bark; ethanol-water, hexane and ethyl acetate fractions of bark and ethyl acetate fraction of leaf of Croton urucurana against the subterranean termite, Heterotermes sulcatus (Hagen). The experiments were performed in the laboratory with 100 foraging workers of this termite using no-choice bioassay method. Filter paper treated with crude extract and fractions of C. urucurana at concentrations of 250, 500, 1000, 3000, 5000, 8000 and 10,000 ppm were used. A piece of filter paper treated with respective solvent only was used as a control e.g., control 1 (water), control 2 (ethanol solvent). The substitute variables evaluated were daily mortality, lethal concentration LC50 and LC95 and lethal time LT50 and LT95. It was found that the crude extract and ethanol-water fraction resulted in the lowest LC50 and LC95 values as well as these formulations also presented lowest LT50 and LT95 values among all the treatments, hence making these formulations most toxic among the tested ones against H. sulcatus, C. urucurana seemed to have bioactive compounds with termiticide effect and it can be considered as potential alternative to synthetic insecticides for the control of termites.

Related Articles in ASCI
Similar Articles in this Journal
Search in Google Scholar
View Citation
Report Citation

  How to cite this article:

Mayra Layra dos Santos Almeida, Angelica Silva Oliveira, Gabriel dos Santos Carvalho, Leonardo Santana da Silva, Luciana Barboza Silva, Eliane Carneiro Bueno dos Santos and Fabiana Elaine Casarin, 2016. Toxicity of Croton urucurana Against the Subterranean Termite Heterotermes sulcatus (Isoptera: Rhinotermitidae). Journal of Entomology, 13: 48-54.

DOI: 10.3923/je.2016.48.54

Received: March 01, 2015; Accepted: December 15, 2015; Published: February 15, 2016


The infraorder Isoptera (Krishna et al., 2013) includes 2,882 termite species catalogued worldwide (Constantino, 2015) in which approximately 10% are considered pests (Wood, 1996; Rouland-Lefevre, 2011). They are pests in the urban, agricultural and forest environment (Logan et al., 1990). Due to feeding habit (Seo et al., 2009), termites have become a major polyphagous agricultural pest, being found in crops such as sugar cane (Saccharum officinarum L.), maize (Zea mays L.), rice (Oryza sativa L.), barley (Hordeum vulgare) and peanuts (Arachis hypogaea L.) (Elango et al., 2012).

Subterranean termites belonging to the genera Reticulitermes, Heterotermes and Coptotermes are among the most damaging (Constantino, 2002). The genus Heterotermes have 51 species, in which 12 are considered urban and/or agricultural pests (Constantino, 2015). In South America, it is found six species, being all of them considered pests (Constantino, 2002). In Brazil, the genus Heterotermes cause damage in agricultural and urban areas. In the cultivation of sugar cane, the losses may reach 10 t ha–1 year–1 (Almeida and Alves, 2009). In the Northeastern region, H. sulcatus is the most destructive species of subterranean termites in urban areas (Vasconcellos et al., 2002). Recently, H. sulcatus was found attacking fruit orchards in the Southern region of Piaui, Brazil, with a considerable loss in production of cashew trees.

The control of termites is made mainly through the application of synthetic insecticides or traditional wood preservatives (Lee and Ryu, 2003; Pandey et al., 2012). However, these insecticides have active ingredients in its composition identified with Persistent Organic Pollutants (POPs) (Verma et al., 2009), which although effective, when applied in a large scale contaminates the soil, can trigger resistance mechanisms of pests to pesticides and reducing the action of natural biological control agents. Thereby, it is necessary to find control strategies that are relevant to the sustainability of agricultural production, added to a philosophy based on Integrated Pest Management (IPM) (De Freitas Bueno et al., 2012). In this context, plant extracts stand out for constituting a rich source of bioactive molecules (Elango et al., 2012), with rapid degradation when compared to organochlorine isecticides, besides being obtained from renewable sources (Roel, 2001). Among the plants that present insecticides activities, the genus Croton (Euphorbiaceae) has been widely studied for constituting several active substances as terpenoids, flavonoids and alkaloids (Braga, 1960; Silva et al., 2012). Croton urucurana and its fractions semi purified showed antibacterial activity against Bacillus subtilis and Escherichia coli (Cai et al., 1993). The methanolic extract of C. urucurana bark inserted in artificial diet of larvae of Dysdercus maurus Distant. (Hemiptera, Pyrrhocoridae) caused 70% mortality after 13 days (Silva et al., 2012).

Considering the advancement of researches on the botanical insecticides and their potential for pest control and the need to find slow action products to be incorporated into baits for control of subterranean termites, the objective of this study was to evaluate the potential termiticide of the ethanolic extract of bark of C. urucurana and their ethanol-water, hexane and bark ethyl acetate and leaf ethyl acetate fractions against subterranean termite H. sulcatus (Isoptera: Rhinotermitidae).


Termites: Subterranean termites, H. sulcatus were collected from corrugated cardboard traps of colonies localized in the city of Cristino Castro (PI, Brazil, 08°04’49’’ S, 44°13’27’’ W). Traps were brought to the laboratory and the termites were transferred to plastic boxes containing moist soil. Only large workers (third instar) were used in the experiments. Termites were used within four days after field collection.

Plant material: The leaves and bark of C. urucurana were collected in May 2011, in the region of Dourados, Mato Grosso do Sul, Brazil. The species was identified by Claudio Conceição, Biology Department, Federal University of Mato Grosso do Sul-UFMS, Campo Grande-MT and a sample has been deposited (no. 5009) at CGMS Herbarium.

Preparation of the extract: In the present study, 350 g of C. urucurana leaves and bark were collected and were separated and dried in forced air circulation oven, for three days at a temperature between 40-50°C. After drying, the materials were shredded and submitted to extraction with 5 L of ethanol (3x), by means of Buchner funnel with filter paper. The filtrate was evaporated to dryness under reduced pressure forming the crude extract. After that, the extract was submitted to chromatography in column for fractions separation. The glass column (8 cm diameter: 60 cm long) was packaged with silica gel (240 g) and a mixture of crude extract with ethanol was held to produce a reddish brown solid (424.13 g). The fractions were collected in 200 mL conical sample bottles and verified by Thin Layer Chromatography (TLC).

Anti-termitic activity: The no-choice bioassay method of Kang et al. (1990) and Cheng et al. (2007) was employed to evaluate the anti-termitic activity of the bark extract of C. urucurana and their fractions.

Table 1: Curve slopes data of concentration-mortality, LC50 and LC95, X2 to the crude extract Croton urucurana and the ethanol-water, hexane, leaf ethyl acetate and bark on Heterotermes sulcatus
EPM: Medio standard error, LC50: Lethal concentration 50%, LC95: Lethal concentration 95%, CI: Confidence interval 95% probability, X2: Chi-square, P: Probability, FEA: Fraction ethanol-water, FHEX: Hexane fraction, FAEFO: Ethyl acetate fraction leaf, FAEC: Ethyl acetate fraction bark

Petri dishes (9 cm in diameter and 1.5 cm high) filled with approximately 15 g of sterilized sand were used to test the toxicity of the extract against the workers of the H. sulcatus. Concentrations of 250, 500, 1000, 3000, 5000, 80000 and 10,0000 ppm of the extract dissolved in 900 μL of ethanol were applied to 1 g filter paper samples (Whatman No. 3 and 8.5 cm in diameter) as shown in Table 1. A blank filter paper and filter paper treated with solvent only were used as the controls. After the solvent was removed from the treated filter papers by air-drying at ambient temperature, 100 active termites (90 workers and 10 soldiers) above the third instar were added to each plate. Drops of water were periodically sprinkled onto the sterilized sand in the dishes to maintain sufficient moisture for the termites. The experimental delineation used was randomized, with six repetitions for each sample. The mortality of termites was evaluated daily for 14 days. Additionally, Lethal Concentrations-LC and Lethal Time-LT were estimated.

Data analysis: The mortality dada corrected were submitted to analysis of variance ANOVA and separated by Tukey HSD (p<0.01, software SISVAR 4.6). The graphics showing the percentage of survival were made using SigmaPlot software system (2.001 thousand SPSS, Chicago, IL, USA). Lethal concentrations-LC50 and LC95 and lethal time-LT50 were calculated by Probit through the procedure PROC PROBIT Systen of Statistical Analyses program SAS.


Mortality of termites: The crude extract of C. urucurana resulted in 100% of mortality at concentrations of 1000, 3000 and 5000 ppm in 10, 6 e 4 days, respectively. At concentrations of 250 and 500 ppm, the activity of the extract was slower but with low mortality of 36 and 35%, respectively, after 15 days (Fig. 1a). In the ethanol-water fraction, at a 3000 ppm concentration was more toxic to termites than other concentrations within five days, thereafter, at a concentration of 5000 ppm resulted in higher percentage of mortality (Fig. 1b). The hexane fraction (Fig. 1c) in 8.000 ppm concentration resulted in 50% mortality of termites after 7 days. For concentrations of 500, 1000 and 3000 ppm, the survival was above 40% (Fig. 1c). The fractions of bark ethyl acetate (Fig. 1d) and leaf ethyl acetate (Fig. 1e) presented themselves efficient in the control of termites in the concentration of 10,000 ppm. The mortality rate of 100% of termites in days 12 and 13 after application of bark ethyl acetate fraction and leaf ethyl acetate fraction, respectively (Fig. 1d and e).

Estimate of lethal concentration: The results of probit analysis for determination of lethal concentrations (LC50 and LC95) showed that LC50 of ethanol-water fraction was the most efficient one. In this fraction, the minimum concentration required to cause 50% of mortality in workers was estimated in 280 ppm with an interval ranging from 235-319 ppm. As for the values of LC95, the ethanol-water fraction (831 ppm) also showed higher toxicity compared to other compounds (Table 2). Among the compounds tested, the leaf ethyl acetate fraction was considered less toxic, with LC50 estimated in 1089 ppm and LC95 in 4150 ppm (Table 2).

Estimating the lethal time: For the analysis of Lethal Time (LT) the crude extract of C. urucurana was the most toxic, with LT50 estimated in 2.6 days in 3,000 ppm concentration. In the same concentration ethanol-water fraction, obtained a LT50 estimated at 3.8 days and also showed high toxicity when compared to the control LT50 (93.5 days). The hexane, bark ethyl acetate, leaf ethyl acetate fractions, in 3000 ppm concentration, presented less toxicity with a LT50 of 14.3, 12.3 and 14 days, respectively, compared to the control (93.5 days). As for the LT95 the results show higher toxicity of crude extract of C. urucurana (5 days) compared to other compounds and lower toxicity to bark ethyl acetate (79.6 days) 3000 ppm concentration (Table 3).

Fig. 1(a-e):
Mortality of the workers of H. sulcatus in contact with filter paper treated with (a) Extracto crud of C. urucurana, (b) Fraction ethanol-water, (c) Hexane fration, (d) Leaf ethyl acetate and (e) Bark ethyl acetate

Table 2: Concentrations used in the different bioassays from the crude extract and semipurified fractions of Croton urucurana
FEA: Ethanol-water fraction, FHEX: Hexane fraction, FAEC: Peel ethyl acetate fraction, FAEFO: Leaf ethyl acetate fraction

Table 3: Termiticide activity (LT50 and LT95/days) of Croton urucurana and their fractions in the concentration of 3000 ppm on Heterotermes sulcatus workers
EPM: Medio standard error, LT50: Lethal time 50%, LT99: Lethal time 99%, IC: Confidence interval 95% probability, X2: Chi-square, P: Probability, FEA: Fraction ethanol-water, FHEX: Hexane fraction, FAEFO: Ethyl acetate fraction leaf, FAEC: Ethyl acetate fraction bark


Survival analyses showed that the crude extract C. urucurana provided higher percentage of mortality of H. sulcatus in less time, when compared to the semipurified fractions. This fact may be related to bioactive compounds with insecticidal effect present in species of the genus Croton as the tannins. This phenolic compound binds readily with proteins to form a complex tannin-protein that reduces, significantly, the growth and survival of insects, once it turns off digestive enzymes and consequently makes it difficult the digestion (Mello and Silva-Filho, 2002). Additionally, the subterranean termites from the family Rhinotermitidae have protozoa and bacteria responsible for most of the digestion of cellulose. The reduction of these endogenous microorganisms decreases considerably the efficiency in cellulose degradation this group of termites and they can die from starvation (Lo et al., 2010).

Ahmed et al. (2006) reported that termites Microtermes obesi (Isoptera: Termitidae) treated with extract obtained from seeds of Croton tiglium L. (Euphorbiaceae) decreased number of colonies of bacteria in the intestinal flora of termites in comparison with those from untreated termites. As the intestines of Termitidae family consists of a consortium of bacteria and endogenous cellulolytic enzymes (Tokuda et al., 2012) responsible for the degradation of cellulose, there has been a reduction in nutrient absorption and consequently on survival.

Lethal concentration analyses showed that the ethanol-water fraction presented the lowest value of LC50 (280 ppm) and LC95 (831 ppm) and it was considered the most toxic fraction for H. sulcatus, followed by crude extract of C. urucurana with LC50 estimated in 304 ppm and LC95 of 881 ppm. These compounds showed symptoms of convulsions, tremor, muscle weakness, indicating the presence of bioactive molecules present in plant secondary metabolites, which may show neurotoxic effect. Ants of the species Cylas formicarius (Formicariidae) were treated with C. cajucara, which presented neurotoxic symptoms (Kubo et al., 1991). In this paper, poisoning symptoms appear rapidly in workers of H. sulcatus, after feeding with extract C. urucurana. According to these authors, the poisoning symptoms of C. cajucara is related to the presence of cis-desidrocrotonine, present in various species of the genus Croton and consequently, can relate to the symptoms observe in H. sulcatus.

According to the results in this work, the leaf ethyl acetate fraction LC50 (1089 ppm) was considered less toxic to H. sulcatus than t he bark ethyl acetate fraction LC50 (886 ppm). The efficiency of a botanical insecticide varies with the concentration (Silva et al., 2012) and the part of the plant from which the toxic metabolite was synthesized (Haas et al., 2002). Therefore, it is likely that the chemicals present in the bark ethyl acetate fraction have the greatest potential termiticide. Such statement is based on chemical studies carried out with the bark ethyl acetate fraction, which resulted in the isolation of phenolic compounds, catechin and gallocatechin (Winkel-Shirley, 2001), which may be involved in insecticidal activity observed on termites.

These condensed tannins are phenolic compounds which when consumed, bind the digestive proteins of insects and reduces their survival (Winkel-Shirley, 2001). In bioassays conducted with H. sulcatus there was total consumption of filter paper treated with these fractions, which can prove that termiticide activity observed for H. sulcatus is a result of the action of the compounds catechin and gallocatechin.

Silva et al. (2009), obtained similar results when they tested the bark ethyl acetate fraction of C. urucurana embedded in artificial diet of A. kuehniella (Lepidoptera: Pyralidae). They tested this fraction in concentration of 1.0% (10000 ppm) and reached an average of 55% mortality of A. kuehniella. For the larvae fed with solutions of this fraction in concentrations of 0.5% and 1.0 (5000 and 10000 ppm), there was a reduction in weight of 54 and 30%, respectively, when compared to the control treatment.

As for lethal time estimates, the crude extract of C. urucurana presented the lowest LT50 (2.6 days) and LT95 (5 days), in a concentration of 3,000 ppm. Ahmed et al. (2007), working with extract of C. tiglium on Odontotermes obesus Rambur (Isoptera: Termitidae). The presented similar effect with this work (of LT50, 1.5 day). However, in higher concentrations (500,000 and 100,000 ppm), the extract of Jatropha curcas L. which also belongs to the family Euphorbiaceae while being tested on O. obesus resulted in higher LT50 (4 days) in a higher concentration (100,000 ppm) when compared to the crude extract of C. urucurana on H. sulcatus.

Croton urucurana and its fractions showed potential termiticide, resulting in a high mortality of H. sulcatus. According to Guerra (1985), the species of Croton have high power insecticide and in some cases are more toxic to insects than the pyrethrum found in chrysanthemum flowers, that offers wide spectrum of action. Thus, these compounds have high probability of being applied in controlling subterranean termites. Future studies are needed to confirm the efficiency of the compounds the C. urucurana against H. sulcatus.

Ahmed, S., M.A. Riaz and M. Shahid, 2006. Response of Microtermes obesi (Isoptera: Termitidae) and its gut bacteria towards some plant extracts. J. Food Agric. Environ., 4: 317-320.
Direct Link  |  

Ahmed, S., M.A. Riaz, A. Malik and M. Shahid, 2007. Effect of seed extracts of Withania somnifera, Croton tiglium and Hygrophila auriculata on behavior and physiology of Odontotermes obesus (Isoptera, Termitidae). Biologia, 62: 770-773.
CrossRef  |  Direct Link  |  

Almeida, J.E.M. and S.B. Alves, 2009. The foraging activity of Heterotermes tenuis (Hagen) (Isoptera: Rhinotermitidae) in sugarcane using the Termitrap® trap. Instituto Biologico Sao Paulo, 76: 613-618.
Direct Link  |  

Braga, R., 1960. Northeastern Plants, Especially the Ceara. 2nd Edn., Official Press, Fortaleza.

Cai, Y., Z.P. Chen and J.D. Phillipson, 1993. Clerodane diterpenoids from Croton lechleri. Phytochemistry, 34: 265-268.
CrossRef  |  Direct Link  |  

Cheng, S.S., H.T. Chang, C.L. Wu and S.T. Chang, 2007. Anti-termitic activities of essential oils from coniferous trees against Coptotermes formosanus. Bioresour. Technol., 98: 456-459.
CrossRef  |  PubMed  |  Direct Link  |  

Constantino, R., 2002. The pest termites of South America: Taxonomy, distribution and status. J. Applied Entomol., 126: 355-365.
CrossRef  |  Direct Link  |  

Constantino, R., 2015. On-line termites database. University of Brasilia.

De Freitas Bueno, R.C.O., J.R.P. Parra and A. de Freitas Bueno, 2012. Trichogramma pretiosum parasitism of Pseudoplusia includens and Anticarsia gemmatalis eggs at different temperatures. Biol. Control, 60: 154-162.
CrossRef  |  Direct Link  |  

Elango, G., A. Abdul Rahuman, C. Kamaraj, A. Bagavan and A. Abduz Zahir et al., 2012. Efficacy of medicinal plant extracts against Formosan subterranean termite, Coptotermes formosanus. Ind. Corps Prod., 36: 524-530.
CrossRef  |  Direct Link  |  

Guerra, M.S., 1985. Alternatives for the Control of Pests and Diseases of Cultivated Plants and their Products. Embrapa, Brasilia, Pages: 165.

Haas, W., H. Sterk and M. Mittelbach, 2002. Novel 12-deoxy-16-hydroxyphorbol diesters isolated from the seed oil of Jatropha curcas. J. Nat. Prod., 65: 1434-1440.
CrossRef  |  Direct Link  |  

Kang, H.Y., N. Matsushima, K. Sameshima and N. Takamura, 1990. Termite resistance tests of hardwoods of Kochi growth. I. The strong termiticidal activity of kagonoki (Litsea coreana). J. Jpn. Wood Res. Soc., 36: 78-84.
Direct Link  |  

Krishna, K., D.A. Grimaldi, V. Krishna and M.S. Engel, 2013. Treatise on the isoptera of the world: Volume 4 Termitidae (Part one). Bull. Am. Museum Nat. History, 377: 973-1495.
CrossRef  |  Direct Link  |  

Kubo, I., Y. Asaka and K. Shibata, 1991. Insect growth inhibitory nor-diterpenes, cis-dehydrocrotonin and trans-dehydrocrotonin, from Croton cajucara. Phytochemistry, 30: 2545-2546.
CrossRef  |  Direct Link  |  

Lee, D.H. and D.P. Ryu, 2003. Termite Ecology and Their Control. Korea Forest Research Institute, Seoul, Republic of Korea, pp: 321.

Lo, N., G. Tokuda and H. Watanabe, 2010. Evolution and Function of Endogenous Termite Cellulases. In: Biology of Termites: A Modern Synthesis, Bignell, D.E., Y. Roisin and N. Lo (Eds.). Springer, London, New York, pp: 51-67.

Logan, J.W.M., R.H. Cowie and T.G. Wood, 1990. Termite (Isoptera) control in agriculture and forestry by non-chemical methods: A review. Bull. Entomol. Res., 80: 309-330.
CrossRef  |  Direct Link  |  

Mello, M.O. and M.C. Silva-Filho, 2002. Plant-insect interactions: An evolutionary arms race between two distinct defense mechanisms. Braz. J. Plant Physiol., 14: 71-81.
CrossRef  |  Direct Link  |  

Pandey, A., P. Chattopadhyay, S. Banerjee, K. Pakshirajan and L. Singh, 2012. Antitermitic activity of plant essential oils and their major constituents against termite Odontotermes assamensis Holmgren (Isoptera: Termitidae) of North East India. Int. Biodeterior. Biodegrad., 75: 63-67.
CrossRef  |  Direct Link  |  

Roel, A.R., 2001. Use of plants with insecticidal properties: A contribution to sustainable rural development. J. Devel. Int. Local, 1: 43-50.

Rouland-Lefevre, C., 2011. Termites as Pests of Agriculture. In: Biology of Termites: A Modern Synthesis, Bignell, D.E., Y. Roisin and N. Lo (Eds.). Vol. 18, Springer, New York, ISBN: 9789048139774, pp: 499-518.

Seo, S.M., J. Kim, S.G. Lee, C.H. Shin, S.C. Shin and I.K. Park, 2009. Fumigant antitermitic activity of plant essential oils and components from ajowan (Trachyspermum ammi), allspice (Pimenta dioica), caraway (Carum carvi), dill (Anethum graveolens), geranium (Pelargonium graveolens) and litsea (Litsea cubeba) oils against Japanese termite (Reticulitermes speratus Kolbe). J. Agric. Food Chem., 57: 6596-6602.
CrossRef  |  Direct Link  |  

Silva, L.B., W. Silva, M.L.R. Macedo and M.T.L.P. Peres, 2009. Effects of Croton urucurana extracts and crude resin on Anagasta kuehniella (Lepidoptera: Pyralidae). Braz. Arch. Biol. Technol., 52: 653-664.
CrossRef  |  Direct Link  |  

Silva, L.B., Z.F. Xavier, C.B. Silva, O. Faccenda, A.C.S. Candido and M.T.L.P. Peres, 2012. Insecticidal effects of Croton urucurana extracts and crude resin on Dysdercus maurus (Hemiptera: Pyrrocoridae). J. Entomol., 9: 98-106.
CrossRef  |  Direct Link  |  

Tokuda, G., H. Watanabe, M. Hojo, A. Fujita and H. Makiya et al., 2012. Cellulolytic environment in the midgut of the wood-feeding higher termite Nasutitermes takasagoensis. J. Insect Physiol., 58: 147-154.
CrossRef  |  Direct Link  |  

Vasconcellos, A., A.G. Bandeira, C.S. Miranda and M.P. Silva, 2002. Termites (Isoptera) pests in buildings in Joao Pessoa, Brazil. Sociobiology, 40: 1-6.

Verma, M., S. Sharma and R. Prasad, 2009. Biological alternatives for termite control: A review. Int. Biodeterior. Biodegrad., 63: 959-972.
CrossRef  |  Direct Link  |  

Winkel-Shirley, B., 2001. Flavonoid biosynthesis. A colorful model for genetics, biochemistry, cell biology and biotechnology. Plant Physiol., 126: 485-493.
CrossRef  |  Direct Link  |  

Wood, T.G., 1996. The agricultural importance of termites in the tropics. Agric. Zool. Rev., 7: 117-155.
Direct Link  |  

©  2019 Science Alert. All Rights Reserved
Fulltext PDF References Abstract