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Original Research Article | OPEN ACCESS

Chemical composition and insecticidal properties of the essential oil of Bidens frondosa L (Asteraceae) against booklice (Liposcelis bostrychophila)

Heng Yu Li1, Xu Bo Chen2, Qi Zhi Liu1, Zhi Long Liu1

1Department of Entomology, China Agricultural University, 2 Yuanmingyuan West Road, Haidian District, Beijing 100193; 2College of Ecology, Lishui University, No. 1 Xueyuan Road, Lishui City, Zhejiang Province, 323000, China.

For correspondence:-  Zhi Liu   Email: zhilongliu@cau.edu.cn   Tel:+861062734458

Received: 13 July 2016        Accepted: 16 December 2016        Published: 31 January 2017

Citation: Li HY, Chen XB, Liu QZ, Liu ZL. Chemical composition and insecticidal properties of the essential oil of Bidens frondosa L (Asteraceae) against booklice (Liposcelis bostrychophila). Trop J Pharm Res 2017; 16(1):171-177 doi: 10.4314/tjpr.v16i1.23

© 2017 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To investigate contact and fumigant toxicity of the essential oil of Bidens frondosa and its isolated constituents against booklice (Liposcelis bostrychophila).
Methods: The essential oil of B. frondosa was obtained by hydro-distillation and analyzed by gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS) with HP-5MS column. The active constituents were purified from the oil by bioactivity-guided fractionation. Contact (impregnated filter paper method) and fumigant toxicity (sealed space) of the oil and its isolates were determined.
Results: Thirty-two compounds, representing 98.88 % of the total oil, were determined and the major constituents of the essential oil were caryophyllene oxide (20.50 %), borneol (17.66 %), 4-terpineol (17.26 %), and β-cedrene (6.94 %). The essential oil displayed fumigant toxicity against booklice, with a median lethal concentration (LC50) of 507.35 μg/L while the isolated constituents, borneol and 4-terpineol, had LC50 values of 2.20 mg/L and 335.24 μg/L against booklice, respectively. The essential oil also exhibited contact toxicity against L. bostrychophila with an LC50 value of 210.73 µg/cm2. Borneol, caryophyllene oxide, β-cedrene, and 4-terpineol showed acute toxicity against booklice with LC50 of 98.04, 84.62, 458.79 and 211.35 µg/cm2, respectively.
Conclusion: The results suggest that the essential oil and its isolates possess potential for cultivation into natural insecticides or fumigants, for control of insects in stored grains.

Keywords: Bidens frondosa, Liposcelis bostrychophila, Contact toxicity, Essential oil, Boolice, Stored grains, Natural insecticides, Fumigants

Introduction

During our screening program for new pesticides from Chinese medicinal herbs and local wild plants, the essential oil of the aerial parts of Bidens frondosa L. (Family: Asteraceae) was found to exhibit acute toxicity against booklice (Liposcelis bostrychophila Badonnel). Common beggar-ticks (B. frondosa) are annual, erect, herbaceous plants arising from a taproot. This herb is usually about 20 to 60 centimeters high, but it can reach 1.8 meters. It is weedy in appearance and extremely prolific.

This species originated from North America and has now became a common invasive plant in China where it is often found in moist woods, meadows, thickets, fields, roadsides, railroads, borders of streams, ponds, sloughs, swamps and ditches [1]. It is presently distributed in Guangdong, Jiangsu, Shanghai, Jiangxi, Zhejiang and Liaoning province, China [1,2]. Fresh leaves and stems of B. frondosa can be used as human food [3]. Chinese traditional medicine made use of the aerial parts of B. frondosa to treat virtual fatigue, night sweat hemoptysis, infantile malnutritioal and dysentery [4]. Various polyacetylenes, acylated glucosides, flavonoids, phenylpropanoids, terpenoids, and sterols were isolated from this plant in the previous phytochemical investigations [5,6]. The composition of the essential oil derived from the leaves of B. frondosa has also been determined previously [3]. However, a literature survey has shown that there is no previous report on the volatile constituents and insecticidal activity of the essential oil of the aerial parts of B. frondosa. The aims of the present project were to determine the composition of the essential oil of B. frondosa and its insecticidal properties against booklice, and to isolate active constituents from the essential oil.

Methods

Plant material and essential oil

Fresh aerial parts of B. frondosa (20 kg) at flowering stage were collected from Lishui City, Zhejiang Province, China (27.54° N and 119.20° E) in September 2014. The plant was classified by Dr. Liu (College of Life Sciences, Beijing Normal University, Beijing 100875, China), and a voucher specimen (no. ENTCAU-Compositae-Dalangba-161) was saved at the museum of Department of Entomology, China Agricultural University, Beijing, China. The plant sample was chopped into small pieces and subjected to hydro distillation for 6 h using a modified Clevenger-type apparatus. n-Hexane was used as a solvent to extract the essential oil from the distilled solution and water was removed from the extract by using anhydrous Na2SO4. The essential oil was then saved in airtight containers in a refrigerator at 4 °C for subsequent experiments.

Analysis of the essential oils

GC analysis was carried out using a Hewlett–Packard 5890 gas chromatograph equipped with HP-5 column (5 % diphenyl and 95 % dimethylpolysyloxane, 30 m × 0.25 mm, 0.25 μm film thickness) with nitogen as the carrier gas and flow rate of 1 mL min1. Oven temperature was programmed from 60 to 280 °C (at a rate of 2 °C min1); injector and detector temperatures were 270 °C and 300 °C, respectively. GC-MS analysis was performed using a Agilent 6890N gas chromatograph connected to Agilent 5973N mass selective detector at 70 eV ionization energy, equipped with an HP-5MS capillary column (5 % diphenyl and 95 % dimethyl-polysyloxane, 30m × 0.25mm × 0.25μm). The carrier gas was helium at a flow rate of 1.0 ml min1. Oven temperature was programmed as follows: the initial temperature was detained at 60 °C for 1 min and increased at 10 °C min1 to 180 °C, remained at 180 °C for 1 min, and then ramped at 20 °C min1 to 280 °C and held there for 15 min. The injector temperature was kept at 270 °C. The samples (1 μL, 1/100, v/v, in acetone) were instilled, with a split ratio of 1:10. Spectra were scanned over the range 20 to 550 m/z at 2 scans s-1. Most constituents were identified by comparison of their retention indices with those reported in the literature or with those of authentic compounds available in our laboratories. Retention indices were determined using retention times of n-alkanes (C8–C24) under the same chromatographic conditions. Further identification was made by comparing the NIST 05 and Wiley 275 library data of the peaks with those reported in literature, mass spectra of the peaks with literature data [7]. Relative percentages of the oil constituents were estimated based on GC peak areas without using correction factors.

Purification and characterization of four constituents 

The crude essential oil of B. frondosa (30 ml) was subjected to column chromatography over silica gel, eluting with a gradient of increasing ethyl acetate in n-hexane (0-100 %, v/v). Fractions of 300 mL each were gathered and distilled at 35 °C, and related fractions as indicated by their TLC profiles were merged to produce 15 fractions. Based on contact bioassay, fractions (4, 6, 9 and 13) were further separated by preparative silica gel column chromatography (PTLC) until to obtain four pure compounds borneol, 4-terpineol, β-cedrene and caryophyllene oxide. The structure of the compounds was determined by using nuclear magnetic resonance. 1H and 13C NMR spectra were detected on Bruker Avance DRX 500 instruments using CDCl3 as solvent with TMS as internal standard.

Insects

The booklice (L. bostrychophila) were provided from a laboratory colony in the dark in incubators at 28-30 °C and 70 - 80 % relative humidity and the artificial diet (1: 1: 1 mixture of milk powder, active yeast, and flour) was provided. All the containers accommodating the insects and the Petri dishes utilized in experiments were made escape-proof with a coating of polytetrafluoroethylene (Fluon®, Blades Biological, Edenbridge, UK). Laboratory bioassays were performed within one week after adult collections.

Contact toxicity test

In a preliminary experiment, suitable testing concentration range of the essential oil of B. frondosa and pure compounds was determined. Acetone was used to dilute the essential oil and compounds. The solution (150 μL, 2.0, 2.4, 2.9, 3.5, 4.2 and 5.0 % in acetone) was applied to a filter paper (Whatman, 3.5 cm in diameter). Then the treated filter paper was treatment with a solid glue (Glue Stick, Jong Ie Nara Co Ltd, Hong Kong) and put in a petri dish (3.5 cm in diameter). Ten booklice were left on the Petri dish. The cover of the Petri dish with several drilled holes drilled into it was placed over it and all the Petri dishes were kept in an incubator at 27 - 29 C, 70 - 80 % RH for 24 h. Acetone was used as a control while pyrethrum extract (25 % pyrethrin I and pyrethrin II, obtained from Fluka Chemie) was adopted as a positive control. Five concentrations and five replicates of each concentration were taken in all treatments and controls. Mortality of insects was examined.

Fumigant toxicity bioassay

The appropriate test concentrations of the essential oil/pure compounds were estimated by range-finding experiments. Ten adults of the booklice were transferred into a small glass bottle (8 mL) by using a fine goat hair brush. Acetone was utilized to dilute the essential oil/compounds. A 10 μL solution (3.1, 3.4, 3.7, 4.1, 4.5 and 5.0 % in acetone) was evenly applied to a filter paper strip (3.5 cm ´ 1.5 cm). The impregnated filter paper was then laid in the bottom cover of a big glass bottle (250 mL). The small bottle was placed in a big bottle, and covered leaving a sealed space. The booklice were exposed for 24 h and the mortality of insects was determined. All the treatments were replicated five times. Acetone was utilized as control and dichlorvos was employed as positive control. Positive control, dichlorvos (99.9 %) was purchased from Aladdin-reagent Company (Shanghai).

Statistical analysis

The LC50 values of the essential oil/compounds and their 95 % confidence intervals were estimated by using PriProbit Program V1.6.3 [8]. Samples for which the 95 % fiducial limits did not overlap were regarded as significantly different.

Results

The content of essential oil of the aerial parts of B. frondosa at flowering stage was 0.03 % (yellow, v/w based on fresh weight) while its density was 0.89 g/ml. A total of 32 components from the essential oil of B. frondosa were detected, representing 98.88 % of the crude essential oil (). The principal constituents of B. frondosa essential oil were caryophyllene oxide (20.50 %), borneol (17.66 %), 4-terpineol (14.56 %), α-terpineol (6.28 %), β-cedrene (6.94 %), spathulenol (4.07 %) and caryophyllene (3.97 %) (). Sesquiterpenoids represented 16 of the 32 constituents, corresponding to 52.14 % of the essential oil while monoterpenoids characterized 12 of the 32 compounds (46.06 % of the crude essential oil).

Borneol. Colorless oil. 1H-NMR (CDCl3, 500 MHz) δ ppm: 4.04 (1H, m, H-1), 2.28 (1H, m, H-5), 1.90 (1H, m, H-6a), 1.70 (2H, m, H-6b, H-4a), 1.62 (1H, t, -OH), 1.25 (2H, m, H-4b, H-3a), 0.95 (1H, dd, H-3b), 0.87 (3H, s, 8-C H3), 0.86 (3H, s, 9-C H3), 0.85 (3H, s, 10-C H3). 13C-NMR (CDCl3, 125MHz) δ ppm: 77.7 (C-1), 49.9 (C-2), 48.2 (C-8), 45.2 (C-5), 39.2 (C-6), 28.5 (C-4), 26.2 (C-3), 20.5 (C-9), 18.9 (C-10), 13.4 (C-7). The spectra data are in agreement with earlier reports [9,10].

4-Terpineol. Colorless oil. 1H-NMR (CDCl3, 500 MHz) δ ppm: 5.32 (1H, m, H-5), 2.17 (2H, m, H-6), 1.94 (2H, m, H-3), 1.71 (3H, s, 4-CH3), 1.67 (1H, m, H-7), 1.58 (2H, m, H-2), 0.97 (3H, d, J = 7.0 Hz, 8-CH3), 0.94 (3H, d, J = 7.0 Hz, 9-CH3). 13C-NMR (CDCl3, 125MHz) δ ppm: 133.9 (C-4), 118.5 (C-5), 71.8 (C-1), 36.8 (C-7), 34.6 (C-2), 30.8 (C-6), 27.1 (4-CH3), 23.3 (C-3), 16.8 (C-8, 9). The spectra data are consistent with the previous reports [9,10].

β-Cedrene. Colorless oil. 1H-NMR (CDCl3, 500 MHz) δ ppm: 4.58 (1H, t, J = 2.2 Hz, H-15a), 4.51 (1H, t, J = 2.2 Hz, H-15b), 2.32 (2H, m, H-4), 2.19 (1H, d, J = 4.4 Hz, H-2), 1.87 (1H, H-8a), 1.82 (1H, H-10), 1.78 (1H, H-1a), 1.69 (1H, H-7), 1.55 (1H, H-9a), 1.48 (1H, H-5a), 1.43 (1H, H-9b), 1.38 (1H, H-5b), 1.30 (1H, H-8b), 1.20 (1H, H-1b), 0.97 (3H, s, 12-CH3), 0.94 (3H, s, 13-CH3), 0.85 (3H, d, J = 6.9 Hz, 14-CH3). 13C-NMR (CDCl3, 125MHz) δ ppm: 151.8 (C-3), 107.6 (C-15), 60.7 (C-2), 56.5 (C-10), 55.4 (C-6), 45.1 (C-1), 42.3 (C-11), 37.0 (C-8), 33.7 (C-8), 33.7 (C-3), 29.7 (C-4), 26.6 (C-12), 25.9 (C-13), 15.7 (C-9), 15.5 (C-14). The spectra data are in agreement with the reported data [10].

Caryophyllene oxide. Colorless oil. 1HNMR (CDCl3, 500MHz) δ: 5.00 (1H, s, H-12), 4.88 (1H, s, H-12), 2.90 (1H, dd, J = 4.1 and 10.7 Hz, H-9), 2.64 (1H, d, J = 9.1 Hz, H-2), 2.33 - 2.37 (1H, m, H-11), 2.28 (1H, dd, J = 3.6 and 8.4 Hz, H-10 ), 2.09 - 2.15 (2H, m, H-7, H-11), 1.72 - 1.74 (1H, m, H-5), 1.69 (1H, br. s., H-3), 1.65 - 1.67 (1H, m, H-6), 1.62 (1H, br. s, H-3), 1.44 (1H, d, J = 2.8 Hz , H-6), 1.36 - 1.39 (1H, m, H-10), 1.23 (3H, s, H-15), 1.03 (3H, s, H-13), 1.01 (3H, s, H-14), 0.99 (1H, br. s., H-7). 13CNMR (CDCl3, 125MHz) δ: 151.8 (C-1), 112.8 (C-12), 63.8 (C-9), 59.9 (C-8), 50.7 (C-5), 48.9 (C-2), 39.7 (C-3), 39.1 (C-7), 34.0 (C-4), 30.2 (C-10), 29.9 (C-14), 29.8 (C-11), 27.2 (C-6), 21.6 (C-13), 17.0 (C-15). The spectra data matched with the previous report [10].

Contact toxicity of the essential oil of B. frondosa was found against L. bostrychophila with an LC50 value of 210.73 mg/cm2 (). Borneol, caryophyllene oxide, β-cedrene, and 4-terpineol exhibited acute toxicity against the booklice with LC50 values of 98.04 mg/cm2, 84.62 mg/cm2, 458.79 mg/cm2, and 211.35 mg/cm2, respectively ().

Significant fumigant toxicity of the essential oil of B. frondosa against booklice (L. bostrychophila) was found with LC50 value of 507.35 μg/L while the two isolated constituents, borneol and 4-terpineol had LC50 values of 2.20 mg/L and 335.24 μg/L against the booklice, respectively (). Caryophyllene oxide and β-cedrene did not show fumigant toxicity against the booklice at the experimental dosage ().

Discussion

The major constituents identified in the essential oil of B. frondosa aerial parts were caryophyllene oxide, borneol, 4-terpineol, α-terpineol, β-cedrene, spathulenol and caryophyllene (3.97 %). The results are different from the essential oil of B. frondosa leaves that were collected from Kyoungsan city, Republic of Korea [3]. β-Caryophyllene (14.3 %), rosefuran (13.5 %), verbenone (11.5 %), spathulenol (6.02 %), caryophyllene oxide (5.49 %), cis-tagetone (5.3 %), α-humulene (4.02 %) and linalool (3.2 %) were determined as the main compounds in the essential oil derived from of the leaves of B. frondosa [3].  

The essential oil of the aerial parts of B. frondosa and its isolates possessed   acute toxicity toward the booklice. Compared with the positive control, pyrethrum extract (LC50 = 18.99 mg/cm2), the contact toxicity was only 11 times less. However, the essential oil of B. frondosa demonstrated stronger contact toxicity against L. bostrychophila adults than several essential oils using the same bioassay, e.g. Artemisia rupestris [11], A. frigida [12], Curcuma wenyujin [13], Foeniculum vulgare [14], and Valeriana jatamansi [15], however, the essential oil of B. frondosa shows less contact toxicity than the essential oils of Illicium henryi [16] and Kaempferia galangal [17]. Among the four isolated constituents, caryophyllene oxide, and borneol displayed stronger contact toxicity (no overlap in 95 % fiducial limit) than the essential oil against the booklice (L. bostrychophila). 4-Terpineol shows the same level of contact toxicity as the oil against booklice but booklice was more susceptible to the essential oil than to β-cedrene (). Therefore, it is suggested that the contact toxicity of the essential oil may be mainly attributed to caryophyllene oxide and borneol as well as 4-terpineol. 

The essential oil of B. frondosa and its two isolates, borneol and 4-terpineol were found to display fumigant toxicity against the booklice (L. bostrychophila).  4-Terpineol exhibited stronger fumigant toxicity (no overlap in 95 % fiducial limit) than the crude oil (). When compared with dichlorvos (LC50 = 1.35 μg/L), the essential oil of B. frondosa and 4-terpineol showed only 375 times and 248 times less toxicity against L. bostrychophila, respectively. However, the essential oil of B. frondosa demonstrated a stronger fumigant toxicity against booklice than several essential oils using the same bioassay, e.g., Artemisia rupestris (LC50 = 6.67 mg/L air) [11], A. frigida (LC50 =1.25 mg/L) [12], C. wenyujin (LC50 = 2.76 mg/L) [13], V. jatamansi (LC50 = 6.0 mg/L) [15], and K. galangal (LC50 = 1.5 mg/L air) [17], but the oil of B. frondosa demonstrated less toxicity than the essential oils of Allium chinense (LC50 = 186.5 mg/L air) [18] and F. vulgare fruits (LC50 = 34.07 μg/L) [14]. However, the currently commercial fumigants (e.g. phosphine and MeBr) are synthetic insecticides and are also extremely poisonous against human beings and other non-target organisms. Thus, it is suggested that fumigant activity of the essential oil of B. frondosa aerial parts and the two isolates, especially 4-terpineol is quite promising.

In the previous studies, 4-terpineol had been demonstrated to possess fumigant toxicity against several grain storage insects, such as Sitophilus granaries, S. oryzae, S. zeamais, Tribolium castaneum, T. confusum, and Rhyzopertha dominica as well as German cockroaches, Blattella germanica [19]. Borneol was also found to exhibit insecticidal activities against several insects and mites [19]. Moreover, it has been shown that caryophyllene oxide exhibited fumigant and contact toxicity as well as repellent activity against several insects and mites [20]. It also displayed larvicidal activity against Aedes aegypti with a LC50 value of 125 ppm [21]. However, this is the first time to report contact toxicity of β-cedrene against grain storage insects. The above findings suggest that the essential oil of B. frondosa aerial parts and the four isolated constituents, especially 4-terpineol show promise for development into possible natural insecticides/fumigants to control stored product insects.

The aerial parts of B. frondosa have been used to treat virtual fatigue, night sweat; hemoptysis, infantile malnutrition and dysentery in traditional Chinese medicine [6] and young leaves of B. frondosa are utilized as human food and tea [3]. It seems that the aerial parts of B. frondosa are quite safe for human consumption. However, there is no experimental data on toxicity of the essential oil of B. frondosa aerial parts and its four isolated constituents to humans to the best of our knowledge.

Conclusion

The essential oil of aerial parts of B. frondosa demonstrates strong contact and fumigant toxicity against booklice. Four active constituents were isolated and identified from the essential oil. The results suggest that the essential oil of B. frondosa aerial parts and the four isolated constituents, especially 4-terpineol have a potential for development into natural insecticides or fumigants for the control of insects in stored grains. However, further evaluation to determine their safety in humans and to optimize their activities is needed.

Declarations

Acknowledgement

This work was funded by National Key Technology Research and Development Program of the Ministry of Science and Technology of China (Grant no. 2014BAD23B02). We thank Dr. Liu QR from the College of Life Sciences, Beijing Normal University, Beijing, China for the identification of the investigated plant.

References

  1. Editorial Committee of Flora of China of Chinese Academy of Sciences. Flora Reipublicae Popularis Sinicae, Science Press, Beijing, China; 1979. 75; 372.
  2. Yan XH, Zeng JJ, Zhou B, Wang N, Xiang HH, Kang YY. Allelopathic potential of the extracts from alien invasive plant Bidens frondosa. J Yangzhou Univ 2012; 33: 88-94 (in Chinese with English abstract)
  3. Rahman A, Bajpai VK, Dung NT, Kang SC. Antibacterial and antioxidant activities of the essential oil and methanol extracts of Bidens frondosa Linn. Int J Food Sci Technol 2011; 46: 1238-1244.
  4. Jiangsu New Medical College. Dictionary of Chinese Herbal Medicine. Shanghai Science & Technology Press, Shanghai, China, 1977, pp 1901-1902.
  5. Karikome H, Ogawa K, Sashida Y. New acylated glucosides of chalcone from the leaves of Bidens frondosa. Chem Pharm Bull 1992; 40: 689-691.
  6. Venkateswarlu S, Panchagnula GK, Subbaraju GV. Synthesis and antioxidative activity of 3',4',6,7-tetrahydroxyaurone, a metabolite of Bidens frondosa. Biosci Biotechnol Biochem 2004; 68: 2183-2185.
  7. Adams RP. Identification of Essential Oil Components by Gas Chromatograph /Mass Spectrometry. 4th ed. Allured Publishing Corporation, Carol Stream, USA, 2007.
  8. Sakuma M. Probit analysis of preference data. Appl Entomol Zool 1998; 33: 339-347.
  9. Bohlmann F, Zeisberg R, Klein E. Naturally occurring terpene derivatives. 13CNMR spectra of monoterpenes. Org Magn Reson 1975; 7: 426-432
  10. Chu SS, Du SS, Liu ZL. Fumigant compounds from the essential oil of Chinese Blumea balsamifera leaves against the maize weevil (Sitophilus zeamais). J Chem 2013; doi:10.1155/2013/289874.
  11. Liu XC, Li XP, Li HQ, Deng, ZW, Zhou L, Liu ZL, Du SS. Identification of repellent and insecticidal constituents of the essential oil of Artemisia rupestris L. aerial parts against Liposcelis bostrychophila Badonnel. Molecules 2013; 18: 10733-10746.
  12. Liu XC, Li YL, Wang TJ, Wang Q, Liu ZL. Chemical composition and insecticidal activity of essential oil of Artemisia frigida Willd. (Compositae) against two grain storage insects. Trop J Pharm Res 2014; 13: 587-592.
  13. Liu ZL, Zhao NN, Liu CM, Zhou L, Jiang GH. Identification of insecticidal constituents of the essential oil of Curcuma wenyujin rhizomes against Liposcelis bostrychophila Badonnel. Molecules 2012; 17: 12049-12060.
  14. Zhao NN, Zhou L, Liu ZL, Du SS, Deng ZW. Evaluation of the toxicity of the essential oils of some common Chinese spices against Liposcelis bostrychophila. Food Control 2012; 26: 486-490.
  15. Liu XC, Zhou L, Liu ZL. Identification of insecticidal constituents from the essential oil of Valeriana jatamansi Jones against Liposcelis bostrychophila Badonnel. J Chem 2013; doi:10.1155/2013/853912.
  16. Liu XC, Liu ZL. Analysis of the essential oil of Illicium henryi Diels root bark and its insecticidal activity against Liposcelis bostrychophila Badonnel. J Food Prot 2015; 78: 772-777.
  17. Liu XC, Liang Y, Shi WP, Liu QZ, Zhou L, Liu ZL. Repellent and insecticidal effects of the essential oil of Kaempferia galanga rhizomes to Liposcelis bostrychophila (Psocoptera: Liposcelidae). J Econ Entomol 2014; 107: 1706-1712.
  18. Liu XC, Lu XN, Liu QZ, Liu ZL. Evaluation of insecticidal activities of the essential oil of Allium chinense G. Don and its major constituents against Liposcelis bostrychophila Badonnel. J Asia-Pacific Entomol 2014; 17: 853-856.
  19. Yeom HJ, Kang J, Kim SW, Park IK. Fumigant and contact toxicity of Myrtaceae plant essential oils and blends of their constituents against adults of German cockroach (Blattella germanica) and their acetylcholinesterase inhibitory activity. Pestic Biochem Physiol 2013; 107: 200-206.
  20. Liu P, Liu XC, Dong HW, Liu ZL, Du SS, Deng ZW. Chemical composition and insecticidal activity of the essential oil of Illicium pachyphyllum fruits against two grain storage insects. Molecules 2012; 17: 4870-14881.
  21. Silva WJ, Doria GAA, Maia RT, Nunes RS, Carvalho GA, Blank AF, Alves PB, Marcal RM, Cavalcanti SCH. Effects of essential oils on Aedes aegypti larvae: Alternatives to environmentally safe insecticides. Bioresour Technol 2008; 99: 3251-3255.
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