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Communication

Screening of the Acaricidal Activity of Essential Oils against Panonychus citri (McGregor) (Acari: Tetranychidae)

1
The Key Laboratory for Quality Improvement of Agricultural Products of Zhejiang Province, College of Advanced Agricultural Sciences, Zhejiang A & F University, Hangzhou 311300, China
2
Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China
3
State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-Products, Institute of Plant Protection and Microbiology, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, China
*
Authors to whom correspondence should be addressed.
Agronomy 2023, 13(2), 397; https://doi.org/10.3390/agronomy13020397
Submission received: 23 December 2022 / Revised: 23 January 2023 / Accepted: 27 January 2023 / Published: 29 January 2023
(This article belongs to the Topic Integrated Pest Management of Crops)

Abstract

:
The citrus red mite, Panonychus citri (McGregor), is an important pest of citrus in China, where pesticides are commonly used in citrus orchards. In order to reduce the use of chemical pesticides against P. citri and the development of resistance, the screening of biological control agents has attracted the attention of students. In this study, seven plant essential oils with high toxicity were selected from 40 plant essential oils by the leaf-dip bioassay, including plant essential oils of lemongrass, patchouli, juniper berry, sage, clove, frankincense, and citrus. The LC50 after 72 h treatment were 3.198 μL/mL, 8.312 μL/mL, 3.244 μL/mL, 6.701 μL/mL, 8.350 μL/mL, 21.953 μL/mL, and 8.788 μL/mL, respectively. According to the LT50, the essential oils’ acute toxicity to P. citri from high to low were lemongrass, juniper berry, patchouli, citrus, sage, vetiver, and frankincense essential oils. In general, lemongrass and juniper berry essential oils have the best acaricidal effect and have high application value for the biological control of P. citri, which provides a basis for the development of botanical acaricides.

1. Introduction

Panonychus citri (McGregor), also known as citrus red mite, is one of the most important pests in citrus orchards all over the world [1] and can harm more than one hundred different plants, including peach, pear, and prickly ash [2]. Adults and larvae of this mite could sting and suck the leaves, new shoots, and fruit skin of citrus, and in severe cases, leaves, withered shoots, and fruit would fall [3,4]. Moreover, it occurs for many generations every year, and the generations overlap, which is very serious for citrus in China [5], affecting the growth of citrus trees and the yield and quality of citrus [6]. Currently, chemical acaricides such as spirodiclofen, bifenazate, hexythiazox, pyridaben, abamectin, and fenpropathrin are mainly used to control P. citri [7].
The use of chemical pesticides in actual production is helpful to increase agricultural output [8]. However, people have a demand for more efficient and sustainable production of crops, thus overusing these chemicals. This situation not only caused huge economic losses, but also made the specific substances in the pesticides exert continuous selection pressure on pests, increased their adaptability and resistance [9,10], and makes the resistance traits be passed on to the next pest generations [11]. At the same time, chemical pesticides have become the main pollution sources in soil and water, destroy the ecological balance, and have high toxicity to humans and animals [12,13]. Therefore, biological control has emerged as the primary research focus in recent years.
To reduce the influence of traditional chemical pesticides, predatory natural enemies [14] and insect pathogenic microorganisms have been used for biological control of P. citri, such as some species of phytoseiid mites [15,16], predatory thrips [17] and Beauveria bassiana [18]. Besides, some natural products such as plant extracts and essential oils were also used to control pests [19]. These botanical pesticides, including veratrine [20] and matrine [21], have unique mechanisms of action, are not easy to produce drug resistance, and have the characteristics of high efficiency, low toxicity, and environmental compatibility [22]. Plant essential oil, as the secondary metabolite of plants, is a compound with special aroma, volatility, and solubility in organic solvents.
In the fields of food preservation, biomedicine, cosmetics, and agriculture, plant essential oils have been used for safe applications [23]. Essential oils are mixed with complex and unique compounds, including alkaloids, monoterpenes, phenolic acids, and aldehydes [24]. Due to different plants, different collection sites, and different extraction methods, there are great differences in the types and contents of compounds. Compared with synthetic pesticides, the cost of extracting and applying essential oils has increased. But for organic agriculture, the application of essential oils can not only solve the problem of pesticide-resistant pests but also avoid the health issues for humans and animals related to pesticide accumulation [25]. Biological pesticides synthesized from essential oils are an effective alternative in crop production and IPM [26,27].
At present, there are numerous studies and applications on the insecticidal activity of plant essential oils. When essential oils extracted from lemongrass, cinnamon, eucalyptus globulus, fennel, and pepper were mixed and compounded with soybean oil, respectively, they demonstrated high ovicidal and repellent activities against Periplaneta americana, with effects comparable to 10% cypermethrin [28]. Neem and tobacco extracts showed considerable mortalities of Phenacoccus solenopsis Tinsley and were safe for natural enemies but low as compared to the synthetic pesticides [29]. Artemisia absinthium essential oil caused significant acute mortalities against Diaphorina citri, especially carvacrol and (−)-α-bisabolol displayed synergistic effects [30]. Compound 1 is an acaricidal substance extracted from the external seed coat. Its toxicity to P. citri is equivalent to pyridaben, and obviously superior to omethoate, which not only has strong contact toxicity but is also quick-acting. At the same time, the compound is corrosive to P. citri but non-toxic to plants [31].
In this study, the acaricidal activity of 40 plant essential oils against P. citri was tested. The LC50 and LT50 of several plant essential oils against P. citri were further determined, and the laboratory toxicity of these plant essential oils was compared. The purpose of this study was to screen out the essential oils that had the effect of controlling P. citri and provide a theoretical basis for the development and application of green pesticides.

2. Materials and Methods

2.1. Testing Mites

P. citri was collected from Lin’an, Hangzhou, China. P. citri in this citrus orchard has several generations per year. The population resistance of P. citri was extremely high due to a large number of pesticides and frequent use. The mite was collected from the citrus orchard, which had been pesticide free for two months. The collected mites were transferred to citrus in the greenhouse to maintain the population.

2.2. Testing Essential Oils

Black pepper (B1), bergamot (B2), basil (B3), cinnamon (C1), clove (C2), cypress (C3), chamomile (C4), citrus (C5), eucalyptus (E1), frankincense (F1), geranium (G1), ginger (G2), grapefruit (G3), juniper berry (J1), jasmine (J2), lavender (L1), lemongrass (L2), lemon (L3), myrrh (M1), melissa (M2), niaouli (N1), neroli (N2), nutmeg (N3), origanum (O1), peppermint (P1), pine needles (P2), patchouli (P3), palmarosa (P4), ravansara (R1), rose (R2), rosemary (R3), sage (S1), sandalwood (S2), sweet fennel (S3), sweet orange (S4), tea tree (T1), thyme (T2), vanilla (V1), vetiver (V2), ylang (Y1) were purchased from ECO WILD. Tween-80 was purchased from Shanghai Macklin Biochemical Technology Co., Ltd.

2.3. Bioassay

The essential oils were dissolved in a 0.1% Tween-80 water solution to prepare different concentrations of the solution [32], and the solution was emulsified by ultrasonic. A leaf-dip bioassay was conducted to evaluate the effects of 40 essential oils on field-collected populations of P. citri [33]. The fresh, mature leaves were cut from the middle of citrus branches and made into 1 cm × 1 cm leaf discs. All leaves are washed with clean water three times and then dried to ensure that there are no arthropods on them. The leaf disc was immersed in the solution for 10 s, and allowed to naturally dry for 3 min. To prevent mites from escaping, a layer of filter paper with a diameter of 30 mm was placed at the bottom of a culture dish with a diameter of 35 mm, water was added to wet it until it was saturated but not dripping, and the leaf disc was placed on the wet filter paper with the leaf back facing up. Twenty female adult mites with similar size and high vitality on each leaf disc were picked, and the culture dish’s edge was sealed with sealing film. The death of the female adult mite was recorded under the stereoscope after 6 h, 12 h, 24 h, 48 h, and 72 h. The mite’s body was touched with a writing brush for judgment. If the mite foot did not move, it was deemed dead. All treatments were placed in an incubator with a temperature of 25 °C, relative humidity of 75%, and illumination of 16 h. Each treatment was repeated 3 times, and 0.1% Tween-80 aqueous solution was used as the control.

2.4. Data Analysis

All statistical analyses were performed using the Polo-Plus program to calculate the LC50 and 95% confidence limits. LT50, the toxicity regression equation, and the correlation coefficient were calculated by Excel software. GraphPad Prism 8.3.0 software was used to perform a one-way ANOVA on the group data and draw charts.

3. Results

3.1. Comparison of Lethal Toxicity of 40 Essential Oils to P. citri

The leaf-dip bioassay of P. citri was conducted with 1 μL/mL plant essential oil solution. The experimental results are shown in Figure 1. After 6 h and 12 h, the mortality rates of the essential oils treated with bergamot, frankincense, ginger, and myrrh differ significantly from the control (p ≤ 0.001), showing certain acute toxicity. However, with the prolonged treatment time, the mortality rates of bergamot and frankincense oil did not differ from those of the control, and there was no significant lethal effect. After 24 h, the essential oils of citrus, ginger, myrrh, sage, and vetiver showed a certain level of toxicity, and the difference was significant (p ≤ 0.0001) compared to the control, and the mortality rate was the highest after treatment with the myrrh essential oil. After 48 h, the mortality rate of each essential oil treatment increased significantly. After 72 h of treatment, there was a certain difference (p ≤ 0.01) compared to 28 essential oils of the control, among which 10 essential oils, including citrus, ginger, grapefruit, juniper berry, lemon, myrrh, sage, sandalwood, sweet orange, and vetiver, had a higher mortality rate, showing an extremely significant difference (p ≤ 0.0001) compared with the control, and the essential oils of ginger, juniper berry, and myrrh had the highest mortality rate.

3.2. Half Lethal Concentration of Seven Essential Oils to P. citri

Through the preliminary experiment, seven plant essential oils with high toxicity to P. citri were further selected from 40 essential oils, including lemongrass, patchouli, juniper, sage, clove, frankincense, and citrus. The results in Table 1 show that the LC50 of lemongrass essential oil was 4.697 μL/mL at 24 h, which was significantly lower than that of several other test essential oils and indicated a high toxicity level. After 24 h, the LC50 of sage essential oil was the highest, at 93.384 μL/mL, and its relative toxicity was relatively poor. Considering the LC50 values at different time points, the lower concentrations of lemongrass and juniper berry essential oils exhibited higher toxicity at 12 h, while the LC50 values of sage and patchouli essential oils were the most affected by time, and the LC50 values at different application time points were significantly different. The indoor toxicity of the seven essential oils to P. citri increased over time, and the toxicity was ranked as follows: lemongrass, juniper berry, sage, patchouli, vetiver, citrus, and frankincense at 72 h from high to low, with lemongrass and juniper berry having the best effect and the lowest LC50.

3.3. Acute Toxicity of Seven Essential Oils to P. citri

When treating P. citri with high-concentration essential oils, as shown in Table 2, the higher the concentration of the essential oil, the shorter the time to half-death (LT50). At the concentration of 16 μL/mL, the LT50 of the seven essential oils was all less than 50 h, with lemongrass essential oil having the lowest LT50, and the death rate could reach half after treating 4.07 h. However, the LT50 of frankincense oil is higher, and only after 88.96 h of treatment can the mites die by half. Other essential oils can reduce the population by half within 1–2 days. In conclusion, compared with a concentration of 1 μL/mL, most essential oils need to exert acute toxicity at a concentration of 16 μL/mL or higher. The results showed that lemongrass essential oil had the best acaricidal effect, followed by juniper berry, patchouli, citrus, sage, vetiver, and frankincense.

4. Discussion

Plant essential oil has many biological characteristics, including insecticidal, bactericidal, and herbicidal activity. Eucalyptus saligna leaf litter essential oil showed phytotoxicity. The effects on Lactuca sativa and Amaranthus viridis were comparable to the effects of the herbicide that was used as a positive control (Logran®) [34]. Thymus zygis (red thyme) essential oil possesses a broad antimicrobial spectrum and may even enhance the effect of certain antimicrobial agents [35]. The chemical components of cumin essential oil can inhibit the growth of Panax notoginseng-associated pathogenic fungi in vitro, and the inhibitory effect of cuminaldehyde was similar to that of hymexazol [36]. These studies verified the potential of plant essential oil as a plant insecticide, fungicide, and herbicide that is environmentally friendly and provide ideas for developing new products to control agricultural pests.
The experimental results of this study showed that essential oils of lemongrass, patchouli, juniper berry, sage, vetiver, frankincense, and citrus had great acaricidal effects on the citrus red mite, among which essential oils of lemongrass, juniper berry, patchouli, and citrus had higher acaricidal activity, and a 1.6% solution of lemongrass berry essential oil had a high mortality rate of over 50% for P. citri after 4 h, showing quick-acting ability.
Several studies have shown that the above essential oils also have contact-killing, fumigation, and repellent activities against other harmful insects. The lemongrass leaf extract has certain fumigation activity on Drosophila melanogaster and can inhibit its acetylcholinesterase and catalase activities [37]. The essential oil extracted from juniper has high larvicidal activity and repellent activity against Aedes albopictus [38]. Solutions with juniper essential oil concentrations of 1%, 2.5%, and 5% have significant repellent and insecticidal activity against Rhopalosiphum padi and Sitobion avenae [39]. Essential oils of vetiver, cinnamon, and lavender show high contact/fumigant toxicity against Musca domestica L. [40]. Ylang-ylang and frankincense essential oils showed significant insecticidal activity against Culex quinquefasciatus larvae and Musca domestica adults [41]. Five citrus essential oils have fumigant activity against the confused flour beetle Tribolium confusum Du Val [42]. Essential oils such as patchouli and sage have repellent activity against Culex quinquefasciatus, and the combination of them can effectively resist Aedes aegypti and Anopheles dirus, thus prolonging the repellent time [43]. The essential oils of patchouli, juniper, frankincense, sage, and lemongrass have repellent effects against Lasioderma serricorne [44]. These results are consistent with the results of this experiment, which fully prove that essential oils such as lemongrass, patchouli, juniper berry, sage, vetiver, frankincense, and citrus can be used as green pesticides to control harmful insects. These plant essential oils are a mixture of a large number of different components, mainly including linalool, limonene, patchouli alcohol, α-pinene, β-caryophyllene, α-thujone, cyclo-isolongifolene, monolinolenin, and so on [39,45,46,47,48,49,50]. Many compounds are common in several essential oils, but the content is different. They often show complex synergistic effects between components. Compared with the single application of one compound, the mixture of two or more compounds shows higher biological activity [45].
In addition, for different pests, the essential oils with insecticidal effects are different. The essential oils extracted from medicinal plants such as oregano, thyme, lavender, and mint have acaricidal activity against adults of Tetranychus cinnabarinus [51]. Essential oils of geranium, cedarwood, cinnamon, citronella, ginger, and lemongrass have certain acaricidal activity against adults of T. urticae [52]. However, in this study, the mortality of P. citri treated with lavender, cinnamon, mint, and geranium essential oils was not significantly different from that of the control.
In this study, the acaricidal activity and median lethal concentration of various plant essential oils against P. citri were determined by the leaf-dip method in the laboratory. Considering the difference of components of different essential oils in the production process, in the follow-up study, it is necessary to further analyze the main chemical components of plant essential oils that play a role in harmful mites and carry out essential oil blending and related greenhouse tests to more accurately evaluate the effects of plant essential oils on P. citri and citrus fruits, and thus provide a scientific basis for developing plant essential oils into green acaricides.

Author Contributions

Conceptualization, Z.Z. and Q.R.; methodology, Y.Z., T.W. and Y.W.; software, Y.Z., L.C. and Y.X.; validation, J.D., Q.R. and Z.Z.; resources, L.C. and Q.R.; data curation, Y.Z. and Q.R; writing—original draft preparation, Y.Z. and T.W.; writing—review and editing, Y.X. and Q.R.; supervision, Q.R.; funding acquisition, Z.Z. and Q.R. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by National Key R&D Program of China, grant number 2019YFD1002100; Science and Technology Commissioner Program, Jiaxing Zhejiang Province, China, grant number 2021K108; the Key Research and Development Program of Zhejiang Province, China, grant number 2021C02003 and the Demonstration and Extension Program of Science and Technology Achievements of Zhejiang Academy of Agricultural Sciences, grant number tg2022008.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data available on request from the authors.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Uri, G. Acarine pests of citrus: Overview and non-chemical control. Syst. Appl. Acarol-UK 2003, 8, 3–12. [Google Scholar] [CrossRef]
  2. Migeon, A.; Nouguier, E.; Dorkeld, F. Spider Mites Web: A comprehensive database for the Tetranychidae. In Trends in Acarology: Proceedings of the 12th International Congress; Springer Science & Business Media: Berlin/Heidelberg, Germany, 2011; pp. 557–560. [Google Scholar]
  3. Henry, Y.F.; Clement, A.; Yingfang, X.; Joseph, A. Field evaluation of predacious mites (Acari: Phytoseiidae) for biological control of citrus red mite, Panonychus citri (Trombidiformes: Tetranychidae). Fla. Entomol. 2013, 96, 80–91. [Google Scholar] [CrossRef]
  4. Fang, X.D.; Ouyang, G.C.; Lu, H.L.; Guo, M.F.; Wu, W.N. Ecological control of citrus pests primarily using predatory mites and the bio-rational pesticide matrine. Int. J. Pest. Manag. 2018, 64, 262–270. [Google Scholar] [CrossRef]
  5. Zhe, L.; Changbao, X.; George, A.B.; Xuying, Z.; Yijing, C. Influence of different fertilizer types on life table parameters of citrus red mite, Panonychus citri (Acari: Tetranychidae). Syst. Appl. Acarol. UK 2019, 24, 2209–2218. [Google Scholar] [CrossRef]
  6. Pan, D.; Dou, W.; Yuan, G.R.; Zhou, Q.H.; Wang, J.J. Monitoring the resistance of the citrus red mite (Acari: Tetranychidae) to four acaricides in different citrus orchards in China. J. Econ. Entomol. 2020, 113, 918–923. [Google Scholar] [CrossRef]
  7. Hu, J.; Wang, C.; Wang, J.; You, Y.; Chen, F. Monitoring of resistance to spirodiclofen and five other acaricides in Panonychus citri collected from Chinese citrus orchards. Pest. Manag. Sci. 2010, 66, 1025–1030. [Google Scholar] [CrossRef] [PubMed]
  8. Aktar, M.W.; Sengupta, D.; Chowdhury, A. Impact of pesticides use in agriculture: Their benefits and hazards. Interdiscip. Toxicol. 2009, 2, 1–12. [Google Scholar] [CrossRef] [Green Version]
  9. Van Leeuwen, T.; Van Nieuwenhuyse, P.; Vanholme, B.; Dermauw, W.; Nauen, R.; Tirry, L. Parallel evolution of cytochrome b mediated bifenazate resistance in the citrus red mite Panonychus citri. Insect. Mol. Biol. 2011, 20, 135–140. [Google Scholar] [CrossRef]
  10. Doker, I.; Kazak, C.; Ay, R. Resistance status and detoxification enzyme activity in ten populations of Panonychus citri (Acari: Tetranychidae) from Turkey. Crop Prot. 2021, 141, 105488. [Google Scholar] [CrossRef]
  11. Miller, A.L.; Tindall, K.; Leonard, B.R. Bioassays for monitoring insecticide resistance. J. Vis. Exp. 2010, 46, e2129. [Google Scholar] [CrossRef]
  12. Kim, K.H.; Kabir, E.; Jahan, S.A. Exposure to pesticides and the associated human health effects. Sci. Total Environ. 2017, 575, 525–535. [Google Scholar] [CrossRef] [PubMed]
  13. Van Leeuwen, T.; Tirry, L.; Yamamoto, A.; Nauen, R.; Dermauw, W. The economic importance of acaricides in the control of phytophagous mites and an update on recent acaricide mode of action research. Pestic. Biochem. Physiol. 2015, 121, 12–21. [Google Scholar] [CrossRef]
  14. Van Lenteren, J.C. The state of commercial augmentative biological control: Plenty of natural enemies, but a frustrating lack of uptake. BioControl 2012, 57, 1–20. [Google Scholar] [CrossRef] [Green Version]
  15. Tsolakis, H.; Principato, D.; Jorda, P.R.; Lombardo, A. Biological and life table parameters of Typhlodromus laurentii and Iphiseius degenerans (Acari, Phytoseiidae) fed on Panonychus citri and pollen of Oxalis pes-caprae under laboratory conditions. Exp. Appl. Acarol. 2016, 70, 205–218. [Google Scholar] [CrossRef]
  16. Kong, C.; Hu, F.; Xu, X.; Zhang, M.; Liang, W. Volatile allelochemicals in the Ageratum conyzoides intercropped citrus orchard and their effects on mites Amblyseius newsami and Panonychus citri. J. Chem. Ecol. 2005, 31, 2193–2203. [Google Scholar] [CrossRef]
  17. Li, Y.; Liu, M.; Yuan, J.; Okonkwo, T.T.; Chen, H.; Liu, H. Evaluation of a philic egg-consumption predatory thrips Scolothrips takahashii for control of the citrus red mite Panonychus citri. Crop Prot. 2021, 140, 105421. [Google Scholar] [CrossRef]
  18. Shi, W.; Feng, M. Field efficacy of application of Beauveria bassiana formulation and low rate pyridaben for sustainable control of citrus red mite Panonychus citri (Acari: Tetranychidae) in orchards. Biol. Control. 2006, 39, 210–217. [Google Scholar] [CrossRef]
  19. Ribeiro, L.P.; Zanardi, O.Z.; Vendramim, J.D.; Yamamoto, P.T. Comparative toxicity of an acetogenin-based extract and commercial pesticides against citrus red mite. Exp. Appl. Acarol. 2014, 64, 87–98. [Google Scholar] [CrossRef]
  20. Norris, E.J.; Bloomquist, J.R. Sodium channel-directed alkaloids synergize the mosquitocidal and neurophysiological effects of natural pyrethrins. Pestic. Biochem. Phys. 2022, 186, 105171. [Google Scholar] [CrossRef] [PubMed]
  21. Kordestani, M.; Mahdian, K.; Baniameri, V.; Garjan, A.S. Proteus, matrine, and pyridalyl toxicity and their sublethal effects on Orius laevigatus (Hemiptera: Anthocoridae). J. Econ. Entomol. 2022, 115, 573–581. [Google Scholar] [CrossRef]
  22. Yang, H.; Hu, J.; Li, Q.; Li, H.; Liu, H.; Yao, T.; Ran, C.; Lei, H. Acaricidal activity of Boenninghausenia sessilicarpa against Panonychus citri. Agric. Sci. China 2009, 8, 1097–1102. [Google Scholar] [CrossRef]
  23. Fierascu, R.C.; Fierascu, I.C.; Dinu-Pirvu, C.E.; Fierascu, I.; Paunescu, A. The application of essential oils as a next-generation of pesticides: Recent developments and future perspectives. Z. Nat. C J. Biosci. 2020, 75, 183–204. [Google Scholar] [CrossRef] [PubMed]
  24. Seow, Y.X.; Yeo, C.R.; Chung, H.L.; Yuk, H.G. Plant essential oils as active antimicrobial agents. Crit. Rev. Food Sci. Nutr. 2014, 54, 625–644. [Google Scholar] [CrossRef] [PubMed]
  25. Mossa, A.T.H. Green Pesticides: Essential Oils as Biopesticides in Insect-pest Management. J. Environ. Sci. Technol. 2016, 9, 354–378. [Google Scholar] [CrossRef] [Green Version]
  26. Werdin, G.J.; Gutierrez, M.M.; Ferrero, A.A.; Fernandez, B.B. Essential oils nanoformulations for stored-product pest control-characterization and biological properties. Chemosphere 2014, 100, 130–138. [Google Scholar] [CrossRef]
  27. Attia, S.; Grissa, K.L.; Lognay, G.; Bitume, E.; Hance, T.; Mailleux, A.C. A review of the major biological approaches to control the worldwide pest Tetranychus urticae (Acari: Tetranychidae) with special reference to natural pesticides. J. Pest Sci. 2013, 86, 361–386. [Google Scholar] [CrossRef]
  28. Soonwera, M.; Moungthipmalai, T.; Takawirapat, W.; Sittichok, S. Ovicidal and repellent activities of several plant essential oils against Periplaneta americana L. and enhanced activities from their combined formulation. Sci. Rep. 2022, 12, 12070. [Google Scholar] [CrossRef]
  29. Rizvi, S.; Ikhlaq, M.N.; Jaffar, S.; Hussain, S. Efficacy of some selected synthetic chemical insecticides and bio-pesticides against cotton mealybug, Phenacoccus solenopsis Tinsley (Sternorrhyncha: Pseudococcidae) under agro ecological conditions of Peshawar, Pakistan. J. Entomol. Zool. Stud. 2015, 3, 223–226. [Google Scholar]
  30. Rizvi, S.A.H.; Ling, S.; Tian, F.; Xie, F.; Zeng, X. Toxicity and enzyme inhibition activities of the essential oil and dominant constituents derived from Artemisia absinthium L. against adult Asian citrus psyllid Diaphorina citri Kuwayama (Hemiptera: Psyllidae). Ind. Crop. Prod. 2018, 121, 468–475. [Google Scholar] [CrossRef]
  31. Pan, W.; Luo, P.; Fu, R.; Gao, P.; Long, Z.; Xu, F.; Xiao, H.; Liu, S. Acaricidal activity against Panonychus citri of a ginkgolic acid from the external seed coat of Ginkgo biloba. Pest. Manag. Sci. 2006, 62, 283–287. [Google Scholar] [CrossRef]
  32. Subaharan, K.; Senthamarai, S.P.; Subramanya, T.M.; Senthoorraja, R.; Manjunath, S.; Das, T.; Pragadheesh, V.S.; Bakthavatsalam, N.; Mohan, M.G.; Senthil-Nathan, S.; et al. Ultrasound-assisted nanoemulsion of Trachyspermum ammi essential oil and its constituent thymol on toxicity and biochemical aspect of Aedes aegypti. Environ. Sci. Pollut. Res. Int. 2022, 29, 71326–71337. [Google Scholar] [CrossRef] [PubMed]
  33. Rizvi, S.; Xie, F.; Ling, S.; Zeng, X. Development and evaluation of emulsifiable concentrate formulation containing Sophora alopecuroides L. extract for the novel management of Asian citrus psyllid. Environ. Sci. Pollut. Res. Int. 2019, 26, 21871–21881. [Google Scholar] [CrossRef] [PubMed]
  34. Silva, E.R.; Igartuburu, J.M.; Overbeck, G.E.; Soares, G.; Macias, F.A. Bioherbicide Potential of Eucalyptus saligna Leaf Litter Essential Oil. Chem. Biodivers. 2020, 17, e2000407. [Google Scholar] [CrossRef] [PubMed]
  35. Coimbra, A.; Ferreira, S.; Duarte, A.P. Biological properties of Thymus zygis essential oil with emphasis on antimicrobial activity and food application. Food Chem. 2022, 393, 133370. [Google Scholar] [CrossRef] [PubMed]
  36. Huo, Y.Y.; Li, T.T.; Yang, J.; Huang, H.Y.; Chen, C.J.; Xu, F.R.; Dong, X. Chemical Constituents of the Essential oil from Cuminum cyminum L. and Its Antifungal Activity against Panax notoginseng Pathogens. Chem. Biodivers. 2021, 18, e2100638. [Google Scholar] [CrossRef]
  37. Johnson, T.O.; Ojo, O.A.; Ikiriko, S.; Ogunkua, J.; Akinyemi, G.O.; Rotimi, D.E.; Oche, J.R.; Adegboyega, A.E. Biochemical evaluation and molecular docking assessment of Cymbopogon citratus as a natural source of acetylcholine esterase (AChE)- targeting insecticides. Biochem. Biophys. Rep. 2021, 28, 101175. [Google Scholar] [CrossRef]
  38. Evergetis, E.; Michaelakis, A.; Papachristos, D.P.; Badieritakis, E.; Kapsaski-Kanelli, V.N.; Haroutounian, S.A. Seasonal variation and bioactivity of the essential oils of two Juniperus species against Aedes (Stegomyia) albopictus (Skuse, 1894). Parasitol. Res. 2016, 115, 2175–2183. [Google Scholar] [CrossRef]
  39. Semerdjieva, I.; Zheljazkov, V.D.; Radoukova, T.; Dincheva, I.; Piperkova, N.; Maneva, V.; Astatkie, T.; Kacaniova, M. Biological Activity of Essential Oils of Four Juniper Species and Their Potential as Biopesticides. Molecules 2021, 26, 6358. [Google Scholar] [CrossRef]
  40. Khater, H.F.; Geden, C.J. Efficacy and repellency of some essential oils and their blends against larval and adult house flies, Musca domestica L. (Diptera: Muscidae). J. Vector. Ecol. 2019, 44, 256–263. [Google Scholar] [CrossRef] [Green Version]
  41. Pavela, R.; Maggi, F.; Giordani, C.; Cappellacci, L.; Petrelli, R.; Canale, A. Insecticidal activity of two essential oils used in perfumery (ylang ylang and frankincense). Nat. Prod. Res. 2021, 35, 4746–4752. [Google Scholar] [CrossRef]
  42. Campolo, O.; Malacrino, A.; Zappala, L.; Laudani, F.; Chiera, E.; Serra, D.; Russo, M.; Palmeri, V. Fumigant bioactivity of five Citrus essential oils against Tribolium confusum. Phytoparasitica 2014, 42, 223–233. [Google Scholar] [CrossRef]
  43. Sutthanont, N.; Sudsawang, M.; Phanpoowong, T.; Sriwichai, P.; Ruangsittichai, J.; Rotejanaprasert, C.; Srisawat, R. Effectiveness of herbal essential oils as single and combined repellents against Aedes aegypti, Anopheles dirus and Culex quinquefasciatus (Diptera: Culicidae). Insects 2022, 13, 658. [Google Scholar] [CrossRef] [PubMed]
  44. Ren, Y.; Wang, T.; Jiang, Y.; Chen, D.; Zuo, W.; Guo, J.; Jin, D. Behavioral Response, Fumigation Activity, and Contact Activity of Plant Essential Oils Against Tobacco Beetle (Lasioderma serricorne (F.)) Adults. Front. Chem. 2022, 10, 880608. [Google Scholar] [CrossRef] [PubMed]
  45. Tak, J.; Jovel, E.; Isman, M.B. Synergistic interactions among the major constituents of lemongrass essential oil against larvae and an ovarian cell line of the cabbage looper, Trichoplusia ni. J. Pest. Sci. 2017, 90, 735–744. [Google Scholar] [CrossRef]
  46. Albuquerque, E.L.; Lima, J.K.; Souza, F.H.; Silva, I.M.; Santos, A.A.; Araujo, A.P.; Blank, A.F.; Lima, R.N.; Alves, P.B.; Bacci, L. Insecticidal and repellence activity of the essential oil of Pogostemon cablin against urban ants species. Acta. Trop. 2013, 127, 181–186. [Google Scholar] [CrossRef] [PubMed]
  47. Campolo, O.; Giunti, G.; Laigle, M.; Michel, T.; Palmeri, V. Essential oil-based nano-emulsions: Effect of different surfactants, sonication and plant species on physicochemical characteristics. Ind. Crop. Prod. 2020, 157, 112935. [Google Scholar] [CrossRef]
  48. Kadarohman, A.; Sardjono, R.E.; Aisyah, S.; Khumaisah, L.L. Biolarvicidal of Vetiver Oil and Ethanol Extract of Vetiver Root Distillation Waste (Vetiveria zizanoides) Effectiveness toward Aedes aegypti, Culex sp., and Anopheles sundaicus. J. Essent. Oil Bear. Pl. 2013, 16, 749–762. [Google Scholar] [CrossRef]
  49. Metayi, M.H.; Abd El-Naby, S.S.; El-Habal, N.A.; Fahmy, H.H.; Abdou, M.S.; Ali, B.; Abdel-Rheim, K.H.; Abdel-Megeed, A. Omani Frankincense nanoemulsion formulation efficacy and its latent effects on biological aspects of the spiny bollworm Earias insulana (Boisd.). Front. Physiol. 2022, 13, 1001136. [Google Scholar] [CrossRef]
  50. Visakh, N.U.; Pathrose, B.; Chellappan, M.; Ranjith, M.T.; Sindhu, P.V.; Mathew, D. Chemical characterisation, insecticidal and antioxidant activities of essential oils from four Citrus spp. fruit peel waste. Food. Biosci. 2022, 50, 102163. [Google Scholar] [CrossRef]
  51. Erdal, S.; Kamuran, K.; Soner, S. Acaricidal activities of the essential oils from several medicinal plants against the carmine spider mite (Tetranychus cinnabarinus Boisd) (Acarina: Tetranychidae). Ind. Crop. Prod. 2009, 31, 107–112. [Google Scholar] [CrossRef]
  52. An, H.; Tak, J. Miticidal and repellent activity of thirty essential oils and their synergistic interaction with vanillin against Tetranychus urticae Koch (Acari: Tetranychidae). Ind. Crop. Prod. 2022, 182, 114872. [Google Scholar] [CrossRef]
Figure 1. The lethal situation of 1μL/mL essential oils against Panonychus citri at different times. (AE) Mortality rates of Panonychus citri in leaf-dip bioassay after 6 h, 12 h, 24 h, 48 h, and 72 h, respectively. The error bars denote the standard deviation. * p ≤ 0.05; ** p ≤ 0.01; *** p ≤ 0.001; **** p ≤ 0.0001.
Figure 1. The lethal situation of 1μL/mL essential oils against Panonychus citri at different times. (AE) Mortality rates of Panonychus citri in leaf-dip bioassay after 6 h, 12 h, 24 h, 48 h, and 72 h, respectively. The error bars denote the standard deviation. * p ≤ 0.05; ** p ≤ 0.01; *** p ≤ 0.001; **** p ≤ 0.0001.
Agronomy 13 00397 g001
Table 1. Median lethal concentration, 95% confidence limit, and toxicity regression equation of Panonychus citri treated with essential oils at different times.
Table 1. Median lethal concentration, 95% confidence limit, and toxicity regression equation of Panonychus citri treated with essential oils at different times.
Essential Oils24 h48 h72 h
LC50
95%CL
Toxicity Regression EquationLC50
95%CL
Toxicity Regression EquationLC50
95%CL
Toxicity Regression Equation
Lemongrass4.697
3.625~7.451
y = 1.0438ln(x) + 3.30474.157
3.190~6.712
y = 0.8098ln(x) + 3.77563.198
2.576~4.197
y = 0.8098ln(x) + 3.7756
Patchouli15.591
10.587~27.506
y = 0.7962ln(x) + 2.84610.065
7.056~13.467
y = 1.3197ln(x) + 2.31418.312
5.333~11.296
y = 1.3839ln(x) + 2.5174
Juniper berry22.484
8.371~1223.728
y = 0.2607ln(x) + 4.171912.322
5.918~117.420
y = 0.2883ln(x) + 4.29073.244
2.156~5.791
y = 0.3765ln(x) + 4.6154
Sage93.384
28.113~14526.685
y = 0.3136ln(x) + 3.573115.753
10.235~35.423
y = 0.4796ln(x) + 3.70356.701
4.794~10.390
y = 0.468ln(x) +4.1938
Vetiver49.293
18.928~4171.676
y = 0.3676ln(x) + 3.571222.277
12.290~111.833
y = 0.4478ln(x) + 3.61878.350
5.919~13.738
y = 0.5757ln(x) + 3.8076
Frankincense30.387
21.232~63.663
y = 1.1291ln(x) + 1.262225.985
18.989~45.749
y = 1.1874ln(x) + 1.235121.953
15.117~44.181
y = 1.0182ln(x) + 1.9698
Citrus62.188
22.156~2665.324
y = 0.2647ln(x) + 3.53619.000
11.419~51.234
y = 0.3869ln(x) + 3.68668.788
5.245~22.605
y = 0.4141ln(x) + 4.1372
Table 2. Median lethal time of Panonychus citri treated with essential oils of 16 μL/mL.
Table 2. Median lethal time of Panonychus citri treated with essential oils of 16 μL/mL.
Essential OilsLT50 (h)
Lemongrass4.07
Patchouli34.25
Juniper berry33.00
Sage45.70
Vetiver49.87
Frankincense88.96
Citrus37.90
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Zhu, Y.; Wu, T.; Xie, Y.; Wu, Y.; Deng, J.; Cao, L.; Zhang, Z.; Rao, Q. Screening of the Acaricidal Activity of Essential Oils against Panonychus citri (McGregor) (Acari: Tetranychidae). Agronomy 2023, 13, 397. https://doi.org/10.3390/agronomy13020397

AMA Style

Zhu Y, Wu T, Xie Y, Wu Y, Deng J, Cao L, Zhang Z, Rao Q. Screening of the Acaricidal Activity of Essential Oils against Panonychus citri (McGregor) (Acari: Tetranychidae). Agronomy. 2023; 13(2):397. https://doi.org/10.3390/agronomy13020397

Chicago/Turabian Style

Zhu, Yijing, Taoqi Wu, Yongjian Xie, Yixuan Wu, Jianyu Deng, Lidong Cao, Zhijun Zhang, and Qiong Rao. 2023. "Screening of the Acaricidal Activity of Essential Oils against Panonychus citri (McGregor) (Acari: Tetranychidae)" Agronomy 13, no. 2: 397. https://doi.org/10.3390/agronomy13020397

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