Next Article in Journal
Effect of Bioactive Phytochemicals from Phlomis viscosa Poiret on Wound Healing
Next Article in Special Issue
Bioactivity of Common Pesticidal Plants on Fall Armyworm Larvae (Spodoptera frugiperda)
Previous Article in Journal
Omics Potential in Herbicide-Resistant Weed Management
Previous Article in Special Issue
Phytochemical Analysis of Tephrosia vogelii across East Africa Reveals Three Chemotypes that Influence Its Use as a Pesticidal Plant
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

United Forces of Botanical Oils: Efficacy of Neem and Karanja Oil against Colorado Potato Beetle under Laboratory Conditions

by
Kateřina Kovaříková
* and
Roman Pavela
Group Secondary Metabolites in Crop Protection, Crop Research Institute, Dmovská 507, 161 06 Praha 6-Ruzyně, Czech Republic
*
Author to whom correspondence should be addressed.
Plants 2019, 8(12), 608; https://doi.org/10.3390/plants8120608
Submission received: 14 November 2019 / Revised: 10 December 2019 / Accepted: 12 December 2019 / Published: 14 December 2019
(This article belongs to the Special Issue Pesticidal Plants: From Smallholder Use to Commercialisation)

Abstract

:
Neem and karanja oil are the most promising botanical insecticides in crop protection nowadays. Given that information about the insecticidal abilities of these oils is lacking, the aim was to explore the effects of neem and karanja oil binary mixtures. The insecticidal activity of NeemAzal T/S (Trifolio-M GmbH, Lahnau, Germany) (neem oil), Rock Effect (Agro CS a.s., Česká Skalice, Czech Republic) (karanja oil), and their binary mixes (at 1:1, 1:2, and 2:1 volume ratios) against the larvae of the Colorado potato beetle (CPB; Leptinotarsa decemlineata) was studied. In our bioassays, a synergistic effect of the mixtures, which was dose-dependent, was observed for the first time against this pest. The most effective blend was the 1:1 ratio. Its efficacy was more or less the same as, or even greater than, the neem oil alone. The LC50 of neem oil two days after application was (0.075 g·L−1) and the LC50 of the mixture was (0.065 g·L−1). The LC50 of karanja oil was (0.582 g·L−1), which was much higher than the LC50 of neem oil. The LC90 of neem oil five days after application was (0.105 g·L−1) and the LC90 of the mixture was (0.037 g·L−1). The LC90 of karanja oil was (1.032 g·L−1). The results demonstrate that it is possible to lower the doses of both oils and get improved efficacy against CPB larvae; nevertheless, further verification of the results in field conditions is necessary.

1. Introduction

The Colorado potato beetle (CPB), (Leptinotarsa decemlineata (Say, 1824), Coleoptera: Chrysomelidae) is one of the most important potato pests. This species is native to North America, from where it has gradually spread across Europe and Asia [1] alongside the expansion of potato cultivation. L. decemlineata is now considered to be the most important insect defoliator of potatoes. Through defoliation, the yield of tubers can be reduced by more than 50% [2]. Moreover, if the pest appears early and in intense numbers, it can destroy the entire production of a potato growing operation. The values of “intense numbers” vary from author to author and correspond with economic (action) thresholds, which were established for optimizing the use of insecticide applications and are unique to certain conditions. For example, Senanayake and Holliday [3] suggest 0.14 to 0.82 larvae per plant. Mailloux and Bostanian [4] stated that a measure based on the level of defoliation is better than one based on pest abundance. These levels were estimated, for example, by Zehnder et al. [5] at 20% leaf loss for young plants, 30% for plants from early bloom to late bloom, and 60% for plants from late bloom to harvest for fields in eastern Virginia. Nevertheless, the CPB larval stage is considered to be the most harmful stage to potato production [4], so we focused our research on the CPB larvae.
Various non-chemical control methods have been introduced since the 19th century to reduce the impact of CPB. Crop rotation, trap crops (eggplant), and other agrotechnical practices were recommended to farmers at that time [6]. In a study by Reed [6], it was concluded that the only two reliable methods were hand picking and the use of Paris Green (a toxic pigment). Hand picking, especially before mating, was considered very effective, but impractical on a larger scale. As such, the majority of alternative methods failed, and the most common method became the use of pesticides. Although pests have developed resistance to many active ingredients of insecticides, the use of chemicals remains the most widely used method against CPB to date (although biological controls are also often applied [7,8,9]).
According to the Arthropod Pesticide Resistance Database [10], CPB has shown resistance to 56 active ingredients of insecticides to date, among them spinosad [11] and Bacillus thuringiensis [12]. Mota-Sanchez et al. [11] also observed cross resistance to nine other neonicotinoids in an imidacloprid-resistant adult population of CPB. As of now, resistance has been recorded to most of the commonly used insecticides, such as pyrethroids, neonicotinoids, diamides, and organophosphates. As Yamamoto et al. [13] stated, it is possible to delay or prevent resistance development of pests via rotating insecticides with different modes of action and using certain combinations of insecticides. Barnes et al. [14] proved that a strategy using mixtures of insecticides is even more effective than the rotation of insecticides, and this is the very essence of botanical insecticides (BIs), which are complex mixtures of many functional secondary metabolites [15,16], in contrast to chemical substances, which are often characterized by one active ingredient, complemented by a number of inactive ingredients to facilitate the application. Moreover, the excessive use of chemical pesticides harms the environment, non-target organisms, and humans. By contrast, botanical pesticides are biodegradable and leave no harmful residues. Unfortunately, the scale of products applicable in organic production is insufficient as well. It is necessary to search for additional environmentally acceptable substances for effective control of CPB, and the use of botanical pesticides is a promising possibility. Chaudhary et al. [17] stated that the use of botanical pesticides is the most efficient means to replace synthetic pesticides, and among those, extracts and oils are the best choices. Neem and karanja oil, in particular, have great potential for use in sustainable integrated pest management.
Neem oil is one of the most promising substances in the current approach to pest control. Neem oil is a product of the Indian neem tree Azadirachta indica (A.) Juss. It possesses a variety of insecticidal properties, such as repellency [18], antifeedancy, toxicity, and growth disruption, against numerous pest species [19]. For example, the biochemical effect (growth inhibition, feeding deterrence, oviposition inhibition) of neem oil against more than 30 Lepidopteran pests [20] has been well documented. The main active ingredient is azadirachtin, a tetranortriterpenoid, which was isolated from the seeds of Azadirachta indica by Butterworth and Morgan [21] and is known to disrupt insects’ metamorphosis [22]. Neem oil is a contact insecticide, but even systemic activity has been documented [23]. Pavela et al. [24] also proved that azadirachtin can be taken up by plant roots and thus affect the population of immature aphids feeding on the treated plant.
Karanja oil is a product of the seeds of a widespread tropical and subtropical tree called Pongamia pinnata (L.) Pierre [25]. Karanja oil is rich in furano-flavonoids [26]. Al Muqarrabun et al. [27] summarized the known attributes of up to 70 flavones and their derivatives that had been isolated from Pongamia pinnata by various authors. Of these, karanjin, which was first discovered by Limaye [28], is particularly effective against a large number of insects [29]. The oil and extract of karanja act as insecticides [30], repellents, antifeedants, and growth regulators [31], and even oviposition deterrents [32].
Some insecticides, in combinations, may exhibit greater-than-additive toxicity, but the prediction of mixture toxicity using a response addition model is not always accurate for active ingredients with different modes of action [33]. In the case of neem and karanja oils, a synergistic effect was found by Kumar et al. [34] in bioassays on aphids and mites. Later, this phenomenon was confirmed by Packiam and Ignacimuthu [35] during experiments on Spodoptera litura. However, although the synergistic effect of insecticides is of great importance in practice, there is still much to be explored in this research area; for example, application doses may be reduced (economic and environmental benefits) and, moreover, multi-substance mixtures prevent the development of resistant populations of pests (anti-resistant strategy).
Although the efficacy of neem extracts on the Colorado potato beetle has already been studied, the efficacy of karanja oil against this pest has not yet been reported. Similarly, a possible synergistic effect of binary mixtures of these oils has also not been studied sufficiently to date. Thus the aim of our research was to evaluate the insecticidal properties of two commercial products (NeemAzal T/S - Trifolio-M GmbH, Lahnau, Germany, Rock Effect - Agro CS a.s., Česká Skalice, Czech Republic)), based on Azadirachta indica seed kernel oil and Pongamia pinnata oil, respectively, against the most destructive stage of CPB and to verify any possible synergistic effects of their binary mixtures in three different ratios with regard to practical use.

2. Results

The insecticidal activity of both tested BIs against CPB larvae was very good; however, significant differences in efficacies were found. From the LC50 (LC90) of Rock Effect (Agro CS a.s., Česká Skalice, Czech Republic) (0.582 g·L−1) and NeemAzal T/S (Trifolio-M GmbH, Lahnau, Germany) (0.075 g·L−1), it is obvious that karanja oil by itself is significantly less effective against larvae of Leptinotarsa decemlineata in comparison with neem oil. Complete results are presented in Table 1.
A comparison of the LC values revealed that both BIs showed significant chronic toxicity, which resulted in an apparent decrease in lethal concentrations over time (Table 1). The LC50 (LC90) values for NeemAzal T/S (Trifolio-M GmbH, Lahnau, Germany) were estimated at 0.075 g·L−1 (0.618 g·L−1) after 48 h and 0.005 g·L−1 (0.029 g·L−1) after 8 days, which is an obviously lower range of concentrations than the estimate for Rock Effect (Agro CS a.s., Česká Skalice, Czech Republic), where the LC50 (LC90) was 0.582 g·L−1 (1.692 g·L−1) after 48 h and 0.259 g·L−1 (0.774 g·L−1) after 8 days.
The insecticidal activity of the mixtures was assessed by the activity of the pure BIs. The LC range of the mixtures was usually within the LC range of NeemAzal T/S (Trifolio-M GmbH, Lahnau, Germany) and Rock Effect (Agro CS a.s., Česká Skalice, Czech Republic). As such, all the mixtures were more efficient than Rock Effect (Agro CS a.s., Česká Skalice, Czech Republic) alone. An exception was found in the case of mixtures after 48 h (acute toxicity), when the LC90 was higher for the mixtures than for the original substances. The LC values of the mixtures decreased over time, as did the LC values of the pure BIs. The LC50 (LC90) of the mixtures (1:1, 1:2, and 2:1 respectively) were estimated as follows: 0.065–0.001 g·L−1 (1.651–0.011 g·L−1), 0.543–0.012 g·L−1 (6.553–0.028 g·L−1), and 0.387–0.015 g·L−1 (6.361–0.059 g·L−1) 48 h to 8 days after treatment.
The order of the tested BIs according to efficacy (LC) is summarized as follows: mixture (1:1), NeemAzal T/S (Trifolio-M GmbH, Lahnau, Germany), mixture (1:2), mixture (2:1), and Rock Effect (Agro CS a.s., Česká Skalice, Czech Republic). The improved efficacy of the mixtures indicates an obvious synergistic effect.

3. Discussion

This experiment involved testing the insecticidal activity of NeemAzal T/S (Trifolio-M GmbH, Lahnau, Germany) (neem oil), Rock Effect (Agro CS a.s., Česká Skalice, Czech Republic) (karanja oil), and three binary mixtures. In the course of the experiment, it was observed that the larvae treated with the oils also showed a reduction in food intake, which resulted in little leaf damage compared to leaves in the control variant. This effect was not a primary target of the testing; nevertheless, antifeedancy has previously been reported for karanja oil [36] as well as neem oil [37].
The efficacy of neem oil was very good even at low concentrations such as 0.1–2 g·L−1 in our bioassays. The efficacy of neem products may vary with respect to concentrations of azadirachtin [38], and thus some authors have stated lower insecticidal activity against CPB [39,40]. However, that was not the case in our study, because the commercial product NeemAzal T/S (Trifolio-M GmbH, Lahnau, Germany) used in the bioassay contains 1% of the purified active ingredient Azadirachtin A, which is a very potent insect growth inhibitor [41] (reviewed in [19,42]). In the case of karanja oil, higher doses were needed to achieve the same mortality of CPB larvae as with neem oil. According to the literature, karanja oil is generally effective at higher doses, from 10 g·L−1 upwards [43,44,45]. Deshmukh and Borle [46] also mentioned that karanja oil has some limits for use at the farmer’s level, because its aqueous suspension is not as effective as that of neem. The higher efficacy of neem oil over karanja oil was also reported by Biswas et al. [47] in the case of Helicoverpa armigera.
Zehnder and Warthen [37] found that azadirachtin caused mortality, and they also observed an antifeedant effect in the case of CPB. Feuerhake and Schmutterer [48] tested neem seed extract formulations and were able to achieve 100% mortality of CPB. Other observed effects of neem oil on CPB are disruption of egg hatching and larvae molting [49]. The repellent effects of neem oil were even observed in laboratory as well as in field conditions [50]. Kaethner [51] observed the effect of fitness reduction in the treated beetles and a lower fecundity of females. Murray et al. [52] confirmed the oviposition effects of citrus limonoids, which are structurally and functionally similar to azadirachtin. The effect of karanja oil on CPB has not been studied to date.
With respect to other insect pests, synergistic effects were reported for both neem and karanja oils. Synergism refers to when the combined effect of two factors is greater than the sum of individual factors. It can occur between various insecticides [14], insecticides and fungicides [53], insecticides and poor nutritional conditions [54], and so on. For example, a synergism was found for the combination of neem oil and Beauveria bassiana on Spodoptera litura Fabricius [55], Tribolium castaneum [56], and aphids [57]. The combination of both oils with some pyrethrins shows synergism as well [36,58]. Synergism was also observed in the combination of neem and karanja oil by Kumar et al. [34], where both oils were found to be highly effective individually and also in combination against mites and aphids. In our case, the most significant synergistic effect was found for the mixture of neem and karanja oil in a 1:1 ratio. In addition, this effect appeared chronically and not acutely, and thus it is possible to use lower doses of insecticides. A notable observation in this experiment was that the individual neem and karanja oil treatments were less effective compared to the mixtures. For example, the toxicity (LC90) five days after treatment with the 1:1 mixture was almost 3-fold higher than for neem oil alone, and up to 28-fold higher than for karanja. The other mixtures showed synergism as well, although the effect was significantly weaker. Packiam and Ignacimuthu [35] came to the same conclusions when testing various combinations of neem and karanja oils against larvae of Spodoptera litura. Thus, it is clear that the strength of the synergistic effect is ratio dependent, and this is the first research paper to describe such a phenomenon in the case of CPB.
Neem and karanja oil seem to provide the perfect solution to all the problems of contemporary crop protection. Nevertheless, the possible cons should be discussed as well. Because it possesses a variety of insecticidal properties, even against some beneficial insects in the juvenile stage [59], the use of neem oil carries a potential risk. Any decision to use neem oil should therefore be made carefully. The same situation occurs in the case of karanja oil, which is considered a broad-spectrum insecticide [36]. On the other hand, Koss et al. [60] and Radkova et al. [61] found that beneficial arthropods in potato fields were more abundant when botanical and selective pesticides were sprayed in contrast to when chemical pesticides were used. Neem oil is considered environmentally friendly because it is free of chloramine, phosphorous, and nitrogen atoms, which are commonly found in synthetic pesticides. Moreover, using neem oil in the field can prevent some other pests from ovipositing [62], thus providing improved crop protection, and due to the synergistic effect of the compounds, a reduced dose is used, significantly reducing toxicity to non-target organisms while also reducing the cost of applications. Generally, neem products can be recommended for many integrated pest management (IPM) programs [63]. The effect of an insecticide based on a combination of neem and karanja oils (PONNEEM#) has already been tested against the hymenopteran parasitoid wasp Trichogramma chilonis, which was not affected from applications with up to a 0.5% concentration [35]. The recommended dose for NeemAzal T/S (Trifolio-M GmbH, Lahnau, Germany) in potatoes is 2.5 L for 300–700 L of water/ha (0.8–0.35% concentration). Because the 1:1 mixture was almost 3 times more effective, we should theoretically recommend the use of a 0.3–0.1% concentration for field application, and thus parasitoids should not be affected.
Field efficacy, however, will still need to be verified by a series of tests before its implementation, because some authors [64] have demonstrated the low stability of neem oil under field conditions due to photodegradation. This issue can be resolved theoretically via nano and micro encapsulation, which improves the stability and efficacy of oils exposed to UV light [65]; on the other hand, this solution is more suitable for soil applications of neem seed oil [66]. Moreover, the cost of such a product will be affected as well. The greater variability of karanja oil efficacy against CPB larvae reveals that this compound is less reliable than neem oil, especially when acute toxicity is concerned. However, Kumar and Singh [36] stated that the persistence of karanja oil is greater than for other botanical insecticides. In addition, the karanja extract is a highly effective UV absorbent [67] and is now being used in cosmetics as a component of modern sunscreen preparations, even for humans. As Wanyika et al. [68] have indicated, stabilization can be developed by adding solar radiation protectants, and therefore the combination of neem and karanja oils seems to be a perfect match, because what is missing in one is replaced by the other.

4. Materials and Methods

4.1. Insecticides

Two botanical insecticides that are suitable for organic farming were used in the bioassays. The first one (NeemAzal T/S) (Trifolio-M GmbH, Lahnau, Germany) was tested at five different doses and the second one (Rock Effect) (Agro CS a.s., Česká Skalice, Czech Republic) was tested at six different doses. Both substances were tested as contact insecticides.
NeemAzal® T/S (Trifolio-M GmbH, Lahnau, Germany) is a commercial formulation of the seed kernel extract of the tree Azadirachta indica (A.) Juss., which contains 1% of the purified active ingredient Azadirachtin A. It is generally used as a 0.3% to 0.5% aqueous solution. In the following text, the term “neem oil” is used.
Rock Effect (Agro CS a.s., Česká Skalice, Czech Republic) is a commercial formulation of Pongamia pinnata (L.) Pierre oil. The oil content is declared as 868.5 g·L−1. It is generally used as a 1% to 3% aqueous solution. In the following text, the term “karanja oil” is used.

4.2. Insects and Plant Material

Newly enclosed second instar larvae of Leptinotarsa decemlineata (Say) (Coleoptera: Chrysomelidae) were obtained from a colony reared on potato, Solanum tuberosum, cv. Agria, in a climate chamber at 22 ± 1 °C, a relative humidity of 40–60%, and a 16:8 (L:D) photoperiod. The colony was established from eggs and adults collected from a potato culture at a local field of the Crop Research Institute in Prague, Czech Republic (50°05′N, 14°18′E, 340 m a.s.l.) in June and August 2019.

4.3. Laboratory Bioassay

A potato leaf with five to seven leaflets was inserted into floral foam supporting moisture (Oasis, Belgium) and placed in a plastic box (16 × 11 × 7 cm). Twenty to twenty-five individuals (L2) of CPB were transferred carefully using a fine brush on each potato leaf. The tested BIs were dissolved in water right before use. NeemAzal T/S (Trifolio-M GmbH, Lahnau, Germany), Rock Effect (Agro CS a.s., Česká Skalice, Czech Republic), and their binary mixtures in three ratios (1:1, 2:1, and 1:2, by volume) were tested. For each BI, at least five concentrations that resulted in more than 0% and less than 100% mortality, based on preliminary assays, were used. The concentration series were 0.1–2 g·L−1 for NeemAzal T/S (Trifolio-M GmbH, Lahnau, Germany), 2–25 g·L−1 for Rock Effect (Agro CS a.s., Česká Skalice, Czech Republic), 0.05–2 g·L−1 for the 1:1 mixture, 0.1–15 g·L−1 for the 2:1 Rock Effect:Neem Azal (RE:NA) mixture, and 0.05–5 g·L−1 for the 1:2 (RE:NA) mixture. To obtain the LC value, the insecticidal activity of the concentration series of each insecticide was tested under laboratory conditions.
Once the larvae began to feed on the leaves, the prepared solutions were sprayed on both sides of the leaves using a hand sprayer. The control variant was sprayed with water only. Each variant was performed in three repetitions. The experiment was run in a climate chamber set at 22 ± 1 °C and 69% ± 6% relative humidity. The mortality rate was evaluated at 48 h, 5 days, and 8 days later. Individuals unable to right themselves when disturbed were counted as dead.

4.4. Statistical Analysis

Abbott’s formula was used to correct the data for control mortality [69]. Probit analysis [70] was used to estimate the doses needed to cause 50% mortality (LC50) and 90% mortality (LC90), as well as the associated 95% confidence limits for each BI, including binary mixtures, using BioStat (version 5.9.8.5).

5. Conclusions

Because of their natural origin and environmental friendliness, botanical pesticides currently have great potential. Furthermore, botanical pesticides are also very potent insecticides and, due to their composition, they can help to fight the global problem of insects developing resistance to insecticides.
Both of the tested BIs (insecticides based on neem oil and karanja oil) were efficient against L. decemlineata larvae at different concentrations. However, the efficacy of karanja oil against CPB larvae showed higher variability than for neem oil, on account of the high azadirachtin content of the commercial neem product and also the slightly different mode of action of both oils. Our experiment demonstrated a synergistic effect of neem and karanja oils against CPB larvae under laboratory conditions—one that was ratio-dependent. The most potent mixture (1:1 ratio) was equally, or even more effective, than neem oil itself. This effect intensified with respect to exposure time and appeared chronically. Five days after application of the mixture, LC90 values were 3-fold higher for neem oil and up to 28-fold higher for karanja oil. Due to these results, the recommended field dose of the mixture was estimated as high as 1.4 L in 500 L of water/ha (0.3%). Nevertheless, further verification in field conditions of the results achieved by this experiment is necessary in order to reach reliable conclusions and implement them into practice, and the effect on beneficial and non-target organisms should be verified.

Author Contributions

Conceptualization: R.P. and K.K.; methodology: R.P. and K.K.; software: R.P.; investigation: K.K.; data curation: R.P.; writing—original draft preparation: K.K.; writing—review and editing: K.K.; visualization: K.K.; supervision: R.P.; project administration: K.K.; funding acquisition: R.P.

Funding

This research was funded by the Ministerstvo Zemědělství - Národní Agentura pro Zemědělský Výzkum, grant number QK1920214.

Acknowledgments

The authors would like to thank the team members for providing the necessary background for running the experiments.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Weber, D. Colorado beetle: Pest on the move. Pestic. Outlook 2003, 14, 256–259. [Google Scholar] [CrossRef]
  2. Ozturk, G.; Yildrim, Z. Effect of bio activators on the tuber yield and tuber size of potatoes. Turk. J. Field Crops 2013, 18, 82–86. [Google Scholar]
  3. Senanayake, D.G.; Holliday, N.J. Economic injury levels for Colorado potato beetle (Coleoptera: Chrysomelidae) on ‘Norland’ potatoes in Manitoba. J. Econ. Entomol. 1989, 83, 2058–2064. [Google Scholar] [CrossRef]
  4. Mailloux, G.; Bostanian, N.J. Effect of manual defoliation on potato yield at maximum abundance of different stages of Colorado potato beetle, Leptinotarsa decemlineata (Say), in the field. J. Agric. Entomol. 1989, 6, 217–226. [Google Scholar]
  5. Zehnder, G.; Encill, A.M.; Speese, J. Action thresholds based on plant defoliation for management of Colorado potato beetle (Coleoptera: Chrysomelidae) in potato. J. Econ. Entomol. 1995, 88, 155–161. [Google Scholar] [CrossRef]
  6. Reed, E.B. Insects injurious to the potato. In Annual Report—Entomological Society of Ontario; Bethune, C.J.S., Saunders, W., Reed, E.B., Eds.; The Society: Toronto, ON, Canada, 1872; Volumes 2–8, pp. 65–79. [Google Scholar]
  7. Trdan, S.; Vidrih, M.; Laznik, Ž. Activity of four entomopathogenic nematode species against different developmental stages of Colorado potato beetle, Leptinotarsa decemlineata (Coleoptera, Chrysomelidae). Helminthologia 2009, 46, 14–20. [Google Scholar] [CrossRef] [Green Version]
  8. Laznik, Ž.; Tóth, T.; Lakatos, T.; Vidrih, M.; Trdan, S. Control of the Colorado potato beetle (Leptinotarsa decemlineata [Say]) on potato under field conditions: A comparison of the efficacy of foliar application of two strains of Steinernema feltiae (Filipjev) and spraying with thiametoxam. J. Plant Dis. Protect. 2010, 117, 129–135. [Google Scholar] [CrossRef]
  9. Weber, D.C. Biological control of potato insect pests. In Insect Pests of Potato; Giordanengo, P., Vincent, C., Alyokhin, A., Eds.; Elsevier: Waltham, MA, USA, 2013; Volume 1, pp. 399–405. [Google Scholar]
  10. Arthropod Pesticide Resistance Database. Available online: http://www.pesticideresistance.org (accessed on 18 September 2019).
  11. Mota-Sanchez, D.; Hollingworth, R.M.; Grafius, E.J.; Moyer, D.D. Resistance and cross-resistance to neonicotinoid insecticides and spinosad in the Colorado potato beetle, Leptinotarsa decemlineata (Say) (Coleoptera: Chrysomelidae). Pest Manag. Sci. 2006, 62, 30–37. [Google Scholar] [CrossRef]
  12. Whalon, M.E.; Miller, D.L.; Hollingworth, R.M.; Grafius, E.J.; Miller, J.R. Selection of a Colorado potato beetle (Coleoptera: Chrysomelidae) strain resistant to Bacillus thuringiensis. J. Econ. Entomol. 1993, 86, 226–233. [Google Scholar] [CrossRef]
  13. Yamamoto, I.; Kyomura, N.; Takahashi, Y. Negatively correlated cross resistance: Combinations of N-methylcarbamate with N-propylcarbamate or oxadiazolone for green rice leafhopper. Arch. Ins. Biochem. Phys. 1993, 22, 277–288. [Google Scholar] [CrossRef]
  14. Barnes, E.H.; Dobson, R.J.; Barger, I.A. Worm control and anthelmintic resistance: Adventures with a model. Parasitol. Today 1995, 11, 56–63. [Google Scholar] [CrossRef]
  15. Lahlou, M. Methods to study the photochemistry and bioactivity of essential oils. Phytother. Res. 2004, 18, 435–448. [Google Scholar] [CrossRef] [PubMed]
  16. Miresmailli, S.; Bradbury, R.; Isman, M.B. Comparative toxicity of Rosmarinus officinalis L. essential oil and blends of its major constituents against Tetranychus urticae Koch (Acari: Tetranychidae) on two different host plants. Pest Manag. Sci. 2006, 62, 366–371. [Google Scholar] [CrossRef] [PubMed]
  17. Chaudhary, S.; Kanwar, R.K.; Sehgal, A.; Cahill, D.M.; Barrow, C.J.; Sehgal, R.; Kanwar, J.R. Progress on Azadirachta indica based biopesticides in replacing synthetic toxic pesticides. Front. Plant. Sci. 2017, 8, 610. [Google Scholar] [CrossRef]
  18. Bina, S.; Javadi, I.; Iravani, O. Evaluation of the repellency effect of neem (Melia azedarach) plant extracts based on the Mittler&Dadd method. J. Agric. Chem. Environ. 2017, 6, 165–174. [Google Scholar] [CrossRef] [Green Version]
  19. Saxena, R.C. Insecticides from neem. In Insecticides of Plant Origin; Arnason, J.T., Philogène, B.J.R., Morand, P., Eds.; American Chemical Society: Washington, DC, USA, 1989; Volume 387, pp. 110–135. [Google Scholar] [CrossRef]
  20. Senthil-Nathan, S. Physiological and biochemical effect of neem and other Meliaceae plants secondary metabolites against Lepidopteran insects. Front. Physiol. 2013, 4, 1–17. [Google Scholar] [CrossRef] [Green Version]
  21. Butterworth, J.H.; Morgan, E.D. Isolation of a substance that suppresses feeding in locusts. Chem. Commun. 1968, 1, 23–24. [Google Scholar] [CrossRef]
  22. Tomlin, C. The Pesticide Manual: A World Compendium: Incorporating the Agrochemicals Handbook, 11th ed.; British Crop Protection Council: Farnham, Surrey; The Royal Society of Chemistry: Cambridge, UK, 1997. [Google Scholar]
  23. Osman, M.Z.; Port, G.R. Systemic action of neem seed substances against Pieris brassicae. Entomol. Exp. Appl. 1990, 54, 297–300. [Google Scholar] [CrossRef]
  24. Pavela, R.; Barnet, M.; Kocourek, F. Effect of azadirachtin applied systemically through roots of plants on the mortality, development and fecundity of the cabbage aphid (Brevicoryne brassicae). Phytoparasitica 2004, 32, 286–294. [Google Scholar] [CrossRef]
  25. Belide, S.; Sajjalaguddam, R.R.; Paladugu, A. Cytokinin preconditioning enhances multiple shoot regeneration in Pongamia pinnata (L.) Pierre—A potential, non-edible tree seed oil source for biodiesel. Electron. J. Biotechn. 2010, 13, 1–8. [Google Scholar] [CrossRef] [Green Version]
  26. Bringi, N.V.; Mukerjee, S.K. Karanja seed (Pongamia glabra) oil. In Non-Traditional Oil Seeds and Oils in India; Bringi, N.V., Ed.; Oxford IBH Publishing Co.: New Delhi, India, 1987; pp. 143–166. [Google Scholar]
  27. Al Muqarrabun, L.M.R.; Ahmat, N.; Ruzaina, S.A.S.; Ismail, N.H.; Sahidin, I. Medicinal uses, phytochemistry and pharmacology of Pongamia pinnata (L.) Pierre: A review. J. Ethnopharmacol. 2013, 150, 395–420. [Google Scholar] [CrossRef] [PubMed]
  28. Limaye, D.B. Karanjin part I: A crystalline constituent of the oil from Pongamia glabra. Proc. 12th Indian Acad. Sci. Congr. 1925, 118–125. [Google Scholar]
  29. Mathur, Y.K.; Srivastava, J.P.; Nigam, S.K.; Banerji, R. Juvenomimetic effects of karanjin on the larval development of flesh fly Sarcophaga ruficornis (Cyclorrhapha: Diptera). J. Ent. Res. 1990, 14, 44–51. [Google Scholar]
  30. Parmar, B.S.; Gulati, K.C. Synergists for pyrethrins (II)-karanjin. Indian J. Entomol. 1969, 31, 239–243. [Google Scholar]
  31. Kumar, V.; Chandrashekar, K.; Sidhu, O.P. Efficacy of karanjin and different extracts of Pongamia pinnata against selected insect pests. J. Ent. Res. 2006, 31, 121–124. [Google Scholar]
  32. Pavela, R.; Herda, G. Effect of pongam oil on adults of the greenhouse whitefly Trialeurodes vaporariorum (Homoptera: Trialeurodidae). Entomol. Gener. 2007, 30, 193–201. [Google Scholar] [CrossRef]
  33. Pape-Lindstrom, P.A.; Lydy, M.J. Synergistic toxicity of atrazine and organophosphate insecticides contravenes the response addition mixture model. Environ. Toxicol. Chem. 1997, 16, 2415–2420. [Google Scholar] [CrossRef]
  34. Kumar, V.; Chandrashekar, K.; Sidhu, O.P. Synergistic action of neem and karanj to aphids and mites. J. Ent. Res. 2007, 31, 121–124. [Google Scholar]
  35. Packiam, S.M.; Ignacimuthu, S. Effect of PONNEEM# on Spodoptera litura (Fab.) and its compatibility with Trichogramma chilonis Ishii. Braz. Arch. Biol. Technol. 2012, 55, 291–298. [Google Scholar]
  36. Kumar, M.; Singh, R. Potential of Pongamia glabra Vent as an insecticide of plant origin. Biol. Agric. Hortic. 2002, 20, 29–50. [Google Scholar] [CrossRef]
  37. Zehnder, G.; Warthen, J.D. Feeding inhibition and mortality effects of neem-seed extract on the Colorado potato beetle (Coleoptera, Chrysomelidae). J. Econ. Entomol. 1988, 81, 1040–1044. [Google Scholar] [CrossRef]
  38. Isman, M.B.; Koul, O.; Luczynski, A.; Kaminski, J. Insecticidal and antifeedant bioactivities of neem oils and their relationship to azadirachtin content. J. Agr. Food Chem. 1990, 38, 1406–1411. [Google Scholar] [CrossRef]
  39. Trdan, S.; Cirar, A.; Bergant, K.; Andjus, L.; Kač, M.; Vidrih, M.; Rozman, L. Effect of temperature on efficacy of three natural substances to Colorado potato beetle, Leptinotarsa decemlineata (Coleoptera: Chrysomelidae). Acta Agr. Scand. 2007, 57, 293–296. [Google Scholar] [CrossRef]
  40. Ropek, D.; Kołodziejczyk, M. Efficacy of selected insecticides and natural preparations against Leptinotarsa decemlineata. Potato Res. 2019, 62, 85–95. [Google Scholar] [CrossRef] [Green Version]
  41. Ruscoe, C.N.E. Growth disruption effects of an insect antifeedant. Nat. N. Biol. 1972, 236, 159–160. [Google Scholar] [CrossRef]
  42. Rembold, H.; Sharma, G.K.; Czoppelt, C.; Schmutterer, H. Azadirachtin: A potent insect growth regulator of plant origin. Z. Ang. Ent. 2009, 93, 12–17. [Google Scholar] [CrossRef]
  43. Ketkar, C.M. Use of tree-derived non edible oils as surface protectants for stored legumes against Callosobruchus maculatus and C. chinensis. In Natural Pesticides from the Neem Tree and Other Tropical Plants, In Proceedings of the 3rd International Neem Conference, Nairobi, Kenya, 10–15 July 1968; Deutsche Gesellschaft für Technische Zusammenarbeit: Eschborn, Germany, 1986; pp. 535–542. [Google Scholar]
  44. Negi, R.S.; Srivastava, M.; Saxena, M.M. Egg laying and adult emergence of Callospbrichus chinensis on green gram (Vigna radiata) treated with pongam oil. Indian J. Entomol. 1997, 59, 362–365. [Google Scholar]
  45. Satpathi, C.R.; Ghatak, S.S.; Bhusan, T.K. Efficacy of some plant extracts against the larvae of Indian meal moth Corcyra cephalonica Staint (Gelechiidae: Lepidoptera). Environ. Ecol. 1991, 9, 687–689. [Google Scholar]
  46. Deshmukh, S.D.; Borle, M.N. Studies on the insecticidal properties of indigenous plant products. Indian J. Entomol. 1976, 37, 11–18. [Google Scholar]
  47. Biswas, D.; Uddin, M.M.; Ahmad, M. Biorational management of tomato fruit borer, Helicoverpa armigera (Hübner) in winter under field condition of Bangladesh. Fundam. Appl. Agric. 2019, 4, 792–797. [Google Scholar] [CrossRef]
  48. Feuerhake, K.; Schmutterer, H. Use of simple methods for extraction of neem seed, formulation of extracts and their effects on various insect pests. Z. Pflanzenkr. Pflanzenschutz 1982, 89, 737–747. [Google Scholar]
  49. National Research Council (US) Panel on Neem. Effects on Insects. In Neem: A Tree for Solving Global Problems; National Academies Press: Washington, DC, USA, 1992. [Google Scholar]
  50. Zabel, A.; Manojlovic, B.; Rajkovic, S.; Stanković, S.; Kostic, A.M. Effect of Neem extract on Lymantria dispar L. (Lepidoptera: Lymantriidae) and Leptinotarsa decemlineata Say. (Coleoptera: Chrysomelidae). Anz. Schädlingskd. J. Pest Sci. 2002, 75, 19–25. [Google Scholar] [CrossRef]
  51. Kaethner, M. Fitness reduction and mortality effects of neem-based pesticides on the Colorado potato beetle Leptinotarsa decemlineata Say (Col., Chrysomelidae). J. Appl. Ent. 1992, 113, 456–465. [Google Scholar] [CrossRef]
  52. Murray, K.D.; Groden, E.; Drummond, F.A.; Alford, A.R.; Conley, S.; Storch, R.H.; Bentley, M.D. Citrus limonoid effects on Colorado potato beetle (Coleoptera: Chrysomelidae) colonization and oviposition. Environ. Entomol. 1995, 24, 1275–1283. [Google Scholar] [CrossRef]
  53. Thompson, H.M.; Fryday, S.L.; Harkin, S.; Milner, S. Potential impacts of synergism in honeybees (Apis mellifera) of exposure to neonicotinoids and sprayed fungicides in crops. Apidologie 2014, 45, 545–553. [Google Scholar] [CrossRef]
  54. Tosi, S.; Nieh, J.C.; Sgolastra, F.; Cabbri, R.; Medrzycki, P. Neonicotinoid pesticides and nutritional stress synergistically reduce survival in honey bees. Proc. R. Soc. B 2017, 284, 20171711. [Google Scholar] [CrossRef] [Green Version]
  55. Mohan, M.C.; Reddy, N.P.; Devi, U.K.; Kongara, R.; Sharma, H.C. Growth and insect assays of Beauveria bassiana with neem to test their compatibility and synergism. Biocontrol. Sci. Techn. 2007, 17, 1059–1069. [Google Scholar] [CrossRef] [Green Version]
  56. Akbar, W.; Lord, J.C.; Nechols, J.R.; Loughin, T.M. Efficacy of Beauveria bassiana for red flour beetle when applied with plant essential oils or in mineral oil and organosilicone carriers. J. Econ. Entomol. 2005, 98, 683–688. [Google Scholar] [CrossRef]
  57. Filotas, M.; Sanderson, J.; Wraight, S.P. Compatibility and potential synergism between the entomopathogenic fungus Beauveria bassiana and the insect growth regulator azadirachtin for control of the greenhouse pests Myzus persicae and Aphis gossypii. In Proceedings of the Society for Invertebrate Pathology Annual Meeting Proceedings, Anchorage, Alaska, 7–11 August 2005; p. 81. [Google Scholar]
  58. Rao, G.R.; Dhingra, S. Synergistic activity of some vegetable oils in mixed formulations with cypermethrin against different instars of Spodoptera litura Fabricius. J. Ent. Res. 1997, 21, 153–160. [Google Scholar]
  59. Zanuncio, J.C.; Mourão, S.A.; Martínez, L.C.; Wilcken, C.F.; Ramalho, F.S.; Plata-Rueda, A.; Soares, M.A.; Serrão, J.E. Toxic effects of the neem oil (Azadirachta indica) formulation on the stink bug predator, Podisus nigrispinus (Heteroptera: Pentatomidae). Sci. Rep. 2016, 6, 30261. [Google Scholar] [CrossRef] [Green Version]
  60. Koss, A.M.; Jensen, A.S.; Schreiber, A.; Pike, K.S.; Snyder, W.E. Comparison of predator and pest communities in Washington potato fields treated with broad-spectrum, selective, or organic insecticides. Environ. Entomol. 2005, 34, 87–95. [Google Scholar] [CrossRef]
  61. Radkova, M.; Kalushkov, P.; Chehlarov, E.; Gueorguiev, B.; Naumova, M.; Ljubomirov, T.; Stoichev, S.; Slavov, S.; Djilianov, D. Beneficial arthropod communities in commercial potato fields. Compt. Rend. Acad. Bulg. Sci. 2017, 70, 309–316. [Google Scholar]
  62. Shah, F.M.; Razaq, M.; Ali, Q.; Shad, S.A.; Aslam, M.; Hardy, I.C.W. Field evaluation of synthetic and neem-derived alternative insecticides in developing action thresholds against cauliflower pests. Sci. Rep. 2019, 9, 1–13. [Google Scholar] [CrossRef] [PubMed]
  63. Schmutterer, H. Properties and potential of natural pesticides from the neem tree, Azadirachta indica. Annu. Rev. Entomol. 1990, 35, 271–297. [Google Scholar] [CrossRef]
  64. Barek, S.; Paisse, O.; Grenier-Loustalot, M.-F. Analysis of neem oils by LC-MS and degradation kinetics of azadirachtin-A in a controlled environment. Characterization of degradation products by HPLC-MS-MS. Anal. Bioanal. Chem. 2004, 378, 753–763. [Google Scholar] [CrossRef]
  65. Riyajan, S.-A.; Sakdapipanich, J.T. Encapsulated neem extract containing Azadirachtin-A within hydrolysed poly(vinylacetate) for controlling its release and photodegradation stability. Chem. Eng. J. 2009, 152, 591–597. [Google Scholar] [CrossRef]
  66. Devi, N.; Maji, T.K. A novel microencapsulation of neem (Azadirachta indica A. Juss.) seed oil (NSO) in polyelectrolyte complex of j-carrageenan and chitosan. J. Appl. Polym. Sci. 2009, 113, 1576–1583. [Google Scholar] [CrossRef]
  67. Buddepu, M.; Sabithadevi, K.; Ashok, V.; Ramprasad, M.V.N.S. Determination of in vitro sunscreen activity of Pongamia pinnata (L.) essential oil. Drug Invent. Today 2011, 3, 197–199. [Google Scholar]
  68. Wanyika, H.N.; Kareru, P.G.; Keriko, J.M.; Gachanja, A.; Kenji, G.M.; Mukiira, N.J. Contact toxicity of some fixed plant oils and stabilized natural pyrethrum extracts against adult maize weevils (Sitophilus zeamais Motschulsky). Afr. J. Pharm. Pharmaco. 2009, 3, 66–69. [Google Scholar]
  69. Abbott, W.S. A method of computing the effectiveness of an insecticide. J. Econ. Entomol. 1925, 18, 265–267. [Google Scholar] [CrossRef]
  70. Finney, D.J. Probit Analysis, 3rd ed.; University Press: Cambridge, UK, 1971; p. 333. [Google Scholar]
Table 1. Toxicity of botanical insecticides (Bis) and their mixtures against Leptinotarsa decemlineata larvae. LC50 and LC90: concentration causing 50% and 90% mortality of insects, respectively. CI95: 95% confidence intervals, insecticide activity is considered significantly different when the 95% CI fails to overlap. Chi = Chi-square value, significant at p < 0.05 level.
Table 1. Toxicity of botanical insecticides (Bis) and their mixtures against Leptinotarsa decemlineata larvae. LC50 and LC90: concentration causing 50% and 90% mortality of insects, respectively. CI95: 95% confidence intervals, insecticide activity is considered significantly different when the 95% CI fails to overlap. Chi = Chi-square value, significant at p < 0.05 level.
InsecticidesDays after TreatmentLC50CI95LC90CI95Chi-Squarep-Value
Neem Azal T/S20.075 ± 0.0110.066–0.1010.618 ± 0.2150.372–1.3230.9880.804
50.021 ± 0.0020.011–0.0210.105 ± 0.0110.082–0.1562.0310.565
80.005 ± 0.0010.003–0.0080.029 ± 0.0040.022–0.0410.0070.999
Rock Effect20.582 ± 0.0930.344–0.8581.692 ± 0.4281.112–4.3192.3160.677
50.371 ± 0.0710.190–0.5531.032 ± 0.2630.672–2.8135.0650.281
80.259 ± 0.0540.119–0.3790.774 ± 0.1760.523–1.1651.8210.768
Rock Effect and NeemAzal T/S 1:220.543 ± 0.1510.367–0.6116.553 ± 2.4415.369–7.9216.5910.252
50.021 ± 0.0050.015–0.0310.151 ± 0.0270.094–0.2115.3980.369
80.012 ± 0.0010.012–0.0170.028 ± 0.0020.024–0.0340.6770.954
Rock Effect and NeemAzal T/S 1:120.065 ± 0.0160.042–0.1131.651 ± 0.3251.354–1.9232.0880.552
50.008 ± 0.0150.001–0.0600.037 ± 0.0230.016–0.0651.5070.681
80.001 ± 0.0010.002–0.0260.011 ± 0.0010.007–0.0160.0520.996
Rock Effect and NeemAzal T/S 2:120.387 ± 0.0520.302–0.5126.361 ± 2.5853.391–7.1825.1260.401
50.053 ± 0.0020.012–0.0910.267 ± 0.0850.168–0.3783.7710.582
80.015 ± 0.0020.011–0.0190.059 ± 0.0070.047–0.0770.3360.996

Share and Cite

MDPI and ACS Style

Kovaříková, K.; Pavela, R. United Forces of Botanical Oils: Efficacy of Neem and Karanja Oil against Colorado Potato Beetle under Laboratory Conditions. Plants 2019, 8, 608. https://doi.org/10.3390/plants8120608

AMA Style

Kovaříková K, Pavela R. United Forces of Botanical Oils: Efficacy of Neem and Karanja Oil against Colorado Potato Beetle under Laboratory Conditions. Plants. 2019; 8(12):608. https://doi.org/10.3390/plants8120608

Chicago/Turabian Style

Kovaříková, Kateřina, and Roman Pavela. 2019. "United Forces of Botanical Oils: Efficacy of Neem and Karanja Oil against Colorado Potato Beetle under Laboratory Conditions" Plants 8, no. 12: 608. https://doi.org/10.3390/plants8120608

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop