Habituation in Frankliniella occidentalis to deterrent plant compounds and their blends.

Feeding and oviposition deterrence of three secondary plant compounds and their 1:1 blends to adult female Frankliniella occidentalis Pergande (Thysanoptera: Thripidae) and the potential for habituation of the thrips to the pure compounds and the 1:1 blends at various concentrations were investigated. In choice assays, we tested dose-dependent feeding and oviposition deterrence of the two fatty acid derivatives methyl jasmonate and cis-jasmone, the phenylpropanoid allylanisole, and their blends when directly applied to bean leaf discs. The concentration required to reduce the feeding damage by 50% relative to the control treatment (FDC50) was lowest for cis-jasmone and highest for allylanisole. The feeding deterrent effect of both jasmonates was increased when blended with allylanisole. Feeding deterrence and oviposition deterrence were strongly correlated. In no-choice assays conducted over four consecutive days, we discovered that dilutions at low concentrations (FDC15) applied to bean leaves resulted in habituation to the deterrents, whereas no habituation occurred at higher concentrations (FDC50). We observed a tendency that the 1:1 blends reduce the probability that thrips habituate to the deterrent compounds. Our results may be useful in the development of integrated crop protection strategies with the implementation of allelochemicals as pest behaviour-modifying agents.

Introduction

Western flower thrips, Frankliniella occidentalis Pergande (Thysanoptera: Thripidae), is one of the most harmful pests on many horticultural and agricultural crops worldwide (Kirk & Terry, 2003). Adults and immature stages both feed on plant tissue by penetrating plant cells and sucking out the cell sap (Childers, 1997). In addition to the direct feeding damage, plants are damaged indirectly because F. occidentalis is a potent vector of plant virus diseases (Wijkamp et al., 1995). Management of F. occidentalis is problematic due to their minute size and their thigmotactic behaviour (Lewis, 1997). Control strategies relying on repeated application of chemical insecticides have resulted in widespread development of resistance in F. occidentalis (e.g., Jensen, 2000). Among possible approaches to thrips control, the integration of secondary plant compounds that disrupt host acceptance behaviours with other control measures into behavioural manipulation strategies is broadly considered to have great potential (Cowles, 2004; Cook et al., 2007).

Plants produce a wide range of secondary compounds that may act as allelochemicals, mediating interactions between insects and plants. Some volatile secondary metabolites act as insect behaviour‐modifying agents or are toxic to various insect species (Renwick, 1999; Kim & Ahn, 2001). Allylanisole or estragole, a volatile phenylpropanoid (Knudsen et al., 1993), is a compound found in the essential oil of Pimpinella anisum L. and Ocimum basilicum L. (Hasegawa et al., 1997; Santos et al., 1998). The essential oil of Foeniculum vulgare Mill. also contains allylanisole and was deterrent to some beetle species (Cosimi et al., 2009). cis‐Jasmone and methyl jasmonate, two volatile fatty acid derivatives (Knudsen et al., 1993), are constituents of various essential oils, for instance from Jasminum, Lonicera, and Philadelphus species (Joulain, 1986; Mookherjee et al., 1990). Being stress‐related secondary plant compounds, both jasmonates are known to play a role in plant defence against herbivores as well (Birkett et al., 2000; Howe & Jander, 2008). Jasmonates were found to be repellent to various aphid species (Birkett et al., 2000; Bruce et al., 2003). Previous findings indicate that F. occidentalis respond negatively to jasmonates: females avoided settling and feeding on methyl jasmonate‐treated chrysanthemum plants (Bruhin, 2009), significantly fewer thrips were found on jasmonic acid‐sprayed plants (Thaler et al., 2001), and jasmonate‐baited traps did not attract F. occidentalis (James, 2005).

Habituation is the waning of a response as a result of repeated presentation of a stimulus (Chapman & Bernays, 1989; Schoonhoven et al., 2005). This type of experience‐based response has been found to occur in phytophagous insects for feeding deterrents and may reduce the effect of behavioural pest control strategies relying on behavioural manipulation of the pest (Jermy et al., 1982; Jermy, 1987; Glendinning & Gonzalez, 1995; Akhtar & Isman, 2003, 2004). Generally, the potential for habituation may be greater in polyphagous species such as F. occidentalis, presumably because they have evolved mechanisms for dealing with plant defensive compounds (Bernays & Chapman, 1994; Bernays et al., 2000). Whether – and to what extent – habituation to plant compounds can develop may also depend on the compound concentration and mixture. Habituation to feeding deterrents applied to plants occurs most readily when a single pure compound provides a weak inhibitory stimulus (Szentesi & Bernays, 1984; Held et al., 2001), whereas complex mixtures of antifeedants can prevent a decrease in feeding deterrent responses (Jermy, 1987; Bomford & Isman, 1996; Renwick & Huang, 1996). Strategies such as the mixture of several deterrents have been shown to have potential for mitigating the decrease in feeding deterrent responses to antifeedants by insects (Akhtar & Isman, 2003).

Here, we study habituation effects of deterrents in a cell sap‐feeding insect species with piercing‐sucking mouthparts. This study investigates the little‐researched responses of adult insects to feeding and oviposition deterrents (Held et al., 2001; Akhtar & Isman, 2004; Liu et al., 2005; Wang et al., 2008). Specifically, we investigate possible deterrent effects of three pure essential oil compounds and their binary (1:1) mixtures, applied directly to bean leaf discs, on adult female F. occidentalis and the potential for habituation of the thrips to the pure and mixed compounds.

Materials and methods

Insects and plants

A greenhouse‐collected strain of F. occidentalis was reared on detached bean leaves [Phaseolus vulgaris L. cv. Borlotto (Fabaceae); Austrosaat, Vienna, Austria] on 1% (wt/vol) water agar (Agar; Sigma‐Aldrich, Vienna, Austria) in plastic Petri dishes (14 cm diameter) in a climate chamber at 24 ± 1 °C, 35 ± 5% r.h., and L16:D8 photoperiod. About 50 adult females were allowed to lay eggs on bean leaves in the Petri dishes. The dishes were closed with lids with central holes covered with a fine mesh to ensure ventilation. After 48 h, the thrips were removed and the leaves with eggs were kept in Petri dishes in the climate chamber until adults emerged. Adults were used to maintain rearing or for the bioassays.

To obtain groups of even‐aged thrips females, thrips pupae were collected from the rearing and transferred to fresh bean leaves on 1% water agar in separate Petri dishes. Females were used in all bioassays 48 h after adult emergence, i.e., at the end of their pre‐oviposition period (van Rijn et al., 1995).

Bean plants used for rearing as well as for testing were grown in a plant growing room at 25 ± 1 °C, at 50 ± 5% r.h., and L16:D8 photoperiod in groups of 13–15 plants per pot. Leaf discs used for the bioassays were punched with a cork borer (1.1 cm diameter) from cotyledons of bean plants 11–13 days after sowing.

Pure compounds and their blends

The pure compounds cis‐jasmone and methyl jasmonate were purchased from Sigma‐Aldrich, and allylanisole from Merck (Darmstadt, Germany). All pure compounds were blended at a ratio of 1:1 (wt/wt), i.e., each compound represents half of the total dose tested. Pure compounds as well as their three blends were diluted in pure ethanol (Merck) at a ratio of 1:10 by volume. Subsequently, the respective amount of distilled water plus Triton X‐100 (0.05%; Sigma‐Aldrich) as surfactant was added to obtain a range of concentrations (0.1–2%). The control solution consisted of ethanol and distilled water with the surfactant at a ratio of 1:10.

General bioassay procedure

Bean leaf discs were put in a glass Petri dish (9 cm diameter) and sprayed with the respective dilution using a Potter Precision Laboratory Spray Tower (Burkard Manufacturing, Rickmansworth, UK) at constant air pressure resulting in an exact wet deposit of 1 μl cm−2 dilution quantity on the upper surface of each leaf disc. Before releasing the test insects, the treated leaf discs were allowed to dry for ca. 10 min and subsequently placed on a 1% water agar layer in glass Petri dishes (6 cm diameter) to prevent the thrips from feeding on the lower leaf surfaces. The units were closed with a plastic sealing film (Carl Roth, Karlsruhe, Germany) which was perforated subsequently by means of insect pins (ca. 10 punctures cm−2) to ensure ventilation.

Feeding and oviposition deterrence index

In a choice assay adapted from Bomford & Isman (1996), a bean leaf disc treated with the control dilution and a leaf disc treated with a compound or blend dilution were placed at a distance of ca. 4 cm to each other on a thin 1% water agar layer in a glass Petri dish (6 cm diameter) to prevent the thrips from feeding on the lower leaf surfaces. A single F. occidentalis female of known age was released in the centre of the Petri dish. The dish was sealed with perforated plastic sealing film as described above and kept in a climate chamber at 24 ± 1 °C, 35 ± 5% r.h., and L16:D8 photoperiod. After 24 h, the female was removed, the area of feeding damage on each leaf disc was measured using a transparent counting grid (0.25 × 0.25 mm; Boraident, Halle, Germany) and a stereo microscope (Stemi 2000; Zeiss, Vienna, Austria). Subsequently, the eggs on each leaf disc were counted using a transmitted light microscope. This procedure was repeated with 4–6 concentrations (0.1, 0.25, 0.5, 0.75, 1, and 2%) of each compound or blend dilution for calculating a feeding or oviposition deterrence index (FDI or ODI), using the formulae FDI = 100 [(FC − FT)/(FC + FT)], where FC and FT are the control and treated leaf areas damaged by the F. occidentalis females (Isman et al., 1990), and ODI = 100 [(OC − OT)/(OC + OT)], where OC and OT are the numbers of eggs laid on the control and treated leaf discs, respectively.

The bioassay was replicated with 25–35 thrips females per concentration of each compound or blend dilution. FDC15, FDC50, or FDC95 (that is, the concentration required to reduce feeding damage on the treated leaf disc by 15, 50, or 95% relative to the control leaf disc) was calculated via linear regression (Seffrin et al., 2010).

Repeated short‐term exposure

In a no‐choice assay adapted from Bomford & Isman (1996), F. occidentalis females were tested for habituation to the pure compounds and their 1:1 blends compared to the control dilution applied to bean leaf discs. The pure compounds were tested at their FDC15 and FDC50, and cis‐jasmone was tested additionally at the FDC95 (see Table 1 for concentrations). The blends were tested at their FDC50.

Table 1

Concentrations (%) of pure compounds and their 1:1 blends required to produce 50% feeding (FDC50) or oviposition (ODC50) deterrence in on bean. Calculations by means of linear regression are based on 4–5 concentrations (n = 25–35 thrips females each) per compound/blend

Pure compound/blend	Feeding deterrence		Oviposition deterrence
	FDC50	r2	ODC50	r2
cis‐Jasmone	0.66	0.86	0.67	0.83
Methyl jasmonate	0.77	0.99	0.60	0.97
Allylanisole	0.94	0.97	0.96	0.99
Methyl jasmonate/cis‐jasmone	0.66	0.68	0.71	0.63
Methyl jasmonate/allylanisole	0.31	0.88	0.29	0.96
cis‐Jasmone/allylanisole	0.51	0.89	0.58	0.98

At 15:00 hours of the 1st day of the bioassay, a F. occidentalis female of known age was placed singly on an untreated leaf disc on water agar in a glass Petri dish as described above and stored in a climate chamber at 24 ± 1 °C, 35 ± 5% r.h., and L16:D8 photoperiod. At 09:00 hours on the following day, the adult female was transferred to a leaf disc treated either with the compound or blend dilution or the control dilution in a glass Petri dish as described above and put back into the climate chamber. Six hours later the female was again transferred to a fresh untreated leaf disc and allowed to feed for 18 h. This procedure was repeated so that each female was exposed to the same treatment for 6 h on each of four consecutive days. Immediately after each transfer of the thrips, the feeding damage was measured and the eggs were counted on the leaf discs as described above. The bioassay was replicated with 23–34 F. occidentalis females for each compound or blend dilution at the respective FDC.

Statistical analysis

The correlation between feeding deterrence and oviposition deterrence was determined by calculating Pearson's correlation coefficient for the data obtained in the feeding/oviposition deterrence choice assay. Data obtained in the assays with repeated short‐term exposures of thrips to pure compounds or their blends, i.e., the mean area damaged by thrips feeding and the mean number of eggs laid on the leaf discs, were analysed using repeated measures ANOVA, separating the means on the consecutive treatment days by Bonferroni post‐hoc tests. Degrees of freedom were corrected using Greenhouse‐Geisser estimates if the assumption of sphericity was violated (Mauchly's test for sphericity). Mean feeding damage/oviposition rates of the test compound treatments were compared to the control treatment using a one‐way ANOVA combined with a Bonferroni or a Games‐Howell post‐hoc test for pairwise comparisons of means. All statistical analyses were performed using the statistical package PASW 18.0.0 (IBM‐SPSS, Armonk, NY, USA).

Results

Feeding and oviposition deterrence

Generally, in all bioassays the feeding deterrence of pure compounds as well as their 1:1 blends was significantly correlated with the respective oviposition deterrence to F. occidentalis on bean leaves (Pearson correlation: r = 0.93, d.f. = 812, P<0.01; Figure 1). The feeding and oviposition deterrent effect on F. occidentalis of the pure compounds methyl jasmonate, cis‐jasmone, and allylanisole as well as their 1:1 blends methyl jasmonate/cis‐jasmone, methyl jasmonate/allylanisole, and cis‐jasmone/allylanisole (Figure 1) applied to leaf discs was dose‐dependent: increasing concentrations resulted in reduced feeding damage and reduced oviposition rate. The application of cis‐jasmone at about 0.66% reduced the feeding damage by 50% on the treated leaf disc compared to the control disc, methyl jasmonate applied at about 0.77% was required to deter thrips feeding by 50%, and allylanisole at about 0.94% reduced feeding damage by 50% (Table 1). The 1:1 blends of allylanisole and methyl jasmonate or cis‐jasmone deterred thrips from feeding at lower concentrations than the jasmonates applied as pure compounds: FDC50 of the 1:1 blend methyl jasmonate/allylanisole was about 0.31%, FDC50 of cis‐jasmone/allylanisole was about 0.51%. The 1:1 blend methyl jasmonate/cis‐jasmone deterred feeding by 50% when applied at about 0.66%. The concentration required to deter oviposition by 50% was about 0.67% for cis‐jasmone, 0.60% for methyl jasmonate, and 0.96% for allylanisole. The 1:1 blend of methyl jasmonate/cis‐jasmone reduced oviposition by 50% at about 0.71%, methyl jasmonate/allylanisole at about 0.29%, and cis‐jasmone/allylanisole at about 0.58%.

Figure 1

Mean (A) feeding deterrence and (B) oviposition deterrence of increasing concentrations of the pure compounds cis‐jasmone (cis‐j), methyl jasmonate (m‐j), and allylanisole (all‐ani), and the 1:1 blends cis‐jasmone/methyl jasmonate, cis‐jasmone/allylanisole, and methyl jasmonate/allylanisole to females on bean leaf discs in choice assays (n = 25–30 thrips females per compound and concentration tested).

Effects within exposure days

The application of cis‐jasmone at the FDC15 (0.29%) reduced feeding damage caused by F. occidentalis females during the 6‐h exposure period on day 2, but on days 1, 3, and 4 no significant reduction in the feeding damage compared to the control treatment was found (Figure 2). cis‐Jasmone at the FDC50 (0.66%) deterred F. occidentalis from feeding on days 1–3. On day 4, no significant reduction in the feeding damage on treated leaf discs was found. cis‐Jasmone at the FDC95 (1.15%) deterred the thrips within all exposure days compared to the control treatment.

Figure 2

Mean (+ SEM) feeding damage caused by during a 6‐h exposure period on four consecutive days on treated bean leaf discs in a no‐choice assay. Bean leaves were treated with ethanol + water (control), cis‐jasmone (cis‐j) at 0.29% (FDC15), 0.66% (FDC50), or 1.15% (FDC95), methyl jasmonate (m‐j) at 0.08% (FDC15) or 0.77% (FDC50), or allylanisole (all‐ani) at 0.17% (FDC15) or 0.94% (FDC50) (n = 24–34 thrips females per dilution tested). Means within a day capped with different letters are significantly different (one‐way ANOVA, followed by Bonferroni pairwise comparisons: P<0.05).

Methyl jasmonate or allylanisole applied at the respective FDC15 (0.08 or 0.17%) to bean leaf discs reduced feeding damage during the 6‐h exposure period on day 2, but not on days 1, 3, and 4 compared to the control treatment. Methyl jasmonate at the FDC50 (0.77%) deterred F. occidentalis females on days 2 and 4. No significant reduction in the feeding damage on treated leaf discs compared to the control discs was found on days 1 and 3. Allylanisole at the FDC50 (0.94%) deterred F. occidentalis females on day 2, on the other days, no significant reduction in the feeding damage on treated leaf discs compared to the control discs was found during 6 h of exposure.

Applications of the 1:1 blends of methyl jasmonate/cis‐jasmone or methyl jasmonate/allylanisole at the respective FDC50 (0.66 or 0.31%) reduced the feeding damage of F. occidentalis females during the 6‐h exposure period significantly compared to the control treatment on day 2, but on days 1, 3, and 4 no significant reduction in the feeding damage on treated leaf discs was found (Figure 3). The 1:1 blend cis‐jasmone/allylanisole applied at FDC50 (0.51%) reduced the feeding damage significantly on days 2, 3, and 4, but not on day 1 in within‐day comparisons to the control treatment.

Figure 3

Mean (+ SEM) feeding damage caused by during a 6‐h exposure period on four consecutive days on treated bean leaf discs in a no‐choice assay. Bean leaves were treated either with ethanol + water (control), the binary mixtures methyl jasmonate/cis‐jasmone (m‐j/cis‐j) at 0.66% (FDC50), cis‐jasmone/allylanisole (cis‐j/all‐ani) at 0.51% (FDC50), or methyl jasmonate/allylanisole (m‐j/all‐ani) at 0.31% (FDC50) (n = 24–34 thrips females per dilution tested). Means within a day capped with different letters are significantly different (one‐way ANOVA, followed by Bonferroni pairwise comparisons: P<0.05).

Effects between exposure days

Generally, the feeding activity of F. occidentalis resulting in damaged areas on control bean leaf discs varied significantly during the 6‐h exposure period among the four consecutive days (ANOVA for repeated measures: F3,72 = 3.64, P = 0.017; Figure 2). Bonferroni post‐hoc pairwise comparisons between days revealed that thrips feeding on the control discs significantly increased on day 2 compared to day 1, but on days 3 and 4 feeding did not differ statistically from days 1 and 2.

Between‐day comparisons revealed that the feeding activity of thrips on leaf discs treated with cis‐jasmone at the FDC15 increased significantly from day 1 to day 2, and on day 3 compared to days 1 and 2. On day 4 feeding differed statistically from day 1, but not from days 2 and 3 (F3,75 = 13.74, P = 0.001). On leaf discs treated with cis‐jasmone at the FDC50, feeding damage increased significantly from day 1 to day 2, but there was no difference between areas of feeding damage on days 2–4 (F3,84 = 10.71, P<0.001). Feeding damage on discs treated with cis‐jasmone at the FDC95 did not significantly increase on four consecutive days (F3,69 = 2.80, P = 0.051).

The deterrent effect of methyl jasmonate in between‐day comparisons at the lower concentration (FDC15) gradually decreased: the amount of feeding damage was significantly lower on day 1 compared to the following 3 days (F3,75 = 15.01, P>0.001). On leaf discs treated with methyl jasmonate at the FDC50, feeding damage increased significantly from day 1 to day 3, but on day 4 feeding damage decreased significantly compared to days 2 and 3 (F3,72 = 13.66, P<0.001).

Between‐day comparisons showed that the feeding activity of thrips on leaf discs treated with allylanisole at the FDC15 increased significantly going from day 1 to day 3. The feeding damage on day 4 was not significantly different from that on day 3 (F3,66 = 13.82, P<0.001). On leaf discs treated with allylanisole at FDC50, feeding damage did not increase. On day 3, the damage increased significantly compared to day 2, the damaged area on day 4 did not differ from that on days 1–3 (F2.01,50.34 = 3.90, P = 0.026).

Between‐day comparisons of methyl jasmonate/cis‐jasmone‐treated leaf discs revealed a significantly increased feeding activity on days 3 and 4 (F3,66 = 7.56, P<0.001; Figure 3). Comparing the feeding activity of thrips on leaf discs treated with methyl jasmonate/allylanisole at the FDC50 on the four consecutive exposure days revealed that the feeding damage increased significantly on day 2 compared to day 1, and on day 3 compared to days 1 and 2. On day 4, the feeding damage did not increase compared to day 3 (F3,75 = 10.64, P<0.001). Bonferroni post‐hoc tests resulted in no significant differences in the feeding damage on leaf discs treated with the 1:1 blend cis‐jasmone/allylanisole at FDC50 (0.51%) over 4 days in between‐day comparisons, although the ANOVA for repeated measures indicated a significant treatment effect (F3,66 = 2.96, P = 0.039).

Discussion

Based on the FDC50 values, cis‐jasmone deterred thrips feeding by 50% at the lowest concentration, followed by methyl jasmonate and allylanisole. The latter was chosen for the bioassays because it belongs to a different chemical class than the jasmonates tested and because of the repellent properties of fennel essential oil and allylanisole against various beetle species (Knudsen et al., 1993; Hayes et al., 1994; Cosimi et al., 2009). It was identified as a thrips deterrent compound for the first time.

As a pure compound, allylanisole displayed a relatively high FDC50 (0.94%) compared to the FDC50 of the pure jasmonates, whereas in blends the FDC50 were comparatively low: methyl jasmonate/allylanisole (0.31%) and cis‐jasmone/allylanisole (0.51%). The blend of the two jasmonates did not show a noticeable increase in deterrent effect compared to the pure compounds. Blending of a jasmonate—belonging to the class of fatty acid derivatives—and allylanisole—a phenylpropanoid (Knudsen et al., 1993)—apparently increased deterrence efficiency. Binary and complex mixtures were reported to be more effective compared to single compounds as deterrents to other insect species, e.g., Locusta migratoria L., Sitophilus granarius L., or Spodoptera litura Fabricius (Adams & Bernays, 1978; Castellanos & Espinosa‐García, 1997; Hummelbrunner & Isman, 2001).

The no‐choice assay for habituation on four consecutive days showed an increased feeding damage on days 2 and 3 in the control treatment, which dropped on day 4. A possible explanation could be the natural reproductive cycle of F. occidentalis females: the oviposition rate peaks 3 days after adult emergence, thus causing the necessity of enhanced food uptake (van Rijn et al., 1995). Feeding and oviposition deterrence were strongly correlated in all bioassays, independently from the treatment. This matches the decreasing reproductive fitness as a result of minor food quality as shown in a study with F. occidentalis by Trichilo & Leigh (1988).

We assessed the potential of F. occidentalis to habituate to secondary plant compounds in repeated exposure bioassays using the deterrent cis‐jasmone at various concentrations as a model compound. Weak stimuli induced habituation, whereas strong stimuli did not, supporting the results of previous studies of Jermy et al. (1982) and Szentesi & Bernays (1984): the lowest concentration of cis‐jasmone (FDC15 = 0.29%) was deterrent only during the first half of the 4‐day testing period, the intermediate concentration (FDC50 = 0.66%) deterred the thrips over a longer period and the highest concentration (FDC95 = 1.15%) did not decrease the deterrent efficiency over all 4 days tested. Methyl jasmonate and allylanisole applied as pure compounds at low (FDC15) and intermediate (FDC50) concentrations supported the thesis that habituation is dose‐dependent in thrips.

We observed a tendency that thrips needed a longer exposure to habituate to the 1:1 blends at the respective FDC50 of the compounds. However, this was not always the case: the two jasmonates applied as single compounds at the respective FDC50 deterred thrips feeding more effectively compared to allylanisole, whereas the 1:1 blend of the jasmonates was deterrent to the thrips only on day 2. The same applies to the blend methyl jasmonate/allylanisole; the blend cis‐jasmone/allylanisole exhibited a deterrent effect on 3 of 4 days. Considering that the quantity of either jasmonate is reduced in their binary mixture, we suppose that this reduced quantity of either deterrent enhances the probability for habituation in thrips. Habituation might occur in bioassays with the two jasmonates in mixture because the two compounds are chemically closely related. In contrast, the blend cis‐jasmone/allylanisole inhibited habituation, although the blend concentration was even lower (0.51%). The prolonged deterrent effect of this blend may be due to the increased complexity of the blend and the presence of cis‐jasmone, the most effective pure deterrent compound tested. However, further research using more and other mixtures is required to better understand the mode of action of the compounds. Methyl jasmonate, however, may be too weak a deterrent stimulus at the low concentration in the binary mixture with allylanisole to maintain the deterrent effect over the 4‐day testing period. Our results correspond to previous studies about the correlation between mixture complexity and habituation potential in insects (Jermy, 1987; Bomford & Isman, 1996).

This study is the first to investigate the habituation potential of a generalist, cell sap‐feeding insect with piercing‐sucking mouthparts to secondary plant compounds. The compounds tested remained deterrent over several days when applied at their respective FDC50. Application at lower concentrations (FDC15) resulted in habituation of the thrips to the pure compounds. The amount of a pure compound used to deter F. occidentalis may be reduced by blending deterrent agents, thus enhancing the chemical complexity and preventing habituation to the compounds. It should be noted that a direct application of jasmonates to crop plants also might induce defence mechanisms in the plant (Farmer & Ryan, 1990; Browse & Howe, 2008). These effects might be considered in further studies. Further experiments should evaluate the long‐term habituation potential of thrips before our results may be used in the development of integrated crop protection strategies with the implementation of allelochemicals as pest behaviour‐modifying agents.