Advertisement
Research Article

Electrophysiological and Behavioral Responses of Male Fall Webworm Moths (Hyphantria cunea) to Herbivory-Induced Mulberry (Morus alba) Leaf Volatiles

  • Rui Tang,

    Affiliations: State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing, People's Republic of China, Graduate University of the Chinese Academy of Sciences (GUCAS), Beijing, People's Republic of China

    X
  • Jin Ping Zhang,

    Affiliation: State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing, People's Republic of China

    X
  • Zhong Ning Zhang mail

    zhangzn@ioz.ac.cn

    Affiliation: State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing, People's Republic of China

    X
  • Published: November 14, 2012
  • DOI: 10.1371/journal.pone.0049256

Abstract

Volatile organic compounds (VOCs) were collected from damaged and intact mulberry leaves (Morus alba L., Moraceae) and from Hyphantria cunea larvae by headspace absorption with Super Q columns. We identified their constituents using gas chromatography-mass spectrometry, and evaluated the responses of male H. cunea antennae to the compounds using gas chromatography-flame ionization detection coupled with electroantennographic detection. Eleven VOC constituents were found to stimulate antennae of male H. cunea moths: β-ocimene, hexanal, cis-3-hexenal, limonene, trans-2-hexenal, cyclohexanone, cis-2-penten-1-ol, 6-methyl-5-hepten-2-one, 4-hydroxy-4-methyl-2-pentanone, trans-3-hexen-1-ol, and 2,4-dimethyl-3-pentanol. Nine of these chemicals were released by intact, mechanically-damaged, and herbivore-damaged leaves, while cis-2-penten-1-ol was released only by intact and mechanically-damaged leaves and β-ocimene was released only by herbivore-damaged leaves. Results from wind tunnel experiments conducted with volatile components indicated that male moths were significantly more attracted to herbivory-induced volatiles than the solvent control. Furthermore, male moths' attraction to a sex pheromone lure was increased by herbivory-induced compounds and β-ocimene, but reduced by cis-2-penten-1-ol. A proof long-range field trapping experiment showed that the efficiency of sex pheromone lures in trapping male moths was increased by β-ocimene and reduced by cis-2-penten-1-ol.

Introduction

The fall webworm, Hyphantria cunea (Drury) (Lepidoptera: Arctiidae), is native to North America but spread into central Europe and eastern Asia in the 1940s [1]. In China, this species was first found in Liaoning Province in 1979 and has since been introduced into other regions, such as Beijing, Tianjin, and Hebei, Shandong, and Shanxi provinces [2]. This polyphagous defoliator has caused huge damage to forests, urban ornamental trees, and agricultural crops in China because of its wide host range [2]. Currently, 175 different plant species within 49 families and 108 genera are known to serve as its hosts [3]. More than 30 years after its initial invasion, H. cunea is now widely distributed in eastern and northeastern China. The major hosts of H. cunea in China are mulberry, poplar and rock maple, which are all different from those in their native area [4]. Mulberry is especially prone to herbivory by H. cunea, because of the plant's high density in China for silkworm breeding and agriculture.

Some of the volatile organic compounds (VOCs) released by herbivore-attacked plants are known to attract arthropod predators and parasitoids in laboratory experiments on agricultural plants [5] and have been shown to function defensively under natural conditions [6]. In some cases, host-related plant volatiles, such as trans-2-hexenal, benzaldehyde, 1-hexenol, cis-3-hexen-1-ol, geraniol, linalool, (+)-limonene, hexenal, and trans-2-hexenol, could increase the sensitivity of insect antennae towards pheromones [7]. Research with H. cunea showed that previous herbivory on red alder may improve food quality for fall webworm larvae [8]. On the other hand, eastern tent caterpillar infestations on black cherry negatively affect fall webworm use of the same trees [9]. Although mulberry volatiles have been identified by some researchers [10][13], the relationship between mulberry VOCs and H. cunea remains unreported. The aims of this study were to identify the bioactive compounds of mulberry leaf volatiles by electrophysiological analysis with H. cunea male moths and to identify blends of volatile emissions with potential effects on pheromone trapping.

Materials and Methods

Moths

Insects were provided by the Chinese Academy of Forestry, which established a laboratory population of H. cunea using wild moths collected in Qinghuangdao, Hebei Province, China. Pupas were kept at 25±1°C under a 16 h light/8 h dark photoperiod in environmental chambers for one week before eclosion. Third-instar larvae were starved for one day before the experiment.

Headspace collection of VOCs

Chemicals used in all experiments are shown in Table 1. All glassware was carefully cleaned, washed with acetone, and heated at 200–230°C overnight before use. The Super Q GC Packed Column (80/100, Alltech, Deerfield, IL, USA) used to collect volatiles in air entrainment experiments was washed with acetone, tested for purity by gas chromatography (GC), and then conditioned by heating overnight in a stream of nitrogen at 100°C.

thumbnail

Table 1. List of chemicals, and their purity and source, used in the experiments.

doi:10.1371/journal.pone.0049256.t001

Mulberry plants were bought from Jiangsu Province and then grown in laboratory conditions with 25°C and 30% relative humidity for 1 month before experiments in order to make them stable. Fully grown, intact plants at a height of 1.2–1.3 m were chosen. Volatiles were collected by encasing all upper parts of each plant in oven bags (turkey size, Reynolds, Richmond, Virginia, USA) during absorption.

We conducted four treatments, each with at least 10 replicates. (1) Intact leaf volatile compounds: odors from intact leaves of natural mulberry plants were collected in situ using oven bags. (2) Mechanically-damaged leaf volatile compounds: 30% of leaves on a mulberry plant were cut in half and volatiles were collected by encasing plants in oven bags. (3) Herbivore-induced leaf volatile compounds: ten H. cunea larvae were put into oven bags with mulberry plants. (4) Larvae: ten third-instar larvae were placed without leaves in oven bags.

For all four treatments, air was collected via an air sampler (QC-1, Beijing Municipal Institute of Labour Protection, Beijing, PRC) and 0.3 g of Super Q absorbent connected to the oven bags. Air flow was at 50 ml/min and air into the bags was purified by an activated carbon sphere on the inlet of the bags. Volatile samples were collected for 24 hours before elution with 2 ml of solvent (70% pentane and 30% diethyl ether), and a total of approximately 72l volume of air was captured through absorbent. Eluted samples were kept in a refrigerator at −20°C prior to subsequent analyses.

Chemical analyses

Samples were analyzed by gas chromatography-mass spectrometry (GC-MS) using an Agilent 5973N (Santa Clara, CA, USA) mass selective detector coupled with an Agilent 6890N network GC system equipped with a quartz capillary column (DB-WAX, 60 m×0.25 mm×0.25 µm; J&W Scientific, Palo Alto, CA, USA). The column oven was maintained at 37°C for 2 min, increased to 150°C at 5°C/min, held for 2 min, increased to 200°C at 10°C/min, held for 5 min, and finally heated to 230°C at 20°C/min, and held for 1 min. The carrier gas was helium at a constant flow rate of 1 ml/min. The injection port was at 250°C with no split-flow.

Electrophysiological analyses

Combined gas chromatography-flame ionization detection coupled with electroantennographic detection (GC-EAD) was used to identify compounds that were electrophysiologically active in male moths. The GC column and temperature program was identical to that of the GC-MS analysis above. Each antenna was prepared by cutting both extremes and immediately mounted between two Ag/AgCl electrodes filled with Kaissling saline (glucose 354 mmol/L, KCl 6.4 mmol/L, KH2PO4 20 mmol/L, MgCl2 12 mmol/L, CaCl2 1 mmol/L, NaCl 12 mmol/L, KOH 9.6 mmol/L, pH 6.5). The electrode at the distal end of the antenna was connected via an interface box to a signal acquisition interface board (IDAC; Syntech, Kirchzarten, Germany) connected to a computer. EAD signals and flame ionization detector (FID) responses from the GC were simultaneously recorded by a computer using AutoSpike software (Syntech).

Wind tunnel experiments

Wind tunnel experiments were conducted with 2–3 day old virgin male moths in a tunnel with a flying section of 90×90×240 cm (Heling Electronics Co. Ltd, Taiwan, China). Filtered air was blown by a centrifugal fan (Chongqing Dema Frequency Motor R & D Co. Ltd, Chongqing, China) at 30 cm/s. The outflowing air was aspired by another fan and released through a pipe. The flight section was lit diffusely from the top at 10 lux, and the room was kept at 23±2°C and 40–60% relative humidity. Experiments were carried out at the 6–7th hour of the dark phase [2].

Intact leaf volatile compounds, mechanically-damaged leaf volatile compounds, herbivory-induced volatile compounds, β-ocimene and cis-2-penten-1-ol were used in wind tunnel experiments. They were used individually as olfactory stimuli and also used as synergists coupled with 1/4 Nitolure synthetic pheromone lures for H. cunea (Nitto Denko, Osaka, Japan).

Gray rubber septa (The West Company, Phoenixville, PA) loaded with 100 µl solutions of compound samples were used in the experiments. β-ocimene and cis-2-penten-1-ol were at a dose of 1000 µg per septum [14]. Solvent and 1/4 pheromone lures for H. cunea were respectively used as a control in each group.

Olfactory stimuli were released from the center of the upwind end of the flight tunnel. Each compound was tested with 50 male moths, which were divided into 10 groups each with 5 individuals. Moths were released at the center of the downwind end in a small metal screen cage and behaviors were recorded for 5 min per moth. An orientation flight (more than 50 cm of tight zigzag flight to within 10 cm of the target) was recorded as positive [15]. Numbers of moths attracted were converted into a percentage and the effects of different compounds on moth attraction were tested using one-way ANOVA. Duncan's multiple-comparison test was used to compare mean differences between groups at P = 0.05. All analyses were performed in SPSS 16.0.

Long-range field experiments

Gray rubber septa loaded with 100 µl solutions of the compounds (with a concentration of 10 mg/ml) were used in the field trials. After evaporation of the solvent, the rubber septa were wrapped in aluminum foil and stored at −20°C until used in field tests.

Field trapping experiments were executed from 3–14 September, 2011 in Laixi, Shandong Province, China, using the 11 active compounds and the headspace mixtures from mechanically- and herbivore-damaged leaves. Each compound was used with Nitolure synthetic pheromone lures for H. cunea in a single unitrap (Pherobio Technology Co., Beijing, China) at a dose of 1000 µg/septum. Nitolures alone were used as control.

Unitraps were hung 1.5–1.8 m above the ground and 50 m or more apart in poplar trees. Daily numbers of moths captured were transformed to log10 (n+1) prior to statistical analysis [16]. The effects of different compounds on the mean number of moths captured were tested using one-way ANOVA. LSD multiple-comparison test was used to compare mean differences between groups at P = 0.1. All analyses were performed in SPSS 16.0.

Ethics Statement

All necessary permits were obtained for the described field studies from the Forest Pest Control and Quarantine Bureau of Shandong Province. These field studies did not involve endangered or protected species.

Results

Chemical and electrophysiological analyses

The GC-MS and GC-EAD analyses showed that 11 compounds elicited electrophysiological responses: hexanal, cis-3-hexenal, limonene, trans-2-hexenal, cyclohexanone, cis-2-penten-1-ol, 6-methyl-5-hepten-2-one, 4-hydroxy-4-methyl-2-pentanone, trans-3-hexen-1-ol, β-ocimene, and 2,4-dimethyl-3-pentanol (Figure 1). No unique volatiles were released by the larvae group (larvae alone). Although limonene and 4-hydroxy-4-methyl-2-pentanone could be detected from larvae, these compounds were also detected from mechanically-damaged leaves. Therefore, we concluded that these 11 active compounds were released by mulberry leaves. Only one compound, cis-2-penten-1-ol, was unique to leaves that had not suffered herbivore damage; it was detected in both intact and mechanically-damaged leaves. Interestingly, β-ocimene could be only detected from herbivore-damaged leaves and at high levels (with an average of 14% of total mass). Intact leaves released four active volatiles: trans-2-hexenal, hexanal, cis-2-penten-1-ol, and 4-hydroxy-4-methyl-2-pentanone. None of these four compounds differed between intact and mechanically-damaged leaves. Damage-induced volatiles that were not released by intact leaves, but could be detected from both mechanically- and herbivore-damaged leaves, were trans-3-hexen-1-ol, cis-3-hexenal, 6-methyl-5-hepten-2-one, 2,4-dimethyl-3-pentanol and cyclohexanene. Herbivory-influenced variation in each compound was tested with independent-samples t-tests (P = 0.05) between groups of mechanically- and herbivore-damaged leaves. Six compounds showed significant herbivory-influenced differences in production: β-ocimene, trans-2-hexenal, hexanal, cis-2-penten-1-ol, cis-3-hexenal and 2,4-dimethyl-3-pentanol (Figure 2). Concentrations of total bioactive compounds were at an average of 10.96 µg/µl and the average of total VOC mass captured by each absorbent was 21.92 mg.

thumbnail

Figure 1. GC-EAD responses of Hyphantria cunea antennae to mulberry leaf volatiles.

(A) Responses of one male moth to mechanically-damaged leaf volatiles. (B) Responses of one male moth to herbivore-damaged leaf volatiles. β-ocimene (5) was only detected from herbivore-damaged leaves (B), while cis-2-penten-1-ol (8) could be detected only in leaves that had not been eaten (A) and mechanical damage showed no influence on release of this compound. 1: hexanal; 2: cis-3-hexenal; 3: limonene; 4: trans-2-hexenal; 5: β-ocimene; 6: cyclohexanene; 7: 2,4-dimethyl-3-pentanol; 8: cis-2-penten-1-ol; 9: 6-methyl-5-hepten-2-one; 10: 4-hydroxy-4-methyl-2-pentanone; 11: trans-3-hexen-1-ol. CG-EAD: combined gas chromatography-flame ionization detection coupled with electroantennographic detection.

doi:10.1371/journal.pone.0049256.g001
thumbnail

Figure 2. Mean values of bioactive components from intact, mechanically-damaged, herbivore-damaged mulberry leaves and Hyphantria cunea larvae.

All 11 bioactive components were determined by gas chromatography-mass spectrometry (GC-MS) and combined gas chromatography-flame ionization detection coupled with electroantennographic detection (CG-EAD). Asterisks indicate significant differences between mechanically- and herbivore-damaged leaves for each compound (independent samples t-test; *, P<0.05 and **, P<0.01).

doi:10.1371/journal.pone.0049256.g002

Wind tunnel experiments

Intact leaf volatiles, mechanically-damaged leaf volatiles and herbivory-induced leaf volatiles were used alone as olfactory stimuli in wind tunnel experiments. Duncan's multiple-comparison test showed that herbivory-induced volatiles were significantly more attractive to male moths than the solvent control (Figure 3). Further wind tunnel experiments were conducted after combining a sex pheromone with each of the following compounds: intact leaf volatiles, mechanically-damaged leaf volatiles, herbivory-induced leaf volatiles, β-ocimene and cis-2-penten-1-ol. Male moth's attraction to the sex pheromone was significantly increased by herbivory-induced volatiles and β-ocimene, but significantly decreased by cis-2-penten-1-ol (Figure 4).

thumbnail

Figure 3. Attraction of male moths to volatile compounds from mulberry leaves in four treatments.

Results from wind tunnel experiments using headspace absorbed volatile compounds. ‘Solvent’ was control, ‘intact’, ‘mechanically-damaged’ and ‘herbivory-damaged’ mulberry leaves were treatment groups. Intact and mechanically-damaged leaf volatiles did not attract male moths compared with solvent control. Herbivory-induced volatiles showed significant attractiveness to male moths (Duncan's multiple comparison tests, P<0.05).

doi:10.1371/journal.pone.0049256.g003
thumbnail

Figure 4. Attraction of male moths to volatile compounds combined with H. cunea sex pheromone lure.

Results from wind tunnel experiments using headspace absorbed volatile compounds grouped into treatments: sex pheromone lure used as control; sex pheromone (SP) plus intact leaf volatiles; sex pheromone (SP) plus mechanically-damaged leaf volatiles (MD); sex pheromone (SP) plus herbivore-induced leaf volatiles (HI); sex pheromone (SP) plus β-ocimene; sex pheromone (SP) plus cis-2-penten-1-ol. Intact and mechanically-damaged leaf volatiles did not affect attraction of male moths to the sex pheromone. Herbivory-induced volatiles and β-ocimene significantly increased attraction of male moths to the sex pheromone, while cis-2-penten-1-ol significantly decreased attraction (Duncan's multiple comparison tests, P<0.05).

doi:10.1371/journal.pone.0049256.g004

Long-range field trapping

A total of 446 moths, all males, were captured in 28 unitraps. Numbers of moths captured by various compounds were compared. Duncan's multiple-comparison test showed that cis-2-penten-1-ol significantly lowered the numbers of moths captured, while β-ocimene significantly increased the numbers of moths captured relative to the sex pheromone control alone (Figure 5).

thumbnail

Figure 5. Long-range attractiveness of 13 volatiles and a sex pheromone to Hyphantria cunea in the field.

Most compounds did not differ significantly from the sex pheromone control. β-Ocimene substantially increased the attractiveness of the sex pheromone, while cis-2-penten-1-ol substantially decreased its attractiveness (Duncan's multiple-comparison tests, P<0.1).

doi:10.1371/journal.pone.0049256.g005

Discussion

Green leaf volatiles are considered to be varieties of kairomones [17]. Many studies have indicated that olfactory reactions of male insects can be heavily affected by leaf volatiles [18][21]. When combined, botanical secondary substances and sex pheromones can attract Helicoverpa armigera moths over large distances [22]. Plant odors can also attract Paralobesia viteana and Lobesia Botrana moths in wind tunnel experiments [23], [24]. In the present study, herbivory-induced leaf volatiles were attractive to male H. cunea moths in wind tunnel experiments. Moreover, herbivory-induced volatiles and compounds like β-ocimene could significantly affect the attraction of moths to sex pheromones. However, when plant odors were used in the field, the majority, with the exception of β-ocimene and cis-2-penten-1-ol, did not significantly affect the attraction of moths to sex pheromones. These results suggest that effects of plant odors may be altered by volatiles emitted from plants in the field. Functions of plant volatiles could be more widespread and complicated in the natural environment. Although blends of mulberry leaf volatiles had significant effects on the attractiveness of the sex pheromone in the laboratory, some individual components did affect sex pheromone attractiveness even in the field. Compounds of VOCs of mulberry leaves, such as β-ocimene and cis-2-penten-1-ol, could potentially affect the location abilities of male H. cunea moths over a larger range than sex pheromones alone. That blends of VOCs showed no effect may be because the different functions of the individual components balanced one another out. Thus, botanical chemicals may have complex effects on this moth species.

The floral scent compound z-ocimene has also been reported to induce herbivory in a wide range of plants [25][28]. Non-specific storage of ocimene, because of its limited volatility, is a common phenomenon [29], and we found significant quantities of ocimene in the VOCs. Ocimene is known to activate defensive responses in Arabidopsis thaliana [27], [30] and functions as a volatile brood pheromone involved in social regulation in honey bee colonies [31]. Thus, ocimene may participate in a wide range of regulatory functions in ecosystems. Because ocimene is a taxonomically-widespread volatile that is induced by herbivory, attraction to it may offer H. cunea a broader range of host plants compared with other pests, which are repelled by herbivory-induced odors. However, herbivory-induced volatiles can also attract parasitic wasps that are known to attack H. cunea. This suggests that H. cunea is more likely to attack plants that have been fed on by other insects and are emitting ocimene, but that they endure a higher risk of being parasitized by natural enemies that are also attracted to those herbivory-damaged plants. We observed that parasitism rates of H. cunea pupae were remarkably high in the wild (personal observation), which supports the assumption above. Conversely, cis-2-penten-1-ol decreased the trapping rate of the sex pheromone lure. This compound is commonly found in plant oils [32] and has been suggested to contribute to the development of unpleasant fishy and rancid odors [33]. Peppermint oil, which also contains cis-2-penten-1-ol, can deter insects [34]. The presence of this component only in volatiles emitted from leaves that were not herbivore damaged could explain the reduction in moth captures by the volatiles from mechanically-damaged leaves combined with the sex pheromone.

Because only male moths were captured in our experiments, we suggest that the sex pheromone repelled female moths, as has been shown in other Lepidoptera species [35]. We speculate that mulberry VOCs were apparently not sufficiently attractive to H. cunea females to overcome the possible repellency of the sex pheromone.

We conclude that the herbivory-induced leaf volatiles of M. alba can attract H. cunea male moths in wind tunnel experiments. Furthermore, a blend of head space absorbed herbivory-induced volatiles and some components of volatiles, including β-ocimene and cis-2-penten-1-ol, could affect attraction of H. cunea sex pheromones. A blend of these volatile compounds could have more complex functions in nature. Mulberry trees contain compounds such as cis-2-penten-1-ol, which act as a natural shield against insects. However, after attack, herbivore-induced volatiles such as β-ocimene may attract male H. cunea by increasing its sensitivity towards sex pheromones. The invasion of China by this insect may differ from the movement patterns of local species because of their attraction to herbivore-induced compounds.

Acknowledgments

We thank the Chinese Academy of Forestry for providing insects. We thank Dr. Mao-wen Su for helping with our field trapping experiments and Mr. Boi Wong for helping maintaining of mulberry plants.

Author Contributions

Conceived and designed the experiments: RT JPZ ZNZ. Performed the experiments: RT. Analyzed the data: RT. Contributed reagents/materials/analysis tools: RT. Wrote the paper: RT ZNZ.

References

  1. 1. Ito Y, Miyashita K (1968) Biology of Hyphantra cunea drury (Lepidoptera: Arctiidae) in Japan. V. preliminary life tables and mortality data in urban areas. Res Popul Ecol (1968) X: 177–209. doi: 10.1007/bf02510872
  2. 2. Su MW, Fang YL, Tao WQ, Yan GZ, Ma WE, et al. (2008) Identification and field evaluation of the sex pheromone of an invasive pest, the fall webworm Hyphantria cunea in China. Chinese Sci Bull 53: 555–560. doi: 10.1007/s11434-008-0124-9
  3. 3. Yang ZQ, Wei JR, Wang XY (2006) Mass rearing and augmentative releases of the native parasitoid Chouioia cunea for biological control of the introduced fall webworm Hyphantria cunea in China. Biocontrol 51: 401–418. doi: 10.1007/s10526-006-9010-z
  4. 4. Jaenike J, Selander RK (1980) On the question of host races in the fall webworm, Hyphantria cunea. Entomol Exp Appl 27: 31–37. doi: 10.1111/j.1570-7458.1980.tb02943.x
  5. 5. Dicke M, Hilker M (2003) Induced plant defences: from molecular biology to evolutionary ecology. Basic Appl Ecol 4: 3–14. doi: 10.1078/1439-1791-00129
  6. 6. Kessler A, Baldwin IT (2001) Defensive function of herbivore-induced plant volatile emissions in nature. Science 291: 2141–2144. doi: 10.1126/science.291.5511.2141
  7. 7. Stelinski L (2003) Increased EAG responses of tortricid moths after prolonged exposure to plant volatiles: evidence for octopamine-mediated sensitization. J Insect Physiol 49: 845–856. doi: 10.1016/s0022-1910(03)00136-7
  8. 8. Williams KS, Myers JH (1984) Previous herbivore attack of red alder may improve food quality for fall wabworm larvae. Oecologia (Berlin) 63: 166–170. doi: 10.1007/bf00379873
  9. 9. Travis HJ (2005) The effect of eastern tent caterpillar (Malacasoma americanum) infestation on fall webworm (Hyphantria cunea) selection of black cherry (Prunus serotina) as a host tree. Am Midl Nat 153: 270–275. doi: 10.1674/0003-0031(2005)153[0270:teoetc]2.0.co;2
  10. 10. Li JH, Chen DW (2007) Analysis of volatile chemical composition in mulberry leaves using microwave assisted extraction associated with solid phase microextraction. Chemistry and Industry of Forest Products 27: 107–110 (In Chinese).
  11. 11. Li WG, Zhang LW, Wang C, Wang YW, Mu ZM, et al. (2009) Analysis of mulberry leaf volatile components by static headspace-gas chromatography-mass spectrometry. Canye Kexue 35: 355–361 (In Chinese).
  12. 12. Cao MQ, Wang HY, Liu SS, Jiang NX, Shen JH (2010) Analysis of volatile components of essential oil from fresh and air-dried mulberry leaves. Territory & Natural Resources Study 2010 No. 2: 86–87 (In Chinese).
  13. 13. Tanaka K, Uda Y, Ono Y, Nakagawa T, Suwa M, et al. (2009) Highly selective tuning of a silkworm olfactory receptor to a key mulberry leaf volatile. Curr Biol 19: 881–890. doi: 10.1016/j.cub.2009.04.035
  14. 14. Tang R, Su MW, Zhang ZN (2012) Electroantennogram responses of an invasive species fall webworm (Hyphantria cunea) to host volatile compounds. Chinese Sci Bull 57 (In press). doi: 10.1007/s11434-012-5356-z
  15. 15. Howard RW, Blomquist GJ (2005) Ecological, behavioral, and biochemical aspects of insect hydrocarbons. Annu Rev Entomol 50: 371–393. doi: 10.1146/annurev.ento.50.071803.130359
  16. 16. Teal PEA, Heath RR, Tumlinson JH, McLaughlin JR (1981) Identification of a sex pheromone of Heliothis subflexa (GN.) (Lepidoptera: Noctuidae) and field trapping studies using different blends of components. J Chem Ecol 7: 1011–1022. doi: 10.1007/bf00987623
  17. 17. Ruther J, Reinecke A, Hilker M (2002) Plant volatiles in the sexual communication of Melolontha hippocastani response towards time-dependent bouquets and novel function of (Z)-3-hexen-1-ol as a sexual kairomone. Ecol Entomol 27: 76–83. doi: 10.1046/j.1365-2311.2002.0373a.x
  18. 18. Dickens JC, Visser JH, van-der-Pers JCN (1993) Detection and deactivation of pheromone and plant odor components by the beet armyworm, Spodoptera exigua (Hübner) (Lepidoptera: Noctuidae). J Insect Physiol 39: 503–516. doi: 10.1016/0022-1910(93)90083-4
  19. 19. Dickens JC, Smith JW, Light DM (1993) Green leaf volatiles enhance sex attractant pheromone of the tobacco budworm, Heliothis virescens (Lep. Noctuidae). Chemoecology 4: 175–177. doi: 10.1007/bf01256553
  20. 20. Dickens JC (1984) Olfaction in the boll weevil Anthonomus grandis Boh. (Coleoptera Curculionidae) electroantennogram studies. J Chem Ecol 10: 1759–1786. doi: 10.1007/bf00987360
  21. 21. Dickens JC (1989) Green leaf volatiles enhance aggregation pheromone of the boll weevil Anthonomus grandis. EntomoL exp appl 52: 191–203. doi: 10.1111/j.1570-7458.1989.tb01268.x
  22. 22. Lu YJ, Zhang XY (2003) Effects of interaction of plant volatiles and sex pheromone on EAG response of Helicoverpa armigera (Huber). Acta Ecologica Sinica 23: 308–313 (In Chinese).
  23. 23. Tasin M, Bäckman A–C, Bengtsson M, Varela N, Ioriatti C, et al. (2006) Wind tunnel attraction of grapevine moth females, Lobesia Botrana, to natural and artificial grape odour. Chemoecology 16: 87–92. doi: 10.1007/s00049-005-0332-6
  24. 24. Cha DH, Hesler SP, Moser CL, Nojima S, Linn CE Jr, et al. (2008) Flight tunnel responses of female grape berry moth (Paralobesia viteana) to host plants. J Chem Ecol 34: 622–627. doi: 10.1007/s10886-008-9474-7
  25. 25. Arimura G, Huber DPW, Bohlmann J (2004) Forest tent caterpillars (Malacosoma disstria) induce local and systemic diurnal emissions of terpenoid volatiles in hybrid poplar (Populus trichocarpa x deltoides): cDNA cloning, functional characterization, and patterns of gene expression of (−)-germacrene D synthase, PtdTPS1. Plant J 37: 603–616. doi: 10.1111/j.1365-313x.2003.01987.x
  26. 26. Arimura G, Ozawa R, Kugimiya S, Takabayashi J, Bohlmann J (2004) Herbivore-induced defense response in a model legume. Two-spotted spider mites induce emission of (E)-beta-ocimene and transcript accumulation of (E)-beta-ocimene synthase in Lotus japonicus. Plant Physiol 135: 1976–1983. doi: 10.1104/pp.104.042929
  27. 27. Kishimoto K, Matsui K, Ozawa R, Takabayashi J (2005) Volatile C6-aldehydes and Allo-ocimene activate defense genes and induce resistance against Botrytis cinerea in Arabidopsis thaliana. Plant Cell Physiol 46: 1093–1102. doi: 10.1093/pcp/pci122
  28. 28. Navia-Giné WG, Yuan JS, Mauromoustakos A, Murphy JB, Chen F, et al. (2009) Medicago truncatula (E)-β-ocimene synthase is induced by insect herbivory with corresponding increases in emission of volatile ocimene. Plant Physiol Bioch 47: 416–425. doi: 10.1016/j.plaphy.2009.01.008
  29. 29. Noe S, Ciccioli P, Brancaleoni E, Loreto F, Niinemets U (2006) Emissions of monoterpenes linalool and ocimene respond differently to environmental changes due to differences in physico-chemical characteristics. Atmos Environ 40: 4649–4662. doi: 10.1016/j.atmosenv.2006.04.049
  30. 30. Kishimoto K, Matsui K, Ozawa R, Takabayashi J (2006) Analysis of defensive responses activated by volatile allo-ocimene treatment in Arabidopsis thaliana. Phytochemistry 67: 1520–1529. doi: 10.1016/j.phytochem.2006.05.027
  31. 31. Maisonnasse A, Lenoir JC, Beslay D, Crauser D, Le Conte Y (2010) E-beta-ocimene, a volatile brood pheromone involved in social regulation in the honey bee colony (Apis mellifera). PLoS One 5 doi: 10.1371/journal.pone.0013531
  32. 32. Angerosa F, Mostallino R, Basti C, Vito R (2000) Virgin olive oil odour notes their relationships with volatile compounds from the lipoxygenase pathway and secoiridoid compounds. Food Chem 68: 283–287. doi: 10.1016/s0308-8146(99)00189-2
  33. 33. Hartvigsen K, Lund P, Hansen LF, Holmer G (2000) Dynamic headspace gas chromatography-mass spectrometry characterization of volatiles produced in fish oil-enriched mayonnaise during storage. J Agri Food Chem 48: 4858–4867. doi: 10.1021/jf991385b
  34. 34. Chen MZ, Trinnaman L, Bardsley K, St Hilaire CJ, Da Costa NC (2011) Volatile compounds and sensory analysis of both harvests of double-cut Yakima peppermint (Mentha piperita L.). J Food Sci 76: C1032–1038. doi: 10.1111/j.1750-3841.2011.02328.x
  35. 35. Saad AD, Scott DR (1981) Repellency of pheromones released by females of Heliothis armigera and Heliothis zea to females of both species. Entomol Exp Appl 30: 123–127. doi: 10.1111/j.1570-7458.1981.tb03085.x