71. Wei J, Wang L, Zhu J (2007) Plants attract parasitic wasps to defend themselves against insect
pests by releasing hexenol. PLoS One 2:1–7. https://doi.org/10.1371/journal.pone.0000852
72. Du YJ, Poppy GM, Powell W (1998) Identification of semiochemicals released during aphid
feeding that attract parasitoid Aphidius ervi. J Chem Ecol 24:1355–1368. https://doi.org/
10.1023/A:1021278816970
73. Yamauchi Y, Matsuda A, Matsuura N (2018) Transcriptome analysis of Arabidopsis thaliana
treated with green leaf volatiles: possible role of green leaf volatiles as self-made damageassociated molecular patterns. J Pestic Sci 43:207–213. https://doi.org/10.1584/jpestics.D18-020
74. Visser JH, Avé DA (1978) General green leaf volatiles in the olfactory orientation of the
Colorado beetle, Leptinotarsa decemlineata. Entomol Exp Appl 24(3):738–749. https://doi.
org/10.1111/j.1570-7458.1978.tb02838.x
75. Whitman DW, Eller FJ (1990) Parasitic wasps orient to green leaf volatiles. Chemoecology
1:69–76. https://doi.org/10.1007/BF01325231
76. Dicke M, Van Beek TA, Posthumus MA (1990) Isolation and identification of volatile
kairomone that affects acarine predator-prey interactions. J Chem Ecol 16:381–396. https://
doi.org/10.1007/BF01021772
77. Rodriguez-Saona C, Kaplan I, Braasch J (2011) Field responses of predaceous arthropods to
methyl salicylate: a meta-analysis and case study in cranberries. Biol Control 59:294–303.
https://doi.org/10.1016/j.biocontrol.2011.06.017
78. Smid HM, Van Loon JJA, Posthumus MA, Vet LEM (2002) GC-EAG-analysis of volatiles
from Brussels sprouts plants damaged by two species of Pieris caterpillars: olfactory receptive
range of a specialist and a generalist parasitoid wasp species. Chemoecology 12:169–176.
https://doi.org/10.1007/PL00012665
79. Gheysen G, Fenoll C (2002) Gene expression in nematode feeding sites. Annu Rev
Phytopathol 40(1):191–219. https://doi.org/10.1146/annurev.phyto.40.121201.093719
80. Fox CW, Stillwell RC, Amarillo-S AR (2004) Genetic architecture of population differences in
oviposition behaviour of the seed beetle Callosobruchus maculatus. J Evol Biol
17:1141–1151. https://doi.org/10.1111/j.1420-9101.2004.00719.x
81. Nealis VG, Nault JR (2005) Seasonal changes in foliar terpenes indicate suitability of
Douglas-fir buds for western spruce budworm. J Chem Ecol 31:683–696. https://doi.org/
10.1007/s10886-005-3538-8
82. Glendinning JI, Davis A, Ramswamy S, Ramaswamy S (2002) Contribution of different taste
cells and signaling pathways to the discrimination of “bitter” taste stimuli by an insect.
J Neurosci 22:7281–7287
83. Zagrobelny M, Bak S, Rasmussen AV (2004) Cyanogenic glucosides and plant-insect interactions. Phytochemistry 65:293–306. https://doi.org/10.1016/j.phytochem.2003.10.016
84. Perkins LE, Cribb BW, Brewer PB (2013) Generalist insects behave in a jasmonatedependent
manner on their host plants, leaving induced areas quickly and staying longer on distant parts.
Proc R Soc Lond B Biol Sci 280:20122646. https://doi.org/10.1098/rspb.2012.2646
85. Valley C, County R, Guthrie FE et al (1960) Feeding sites of the green peach aphid with
respect to its adaptation to tobacco. Ann Entomol Soc Am 55(1):42–46. https://doi.org/
10.1093/aesa/55.1.42
86. Rathcke BJ, Poole RW (1975) Coevolutionary race continues: butterfly larval adaptation to
plant trichomes. Science 187(80):175–176. https://doi.org/10.1126/science.187.4172.175
87. Dussourd DE (2017) Behavioral sabotage of plant defenses by insect folivores. Annu Rev
Entomol 62:15–34. https://doi.org/10.1146/annurev-ento-031616-035030
88. Becerra JX (2003) Synchronous coadaptation in an ancient case of herbivory. Proc Natl Acad
Sci 100:12804–12807. https://doi.org/10.1073/pnas.2133013100
89. Li X, Schuler MA, Berenbaum MR (2007) Molecular mechanisms of metabolic resistance to
synthetic and natural xenobiotics. Annu Rev Entamol 52:231–253. https://doi.org/10.1146/
annurev.ento.51.110104.151104
90. Feyereisen R (2012) Insect CYP genes and P450 enzymes. In: Insect molecular biology and
biochemistry, pp 236–316). https://doi.org/10.1016/B978-0-12-384747-8.10008-X
91. Hung CF, Berenbaum MR, Schuler MA (1997) Isolation and characterization of CYP6B4, a
furanocoumarin-inducible cytochrome P450 from a polyphagous caterpillar (Lepidoptera:
42
S. S. Zunjarrao et al.
pests by releasing hexenol. PLoS One 2:1–7. https://doi.org/10.1371/journal.pone.0000852
72. Du YJ, Poppy GM, Powell W (1998) Identification of semiochemicals released during aphid
feeding that attract parasitoid Aphidius ervi. J Chem Ecol 24:1355–1368. https://doi.org/
10.1023/A:1021278816970
73. Yamauchi Y, Matsuda A, Matsuura N (2018) Transcriptome analysis of Arabidopsis thaliana
treated with green leaf volatiles: possible role of green leaf volatiles as self-made damageassociated molecular patterns. J Pestic Sci 43:207–213. https://doi.org/10.1584/jpestics.D18-020
74. Visser JH, Avé DA (1978) General green leaf volatiles in the olfactory orientation of the
Colorado beetle, Leptinotarsa decemlineata. Entomol Exp Appl 24(3):738–749. https://doi.
org/10.1111/j.1570-7458.1978.tb02838.x
75. Whitman DW, Eller FJ (1990) Parasitic wasps orient to green leaf volatiles. Chemoecology
1:69–76. https://doi.org/10.1007/BF01325231
76. Dicke M, Van Beek TA, Posthumus MA (1990) Isolation and identification of volatile
kairomone that affects acarine predator-prey interactions. J Chem Ecol 16:381–396. https://
doi.org/10.1007/BF01021772
77. Rodriguez-Saona C, Kaplan I, Braasch J (2011) Field responses of predaceous arthropods to
methyl salicylate: a meta-analysis and case study in cranberries. Biol Control 59:294–303.
https://doi.org/10.1016/j.biocontrol.2011.06.017
78. Smid HM, Van Loon JJA, Posthumus MA, Vet LEM (2002) GC-EAG-analysis of volatiles
from Brussels sprouts plants damaged by two species of Pieris caterpillars: olfactory receptive
range of a specialist and a generalist parasitoid wasp species. Chemoecology 12:169–176.
https://doi.org/10.1007/PL00012665
79. Gheysen G, Fenoll C (2002) Gene expression in nematode feeding sites. Annu Rev
Phytopathol 40(1):191–219. https://doi.org/10.1146/annurev.phyto.40.121201.093719
80. Fox CW, Stillwell RC, Amarillo-S AR (2004) Genetic architecture of population differences in
oviposition behaviour of the seed beetle Callosobruchus maculatus. J Evol Biol
17:1141–1151. https://doi.org/10.1111/j.1420-9101.2004.00719.x
81. Nealis VG, Nault JR (2005) Seasonal changes in foliar terpenes indicate suitability of
Douglas-fir buds for western spruce budworm. J Chem Ecol 31:683–696. https://doi.org/
10.1007/s10886-005-3538-8
82. Glendinning JI, Davis A, Ramswamy S, Ramaswamy S (2002) Contribution of different taste
cells and signaling pathways to the discrimination of “bitter” taste stimuli by an insect.
J Neurosci 22:7281–7287
83. Zagrobelny M, Bak S, Rasmussen AV (2004) Cyanogenic glucosides and plant-insect interactions. Phytochemistry 65:293–306. https://doi.org/10.1016/j.phytochem.2003.10.016
84. Perkins LE, Cribb BW, Brewer PB (2013) Generalist insects behave in a jasmonatedependent
manner on their host plants, leaving induced areas quickly and staying longer on distant parts.
Proc R Soc Lond B Biol Sci 280:20122646. https://doi.org/10.1098/rspb.2012.2646
85. Valley C, County R, Guthrie FE et al (1960) Feeding sites of the green peach aphid with
respect to its adaptation to tobacco. Ann Entomol Soc Am 55(1):42–46. https://doi.org/
10.1093/aesa/55.1.42
86. Rathcke BJ, Poole RW (1975) Coevolutionary race continues: butterfly larval adaptation to
plant trichomes. Science 187(80):175–176. https://doi.org/10.1126/science.187.4172.175
87. Dussourd DE (2017) Behavioral sabotage of plant defenses by insect folivores. Annu Rev
Entomol 62:15–34. https://doi.org/10.1146/annurev-ento-031616-035030
88. Becerra JX (2003) Synchronous coadaptation in an ancient case of herbivory. Proc Natl Acad
Sci 100:12804–12807. https://doi.org/10.1073/pnas.2133013100
89. Li X, Schuler MA, Berenbaum MR (2007) Molecular mechanisms of metabolic resistance to
synthetic and natural xenobiotics. Annu Rev Entamol 52:231–253. https://doi.org/10.1146/
annurev.ento.51.110104.151104
90. Feyereisen R (2012) Insect CYP genes and P450 enzymes. In: Insect molecular biology and
biochemistry, pp 236–316). https://doi.org/10.1016/B978-0-12-384747-8.10008-X
91. Hung CF, Berenbaum MR, Schuler MA (1997) Isolation and characterization of CYP6B4, a
furanocoumarin-inducible cytochrome P450 from a polyphagous caterpillar (Lepidoptera:
42
S. S. Zunjarrao et al.