Barker AM, Molotsane R, Müller C, Schaffner U, Städler E (2006) Chemosensory and behavioural responses of the turnip sawfly, Athalia rosae, to glucosinolates and isothiocyanates. Chemoecology 16(4):209–218. https://doi.org/10.1007/s00049-006-0349-5

Article  CAS  Google Scholar 

Bernays EA (1991) Relationship between deterrence and toxicity of plant secondary compounds for the grasshopper Schistocerca americana. J Chem Ecol 17:2519–2526. https://doi.org/10.1007/Bf00994599

Article  CAS  PubMed  Google Scholar 

Bernays EA (2001) Neural limitations in phytophagous insects: Implications for diet breadth and evolution of host affiliation. Annu Rev Entomol 46:703–727. https://doi.org/10.1146/annurev.ento.46.1.703

Article  CAS  PubMed  Google Scholar 

Bernays EA, Chapman RF (1994) Host-plant selection by phytophagous insects. Chapman & Hall, New York

Book  Google Scholar 

Bernays EA, Hartmann T, Chapman RF (2004) Gustatory responsiveness to pyrrolizidine alkaloids in the Senecio specialist, Tyria jacobaeae (Lepidoptera, Arctiidae). Physiol Entomol 29:67–72. https://doi.org/10.1111/j.1365-3032.2004.0366.x

Article  Google Scholar 

Chapman RF (2003) Contact chemoreception in feeding by phytophagous insects. Annu Rev Entomol 48:455–484. https://doi.org/10.1146/annurev.ento.48.091801.112629

Article  CAS  PubMed  Google Scholar 

del Campo ML, Miles CI, Schroeder FC, Müller C, Booker R, Renwick JA (2001) Host recognition by the tobacco hornworm is mediated by a host plant compound. Nature 411:186–189. https://doi.org/10.1038/35075559

Article  CAS  PubMed  Google Scholar 

Dethier VG (1941) Chemical factors determining the choice of food plants by Papilio larvae. Am Nat 75:61–73. https://doi.org/10.1086/280929

Article  Google Scholar 

Dethier VG (1954) Evolution of feeding preferences in phytophagous insects. Evolution 8:33–54. https://doi.org/10.1111/j.1558-5646.1954.tb00107.x

Article  Google Scholar 

Dethier VG (1959) Food-plant distribution and density and larval dispersal as factors affecting insect populations. Can Entomol 91:581–596. https://doi.org/10.4039/Ent91581-9

Article  Google Scholar 

Dethier VG, Crnjar RM (1982) Candidate codes in the gustatory system of caterpillars. J Gen Physiol 79:549–569. https://doi.org/10.1085/jgp.79.4.549

Article  CAS  PubMed  Google Scholar 

Ehrlich PR, Raven PH (1964) Butterflies and plants: a study in coevolution. Evolution 18:586–608

Article  Google Scholar 

Feeny P, Sachdev K, Rosenberry L, Carter M (1988) Luteolin 7-O-(6″-O-malonyl)-β-D-glucoside and trans-chlorogenic acid: Oviposition stimulants for the black swallowtail butterfly. Phytochemistry 27:3439–3448. https://doi.org/10.1016/0031-9422(88)80745-3

Article  CAS  Google Scholar 

Fraenkel GS (1959) The raison d’être of secondary plant substances. Science 129(3361):1466–1470. https://doi.org/10.1126/science.129.3361.1466

Article  CAS  PubMed  Google Scholar 

Fraenkel GS (1981) Importance of allelochemics in plant insect relations: Personal reminiscences. In: Labeyrie V (ed) The Ecology of Bruchids Attacking Legumes (Pulses) Proceedings of the International Symposium held at Tours (France), pp. 1466–1470

Hicks KL (1974) Mustard oil glucosides—feeding stimulants for adult cabbage flea beetles, Phyllotreta-Cruciferae (Coleoptera-Chrysomelidae). Ann Entomol Soc Am 67:261–264. https://doi.org/10.1093/aesa/67.2.261

Article  CAS  Google Scholar 

Hodgson ES, Lettvin JY, Roeder KD (1955) Physiology of a primary chemoreceptor unit. Science 122(3166):417–418. https://doi.org/10.1126/science.122.3166.417-a

Article  CAS  PubMed  Google Scholar 

Hopkins RJ, van Dam NM, Van Loon JJA (2009) Role of glucosinolates in insect-plant relationships and multitrophic interactions. Annu Rev Entomol 54:57–83. https://doi.org/10.1146/annurev.ento.54.110807.090623

Article  CAS  PubMed  Google Scholar 

Ishikawa S (1966) Electrical response and function of a bitter substance receptor associated with the maxillary sensilla of the larva of the silkworm, Bombyx mori L. J Cell Physiol 67:1–11. https://doi.org/10.1002/jcp.1040670102

Article  CAS  PubMed  Google Scholar 

Kennedy JS (1958) Physiological condition of the host-plant and susceptibility to aphid attack. Entomol Exp Appl 1:50–65. https://doi.org/10.1111/j.1570-7458.1958.tb00009.x

Article  Google Scholar 

Larsen LM, Nielsen JK, Sørensen H (1992) Host plant recognition in monophagous weevils—Specialization of Ceutorhynchus inaffectatus to glucosinolates from its host plant Hesperis matronalis. Entomol Exp Appl 64:49–55. https://doi.org/10.1111/j.1570-7458.1992.tb01593.x

Article  CAS  Google Scholar 

Lipke H, Fraenkel G (1956) Insect nutrition. Annu Rev Entomol 1:17–44. https://doi.org/10.1146/annurev.en.01.010156.000313

Article  Google Scholar 

Louda S, Mole S (1991) Glucosinolates: chemistry and ecology. In: Rosenthal GA, Berenbaum M (eds) Herbivores: their interactions with secondary plant metabolites, vol 1. Academic Press, San Diego, pp 123–164

Chapter  Google Scholar 

Metcalf RL, Metcalf RA, Rhodes AM (1980) Cucurbitacins as kairomones for diabroticite beetles. PNAS 77:3769–3772. https://doi.org/10.1073/pnas.77.7.3769

Article  CAS  PubMed  PubMed Central  Google Scholar 

Mullin CA, Chyb S, Eichenseer H, Hollister B, Frazier JL (1994) Neuroreceptor mechanisms in insect gustation: a pharmacological approach. J Insect Physiol 40:913–931. https://doi.org/10.1016/0022-1910(94)90130-9

Article  CAS  Google Scholar 

Nair KSS, McEwen FL (1976) Host selection by the adult cabbage maggot, Hylemya brassicae (Diptera: Anthomyiidae): Effect of glucosinolates and common nutrients on oviposition. Can Entomol 108:1021–1030. https://doi.org/10.4039/Ent1081021-10

Article  CAS  Google Scholar 

Nielsen JK (1978a) Host plant-selection of monophagous and oligophagous flea beetles feeding on crucifers. Entomol Exp Appl 24:562–569. https://doi.org/10.1111/j.1570-7458.1978.tb02817.x

Article  CAS  Google Scholar 

Nielsen JK (1978b) Host plant discrimination within Cruciferae: Feeding responses of 4 leaf beetles (Coleoptera: Chrysomelidae) to glucosinolates, cucurbitacins and cardenolides. Entomol Exp Appl 24:41–54. https://doi.org/10.1111/j.1570-7458.1978.tb02755.x

Article  CAS  Google Scholar 

Nielsen JK, Dalgaard L, Larsen LM, Sørensen H (1979) Host plant selection of the horse-radish flee beetle Phyllotreta armoraciae (Coleoptera: Chrysomelidae): Feeding responses to glucosinolates from several crucifers. Entomol Exp Appl 25:227–239. https://doi.org/10.1111/j.1570-7458.1979.tb02875.x

Article  Google Scholar 

Ohsugi T, Nishida R, Fukami H (1991) Multi-component system of oviposition stimulants for a Rutaceae-feeding swallowtail butterfly, Papilio xuthus (Lepidoptera:Papilionidae). Appl Entomol Zool 26:29–40. https://doi.org/10.1303/aez.26.29

Article  CAS  Google Scholar 

Ozaki K, Ryuda M, Yamada A, Utoguchi A, Ishimoto H, Calas D, Marion-Poll F, Tanimura T, Yoshikawa H (2011) A gustatory receptor involved in host plant recognition for oviposition of a swallowtail butterfly. Nat Commun 2:542. https://doi.org/10.1038/ncomms1548

Article  CAS  PubMed  Google Scholar 

Rask L, Andreasson E, Ekbom B, Eriksson S, Pontoppidan B, Meijer J (2000) Myrosinase: gene family evolution and herbivore defense in Brassicaceae. Plant Mol Biol 42(1):93–113. https://doi.org/10.1023/A:1006380021658

Article  CAS  PubMed  Google Scholar 

Rees CJC (1969) Chemoreceptor specificity associated with choice of feeding site by beetle, Chrysolina brunsvicensis on its roodplant, Hypericum hirsutum. Entomol Exp Appl 12:565–583. https://doi.org/10.1111/j.1570-7458.1969.tb02554.x

Article  Google Scholar 

Reifenrath K, Müller C (2008) Multiple feeding stimulants in Sinapis alba for the oligophagous leaf beetle Phaedon cochleariae. Chemoecology 18:19–27. https://doi.org/10.1007/s00049-007-0389-5

Article  CAS  Google Scholar 

Renwick JAA (2002) The chemical world of crucivores: lures, treats and traps. Entomol Exp Appl 104:35–42. https://doi.org/10.1046/j.1570-7458.2002.00988.x

Article  CAS  Google Scholar 

Renwick JAA, Radke CD, Sachdev-Gupta K, Städler E (1992) Leaf surface chemicals stimulating oviposition by Pieris rapae (Lepidoptera: Pieridae) on cabbage. Chemoecology 3:33–38. https://doi.org/10.1007/BF01261454

Article  CAS  Google Scholar 

Roessingh P, Städler E, Schoni R, Feeny P (1991) Tarsal contact chemoreceptors of the black swallowtail butterfly Papilio polyxenes: responses to phytochemicals from host- and non-host plants. Physiol Entomol 16:485–495. https://doi.org/10.1111/j.1365-3032.1991.tb00588.x

Article  Google Scholar 

Schoonhoven LM (1967) Chemoreception of mustard oil glucosides in larvae of Pieris brassicae. Kon Nederl Akad Wetensch Amsterdam Proc Ser C70:556–568

Google Scholar 

Schoonhoven LM, Blom F (1988) Chemoreception and feeding behavior in a caterpillar: towards a model of brain functioning in insects. Entomol Exp Appl 49:123–129. https://doi.org/10.1111/j.1570-7458.1988.tb02483.x

Article  Google Scholar 

Schoonhoven LM, Van Loon JJA, Dicke M (2005) Insect-Plant Biology, 2nd edn. Oxford University Press, Oxford

Book  Google Scholar 

Städler E (1978) Chemoreception of host plant chemicals by ovipositing females of Delia (Hylemya) brassicae. Entomol Exp Appl 24(3):511–520. https://doi.org/10.1111/j.1570-7458.1978.tb02835.x

Article