Hostname: page-component-586b7cd67f-g8jcs Total loading time: 0 Render date: 2024-11-20T21:03:29.230Z Has data issue: false hasContentIssue false

Short-range attraction and oviposition stimulant of a biocontrol agent, Galerucella placida Baly (Coleoptera: Chrysomelidae) toward weed leaf surface waxes

Published online by Cambridge University Press:  27 August 2021

Anamika Koner
Affiliation:
Department of Zoology, Ecology Research Laboratory, The University of Burdwan, Burdwan713 104, West Bengal, India
Swati Das
Affiliation:
Department of Zoology, Ecology Research Laboratory, The University of Burdwan, Burdwan713 104, West Bengal, India
Syed Husne Mobarak
Affiliation:
Department of Zoology, Ecology Research Laboratory, The University of Burdwan, Burdwan713 104, West Bengal, India
Anandamay Barik*
Affiliation:
Department of Zoology, Ecology Research Laboratory, The University of Burdwan, Burdwan713 104, West Bengal, India
*
Author for correspondence: Anandamay Barik, Email: anandamaybarik@yahoo.co.in

Abstract

Two Polygonaceae weeds, Rumex dentatus L. and Polygonum glabrum Willd. are abundant in wheat- and rice-fields, respectively, in India. Galerucella placida Baly (Coleoptera: Chrysomelidae) is a biocontrol agent of these two weeds. The importance of long-chain alkanes and free fatty acids present in leaf surface waxes of these weeds was assessed as short-range attractant and ovipositional stimulant in G. placida females. Extraction, TLC, GC-MS and GC-FID analyses demonstrated 19 n-alkanes from n-C14 to n-C35 and 14 free fatty acids from C12:0 to C22:0 in leaf surface waxes. Hentriacontane was predominant among alkanes in both weeds, while oleic acid and docosanoic acid were predominant among free fatty acids in R. dentatus and P. glabrum, respectively. Females of G. placida were attracted toward one leaf equivalent surface wax of both weeds against the control solvent (petroleum ether) in a short Y-tube olfactometer bioassay. But, the insect could not differentiate between one leaf equivalent surface wax of R. dentatus and P. glabrum, indicating that both weed leaves were equally attractive in females. A synthetic blend of either 2.44, 35.57 and 23.58 μg ml−1 of octadecane, heptacosane and nonacosane, respectively, resembling the amounts present in one leaf equivalent surface wax of R. dentatus or 4.08, 19.54 and 23.58 μg ml−1 of octadecane, palmitoleic acid and docosanoic acid, respectively, resembling the amounts present in one leaf equivalent surface wax of P. glabrum acted as short-range attractant and ovipositional stimulant in G. placida. These results could be a basis for host plant specificity of the biocontrol agent.

Type
Research Paper
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Abbas, G, Ali, MA, Abbas, Z, Aslam, M and Akram, M (2009) Impact of different herbicides on broadleaf weeds and yield of wheat. Pakistan Journal of Weed Science Research 15, 110.Google Scholar
Abbas, T, Tanveer, A, Khaliq, A and Safdar, ME (2016) Comparative allelopathic potential of native and invasive weeds in rice ecosystem. Pakistan Journal of Weed Science Research 22, 269283.Google Scholar
Al-Sherif, EA, Ismael, MA, Karam, MA and Elfayoumi, HH (2018) Weed flora of Fayoum (Egypt), one of the oldest agricultural regions in the world. Planta Daninha 36, e0181719990.CrossRefGoogle Scholar
Anjum, T and Bajwa, R (2010) Competition losses caused by Rumex dentatus L. and Chenopodium album L. in wheat (Triticum aestivum L.). Philippine Agricultural Scientist 93, 365368.Google Scholar
Beenen, R (1998) Galerucella placida a proper species from South East Asia (Coleoptera: Chrysomelidae: Galerucinae). Serangga 31, 107110.Google Scholar
Bruce, TJA and Pickett, JA (2011) Perception of plant volatile blends by herbivorous insects − finding the right mix. Phytochemistry 72, 16051611.CrossRefGoogle ScholarPubMed
Bruce, TJA, Wadhams, LJ and Woodcock, CM (2005) Insect host location: a volatile situation. Trends in Plant Science 10, 269274.CrossRefGoogle ScholarPubMed
Culliney, TW (2005) Benefits of classical biological control for managing invasive plants. Critical Reviews in Plant Sciences 24, 131150.CrossRefGoogle Scholar
Das, S, Koner, A and Barik, A (2019a) Biology and life history of Lema praeusta (Fab.) (Coleoptera: Chrysomelidae), a biocontrol agent of two Commelinaceae weeds, Commelina benghalensis and Murdannia nudiflora. Bulletin of Entomological Research 109, 463471.CrossRefGoogle Scholar
Das, S, Koner, A and Barik, A (2019b) A beetle biocontrol agent of rice-field weeds recognizes its host plants by surface wax long-chain alkanes and free fatty acids. Chemoecology 29, 155170.CrossRefGoogle Scholar
Deka, J and Barua, IC (2015) Problem weeds and their management in the North-East Himalayas. Indian Journal of Weed Science 47, 296305.Google Scholar
Ding, J, Fu, W, Reardon, R, Wu, Y and Zhang, G (2004) Exploratory survey in China for potential insect biocontrol agents of mile-a-minute weed, Polygonum perfoliatum L., in Eastern USA. Biological Control 30, 487495.CrossRefGoogle Scholar
Eastop, VF (1973) Biotypes of aphids. Bulletin of the Entomological Society of New Zealand 2, 4051.Google Scholar
Eigenbrode, SD and Espelie, KE (1995) Effects of plant epicuticular lipids on insect herbivores. Annual Review of Entomology 40, 171194.CrossRefGoogle Scholar
Elzaawely, AA and Tawata, S (2012) Antioxidant capacity and phenolic content of Rumex dentatus L. grown in Egypt. Journal of Crop Science & Biotechnology 15, 5964.CrossRefGoogle Scholar
Galizia, CG and Rӧssler, W (2010) Parallel olfactory systems in insects: anatomy and function. Annual Review of Entomology 55, 399420.CrossRefGoogle ScholarPubMed
Grant, GG, Zhao, B and Langevin, D (2000) Oviposition response of spruce budworm (Lepidoptera: Tortricidae) to aliphatic carboxylic acids. Environmental Entomology 29, 164170.CrossRefGoogle Scholar
Gupta, A, Verma, A, Chhokar, RS, Sheoran, S, Sendhil, R and Sharma, I (2013) Annual Report 2012–2013. Karnal, Haryana, India. Directorate of Wheat Research (Indian Council of Agricultural Research).Google Scholar
Hadjichambis, ACH, Paraskeva-Hadjichambi, D, Della, A, Giusti, ME, De Pasquale, C, Lenzarini, C, Censorii, E, Gonzales-Tejero, MR, Sanchez-Rojas, CP, Ramiro-Gutierrez, JM, Skoula, M, Johnson, C, Sarpaki, A, Hmamouchi, M, Jorhi, S, El-Demerdash, M, El-Zayat, M and Pieroni, A (2008) Wild and semi-domesticated food plant consumption in seven circum-Mediterranean areas. International Journal of Food Sciences and Nutrition 59, 383414.CrossRefGoogle ScholarPubMed
Hnatiuk, RJ (1990) Australian Flora and Fauna Series Number 11: Census of Australian Vascular Plants. Canberra: Australian Government Publishing Service.Google Scholar
Jetter, R and Schäffer, S (2001) Chemical composition of the Prunus laurocerasus leaf surface. Dynamic changes of the epicuticular wax film during leaf development. Plant Physiology 126, 17251737.CrossRefGoogle ScholarPubMed
Jetter, R, Schäffer, S and Riederer, M (2000) Leaf cuticular waxes are arranged in chemically and mechanically distinct layers: evidence from Prunus laurocerasus L. Plant, Cell & Environment 23, 619628.CrossRefGoogle Scholar
Kanatas, P, Travlos, IS, Gazoulis, I, Tataridas, A, Tsekoura, A and Antonopoulos, N (2020) Benefits and limitations of decision support systems (DSS) with a special emphasis on weeds. Agronomy 10, 548.CrossRefGoogle Scholar
Karmakar, A, Malik, U and Barik, A (2016) Effects of leaf epicuticular wax compounds from Solena amplexicaulis (Lam.) Gandhi on olfactory responses of a generalist insect herbivore. Allelopathy Journal 37, 253272.Google Scholar
Karmakar, A, Mitra, P, Koner, A, Das, S and Barik, A (2020) Fruit volatiles of creeping cucumber (Solena amplexicaulis) attract a generalist insect herbivore. Journal of Chemical Ecology 46, 275287.CrossRefGoogle ScholarPubMed
Kimoto, S (1989) Chrysomelidae (Coleoptera) of Thailand, Cambodia, Laos and Vietnam. IV. Galerucinae. Esakia 27, 1241.CrossRefGoogle Scholar
Koner, A, Debnath, R and Barik, A (2019) Age-stage, two-sex life table and food utilization efficiencies of Galerucella placida Baly (Coleoptera: Chrysomelidae) on two Polygonaceae weeds. Journal of Asia-Pacific Entomology 22, 11361144.CrossRefGoogle Scholar
Li, G and Ishikawa, Y (2006) Leaf epicuticular wax chemicals of the Japanese knotweed Fallopia japonica as oviposition stimulants for Ostrinia latipennis. Journal of Chemical Ecology 32, 595604.CrossRefGoogle ScholarPubMed
Macel, M, Visschers, IGS, Peters, JL, van Dam, NM and de Graaf, RM (2020) High concentrations of very long chain leaf wax alkanes of thrips susceptible pepper accessions (Capsicum spp). Journal of Chemical Ecology 46, 10821089.CrossRefGoogle Scholar
Malik, U and Barik, A (2015) Free fatty acids from the weed, Polygonum orientale leaves for attraction of the potential biocontrol agent, Galerucella placida (Coleoptera: Chrysomelidae). Biocontrol Science & Technology 25, 593607.CrossRefGoogle Scholar
Malik, U, Mitra, S and Barik, A (2017) Attraction of the biocontrol agent, Galerucella placida Baly (Coleoptera: Chrysomelidae) to the leaf surface alkanes of the weed, Polygonum orientale L. Allelopathy Journal 40, 103116.CrossRefGoogle Scholar
Malik, U, Das, S and Barik, A (2018) Biology of Galerucella placida Baly (Coleoptera: Chrysomelidae) on the rice-field weed Polygonum orientale L. (Polygonaceae). Proceedings of the Zoological Society 71, 257264.CrossRefGoogle Scholar
Manosalva, L, Pardo, F, Perich, F, Mutis, A, Parra, L, Ortega, F, Isaacs, R and Quiroz, A (2011) Behavioral responses of clover root borer to long-chain fatty acids from young red clover (Trifolium pratense) roots. Environmental Entomology 40, 399404.CrossRefGoogle Scholar
Mitra, S, Sarkar, N and Barik, A (2017) Long-chain alkanes and fatty acids from Ludwigia octovalvis weed leaf surface waxes as short-range attractant and ovipositional stimulant to Altica cyanea (Weber) (Coleoptera: Chrysomelidae). Bulletin of Entomological Research 107, 391400.CrossRefGoogle Scholar
Mitra, P, Das, S and Barik, A (2020) Leaf waxes from Lathyrus sativus: short-range attractant and stimulant for nymph laying in a viviparous insect. Chemoecology 30, 117129.CrossRefGoogle Scholar
Mitra, S, Mobarak, SH and Barik, A (2021) Age-stage, two-sex life table of the biocontrol agent, Altica cyanea on three Ludwigia species. Biologia 76, 101112.CrossRefGoogle Scholar
Mobarak, SH, Koner, A, Mitra, S, Mitra, P and Barik, A (2020) The importance of leaf surface wax as short-range attractant and oviposition stimulant in a generalist Lepidoptera. Journal of Applied Entomology 144, 616631.CrossRefGoogle Scholar
Mukherjee, A, Sarkar, N and Barik, A (2013) Alkanes in flower surface waxes of Momordica cochinchinensis influence attraction to Aulacophora foveicollis Lucas (Coleoptera: Chrysomelidae). Neotropical Entomology 42, 366371.CrossRefGoogle Scholar
Mukherjee, A, Sarkar, N and Barik, A (2014) Long-chain free fatty acids from Momordica cochinchinensis leaves as attractants to its insect pest, Aulacophora foveicollis Lucas (Coleoptera: Chrysomelidae). Journal of Asia-Pacific Entomology 17, 229234.CrossRefGoogle Scholar
Mukherjee, A, Sarkar, N and Barik, A (2015) Momordica cochinchinensis (Cucurbitaceae) leaf volatiles: semiochemicals for host location by the insect pest, Aulacophora foveicollis (Coleoptera: Chrysomelidae). Chemoecology 25, 93104.CrossRefGoogle Scholar
Muller, J (1981) Fossil pollen records of extant angiosperms. The Botanical Review 47, 1142.CrossRefGoogle Scholar
Müller, C (2006) Plant–insect interactions on cuticular surfaces. In Riederer, M and Müller, C (eds), Biology of the Plant Cuticle. Oxford: Blackwell Publishing, pp. 398422.CrossRefGoogle Scholar
Müller, C and Hilker, M (2001) Host finding and oviposition behavior in a chrysomelid specialist–the importance of host plant surface waxes. Journal of Chemical Ecology 27, 985994.CrossRefGoogle Scholar
Najar-Rodriguez, AJ, Galizia, CG, Stierle, J and Dorn, S (2010) Behavioural and neurophysiological responses of an insect to changing ratios of constituents in host plant-derived volatile mixtures. The Journal of Experimental Biology 213, 33883397.CrossRefGoogle ScholarPubMed
Naseer-ud-Din, GM, Shehzad, MA and Nasrullah, HM (2011) Efficacy of various pre and post-emergence herbicides to control weeds in wheat. Pakistan Journal of Agricultural Sciences 48, 185190.Google Scholar
Padovan, A, Keszei, A, Köllner, TG, Degenhardt, J and Foley, WJ (2010) The molecular basis of host plant selection in Melaleuca quinquenervia by a successful biological control agent. Phytochemistry 71, 12371244.CrossRefGoogle ScholarPubMed
Parr, MJ, Tran, BMD, Simmonds, MSJ, Kite, GC and Credland, PF (1998) Influence of some fatty acids on oviposition by the bruchid beetle, Callosobruchus maculatus. Journal of Chemical Ecology 24, 15771593.CrossRefGoogle Scholar
Reid, CAM (2001) Galerucella placida Baly in Australia (Coleoptera: Chrysomelidae: Galerucinae). Australian Journal of Entomology 40, 331334.CrossRefGoogle Scholar
Riffell, JA, Lei, H, Christensen, TA and Hildebrand, JG (2009a) Characterization and coding of behaviorally significant odor mixtures. Current Biology 19, 335340.CrossRefGoogle Scholar
Riffell, JA, Lei, H and Hildebrand, JG (2009b) Neural correlates of behavior in the moth Manduca sexta in response to complex odors. Proceedings of the National Academy of Sciences of the USA 106, 1921919226.CrossRefGoogle Scholar
Sambamurty, AVSS (2005) Taxonomy of Angiosperms. New Delhi, India: I.K. International Pvt. Ltd.Google Scholar
Sarkar, N and Barik, A (2015) Free fatty acids from Momordica charantia L. flower surface waxes influencing attraction of Epilachna dodecastigma (Wied.) (Coleoptera: Coccinellidae). International Journal of Pest Management 61, 4753.CrossRefGoogle Scholar
Sarkar, N, Mukherjee, A and Barik, A (2013) Long-chain alkanes: allelochemicals for host location by the insect pest, Epilachna dodecastigma (Coleoptera: Coccinellidae). Applied Entomology & Zoology 48, 171179.CrossRefGoogle Scholar
Sarkar, N, Malik, U and Barik, A (2014) n-alkanes in epicuticular waxes of Vigna unguiculata (L.) Walp. leaves. Acta Botanica Gallica 161, 373377.CrossRefGoogle Scholar
Sarkar, N, Mukherjee, A and Barik, A (2015) Attraction of Epilachna dodecastigma (Coleoptera: Coccinellidae) to Momordica charantia (Cucurbitaceae) leaf volatiles. The Canadian Entomologist 147, 169180.CrossRefGoogle Scholar
Singh, V, Gupta, S, Singh, H and Raghubanshi, AS (2015) Ecophysiological characteristics of five weeds and a wheat crop in the Indo-Gangetic Plains, India. Weed Biology & Management 15, 102112.CrossRefGoogle Scholar
Smith, L and Beck, JJ (2013) Effect of mechanical damage on emission of volatile organic compounds from plant leaves and implications for evaluation of host plant specificity of prospective biological control agents of weeds. Biocontrol Science & Technology 23, 880907.CrossRefGoogle Scholar
Tomasi, P, Dyer, JM, Jenks, MA and Abdel-Haleem, H (2018) Characterization of leaf cuticular wax classes and constituents in a spring Camelina sativa diversity panel. Industrial Crops & Products 112, 247251.CrossRefGoogle Scholar
Udayagiri, S and Mason, CE (1997) Epicuticular wax chemicals in Zea mays influence oviposition in Ostrinia nubilalis. Journal of Chemical Ecology 23, 16751687.CrossRefGoogle Scholar
Waheed, Z, Usman, K and Ali, I (2017) Response of wheat to varying densities of Rumex dentatus under irrigated condition of Dera Ismail Khan, Pakistan. Sarhad Journal of Agriculture 33, 17.CrossRefGoogle Scholar
Weber, J and Schwark, L (2020) Epicuticular wax lipid composition of endemic European Betula species in a simulated ontogenetic/diagenetic continuum and its application to chemotaxonomy and paleobotany. Science of the Total Environment 730, 138324.CrossRefGoogle Scholar
Wheeler, GS and Schaffner, U (2013) Improved understanding of weed biological control safety and impact with chemical ecology: a review. Invasive Plant Science & Management 6, 1629.CrossRefGoogle Scholar
Zar, JH (1999) Biostatistical Analysis. New Jersey: Prentice-Hall.Google Scholar
Supplementary material: File

Koner et al. supplementary material

Koner et al. supplementary material

Download Koner et al. supplementary material(File)
File 595.5 KB