Intraspecific Facilitation Through Host Plant Quality Improvement? Observations on the Aggregation Behaviour and Population Biology of the Senescence Inducing Phloem Feeder (Ischnodemus Sabuleti)
DOI:
https://doi.org/10.33038/jcegi.4529Keywords:
Ischnodemus sabuleti, Heteroptera, Blissidae, Glyceria maxima, intraspecific facilitation, aggregation behaviourAbstract
The aggregation behaviour and the senescence inducing effect on its host plants (Glyceria spp.) of the European chinch bug (Ischnodemus sabuleti) is documented in several Hungarian high- density populations. The hypothesis of intraspecific facilitation through host plant quality improvement is formulated and discussed in detail. We suggest that drought stressed host plants improve the performance of I. sabuleti and facilitate the local population outbreaks. We suggest that the optimal host plant drought stress level is higher for senescence feeding herbivores than for the flush feeding herbivores.
References
ADDESSO, K. M. – MCAUSLANE, H. J. – CHERRY, R. (2012): Aggregation behaviour of the Southern chinch bug (Hemiptera: Blissidae), Environmental Entomology, 41, 887–895. DOI: https://doi.org/10.1603/EN11145
BACKUS, E. A. (1988): Sensory systems and behaviours which mediate hemipteran plant-feeding: A taxonomic overview, Journal of Insect Physiology, 34, 151–165. DOI: https://doi.org/10.1016/0022-1910(88)90045-5
BACKUS, E. A. – RANGASAMY, M. – STAMM, M. – MCAUSLANE, H.J. – CHERRY, R. (2013): Waveform library for chinch bugs (Hemiptera: Heteroptera: Blissidae): Characterization of electrical penetration graph waveforms at multiple input impedances. Annals of the Entomological Society of America, 106: 524–539. https://doi.org/10.1603/AN13015
BANFIELD-ZANIN, J. – LEATHER, S. (2015): Drought intensity and frequency have contrasting effects on development time and survival of the green spruce aphid. Agricultural and Forest Entomology, 17, 309–316. https://doi.org/17.10.1111/afe.12109.
CAO, H. H, – LIU, H. R. – ZHANG, Z. F. – LIU, T. X. (2016): The green peach aphid Myzus persicae perform better on pre-infested Chinese cabbage Brassica pekinensis by enhancing host plant nutritional quality. Scientific Reports, 6, 21954. https://doi.org/10.1038/srep21954
CHALKER-SCOTT, L. (1999): Environmental Significance of Anthocyanins in Plant Stress Responses. Photochemistry and Photobiology, 70, 1–9. https://doi.org/10.1111/j.1751-1097.1999.tb01944.x
CHERRY, R. (2001): Spatial distribution of southern chinch bugs (Hemiptera, Lygaeidae) in St. Augustinegrass. The Florida Entomologist, 84, 151–153. https://doi.org/10.2307/3496677
CHERRY, R. - WRIGHT, A. – LU, H. & LUO, Y. – ARTHURS, S. (2013): Morphological and nutrient changes in St. Augustinegrass caused by Southern chinch bug (Hemiptera: Blissidae) feeding damage. Journal of Entomological Science, 48, 327–331. https://doi.org/10.18474/0749-8004-48.4.327
CLIFTON, E.H. – JARONSKI, S.T. – COATES, B. S. – HODGSON, E.W. – GASSMANN, A. J. (2018): Effects of endophytic entomopathogenic fungi on soybean aphid and identification of Metarhizium isolates from agricultural fields. PLoS One. 2018 Mar 22;13, e0194815. https://doi.org/10.1371/journal.pone.0194815.
COCKFIELD, S.D. – POTTER, D.A. – HOUTZ, R.L. (1987): Chlorosis and reduced CO2 assimilation of Euonymus fortunei infested with euonymus scale (Homoptera: Diaspididae). Environmental Entomology, 16, 1314–1318. https://doi.org/10.1093/ee/16.6.1314
COURCHAMP, F. – GRENFELL, B.T. – CLUTTON-BROCK, T. (1999). Population Dynamics of Obligate Cooperators. Proceedings of the Royal Society B: Biological Sciences. 266. https://doi.org/10.1098/rspb.1999.0672
COTTRELL, T.E. – WOOD, B.W. – NI, X. (2009): Chlorotic feeding injury by the black pecan aphid (Hemiptera: Aphididae) to pecan foliage promotes aphid settling and nymphal development. Environmental Entomology, 38, 411–416. https://doi.org/10.1603/022.038.0214
CRAWFORD, S.A – WILKENS, S (1996): Ultrastructural aspects of damage to leaves of Eucalyptus camaldulensis by the psyllid Cardiaspina retator. Micron, 27, 359–366. https://doi.org/10.1016/S0968-4328(96)00036-4
DILLWITH, J.W. – BERBERET, R.C. – BERGMAN, D.K. – NEESE, P.A. – EDWARDS, R.M. – MCNEW, R.W. (1991): Plant biochemistry and aphid populations: Studies on the spotted alfalfa aphid, Therioaphis maculata. Archives of Insect Biochemistry and Physiology, 17, 235–251. https://doi.org/10.1002/arch.940170407
DORSCHNER, K.W. – RYAN, J. D. – JOHNSON, R.C – EIKENBARY, R. D. (1987): Modification of host nitrogen levels by the greenbug (Homoptera: Aphididae): its role in resistance of winter wheat to aphids. Environmental Entomology, 16, 1007–1011. https://doi.org/10.1093/ee/16.4.1007
ELZINGA, D.A. – JANDER, G. (2013): The role of protein effectors in plant-aphid interactions. Current Opinion in Plant Biology, 16, 451–456. https://doi.org/10.1016/j.pbi.2013.06.018
FISCHER, M. (1987): The effect of previously infested spruce needles on the growth of the green spruce aphid, Elatobium abietinum, and the effect of the aphid on the amino acid balance of the host plant. Annals of Applied Biology, 111, 33–41. https://doi.org/10.1111/j.1744-7348.1987.tb01430.x
FUCARINO, A. – MILLAR, J.G. – MCELFRESH, J.S. – COLAZZA, S. (2004): Chemical and physical signals mediating conspecific and heterospecific aggregation behavior of first instar stink bugs. Journal of Chemical Ecology 30, 1257–1269. https://doi.org/10.1023/B:JOEC.0000030276.32665.cb
FUJISAKI, K. (1989): Wing form determination and sensitivity of stages to environmental factors in the oriental chinch bug, Cavelerius saccharivorus Okajima (Heteroptera : Lygaeidae). Applied Entomology and Zoology, 24, 287–294. https://doi.org/10.1303/aez.24.287
GELY, C. – LAURANCE, S.G.W. – STORK, N.E. (2020):, How do herbivorous insects respond to drought stress in trees? Biological Reviews, 95, 434–448. https://doi.org/10.1111/brv.12571
GIDÓ, ZS. (2022): Range expansion and invasive capacity of the wing di- and polymorphic insects: a short review. Journal of Central European Green Innovation, 10, 51–62. https://doi.org/10.33038/jcegi.3473
GIDÓ, ZS. (2023a): Wing dimorphism/polymorphism in true bugs (Heteroptera) from a functional viewpoint: a review. Part I: Non-phytophagous species. Journal of Central European Green Innovation, 11, 39–54. https://doi.org/10.33038/jcegi.4491
GIDÓ, ZS. (2023b): Wing dimorphism/polymorphism in true bugs (Hemiptera: Heteroptera) from a functional viewpoint: a review. Part II: Phytophagous species. Journal of Central European Green Innovation, 11(2), 68–85. https://doi.org/10.33038/jcegi.4854
GONZALES, W. – RAMÍREZ, C. – OLEA, N. – NIEMEYER, H. (2002): Host plant changes produced by the aphid Sipha flava: Consequences for aphid feeding behaviour and growth. Entomologia Experimentalis et Applicata, 103, 107–113. https://doi.org/10.1023/A:1020303817697
GRIPENBERG, S. – MAYHEW, P.J. – PARNELL, M. – ROSLIN, T. (2010): A meta-analysis of preference–performance relationships in phytophagous insects. Ecology Letters, 13: 383–393. https://doi.org/10.1111/j.1461-0248.2009.01433.x
HALE, B. K. – BALE, J. S. – PRITCHARD, J. – MASTERS, G. J. – BROWN, V. K. (2003): Effects of host plant drought stress on the performance of the bird cherry-oat aphid. Ecological Entomology, 28, 666–677. https://doi.org/10.1111/j.1365-2311.2003.00563.x
HE, Y. – JIANG, W. – DING, W. – CHEN, W. – ZHAO, D. (2022): Effects of PVY-infected tobacco plants on the adaptation of Myzus persicae (Hemiptera: Aphididae). Insects, 13, 1120. https://doi.org/10.3390/insects13121120
HENG-MOSS, T. – BAXENDALE, F. – NOVAK, D. – BOSE, S. – NI, X. – QUISENBERRY, S. (2004): Characterization of oxidative enzyme changes in buffalograsses challenged by Blissus occiduus. Journal of Economic Entomology, 97,1086–1095. https://doi.org/10.1093/jee/97.3.1086
HOPMANS, P. – COLLETT, N.C. – SMITH, I.W. – ELMS, S.R. (2008): Growth and nutrition of Pinus radiata in response to fertilization applied after thinning and interaction with defoliation associated with Essigella californica. Forest Ecology and Management, 255, 2118–2128. https://doi.org/10.1016/j.foreco.2007.12.020
HUBERTY, A.F. – DENNO, R.F. (2004): Plant water stress and its consequences for herbivorous insects: a new synthesis. Ecology, 85: 1383–1398. https://doi.org/10.1890/03-0352
KAMPS, B.B.J. – POELMAN, E.H. (2023): Adaptations to water gradient in three Rorippa plant species correspond with plant resistance against insect herbivory under drought and waterlogged conditions. Ecological Entomology, 1–9. https://doi.org/10.1111/een.13273
KANSMAN, J.T. – BASU, S. – CASTEEL, C. L. – CROWDER, D.W. – LEE, B. W. – NIHRANZ, C. T. – FINKE, D. L (2022): Plant water stress reduces aphid performance: exploring mechanisms driven by water stress intensity. Frontiers in Ecology and Evolution, 10, https://doi.org/10.3389/fevo.2022.846908
KAPLAN, I. – DENNO, R.F. (2007): Interspecific interactions in phytophagous insects revisited: a quantitative assessment of competition theory. Ecology Letters, 10: 977–994. https://doi.org/10.1111/j.1461-0248.2007.01093.x
KERSCH-BECKER, M.F. – THALER, J.S. (2014): Virus strains differentially induce plant susceptibility to aphid vectors and chewing herbivores. Oecologia, 174, 883–892. https://doi.org/10.1007/s00442-013-2812-7
KHAN, M. A. M. – ULRICHS, C. – MEWIS, I. (2011): Drought stress– impact on glucosinolate profile and performance of phloem feeding cruciferous insects. Acta horticulturae, 917, 111–117. https://doi.org/10.17660/ActaHortic.2011.917.13
KMENT, P. – CUNEV, J. – HEMALA, V. – RĂDAC, I. A. – KONDOROSY, E. (2023): Dimorphopterus blissoides (Hemiptera: Heteroptera: Blissidae): recent spreading of a neonative species in the Pannonian Basin. Zootaxa, 5382 (1): 108–119. https://doi.org/10.11646/zootaxa.5382.1.12
LIN, X. – XU, Y. – JIANG, J. – LAVINE, M. – LAVINE, L. C. (2018): Host quality induces phenotypic plasticity in a wing polyphenic insect. Proceedings of the National Academy of Sciences, 115, 7563–7568. http://dx.doi.org/10.1073/pnas.1721473115
LIU, J. – LIU, Y. – DONKERLEY, P – DONG, Y. – CHEN, X. – ZANG, Y. – XU, P. – REN, G. (2019): Preference of the aphid Myzus persicae (Hemiptera: Aphididae) for tobacco plants at specific stages of potato virus Y infection. Archives of Virology, 164, 1567–1573. https://doi.org/10.1007/s00705-019-04231-y
LOCKWOOD, J. A – STORY, R.N. (1986): Adaptive functions of nymphal aggregation in the Southern green stink bug, Nezara viridula (L.) (Hemiptera: Pentatomidae). Environmental Entomology, 15, 739–749. https://doi.org/10.1093/ee/15.3.739
MODY, K. – EICHENBERGER, D. – DORN, S. (2009): Stress magnitude matters: Different intensities of pulsed water stress produce non-monotonic resistance responses of host plants to insect herbivores. Ecological Entomology, 34, 133–143. https://doi.org/10.1111/j.1365-2311.2008.01053.x
MORATH, S.U. – PRATT, P. D. – SILVERS, C.S. – CENTER, T. D. (2006): Herbivory by Boreioglycaspis melaleucae (Hemiptera: Psyllidae) accelerates foliar senescence and abscission in the invasive tree Melaleuca quinquenervia, Environmental Entomology, 35, 1372–1378, https://doi.org/10.1093/ee/35.5.1372
NALAM, V. – LOUIS, J. – SHAH, J. (2019): Plant defense against aphids, the pest extraordinaire. Plant Science, 279:96–107. https://doi.org/10.1016/j.plantsci.2018.04.027
OKOSUN, O.O. (2012): Chemical ecology and eco-physiology of the grain chinch bug, Macchiademus diplopterus (Distant) (Hemiptera: Lygaeidae: Blissinae), a phytosanitary pest of South African export fruit. MSc Thesis, Stellenbosch University.
OVERHOLT, W. – EWE, S.M.L. – DIAZ, R. – MORGAN, E. – MOERI, O.E. (2004): Feeding effects of Ischnodemus variegatus (Hemiptera: Blissidae) on photosynthesis and growth of Hymenachne amplexicaulis (Poaceae). Florida Entomologist,87, 312–316. https://doi.org/87.312-316.10.1653/0015-4040(2004)087[0312:FEOIVH]2.0.CO;2.
PARRY, W.H. (1979): Summer survival of the green spruce aphid Elatobium abietinum in north-east Scotland, UK. Oecologia 4, 235–244. https://doi.org/10.1007/BF00345005
PEGADARAJU, V. – KNEPPER, C. – REESE, J. – SHAH, J. (2005): Premature leaf senescence modulated by the Arabidopsis PHYTOALEXIN DEFICIENT4 gene is associated with defense against the phloem-feeding green peach aphid. Plant Physiology, 139(4):1927–1934. https://doi.org/10.1104/pp.105.070433
PÉRICART, J. (1999): Hémiptères Lygaeidae euro-méditerranéens. Faune de France, 1 84A, i-xx, 1–468.
PUTSKOV, V.G. (1969): Vypusk 2: Ligeïdi. In Fauna Ukraïni, 21, Kiev, 388 pp.
RAMM, C. – WAYANDANDE, A. – BAIRD, L. – NANDAKUMAR R. – MADAYIPUTHIVA N. – AMUNDSEN, K. - DONZE-REINER T. – BAXENDALE, F. – SARATH, G. – HENG-MOSS, T. (2015): Morphology and Proteome Characterization of the Salivary Glands of the Western Chinch Bug (Hemiptera: Blissidae). Journal of Economical Entomology, 108, 2055–64. https://doi.org/10.1093/jee/tov149
RANGASAMY, M. – MCAUSLANE, H. – BACKUS, E. – CHERRY, R. (2015): Differential Probing Behavior of Blissus insularis (Hemiptera: Blissidae) on Resistant and Susceptible St. Augustinegrasses. Journal of Economic Entomology, 108, 780–788. https://doi.org/10.1093/jee/tou061
REAGAN, T.E. – AKBAR, W. – SHOWLER, A.T. (2011): A nutritional perspective of sugarcane resistance to stalk borers and sap feeders. International Sugar Journal, 113, 220–223.
REINERT, J. – CHANDRA, A. – ENGELKE, M.C. (2011): Susceptibility of Genera and Cultivars of Turfgrass to Southern Chinch Bug Blissus insularis (Hemiptera: Blissidae). Florida Entomologist, 97, 158–163. https://doi.org/10.1653/024.094.0206.
REITHEL, J. (2009): Effects of aggregation size and host plant on the survival of an ant-tended membracid (Hemiptera: Membracidae): potential roles in selecting for generalized host plant use. Annals of the Entomological Society of America, 101, 70–78. https://doi.org/10.1603/0013-8746(2008)101[70:EOASAH]2.0.CO;2
RICHMOND, D. – SHETLAR, D. (2000): Hairy Chinch Bug (Hemiptera: Lygaeidae) Damage, Population Density, and Movement in Relation to the Incidence of Perennial Ryegrass Infected by Neotyphodium Endophytes. Journal of economic entomology, 93, 1167–1172. https://doi.org/10.1603/0022-0493-93.4.1167
SANDSTRÖM, J. – TELANG, A. – MORAN, N.A, (2000): Nutritional enhancement of host plants by aphids – a comparison of three aphid species on grasses. Journal of Insect Physiology, 46, 33–40. https://doi.org/10.1016/S0022-1910(99)00098-0
SLATER, J. A. (1976): Monocots and chinch bugs: a study of host plant relationships in the lygaeid subfamily Blissinae (Hemiptera: Lygaeidae). Biotropica 8:143–165. https://doi.org/10.2307/2989681
SRINIVASAN, T.S. – ALMAZAN, M.L.P. – BERNAL, C.C. – RAMAL, A.F. (2016): Interactions between nymphs of Nilaparvata lugens and Sogatella furcifera (Hemiptera: Delphacidae) on resistant and susceptible rice varieties. Applied Entomology and Zoology, 51, 81–90 (2016). https://doi.org/10.1007/s13355-015-0373-4
STEINBAUR, M.J. – BURNS, A.E. – HALL, A. – RIEGLER, M. – TAYLOR, G. S. (2014): Nutritional enhancement of leaves by a psyllid through senescence-like processes: insect manipulation or plant defence? Oecologia, 176, 1061–1074. https://doi.org/10.1007/s00442-014-3087-3
TARIQ, M. – WRIGHT, D. – ROSSIOTER, J. – STALEY, J. (2012): Aphids in a changing world: Testing the plant stress, plant vigour and pulsed stress hypotheses. Agricultural and Forest Entomology, 14. https://doi.org/10.1111/j.1461-9563.2011.00557.x.
TELANG, A. – SANDSTRÖM, J. – DYRESON, E. – MORAN, N.A. (1999): Feeding damage by Diuraphis noxia results in a nutritionally enhanced phloem diet. Entomologia Experimentalis et Applicata, 91: 403–412. https://doi.org/10.1046/j.1570-7458.1999.00508.x
TISCHLER, W. (1960): Studien zur Bionomie und Ökologie der Schmalwanze Ischnodemus sabuleti Fall. (Hem., Lygaeidae). Zeitschrift für Wissenschaftliche Zoologie, 163, 168–209.
TISCHLER, W. (1963): Weitere Untersuchungen zur Ökologie der Schmalwanze Ischnodemus sabuleti Fall. (Hem., Lygaeidae). Zoologischer Anzeiger, 171, 339–349. https://eurekamag.com/research/024/131/024131613.php
VARENHORST, A.J. – MCCARVILLE, M.T. – O’NEAL, M.E. (2015): Determining the duration of Aphis glycines (Hemiptera: Aphididae) induced susceptibility effect in soybean. Arthropod-Plant Interactions, 9, 457–464. https://doi.org/10.1007/s11829-015-9395-7
WHITE, T.C.R. (2015): Senescence-feeders: a new trophic sub-guild of insect herbivores. Journal of Applied Entomology, 139: 11–22. https://doi.org/10.1111/jen.12147
ZHANG, Y. – FU, Y. – FAN J. – LI, Q. – FRANCIS, F. – CHEN, J. (2019): Comparative transcriptome and histological analyses of wheat in response to phytotoxic aphid Schizaphis graminum and non-phytotoxic aphid Sitobion avenae feeding. BMC Plant Biology 19, 547 (2019). https://doi.org/10.1186/s12870-019-2148-5
Downloads
Published
Issue
Section
License
Copyright (c) 2023 Journal of Central European Green Innovation
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.