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Host range expansion of a Polygonaceae-associated leaf beetle to an invasive aquatic plant Myriophyllum aquaticum (Haloragaceae)

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Abstract

The expansion of available resources leads organisms to adapt to novel niches and create new biological interactions. Galerucella grisescens (Coleoptera: Chrysomelidae) is usually associated with Polygonaceae in Japan but a population feeding on an invasive plant species Myriophyllum aquaticum (Haloragaceae) was found in Chiba Prefecture, Honshu. To infer the process of host range expansion and possible rapid adaptations of G. grisescens to M. aquaticum, we studied larval host plant suitability and female oviposition site preference by G. grisescens in different strains. In laboratory rearing experiments, adult body weight and egg mass size of G. grisescens were smaller on M. aquaticum than on the native host Persicaria lapathifolia (Polygonaceae), suggesting that Polygonaceae are more suitable hosts for G. grisescens than M. aquaticum. On M. aquaticum, the larval survival rate was significantly higher in the Chiba strain collected from M. aquaticum than in the Saga strain originating from Polygonaceae. This raises the possibility that the Chiba strain rapidly adapted to M. aquaticum and improved survival rate on the plant. Oviposition site preference of G. grisescens females was slightly different between individuals reared on Polygonaceae and M. aquaticum. These results suggest that G. grisescens represents early stages of ecological adaptation to the introduced plant and it is a possible biological control agent against M. aquaticum.

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References

  • Adachi S, Shirahama S, Tokuda M (2016) Seasonal occurrence of Uroleucon nigrotuberculatum (Hemiptera: Aphididae) in northern Kyushu and mechanisms of its summer disappearance. Environ Entomol 45:16–23

    PubMed  Google Scholar 

  • Adachi S, Kidokoro T, Chiba M, Tokuda M (2018) Comparisons of seasonal fluctuations in Uroleucon nigrotuberculatum (Hemiptera: Aphididae) densities between 2003–04 and 2015–16 at northern areas of its distribution range in Japan. Appl Entomol Zool 53:243–252

    Google Scholar 

  • Agosta SJ (2006) On ecological fitting, plant–insect associations, herbivore host shifts, and host plant selection. Oikos 114:556–565

    Google Scholar 

  • Agosta SJ, Klemens JA (2008) Ecological fitting by phenotypically flexible genotypes: implications for species associations, community assembly and evolution. Ecol Lett 11:1123–1134

    PubMed  Google Scholar 

  • Agosta SJ, Janz N, Brooks DR (2010) How specialists can be generalists: resolving the “parasite paradox” and implications for emerging infectious disease. Zoologia 27:151–162

    Google Scholar 

  • Bezemer TM, Harvey JA, Cronin JT (2014) Response of native insect communities to invasive plants. Annu Rev Entomol 59:119–141

    CAS  PubMed  Google Scholar 

  • Carroll SP, Boyd C (1992) Host race radiation in the soapberry bug: natural history with the history. Evolution 46:1052–1069

    PubMed  Google Scholar 

  • Carroll SP, Dingle H, Klassen SP (1997) Genetic differentiation of fitness-associated traits among rapidly evolving populations of the soapberry bug. Evolution 51:1182–1188

    PubMed  Google Scholar 

  • Carroll SP, Klassen SP, Dingle H (1998) Rapidly evolving adaptations to host ecology and nutrition in the soapberry bug. Evol Ecol 12:955–968

    Google Scholar 

  • Carroll SP, Marler M, Winchell R, Dingle H (2003) Evolution of cryptic flight morph and life history differences during host race radiation in the soapberry bug, Jadera haematoloma Herrich-Schaeffer (Hemiptera: Rhopalidae). Ann Entomol Soc Am 96:135–143

    Google Scholar 

  • Carroll SP, Loye JE, Dingle H, Mathieson M, Famula TR, Zalucki MP (2005) And the beak shall inheritevolution in response to invasion. Ecol Lett 8:944–951

    PubMed  Google Scholar 

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

    Google Scholar 

  • Feder JL, Chilcote CA, Bush GL (1988) Genetic differentiation between sympatric host races of the apple maggot fly Rhagoletis pomonella. Nature 336:61–64

    Google Scholar 

  • Forister ML, Wilson JS (2013) The population ecology of novel plant–herbivore interactions. Oikos 122:657–666

    Google Scholar 

  • Futuyma DJ, Keese MC (1992) Evolution and coevolution of plants and phytophagous arthropods. In: Berenbaum MR, Rosenthal GA (eds) Herbivores: their interactions with secondary plant metabolites, vol 2. Academic Press, New York, pp 439–475

    Google Scholar 

  • Ghalambor CK, McKay JK, Carroll SP, Reznick DN (2007) Adaptive versus non-adaptive phenotypic plasticity and the potential for contemporary adaptation in new environments. Funct Ecol 21:394–407

    Google Scholar 

  • Gratton C, Welter SC (1998) Oviposition preference and larval performance of Liriomyza helianthi (Diptera: Agromyzidae) on normal and novel host plants. Environ Entomol 27:926–935

    Google Scholar 

  • Graves SD, Shapiro AM (2003) Exotics as host plants of the California butterfly fauna. Biol Conserv 110:413–433

    Google Scholar 

  • Henniges-Janssen K, Heckel DG, Groot AT (2017) Preference of diamondback moth larvae for novel and original host plant after host range expansion. Insects 5:793–804

    Google Scholar 

  • Jahner JP, Bonilla MM, Badik KJ, Shapiro AM, Forister ML (2011) Use of exotic hosts by Lepidoptera: widespread species colonize more novel hosts. Evolution 65:2719–2724

    PubMed  Google Scholar 

  • Janz N, Nylin S (2008) The oscillation hypothesis of host-plant range and speciation. In: Tilmon KJ (ed) Specialization, speciation, and radiation: the evolutionary biology of herbivorous insects. University of California Press, Berkeley, pp 203–215

    Google Scholar 

  • Janz N, Nylin S, Wahlberg N (2006) Diversity begets diversity: host expansions and the diversification of plant-feeding insects. BMC Evol Biol 6:4

    PubMed  PubMed Central  Google Scholar 

  • Japan Wild Research Center (2008) A photographic guide to the invasive alien species in Japan. Heibonsha, Tokyo

    Google Scholar 

  • Jermy T (1984) Evolution of insect host plant relationships. Am Nat 124:609–630

    Google Scholar 

  • Jigins CD, Bridle JR (2004) Speciation in the apple maggot fly: a blend of vintages? Trends Ecol Evol 19:111–114

    Google Scholar 

  • Kanamaru T, Sawada Y, Yamamoto S, Fujihara M, Oyabu T, Uehara T (2014) Test for exterminating the invasive aquatic plant Parrotfeather (Myriophyllum acuaticum (Vell.) Verdc.). J Jpn Soc Reveg Technol 40:437–445

    Google Scholar 

  • Kimoto K, Takizawa H (1994) Leaf beetles (Chrysomelidae) of Japan. Tokai University Press, Hatano (In Japanese)

    Google Scholar 

  • Lee JE (1990) Morphological studies on the immature stages of two Japanese species of the genus Galerucella (Coleoptera, Chrysomelidae). Jpn J Entomol 58:425–439

    Google Scholar 

  • National Institute of Environmental Studies (2018) Invasive species of Japan. https://www.nies.go.jp/biodiversity/invasive/DB/detail/80250e.html. Accessed 8 Feb 2018

  • Ohshima I (2007) Host race formation in the leaf-mining moth Acrocercops transecta (Lepidoptera: Gracillariidae). Biol J Lin Soc 93:135–145

    Google Scholar 

  • Ohshima I (2010) Host-associated pre-mating reproductive isolation between host races of Acrocercops transecta: mating site preferences and effect of host presence on mating. Ecol Entomol 35:253–257

    Google Scholar 

  • Ohshima I (2012) Genetic mechanisms preventing the fusion of ecotypes even in the face of gene flow. Sci Rep 2:506

    PubMed  PubMed Central  Google Scholar 

  • Ohta I, Matsuda K, Matsumoto Y (1998) Feeding stimulation of strawberry leaf beetle, Galerucella vittaticollis Baly (Coleoptera: Chrysomelidae) by quercetin glycosides in polygonaceous plants. Jpn J Appl Entomol Zool 2:45–49 (In Japanese with English summary)

    Google Scholar 

  • R Core Team (2018) R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. https://www.R-project.org/

  • Roff D (1980) Optimizing development time in a seasonal environment: the ‘ups and downs’ of clinal variation. Oecologia 45:202–208

    PubMed  Google Scholar 

  • Sakata Y, Ohgushi T, Isagi Y (2013) Geographic variations in phenotypic traits of the exotic herb Solidago altissima and abundance of recent established exotic herbivorous insects. J Plant Interact 8:216–218

    Google Scholar 

  • Sakata Y, Yamasaki M, Isagi Y, Ohgushi T (2014) An exotic herbivorous insect drives the evolution of resistance in the exotic perennial herb Solidago altissima. Ecology 95:2569–2578

    Google Scholar 

  • Sakata Y, Craig TP, Itami JK, Yamasaki M, Ohgushi T (2017) Parallel environmental factors drive variation in insect density and plant resistance in the native and invaded ranges. Ecology 98:2873–2884

    PubMed  Google Scholar 

  • Shirahama S, Yamawo A, Tokuda M (2017) Dimorphism in trichome production of Persicaria lapathifolia var. lapathifolia and its multiple effects on a leaf beetle. Arthropod Plant Interact 11:683–690

    Google Scholar 

  • Strauss SY, Lau JA, Carroll SP (2006) Evolutionary responses of natives to introduced species: what do introductions tell us about natural communities. Ecol Lett 9:357–374

    PubMed  Google Scholar 

  • Suzuki N (1985) Resource utilization of three chrysomelid beetles feeding on Rumex plants with diverse vegetational background. Jpn J Ecol 35:225–234

    Google Scholar 

  • Suzuki N (1986) Interspecific competition and coexistence of the two chrysomelids, Gastrophysa atrocyanea Motschulsky and Galerucella vittaticollis Baly (Coleoptera: Chrysomelidae), under limited food resource conditions. Ecol Res 1:259–268

    Google Scholar 

  • Suzuki N (1987) Chrysomelid communities on Rumex japonicus. In: Kimoto S, Takeda H (eds) Insect communities in Japan. Tokai University Press, Tokyo, pp 141–148 (In Japanese.)

    Google Scholar 

  • The Angiosperm Phylogeny Group (2016) An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV. Bot J Linn Soc 181:1–20

    Google Scholar 

  • Tokuda M (2015) Host specificity and wing polymorphism in Galerucella Grisescens (Coleoptera: Chrysomelidae). Nat Insects 50(12):8–12 (In Japanese.)

    Google Scholar 

Download references

Acknowledgements

This study was supported in part by JSPS KAKENHI Grant Number 26870435 to MT. Laboratory rearing of M. aquaticum was conducted with permission from the Ministry of Environment. The experiments complied with the current laws of Japan. We declare no conflicts of interest.

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MT, HM, and UO conceived and designed experiments. UO, SS, SN, HM, and MT collected materials from the field. UO, SS, and SN reared insects in the laboratory. UO, SS, and SN performed laboratory experiments. UO and MT analyzed the data and wrote the manuscript.

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Correspondence to Makoto Tokuda.

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Okamoto, U., Shirahama, S., Nasu, S. et al. Host range expansion of a Polygonaceae-associated leaf beetle to an invasive aquatic plant Myriophyllum aquaticum (Haloragaceae). Arthropod-Plant Interactions 14, 491–497 (2020). https://doi.org/10.1007/s11829-020-09764-7

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  • DOI: https://doi.org/10.1007/s11829-020-09764-7

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