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Disturbance induced dynamics of a tritrophic novel ecosystem

Published online by Cambridge University Press:  26 July 2017

K.T. Lakatos ,
Z. László  and
B. Tóthmérész
K.T. Lakatos
Affiliation:
Department of Ecology, University of Debrecen, Debrecen, Egyetem square 1, H-4032, Hungary
Z. László*
Affiliation:
Hungarian Department of Biology and Ecology, Babeş-Bolyai University, Str. Clinicilor nr. 5–7, 400006 Cluj-Napoca, Romania
B. Tóthmérész
Affiliation:
MTA-DE Biodiversity and Ecosystem Services Research Group, Debrecen, Egyetem square 1, H-4032, Hungary
*
*Author for correspondence Tel: 0742 496 330 Fax: 0264 431 858 Email: [email protected]
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Abstract

Novel ecosystems formed by invasive plants provide a good opportunity to get insight into early dynamics and pattern formation of these ecosystems. The invasive black locust as host plant, Bruchophagus robiniae as host-specific seed predator and its parasitoids were the components of the studied tritrophic system. To investigate disturbance-driven dynamics of this system we created seed-vacated host plant patches in a field experiment. We removed all pods from selected patches of black locust resulting in an induced local extinction of seed predators and their parasitoids. We hypothesized that disturbance enhances top-down control by parasitoids; this enhanced top-down control decreases seed predation, facilitating the host plant's spread. We found that disturbance modified only parasitism after controlling with year effect: in vacated patches median parasitism was higher than in control patches. Seed predation exceeded its initial level in vacated patches in the third year after the disturbance, but in the fourth year it dropped again presumably due to the strong top-down control. Our findings also suggested that the seed predator was also affected by the bottom-up control of its host plant's density. We found that in the studied new ecosystem the top-down control was strengthened by the disturbance. Since the host plant of the tritrophic system is an invasive species, partial habitat disturbance of such species may increase the severity of parasitoid top-down control, which may reduce seed predation by the herbivores.

Keywords

black locustinvasive speciesfield experimenthost–parasitoid dynamicsseed predatorsvacated host plant patches
Type
Research Papers
Information
Bulletin of Entomological Research , Volume 108 , Issue 2 , April 2018 , pp. 158 - 165
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Copyright
Copyright © Cambridge University Press 2017 

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References

Arista, M. & Talavera, S. (1996) Density effect on the fruit-set, seed crop viability and seedling vigour of Abies pinsapo . Annals of Botany 77, 187–192.Google Scholar
Bartha, D., Csiszár, Á. & Zsigmond, V. (2008) Black Locust. pp. 63–76 in Botta-Dukát, Z. & Balogh, L. (Eds) The Most Important Invasive Plants in Hungary. Vácrátót, Hungary, Institute of Ecology and Botany, Hungarian Academy of Sciences.Google Scholar
Bates, D., Maechler, M. & Bolker, B. (2012) lme4: Linear mixed-effects models using S4 classes. . R Package version 0.999999-2.Google Scholar
Batiste, W.C. (1967) Humidity and the emergence of Bruchophagus kolobovae (Hymenoptera: Eurytomidae) and its parasites from trefoil seeds. Annals of the Entomological Society of America 60(4), 752–756.CrossRefGoogle Scholar
Bezemer, T.M., Harvey, J.A. & Cronin, J.T. (2014) Response of native insect communities to invasive plants. Annual Review of Entomology 59, 119–41.Google Scholar
Chase, J.M., Burgett, A.A. & Biro, E.G. (2010) Habitat isolation moderates the strength of top-down control in experimental pond food webs. Ecology 91(3), 637–643.Google Scholar
Cohen, A.N. (2002) Success factors in the establishment of human-dispersed organisms. pp. 374–394 in Bullock, R., Kenward, J.M. & Hails, R.E. (Eds) Dispersal Ecology. Oxford, Blackwell Publishing.Google Scholar
Compton, S.G. (2002) Sailing with wind: dispersal by small flying insects. pp. 113–133 in Bullock, R.S., Kenward, J.M. & Hails, R.E. (Eds) Dispersal Ecology. Oxford, British Ecological Society, Blackwell Publishing.Google Scholar
Crawley, M.J. (2012) The R Book. Chichester, John Wiley & Sons.Google Scholar
Cronin, J.T. & Haynes, K.J. (2004) An invasive plant promotes unstable host-parasitoid patch dynamics. Ecology 85(10), 2772–2782.Google Scholar
Denno, R.F., Gratton, C., Hartmut, D. & Finke, D.L. (2003) Predation risk affects relative strength of top-down and bottom-up impacts on insect herbivores. Ecology 84(4), 1032–1044.Google Scholar
Elzinga, J.A., van Nouhuys, S., van Leeuwen, D.-J. & Biere, A. (2007) Distribution and colonisation ability of three parasitoids and their herbivorous host in a fragmented landscape. Basic and Applied Ecology 8(1), 75–88.Google Scholar
Hargrove, W.W. (1986) An annoted species list of insect herbivores commonly associated with black locust, Robinia pseudoacacia, in the Southern Appalachians. Entomological News 97(1), 36–40.Google Scholar
Hobbs, R.J. & Huenneke, L.F. (1992) Disturbance, diversity, and invasion: implications for conservation. Conservation Biology 6(3), 324–337.Google Scholar
Hothorn, T., Bretz, F. & Westfall, P. (2008) Simultaneous inference in general parametric models. Biometrical Journal 50(3), 346–363.Google Scholar
Kamm, J.A. (1989) In-flight assessment of host and Nonhost Odors by Alfalfa Seed Chalcid (Hymenoptera: Eurytomidae). Environmental Entomology 18(1), 56–60.Google Scholar
Kareiva, P. (1983) Influence of vegetation texture on herbivore populations: resource concentration and herbivore movement. pp. 259–289 in Denno, R.F. & McClure, M.S. (Eds) Variable Plants and Herbivores in Natural and Managed Systems. New York, Academic Press, Inc.CrossRefGoogle Scholar
Lakatos, T.K., László, Z. & Tóthmérész, B. (2016) Resource dependence in a new ecosystem: a host plant and its colonizing community. Acta Oecologica, 73, 80–86.CrossRefGoogle Scholar
Lambdon, P., Pyšek, P., Basnou, C., Hejda, M., Arianoutsou, M., Essl, F., Jarošik, V., Pergl, J., Winter, M., Anastasiu, P., Andriopoulos, P., Bazos, I., Brundu, G., Celesti-Grapow, L., Chassot, P., Delipetrou, P., Josefsson, M., Kark, S., Klotz, S., Kokkoris, Y., Kühn, I., Marchante, H., Perglová, I., Pino, J., Vilá, M., Zikos, A., Roy, D. & Hulme, P. (2008) Alien flora of Europe: species diversity, temporal trends, geographical patterns and research needs. Preslia 80, 101–149.Google Scholar
Neser, O.C. & Prinsloo, G.L. (2004) Seed-feeding species of Bruchophagus Ashmead (Hymenoptera: Eurytomidae) associated with native Australian acacias that are invasive in South Africa, with the description of two new species. Australian Journal of Entomology 43(1), 46–56.Google Scholar
Nylin, S. (2001) Life history perspectives on pest insects: what's the use? Austral Ecology 26, 507–517.Google Scholar
Osborne, J.L., Loxdale, H.D. & Woiwod, I.P. (2002) Monitoring insect dispersal: methods and approaches. pp. 24–49 in Bullock, R., Kenward, J.M. & Hails, R.E. (Eds) Dispersal Ecology. Oxford, Blackwell Publishing.Google Scholar
Pannell, J.R. & Obbard, D.J. (2003) Probing the primacy of the patch: what makes a metapopulation? Journal of Ecology 91(3), 485–488.Google Scholar
Perju, T. (1998) The pest of the white acacia (Robinia pseudoacacia L.). Buletin de informare Societatea Lepidopterologica Romana 9(3–4), 291–295.Google Scholar
Price, P.W., Bouton, C.E., Gross, P., Mcpheron, B.A., Thompson, J.N. & Weis, A.E. (1980) Interactions among three trophic levels: influence of plants on interactions between insect herbivores and natural enemies. Annual Review of Ecology and Systematics 11, 41–65.Google Scholar
QGIS Development Team (2015) QGIS Geographic Information System. Open Source Geospatial Foundation Project, http://qgis.osgeo.org Google Scholar
R Development Core Team (2013) R: A language and environment for statistical computing.Google Scholar
Rédei, K., Csiha, I., Keserû, Z., Kamandiné Végh, Á. & Győri, J. (2011) The Silviculture of Black Locust (Robinia pseudoacacia L.) in Hungary: a Review. South-East European Forestry 2(2), 101–107.Google Scholar
Shea, K., Smyth, M., Sheppard, A., Morton, R. & Chalimbaud, J. (2000) Effect of patch size and plant density of Paterson's curse (Echium plantagineum) on the oviposition of a specialist weevil, Mogulones larvatus . Oecologia 124, 615–621.Google Scholar
Soroka, J. & Otani, J. (2011) Arthropods of legume forage crops. pp. 239–264 in Floate, K.D. (Ed) Arthropods of Canadian Grasslands (Volume 2): Inhabitants of a Changing Landscape. Ottawa, ON, Biological Survey of Canada.Google Scholar
Traveset, A. (1995) Spatio-temporal variation in pre-dispersal reproductive losses of a Mediterranean shrub. Euphorbia dendroides L. Oecologia 103, 118–126.Google Scholar
Underwood, N. & Halpern, S.L. (2012) Insect herbivores, density dependence, and the performance of the perennial herb Solanum carolinense . Ecology 93(5), 1026–1035.Google Scholar
Wilkinson, E.B. & Feener, D.H. (2007) Habitat complexity modifies ant-parasitoid interactions: implications for community dynamics and the role of disturbance. Oecologia 152(1), 151–161.Google Scholar
Yu, H.L., Zhang, Y.J., Wu, K.M., Wyckhuys, K.A.G. & Guo, Y.Y. (2009) Flight potential of Microplitis mediator, a parasitoid of various lepidopteran pests. BioControl 54, 183–193.Google Scholar