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The ghost of disturbance past: long-term effects of pulse disturbances on community biomass and composition
Jacquet, C., & Altermatt, F. (2020). The ghost of disturbance past: long-term effects of pulse disturbances on community biomass and composition. Proceedings of the Royal Society B: Biological Sciences, 287(1930), 20200678 (8 pp.). https://doi.org/10.1098/rspb.2020.0678
Behavior out of control: experimental evolution of resistance to host manipulation
Hafer‐Hahmann, N. (2019). Behavior out of control: experimental evolution of resistance to host manipulation. Ecology and Evolution, 9(12), 7237-7245. https://doi.org/10.1002/ece3.5294
Defensive symbionts mediate species coexistence in phytophagous insects
Hertäg, C., & Vorburger, C. (2018). Defensive symbionts mediate species coexistence in phytophagous insects. Functional Ecology, 32, 1057-1064. https://doi.org/10.1111/1365-2435.13040
Rapid evolution of symbiont-mediated resistance compromises biological control of aphids by parasitoids
Käch, H., Mathé-Hubert, H., Dennis, A. B., & Vorburger, C. (2018). Rapid evolution of symbiont-mediated resistance compromises biological control of aphids by parasitoids. Evolutionary Applications, 11(2), 220-230. https://doi.org/10.1111/eva.12532
The role of defensive symbionts in host-parasite coevolution
Vorburger, C., & Perlman, S. J. (2018). The role of defensive symbionts in host-parasite coevolution. Biological Reviews, 93(4), 1747-1764. https://doi.org/10.1111/brv.12417
Environmental context and magnitude of disturbance influence trait-mediated community responses to wastewater in streams
Burdon, F. J., Reyes, M., Alder, A. C., Joss, A., Ort, C., Räsänen, K., … Stamm, C. (2016). Environmental context and magnitude of disturbance influence trait-mediated community responses to wastewater in streams. Ecology and Evolution, 6(12), 3923-3939. https://doi.org/10.1002/ece3.2165
Are aphid parasitoids locally adapted to the prevalence of defensive symbionts in their hosts?
Vorburger, C., & Rouchet, R. (2016). Are aphid parasitoids locally adapted to the prevalence of defensive symbionts in their hosts? BMC Evolutionary Biology, 16, 271 (11pp.). https://doi.org/10.1186/s12862-016-0811-0
Assessing antibiotic resistance of microorganisms in sanitary sewage
Kaeseberg, T., Blumensaat, F., Zhang, J., & Krebs, P. (2015). Assessing antibiotic resistance of microorganisms in sanitary sewage. Water Science and Technology, 71(2), 168-173. https://doi.org/10.2166/wst.2014.467
Gallium-mediated siderophore quenching as an evolutionarily robust antibacterial treatment
Ross-Gillespie, A., Weigert, M., Brown, S. P., & Kümmerli, R. (2014). Gallium-mediated siderophore quenching as an evolutionarily robust antibacterial treatment. Evolution, Medicine and Public Health, 2014(1), 18-29. https://doi.org/10.1093/emph/eou003
The evolutionary ecology of symbiont-conferred resistance to parasitoids in aphids
Vorburger, C. (2014). The evolutionary ecology of symbiont-conferred resistance to parasitoids in aphids. Insect Science, 21(3), 251-264. https://doi.org/10.1111/1744-7917.12067
Comparing constitutive and induced costs of symbiont-conferred resistance to parasitoids in aphids
Vorburger, C., Ganesanandamoorthy, P., & Kwiatkowski, M. (2013). Comparing constitutive and induced costs of symbiont-conferred resistance to parasitoids in aphids. Ecology and Evolution, 3(3), 706-713. https://doi.org/10.1002/ece3.491
Development, specificity and sublethal effects of symbiont-conferred resistance to parasitoids in aphids
Schmid, M., Sieber, R., Zimmermann, Y. S., & Vorburger, C. (2012). Development, specificity and sublethal effects of symbiont-conferred resistance to parasitoids in aphids. Functional Ecology, 26(1), 207-215. https://doi.org/10.1111/j.1365-2435.2011.01904.x
Versteckte Helfer: Symbionten und ihr Einfluss auf Wirt-Parasit-Beziehungen bei Insekten
Vorburger, C. (2011). Versteckte Helfer: Symbionten und ihr Einfluss auf Wirt-Parasit-Beziehungen bei Insekten. Vierteljahrsschrift der Naturforschenden Gesellschaft in Zürich, 156(3-4), 89-97.
UV-C inactivation in <I>Escherichia coli</I> is affected by growth conditions preceding irradiation, in particular by the specific growth rate
Bucheli-Witschel, M., Bassin, C., & Egli, T. (2010). UV-C inactivation in Escherichia coli is affected by growth conditions preceding irradiation, in particular by the specific growth rate. Journal of Applied Microbiology, 109(5), 1733-1744. https://doi.org/10.1111/j.1365-2672.2010.04802.x
Ample genetic variation but no evidence for genotype specificity in an all-parthenogenetic host–parasitoid interaction
Sandrock, C., Gouskov, A., & Vorburger, C. (2010). Ample genetic variation but no evidence for genotype specificity in an all-parthenogenetic host–parasitoid interaction. Journal of Evolutionary Biology, 23(3), 578-585. https://doi.org/10.1111/j.1420-9101.2009.01925.x
Adaptation to UVA radiation of <I>E. coli</I> growing in continuous culture
Berney, M., Weilenmann, H. U., & Egli, T. (2007). Adaptation to UVA radiation of E. coli growing in continuous culture. Journal of Photochemistry and Photobiology B: Biology, 86(2), 149-159. https://doi.org/10.1016/j.jphotobiol.2006.08.014
Efficacy of solar disinfection of <I>Escherichia coli</I>, <I>Shigella flexneri</I>, <I>Salmonella</I> Typhimurium and <I>Vibrio cholerae</I>
Berney, M., Weilenmann, H. U., Simonetti, A., & Egli, T. (2006). Efficacy of solar disinfection of Escherichia coli, Shigella flexneri, Salmonella Typhimurium and Vibrio cholerae. Journal of Applied Microbiology, 101(4), 828-836. https://doi.org/10.1111/j.1365-2672.2006.02983.x