Krishnan Anusha, Ghara Mahua, Kasinathan Srinivasan, Pramanik Gautam Kumar, Revadi Santosh, Borges Renee M
Centre for Ecological Sciences, Indian Institute of Science, Bangalore, 560 012, India.
Botanical Garden, Department of Molecular Biology and Ecology of Plants, George Wise Faculty of Life Science, Tel Aviv University, 69978, Tel Aviv, Israel.
Oecologia. 2015 Nov;179(3):797-809. doi: 10.1007/s00442-015-3372-9. Epub 2015 Jul 11.
Plants, herbivores and parasitoids affect each other directly and indirectly; however, feedback effects mediated by host plant traits have rarely been demonstrated in these tritrophic interactions. Brood-site pollination mutualisms (e.g. those involving figs and fig wasps) represent specialised tritrophic communities where the progeny of mutualistic pollinators and of non-mutualistic gallers (both herbivores) together with that of their parasitoids develop within enclosed inflorescences called syconia (hence termed brood-sites or microcosms). Plant reproductive phenology (which affects temporal brood-site availability) and inflorescence size (representing brood-site size) are plant traits that could affect reproductive resources, and hence relationships between trees, pollinators and non-pollinating wasps. Analysing wasp and seed contents of syconia, we examined direct, indirect, trophic and non-trophic relationships within the interaction web of the fig-fig wasp community of Ficus racemosa in the context of brood site size and availability. We demonstrate that in addition to direct resource competition and predator-prey (host-parasitoid) interactions, these communities display exploitative or apparent competition and trait-mediated indirect interactions. Inflorescence size and plant reproductive phenology impacted plant-herbivore and plant-parasitoid associations. These plant traits also influenced herbivore-herbivore and herbivore-parasitoid relationships via indirect effects. Most importantly, we found a reciprocal effect between within-tree reproductive asynchrony and fig wasp progeny abundances per syconium that drives a positive feedback cycle within the system. The impact of a multitrophic feedback cycle within a community built around a mutualistic core highlights the need for a holistic view of plant-herbivore-parasitoid interactions in the community ecology of mutualisms.
植物、食草动物和寄生蜂直接或间接地相互影响;然而,在这些三营养级相互作用中,由寄主植物性状介导的反馈效应却鲜有证据。巢址传粉共生关系(例如涉及榕树和榕小蜂的关系)代表了特殊的三营养级群落,其中互利传粉者和非互利造瘿昆虫(均为食草动物)的后代及其寄生蜂的后代在称为隐头花序的封闭花序内发育(因此称为巢址或微观世界)。植物繁殖物候(影响巢址的时间可用性)和花序大小(代表巢址大小)是可能影响繁殖资源的植物性状,进而影响树木、传粉者和非传粉黄蜂之间的关系。通过分析隐头花序中的黄蜂和种子含量,我们在巢址大小和可用性的背景下,研究了总状花序榕榕小蜂群落相互作用网络中的直接、间接、营养和非营养关系。我们证明,除了直接的资源竞争和捕食者 - 猎物(寄主 - 寄生蜂)相互作用外,这些群落还表现出剥削性或表观竞争以及性状介导的间接相互作用。花序大小和植物繁殖物候影响了植物 - 食草动物和植物 - 寄生蜂的关联。这些植物性状还通过间接效应影响了食草动物 - 食草动物和食草动物 - 寄生蜂的关系。最重要的是,我们发现树内繁殖异步性与每个隐头花序中榕小蜂后代丰度之间存在相互作用,这在系统内驱动了一个正反馈循环。围绕互利核心构建的群落中多营养级反馈循环的影响凸显了在互利共生群落生态学中对植物 - 食草动物 - 寄生蜂相互作用进行整体观的必要性。