Hannah B. Shulman, Emma L. Aronson, Diego Dierick, Andrian A. Pinto-Tomás, Jon K. Botthoff, Allan Artavia-León, Michael F. Allen
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引用次数: 0
摘要
在厄尔尼诺南方涛动事件的整个干旱阶段,我们在哥斯达黎加的一个新热带雨林开展了一项研究活动,以确定微生物群落动态和土壤碳通量。我们的研究包括切叶蚁 Atta cephalotes 的巢穴,因为这些生态系统工程师对土壤的扰动可能会影响微生物对干旱的反应。干旱降低了微生物的多样性和核心微生物群分类群的丰度,包括疣状微生物细菌和脊索真菌。尽管最初的反应是多样性减少和组成改变,但干旱后 6 个月,微生物群落与干旱前的情况相似,这表明土壤微生物群落对干旱事件的恢复能力很强。头状菌巢穴改变了周围土壤中的真菌组成,并降低了真菌死亡率和干旱后酸性杆菌的生长。由于土壤湿度较低,干旱增加了土壤中的甲烷消耗量,而头足椿巢穴降低了某些类型土壤中甲烷排放量的变化。甲烷营养细菌的丰度和真菌的组成跟踪了CH4的排放。这些结果描述了干旱期间热带土壤微生物组在时间和空间上的特征,并为切叶蚁巢穴在塑造土壤微生物组和增强微生物在气候扰动期间的恢复力方面的重要性提供了证据。
Leafcutter ants enhance microbial drought resilience in tropical forest soil
We conducted a research campaign in a neotropical rainforest in Costa Rica throughout the drought phase of an El-Nino Southern Oscillation event to determine microbial community dynamics and soil C fluxes. Our study included nests of the leafcutter ant Atta cephalotes, as soil disturbances made by these ecosystem engineers may influence microbial drought response. Drought decreased the diversity of microbes and the abundance of core microbiome taxa, including Verrucomicrobial bacteria and Sordariomycete fungi. Despite initial responses of decreasing diversity and altered composition, 6 months post-drought the microbiomes were similar to pre-drought conditions, demonstrating the resilience of soil microbial communities to drought events. A. cephalotes nests altered fungal composition in the surrounding soil, and reduced both fungal mortality and growth of Acidobacteria post-drought. Drought increased CH4 consumption in soils due to lower soil moisture, and A. cephalotes nests decrease the variability of CH4 emissions in some soil types. CH4 emissions were tracked by the abundance of methanotrophic bacteria and fungal composition. These results characterize the microbiome of tropical soils across both time and space during drought and provide evidence for the importance of leafcutter ant nests in shaping soil microbiomes and enhancing microbial resilience during climatic perturbations.
期刊介绍:
The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side.
Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following:
the structure, activities and communal behaviour of microbial communities
microbial community genetics and evolutionary processes
microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors
microbes in the tree of life, microbial diversification and evolution
population biology and clonal structure
microbial metabolic and structural diversity
microbial physiology, growth and survival
microbes and surfaces, adhesion and biofouling
responses to environmental signals and stress factors
modelling and theory development
pollution microbiology
extremophiles and life in extreme and unusual little-explored habitats
element cycles and biogeochemical processes, primary and secondary production
microbes in a changing world, microbially-influenced global changes
evolution and diversity of archaeal and bacterial viruses
new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.