山区不同排水条件下表土和底土细菌群落组合。

IF 4.3 2区 生物学 Q1 BIOLOGY Biological Research Pub Date : 2023-06-24 DOI:10.1186/s40659-023-00445-2
Constanza Aguado-Norese, Valentina Cárdenas, Alexis Gaete, Dinka Mandakovic, Javiera Vasquez-Dean, Christian Hodar, Marco Pfeiffer, Mauricio Gonzalez
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引用次数: 1

摘要

背景:高山环境对生命和人类社会起着至关重要的作用,同时也是极易受到气候变化和土地利用集约化影响的环境,因此受到特别关注。尽管如此,我们对南美洲高山土壤及其微生物群落结构的了解非常少,考虑到依赖这些地区提供的生态系统服务的大量人口,这一点更值得关注。相反,位于智利地中海地区的中安第斯山脉长期以来一直因其独特的植物群而受到研究,其多样性和地方性归因于特殊的地质历史和短距离内明显的环境梯度。在33.5˚S的低高山植被带(~2500 m a.s.l.),我们研究了安第斯山谷中保存完好的土壤性质和微生物群落结构。这提供了一个机会,以确定在高度异质环境的土壤深度剖面中,不同类型的土壤及其不同层的总体细菌群落结构的变化。结果:共检测到55个门的18427个扩增子序列变异(Amplicon Sequence Variant, asv)。同一层位内的细菌群落结构非常相似,验证了土壤取样方法。Bray-Curtis差异分析表明,浅层(表土)细菌群落结构与深层(底土)细菌群落结构存在位点特异性差异。然而,表层土壤微生物群落之间的总体关系比下层土壤微生物群落之间的关系更密切。表层土壤细菌群落的α多样性高于底土,表层土壤细菌相互作用较多,平均连通性较高。最后,特定类群的丰度可以作为表层土壤向下层土壤过渡的生物学标志,如浅层土壤中的纤维杆菌群、变形杆菌群、拟杆菌群,以及深层土壤中的绿杆菌群、晚孢杆菌群和亚硝基螺旋体。结论:土壤排水条件对细菌群落组成具有重要意义,其结构信息及其可能的生态关系可能有助于厘清山区表土-底土过渡边缘的位置。
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Topsoil and subsoil bacterial community assemblies across different drainage conditions in a mountain environment.

Background: High mountainous environments are of particular interest as they play an essential role for life and human societies, while being environments which are highly vulnerable to climate change and land use intensification. Despite this, our knowledge of high mountain soils in South America and their microbial community structure is strikingly scarce, which is of more concern considering the large population that depends on the ecosystem services provided by these areas. Conversely, the Central Andes, located in the Mediterranean region of Chile, has long been studied for its singular flora, whose diversity and endemism has been attributed to the particular geological history and pronounced environmental gradients in short distances. Here, we explore soil properties and microbial community structure depending on drainage class in a well-preserved Andean valley on the lower alpine vegetation belt (~2500 m a.s.l.) at 33.5˚S. This presents an opportunity to determine changes in the overall bacterial community structure across different types of soils and their distinct layers in a soil depth profile of a highly heterogeneous environment.

Methods: Five sites closely located (<1.5 km) and distributed in a well preserved Andean valley on the lower alpine vegetation belt (~2500 m a.s.l.) at 33.5˚S were selected based on a pedological approach taking into account soil types, drainage classes and horizons. We analyzed 113 soil samples using high-throughput sequencing of the 16S rRNA gene to describe bacterial abundance, taxonomic composition, and co-occurrence networks.

Results: Almost 18,427 Amplicon Sequence Variant (ASVs) affiliated to 55 phyla were detected. The bacterial community structure within the same horizons were very similar validating the pedological sampling approach. Bray-Curtis dissimilarity analysis revealed that the structure of bacterial communities in superficial horizons (topsoil) differed from those found in deep horizons (subsoil) in a site-specific manner. However, an overall closer relationship was observed between topsoil as opposed to between subsoil microbial communities. Alpha diversity of soil bacterial communities was higher in topsoil, which also showed more bacterial members interacting and with higher average connectivity compared to subsoils. Finally, abundances of specific taxa could be considered as biological markers in the transition from topsoil to subsoil horizons, like Fibrobacterota, Proteobacteria, Bacteroidota for shallower soils and Chloroflexi, Latescibacterota and Nitrospirota for deeper soils.

Conclusions: The results indicate the importance of the soil drainage conditions for the bacterial community composition, suggesting that information of both structure and their possible ecological relationships, might be useful in clarifying the location of the edge of the topsoil-subsoil transition in mountainous environments.

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来源期刊
Biological Research
Biological Research 生物-生物学
CiteScore
10.10
自引率
0.00%
发文量
33
审稿时长
>12 weeks
期刊介绍: Biological Research is an open access, peer-reviewed journal that encompasses diverse fields of experimental biology, such as biochemistry, bioinformatics, biotechnology, cell biology, cancer, chemical biology, developmental biology, evolutionary biology, genetics, genomics, immunology, marine biology, microbiology, molecular biology, neuroscience, plant biology, physiology, stem cell research, structural biology and systems biology.
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