Prokaryotic biogeography across atmospheric, aquatic, and terrestrial ecosystems in the Mount Everest region

IF 20.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Science Bulletin Pub Date : 2026-10-15 Epub Date: 2026-07-28 DOI:10.1016/j.scib.2026.07.065
Yongqin Liu, Mukan Ji, Yuying Chen, Keshao Liu, Pengfei Liu, Yang Liu, Tandong Yao
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Abstract

The Mount Everest region encompasses one of the world’s most fragile cryospheric landscapes, comprising diverse and interconnected habitats across atmospheric, aquatic, and terrestrial ecosystems. Despite growing interest in high-mountain microbial ecology, basin-scale assessments remain scarce. Here, we conducted a microbial survey in the Rongbuk River basin (3699–7000 m a.s.l.), analyzing 677 samples from aerosols, snow, stream water, stream sediments, and soils via 16S rRNA gene amplicon sequencing. We identified 58,141 operational taxonomic units (OTUs) across 67 prokaryotic phyla, dominated by Pseudomonadota, Actinomycetota, and Bacteroidota. Elevational diversity patterns were ecosystem-specific: richness declined with elevation in aerosols and stream water, showed a U-shaped pattern in snow, peaked at mid-elevations in soils, and remained stable in stream sediments. Evenness and Shannon diversity, however, displayed distinct elevational trends and environmental determinants compared to richness. Community assembly was largely stochastic in snow, aquatic, and soils but strongly deterministic in aerosols. Source-tracking analysis revealed strong landscape-scale connectivity, with snow serving as a microbial vector linking atmospheric inputs to downstream ecosystems (contributing 1.4%–12.0%). Soils served as a potential microbial reservoir, harboring 42% of the unique OTUs and contributing 3%–11.8% of communities to other habitats. While stream water and sediments showed reciprocal exchange, aerosols remained largely uncharacterized in terms of their sources. Collectively, these findings demonstrate that although prokaryotic responses to elevation are ecosystem-specific, these habitats are ecologically interconnected across the high-mountain landscape, providing a comprehensive overview of the prokaryotic biogeography of the region.
珠穆朗玛峰地区大气、水生和陆地生态系统的原核生物地理学。
珠穆朗玛峰地区拥有世界上最脆弱的冰冻圈景观之一,包括大气、水生和陆地生态系统中多种多样且相互关联的栖息地。尽管人们对高山微生物生态学的兴趣日益浓厚,但流域尺度的评估仍然很少。本研究在绒北江流域(海拔3699 ~ 7000米)开展了微生物调查,通过16S rRNA基因扩增子测序,分析了来自气溶胶、雪、溪水、溪流沉积物和土壤的677个样品。我们在67个原核生物门中鉴定出58,141个操作分类单位(OTUs),以假单胞菌门、放线菌门和拟杆菌门为主。海拔多样性模式具有生态系统特异性:气溶胶和溪流水的丰富度随海拔高度而下降,在雪中呈u形分布,在土壤中达到峰值,在溪流沉积物中保持稳定。与丰富度相比,均匀度和香农多样性表现出明显的海拔变化趋势和环境决定因素。群落聚集在雪、水和土壤中主要是随机的,但在气溶胶中具有很强的确定性。来源跟踪分析显示,景观尺度上的连通性很强,雪作为连接大气输入和下游生态系统的微生物载体(贡献6.6%-12.0%)。土壤是潜在的微生物库,拥有42%的独特otu,并为其他栖息地贡献了3%-11.8%的群落。虽然水流和沉积物表现出相互交换,但就其来源而言,气溶胶在很大程度上仍未得到表征。总的来说,这些发现表明,尽管原核生物对海拔的反应是生态系统特异性的,但这些栖息地在高山景观中具有生态联系,为该地区的原核生物地理学提供了全面的概述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Science Bulletin
Science Bulletin MULTIDISCIPLINARY SCIENCES-
CiteScore
24.60
自引率
2.10%
发文量
8092
期刊介绍: Science Bulletin (Sci. Bull., formerly known as Chinese Science Bulletin) is a multidisciplinary academic journal supervised by the Chinese Academy of Sciences (CAS) and co-sponsored by the CAS and the National Natural Science Foundation of China (NSFC). Sci. Bull. is a semi-monthly international journal publishing high-caliber peer-reviewed research on a broad range of natural sciences and high-tech fields on the basis of its originality, scientific significance and whether it is of general interest. In addition, we are committed to serving the scientific community with immediate, authoritative news and valuable insights into upcoming trends around the globe.
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