Biodiversity and potential functionality of biofilm-sediment biotope in La Muerte lagoon, Monegros Desert, Spain

IF 2.4 3区 环境科学与生态学 Q2 ECOLOGY
Mercedes Berlanga, Pere Picart, Arnau Blasco, Robert Benaiges-Fernandez, Ricardo Guerrero, Andrea Butturini, Jordi Urmeneta
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Abstract

La Muerte lagoon is an ephemeral endorheic water body located in the Monegros desert, Zaragoza, Spain. Amplicon sequencing of the 16S rRNA gene was performed to analyze the bacterial and archaeal communities in biofilm-sediment samples over three years, to understand the dynamic changes in the microbial community. PICRUSt and shotgun metagenomics were used to examine energy production and carbohydrate metabolism pathways. The dominant bacterial phyla were Actinobacteriota, Bacteroidota, Cyanobacteriota, and Pseudomonadota, while Halobacteriota was the predominant archaeal phylum. Despite seasonal environmental fluctuations, the biofilm community remained stable over time, suggesting resilience. The Calvin-Benson cycle was the main carbon fixation pathway, carried out by Cyanobacteria and purple non-sulfur bacteria. Nitrogen fixation by diazotrophs supplied an important nitrogen source. Organic carbon was derived primarily from autotrophs, with little use of allochthonous plant material. The comparison of biofilm-sediment and water column biotopes showed distinct but related prokaryote communities. Biofilm-sediments showed higher taxonomic diversity and different proportions of microbial phyla compared to the water column. This study provides initial insights into the complex microbial life in endorheic lagoons and underscores the importance of protecting these globally threatened habitats. The limited sample size in this study warrants further investigation with a more comprehensive sampling strategy to fully characterize the microbial communities and their functional roles in the different biotopes of La Muerte lagoon.
西班牙莫内格罗斯沙漠 La Muerte 泻湖生物膜-沉积物生物群落的生物多样性和潜在功能
La Muerte泻湖位于西班牙萨拉戈萨的莫内格罗斯沙漠,是一个短暂的内流水体。为了了解微生物群落的动态变化,对生物膜沉积物样本中的细菌和古细菌群落进行了 16S rRNA 基因扩增子测序分析。利用 PICRUSt 和枪式元基因组学研究了能量生产和碳水化合物代谢途径。主要的细菌门为放线菌门、类杆菌门、蓝藻菌门和假单胞菌门,而卤杆菌门是主要的古细菌门。尽管存在季节性环境波动,但生物膜群落在一段时间内保持稳定,这表明生物膜群落具有恢复能力。卡尔文-本森循环是主要的碳固定途径,由蓝细菌和紫色非硫细菌进行。重氮菌的固氮作用提供了重要的氮源。有机碳主要来自自养菌,很少利用同源植物材料。生物膜-沉积物和水柱生物群落的比较显示了不同但相关的原核生物群落。与水柱相比,生物膜沉积物显示出更高的分类多样性和不同的微生物门类比例。这项研究初步揭示了内河泻湖中复杂的微生物生命,并强调了保护这些受到全球威胁的栖息地的重要性。这项研究的样本量有限,需要采用更全面的取样策略进行进一步调查,以全面了解拉穆埃尔特泻湖不同生物群落的微生物群落特征及其功能作用。
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来源期刊
Frontiers in Ecology and Evolution
Frontiers in Ecology and Evolution Environmental Science-Ecology
CiteScore
4.00
自引率
6.70%
发文量
1143
审稿时长
12 weeks
期刊介绍: Frontiers in Ecology and Evolution publishes rigorously peer-reviewed research across fundamental and applied sciences, to provide ecological and evolutionary insights into our natural and anthropogenic world, and how it should best be managed. Field Chief Editor Mark A. Elgar at the University of Melbourne is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics and the public worldwide. Eminent biologist and theist Theodosius Dobzhansky’s astute observation that “Nothing in biology makes sense except in the light of evolution” has arguably even broader relevance now than when it was first penned in The American Biology Teacher in 1973. One could similarly argue that not much in evolution makes sense without recourse to ecological concepts: understanding diversity — from microbial adaptations to species assemblages — requires insights from both ecological and evolutionary disciplines. Nowadays, technological developments from other fields allow us to address unprecedented ecological and evolutionary questions of astonishing detail, impressive breadth and compelling inference. The specialty sections of Frontiers in Ecology and Evolution will publish, under a single platform, contemporary, rigorous research, reviews, opinions, and commentaries that cover the spectrum of ecological and evolutionary inquiry, both fundamental and applied. Articles are peer-reviewed according to the Frontiers review guidelines, which evaluate manuscripts on objective editorial criteria. Through this unique, Frontiers platform for open-access publishing and research networking, Frontiers in Ecology and Evolution aims to provide colleagues and the broader community with ecological and evolutionary insights into our natural and anthropogenic world, and how it might best be managed.
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