纬度梯度河流中氨氧化和反硝化微生物群落β多样性的物种库和局部聚集过程。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xiang Xiong, Lian Feng, Jieya Huang, Wenjie Wan, Yuyi Yang, Wenzhi Liu
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引用次数: 0

摘要

区域物种库和地方群落集结机制都驱动着不同地理梯度的微生物多样性模式。然而,很少有人研究它们对河流生态系统中参与氮(N)循环的微生物群落的β多样性模式的影响。在此,我们利用高通量测序的古菌amoA、细菌amoA、nirK和nirS基因、空模型和中性群落模型来区分物种池和局部组装过程对中国东部纬度梯度河流湿地中氨氧化和反硝化群落的相对重要性。结果表明,nirS型反硝化群落的β多样性与γ多样性和环境异质性共同变化,这意味着区域物种库和异质性选择解释了β多样性的变化。然而,氨氧化和 nirK 型反硝化群落的 β 多样性与 γ 多样性和环境异质性不相关。β偏差沿纬度梯度的连续驼峰分布和较低的物种扩散率表明,扩散限制决定了氨氧化和 nirK 型反硝化群落 β 多样性的变化。此外,生物相互作用通过影响物种共存模式驱动了氨氧化和 nirS 型反硝化群落。我们的研究强调了区域物种库和地方群落组装过程在形成氮循环微生物地理模式方面的重要性,并扩展了它们对大规模持续变化环境的适应性的知识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Species pool and local assembly processes drive β diversity of ammonia-oxidizing and denitrifying microbial communities in rivers along a latitudinal gradient

Both regional species pool and local community assembly mechanism drive the microbial diversity patterns across geographical gradients. However, little has been done to separate their effects on the β diversity patterns of microbial communities involved in nitrogen (N) cycling in river ecosystems. Here, we use high-throughput sequencing of the archaeal amoA, bacterial amoA, nirK, and nirS genes, null model, and neutral community model to distinguish the relative importance of species pool and local assembly processes for ammonia-oxidizing and denitrifying communities in river wetlands along a latitudinal gradient in eastern China. Results indicated that the β diversity of the nirS-type denitrifying community co-varied with γ diversity and environmental heterogeneity, implying that regional species pool and heterogeneous selection explained variation in β diversity. However, the β diversity of ammonia-oxidizing and nirK-type denitrifying communities did not correlate with γ diversity and environmental heterogeneity. The continuous hump distribution of β deviation along the latitudinal gradient and the lower species dispersal rate indicated that the dispersal limitation shaped the variation in β diversity of ammonia-oxidizing and nirK-type denitrifying communities. Additionally, biotic interactions drove ammonia-oxidizing and nirS-type denitrifying communities by influencing species co-occurrence patterns. Our study highlights the importance of regional species pool and local community assembly processes in shaping geographical patterns of N-cycling microorganisms and extends knowledge of their adaptability to a continuously changing environment on a large scale.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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