甲烷营养群落在稻田土壤大气甲烷氧化中的作用。

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2024-11-06 eCollection Date: 2024-01-01 DOI:10.3389/fmicb.2024.1481044
Yan Zheng, Yuanfeng Cai, Zhongjun Jia
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引用次数: 0

摘要

湿地系统是已知的甲烷(CH4)来源。然而,被水淹没的稻田会定期排水。由于存在高亲和力甲烷氧化细菌(甲烷营养菌),水稻田土壤在旱季可吸收大气中的 CH4。水稻田土壤中高浓度 CH4 的低亲和性氧化作用可诱导大气中 CH4 的吸收。多种相互作用的因素控制着土壤生态系统对大气中 CH4 的吸收。我们需要更广泛的生物地理数据来完善我们对水稻田土壤吸收大气中 CH4 的相关生物和非生物因素的理解。因此,我们旨在评估中国九种不同地理位置的水稻田土壤中高亲和性 CH4 氧化活性,并探索活跃的大气甲烷营养体的群落组成。我们的研究结果表明,传统甲烷营养体消耗 10,000 ppmv 高浓度 CH4 后,可迅速诱导 1.86 ppmv(体积分数)CH4 的高亲和性氧化。在所有具有高亲和力 CH4 氧化活性的酸中性土壤(不包括碱性土壤)中,II 型甲烷营养体的 16S rRNA 与 rRNA 基因(rDNA)之比均高于 I 型甲烷营养体。II 型甲烷营养体的 16S rRNA:rDNA 比率和 13C 标记的 II 型甲烷营养体的丰度均与高亲和性 CH4 氧化活性呈正相关。土壤非生物因素可调控水稻田土壤中的甲烷营养群落组成和对大气中CH4的吸收。高亲和力甲烷氧化活性和 II 型甲烷营养体的丰度与土壤 pH 值呈负相关,而与土壤养分供应量(土壤有机碳、全氮和铵态氮)呈正相关。我们的研究结果表明了 II 型甲烷营养体和非生物因素在水稻田土壤吸收大气中的甲烷的重要性。我们的研究结果为水稻田土壤吸收大气中的 CH4 提供了更广阔的生物地理学视角。这为定期排水的稻田可作为旱季甲烷吸收汇提供了证据。预计这项研究将有助于通过有效的稻田农业管理来确定和制定温室气体减排策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of methanotrophic communities in atmospheric methane oxidation in paddy soils.

Wetland systems are known methane (CH4) sources. However, flooded rice fields are periodically drained. The paddy soils can absorb atmospheric CH4 during the dry seasons due to high-affinity methane-oxidizing bacteria (methanotroph). Atmospheric CH4 uptake can be induced during the low-affinity oxidation of high-concentration CH4 in paddy soils. Multiple interacting factors control atmospheric CH4 uptake in soil ecosystems. Broader biogeographical data are required to refine our understanding of the biotic and abiotic factors related to atmospheric CH4 uptake in paddy soils. Thus, here, we aimed to assess the high-affinity CH4 oxidation activity and explored the community composition of active atmospheric methanotrophs in nine geographically distinct Chinese paddy soils. Our findings demonstrated that high-affinity oxidation of 1.86 parts per million by volume (ppmv) CH4 was quickly induced after 10,000 ppmv high-concentration CH4 consumption by conventional methanotrophs. The ratios of 16S rRNA to rRNA genes (rDNA) for type II methanotrophs were higher than those for type I methanotrophs in all acid-neutral soils (excluding the alkaline soil) with high-affinity CH4 oxidation activity. Both the 16S rRNA:rDNA ratios of type II methanotrophs and the abundance of 13C-labeled type II methanotrophs positively correlated with high-affinity CH4 oxidation activity. Soil abiotic factors can regulate methanotrophic community composition and atmospheric CH4 uptake in paddy soils. High-affinity methane oxidation activity, as well as the abundance of type II methanotroph, negatively correlated with soil pH, while they positively correlated with soil nutrient availability (soil organic carbon, total nitrogen, and ammonium-nitrogen). Our results indicate the importance of type II methanotrophs and abiotic factors in atmospheric CH4 uptake in paddy soils. Our findings offer a broader biogeographical perspective on atmospheric CH4 uptake in paddy soils. This provides evidence that periodically drained paddy fields can serve as the dry-season CH4 sink. This study is anticipated to help in determining and devising greenhouse gas mitigation strategies through effective farm management in paddy fields.

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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University 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, clinicians and the public worldwide.
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