Microbial life-history strategies mediate microbial carbon pump efficacy in response to N management depending on stoichiometry of microbial demand

IF 10.8 1区 环境科学与生态学 Q1 BIODIVERSITY CONSERVATION
Liyang Yang, Alberto Canarini, Wushuai Zhang, Ming Lang, Yuanxue Chen, Zhenling Cui, Yakov Kuzyakov, Andreas Richter, Xinping Chen, Fusuo Zhang, Jing Tian
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Abstract

The soil microbial carbon pump (MCP) is increasingly acknowledged as being directly linked to soil organic carbon (SOC) accumulation and stability. Given the close coupling of carbon (C) and nitrogen (N) cycles and the constraints imposed by their stoichiometry on microbial growth, N addition might affect microbial growth strategies with potential consequences for necromass formation and carbon stability. However, this topic remains largely unexplored. Based on two multi-level N fertilizer experiments over 10 years in two soils with contrasting soil fertility located in the North (Cambisol, carbon-poor) and Southwest (Luvisol, carbon-rich), we hypothesized that different resource demands of microorganism elicit a trade-off in microbial growth potential (Y-strategy) and resource-acquisition (A-strategy) in response to N addition, and consequently on necromass formation and soil carbon stability. We combined measurements of necromass metrics (MCP efficacy) and soil carbon stability (chemical composition and mineral associated organic carbon) with potential changes in microbial life history strategies (assessed via soil metagenomes and enzymatic activity analyses). The contribution of microbial necromass to SOC decreased with N addition in the Cambisol, but increased in the Luvisol. Soil microbial life strategies displayed two distinct responses in two soils after N amendment: shift toward A-strategy (Cambisol) or Y-strategy (Luvisol). These divergent responses are owing to the stoichiometric imbalance between microbial demands and resource availability for C and N, which presented very distinct patterns in the two soils. The partial correlation analysis further confirmed that high N addition aggravated stoichiometric carbon demand, shifting the microbial community strategy toward resource-acquisition which reduced carbon stability in Cambisol. In contrast, the microbial Y-strategy had the positive direct effect on MCP efficacy in Luvisol, which greatly enhanced carbon stability. Such findings provide mechanistic insights into the stoichiometric regulation of MCP efficacy, and how this is mediated by site-specific trade-offs in microbial life strategies, which contribute to improving our comprehension of soil microbial C sequestration and potential optimization of agricultural N management.

Abstract Image

微生物的生活史策略介导微生物碳泵的功效,以应对氮管理,这取决于微生物需求的化学计量法
人们越来越认识到,土壤微生物碳泵(MCP)与土壤有机碳(SOC)的积累和稳定性直接相关。鉴于碳(C)和氮(N)循环的密切耦合以及它们的化学计量对微生物生长的限制,氮的添加可能会影响微生物的生长策略,从而对新陈代谢的形成和碳的稳定性产生潜在影响。然而,这一课题在很大程度上仍未得到探讨。基于在北方(寒武纪,碳贫瘠)和西南(卢维索尔,碳丰富)两种土壤肥力对比强烈的土壤中进行的为期 10 年的两次多级氮肥实验,我们假设微生物的不同资源需求会引起微生物生长潜力(Y 级策略)和资源获取(A 级策略)的权衡,以应对氮的添加,并进而影响坏死物质的形成和土壤碳的稳定性。我们将坏死物质指标(MCP 效能)和土壤碳稳定性(化学成分和与矿物相关的有机碳)的测量结果与微生物生活史策略的潜在变化(通过土壤元基因组和酶活性分析进行评估)相结合。在 Cambisol,微生物坏死物质对 SOC 的贡献随着氮的添加而减少,但在 Luvisol 则有所增加。氮添加后,两种土壤中的土壤微生物生命策略表现出两种截然不同的反应:转向 A 策略(寒武纪土壤)或 Y 策略(路维索尔土壤)。这些不同的反应是由于微生物对碳和氮的需求与资源可用性之间的化学计量失衡造成的,在两种土壤中呈现出截然不同的模式。偏相关分析进一步证实,高氮添加量加剧了碳的化学计量需求,使微生物群落策略转向资源获取,从而降低了寒武壤中碳的稳定性。与此相反,微生物的 Y 战略对 Luvisol 中的 MCP 效能有直接的积极影响,从而大大提高了碳的稳定性。这些发现从机理上揭示了 MCP 效能的化学计量调控,以及如何通过特定地点的微生物生命策略权衡来实现这一调控,有助于提高我们对土壤微生物固碳的理解,并为农业氮管理的潜在优化做出贡献。
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来源期刊
Global Change Biology
Global Change Biology 环境科学-环境科学
CiteScore
21.50
自引率
5.20%
发文量
497
审稿时长
3.3 months
期刊介绍: Global Change Biology is an environmental change journal committed to shaping the future and addressing the world's most pressing challenges, including sustainability, climate change, environmental protection, food and water safety, and global health. Dedicated to fostering a profound understanding of the impacts of global change on biological systems and offering innovative solutions, the journal publishes a diverse range of content, including primary research articles, technical advances, research reviews, reports, opinions, perspectives, commentaries, and letters. Starting with the 2024 volume, Global Change Biology will transition to an online-only format, enhancing accessibility and contributing to the evolution of scholarly communication.
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