美国表土中细菌和真菌的宏观生态学分化

IF 5.4 2区 地球科学 Q1 ENVIRONMENTAL SCIENCES Global Biogeochemical Cycles Pub Date : 2023-10-26 DOI:10.1029/2023GB007706
Liyuan He, Nicolas Viovy, Xiaofeng Xu
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引用次数: 0

摘要

细菌和真菌具有不同的生理特性。它们的宏观生态学对于碳循环等生态系统功能至关重要。然而,细菌和真菌的生物地理学及其潜在机制仍然难以捉摸。在这项研究中,我们通过整合微生物显式模型CLM Microbe与34个近地天体站点的真菌(FBC)和细菌生物量碳(BBC),研究了细菌与真菌的宏观生态学。FBC、BBC和FBC:BC(F:B)比率在不同地点的分布得到了很好的模拟,CLM-Microbe模型分别解释了99%(P<;0.001)、97%(P<)和99%(P>;0.001)的变化。我们发现,在美国各地,相对于BBC,FBC的生物地理模式更强。真菌和细菌的更替率在纬度上显示出相似的趋势。然而,细菌和真菌之间其成分通量(碳同化、呼吸和尸体大量产生)的纬度趋势是不同的,这些纬度趋势遵循真菌的反单峰模式,并显示出细菌的指数下降反应。碳同化受植被生产力的支配,呼吸受细菌和真菌的年平均温度的支配。它们大量繁殖的主导因素各不相同,土壤因素控制真菌,年均温度控制细菌过程。对真菌和细菌宏观生态学的理解是将微生物代谢与土壤生物地球化学过程联系起来的重要一步。独特的真菌和细菌宏观生态学有助于微生物生态学,特别是在微生物群落结构及其与空间生态系统碳循环的关系方面。
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Macroecology Differentiation Between Bacteria and Fungi in Topsoil Across the United States

Bacteria and fungi possess distinct physiological traits. Their macroecology is vital for ecosystem functioning such as carbon cycling. However, bacterial and fungal biogeography and underlying mechanisms remain elusive. In this study, we investigated bacterial versus fungal macroecology by integrating a microbial-explicit model—CLM-Microbe—with measured fungal (FBC) and bacterial biomass carbon (BBC) from 34 NEON sites. The distribution of FBC, BBC, and FBC: BBC (F:B) ratio was well simulated across sites, with variations in 99% (P < 0.001), 97% (P < 0.001), and 99% (P < 0.001) being explained by the CLM-Microbe model, respectively. We found stronger biogeographic patterns of FBC relative to BBC across the United States. Fungal and bacterial turnover rates showed similar trends along latitude. However, latitudinal trends of their component fluxes (carbon assimilation, respiration, and necromass production) were distinct between bacteria and fungi, with those latitudinal trends following inverse unimodal patterns for fungi and showing exponential declining responses for bacteria. Carbon assimilation was dominated by vegetation productivity, and respiration was dominated by mean annual temperature for bacteria and fungi. The dominant factor for their necromass production differs, with edaphic factors controlling fungal and mean annual temperature controlling bacterial processes. The understanding of fungal and bacterial macroecology is an important step toward linking microbial metabolism and soil biogeochemical processes. Distinct fungal and bacterial macroecology contributes to the microbial ecology, particularly on microbial community structure and its association with ecosystem carbon cycling across space.

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来源期刊
Global Biogeochemical Cycles
Global Biogeochemical Cycles 环境科学-地球科学综合
CiteScore
8.90
自引率
7.70%
发文量
141
审稿时长
8-16 weeks
期刊介绍: Global Biogeochemical Cycles (GBC) features research on regional to global biogeochemical interactions, as well as more local studies that demonstrate fundamental implications for biogeochemical processing at regional or global scales. Published papers draw on a wide array of methods and knowledge and extend in time from the deep geologic past to recent historical and potential future interactions. This broad scope includes studies that elucidate human activities as interactive components of biogeochemical cycles and physical Earth Systems including climate. Authors are required to make their work accessible to a broad interdisciplinary range of scientists.
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