Johanna Pausch, Maire Holz, Biao Zhu, Weixin Cheng
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引用次数: 0
摘要
根圈中氮的供应依赖于根-微生物的相互作用,根系渗出物通过根圈启动效应(RPE)引发土壤有机质(SOM)分解。虽然微生物坏死物质对有机结合土壤氮(N)的贡献很大,但 RPE 在调节坏死物质循环和植物氮获取方面的作用却很少受到关注。与其他土壤氮形式相比,坏死物质富含 15 N,因此我们使用 15 N 自然丰度作为坏死物质氮的替代物。我们合并了采用相同实验设计对不同植物物种和相同土壤类型进行连续 13 CO2 标记的研究,但考虑到了表土和底土。RPE 被量化为种植土壤与未种植土壤之间 SOM 分解的差异。结果表明,随着 RPE 的增加,植物的氮吸收量也随之增加。芽和根的 15 N 富集与 RPE 之间的正相关关系表明,RPE 增强了坏死-N 的转化。此外,我们的数据还显示,在表土中,随着碳(C)输入量的增加,RPE 通过根瘤沉积达到饱和。在底土中,RPE 在较小的碳输入范围内呈线性增长,这表明根释放的碳对较深土壤层的分解速率有很大影响。总之,这项研究证实了根瘤菌释放的 C 对植物获取氮具有重要作用,因为根瘤菌增强了新陈代谢。
Rhizosphere priming promotes plant nitrogen acquisition by microbial necromass recycling
Nitrogen availability in the rhizosphere relies on root-microorganism interactions, where root exudates trigger soil organic matter (SOM) decomposition through the rhizosphere priming effect (RPE). Though microbial necromass contribute significantly to organically bound soil nitrogen (N), the role of RPEs in regulating necromass recycling and plant nitrogen acquisition has received limited attention. We used 15N natural abundance as a proxy for necromass-N since necromass is enriched in 15N compared to other soil-N forms. We combined studies using the same experimental design for continuous 13CO2 labelling of various plant species and the same soil type, but considering top- and subsoil. RPE were quantified as difference in SOM-decomposition between planted and unplanted soils. Results showed higher plant N uptake as RPEs increased. The positive relationship between 15N-enrichment of shoots and roots and RPEs indicated an enhanced necromass-N turnover by RPE. Moreover, our data revealed that RPEs were saturated with increasing carbon (C) input via rhizodeposition in topsoil. In subsoil, RPEs increased linearly within a small range of C input indicating a strong effect of root-released C on decomposition rates in deeper soil horizons. Overall, this study confirmed the functional importance of rhizosphere C input for plant N acquisition through enhanced necromass turnover by RPEs.
期刊介绍:
Plant, Cell & Environment is a premier plant science journal, offering valuable insights into plant responses to their environment. Committed to publishing high-quality theoretical and experimental research, the journal covers a broad spectrum of factors, spanning from molecular to community levels. Researchers exploring various aspects of plant biology, physiology, and ecology contribute to the journal's comprehensive understanding of plant-environment interactions.