Abstract
Microbes are the drivers of soil phosphorus (P) cycling in terrestrial ecosystems; however, the role of soil microbes in mediating P cycling in P-rich soils during primary succession remains uncertain. This study examined the impacts of bacterial community structure (diversity and composition) and its functional potential (absolute abundances of P-cycling functional genes) on soil P cycling along a 130-year glacial chronosequence on the eastern Tibetan Plateau. Bacterial community structure was a better predictor of soil P fractions than P-cycling genes along the chronosequence. After glacier retreat, the solubilization of inorganic P and the mineralization of organic P were significantly enhanced by increased bacterial diversity, changed interspecific interactions, and abundant species involved in soil P mineralization, thereby increasing P availability. Although 84% of P-cycling genes were associated with organic P mineralization, these genes were more closely associated with soil organic carbon than with organic P. Bacterial carbon demand probably determined soil P turnover, indicating the dominant role of organic matter decomposition processes in P-rich alpine soils. Moreover, the significant decrease in the complexity of the bacterial co-occurrence network and the taxa-gene-P network at the later stage indicates a declining dominance of the bacterial community in driving soil P cycling with succession. Our results reveal that bacteria with a complex community structure have a prominent potential for biogeochemical P cycling in P-rich soils during the early stages of primary succession.
| Original language | English |
|---|---|
| Article number | e2024GB008174 |
| Number of pages | 16 |
| Journal | Global Biogeochemical Cycles |
| Volume | 38 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - Oct 2024 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2024. American Geophysical Union. All Rights Reserved.
Keywords
- bacterial community structure
- functional genes
- glacier forefield
- microbial carbon demand
- phosphorus cycling
- primary succession