Coastal blue carbon (C) ecosystems are recognized as efficient natural C sinks and play key roles in mitigating global climate change. Microbially driven C, nitrogen (N) and sulphur (S) cycles are crucial for ecosystem functioning, but how microorganisms drive C sink formation and C sequestration in coastal sediments remains unclear.
In this study, we conducted a comprehensive analysis of amino sugars, C, N and S cycling genes/pathways and their associated taxa in coastal sediments of native (Cyperus malaccensis and Kandelia obovata) and alien (Spartina alterniflora and Sonneratia apetala) vegetation.
Compared to the alien‐vegetated coastal sediment, the native‐vegetated coastal sediment had significantly (p < 0.05) higher microbial necromass C and higher functional potentials of chemoautotrophic C fixation, C degradation, methane cycling, N2 fixation, S oxidation and sulphate reduction. Also, our analysis of coastal sediment microbiomes showed that S oxidation could be coupled with C fixation and/or nitrate/nitrite reduction. S oxidation, C degradation and C fixation were found to be key functional pathways for predicting sediment microbial necromass C. Additionally, the sulphur‐oxidizing Burkholderiales metagenome‐assembled genomes (MAGs) were a key functional group that dominated chemoautotrophic C fixation in coastal sediments.
These results suggested that chemoautotrophic S oxidizers, in particular Burkholderiales with a novel lineage, might be the key microbial group that dominates microbial necromass C formation in coastal sediments through microbial anabolism (C fixation);the coupling of microbially driven C, N and S cycling processes; and the deposition of microbially derived C. This study provides novel insights into the importance of chemoautotrophic S oxidizers for microbial necromass formation and shed new light on the microbial mechanism of C sink formation in coastal ecosystems, which also has important implications for enhancing C sequestration in coastal wetlands.
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