EGU24-493, updated on 08 Mar 2024
https://doi.org/10.5194/egusphere-egu24-493
EGU General Assembly 2024
© Author(s) 2024. This work is distributed under
the Creative Commons Attribution 4.0 License.

Nitrogen removal and carbon mineralization under coastal salinity intrusion

Ziyan Wang1 and Benoit Thibodeau1,2
Ziyan Wang and Benoit Thibodeau
  • 1School of Life Sciences, The Chinese University of Hong Kong, Hong Kong, China (1155186101@link.cuhk.edu.hk)
  • 2Earth and Environmental Sciences Programme, the Chinese University of Hong Kong, Hong Kong, China (benoit.thibodeau@cuhk.edu.hk)

Rapid population growth and intensification of human activities have led to a massive increase in the release of nitrogen (N) to the environment, often ending up in aquatic ecosystems. Coastal wetlands, a transition ecosystem in the freshwater-to-marine continuum, play a vital role in reducing nitrogen through natural processes, including denitrification and anaerobic ammonium oxidation (anammox). Considering denitrification's risk of producing nitrous oxide—a potent greenhouse gas—and anammox's efficient co-removal of ammonium and nitrite, it's crucial to identify what controls the balance between these two key processes. However, the identity of the drivers controlling the relative abundance of these two N-removal processes and their respective interactions with carbon (C) and sulfur cycles are not well-documented, especially in coastal wetlands.

This study investigated salinity's role in N reduction with carbon remineralization in coastal wetlands facing salinity intrusion. Using air-dried mangrove sediments mixed with anoxic artificial seawater of contrasting salinities (0, 10, 20, and 30 ppt) over a 28-day period, we monitored N and C transformation by the concentration of NH4+, NO2-, NO3-, dissolved inorganic carbon (DIC) and total alkalinity in the supernatant, and microbial community adaptation in sediment by molecular analysis. We applied the revised 15N-paring isotope technique in slurry incubation to quantify the potential of N loss pathways.

Preliminary results indicate that significant N removal starts after a week of internal cycling between organic and inorganic N, with the maximum removal potential at 30 ppt salinity. Depletion of NO3- in the last week of incubation makes anammox stand out by utilizing NH4+ and NO2-. The rate of DIC release decreased with increasing salinity, displaying an inverse pattern to that of N species. This decoupling points to the co-existence of autotrophic anammox, heterotrophic denitrification, and sulfate reduction processes. The stoichiometric ratio of total alkalinity to DIC suggests a shift of the predominant carbon decomposition process as salinity increased, from denitrification to sulfate reduction. This shift could enhance the total nitrogen removal potential while slowing carbon remineralization, indicating a positive feedback loop for both nitrogen removal and blue carbon storage in response to salinity intrusion. We will further focus on 15N2 samples and microbial evidence to elucidate the interplay among nitrogen removal processes.

How to cite: Wang, Z. and Thibodeau, B.: Nitrogen removal and carbon mineralization under coastal salinity intrusion, EGU General Assembly 2024, Vienna, Austria, 14–19 Apr 2024, EGU24-493, https://doi.org/10.5194/egusphere-egu24-493, 2024.