Abstract
Sinking diatom aggregates are important components of vertical elemental fluxes and represent ‘hotspots’ of microbial-driven remineralization in the water column. A combined analytical approach of microsensors and fluorometry was used to measure oxygen (O2) and ammonium (NH4+) concentrations in sinking diatom aggregates as a function of the ambient O2 concentrations. Diffusive fluxes of O2 and NH4+ within and around sinking aggregates were subsequently analyzed using a diffusion–reaction model. Diffusion limitation of O2 within the diatom aggregates occurred when ambient O2 concentrations decreased beneath 100μM. At ambient O2 concentrations of 20μM, the measured flux of O2 to aggregates was equivalent to 33% of fluxes when O2 concentrations were in equilibrium with the atmosphere and approximately 50% of the aggregate volume was anoxic. When the diatom aggregates were maintained under hypoxic conditions, NH4+ was produced in a ratio of −8.9mol O2 consumed:1mol NH4+ produced which is within the expected range during ammonification. The average POC-specific respiration rate and the average PON-specific NH4+ production rate under hypoxic conditions were 0.065d−1 and 0.052d−1, respectively. Under anoxic conditions, the NH4+ release was 18% of that measured under hypoxic conditions. Our empirical and modeled data revealed diatom aggregates to be microenvironments of elevated NH4+ concentrations ranging from 1 to 8μM and therefore to be potential sources of NH4+ in the oxygen minimum zones in the ocean.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.