Wanxuan Yao

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Marine carbon dioxide removal (mCDR) and geological carbon storage in the marine environment (mCS) promise to contribute to the mitigation of global climate change in combination with drastic emission reductions. However, the implementable potential of mCDR and mCS depends, apart from technology readiness, also on site-specific conditions. In this paper, we explore different options for mCDR and mCS, using the German context as a case study. We challenge each option to remove 10 Mt CO2 yr-1, which accounts for 8-22% of projected hard-to-abate and residual emissions of Germany in 2045. We focus on the environmental, resource, and infrastructure requirements of individual mCDR and mCS options at a specific site, within the German jurisdiction when possible. Furthermore, we discuss main uncertainty factors and research needs, and, where possible, cost estimates, expected environmental effects, and monitoring approaches. In total, we describe ten mCDR and mCS options; four aim at enhancing the chemical carbon uptake of the ocean through alkalinity enhancement, four aim at enhancing blue carbon ecosystems’ sink capacity, and two employ geological off-shore storage. Our results indicate that five out of ten options would potentially be implementable within German jurisdiction, and three of them could potentially rise to the challenge. This exercise provides a basis for further studies to assess the socio-economic, ethical, political, and legal aspects for such implementations.
Iron is a key micronutrient controlling phytoplankton growth in vast regions of the global ocean. Despite its importance, uncertainties remain high regarding external iron source fluxes and internal cycling on a global scale. In this study, we used a global dissolved iron dataset, including GEOTRACES measurements, to constrain source and scavenging fluxes in the marine iron component of a global ocean biogeochemical model. Our model simulations tested three key uncertainties: source inputs of atmospheric soluble iron deposition (varying from 1.4 - 3.4 Gmol/yr), reductive sedimentary iron release (14 - 117 Gmol/yr), and compare a variable ligand parameterization to a constant distribution. In each simulation, scavenging rates were adjusted to reproduce the observed global mean iron inventory for consistency. The apparent oxygen utilization term in the variable ligand parameterization significantly improved the model-data misfit, suggesting that heterotrophic bacteria are an important source of ligands to the ocean. Model simulations containing high source fluxes of atmospheric soluble iron deposition (3.4 Gmol/yr) and reductive sedimentary iron release (114 Gmol/yr) further improved the model, which then required high scavenging rates to maintain the observed iron inventory in these high source scenarios. Our model-data analysis suggests that the global marine iron cycle operates with high source fluxes and high scavenging rates, resulting in relatively short surface and global ocean mean residence times of 0.83 and 7.5 years, respectively, which are on the low-end of previous model estimates. Model biases and uncertainties remain high and are discussed to help improve global marine iron cycle models.