Meridional eddy transport across the Antarctic Circumpolar Current is an essential component of the global meridional overturning circulation and the transport of climate relevant tracers. Challenges in comparing model and observational estimates of the transport arise from varying methodologies describing ‘eddy’ processes. We reconcile the approach used in shipboard surveys of eddies, complemented by satellite eddy tracking, with Reynolds decomposition applied to model outputs. This allows us to estimate the fraction of total meridional tracer transport attributed to coherent eddies in a global 0.1$^\circ$ ocean model. The model realistically simulates observed eddy kinetic energy and three-dimensional characteristics, particularly in representing an observed cyclonic eddy near 150 \degrees E, a hotspot for poleward heat flux. Annual meridional transports due to coherent eddies crossing the Subantarctic Front are estimated by vertically and radially integrating the tracer contents of all eddies. Notably, only cyclonic eddies moving equatorward across the Subantarctic Front contribute to the coherent eddy transport, with no anticyclonic eddies found to cross the front poleward in this region. Applying Reynolds decomposition, our study reveals predominantly poleward meridional transports due to all transient processes in a standing meander, particularly between the northern and southern branches of the Subantarctic Front. Coherent, long-lived eddies tracked from satellite data contribute less than 20\% to transient poleward heat transport, and equatorward nitrate transport in the model. Furthermore, we demonstrate that the integrated surface elevation of mesoscale eddies serves as a reliable proxy for inferring subsurface eddy content.

Tyler Rohr

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For nearly a century, the functional response curves, which describe how predation rates vary with prey density, have been a mainstay of ecological modelling. While originally derived to describe terrestrial interactions, they have been adopted to characterize aquatic systems in marine biogeochemical, size-spectrum, and population models. However, marine ecological modellers disagree over the qualitative shape of the curve (e.g. Type II vs. III), whether its parameters should be mechanistically or empirically defined (e.g. disk vs. Michaelis-Menten scheme), and the most representative value of those parameters. As a case study, we focus on marine biogeochemical models, providing a comprehensive theoretical, empirical, and numerical road-map for interpreting, formulating, and parameterizing the functional response when used to prescribe zooplankton specific grazing rates on a single prey source. After providing a detailed derivation of each of the canonical functional response types explicitly for aquatic systems, we review the literature describing their parameterization. Empirical estimates of each parameter vary by over three orders of magnitude across 10 orders of magnitude in zooplankton size. However, the strength and direction of the allometric relationship between each parameter and size differs depending on the range of sizes being considered. In models, which must represent the mean state of different functional groups, size spectra or in many cases the entire ocean’s zooplankton population, the range of parameter values is smaller, but still varies by two to three orders of magnitude. Next, we conduct a suite of 0-D NPZ simulations to isolate the sensitivity of phytoplankton population size and stability to the grazing formulation. We find that the disk parameterizations scheme is much less sensitive to it parameterization than the Michaelis-Menten scheme, and quantify the range of parameters over which the Type II response, long known to have destabilizing properties, introduces dynamic instabilities. Finally, we use a simple theoretical model to show how the mean apparent functional response, averaged across sufficient sub-grid scale heterogeneity diverges from the local response. Collectively, we recommend using a type II disk response for models with smaller scales and finer resolutions but suggest that a type III Michaelis-Menten response may do a better job of capturing the complexity of all processes being averaged across in larger scale and coarser resolution modal, not just local consumption and capture rates. While we focus specifically on the grazing formulation in marine biogeochemical models, we believe these recommendations are robust across a much broader range of ecosystem models.