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Abstract The enzyme carbonic anhydrase (CA) is crucial to many physiological processes involvingCO2, from photosynthesis and respiration, to calcification andCaCO3dissolution. We present new measurements of CA activity along a North Pacific transect, on samples from in situ pumps, sediment traps, discreet plankton samples from the ship's underway seawater line, plankton tows, and surface sediment samples from multicores. CA activity is highest in the surface ocean and decreases with depth, both in suspended and sinking particles. Subpolar gyre surface particles exhibit 10× higher CA activity per liter of seawater compared to subtropical gyre surface particles. Activity persists to 4700 m in the subpolar gyre, but only to 1000 m in the subtropics. All sinking CA activity normalized to particulate organic carbon (POC) follows a single relationship (CA/POC = 1.9 ± 0.2 × 10−7mol mol−1). This relationship is consistent with CA/POC values in subpolar plankton tow material, suspended particles, and core top sediments. We hypothesize that most subpolar CA activity is associated with rapidly sinking diatom blooms, consistent with a large mat of diatomaceous material identified on the seafloor. Compared to the basin‐wide sinking CA/POC relationship, a lower subtropical CA/POC suggests that the inventory of subtropical biomass is different in composition from exported material. Pteropods also demonstrate substantial CA activity. Scaled to the volume within pteropod shells, first‐orderCO2hydration rate constants are elevated ≥ 1000× above background. This kinetic enhancement is large enough to catalyze carbonate dissolution within microenvironments, providing observational evidence for CA‐catalyzed, respiration‐drivenCaCO3dissolution in the shallow North Pacific.
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What Controls the Large‐Scale Efficiency of Carbon Transfer Through the Ocean's Mesopelagic Zone? Insights From a New, Mechanistic Model (MSPACMAM)
Abstract A key challenge for current‐generation Earth system models (ESMs) is the simulation of the penetration of sinking particulate organic carbon (POC) into the ocean interior, which has implications for projections of future oceanic carbon sequestration in a warming climate. This paper presents a new, cost‐efficient, mechanistic 1D model that prognostically calculates POC fluxes by carrying four component particles in two different size classes. Gravitational settling and removal/transformation processes are represented explicitly through parameterizations that incorporate the effects of particle size and density, dissolved oxygen, calcite and aragonite saturation states, and seawater temperature, density, and viscosity. The model reproduces the observed POC flux attenuation at 22 locations in the North Atlantic and North Pacific. The model is applied over a global ocean domain with seawater properties prescribed from observation‐based climatologies in order to address an important scientific question: What controls the spatial pattern of mesopelagic POC transfer efficiency? The simulated vertical POC transfer is more efficient at high latitudes than at low latitudes with the exception of oxygen minimum zones, which is consistent with recent inverse modeling and neutrally buoyant sediment trap studies. Here, model experiments show that the relative abundance of large‐sized, rapidly sinking particles and the slower rate of remineralization at high latitudes compensate for the region's lack of calcium carbonate ballast and the cold‐water viscous resistance, leading to higher transfer efficiencies compared to low‐latitude regions. The model could be deployed in ESMs in order to diagnose the impacts of climate change on oceanic carbon sequestration and vice versa.
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- Award ID(s):
- 2019589
- PAR ID:
- 10559555
- Publisher / Repository:
- AGU Publications
- Date Published:
- Journal Name:
- Global Biogeochemical Cycles
- Volume:
- 36
- Issue:
- 10
- ISSN:
- 0886-6236
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1029/2021GB007131
