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Sinking particles play a key role in the biological carbon pump. While previous studies have analyzed particulate carbon flux over timescales of days to years, few have been able to resolve flux variability on shorter, hourly scales at multiple depths simultaneously. This study uses an array of upward‐facing cameras, built from off‐the‐shelf components for under $500 each, to visualize particle fluxes at multiple depths during the EXPORTS campaign in 2018 in the North Pacific. This manuscript is the first comprehensive description of this tool, called GelCam, which captures a time‐lapse image sequence at 20‐min intervals of particles that settle into a polyacrylamide gel layer located at the base of a sediment trap tube. Methods are described for the design and post‐processing pipeline, in addition to two proxy methods for estimating the total particulate organic carbon flux. The GelCam‐derived fluxes modeled from individual particle images show strong agreement with the ground‐truth data obtained from coincident trap measurements. This approach helps address the need for accessible, open‐source tools to more broadly observe and quantify the role of episodic particle flux events across the global oceans. 

Measurements of particulate organic carbon (POC) are critical for understanding the ocean carbon cycle, including biogenic particle formation and removal processes, and for constraining models of carbon cycling at local, regional, and global scales. Despite the importance and ubiquity of POC measurements, discrepancies in methods across platforms and users, necessary to accommodate a multitude of needs and logistical constraints, commonly result in disparate results. Considerations of filter type and pore size, sample volume, collection method, and contamination sources underscore the potential for dissimilar measurements of the same variable assessed using similar and different approaches. During the NASA EXport Processes in the Ocean from RemoTe Sensing (EXPORTS) 2018 field campaign in the North Pacific Ocean, multiple methodologies and sampling approaches for determining POC were applied, including surface inline flow-through systems and depth profiles using Niskin bottles, in situ pumps, and Marine Snow Catchers. A comparison of results from each approach and platform often resulted in significant differences. Supporting measurements, however, provided the means to normalize results across datasets. Using knowledge of contrasting protocols and synchronous or near-synchronous measurements of associated environmental variables, we were able to reconcile dataset differences to account for undersampling of some particle types and sizes, possible sample contamination and blank corrections. These efforts resulted in measurement agreement between initially contrasting datasets and insights on long-acknowledged but rarely resolved discrepancies among contrasting methods for assessing POC concentrations in the ocean. 

Abstract Particulate organic matter settling out of the euphotic zone is a major sink for atmospheric carbon dioxide and serves as a primary food source to mesopelagic food webs. Degradation of this organic matter encompasses a suite of mechanisms that attenuate flux, including heterotrophic metabolic processes of microbes and metazoans. The relative contributions of microbial and metazoan heterotrophy to flux attenuation, however, have been difficult to determine. We present results of compound specific nitrogen isotope analysis of amino acids of sinking particles from sediment traps and size‐fractionated particles from in situ filtration between the surface and 500 m at Ocean Station Papa, collected during NASA EXPORTS (EXport Processes in the Ocean from RemoTe Sensing). With increasing depth, we observe: (1) that, based on theδ¹⁵N values of threonine, fecal pellets dominate the sinking particle flux and that attenuation of downward particle flux occurs largely via disaggregation in the upper mesopelagic; (2) an increasing trophic position of particles in the upper water column, reflecting increasing heterotrophic contributions to the nitrogen pool and the loss of particles via remineralization; and (3) increasingδ¹⁵N values of source amino acids in submicron and small (1–6μm) particles, reflecting microbial particle solubilization. We further employ a Bayesian mixing model to estimate the relative proportions of fecal pellets, phytodetritus, and microbially degraded material in particles and compare these results and our interpretations of flux attenuation mechanisms to other, independent methods used during EXPORTS. 

Abstract Sinking particles strongly regulate the distribution of reactive chemical substances in the ocean, including particulate organic carbon and other elements (e.g., P, Cd, Mn, Cu, Co, Fe, Al, and²³²Th). Yet, the sinking fluxes of trace elements have not been well described in the global ocean. The U.S. GEOTRACES campaign in the North Atlantic (GA03) offers the first data set in which the sinking flux of carbon and trace elements can be derived using four different radionuclide pairs (²³⁸U^:234Th^;210Pb:²¹⁰Po;²²⁸Ra:²²⁸Th; and²³⁴U:²³⁰Th) at stations co‐located with sediment trap fluxes for comparison. Particulate organic carbon, particulate P, and particulate Cd fluxes all decrease sharply with depth below the euphotic zone. Particulate Mn, Cu, and Co flux profiles display mixed behavior, some cases reflecting biotic remineralization, and other cases showing increased flux with depth. The latter may be related to either lateral input of lithogenic material or increased scavenging onto particles. Lastly, particulate Fe fluxes resemble fluxes of Al and²³²Th, which all have increasing flux with depth, indicating a dominance of lithogenic flux at depth by resuspended sediment transported laterally to the study site. In comparing flux estimates derived using different isotope pairs, differences result from different timescales of integration and particle size fractionation effects. The range in flux estimates produced by different methods provides a robust constraint on the true removal fluxes, taking into consideration the independent uncertainties associated with each method. These estimates will be valuable targets for biogeochemical modeling and may also offer insight into particle sinking processes.