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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. 

Imaging FlowCytobot (IFCB) deployments have been conducted since June 2006 at the Martha’s Vineyard Coastal Observatory (MVCO; 41° 19.5’ N, 70° 34.0’ W). IFCB, an automated submersible imaging-in-flow cytometer, is specially designed to operate in the ocean and image plankton and other particulate material approximately 5 to 200 micrometers in length. In conjunction with image acquisition, IFCB also uses a diode laser to measure the chlorophyll fluorescence and light scattering associated each imaged target. IFCB typically produces thousands of photomicrographs and associated laser signals each hour. The web-based IFCB dashboard provides browse capability and access to the entire image data set.