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Comprehensive field observations characterizing the biological carbon pump (BCP) provide the foundation needed to constrain mechanistic models of downward particulate organic carbon (POC) flux in the ocean. Sediment traps were deployed three times during the EXport Processes in the Ocean from RemoTe Sensing campaign at Ocean Station Papa in August–September 2018. We propose a new method to correct sediment trap sample contamination by zooplankton “swimmers.” We consider the advantages of polyacrylamide gel collectors to constrain swimmer influence and estimate the magnitude of possible trap biases. Measured sediment trap fluxes of thorium-234 are compared to water column measurements to assess trap performance and estimate the possible magnitude of fluxes by vertically migrating zooplankton that bypassed traps. We found generally low fluxes of sinking POC (1.38 ± 0.77 mmol C m–2 d–1 at 100 m, n = 9) that included high and variable contributions by rare, large particles. Sinking particle sizes generally decreased between 100 and 335 m. Measured 234Th fluxes were smaller than water column 234Th fluxes by a factor of approximately 3. Much of this difference was consistent with trap undersampling of both small (<32 μm) and rare, large particles (>1 mm) and with zooplankton active migrant fluxes. The fraction of net primary production exported below the euphotic zone (0.1% light level; Ez-ratio = 0.10 ± 0.06; ratio uncertainties are propagated from measurements with n = 7–9) was consistent with prior, late summer studies at Station P, as was the fraction of material exported to 100 m below the base of the euphotic zone (T100, 0.55 ± 0.35). While both the Ez-ratio and T100 parameters varied weekly, their product, which we interpret as overall BCP efficiency, was remarkably stable (0.055 ± 0.010), suggesting a tight coupling between production and recycling at Station P.

Atmospheric deposition is an important input route of trace elements (TEs) to the global ocean. As atmospheric inputs impact phytoplankton community health and dynamics, atmospheric TE fluxes, and in particular atmospheric iron fluxes, are a key component of marine biogeochemical models. Trace element concentrations were determined in dry (aerosols) and wet (precipitation) deposition samples from the North Atlantic, north of 40°N, during the GEOVIDE cruise (GEOTRACES cruise GA01) in May/June 2014. Atmospheric aerosol loading in the study region was low (~2-500 ng m -3 ) throughout the cruise, as inferred from the very low aerosol Ti concentrations determined (0.0084-1.9 ng m -3 ). Wet deposition appeared to be of roughly equal or greater importance than dry deposition to the total depositional flux of TEs, which is consistent with other regions of the Atlantic Ocean outside of the influence of the Saharan plume.It can be challenging to convert aerosol chemical composition data into reliable flux estimates, due to the uncertainties associated with the parameterisation of dry deposition velocity, and precipitation rate.Therefore, the goal of this study was to compare TE flux estimates derived from two different techniques: (1) the traditional approach of summed wet and dry deposition TE fluxes, using concentration data, precipitation rates, and dry deposition velocities and, (2) using the inventory of the cosmogenic radioisotope beryllium-7 ( 7 Be) in the upper ocean as a proxy for atmospheric deposition. These two approaches yielded TE flux estimates that were in excellent agreement (within one standard deviation) for about half of the TEs under investigation. However, for the remaining TEs differences between the flux estimates ranged from two to forty times, with the traditional approach generally being the higher of the two estimates. Therefore, factors that may contribute to this variation, such as differences in the timescale of integration and selection of representative deposition velocities and precipitation rates, are discussed. Our results suggest that the 7 Be approach continues to show promise in this application, particularly in regions where precipitation samples cannot be routinely collected.

The goal of the EXport Processes in the Ocean from RemoTe Sensing (EXPORTS) field campaign is to develop a predictive understanding of the export, fate, and carbon cycle impacts of global ocean net primary production. To accomplish this goal, observations of export flux pathways, plankton community composition, food web processes, and optical, physical, and biogeochemical (BGC) properties are needed over a range of ecosystem states. Here we introduce the first EXPORTS field deployment to Ocean Station Papa in the Northeast Pacific Ocean during summer of 2018, providing context for other papers in this special collection. The experiment was conducted with two ships: a Process Ship, focused on ecological rates, BGC fluxes, temporal changes in food web, and BGC and optical properties, that followed an instrumented Lagrangian float; and a Survey Ship that sampled BGC and optical properties in spatial patterns around the Process Ship. An array of autonomous underwater assets provided measurements over a range of spatial and temporal scales, and partnering programs and remote sensing observations provided additional observational context. The oceanographic setting was typical of late-summer conditions at Ocean Station Papa: a shallow mixed layer, strong vertical and weak horizontal gradients in hydrographic properties, sluggish sub-inertial currents, elevated macronutrient concentrations and low phytoplankton abundances. Although nutrient concentrations were consistent with previous observations, mixed layer chlorophyll was lower than typically observed, resulting in a deeper euphotic zone. Analyses of surface layer temperature and salinity found three distinct surface water types, allowing for diagnosis of whether observed changes were spatial or temporal. The 2018 EXPORTS field deployment is among the most comprehensive biological pump studies ever conducted. A second deployment to the North Atlantic Ocean occurred in spring 2021, which will be followed by focused work on data synthesis and modeling using the entire EXPORTS data set.

The Arctic sea‐ice extent reached a record minimum in September 2012. Sea‐ice decline increases the absorption of solar energy in the Arctic Ocean, affecting primary production and the plankton community. How this will modulate the sinking of particulate organic carbon (POC) from the ocean surface remains a key question. We use the 234Th/238U and 210Po/210Pb radionuclide pairs to estimate the magnitude of the POC export fluxes in the upper ocean of the central Arctic in summer 2012, covering time scales from weeks to months. The 234Th/238U proxy reveals that POC fluxes at the base of the euphotic zone were very low (2 ± 2 mmol C m−2 d−1) in late summer. Relationships obtained between the 234Th export fluxes and the phytoplankton community suggest that prasinophytes contributed significantly to the downward fluxes, likely via incorporation into sea‐ice algal aggregates and zooplankton‐derived material. The magnitude of the depletion of 210Po in the upper water column over the entire study area indicates that particle export fluxes were higher before July/August than later in the season. 210Po fluxes and 210Po‐derived POC fluxes correlated positively with sea‐ice concentration, showing that particle sinking was greater under heavy sea‐ice conditions than under partially ice‐covered regions. Although the POC fluxes were low, a large fraction of primary production (>30%) was exported at the base of the euphotic zone in most of the study area during summer 2012, indicating a high export efficiency of the biological pump in the central Arctic.