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The oceans teem with heterotrophic bacterioplankton that play an appreciable role in the uptake of dissolved organic carbon (DOC) derived from phytoplankton net primary production (NPP). As such, bacterioplankton carbon demand (BCD), or gross heterotrophic production, represents a major carbon pathway that influences the seasonal accumulation of DOC in the surface ocean and, subsequently, the potential vertical or horizontal export of seasonally accumulated DOC. Here, we examine the contributions of bacterioplankton and DOM to ecological and biogeochemical carbon flow pathways, including those of the microbial loop and the biological carbon pump, in the Western North Atlantic Ocean (∼39-54°N along ∼40°W) over a composite annual phytoplankton bloom cycle. Combining field observations with data collected from corresponding DOC remineralization experiments, we estimate the efficiency at which bacterioplankton utilize DOC, demonstrate seasonality in the fraction of NPP that supports BCD, and provide evidence for shifts in the bioavailability and persistence of the seasonally accumulated DOC. Our results indicate that while the portion of DOC flux through bacterioplankton relative to NPP increased as seasons transitioned from high to low productivity, there was a fraction of the DOM production that accumulated and persisted. This persistent DOM is potentially an important pool of organic carbon available for export to the deep ocean via convective mixing, thus representing an important export term of the biological carbon pump.

Four North Atlantic Aerosol and Marine Ecosystems Study (NAAMES) field campaigns from winter 2015 through spring 2018 sampled an extensive set of oceanographic and atmospheric parameters during the annual phytoplankton bloom cycle. This unique dataset provides four seasons of open-ocean observations of wind speed, sea surface temperature (SST), seawater particle attenuation at 660 nm (cp,660, a measure of ocean particulate organic carbon), bacterial production rates, and sea-spray aerosol size distributions and number concentrations (NSSA). The NAAMES measurements show moderate to strong correlations (0.56 < R < 0.70) between NSSA and local wind speeds in the marine boundary layer on hourly timescales, but this relationship weakens in the campaign averages that represent each season, in part because of the reduction in range of wind speed by multiday averaging. NSSA correlates weakly with seawater cp,660 (R = 0.36, P << 0.01), but the correlation with cp,660, is improved (R = 0.51, P < 0.05) for periods of low wind speeds. In addition, NAAMES measurements provide observational dependence of SSA mode diameter (dm) on SST, with dm increasing to larger sizes at higher SST (R = 0.60, P << 0.01) on hourly timescales. These results imply that climate models using bimodal SSA parameterizations to wind speed rather than a single SSA mode that varies with SST may overestimate SSA number concentrations (hence cloud condensation nuclei) by a factor of 4 to 7 and may underestimate SSA scattering (hence direct radiative effects) by a factor of 2 to 5, in addition to overpredicting variability in SSA scattering from wind speed by a factor of 5.

Four North Atlantic Aerosol and Marine Ecosystems Study (NAAMES) field campaigns from winter 2015 through spring 2018 sampled an extensive set of oceanographic and atmospheric parameters during the annual phytoplankton bloom cycle. This unique dataset provides four seasons of open-ocean observations of wind speed, sea surface temperature (SST), seawater particle attenuation at 660 nm (c p,660, a measure of ocean particulate organic carbon), bacterial production rates, and sea-spray aerosol size distributions and number concentrations (N SSA). The NAAMES measurements show moderate to strong correlations (0.56 < R < 0.70) between N SSA and local wind speeds in the marine boundary layer on hourly timescales, but this relationship weakens in the campaign averages that represent each season, in part because of the reduction in range of wind speed by multiday averaging. N SSA correlates weakly with seawater cp,660 (R = 0.36, P << 0.01), but the correlation with cp,660, is improved (R = 0.51, P < 0.05) for periods of low wind speeds. In addition, NAAMES measurements provide observational dependence of SSA mode diameter (d m) on SST, with d m increasing to larger sizes at higher SST (R = 0.60, P << 0.01) on hourly timescales. These results imply that climate models using bimodal SSA parameterizations to wind speed rather than a single SSA mode that varies with SST may overestimate SSA number concentrations (hence cloud condensation nuclei) by a factor of 4 to 7 and may underestimate SSA scattering (hence direct radiative effects) by a factor of 2 to 5, in addition to overpredicting variability in SSA scattering from wind speed by a factor of 5.

The oceans teem with heterotrophic bacterioplankton that play an appreciable role in the uptake of dissolved organic carbon (DOC) derived from phytoplankton net primary production (NPP). As such, bacterioplankton carbon demand (BCD), or gross heterotrophic production, represents a major carbon pathway that influences the seasonal accumulation of DOC in the surface ocean and, subsequently, the potential vertical or horizontal export of seasonally accumulated DOC. Here, we examine the contributions of bacterioplankton and DOM to ecological and biogeochemical carbon flow pathways, including those of the microbial loop and the biological carbon pump, in the Western North Atlantic Ocean (∼39–54°N along ∼40°W) over a composite annual phytoplankton bloom cycle. Combining field observations with data collected from corresponding DOC remineralization experiments, we estimate the efficiency at which bacterioplankton utilize DOC, demonstrate seasonality in the fraction of NPP that supports BCD, and provide evidence for shifts in the bioavailability and persistence of the seasonally accumulated DOC. Our results indicate that while the portion of DOC flux through bacterioplankton relative to NPP increased as seasons transitioned from high to low productivity, there was a fraction of the DOM production that accumulated and persisted. This persistent DOM is potentially an important pool of organic carbon available for export to the deep ocean via convective mixing, thus representing an important export term of the biological carbon pump.

Mesoscale eddies play a key role in structuring open ocean ecosystems, affecting the entire trophic web from primary producers to large pelagic predators including sharks and elephant seals. Recent advances in the tracking of pelagic predators have revealed that these animals forage in the mesopelagic and the depth and duration of their foraging dives are affected by the presence of eddies. The ways in which eddies impact the distribution of mesopelagic micronekton, however, remain largely unknown. During a multi-seasonal experiment we used a shipboard scientific echosounder transmitting at 38 kHz to observe the distribution of acoustic backscattering in the energetic mesoscale eddy field of the northwestern Atlantic. Observations were collected at 24 stations with 6 located in anticyclonic and 7 in cyclonic eddies. The sampled anticyclonic eddies are characterized by intense acoustic backscattering in the mesopelagic and changes in the intensity of acoustic backscattering layers match gradients of surface properties. Furthermore, mesopelagic daytime backscattering is positively correlated with sea level anomaly. These results suggest that anticyclonic eddies in the northwestern Atlantic impact the distribution of mesopelagic micronekton and may have the potential to locally enhance or structure spatially mesopelagic communities.

The majority of the aerosol particle number (condensation nuclei or CN) in the marine boundary layer (MBL) consists of sulfate and organic compounds that have been shown to provide a large fraction of the cloud condensation nuclei (CCN). Here we use submicron non‐refractory Aerosol Mass Spectrometer (AMS) and filter measurements of organic and sulfate components of aerosol particles measured during four North Atlantic Aerosol and Marine Ecosystems Study (NAAMES) research cruises to assess the sources and contributions of submicron organic and sulfate components for CCN concentrations in the MBL during four different seasons. Submicron hydroxyl group organic mass (OM) correlated strongly to sodium concentrations during clean marine periods (R = 0.9), indicating that hydroxyl group OM can serve as a proxy for sea‐spray OM in ambient measurements. Sea‐spray OM contributed 45% of the sum of sea‐spray OM and sea salt during late spring (biomass climax phase) compared to <20% for other seasons, but the seasonal difference was not statistically significant. The contribution of non‐combustion sources during clean marine periods to submicron OM was 47 to 88% and to non‐sea‐salt sulfate 31 to 86%, with likely sources being marine and biogenic. The remaining submicron OM and sulfate were likely associated with ship or continental sources, including biomass burning, even during clean marine periods. The seasonal contribution from secondary sulfate and OM components to submicron aerosol mass was highest during late spring (60%), when biogenic emissions are expected to be highest, and lowest during winter (18%). Removing submicron sea‐spray OM decreased CCN concentrations by <10% because of competing effects from increased hygroscopicity and decreased particle size. During all seasons, adding biogenic secondary sulfate increased hygroscopicity, particle size, and CCN concentrations at 0.1–0.3% supersaturations by 5–66%. The largest change was during early spring when the fraction of hygroscopic sulfate components in the 0.1–0.2 μm size range was highest (80%). During continental periods, the increased contribution from low‐hygroscopicity organic components to 0.1–0.2 μm diameter particles reduces the CCN/CN by 20–100% for three seasons despite the increased CN and mass concentrations. These results illustrate the important role of the chemical composition of particles with diameters 0.1–0.2 μm for controlling CCN in the MBL. Key Points: Ambient hydroxyl group mass correlated strongly to sodium, and their ratio for the limited samples available correlated to dissolved organic carbon normalized by salinity for generated sea spray aerosolNon‐combustion, likely secondary biogenic, sources contribute 47–88% of submicron organic mass and 21–86% of submicron sulfate during marine periodsThe fraction of particles in the 0.1–0.2 μm size range that were cloud condensation nuclei was highest during early spring due to a larger fraction of hygroscopic sulfate [ABSTRACT FROM AUTHOR]

The oceans teem with heterotrophic bacterioplankton that play an appreciable role in the uptake of dissolved organic carbon (DOC) derived from phytoplankton net primary production (NPP). As such, bacterioplankton carbon demand (BCD), or gross heterotrophic production, represents a major carbon pathway that influences the seasonal accumulation of DOC in the surface ocean and, subsequently, the potential vertical or horizontal export of seasonally accumulated DOC. Here, we examine the contributions of bacterioplankton and DOM to ecological and biogeochemical carbon flow pathways, including those of the microbial loop and the biological carbon pump, in the Western North Atlantic Ocean (∼39-54°N along ∼40°W) over a composite annual phytoplankton bloom cycle. Combining field observations with data collected from corresponding DOC remineralization experiments, we estimate the efficiency at which bacterioplankton utilize DOC, demonstrate seasonality in the fraction of NPP that supports BCD, and provide evidence for shifts in the bioavailability and persistence of the seasonally accumulated DOC. Our results indicate that while the portion of DOC flux through bacterioplankton relative to NPP increased as seasons transitioned from high to low productivity, there was a fraction of the DOM production that accumulated and persisted. This persistent DOM is potentially an important pool of organic carbon available for export to the deep ocean via convective mixing, thus representing an important export term of the biological carbon pump., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2021 Baetge, Behrenfeld, Fox, Halsey, Mojica, Novoa, Stephens and Carlson.)

Sea spray aerosol (SSA) consists of both sea salt and organic components. These aerosols affect Earth's climate by scattering solar radiation and by altering cloud properties. Here we present observations of SSA particles generated at sea using an over‐the‐side bubbling system (Sea Sweep) and an onboard plunging wave mesocosm (Marine Aerosol Reference Tank—MART) during five cruises in the North Atlantic. The cruises were timed to sample different stages of the North Atlantic plankton bloom and included transects from the oligotrophic Sargasso Sea to the biologically productive western subarctic. The results show that the North Atlantic plankton bloom has little effect on the emission flux, organic fraction, or cloud condensation nuclei (CCN) activity of SSA, and therefore, plankton ecosystems do not need to be included in modeling aerosol indirect effects of primary SSA in global climate models or in chemical transport models. Plain Language Summary: Breaking waves on the ocean surface emit sea spray aerosol (SSA) to the atmosphere. These particles affect Earth's climate by scattering solar radiation and altering cloud properties (e.g., cloud brightness, extent, and rain). SSA consists of both sea salt and organic components. A key question in chemical transport and climate models is whether marine plankton ecosystems affect the organic component of SSA. The results presented here show that marine plankton ecosystems have little effect on SSA and that the ocean source of organic SSA comes from the large pool of dissolved organic carbon in the ocean. Chemical transport and climate models, therefore, can treat the ocean as a uniform organic SSA source, affected only by sea surface temperature. Key Points: Marine plankton ecosystems do not directly affect sea spray aerosolChemical transport and climate models do not need to incorporate plankton ecosystems in modeling sea spray aerosol [ABSTRACT FROM AUTHOR]