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Motivated by the need to predict how the Arctic atmosphere will change in a warming world, this article summarizes recent advances made by the research consortium NETCARE (Network on Climate and Aerosols: Addressing Key Uncertainties in Remote Canadian Environments) that contribute to our fundamental understanding of Arctic aerosol particles as they relate to climate forcing. The overall goal of NETCARE research has been to use an interdisciplinary approach encompassing extensive field observations and a range of chemical transport, earth system, and biogeochemical models. Several major findings and advances have emerged from NETCARE since its formation in 2013. (1) Unexpectedly high summertime dimethyl sulfide (DMS) levels were identified in ocean water (up to 75 nM) and the overlying atmosphere (up to 1 ppbv) in the Canadian Arctic Archipelago (CAA). Furthermore, melt ponds, which are widely prevalent, were identified as an important DMS source (with DMS concentrations of up to 6 nM and a potential contribution to atmospheric DMS of 20 % in the study area). (2) Evidence of widespread particle nucleation and growth in the marine boundary layer was found in the CAA in the summertime, with these events observed on 41 % of days in a 2016 cruise. As well, at Alert, Nunavut, particles that are newly formed and grown under conditions of minimal anthropogenic influence during the months of July and August are estimated to contribute 20 % to 80 % of the 30-50 nm particle number density. DMS-oxidation-driven nucleation is facilitated by the presence of atmospheric ammonia arising from seabird-colony emissions, and potentially also from coastal regions, tundra, and biomass burning. Via accumulation of secondary organic aerosol (SOA), a significant fraction of the new particles grow to sizes that are active in cloud droplet formation. Although the gaseous precursors to Arctic marine SOA remain poorly defined, the measured levels of common continental SOA precursors (isoprene and monoterpenes) were low, whereas elevated mixing ratios of oxygenated volatile organic compounds (OVOCs) were inferred to arise via processes involving the sea surface microlayer. (3) The variability in the vertical distribution of black carbon (BC) under both springtime Arctic haze and more pristine summertime aerosol conditions was observed. Measured particle size distributions and mixing states were used to constrain, for the first time, calculations of aerosol-climate interactions under Arctic conditions. Aircraft- and ground-based measurements were used to better establish the BC source regions that supply the Arctic via long-range transport mechanisms, with evidence for a dominant springtime contribution from eastern and southern Asia to the middle troposphere, and a major contribution from northern Asia to the surface. (4) Measurements of ice nucleating particles (INPs) in the Arctic indicate that a major source of these particles is mineral dust, likely derived from local sources in the summer and long-range transport in the spring. In addition, INPs are abundant in the sea surface microlayer in the Arctic, and possibly play a role in ice nucleation in the atmosphere when mineral dust concentrations are low. (5) Amongst multiple aerosol components, BC was observed to have the smallest effective deposition velocities to high Arctic snow (0.03 cm s1).

Abstract. Motivated by the need to predict how the Arctic atmosphere will change in a warming world, this article summarizes recent advances made by the research consortium NETCARE (Network on Climate and Aerosols: Addressing Key Uncertainties in Remote Canadian Environments) that contribute to our fundamental understanding of Arctic aerosol particles as they relate to climate forcing. The overall goal of NETCARE research has been to use an interdisciplinary approach encompassing extensive field observations and a range of chemical transport, earth system, and biogeochemical models. Several major findings and advances have emerged from NETCARE since its formation in 2013 . (1) Unexpectedly high summertime dimethyl sulfide (DMS) levels were identified in ocean water and the overlying atmosphere in the Canadian Arctic Archipelago (CAA). Furthermore, melt ponds, which are widely prevalent, were identified as an important DMS source. (2) Evidence was found of widespread particle nucleation and growth in the marine boundary layer in the CAA in the summertime. DMS-oxidation-driven nucleation is facilitated by the presence of atmospheric ammonia arising from sea bird colony emissions, and potentially also from coastal regions, tundra, and biomass burning. Via accumulation of secondary organic material (SOA), a significant fraction of the new particles grow to sizes that are active in cloud droplet formation. Although the gaseous precursors to Arctic marine SOA remain poorly defined, the measured levels of common continental SOA precursors (isoprene and monoterpenes) were low, whereas elevated mixing ratios of oxygenated volatile organic compounds were inferred to arise via processes involving the sea surface microlayer. (3) The variability in the vertical distribution of black carbon (BC) under both springtime Arctic haze and more pristine summertime aerosol conditions was observed. Measured particle size distributions and mixing states were used to constrain, for the first time, calculations of aerosol–climate interactions under Arctic conditions. Aircraft- and ground-based measurements were used to better establish the BC source regions that supply the Arctic via long-range transport mechanisms. (4) Measurements of ice nucleating particles (INPs) in the Arctic indicate that a major source of these particles is mineral dust, likely derived from local sources in the summer and long-range transport in the spring. In addition, INPs are abundant in the sea surface microlayer in the Arctic, and possibly play a role in ice nucleation in the atmosphere when mineral dust concentrations are low. (5) Amongst multiple aerosol components, BC was observed to have the smallest effective deposition velocities to high Arctic snow.

Over the past two decades, with recognition that the ocean's sea-ice cover is neither insensitive to climate change nor a barrier to light and matter, research in sea-ice biogeochemistry has accelerated significantly, bringing together a multi-disciplinary community from a variety of fields. This disciplinary diversity has contributed a wide range of methodological techniques and approaches to sea-ice studies, complicating comparisons of the results and the development of conceptual and numerical models to describe the important biogeochemical processes occurring in sea ice. Almost all chemical elements, compounds, and biogeochemical processes relevant to Earth system science are measured in sea ice, with published methods available for determiningbiomass, pigments, net community production, primary production, bacterial activity, macronutrients, numerous natural and anthropogenic organic compounds, trace elements, reactive and inert gases, sulfur species, the carbon dioxide system parameters, stable isotopes, and water-ice-Atmosphere fluxes of gases, liquids, and solids. For most of these measurements, multiple sampling and processing techniques are available, but to date there has been little intercomparison or intercalibration between methods. In addition, researchers collect different types of ancillary data and document their samples differently, further confounding comparisons between studies. These problems are compounded by the heterogeneity of sea ice, in which even adjacent cores can have dramatically different biogeochemical compositions. We recommend that, in future investigations, researchers design their programs based on nested sampling patterns, collect a core suite of ancillary measurements, and employ a standard approach for sample identification and documentation. In addition, intercalibration exercises are most critically needed for measurements of biomass, primary production, nutrients, dissolved and particulate organic matter (including exopolymers), the CO2 system, air-ice gas fluxes, and aerosol production. We also encourage the development of in situ probes robust enough for long-Term deployment in sea ice, particularly for biological parameters, the CO2 system, and other gases.

The Arctic Ocean is currently undergoing significant transformations due to climate change, leading to profound changes in its microbial planktonic communities. These communities consist of a wide range of organisms, including photoautotrophic prokaryotes and eukaryotes, as well as heterotrophic, phagotrophic, and mixotrophic protistan species. Here, for simplicity, we refer to these single-celled species as phytoplankton. Within this diversity, potentially toxic and/or harmful algal species (hereafter abbreviated as "HA") are of particular concern. These organisms have the potential to spread into Arctic waters, posing threats to both human and ecosystem health. Despite their importance, the spatial and temporal distribution of phytoplankton communities, including HA species, in the North American Arctic, remains poorly understood. To address this gap, we compiled and synthesized the largest possible body of data from different databases, individual published and unpublished datasets, and partitioned it into nine regions based on the Large Marine Ecosystem classification. Our dataset contains 385 800 individual georeferenced data points and 18 268 unique sampling events, revealing greater diversity than previously thought, with 1445 unique taxa. Heterokontophyta (which notably included diatoms) and Dinoflagellata were the most dominant phyla. Our results indicate distinct spatial patterns of diversity, with the highest diversity observed in Atlantic-influenced regions of the North American Arctic. For most of the HA species recorded in our database, no evidence was found for an increase in the northernmost latitude where HA species are observed over the years, meaning that there is no substantial spread of HA species into the North American part of the Arctic. Our study challenges the traditional view of the Arctic as being unsuitable for toxin-producing and harmful algae and highlights the importance of extensive and long-term sampling efforts to understand the region's biodiversity. Overall, our findings provide new insights into the spatial patterns and biodiversity of phytoplankton and other protists in the North American Arctic and have implications for understanding the ecological functioning and response of this region to ongoing climate change. [ABSTRACT FROM AUTHOR]

Submarine canyons enhance shelf–slope sediment exchange and influence hydrodynamic processes, with consequences for biogeochemical cycles. This work documents variations in the vertical export of biogenic matter on the northern shore of the lower St. Lawrence Estuary (LSLE, Quebec, eastern Canada), which is characterized by the presence of an active submarine canyon system. A total of three moorings were deployed from November 2020 to September 2021. One nearshore mooring (PDMc) was deployed in the main axis of the Pointe-des-Monts (PDM) canyon system and was equipped with an acoustic Doppler current profiler (ADCP), and two moorings equipped with sediment traps were deployed in the distal PDM canyon system (PDM-154, PDM-224) and offshore Baie-Comeau (BC-133). The ADCP data revealed the occurrence of a minor sediment remobilization event (December 2020) and a small turbidity current (February 2021) in the canyon. Concurrent elevated fluxes of total particulate matter, particulate organic carbon, particulate nitrogen, and chloropigments showed that these events left a signature in sediment traps PDM-154 and PDM-224 located > 2.6 km further offshore by enhancing lateral dispersion of resuspended sediments. The composition of diatom and dinoflagellate assemblages was similar in the canyon system and offshore BC, but the diatom bloom occurred 2 weeks earlier (in mid-April) at the PDM site. A bloom of the potentially toxic diatom Pseudo-nitzschia seriata was also observed during the second half of September 2021 at the BC site. Annual diatom and dinoflagellate fluxes were almost 2 times lower at the PDM site than at the BC site, possibly due to differences in riverine input and the structure of the water column, as well as increased sediment input and resuspension at the PDM site, leading to limited light availability. This study notably helps identify the relationship between near-bed canyon processes and biogenic matter export in the water column, thereby directly influencing the ecosystem offshore PDM. The study period further covered an anomalously nearly ice-free winter, and thus, in the context of climate change, it provides valuable insight into future trends of biogenic matter export in the LSLE. [ABSTRACT FROM AUTHOR]

The complex topography surrounding submarine canyons influences local hydrodynamics. For example, canyon-induced upwelling can supply nutrients to the surface waters and stimulate biological productivity. Canyons may also represent hazard hotspots [...]

The coastal shelf of Pointe-des-Monts (PDM), located on the northern shore of the Lower St. Lawrence Estuary (LSLE), is characterized by active submarine canyons. Despite the presence of regional biological [...]