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 (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 s−1).
The influence of local oil exploration, regional wildfires, and long
range transport on summer 2015 aerosol over the North Slope of
Alaska
