Abstract

Abstract. Motivated by increasing levels of open ocean in the Arctic summer and the lack of prior altitude-resolved studies, extensive aerosol measurements were made during 11 flights of the NETCARE July 2014 airborne campaign from Resolute Bay, Nunavut. Flights included vertical profiles (60 to 3000 m above ground level) over open ocean, fast ice, and boundary layer clouds and fogs. A general conclusion, from observations of particle numbers between 5 and 20 nm in diameter (N5 − 20), is that ultrafine particle formation occurs readily in the Canadian high Arctic marine boundary layer, especially just above ocean and clouds, reaching values of a few thousand particles cm−3. By contrast, ultrafine particle concentrations are much lower in the free troposphere. Elevated levels of larger particles (for example, from 20 to 40 nm in size, N20 − 40) are sometimes associated with high N5 − 20, especially over low clouds, suggestive of aerosol growth. The number densities of particles greater than 40 nm in diameter (N > 40) are relatively depleted at the lowest altitudes, indicative of depositional processes that will lower the condensation sink and promote new particle formation. The number of cloud condensation nuclei (CCN; measured at 0.6 % supersaturation) are positively correlated with the numbers of small particles (down to roughly 30 nm), indicating that some fraction of these newly formed particles are capable of being involved in cloud activation. Given that the summertime marine Arctic is a biologically active region, it is important to better establish the links between emissions from the ocean and the formation and growth of ultrafine particles within this rapidly changing environment.

Highlights

  • Surface temperatures within the Arctic are rising almost twice as fast as in any other region of the world

  • We focus especially on ultrafine particles (UFPs) (5–20 nm in diameter) and address the following questions: what are the concentrations of UFPs in the Arctic summertime, and what is their vertical distribution? What are the environmental conditions that favour occurrence of UFPs and is there evidence for growth of UFP to cloud condensation nuclei (CCN) sizes? Aside from the studies conducted near Svalbard, we believe this is the first aircraft study in the high Arctic to systematically address these specific questions

  • Bursts of N5−20 > 2000 cm−3 were observed over polynyas, which were consistent with previous observations (Leaitch et al, 1984, 1994), in Lancaster Sound and south of Resolute Bay

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Summary

Introduction

Surface temperatures within the Arctic are rising almost twice as fast as in any other region of the world. Leck and Bigg (2010) highlighted that nucleation events in the high Arctic do not follow the classical banana shaped growth curve (Kulmala et al, 2001) but enhanced levels of ultrafine particles rather appear simultaneously in distinct size ranges (Karl et al, 2012). Such events could not be modelled with the selected empirical nucleation mechanism for the extremely low DMS concentrations in this region (Karl et al, 2013). This work provides a comprehensive picture of UFPs observed during the campaign whereas a prior publication from Willis et al (2016) detailed one UFP formation and growth event observed over Lancaster Sound

Sampling platform Polar 6
Meteorological parameters and state parameters
Aerosol physical and chemical properties
Trace gases
Data analysis and nomenclature of particle size data
FLEXPART-WRF Simulations
Study area and flight tracks
Meteorological and atmospheric conditions
Frequency of ultrafine particle events
Arctic air mass period: 4 July to 12 July
Transition day on 17 July
19 July–21 July
Case study: 8 July
CCN activity
Discussion and conclusions
Full Text
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