ALBERT

Description: Most estimates of sea spray aerosol source functions have used indirect means to infer the rate of production as a function of wind speed. Only recently has the technology become available to make high frequency measurements of aerosol spectra suitable for direct eddy correlation determination of the sea spray particle flux. This was accomplished in this study by combining a newly developed fast aerosol particle counter with an ultrasonic anemometer which allowed for eddy covariance measurements of size-segregated particle fluxes. The aerosol instrument is the Compact Lightweight Aerosol Spectrometer Probe (CLASP) – capable of measuring 8-channel size spectra for mean radii between 0.15 and 3.5 µm at 10 Hz. The first successful measurements were made during the Waves, Air Sea Fluxes, Aerosol and Bubbles (WASFAB) field campaign in October 2005 in Duck (NC, USA). The method and initial results are presented and comparisons are made with recent sea spray source functions from the literature.

Description: Unique measurements of vertical size-resolved aerosol particle concentrations, trace gas concentrations and meteorological data were obtained during the Arctic Summer Cloud Ocean Study (ASCOS, www.ascos.se), an International Polar Year project aimed at establishing the processes responsible for formation and evolution of low-level clouds over the high Arctic summer pack ice. The experiment was conducted from on board the Swedish icebreaker Oden, and provided both ship- and helicopter-based measurements. This study focuses on the vertical helicopter profiles and onboard measurements obtained during a three-week period when Oden was anchored to a drifting ice floe, and sheds light on the characteristics of Arctic aerosol particles and their distribution throughout the lower atmosphere. Distinct differences in aerosol particle characteristics within defined atmospheric layers are identified. Within the lowermost couple hundred metres, transport from the marginal ice zone (MIZ), condensational growth and cloud processing develop the aerosol population. During two of the four representative periods defined in this study, such influence is shown. At altitudes above about 1 km, long-range transport occurs frequently. However, only infrequently does large-scale subsidence descend such air masses to become entrained into the mixed layer in the high Arctic, and therefore long-range transport plumes are unlikely to directly influence low-level stratiform cloud formation. Nonetheless, such plumes can influence the radiative balance of the planetary boundary layer (PBL) by influencing formation and evolution of higher clouds, as well as through precipitation transport of particles downwards. New particle formation was occasionally observed, particularly in the near-surface layer. We hypothesize that the origin of these ultrafine particles could be in biological processes, both primary and secondary, within the open leads between the pack ice and/or along the MIZ. In general, local sources, in combination with upstream boundary-layer transport of precursor gases from the MIZ, are considered to constitute the origin of cloud condensation nuclei (CCN) particles and thus be of importance for the formation of interior Arctic low-level clouds during summer, and subsequently, through cloud influences, for the melting and freezing of sea ice.

Description: The first measurements of bubble size spectra within the near-surface waters of open leads in the central Arctic pack ice were obtained during the Artic Summer Cloud-Ocean Study (ASCOS) in August 2008 at 87–87.6° N, 1–11° W. A significant number of small bubbles (30–100 μm diameter) were present, with concentration decreasing rapidly with size from 100–560 μm; no bubbles larger than 560 μm were observed. The bubbles were present both during periods of low wind speed (U 〈 6 m/s) and when ice covered the surface of the lead. The low wind and short open-water fetch precludes production of bubbles by wave breaking suggesting that the bubbles are generated by processes below the surface. When the surface water was open to the atmosphere bubble concentrations increased with increasing heat loss to the atmosphere. The presence of substantial numbers of bubbles is significant because the bursting of bubbles at the surface provides a mechanism for the generation of aerosol and the ejection of biological material from the ocean into the atmosphere. Such a transfer has previously been proposed as a potential climate feedback linking marine biology and Arctic cloud properties.

Description: The first measurements of bubble size spectra within the near-surface waters of open leads in the central Arctic pack ice were obtained during the Arctic Summer Cloud-Ocean Study (ASCOS) in August 2008 at 87–87.6° N, 1–11° W. A significant number of small bubbles (30–100 μm diameter) were present, with concentration decreasing rapidly with size from 100–560 μm; no bubbles larger than 560 μm were observed. The bubbles were present both during periods of low wind speed (U

Description: Simultaneous measurements of near-surface aerosol and bubble spectra were made during five buoy deployments in the open ocean of the North Atlantic and used to estimate aerosol fluxes per unit area of whitecap. The measurements were made during two cruises as part of the SEASAW project, a UK contribution to the international SOLAS program. The mean bubble number concentrations for each deployment are in broad agreement with other open ocean spectra and are consistently one to two orders of magnitude lower than previous laboratory and surf zone studies. This suggests that the aerosol fluxes estimated above open ocean whitecaps will differ to those from over the surf zone and laboratory whitecaps due to the differences in the size and number of bursting bubbles. Production fluxes per unit area of whitecap are estimated from the mean aerosol concentration for each buoy deployment. They are found to increase with wind speed, and span the range of values found by previous laboratory and surf-zone studies for particles with radius at 80% humidity, R80 〈 1 μm, but to drop off more rapidly with increasing size for larger particles. A possible cause of this difference in behavior is the significant difference in bubble spectra. Estimates of the mean sea spray flux were made by scaling the whitecap production fluxes with in-situ estimates of whitecap fraction. The sea spray fluxes are also compared with simultaneous individual eddy covariance flux estimates made during the cruise, and with a sea spray source function derived from them.

Description: Simultaneous measurements of near-surface aerosol (0.12 〈 R 〈 9.25 μm) and bubble spectra (13 〈 R 〈 620 μm) were made during five buoy deployments in the open ocean of the North Atlantic and used to estimate aerosol fluxes per unit area of whitecap. The measurements were made during two cruises as part of the Sea Spray, Gas Flux, and Whitecaps (SEASAW) project, a UK contribution to the international Surface Ocean Lower Atmosphere Study (SOLAS) program. The mean bubble number concentrations for each deployment are in broad agreement with other open ocean spectra and are consistently one to two orders of magnitude lower than surf zone studies. Production fluxes per unit area of whitecap are estimated from the mean aerosol concentration for each buoy deployment. They are found to increase with wind speed, and span the range of values found by previous laboratory and surf-zone studies for particles with radius at 80% relative humidity, R80 〈 1 μm, but to drop off more rapidly with increasing particle size for larger particles. Estimates of the mean sea spray flux were made by scaling the whitecap production fluxes with in situ estimates of whitecap fraction. The sea spray fluxes are also compared with simultaneous individual eddy covariance flux estimates, and with a sea spray source function derived from them.

Description: Direct measurements of the turbulent air–sea fluxes of momentum, heat, moisture and gases. are often made using sensors mounted on ships. Ship-based turbulent wind measurements are corrected for platform motion using well established techniques, but biases at scales associated with wave and platform motion are often still apparent in the flux measurements. It has been uncertain whether this signal is due to time-varying distortion of the air flow over the platform, or to wind–wave interactions impacting the turbulence. Methods for removing such motion-scale biases from scalar measurements have previously been published but their application to momentum flux measurements remains controversial. Here we show that the measured motion-scale bias has a dependence on the horizontal ship velocity, and that a correction for it reduces the dependence of the measured momentum flux on the orientation of the ship to the wind. We conclude that the bias is due to experimental error, and that time-varying motion-dependent flow distortion is the likely source.

Description: The climate in the Arctic is changing faster than anywhere else on Earth. Poorly understood feedback processes relating to Arctic clouds and aerosol-cloud interactions contribute to a poor understanding of the present changes in the Arctic climate system, and also to a large spread in projections of future climate in the Arctic. The problem is exacerbated by the paucity of research-quality observations in the central Arctic. Improved formulations in climate models require such observations, which can only come from measurements in-situ in this difficult to reach region with logistically demanding environmental conditions. The Arctic Summer Cloud-Ocean Study (ASCOS) was the most extensive central Arctic Ocean expedition with an atmospheric focus during the International Polar Year (IPY) 2007–2008. ASCOS focused on the study of the formation and life cycle of low-level Arctic clouds. ASCOS departed from Longyearbyen on Svalbard on 2 August and returned on 9 September 2008. In transit into and out of the pack ice, four short research stations were undertaken in the Fram Strait; two in open water and two in the marginal ice zone. After traversing the pack-ice northward an ice camp was set up on 12 August at 87°21' N 01°29' W and remained in operation through 1 September, drifting with the ice. During this time extensive measurements were taken of atmospheric gas and particle chemistry and physics, mesoscale and boundary-layer meteorology, marine biology and chemistry, and upper ocean physics. ASCOS provides a unique interdisciplinary data set for development and testing of new hypotheses on cloud processes, their interactions with the sea ice and ocean and associated physical, chemical, and biological processes and interactions. For example, the first ever quantitative observation of bubbles in Arctic leads, combined with the unique discovery of marine organic material, polymer gels with an origin in the ocean, inside cloud droplets suggest the possibility of primary marine organically derived cloud condensation nuclei in Arctic stratocumulus clouds. Direct observations of surface fluxes of aerosols could, however, not explain observed variability in aerosol concentrations and the balance between local and remote aerosols sources remains open. Lack of CCN was at times a controlling factor in low-level cloud formation, and hence for the impact of clouds on the surface energy budget. ASCOS provided detailed measurements of the surface energy balance from late summer melt into the initial autumn freeze-up, and documented the effects of clouds and storms on the surface energy balance during this transition. In addition to such process-level studies, the unique, independent ASCOS data set can and is being used for validation of satellite retrievals, operational models, and reanalysis data sets.

Description: Unique measurements of vertical size resolved aerosol particle concentrations, trace gas concentrations and meteorological data were obtained during the Arctic Summer Cloud Ocean Study (ASCOS, http://www.ascos.se), an International Polar Year project aimed at establishing the processes responsible for formation and evolution of low-level clouds over the high Arctic summer pack ice. The experiment was conducted from onboard the Swedish icebreaker Oden, and provided both ship- and helicopter-based measurements. This study focuses on the vertical helicopter profiles and onboard measurements obtained during a three-week period when Oden was anchored to a drifting ice floe, and sheds light on the characteristics of Arctic aerosol particles and their distribution throughout the lower atmosphere. Distinct differences in aerosol particle characteristics within defined atmospheric layers are identified. Near the surface (lowermost couple hundred meters), transport from the marginal ice zone (MIZ), if sufficiently short (less than ca. 2 days), condensational growth and cloud-processing develop the aerosol population. During two of the four representative periods defined in this study, such influence is shown. At altitudes above about 1 km, long-range transport occurs frequently. However, only infrequently does large-scale subsidence descend such air masses to become entrained into the mixed layer in the high Arctic, and therefore they are unlikely to directly influence low-level stratiform cloud formation. Nonetheless, long-range transport plumes can influence the radiative balance of the PBL by influencing formation and evolution of higher clouds, as well as through precipitation transport of particles downwards. New particle formation was occasionally observed, particularly in the near-surface layer. We hypothesize that the origin of these ultrafine particles can be from biological processes, both primary and secondary, within the open leads between the pack ice and/or along the MIZ. In general, local sources, in combination with upstream boundary layer transport of precursor gases from the MIZ, are suggested to constitute the origin of CCN particles and thus be of importance for the formation of interior Arctic low level clouds during summer, and subsequently, through cloud influences, on the melting and freezing of sea ice.

Description: The eddy covariance technique is the most direct of the methods that have been used to measure the flux of sea-spray aerosol between the ocean and atmosphere, but has been applied in only a handful of studies. However, unless the aerosol is dried before the eddy covariance measurements are made, the hygroscopic nature of sea-spray may combine with a relative humidity flux to result in a bias in the calculated aerosol flux. "Bulk" methods have been presented to account for this bias, however they rely on assumptions of the shape of the aerosol spectra which may not be valid for near-surface measurements of sea-spray. Here we describe a method of correcting aerosol spectra for relative humidity induced size variations at the high frequency (10 Hz) measurement timescale, where counting statistics are poor and the spectral shape cannot be well represented by a simple power law. Such a correction allows the effects of hygroscopicity and relative humidity flux on the aerosol flux to be explicitly evaluated and compared to the bulk corrections, both in their original form and once reformulated to better represent the measured mean aerosol spectra. In general, the bulk corrections – particularly when reformulated for the measured mean aerosol spectra – perform relatively well, producing flux corrections of the right sign and approximate magnitude. However, there are times when the bulk methods either significantly over- or underestimate the required flux correction. We thus conclude that, where possible, relative humidity corrections should be made at the measurement frequency.