scholarly journals Ice nucleating particles in the marine boundary layer in the Canadian Arctic during summer 2014

2018 ◽  
Author(s):  
Victoria E. Irish ◽  
Sarah J. Hanna ◽  
Megan D. Willis ◽  
Swarup China ◽  
Jennie L. Thomas ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Surface Area ◽  
Marine Boundary Layer ◽  
Mineral Dust ◽  
Canadian Arctic ◽  
Particle Dispersion ◽  
Sea Spray ◽  
Dispersion Modelling ◽  
Air Mass ◽  
Sea Spray Aerosol

Abstract. Ice nucleating particles (INPs) in the Arctic can influence climate and precipitation in the region; yet our understanding of the concentrations and sources of INPs in this region remain uncertain. In the following we (1) measured concentrations of INPs in the Canadian Arctic marine boundary layer during summer 2014 on board the CCGS Amundsen, (2) determined ratios of surface areas of mineral dust aerosol to sea spray aerosol, and (3) investigated the source region of the INPs using particle dispersion modelling. Average concentrations of INPs at −15, −20 and −25 °C were 0.005, 0.044, and 0.154 L−1, respectively. These concentrations fall within the range of INP concentrations measured in other marine environments. For the samples investigated the ratio of mineral dust surface area to sea spray surface area ranged from 0.03 to 0.09. Based on these ratios and the ice active surface site densities of mineral dust and sea spray aerosol determined in previous laboratory studies, our results suggest that mineral dust is a more important contributor to the INP population than sea spray aerosol for the samples analysed. Based on particle dispersion modelling, the highest concentrations of INPs were often associated with lower latitude source regions such as the Hudson Bay area, eastern Greenland, or northwestern continental Canada. On the other hand, the lowest concentrations were often associated with regions further north of the sampling sites and over Baffin Bay. A weak correlation was observed between INP concentrations and the time the air mass spent over bare land, and a weak negative correlation was observed between INP concentrations and the time the air mass spent over ice and open water. These combined results suggest that mineral dust from local sources is an important contributor to the INP population in the Canadian Arctic marine boundary layer during summer 2014.

scholarly journals Ice nucleating particles in the marine boundary layer in the Canadian Arctic during summer 2014

2019 ◽  
Vol 19 (2) ◽  
pp. 1027-1039 ◽  
Author(s):  
Victoria E. Irish ◽  
Sarah J. Hanna ◽  
Megan D. Willis ◽  
Swarup China ◽  
Jennie L. Thomas ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Surface Area ◽  
Marine Boundary Layer ◽  
Mineral Dust ◽  
Canadian Arctic ◽  
Particle Dispersion ◽  
Sea Spray ◽  
Dispersion Modelling ◽  
Air Mass ◽  
Sea Spray Aerosol

Abstract. Ice nucleating particles (INPs) in the Arctic can influence climate and precipitation in the region; yet our understanding of the concentrations and sources of INPs in this region remain uncertain. In the following, we (1) measured concentrations of INPs in the immersion mode in the Canadian Arctic marine boundary layer during summer 2014 on board the CCGS Amundsen, (2) determined ratios of surface areas of mineral dust aerosol to sea spray aerosol, and (3) investigated the source region of the INPs using particle dispersion modelling. Average concentrations of INPs at −15, −20, and −25 ∘C were 0.005, 0.044, and 0.154 L−1, respectively. These concentrations fall within the range of INP concentrations measured in other marine environments. For the samples investigated the ratio of mineral dust surface area to sea spray surface area ranged from 0.03 to 0.09. Based on these ratios and the ice active surface site densities of mineral dust and sea spray aerosol determined in previous laboratory studies, our results suggest that mineral dust is a more important contributor to the INP population than sea spray aerosol for the samples analysed. Based on particle dispersion modelling, the highest concentrations of INPs were often associated with lower-latitude source regions such as the Hudson Bay area, eastern Greenland, or north-western continental Canada. On the other hand, the lowest concentrations were often associated with regions further north of the sampling sites and over Baffin Bay. A weak correlation was observed between INP concentrations and the time the air mass spent over bare land, and a weak negative correlation was observed between INP concentrations and the time the air mass spent over ice and open water. These combined results suggest that mineral dust from local sources is an important contributor to the INP population in the Canadian Arctic marine boundary layer during summer 2014.

scholarly journals Concentrations, composition, and sources of ice-nucleating particles in the Canadian High Arctic during spring 2016

2019 ◽  
Vol 19 (5) ◽  
pp. 3007-3024 ◽  
Author(s):  
Meng Si ◽  
Erin Evoy ◽  
Jingwei Yun ◽  
Yu Xi ◽  
Sarah J. Hanna ◽  
...  
Keyword(s):  
Hydrological Cycle ◽  
Mineral Dust ◽  
Ground Level ◽  
Particle Dispersion ◽  
The Arctic ◽  
Sea Spray ◽  
Gobi Desert ◽  
Anthropogenic Aerosol ◽  
Sea Spray Aerosol ◽  
Immersion Freezing

Abstract. Modelling studies suggest that the climate and the hydrological cycle are sensitive to the concentrations of ice-nucleating particles (INPs). However, the concentrations, composition, and sources of INPs in the atmosphere remain uncertain. Here, we report daily concentrations of INPs in the immersion freezing mode and tracers of mineral dust (Al, Fe, Ti, and Mn), sea spray aerosol (Na+ and Cl−), and anthropogenic aerosol (Zn, Pb, NO3-, NH4+, and non-sea-salt SO42-) at Alert, Canada, during a 3-week campaign in March 2016. In total, 16 daily measurements of INPs are reported. The average INP concentrations measured in the immersion freezing mode were 0.005±0.002, 0.020±0.004, and 0.186±0.040 L−1 at −15, −20, and −25 ∘C, respectively. These concentrations are within the range of concentrations measured previously in the Arctic at ground level or sea level. Mineral dust tracers all correlated with INPs at −25 ∘C (correlation coefficient, R, ranged from 0.70 to 0.76), suggesting that mineral dust was a major contributor to the INP population at −25 ∘C. Particle dispersion modelling suggests that the source of the mineral dust may have been long-range transport from the Gobi Desert. Sea spray tracers were anti-correlated with INPs at −25 ∘C (R=-0.56). In addition, INP concentrations at −25 ∘C divided by mass concentrations of aluminum were anti-correlated with sea spray tracers (R=-0.51 and −0.55 for Na+ and Cl−, respectively), suggesting that the components of sea spray aerosol suppressed the ice-nucleating ability of mineral dust in the immersion freezing mode. Correlations between INPs and anthropogenic aerosol tracers were not statistically significant. These results will improve our understanding of INPs in the Arctic during spring.

scholarly journals Sea spray aerosol as a unique source of ice nucleating particles

2015 ◽  
Vol 113 (21) ◽  
pp. 5797-5803 ◽  
Author(s):  
Paul J. DeMott ◽  
Thomas C. J. Hill ◽  
Christina S. McCluskey ◽  
Kimberly A. Prather ◽  
Douglas B. Collins ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Radiative Forcing ◽  
Marine Boundary Layer ◽  
Strong Increase ◽  
Sea Spray ◽  
Surface Boundary ◽  
Surface Boundary Layer ◽  
Surface Areas ◽  
Order Of Magnitude ◽  
Sea Spray Aerosol

Ice nucleating particles (INPs) are vital for ice initiation in, and precipitation from, mixed-phase clouds. A source of INPs from oceans within sea spray aerosol (SSA) emissions has been suggested in previous studies but remained unconfirmed. Here, we show that INPs are emitted using real wave breaking in a laboratory flume to produce SSA. The number concentrations of INPs from laboratory-generated SSA, when normalized to typical total aerosol number concentrations in the marine boundary layer, agree well with measurements from diverse regions over the oceans. Data in the present study are also in accord with previously published INP measurements made over remote ocean regions. INP number concentrations active within liquid water droplets increase exponentially in number with a decrease in temperature below 0 °C, averaging an order of magnitude increase per 5 °C interval. The plausibility of a strong increase in SSA INP emissions in association with phytoplankton blooms is also shown in laboratory simulations. Nevertheless, INP number concentrations, or active site densities approximated using “dry” geometric SSA surface areas, are a few orders of magnitude lower than corresponding concentrations or site densities in the surface boundary layer over continental regions. These findings have important implications for cloud radiative forcing and precipitation within low-level and midlevel marine clouds unaffected by continental INP sources, such as may occur over the Southern Ocean.

scholarly journals Concentrations, composition, and sources of ice-nucleating particles in the Canadian High Arctic during spring 2016

2018 ◽  
Author(s):  
Meng Si ◽  
Erin Evoy ◽  
Jingwei Yun ◽  
Yu Xi ◽  
Sarah Hanna ◽  
...  
Keyword(s):  
Hydrological Cycle ◽  
Mineral Dust ◽  
Ground Level ◽  
Particle Dispersion ◽  
The Arctic ◽  
Sea Spray ◽  
Gobi Desert ◽  
Anthropogenic Aerosol ◽  
Sea Spray Aerosol ◽  
Immersion Freezing

Abstract. Modelling studies suggest that the climate and the hydrological cycle are sensitive to the concentrations of ice-nucleating particles (INPs). However, the concentrations, composition, and sources of INPs in the atmosphere remain uncertain. Here we report daily concentrations of INPs and tracers of mineral dust (Al, Fe, Ti, and Mn), sea spray aerosol (Na+ and Cl−), and anthropogenic aerosol (Zn, Pb, NO3−, NH4+, and non-sea-salt SO42−) at Alert, Canada during a three-week campaign in March 2016. The average INP concentrations measured in the immersion freezing mode were approximately 0.005 ± 0.002 L−1, 0.020 ± 0.004 L−1, and 0.186 ± 0.040 L−1 at −15 ºC, −20 ºC, and −25 ºC, respectively. These concentrations are within the range of concentrations measured previously in the Arctic at ground level or sea level. Mineral dust tracers all correlated with INPs at −25 ºC (correlation coefficient, R, ranged from 0.70 to 0.76), suggesting that mineral dust was a major contributor to the INP population. Particle dispersion modelling suggests that the source of the mineral dust may have been the long-range transported dust from the Gobi desert. Sea spray tracers were anti-correlated with INPs at −25 ºC (R = −0.56). In addition, INP concentrations at −25 ºC divided by mass concentrations of aluminum were anti-correlated with sea spray tracers (R = −0.51 and −0.55 for Na+ and Cl−, respectively), suggesting that the components of sea spray aerosol suppressed the ice-nucleating ability of mineral dust in the immersion freezing mode. Correlations between INPs and anthropogenic aerosol tracers were not statistically significant. These results will improve our understanding of INPs in the Arctic during spring.

scholarly journals Sea State and Boundary Layer Stability Limit Sea Spray Aerosol Lifetime over the Southern Ocean

2020 ◽  
Author(s):  
Sebastian Landwehr ◽  
Michele Volpi ◽  
Marzieh H Derkani ◽  
Filippo Nelli ◽  
Alberto Alberello ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Southern Ocean ◽  
Stability Limit ◽  
Sea Spray ◽  
Boundary Layer Stability ◽  
Sea State ◽  
Sea Spray Aerosol

scholarly journals Supplementary material to "Ice nucleating particles in the marine boundary layer in the Canadian Arctic during summer 2014"

2018 ◽  
Author(s):  
Victoria E. Irish ◽  
Sarah J. Hanna ◽  
Megan D. Willis ◽  
Swarup China ◽  
Jennie L. Thomas ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Marine Boundary Layer ◽  
Canadian Arctic ◽  
Supplementary Material

scholarly journals The North Atlantic Marine Boundary Layer Experiment(NAMBLEX). Overview of the campaign held at Mace Head, Ireland, in summer 2002

2006 ◽  
Vol 6 (8) ◽  
pp. 2241-2272 ◽  
Author(s):  
D. E. Heard ◽  
K. A. Read ◽  
J. Methven ◽  
S. Al-Haider ◽  
W. J. Bloss ◽  
...  
Keyword(s):  
Boundary Layer ◽  
North Atlantic ◽  
Marine Boundary Layer ◽  
Numerical Models ◽  
Measurement Data ◽  
Air Mass ◽  
The North ◽  
Trace Species ◽  
Wide Range ◽  
The North Atlantic

Abstract. The North Atlantic Marine Boundary Layer Experiment (NAMBLEX), involving over 50 scientists from 12 institutions, took place at Mace Head, Ireland (53.32° N, 9.90° W), between 23 July and 4 September 2002. A wide range of state-of-the-art instrumentation enabled detailed measurements of the boundary layer structure and atmospheric composition in the gas and aerosol phase to be made, providing one of the most comprehensive in situ studies of the marine boundary layer to date. This overview paper describes the aims of the NAMBLEX project in the context of previous field campaigns in the Marine Boundary Layer (MBL), the overall layout of the site, a summary of the instrumentation deployed, the temporal coverage of the measurement data, and the numerical models used to interpret the field data. Measurements of some trace species were made for the first time during the campaign, which was characterised by predominantly clean air of marine origin, but more polluted air with higher levels of NOx originating from continental regions was also experienced. This paper provides a summary of the meteorological measurements and Planetary Boundary Layer (PBL) structure measurements, presents time series of some of the longer-lived trace species (O3, CO, H2, DMS, CH4, NMHC, NOx, NOy, PAN) and summarises measurements of other species that are described in more detail in other papers within this special issue, namely oxygenated VOCs, HCHO, peroxides, organo-halogenated species, a range of shorter lived halogen species (I2, OIO, IO, BrO), NO3 radicals, photolysis frequencies, the free radicals OH, HO2 and (HO2+Σ RO2), as well as a summary of the aerosol measurements. NAMBLEX was supported by measurements made in the vicinity of Mace Head using the NERC Dornier-228 aircraft. Using ECMWF wind-fields, calculations were made of the air-mass trajectories arriving at Mace Head during NAMBLEX, and were analysed together with both meteorological and trace-gas measurements. In this paper a chemical climatology for the duration of the campaign is presented to interpret the distribution of air-mass origins and emission sources, and to provide a convenient framework of air-mass classification that is used by other papers in this issue for the interpretation of observed variability in levels of trace gases and aerosols.

scholarly journals The importance of alkyl nitrates and sea ice emissions to atmospheric NO<sub>x</sub> sources and cycling in the summertime Southern Ocean marine boundary layer

2021 ◽  
Author(s):  
Jessica Mary Burger ◽  
Julie Granger ◽  
Emily Joyce ◽  
Meredith Galanter Hastings ◽  
Kurt Angus McDonald Spence ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Southern Ocean ◽  
Sea Ice ◽  
Marine Boundary Layer ◽  
Weddell Sea ◽  
Alkyl Nitrates ◽  
Air Mass ◽  
Surface Ocean ◽  
Alkyl Nitrate ◽  
Atmospheric Nitrate

Abstract. Atmospheric nitrate originates from the oxidation of nitrogen oxides (NOx = NO + NO2) and impacts both tropospheric chemistry and climate. NOx sources, cycling, and NOx to nitrate formation pathways are poorly constrained in remote marine regions, especially the Southern Ocean where pristine conditions serve as a useful proxy for the preindustrial atmosphere. Here, we measured the isotopic composition (δ15N and δ18O) of atmospheric nitrate in coarse-mode (> 1 μm) aerosols collected in the summertime marine boundary layer of the Atlantic Southern Ocean from 34.5° S to 70° S, and across the northern edge of the Weddell Sea. The δ15N-NO3− decreased with latitude from −2.7 ‰ to −43.1 ‰. The decline in δ15N with latitude is attributed to changes in the dominant NOx sources: lightning at the low latitudes, oceanic alkyl nitrates at the mid latitudes, and photolysis of nitrate in snow at the high latitudes. There is no evidence of any influence from anthropogenic NOx sources or equilibrium isotopic fractionation. Using air mass back trajectories and an isotope mixing model, we calculate that oceanic alkyl nitrate emissions have a δ15N signature of −22.0 ‰ ± 7.5 ‰. Given that measurements of alkyl nitrate contributions to remote nitrogen budgets are scarce, this may be a useful tracer for detecting their contribution in other oceanic regions. The δ18O-NO3− was always less than 70 ‰, indicating that daytime processes involving OH are the dominant NOx oxidation pathway during summer. Unusually low δ18O-NO3− values (less than 31 ‰) were observed at the western edge of the Weddell Sea. The air mass history of these samples indicates extensive interaction with sea ice covered ocean, which is known to enhance peroxy radical production. The observed low δ18O-NO3− is therefore attributed to increased exchange of NO with peroxy radicals, which have a low δ18O, relative to ozone, which has a high δ18O. This study reveals that the mid- and high-latitude surface ocean may serve as a more important NOx source than previously thought, and that the ice-covered surface ocean impacts the reactive nitrogen budget as well as the oxidative capacity of the marine boundary layer.

scholarly journals Meridional and vertical variations of the water vapour isotopic composition in the marine boundary layer over the Atlantic and Southern Ocean

2020 ◽  
Vol 20 (9) ◽  
pp. 5811-5835 ◽  
Author(s):  
Iris Thurnherr ◽  
Anna Kozachek ◽  
Pascal Graf ◽  
Yongbiao Weng ◽  
Dimitri Bolshiyanov ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Time Series ◽  
Wind Speed ◽  
Southern Ocean ◽  
Water Vapour ◽  
Turbulent Mixing ◽  
Large Scale ◽  
Marine Boundary Layer ◽  
Sea Spray ◽  
Moisture Source

Abstract. Stable water isotopologues (SWIs) are useful tracers of moist diabatic processes in the atmospheric water cycle. They provide a framework to analyse moist processes on a range of timescales from large-scale moisture transport to cloud formation, precipitation and small-scale turbulent mixing. Laser spectrometric measurements on research vessels produce high-resolution time series of the variability of the water vapour isotopic composition in the marine boundary layer. In this study, we present a 5-month continuous time series of such ship-based measurements of δ2H and δ18O from the Antarctic Circumnavigation Expedition (ACE) in the Atlantic and the Southern Ocean in the time period from November 2016 to April 2017. We analyse the drivers of meridional SWI variations in the marine boundary layer across diverse climate zones in the Atlantic and Southern Ocean using Lagrangian moisture source diagnostics and relate vertical SWI differences to near-surface wind speed and ocean surface state. The median values of δ18O, δ2H and deuterium excess during ACE decrease continuously from low to high latitudes. These meridional SWI distributions reflect climatic conditions at the measurement and moisture source locations, such as air temperature, specific humidity and relative humidity with respect to sea surface temperature. The SWI variability at a given latitude is highest in the extratropics and polar regions with decreasing values equatorwards. This meridional distribution of SWI variability is explained by the variability in moisture source locations and its associated environmental conditions as well as transport processes. The westward-located moisture sources of water vapour in the extratropics are highly variable in extent and latitude due to the frequent passage of cyclones and thus widen the range of encountered SWI values in the marine boundary layer. Moisture loss during transport further contributes to the high SWI variability in the extratropics. In the subtropics and tropics, persistent anticyclones lead to well-confined narrow easterly moisture source regions, which is reflected in the weak SWI variability in these regions. Thus, the expected range of SWI signals at a given latitude strongly depends on the large-scale circulation. Furthermore, the ACE SWI time series recorded at 8.0 and 13.5 m above the ocean surface provide estimates of vertical SWI gradients in the lowermost marine boundary layer. On average, the vertical gradients with height found during ACE are -0.1‰m-1 for δ18O, -0.5‰m-1 for δ2H and 0.3 ‰ m−1 for deuterium excess. Careful calibration and post-processing of the SWI data and a detailed uncertainty analysis provide a solid basis for the presented gradients. Using sea spray concentrations and sea state conditions, we show that the vertical SWI gradients are particularly large during high wind speed conditions with increased contribution of sea spray evaporation or during low wind speed conditions due to weak vertical turbulent mixing. Although further SWI measurements at a higher vertical resolution are required to validate these findings, the simultaneous SWI measurements at several heights during ACE show the potential of SWIs as tracers for vertical mixing and sea spray evaporation in the lowermost marine boundary layer.

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