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A new bubble-generating glass chamber with an extensive set of aerosol production experiments is presented. Compared to the experiments described in the literature since the ground-setting works of Edward C.​​​​​​​ Monahan et al. in 1980s, the current setup is among the medium-sized installations allowing for accurate control of the air discharge, water temperature, and salinity. The size and material of the chamber offer a variety of applications due to its portability, measurement setup adjustability, and sterilization option. The experiments have been conducted in a cylindrical bubbling tank of 10 L volume that was filled by ∼ 30 %–40 % with water of controlled salt content and temperature and covered with a hermetic lid. The chamber was used to study the characteristics of aerosols produced by bursting bubbles under different conditions. In line with previous findings, the sea spray aerosol production was shown to depend linearly on the surface area covered by the bubbles, which in turn is a near-linear function of the air discharge through the water. Observed dependencies of the aerosol size spectra and particle fluxes on water salinity and temperature, being qualitatively comparable with the previous experiments, substantially refined the existing parameterizations. In particular, the bubble size was practically independent from the air discharge through the water body, except in the case of very small flows. Also, the dependence of aerosol spectrum and amount on salinity was much weaker than suggested in some previous experiments. The temperature dependence, to the contrary, was significant and consistent, with a transition in the spectrum shape at ∼ 10 ∘C. Theoretical analysis based on the basic conservation laws supported the main results of the experiments but also highlighted the need for a better understanding of the aerosol production from a cold water surface.

Ground-based observations of 11.072 GHz atmospheric ozone (O3) emission have been made using the Ny-Ålesund Ozone in the Mesosphere Instrument (NAOMI) at the UK Arctic Research Station (latitude 78∘55′0′′ N, longitude 11∘55′59′′ E), Spitsbergen. Seasonally averaged O3 vertical profiles in the Arctic polar mesosphere–lower thermosphere region for night-time and twilight conditions in the period 15 August 2017 to 15 March 2020 have been retrieved over the altitude range 62–98 km. NAOMI measurements are compared with corresponding, overlapping observations by the Sounding of the Atmosphere using Broadband Emission Radiometry (SABER) satellite instrument. The NAOMI and SABER version 2.0 data are binned according to the SABER instrument 60 d yaw cycles into nominal 3-month “winter” (15 December–15 March), “autumn” (15 August–15 November), and “summer” (15 April–15 July) periods. The NAOMI observations show the same year-to-year and seasonal variabilities as the SABER 9.6 µm O3 data. The winter night-time (solar zenith angle, SZA ≥ 110∘) and twilight (75∘ ≤ SZA ≤ 110∘) NAOMI and SABER 9.6 µm O3 volume mixing ratio (VMR) profiles agree to within the measurement uncertainties. However, for autumn twilight conditions the SABER 9.6 µm O3 secondary maximum VMR values are higher than NAOMI over altitudes 88–97 km by 47 % and 59 %, respectively in 2017 and 2018. Comparing the two SABER channels which measure O3 at different wavelengths and use different processing schemes, the 9.6 µm O3 autumn twilight VMR data for the three years 2017–2019 are higher than the corresponding 1.27 µm measurements with the largest difference (58 %) in the 65–95 km altitude range similar to the NAOMI observation. The SABER 9.6 µm O3 summer daytime (SZA < 75∘) mesospheric O3 VMR is also consistently higher than the 1.27 µm measurement, confirming previously reported differences between the SABER 9.6 µm channel and measurements of mesospheric O3 by other satellite instruments.

During the Multidisciplinary drifting Observatory for the Study of Arctic Climate (MOSAiC) expedition, meteorological conditions over the lowest 1 km of the atmosphere were sampled with the DataHawk2 (DH2) fixed-wing uncrewed aircraft system (UAS). These in situ observations of the central Arctic atmosphere are some of the most extensive to date and provide unique insight into the atmospheric boundary layer (ABL) structure. The ABL is an important component of the Arctic climate, as it can be closely coupled to cloud properties, surface fluxes, and the atmospheric radiation budget. The high temporal resolution of the UAS observations allows us to manually identify the ABL height (ZABL) for 65 out of the total 89 flights conducted over the central Arctic Ocean between 23 March and 26 July 2020 by visually analyzing profiles of virtual potential temperature, humidity, and bulk Richardson number. Comparing this subjective ZABL with ZABL identified by various previously published automated objective methods allows us to determine which objective methods are most successful at accurately identifying ZABL in the central Arctic environment and how the success of the methods differs based on stability regime. The objective methods we use are the Liu–Liang, Heffter, virtual potential temperature gradient maximum, and bulk Richardson number methods. In the process of testing these objective methods on the DH2 data, numerical thresholds were adapted to work best for the UAS-based sampling. To determine if conclusions are robust across different measurement platforms, the subjective and objective ZABL determination processes were repeated using the radiosonde profile closest in time to each DH2 flight. For both the DH2 and radiosonde data, it is determined that the bulk Richardson number method is the most successful at identifying ZABL, while the Liu–Liang method is least successful. The results of this study are expected to be beneficial for upcoming observational and modeling efforts regarding the central Arctic ABL.

Meteor radars have become widely used instruments to study atmospheric dynamics, particularly in the 70 to 110 km altitude region. These systems have been proven to provide reliable and continuous measurements of horizontal winds in the mesosphere and lower thermosphere. Recently, there have been many attempts to utilize specular and/or transverse scatter meteor measurements to estimate vertical winds and vertical wind variability. In this study we investigate potential biases in vertical wind estimation that are intrinsic to the meteor radar observation geometry and scattering mechanism, and we introduce a mathematical debiasing process to mitigate them. This process makes use of a spatiotemporal Laplace filter, which is based on a generalized Tikhonov regularization. Vertical winds obtained from this retrieval algorithm are compared to UA-ICON model data. This comparison reveals good agreement in the statistical moments of the vertical velocity distributions. Furthermore, we present the first observational indications of a forward scatter wind bias. It appears to be caused by the scattering center's apparent motion along the meteor trajectory when the meteoric plasma column is drifted by the wind. The hypothesis is tested by a radiant mapping of two meteor showers. Finally, we introduce a new retrieval algorithm providing a physically and mathematically sound solution to derive vertical winds and wind variability from multistatic meteor radar networks such as the Nordic Meteor Radar Cluster (NORDIC) and the Chilean Observation Network De meteOr Radars (CONDOR). The new retrieval is called 3DVAR+DIV and includes additional diagnostics such as the horizontal divergence and relative vorticity to ensure a physically consistent solution for all 3D winds in spatially resolved domains. Based on this new algorithm we obtained vertical velocities in the range of w = ± 1–2 m s−1 for most of the analyzed data during 2 years of collection, which is consistent with the values reported from general circulation models (GCMs) for this timescale and spatial resolution.

Ground based observations of 11.072 GHz atmospheric ozone (O3) emission have been made using the Ny Ålesund Ozone in the Mesosphere Instrument (NAOMI) at the UK Arctic Research Station (latitude 78°55’0” N, longitude 11°55’59” E), Spitsbergen. Seasonally averaged O3 vertical profiles in the Arctic polar mesosphere lower thermosphere region for night-time and twilight conditions in the period 15 August 2017 to 15 March 2020 have been retrieved over the altitude range 62–98 km. NAOMI measurements are compared with corresponding, overlapping observations by the Sounding of the Atmosphere using Broadband Emission Radiometry (SABER) satellite instrument. The NAOMI and SABER data are binned according to the SABER instrument 60 day yaw cycles into 3 month ‘winter’ (15 December–15 March), ‘autumn’ (15 August–15 November), and ‘summer’ (15 April–15 July) periods. The NAOMI observations show the same year-to-year and seasonal variabilities as the SABER 9.6 μm O3 data. The winter night-time (solar zenith angle, SZA ≥ 110°) and twilight (75° ≤ SZA ≤ 110°) NAOMI and SABER 9.6 μm O3 volume mixing ratio (VMR) profiles agree to within the measurement uncertainties. However, for autumn twilight conditions the SABER 9.6 μm O3 secondary maximum VMR values are higher than NAOMI over altitudes 88–97 km by 47 % and 59 % respectively in 2017 and 2018. Comparing the two SABER channels which measure O3 at different wavelengths and use different processing schemes, the 9.6 μm O3 autumn twilight VMR data for the three years 2017–19 are higher than the corresponding 1.27 μm measurements with the largest difference (58 %) in the 65–95 km altitude range similar to the NAOMI observation. The SABER 9.6 μm O3 summer daytime (SZA < 75°) mesospheric O3 VMR is also consistently higher than the 1.27 μm measurement, confirming previously reported differences between the SABER 9.6 μm channel and measurements of mesospheric O3 by other satellite instruments.

Emissions of methane (CH4) from offshore oil and gas installations are poorly ground-truthed, and quantification relies heavily on the use of emission factors and activity data. As part of the United Nations Climate & Clean Air Coalition (UN CCAC) objective to study and reduce short-lived climate pollutants (SLCPs), a Twin Otter aircraft was used to survey CH4 emissions from UK and Dutch offshore oil and gas installations. The aims of the surveys were to (i) identify installations that are significant CH4 emitters, (ii) separate installation emissions from other emissions using carbon-isotopic fingerprinting and other chemical proxies, (iii) estimate CH4 emission rates, and (iv) improve flux estimation (and sampling) methodologies for rapid quantification of major gas leaks. In this paper, we detail the instrument and aircraft set-up for two campaigns flown in the springs of 2018 and 2019 over the southern North Sea and describe the developments made in both the planning and sampling methodology to maximise the quality and value of the data collected. We present example data collected from both campaigns to demonstrate the challenges encountered during offshore surveys, focussing on the complex meteorology of the marine boundary layer and sampling discrete plumes from an airborne platform. The uncertainties of CH4 flux calculations from measurements under varying boundary layer conditions are considered, as well as recommendations for attribution of sources through either spot sampling for volatile organic compounds (VOCs) ∕ δ13CCH4 or using in situ instrumental data to determine C2H6–CH4 ratios. A series of recommendations for both planning and measurement techniques for future offshore work within marine boundary layers is provided. Atmospheric Measurement Techniques, 14 (1) ISSN:1867-8548 ISSN:1867-1381

Atmospheric ethane can be used as a tracer to distinguish methane sources, both at the local and global scale. Currently, ethane can be measured in the field using flasks or in situ analyzers. In our study, we characterized the CRDS Picarro G2201-i instrument, originally designed to measure isotopic CH4 and CO2, for measurements of ethane-to-methane ratio in mobile-measurement scenarios, near sources and under field conditions. We evaluated the limitations and potential of using the CRDS G2201-i to measure the ethane-to-methane ratio, thus extending the instrument application to simultaneously measure two methane source proxies in the field: carbon isotopic ratio and the ethane-to-methane ratio. First, laboratory tests were run to characterize the instrument in stationary conditions. Subsequently, the instrument performance was tested in field conditions as part of a controlled release experiment. Finally, the instrument was tested during mobile measurements focused on gas compressor stations. The results from the field were afterwards compared with the results obtained from instruments specifically designed for ethane measurements. Our study shows the potential of using the CRDS G2201-i instrument in a mobile configuration to determine the ethane-to-methane ratio in methane plumes under measurement conditions with an ethane uncertainty of 50 ppb. Assuming typical ethane-to-methane ratios ranging between 0 and 0.1 ppb ppb−1, we conclude that the instrument can accurately estimate the “true” ethane-to-methane ratio within 1σ uncertainty when CH4 enhancements are at least 1 ppm, as can be found in the vicinity of strongly emitting sites such as natural gas compressor stations and roadside gas pipeline leaks.