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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.

This paper investigates the scientific value of retrieving H218O and HDO columns in addition to H216O columns from high-resolution ground-based near-infrared spectra. We present a set of refined H216O, H218O, and HDO spectral windows. The retrieved H216O, H218O, and HDO columns are used for an a posteriori calculation of columnar δD and δ18O. We estimate the uncertainties for the so-calculated columnar δD and δ18O values. These estimations include uncertainties due to the measurement noise, errors in the a priori data, and uncertainties in spectroscopic parameters. Time series of δ18O obtained from ground-based FTIR (Fourier transform infrared) spectra are presented for the first time. For our study we use a full physics isotopic general circulation model (ECHAM5-wiso). We show that the full physics simulation of HDO and H218O can already be reasonably predicted from the H216O columns by a simple linear regression model (scatter values between full physics and linear regression simulations are 35 and 4‰ for HDO and H218O, respectively). We document that the columnar δD and δ18O values as calculated a posteriori from the retrievals of H216O, H218O, and HDO show a better agreement with the ECHAM5-wiso simulation than the δD and δ18O values as calculated from the H216O retrievals and the simple linear regression model. This suggests that the H218O and HDO column retrievals add complementary information to the H216O retrievals. However, these data have to be used carefully, because of the different vertical sensitivity of the H216O, H218O, and HDO columnar retrievals. Furthermore, we have to note that the retrievals use reanalysis humidity profiles as a priori input and the results are thus not independent of the reanalysis data.

Abstract. The present study investigates for the first time, the ground and flight performances of three miniaturized aerosol absorption sensors integrated on-board of Unmanned Aerial Systems (UAS). These sensors were evaluated during two contrasted field campaigns performed respectively at an urban site (Athens, Greece) impacted mainly by local traffic and domestic wood burning sources and at a remote regional background site (Agia Marina, Cyprus) impacted by long-range transported sources including dust. The three sensors were intercompared at the ground level against two commercially available instruments (MAAP and AE33) used as a reference. The measured signal of the three sensors was converted into absorption coefficient, equivalent black carbon concentration (eBC) and, when applicable, to signal saturation corrections following the suggestions of the manufacturers. Despite the diversity of the aerosol origin, chemical composition, sources and concentration levels during the two campaigns, the aerosol absorption sensors exhibited similar behavior against the reference instruments. The deviation from the reference during both campaigns concerning (eBC) mass was less than 8 %, suggesting that those miniature sensors that report BC mass are tuned/corrected to measure more accurately eBC rather than the absorption coefficient which deviated at least 15 %. The overall potential use of miniature aerosol absorption sensor on-board UAS is also illustrated here. UAS-based absorption measurements were used to investigate the vertical distribution of eBC over Athens up to 1 km above sea level during January 2016, reaching the top of the planetary boundary layer (PBL). Our results highlighted a heterogeneous boundary layer concentration of absorbing aerosol, especially in the early morning hours with the concurrent peak traffic emissions at ground-level and fast development of the boundary layer. Vertical homogeneity was achieved when the boundary layer depth became stable.

Abstract. Atmospheric aerosol particles are important for our planet’s climate because they interact with radiation and clouds. Hence, having characterised methods to collect aerosol from aircraft for detailed offline analysis are valuable. However, collecting aerosol, particularly coarse mode aerosol, onto substrates from a fast moving aircraft is challenging and can result in both losses and enhancement in aerosol. Here we present the characterisation of an inlet system designed for collection of aerosol onto filters on board the UK’s BAe 146 Facility for Airborne Atmospheric Measurements (FAAM) research aircraft. We also present an offline Scanning Electron Microscopy (SEM) technique for quantifying both the size distribution and size resolved composition of the collected aerosol. We use this SEM technique in parallel with online underwing optical probes in order to experimentally characterise the efficiency of the inlet system. We find that the coarse mode aerosol is sub-isokinetically enhanced, with a peak enhancement at around 10 μm up to a factor of three under typical operating conditions. Calculations show that the efficiency of collection then decreases rapidly at larger sizes. In order to minimise the isokinetic enhancement of coarse mode aerosol we recommend sampling with total flow rates above 50 L min−1; operating the inlet with the bypass fully open helps achieve this by increasing the flow rate through the inlet nozzle. With the inlet characterised, we also present single particle chemical information obtained from X-ray spectroscopy analysis which allows us to group the particles into composition categories. Our intention is to use the composition information in parallel with filter based ice nucleating particle measurements in order to correlate composition and ice nucleating particle concentrations.

Low-level flights over tundra wetlands in Alaska and Canada have been conducted during the Airborne Measurements of Methane Emissions (AirMeth) campaigns to measure turbulent methane fluxes in the atmosphere. In this paper we describe the instrumentation and new calibration procedures for the essential pressure parameters required for turbulence sensing by aircraft that exploit suitable regular measurement flight legs without the need for dedicated calibration patterns. We estimate the accuracy of the mean wind and the turbulence measurements. We show that airborne measurements of turbulent fluxes of methane and carbon dioxide using cavity ring-down spectroscopy trace gas analysers together with established turbulence equipment achieve a relative accuracy similar to that of measurements of sensible heat flux if applied during low-level flights over natural area sources. The inertial subrange of the trace gas fluctuations cannot be resolved due to insufficient high-frequency precision of the analyser, but, since this scatter is uncorrelated with the vertical wind velocity, the covariance and thus the flux are reproduced correctly. In the covariance spectra the -7/3 drop-off in the inertial subrange can be reproduced if sufficient data are available for averaging. For convective conditions and flight legs of several tens of kilometres we estimate the flux detection limit to be about 4 mg m−2 d−1 for w′CH4′‾, 1.4 g m−2 d−1 for w′CO2′‾ and 4.2 W m−2 for the sensible heat flux.

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.

The SPectrometer for Ice Nuclei (SPIN) is a commercially available ice nucleating particle (INP) counter manufactured by Droplet Measurement Technologies in Boulder, CO. The SPIN is a continuous flow diffusion chamber with parallel plate geometry based on the Zurich Ice Nucleation Chamber and the Portable Ice Nucleation Chamber. This study presents a standard description for using the SPIN instrument and also highlights methods to analyze measurements in more advanced ways. It characterizes and describes the behavior of the SPIN chamber, reports data from laboratory measurements, and quantifies uncertainties associated with the measurements. Experiments with ammonium sulfate are used to investigate homogeneous freezing of deliquesced haze droplets and droplet breakthrough. Experiments with kaolinite, NX illite, and silver iodide are used to investigate heterogeneous ice nucleation. SPIN nucleation results are compared to those from the literature. A machine learning approach for analyzing depolarization data from the SPIN optical particle counter is also presented (as an advanced use). Overall, we report that the SPIN is able to reproduce previous INP counter measurements. Atmospheric Measurement Techniques, 9 (7) ISSN:1867-8548 ISSN:1867-1381