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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.

The Ku-band microwave frequencies (10.70–14.25 GHz) overlap emissions from ozone (O3) at 11.072 GHz and hydroxyl radical (OH) at 13.441 GHz. These important chemical species in the polar middle atmosphere respond strongly to high-latitude geomagnetic activity associated with space weather. Atmospheric model calculations predict that energetic electron precipitation (EEP) driven by magnetospheric substorms produces large changes in polar mesospheric O3 and OH. The EEP typically peaks at geomagnetic latitudes of ∼65∘ and evolves rapidly with time longitudinally and over the geomagnetic latitude range 60–80∘. Previous atmospheric modelling studies have shown that during substorms OH abundance can increase by more than an order of magnitude at 64–84 km and mesospheric O3 losses can exceed 50 %. In this work, an atmospheric simulation and retrieval study has been performed to determine the requirements for passive microwave radiometers capable of measuring diurnal variations in O3 and OH profiles from high-latitude Northern Hemisphere and Antarctic locations to verify model predictions. We show that, for a 11.072 GHz radiometer making 6 h spectral measurements with 10 kHz frequency resolution and root-mean-square baseline noise of 1 mK, O3 could be profiled over 8×10-4–0.22 hPa (∼98–58 km) with 10–17 km height resolution and ∼1 ppmv uncertainty. For the equivalent 13.441 GHz measurements with vertical sensor polarisation, OH could be profiled over 3×10-3–0.29 hPa (∼90–56 km) with 10–17 km height resolution and ∼3 ppbv uncertainty. The proposed observations would be highly applicable to studies of EEP, atmospheric dynamics, planetary-scale circulation, chemical transport, and the representation of these processes in polar and global climate models. Such observations would provide a relatively low-cost alternative to increasingly sparse satellite measurements of the polar middle atmosphere, extending long-term data records and also providing “ground truth” calibration data.

We report the first ground‐based passive microwave observations made from Troll station, Antarctica, which show enhanced mesospheric nitric oxide (NO) volume mixing ratio reaching levels of 1.2 ppmv, or 2–3 orders of magnitude above background, at 70–80 km during small, relatively isolated geomagnetic storms in 2008. The mesospheric NO peaked 2 days after enhanced NO at higher altitudes (110–150 km) measured by the SABER satellite, and 2 days after peaks in the >30 keV and >300 keV electron flux measured by POES, although the 300 keV electron flux remained high. High time resolution data shows that mesospheric NO was enhanced at night and decayed during the day and built up to high levels over a period of 3–4 days. The altitude profile of mesospheric NO suggests direct production by ∼300 keV electron precipitation. Simulations using the Sodankylä Ion and Neutral Chemistry model show that the delay between thermospheric and mesospheric NO enhancements was primarily a result of the weaker production rate at lower altitudes by ∼300 keV electrons competing against strong day‐time losses. Key Points Polar mesospheric NO is significantly enhanced during small geomagnetic storms NO is produced directly in the mesosphere at 70–85 km by 300 keV electrons Weak NO production by 300 keV electrons and strong day time losses

This study presents a new ion-neutral chemical model coupled into the Whole Atmosphere Community Climate Model (WACCM). The ionospheric D-region (altitudes ∼ 50-90 km) chemistry is based on the Sodankylä Ion Chemistry (SIC) model, a one-dimensional model containing 307 ion-neutral and ion recombination, 16 photodissociation and 7 photoionization reactions of neutral species, positive and negative ions, and electrons. The SIC mechanism was reduced using the simulation error minimization connectivity method (SEM-CM) to produce a reaction scheme of 181 ion-molecule reactions of 181 ion-molecule reactions of 27 positive and 18 negative ions. This scheme describes the concentration profiles at altitudes between 20 km and 120 km of a set of major neutral species (HNO3, O3, H2O2, NO, NO2, HO2, OH, N2O5) and ions (O2+, O4+, NO+, NO+(H2O), O2+(H2O), H+(H2O), H+(H2O)2, H+(H2O)3, H+(H2O)4, O3, NO2, O, O2, OH, O2(H2O), O2(H2O)2, O4, CO3, CO3(H2O), CO4, HCO3, NO2, NO3, NO3(H2O), NO3(H2O)2, NO3(HNO3), NO3(HNO3)2, Cl, ClO), which agree with the full SIC mechanism within a 5 % tolerance. Four 3-D model simulations were then performed, using the impact of the January 2005 solar proton event (SPE) on D-region HOx and NOx chemistry as a test case of four different model versions: the standard WACCM (no negative ions and a very limited set of positive ions); WACCM-SIC (standard WACCM with the full SIC chemistry of positive and negative ions); WACCM-D (standard WACCM with a heuristic reduction of the SIC chemistry, recently used to examine HNO3 formation following an SPE); and WACCM-rSIC (standard WACCM with a reduction of SIC chemistry using the SEM-CM method). The standard WACCM misses the HNO3 enhancement during the SPE, while the full and reduced model versions predict significant NOx, HOx and HNO3 enhancements in the mesosphere during solar proton events. The SEM-CM reduction also identifies the important ion-molecule reactions that affect the partitioning of odd nitrogen (NOx), odd hydrogen (HOx) and O3 in the stratosphere and mesosphere.

The submillimetre is an understudied region of the Earth's atmospheric electromagnetic spectrum. Prior technological gaps and relatively high opacity due to the prevalence of rotational water vapour lines at these wavelengths have slowed progress from a ground-based remote sensing perspective; however, emerging superconducting detector technologies in the fields of astronomy offer the potential to address key atmospheric science challenges with new instrumental methods. A site study, with a focus on the polar regions, is performed to assess theoretical feasibility by simulating the downwelling (zenith angle = 0°) clear-sky submillimetre spectrum from 30 mm (10 GHz) to 150 µm (2000 GHz) at six locations under annual mean, summer, winter, daytime, night-time and low-humidity conditions. Vertical profiles of temperature, pressure and 28 atmospheric gases are constructed by combining radiosonde, meteorological reanalysis and atmospheric chemistry model data. The sensitivity of the simulated spectra to the choice of water vapour continuum model and spectroscopic line database is explored. For the atmospheric trace species hypobromous acid (HOBr), hydrogen bromide (HBr), perhydroxyl radical (HO2) and nitrous oxide (N2O) the emission lines producing the largest change in brightness temperature are identified. Signal strengths, centre frequencies, bandwidths, estimated minimum integration times and maximum receiver noise temperatures are determined for all cases. HOBr, HBr and HO2 produce brightness temperature peaks in the mK to µK range, whereas the N2O peaks are in the K range. The optimal submillimetre remote sensing lines for the four species are shown to vary significantly between location and scenario, strengthening the case for future hyperspectral instruments that measure over a broad wavelength range. The techniques presented here provide a framework that can be applied to additional species of interest and taken forward to simulate retrievals and guide the design of future submillimetre instruments.

Meteorological and atmospheric models are being extended up to 80 km altitude but there are very few observing techniques that can measure stratospheric–mesospheric winds at altitudes between 20 and 80 km to verify model datasets. Here we demonstrate the feasibility of horizontal wind profile measurements using ground-based passive millimetre-wave spectroradiometric observations of ozone lines centred at 231.28, 249.79, and 249.96 GHz. Vertical profiles of horizontal winds are retrieved from forward and inverse modelling simulations of the line-of-sight Doppler-shifted atmospheric emission lines above Halley station (75°37′ S, 26°14′ W), Antarctica. For a radiometer with a system temperature of 1400 K and 30 kHz spectral resolution observing the ozone 231.28 GHz line we estimate that 12 h zonal and meridional wind profiles could be determined over the altitude range 25–74 km in winter, and 28–66 km in summer. Height-dependent measurement uncertainties are in the range 3–8 m s−1 and vertical resolution  ∼  8–16 km. Under optimum observing conditions at Halley a temporal resolution of 1.5 h for measuring either zonal or meridional winds is possible, reducing to 0.5 h for a radiometer with a 700 K system temperature. Combining observations of the 231.28 GHz ozone line and the 230.54 GHz carbon monoxide line gives additional altitude coverage at 85 ± 12 km. The effects of clear-sky seasonal mean winter/summer conditions, zenith angle of the received atmospheric emission, and spectrometer frequency resolution on the altitude coverage, measurement uncertainty, and height and time resolution of the retrieved wind profiles have been determined.

Christmas comes but once a year, and when it does, it brings high blood pressure. I should know. As luck would have it, my half-yearly check-up always coincides with the festive season. Bah humbug.

I am big in Bangalore. In Auckland, I am quoted at dinner parties. As for Johannesburg, well, I am almost a household name. This, at least, is what the emails imply - the ones that began arriving after my 60th birthday.