Editor’s note: For easy download the posted pdf of the State of the Climate for 2019 is a low-resolution file. A high-resolution copy of the report is available by clicking here. Please be patient as it may take a few minutes for the high-resolution file to download.

Abstract. This study describes a retrieval algorithm developed at the University of Bremen to obtain vertical profiles of ozone from limb observations performed by the Ozone Mapper and Profiler Suite (OMPS). This algorithm is based on the technique originally developed for use with data from the SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY) instrument. As both instruments make limb measurements of the scattered solar radiation in the ultraviolet (UV) and visible (Vis) spectral ranges, an underlying objective of the study is to obtain consolidated and consistent ozone profiles from the two satellites and to produce a combined data set. The retrieval algorithm uses radiances in the UV and Vis wavelength ranges normalized to the radiance at an upper tangent height to obtain ozone concentrations in the altitude range of 12–60 km. Measurements at altitudes contaminated by clouds in the instrument field of view are identified and filtered out. An independent aerosol retrieval is performed beforehand and its results are used to account for the stratospheric aerosol load in the ozone inversion. The typical vertical resolution of the retrieved profiles varies from  ∼  2.5 km at lower altitudes ( < 30 km) to  ∼  1.5 km (about 45 km) and becomes coarser at upper altitudes. The retrieval errors resulting from the measurement noise are estimated to be 1–4 % above 25 km, increasing to 10–30 % in the upper troposphere. OMPS data are processed for the whole of 2016. The results are compared with the NASA product and validated against profiles derived from passive satellite observations or measured in situ by balloon-borne sondes. Between 20 and 60 km, OMPS ozone profiles typically agree with data from the Microwave Limb Sounder (MLS) v4.2 within 5–10 %, whereas in the lower altitude range the bias becomes larger, especially in the tropics. The comparison of OMPS profiles with ozonesonde measurements shows differences within ±5 % between 13 and 30 km at northern middle and high latitudes. At southern middle and high latitudes, an agreement within 5–7 % is also achieved in the same altitude range. An unexpected bias of approximately 10–20 % is detected in the lower tropical stratosphere. The processing of the 2013 data set using the same retrieval settings and its validation against ozonesondes reveals a much smaller bias; a possible reason for this behaviour is discussed.

Abstract. This paper presents vertically and zonally resolved merged ozone time series from limb measurements of the SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY) and the Ozone Mapping and Profiler Suite (OMPS) Limb Profiler (LP). In addition, we present the merging of the latter two data sets with zonally averaged profiles from Stratospheric Aerosol and Gas Experiment (SAGE) II. The retrieval of ozone profiles from SCIAMACHY and OMPS-LP is performed using an inversion algorithm developed at the University of Bremen. To optimize the merging of these two time series, we use data from the Microwave Limb Sounder (MLS) as a transfer function and we follow two approaches: (1) a conventional method involving the calculation of deseasonalized anomalies and (2) a “plain-debiasing” approach, generally not considered in previous similar studies, which preserves the seasonal cycles of each instrument. We find a good correlation and no significant drifts between the merged and MLS time series. Using the merged data set from both approaches, we apply a multivariate regression analysis to study ozone changes in the 20–50 km range over the 2003–2018 period. Exploiting the dense horizontal sampling of the instruments, we investigate not only the zonally averaged field, but also the longitudinally resolved long-term ozone variations, finding an unexpected and large variability, especially at mid and high latitudes, with variations of up to 3 %–5 % per decade at altitudes around 40 km. Significant positive linear trends of about 2 %–4 % per decade were identified in the upper stratosphere between altitudes of 38 and 45 km at mid latitudes. This is in agreement with the predicted recovery of upper stratospheric ozone, which is attributed to both the adoption of measures to limit the release of halogen-containing ozone-depleting substances (Montreal Protocol) and the decrease in stratospheric temperature resulting from the increasing concentration of greenhouse gases. In the tropical stratosphere below 25 km negative but non-significant trends were found. We compare our results with previous studies and with short-term trends calculated over the SCIAMACHY period (2002–2012). While generally a good agreement is found, some discrepancies are seen in the tropical mid stratosphere. Regarding the merging of SAGE II with SCIAMACHY and OMPS-LP, zonal mean anomalies are taken into consideration and ozone trends before and after 1997 are calculated. Negative trends above 30 km are found for the 1985–1997 period, with a peak of −6 % per decade at mid latitudes, in agreement with previous studies. The increase in ozone concentration in the upper stratosphere is confirmed over the 1998–2018 period. Trends in the tropical stratosphere at 30–35 km show an interesting behavior: over the 1998–2018 period a negligible trend is found. However, between 2004 and 2011 a negative long-term change is detected followed by a positive change between 2012 and 2018. We attribute this behavior to dynamical changes in the tropical middle stratosphere.

Abstract. We report on updated trends using different merged zonal mean total ozone datasets from satellite and ground-based observations for the period from 1979 to 2020. This work is an update of the trends reported in Weber et al. (2018) using the same datasets up to 2016. Merged datasets used in this study include NASA MOD v8.7 and NOAA Cohesive Data (COH) v8.6, both based on data from the series of Solar Backscatter Ultraviolet (SBUV), SBUV-2, and Ozone Mapping and Profiler Suite (OMPS) satellite instruments (1978–present), as well as the Global Ozone Monitoring Experiment (GOME)-type Total Ozone – Essential Climate Variable (GTO-ECV) and GOME-SCIAMACHY-GOME-2 (GSG) merged datasets (both 1995–present), mainly comprising satellite data from GOME, SCIAMACHY, OMI, GOME-2A, GOME-2B, and TROPOMI. The fifth dataset consists of the annual mean zonal mean data from ground-based measurements collected at the World Ozone and Ultraviolet Radiation Data Centre (WOUDC). Trends were determined by applying a multiple linear regression (MLR) to annual mean zonal mean data. The addition of 4 more years consolidated the fact that total ozone is indeed slowly recovering in both hemispheres as a result of phasing out ozone-depleting substances (ODSs) as mandated by the Montreal Protocol. The near-global (60∘ S–60∘ N) ODS-related ozone trend of the median of all datasets after 1995 was 0.4 ± 0.2 (2σ) %/decade, which is roughly a third of the decreasing rate of 1.5 ± 0.6 %/decade from 1978 until 1995. The ratio of decline and increase is nearly identical to that of the EESC (equivalent effective stratospheric chlorine or stratospheric halogen) change rates before and after 1995, confirming the success of the Montreal Protocol. The observed total ozone time series are also in very good agreement with the median of 17 chemistry climate models from CCMI-1 (Chemistry-Climate Model Initiative Phase 1) with current ODS and GHG (greenhouse gas) scenarios (REF-C2 scenario). The positive ODS-related trends in the Northern Hemisphere (NH) after 1995 are only obtained with a sufficient number of terms in the MLR accounting properly for dynamical ozone changes (Brewer–Dobson circulation, Arctic Oscillation (AO), and Antarctic Oscillation (AAO)). A standard MLR (limited to solar, Quasi-Biennial Oscillation (QBO), volcanic, and El Niño–Southern Oscillation (ENSO)) leads to zero trends, showing that the small positive ODS-related trends have been balanced by negative trend contributions from atmospheric dynamics, resulting in nearly constant total ozone levels since 2000.

Despite the recently reported beginning of a recovery in global stratospheric ozone (O 3 ), an unexpected O 3 decline in the tropical mid-stratosphere (around 30-35 km altitude) was observed in satellite measurements during the first decade of the 21st century. We use SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY) measurements for the period 2004-2012 to confirm the significant O 3 decline. The SCIAMACHY observations show that the decrease in O 3 is accompanied by an increase in NO 2 .To reveal the causes of these observed O 3 and NO 2 changes, we performed simulations with the TOMCAT 3-D chemistry-transport model (CTM) using different chemical and dynamical forcings. For the 2004-2012 time period, the TOMCAT simulations reproduce the SCIAMACHYobserved O 3 decrease and NO 2 increase in the tropical mid-stratosphere. The simulations suggest that the positive changes in NO 2 (around 7 % decade −1 ) are due to similar positive changes in reactive odd nitrogen (NO y ), which are a result of a longer residence time of the source gas N 2 O and increased production via N 2 O + O( 1 D). The model simulations show a negative change of 10 % decade −1 in N 2 O that is most likely due to variations in the deep branch of the Brewer-Dobson Circulation (BDC). Interestingly, modelled annual mean "age of air" (AoA) does not show any sig-nificant changes in transport in the tropical mid-stratosphere during 2004-2012.However, further analysis of model results demonstrates significant seasonal variations. During the autumn months (September-October) there are positive AoA changes that imply transport slowdown and a longer residence time of N 2 O allowing for more conversion to NO y , which enhances O 3 loss. During winter months (January-February) there are negative AoA changes, indicating faster N 2 O transport and less NO y production. Although the variations in AoA over a year result in a statistically insignificant linear change, nonlinearities in the chemistry-transport interactions lead to a statistically significant negative N 2 O change.