Solar cycle response and long-term trends in the mesospheric metal layers

The meteoric metal layers (Na, Fe, and K)—which form as a result of the ablation of incoming meteors—act as unique tracers for chemical and dynamical processes that occur within the upper mesosphere/lower thermosphere region. In this work, we examine whether these metal layers are sensitive indicators of decadal long-term changes within the upper atmosphere. Output from a whole-atmosphere climate model is used to assess the response of the Na, K, and Fe layers across a 50 year period (1955–2005). At short timescales, the K layer has previously been shown to exhibit a very different seasonal behavior compared to the other metals. Here we show that this unusual behavior is also exhibited at longer timescales (both the ~11 year solar cycle and 50 year periods), where K displays a much more pronounced response to atmospheric temperature changes than either Na or Fe. The contrasting solar cycle behavior of the K and Na layers predicted by the model is confirmed using satellite and lidar observations for the period 2004–2013

Analysis and attribution of total column ozone changes over the Tibetan Plateau during 1979–2017

Various observation-based datasets have confirmed positive zonal mean column ozone trends at midlatitudes as a result of the successful implementation of the Montreal Protocol. However, there is still uncertainty about the longitudinal variation of these trends and the direction and magnitude of ozone changes at low latitudes. Here, we use the extended Copernicus Climate Change Service (C3S) dataset (1979–2017) to investigate the long-term variations in total column ozone (TCO) over the Tibetan Plateau (TP) for different seasons. We use piecewise linear trend (PWLT) and equivalent effective stratospheric chlorine loading (EESC)-based multivariate regression models with various proxies to attribute the influence of dynamical and chemical processes on the TCO variability. We also compare the seasonal behaviour of the relative total ozone low (TOL) over the TP with the zonal mean at the same latitude. Both regression models show that the TP column ozone trends change from negative trends from 1979 to 1996 to small positive trends from 1997 to 2017, although the later positive trend based on PWLT is not statistically significant. The wintertime positive trend starting from 1997 is larger than that in summer, but both seasonal TP recovery rates are smaller than the zonal means over the same latitude band. For TP column ozone, both regression models suggest that the geopotential height at 150 hPa (GH150) is a more suitable and realistic dynamical proxy compared to a surface temperature proxy used in some previous studies. Our analysis also shows that the wintertime GH150 plays an important role in determining summertime TCO over the TP through persistence of the ozone signal. For the zonal mean column ozone at this latitude, the quasi-biennial oscillation (QBO) is nonetheless the dominant dynamical proxy. We also use a 3-D chemical transport model to diagnose the contributions of different proxies for the TP region. The role of GH150 variability is illustrated by using two sensitivity experiments with repeating dynamics of 2004 and 2008. The simulated ozone profiles clearly show that wintertime TP ozone concentrations are largely controlled by tropics to midlatitude pathways, whereas in summer variations associated with tropical processes play an important role. These model results confirm that the long-term trends of TCO over the TP are dominated by different processes in winter and summer. The different TP recovery rates relative to the zonal means at the same latitude band are largely determined by wintertime dynamical processes

The near-global mesospheric potassium layer: Observations and modeling

The meteoric metal layers act as unique tracers of chemistry and dynamics in the upper atmosphere. Existing lidar studies from a few locations show that K exhibits a semiannual seasonality (winter and summer maxima), quite unlike the annual seasonality (winter maximum and summer minimum) seen with Na and Fe. This work uses spaceborne observations made with the Optical Spectrograph and InfraRed Imager System instrument on the Odin satellite to retrieve the near-global K layer for the first time. The satellite data (2004 to mid-2013) are used to validate the implementation of a recently proposed potassium chemistry scheme in a whole atmosphere chemistry climate model, which provides a chemical basis for this semiannual seasonal behavior. The satellite and model data show that this semiannual seasonality is near global in extent, with the strongest variation at middle and high latitudes. The column abundance, centroid layer height, and root-mean-square width of the K layer are consistent with the limited available lidar record. The K data set is then used to investigate the impact of polar mesospheric clouds on the metal layers at high latitudes during summer. Finally, the occurrence frequency of sporadic K layers and their possible link to sporadic E layers are examined

D-region ion–neutral coupled chemistry (Sodankylä Ion Chemistry, SIC) within the Whole Atmosphere Community Climate Model (WACCM 4) – WACCM-SIC and WACCM-rSIC

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

Global investigation of the Mg atom and ion layers using SCIAMACHY/Envisat observations between 70 and 150 km altitude and WACCM-Mg model results

Mg and Mg+ concentration fields in the upper mesosphere/lower thermosphere (UMLT) region are retrieved from SCIAMACHY/Envisat limb measurements of Mg and Mg+ dayglow emissions using a 2-D tomographic retrieval approach. The time series of monthly mean Mg and Mg+ number density and vertical column density in different latitudinal regions are presented. Data from the limb mesosphere–thermosphere mode of SCIAMACHY/Envisat are used, which cover the 50 to 150 km altitude region with a vertical sampling of ≈3.3 km and latitudes up to 82°. The high latitudes are not observed in the winter months, because there is no dayglow emission during polar night. The measurements were performed every 14 days from mid-2008 until April 2012. Mg profiles show a peak at around 90 km altitude with a density between 750 cm−3 and 1500 cm−3. Mg does not show strong seasonal variation at latitudes below 40°. For higher latitudes the density is lower and only in the Northern Hemisphere a seasonal cycle with a summer minimum is observed. The Mg+ peak occurs 5–15 km above the neutral Mg peak altitude. These ions have a significant seasonal cycle with a summer maximum in both hemispheres at mid and high latitudes. The strongest seasonal variations of Mg+ are observed at latitudes between 20 and 40° and the density at the peak altitude ranges from 500 cm−3 to 4000 cm−3. The peak altitude of the ions shows a latitudinal dependence with a maximum at mid latitudes that is up to 10 km higher than the peak altitude at the equator. The SCIAMACHY measurements are compared to other measurements and WACCM model results. The WACCM results show a significant seasonal variability for Mg with a summer minimum, which is more clearly pronounced than for SCIAMACHY, and globally a higher peak density than the SCIAMACHY results. Although the peak density of both is not in agreement, the vertical column density agrees well, because SCIAMACHY and WACCM profiles have different widths. The agreement between SCIAMACHY and WACCM results is much better for Mg+ with both showing the same seasonality and similar peak density. However, there are also minor differences, e.g. WACCM showing a nearly constant altitude of the Mg+ layer's peak density for all latitudes and seasons

Attribution of the Hemispheric Asymmetries in Trends of Stratospheric Trace Gases Inferred From Microwave Limb Sounder (MLS) Measurements

Using Microwave Limb Sounder (MLS) satellite observations, ERA‐Interim reanalysis data, and a chemistry transport model simulation, we analyze and investigate the causes of the asymmetric hemispheric trends of N2O, CH4, and HCl in the stratosphere during the period 2004–2012. We find significant hemispheric asymmetries in the trends of these trace gases in the midlatitude middle and lower stratosphere. With regard to N2O and CH4, the enhanced downwelling branch of the residual circulation in the Northern Hemisphere (NH) middle and upper stratosphere transports more N2O/CH4‐poor air from the upper stratosphere to the lower stratosphere. The enhanced poleward meridional branch of the residual circulation in the Southern Hemisphere (SH) stratosphere brings more N2O/CH4‐rich air from lower to middle latitudes. These processes therefore contribute to the negative trends of N2O and CH4 in the NH lower stratosphere and the positive trends in the SH middle stratosphere. A corresponding positive trend is found for HCl in the NH, where the deep branch of the residual circulation located in the middle and upper stratosphere strengthens, bringing more HCl‐rich air downward to the lower stratosphere, while the shallow branch of the residual circulation in the lower stratosphere weakens and leads to enhanced conversion of chlorine‐containing source gases of different lifetimes to HCl. A reversed picture emerges in the SH, where the deep branch of the residual circulation in the middle and upper stratosphere weakens, while the shallow branch in the lower stratosphere strengthens, resulting in less HCl there. In addition, the southward shift of the upwelling branch of the residual circulation in recent decades can partly explain trace gas trends above 20 hPa, while the eddy mixing has a small effect on the trends. Understanding these contributions from different processes to the hemispheric asymmetries in trends of these trace gases can help us to evaluate more accurately future changes in stratospheric composition

Determination of the atmospheric lifetime and global warming potential of sulfur hexafluoride using a three-dimensional model

We have used the Whole Atmosphere Community Climate Model (WACCM), with an updated treatment of loss processes, to determine the atmospheric lifetime of sulfur hexafluoride (SF6). The model includes the following SF6 removal processes: photolysis, electron attachment and reaction with mesospheric metal atoms. The Sodankylä Ion Chemistry (SIC) model is incorporated into the standard version of WACCM to produce a new version with a detailed D region ion chemistry with cluster ions and negative ions. This is used to determine a latitude- and altitude-dependent scaling factor for the electron density in the standard WACCM in order to carry out multi-year SF6 simulations. The model gives a mean SF6 lifetime over an 11-year solar cycle (τ) of 1278 years (with a range from 1120 to 1475 years), which is much shorter than the currently widely used value of 3200 years, due to the larger contribution (97.4 %) of the modelled electron density to the total atmospheric loss. The loss of SF6 by reaction with mesospheric metal atoms (Na and K) is far too slow to affect the lifetime. We investigate how this shorter atmospheric lifetime impacts the use of SF6 to derive stratospheric age of air. The age of air derived from this shorter lifetime SF6 tracer is longer by 9 % in polar latitudes at 20 km compared to a passive SF6 tracer. We also present laboratory measurements of the infrared spectrum of SF6 and find good agreement with previous studies. We calculate the resulting radiative forcings and efficiencies to be, on average, very similar to those reported previously. Our values for the 20-, 100- and 500-year global warming potentials are 18 000, 23 800 and 31 300, respectively

Identifying chemokines as therapeutic targets in renal disease: Lessons from antagonist studies and knockout mice

Chemokines, in concert with cytokines and adhesion molecules, play multiple roles in local and systemic immune responses. In the kidney, the temporal and spatial expression of chemokines correlates with local renal damage and accumulation of chemokine receptor-bearing leukocytes. Chemokines play important roles in leukocyte trafficking and blocking chemokines can effectively reduce renal leukocyte recruitment and subsequent renal damage. However, recent data indicate that blocking chemokine or chemokine receptor activity in renal disease may also exacerbate renal inflammation under certain conditions. An increasing amount of data indicates additional roles of chemokines in the regulation of innate and adaptive immune responses, which may adversively affect the outcome of interventional studies. This review summarizes available in vivo studies on the blockade of chemokines and chemokine receptors in kidney diseases, with a special focus on the therapeutic potential of anti-chemokine strategies, including potential side effects, in renal disease. Copyright (C) 2004 S. Karger AG, Basel

Substantial Increases in Eastern Amazon and Cerrado Biomass Burning‐Sourced Tropospheric Ozone

The decline in Amazonian deforestation rates and biomass burning activity (2001–2012) has been shown to reduce air pollutant emissions (e.g., aerosols) and improve regional air quality. However, in the Cerrado region (savannah grasslands in northeastern Brazil), satellite observations reveal increases in fire activity and tropospheric column nitrogen dioxide (an ozone precursor) during the burning season (August‐October, 2005–2016), which have partially offset these air quality benefits. Simulations from a 3‐D global chemistry transport model (CTM) capture this increase in NO2 with a surface increase of ~1 ppbv per decade. As there are limited long‐term observational tropospheric ozone records, we utilize the well‐evaluated CTM to investigate changes in ozone. Here, the CTM suggests that Cerrado region surface ozone is increasing by ~10 ppbv per decade. If left unmitigated, these positive fire‐sourced ozone trends will substantially increase the regional health risks and impacts from expected future enhancements in South American biomass burning activity under climate change