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At least 307 records · Page 17

Long-Term Changes in Lower Tropospheric Baseline Ozone Concentrations:

Two recent papers have quantified long-term ozone (O3) changes observed at northernmidlatitude sites that are believed to represent baseline (here understood as representative of continental to hemispheric scales) conditions. Three chemistry-climate models (NCAR CAM-chem, GFDL-CM3, and GISS-E2-R) have calculated retrospective tropospheric O3 concentrations as part of the Atmospheric Chemistry and Climate Model Intercomparison Project and Coupled Model Intercomparison Project Phase 5 model intercomparisons. We present an approach for quantitative comparisons of model results with measurements for seasonally averaged O3 concentrations. There is considerable qualitative agreement between the measurements and the models, but there are also substantial and consistent quantitative disagreements. Most notably, models (1) overestimate absolute O3 mixing ratios, on average by approximately 5 to 17 ppbv in the year 2000, (2) capture only approximately 50% of O3 changes observed over the past five to six decades, and little of observed seasonal differences, and (3) capture approximately 25 to 45% of the rate of change of the long-term changes. These disagreements are significant enough to indicate that only limited confidence can be placed on estimates of present-day radiative forcing of tropospheric O3 derived from modeled historic concentration changes and on predicted future O3 concentrations. Evidently our understanding of tropospheric O3, or the incorporation of chemistry and transport processes into current chemical climate models, is incomplete. Modeled O3 trends approximately parallel estimated trends in anthropogenic emissions of NO(sub x), an important O3 precursor, while measured O3 changes increase more rapidly than these emission estimates.

atmospheric composition↗

Tropospheric Ozonesonde Profiles at Long-Term U.S. Monitoring Sites: 2. Links Between Trinidad Head, CA, Profile Clusters and Inland Surface Ozone Measurements

Much attention has been focused on the transport of ozone (O3) to the western U.S., particularly given the latest revision of the National Ambient Air Quality Standard to 70 parts per billion by volume (ppbv) of O3. This makes quantifying the contributions of stratosphere-to-troposphere exchange, local pollution, and pollution transport to this region essential. To evaluate free-tropospheric and surface O3 in the western U.S., we use self-organizing maps to cluster 18 years of ozonesonde profiles from Trinidad Head, CA. Three of nine O3 mixing ratio profile clusters exhibit thin laminae of high O3 above Trinidad Head. The high O3 layers are located between 1 and 6 km above mean sea level and reside above an inversion associated with a northern location of the Pacific subtropical high. Ancillary data (reanalyses, trajectories, and remotely sensed carbon monoxide) help identify the high O3 sources in one cluster, but distinguishing mixed influences on the elevated O3 in other clusters is difficult. Correlations between the elevated tropospheric O3 and surface O3 at high-altitude monitors at Lassen Volcanic and Yosemite National Parks, and Truckee, CA, are marked and long lasting. The temporal correlations likely result from a combination of transport of baseline O3 and covarying meteorological parameters. Days corresponding to the high O3 clusters exhibit hourly surface O3 anomalies of +5-10 ppbv compared to a climatology; the positive anomalies can last up to 3 days after the ozonesonde profile. The profile and surface O3 links demonstrate the importance of regular ozonesonde profiling at Trinidad Head.

STE↗

Overview of Large-scale Tropospheric Transport in the Chemistry Climate Model Initiative (CCMI) Simulations

The transport of chemicals is a major uncertainty in the modeling of tropospheric composition. Here we compare the large-scale tropospheric transport properties among different models in the Chemistry Climate Modeling Initiative (CCMI) with a focus on transport defined with respect to the Northern Hemisphere (NH) midlatitude surface. Among simulations of the recent past (1980-2010) we show that there are substantial differences in their global-scale tropospheric transport properties. For example, the mean transit time since southern hemisphere air last contacted the NH midlatitude surface differs by ~30-40% among simulations. We show that these differences are most likely associated with differences in parameterized convection over the oceans, such that the spread in transport among simulations constrained with analysis fields is as large as the spread among free-running simulations.

large-scale tropospheric transport↗

Evaluation of Stratospheric Intrusions and Biomass Burning Plumes on the Vertical Distribution of Tropospheric Ozone Over the Midwestern U.S.

Naturally occurring ozone rich Stratosphere-to-Troposphere Transport (STT) intrusions and biomass burning plumes reaching the surface can contribute to exceedances of the U.S. National Ambient Air Quality Standards (NAAQS) for ground-level ozone (70 ppbv implemented in 2015). In addition, fires can inject significant pollution into the free troposphere where it can be transported long distances. The combined air quality impacts from these sources on ozone has only been analyzed in a few case studies for the Midwest U.S. Here we study ozone impacts in a major Midwestern city, for the first time in St. Louis, Missouri, using a series of ozonesonde profiles taken during the SEAC4RS (Studies of Emissions and Atmospheric Composition, Clouds and Climate Coupling by Regional Surveys) field campaign in August-September 2013. All ozonesondes showed some enhancements above the background profile levels (~55 ppbv) throughout each tropospheric column. Two models were used to estimate and quantify ozone origins within the columns. A chemical transport model identified enhancements from STT equivalent to 10to15 ppbv over the background with a 10 to15% contribution overall to the column. Two FLEXPART-WRF simulations, one with smoke in the boundary layer and the other with smoke above, identified enhancements from biomass burning equivalent to 10to 80 ppbv. Overall, the total biomass burning contribution is 15to 30% of the total column. Five ozonesondes showed signatures of mixed biomass burning plumes and STT intrusions. During this study period, biomass burning in the western U.S. contributed 70% to ozone enhancements in the total column compared to 3% from the central U.S and 27% from other areas.

National Ambient Air Quality Standards for ground‐↗

Heterogeneity and Chemical Reactivity of the Remote Troposphere Defined By Aircraft Measurements - Corrected

The NASA Atmospheric Tomography (ATom) mission built a photochemical climatology of air parcels based on in situ measurements with the NASA DC-8 aircraft along objectively planned profiling transects through the middle of the Pacific and Atlantic oceans. In this paper we present and analyze a data set of 10 s (2 km) merged and gap-filled observations of the key reactive species driving the chemical budgets of O3 and CH4 (O3, CH4, CO, H2O, HCHO, H2O2, CH3OOH, C2H6, higher alkanes, alkenes, aromatics, NOx, HNO3, HNO4, peroxyacetyl nitrate, and other organic nitrates), consisting of 146 494 distinct air parcels from ATom deployments 1 through 4. Six models calculated the O3 and CH4 photochemical tendencies from this modeling data stream for ATom 1. We find that 80 %–90 % of the total reactivity lies in the top 50 % of the parcels and 25 %–35 % in the top 10 %, supporting previous model-only studies that tropospheric chemistry is driven by a fraction of all the air. Surprisingly, the probability densities of species and reactivities averaged on a model scale (100 km) differ only slightly from the 2 km ATom 10 s data, indicating that much of the heterogeneity in tropospheric chemistry can be captured with current global chemistry models. Comparing the ATom reactivities over the tropical oceans with climatological statistics from six global chemistry models, we find generally good agreement with the reactivity rates for O3 and CH4. Models distinctly underestimate O3 production below 2 km relative to the mid-troposphere, and this can be traced to lower NOx levels than observed. Attaching photochemical reactivities to measurements of chemical species allows for a richer, yet more constrained-to-what-matters, set of metrics for model evaluation.

Tropospheric Chemistry↗

Stratospheric ozone - The possible effects of tropospheric-stratospheric feedback

The existence of tropospheric-stratospheric feedback mechanisms affecting variations in stratospheric ozone indicates the need to model the complete tropospheric-stratospheric system. For instance, a decrease in stratospheric ozone results in increased photolytic destruction of nitrous oxide in the troposphere and thereby reduced production of nitric oxide in the stratosphere. Estimates indicate that this mechanism will result in a recovery in atmospheric ozone of about 6 to 13 percent of the initial perturbation.

Chameides, W. L.↗

Effects of tropospheric and ionospheric refraction errors in the utilization of GEOS-C altimeter data

The effects of tropospheric and ionospheric refraction errors are analyzed for the GEOS-C altimeter project in terms of their resultant effects on C-band orbits and the altimeter measurement itself. Operational procedures using surface meteorological measurements at ground stations and monthly means for ocean surface conditions are assumed, with no corrections made for ionospheric effects. Effects on the orbit height due to tropospheric errors are approximately 15 cm for single pass short arcs (such as for calibration) and 10 cm for global orbits of one revolution. Orbit height errors due to neglect of the ionosphere have an amplitude of approximately 40 cm when the orbits are determined from C-band range data with predominantly daylight tracking. Altimeter measurement errors are approximately 10 cm due to residual tropospheric refraction correction errors. Ionospheric effects on the altimeter range measurement are also on the order of 10 cm during the GEOS-C launch and early operation period.

Goad, C. C.↗

Upper tropospheric dynamics as reflected in Nimbus 4 THIR 6.7-micron data

An investigation was conducted of the spatial and temporal relationships existing between the radiometrically observed water vapor patterns in cloud free areas and the conventionally derived water vapor patterns. The upper and middle tropospheric water vapor budget and the associated dynamics were examined to obtain a basis for a more definite evaluation of the significance of the Nimbus 4 radiometric 6.7-micrometer observations for the study of tropospheric dynamics in cloud free areas. A large-amplitude trough situated to the lee of the Rocky Mountains over the central U.S. between April 30 and May 1, 1970, was selected for the investigation because it best illustrated large upper tropospheric dynamic variations.

Rodgers, E. B.↗

Tropospheric effects on the middle atmosphere and vice-versa

The mechanisms by which phenomena occurring in the troposphere can affect that atmospheric region lying above the tropopause and below the mesopause are discussed as well as mechanisms by which middle atmospheric phenomena affect the tropospheric circulation, and how the middle atmosphere may act as a medium by which extraterrestrial effects may give rise to changes in tropospheric circulation. Energetics and external energy sources are considered. Aspects of vertical coupling examined include upward, downward, radiational, chemical, and electrical modes.

Geller, M. A.↗

Tropospheric limitations on the accuracy of phase measurement of coordinates in astronomy

The effect of tropospheric fluctuation on the accuracy of phase measurements of coordinates is discussed. The nature of the averaging of the tropospheric effects, if N coordinate measurements of duration T with period mu are made, is investigated. Various averaging modes depending on the relation of the various time parameters are investigated. Equations taking into account the correlations between individual observations are presented. It is shown that the correlation interval between the individual observations is always greater than the fluctuation period of tropospheric inhomogeneities typical for a given baseline.

Dravskikh, A. F.↗

Global atmospheric sampling program - Prospects for establishing a tropospheric ozone budget from commercial aircraft data

A preliminary analysis of zonally averaged, ozone concentration data obtained from commercial (GASP) aircraft between the equator and 60 deg North indicates that ozone in the upper troposphere exhibits a primary maximum during the spring, and, in middle latitudes, a secondary maximum in the summer of both 1975 and 1976. A late-fall/early-winter minimum also appears and seems consistent with previous upper air measurements. The April ozone maximum has been well documented and appears at the time when the stratospheric ozone content is greatest and cyclogenetic activity is most vigorous. However, the secondary maximum in June has not been widely observed or quoted as a unique feature. It is hypothesized that the rapid ascent of the tropopause between midspring and summer could account for the incorporation of ozone-rich, stratospheric air into the upper troposphere with a subsequent dilution during the following months. This may explain certain aspects of the annual ozone cycle in the lower troposphere which occasionally exhibit a bimodal distribution during the warm season.

Falconer, P. D.↗

Application of a microprocessor controlled lidar to tropospheric ozone measurements

A microprocessor controlled lidar system under construction at the NASA Goddard Space Flight Center is described and the problems in making space-based measurements of tropospheric ozone are considered. The differential absorption lidar using a dual wavelength, pulsed CO2 laser and direct detection receiver can significantly improve the existing global data base on tropospheric ozone burden. Sensitivity to tropospheric ozone can be obtained in the spaceborne version of lidar by selecting laser lines located in the wings of the target zone lines. Simulation studies using various laser line pairs in the P-branch of the CO2 9.4 micron band show that the ozone burden retrieval may be weighted to particular altitude regions. These simulation studies are based on numerical integration of differences in absorption coefficient at the two selected laser wavelengths using the AFGL absorption line parameter compilations, U.S. Standard Atmosphere ozone profile, and laser software. Simulation, data collection and reduction are performed by a microprocessor subsystem of the CO2 lidar.

Stewart, R. W.↗

Mark 3 VLBI system: Tropospheric calibration subsystems

Tropospheric delay calibrations are implemented in the Mark 3 system with two subsystems. Estimates of the dry component of tropospheric delay are provided by accurate barometric data from a subsystem of surface meteorological sensors (SMS). An estimate of the wet component of tropospheric delay is provided by a water vapor radiometer (WVR). Both subsystems interface directly to the ASCII Transceiver bus of the Mark 3 system and are operated by the control computer. Seven WVR's under construction are designed to operate in proximity to a radio telescope and can be commanded to point along the line-of-sight to a radio source. They should provide a delay estimate that is accurate to the + or - 2 cm level.

Resch, G. M.↗

Overview of the NASA tropospheric environmental quality remote sensing program

This paper will summarize the current NASA Tropospheric Environmental Quality Remote Sensing Program for studying the global and regional troposphere from space, airborne and ground-based platforms. As part of the program to develop remote sensors for utilization from space, NASA has developed a series of passive and active remote sensors which have undergone field test measurements from airborne and ground platforms. Recent measurements with active lidar and passive gas filter correlation and infrared heterodyne techniques will be summarized for measurements of atmospheric aerosols, CO, SO2, O3, and NH3. These measurements provide the data base required to assess the sensitivity of remote sensors for applications to urban and regional field measurement programs. Studies of Earth Observation Satellite Systems are currently being performed by the scientific community to assess the capability of satellite imagery to detect regions of elevated pollution in the troposphere. The status of NASA sponsored research efforts in interpreting satellite imagery for determining aerosol loadings over land and inland bodies of water will be presented, and comments on the potential of these measurements to supplement in situ and airborne remote sensors in detecting regional haze will be made.

Allario, F.↗

The sulfur budget of the troposphere

A one dimensional photochemical tropospheric model was used to calculate the vertical profiles of tropospheric species. Particular attention is focused on the recent inclusion of the chemistry of the sulfur group, which consists of 13 species involving a total of 45 chemical reactions. It is found that the chemistry of the sulfur species, because it is largely anthropogenic, plays an increasingly important role in the distribution of tropospheric gases. The calculated vertical profiles were compared to available measurements and generally found to be in good agreement.

Tiwari, S. N.↗

Tropospheric passive remote sensing: Introduction

Measurement needs regarding chemical and transport parameters were identified. Measurement of those gases involved in tropospheric photochemistry (O3, CO, CH4, NOx, HNO3, SO2, NH3, and CH3CCl3) and quantification of their sources and sinks, as well as a fundamental understanding of atmospheric chemical transformations were discussed. The photochemistry of OH and its role as a sink are summarized. The concentrations and lifetimes of the tropospheric gases were considered. Major concerns in tropospheric transport are the making of representative remote measurements of trace gases and aerosols and the dependence of these measurements on structural differences in the atmosphere.

Source record↗

The Seasat altimeter wet tropospheric range correction

It is found that the difference between the wet tropospheric corrections obtained with the Seasat Multichannel Microwave Radiometer (SMMR) algorithm and corrections based on near-coincident radiosonde meteorological measurements has a standard deviation of 2.79 cm, which is consistent with the independent value for water vapor determination accuracy reported by the SMMR Evaluation Team. Because the difference between the radiosonde corrections and those obtained by means of interpolated surface meteorological data has a standard deviation of 5.73 cm, the SMMR wet tropospheric correction is recommended for investigations sensitive to the wet tropospheric height correction accuracy.

Tapley, B. D.↗

The effects of isotropic multiple scattering and surface albedo on the photochemistry of the troposphere

The present study is believed to be the first investigation which combines a detailed tropospheric photochemical model with a radiative code that realistically considers the important physical processes in the cloudless troposphere which control the transfer of incoming solar radiation. It is found in most cases that the inclusion of the multiple scattering code significantly alters the photolytic reaction frequencies. This in turn alters the vertical distribution of some key tropospheric species. In the case of ozone a decrease was found, while O(1D) and OH showed increased concentrations. The increases are especially evident for the species which are highly dependent on photolysis processes that occur shortward of about 320 nm. The photolysis frequencies for ozone photolysis calculated with the Anderson-Meier model are in general in excellent agreement with recent measurements

Augustsson, T. R.↗