Measurements Of Ozone Vertical Profiles Research Articles

Measurements of Ozone Vertical Profiles in the Upper Troposphere–Stratosphere over Western Siberia by DIAL, MLS, and IASI

The purpose of this work is to measure the ozone vertical distribution (OVD) in the upper troposphere–stratosphere by differential absorption lidar (DIAL) at 299/341 nm and 308/353 nm and to compare and analyze the results against satellite data. А lidar complex for measuring the OVD in the altitude range ≈(5–45) km has been created. Here we analyze the results of ozone lidar measurements at wavelengths of 299/341 nm and 308/353 nm in 2018 at Siberian Lidar Station (SLS) and compare them with satellite (MLS/Aura and IASI/MetOp) measurements of OVD. The retrieved lidar OVD profiles in the upper troposphere–stratosphere in comparison with MLS/Aura and IASI/MetOp profiles, as well as the stitched OVD profile in comparison with the mid-latitude Krueger model, confirm the prospects of using the pairs of ozone sounding wavelengths 299/341 and 308/353 nm.

Intercomparison of Ozone Vertical Profile Measurements by Differential Absorption Lidar and IASI/MetOp Satellite in the Upper Troposphere–Lower Stratosphere

This paper introduces the technique of retrieving the profiles of vertical distribution of ozone considering temperature and aerosol correction in DIAL sounding of the atmosphere. The authors determine wavelengths, which are promising for measurements of ozone profiles in the upper troposphere–lower stratosphere. An ozone differential absorption lidar is designed for the measurements. The results of applying the developed technique to the retrieval of the vertical profiles of ozone considering temperature and aerosol correction in the altitude range 6–15 km in DIAL sounding of the atmosphere confirm the prospects of ozone sounding at selected wavelengths of 341 and 299 nm with the proposed lidar. The 2015 ozone profiles retrieved were compared with satellite IASI data and the Kruger model.

Impact of sampling frequency in the analysis of tropospheric ozone observations

Abstract. Measurements of ozone vertical profiles are valuable for the evaluation of atmospheric chemistry models and contribute to the understanding of the processes controlling the distribution of tropospheric ozone. The longest record of ozone vertical profiles is provided by ozone sondes, which have a typical frequency of 4 to 12 profiles a month. Here we quantify the uncertainty introduced by low frequency sampling in the determination of means and trends. To do this, the high frequency MOZAIC (Measurements of OZone, water vapor, carbon monoxide and nitrogen oxides by in-service AIrbus airCraft) profiles over airports, such as Frankfurt, have been subsampled at two typical ozone sonde frequencies of 4 and 12 profiles per month. We found the lowest sampling uncertainty on seasonal means at 700 hPa over Frankfurt, with around 5% for a frequency of 12 profiles per month and 10% for a 4 profile-a-month frequency. However the uncertainty can reach up to 15 and 29% at the lowest altitude levels. As a consequence, the sampling uncertainty at the lowest frequency could be higher than the typical 10% accuracy of the ozone sondes and should be carefully considered for observation comparison and model evaluation. We found that the 95% confidence limit on the seasonal mean derived from the subsample created is similar to the sampling uncertainty and suggest to use it as an estimate of the sampling uncertainty. Similar results are found at six other Northern Hemisphere sites. We show that the sampling substantially impacts on the inter-annual variability and the trend derived over the period 1998–2008 both in magnitude and in sign throughout the troposphere. Also, a tropical case is discussed using the MOZAIC profiles taken over Windhoek, Namibia between 2005 and 2008. For this site, we found that the sampling uncertainty in the free troposphere is around 8 and 12% at 12 and 4 profiles a month respectively.

Background ozone levels of air entering the west coast of the US and assessment of longer-term changes

An analysis of surface ozone measurements at a west coast site in northern California (Trinidad Head) demonstrates that this location is well situated to sample air entering the west coast of the US from the Pacific Ocean. During the seasonal maximum in the spring, this location regularly observes hourly average ozone mixing ratios ⩾50 ppbv in air that is uninfluenced by the North American continent. Mean daytime values in the spring exceed 40 ppbv. A location in southern California (Channel Islands National Park) demonstrates many of the characteristics during the spring as Trinidad Head in terms of air flow patterns and ozone amounts suggesting that background levels of ozone entering southern California from the Pacific Ocean are similar to those in northern California. Two inland locations (Yreka and Lassen Volcanic National Park) in northern California with surface ozone data records of 20 years or more are more difficult to interpret because of possible influences of local or regional changes. They show differing results for the long-term trend during the spring. The 10-year ozone vertical profile measurements obtained with weekly ozonesondes at Trinidad Head show no significant longer-term change in tropospheric ozone.

Ground-level ozone and ozone vertical profile measurements close to the foothills of the Guadarrama mountain range (Spain)

Continuous measurements of ozone vertical profiles, OVP, in the low troposphere (around 500–2400 m) using an unattended commercial ozone profiler DIAL, were conducted during June–July 2004 in Segovia, SG, a small city in the upper plateau located close to the foothills of the Guadarrama mountain range, Guadarrama, in the Central Massif. The data obtained over almost 37 complete days have enabled us to characterise the ozone vertical exchange, describe the phenomenology of the main ozone peaks, OP, recorded in the city and their relationship with ozone transport/formation from the gas precursor emissions of the greater Madrid area across Guadarrama. To achieve the last objective concurrent measurements of ground-level ozone in SG and a representative monitoring station upwind from Guadarrama, Buitrago de Lozoya, BL, have been used. 72.2% of the concurrent maximum diurnal ozone peaks exceeding the 95 percentile hourly value in SG (OPSG) and BL (OPBL) were linked to ozone transport and formation from the greater Madrid area towards Guadarrama. An estimate of the contribution of the greater Madrid area on OPSG yielded 28 μg m −3. The most prominent ozone vertical stratification was linked to the mixing height, MH, and a frequent nocturnal stable layer formed, NSL. Three small ozone enriched-layers were identified at mean heights of 500, 700 and 1000 m, respectively. Ozone tended to decline versus altitude. The hourly patterns of the three layers showed two peak occurrences of similar amplitude in the early morning, 7–8 h, and mid-afternoon, 14–16 h. A minimum was also observed during daytime, 10–11 h, its origin being attributed to a dilution process induced by the “chimney effect” caused by the slopes heating during this period. The comparison between OPSG, and the maximum diurnal ozone peaks in the first layer, OL1P, showed a satisfactory relationship, correlation coefficient, r, of the linear fit 0.77, and comparable mean values, 127 and 130 μg m −3, respectively, revealing the presence of an uniform ozone vertical distribution in the 500 m atmospheric layer above ground level during mid-afternoon.

Tropospheric ozone over the North Pacific from ozonesonde observations

As part of the Transport and Chemical Evolution over the Pacific (TRACE‐P) mission, ozonesondes were used to make ozone vertical profile measurements at nine locations in the North Pacific. At most of the sites there is a multiyear record of observations. From locations in the western Pacific (Hong Kong; Taipei; Jeju Island, Korea; and Naha, Kagoshima, Tsukuba, and Sapporo, Japan), a site in the central Pacific (Hilo, Hawaii), and a site on the west coast of the United States (Trinidad Head, California) both a seasonal and event specific picture of tropospheric ozone over the North Pacific emerges. Ozone profiles over the North Pacific generally show a prominent spring maximum throughout the troposphere. This maximum is tied to the location of the jet stream and its influence on stratosphere‐troposphere exchange and the increase in photochemical ozone production through the spring. Prominent layers of enhanced ozone in the middle and upper troposphere north of about 30°N seem to be more closely tied to stratospheric intrusions while biomass burning leads to layers of enhanced ozone in the lower and upper troposphere at Hong Kong (22°N) and Taipei (25°N). The lower free tropospheric layers at Hong Kong are associated with burning in SE Asia, but the upper layer may be associated with either equatorial Northern Hemisphere burning in Africa or SE Asian biomass burning. In the boundary layer at Taipei very high mixing ratios of ozone were observed that result from pollution transport from China in the spring and local urban pollution during the summer. At the ozonesonde site near Tokyo (Tsukuba, 36°N) very large enhancements of ozone are seen in the boundary layer in the summer that are characteristic of urban air pollution. At sites in the mid and eastern Pacific the signature of transport of polluted air from Asia is not readily identifiable from the ozonesonde profile. This is likely due to the more subtle signal and the fact that from the ozone profile and meteorological data by themselves it is difficult to identify such a signal. During the TRACE‐P intensive campaign period (February–April 2001), tropospheric ozone amounts were generally typical of those seen in the long‐term records of the stations with multiyear soundings. The exception was the upper troposphere over Hong Kong and Taipei where ozone amounts were lower in 2001.

Ozone in the Pacific tropical troposphere from ozonesonde observations

Ozone vertical profile measurements obtained from ozonesondes flown at Fiji, Samoa, Tahiti, and the Galapagos are used to characterize ozone in the troposphere over the tropical Pacific. There is a significant seasonal variation at each of these sites. At sites in both the eastern and western Pacific, ozone mixing ratios are greatest at almost all levels in the troposphere during the September‐November season and smallest during March‐May. The vertical profile has a relative maximum at all of the sites in the midtroposphere throughout the year (the largest amounts are usually found near the tropopause). This maximum is particularly pronounced during the September‐November season. On average, throughout the troposphere, the Galapagos has larger ozone amounts than the western Pacific sites. A trajectory climatology is used to identify the major flow regimes that are associated with the characteristic ozone behavior at various altitudes and seasons. The enhanced ozone seen in the midtroposphere during September‐November is associated with flow from the continents. In the western Pacific this flow is usually from southern Africa (although 10‐day trajectories do not always reach the continent) but also may come from Australia and Indonesia. In the Galapagos the ozone peak in the midtroposphere is seen in flow from the South American continent and particularly from northern Brazil. High ozone concentrations within potential source regions and flow characteristics associated with the ozone mixing ratio peaks seen in both the western and eastern Pacific suggest that these enhanced ozone mixing ratios result from biomass burning. In the upper troposphere, low ozone amounts are seen with flow that originates in the convective western Pacific.

Trends of ozone in the troposphere

Using a set of selected surface ozone (nine stations) and ozone vertical profile measurements (from six stations), we have documented changes in tropospheric ozone at a number of locations. From two stations at high northern hemisphere (NH) latitudes there has been a significant decline in ozone amounts throughout the troposphere since the early 1980s. At midlatitudes of the NH where data are the most abundant, on the other hand, important regional differences prevail. The two stations in the eastern United States show that changes in ozone concentrations since the early 1970s have been relatively small. At the two sites in Europe, however, ozone amounts increased rapidly into the mid‐1980s, but have increased less rapidly (or in some places not at all) since then. Increases at the Japanese ozonesonde station have been largest in the lower troposphere, but have slowed in the recent decade. The tropics are sparsely sampled but do not show significant changes. Small increases are suggested at southern hemisphere (SH) midlatitudes by the two surface data records. In Antarctica large declines in the ozone concentration are noted in the South Pole data, and like those at high latitudes of the NH, seem to parallel the large decreases in the stratosphere.

Mid stratospheric ozone minima in polar regions

Recent springtime measurements of ozone vertical profiles in polar regions have revealed local ozone depressions of about 25% at altitudes near 30 km. Similar features are also identified in three‐dimensional photochemical model results. The modeled ozone depressions are local and temporary, often associated with stratospheric warming events which transport air from low latitudes, altering its photochemical history. The feature may be a component of the climatology of the region, but occurs less frequently in the model, possibly because of the long‐standing problem of the underprediction of upper stratospheric ozone.

Toward an improved global network for determination of tropospheric ozone climatology and trends

An examination of typical tropospheric ozone variability on daily, monthly, annual and interannual timescales and instrumental precision indicates that the current ozonesonde network is insufficient to detect a trend in tropospheric ozone of ≤1% per year at the 2σ level even at stations with records a decade in length. From a trend prediction analysis we conclude that in order to detect a 1% per year trend in a decade or less it will be necessary to decrease the time between observations from its present value of 3–7 days to 1 day or less. The spatial distribution of the current ozonesonde stations is also inadequate for determining the global climatology of ozone. We present a quantitative theory taking into account photochemistry, surface deposition, and wind climatology to define the ‘effectively sampled region’ for an observing station which, used in conjunction with the instrumental precision and the above prediction analysis, forms the basis for defining a suitable global network for determining regional and global ozone climatology and trends. At least a doubling of the present number of stations is necessary, and the oceans, most of Asia, Africa, and South America are areas where more stations are most needed. Differential absorption lidar ozone instruments have the potential for far more frequent measurements of ozone vertical profiles and hence potentially more accurate climatology and trend determinations than feasible with ozonesondes but may produce a (fair weather) biased data set above the cloud base. A strategy for cloudy regions in which either each station utilizes both lidars and sondes or each station is in fact a ‘doublet’ comprised of a near-sea-level lidar and a proximal-mountain-top lidar could serve to minimize this bias.

Lidar measurements of ozone vertical profiles

Remote measurements of trace constituents using an active technique such as lidar have been made possible for the rapid development of powerful tunable laser sources. This paper, originally presented at the OSA Topical Meeting on Optical Remote Sensing of the Atmosphere, in January 1985, illustrates the differential absorption lidar technique used for the measurement of the ozone vertical distribution in the troposphere and the atmosphere.