Ziemke, J. R., S. Chandra, and P. K.
Bhartia, A 25-year data record of stratospheric and tropospheric
ozone from TOMS Cloud Slicing: Implications for stratospheric
ozone recovery,
J. Geophys. Res. , submitted, 2004.
Abstract. The newly reprocessed Solar Backscatter Ultraviolet (SBUV)
and Total Ozone Mapping Spectrometer (TOMS) data from 1978 to 2003 are
used to estimate the seasonal cycle, latitude dependence and long-term
trends in ozone in three broad layers of the atmosphere: upper
stratosphere (32 hPa and above), lower stratosphere (32 hPa to
tropopause), and the troposphere. The ozone amount in these layers is
derived by first determining stratospheric column ozone (SCO) from
TOMS using deep convective clouds in the Pacific. The validity of
this "Cloud Slicing" technique is extensively tested using SCO derived
from Stratospheric Aerosols and Gas Experiment (SAGE) data.
Tropospheric column ozone (TCO) is then derived by taking the
difference between total column ozone and SCO. The validity of the
Cloud Slicing technique for obtaining TCO is also tested using
extensive data from the Southern Hemisphere Additional Ozonesondes
(SHADOZ) ozonesonde network. SBUV ozone data are used to estimate
upper stratospheric column ozone (USCO). Finally, lower stratospheric
column ozone (LSCO) is derived from the difference between SCO and
USCO. This process yields a unique 25-year long record of ozone in
three atmospheric layers covering all latitudes and seasons. By
contrast, SAGE provides limited spatial and temporal coverage of the
stratosphere, albeit at much higher vertical resolution. Our analysis
shows that the seasonal cycle, latitude dependence, and trends of
USCO, LSCO, and TCO are quite different. In particular, the
decreasing trends in USCO have moderated in recent years, while LSCO
trends are continuing. In the troposphere, the TCO shows a
statistically significant upward trend in mid-latitudes of both
hemispheres, but not in the tropics.
Chandra, S., J. R. Ziemke, X. Tie,
and G. Brasseur, Elevated ozone in the troposphere over the Atlantic
and Pacific oceans in the Northern Hemisphere,
Geophys. Res. Lett. , Vol. 31, L23102,
doi:10.1029/2004GL020821, 2004.
Abstract. Tropospheric column ozone (TCO) is derived from differential
measurements of total column ozone from Total Ozone Mapping
Spectrometer (TOMS), and stratospheric column ozone (SCO) from the
Microwave Limb Sounder (MLS) instrument on the Upper Atmosphere
Research Satellite (UARS). It is shown that TCO during late spring
and summer months over the Atlantic and Pacific Oceans at northern
mid-latitudes is about 50-60 Dobson Units (DU) which is about the same
as over the continents of North America, Europe and Asia (except high
altitude mountain regions), where surface emissions of NOx from
industrial sources, biomass and biofuel burning, and biogenic
emissions are significantly larger. The zonal characteristics of TCO
derived from satellite measurements are generally simulated by a
global chemical transport model called MOZART-2, but some
discrepancies are also shown. The model results are analyzed to
delineate the relative importance of surface NOx emission, lightning
NOx and stratospheric flux.
Ziemke, J. R., and S. Chandra, A
Madden-Julian Oscillation in Tropospheric Ozone, Geophys. Res. Lett. , Vol. 30,
No. 23, 2182, 10.1029/2003GL018523, 2003.
Abstract. This study shows evidence of a Madden-Julian Oscillation
(MJO) in tropospheric ozone. Tropospheric ozone is derived using
differential measurements of total column ozone and stratospheric
column ozone measured from total ozone mapping spectrometer (TOMS) and
microwave limb sounder (MLS) instruments. Two broad regions of
significant MJO signal are identified in the tropics, one in the
western Pacific and the other in the eastern Pacific. Over both
regions, MJO variations in tropospheric ozone represent 5-10 Dobson
Unit (DU) peak-to-peak anomalies. These variations are significant
compared to mean background amounts of 20 DU or less over most of the
tropical Pacific. MJO signals of this magnitude would need to be
considered when investigating and interpreting particular pollution
events since ozone is a precursor of the hydroxyl (OH) radical, the
main oxidizing agent of pollutants in the lower atmosphere.
Ahn, C., J. R. Ziemke, S. Chandra, and
P. K. Bhartia, Derivation of tropospheric column ozone from the Earth
Probe TOMS/GOES co-located data sets using the Cloud Slicing
technique, J. Atmos. Sol. Terr. Phys.
, 65 (10), 1127-1137, 2003.
Abstract. A recently developed technique called cloud slicing used
for deriving upper tropospheric ozone from the Nimbus 7 Total Ozone
Mapping Spectrometer (TOMS) instrument combined with
temperature-humidity and infrared radiometer (THIR) is not applicable
to the Earth Probe TOMS (EP TOMS) because this satellite platform does
not have an instrument to measure cloud-top temperatures. For
continuing monitoring of tropospheric ozone between 200-500hPa and
testing the feasibility of this technique across spacecrafts, EP TOMS
data are co-located in time and space with the Geostationary
Operational Environmental Satellite (GOES)-8 infrared data for year
2001 and early 2002, covering most of North and South America (45S-45N
and 120W-30W). Results show that the maximum column amounts for the
mid-latitudinal sites of the northern hemisphere are found in the
March-May season. For the mid-latitudinal sites in the southern
hemisphere, the highest column amounts are found in the
September-November season with overall seasonal variability smaller
than that in the northern hemisphere. The tropical sites show weaker
seasonal variability compared to higher latitudes. The derived
results for selected sites are cross-validated qualitatively with the
seasonality of ozonesonde observations and the results from THIR
analyses over the 1979-1984 time period. These comparisons show a
reasonably good agreement among THIR, ozonesonde observations, and
cloud slicing-derived column ozone. Cloud slicing measurements from
TOMS coincide with large-scale convection events, especially in
regions of the tropospheric wind jets (around +/-30 degrees latitude).
In these cases they may not be representative of typical conditions in
the atmosphere. Two new variant approaches, High-Low (HL) cloud
slicing and ozone profile derivation from cloud slicing are introduced
to estimate column ozone amounts using the entire cloud information in
the troposphere. A future satellite platform such as the Earth
Observing System (EOS) Aura with the ozone monitoring instrument (OMI)
can provide better statistics of derived ozone because of improved
spatial resolution and improved measurements of cloud-top pressures.
Ziemke, J. R., S. Chandra, and P. K.
Bhartia, Upper tropospheric ozone derived from Cloud Slicing
technique: Implications for large-scale convection, J. Geophys. Res. , Vol. 108,
No. D13, 4390, 10.1029/2002JD002919, 2003.
Abstract. This study evaluates the spatial distributions and seasonal
cycles in upper tropospheric ozone (pressure range 200-500 hPa) from
low to high latitudes (60S to 60N) derived from the satellite
retrieval method called "Cloud Slicing". The Cloud Slicing method
determines ozone profile information in the troposphere by combining
co-located measurements of cloud-top pressure and above-cloud column
ozone. Measurements of Nimbus 7 Total Ozone Mapping Spectrometer
(TOMS) above-cloud column ozone and N imbus 7 Temperature Humidity
Infrared Radiometer (THIR) cloud-top pressure during 1979-1984 were
merged to derive upper tropospheric ozone. Because of large footprint
measurements from TOMS (~100 km diameter on average), upper
tropospheric ozone derived from Cloud Slicing coincides with
large-scale convection events. These events are not necessarily
representative of average atmospheric conditions in regions near and
poleward of the tropospheric wind jets (around +/-30 degrees
latitude), especially in winter and spring seasons when dynamical wave
activity in the troposphere and lower stratosphere is most intense.
The Cloud Slicing method with Nimbus 7 geometry in any case provides a
unique opportunity to investigate the behavior of upper tropospheric
ozone under condition of intense broad-scale convection. In the
tropics the measured upper tropospheric ozone shows year-round
enhancement in the Atlantic region and evidence of a possible
semiannual variability. Outside the tropics upper tropospheric ozone
from Cloud Slicing shows greatest abundance in winter and spring
seasons in both hemispheres with largest variance and largest amounts
in the northern hemisphere. This seasonal cycle behavior under
conditions of intense convection is different from general ozonesonde
climatology which shows instead upper tropospheric ozone maximizing
around early-to-mid summer months. The seasonal cycles and spatial
characteristics in upper tropospheric ozone from Cloud Slicing are
similar to lower stratospheric ozone. It is suggested that the
large-scale convection events with Cloud Slicing coincide with an
occurrence of stratosphere-troposphere exchange (STE).
Chandra, S., J. R. Ziemke, and R.
V. Martin, Tropospheric ozone at tropical and middle latitudes derived
from TOMS/MLS residual: Comparison with a global model, J. Geophys. Res. , Vol. 108, No. D9,
4291, 10.1029/2002JD002912, 2003.
Abstract. The tropospheric ozone residual method is used to derive
zonal maps of tropospheric column ozone using concurrent measurements
of total column ozone from Nimbus 7 and Earth Probe (EP) Total Ozone
Mapping Spectrometer (TOMS) and stratospheric column ozone from the
Microwave Limb Sounder (MLS) instrument on the Upper Atmosphere
Research Satellite (UARS). Our study shows that the zonal variability
in TOMS total column ozone at tropical and sub-tropical latitudes is
mostly of tropospheric origin. The seasonal and zonal variability
in tropospheric column ozone (TCO), derived from the TOMS/MLS
residual, are consistent with that derived from the convective cloud
differential (CCD) method and ozonesonde measurements in regions where
these data overlap. A comparison of TCO derived from the TOMS/MLS
residual and a global 3D model of tropospheric chemistry (GEOS-CHEM)
for 1996-1997 shows good agreement in the tropics south of the
equator. Both the model and observations show similar zonal and
seasonal characteristics including an enhancement of TCO in the
Indonesian region associated with the 1997 El Nino. Both show the
decline of the wave-1 pattern from the tropics to the extratropics as
lightning activity and the Walker circulation decline. Both show
enhanced ozone in the downwelling branches of the Hadley Circulation
near +/-30 degrees latitude. Model and observational differences
increase with latitude during winter and spring.
Ziemke, J. R., and S. Chandra,
La Nina and El Nino-induced variabilities of ozone in the tropical
lower atmosphere during 1970-2001,
Geophys. Res. Lett. , Vol 30, No. 3, 1142,
10.1029/2002GL016387, 2003.
Abstract. This study provides the first evidence from several decades
of satellite measurements that both La Nina and El Nino events have a
comparable and dramatic impact in altering the interannual variability
and distribution of tropospheric ozone in the tropics. Measurements
of tropospheric ozone were combined from several total ozone mapping
spectrometer (TOMS) and backscatter ultraviolet (BUV) satellite
instruments to establish long time series in the tropics extending
from April 1970 through December 2001. The changes in tropospheric
column ozone (TCO) for both La Nina and El Nino are sizeable when
compared to local values which average from less than 15 Dobson Units
(DU) up to 25 DU over the year. It is suggested that interannual
changes in TCO from combined La Nina and El Nino are the dominant
source of decadal variability in the tropics.
Chandra, S., J. R. Ziemke, P. K. Bhartia,
and R. V. Martin, Tropical tropospheric ozone: Implications for
dynamics and biomass burning, J. Geophys.
Res. , Vol. 107, D14, 10.1029/2001JD000447, 2002.
Abstract. This paper studies the significance of large scale
transport and pyrogenic (e.g., biomass burning) emissions in the
production of tropospheric ozone in the tropics. Using aerosol index
(AI) and tropospheric column ozone (TCO) time series from 1979 to 2000
derived from the Nimbus 7 and Earth Probe TOMS measurements, our study
shows significant differences in the seasonal and spatial
characteristics of pyrogenic emissions north and south of the equator
in the African region and Brazil in South America. Notwithstanding
these differences, most of the observed seasonal characteristics are
well simulated by the GEOS-CHEM global model of tropospheric
chemistry. The only exception is the northern African region where
modeled and observed TCO differ signficantly. In the Indonesian
region, the most significant increase in TCO occurred during
September-December 1997, folllowing large-scale forest and savanna
fires associated with the El Nino-induced dry condition. The increase
in TCO extended over most of the western Pacific well outside the
burning region and was accompanied by a decrease in the eastern
Pacific resembling a west-to-east dipole about the dateline. These
features are well simulated in the GEOS-CHEM model which suggests that
both the biomass burning and changes in meteorological conditions
during El Nino period contributed almost equally to the observed
increase in TCO in the Indonesian region. During 1997, the net
increase in TCO integrated over the tropical region between 15N and
15S was about 6-8 Tg (1 Tg = 10^12 gm) over the mean climatological
value of about 77 Tg. The GEOS-CHEM model suggests that most of this
increase may have been caused by biomass burning in the Indonesian
region. However the interannual variability in the area-averaged
column ozone in the tropics is influenced by a number of factors
including the quasi-biennial oscillation and solar cycle.
Ziemke, J. R., S. Chandra, and P. K.
Bhartia, "Cloud Slicing": A new technique to derive upper tropospheric
ozone from satellite measurements, J.
Geophys. Res., 106, 9853-9867, 2001.
Abstract. A new technique denoted cloud slicing has been developed
for measuring upper tropospheric ozone. Cloud slicing takes advantage
of the opaque property of water vapor clouds to ultraviolet wavelength
radiation. Measurements of above-cloud column ozone from the Nimbus 7
total ozone mapping spectrometer (TOMS) instrument are combined
together with Nimbus 7 temperature humidity and infrared radiometer
(THIR) cloud-top pressure data to derive ozone column amounts in the
upper troposphere. In this study tropical TOMS and THIR data for the
period 1979-1984 are analyzed. By combining total tropospheric column
ozone (denoted TCO) measurements from the convective cloud
differential (CCD) method with 100-400 hPa upper tropospheric column
ozone amounts from cloud slicing, it is possible to estimate 400-1000
hPa lower tropospheric column ozone and evaluate its spatial and
temporal variability. Results for both the upper and lower tropical
troposphere show a year-round zonal wavenumber 1 pattern in column
ozone with largest amounts in the Atlantic region (up to around 15 DU
in the 100-400 hPa pressure band and around 25-30 DU in the 400-1000
hPa pressure band). Upper tropospheric ozone derived from cloud
slicing shows maximum column amounts in the Atlantic region in the
June-August and September-November seasons which is similar to the
seasonal variability of CCD derived TCO in the region. For the lower
troposphere, largest column amounts occur in the September-November
season over Brazil in South America and also southern Africa.
Localized increases in the tropics in lower tropospheric ozone are
found over the northern region of South America around August and off
the west coast of equatorial Africa in the March-May season. Time
series analysis for several regions in South America and Africa show
an anomalous increase in ozone in the lower troposphere around the
month of March which is not observed in the upper troposphere. The
eastern Pacific indicates weak seasonal variability of upper, lower,
and total tropospheric ozone compared to the western Pacific which
shows largest TCO amounts in both hemispheres around spring months.
ozone variability in the western Pacific is expected to have greater
variability caused by strong convection, pollution and biomass
burning, land/sea contrast and monsoon developments.
Martin, R. V., D. J. Jacob, J. A. Logan,
J. R. Ziemke, and R. Washington, Detection of lightning influence on
tropical tropospheric ozone, Geophys. Res. Lett., 11, 1639-1642,
2000.
Abstract. Empirical orthogonal functions (EOFs) are used to analyze a
14-year record of tropical tropospheric ozone columns (TTOCs)
determined from satellite measurements. The first EOF explains 54% of
TTOC variance and represents biomass burning in Africa and South
America. The second EOF explains 20% of the variance and has a
distinct lightning signature.
Ziemke, J. R., S. Chandra, and P. K. Bhartia,
A new NASA data product: Tropospheric and stratospheric column ozone in
the tropics derived from TOMS measurements, Bull.
Amer. Meteorol. Soc., 81, 580-583, March, 2000.
Abstract. Tropospheric and stratospheric column ozone data in the
tropics for 1979-present are now available for the general scientific
community for the first time. These data are derived at NASA Goddard
Space Flight Center and may be obtained via either direct ftp,
world-wide-web, or electronic mail. The objective of this note is to
provide information about the data including an overview of the
method, validation efforts, and adjustments. Tropospheric column ozone
time series are shown to compare well with recent 1998-1999 ozonesonde
measurements from the Southern Hemisphere ADditional OZonesondes
(SHADOZ) project. An important adjustment made to this new data set is
a correction for absorbing aerosols (e.g., smoke, dust) in the
troposphere. The presence of absorbing aerosols produces an
underdetermination of tropospheric column ozone amounts. The new data
products of tropospheric and stratospheric column ozone provide useful
information on variabilities from monthly to decadal
timescales. Previous analyses of the data indicate the first detected
solar-cycle signal (2-3 DU peak-to-peak) and also a robust El
Nino-induced signal (5-10 Dobson units) in tropospheric column
ozone. It is anticipated that these new data products from NASA will
prove beneficial for the study and modeling of ozone in the
tropics.
Ziemke, J. R., and S. Chandra, Seasonal and
interannual variabilities in tropical tropospheric ozone, J.
Geophys. Res., 104, 21,425-21,442, 1999.
Abstract. This paper presents the first detailed characterization of
seasonal and interannual variability in tropical tropospheric column
ozone (TCO) to delineate the relative importance of biomass burning
and large-scale transport. TCO time series are derived from 20 years
(1979-1998) of total ozone mapping spectrometer (TOMS) data using the
convective cloud differential (CCD) method. Our study identifies three
regions in the tropics with distinctly different characteristics
related to seasonal and interannual variability. These three regions
are the eastern Pacific, Atlantic, and western Pacific. TCO in the
Atlantic region peaks at about the same time (September-October) both
north and south of the Equator, while the annual-cycle amplitude in
TCO varies from about 3 to 6 Dobson units (DU) from north to south of
the Equator. In comparison, annual cycles in TCO in both the eastern
and western Pacific are generally weak with largest TCO amount
occurring around March-April in the northern hemisphere and
September-November in the southern hemisphere. Interannual
variabilities in these three regions are also very different. The
Atlantic region indicates a quasi-biennial oscillation (QBO) in TCO
which is out of phase with the QBO in stratospheric ozone. This is
consistent with the photochemical control of this region by
ozone-producing precursors. The observed pattern however does not
seem to be related to interannual variability in ozone precursors
related to biomass burning. Instead it appears to be a manifestation
of the UV modulation of upper tropospheric chemistry on a QBO time
scale caused by stratospheric ozone. During El Nino events there is
anomalously low TCO in the eastern Pacific and high values in the
western Pacific, indicating the effects of convectively-driven
transport. The observed increase of 10-20 DU in TCO in the Indonesian
region in the western Pacific during the recent 1997-1998 El Nino was
associated with large-scale fires which may have contributed 5-10 DU
of the total increase. Finally, a simplified tropospheric ozone
residual (STOR) method is proposed in this study to derive
high-resolution maps of TCO in the tropics even in the absence of
tropopause-level clouds.
Chandra, S., J. R. Ziemke, and R. W. Stewart,
An 11-year solar cycle in tropospheric ozone from TOMS measurements, Geophys.
Res. Lett., 26, 185-188, 1999.
Abstract. Tropospheric column ozone derived from Nimbus 7 total ozone
mapping spectrometer (TOMS) footprint measurements from 1979 to 1992
provide the first observational evidence of changes in tropospheric
ozone in the marine atmosphere of the tropics which are out of phase
with stratospheric ozone changes on a time scale of a solar cycle. The
estimated changes in tropospheric and stratospheric column ozone over
a solar cycle are respectively -2.98 +/-1.31 and +8.63 +/-1.99 Dobson
units (DU), or equivalently -12.6 +/-5.6 and +3.69 +/-0.86 % from
solar minimum to solar maximum. These values are statistically
significant at the 2-sigma level. In comparison, linear trends in
tropical tropospheric ozone are not statistically significant. These
observations are qualitatively consistent with a modulation effect on
tropospheric ozone photochemistry by UV-induced changes in
stratospheric ozone. However, in the low NOx regime of the marine
atmosphere the observed changes are signficantly larger than estimated
from a photochemical model.
Chandra, S., J. R. Ziemke, W. Min, and W. G.
Read, Effects of 1997-1998 El Nino on tropospheric ozone and water vapor,
Geophys.
Res. Lett., 3867-3870, 1998.
Abstract. This paper analyzes the impact of the 1997-1998 El Nino on
tropospheric column ozone (TCO) and tropospheric H2O derived from the
earth probe (EP) total ozone mapping spectrometer (TOMS) and Upper
Atmosphere Research Satellite (UARS) microwave limb sounder (MLS)
instruments, respectively. The 1997-1998 El Nino, characterized by an
anomalous increase in sea-surface temperature (SST) across the eastern
and central tropical Pacific Ocean, is one of the strongest El Nino
Southern Oscillation (ENSO) events of the century, comparable in
magnitude to the 1982-83 episode. The major impact of the SST change
has been a shift in the convection pattern from the western to the
eastern Pacific affecting the response of the rain-producing
cumulonimbus. As a result, there has been a significant increase in
rainfall over the eastern Pacific and decrease over the western
Pacific and Indonesia. The dryness in the Indonesian region has
contributed to large scale burning by uncontrolled wildfires in the
tropical rainforests of Sumatra and Borneo. Our study shows that TCO
decreased by 4-8 Dobson units (DU) in the eastern Pacific and
increased by about 10-20 DU in the western Pacific as a result of the
eastward whift of the tropical convective activity. The effect of this
shift is also evident in upper tropospheric H2O which varies inversely
as ozone. Our study suggests that a significant increase in TCO and
decrease in tropospheric H2O in this region is related to El
Nino-induced changes in the Walker circulation as inferred from the
National Oceanic and Atmospheric Administration (NOAA) outgoing
longwave radiation (OLR) and Geostationary Earth Orbiting Satellite-1
(GEOS-1) zonal and vertical wind data. This does not exclude the
possibility that some increase in TCO may have been caused by biomass
burning in the Indonesian region.
Ziemke, J. R., S. Chandra, and P. K. Bhartia,
Two new methods for deriving tropospheric column ozone from TOMS measurements:
The assimilated UARS MLS/HALOE and convective-cloud differential techniques,
J.
Geophys. Res., 103, 22,115-22,127, 1998.
Abstract. This study introduces two new approaches for determining
tropospheric column ozone from satellite data. In the first method,
stratospheric column ozone is derived by combining Upper Atmospheric
Research Satellite (UARS) halogen occultation experiment (HALOE) and
microwave limb sounder (MLS) ozone measurements. Tropospheric column
ozone is then obtained by subtracting these stratospheric amounts from
the total column. Total column ozone in this study include retrievals
from Nimbus-7 (November 1978-May 1993) and earth probe (July
1996-present) total ozone mapping spectrometer (TOMS). Data from HALOE
are used in this first method to extend the vertical span of MLS
(highest pressure level 46 hPa) using simple regression. This
assimilation enables high-resolution daily maps of stratospheric ozone
which is not possible from solar occultation measurements alone, such
as from HALOE or Stratospheric Aerosols and Gas Experiment (SAGE). We
also examine another new and promising technique that yields
tropospheric column ozone directly from TOMS high-density footprint
measurements in regions of high convective clouds. We define this
method as the convective-cloud differential (CCD) technique. The CCD
method is shown to provide long time series (essentially late 1978 to
the present) of tropospheric ozone in regions dominated by persistent
high tropopause-level clouds, such as the maritime tropical Pacific
and within or near midlatitude continental landmasses. This method
also indicates a dominant coupling of tropospheric ozone in the
tropical Pacific region with the El Nino and La Nina events. For
validation purposes, both the CCD and assimilated UARS MLS/HALOE
results are compared with ozonesonde data from several southern
tropical stations. Despite all three measurements being distinctly
different in sampling and technique, all three show good qualitative
aggreement.
Ziemke, J. R., and S. Chandra,
Comment on "Tropospoheric ozone derived from TOMS/SBUV measurements
during TRACE A", by J. Fishman et al., J.
Geophys. Res., 103, 13,903-13,906, 1998.
Abstract. Recently, Fishman et al. [1996] combined Nimbus 7 total
ozone mapping spectrometer (TOMS) total ozone with vertical ozone
profiles from the NOAA 11 solar backscatter ultraviolet 2 (SBUV2)
instrument in an effort to estimate tropospheric ozone residuals
(TOR). They included tropopause height fields from the National
Meteorological Center (NMC) to calculate stratospheric column ozone
from the SBUV2 profiles. TOR was then calculated by subtracting
stratospheric column ozone from TOMS total ozone. We note that this
same method for deriving TOR was used earlier by Vukovich et
al. [1996]. A more recent study by Vukovich et al. [1997] describes
the potentially large errors using this method by comparing one-to-one
with ground-based ozonesonde data. In our short comment we focus on
tropical latitudes and illustrate that significant errors arise in
stratospheric column ozone derived from SBUV because of the
combination of vertical weighting functions and the inversion
algorithm.
Ziemke, J. R., and S. Chandra, On
tropospheric ozone and the tropical wave 1 in total ozone, Atmospheric Ozone, Vol. 1 ,
Ed. R. D. Bojkov and G. Visconti, pp. 447-450, 1998.
Abstract. Studies have shown that total ozone in the southern tropics
exhibits a year-round stationary wave 1 pattern with maximum
peak-to-peak amplitudes ~20-30 Dobson units (DU) during southern
spring (September-October). The crest of this wave occurs in the
south Atlantic region with largest amplitudes occurring within the
months of intense biomass burning in South America and Africa from
July-October. However, because the wave exists in all months of the
year (weakest in May-June with peak-to-peak amplitudes ~10-12 DU),
this indicates the presence of a persistent dynamical forcing
mechanism. The present study investigates the persistence of the
wave, combining ozonesonde data from several tropical stations with 14
years (1979-1992) of both Nimbus 7 total ozone mapping spectrometer
(TOMS) ozone and National Centers for Environmental Prediction (NCEP)
geopotential height analyses. The limited number of ozonesonde
profiles in the tropics indicates that the primary contribution to
both tropospheric column ozone and the TOMS ozone wave 1 lies in the
low to middle troposphere, maximizing around altitudes 4-5 km. Near
this maxima, 500 hPa (~5 km altitude) geopotential heights show a
persistent (year-round) wave 1 pattern in the south Atlantic similar
to TOMS ozone, indicating both equatorward transport of subtropical
ozone into the region and a potential for planetary scale subsidence
effects. This is the first study providing evidence that lower
tropospheric ozone and dynamical transport have major roles in
establishing persistence of the wave 1 anomaly in total ozone.
Ziemke, J. R., S. Chandra, A. M. Thompson,
and D. P. McNamara, Zonal asymmetries in southern hemisphere column
ozone: Implications of biomass burning, J. Geophys. Res., 101, 14,421-14,427,
1996.
Abstract. Studies have shown that total ozone in the southern tropics
exhibits a year-round stationary wave 1 pattern with maximum
peak-to-peak amplitudes ~20-30 Dobson units (DU) during southern
spring (September-October). The crest of this wave occurs in the
south Atlantic region with largest amplitudes occurring within the
months of intense biomass burning in South America and Africa from
July-October. However, because the wave exists in all months of the
year (weakest in May-June with peak-to-peak amplitudes ~10-12 DU),
this indicates the presence of a persistent dynamical forcing
mechanism. The present study investigates the persistence of the
wave, combining ozonesonde data from several tropical stations with 14
years (1979-1992) of both Nimbus 7 total ozone mapping spectrometer
(TOMS) ozone and National Centers for Environmental Prediction (NCEP)
geopotential height analyses. The limited number of ozonesonde
profiles in the tropics indicates that the primary contribution to
both tropospheric column ozone and the TOMS ozone wave 1 lies in the
low to middle troposphere, maximizing around altitudes 4-5 km. Near
this maxima, 500 hPa (~5 km altitude) geopotential heights show a
persistent (year-round) wave 1 pattern in the south Atlantic similar
to TOMS ozone, indicating both equatorward transport of subtropical
ozone into the region and a potential for planetary scale subsidence
effects. This is the first study providing evidence that lower
tropospheric ozone and dynamical transport have major roles in
establishing persistence of the wave 1 anomaly in total ozone.