1996 Progress Report on EOS IDS
Steve E. Cohn, Goddard Space Flight Center
Anne R. Douglass, Goddard Space Flight Center
James Gleason, Goddard Space Flight Center
Charles H. Jackman, Goddard Space Flight Center
Leslie R. Lait, Hughes STX, Landover, MD
Paul A. Newman, Goddard Space Flight Center
Richard B. Rood, Goddard Space Flight Center
Joan E. Rosenfield, Goddard Space Flight Center
Richard S. Stolarski, Goddard Space Flight Center
Anne M. Thompson, Goddard Space Flight Center
Marvin A. Geller, State University of New York-Stony Brook
Robert D. Hudson, University of Maryland-College Park
Our research efforts achieved the major goal of completing the first of the Multiyear Ozone Depletion Experiments (MODE) which has been recently published in JGR. The goal of MODE is to model the development of the polar ozone depletions using satellite and ground based data. The cover figure and Figure 2.2.1-1 (and enclosed viewgraph) summarize the Antarctic results of MODE which reproduce the development of the ozone hole. The MODE trajectory technique is now being extended to study the northern hemisphere.
We have also achieved a milestone with our 2D interactive model. Our Pinatubo studies (Figures 2.2.5-1,2) show good agreement with observations - probably the best achieved yet with a 2D model with interactive dynamics. We are now turning our attention to climate studies (CO2 doubling).
The main thrust of the 3D chemical modelling effort (partially supported under this IDS) is to understand the impact of the EOS assimilation winds on the transport of long lived tracers. These studies and direct constituent assimilation studies described below are having a positive impact on the stratospheric assimilation.
Aircraft data analysis has always been a central theme of the proposal. We are now just beginning to analyze the TOTE/VOTE data in conjunction with our ongoing STRAT data analysis. Part of our effort is to focus on tropical dynamics and implications for mixing. We have been modelling the QBO as well as estimation the mixing from the tracer-wind correlations.
Our analysis of tropospheric ozone continues, and we are looking at an improvement to the Fishman residual technique to estimate tropospheric ozone from TOMS and SAGE data. In the first part of this effort, we are building a climatology of lower stratospheric ozone using trajectory mapping (developed under this IDS). We are also approaching the problem using potential vorticity - potential temperature binning. In the text below we describe work with tropical TOMS measurements and estimates of tropospheric ozone from that data.
Using the UARS and aircraft data along with high resolution trajectory studies, we are also investigating the fundamental mixing processes of the stratosphere.
Finally, we continue to support the trajectory automailer which is heavily used by the community (53% increase in 1995 over 1994). The automailer statistics are shown at the end of this report. Eighteen publications were associated with this IDS in FY 1996.
This report is located at http://hyperion.gsfc.nasa.gov/EOS/report_1996/report.html
Our 1995 report is located on the world-wide web at
http://hyperion.gsfc.nasa.gov/EOS/report_1995/report.html
The introduction to the 1995 report summarizes our main research goals and progress up
through 1995. This report stands as an update of the 1995 report. The sectional structure is
similar to the 1995 report so that the reader can compare this report to the 1995 report section
by section except were indicated.
The goal of MODE under this IDS is to simulate the observed long-term change in ozone
within the polar vortex. The first phase of this experiment involved simulating the growth of
the Antarctic ozone hole. This phase has been completed and published in Schoeberl et al.
[1996].We have now begun to simulate the Arctic ozone loss as described below. The
MODE project is central to the IDS goal of isolating anthropogenic and natural changes in
ozone.
To address the Antarctic problem, we concentrated on simulating the UARS observed changes
in ozone using the Lagrangian chemistry model. The procedure was as follows: first,
Cryogenic Limb Array Talon Spectrometer (CLAES) and Microwave Limb Sounder (MLS)
data are mapped into potential vorticity space for data collected on August 17, 1992. Halogen
Occultation Experiment (HALOE) HCl data is used from the entire previous month (because
HALOE data is collected more slowly than CLAES and MILS data, we have to include the
data over a longer period to get sufficient sampling with respect to potential vorticity). The
UARS data are then used to initialize the Lagrangian chemical model. The model is then run
forward for a month for 625 regularly spaced isentropic trajectories. The isentropic
assumption is appropriate for the Antarctic vortex, as diabatic cooling rates are small in late
winter. After validating the 1992 ozone loss we ran the model for all the TOMS years to see
if we could reproduce the chlorine trends. The year to year variability was difficult to
reproduce but the overall development of the ozone hole
The Antarctic MODE results were published in Schoeberl et al. [1996].
Figure 2.1.1-1 shows
the long term changes in Antarctic ozone from the MODE Antarctic experiment.
We are now gearing up for a MODE Arctic experiment. To do this, a number of significant
model changes had to be made because of the larger diabatic descent. A preliminary January
1993 experiment has been performed.
Figure 2.1.2-1a and
Figure 2.1.2-1b
show the results of the experiment,
comparing the Arctic ozone loss at a single isentropic level. Future tasks include full diabatic
runs and a simplified denitrification scheme.
This section describes some of the other chemical and dynamical activities supported under
this IDS. The testing and development of models as tools for our science objectives and
analysis of EOS data is a critical activity in the pre-EOS time frame. Most of our activity
centers around analysis of satellite and aircraft data sets.
The three-dimensional chemical model is being developed under funding from the
Atmospheric Chemistry Modeling and Analysis Program. The chemical package and
transport scheme eventually will be used in the chemical assimilation effort. Thus, scientific
testing of the 3-D chemical model is essential for the success of the IDS assimilation program
and also allows us to move toward our goal of using the 3-D chemical model for interpreting
long-term trends.
There have been substantial improvements to the 3-D chemistry and transport model in the
last year. Development of a complete scheme for stratospheric photochemical processes,
including gas-phase and heterogeneous reactions and a model for PSC formation, allows a
more complete comparison of modeled physical processes with observations. A simulation
for the period November 15, 1991-May 31, 1992 has been completed. Ozone, constituents
directly important to the ozone evolution such as nitrogen dioxide and chlorine monoxide, and
long lived constituents such as nitrous oxide and methane are included in the simulation.
Because the winds and temperatures used in this off-line simulation are taken from the
GEOS-1 data assimilation system, the calculated constituent evolution is sensibly compared
with observations. To date, such comparisons emphasize observations from the UARS
satellite.
The performance of this CTM is evaluated by comparison of model and observations through
interpolation of model fields to the times and locations of the satellite observations. Scatter
plots for 6.8 hPa ozone observations, poleward of 30N and outside the polar vortex, are given
for UARS instruments HALOE, CLAES, and MILS in
Figure 2.2.1-1. For all three
instruments the model values show good correlation with the observations. The model field
for February 19 at 7 hPa is given in
Figure 2.2.1-2; the model field shows spatial variability
outside the tropics and the polar vortex which is reflected in the observations. The model
shows two areas of low ozone mixing ratios within the polar vortex and between about 140E
and 210E, associated with the Aleutian anticyclone. Manney et al. [1995] examine similar
low ozone "pockets" and show that these are most likely produced photochemically. Douglass
et al. [1996] confirm that when air is confined to the Aleutian anticyclone the ozone
decreases photochemically, and show that horizontal transport is essential to maintain the
winter ozone above its photochemical equilibrium mixing ratio at 7 hPa throughout the middle latitudes.
This analysis shows that the model ozone evolution at middle latitudes
parallels the observed ozone evolution, indicating an appropriate model balance between
photochemical processes and horizontal waves transports.
The same analysis reveals flaws in the model transport. The sharp gradients observed by
CLAES in long-lived constituents such as nitrous oxide are not maintained by the model,
which leads to excessively high model mixing ratios in the subtropics and at middle latitudes.
This problem, which is produced by the model wind fields, is being addressed both through
improvements in using the assimilation wind fields in the model and through improvements to
the assimilation system.
One of the current issues in stratospheric dynamics is the rate at which material mixes into
the tropical stratosphere from midlatitudes. It turns out that an upper limit on the rate of
mixing can be estimated from the tracer correlations with the tropical QBO winds.
Figure 2.2.2.1-1
shows the ratio of N2O to CH4 from CLAES and an overlay of the QBO
Singapore. The close correlation of the descent of the QBO zero wind line and the change in
the trace gas ratio suggests that little air is mixing in from mid-latitudes. We estimate that the
mixing coefficient for air from mid-latitudes is no greater than about 7x10^8 cm^2/sec which
is much lower that used in most 2D models. These results are in press in GRL [Schoeberl et
al., 1996]
We are currently investigating the movement of dry air from the tropics to midlatitudes using
high vertical resolution HALOE data from UARS.
A paper was submitted to and accepted by the Journal of the Atmospheric Sciences titled,
"Calculations of the Stratospheric QBO for Time-Varying Wave Forcing", by M. A. Geller,
W. Shen, M. Zhang, and W.Wu. The research in this paper started off with the premise that
tropospherically forced atmospheric waves in the equatorial region force the observed
quasi-biennial oscillation (QBO) in lower stratospheric winds in equatorial regions. This is
the accepted mechanism. We then noted that the state of sea-surface temperatures(SSTs),
very likely, is important in determining the nature of these equatorial waves. Thus, it is
likely that there is a physical link between SSTs and the QBO. Yet, previous studies had
indicated that time series of equatorial SSTs appear to be unrelated to QBO behavior. Noting
that wave forcing of the QBO is an inherently nonlinear problem, we carried out idealized
models (of the nature done earlier by Holton and Lindzen, for example) with sinusoidally
varying equatorial wave behavior of different periods. The QBO response differed depending
on the ratio of the time varying forcing to the steady forcing, the period of the equatorial
wave modulation, and the phase relationship between the time variation of the easterly and
westerly momentum fluxes by the waves. We then tried a hypothesized time variation for the
equatorial wave momentum fluxes that were straight forwardly related to observed SST variations.
Our derived period of the QBO showed little relation to the original time variation
of the momentum fluxes (i. e., the SSTs) but did show great resemblance to the observed
behavior of the QBO. Thus, we concluded that: (1) In a nonlinear phenomenon, such as the
QBO, there is no reason to expect the QBO response to resemble the time variation of the
forcing. (2) It is very likely that equatorial SST variations play a large part in controlling the
time variation of the QBO. (3) It is likely that the SST control of equatorial wave momentum
fluxes results in the easterly and westerly momentum fluxes varying out of phase with one
another.
While SBUV measurements provide daily, near global coverage of ozone, these instruments
are unable to provide reliable profiles of ozone below the ozone peak. HALOE and SAGE
are high resolution profile instruments and are able to provide information on the shape of the
ozone profile below the peak. They both make their measurements, however, using a solar
occultation technique. This technique limits measurements to two narrow latitude bands of
observations each day: one in the location of sunsets, the other in the location of sunrises.
Data coverage, therefore, is relatively sparse.
Combined, the SBUV and HALOE/SAGE data sets provide us with all the information on
ozone we desire: global coverage with excellent vertical resolution from the tropopause into
the mesosphere. To make the HALOE/SAGE data useful, we need to produce synoptic maps
with global coverage. Because ozone behaves like a conserved trace gas in the lower
stratosphere, we can apply the trajectory mapping technique [Morris et al., 1995] to an entire
month of HALOE or SAGE measurements and produce the desired synoptic maps.
To derive our estimates of column ozone from the HALOE and SAGE measurements, we
produce isentropic trajectory maps on eight potential temperature surfaces between 400K
(20km) and 1200K (36km). Most of the ozone can be found between these levels (as shown
in
Figure 2.2.3-1).
We then advect the measurements from an entire month of sampling to a
specified date and time. The data on each level are gridded using a Barnes' scheme and then
integrated vertically.
Figure 2.2.3-2
shows such a map from a combination of HALOE and
SAGE data in September 1994. We have found that combining HALOE and SAGE data for
use in the production of a single map is not unwarranted.
Figure 2.2.3-3 shows a comparison
of HALOE and SAGE measurements from one of the potential temperature surfaces used for
the integration. The agreement between HALOE and SAGE is quite good with only a small
offset. Similar agreement is observed at other vertical levels.
Figure 2.2.3-4 shows the
TOMS total ozone field for the same date as the combine HALOE/SAGE field shown in
Figure 2.2.3-2.
Good agreement between the features in the two data sets is apparent. The
lack of inclusion of tropospheric ozone in the HALOE/SAGE map is largely responsible for
the observed offset although systematic bias between HALOE/SAGE and TOMS must also be
considered.
Our future research on this project will be directed toward a number of goals: to expand our
technique and produce combined HALOE/SAGE/SBUV2 profiles; to improve the first guess
profiles for the SBUV2 retrievals; to derive tropospheric ozone through a subtraction of our
stratospheric column maps of HALOE/SAGE from the TOMS total ozone fields; and to
improve data assimilation products through the provision of accurate, high resolution ozone
profiles. Our early efforts appear very promising.
The measurements of EOS AM's Measurements of Pollution in the Troposphere (MOPITT)
instrument will produce low vertical resolution CO profiles and column CH4 measurements.
The Ozone Dynamic Ultraviolet Spectrometer (ODUS), scheduled for the EOS CHEM
payload, will produce column ozone. We have developed a new method using trajectories
which allows us to reconstruct the vertical structure of trace gases from column measurements
under certain conditions. The column can be thought of as a shadow or projection of the
three-dimensional field. The time evolution of the projection along with the column
information can be used to reconstruct the three-dimensional field. We combine the various
projections (like a medical CAT scan) to estimate the three-dimensional structure. The
technique is an improvement of the method originally developed by Schoeberl et al. [1992c].
The new technique has been applied to the SO2 field from the Pinatubo cloud as measured by
TOMS with excellent results. We are currently preparing a paper on the technique.
As an outgrowth of studies started under the AEAP program and continued with ACMAP
funding, we are now applying our Monte Carlo uncertainty study to 2D modeling of the
evolution of ozone over the past two decades. As we try to understand the detailed
mechanism responsible for the observed trend in ozone, it is important to consider the
uncertainties inherent in the modeling as well as those in the measurements and the trend
analysis. We have focussed thus far on the quantifiable part of model prediction uncertainty;
that is the uncertainties due to input gas-phase chemical reaction rates, photolysis coefficients,
heterogeneous reaction rates, and polar stratospheric cloud microphysics parameters. These
have been propagated through a model calculation of the evolution of ozone over the past two
decades. This model calculation included a realistic solar cycle and stratospheric sulfate
aerosol variability. Figure 2.2.5.1-1
shows the calculated time evolution of global total ozone
from the nominal model using the accepted "best" values for input parameters compared to
the TOMS version 7 data. Also shown are the 1-sigma uncertainty bounds using the
estimated uncertainties in input parameters and the most extreme cases found.
The model calculated total ozone trend agrees quite well with the TOMS version 7
measurements. The differences between the model and measurements is less than the 1-sigma
uncertainty of the model calculation. However, the model calculates a very small seasonal
variation of the trend in the northern hemisphere midlatitudes in contrast to the data. This
difference is many sigma from the mean calculated seasonal variation and cannot be attributed
to input parameter uncertainties and there for most likely due to a deficiency of the model.
Under this IDS, we have developed an interactive 2-D model based on the dynamics package
of Bacmeister and Schoeberl [Bacmeister et al., 1995] to study long-term trends in trace
gases. This model fully couples chemistry dynamics and radiation, and thus can be used to
study the feedbacks between the processes which we have not been able to study with the
fixed circulation 2-D model. Over the last year, several improvements have been made in the
model. A new parameterization for chemistry occurring on the surfaces of polar stratospheric
clouds has been added to the chemistry package, allowing the model to predict the Antarctic
ozone hole. Extensive tuning of the planetary wave forcing parameters was carried out in
order to improve the breakup of the southern hemisphere polar vortex. A gravity wave
scheme has been added to the dynamics package (Bacmeister et al., 1995). The CO2 infrared
cooling parameterization of M.D. Chou and Kouvaris (1991) has been added to the radiation
package, allowing the variation of the CO2 heating rate calculation. The parameterization of
Rosenfield (1992) for the radiative heating due to water ice and nitric acid trihydrate
stratospheric clouds has been included. The chemistry package has been upgraded and is now
compatible with that used by the 2-D assessment model.
The 2-D interactive model was used to study the effects of the sulfate aerosol cloud formed
by the eruption of Mt. Pinatubo in June 1991 on stratospheric temperatures, dynamics, and
chemistry (Rosenfield et al., 1996). Aerosol extinctions and surface area densities,
constrained by satellite observations, were used to compute the aerosol effects on radiative
heating rates, photolysis rates, and heterogeneous chemistry. The net predicted perturbations
to the column ozone amount, shown in
Fig. 2.2.5.2-1,
were low latitude depletions of 2-3%
and northern and southern high latitude depletions of 10-12%, in good agreement with
observations. In the low latitudes a depletion of roughly 1-2% was due to the altered
circulation (increased upwelling) resulting from the perturbation of the heating rates, with the
heterogeneous chemistry and photolysis rate perturbations contribution roughly 0.5% each. In
the high latitudes the computed ozone column depletions were mainly a result of
heterogeneous chemistry occurring on the surfaces of the volcanic aerosol. Computed global
average ozone losses
(Fig. 2.2.5.2-2)
reached 1% at the end of 1991, and fell to a low of
3.2% around September 1992, after which the ozone began recovering. These computed
global ozone changes were generally within 1% in absolute magnitude of those observed by
the TOMS instrument except in early 1993 when the model ozone starts recovering faster
than the observations indicate.
A significant effort has been devoted to an investigation of the vertical mixing of tracers
which arises from the variability in the radiative heating of air parcels. Air parcels starting
on a given isentropic surface experience different time histories of diabatic heating which
causes irreversible vertical mixing across isentropic surfaces. We refer to this process as
"diabatic dispersion".
We have investigated diabatic dispersion in the lower stratosphere by computing parcel
trajectories initialized uniformly over the 500K surface on 1 Jan 1993. Parcels were followed
for two months using analyzed winds and diabatic heating rates computed from analyzedtemperatures.
Two independent data sets and radiative calculations were used. The trajectory
statistics suggest that the four regions, polar vortex, winter hemisphere surf zone, tropics and
extratropical summer hemisphere, are to some extent isolated from each other by eddy
transport barriers. By looking at the mixing in each of these regions separately, we were able
to establish the dependence of the vertical mixing on the horizontal transport and the spatial
structure of the diabatic heating. We have found that the character and magnitude of the
diabatic dispersion for parcels remaining in each of these four regions is distinctly different.
The dispersion in both the surf zone and southern hemisphere extratropics is initially
advective, but becomes diffusive after about one month with a diffusivity in the range 3-6
K^2/day. Diabatic dispersion within the tropics and polar vortex over the two month period
is more than an order of magnitude smaller and is less clearly diffusive. The potential
temperature variance for the entire ensemble is dominated by differential advection associated
with the mean diabatic circulation and increases quadratically with time. Our results therefore
do not support the notion of global diffusive dispersion, at least not on seasonal time scales.
Other projects are underway which utilize the statistical information contained in observations
of tracer and dynamical variability. The results of these investigations will be useful for a
number of problems. As an example, we show here how a statistical comparison of tropical
and midlatitude variability can be used to extract information about the strength of the
transport barrier between the tropics and the northern midlatitudes.
Figure 2.2.6-1 shows the
tropical and midlatitude mixing ratio PDFs (probability distribution functions) of N20
observations taken by the CLAES instrument on UARS. The tropical and midlatitude PDFs
shown here are histograms of N20 observations in the latitude ranges 15S-15N and 15N-55N,
respectively, at the altitudes 24,30 and 38 km, and during the period March 8-14, 1993. A
scatter plot of mixing ratio versus latitude of the observations is shown below each PDF plot.
The tropics and midlatitudes, as defined here, are also indicated on the plot.
The distributions are clearly more distinct at 30 km relative to the other two levels, indicating
a stronger barrier to mixing across the latitude 15N. A measure of the barrier strength might
be defined by quantifying the extent to which the tropical and midlatitude regions are
chemically distinct, that is, the extent to which the two PDFs are resolved. A standard
measure of the degree to which two overlapping distributions are distinct is the quantity ``d''
which is the absolute value of the difference in the mean values for each distribution, divided
by the geometric mean of the variances of the distributions.
We have computed d as a function of altitude from CLAES N20 observations for two
different north facing periods Dec 8-15 1992, and March 8-14, 1993. The results are shown
in
Figure 2.2.6-2
and indicate that the tropics and midlatitudes are most chemically distinct
near 30km for the early March period. For the early December period on the other hand, d
depends weakly on altitude in the range 25-35 km. In both cases, d decreases with increasing
altitude. While this is partly due to the weakening of the transport barrier, it is also due to the
greater photochemical loss of N20 in the tropics. This causes the tropical PDF to move
toward lower midlatitude values which also causes the regions to become less chemically
distinct. All of these results are fairly insensitive to the choice of the northern tropical
boundary, provided it is in the range 10N-20N.
The CLAES observations can be directly compared to model data by a similar analysis
applied to model tracer fields interpolated to UARS measurement locations. Preliminary
results indicate for example that the barrier strength in the GSFC chemistry and transport
model during northern hemisphere winter is strongest at 25 km.
In the last EOS IDS report, the development of the Kalman filter for stratospheric constituent
assimilation was reported. This work is now accepted for publication [Lyster et al. 1996]..
The initial results for constituent assimilation were also presented at an international
conference [Menard et al., 1995].
Since the last EOS IDS report we have performed extensive runs using real winds and data
that have been retrieved from the UARS satellite. These runs are validations of the
effectiveness of the Kalman filter approach. For example, a distinctive wave-breaking event
is evident in stratospheric constituent observations in the period September 6-14 1992.
Figure 2.3.1-1
shows an attempt to reproduce this event using a pure forecast of methane from
simple (zonally averaged) initial conditions.
Figure 2.3.1-2 shows an assimilation using the
Kalman filter with a limited data set from the HALOE instrument (the black triangles show
the locations of the observations). The wave-breaking is evident in the southern hemisphere,
and it is absent from the first figure. A validation against CLAES data show that the
structure of the event is being reproduced even where HALOE observations are not present.
Apart from the work using real data, there has been development in the methodology of the
constituent Kalman filter. A key advantage of the Kalman filter is the ability to assess the
accuracy of the assimilation (i.e., to calculate the error bars). We have implemented an
approach for including the effects of errors in the assimilating wind. The winds are obtained
from the DAO assimilation system (GEOS DAS) and the appropriate inclusion of their errors
must be done in order to properly interpret the results of the constituent assimilation. Also, a
common assumption in data assimilation is that errors are normally (Gaussian) distributed.
This is inappropriate for constituent assimilation because the resulting field is (by definition)
positive. We have developed a methodology for the log normal filter [Cohn, 1995] that
removes this problem by transporting and assimilating the logarithm of the constituent field.
We are also in the process of developing an extension to trajectory mapping called the
Lagrangian filter. This approach to constituent assimilation takes into account the statistics of
errors of the observations and the spatial correlation in the tracer field; in this approach
observations now update the field in a group of neighboring parcels.
We have initiated a project to use the Kalman filter to map the three-dimensional structure of
ozone in the lower stratosphere. This is a difficult project because of the spatial and temporal
sparsity of data from satellites such as HALOE and SAGE. Also, the retrieval algorithms for
these instruments have reduced accuracy in the vicinity of and below the ozone maximum in
the lower stratosphere. We will use the Kalman filter to study the three dimensional
development of structures such as the one shown in Figure 2.3-2. Ultimately data such asthese and
total ozone measurements from TOMS instruments might be useful for mapping the
distributions of tropospheric ozone. This approach will also be investigated.
A part of this IDS consists of diagnostic and transport studies designed to provide guidance to
the DAO's data assimilation system development. These IDS studies make use of the
available assimilation runs, completed for the UARS mission and aircraft missions, as well as
special assimilation development runs. The diagnostic studies include the calculation of the
residual mean circulation and comparisons of assimilation produced potential vorticity (pv)
fields with tracer measurements from UARS. DAO winds and temperatures have been
compared with UKMO winds and temperatures (Coy and Swinbank, submitted to JGR), with
respect to diagnostic transport quantities, such as the representation of the polar pv barrier and
the mean transport circulation. RDF trajectory model runs conserving pv and the 3D
chemistry transport model for N2O have been run for several DAO assimilations of a given
time period, each experiment varying an aspect of the data assimilation system. Transport
and trajectory studies based on changing the horizontal resolution of the analysis have shown
that alternate methods of data insertion, such as BIAU (Balanced Incremental Analysis
Update), can reduce unphysical small scale structure in the assimilation produced winds
without adversely affecting the transport results.
The stratospheric trajectory, transport, and diagnostic studies associated with this IDS, have
played a large role in the development of the DAO's data assimilation system. One dramatic
past improvement of the data assimilation system's GCM (General Circulation Model) has
been the development and inclusion of the rotated computational pole. Moving the
computational pole away from the geographic pole was done in direct response to
stratospheric transport needs for clean cross polar transport during large amplitude
stratospheric wave events. More recently, difficulties with 3D transport near the upper level
of the transport model has been the major reason for the vertical expansion of the
assimilation system's GCM from 60 to 80 km. In addition, the lack of polar vortex descent
in the 3D transport model has required the inclusion of a simple orographic gravity wave
model and a mesospheric Rayleigh friction drag term. The newest DAO assimilation system
(GEOS-2) will contain all of the above GCM improvements. Moreover, trajectory, transport,
and diagnostic studies done under this IDS have also highlighted problems with the
assimilation's tropical wind analyses. These assimilation driven results generally show more
small scale structure than is observed. Such results are believed to highlight a fundamental
limitation of the current analysis system and have been a part of the rationale for using a
completely new analysis system, PSAS (Physical space Statistical Analysis System), in the
developing GEOS-2 assimilation system. Work under this IDS will continue, in collaboration
with the DAO, to assess of the ability of assimilation winds to drive realistic transport and to
provide supporting evidence from such studies to help guide future improvements to the data
assimilation system.
We have continued developing methods to derive tropical tropospheric ozone maps from
TOMS and other satellites. As per last year's progress report, our first FY96 activity was to
extend the method of Kim et al [1996] for deriving monthly averaged tropospheric ozone
maps from TOMS between 10N and 10S to all of 1992 [Hudson and Thompson, 1996]. This
latitude range is selected to correspond to tropical air masses only because studies with
geopotential height show that sub-tropical air frequently penetrates equatorward of 15 degrees
[Frolov and Hudson, 1996]. Accurate retrieval of time-averaged tropospheric ozone from
TOMS requires stratospheric ozone to be relatively constant over time, which is the case in
the tropics. Furthermore, because the stratospheric ozone retrieval is 100% efficient in the
tropics, tropospheric ozone column amount can be derived without detailed knowledge of the
stratospheric ozone profile [Hudson and Kim, 1994].
For tropospheric air masses, a good assumption is that the minimum tropospheric ozone
column in the tropics is 26 DU [Komhyr et al, 1994;Thompson et al, 1996a], although some
tropical ozonesondes launched over the Indian and central Pacific Oceans been as low as 10
DU [R. R. Dickerson, personal communication, 1995]. In addition, a striking feature of total
ozone is a year- round wave-one pattern, with a maximum over the central Atlantic and a
minimum over the central Pacific [Hudson and Thompson, 1996; Ziemke et al, 1996]. This
can be verified with the tropical ozonesonde record, although the latter is very incomplete.
For the years, 1991-1992, for which sonde coverage at Natal (5.5S, 35W), Ascension (8S,
14W), and Brazzaville (4S, 15E)captures total ozone over the Atlantic [Thompson et al,
1996a,b], there are no Pacific sondes. For 1986-1990 there is a record at American Samoa
(14S, 174W) [Komhyr et al, 1994], but this site is not always in the tropical band.
The wave-like pattern is used to derive a tropospheric ozone field by two methods [Kim et al,
1996], with an efficiency correction for low-lying ozone at high concentrations, as observed
during biomass burning [Thompson et al, 1996b]. In one method, it is assumed (1) that the
background total ozone column over the Pacific, consists of Strat. O3 Col. + 26 DU, and is
zonally constant, and (2) that any excess ozone beyond that amount is in the troposphere.
This implies, however, that tropospheric column ozone is > 65 DU over Africa during the
August-October biomass burning period
(Fig. 2.4-1), with an Indian Ocean background of 45
DU. These levels are 15-20 DU higher than suggested by in-situ measurements during
TRACE-A [Baldy et al, 1996;Fishman et al, 1996; Browell et al, 1996; Thompson et al,
1996b].
The alternative technique assumes that the total "background ozone"consists of a stratospheric
wave, plus a zonally constant 26 DU. During biomass burning season, an additional "hump"
is superimposed on the background wave over the Atlantic and tropospheric column ozone
over the burning regions of Africa and South America is 45-50 DU during 1992, for example,
in agreement with the sonde record
(Fig. 2.4-1; Kimet al, 1996). The picture obtained
assuming a stratospheric wave in March-April-May also agrees very well with the Ascension,
Brazzaville and Natal sondes in 1992, whereas the tropospheric wave assumption does not
Fig. 2.4-2).
These results appear to contradict the inferences from the sondes, as described by
Ziemke et al [1996], and we are seeking independent approaches to determining the nature of
the wave-like pattern. These include further analysis with sample tropospheric ozone profiles
- what radiances and total ozone are derived, given various assumptions of stratosphericozone?
In addition, we will start to look at ozone in the tropical lower stratosphere-upper
troposphere from the 3D chemical model for insight into dynamical contributions to the wave
pattern.
One thing is certain from the analyses to date. Validation of alternative approaches for
deriving tropospheric ozone requires a good ozonesonde network in the tropics. The record
coincident with Nimbus 7 TOMS is too spotty. During its 14-plus- year record, Natal was
the only continuously operational sounding station within 10 degrees of the equator. Also
needed are a central Atlantic and/or Africa site (Ascension is ideal; Brazzaville would also
work, although it suffers from more variable cloud effects; Thompson et al, 1996b). In the
Pacific, locations that have been suggested are Galapagos, Christmas Island (F. Hasebe
personal communication, 1996) and Tarawa (W. A. Matthews, personal communication,
1996). Now that ADEOS- and EarthProbe-TOMS are operational, we can continue
development of tropical tropospheric ozone retrievals on a firmer basis if the sonde network is
enhanced.
The second FY96 activity is the production of the entire 14- year Nimbus 7 TOMS tropical
tropospheric ozone map record to see if there are trends discernable during this time. Total
ozone maps, prepared as in Kim et al [1996], have just been completed.
As part of this IDS, complementary activities to the production of tropospheric ozone maps
are analyses of in-situ tropospheric ozone and related data and modeling and analysis of the
convection-ozone link. Three recently completed papers on transport and chemistry associated
with southern African ozone (south of 20S) [Swap et al, 1996; Thompson et al, 1996c; Tyson
et al, 1996] further elucidated the photochemical origins of persistent ozone layers over the
subtropics during the SAFARI/TRACE-A period (September-October 1992). African biomass
burning is not the only source. Near-surface tracer measurements at Etosha Park signified
industrial and/or biogenic sources as well [Swapet al, 1996]. In the upper troposphere (10-15
km) ozonesondes at Pretoria (25S, 28E) and Etosha Park (19S, 16E) averaged 3-4 D Uricher
in September-October 1992 than in March- April-May and back trajectories for every one of
the 30 sondes taken during SAFARI/TRACE-A showed origins 4-8 days earlier over South
America. The mechanism for this ozone source is presumably post-convective ozone
formation from pyrogenic, biogenic and/or urban NOx and CO sources.
We are looking at ozone and biomass fire links in SCAR-B [Smoke, Clouds, Aerosols, and
Radiation-Brazil, M. King and Y. Kaufman, NASAPIs], a MODIS-sponsored biomass
burning experiment conducted in August-September 1995 [Thompson et al, 1996d].
Unfortunately, SCAR-B occurred during the gap between Nimbus/Meteor TOMS coverage
and EP/ ADEOS TOMS so it does not help in further TOMS tropospheric ozone map
development. As part of this IDS, improvements to the GEOS-1 tracer model convective
parameterization were performed [Allen et al., 1996] and a review paper on the tropical
ozone-convection link was completed [Thompson et al., 1996e].
The section below summarizes some of the other activities supported by this IDS. These
research efforts do not fall under the categories described above but are an important part of
this investigation.
During the December 1995/ January-February 1996, the PI was also the Project Scientist for
the Tropical Ozone Transport Experiment/Vortex Ozone Transport Experiment
(TOTE/VOTE). We are now beginning to analyze the data from that mission..One of the
most interesting observations made was the presence of sub-visible cirrus south of 18N at the
longitude of Hawaii.
Figure 2.5.1-1
shows an example of the DIAL aerosol observations made
on the flight. Jensen et al [1996] have speculated that subvisible cirrus near the tropopause
might generate broad scale uplift and hence allow air to enter the stratosphere. This
hypothesis is a variant on Danielsen's idea that the heating of the cirrus shields in tropical
systems can radiatively lift air to stratospheric potential temperatures. The exciting discovery
here is that the cirrus observed is not attached to any nearby convective systems.
We are also analyzing other aspects of the TOTE/VOTE data including polar ozone depletion,
mixing in the stratosphere, and aircraft exhaust studies.
The HIRDLS instrument on the EOS CHEM platform is designed to make horizontal and
vertical observations at higher resolutions than have previously been made, while observing
the upper troposphere and lower stratosphere with improved sensitivity and accuracy. The
higher horizontal resolution is achieved by azimuthal scanning of the instrument's field of
view. Previous limb-viewing sounders (LIMS, ISAMS, CLAES, MILS, etc.) did not have this
azimuthal scanning capability and thus were unable to sample a given latitude circle more
than twice per orbit.
High-resolution (1 degree by 1 degree) global RDF fields have now been generated on the
560 K isentropic surface, covering every six hours for 30 days, from February 19, 1992, to
March 19, 1992. The fields are currently being used to examine scale-dependent statistics.
These fields will be used for simulations of satellite sampling strategies, permitting more
realistic investigations of how satellite instruments sample an evolving high-resolution
meteorological field. The results of this work culminated in a M.S. Thesis.
Aside from UARS data, investigators under this IDS spend some time looking at TOMS data
and performing analysis of global ozone amounts. Simulations of ozone change have to fit
within the TOMS observational set. A TOMS-like instrument (ODUS) will be launched on
EOS CHEM. We are currently analyzing new data from ADEOS and Earth Probe TOMS,
Figure 2.5.3-1
shows differences between the data sets. Most of the differences can be
accounted for by changes in small scale meteorological processes that occur between satellite
crossing times. However there are larger scale differences that are still under investigation.
CRISTA is an IR limb stratosphere chemistry sounder which flew on the shuttle ATLAS
missions. We have been working with Dr. Offermann of Wuppertal University to help
analyze the data. Preliminary calculations show good agreement between the high horizontal
resolution CRISTA data and RDF simulations of tracer fields. Unfortunately the first
CRISTA data set has not been released (release was targeted for June 1996) so the analysis
has not been completed.
Fig. 2.1.1-1 Summary of model results from MODE [Schoeberl et al., 1996] showing the
change in total ozone as a function of year for the Antarctic ozone hole.
Fig. 2.1.2-1a and
Fig. 2.1.2-1b
Summary of preliminary Arctic model results from MODE showing the change in
ozone and other trace gases compared with observations from Jan. to Feb. 1993. Part a, ozone
comparisons; part b, ClONO2, HNO3, HCl and PV.
Fig. 2.2.1-1 Observations of ozone from HALOE (month of February), CLAES (Feb. 19)and
MILS (Feb. 19) compared with model mixing ratios interpolated to the time and location of
the satellite measurements.
Fig. 2.2.1-2 The model ozone at 6.8 hPa illustrating horizontal variability. This variability is
reflected in the model/observation comparisons shown in Figure 2.2.1-1.
Fig. 2.2.2.1-1 The ratio of CLAES N2O/CH4 averaged between 8N and 8S(in color) with
time mean removed (at right). Dark lines show the Singapore zonal winds. Phase lags/leads
of one and two months are shown in white.
Fig. 2.2.3-1 Typical midlatitude SAGE ozone profile showing number density as a function
of altitude. Most of the ozone falls between the 400K (20km)and 1200K (36km) potential
temperature levels (marked in the figure).
Fig. 2.2.3-2 Total column ozone as derived from combined stratospheric measurements made
by SAGE and HALOE. The trajectory mapping technique has been applied to data from both
instruments to produce this synoptic map of the ozone distribution in September 1994.
Fig. 2.2.3-3 Comparison of HALOE and SAGE ozone measurements at 600K (26km) using
the trajectory mapping technique.
Fig. 2.2.3-4. TOMS total ozone field for the same date shown using the HALOE/SAGE data
in Figure 2.
Fig. 2.2.5.1-1 The calculated time evolution of global total ozone from the nominal 2D model
using the accepted "best" values for input parameters compared to the TOMS version 7 data
(solid line), 1-sigma uncertainty bounds using the estimated uncertainties (dashed line) in
input parameters, and the most extreme cases found (dotted lines).
Fig. 2.2.5.2-1 Percent changes in column ozone due to full chemistry and radiation
perturbation. Contour intervals are -28, -24, -20, -16,-12, -8, -4, -3, -2, 0, 2, 4.
Fig. 2.2.5.2-2 Global average ozone percent changes with full perturbation compared to
TOMS.
Figure 2.2.6-1 Tropical and midlatitude CLAES v.7 N20 PDFs (probability distribution
functions) and latitude/mixing ratio scatter plots at vertical levels 24, 30 and 38 km, for
March 8-15, 1993. The vertical lines in the scatter plots indicate the boundaries of the tropics
and midlatitudes as defined here.
Figure 2.2.6-2 The altitude dependence of the difference between the tropical and northern
midlatitude N20 tracer distributions. CLAES vs N20, March 8-15, 1993.
Fig. 2.3.1-1 A constituent forecast of methane from simple (zonally averaged) initial
conditions.
Fig. 2.3.1-2 An assimilation of CH4 using the Kalman filter with a limited data set from the
HALOE instrument (the black triangles show the locations of the observations).
Fig. 2.4-1 Two maps of tropospheric ozone column for October 1992 in Dobson units (DU)
[Hudson and Thompson, 1996]. Methods of deriving the maps are described in Kim et al
[1996]. The upper frame is based on assuming the wavelike pattern in total ozone is due to a
tropospheric wave. The lower frame assumes that the Two maps of tropospheric ozone
column for May 1992 in Dobson
units (DU) [Hudson and Thompson, 1996].
Fig. 2.4-2 Two maps of tropospheric ozone column for May 1992 in Dobson units (DU)
[Hudson and Thompson, 1996]. Methods of deriving the maps are described in Kim et al
[1996]. The upper frame is based on assuming the wavelike pattern in total ozone is due to a
tropospheric wave. The lower frame assumes that the wavelike pattern is in the stratosphere.
Ozonesonde data in March-April-May for 1992 shows average tropospheric ozone column at
Ascension Island (8S, 14W) was 30 DU and at Brazzaville (4S, 15E), the sondes averaged 34
DU. These values agree better
Fig. 2.5.1-1 DIAL observations of aerosols for the TOTE flight of Dec. 15, 1995. Overlayed
are the MTP temperatures. The high scattering features show sub-visible cirrus near the
tropopause.
Fig. 2.5.3-1 Column ozone differences between Earth Probe and ADEOS TOMS on Oct. 1,
1996. Because of the lower orbit altitude, Earth Probe TOMS cannot scan from orbit track to
orbit track.
Allen, D. J., P. Kasibhatla, A. M. Thompson, R. B. Rood, B. Doddridge, K. E. Pickering, R.
D. Hudson and S-J. Lin, J. Geophys. Res., Transport-induced interannual variability of carbon
monoxide determined with a chemistry and transport model, J. Geophys. Res., submitted,
1996.
Bacmeister, J.T., M.R. Schoeberl, M.E. Summers, J.E. Rosenfield, and X. Zhu,
Descent of long-lived trace gases in the winter polar vortex, J. Geophys.
Res., 100, 11,669-11,684, 1
Bacmeister, J. T., S. D. Eckermann, L. Sparling, K. R. Chan, M .Loewenstein, and M. H.
Proffitt, 1996: Analysis of intermittency in aircraft measurements of velocity, temperature and
atmospheric tracers using wavelet transforms, To appear in NATO ASI Series, Vol. 1, Gravity
Wave Processes and their Parameterization in Global Climate Models, ed. K. P. Hamilton,
Springer Verlag, Heidelberg.
Browell, E. V., et al, Air mass characteristics observed over the tropical Atlantic, Africa, and
Brazil during TRACE-A, J. Geophys. Res., in press, 1996.
Chou, M.-D., and L. Kouvaris, Calculations of transmission functions in the
infrared CO2 and O3 bands, J. Geophys. Res., 96, 9003-9012, 1991.
995.
Cohn, S.E., 1996: An introduction to estimation theory. Special issue dedicated to data
assimilation in meteorology and oceanography: theory an practice, submitted to J. Met. Soc.
Japan.
Considine, D.B., R.S. Stolarski, C.H. Jackman, J.E. Rosenfield, and E.L. Fleming,
"Uncertainty in the response of ozone to chlorine increases in a 2D model of stratospheric
photochemistry", submitted to the proceedings of the Quadrennial Ozone Symposium,
L'Aquila, Italy, September, 1996.
Coy, L., and R. Swinbank, The characteristics of stratospheric winds and temperatures
produced by data assimilation, submitted to JGR.
Douglass, A. R., R. B. Rood, S. R. Kawa, D. J. Allen, M. C. Cerniglia, Simulation of the
evolution of the middle latitude winter ozone in the middle stratosphere, submitted (almost) to
J. Geophys. Res., 1996.
Fishman, J., V. G. Brackett, E. V. Browell, and W. B. Grant, Tropospheric ozone derived
from TOMS/SBUV measurements during TRACE-A, J. Geophys. Res., in press, 1996.
Frolov, A. D., and R. D. Hudson, Correlation of northern hemisphere total ozone and
geopotential height fields, in XVIII Quadrennial Ozone Symposium Abstract Volume,
L'Aquila, Italy, 12-21 Sept. 1996, p. 173.
Hudson, R. D., and J. Kim, Direct measurements of tropospheric O3 using TOMS data, in
Ozone in the Troposphere and Stratosphere, ed. R. D. Hudson, NASA Conf. Pub. 3266,
pp.119-121, 1994.
Hudson R. D., J-H. Kim, and A. M. Thompson, On the derivation of tropospheric column
ozone from radiances measured by the Total Ozone Mapping Spectrometer, J. Geophys. Res.,
100, 11137-11146, 1995.
Hudson, R. D., and A. M. Thompson, Annual cycle of tropospheric ozone in the tropics, in
XVIII Quadrennial Ozone Symposium Abstract Volume, L'Aquila, Italy, 12-21 Sept. 1996, p.
240.
Jensen, E. J., O. B. Toon, J. D. Spinhirne and H. B. Selkirk, On the formation and persistence
of subvisible cirrus clouds near the tropical tropopause, J. Geophys. Res., in press, 1996.
Kim J. H., R. D. Hudson, and A. M. Thompson, Derivation of time-averaged tropospheric
column ozone from radiances measured by the Total Ozone Mapping Spectrometer:
Intercomparison and analysis, J. Geophys. Res., 101, in press, 1996.
Komhyr, W. D., S. J. Oltmans, J. A. Lathrop, J. B. Kerr, and W.A. Mathews, The latitudinal
distribution of ozone to 35 km altitude from ECC ozonesonde observations: 1982-1990, in
Ozone in the Troposphere and Stratosphere, ed. by R. D.Hudson, NASA Conf. Pub. 3266, pp.
858-862, 1994.
Lyster, P.M. , S.E. Cohn, R. Menard, L.-P. Chang, S.-J. Lin, R. Olsen, 1996: Parallel
Implementation of a Kalman Filter for Constituent Data Assimilation, accepted for publication
in Mon. Wea. Rev., 1996.
Manney, G. L., L. Froidevaux, J. W. Waters, R. W. Zurek, J. C. Gille, J. B. Kumer, J. L.
Mergenthaler, A. E. Roche, A. O'Neill, R. Swinbank, Formation of low-ozone pockets in the
middle stratospheric anticyclone during winter, J. Geophys. Res., 100, 13,939-13,950, 1995
Menard, R., P.M. Lyster, L.-P. Chang, and S.E. Cohn, 1995: Middle atmosphere assimilation
of UARS constituent data using Kalman filtering: preliminary results. Second International
Symposium on Assimilation of Observations in Meteorology and Oceanography, Tokyo,
13-17 March 1995, World Meteorological Organization, pp 235-238.
Morris, G.A., et al., Trajectory mapping and applications to data from the Upper Atmosphere
Research Satellite, J. Geophys. Res., 100,16,491--16,505, 1995.
Rosenfield, J.E., Radiative effects of polar stratospheric clouds during the
Airborne Antarctic Ozone Experiment and the Airborne Arctic Stratospheric
Expedition, J. Geophys. Res., 7841-7858, 1992.
Schoeberl, M. R. et al., An estimate of the dynamical isolation of the tropical lower
stratosphere using UARS wind and trace gas observations of the Quasi-biennial Oscillation,
Geophys. Res. Lett., (in press), 1996.
Schoeberl, M. R. et al., Development of the Antarctic ozone hole, J. Geophys. Res., 101,
20909-20924, 1996.
Swap, R. J., A. M. Thompson, M. Garstang, and S. A. Macko, Multiple sources of southern
African ozone in the lower troposphere during biomass burning, Geophys. Res. Lett.,
submitted, 1996.
Thompson, A. M., R. D. Diab, G. E. Bodeker, M. Zunckel, G. J. R.Coetzee, C. B. Archer, D.
P. McNamara, K. E. Pickering, J. B.Combrink, J. Fishman, and D. Nganga, Ozone over
southern Africa during SAFARI/TRACE-A, J. Geophys. Res., in press, 1996a.
Thompson, A. M., K. E. Pickering, D. P. McNamara, M. R. Schoeberl, R. D. Hudson, J. H.
Kim, E. V. Browell, V. W. J.H. Kirchhoff, and D. Nganga, Where did tropospheric ozone
over southern Africa and the tropical Atlantic come from in October 1992? Insights from
TOMS, GTE/TRACE-A and SAFARI-92, J. Geophys. Res., in press, 1996b.
Thompson, A. M., D. P. McNamara, R. J. Swap, J. Combrink, and R. D. Diab, Sources of
free tropospheric ozone in subtropical southern Africa during SAFARI-92/TRACE-A: Intra-
and inter-continental transport, J. Geophys. Res., submitted, 1996c.
Thompson, A. M., D. P. McNamara, V. W. J. H. Kirchhoff, and A. Setzer, Tropospheric
ozone at Cuiabá during SCAR-B and TRACE-A, in Proceedings of SCAR-B AEB Workshop,
Fortaleza, Brazil, Nov. 1996d.
Thompson, A. M., W.-K. Tao, K. E. Pickering, J. R. Scala, and J. Simpson, Tropical deep
convection and ozone formation, Bull.Am. Meteor. Soc., submitted, 1996e.
Tyson, P. D., M. Garstang, A. M. Thompson, P. C. D'Abreton, R. D. Diab and E. V. Browell,
Transport and photochemistry of ozone over south central southern Africa during SAFARI, J.
Geophys. Res., submitted, 1996.
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,
14421-14427, 1996.
(1)Calculations of the Stratospheric QBO for Time-Varying Wave Forcing, by M. A. Geller,
W. Shen, M. Zhang, and W. Wu, To appear in J. Atmos Sci., 1996.
(2) Stratospheric Acceleration from Tropical Waves Driven by Moist Convection and
Extratropical Wave Forcings, by W. Shen and M. A. Geller, submitted to J. Atmos. Sci.,
1996.
(3) Lyster, P.M. , S.E. Cohn, R. Menard, L.-P. Chang, S.-J. Lin, R.Olsen, 1996: Parallel
Implementation of a Kalman Filter for Constituent Data Assimilation, accepted for publication
in Mon. Wea. Rev., 1996.
(4) Schoeberl, M. R. et al., An estimate of the dynamical isolation of the tropical lower
stratosphere using UARS wind and trace gas observations of the Quasi-biennial Oscillation,
Geophys. Res. Lett., (in press),1996.
(5) Schoeberl, M. R. et al., Development of the Antarctic ozone hole, J. Geophys. Res., 101,
20909-20924, 1996.
(6) Sparling, L. C., J. A. Kettleborough, P. H. Haynes, M. E. McIntyre, J. E. Rosenfield, P.
A. Newman and M. R. Schoeberl, Diabatic dispersion in the lower stratosphere, Journal of
Atmospheric Sciences, submitted, 1966
(7) Allen, D. J., P. Kasibhatla, A. M. Thompson, R. B. Rood, B.Doddridge, K. E. Pickering,
R. D. Hudson and S-J. Lin, J. Geophys. Res., Transport-induced interannual variability of
carbon monoxide determined with a chemistry and transport model, J. Geophys. Res.,
submitted, 1996.
(8) Thompson, A. M., W.-K. Tao, K. E. Pickering, J. R. Scala, and J. Simpson, Tropical deep
convection and ozone formation, Bull.Am. Meteor. Soc., submitted, 1996e.
(9) Thompson, A. M., D. P. McNamara, R. J. Swap, J. Combrink, and R. D. Diab, Sources of
free tropospheric ozone in subtropical southern Africa during SAFARI-92/TRACE-A: Intra-
and inter-continental transport, J. Geophys. Res., submitted, 1996c.
(10) Lyster, P.M. , S.E. Cohn, R. Menard, L.-P. Chang, S.-J. Lin, R. Olsen, 1996: Parallel
Implementation of a Kalman Filter for
Constituent Data Assimilation, accepted for publication in Mon. Wea.
Rev., 1996.
(11) Bacmeister, J. T., S. D. Eckermann, L. Sparling, K. R. Chan, M.Loewenstein, and M. H.
Proffitt, 1996: Analysis of intermittency in aircraft measurements of velocity, temperature and
atmospheric tracers using wavelet transforms, To appear in NATO ASI Series, Vol. 1, Gravity
Wave Processes and their Parameterization in Global Climate Models, ed. K. P. Hamilton,
Springer Verlag, Heidelberg.
(12) Jackman, C.H., E.L. Fleming, S. Chandra, D.B. Considine, and J.E. Rosenfield, Past,
present, and future modelled ozone trends with comparisons to observed trends, J. Geophys.
Res., 1996, in press.
(13) Nash, E.R., P.A. Newman, J.E. Rosenfield, and M.R. Schoeberl, An objective
determination of the polar vortex using Ertel's potential vorticity, J. Geophys. Res., 101,
9471-9478, 1996.
(14) Newman, P.A. and J.E. Rosenfield, Stratospheric thermal damping times,
Geophys. Res. Lett., 1996, submitted.
(15) Rosenfield, J.E., D.B. Considine, P.E. Meade, J.T. Bacmeister, C.H. Jackman,
and M.R. Schoeberl, Stratospheric effects of the Mt. Pinatubo aerosol studied with a coupled
two-dimensional model, J. Geophys. Res., 1996, submitted.
or Constituent Data Assimilation, accepted for publication in Mon. Wea. Rev., 1996.
(16) Newman et al. Measurements of polar vortex air in the midlatitudes, J. Geophys. Res.,
101, 12879-12891, 1996.
(17) Tabazadeh, A., O. B. Toon, B. L. Gary, J. T. Bacmeister, and M. R. Schoeberl,
Observational constraints on the formation of Type 1a polar stratospheric clouds, Geophys.
Res. Lett., 23, 2109-2112, 1996.
(18) Coy, L., and R. Swinbank, The characteristics of stratospheric winds and
temperatures produced by data assimilation, submitted to JGR, 1996.
1.0 Background
2.0 Scientific Activities
2.1 Multiyear Ozone Depletion Experiment (MODE)
2.1.1 Antarctic Experiment
2.1.2 Arctic Experiment
2.2 Stratospheric Chemical and Dynamical Modeling
2.2.1 Simulation of stratospheric constituents using the 3-D chemical model
2.2.2 Quasi-biennial Oscillation (new section)
2.2.2.1 Using the QBO to assess mixing
2.2.2.2 Models of the QBO
2.2.3 Trajectory Mapping
2.2.4 Evolution of the Pinatubo Cloud
2.2.5 Two Dimensional Modelling studies
2.2.5.1 Monte Carlo studies (new section)
2.2.5.2 Interactive Two Dimensional Model Studies
2.2.6 Mixing and Dynamics in the Stratosphere (New Section)
2.3 Stratospheric Data Assimilation
2.3.1 Chemical Assimilation
2.3.2 Improvements to Assimilation System
2.4 Tropospheric Chemistry Studies
2.5 Other Activities
2.5.1 TOTE/VOTE Analysis (New Section)
2.5.2 HIRDLS simulation studies
2.5.3 TOMS data
2.5.4 Analysis of CRISTA data
FIGURE CAPTIONS
References
New Publications under this IDS