GISS Model E2.2: A Climate Model Optimized for the Middle Atmosphere—Model Structure, Climatology, Variability, and Climate Sensitivity

2020 ◽  
Vol 125 (10) ◽  
Author(s):  
D. Rind ◽  
C. Orbe ◽  
J. Jonas ◽  
L. Nazarenko ◽  
T. Zhou ◽  
...  
2007 ◽  
Vol 7 (2) ◽  
pp. 485-493 ◽  
Author(s):  
S. Tegtmeier ◽  
T. G. Shepherd

Abstract. The persistence and decay of springtime total ozone anomalies over the entire extratropics (midlatitudes plus polar regions) is analysed using results from the Canadian Middle Atmosphere Model (CMAM), a comprehensive chemistry-climate model. As in the observations, interannual anomalies established through winter and spring persist with very high correlation coefficients (above 0.8) through summer until early autumn, while decaying in amplitude as a result of photochemical relaxation in the quiescent summertime stratosphere. The persistence and decay of the ozone anomalies in CMAM agrees extremely well with observations, even in the southern hemisphere when the model is run without heterogeneous chemistry (in which case there is no ozone hole and the seasonal cycle of ozone is quite different from observations). However in a version of CMAM with strong vertical diffusion, the northern hemisphere anomalies decay far too rapidly compared to observations. This shows that ozone anomaly persistence and decay does not depend on how the springtime anomalies are created or on their magnitude, but reflects the transport and photochemical decay in the model. The seasonality of the long-term trends over the entire extratropics is found to be explained by the persistence of the interannual anomalies, as in the observations, demonstrating that summertime ozone trends reflect winter/spring trends rather than any change in summertime ozone chemistry. However this mechanism fails in the northern hemisphere midlatitudes because of the relatively large impact, compared to observations, of the CMAM polar anomalies. As in the southern hemisphere, the influence of polar ozone loss in CMAM increases the midlatitude summertime loss, leading to a relatively weak seasonal dependence of ozone loss in the Northern Hemisphere compared to the observations.


1988 ◽  
Vol 45 (3) ◽  
pp. 329-370 ◽  
Author(s):  
D. Rind ◽  
R. Suozzo ◽  
N. K. Balachandran ◽  
A. Lacis ◽  
G. Russell

2006 ◽  
Vol 6 (2) ◽  
pp. 3403-3417 ◽  
Author(s):  
S. Tegtmeier ◽  
T. G. Shepherd

Abstract. The persistence and decay of springtime total ozone anomalies over the entire extratropics (midlatitudes plus polar regions) is analysed using results from the Canadian Middle Atmosphere Model (CMAM), a comprehensive chemistry-climate model. As in the observations, interannual anomalies established through winter and spring persist with very high correlation coefficients (above 0.8) through summer until early autumn, while decaying in amplitude as a result of photochemical relaxation in the quiescent summertime stratosphere. The persistence and decay of the ozone anomalies in CMAM agrees extremely well with observations, even in the southern hemisphere when the model is run without heterogeneous chemistry (in which case there is no ozone hole and the seasonal cycle of ozone is quite different from observations), and even in the northern hemisphere where this version of CMAM (run with fixed external forcing) strongly underestimates the observed interannual variability. This shows that ozone anomaly persistence and decay does not depend on how the springtime anomalies are created or on their magnitude, but reflects the transport and photochemical decay in the model. It is thus a robust diagnostic of model performance.


2020 ◽  
Vol 125 (24) ◽  
Author(s):  
Clara Orbe ◽  
David Rind ◽  
Jeffrey Jonas ◽  
Larissa Nazarenko ◽  
Greg Faluvegi ◽  
...  

Atmosphere ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 133
Author(s):  
Ji-Hee Lee ◽  
Geonhwa Jee ◽  
Young-Sil Kwak ◽  
Heejin Hwang ◽  
Annika Seppälä ◽  
...  

Energetic particle precipitation (EPP) is known to be an important source of chemical changes in the polar middle atmosphere in winter. Recent modeling studies further suggest that chemical changes induced by EPP can also cause dynamic changes in the middle atmosphere. In this study, we investigated the atmospheric responses to the precipitation of medium-to-high energy electrons (MEEs) over the period 2005–2013 using the Specific Dynamics Whole Atmosphere Community Climate Model (SD-WACCM). Our results show that the MEE precipitation significantly increases the amounts of NOx and HOx, resulting in mesospheric and stratospheric ozone losses by up to 60% and 25% respectively during polar winter. The MEE-induced ozone loss generally increases the temperature in the lower mesosphere but decreases the temperature in the upper mesosphere with large year-to-year variability, not only by radiative effects but also by adiabatic effects. The adiabatic effects by meridional circulation changes may be dominant for the mesospheric temperature changes. In particular, the meridional circulation changes occasionally act in opposite ways to vary the temperature in terms of height variations, especially at around the solar minimum period with low geomagnetic activity, which cancels out the temperature changes to make the average small in the polar mesosphere for the 9-year period.


2011 ◽  
Vol 11 (10) ◽  
pp. 5045-5077 ◽  
Author(s):  
K. Semeniuk ◽  
V. I. Fomichev ◽  
J. C. McConnell ◽  
C. Fu ◽  
S. M. L. Melo ◽  
...  

Abstract. The impact of NOx and HOx production by three types of energetic particle precipitation (EPP), auroral zone medium and high energy electrons, solar proton events and galactic cosmic rays on the middle atmosphere is examined using a chemistry climate model. This process study uses ensemble simulations forced by transient EPP derived from observations with one-year repeating sea surface temperatures and fixed chemical boundary conditions for cases with and without solar cycle in irradiance. Our model results show a wintertime polar stratosphere ozone reduction of between 3 and 10 % in agreement with previous studies. EPP is found to modulate the radiative solar cycle effect in the middle atmosphere in a significant way, bringing temperature and ozone variations closer to observed patterns. The Southern Hemisphere polar vortex undergoes an intensification from solar minimum to solar maximum instead of a weakening. This changes the solar cycle variation of the Brewer-Dobson circulation, with a weakening during solar maxima compared to solar minima. In response, the tropical tropopause temperature manifests a statistically significant solar cycle variation resulting in about 4 % more water vapour transported into the lower tropical stratosphere during solar maxima compared to solar minima. This has implications for surface temperature variation due to the associated change in radiative forcing.


2012 ◽  
Vol 2012 ◽  
pp. 1-7
Author(s):  
T. Egorova ◽  
E. Rozanov ◽  
A. V. Shapiro ◽  
W. Schmutz

We have applied chemistry-climate model (CCM) SOCOL to simulate the distribution of the temperature and gas species in the upper stratosphere and mesosphere. As an input for the simulation, we employ daily spectral solar UV irradiance measured by SUSIM instrument onboard UARS satellite in January 1992. We have carried out an ensemble of nine 1-month long simulations using slightly different initial states of the atmosphere. We have compared the obtained time evolution of the simulated species and temperature with available satellite measurements. The obtained results allowed us to define the areas where the nowcast and short-term forecast of the atmospheric species with CCM SOCOL could be successful.


2012 ◽  
Vol 12 (1) ◽  
pp. 1553-1584
Author(s):  
R. W. Saunders ◽  
S. Dhomse ◽  
W. S. Tian ◽  
M. P. Chipperfield ◽  
J. M. C. Plane

Abstract. Nano-sized meteoric smoke particles (MSPs) with iron-magnesium silicate compositions, formed in the upper mesosphere as a result of meteoric ablation, may remove sulphuric acid from the gas-phase above 40 km and may also affect the composition and behaviour of supercooled H2SO4-H2O droplets in the global stratospheric aerosol (Junge) layer. This study describes a time-resolved spectroscopic analysis of the evolution of the ferric (Fe3+) ion originating from amorphous ferrous (Fe2+)-based silicate powders dissolved in varying Wt % sulphuric acid (30–75%) solutions over a temperature range of 223–295 K. Complete dissolution of the particles was observed under all conditions. The first-order rate coefficient for dissolution decreases at higher Wt % and lower temperature, which is consistent with the increased solution viscosity limiting diffusion of H2SO4 to the particle surfaces. Dissolution under stratospheric conditions should take less than a week, and is much faster than the dissolution of crystalline Fe2+ compounds. The chemistry climate model UMSLIMCAT (based on the UKMO Unified Model) was then used to study the transport of MSPs through the middle atmosphere. A series of model experiments were performed with different uptake coefficients. Setting the concentration of 1.5 nm radius MSPs at 80 km to 3000 cm−3 (based on rocket-borne charged particle measurements), the model matches the reported Wt % Fe values of 0.5–1.0 in Junge layer sulphate particles, and the MSP optical extinction between 40 and 75 km measured by a satellite-borne spectrometer, if the global meteoric input rate is about 20 t d−1. The model indicates that an uptake coefficient ≥0.01 is required to account for the observed two orders of magnitude depletion of H2SO4 vapour above 40 km.


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