Abstract

The chemistry climate model ECHAM-HAMMOZ contains a detailed representation of tropospheric and stratospheric reactive chemistry and state-of-the-art parametrisations of aerorols using either a modal scheme (M7) or a bin scheme (SALSA). This article describes and evaluates the model version ECHAM6.3-HAM2.3-MOZ1.0 with a focus on the tropospheric gas-phase chemistry. A ten-year model simulation was performed to test the stability of the model and provide data for its evaluation. The comparison to observations concentrates on the year 2008 and includes total column observations of ozone (O<sub>3</sub>) and carbon monoxide (CO) from Infrared Atmospheric Sounding Interferometer (IASI) and Ozone Monitoring Instrument (OMI), Microwave Limb Sounder (MLS) observations of temperature, nitric acid (HNO<sub>3</sub>), chlorine monoxide (ClO), and O<sub>3</sub> for the evaluation of polar stratospheric processes, an ozone sonde climatology, surface ozone observations from the Tropospheric Ozone Assessment Report (TOAR) database, and surface CO data from the Global Atmosphere Watch network. Global budgets of ozone, hydroxide (OH), nitrogen oxides (NO<sub>x</sub>), aerosols, clouds, and radiation are analyzed and compared to the literature. ECHAM-HAMMOZ performs well in many aspects. However, in the base simulation, lightning NO<sub>x</sub> emissions are very low, and the impact of the heterogeneous reaction of HNO<sub>3</sub> on dust and seasalt aerosol is too strong. Sensitivity simulations with increased lightning NOx or modified heterogeneous chemistry deteriorate the comparison with observations and yield excessively large ozone budget terms and too much OH. We hypothesize that this is an impact of potential issues with tropical convection in the ECHAM model.

Highlights

  • Global chemistry–climate models have become indispensable tools for the investigation of interactions between atmospheric chemistry and various aspects of the physical and biogeochemical climate system

  • We describe and evaluate a new chemistry–climate model based on the general circulation model ECHAM6.3 (Stevens et al, 2013), the Hamburg Aerosol Model (HAM) version 2.3 (Tegen et al, 2018; Stier et al, 2005; Zhang et al, 2012), and the gas-phase tropospheric and stratospheric module MOZ1.0

  • All emissions in the ECHAM-HAMMOZ model are controlled via a single “emi_spec” file, which provides a simple and compact way to define all trace gas and aerosol emissions used in a model simulation and ensures proper documentation of the emissions used in a specific run

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Summary

Introduction

Global chemistry–climate models have become indispensable tools for the investigation of interactions between atmospheric chemistry and various aspects of the physical and biogeochemical climate system. We describe and evaluate a new chemistry–climate model based on the general circulation model ECHAM6.3 (Stevens et al, 2013), the Hamburg Aerosol Model (HAM) version 2.3 (Tegen et al, 2018; Stier et al, 2005; Zhang et al, 2012), and the gas-phase tropospheric and stratospheric module MOZ1.0. Several studies were performed with the aerosol climate model ECHAM-HAM, which uses trace gas climatologies from ECHAM-HAMMOZ to constrain aerosol nucleation (e.g., Jiao et al, 2014; Neubauer et al, 2014; Stanelle et al, 2014; Ghan et al, 2016; Zhang et al, 2016).

Model description
Emissions
Lightning
Lower boundary conditions for long-lived stratospheric species
Photolysis
Dry deposition
Wet deposition and scavenging
Simulation setup
Total column ozone and stratospheric processes
Tropospheric ozone
Surface ozone
Total column CO
Surface CO
Ozone and OH
NOx budget
Findings
Conclusions

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