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Abstract. Reactive gases and aerosols are produced by terrestrial ecosystems, processed within plant canopies, and can then be emitted into the above-canopy atmosphere. Estimates of the above-canopy fluxes are needed for quantitative earth system studies and assessments of past, present and future air quality and climate. The Model of Emissions of Gases and Aerosols from Nature (MEGAN) is described and used to quantify net terrestrial biosphere emission of isoprene into the atmosphere. MEGAN is designed for both global and regional emission modeling and has global coverage with ∼1 km 2 spatial resolution. Field and laboratory investigations of the processes controlling isoprene emission are described and data available for model development and evaluation are summarized. The factors controlling isoprene emissions include biological, physical and chemical driving variables. MEGAN driving variables are derived from models and satellite and ground observations. Tropical broadleaf trees contribute almost half of the estimated global annual isoprene emission due to their relatively high emission factors and because they are often exposed to conditions that are conducive for isoprene emission. The remaining flux is primarily from shrubs which have a widespread distribution. The annual global isoprene emission estimated with MEGAN ranges from about 500 to 750 Tg isoprene (440 to 660 Tg carbon) depending on the driving variables which include temperature, solar radiation, Leaf Area Index, and plant functional type. The global annual isoprene emission estimated using the standard driving variables is ∼600 Tg isoprene. Differences in driving variables result in emission estimates that differ by more than a factor of three for specific times and locations. It is difficult to evaluate isoCorrespondence to: A. Guenther (guenther@ucar.edu) prene emission estimates using the concentration distributions simulated using chemistry and transport models, due to the substantial uncertainties in other model components, but at least some global models produce reasonable results when using isoprene emission distributions similar to MEGAN estimates. In addition, comparison with isoprene emissions estimated from satellite formaldehyde observations indicates reasonable agreement. The sensitivity of isoprene emissions to earth system changes (e.g., climate and land-use) demonstrates the potential for large future changes in emissions. Using temperature distributions simulated by global climate models for year 2100, MEGAN estimates that isoprene emissions increase by more than a factor of two. This is considerably greater than previous estimates and additional observations are needed to evaluate and improve the methods used to predict future isoprene emissions.

Abstract. The Model of Emissions of Gases and Aerosolsfrom Nature version 2.1 (MEGAN2.1) is a modeling framework for estimating fluxes of biogenic compounds between terrestrial ecosystems and the atmosphere using simple mechanistic algorithms to account for the major known processes controlling biogenic emissions. It is available as an offline code and has also been coupled into land surface and atmospheric chemistry models. MEGAN2.1 is an update from the previous versions including MEGAN2.0, which was described for isoprene emissions by Guenther et al. (2006) and MEGAN2.02, which was described for monoterpene and sesquiterpene emissions by Sakulyanontvittaya et al. (2008). Isoprene comprises about half of the total global biogenic volatile organic compound (BVOC) emission of 1 Pg (1000 Tg or 10 15 g) estimated using MEGAN2.1. Methanol, ethanol, acetaldehyde, acetone, α-pinene, β-pinene, t-β-ocimene, limonene, ethene, and propene together contribute another 30 % of the MEGAN2.1 estimated emission. An additional 20 compounds (mostly terpenoids) are associated with the MEGAN2.1 estimates of another 17 % of the total emission with the remaining 3 % distributed among >100 compounds. Emissions of 41 monoterpenes and 32 sesquiterpenes together comprise about 15 % and 3 %, respectively, of the estimated total global BVOC emission. Tropical trees cover about 18 % of the global land surface and are estimated to be responsible for ∼ 80 % of terpenoid emissions and ∼ 50 % of other VOC emissions. Other trees cover about the same area but are estimated to contribute only about 10 % of total emissions. The magnitude of the emissions estimated with MEGAN2.1 are within the range of estimates reported using other approaches and much of the differences between reported values can be attributed to land cover and meteorological driving variables. The offline version of MEGAN2.1 source code and driving variables is available from http://bai.acd.ucar.edu/MEGAN/ and the version integrated into the Community Land Model version 4 (CLM4) can be downloaded from http://www.cesm. ucar.edu/.

The emission of isoprene and monoterpenes from plants is influenced by light and leaf temperature, which account for almost all short‐term variations (minutes to days) and a large part of spatial and long‐term variations. The temperature dependence of monoterpene emission varies among monoterpenes, plant species, and other factors, but a simple exponential relationship between emission rate (E) and leaf temperature (T), E = Es [exp (β(T − Ts))], provides a good approximation. A review of reported measurements suggests a best estimate of β = 0.09 K−1 for all plants and monoterpenes. Isoprene emissions increase with photosynthetically active radiation up to a saturation point at 700–900 μmol m−2 s−1. An exponential increase in isoprene emission is observed at leaf temperatures of less than 30°C. Emissions continue to increase with higher temperatures until a maximum emission rate is reached at about 40°C, after which emissions rapidly decline. This temperature dependence can be described by an enzyme activation equation that includes denaturation at high temperature. Algorithms developed to simulate these light and temperature responses perform well for a variety of plant species under laboratory and field conditions. Evaluations with field measurements indicate that these algorithms perform significantly better than earlier models which have previously been used to simulate isoprene emission rate variation. These algorithms account for about 90% of observed diurnal variability and can predict diurnal variations in hourly averaged isoprene emissions to within 35%.

Abstract. The Model for Ozone and Related chemical Tracers, version 4 (MOZART-4) is an offline global chemical transport model particularly suited for studies of the troposphere. The updates of the model from its previous version MOZART-2 are described, including an expansion of the chemical mechanism to include more detailed hydrocarbon chemistry and bulk aerosols. Online calculations of a number of processes, such as dry deposition, emissions of isoprene and monoterpenes and photolysis frequencies, are now included. Results from an eight-year simulation (2000)(2001)(2002)(2003)(2004)(2005)(2006)(2007) are presented and evaluated. The MOZART-4 source code and standard input files are available for download from the NCAR Community Data Portal (http://cdp.ucar.edu).