Baerbel Langmann

A comparison of satellite‐ and ground‐based measurements of SO2 emissions from Tungurahua volcano, Ecuador

Satellite-measured SO2 mass loadings and ground-based measurements of SO2 emission rate are not directly comparable, with ∼40% differences between mean emissions reported by each technique from Tungurahua volcano, Ecuador, during late 2007. Numerical simulations of postemission processing and dispersal of Tungurahuas SO2 emissions enable more effective comparison of ground- and satellite-based SO2 data sets, reducing the difference between them and constraining the impact of plume processing on satellite SO2 observations. Ground-based measurements of SO2 emission rate are used as the model input, and simulated SO2 mass loadings are compared to those measured by the Ozone Monitoring Instrument (OMI). The changing extent of SO2 processing has a significant impact on daily variation in SO2 mass loading for a fixed volcanic emission rate. However, variations in emission rate at Tungurahua are large, suggesting that overall volcanic source strength and not subsequent processing is more likely to be the dominant control on atmospheric mass loading. SO2 emission rate estimates are derived directly from the OMI observations using modeled SO2 lifetime. Good agreement is achieved between both observed and simulated mass loadings (∼21%) and satellite-derived and ground-measured SO2 emission rates (∼18%), with a factor of 2 improvement over the differences found by simple direct comparison. While the balance of emission source strength and postemission processing will differ between volcanoes and regions, under good observation conditions and where SO2 lifetime is ∼24 hours, satellite-based sensors like OMI may provide daily observations of SO2 mass loading which are a good proxy for volcanic source strength.

Ocean–Atmosphere Interactions of Particles

This chapter provides an overview of the current knowledge on aerosols in the marine atmosphere and the effects of aerosols on climate and on processes in the oceanic surface layer. Aerosol particles in the marine atmosphere originate predominantly from direct production at the sea surface due to the interaction between wind and waves (sea spray aerosol, or SSA) and indirect production by gas to particle conversion. These aerosols are supplemented by aerosols produced over the continents, as well as aerosols emitted by volcanoes and ship traffic, a large part of it being deposited to the ocean surface by dry and wet deposition. The SSA sources, chemical composition and ensuing physical and optical effects, are discussed. An overview is presented of continental sources and their ageing and mixing processes during transport. The current status of our knowledge on effects of marine aerosols on the Earth radiative balance, both direct by their interaction with solar radiation and indirect through their effects on cloud properties, is discussed. The deposition on the ocean surface of some key species, such as nutrients, their bioavailability and how they impact biogeochemical cycles are shown and discussed through different time and space scales approaches.

On the role of climate forcing by volcanic sulphate and volcanic ash

There is overall agreement that volcanic sulphate aerosols in the stratosphere can reduce solar radiation reaching the earth’s surface for years, thereby reducing surface temperatures, affecting global circulation patterns and generally the global climate system. However, the response of the climate system after large volcanic eruptions is not fully understood and global climate models have difficulties to reproduce the observed variability of the earth system after large volcanic eruptions until now. For geological timescales, it has been suggested that, in addition to the stratospheric climate forcing by volcanic sulphate aerosols, volcanic ash affects climate by modifying the global carbon cycle through iron fertilising the surface ocean and stimulating phytoplankton growth. This process has recently also been observed after the eruption of the volcano Kasatochi on the Aleutian Islands in summer 2008. To trigger future research on the effect of volcanic ash on the climate system via ocean iron fertilisation, this review paper describes the formation processes and atmospheric life cycles of volcanic sulphate and volcanic ash, contrasts their impact on climate, and emphasises current limitations in our understanding.

Contribution of Isoprene Oxidation Products to Marine Aerosol over the North-East Atlantic

Secondary organic aerosol (SOA) formation through isoprene oxidation was investigated with the regional-scale climate model REMOTE. The applied modeling scheme includes a treatment for marine primary organic aerosol emissions, aerosol microphysics, and SOA formation through the gas/particle partitioning of semivolatile, water-soluble oxidation products. The focus was on SOA formation taking place over the North-East Atlantic during a period of high biological activity. Isoprene SOA concentrations were up to ~5 ng over North Atlantic in the base case model runs, and isoprene oxidation made a negligible contribution to the marine organic aerosol (OA) mass. In particular, isoprene SOA did not account for the observed water-soluble organic carbon (WSOC) concentrations over North Atlantic. The performed model calculations, together with results from recent field measurements, imply a missing source of SOA over remote marine areas unless the isoprene oxidation products are considerably less volatile than the current knowledge indicates.

Asian Dust Transport in China: A Palaeoclimate and Modeling Study

We evaluate the ability of the regional chemistry/aerosol climate model REMOTE to simulate Asian dust transport over China in response to changing Asian monsoon conditions. Applied to years of different monsoon strength, model results are compared to dust fluxes measured in a 9.5 kyr peat core from NW Szechuan. This palaeoclimate archive provides an uninterrupted history of Holocene monsoon conditions and dust fluxes to the Eastern Tibetan Plateau and represents a solid long-term framework for evaluating model responses to climate change. We present preliminary model results for selected months of the year 1996, which displayed normal monsoon conditions. Simulation results suggest that dust deposition to the Eastern Tibetan Plateau is dominated by wet deposition during monsoon and pre-monsoon months. Model deposition fluxes agree within a factor of two with fluxes from relevant sections of the peat core, providing encouraging new data in the bid to assess future impacts of dust on climate. The yearly simulations must henceforth be carried out under dry and wet monsoon conditions and compared to relevant sections of the core.