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Bernd R.T. Simoneit

Bio: Bernd R.T. Simoneit is an academic researcher from Oregon State University. The author has contributed to research in topics: Organic matter & Hydrothermal circulation. The author has an hindex of 98, co-authored 435 publications receiving 40940 citations. Previous affiliations of Bernd R.T. Simoneit include University of Bristol & Hokkaido University.


Papers
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Journal ArticleDOI
16 Mar 1978-Nature
TL;DR: In this article, the role of oxic and anoxic sedimentary environments is evaluated using a combination of geochemical parameters such as lipid composition, sulphur and organic pigments.
Abstract: Our increasing knowledge of the geochemical processes of present-day sedimentation conditions provides a basis for evaluating the role of oxic and anoxic sedimentary environments. In particular, there are organic geochemical parameters, such as lipid composition, sulphur and organic pigments, which link Recent sediments with their geologically older counterparts, and these may therefore be used to assign the depositional palaeoenvironments of ancient sediments and petroleums.

1,902 citations

Journal ArticleDOI
TL;DR: In this paper, a chemical mass balance receptor model based on organic compounds was developed that relates sours; contributions to airborne fine particle mass concentrations and revealed source contributions to the concentrations of specific organic compounds.

1,396 citations

Journal ArticleDOI
TL;DR: In this article, the authors search for conservative marker compounds suitable for tracing the presence of vehicular particulate exhaust emissions in the urban atmosphere, compile quantitative source profiles, and study the contributions of fine organic particulate vehicular exhaust to the Los Angeles atmosphere.
Abstract: Gasoline- and diesel-powered vehicles are known to contribute appreciable amounts of inhalable fine particulate matter to the atmosphere in urban areas. Internal combustion engines burning gasoline and diesel fuel contribute more than 21% of the primary fine particulate organic carbon emitted to the Los Angeles atmosphere. In the present study, particulate (d[sub p] [le] 2 [mu]m) exhaust emissions from six noncatalyst automobiles, seven catalyst-equipped automobiles, and two heavy-duty diesel trucks are examined by gas chromatography/mass spectrometry. The purposes of this study are as follows: (a) to search for conservative marker compounds suitable for tracing the presence of vehicular particulate exhaust emissions in the urban atmosphere, (b) to compile quantitative source profiles, and (c) to study the contributions of fine organic particulate vehicular exhaust to the Los Angeles atmosphere. More than 100 organic compounds are quantified, including n-alkanes, n-alkanoic acids, benzoic acids, benzaldehydes, PAH, oxy-PAH, steranes, pentacyclic triterpanes, azanaphthalenes, and others. Although fossil fuel markers such as steranes and pentacyclic triterpanes can be emitted from other sources, it can be shown that their ambient concentrations measured in the Los Angeles atmosphere are attributable mainly to vehicular exhaust emissions. 102 refs., 9 figs., 6 tabs.

1,343 citations

Journal ArticleDOI
TL;DR: In this paper, a brief review of the organic matter composition in aerosols derived from the major sources is also given, with emphasis on the detection of biomass burning components, and a long range transport of smoke particulate matter with the associated organic compounds is also discussed.

1,325 citations

Journal ArticleDOI
TL;DR: The major organic components of smoke particles from biomass burning are monosaccharide derivatives from the breakdown of cellulose, accompanied by generally lesser amounts of straight-chain, aliphatic and oxygenated compounds and terpenoids from vegetation waxes, resins/gums, and other biopolymers.

1,292 citations


Cited by
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Journal ArticleDOI
TL;DR: In this paper, the authors provided an assessment of black-carbon climate forcing that is comprehensive in its inclusion of all known and relevant processes and that is quantitative in providing best estimates and uncertainties of the main forcing terms: direct solar absorption; influence on liquid, mixed phase, and ice clouds; and deposition on snow and ice.
Abstract: Black carbon aerosol plays a unique and important role in Earth's climate system. Black carbon is a type of carbonaceous material with a unique combination of physical properties. This assessment provides an evaluation of black-carbon climate forcing that is comprehensive in its inclusion of all known and relevant processes and that is quantitative in providing best estimates and uncertainties of the main forcing terms: direct solar absorption; influence on liquid, mixed phase, and ice clouds; and deposition on snow and ice. These effects are calculated with climate models, but when possible, they are evaluated with both microphysical measurements and field observations. Predominant sources are combustion related, namely, fossil fuels for transportation, solid fuels for industrial and residential uses, and open burning of biomass. Total global emissions of black carbon using bottom-up inventory methods are 7500 Gg yr−1 in the year 2000 with an uncertainty range of 2000 to 29000. However, global atmospheric absorption attributable to black carbon is too low in many models and should be increased by a factor of almost 3. After this scaling, the best estimate for the industrial-era (1750 to 2005) direct radiative forcing of atmospheric black carbon is +0.71 W m−2 with 90% uncertainty bounds of (+0.08, +1.27) W m−2. Total direct forcing by all black carbon sources, without subtracting the preindustrial background, is estimated as +0.88 (+0.17, +1.48) W m−2. Direct radiative forcing alone does not capture important rapid adjustment mechanisms. A framework is described and used for quantifying climate forcings, including rapid adjustments. The best estimate of industrial-era climate forcing of black carbon through all forcing mechanisms, including clouds and cryosphere forcing, is +1.1 W m−2 with 90% uncertainty bounds of +0.17 to +2.1 W m−2. Thus, there is a very high probability that black carbon emissions, independent of co-emitted species, have a positive forcing and warm the climate. We estimate that black carbon, with a total climate forcing of +1.1 W m−2, is the second most important human emission in terms of its climate forcing in the present-day atmosphere; only carbon dioxide is estimated to have a greater forcing. Sources that emit black carbon also emit other short-lived species that may either cool or warm climate. Climate forcings from co-emitted species are estimated and used in the framework described herein. When the principal effects of short-lived co-emissions, including cooling agents such as sulfur dioxide, are included in net forcing, energy-related sources (fossil fuel and biofuel) have an industrial-era climate forcing of +0.22 (−0.50 to +1.08) W m−2 during the first year after emission. For a few of these sources, such as diesel engines and possibly residential biofuels, warming is strong enough that eliminating all short-lived emissions from these sources would reduce net climate forcing (i.e., produce cooling). When open burning emissions, which emit high levels of organic matter, are included in the total, the best estimate of net industrial-era climate forcing by all short-lived species from black-carbon-rich sources becomes slightly negative (−0.06 W m−2 with 90% uncertainty bounds of −1.45 to +1.29 W m−2). The uncertainties in net climate forcing from black-carbon-rich sources are substantial, largely due to lack of knowledge about cloud interactions with both black carbon and co-emitted organic carbon. In prioritizing potential black-carbon mitigation actions, non-science factors, such as technical feasibility, costs, policy design, and implementation feasibility play important roles. The major sources of black carbon are presently in different stages with regard to the feasibility for near-term mitigation. This assessment, by evaluating the large number and complexity of the associated physical and radiative processes in black-carbon climate forcing, sets a baseline from which to improve future climate forcing estimates.

4,591 citations

Journal ArticleDOI

3,734 citations

Journal ArticleDOI
TL;DR: In this paper, parent and alkyl PAHs were quantified in suspended particulates and sediments (345 samples) from the Fraser River system, British Columbia, Canada, and the best potential to distinguish natural and anthropogenic sources is exhibited by ratios of the principal mass 178, 202, 228 and 276 parent PAH, 1,7/2,6+1,7-DMP (dimethylphenanthrene), the phenanthrene/anthracene and fluoranthene/pyrene alkyal PAH series and several less commonly applied PA

3,527 citations

Journal ArticleDOI
TL;DR: In this article, an overview of the atmospheric degradation mechanisms for SOA precursors, gas-particle partitioning theory and analytical techniques used to determine the chemical composition of SOA is presented.
Abstract: Secondary organic aerosol (SOA) accounts for a significant fraction of ambient tropospheric aerosol and a detailed knowledge of the formation, properties and transformation of SOA is therefore required to evaluate its impact on atmospheric processes, climate and human health. The chemical and physical processes associated with SOA formation are complex and varied, and, despite considerable progress in recent years, a quantitative and predictive understanding of SOA formation does not exist and therefore represents a major research challenge in atmospheric science. This review begins with an update on the current state of knowledge on the global SOA budget and is followed by an overview of the atmospheric degradation mechanisms for SOA precursors, gas-particle partitioning theory and the analytical techniques used to determine the chemical composition of SOA. A survey of recent laboratory, field and modeling studies is also presented. The following topical and emerging issues are highlighted and discussed in detail: molecular characterization of biogenic SOA constituents, condensed phase reactions and oligomerization, the interaction of atmospheric organic components with sulfuric acid, the chemical and photochemical processing of organics in the atmospheric aqueous phase, aerosol formation from real plant emissions, interaction of atmospheric organic components with water, thermodynamics and mixtures in atmospheric models. Finally, the major challenges ahead in laboratory, field and modeling studies of SOA are discussed and recommendations for future research directions are proposed.

3,324 citations

Book ChapterDOI
TL;DR: The most consistent and pervasive effect is an increase in impervious surface cover within urban catchments, which alters the hydrology and geomorphology of streams as discussed by the authors, which results in predictable changes in stream habitat.
Abstract: The world’s population is concentrated in urban areas. This change in demography has brought landscape transformations that have a number of documented effects on stream ecosystems. The most consistent and pervasive effect is an increase in impervious surface cover within urban catchments, which alters the hydrology and geomorphology of streams. This results in predictable changes in stream habitat. In addition to imperviousness, runoff from urbanized surfaces as well as municipal and industrial discharges result in increased loading of nutrients, metals, pesticides, and other contaminants to streams. These changes result in consistent declines in the richness of algal, invertebrate, and fish communities in urban streams. Although understudied in urban streams, ecosystem processes are also affected by urbanization. Urban streams represent opportunities for ecologists interested in studying disturbance and contributing to more effective landscape management.

3,007 citations