PM anomaly detection for exceptional event demonstrations: A Texas case study.

The shifting frontiers of air pollution emission sources contribute to stagnation or reversal of air quality gains across the United States (US). The frequency and possible duration of Exceptional Events - driven primarily by wildfires and dust storms - have significantly increased in the US over the past decade. Combined with the US Environmental Protection Agency (EPA) final rule strengthening primary annual National Ambient Air Quality Standards (NAAQS) for PM by 25%, communities will need to reevaluate domestic and international sources of PM.

Aging Effects on Biomass Burning Aerosol Mass and Composition: A Critical Review of Field and Laboratory Studies.

Biomass burning is a major source of atmospheric particulate matter (PM) with impacts on health, climate, and air quality. The particles and vapors within biomass burning plumes undergo chemical and physical aging as they are transported downwind. Field measurements of the evolution of PM with plume age range from net decreases to net increases, with most showing little to no change.

Sources of Black Carbon Deposition to the Himalayan Glaciers in Current and Future Climates.

WRF-Chem and a modified version of the ECLIPSE 5a emission inventory were used to investigate the sources impacting black carbon (BC) deposition to the Himalaya, Karakoram, and Hindu Kush (HKHK) region. This work extends previous studies by simulating deposition to the HKHK region not only under current conditions, but also in the 2040-2050 period under two realistic emission scenarios and in three different phases of the El Niño-Southern Oscillation (ENSO). Under current conditions, sources from outside our South Asian modelling domain have a similar impact on total BC deposition to the HKHK region (35-87%, varying with month) as South Asian anthropogenic sources (13-62%).

Southeast Atmosphere Studies: learning from model-observation syntheses.

Concentrations of atmospheric trace species in the United States have changed dramatically over the past several decades in response to pollution control strategies, shifts in domestic energy policy and economics, and economic development (and resulting emission changes) elsewhere in the world. Reliable projections of the future atmosphere require models to not only accurately describe current atmospheric concentrations, but to do so by representing chemical, physical and biological processes with conceptual and quantitative fidelity. Only through incorporation of the processes controlling emissions and chemical mechanisms that represent the key transformations among reactive molecules can models reliably project the impacts of future policy, energy and climate scenarios.

The spectroscopic foundation of radiative forcing of climate by carbon dioxide.

The radiative forcing (RF) of carbon dioxide (CO) is the leading contribution to climate change from anthropogenic activities. Calculating CO RF requires detailed knowledge of spectral line parameters for thousands of infrared absorption lines. A reliable spectroscopic characterization of CO forcing is critical to scientific and policy assessments of present climate and climate change.

Development and recent evaluation of the MT_CKD model of continuum absorption.

Water vapour continuum absorption is an important contributor to the Earth's radiative cooling and energy balance. Here, we describe the development and status of the MT_CKD (MlawerTobinCloughKneizysDavies) water vapour continuum absorption model. The perspective adopted in developing the MT_CKD model has been to constrain the model so that it is consistent with quality analyses of spectral atmospheric and laboratory measurements of the foreign and self continuum.

Emission Ratios for Ammonia and Formic Acid and Observations of Peroxy Acetyl Nitrate (PAN) and Ethylene in Biomass Burning Smoke as Seen by the Tropospheric Emission Spectrometer (TES).

We use the Tropospheric Emission Spectrometer (TES) aboard the NASA Aura satellite to determine the concentrations of the trace gases ammonia (NH) and formic acid (HCOOH) within boreal biomass burning plumes, and present the first detection of peroxy acetyl nitrate (PAN) and ethylene (CH) by TES. We focus on two fresh Canadian plumes observed by TES in the summer of 2008 as part of the Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS-B) campaign. We use TES retrievals of NH and HCOOH within the smoke plumes to calculate their emission ratios (1.