Marked long-term decline in ambient CO mixing ratio in SE England, 1997-2014: evidence of policy success in improving air quality.

Atmospheric CO at Egham in SE England has shown a marked and progressive decline since 1997, following adoption of strict controls on emissions. The Egham site is uniquely positioned to allow both assessment and comparison of 'clean Atlantic background' air and CO-enriched air downwind from the London conurbation. The decline is strongest (approximately 50 ppb per year) in the 1997-2003 period but continues post 2003. A 'local CO increment' can be identified as the residual after subtraction of contemporary background Atlantic CO mixing ratios from measured values at Egham. This increment, which is primarily from regional sources (during anticyclonic or northerly winds) or from the European continent (with easterly air mass origins), has significant seasonality, but overall has declined steadily since 1997. On many days of the year CO measured at Egham is now not far above Atlantic background levels measured at Mace Head (Ireland). The results are consistent with MOPITT satellite observations and 'bottom-up' inventory results. Comparison with urban and regional background CO mixing ratios in Hong Kong demonstrates the importance of regional, as opposed to local reduction of CO emission. The Egham record implies that controls on emissions subsequent to legislation have been extremely successful in the UK.

Application of gas chromatography with a pulsed discharge helium ionization detector for measurements of molecular hydrogen in the atmosphere.

The Earth's troposphere contains approximately 160 Tg H2 with an average surface mixing ratio approximately 530 nmole mole(-1) (ppb) and lifetime of 2 years. Atmospheric H2 is typically measured using gas chromatography (GC) followed by hot mercuric oxide reduction detection (GC-HgO). Here we describe an alternate method using GC with a pulsed-discharge helium ionization detector (HePPD). HePPD is a universal detector; when applied to H2, the GC-HePDD provides a wide linear range (0.3% over a range of 2000 ppb), a detection limit of approximately 0.03 pg, high precision (0.12%) and a stable response (+/-1.6% over nearly one year). HePPD is compared to HgO reduction using a suite of gravimetrically prepared reference gases spanning remote to urban concentrations. The method is excellent for atmospheric measurements as it provides a wide linear range with high precision, stability and reproducibility. We suggest these characteristics will improve the ability to maintain reference gases and improve measurements of atmospheric H2, thus providing better constraints on potential future changes in its sources and sinks.

Recent changes in atmospheric carbon monoxide.

Measurements of carbon monoxide (CO) in air samples collected from 27 locations between 71 degrees N and 41 degrees S show that atmospheric levels of this gas have decreased worldwide over the past 2 to 5 years. During this period, CO decreased at nearly a constant rate in the high northern latitudes. In contrast, in the tropics an abrupt decrease occurred beginning at the end of 1991. In the Northern Hemisphere, CO decreased at a spatially and temporally averaged rate of 7.3 (+/-0.9) parts per billion per year (6.1 percent per year) from June 1990 to June 1993, whereas in the Southern Hemisphere, CO decreased 4.2 (+/-0.5) parts per billion per year (7.0 percent per year). This recent change is opposite a long-term trend of a 1 to 2 percent per year increase inferred from measurements made in the Northern Hemisphere during the past 30 years.