Karl B. Haase

Unexpected consequences of increasing CO2 and ocean acidity on marine production of DMS and CH2ClI: potential climate impacts

Increasing atmospheric mixing ratios of CO2 have already lowered surface ocean pH by 0.1 units compared to preindustrial values and pH is expected to decrease an additional 0.3 units by the end of this century. Pronounced physiological changes in some phytoplankton have been observed during previous CO2 perturbation experiments. Marine microorganisms are known to consume and produce climate-relevant organic gases. Concentrations of (CH3)2S (DMS) and CH2ClI were quantified during the Third Pelagic Ecosystem CO2 Enrichment Study. Positive feedbacks were observed between control mesocosms and those simulating future CO2. Dimethyl sulfide was 26% (±10%) greater than the controls in the 2x ambient CO2 treatments, and 18% (±10%) higher in the 3xCO2 mesocosms. For CH2ClI the 2xCO2 treatments were 46% (±4%) greater than the controls and the 3xCO2 mesocosms were 131% (±11%) higher. These processes may help contribute to the homeostasis of the planet.

Calibration and intercomparison of acetic acid measurements using proton-transfer-reaction mass spectrometry (PTR-MS)

Acetic acid is one of the most abundant organic acids in the ambient atmosphere, with maximum mixing ratios reaching into the tens of parts per billion by volume (ppbv) range. The identities and associated magnitudes of the major sources and sinks for acetic acid are poorly characterized, due in part to the limitations of available measurement techniques. This paper demonstrates that, when properly calibrated, proton-transfer-reaction mass spectrometry (PTR-MS) can be a valuable technique for fast response, accurate quantification of acetic acid in ambient air. Three different PTR-MS configurations were calibrated at low ppbv mixing ratios using permeation tubes, which yielded calibration factors between 7.0 and 10.9 normalized counts per second per ppbv (ncps ppbv −1) at a drift tube field strength of 132 Townsend (Td). Detection limits ranged from 0.06 to 0.32 ppbv with dwell times of 5 s. These calibration factors showed negligible humidity dependence. Acetic acid was measured with PTR-MS on Appledore B Island, ME, during the International Consortium for Atmospheric Research on Transport and Transformation (ICARTT) campaign and validated based on acetic acid measured in parallel using tandem mist chambers coupled with ion chromatography (MC/IC). Mixing ratios ranged from a minimum of 0.075± 0.004 ppbv to 3.555 ± 0.171 ppbv, with a median mixing ratio of 0.530 ± 0.025 ppbv. An orthogonal least squares linear regression of paired data yielded a slope of 1.14± 0.06 (2σ ), an intercept of 0.049 ± 0.020 (2σ ) ppbv, and anR2 of 0.78.