Hui Kang

Secondary organic aerosols over oceans via oxidation of isoprene and monoterpenes from Arctic to Antarctic

Isoprene and monoterpenes are important precursors of secondary organic aerosols (SOA) in continents. However, their contributions to aerosols over oceans are still inconclusive. Here we analyzed SOA tracers from isoprene and monoterpenes in aerosol samples collected over oceans during the Chinese Arctic and Antarctic Research Expeditions. Combined with literature reports elsewhere, we found that the dominant tracers are the oxidation products of isoprene. The concentrations of tracers varied considerably. The mean average values were approximately one order of magnitude higher in the Northern Hemisphere than in the Southern Hemisphere. High values were generally observed in coastal regions. This phenomenon was ascribed to the outflow influence from continental sources. High levels of isoprene could emit from oceans and consequently have a significant impact on marine SOA as inferred from isoprene SOA during phytoplankton blooms, which may abruptly increase up to 95u2005ng/m3 in the boundary layer over remote oceans.

Levoglucosan indicates high levels of biomass burning aerosols over oceans from the Arctic to Antarctic

Biomass burning is known to affect air quality, global carbon cycle, and climate. However, the extent to which biomass burning gases/aerosols are present on a global scale, especially in the marine atmosphere, is poorly understood. Here we report the molecular tracer levoglucosan concentrations in marine air from the Arctic Ocean through the North and South Pacific Ocean to Antarctica during burning season. Levoglucosan was found to be present in all regions at ng/m3 levels with the highest atmospheric loadings present in the mid-latitudes (30°–60° N and S), intermediate loadings in the Arctic, and lowest loadings in the Antarctic and equatorial latitudes. As a whole, levoglucosan concentrations in the Southern Hemisphere were comparable to those in the Northern Hemisphere. Biomass burning has a significant impact on atmospheric Hg and water-soluble organic carbon (WSOC) from pole-to-pole, with more contribution to WSOC in the Northern Hemisphere than in the Southern Hemisphere.

Atmospheric HCH concentrations over the marine boundary layer from Shanghai, China to the Arctic Ocean: role of human activity and climate change.

From July to September 2008, air samples were collected aboard the research expedition icebreaker XueLong (Snow Dragon) as part of the 2008 Chinese Arctic Research Expedition Program. Hexachlorocyclohexane (HCH) concentrations were analyzed in all of the samples. The average concentrations (± standard deviation) over the entire period were 33 ± 16, 5.4 ± 3.0, and 13 ± 7.5 pg m⁻³ for α-, β- and γ-HCH, respectively. Compared to previous studies in the same areas, total HCH (ΣHCH, the sum of α-, β-, and γ-HCH) levels declined by more than 10 × compared to those observed in the 1990s, but were approximately 4 × higher than those measured by the 2003 China Arctic Research Expedition, suggesting the increase of atmospheric ΣHCH recently. Because of the continuing use of lindane, ratios of α/γ-HCH showed an obvious decrease in North Pacific and Arctic region compared with those for 2003 Chinese Arctic Research Expedition. In Arctic, the level of α-HCH was found to be linked to sea ice distribution. Geographically, the average concentration of α-HCH in air samples from the Chukchi and Beaufort Seas, neither of which contain sea ice, was 23 ± 4.4 pg m⁻³, while samples from the area covered by seasonal ice (∼75°N to ∼83°N), the so-called floating sea ice region, contained the highest average levels of α-HCH at 48 ± 12 pg m⁻³, likely due to emission from sea ice and strong air-sea exchange. The lowest concentrations of α-HCH were observed in the pack ice region in the high Arctic covered by multiyear sea ice (∼83°N to ∼86°N). This phenomenon implies that the re-emission of HCH trapped in ice sheets and Arctic Ocean may accelerate during the summer as ice coverage in the Arctic Ocean decreases in response to global climate change.

High variability of atmospheric mercury in the summertime boundary layer through the central Arctic Ocean

The biogeochemical cycles of mercury in the Arctic springtime have been intensively investigated due to mercury being rapidly removed from the atmosphere. However, the behavior of mercury in the Arctic summertime is still poorly understood. Here we report the characteristics of total gaseous mercury (TGM) concentrations through the central Arctic Ocean from July to September, 2012. The TGM concentrations varied considerably (from 0.15u2005ng/m3 to 4.58u2005ng/m3), and displayed a normal distribution with an average of 1.23 ± 0.61u2005ng/m3. The highest frequency range was 1.0–1.5u2005ng/m3, lower than previously reported background values in the Northern Hemisphere. Inhomogeneous distributions were observed over the Arctic Ocean due to the effect of sea ice melt and/or runoff. A lower level of TGM was found in July than in September, potentially because ocean emission was outweighed by chemical loss.

Atmospheric hexachlorobenzene determined during the third China arctic research expedition: Sources and environmental fate

Abstract In July to September 2008, air samples were collected aboard a research expedition icebreaker, Xuelong (Snow Dragon), under the support of the 2008 Chinese Arctic Research Expedition Program. All the air samples were analyzed for determination of the concentrations of Hexachlorobenzene (HCB). The levels of HCB ranged from 24 to 180xa0pg m −3 , with an average concentration of 88xa0pg m −3 . Generally, HCB were more uniform than other organchlorine pollutants in the North Pacific Ocean and the Arctic Ocean. Geographically, the average concentrations of HCB from high to low were in the following order: the Central Arctic Ocean (110xa0±xa057xa0pg m −3 ), the Chukchi and Beaufort Seas (93xa0±xa029xa0pg m −3 ), the East Asia (75xa0±xa049xa0pg m −3 ) and the North Pacific Ocean (69xa0±xa038xa0pg m −3 ). In the East Asia Sea and the North Pacific Ocean, both primary and secondary emissions of HCB from the nearby continents and/or oceans might contribute to the atmospheric HCB. In the Arctic, intense sea–ice melting in the summer of 2008 might result in the remobilization of HCB and enhance its atmospheric levels in this region.

Characterization of atmospheric mercury at a suburban site of central China from wintertime to springtime

Abstract Atmospheric mercury exits primarily as gaseous mercury and particulate mercury (PHg). Change in the species of atmospheric mercury will pose significant impact on the biogeochemical process of mercury. Here total gaseous mercury (TGM) and total particulate mercury (TPM) were measured from heating season in wintertime to springtime with frequent dust storm during February to May 2009 in the suburban of Hefei, central China, where atmospheric mercury measurements were completely absent. The average concentrations of TGM and TPM were 2.57xa0±xa01.37xa0ng/m 3 and 0.32xa0±xa00.10xa0ng/m 3 , respectively. Variations in the TGM were affected by both emissions and meteorological parameters. In the heating period (February), due to coal combustion TGM concentrations were significantly higher than those in the spring (March, April and May). A clear different diurnal variation in TGM concentration was also observed both in late winter and in spring, accompanying with the advance of sunrise. The percentage of total particulate mercury (TPM) in total atmospheric Hg ranged from 5.8%–19.2%, with relatively high levels appeared in March and April. PHg was mainly derived from direct emissions by coal combustion in February and May, while it was dominated by transformation from gaseous Hg on particles in March and April due to dust storms, which may result in more deposition of mercury to ecosystem.

δ 13 C-CH4 reveals CH4 variations over oceans from mid-latitudes to the Arctic

The biogeochemical cycles of CH4 over oceans are poorly understood, especially over the Arctic Ocean. Here we report atmospheric CH4 levels together with δ13C-CH4 from offshore China (31°N) to the central Arctic Ocean (up to 87°N) from July to September 2012. CH4 concentrations and δ13C-CH4 displayed temporal and spatial variation ranging from 1.65 to 2.63 ppm, and from −50.34% to −44.94% (mean value: −48.55u2009±u20090.84%), respectively. Changes in CH4 with latitude were linked to the decreasing input of enriched δ13C and chemical oxidation by both OH and Cl radicals as indicated by variation of δ13C. There were complex mixing sources outside and inside the Arctic Ocean. A keeling plot showed the dominant influence by hydrate gas in the Nordic Sea region, while the long range transport of wetland emissions were one of potentially important sources in the central Arctic Ocean. Experiments comparing sunlight and darkness indicate that microbes may also play an important role in regional variations.

Monocarboxylic and dicarboxylic acids over oceans from the East China Sea to the Arctic Ocean: Roles of ocean emissions, continental input and secondary formation

Organic acids are major components in marine organic aerosols. Many studies on the occurrence, sources and sinks of organic acids over oceans in the low and middle latitudes have been conducted. However, the understanding of relative contributions of specific sources to organic acids over oceans, especially in the high latitudes, is still inadequate. This study measured organic acids, including C14:0 - C32:0 saturated monocarboxylic acids (MCAs), C16:1, C18:1 and C18:2 unsaturated MCAs, and di-C4 - di-C10 dicarboxylic acids (DCAs), in the marine boundary layer from the East China Sea to the Arctic Ocean during the 3rd Chinese Arctic Research Expedition (CHINARE 08). The average concentrations were 18u202f±u202f16u202fng/m3 and 11u202f±u202f5.4u202fng/m3 for ΣMCA and ΣDCA, respectively. The levels of saturated MCAs were much higher than those of unsaturated DCAs, with peaks at C16:0, C18:0 and C14:0. DCAs peaked at di-C4, followed by di-C9 and di-C8. Concentrations of MCAs and DCAs generally decreased with increasing latitudes. Sources of MCAs and DCAs were further investigated using principal component analysis with a multiple linear regression (PCA-MLR) model. Overall, carboxylic acids originated from ocean emissions, continental input (including biomass burning, anthropogenic emissions and terrestrial plant emissions), and secondary formation. All the five sources contributed to MCAs with ocean emissions as the predominant source (48%), followed by biomass burning (20%). In contrast, only 3 sources (i.e., secondary formation (50%), anthropogenic emissions (41%) and biomass burning (9%)) contributed to DCAs. Furthermore, the sources varied with regions. Over the Arctic Ocean, only secondary formation and anthropogenic emissions contributed to MCAs and DCAs.