Ayako Yoshino

Development of a measurement system of OH reactivity in the atmosphere by using a laser-induced pump and probe technique

A novel instrument for measuring OH reactivity in the troposphere has been developed by using a laser-induced pump and probe technique. Air was introduced into a flow tube and OH was produced artificially using O3 photolysis by 266 nm laser. The OH decay rate in the flow tube was monitored by the time-resolved laser-induced fluorescence technique. In this article, the instrument, that is, the measurement principle, the flow tube and the fluorescence detection cell, is presented in detail. Interference by absorption of the 266 nm laser light by O3, and photolysis of NO2 and HCHO was found to be negligible. The influence of recycled OH from the HO2+NO reaction on the measured OH reactivity was estimated by a box model calculation. The systematic error of the measured decay rate was found to be less than 5% even in high NO condition ([NO]=20 ppbv). The dependence of the measured decay rate on the flow rate in the reaction tube was investigated. A slight change in the total flow rate does not influence the me...

Gas-aerosol partitioning of semi volatile carbonyls in polluted atmosphere in Hachioji, Tokyo

Gaseous and particulate semi volatile carbonyls have been measured in urban air using an annular denuder sampling system. Three dicarbonyls, five aliphatic aldehydes and two hydroxy carbonyls were observed. Concentrations of other biogenic and anthropogenic volatile organic compounds (VOCs), SO2, CO, NO2 and particle concentration were also measured. Estimated gas-aerosol equilibrium constants for the carbonyls showed an inverse correlation with the concentrations of anthropogenic pollutants such as benzene, isopentane and SO2. This suggests that the increase in the fraction of non-polar anthropogenic particles in the atmosphere could change the average property of the ambient aerosols and drive the gas particle equilibrium of the carbonyls to the gas phase. This trend is uncommon in remote forest air. In this study, we examined the factors controlling the equilibrium in the polluted atmosphere and show that there is a difference in gas-aerosol partition between polluted and clean air.

Aerosol Health Effects from Molecular to Global Scales

Poor air quality is globally the largest environmental health risk. Epidemiological studies have uncovered clear relationships of gaseous pollutants and particulate matter (PM) with adverse health outcomes, including mortality by cardiovascular and respiratory diseases. Studies of health impacts by aerosols are highly multidisciplinary with a broad range of scales in space and time. We assess recent advances and future challenges regarding aerosol effects on health from molecular to global scales through epidemiological studies, field measurements, health-related properties of PM, and multiphase interactions of oxidants and PM upon respiratory deposition. Global modeling combined with epidemiological exposure-response functions indicates that ambient air pollution causes more than four million premature deaths per year. Epidemiological studies usually refer to PM mass concentrations, but some health effects may relate to specific constituents such as bioaerosols, polycyclic aromatic compounds, and transition metals. Various analytical techniques and cellular and molecular assays are applied to assess the redox activity of PM and the formation of reactive oxygen species. Multiphase chemical interactions of lung antioxidants with atmospheric pollutants are crucial to the mechanistic and molecular understanding of oxidative stress upon respiratory deposition. The role of distinct PM components in health impacts and mortality needs to be clarified by integrated research on various spatiotemporal scales for better evaluation and mitigation of aerosol effects on public health in the Anthropocene.

Current situation of atmospheric nanoparticles in Fukue Island, Japan

Abstract Emissions of polluted air in East Asia have gradually decreased over the last decade. Those air pollutants have been transported over long distances and influenced new particle formation (NPF) in the downstream region. We obtained 5-year data of the mobility size distribution and SO2 and particulate (PM2.5) emissions on Fukue Island (32.75°N, 128.68°E), Japan. Frequent NPF events in the 2013 campaign were observed around 60% under the transboundary transport of polluted air by northwesterly wind. In contrast to the data obtained in the last 2-year campaign (2016–2017), these NPF events (<25%) may reflect a relatively clean environment. The daily average SO2 and PM2.5 concentrations over the campaign periods are 2.3 ± 2.2 ppb and 17.6 ± 8.5 µg·m−3 (February 23 to March 7, 2013), 1.3 ± 0.9 ppb and 13.8 ± 4.7 µg·m−3 (February 27 to March 18, 2015), 0.8 ± 0.5 ppb and 14.7 ± 5.3 µg·m−3 (February 27 to March 25, 2016), and 0.5 ± 0.5 ppb and 12.1 ± 4.6 µg·m−3 (January 28 to April 19, 2017), respectively. These reductions of emissions may be due to the measures implemented by the local government in the source region to handle the adverse impacts of environmental pollution. The latest condition of atmospheric nanoparticles on Fukue Island can be used as an indicator to determine the concentration levels of regional air pollutants in East Asia.

Concentrations of metallic elements in long-range-transported aerosols measured simultaneously at three coastal sites in China and Japan

To determine the effects of long-range transport of aerosols from an upwind area in East Asia to a downwind area in Japan, we chemically analyzed aerosols collected simultaneously on Tuoji Island (Shandong Province, China), Fukue Island (Nagasaki Prefecture, Japan), and Cape Hedo (Okinawa Prefecture, Japan). We focused on changes in the metallic composition of PM2.5 aerosols during long-range transport. The average mass concentrations of PM2.5 at the three sites decreased in the order Tuoji Island > Fukue Island ≈ Cape Hedo (48.3 ± 4.5, 13.9 ± 1.5, and 13.2 ± 0.9 μg/m3, respectively). The fraction of coarse particles in total suspended particles estimated by (1–PM2.5/TSP) was highest on Cape Hedo, indicating that the contribution of sea salts was increased by long-range transport of the aerosols over the ocean. Enrichment factor analysis revealed that at all three sites, Al, K, Ca, Mn, Fe, Co, Sr, and Ba originated from soil; whereas Cr, Ni, Cu, Zn, As, Mo, Ag, Cd, Sn, Sb, Tl, and P appeared to be of anthropogenic origin. Na was the most abundant element on Cape Hedo, indicating the addition of sea salts during aerosol transport. The V concentration was highest at Fukue Island, which was ascribed to V emission from ships. Sixty-one percent of the V on Fukue Island and 62% of the V on Cape Hedo were determined to have originated from ships, implicating of data obtained on dates during which backward trajectory analysis indicated that the same air mass passed over Tuoji Island, Fukue Island, and Cape Hedo in that order.