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Yutaka Matsumi

Bio: Yutaka Matsumi is an academic researcher from Nagoya University. The author has contributed to research in topics: Photodissociation & Laser-induced fluorescence. The author has an hindex of 37, co-authored 215 publications receiving 4730 citations. Previous affiliations of Yutaka Matsumi include Hokkaido University & University of Southern Denmark.


Papers
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Proceedings ArticleDOI
20 Jun 1989
TL;DR: In this paper, an imaging system with a two dimensional photo diode array was developed for the excimer laser beam diagnostics, which is featured with a fast frame rate, high spacial resolution, and responsibity at the uv wave length.
Abstract: An imaging system with a two dimensional photo diode array was developed for the excimer laser beam diagnostics. It is featured with a fast frame rate, high spacial resolution, and responsibity at the uv wave length. With a simple optical set up for the imager, we measured a near and a far field pattern simultaneously and the spectral band width of the consecutive KrF excimer laser pulses at 250Hz. These measurements shows our imaging system possesses enough spacial resolution for the beam pattern and spectral measurements.

3 citations

Journal ArticleDOI
TL;DR: In this paper, the authors measured the concentrations of total reactive nitrogen (NOy), nitric oxide (NO) and nitrogen dioxides (NO2) and then obtained NOx oxidation products at a station at the top of Mount Fuji during the summer of 2017.
Abstract: Lightning is an important source of nitrogen oxides (LNOx). The actual global production of LNOx is still largely uncertain. One of the reasons for this uncertainty is the limited available observation data. We measured the concentrations of total reactive nitrogen (NOy), nitric oxide (NO) and nitrogen dioxides (NO2) and then obtained NOx oxidation products (NOz: NOz = NOy - NOx) at a station at the top of Mount Fuji (3776 m a.s.l.) during the summer of 2017. Increases in NOy and NO2 were observed on 22 August 2017. These peaks were unaccompanied by increases in CO, which suggested that the observed air mass did not contain emissions from combustion. The backward trajectories of the above air mass indicated that it moved across areas where lightning occurred. The NOy concentration was also calculated by using a chemical transport model, which did not take NOx produced by lightning into account. Therefore, the NOy concentration due to lightning can be inferred by subtracting the calculated NOy from the observed NOy concentrations. The concentration of NOy at 13:00 on 22 August 2017 originating from lightning was estimated to be 1.11 ± 0.02 ppbv, which comprised 97 ± 2% of the total NOy concentration. The fractions of NO2 and NOz in the total NOy were 0.54 ± 0.01 and 0.46 ± 0.03, respectively. The NO concentration was below the detection limit. We firstly observed increase of concentrations of NOy originating from lightning by ground-based observation and demonstrated the quantitative estimates of LNOx using model-based calculation.

3 citations

Journal ArticleDOI
20 Apr 2018
TL;DR: In this paper, PM2.5 pollution of indoor and outdoor ambience has been measured on a household which is located between the Ger area and the residential district at simultaneous duration and point.
Abstract: In this study, PM2.5 pollution of indoor and outdoor ambience has been measured on a household which is located between the Ger area and the residential district at simultaneous duration and point. In order to analyze, we used n = 3,119,500 data which was measured at each 10 second during 24 hours period. The instrument that was used to study, created by Nagoya University and Panasonic Corporation. In recent years, the capital of Ulaanbaatar, Mongolia, is leading the air pollution during the winter in the world, and the majority of this pollution is comprised of PM2.5 . Fine particles are very harmful to human health, and people spend approximately 90% of their lives in the indoor ambient. Thus, it is important to measure continuously the amount of indoor and outdoor PM2.5, so we have selected two points and indicated some statistical analysis on indoor and outdoor ambient. The results of this study indicate the PM2.5 concentrations of air in Ulaanbaatar are higher than the air quality standard in October and peak in the December and January. Also, due to the feature of the sites being measured, pollution of indoor ambient was demonsrated strong or weak level, which is depended on outdoor ambient pollution. The measurements of the majority days were a high level of pollution from at 00:00 to 04:00 pm, however, it was decreased at 5:00 pm, but it started to increase around 07:00 to 09:00 in the morning, and it decreased from 10:00 am to low level of the pollution whole day. At 18 o’clock in the evening, the pollution was increasing and at the peak of the day, the fine particle pollution up to 02:00 on the next day.

3 citations

Journal ArticleDOI
TL;DR: Continuous, high time-resolution measurements of CO2 and water vapour isotopologues in a red pine forest at the foot of Mt. Fuji found that the air masses with different water vapours isotopic ratios moved into the forest, and changed the atmosphere of the forest.
Abstract: We conducted continuous, high time-resolution measurements of CO2 and water vapour isotopologues ((16)O(12)C(16)O, (16)O(13)C(16)O and (18)O(12)C(16)O for CO2, and H2(18)O for water vapour) in a red pine forest at the foot of Mt. Fuji for 9 days from the end of July 2010 using in situ absorption laser spectroscopy. The δ(18)O values in water vapour were estimated using the δ(2)H-δ(18)O relationship. At a scale of several days, the temporal variations in δ(18)O-CO2 and δ(18)O-H2O are similar. The orders of the daily Keeling plots are almost identical. A possible reason for the similar behaviour of δ(18)O-CO2 and δ(18)O-H2O is considered to be that the air masses with different water vapour isotopic ratios moved into the forest, and changed the atmosphere of the forest. A significant correlation was observed between δ(18)O-CO2 and δ(13)C-CO2 values at nighttime (r(2)≈0.9) due to mixing between soil (and/or leaf) respiration and tropospheric CO2. The ratios of the discrimination coefficients (Δa/Δ) for oxygen (Δa) and carbon (Δ) isotopes during photosynthesis were estimated in the range of 0.7-1.2 from the daytime correlations between δ(18)O-CO2 and δ(13)C-CO2 values.

2 citations

Journal ArticleDOI
TL;DR: In this paper, a new technique using laser flash photolysis in conjunction with laser-induced fluorescence spectroscopy to investigate the reaction kinetics of metastable O( 1 S) atom with atmospheric molecules has been demonstrated.

2 citations


Cited by
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Journal ArticleDOI
TL;DR: In this paper, the photodissociation processes occurring in molecular oxygen following the two-photon 3dπ(3Σ1g −) Rydberg excitation around 225 nm are presented to show the improvement in spatial resolution in the ion and electron images.
Abstract: The application of electrostatic lenses is demonstrated to give a substantial improvement of the two-dimensional (2D) ion/electron imaging technique. This combination of ion lens optics and 2D detection makes “velocity map imaging” possible, i.e., all particles with the same initial velocity vector are mapped onto the same point on the detector. Whereas the more common application of grid electrodes leads to transmission reduction, severe trajectory deflections and blurring due to the non-point source geometry, these problems are avoided with open lens electrodes. A three-plate assembly with aperture electrodes has been tested and its properties are compared with those of grid electrodes. The photodissociation processes occurring in molecular oxygen following the two-photon 3dπ(3Σ1g −)(v=2, N=2)←X(3Σg −) Rydberg excitation around 225 nm are presented here to show the improvement in spatial resolution in the ion and electron images. Simulated trajectory calculations show good agreement with experiment and ...

2,430 citations

Journal ArticleDOI
TL;DR: An overview of PFASs detected in the environment, wildlife, and humans, and recommend clear, specific, and descriptive terminology, names, and acronyms for PFAS, can be found in this article.
Abstract: The primary aim of this article is to provide an overview of perfluoroalkyl and polyfluoroalkyl substances (PFASs) detected in the environment, wildlife, and humans, and recommend clear, specific, and descriptive terminology, names, and acronyms for PFASs. The overarching objective is to unify and harmonize communication on PFASs by offering terminology for use by the global scientific, regulatory, and industrial communities. A particular emphasis is placed on long-chain perfluoroalkyl acids, substances related to the long-chain perfluoroalkyl acids, and substances intended as alternatives to the use of the long-chain perfluoroalkyl acids or their precursors. First, we define PFASs, classify them into various families, and recommend a pragmatic set of common names and acronyms for both the families and their individual members. Terminology related to fluorinated polymers is an important aspect of our classification. Second, we provide a brief description of the 2 main production processes, electrochemical fluorination and telomerization, used for introducing perfluoroalkyl moieties into organic compounds, and we specify the types of byproducts (isomers and homologues) likely to arise in these processes. Third, we show how the principal families of PFASs are interrelated as industrial, environmental, or metabolic precursors or transformation products of one another. We pay particular attention to those PFASs that have the potential to be converted, by abiotic or biotic environmental processes or by human metabolism, into long-chain perfluoroalkyl carboxylic or sulfonic acids, which are currently the focus of regulatory action. The Supplemental Data lists 42 families and subfamilies of PFASs and 268 selected individual compounds, providing recommended names and acronyms, and structural formulas, as well as Chemical Abstracts Service registry numbers. Integr Environ Assess Manag 2011;7:513–541. © 2011 SETAC

2,356 citations

Journal Article
TL;DR: Denman et al. as discussed by the authors presented the Couplings between changes in the climate system and biogeochemistry Coordinating Lead Authors: Kenneth L. Denman (Canada), Guy Brasseur (USA, Germany), Amnat Chidthaisong (Thailand), Philippe Ciais (France), Peter M. Cox (UK), Robert E. Austin (USA), D.B. Wofsy (USA) and Xiaoye Zhang (China).
Abstract: Couplings Between Changes in the Climate System and Biogeochemistry Coordinating Lead Authors: Kenneth L. Denman (Canada), Guy Brasseur (USA, Germany) Lead Authors: Amnat Chidthaisong (Thailand), Philippe Ciais (France), Peter M. Cox (UK), Robert E. Dickinson (USA), Didier Hauglustaine (France), Christoph Heinze (Norway, Germany), Elisabeth Holland (USA), Daniel Jacob (USA, France), Ulrike Lohmann (Switzerland), Srikanthan Ramachandran (India), Pedro Leite da Silva Dias (Brazil), Steven C. Wofsy (USA), Xiaoye Zhang (China) Contributing Authors: D. Archer (USA), V. Arora (Canada), J. Austin (USA), D. Baker (USA), J.A. Berry (USA), R. Betts (UK), G. Bonan (USA), P. Bousquet (France), J. Canadell (Australia), J. Christian (Canada), D.A. Clark (USA), M. Dameris (Germany), F. Dentener (EU), D. Easterling (USA), V. Eyring (Germany), J. Feichter (Germany), P. Friedlingstein (France, Belgium), I. Fung (USA), S. Fuzzi (Italy), S. Gong (Canada), N. Gruber (USA, Switzerland), A. Guenther (USA), K. Gurney (USA), A. Henderson-Sellers (Switzerland), J. House (UK), A. Jones (UK), C. Jones (UK), B. Karcher (Germany), M. Kawamiya (Japan), K. Lassey (New Zealand), C. Le Quere (UK, France, Canada), C. Leck (Sweden), J. Lee-Taylor (USA, UK), Y. Malhi (UK), K. Masarie (USA), G. McFiggans (UK), S. Menon (USA), J.B. Miller (USA), P. Peylin (France), A. Pitman (Australia), J. Quaas (Germany), M. Raupach (Australia), P. Rayner (France), G. Rehder (Germany), U. Riebesell (Germany), C. Rodenbeck (Germany), L. Rotstayn (Australia), N. Roulet (Canada), C. Sabine (USA), M.G. Schultz (Germany), M. Schulz (France, Germany), S.E. Schwartz (USA), W. Steffen (Australia), D. Stevenson (UK), Y. Tian (USA, China), K.E. Trenberth (USA), T. Van Noije (Netherlands), O. Wild (Japan, UK), T. Zhang (USA, China), L. Zhou (USA, China) Review Editors: Kansri Boonpragob (Thailand), Martin Heimann (Germany, Switzerland), Mario Molina (USA, Mexico) This chapter should be cited as: Denman, K.L., G. Brasseur, A. Chidthaisong, P. Ciais, P.M. Cox, R.E. Dickinson, D. Hauglustaine, C. Heinze, E. Holland, D. Jacob, U. Lohmann, S Ramachandran, P.L. da Silva Dias, S.C. Wofsy and X. Zhang, 2007: Couplings Between Changes in the Climate System and Biogeochemistry. In: Climate Change 2007: The Physical Science Basis. Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change [Solomon, S., D. Qin, M. Manning, Z. Chen, M. Marquis, K.B. Averyt, M.Tignor and H.L. Miller (eds.)]. Cambridge University Press, Cambridge, United Kingdom and New York, NY, USA.

2,208 citations