Biogenic volatile compound emissions from a temperate forest, China: model simulation

被引:10
作者
Bai, Jianhui [1 ]
Duhl, Tiffany [2 ]
Hao, Nan [3 ]
机构
[1] Chinese Acad Sci, Inst Atmospher Phys, LAGEO, Beijing 100029, Peoples R China
[2] Natl Ctr Atmospher Res, POB 3000, Boulder, CO 80307 USA
[3] Deutsch Zentrum Luft & Raumfahrt eV DLR, Remote Sensing Technol Inst, D-82234 Oberpfaffenhofen, Wessling, Germany
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
Biogenic volatile organic compounds; Isoprene; Monoterpene; Emission flux; Photosynthetically active radiation; GOME-2; QUERCUS-ILEX L; TERRESTRIAL ISOPRENE EMISSIONS; ABSORPTION CROSS-SECTIONS; RELAXED EDDY ACCUMULATION; MONOTERPENE EMISSIONS; CLIMATE VARIABILITY; OXIDATION-PRODUCTS; ORGANIC-COMPOUNDS; MIXED FOREST; PHOTON FLUX;
D O I
10.1007/s10874-015-9315-3
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Emissions of biogenic volatile organic compounds (BVOC) were measured using a relaxed eddy accumulation (REA) technique on an above-canopy tower in a temperate forest (Changbai Mountain, Jilin province, China) during the 2010 and 2011 summer seasons. Solar global radiation and photosynthetically active radiation (PAR) were also measured. Based on PAR energy dynamic balance, an empirical BVOC emission and PAR transfer model was developed that includes the processes of BVOC emissions and PAR transfer above the canopy level, including PAR absorption and consumption, and scattering by gases, liquids, and particles (GLPs). Simulated emissions of isoprene and monoterpenes were in agreement with observations. The averages of the relative estimator biases for the flux were 39.3 % for isoprene, and 27.1 % for monoterpenes in the 2010 and 2011 growing seasons, with NMSE (normalized mean square error) values of 0.133 and 0.101, respectively. The observed and simulated mean diurnal variations of isoprene and monoterpenes in the 2010 and 2011 growing seasons were evaluated for the validation of the empirical model. Under observed atmospheric conditions, the sensitivity analysis showed that emissions of isoprene and monoterpenes were more sensitive to changes in PAR than to water vapor content or to the magnitude of the scattering factor. The emissions of isoprene and monoterpenes in the 2010 and 2011 growing seasons (from June to September) were estimated using this empirical model along with hourly observational data, with mean hourly emissions of 1.71 and 1.55 mg m(-2) h(-1) for isoprene, and 0.48 and 0.47 mg m(-2) h(-1) for monoterpenes in 2010 and 2011, respectively. As formaldehyde (HCHO) is considered as the main oxidation product of isoprene and monoterpenes, it is necessary to investigate the link between HCHO and BVOC emissions. GOME-2 HCHO vertical column densities (VCDs) can be used to estimate BVOC emission fluxes in the Changbai Mountain temperate forest.
引用
收藏
页码:29 / 59
页数:31
相关论文
共 112 条
  • [51] Formation of organic aerosols from the oxidation of biogenic hydrocarbons
    Hoffmann, T
    Odum, JR
    Bowman, F
    Collins, D
    Klockow, D
    Flagan, RC
    Seinfeld, JH
    [J]. JOURNAL OF ATMOSPHERIC CHEMISTRY, 1997, 26 (02) : 189 - 222
  • [52] Seasonal variability of monoterpene emission factors for a Ponderosa pine plantation in California
    Holzinger, R
    Lee, A
    McKay, M
    Goldstein, AH
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2006, 6 : 1267 - 1274
  • [53] Observations of oxidation products above a forest imply biogenic emissions of very reactive compounds
    Holzinger, R
    Lee, A
    Paw, KT
    Goldstein, AH
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2005, 5 : 67 - 75
  • [54] The UV-VIS absorption cross sections of the α-dicarbonyl compounds:: Pyruvic acid, biacetyl and glyoxal
    Horowitz, A
    Meller, R
    Moortgat, GK
    [J]. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2001, 146 (1-2) : 19 - 27
  • [55] The impact of nonmethane hydrocarbon compounds on tropospheric photochemistry
    Houweling, S
    Dentener, F
    Lelieveld, J
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D9) : 10673 - 10696
  • [56] Actinic radiation and photolysis processes in the lower troposphere:: Effect of clouds and aerosols
    Junkermann, W
    Brühl, C
    Perner, D
    Eckstein, E
    Trautmann, T
    Früh, B
    Dlugi, R
    Gori, T
    Ruggaber, A
    Reuder, J
    Zelger, M
    Hofzumahaus, A
    Kraus, A
    Rohrer, F
    Brüning, D
    Moortgat, G
    Horowitz, A
    Tadic, J
    [J]. JOURNAL OF ATMOSPHERIC CHEMISTRY, 2002, 42 (01) : 413 - 441
  • [57] Organic aerosol and global climate modelling: a review
    Kanakidou, M
    Seinfeld, JH
    Pandis, SN
    Barnes, I
    Dentener, FJ
    Facchini, MC
    Van Dingenen, R
    Ervens, B
    Nenes, A
    Nielsen, CJ
    Swietlicki, E
    Putaud, JP
    Balkanski, Y
    Fuzzi, S
    Horth, J
    Moortgat, GK
    Winterhalter, R
    Myhre, CEL
    Tsigaridis, K
    Vignati, E
    Stephanou, EG
    Wilson, J
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2005, 5 : 1053 - 1123
  • [58] Exchange processes of volatile organic compounds above a tropical rain forest: Implications for modeling tropospheric chemistry above dense vegetation
    Karl, T
    Potosnak, M
    Guenther, A
    Clark, D
    Walker, J
    Herrick, JD
    Geron, C
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2004, 109 (D18) : D183061 - 19
  • [59] Rapid formation of isoprene photo-oxidation products observed in Amazonia
    Karl, T.
    Guenther, A.
    Turnipseed, A.
    Tyndall, G.
    Artaxo, P.
    Martin, S.
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2009, 9 (20) : 7753 - 7767
  • [60] Measurement of atmospheric sesquiterpenes by proton transfer reaction-mass spectrometry (PTR-MS)
    Kim, S.
    Karl, T.
    Helmig, D.
    Daly, R.
    Rasmussen, R.
    Guenther, A.
    [J]. ATMOSPHERIC MEASUREMENT TECHNIQUES, 2009, 2 (01) : 99 - 112