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BVOC ecosystem flux measurements at a high latitude wetland site

机译:BVOC生态系统助焊场测量在高纬度湿地部位

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In this study, we present summertime concentrations and fluxes of biogenic volatile organic compounds (BVOCs) measured at a sub-arctic wetland in northern Sweden using a disjunct eddy-covariance (DEC) technique based on a proton transfer reaction mass spectrometer (PTR-MS). The vegetation at the site was dominated by Sphagnum, Carex and extit{Eriophorum} spp. The measurements reported here cover a period of 50 days (1 August to 19 September 2006), approximately one half of the growing season at the site, and allowed to investigate the effect of day-to-day variation in weather as well as of vegetation senescence on daily BVOC fluxes, and on their temperature and light responses. The sensitivity drift of the DEC system was assessed by comparing H3O+-ion cluster formed with water molecules (H3O+(H2O) at m37) with water vapour concentration measurements made using an adjacent humidity sensor, and the applicability of the DEC method was analysed by a comparison of sensible heat fluxes for high frequency and DEC data obtained from the sonic anemometer. These analyses showed no significant PTR-MS sensor drift over a period of several weeks and only a small flux-loss due to high-frequency spectrum omissions. This loss was within the range expected from other studies and the theoretical considerations. Standardised (20 C and 1000 mol m2 s1 PAR) summer isoprene emission rates found in this study of 329 g C m2 (ground area) h1 were comparable with findings from more southern boreal forests, and fen-like ecosystems. On a diel scale, measured fluxes indicated a stronger temperature dependence than emissions from temperate or (sub)tropical ecosystems. For the first time, to our knowledge, we report ecosystem methanol fluxes from a sub-arctic ecosystem. Maximum daytime emission fluxes were around 270 g m2 h1 (ca. 100 g C m2 h1), and during most nights small negative fluxes directed from the atmosphere to the surface were observed.
机译:在这项研究中,我们使用基于质子转移反应质谱仪(PTR-MS的PTR-MS,所述夏季挥发性有机化合物(BVOCs)呈现在瑞典北极湿地的生物挥发性有机化合物(BVOCs)的汇编和助熔剂(BVOC)(PTR-MS )。该网站的植被由Sphagnum,Carex和 Texit {Eriophorum} SPP主导。这里报告的测量结果涵盖了50天(2006年8月1日至19日至19日),大约在该网站上生长季节的一半,并允许调查天气日常变异的影响以及植被每日BVOC通量的衰老,以及它们的温度和光反应。通过将形成的H3O +(H2O)在M37处的H3O +(H2O)的簇比较使用使用相邻的湿度传感器进行的水蒸气浓度测量来评估DEC系统的敏感性漂移,并通过A的DEC方法的适用性进行分析高频和DEC数据的明智热通量的比较。这些分析显示出在几周内没有显着的PTR-MS传感器漂移,并且由于高频频谱省略而仅具有小的磁通量损耗。这种损失在其他研究的范围内和理论考虑的范围内。标准化(20℃和1000 mol M2 S1 par)夏季异戊二烯排放率在本研究中发现了329g C m 2(地面)H1与来自更多南方北部森林的调查结果和芬太有的生态系统相当。在Diel刻度上,测量的助熔剂表明比来自温带或(亚)热带生态系统的排放更强的温度依赖性。我们的知识首次从亚北极生态系统中报告生态系统甲醇通量。最大的白昼排放助熔剂约为270g M2 H1(约100g C m 2 H1),并且在大多数夜间期间,观察到从大气中指向表面的小阴性助熔剂。

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