Alonso Rocío, Bytnerowicz Andrzej, Arbaugh Michael
USDA Forest Service, Pacific Southwest Research Station, 4955 Canyon Crest Drive, Riverside, CA 92507, USA.
ScientificWorldJournal. 2002 Jan 5;2:10-26. doi: 10.1100/tsw.2002.73.
Information about spatial and temporal distribution of air pollutants is essential for better understanding of environmental stresses affecting forests and estimation of potential risks associated with air pollutants. Ozone and nitrogenous air pollutants were monitored along an elevation gradient in the Class I San Gorgonio Wilderness area (San Bernardino Mountains, California, U.S.) during the summer of 2000 (mid-June to mid-October). Passive samplers were exposed for 2-week periods at six sampling sites located at 300 m intervals ranging from 1200 to 2700 m elevation. Elevated concentrations of ozone were found in this area with summer 24-h hourly means ranging from 53 to 59 ppb. The highest ozone concentrations were detected in the period July 25-August 8, reaching values of 64 to 72 ppb expressed as 2-week mean. Passive-sampler ozone data did not show a clear relationship with elevation, although during the periods with higher ozone levels, ozone concentrations were higher at those sites below 2000 m than at sites located above that elevation. All nitrogenous pollutants studied showed a consistent decrease of concentrations with elevation. Nitrogen dioxide (NO2) levels were low, decreasing with increasing elevation from 6.4 to 1.5 ppb summer means. Nitric oxide (NO) concentrations were around 1 to 2 ppb, which is within the range of the detection levels of the devices used. Nitric acid (HNO3) vapor concentrations were lower at higher elevations (summer means 1.9-2.5 microg m(-3) than at lower elevations (summer means 4.3-5.1 microg m(-3). Summer concentrations of ammonia (NH3) were slightly higher than nitric acid ranging from 6 microg m(-3) at the lowest site to 2.5 microg m(-3) registered at the highest elevation. Since complex interactions between ozone and nitrogenous air pollutants have already been described for forests, simultaneous information about the distribution of these pollutants is needed. This is particularly important in mountain terrain where no reliable models of air pollutant distribution exist.
了解空气污染物的时空分布信息,对于更好地理解影响森林的环境压力以及评估与空气污染物相关的潜在风险至关重要。2000年夏季(6月中旬至10月中旬),在美国加利福尼亚州圣贝纳迪诺山脉的一级圣戈尔戈尼奥荒野地区,沿着海拔梯度对臭氧和含氮空气污染物进行了监测。被动采样器在海拔1200至2700米、间隔300米的六个采样点暴露两周。该地区臭氧浓度升高,夏季24小时每小时平均值在53至59 ppb之间。7月25日至8月8日期间检测到最高臭氧浓度,以两周平均值表示,达到64至72 ppb。被动采样器的臭氧数据与海拔没有明显关系,尽管在臭氧水平较高的时期,海拔2000米以下站点的臭氧浓度高于该海拔以上的站点。所有研究的含氮污染物浓度均随海拔升高而持续下降。二氧化氮(NO2)水平较低,夏季平均值从6.4 ppb降至1.5 ppb,随海拔升高而降低。一氧化氮(NO)浓度约为1至2 ppb,在所用设备的检测水平范围内。硝酸(HNO3)蒸汽浓度在较高海拔处较低(夏季平均值1.9 - 2.5微克/立方米),而在较低海拔处较高(夏季平均值4.3 - 5.1微克/立方米)。夏季氨(NH3)浓度略高于硝酸,最低站点为6微克/立方米,最高海拔处记录为2.5微克/立方米。由于已经描述了森林中臭氧与含氮空气污染物之间的复杂相互作用,因此需要这些污染物分布的同步信息。这在没有可靠空气污染物分布模型的山区尤为重要。