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首页> 外文期刊>Environmental Science & Technology >Enantiomeric Signatures Of Organochlorine Pesticides In Asian, Trans-pacific, And Western U.s. Air Masses
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Enantiomeric Signatures Of Organochlorine Pesticides In Asian, Trans-pacific, And Western U.s. Air Masses

机译:亚洲,跨太平洋和美国西部地区有机氯农药的对映体签名空气质量

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摘要

The enantiomeric signatures of organochlorine pesticides were measured in air masses from Okinawa, Japan and three remote locations in the Pacific Northwestern United States: Cheeka Peak Observatory (CPO), a marine boundary layer site on the Olympic Peninsula of Washington at 500 m above sea level (m.a.s.l); Mary's Peak Observatory (MPO), a site at 1250 m.a.s.l in Oregon's Coast range; and Mt. Bachelor Observatory (MBO), a site at 2763 m.a.s.l in Oregon's Cascade range. The enantiomeric signatures of composite soil samples, collected from China, South Korea, and the western U.S. were also measured. The data from chiral analysis was expressed as the enantiomeric fraction, defined as (+) enantiomer/(sum of the (+) and (-) enantiomers), where a racemic composition has EF = 0.5. Racemic a-hexachlorocyclohexane (a-HCH) was measured in Asian air masses at Okinawa and in Chinese and South Korean soils. Nonracemic α-HCH (EF = 0.528 ± 0.0048) was measured in regional air masses at CPO, and may reflect volatilization from the Pacific Ocean and regional soils. However, during trans-Pacific transport events at CPO, the a-HCH EFs were significantly more racemic (EF = 0.513 ± 0.0003, p < 0.001). Racemic a-HCH was consistently measured at MPO and MBO in trans-Pacific air masses that had spent considerable time in the free troposphere. The a-HCH EFs in CPO, MPO, and MBO air masses were negatively correlated (p = 0.0017) with the amount of time the air mass spent above the boundary layer, along the 10-day back air mass trajectory, prior to being sampled. This suggests that, on the West coast of the U.S., the α-HCH in the free troposphere is racemic. Racemic signatures of cis- and frans-chlordane were measuredrnin air masses at all four air sampling sites, suggesting that Asian and U.S. urban areas continue to be sources of chlordane that has not yet been biotransformed.
机译:在来自日本冲绳和美国西北太平洋三个偏远地区的空气质量中测量了有机氯农药的对映体特征:Cheeka Peak天文台(CPO),华盛顿奥林匹克半岛海拔500 m的海洋边界层场地(masl);玛丽山顶天文台(MPO),位于俄勒冈州海岸山脉1250 m.a.s.l;和山学士天文台(MBO),位于俄勒冈州喀斯喀特山脉2763m.a.s.l。还测量了从中国,韩国和美国西部收集的复合土壤样品的对映体特征。来自手性分析的数据表示为对映体分数,定义为(+)对映体/((+)和(-)对映体的总和),其中外消旋组合物的EF = 0.5。在冲绳的亚洲空气质量团以及中国和韩国的土壤中测量了外消旋的α-六氯环己烷(a-HCH)。在CPO的区域空气质量中测量了非外消旋的α-HCH(EF = 0.528±0.0048),这可能反映了太平洋和区域土壤的挥发。但是,在CPO的跨太平洋运输事件中,a-HCH EF的外消旋性更高(EF = 0.513±0.0003,p <0.001)。在跨太平洋气团中,MPO和MBO一直测量外消旋a-HCH,这些气团在自由对流层中度过了很长时间。 CPO,MPO和MBO空气质量中的a-HCH EFs与空气质量在采样之前沿边界层上方沿边界层上方停留的时间量呈负相关(p = 0.0017) 。这表明,在美国西海岸,自由对流层中的甲型六氯环己烷是外消旋的。在所有四个空气采样点的空气质量中测量了顺式和氟烷的外消旋特征,这表明亚洲和美国城市地区仍然是尚未经过生物转化的氯丹来源。

著录项

  • 来源
    《Environmental Science & Technology》 |2009年第8期|2806-2811|共6页
  • 作者单位

    Department of Chemistry, Oregon State University, Corvallis, Oregon;

    Department of Chemistry, Oregon State University, Corvallis, Oregon Department of Environmental and Molecular Toxicology, Oregon State University, Corvallis, Oregon;

    Department of Chemistry, Oregon State University, Corvallis, Oregon;

    Science and Technology Branch, Environment Canada;

    Science and Technology Branch, Environment Canada;

    Center for Atmospheric Research, Egbert, Ontario, Andong National University, Andong, South Korea;

    College of Environmental Science, Peking University, Beijing, China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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