Suppr超能文献

美国边境口岸车辆排放造成的空气有毒物质暴露:布法罗和平桥研究

Air toxics exposure from vehicle emissions at a U.S. border crossing: Buffalo Peace Bridge Study.

作者信息

Spengler John, Lwebuga-Mukasa Jamson, Vallarino Jose, Melly Steve, Chillrud Steve, Baker Joel, Minegishi Taeko

机构信息

Department of Environmental Health, Harvard School of Public Health, Boston, Massachusetts 02215, USA.

出版信息

Res Rep Health Eff Inst. 2011 Jul(158):5-132.

Abstract

The Peace Bridge in Buffalo, New York, which spans the Niagara River at the east end of Lake Erie, is one of the busiest U.S. border crossings. The Peace Bridge plaza on the U.S. side is a complex of roads, customs inspection areas, passport control areas, and duty-free shops. On average 5000 heavy-duty diesel trucks and 20,000 passenger cars traverse the border daily, making the plaza area a potential "hot spot" for emissions from mobile sources. In a series of winter and summer field campaigns, we measured air pollutants, including many compounds considered by the U.S. Environmental Protection Agency (EPA*) as mobile-source air toxics (MSATs), at three fixed sampling sites: on the shore of Lake Erie, approximately 500 m upwind (under predominant wind conditions) of the Peace Bridge plaza; immediately downwind of (adjacent to) the plaza; and 500 m farther downwind, into the community of west Buffalo. Pollutants sampled were particulate matter (PM) < or = 10 microm (PM10) and < or = 2.5 microm (PM2.5) in aerodynamic diameter, elemental carbon (EC), 28 elements, 25 volatile organic compounds (VOCs) including 3 carbonyls, 52 polycyclic aromatic hydrocarbons (PAHs), and 29 nitrogenated polycyclic aromatic hydrocarbons (NPAHs). Spatial patterns of counts of ultrafine particles (UFPs, particles < 0.1 microm in aerodynamic diameter) and of particle-bound PAH (pPAH) concentrations were assessed by mobile monitoring in the neighborhood adjacent to the Peace Bridge plaza using portable instruments and Global Positioning System (GPS) tracking. The study was designed to assess differences in upwind and downwind concentrations of MSATs, in areas near the Peace Bridge plaza on the U.S. side of the border. The Buffalo Peace Bridge Study featured good access to monitoring locations proximate to the plaza and in the community, which are downwind with the dominant winds from the direction of Lake Erie and southern Ontario. Samples from the lakeside Great Lakes Center (GLC), which is upwind of the plaza with dominant winds, were used to characterize contaminants in regional air masses. On-site meteorologic measurements and hourly truck and car counts were used to assess the role of traffic on UFP counts and pPAH concentrations. The array of parallel and perpendicular residential streets adjacent to the plaza provided a grid on which to plot the spatial patterns of UFP counts and pPAH concentrations to determine the extent to which traffic emissions from the Peace Bridge plaza might extend into the neighboring community. For lake-wind conditions (southwest to northwest) 12-hour integrated daytime samples showed clear evidence that vehicle-related emissions at the Peace Bridge plaza were responsible for elevated downwind concentrations of PM2.5, EC, and benzene, toluene, ethylbenzene, and xylenes (BTEX), as well as 1,3-butadiene and styrene. The chlorinated VOCs and aldehydes were not differentially higher at the downwind site. Several metals (aluminum, calcium, iron, copper, and antimony) were two times higher at the site adjacent to the plaza as they were at the upwind GLC site on lake-wind sampling days. Other metals (beryllium, sodium, magnesium, potassium, titanium, manganese, cobalt, strontium, tin, cesium, and lanthanum) showed significant increases downwind as well. Sulfur, arsenic, selenium, and a few other elements appeared to be markers for regional transport as their upwind and downwind concentrations were correlated, with ratios near unity. Using positive matrix factorization (PMF), we identified the sources for PAHs at the three fixed sampling sites as regional, diesel, general vehicle, and asphalt volatilization. Diesel exhaust at the Peace Bridge plaza accounted for approximately 30% of the PAHs. The NPAH sources were identified as nitrate (NO3) radical reactions, diesel, and mixed sources. Diesel exhaust at the Peace Bridge plaza accounted for 18% of the NPAHs. Further evidence for the impact of the Peace Bridge plaza on local air quality was found when the differences in 10-minute average UFP counts and pPAH concentrations were calculated between pairs of sites and displayed by wind direction. With winds from approximately 160 degrees through 220 degrees, UFP counts adjacent to the plaza were 10,000 to 20,000 particles/cm3 higher than those upwind of the plaza. A similar pattern was displayed for pPAH concentrations adjacent to the plaza, which were between 10 and 20 ng/m3 higher than those at the upwind GLC site. Regression models showed better correlation with traffic variables for pPAHs than for UFPs. For pPAHs, truck counts and car counts had significant positive correlations, with similar magnitudes for the effects of trucks and cars, despite lower truck counts. Examining all traffic variables, including traffic counts and counts divided by wind speed, the multivariate regression analysis had an adjusted coefficient of determination (R2) of 0.34 for pPAHs, with all terms significant at P < 0.002. Study staff members traversed established routes in the neighborhood while carrying instruments to record continuous UFP and pPAH values. They also carried a GPS, which was used to provide location-specific time-stamped data. Analyses using a geographic information system (GIS) demonstrated that emissions at the Peace Bridge plaza, at times, affected ambient air quality over several blocks (a few hundred meters). Under lake-wind conditions, overall spatial patterns in UFP and pPAH levels were similar for summer and winter and for morning and afternoon sampling sessions. The Buffalo Peace Bridge Study demonstrated that a concentration of motor vehicles resulted in elevated levels of mobile-source-related emissions downwind, to distances of 300 m to 600 m. The study provides a unique data set to assess interrelationships among MSATs and to ascertain the impact of heavy-duty diesel vehicles on air quality.

摘要

纽约州布法罗市的和平桥横跨伊利湖东端的尼亚加拉河,是美国最繁忙的边境口岸之一。美国一侧的和平桥广场是一个由道路、海关检查区、护照管制区和免税商店组成的综合体。平均每天有5000辆重型柴油卡车和20000辆乘用车通过边境,使得广场区域成为移动源排放的潜在“热点”。在一系列冬季和夏季实地监测活动中,我们在三个固定采样点测量了空气污染物,其中包括许多被美国环境保护局(EPA*)视为移动源空气有毒物质(MSATs)的化合物:在伊利湖岸边,距离和平桥广场上风方向约500米处(在主要风向条件下);广场紧邻的下风方向;以及再向下风方向500米处,进入布法罗西部社区。采样的污染物包括空气动力学直径小于或等于10微米(PM10)和小于或等于2.5微米(PM2.5)的颗粒物、元素碳(EC)、28种元素、25种挥发性有机化合物(VOCs)(包括3种羰基化合物)、52种多环芳烃(PAHs)以及29种含氮多环芳烃(NPAHs)。使用便携式仪器和全球定位系统(GPS)跟踪,通过在和平桥广场附近社区的移动监测,评估了超细颗粒物(UFPs,空气动力学直径小于0.1微米的颗粒物)数量和颗粒结合多环芳烃(pPAH)浓度的空间分布模式。该研究旨在评估边境美国一侧和平桥广场附近区域MSATs在上风方向和下风方向浓度的差异。布法罗和平桥研究的优势在于能够很好地进入广场附近和社区的监测地点,这些地点处于来自伊利湖和安大略湖以南方向主导风的下风方向。来自广场上风方向主导风处的湖滨大湖中心(GLC)的样本,用于表征区域气团中的污染物。现场气象测量以及每小时的卡车和汽车流量计数,用于评估交通对超细颗粒物数量和颗粒结合多环芳烃浓度的影响。广场附近平行和垂直的住宅街道形成了一个网格,可用于绘制超细颗粒物数量和颗粒结合多环芳烃浓度的空间分布模式,以确定和平桥广场的交通排放可能延伸到邻近社区的范围。对于湖风条件(西南风至西北风),12小时综合白天样本显示,有明确证据表明和平桥广场与车辆相关的排放导致下风方向的PM2.5、EC、苯、甲苯、乙苯和二甲苯(BTEX)以及1,3 - 丁二烯和苯乙烯浓度升高。下风方向站点的氯化挥发性有机化合物和醛类并没有明显更高。在湖风采样日,几种金属(铝、钙、铁、铜和锑)在广场附近站点的含量是上风方向GLC站点的两倍。其他金属(铍、钠、镁、钾、钛、锰、钴、锶、锡、铯和镧)在下风方向也有显著增加。硫、砷、硒和其他一些元素似乎是区域传输的标志物,因为它们在上风方向和下风方向的浓度相关,比率接近1。使用正定矩阵因子分解(PMF),我们确定了三个固定采样点多环芳烃的来源为区域源、柴油源、一般车辆源和沥青挥发源。和平桥广场的柴油排放约占多环芳烃的30%。含氮多环芳烃的来源被确定为硝酸根(NO3)自由基反应、柴油和混合源。和平桥广场的柴油排放占含氮多环芳烃的18%。当计算各站点对之间10分钟平均超细颗粒物数量和颗粒结合多环芳烃浓度的差异,并按风向显示时,发现了和平桥广场对当地空气质量影响的进一步证据。当风向约为160度至220度时,广场附近的超细颗粒物数量比广场上风方向高10000至20000个/立方厘米。广场附近颗粒结合多环芳烃浓度也呈现类似模式,比上风方向GLC站点高10至20纳克/立方米。回归模型显示,颗粒结合多环芳烃与交通变量的相关性优于超细颗粒物。对于颗粒结合多环芳烃,卡车流量和汽车流量具有显著正相关,尽管卡车流量较低,但卡车和汽车的影响幅度相似。在检查所有交通变量(包括交通流量和流量除以风速)时,多元回归分析对于颗粒结合多环芳烃的调整决定系数(R2)为0.34,所有项在P < 0.002时均显著。研究人员携带仪器沿着社区既定路线行走,记录连续的超细颗粒物和颗粒结合多环芳烃值。他们还携带了GPS,用于提供特定位置的时间标记数据。使用地理信息系统(GIS)进行的分析表明,和平桥广场的排放有时会影响几个街区(几百米)范围内的环境空气质量。在湖风条件下,夏季和冬季以及上午和下午采样时段,超细颗粒物和颗粒结合多环芳烃水平的总体空间分布模式相似。布法罗和平桥研究表明,机动车的集中导致下风方向300米至600米范围内与移动源相关的排放水平升高。该研究提供了一个独特的数据集,用于评估移动源空气有毒物质之间的相互关系,并确定重型柴油车辆对空气质量的影响。

引用本文的文献

2
Metallic elements and oxides and their relevance to Laurentian Great Lakes geochemistry.
PeerJ. 2020 May 6;8:e9053. doi: 10.7717/peerj.9053. eCollection 2020.
3
Occupational exposure and respiratory health of workers at small scale industries.
Saudi J Biol Sci. 2020 Mar;27(3):985-990. doi: 10.1016/j.sjbs.2020.01.019. Epub 2020 Jan 27.
4
Use of honeybees (Apis mellifera L.) as bioindicators for assessment and source appointment of metal pollution.
Environ Sci Pollut Res Int. 2017 Nov;24(33):25828-25838. doi: 10.1007/s11356-017-0196-7. Epub 2017 Sep 21.

本文引用的文献

2
Sources of fine organic aerosol. 6. Cigaret smoke in the urban atmosphere.
Environ Sci Technol. 1994 Jul 1;28(7):1375-88. doi: 10.1021/es00056a030.
4
Residential traffic and children's respiratory health.
Environ Health Perspect. 2008 Sep;116(9):1274-9. doi: 10.1289/ehp.10735.
6
Prenatal exposure to airborne polycyclic aromatic hydrocarbons and risk of intrauterine growth restriction.
Environ Health Perspect. 2008 May;116(5):658-65. doi: 10.1289/ehp.10958.
7
Ischemic and thrombotic effects of dilute diesel-exhaust inhalation in men with coronary heart disease.
N Engl J Med. 2007 Sep 13;357(11):1075-82. doi: 10.1056/NEJMoa066314.
8
Factors influencing the spatial extent of mobile source air pollution impacts: a meta-analysis.
BMC Public Health. 2007 May 22;7:89. doi: 10.1186/1471-2458-7-89.
9
Factor analysis of submicron particle size distributions near a major United States-Canada trade bridge.
J Air Waste Manag Assoc. 2007 Feb;57(2):190-203. doi: 10.1080/10473289.2007.10465316.
10
Effect of exposure to traffic on lung development from 10 to 18 years of age: a cohort study.
Lancet. 2007 Feb 17;369(9561):571-7. doi: 10.1016/S0140-6736(07)60037-3.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验