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评估新西兰奥克兰市多种污染物的空间变异性。

Assessment of Spatial Variability across Multiple Pollutants in Auckland, New Zealand.

机构信息

National Institute of Water and Atmospheric Research (NIWA), Private Bag 99940, Newmarket, Auckland 1149, New Zealand.

University of Pittsburgh Graduate School of Public Health, Department of Environmental and Occupational Health, Pittsburgh, PA 15219, USA.

出版信息

Int J Environ Res Public Health. 2019 May 5;16(9):1567. doi: 10.3390/ijerph16091567.

DOI:10.3390/ijerph16091567
PMID:31060269
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6539388/
Abstract

Spatial saturation studies using source-specific chemical tracers are commonly used to examine intra-urban variation in exposures and source impacts, for epidemiology and policy purposes. Most such studies, however, has been performed in North America and Europe, with substantial regional combustion-source contributions. In contrast, Auckland, New Zealand, a large western city, is relatively isolated in the south Pacific, with minimal impact from long-range combustion sources. However, fluctuating wind patterns, complex terrain, and an adjacent major port complicate pollution patterns within the central business district (CBD). We monitored multiple pollutants (fine particulate matter (PM), black carbon (BC), elemental composition, organic diesel tracers (polycyclic aromatic hydrocarbons (PAHs), hopanes, steranes), and nitrogen dioxide (NO)) at 12 sites across the ~5 km CBD during autumn 2014, to capture spatial variation in traffic, diesel, and proximity to the port. PM concentrations varied 2.5-fold and NO concentrations 2.9-fold across the CBD, though constituents varied more dramatically. The highest-concentration constituent was sodium (Na), a distinct non-combustion-related tracer for sea salt (µ = 197.8 ng/m (SD = 163.1 ng/m)). BC, often used as a diesel-emissions tracer, varied more than five-fold across sites. Vanadium (V), higher near the ports, varied more than 40-fold across sites. Concentrations of most combustion-related constituents were higher near heavy traffic, truck, or bus activity, and near the port. Wind speed modified absolute concentrations, and wind direction modified spatial patterns in concentrations (i.e., ports impacts were more notable with winds from the northeast).

摘要

使用源特异性化学示踪剂进行空间饱和度研究常用于检查城市内部暴露和源影响的变化,以进行流行病学和政策研究。然而,大多数此类研究都在北美和欧洲进行,这些地区的燃烧源贡献较大。相比之下,新西兰奥克兰是一个位于南太平洋的大型西部城市,与远程燃烧源的影响相对隔绝。然而,波动的风向模式、复杂的地形以及毗邻的主要港口使市中心商务区(CBD)内的污染模式变得复杂。我们在 2014 年秋季在 CBD 的 12 个地点监测了多种污染物(细颗粒物(PM)、黑碳(BC)、元素组成、有机柴油示踪剂(多环芳烃(PAHs)、藿烷、甾烷)和二氧化氮(NO )),以捕捉交通、柴油和靠近港口的空间变化。PM 浓度在 CBD 内变化了 2.5 倍,NO 浓度变化了 2.9 倍,尽管成分变化更为显著。浓度最高的成分是钠(Na),一种明显的非燃烧相关的海盐示踪剂(µ=197.8ng/m(SD=163.1ng/m))。BC 通常用作柴油排放示踪剂,在各站点之间变化超过五倍。靠近港口的钒(V)变化超过 40 倍。大多数与燃烧有关的成分的浓度在交通繁忙、卡车或公共汽车活动以及靠近港口的地方较高。风速改变了绝对浓度,风向改变了浓度的空间分布(即,来自东北风时港口的影响更为明显)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/6539388/1f107b72b696/ijerph-16-01567-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/6539388/42c0353887d1/ijerph-16-01567-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/6539388/c62a3e24ec69/ijerph-16-01567-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/6539388/a10a5f12f3b4/ijerph-16-01567-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/6539388/55b89d33ea33/ijerph-16-01567-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/6539388/da3e36d7e6bd/ijerph-16-01567-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/6539388/1f107b72b696/ijerph-16-01567-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/6539388/42c0353887d1/ijerph-16-01567-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/6539388/c62a3e24ec69/ijerph-16-01567-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/6539388/a10a5f12f3b4/ijerph-16-01567-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/6539388/55b89d33ea33/ijerph-16-01567-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/6539388/da3e36d7e6bd/ijerph-16-01567-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/6539388/1f107b72b696/ijerph-16-01567-g006.jpg

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