GSTDTAP  > 地球科学
DOI10.5194/acp-18-13787-2018
Characterization of trace gas emissions at an intermediate port
Wiacek, Aldona1,2; Li, Li1; Tobin, Keane1; Mitchell, Morgan1
2018-10-01
发表期刊ATMOSPHERIC CHEMISTRY AND PHYSICS
ISSN1680-7316
EISSN1680-7324
出版年2018
卷号18期号:19页码:13787-13812
文章类型Article
语种英语
国家Canada
英文摘要

Growing ship traffic in Atlantic Canada strengthens the local economy but also plays an important role in greenhouse gas and air pollutant emissions in this coastal environment. A mobile open-path Fourier transform infrared (OP-FTIR; acronyms defined in Appendix A) spectrometer was set up in Halifax Harbour (Nova Scotia, Canada), an intermediate harbour integrated into the downtown core, to measure trace gas concentrations in the vicinity of marine vessels, in some cases with direct or near-direct marine combustion plume intercepts. This is the first application of the OP-FTIR measurement technique to real-time, spectroscopic measurements of CO2, CO, O-3, NO2, NH3, CH3OH, HCHO, CH4 and N2O in the vicinity of harbour emissions originating from a variety of marine vessels, and the first measurement of shipping emissions in the ambient environment along the eastern seaboard of North America outside of the Gulf Coast. The spectrometer, its active mid-IR source and its detector were located on shore while the passive retroreflector was on a nearby island, yielding a 455 m open path over the ocean (910 m two-way). Atmospheric absorption spectra were recorded during day, night, sunny, cloudy and substantially foggy or precipitating conditions, with a temporal resolution of 1 min or better. A weather station was co-located with the retroreflector to aid in the processing of absorption spectra and the interpretation of results, while a webcam recorded images of the harbour once per minute. Trace gas concentrations were retrieved from spectra by the MALT non-linear least squares iterative fitting routine. During field measurements (7 days in July-August 2016; 12 days in January 2017) AIS information on nearby ship activity was manually collected from a commercial website and used to calculate emission rates of shipping combustion products (CO2, CO, NOx, HC, SO2), which were then linked to measured concentration variations using ship position and wind information. During periods of low wind speed we observed extended (similar to 9h) emission accumulations combined with near-complete O-3 titration, both in winter and in summer. Our results compare well with a NAPS monitoring station similar to 1 km away, pointing to the extended spatial scale of this effect, commonly found in much larger European shipping channels.


We calculated total marine sector emissions in Halifax Harbour based on a complete AIS dataset of ship activity during the cruise ship season (May-October 2015) and the remainder of the year (November 2015-April 2016) and found trace gas emissions (tonnes) to be 2.8 % higher on average during the cruise ship season, when passenger ship emissions were found to contribute 18 % of emitted CO2, CO, NOx, SO2 and HC (0.5 % in the off season due to occasional cruise ships arriving, even in April) Similarly, calculated particulate emissions are 4.1 % higher during the cruise ship season, when passenger ship emissions contribute 18 % of the emitted particulate matter (PM) (0.5 % in the off season). Tugs were found to make the biggest contribution to harbour emissions of trace gases in both cruise ship season (23 % NOx, 24 % SO2) and the off season (26 % of both SO2 and NOx), followed by container ships (25 % NOx and SO2 in the off season, 21 % NOx and SO2 in cruise ship season). In the cruise ship season cruise ships were observed to be in third place regarding trace gas emissions, whilst tankers were in third place in the off season, with both being responsible for 18 % of the calculated emissions. While the concentrations of all regulated trace gases measured by OP-FTIR as well as the nearby in situ NAPS sensors were well below maximum hourly permissible levels at all times during the 19-day measurement period, we find that AIS-based shipping emissions of NOx over the course of 1 year are 4.2 times greater than those of a nearby 500 MW stationary source emitter and greater than or comparable to all vehicle NOx emissions in the city. Our findings highlight the need to accurately represent emissions from the shipping and marine sectors at intermediate ports integrated into urban environments. Emissions can be represented as pseudo-stationary and/or pseudo-line sources.


领域地球科学
收录类别SCI-E
WOS记录号WOS:000446097000001
WOS关键词MARINE BOUNDARY-LAYER ; SHIP EMISSIONS ; EXHAUST EMISSIONS ; AIR-POLLUTION ; DIESEL-ENGINE ; PARTICULATE MATTER ; PARTICLE EMISSIONS ; DOAS MEASUREMENTS ; PLUME INTERCEPTS ; FUEL QUALITY
WOS类目Environmental Sciences ; Meteorology & Atmospheric Sciences
WOS研究方向Environmental Sciences & Ecology ; Meteorology & Atmospheric Sciences
引用统计
文献类型期刊论文
条目标识符http://119.78.100.173/C666/handle/2XK7JSWQ/21691
专题地球科学
作者单位1.St Marys Univ, Dept Environm Sci, Halifax, NS, Canada;
2.St Marys Univ, Dept Astron & Phys, Halifax, NS, Canada
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Wiacek, Aldona,Li, Li,Tobin, Keane,et al. Characterization of trace gas emissions at an intermediate port[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2018,18(19):13787-13812.
APA Wiacek, Aldona,Li, Li,Tobin, Keane,&Mitchell, Morgan.(2018).Characterization of trace gas emissions at an intermediate port.ATMOSPHERIC CHEMISTRY AND PHYSICS,18(19),13787-13812.
MLA Wiacek, Aldona,et al."Characterization of trace gas emissions at an intermediate port".ATMOSPHERIC CHEMISTRY AND PHYSICS 18.19(2018):13787-13812.
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