scholarly journals Long-term observations of tropospheric particle number size distributions and equivalent black carbon mass concentrations in the German Ultrafine Aerosol Network (GUAN)

2016 ◽  
Vol 8 (2) ◽  
pp. 355-382 ◽  
Author(s):  
Wolfram Birmili ◽  
Kay Weinhold ◽  
Fabian Rasch ◽  
André Sonntag ◽  
Jia Sun ◽  
...  

Abstract. The German Ultrafine Aerosol Network (GUAN) is a cooperative atmospheric observation network, which aims at improving the scientific understanding of aerosol-related effects in the troposphere. The network addresses research questions dedicated to both climate- and health-related effects. GUAN's core activity has been the continuous collection of tropospheric particle number size distributions and black carbon mass concentrations at 17 observation sites in Germany. These sites cover various environmental settings including urban traffic, urban background, rural background, and Alpine mountains. In association with partner projects, GUAN has implemented a high degree of harmonisation of instrumentation, operating procedures, and data evaluation procedures. The quality of the measurement data is assured by laboratory intercomparisons as well as on-site comparisons with reference instruments. This paper describes the measurement sites, instrumentation, quality assurance, and data evaluation procedures in the network as well as the EBAS repository, where the data sets can be obtained (doi:10.5072/guan).

2015 ◽  
Vol 8 (2) ◽  
pp. 935-993 ◽  
Author(s):  
W. Birmili ◽  
K. Weinhold ◽  
M. Merkel ◽  
F. Rasch ◽  
A. Sonntag ◽  
...  

Abstract. The German Ultrafine Aerosol Network (GUAN) is a cooperative atmospheric observation network, which aims at improving the scientific understanding of aerosol-related effects in the troposphere. The network addresses research questions dedicated to both, climate and health related effects. GUAN's core activity has been the continuous collection of tropospheric particle number size distributions and black carbon mass concentrations at seventeen observation sites in Germany. These sites cover various environmental settings including urban traffic, urban background, rural background, and Alpine mountains. In association with partner projects, GUAN has implemented a high degree of harmonisation of instrumentation, operating procedures, and data evaluation procedures. The quality of the measurement data is assured by laboratory intercomparisons as well as on-site comparisons with reference instruments. This paper describes the measurement sites, instrumentation, quality assurance and data evaluation procedures in the network as well as the EBAS repository, where the data sets can be obtained (doi:10.5072/guan).


2019 ◽  
Vol 12 (9) ◽  
pp. 4697-4712 ◽  
Author(s):  
Honey Dawn C. Alas ◽  
Kay Weinhold ◽  
Francesca Costabile ◽  
Antonio Di Ianni ◽  
Thomas Müller ◽  
...  

Abstract. Measurements of air pollutants such as black carbon (BC) and particle mass concentration in general, using mobile platforms equipped with high-time-resolution instruments, have gained popularity over the last decade due to their wide range of applicability. Assuring the quality of mobile measurement, data have become more essential, particularly when the personal exposure to pollutants is related to their spatial distribution. In the following, we suggest a methodology to achieve data from mobile measurements of equivalent black carbon (eBC) and PM2.5 mass concentrations with high data quality. Besides frequent routine quality assurance measures of the instruments, the methodology includes the following steps: (a) measures to ensure the quality of mobile instruments through repeated collocated measurements using identical instrumentation, (b) inclusion of a fixed station along the route containing quality-assured reference instruments, and (c) sufficiently long and frequent intercomparisons between the mobile and reference instruments to correct the particle number and mass size distributions obtained from mobile measurements. The application of the methodology can provide the following results. First, collocated mobile measurements with sets of identical instruments allow identification of undetected malfunctions of the instruments. Second, frequent intercomparisons against the reference instruments will ensure the quality of the mobile measurement data of the eBC mass concentration. Third, the intercomparison data between the mobile optical particle size spectrometer (OPSS) and a reference mobility particle size spectrometer (MPSS) allow for the adjustment of the OPSS particle number size distribution using physically meaningful corrections. Matching the OPSS and MPSS volume particle size distributions is crucial for the determination of PM2.5 mass concentration. Using size-resolved complex refractive indices and time-resolved fine-mode volume correction factors of the fine-particle range, the calculated PM2.5 from the OPSS was within 5 % of the reference instruments (MPSS+APSS). However, due to the nonsphericity and an unknown imaginary part of the complex refractive index of supermicrometer particles, a conversion to a volume equivalent diameter yields high uncertainties of the particle mass concentration greater than PM2.5. The proposed methodology addresses issues regarding the quality of mobile measurements, especially for health impact studies, validation of modeled spatial distribution, and development of air pollution mitigation strategies.


2019 ◽  
Author(s):  
Honey Dawn C. Alas ◽  
Kay Weinhold ◽  
Francesca Costabile ◽  
Antonio Di Ianni ◽  
Thomas Müller ◽  
...  

Abstract. Measurements of air pollutants such as black carbon (BC) and particle mass concentration in general, using mobile platforms equipped with high time-resolution instruments have gained popularity over the last decade due to its wide range of applicability. Assuring the quality of mobile measurement, data has become more essential particularly, when the personal exposure to pollutants is related to its spatial distribution. In the following, we suggest a methodology to achieve data from mobile measurements of equivalent black carbon (eBC) and PM2.5 mass concentrations with high data quality. Besides frequent routine quality assurance measures of the instruments, the methodology includes the following steps. a) Measures to ensure the quality of mobile instruments through repeated collocated measurements using identical instrumentation, b) inclusion of a fixed station along the route containing quality-assured reference instruments and c) sufficiently long and frequent intercomparisons between the mobile and reference instruments to correct the particle number and mass size distributions obtained from mobile measurements. The application of the methodology can provide following results. First, collocated mobile measurements with sets of identical instruments allow identification of undetected malfunctions of the instruments. Second, frequent intercomparisons against the reference instruments will ensure the quality of the mobile measurement data of the eBC mass concentration. Third, the intercomparison data between the mobile optical particle size spectrometer (OPSS) and a reference mobility particle size spectrometer (MPSS) allows for the adjustment of the OPSS particle number size distribution using physical meaningful corrections. Matching the OPSS and MPSS volume particle size distributions is crucial for the determination of PM2.5 mass concentration. Using size-resolved complex refractive indices and time-resolved fine mode volume correction factors of the fine particle range, the calculated PM2.5 was within 5 % of the reference instruments (MPSS+APSS). However, due to the non-sphericity and an unknown imaginary part of the complex refractive index of supermicrometer particles, a conversion to a volume equivalent diameter yields high uncertainties of the particle mass concentration greater than PM2.5. The proposed methodology addresses issues regarding the quality of mobile measurements, especially for health impact studies, validation of modelled spatial distribution, and development of air pollution mitigation strategies.


2016 ◽  
Author(s):  
Kgaugelo Euphinia Chiloane ◽  
Johan Paul Beukes ◽  
Pieter Gideon van Zyl ◽  
Petra Maritz ◽  
Ville Vakkari ◽  
...  

Abstract. After carbon dioxide (CO2), aerosol black carbon (BC) is considered to be the second most important contributor to global warming. Africa is one of the least studied continents, although it is regarded as the largest source region of atmospheric BC. Southern Africa is an important sub-source region, with savannah and grassland fires likely to contribute to elevated BC mass concentration levels. South Africa is the economic and industrial hub of southern Africa. To date, little BC mass concentration data have been presented for South Africa in the peer-reviewed public domain. This paper presents equivalent black carbon (eBC) (derived from an optical absorption method) data collected from three sites, where continuous measurements have been conducted, i.e. Elandsfontein (EL), Welgegund (WG) and Marikana (MA), as well elemental carbon (EC) (determined by evolved carbon method) at five sites where samples were collected once a month on a filter and analysed off-line, i.e. Louis Trichardt (LT), Skukuza (SK), Vaal Triangle (VT), Amersfoort (AM) and Botsalano (BS). All these sites are located in the interior of South Africa. Analyses of eBC and EC spatial mass concentration patterns across the eight sites indicate that the mass concentrations in the South African interior are in general higher than what has been reported for the developed world and that different sources are likely to influence different sites. The mean eBC or EC mass concentrations for the background sites (WG, LT, SK, BS) and sites influenced by industrial activities and/or nearby settlements (EL, MA, VT and AM) ranged between 0.7 and 1.1, and 1.3 and 1.4 µg/m3, respectively. Similar seasonal patterns were observed at all three sites where continuous measurement data were collected (EL, MA and WG), with the highest eBC mass concentrations measured during June to October, indicating contributions from household combustion in the cold winter months (June–August), as well as savannah and grassland fires during the dry season (May to mid-October). Diurnal patterns of eBC at EL, MA and WG indicated maximum concentrations in the early mornings and late evenings, and minima during daytime. From the patterns it could be deduced that for MA and WG, household combustion and savannah, and grassland fires were the most significant sources, respectively. Possible contributing sources were explored in greater detail for EL, with five main sources being identified as coal-fired power stations, pyrometallurgical smelters, traffic, household combustion, as well as savannah and grassland fires. Industries on the Mpumalanga Highveld are often blamed for all forms of pollution, due to the NO2 hotspot over this area that is attributed to NOx emissions from industries and vehicle emissions from the Johannesburg-Pretoria megacity. However, a comparison of source strengths indicated that household combustion, and savannah and grassland fires were the most significant sources of eBC, particularly during winter and spring months, while coal-fired power stations, pyro-metallurgical smelters and traffic contribute to eBC mass concentration levels year round.


2005 ◽  
Vol 39 (22) ◽  
pp. 8653-8663 ◽  
Author(s):  
Michael D. Geller ◽  
Satya Brata Sardar ◽  
Harish Phuleria ◽  
Philip M. Fine ◽  
Constantinos Sioutas

2020 ◽  
Vol 20 (14) ◽  
pp. 8593-8610 ◽  
Author(s):  
Mukunda Madhab Gogoi ◽  
Venugopalan Nair Jayachandran ◽  
Aditya Vaishya ◽  
Surendran Nair Suresh Babu ◽  
Sreedharan Krishnakumari Satheesh ◽  
...  

Abstract. During the combined South-West Asian Aerosol–Monsoon Interactions and Regional Aerosol Warming Experiment (SWAAMI–RAWEX), collocated airborne measurements of aerosol number–size distributions in the size (diameter) regime 0.5 to 20 µm and black carbon (BC) mass concentrations were made across the Indo-Gangetic Plain (IGP), for the first time, from three distinct locations, just prior to the onset of the Indian summer monsoon. These measurements provided an east–west transect of region-specific properties of aerosols as the environment transformed from mostly arid conditions of the western IGP (represented by Jodhpur, JDR) having dominance of natural aerosols to the central IGP (represented by Varanasi, VNS) having very high anthropogenic emissions, to the eastern IGP (represented by the coastal station Bhubaneswar, BBR) characterized by a mixture of the IGP outflow and marine aerosols. Despite these, the aerosol size distribution revealed an increase in coarse mode concentration and coarse mode mass fraction (fractional contribution to the total aerosol mass) with the increase in altitude across the entire IGP, especially above the well-mixed region. Consequently, both the mode radii and geometric mean radii of the size distributions showed an increase with altitude. However, near the surface and within the atmospheric boundary layer (ABL), the features were specific to the different subregions, with the highest coarse mode mass fraction (FMC∼72 %) in the western IGP and highest accumulation fraction in the central IGP with the eastern IGP in between. The elevated coarse mode fraction is attributed to mineral dust load arising from local production as well as due to advection from the west. This was further corroborated by data from the Cloud-Aerosol Transport System (CATS) on board the International Space Station (ISS), which also revealed that the vertical extent of dust aerosols reached as high as 5 km during this period. Mass concentrations of BC were moderate (∼1 µg m−3) with very little altitude variation up to 3.5 km, except over VNS where very high concentrations were seen near the surface and within the ABL. The BC-induced atmospheric heating rate was highest near the surface at VNS (∼0.81 K d−1), while showing an increasing pattern with altitude at BBR (∼0.35 K d−1 at the ceiling altitude).


2008 ◽  
Vol 8 (5) ◽  
pp. 18155-18217 ◽  
Author(s):  
F. Costabile ◽  
W. Birmili ◽  
S. Klose ◽  
T. Tuch ◽  
B. Wehner ◽  
...  

Abstract. Due to the presence of diffusive anthropogenic sources in urban areas, the spatio-temporal variability of fine (diameter <1 μm) and ultrafine (<0.1 μm) aerosol particles has been a challenging issue in particle exposure assessment as well as atmospheric research in general. We examined number size distributions of atmospheric aerosol particles (size range 3–800 nm) that were measured simultaneously at a maximum of eight observation sites in and around a city in Central Europe (Leipzig, Germany). Two main experiments were conducted with different time span and number of observation sites (2 years at 3 sites; 1 month at 8 sites). A general observation was that the particle number size distribution varied in time and space in a complex fashion as a result of interaction between local and far-range sources, and the meteorological conditions. To identify statistically independent factors in the urban aerosol, different runs of principal component analysis were conducted encompassing aerosol, gas phase, and meteorological parameters from the multiple sites. Several of the resulting principal components, outstanding with respect to their temporal persistence and spatial coverage, could be associated with aerosol particle modes: a first accumulation mode ("droplet mode", 300–800 nm), considered to be the result of liquid phase processes and far-range transport; a second accumulation mode (centered around diameters 90–250 nm), considered to result from primary emissions as well as aging through condensation and coagulation; an Aitken mode (30–200 nm) linked to urban traffic emissions in addition to an urban and a rural Aitken mode; a nucleation mode (5–20 nm) linked to urban traffic emissions; nucleation modes (3–20 nm) linked to photochemically induced particle formation; an aged nucleation mode (10–50 nm). A number of additional components were identified to represent only local sources at a single site each, or infrequent phenomena. In summary, the analysis of size distributions of high time and size resolution yielded a surprising wealth of statistical aerosol components occurring in the urban atmosphere over one single city. Meanwhile, satisfactory physical explanations could be found for the components with the greatest temporal persistence and spatial coverage. Therefore a paradigm on the behaviour of sub-μm urban aerosol particles is proposed, with recommendations how to efficiently monitor individual sub-fractions across an entire city.


2019 ◽  
Vol 697 ◽  
pp. 133934 ◽  
Author(s):  
Francisco Cereceda-Balic ◽  
Tamara Gorena ◽  
Camila Soto ◽  
Victor Vidal ◽  
Magín Lapuerta ◽  
...  

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