Temporal Trend and Spatial Distribution of Speciated Atmospheric Mercury Emissions in China During 1978–2014

2016 ◽  
Vol 50 (24) ◽  
pp. 13428-13435 ◽  
Author(s):  
Qingru Wu ◽  
Shuxiao Wang ◽  
Guoliang Li ◽  
Sai Liang ◽  
Che-Jen Lin ◽  
...  
2021 ◽  
pp. 125060
Author(s):  
Yaqin Guo ◽  
Lin Xiao ◽  
Bin Chen ◽  
Zhujuan Wu ◽  
Huanxin Chen ◽  
...  

2015 ◽  
Vol 18 (2) ◽  
pp. 313-325 ◽  
Author(s):  
Mayrla Lima Pinto ◽  
Talina Carla da Silva ◽  
Lidiane Cristina Félix Gomes ◽  
Maria Rita Bertolozzi ◽  
Lourdes Milagros Mendoza Villavicencio ◽  
...  

OBJECTIVE: to analyze the spatial distribution of tuberculosis in Crato, Ceará, Brazil, from 2002 to 2011, aiming to check for a point pattern. METHODS: This is an ecological, temporal trend and hybrid design study, with a quantitative approach. A total of 261 cases of tuberculosis were geo-referenced and 20 (7.1%) were considered as losses due to the lack of address. The profile of patients in 10 years of study was in accordance with the following pattern: men aged between 20 and 59 years, with low schooling, affected by the pulmonary form of tuberculosis and who were cured from the disease. RESULTS: The analysis of the spatial distribution of tuberculosis points out that in the period of study, new cases of the disease were not distributed on a regular basis, indicating a clustered spatial pattern, confirmed by the L-function. The map with the density of new cases estimated by the Kernel method showed that the "hot" areas are more concentrated in the vicinity of the central urban area. CONCLUSION: The study allowed pointing out areas of higher and lower concentration of tuberculosis, identifying the spatial pattern, but it also recognized that the disease has not reached all of the population groups with the same intensity. Those who were most vulnerable were the ones who lived in regions with higher population densities, precarious living conditions, and with intense flow of people.


2016 ◽  
Author(s):  
Qianqian Hong ◽  
Zhouqing Xie ◽  
Cheng Liu ◽  
Feiyue Wang ◽  
Pinhua Xie ◽  
...  

Abstract. Long-term continuous measurements of speciated atmospheric mercury were conducted at Hefei, a mid-latitude inland city in east central China, from July 2013 to June 2014. The mean concentrations (± standard deviation) of gaseous elemental mercury (GEM), reactive gaseous mercury (RGM) and particle-bound mercury (PBM) were 3.95 ± 1.93 ng m−3, 2.49 ± 2.41 pg m−3 and 23.3 ± 90.8 pg m−3, respectively, during non-haze days, and 4.74 ± 1.62 ng m−3, 4.32 ± 8.36 pg m−3 and 60.2 ± 131.4 pg m−3, respectively, during haze days. Potential source contribution function (PSCF) analysis suggested that the atmospheric mercury pollution during haze days was caused primarily by local mercury emissions, instead of via long-range mercury transport. In addition, the disadvantageous diffussion during haze days will also enhance the level of atmospheric mercury. Compared to the GEM and RGM, change in PBM was more sensitive to the haze pollution. The mean PBM concentration during haze days was 2.5 times that during non-haze days due to elevated concentrations of particulate matter. A remarkable seasonal trend in PBM was observed with concentration decreasing in the following order in response to the frequency of haze days: autumn, winter, spring, summer. A distinct diurnal relationship was found between GEM and RGM during haze days, with the peak values of RGM coinciding with the decline in GEM. Using HgOH as an intermediate product during GEM oxidation, our results suggest that NO2 aggregation with HgOH could explain the enhanced production of RGM during the daytime in haze days. Increasing level of NOx will potentially accelerate the oxidation of GEM despite the decrease of solar radiation.


2010 ◽  
Vol 7 (6) ◽  
pp. 537 ◽  
Author(s):  
Anne L. Soerensen ◽  
Henrik Skov ◽  
Matthew S. Johnson ◽  
Marianne Glasius

Environmental context Mercury is a neurotoxin that bioaccumulates in the aquatic food web. Atmospheric emissions from urban areas close to the coast could cause increased local mercury deposition to the ocean. Our study adds important new data to the current limited knowledge on atmospheric mercury emissions and dynamics in coastal urban areas. Abstract Approximately 50% of primary atmospheric mercury emissions are anthropogenic, resulting from e.g. emission hotspots in urban areas. Emissions from urban areas close to the coast are of interest because they could increase deposition loads to nearby coastal waters as well as contribute to long range transport of mercury. We present results from measurements of gaseous elemental mercury (GEM) and reactive gaseous mercury (RGM) in 15 coastal cities and their surrounding marine boundary layer (MBL). An increase of 15–90% in GEM concentration in coastal urban areas was observed compared with the remote MBL. Strong RGM enhancements were only found in two cities. In urban areas with statistically significant GEM/CO enhancement ratios, slopes between 0.0020 and 0.0087 ng m–3 ppb–1 were observed, which is consistent with other observations of anthropogenic enhancement. The emission ratios were used to estimate GEM emissions from the areas. A closer examination of data from Sydney (Australia), the coast of Chile, and Valparaiso region (Chile) in the southern hemisphere, is presented.


2011 ◽  
Vol 11 (11) ◽  
pp. 30053-30089 ◽  
Author(s):  
X. W. Fu ◽  
X. Feng ◽  
P. Liang ◽  
H. Zhang ◽  
J. Ji ◽  
...  

Abstract. Measurements of speciated atmospheric mercury were conducted at a remote mountain-top station (WLG) at the edge of northeastern part of the Qinghai-Xizang Plateau, western China. Mean concentrations of total gaseous mercury (TGM), particulate mercury (PHg), and reactive gaseous mercury (RGM) during the whole sampling campaign were 1.98 ± 0.98 ng m−3, 19.4 ± 18.1 pg m−3, and 7.4 ± 4.8 pg m−3, respectively. Levels of speciated Hg at WLG were slightly higher than those reported from remote areas of North America and Europe. Both regional emissions and long-rang transport played a remarkable role in the distribution of TGM and PHg in ambient air at WLG, whereas RGM showed major links to the regional sources, likely as well as the in-situ productions by photochemical processes. Regional sources for speciated Hg were mostly located to the east of WLG, which is the most developed areas of Qinghai province and accounted for most of the province's anthropogenic Hg emissions. Potential source contribution function (PSCF) results showed a strong impact of long-range transport from eastern Gansu, western Ningxia and Shanxi Province, with good accordance with locations of urban areas and industrial centers. Moreover, we found that northern India was also an important source region of WLG during the sampling campaign, and this is the first time of direct evidence of long-range transport of atmospheric Hg from India to northeastern Tibetan Plateau. Seasonal and diurnal variations of TGM were in contrast with most of the previous studies in China, with relatively higher levels in warm seasons and night, respectively. The temporal trend of TGM also highlighted the impact of long-range transport on the distribution of TGM in ambient air at WLG.


2013 ◽  
Vol 125 ◽  
pp. 69-74 ◽  
Author(s):  
L. Fantozzi ◽  
R. Ferrara ◽  
F. Dini ◽  
L. Tamburello ◽  
N. Pirrone ◽  
...  

2003 ◽  
Vol 43 (3) ◽  
pp. 339-351 ◽  
Author(s):  
Sexauer M. Gustin ◽  
M. Coolbaugh ◽  
M. Engle ◽  
B. Fitzgerald ◽  
R. Keislar ◽  
...  

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Long Chen ◽  
Sai Liang ◽  
Maodian Liu ◽  
Yujun Yi ◽  
Zhifu Mi ◽  
...  

Sensors ◽  
2020 ◽  
Vol 20 (2) ◽  
pp. 387
Author(s):  
Linghui Meng ◽  
Charles T. Driscoll ◽  
Mario Montesdeoca ◽  
Huiting Mao

In order to obtain a better perspective of the impacts of brownfields on the land–atmosphere exchange of mercury in urban areas, total gaseous mercury (TGM) was measured at two heights (1.8 m and 42.7 m) prior to 2011–2012 and after 2015–2016 for the remediation of a brownfield and installation of a parking lot adjacent to the Syracuse Center of Excellence in Syracuse, NY, USA. Prior to brownfield remediation, the annual average TGM concentrations were 1.6 ± 0.6 and 1.4 ± 0.4 ng · m − 3 at the ground and upper heights, respectively. After brownfield remediation, the annual average TGM concentrations decreased by 32% and 22% at the ground and the upper height, respectively. Mercury soil flux measurements during summer after remediation showed net TGM deposition of 1.7 ng · m − 2 · day − 1 suggesting that the site transitioned from a mercury source to a net mercury sink. Measurements from the Atmospheric Mercury Network (AMNet) indicate that there was no regional decrease in TGM concentrations during the study period. This study demonstrates that evasion from mercury-contaminated soil significantly increased local TGM concentrations, which was subsequently mitigated after soil restoration. Considering the large number of brownfields, they may be an important source of mercury emissions source to local urban ecosystems and warrant future study at additional locations.


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