scholarly journals In situ measurements of speciated atmospheric mercury and the identification of source regions in the Mexico City Metropolitan Area

2009 ◽  
Vol 9 (1) ◽  
pp. 207-220 ◽  
Author(s):  
A. P. Rutter ◽  
D. C. Snyder ◽  
E. A. Stone ◽  
J. J. Schauer ◽  
R. Gonzalez-Abraham ◽  
...  

Abstract. In order to expand the currently limited understanding of atmospheric mercury source-receptor relationships in the Mexico City Metropolitan Area, real time measurements of atmospheric mercury were made at a downtown urban site, and a rural site on the outskirts of Mexico City, during March 2006. Numerous short-lived increases in particulate mercury (PHg) and reactive gaseous mercury (RGM) concentrations were observed at the urban site during the 17 day study, and less frequent increases in gaseous elemental mercury (GEM) concentrations were measured at both the urban and rural sites. The episodic increases observed were attributed to plume impacts from industrial point source emissions in and around Mexico City. Average concentrations and standard deviations measured during the study were as follows: i) urban site; PHg=187±300 pg m−3, RGM=62±64 pg m−3, GEM=7.2±4.8 ng m−3, and; ii) rural site; GEM=5.0±2.8 ng m−3. Several source regions of atmospheric mercury to the urban and rural sites were determined using Concentration Field Analysis, in which atmospheric mercury measurements were combined with back trajectory data to determine source regions. Only some source regions correlated to mercury emission sources listed in the Federal Pollutant Release and Transfer Register, leaving the rest unaccounted for. Contributions of anthropogenic mercury point sources in and around Mexico City to concentration averages measured at the urban site during the study were estimated to be: 93±3% of reactive mercury (PHg and RGM), and; 81±0.4% of GEM. Point source contributions to GEM measured at the rural site were 72±1%. GEM and reactive mercury (PHg+RGM) were not found to correlate with biomass burning at either of the measurement sites.

2008 ◽  
Vol 8 (4) ◽  
pp. 13125-13157
Author(s):  
A. P. Rutter ◽  
D. C. Snyder ◽  
E. A. Stone ◽  
J. J. Schauer ◽  
R. Gonzalez-Abraham ◽  
...  

Abstract. In order to expand the currently limited understanding of atmospheric mercury source-receptor relationships in the Mexico City Metropolitan Area, real time measurements of atmospheric mercury were made at a downtown urban site, and a rural site on the outskirts of Mexico City, during March, 2006. Numerous short-lived increases in particulate mercury (PHg) and reactive gaseous mercury (RGM) concentrations were observed at the urban site during the 17 day study, and less frequent increases in gaseous elemental mercury (GEM) concentrations were measured at both the urban and rural sites. The episodic increases observed were attributed to plume impacts from industrial point source emissions in and around Mexico City. Average concentrations and standard deviations measured during the study were as follows: i) Urban site: PHg=187±300 pg m−3, RGM=62±64 pg m−3, GEM=7.2±4.8 ng m−3. ii) Rural site: GEM=5.0±2.8 ng m−3. Several source regions of atmospheric mercury to the urban and rural sites were determined using Concentration Field Analysis, in which atmospheric mercury measurements were combined with back trajectory data to determine source regions. Only some source regions correlated to mercury emission sources listed in the Federal Pollutant Release and Transfer Register, leaving the rest unaccounted for. Contributions of anthropogenic mercury point sources in and around Mexico City to concentration averages measured at the urban site during the study were estimated to be: 93±3% of reactive mercury (PHg and RGM), and; 81±0.4% of GEM. Point source contributions to GEM measured at the rural site were 72±1%. GEM and reactive mercury (PHg and RGM) were not found to correlate with biomass burning at either of the measurement sites.


2016 ◽  
Author(s):  
Xuewu Fu ◽  
Yang Xu ◽  
Xiaofang Lang ◽  
Jun Zhu ◽  
Hui Zhang ◽  
...  

Abstract. Mercury (Hg) concentrations and deposition fluxes in precipitation and litterfall were measured at multiple sites (six rural sites and an urban site) across a broad geographic area in China. The annual deposition fluxes of Hg in precipitation at rural sites and an urban site were 2.0 to 7.2 µg m−2 yr−1 and 12.6 ± 6.5 µg m−2 yr−1, respectively. Wet deposition fluxes of Hg at rural sites showed a clear regional difference with elevated deposition fluxes in the subtropical zone, followed by the temporal zone and arid/semi-arid zone. Precipitation depth is the primary influencing factor causing the variation of wet deposition. Hg fluxes through litterfall ranged from 22.8 to 62.8 µg m−2 yr−1, higher than the wet deposition by a factor of 3.9 to 8.7 fluxes and representing approximately 75 % of the total Hg deposition at the forest sites in China. This suggests that uptake of atmospheric Hg by foliage is the dominant pathway to remove atmospheric mercury in forest ecosystems in China. Wet deposition fluxes of Hg at rural sites of China were generally lower compared to those in North America and Europe, possibly due to a combination of lower precipitation depth, lower GOM concentrations in the troposphere and the generally lower cloud base heights at most sites that washout a smaller amount of GOM and PBM during precipitation events.


PLoS Medicine ◽  
2021 ◽  
Vol 18 (9) ◽  
pp. e1003681
Author(s):  
Bich-Tram Huynh ◽  
Elsa Kermorvant-Duchemin ◽  
Rattanak Chheang ◽  
Frederique Randrianirina ◽  
Abdoulaye Seck ◽  
...  

Background Severe bacterial infections (SBIs) are a leading cause of neonatal deaths in low- and middle-income countries (LMICs). However, most data came from hospitals, which do not include neonates who did not seek care or were treated outside the hospital. Studies from the community are scarce, and few among those available were conducted with high-quality microbiological techniques. The burden of SBI at the community level is therefore largely unknown. We aimed here to describe the incidence, etiology, risk factors, and antibiotic resistance profiles of community-acquired neonatal SBI in 3 LMICs. Methods and findings The BIRDY study is a prospective multicentric community-based mother and child cohort study and was conducted in both urban and rural areas in Madagascar (2012 to 2018), Cambodia (2014 to 2018), and Senegal (2014 to 2018). All pregnant women within a geographically defined population were identified and enrolled. Their neonates were actively followed from birth to 28 days to document all episodes of SBI. A total of 3,858 pregnant women (2,273 (58.9%) in Madagascar, 814 (21.1%) in Cambodia, and 771 (20.0%) in Senegal) were enrolled in the study, and, of these, 31.2% were primigravidae. Women enrolled in the urban sites represented 39.6% (900/2,273), 45.5% (370/814), and 61.9% (477/771), and those enrolled in the rural sites represented 60.4% (1,373/2,273), 54.5% (444/814), and 38.1% (294/771) of the total in Madagascar, Cambodia, and Senegal, respectively. Among the 3,688 recruited newborns, 49.6% were male and 8.7% were low birth weight (LBW). The incidence of possible severe bacterial infection (pSBI; clinical diagnosis based on WHO guidelines of the Integrated Management of Childhood Illness) was 196.3 [95% confidence interval (CI) 176.5 to 218.2], 110.1 [88.3 to 137.3], and 78.3 [59.5 to 103] per 1,000 live births in Madagascar, Cambodia, and Senegal, respectively. The incidence of pSBI differed between urban and rural sites in all study countries. In Madagascar, we estimated an incidence of 161.0 pSBI per 1,000 live births [133.5 to 194] in the urban site and 219.0 [192.6 to 249.1] pSBI per 1,000 live births in the rural site (p = 0.008). In Cambodia, estimated incidences were 141.1 [105.4 to 189.0] and 85.3 [61.0 to 119.4] pSBI per 1,000 live births in urban and rural sites, respectively (p = 0.025), while in Senegal, we estimated 103.6 [76.0 to 141.2] pSBI and 41.5 [23.0 to 75.0] pSBI per 1,000 live births in urban and rural sites, respectively (p = 0.006). The incidences of culture-confirmed SBI were 15.2 [10.6 to 21.8], 6.5 [2.7 to 15.6], and 10.2 [4.8 to 21.3] per 1,000 live births in Madagascar, Cambodia, and Senegal, respectively, with no difference between urban and rural sites in each country. The great majority of early-onset infections occurred during the first 3 days of life (72.7%). The 3 main pathogens isolated were Klebsiella spp. (11/45, 24.4%), Escherichia coli (10/45, 22.2%), and Staphylococcus spp. (11/45, 24.4%). Among the 13 gram-positive isolates, 5 were resistant to gentamicin, and, among the 29 gram-negative isolates, 13 were resistant to gentamicin, with only 1 E. coli out of 10 sensitive to ampicillin. Almost one-third of the isolates were resistant to both first-line drugs recommended for the management of neonatal sepsis (ampicillin and gentamicin). Overall, 38 deaths occurred among neonates with SBI (possible and culture-confirmed SBI together). LBW and foul-smelling amniotic fluid at delivery were common risk factors for early pSBI in all 3 countries. A main limitation of the study was the lack of samples from a significant proportion of infants with pBSI including 35 neonatal deaths. Without these samples, bacterial infection and resistance profiles could not be confirmed. Conclusions In this study, we observed a high incidence of neonatal SBI, particularly in the first 3 days of life, in the community of 3 LMICs. The current treatment for the management of neonatal infection is hindered by antimicrobial resistance. Our findings suggest that microbiological diagnosis of SBI remains a challenge in these settings and support more research on causes of neonatal death and the implementation of early interventions (e.g., follow-up of at-risk newborns during the first days of life) to decrease the burden of neonatal SBI and associated mortality and help achieve Sustainable Development Goal 3.


2012 ◽  
Vol 12 (1) ◽  
pp. 2131-2166 ◽  
Author(s):  
T. Holloway ◽  
C. Voigt ◽  
J. Morton ◽  
S. N. Spak ◽  
A. P. Rutter ◽  
...  

Abstract. Quantitative analysis of three atmospheric mercury species – gaseous elemental mercury (Hg0), reactive gaseous mercury (RGHg) and particulate mercury (PHg) – has been limited to date by lack of ambient measurement data as well as by uncertainties in numerical models and emission inventories. This study employs the Community Multiscale Air Quality Model version 4.6 with mercury chemistry (CMAQ-Hg), to examine how local emissions, meteorology, atmospheric chemistry, and deposition affect mercury concentration and deposition the Great Lakes Region (GLR), and two sites in Wisconsin in particular: the rural Devil's Lake site and the urban Milwaukee site. Ambient mercury exhibits significant biases at both sites. Hg0 is too low in CMAQ-Hg, with the model showing a 6% low bias at the rural site and 36% low bias at the urban site. Reactive mercury (RHg = RGHg + PHg) is over-predicted by the model, with annual average biases >250%. Performance metrics for RHg are much worse than for mercury wet deposition, ozone (O3), nitrogen dioxide (NO2), or sulfur dioxide (SO2). Sensitivity simulations to isolate background inflow from regional emissions suggests that oxidation of imported Hg0 dominates model estimates of RHg at the rural study site (91% of base case value), and contributes 55% to the RHg at the urban site (local emissions contribute 45%). Limited evidence on the lifetime of RHg transported to the rural site suggests that modeled dry deposition rates are too high, possibly compensating for the erroneously high RHg values.


2020 ◽  
Vol 20 (3) ◽  
pp. 1233-1254 ◽  
Author(s):  
Marco Paglione ◽  
Stefania Gilardoni ◽  
Matteo Rinaldi ◽  
Stefano Decesari ◽  
Nicola Zanca ◽  
...  

Abstract. The Po Valley (Italy) is a well-known air quality hotspot characterized by particulate matter (PM) levels well above the limit set by the European Air Quality Directive and by the World Health Organization, especially during the colder season. In the framework of Emilia-Romagna regional project “Supersito”, the southern Po Valley submicron aerosol chemical composition was characterized by means of high-resolution aerosol mass spectroscopy (HR-AMS) with the specific aim of organic aerosol (OA) characterization and source apportionment. Eight intensive observation periods (IOPs) were carried out over 4 years (from 2011 to 2014) at two different sites (Bologna, BO, urban background, and San Pietro Capofiume, SPC, rural background), to characterize the spatial variability and seasonality of the OA sources, with a special focus on the cold season. On the multi-year basis of the study, the AMS observations show that OA accounts for averages of 45±8 % (ranging from 33 % to 58 %) and 46±7 % (ranging from 36 % to 50 %) of the total non-refractory submicron particle mass (PM1-NR) at the urban and rural sites, respectively. Primary organic aerosol (POA) comprises biomass burning (23±13 % of OA) and fossil fuel (12±7 %) contributions with a marked seasonality in concentration. As expected, the biomass burning contribution to POA is more significant at the rural site (urban / rural concentration ratio of 0.67), but it is also an important source of POA at the urban site during the cold season, with contributions ranging from 14 % to 38 % of the total OA mass. Secondary organic aerosol (SOA) contributes to OA mass to a much larger extent than POA at both sites throughout the year (69±16 % and 83±16 % at the urban and rural sites, respectively), with important implications for public health. Within the secondary fraction of OA, the measurements highlight the importance of biomass burning aging products during the cold season, even at the urban background site. This biomass burning SOA fraction represents 14 %–44 % of the total OA mass in the cold season, indicating that in this region a major contribution of combustion sources to PM mass is mediated by environmental conditions and atmospheric reactivity. Among the environmental factors controlling the formation of SOA in the Po Valley, the availability of liquid water in the aerosol was shown to play a key role in the cold season. We estimate that the organic fraction originating from aqueous reactions of biomass burning products (“bb-aqSOA”) represents 21 % (14 %–28 %) and 25 % (14 %–35 %) of the total OA mass and 44 % (32 %–56 %) and 61 % (21 %–100 %) of the SOA mass at the urban and rural sites, respectively.


2012 ◽  
Vol 12 (15) ◽  
pp. 7117-7133 ◽  
Author(s):  
T. Holloway ◽  
C. Voigt ◽  
J. Morton ◽  
S. N. Spak ◽  
A. P. Rutter ◽  
...  

Abstract. Quantitative analysis of three atmospheric mercury species – gaseous elemental mercury (Hg0), reactive gaseous mercury (RGHg) and particulate mercury (PHg) – has been limited to date by lack of ambient measurement data as well as by uncertainties in numerical models and emission inventories. This study employs the Community Multiscale Air Quality Model version 4.6 with mercury chemistry (CMAQ-Hg), to examine how local emissions, meteorology, atmospheric chemistry, and deposition affect mercury concentration and deposition the Great Lakes Region (GLR), and two sites in Wisconsin in particular: the rural Devil's Lake site and the urban Milwaukee site. Ambient mercury exhibits significant biases at both sites. Hg0 is too low in CMAQ-Hg, with the model showing a 6% low bias at the rural site and 36% low bias at the urban site. Reactive mercury (RHg = RGHg + PHg) is over-predicted by the model, with annual average biases >250%. Performance metrics for RHg are much worse than for mercury wet deposition, ozone (O3), nitrogen dioxide (NO2), or sulfur dioxide (SO2). Sensitivity simulations to isolate background inflow from regional emissions suggests that oxidation of imported Hg0 dominates model estimates of RHg at the rural study site (91% of base case value), and contributes 55% to the RHg at the urban site (local emissions contribute 45%).


2021 ◽  
Author(s):  
Gloria Dada Chechet ◽  
Jacob KP Kwaga ◽  
Joseph Yahaya ◽  
Annette MacLeod ◽  
Walt E Adamson

Nigeria is the most populated country in Africa with an estimated ~213 million inhabitants. As of November 2021 there have been three waves of SARS-CoV-2 infection in Nigeria but there has been only one seroprevalence survey conducted to assess the proportion of a population that have been infected, which was performed in December 2020 after the first wave of infection. To provide an update on seroprevalence in Nigeria, we conducted survey at one urban site (n=400) and one rural site (n=402) in Kaduna State, Nigeria during October and November 2021 following the third wave of infection. Seroprevalence for the urban and rural sites was 42.5% and 53.5% respectively (mean 48.0%). Symptoms associated with seropositivity were identified for each site. The overall seroprevalence among unvaccinated individuals was 45.4%. The data indicates an infection rate in Kaduna State at least 387 times greater than that derived from cases confirmed by PCR. Extrapolating to the whole of Nigeria, it would suggest there has been at least 96.7 million infections (compared to 206,138 confirmed cases at the time of surveillance). The work presented here will inform public health policy and deployment strategies for testing, treatment, and vaccination in Nigeria, and provide a baseline for SARS-CoV-2 seroprevalence in Nigeria immediately prior to the spread of the Omicron variant.


2020 ◽  
Author(s):  
Annkatrin Burgstall ◽  
Ana Casanueva ◽  
Elke Hertig ◽  
Erich Fischer ◽  
Reto Knutti ◽  
...  

<p>An increasing fraction of people living in urban areas and the expected increase in long lasting heat waves highlight the important role of urban climates in terms of future climate change impacts, especially with relation to the heat-health sector. Due to the urban heat island (UHI) effect and its (generally) increased intensity particularly during nighttime, people living in urban areas happen to be more affected by heat-related discomfort and health risks than those in non-urban regions. In this contribution, temperatures of both rural and urban sites (station couples) in Switzerland and Southern Germany are analyzed, using (i) observed as well as (ii) bias-corrected and downscaled climate model data for daily minimum (tmin) and daily maximum temperature (tmax) to account for the UHI in future climates. As meteorological data are often restricted to locations of long-term measurements at rural sites only, they need to be transferred to urban sites first. For this purpose, the well-established quantile mapping technique (QM) is tested in a two-step manner. The resulting products are urban time series at daily resolution for tmin and tmax. By analyzing the temperature differences of the observed climate at rural sites and their respective urban counterparts and by assuming a stationary relationship between both, we can represent the UHI in future climates, which is quantified in terms of heat indices based on tmin and tmax (tropical nights, summer days, hot days).</p><p>The QM performance is evaluated using long-term weather station data of a Zurich station couple in a comprehensive cross-validation framework. Results reveal a promising performance in the present-day climate, given very low biases in the validation.</p><p>Applying the proposed method to the employed station couples, projections indicate distinct urban-rural temperature differences (UHI) during nighttime (considering the frequency of tropical nights based on tmin) compared to weak differences during the day (considering the frequency of summer days and hot days based on tmax). Moreover, scenarios suggest the frequency of all indices to dramatically rise at the urban site by the end of the century under a strong emission scenario (RCP8.5): compared to the rural site, the number of tropical nights almost doubles while the number of summer days reveals about 15% more days at the urban site when focusing on the station couple in Zurich and the late scenario period. The lack of nighttime relief, indicated by tmin not falling below 20°C (i.e. a tropical night), is especially problematic in terms of human health and makes the study of the urban climate in general and the UHI effect in particular indispensable.</p>


2017 ◽  
Vol 74 (9) ◽  
pp. 2937-2947 ◽  
Author(s):  
Irene Cheng ◽  
Leiming Zhang ◽  
Mark Castro ◽  
Huiting Mao

Abstract To investigate the effectiveness of emission reductions on the concentrations of gaseous elemental mercury (GEM), gaseous oxidized mercury (GOM), and particulate-bound mercury (PBM) at a rural site in Maryland (MD08), long-term (2005–14) measurements of speciated atmospheric mercury were analyzed using concentration-weighted trajectory (CWT) analysis. CWT results suggested that the number of major source regions contributing to GEM, GOM, and reactive mercury (RM = GOM + PBM) over the eastern United States and southeastern Canada declined over time. Across much of these regions, source contributions in 2011–14 decreased by up to 20% for GEM, by greater than 60% for GOM, and by 20%–60% for PBM compared to 2006–08, largely because of the decreases in power-plant mercury emissions since 2009. Changes in the spatial distribution of the source regions were also observed over time. Increases in source contributions of GEM after 2011 over the northeastern United States and southeastern Canada were predominantly from emission increases in metal and steel production and forest fires. Source contribution increases in PBM were more widespread, which can be attributed potentially to mercury transformation processes in the air or wood combustion rather than industrial sources.


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