Organochlorine pesticides in the ambient air of Chiapas, Mexico

Organochlorine (OC) pesticides were measured in the ambient air of Chiapas, Mexico during 2000-2001. Concentrations of some OC pesticides (DDTs, chlordanes, toxaphene) were elevated compared with levels in the Great Lakes region, while those of other pesticides were not (hexachlorocyclohexanes, dieldrin). While this suggests southern Mexico as a source region for the former group of chemicals, comparably high levels have also been reported in parts of the southern United States, where their suspected sources are soil emissions (DDTs, toxaphene) and termiticide usage (chlordane). Ratios of p,p'-DDT/p,p'-DDE and trans-chlordane/cis-chlordane/trans-nonachlor (TC/CC/TN) in Chiapas suggest a mixture of fresh and weathered sources, while congener profiles of toxaphene suggest emission of old residues from soils. This is supported by air parcel back trajectory analysis, which indicated that air masses over Chiapas at the time of sampling had previously passed over areas of continuing or recent use of some OC pesticides as well as areas of past use.     

Impact of emissions controls on ambient carbonyls during the Asia-Pacific Economic Cooperation summit in Beijing,China

Environmental Science and Pollution Research - Beijing and its surrounding areas implemented a series of stringent measures to ensure good air quality during the Asia-Pacific Economic Cooperation...     

Polychlorinated biphenyls (PCBs) residues in milk from an agroindustrial zone of Tuxpan, Veracruz, Mexico

The coasts of the Gulf of Mexico are zones exposed to the exploration and exploitation of petroleum sources, and the products generated in agricultural zones may become contaminated by persistent organic pollutants (POPs). The objective of the present study was to evaluate the presence of polychlorinated biphenyl compounds (PCBs) in milk from dairy production units near sources of environmental pollutants. It was confirmed that the seven congeners of nondioxin-like PCBs (NDL-PCBs) are present in milk where compounds PCB101, PCB118, PCB153 and PCB180 appear in 100% of the samples analyzed, the rank of concentration for the sum of the seven congeners fluctuating between 2.6 and 26 ng g⁻¹ with a median of 6 ng g⁻¹. None of the samples surpassed the provisional value established by the EU of 40 ng g⁻¹ of milk fat for the sum of the seven congeners, indicator that was not affected by the season of the year (p < 0.05), whose median of 8.6 ng g⁻¹ and 6.3 ng g⁻¹ for rain and drought respectively. The concentrations of NDL-PCBs found in milk do not represent a problem for human health; however, they alert the existence of spontaneously generated, uncontrolled sources that may represent a potential danger for human and animal health.     

Formaldehyde levels in air and wet precipitation at Mexico City, Mexico

Formaldehyde concentrations in ambient air and in rain water were measured at the University of Mexico, Mexico City. Air samples were taken twice a day, from 9:00 to 13:00 h and from 13:00 to 16:00 h local time from July to December 1985. Rain water was collected on daily bases from July to October, i.e. during the rainy season. The ambient air mean value was 24.4 x 10(-3) ppmv for morning hours, while the afternoon mean value was 18.5 x 10(-3) ppmv. The formaldehyde concentration in wet precipitation ranged from 0.10 to 0.80 mg liter(-1) (3.3 to 26.6 micromoles liter(-1)) 0.41 mg liter(-1) (13.7 microoles liter(-1)). A comparison of the results of this study with some measurements made at remote maritime sites, rural and urban areas, indicated that the formaldehyde levels in the atmosphere and rain water of Mexico City are among the highest reported in the literature, including the data reported by Grosjean (1982) for Los Angeles, California, during severe photochemical pollution conditions.     

Diurnal and seasonal variations of carbonyls and their effect on ozone concentrations in the atmosphere of Monterrey,Mexico

Few studies have been made regarding carbonyl concentrations in Monterrey, México. The Monterrey Metropolitan Area (MMA) has the third largest population in the country and has increasing pollution issues. The concentrations of 10 aldehydes and two ketones were measured in the MMA, in the spring and fall of 2011 and 2012. Formaldehyde (16–42 ppbv) was the most abundant carbonyl, followed by acetaldehyde (5–15 ppbv) and acetone (7–15 ppbv). The concentrations showed marked diurnal trends with maximum values between 10:00 a.m. and 2:00 p.m., when photochemical activity is intense. Thus, secondary production of carbonyls is statistically significant in the city. Biogenic production of several carbonyls, such as 2-butanone, was supported by their mid correlation with solar radiation and low correlation with propionaldehyde, which is mainly emitted by anthropogenic sources. The seasonal variability of the concentrations was observed in the first three samplings, with the highest levels reached in the fall. The rainy conditions during the fourth sampling did not allow comparison. Carbonyl–NOx–O₃ analysis was made. Results indicated a carbonyl-sensitive atmosphere, especially during the midday samplings of 10:00 a. m. to 2:00 p.m. and 2:00 p.m. and 6:00 p.m. because of the intense solar radiation during these periods.

Implications:?Monitoring of carbonyls in Monterrey, Mexico, was performed to quantify the pollutant concentration in the city’s atmosphere. Although primary emission is significantly important, the secondary production of the pollutants, along with ozone production being carbonyl sensitive, indicates that air pollution controls must address the direct sources and the precursors of the pollutants to achieve air quality.     

Evaluation of human exposure to ambient PM10 in the metropolitan area of Mexico City using a GIS-based methodology.

The main goal of this study was to evaluate the magnitude of outdoor exposure to fine particulate matter (PM10) potentially experienced by the population of metropolitan Mexico City. With the use of a geographic information system (GIS), spatially resolved PM10 distributions were generated and linked to the local population. The PM10 concentration exceeded the 24-hr air quality standard of 150 microg/m3 on 16% of the days, and the annual air quality standard of 50 microg/m3 was exceeded by almost twice its value in some places. The basic methodology described in this paper integrates spatial demographic and air quality databases, allowing the evaluation of various air pollution reduction scenarios. Achieving the annual air quality standard would represent a reduction in the annual arithmetic average concentration of 14 microg/m3 for the typical inhabitant. Human exposure to particulate matter (PM) has been associated with mortality and morbidity in Mexico City; reducing the concentration levels of this pollutant would represent a reduction in mortality and morbidity and the associated cost of such impacts. This methodology is critical to assessing the potential benefits of the current initiative to improve air quality implemented by the Environmental Metropolitan Commission of Mexico City.     

PBDEs, PCBs, and DDE in eggs and their impacts on aplomado falcons (Falco femoralis) from Chihuahua and Veracruz, Mexico

Eggs from aplomado falcons (Falco femoralis septentrionalis) nesting in Chihuahua and Veracruz, Mexico, were analyzed for organochlorine pesticides, PCBs, and PBDEs. p,p′-DDE was the only organochlorine found in all eggs at concentrations ranging from 0.13 to 7.85 μg/g wet weight. PCBs ranged from 0.04 to 2.80 μg/g wet weight and PBDEs from 62 to 798 ng/g lipid weight. DDE concentrations in eggs were not significantly different among regions; however, PCBs were significantly greater (P = 0.015) in Tinaja Verde, Chihuahua than in the other three regions. Also, PBDEs were significantly higher (P < 0.0001) in eggs from Veracruz than in those from Chihuahua. DDE concentrations in eggs were much lower than those associated with eggshell thinning. PBDEs and PCBs were lower than those reported in raptors from industrialized countries. Overall, contaminant concentrations observed suggest no likely impact on hatching success. The PBDE concentrations are among the first to be reported in raptor species in Mexico.     

Fuel reformulation in the Metropolitan Area of Mexico City

Two models frequently used to simulate the dispersion of pollutants in the atmosphere have been compared. This is necessary because only a well-tested and well-calibrated simulation model can be a good representation of the reality of the dispersion of pollutants. The models evaluated (HYSPLIT_4 with its four variants and MEDIA) were run using as input parameters the same meteorological dataset (for 23-26 October 1994) from the French model ARPEGE. The following statistical criteria were compared: the space and time evolution of the pollutant cloud; the variation of statistical parameters in time and space; and the differences between the simulated and measured values of concentration in time for six different stations. The results emphasise the characteristics of the two models and their abilities in the framework of the air quality monitoring.     

Carbon Monoxide Trend,Meteorology, and Three-Way Catalysts in Mexico City

ABSTRACT

From the analysis of data of the Inspection/Maintenance (I/M) program, and of the long-term trend of ambient CO concentrations in Mexico City, it is inferred that three-way catalysts (TWCs) have a 45% efficiency, well below the expected 90% value. The most probable causes are sulfur poisoning, lead contamination, and ceramic breakage due to bumps and potholes on the streets. Also, we have found a ratio between the average daily peak value of atmospheric CO and gasoline consumption: (11 ± 1) ppbCO/MLm (million liters of gasoline per month) in 1988 decaying to (10 ±1) in 1991 for Mexico City before the introduction of TWCs. In addition, we found a correlation between the monthly averages of CO daily peak and meteorological variables, explaining most of the seasonal changes using only the intensity of the inversion layer and surface wind speed.     

Temporal variations of atmospheric carbonyls in urban ambient air and street canyons of a Mountainous city in Southwest China

Carbonyl compounds in urban ambient air and street canyons were measured from December 2008 to August 2009 in a mountainous city in southwest China (Guiyang). The formaldehyde yield from the photo-oxidation of isoprene emitted by vegetation was estimated to be in the range of 0.63–3.62 μg m^?3 from May to August, which accounted for 28.8–33.4% of ambient formaldehyde. Based on the calculation of photolysis rates and rates of reaction with the OH radical, it was found that photolysis was the predominant sink for formaldehyde and acetone in both summer and winter. For acetaldehyde, photo-oxidation by OH radicals and photolysis were the major sinks in summer while photo-oxidation by OH radicals was the dominant sink in winter. Wet precipitation was found to be an important removal process for the atmospheric carbonyls. In the urban ambient air, the average concentrations of formaldehyde, acetaldehyde, acetone and all carbonyls were 4.8 ± 2.1, 5.7 ± 3.3, 5.1 ± 2.5, and 25.1 ± 9.2 μg m^?3 (n = 139), respectively. The average concentrations of these species in street canyons were 18.8 ± 6.5, 9.4 ± 3.2, 10.9 ± 2.1, and 64.1 ± 16.3 μg m^?3 (n = 62), respectively. The significantly higher carbonyl levels on weekdays (compared to weekends) highlight the contribution of vehicle emissions to carbonyls in the street canyons.     

Variation of Different Pollutants in the Atmosphere of Mexico City

The first regional warning system was developed by the New York-New Jersey Cooperative Committee on Air Pollution and was put into operation in 1964. In 1967, new criteria were adopted based on recommendations of a workshop sponsored by City College of New York at the request of State agencies. With the passage of time, it has been recognized that the criteria necessary to call an alert required updating and strengthening. In recognition of this, the Commission sponsored a workshop of government officials to evaluate the criteria and levels of the sulfur dioxide, carbon monoxide, and particulate parameters used in the system and to consider the addition of other parameters.     

Emission Characteristics of Mexico City Vehicles

The University of Denver remote sensor for automobile exhaust was set up for nine days at five locations in the Mexico City area. A total of 31,838 valid readings for CO and HC emissions were obtained. The emissions distribution was unlike any other we have observed in North America or Europe, in that the emissions for both CO and HC were vastly greater than seen elsewhere. The readings are discussed in terms of the fraction of CO and HC which would be measured by a tailpipe probe, and in terms of grams emitted per gallon of gasoline. The median CO emission was 3.8 percent, with half of the CO emissions coming from the 24 percent of the fleet with over 6.6 percent CO in the exhaust. The median HC emission was 1,100 parts per million measured as propane equivalent, while half the emissions come from twelve percent of the fleet with more than 4,000 ppm propane equivalent in the exhaust.     

Fine Particle Receptor Modeling in the Atmosphere of Mexico City

Abstract

Source apportionment analyses were carried out by means of receptor modeling techniques to determine the contribution of major fine particulate matter (PM_2.5) sources found at six sites in Mexico City. Thirty-six source profiles were determined within Mexico City to establish the fingerprints of particulate matter sources. Additionally, the profiles under the same source category were averaged using cluster analysis and the fingerprints of 10 sources were included. Before application of the chemical mass balance (CMB), several tests were carried out to determine the best combination of source profiles and species used for the fitting. CMB results showed significant spatial variations in source contributions among the six sites that are influenced by local soil types and land use. On average, 24-hr PM_2.5 concentrations were dominated by mobile source emissions (45%), followed by secondary inorganic aerosols (16%) and geological material (17%). Industrial emissions representing oil combustion and incineration contributed less than 5%, and their contribution was higher at the industrial areas of Tlalnepantla (11%) and Xalostoc (8%). Other sources such as cooking, biomass burning, and oil fuel combustion were identified at lower levels. A second receptor model (principal component analysis, [PCA]) was subsequently applied to three of the monitoring sites for comparison purposes. Although differences were obtained between source contributions, results evidence the advantages of the combined use of different receptor modeling techniques for source apportionment, given the complementary nature of their results. Further research is needed in this direction to reach a better agreement between the estimated source contributions to the particulate matter mass.     

Concentrations and distributions of carbonaceous species in ambient particles in Kaohsiung City,Taiwan

Concentrations and distributions of elemental carbon (EC) and organic carbon (OC) in particles were measured in Kaohsiung City, Taiwan. PM₁₀ and PM_2.5 samples were collected using a dichotomous sampler from November 1998 to April 1999 and were analyzed for carbonaceous species with an elemental analyzer. The concentrations of carbonaceous species in Kaohsiung City were comparable to those at other urban locations in the world. On average, carbonaceous species accounted for 21.2% of the PM_2.5 and 18.1% of the PM₁₀. It was found that organic carbon dominated the carbonaceous species and was 72.2 and 70.4% of total carbon (TC) for PM_2.5 and PM₁₀. The secondary organic carbon formed through the volatile organic compound gas-to-particle conversion was estimated from the minimum ratio between elemental and organic carbon obtained in this study, and was found to constitute 40.0 and 32.4% of the total organic carbon particle for PM_2.5 and PM₁₀ (or 6.6 and 4.5% of the total particle mass).     

Spatial differences in ambient coarse and fine particles in the Monterrey metropolitan area,Mexico: Implications for source contribution

The ambient air of the Monterrey Metropolitan Area (MMA) in Mexico frequently exhibits high levels of PM₁₀ and PM_2.5. However, no information exists on the chemical composition of coarse particles (PM_c = PM₁₀ – PM_2.5). A monitoring campaign was conducted during the summer of 2015, during which 24-hr average PM₁₀ and PM_2.5 samples were collected using high-volume filter-based instruments to chemically characterize the fine and coarse fractions of the PM. The collected samples were analyzed for anions (Cl^–, NO₃^–, SO₄^2–), cations (Na⁺, NH₄⁺, K⁺), organic carbon (OC), elemental carbon (EC), and 35 trace elements (Al to Pb). During the campaign, the average PM_2.5 concentrations did not showed significance differences among sampling sites, whereas the average PM_c concentrations did. In addition, the PM_c accounted for 75% to 90% of the PM₁₀ across the MMA. The average contribution of the main chemical species to the total mass indicated that geological material including Ca, Fe, Si, and Al (45%) and sulfates (11%) were the principal components of PM_c, whereas sulfates (54%) and organic matter (30%) were the principal components of PM_2.5. The OC-to-EC ratio for PM_c ranged from 4.4 to 13, whereas that for PM_2.5 ranged from 3.97 to 6.08. The estimated contribution of Secondary Organic Aerosol (SOA) to the total mass of organic aerosol in PM_2.5 was estimated to be around 70–80%; for PM_c, the contribution was lower (20–50%). The enrichment factors (EF) for most of the trace elements exhibited high values for PM_2.5 (EF: 10–1000) and low values for PM_c (EF: 1–10). Given the high contribution of crustal elements and the high values of EFs, PM_c is heavily influenced by soil resuspension and PM_2.5 by anthropogenic sources. Finally, the airborne particles found in the eastern region of the MMA were chemically distinguishable from those in its western region.

Implications: Concentration and chemical composition patterns of fine and coarse particles can vary significantly across the MMA. Public policy solutions have to be built based on these observations. There is clear evidence that the spatial variations in the MMA’s coarse fractions are influenced by clearly recognizable primary emission sources, while fine particles exhibit a homogeneous concentration field and a clear spatial pattern of increasing secondary contributions. Important reductions in the coarse fraction can come from primary particles’ emission controls; for fine particles, control of gaseous precursors—particularly sulfur-containing species and organic compounds—should be considered.     

Continuous determination of gaseous ammonia in the ambient atmosphere using fluorescence derivatization

A method for continuous determination of ambient ammonia levels employing o-phthalaldehyde fluorescence derivatization is described. A simplified Venturi scrubber and gas-liquid separator have been employed for reproducible measurements of ⩾ 0.1 ppb ambient ammonia with less than 2 min time resolution. The scrubbing efficiency of the ammonia gas collection system was determined to be 29 ± 1 %. During 4 d in August 1979 ambient ammonia levels at the Brookhaven National Laboratory site averaged about 1.5 ± 1.1 ppb during afternoon daylight hours.     

Measurements of formaldehyde and acetaldehyde in the atmosphere of Mexico City

Ambient levels of carbonyls were measured at the University of Mexico campus, Mexico City. Only formaldehyde and acetaldehyde were measured, since aldehydes with higher molecular weight were not detected. The most abundant aldehyde was formaldehyde, with an overall ratio CH3CHO/H2CO of 0.43. Maximum concentrations occurred for formaldehyde at 10:00 h while for acetaldehyde at 8:00 h. Comparing the concentration measured in this work with those in urban areas it was found that the formaldehyde and acetaldehyde levels in Mexico City are among the highest reported in the literature.     

Impact of wildfires on the air quality of Mexico City, 1992-1999

Wildfires in Mexico increased in 1998, compared to information for the last 6 years. The average number of wildfires in the Mexico City Metropolitan Area (MCMA) for this year (1998) were 58% (1916 events) more events than the 1992-1997 (average cases 1217 events). Mexico City affected area corresponds to 1.3% of the national affected area. The purpose of this paper is to evaluate the impact on the particles air quality due to the wildfire emissions at the MCMA and surrounding areas. Using the corresponding US EPA emission factors for wildfires, the tons of particulate matter, nitrogen oxides, carbon monoxide, and total hydrocarbons emitted by this source for the MCMA case were obtained. The calculated emissions during wildfires were correlated with the levels of particles present in the atmosphere. A comparison of the concentration levels of particles, both as PM10 as well as TSP, were made for the years 1992-1998, during wet and dry season, being March, April, and May the critical months due to the presence of wildfires. A good correlation is observed between particulate wildfire emissions and particulate air quality, being stronger for TSP. A clear impact on the particles air quality due to the increase of wildfires in 1998, is observed when this year is compared with 1997, presenting an increment of 200-300% for some monitoring stations.     

化学滴液电极对废水中Pb~(2+)测定的初步研究

利用自制的滴液电极,运用循环伏安和方波伏安法,对Pb~(2+)在水/甲基异丁基酮(MIBK)界面上通过双硫腙(HDz)促迁移的反应机制进行了研究.结果表明,该迁移过程为不可逆过程,Pb~(2+)的迁移峰电位为0.122 V,且当Pb~(2+)摩尔浓度为5.0×10~(-7)～4.0×10~(-5)mol/L时,峰电流和Pb~(2+)浓度呈线性相关关系;水相中常见的Na~+等金属离子浓度比Pb~(2+)浓度大百倍时,或水相中常见的Mg~(2+)、Ni~(2+)浓度与Pb~(2+)浓度相同时,对峰电流测定结果产生的干扰都较小(相对误差小于10.0%),但当水相中有Zn~(2+)、Cu~(2+)、Fe~(3+)存在时,即使其浓度都与Pb~(2+)浓度相同,也会对峰电流测定结果产生明显干扰(相对误差分别为-12.2%、-28.7%、-60.3%);以方波伏安法取代循环伏安法进行峰电流测定,以新型绿色溶剂室温离子液体(RTILs)取代四苯硼四丁基铵作为有机相电解质,能极大提高Pb~(2+)浓度测定的灵敏度.     

Partitioning of nitrate and ammonium between the gas and particulate phases during the 1997 IMADA-AVER study in Mexico City

The partitioning of nitrate and ammonium between the gas and particulate phases is studied combining available equilibrium models and measurements taken in Mexico City during the 1997 IMADA-AVER field campaign. Based on this analysis, there are no significant differences in model predictions, but some discrepancies exist between predictions and observations. The inclusion of crustal elements in the modeling framework improves agreement of model predictions for particulate nitrate against measurements by approximately 5%. Although some equilibrium aerosol models do not explicitly treat crustal elements, these species can be treated as equivalent concentrations of sodium. Atmospheric equilibrium models predict daily average PM_2.5 nitrate concentrations within 20% of the IMADA-AVER measurements at the MER site. Six-hour average PM_2.5 nitrate concentrations are predicted within 30–50% on average except for the afternoon sampling periods (12:00–18:00 h). Investigating the possible sources of these discrepancies, it appears that a dynamic instead of an equilibrium approach is more suitable in reproducing aerosol behavior during these afternoon periods. By applying the Multicomponent Aerosol Dynamic Model (MADM), model performance in predicting concentrations of particulate nitrate significantly improves during the afternoon periods.