Spatial concentration distributions of sulfur dioxide and nitrogen oxides in Patras, Greece, in a winter period

An economic and quick methodology for performing a preliminary spatial assessment of a city air quality with the purpose to identify locations and zones susceptible to high pollution levels is proposed. A Patras case-study is selected, regarding the air pollutants of sulfur dioxide (SO₂) and oxides of nitrogen (NO_x). A total number of 451 samples of short duration, of which 225 were randomly picked in morning rush hours and 226 within evening rush hours, were collected from 50 locations of the major Patras area during a year period, when peaks of primary air pollutants usually occur. Concentration measurements at prescribed locations used to statistically calculate spatial average concentrations approximating 1-h mean values with mean probable errors less than 25.9% for SO₂, NO and NO_x and less than 15.5% for NO₂. Then iso-concentration contour diagrams plotted indicate high pollution zones and possibly appropriate locations for continuous or random monitoring according to the European Community (EC) Directives. The 1-h mean concentrations were in good correlation to the corresponding traffic rates and useful relationships are given (0.54 ≤ r ≤ 0.63). In addition, comparisons with data available for other cities, as well as with the limit and guide values provided by the EC and the World Health Organization (WHO) were given. The present data could be useful for the design and optimization of a city network of stations for monitoring air quality, for environmental impact assessments, future reference and comparisons due to city development needs, as well as for validating dispersion models.     

Validation of a passive atmospheric deposition sampler for polybrominated diphenyl ethers

An atmospheric deposition sampler was validated with respect to polybrominated diphenyl ethers (PBDEs), a compound group that is widely used as flame retardants in many types of consumer products. The deposition sampler consists of an adsorption cartridge that is connected to a glass funnel. Extraction tests with spiked cartridges using soxhlet extraction with acetone revealed recoveries of >80% for all of the investigated PBDEs. Once adsorbed, PBDEs are stable, as proven by extractions of spiked cartridges that were stored outdoors and collected after different periods of time, up to 84 days. High recoveries indicate that degradation of adsorbed PBDEs does not play a role under realistic field conditions. Bulk deposition rates of PBDEs were determined in a field test with 3 replicates, and a possible breakthrough of target compounds was assessed in the field using a second adsorption cartridge in series. No breakthrough of target compounds could be observed within a sampling period of 61 days, and a bulk deposition rate of approximately 1 ng m(-2) day(-1) for the sum of all analysed PBDEs was measured. The highest deposition rates were measured for octa-brominated congeners, followed by BDEs 99, 183, 153, and 47. Overall, the sampler was successfully validated regarding the atmospheric deposition of PBDEs.     

Simultaneous determination of hydroxylamine and phenol using a nanostructure-based electrochemical sensor

The electrochemical oxidation of hydroxylamine on the surface of a carbon paste electrode modified with carbon nanotubes and 2,7-bis(ferrocenyl ethyl)fluoren-9-one is studied. The electrochemical response characteristics of the modified electrode toward hydroxylamine and phenol were investigated. The results showed an efficient catalytic activity of the electrode for the electro-oxidation of hydroxylamine, which leads to lowering its overpotential. The modified electrode exhibits an efficient electron-mediating behavior together with well-separated oxidation peaks for hydroxylamine and phenol. Also, the modified electrode was used for determination of hydroxylamine and phenol in some real samples.     

Seasonal trends of atmospheric nitrogen dioxide and sulfur dioxide over North Santa Clara, Cuba

Atmospheric nitrogen dioxide (NO₂) and sulfur dioxide (SO₂) levels were monitored simultaneously by means of Radiello passive samplers at six sites of Santa Clara city, Cuba, in the cold and the warm seasons in 2010. The dissolved ionic forms of NO₂ and SO₂ as nitrate and sulfite plus sulfate, respectively, were determined by means of ion chromatography. Analysis of NO₂ as nitrite was also performed by UV–Vis spectrophotometry. For NO₂, significant t tests show good agreement between the results of IC and UV–Vis methods. The NO₂ and SO₂ concentrations peaked in the cold season, while their minimum levels were experienced in the warm season. The pollutant levels do not exceed the maximum allowable limit of the Cuban Standard 39:1999, i.e., 40 μg/m³ and 50 μg/m³ for NO₂ and SO₂, respectively. The lowest pollutant concentrations obtained in the warm season can be attributed to an increase in their removal via precipitation (scavenging) while to the decreased traffic density and industrial emission during the summer holidays (e.g., July and August).     

Performances and application of a passive sampling method for the simultaneous determination of nitrogen dioxide and sulfur dioxide in ambient air

The performances and applicability of a diffusion tubesampler for the simultaneous measurements of NO₂ andSO₂ in ambient air were evaluated. SO₂ andNO₂are collected by the passive sampler using triethanolamine astrapping agent and are determined as sulphate and nitrite withion chromatography. The detection limit (2.3 g m^-3 ofNO₂ and 4.2 g m^-3 of SO₂ for two weekssampling) is adequate for the determination of concentrationsin urban and industrial areas. Precision of the method as RSDis in mean 5% for NO₂ and 12% for SO₂ at theconcentration levels in urban areas. Calibration of the methodwas performed in the field conditions by comparison between theresponses of sampler and the concentrations measured by thecontinuous monitors. High degree of linearity (correlationcoefficients > 0.8) is found between the passive sampler tubeand the continuous monitor data for both NO₂ and SO₂.To reduce the wind velocity influence on passive sampling ofdiffusion tubes, a protective shelter was tested in this study.The overall uncertainty of one measure for the optimised methodis estimated at 5 g m^-3 for NO₂ and 6g m^-3 for SO₂. Suitability of this passivesampling method for air pollution monitoring in urban areas wasdemonstrated by the results shown in this paper on a campaigncarried out in the French agglomeration.     

Development of a personal monitoring method for nitrogen dioxide and sulfur dioxide with Sep-Pak C18 cartridge sampling and ion chromatographic determination

Personal monitoring methods for the determination of hourly integrated concentrations of NO2 and SO2 in ambient air have been developed. Triethanolamine (TEA)-impregnated C18 Sep-Pak cartridges were used to collect NO2 and SO2 simultaneously. After sampling, NO2 and SO2 as their nitrite, nitrate, sulfite and sulfate analogues were stripped from the cartridges with a solution of 5% methanol in distilled, deionized water (DDW) and then determined by ion chromatography. Laboratory tests were conducted to evaluate the sampling rate, collection and recovery efficiencies, breakthrough volumes, absorption capacity, interference and sample stability on the cartridge during storage. NO2 and SO2 detection limits of 0.3 and 0.4 ppb respectively for 1 h samples were obtained. Recoveries for both NO2 and SO2 exceeded 85%.     

Simultaneous monitoring of atmospheric methane and speciated non-methane hydrocarbon concentrations using Peltier effect sub-ambient pre-concentration and gas chromatography

Sub-ambient trapping, used to pre-concentrate atmospheric samples for non-methane hydrocarbon (NMHC) analysis by gas chromatography, can also be used to measure ambient methane concentrations. Above a sample volume of 40 ml, a dynamic equilibrium is established between ambient and trapped methane allowing for simultaneous quantitative determinations of methane and NMHC. The temperature stability of the trap is critical for quantitative methane analysis and this can be achieved by Peltier effect cooling. Simultaneous measurements of methane and NMHC reduce the equipment required for field trips and can ease the interpretation and modelling of atmospheric data. The feasibility for deployment of the system in remote locations was demonstrated by running the apparatus virtually unattended for a 5-day period. The correlations between the concentrations of methane, ethane and ethene measured during this period are discussed.     

硫化物测定的新的标准溶液──硫代乙酰胺

根据在盐酸羟胺存在下硫代乙酰胺（ＴＡ）能够与锌发生均相沉淀的理论,选用了硫代乙酰胺作为硫化物测定的标准溶液,并利用正交试验设计进一步探讨了最佳实验条件。此方法简单、准确、重现性好,线性范围为０～０．２ｍｇ／ＬＳ２－适合于各种水样的测定。     

Wet deposition of nitrogen and sulfur in Guangzhou, a subtropical area in South China

Understanding the exchange mechanism between stratosphere and troposphere is one of the most important concerns of meteorologists and climatologists for decades. Different methods are being adopted to study those mechanisms. One of those methods is the study upon the tropospheric concentration of conserve or passive entities with stratospheric origin. One of those passive entities is ⁷Be that is produced upon the incident of cosmic rays on light atmospheric nuclei in the stratosphere. The availability of 5 years observations of ⁷Be concentration in surface air in Tehran (35°41^′ N, 51°18^′ E) encouraged us to investigate meteorological condition effect on the surface concentration of ⁷Be. Also, the intention was to see if there was any intrusion of stratospheric air into the troposphere at the time of high surface concentration of ⁷Be and scavenging mechanism when the concentration was low. During the course of this study, it has been found that ⁷Be concentration is high whenever there is a jet stream over Tehran. Since high-level jet streams normally form near tropopause folding, it could be interpreted as a sign of the intrusion of stratospheric air into the troposphere. It was also found that high concentration of ⁷Be in the Tehran surface air in summer is associated with an upper ridge on 500 hPa surface located east of the city, and low concentration in winter is associated with an upper trough. The latter normally is seen whenever there is precipitation that suggests wet scavenging could be the reason for that observed low concentration.     

Design and validation of a passive deposition sampler

A new, passive particle deposition air sampler, called the Einstein-Lioy Deposition Sampler (ELDS), has been developed to fill a gap in passive sampling for near-field particle emissions. The sampler can be configured in several ways: with a protective hood for outdoor sampling, without a protective hood, and as a dust plate. In addition, there is an XRF-ready option that allows for direct sampling onto a filter-mounted XRF cartridge which can be used in conjunction with all configurations. A wind tunnel was designed and constructed to test the performance of different sampler configurations using a test dust with a known particle size distribution. The sampler configurations were also tested versus each other to evaluate whether or not the protective hood would affect the collected particle size distribution. A field study was conducted to test the sampler under actual environmental conditions and to evaluate its ability to collect samples for chemical analysis. Individual experiments for each configuration demonstrated precision of the sampler. The field experiment demonstrated the ability of the sampler to both collect mass and allow for the measurement of an environmental contaminant i.e. Cr(6+). The ELDS was demonstrated to be statistically not different for Hooded and Non-Hooded models, compared to each other and the test dust; thus, it can be used indoors and outdoors in a variety of configurations to suit the user's needs.     

Testing the validity of a critical sulfur and nitrogen load model in southern Ontario, Canada, using soil chemistry data from MARYP

The validity of a steady-state massbalance model (Arp et al., 1996; referred to asARP) was tested using physicochemical soil data fromthe Monitoring Acid Rain Youth Program (MARYP). FourARP sites were matched with ten MARYP sites accordingto proximity, bedrock type and subsoil pH to test thevalidity of the ARP model for critical loadexceedances. Soil solution pH, base concentration andAl concentration from MARYP sites, which were wellmatched to ARP sites, validated the modelled criticalload exceedances. Higher exceedance areas wereassociated with more acidic pH and lower base andhigher Al concentrations from matched MARYP sites andvice versa. One ARP site was inappropriately matchedwith MARYP sites and could not be validated using baseand Al concentrations. This study also confirmed thesouthern limit of the zero critical load exceedanceisopleth from the model. However, variability of theother exceedance isopleths was noted due to thelimited number of sites used in the model. Thevalidation of these sites in the ARP model and thezero critical load exceedance isopleth nonethelessallows greater confidence in using this model as amanagement tool for acidic deposition.     

Monitoring of atmospheric nitrogen dioxide by long-path pulsed differential optical absorption spectroscopy using two different light paths

Measurements of the local distribution of atmospheric nitrogen dioxide (NO(2)) by long-path pulsed differential optical absorption spectroscopy (LP-PDOAS) in Tokyo during August 2008 are presented. Two LP-PDOAS systems simultaneously measured average NO(2) temporal mixing ratios along two different paths from a single observation point. Two flashing aviation obstruction lights, located 7.0 km north and 6.3 km east from the observation point, were used as light sources, allowing spatiotemporal variations of NO(2) in Tokyo to be inferred. The LP-PDOAS data were compared with ground-based data measured using chemiluminescence. Surface wind data indicated that large inhomogeneities were present in the spatial NO(2) distributions under southerly wind conditions, while northerly wind conditions displayed greater homogeneity between the two systems. The higher correlation in the NO(2) mixing ratio between the two LP-PDOAS systems was observed under northerly wind conditions with a correlation factor R(2) = 0.88. We demonstrated that the combined deployment of two LP-PDOAS systems oriented in different directions provides detailed information on the spatial distribution of NO(2).     

光离子化检测器便携式气相色谱仪快速测定空气中苯系物

本文研究了使用光离子化检测器便携式气相色谱仪,直接测定空气中ｍｇ／ｍ３级苯系物（苯、甲苯、乙苯、邻、间、对位的二甲苯及异丙苯）的快速分析方法。方法的线性范围为０～１００ｍｇ／ｍ３,相关系数均在０．９９９以上,方法的变异系数分别为２．９～１２．５％（５ｍｇ／ｍ３）,３．４～７．９％（３０ｍｇ／ｍ３）,方法最低检测限达０．２～１．０ｍｇ／ｍ３。     

Field evaluation of a tailor-made new passive sampler for the determination of NO2 levels in ambient air

This study describes the field evaluation of a tailor-made new glass passive sampler developed for the determination of NO(2), based on the collection on triethanolemine (TEA)-coated fibre filter paper. The sampler has been derived from a Palmes design. The overall uncertainty of the sampler was determined by using Griess-Saltzman ASTM D 1607 standard test method as a reference method. The agreement between the results of the passive sampler and the reference method was +/-7.90% with the correlation coefficient of 0.90. Method precision in terms of coefficient of variance (CV) for three simultaneously applied passive samplers was 8.80%. The uptake rate of NO(2) was found to be 2.49 ml/min in a very good agreement with the value calculated from theory (2.63 ml/min). Sampler detection limit was 1.99 microg/m(3) for an exposure period of 1 week and the sampler can be stored safely for a period of up to 6 weeks before exposure. A comparison of the sampler performance was conducted against a commercially available diffusion tube (Gradko diffusion tube). The results from the applied statistical paired t test indicated that there was no significant difference between the performances of two passive samplers (R (2) > 0.90). Also, another statistical comparison was carried out between the dark and transparent glass passive samplers. The results from the dark-colour sampler were higher than that from the transparent sampler (approximately 25%) during the summer season because of the possible photodegradation of NO(2)-TEA complex.     

Monitoring of bioaerosol inhalation risks in different environments using a six-stage Andersen sampler and the PCR-DGGE method

Increasing evidences show that inhalation of indoor bioaerosols has caused numerous adverse health effects and diseases. However, the bioaerosol size distribution, composition, and concentration level, representing different inhalation risks, could vary with different living environments. The six-stage Andersen sampler is designed to simulate the sampling of different human lung regions. Here, the sampler was used in investigating the bioaerosol exposure in six different environments (student dorm, hospital, laboratory, hotel room, dining hall, and outdoor environment) in Beijing. During the sampling, the Andersen sampler was operated for 30 min for each sample, and three independent experiments were performed for each of the environments. The air samples collected onto each of the six stages of the sampler were incubated on agar plates directly at 26 °C, and the colony forming units (CFU) were manually counted and statistically corrected. In addition, the developed CFUs were washed off the agar plates and subjected to polymerase chain reaction (PCR)-denaturing gradient gel electrophoresis (DGGE) for diversity analysis. Results revealed that for most environments investigated, the culturable bacterial aerosol concentrations were higher than those of culturable fungal aerosols. The culturable bacterial and fungal aerosol fractions, concentration, size distribution, and diversity were shown to vary significantly with the sampling environments. PCR-DGGE analysis indicated that different environments had different culturable bacterial aerosol compositions as revealed by distinct gel band patterns. For most environments tested, larger (>3 μm) culturable bacterial aerosols with a skewed size distribution were shown to prevail, accounting for more than 60 %, while for culturable fungal aerosols with a normal size distribution, those 2.1–4.7 μm dominated, accounting for 20–40 %. Alternaria, Cladosporium, Chaetomium, and Aspergillus were found abundant in most environments studied here. Viable microbial load per unit of particulate matter was also shown to vary significantly with the sampling environments. The results from this study suggested that different environments even with similar levels of total microbial cuturable aerosol concentrations could present different inhalation risks due to different bioaerosol particle size distribution and composition. This work fills literature gaps regarding bioaerosol size and composition-based exposure risks in different human dwellings in contrast to a vast body of total bioaerosol levels.     

The epiphytic lichen hypogymnia physodes as a biomonitor of atmospheric nitrogen and sulphur deposition in Norway

Hypogymnia physodes was sampled from 179 sites of Scots pine forests regularly distributed throughout Norway. The purpose was to map the nitrogen and sulphur contents of lichen thalli on a large-scale geographical basis, and to relate these values to differences in atmospheric deposition and climate.The lichen nitrogen and sulphur concentrations showed large differences; the highest concentration values being 4–5 times greater than the lowest. The highest nitrogen and sulphur values occurred along the coast of southern Norway and on some sites in the inland of southern Norway. There was a close correlation between the two elements. The lichen N/S ratio decreased with increasing latitude.The nitrogen and sulphur contents ofHypogymnia physodes were both significantly correlated to estimated atmospheric deposition of these two elements in Norway. The degree of explanation improved when climatic variables such as temperature sum, altitude, annual precipitation and temperature were included. Factors promoting growth, such as high bark pH, mild winters, hot summers, high precipitation, high ammonium deposition and high evapotranspiration, were all associated with lower lichen nitrogen and/or sulphur concentrations. Unfavourable growth conditions, such as at high altitude, was related to higher concentrations than expected from deposition models. This indicates that differences in element concentration between nearby localities might be related to local differences in climate and lichen growth conditions. This should be taken into consideration whenever using lichens for biomonitoring.     

昌吉市NO_x排放现状调查与分析

结合国内近两年NO_x的调查现状介绍了NO_x的来源与危害,并对昌吉市NO_x的排放现状、变化情况、新增排放量预测和减排潜力分析进行了阐述。提出了昌吉市控制NO_x目前面临的问题和困难,讨论了NO_x治理的对策,及对昌吉市经济、社会发展和环境空气质量改善的重要现实意义。     

Dry deposition velocity of atmospheric nitrogen in a typical red soil agro-ecosystem in Southeastern China

Atmospheric dry deposition is an important nitrogen (N) input to farmland ecosystems. The main nitrogen compounds in the atmosphere include gaseous N (NH₃, NO₂, HNO₃) and aerosol N (NH₄ ⁺/NO₃ ^?). With the knowledge of increasing agricultural effects by dry deposition of nitrogen, researchers have paid great attention to this topic. Based on the big-leaf resistance dry deposition model, dry N deposition velocities (V _d) in a typical red soil agro-ecosystem, Yingtan, Jiangxi, Southeastern China, were estimated with the data from an Auto-Meteorological Experiment Station during 2004–2007. The results show that hourly deposition velocities (V _dh) were in the range of 0.17–0.34, 0.05–0.24, 0.57–1.27, and 0.05–0.41 cm/s for NH₃, NO₂, HNO₃, and aerosol N, respectively, and the V _dh were much higher in daytime than in nighttime and had a peak value around noon. Monthly dry deposition velocities (V _dm) were in the range of 0.14–0.36, 0.06–0.18, and 0.07–0.25 cm/s for NH₃, NO₂, and aerosol N, respectively. Their minimum values appeared from June to August, while their maximum values occurred from February to March each year. The maximum value for HNO₃ deposition velocities appeared in July each year, and V _dm(HNO₃) ranged from 0.58 to 1.31 cm/s during the 4 years. As for seasonal deposition velocities (V _ds), V _ds(NH₃), V _ds(NO₂), and V _ds(aerosol N) in winter or spring were significantly higher than those in summer or autumn, while V _ds(HNO₃) in summer were higher than that in winter. In addition, there is no significant difference among all the annual means for deposition velocities (V _da). The average values for NH₃, NO₂, HNO₃, and aerosol N deposition velocities in the 4 years were 0.26, 0.12, 0.81, and 0.16 cm/s, respectively. The model is convenient and feasible to estimate dry deposition velocity of atmospheric nitrogen in the typical red soil agro-ecosystem.     

A comparison of portable XRF and ICP-OES analysis for lead on air filter samples from a lead ore concentrator mill and a lead-acid battery recycler

Personal and area samples for airborne lead were taken at a lead mine concentrator mill, and at a lead-acid battery recycler. Lead is mined as its sulfidic ore, galena, which is often associated with zinc and silver. The ore typically is concentrated, and partially separated, on site by crushing and differential froth flotation of the ore minerals before being sent to a primary smelter. Besides lead, zinc and iron are also present in the airborne dusts, together with insignificant levels of copper and silver, and, in one area, manganese. The disposal of used lead-acid batteries presents environmental issues, and is also a waste of recoverable materials. Recycling operations allow for the recovery of lead, which can then be sold back to battery manufacturers to form a closed loop. At the recycling facility lead is the chief airborne metal, together with minor antimony and tin, but several other metals are generally present in much smaller quantities, including copper, chromium, manganese and cadmium. Samplers used in these studies included the closed-face 37 mm filter cassette (the current US standard method for lead sampling), the 37 mm GSP or "cone" sampler, the 25 mm Institute of Occupational Medicine (IOM) inhalable sampler, the 25 mm Button sampler, and the open-face 25 mm cassette. Mixed cellulose-ester filters were used in all samplers. The filters were analyzed after sampling for their content of the various metals, particularly lead, that could be analyzed by the specific portable X-ray fluorescence (XRF) analyzer under study, and then were extracted with acid and analyzed by inductively coupled plasma optical emission spectroscopy (ICP-OES). The 25 mm filters were analyzed using a single XRF reading, while three readings on different parts of the filter were taken from the 37 mm filters. For lead at the mine concentrate mill, all five samplers gave good correlations (r2 > 0.96) between the two analytical methods over the entire range of found lead mass, which encompassed the permissible exposure limit of 150 mg m(-3) enforced in the USA by the Mine Safety and Health Administration (MSHA). Linear regression on the results from most samplers gave almost 1 ratio 1 correlations without additional correction, indicating an absence of matrix effects from the presence of iron and zinc in the samples. An approximately 10% negative bias was found for the slope of the Button sampler regression, in line with other studies, but it did not significantly affect the accuracy as all XRF results from this sampler were within 20% of the corresponding ICP values. As in previous studies, the best results were obtained with the GSP sampler using the average of three readings, with all XRF results within 20% of the corresponding ICP values and a slope close to 1 (0.99). Greater than 95% of XRF results were within 20% of the corresponding ICP values for the closed-face 37 mm cassette using the OSHA algorithm, and the IOM sampler using a sample area of 3.46 cm2. As in previous studies, considerable material was found on the interior walls of all samplers that possess an internal surface for deposition, at approximately the same proportion for all samplers. At the lead-acid battery recycler all five samplers in their optimal configurations gave good correlations (r2 > 0.92) between the two analytical methods over the entire range of found lead mass, which included the permissible exposure limit enforced in the USA by the Occupational Safety and Health Administration (OSHA). Linear regression on the results from most samplers gave almost 1 ratio 1 correlations (except for the Button sampler), indicating an absence of matrix effects from the presence of the smaller quantities of the other metals in the samples. A negative bias was found for the slope of the button sampler regression, in line with other studies. Even though very high concentrations of lead were encountered (up to almost 6 mg m(-3)) no saturation of the detector was observed. Most samplers performed well, with >90% of XRF results within +/- 25% of the corresponding ICP results for the optimum configurations. The OSHA algorithm for the CFC worked best without including the back-up pad with the filter.     

Streamwater acid-base chemistry and critical loads of atmospheric sulfur deposition in Shenandoah National Park, Virginia

A modeling study was conducted to evaluate the acid-base chemistry of streams within Shenandoah National Park, Virginia and to project future responses to sulfur (S) and nitrogen (N) atmospheric emissions controls. Many of the major stream systems in the park have acid neutralizing capacity (ANC) less than 20 μeq/L, levels at which chronic and/or episodic adverse impacts on native brook trout are possible. Model hindcasts suggested that none of these streams had ANC less than 50 μeq/L in 1900. Model projections, based on atmospheric emissions controls representative of laws already enacted as of 2003, suggested that the ANC of those streams simulated to have experienced the largest historical decreases in ANC will increase in the future. The levels of S deposition that were simulated to cause streamwater ANC to increase or decrease to three specified critical levels (0, 20, and 50 μeq/L) ranged from less than zero (ANC level not attainable) to several hundred kg/ha/year, depending on the selected site and its inherent acid-sensitivity, selected ANC endpoint criterion, and evaluation year for which the critical load was calculated. Several of the modeled streams situated on siliciclastic geology exhibited critical loads <0 kg/ha/year to achieve ANC >50 μeq/L in the year 2040, probably due at least in part to base cation losses from watershed soil. The median modeled siliciclastic stream had a calculated critical load to achieve ANC >50 μeq/L in 2100 that was about 3 kg/ha/year, or 77% lower than deposition in 1990, representing the time of model calibration.