Fluoride pollution of atmospheric precipitation and its relationship with air circulation and weather patterns (Wielkopolski National Park, Poland)

A 2-year study (2010–2011) of fluorides in atmospheric precipitation in the open area and in throughfall in Wielkopolski National Park (west-central Poland) showed their high concentrations, reaching a maximum value of 2 mg/l under the tree crowns. These high values indicate substantial deposition of up to 52 mg/m²/year. In 2011, over 51 % of open area precipitation was characterized by fluoride concentration higher than 0.10 mg/l, and in throughfall such concentrations were found in more than 86 % of events. In 2010, a strong connection was evident between fluoride and acid-forming ions, and in 2011, a correlation between phosphate and nitrite ions was seen. Analysis of available data on F^? concentrations in the air did not show an unequivocal effect on F^? concentrations in precipitation. To find reasons for and source areas of high fluoride pollution, the cases of extreme fluoride concentration in rainwater were related to atmospheric circulation and weather patterns. Weather conditions on days of extreme pollution were determined by movement of weather fronts over western Poland, or by small cyclonic centers with meteorological fronts. Macroscale air advection over the sampling site originated in the western quadrant (NW, W, and SW), particularly in the middle layers of the troposphere (2,500–5,000 m a.s.l.). Such directions indicate western Poland and Germany as possible sources of the pollution. At the same time in the lower troposphere, air inflow was frequently from the north, showing short distance transport from local emitters, and from the agglomeration of Poznań.     

Observational and modeling study of dry deposition on surrogate surfaces in a South China city: implication of removal of atmospheric crustal particles

Dry deposition samples collected during 1999–2001 at a South China site using surrogate surfaces were analyzed by capillary electrophoresis. Collector surface properties played important roles to the dry deposition. The deposition velocities for various species ranged from 0.02 to 1.69 cm s^???1, in general agreement with literature values. More than 90% of Ca^2?+? was deposited by sedimentation and its comparable values of dry or wet removal residence times imply that dry deposition is an important atmospheric removal process for the ubiquitous crustal species in South China, compared with precipitation scavenging. Relatively good agreement was found when the species deposition velocities were modeled based on up-to-date knowledge of particle dry deposition. The total depositions for anthropogenic and crustal species in northern China are likely to be much higher than those in the south, including our site where the fluxes of the acidic species SO₄ ^2??? and NO₃ ^??? were 4.4 and 2.2 g m^???2 year^???1, respectively. The sum of dry deposition for cations Na^?+?, Ca^2?+?, Mg^2?+?, and K^?+? contributes 44% of the total flux, which is equivalent to the value estimated in Europe.     

Controls on Mercury and Methylmercury Deposition for Two Watersheds in Acadia National Park, Maine

Throughfall and bulk precipitation samples were collected for two watersheds at Acadia National Park, Maine, from 3 May to 16 November 2000, to determine which landscape factors affected mercury (Hg) deposition. One of these watersheds, Cadillac Brook, burned in 1947, providing a natural experimental design to study the effects of forest type on deposition to forested watersheds. Sites that face southwest received the highest Hg deposition, which may be due to the interception of cross-continental movement of contaminated air masses. Sites covered with softwood vegetation also received higher Hg deposition than other vegetation types because of the higher scavenging efficiency of the canopy structure. Methyl mercury (MeHg) deposition was not affected by these factors. Hg deposition, as bulk precipitation and throughfall was lower in Cadillac Brook watershed (burned) than in Hadlock Brook watershed (unburned) because of vegetation type and watershed aspect. Hg and MeHg inputs were weighted by season and vegetation type because these two factors had the most influence on deposition. Hg volatilization was not determined. The total Hg deposition via throughfall and bulk precipitation was 9.4 μg/m²/year in Cadillac Brook watershed and 10.2 μg/m²/year in Hadlock Brook watershed. The total MeHg deposition via throughfall and bulk precipitation was 0.05 μg/m²/year in Cadillac Brook watershed and 0.10 μg/m²/year in Hadlock Brook watershed.     

Analysis of Wet Precipitation of Air Pollutants in Mumbai (India)

Bulk precipitation samples at Mumbai (India) were collectedduring the monsoon seasons of 1991 to 1996 and analysed forionic concentrations using an Ion Chromatograph DIONEX model100. The variability of sulphate to nitrate ratio in rainwaterfluctuates in a wide range from 1.5 to 20 and governed by thesulphate concentrations in the sample. The regression analysisof the data reveals that in the bulk precipitation at Mumbai, SO₄ ^2- is becoming increasingly important relative toNO₃ ^-. The role of meteorological influences onscavenging of air pollutants by rain water has been tried toexplain the phenomena. The computed wet deposition rates for Sand N during 1991–1996 show that the S deposition is higherthan N in all the years. There is a wide fluctuation indeposition rates of S ranging from 2 to 55 kg km² per annum.     

Monitoring nitrogen deposition in typical forest ecosystems along a large transect in China

The nitrogen (N) deposition fluxes were investigated in eight typical forest ecosystems along the North–South Transect of Eastern China (NSTEC; based on the ChinaFLUX network) by ion-exchange resin (IER) columns from May 2008 to April 2009. Our results demonstrated that the method of IER columns was both labor cost saving and reliable for measuring dissolved inorganic nitrogen (DIN) deposition at the remote forest stations. The deposition of DIN in the throughfall ranged from 1.3 to 29.5 kg N ha^?1 a^?1, increasing from north to south along NSTEC. The relatively high average ratio of ammonium to nitrate in deposition (1.83) indicated that the N deposition along the NSTEC in China mostly originated in farming and animal husbandry rather than in industry and vehicle activities. For seasonal variability, the DIN deposition showed a single peak in the growing season in the northern part of NSTEC, while, in the southern part, it exhibited double-peaks in the early spring and the mid-summer, respectively. On the annual scale, the DIN deposition variations of the eight sites could be mainly explained by precipitation and the distances from forest stations to provincial capital cities.     

Uptake of metal ions in moss from artificial precipitation

Uptake in Hylocomium splendens and Sphagnum fuscum, of Zn, Cu, Cd, and Pb from artificial solutions of precipitation at ambient concentration levels was investigated. The primary objective was to study to what extent major cations and possibility anions in the precipitation might affect the uptake by competition or possibly by complexing reactions. In addition the effect on metal uptake of pH and temperature was studied. The uptake of Zn and partly Cu was lower from precipitation with a high content of seasalt. With increasing metal concentration an increasing amount of Zn and Cu accumulated in the moss. These observations suggest that cations in the precipitation such as Na⁺ and Mg²⁺ may affect the uptake by competition. Possibly also Cl^- may interfere by complexing reactions. Uptake of Zn and Cd was pH dependent. The uptake of all four metals increased with temperature. The results from this work appear to be significant with respect to the interpreation of data from atmospheric deposition surveys based on moss analysis.     

Atmospheric deposition of major and trace elements in Amman, Jordan

Wet and dry deposition samples were collected in the capital of Jordan, Amman. Concentrations of Al, Ba, Bi, Cd, Co, Cr, Cu, Mn, Mo, Ni, Pb, Sb, V, Zn, Fe, Sr, Mg²⁺, Ca²⁺, Na⁺, K⁺, Cl⁻, NO₃ ⁻ and SO₄ ²⁻, along with pH were determined in collected samples. Mean trace metal concentrations were similar or less than those reported for other urban regions worldwide, while concentrations of Ca²⁺ and SO₄ ²⁻ were among the highest. High Ca²⁺ concentrations were attributed to the calcareous nature of the local soil and to the influence of the Saharan dust. However, high SO₄ ²⁻ concentrations were attributed to the influence of both anthropogenic and natural sources. Except for Cl⁻, NO₃ ⁻, SO₄ ²⁻ and Cu, monthly dry deposition fluxes of all measured species were higher than wet deposition fluxes. The annual wet deposition fluxes of trace metals were much lower than those reported for other urban areas worldwide.     

Modelling the contribution of different sources of sulphur to atmospheric deposition in the United Kingdom

In order to understand relationships between sources and receptors of atmospheric deposition, computer models must be used. This paper describes a Lagrangian acid deposition model that represents emissions of trace species across Northern Europe. The chemistry of sulphur dioxide, dimethyl sulphide and hydrogen sulphide is represented and the model tested against estimates of UK wet and dry deposition. Mean UK wet and dry deposition for the period 1992–1994 was 206 and 145 ktonne S yr^-1, respectively. The model predicted wet and dry deposition of 222 and 166 ktonne S yr^-1, in good agreement with measurements. The model has been used to examine the sources of deposited S to the UK. For a base year of 1992, 86% of the UK's SO₂ emissions are exported. The S deposition attributable from mainland European sources was 36% of the UK total S deposition, in good agreement with other UK models but this differs substantially from the calculations of the EMEP model. Natural sources of S deposition from planktonic emissions of dimethyl sulphide, biological emissions of hydrogen sulphide and non-eruptive volcanic emissions of sulphur dioxide contributed approximately 1% of the modelled UK S deposition, of which 95% originated from dimethyl sulphide. The explicit chemical scheme for dimethyl sulphide incorporated into the model showed that 24% of the resultant deposited S was methane sulphonic acid. Boundary conditions of the model were tested and it was found that initialisation of sulphur dioxide and sulphate concentrations to representative ambient conditions had a very small effect. The modelled contribution of UK and European sources to UK S deposition was approximately 40 and 60%, respectively, showing the dramatic change arising from projected UK SO₂ emissions in 2010. This revised version was published online in July 2006 with corrections to the Cover Date.     

Hydrochemistry of Wet Atmospheric Precipitation Over an Urban Area in Northern Indo-Gangetic Plains

Rain water samples were collected to study the chemical composition of wet atmospheric precipitation (first event) over the Lucknow city in the northern Indo-gangetic alluvial plains. The samples were collected in the month of July, 2005 from different sites. The wet precipitation samples were analyzed for pH, EC, major ions (, Cl⁻, , , , F⁻, Na⁺, K⁺, Ca²⁺, Mg²⁺, ) and heavy metals (As, Cd, Al, Co, Cr, Cu, Fe, Mn, Mo, Ni, Hg, Pb, Se, Sn, Ti, V, Zn). The pH values of wet precipitation samples ranged between 6.5 and 8.7. The analysis of linear regression applied to the set of studied variables and computation of neutralization factors showed that neutralization occurred in precipitation samples and Ca²⁺ had the maximum neutralization capacity. It was found that Cl⁻, , Ca²⁺, Mg²⁺, Na⁺ and K⁺ in the precipitation samples originated mainly from crustal/anthropogenic sources in the region. On an average Fe, and Al accounted for >72% of the total concentration of trace metals in the wet precipitation samples followed by Zn (>10%). Enrichment factors calculated for heavy metals over reference background level in seawater and Earth’s crust showed relatively higher enrichment of Zn. The principal component analysis (PCA) identified the possible sources of ionic species and heavy metals in the wet precipitation samples.     

Deposition and storage of solid-bound heavy metals in the floodplains of the River Geul (the Netherlands)

Because of past mining activities, the floodplains of the River Geul are polluted with heavy metals. The continuous supply of fresh sediments during floods has caused the floodplain soils to exhibit large quality variations in time. By measurements of ¹³⁷Cs deposition rates in part of the floodplain area were determined at 0.4 to 2.7 cm yr^–1. Analysis of soil metal concentrations at various depths at 65 locations, revealed that the upper 40 cm of the soil profile deposited during the past 30–45 yr, exhibit the highest metal levels. The geostatistical interpolation technique kriging was used to map actual and past pollution patterns. It was shown that, as a result of variable deposition rates, the spatial correlation structure of soil metal concentrations becomes less clear with increasing depth/age. Kriged maps of average metal concentrations in the upper 100 cm of the soil profile provided the basis for the calculation of the mass storage of heavy metals.     

Interactions of Atmospheric Deposition with Coniferous Canopies in Estonia

Throughfall and open field bulk precipitation were measured at three coniferous sites during 1995–2002 in the framework of ICP Integrated Monitoring and at five coniferous sites during 1996–2002 in the framework of ICP Forests (Level II). The coniferous canopies acted as a sink for nitrate and ammonium and as a source for base cations: Ca²⁺, Mg²⁺ and K⁺. The estimated share of SO₄–S dry deposition from total deposition was 1.5–4 times higher for dormant period compared to growing period. During the study period average annual throughfall and bulk deposition of SO₄–S decreased significantly, 2.8 and 2.3 times, respectively. Throughfall enrichment with base cations increased in the order Mg < Na < Ca < K. Using Na as a tracer ion, average dry deposition and canopy leaching were calculated. Leaching was the dominant process for TF enrichment by potassium. Leaching of base cations occurred during growing as well as dormant period. The calculated internal flux of Ca²⁺ and Mg²⁺ varied in the range of 0.6–2.0 and 0.6–1.2 kg ha⁻¹ per year in spruce and pine stands, respectively. The internal circulation of K⁺ was significantly higher (8.9–10.9 kg ha⁻¹ per year) in spruce stands than in pine stands (2.7–4.4 kg ha⁻¹ per year).     

2003—2018年全国酸雨状况变化趋势研究

基于2003—2018年全国291个城市降水监测结果的分析表明:全国降水酸度明显降低,其中,2003—2006年有所升高,2006年之后呈降低趋势；酸雨区面积呈减小趋势,共减少约97万km²,酸雨发生频率超过5%的面积减少了20.9个百分点；全国酸雨城市比例为21.3%～40.9%,2009年开始总体呈下降趋势,2018年降为21.6%,重酸雨城市比例在2005年之后总体呈下降趋势；全国平均酸雨频率为11.7%～25.6%,2006年之后总体呈下降趋势,2018年酸雨频率在50%以上的城市比例较2006年下降了13.9个百分点。基于174个城市的降水离子组分分析结果显示:我国降水中的主要阴离子为硫酸根,其离子当量浓度占比为19.4%～32.9%,2003年以来年平均降低0.6个百分点；降水中的主要阳离子为钙离子和铵离子；硫酸根沉降通量年平均下降0.68 t/km²,硝酸根沉降通量年平均降低0.05 t/km²,全国SO₂浓度变化趋势与硫酸根沉降通量变化趋势基本一致；我国降水中的硝酸根与硫酸根离子当量浓度比值总体呈升高趋势,表明硝酸根离子对降水酸度的影响逐渐增加,酸雨类型正由硫酸型向硫酸-硝酸混合型转变。     

Modeling of oak pollen dispersal on the landscape level with a mesoscale atmospheric model

We present the extension and application of the mesoscale atmospheric meteorology model METRAS for dispersion of oak pollen. We incorporated functions for pollen emission, pollen viability and pollen deposition into METRAS and simulated pollen dispersal on a scale of up to 200 km. The basis of the simulations is a real landscape structure that includes topography, land use, and the location and size of oak stands. We simulated the oak pollen dispersion of one single oak stand with an estimated annual pollen production of 1 billion pollen grains/m² forest surface on two exemplary days of the flowering season in 2000. Depending on the meteorological situation of the simulated days, a pollen cloud with about 10 pollen/m³ may extend up to 30 km from the source. Downstream of the oak stand, approximately 1,000 pollen/m² deposited up to a distance of 25 km, and lower amounts of pollen deposited up to 100 km away. These values of pollen concentration and deposition lay within the range of published field studies. Overall, it is shown that mesoscale atmospheric models are applicable to simulate pollen dispersal on the landscape level.     

Long-term transfer of global fallout 137Cs to cow’s milk in Iceland

The aim of this study was to provide improved information on the long-term transfer of global nuclear weapons ¹³⁷Cs fallout to cow’s milk in Iceland many years after deposition. The spatial variation in deposition was confirmed to be explained by precipitation. Soil samples showed a significant difference in ¹³⁷Cs deposition density between the main agricultural areas, with the South having the highest values, then the West and North and the lowest in the Northeast. There was no significant difference between the effective half-lives in ¹³⁷Cs activity concentrations in milk and milk powder from the main dairies in Iceland based on data for milk from 1990 to 2007 and for milk powder from 1986 to 2007. There was, however, a significant difference between the effective half-lives obtained for these two regions, 13.5?years for the Northern and 10.5?years for the Southern regions. These half-lives for global fallout are longer than those previously reported for similar time periods in other Arctic areas. The transfer of ¹³⁷Cs to cow’s milk was quantified for different agricultural regions using aggregated transfer coefficients (T _ag) for the period of peak global fallout soil inventory in 1965–1967. The values ranged from 2.8?×?10^?3 to 10.6?×?10^?3?m²?kg^?1. By 2001–2004, the T _ag values had only declined, in the main agricultural areas, to 0.6?×?10^?3–1.0?×?10^?3?m²?kg^?1. Long-term transfer rates to milk many years after deposition were high in Iceland compared with most other reported data. The transfer is potentially relevant for some of the contaminated areas around the Fukushima Nuclear Power Plant after the accident in March 2011 since limited information is available on uptake from Andosols and associated effective half-lives.     

Evaluation of the effects of acid precipitation in eastern Canada using the raison system

Evaluations have been made of the key chemical factors in the aquatic effects upon surface waters due to acidic precipitation in eastern Canada. The region of Canada east of the Manitoba/Ontario border was divided into 22 aggregates and assessments of inorganic and organic ion chemistry appraised relative to sulphate deposition rates and distributions. Aquatic sensitivity is largely dominated by the concentration, distribution and magnitude of SO _inf4 ^sup2- (sulphate) deposition and by the prevalent geology and derived soils found in each aggregate. The RAISON system provided an adaptable and highly flexible platform to evaluate interactively, multiple data sets of divergent characteristics. Attributes usually associated with geographical information systems are significantly augmented by quantitative numerical and stochastic capabilities that were used extensively in this study.     

Assessment of the redistribution of soil carbon using a new index—a case study in the Haihe River Basin,North China

Soil carbon redistribution is an important process in the terrestrial carbon cycle. This study describes a new index, soil carbon redistribution (SCR) index, that can be used to assess long-term soil carbon redistribution at a large watershed scale. The new index is based on the theoretical preconditions that soil carbon redistribution is mainly controlled by vegetation type, precipitation, topography/slope, and soil carbon concentration. The Haihe River Basin served as an example for this analysis. The SCR index was calculated, and a GIS-based map shows its spatial patterns. The results suggested that soil carbon was usually prone to being carried away from mountainous regions with natural vegetation, while it was prone to deposition in the plain and plateau regions with cultivated vegetation. The methods in the paper offer a tool that can be used to quantify the potential risk where soil carbon is prone to being carried away and deposited in a large watershed.     

Improved mapping of National Atmospheric Deposition Program wet-deposition in complex terrain using PRISM-gridded data sets

High-elevation regions in the United States lack detailed atmospheric wet-deposition data. The National Atmospheric Deposition Program/National Trends Network (NADP/NTN) measures and reports precipitation amounts and chemical constituent concentration and deposition data for the United States on annual isopleth maps using inverse distance weighted (IDW) interpolation methods. This interpolation for unsampled areas does not account for topographic influences. Therefore, NADP/NTN isopleth maps lack detail and potentially underestimate wet deposition in high-elevation regions. The NADP/NTN wet-deposition maps may be improved using precipitation grids generated by other networks. The Parameter-elevation Regressions on Independent Slopes Model (PRISM) produces digital grids of precipitation estimates from many precipitation-monitoring networks and incorporates influences of topographical and geographical features. Because NADP/NTN ion concentrations do not vary with elevation as much as precipitation depths, PRISM is used with unadjusted NADP/NTN data in this paper to calculate ion wet deposition in complex terrain to yield more accurate and detailed isopleth deposition maps in complex terrain. PRISM precipitation estimates generally exceed NADP/NTN precipitation estimates for coastal and mountainous regions in the western United States. NADP/NTN precipitation estimates generally exceed PRISM precipitation estimates for leeward mountainous regions in Washington, Oregon, and Nevada, where abrupt changes in precipitation depths induced by topography are not depicted by IDW interpolation. PRISM-based deposition estimates for nitrate can exceed NADP/NTN estimates by more than 100% for mountainous regions in the western United States.     

A Comparison of Precipitation Sensors Used on the Wet-Only Collectors

The variability in performance of three precipitation sensor types, mounted on three identical wet-only collectors, has been compared for eight months at a single site. The catch efficiencies, determined from the sample volumes, are relatively high for these three apparatuses, since they exceed 89% on average. The recorded data of openings and closings of collector lids reveal that the highest losses of collection efficiency, observed for rainfalls of low intensity and low amount, are largely imputable to design and running characteristics of each sensor. Ionic compositions between the samples of these three collectors are relatively close, although significant differences are especially found for H⁺, Ca²⁺, Mg²⁺ and K⁺, suggesting that these apparatuses are differently exposed to the dry deposition of soil particles. The RS 85 sensor seems to be the most suitable one of the three, since it ensures a high catch efficiency for all rain types and tends to limit the exposures of funnel to the dry deposition.     

Acid soil indicators in forest soils of the Cherry River Watershed, West Virginia

Declining forest health has been observed during the past several decades in several areas of the eastern USA, and some of this decline is attributed to acid deposition. Decreases in soil pH and increases in soil acidity are indicators of potential impacts on tree growth due to acid inputs and Al toxicity. The Cherry River watershed, which lies within the Monongahela National Forest in West Virginia, has some of the highest rates of acid deposition in Appalachia. East and West areas within the watershed, which showed differences in precipitation, stream chemistry, and vegetation composition, were compared to evaluate soil acidity conditions and to assess their degree of risk on tree growth. Thirty-one soil pits in the West area and 36 pits in the East area were dug and described, and soil samples from each horizon were analyzed for chemical parameters. In A horizons, East area soils averaged 3.7 pH with 9.4 cmol_c kg^???1 of acidity compared to pH 4.0 and 6.2 cmol_c kg^???1 of acidity in West area soils. Extractable cations (Ca, Mg, and Al) were significantly higher in the A, transition, and upper B horizons of East versus West soils. However, even with differences in cation concentrations, Ca/Al molar ratios were similar for East and West soils. For both sites using the Ca/Al ratio, a 50% risk of impaired tree growth was found for A horizons, while a 75% risk was found for deeper horizons. Low concentrations of base cations and high extractable Al in these soils translate into a high degree of risk for forest regeneration and tree growth after conventional tree harvesting.     

Spatial variability of soil <Superscript>137</Superscript>Cs in the South Caspian region

In a comprehensive program of environmental radioactivity survey in South Caspian region,¹³⁷Cs inventories in soil has been measured at more than 50 sites in the Iranian northern province of Guilan. This has been the first wide-range survey of soil radionuclide inventories in the narrow band sensitive ecosystem of south Caspian shore. Radioactivity measurements were carried out using HPGe gamma-spectrometry system. The activity concentration of ¹³⁷Cs in surface soil exhibits a mean value of 17.6 ± 9.4 Bq kg⁻¹, with a range of 2.3–41.7 Bq kg⁻¹. In many sites, split-level sampling method has been applied down to a depth of 20 cm. There were found generally two profiles. Most profiles exhibit a negative exponential distribution, while others revealed a clear subsurface peak in 5–10-cm layer. Cesium deposition in the study area has been estimated to be in the range of 0.38–2.9 kBq m⁻² with a mean value of 1.7 kBq m⁻². Distribution patterns of ¹³⁷Cs concentration levels and deposition values have been estimated using Kriging interpolation method. Observed hotspots in deposition pattern coincide with areas of higher precipitation.