Sulphate, Nitrogen and Base Cation Budgets at 21 Forested Catchments in Canada, the United States and Europe

To assess the concern over declining base cation levels in forest soils caused by acid deposition, input-output budgets (1990s average) for sulphate (SO₄), inorganic nitrogen (NO₃-N; NH₄-N), calcium (Ca), magnesium (Mg) and potassium (K) were synthesised for 21 forested catchments from 17 regions in Canada, the United States and Europe. Trend analysis was conducted on monthly ion concentrations in deposition and runoff when more than 9 years of data were available (14 regions, 17 sites). Annual average SO₄ deposition during the 1990s ranged between 7.3 and 28.4 kg ha⁻¹ per year, and inorganic nitrogen (N) deposition was between 2.8 and 13.8 kg ha⁻¹ per year, of which 41–67% was nitrate (NO₃-N). Over the period of record, SO₄ concentration in deposition decreased in 13/14 (13 out of 14 total) regions and SO₄ in runoff decreased at 14/17 catchments. In contrast, NO₃-N concentrations in deposition decreased in only 1/14 regions, while NH₄-N concentration patterns varied; increasing at 3/14 regions and decreasing at 2/14 regions. Nitrate concentrations in runoff decreased at 4/17 catchments and increased at only 1 site, whereas runoff levels of NH₄-N increased at 5/17 catchments. Decreasing trends in deposition were also recorded for Ca, Mg, and K at many of the catchments and on an equivalent basis, accounted for up to 131% (median 22%) of the decrease in acid anion deposition. Base cation concentrations in streams generally declined over time, with significant decreases in Ca, Mg and K occurring at 8, 9 and 7 of 17 sites respectively, which accounted for up to 133% (median 48%) of the decrease in acid anion concentration. Sulphate export exceeded input at 18/21 catchments, likely due to dry deposition and/or internal sources. The majority of N in deposition (31–100%; median 94%) was retained in the catchments, although there was a tendency for greater NO₃-N leaching at sites receiving higher (<7 kg ha^-1 per year) bulk inorganic N deposition. Mass balance calculations show that export of Ca and Mg in runoff exceeds input at all 21 catchments, but K export only exceeds input at 16/21 sites. Estimates of base cation weathering were available for 18 sites. When included in the mass balance calculation, Ca, Mg and K exports exceeded inputs at 14, 10 and 2 sites respectively. Annual Ca and Mg losses represent appreciable proportions of the current exchangeable soil Ca and Mg pools, although losses at some of the sites likely occur from weathering reactions beneath the rooting zone and there is considerable uncertainty associated with mineral weathering estimates. Critical loads for sulphur (S) and N, using a critical base cation to aluminium ratio of 10 in soil solution, are currently exceeded at 7 of the 18 sites with base cation weathering estimates. Despite reductions in SO₄ and H⁺ deposition, mass balance estimates indicate that acid deposition continues to acidify soils in many regions with losses of Ca and Mg of primary concern. The U.S. Government's right to retain a non-exclusive, royalty free licence in and to any copyright is acknowledged. The Canadian Crown reserves the right to retain a non-exclusive, royalty free licence in and to any copyright.     

Does stream water chemistry reflect watershedcharacteristics?

In this study, we investigated the relationships between stream water chemistry and watershed characteristics (topography—mean altitude and slope; climate—mean annual temperature and precipitation; geology—geochemical reactivity; land cover; inhabitation—population density, road density and number of municipalities). We analyzed the concentrations of the major anions (Cl, F, NO₃, SO₄, SiO₂), cations (Ca, Mg, Na, K, Mn, Fe, Al), trace elements (Li, Sr, Cu), ABS₂₄₅, TDP (total dissolved phosphorus), pH, and conductivity at 3,220 diverse watersheds covering a wide variety of watershed characteristics in the Czech Republic. We used marginal and partial multivariate analyses to reveal the most important variables. The partial analysis showed that only 14 % of the variance could be assigned to a specific factor and that 41 % of the variance is shared among the factors, which indicated complex interactions between the watershed characteristics.     

Applications of behavioral science to biodiversity management in agricultural landscapes: conceptual mapping and a California case study

Regime shifts of major salinity constituents (Ca, Mg, Na, K, SO₄, Cl, HCO₃, and NO₃) in the lower Salinas River, an agricultural ecosystem, can have major impacts on ecosystem services central to continued agricultural production in the region. Regime shifts are large, persistent, and often abrupt changes in the structure and dynamics of social-ecological systems that occur when there is a reorganization of the dominant feedbacks in the system. Monitoring information on changes in the system state, controlling variables, and feedbacks is a crucial contributor to applying sustainability and ecosystem resilience at an operational level. To better understand the factors driving salinization of the lower Salinas River on the central coast of California, we examined a 27-year record of concentrations of major salinity constituents in the river. Although limited in providing an understanding of solute flux behavior during storm events, long-term “grab sampling” datasets with accompanying stream discharges can be used to estimate the actual history of concentrations and fluxes. We developed new concentration–discharge relationships to evaluate the dynamics of chemical weathering, hydrological processes, and agricultural practices in the watershed. Examinations of long-term records of surface water and groundwater salinity are required to provide both understanding and perspective towards managing salinity in arid and semi-arid regions while also enabling determination of the influence of external climatic variability and internal drivers in the system. We found that rock weathering is the main source of Ca, Mg, Na, HCO₃, and SO₄ in the river that further enables ion exchange between Ca, Mg, and Na. River concentrations of K, NO₃, and Cl were associated with human activities while agricultural practices were the major source of K and NO₃. A more direct anthropogenic positive trend in NO₃ that has persisted since the mid-1990s is associated with the lag or memory effects of field cropping and use of flood irrigation. Event to inter-year scale patterns in the lower Salinas River salinity are further controlled by antecedent hydrologic conditions. This study underscores the importance of obtaining long-term monitoring records towards understanding watershed changes-of-state and time constants on the range of driving processes.

     

The evolution of the science of Bear Brook Watershed in Maine, USA

The Bear Brook Watershed in Maine (BBWM), USA is a paired watershed study with chemical manipulation of one watershed (West Bear = WB) while the other watershed (East Bear = EB) serves as a reference. Characterization of hydrology and chemical fluxes occurred in 1987–1989 and demonstrated the similarity of the ca. 10 ha adjacent forested watersheds. From 1989–2010, we have added 1,800 eq (NH₄)₂SO₄ ha^???1 y^???1 to WB. EB runoff has slowly acidified even as atmospheric deposition of SO $_{4}^{2-}$ has declined. EB acidification included decreasing pH, base cation concentrations, and alkalinity, and increasing inorganic Al concentration, as SO $_{4}^{2-}$ declined. Organic Al increased. WB has acidified more rapidly, including a 6-year period of increasing leaching of base cations, followed by a long-term decline of base cations, although still elevated over pretreatment values, as base saturation declined in the soils. Sulfate in WB has not increased to a new steady state because of increased anion adsorption accompanying soil acidification. Dissolved Al has increased dramatically in WB; increased export of particulate Al and P has accompanied the acidification in both watersheds, WB more than EB. Nitrogen retention in EB increased after 3 years of study, as did many watersheds in the northeastern USA. Nitrogen retention in WB still remains at over 80%, in spite of 20+ years of N addition. The 20-year chemical treatment with continuous measurements of critical variables in both watersheds has enabled the identification of decadal-scale processes, including ecosystem response to declining SO $_{4}^{-2}$ in ambient precipitation in EB and evolving mechanisms of treatment response in WB. The study has demonstrated soil mechanisms buffering pH, declines in soil base saturation, altered P biogeochemistry, unexpected mechanisms of storage of S, and continuous high retention of treatment N.     

Water pollution in relation to mineral exploration: a case study from Alayi-Ovim area of Southeastern Nigeria

Water samples from rivers, streams, springs, and shallow wells in Alayi-Ovim area of southeast Nigeria have been analyzed for Pb, Ca, Mg, Fe, Mg, PO₄, NO₃, CO₃, SO₄, Cl, and pH. The analyses were carried out using atomic absorption spectrometer and Hach Direct Reading Equipment. Results of the analyses from the area conform to the WHO (1995) standards for drinking water. However, the results show relative enrichment of Ca, pH, Mg, CO₃, and Cl. Low values were obtained for Fe, SO₄, and NO₃. While the Cl and Pb enrichment in the area north of Alayi-Ovim axis is attributed to proximity to the lead–zinc and chloride-rich formations of the Turonian Eze-Aku and the Albian Asu River; the Ca, Mg, SO₄, and CO₃ enrichment in Southern part of Alayi-Ovim is due to the limestone-bearing Late Maastrichtian Nsukka Formation. Furthermore, the very low values of less than 5 ppm for these characters in water in the central region correlate well with the relatively clean Maastrichtian quartz arenite Ajali Sandstone Formation. The Pb–Zn and Cl incursions into the water system from the Older Albian Asu River/Turonian Eze-Aku Formations in the northern part of Alayi-Ovim area and the leaching of Mg, and Ca into the water system in the Maastrichtian limestone area in the south thus constitute geochemical indices for chemical pollution and mineral exploration for brine and dolomitic limestone in the area.     

The Rengen Grassland experiment: bryophytes biomass and element concentrations after 65 years of fertilizer application

The Rengen Grassland Experiment in Germany, established in 1941, consists of the following fertilizer treatments applied under a two cut management: control, Ca, CaN, CaNP, CaNP-KCl, and CaNP-K₂SO₄. The aim of this study was (1) to identify effects of fertilizer application on biomass and species composition of bryophytes and (2) to investigate the impact of fertilizer application on macro- (N, P, K, Ca, Mg), micro- (Cu, Fe, Mn, Zn), and toxic (As, Cd, Cr, Pb, Ni) element concentrations in bryophyte biomass. In June 2006, Rhytidiadelphus squarrosus was the only bryophyte species recorded in the control. In treatment Ca, R. squarrosus was the dominant bryophyte species whereas Brachythecium rutabulum occurred sporadically only in a single plot of that treatment. The latter was the only bryophyte species collected in CaN, CaNP, CaNP-KCl, and CaNP-K₂SO₄ treatments. Dry matter accumulation of bryophytes was highest in the control (180 g m^???2) followed by Ca (46 g m^???2), CaNP (25 g m^???2), CaNP-KCl (15 g m^???2), CaNP-K₂SO₄ (9 g m^???2), and CaN (2 g m^???2) treatments. A negative correlation between biomass production of bryophytes and dry matter production of vascular plants was revealed up to a threshold value of 400 g m^???2. Above this limit, biomass production of bryophytes remained obviously unaffected by further increase in biomass production of vascular plants. A significant effect of treatment on As, Cd, Cr, Fe, Mn, Ni, Pb, P, Ca, Mg, K, and N concentrations was revealed. Concentrations of these elements were a function of amount of elements supplied with fertilizers. Bryophytes seem to be promising bio-indicators not only for airborne deposition of toxic element but also for fertilizer introduced as well.     

Vertical gradients of mineral elements in Pinus sylvestris crown in alkalised soil

Alkalisation of soil has been assumed to be the principal cause of changes in vertical gradients of nutrients in Pinus sylvestris crown. The long-term influence of alkaline dust pollution ( ${\rm {pH}}_{{\rm H}_{2}{\rm O}}$  12.3–12.6) emitted from a cement plant on the element composition of soil and needles of Scots pine in different canopy layers was studied. In the polluted area, the pH of soils was >7, and high amounts of Ca, K and Mg were measured in the upper layers of soil (0–30 cm), while the mobility and solubility of some contaminants have decreased, nutrition processes have become complicated, and imbalance of mineral composition of trees was revealed. Reduced N and increased K, Ca and Mg concentrations in needles were observed in the heavily polluted area. Vertical gradients of elements and their ratios in canopies varied depending on the alkalisation level of soil. Needles on the upper-crown shoots had higher concentrations of N, C, Ca and Mg and lower concentrations of P and K compared to the lower layer of the crown. In the unpolluted area, higher concentrations of N, P, K and Ca were found in lower-crown needles and of C and Mg in needles at the top of the canopy. The P/N ratio below 0.125 indicated P deficiency in pines. The ratios N/Ca, N/Mg and N/K had significantly decreased, while the ratios Ca/Mg, K/Mg and K/Ca had a tendency to increase in heavily polluted sample plots. Magnitude of changes of element ratios indicates on the disbalances of availability and translocation of nutrients in the crown of trees.     

An application of multivariate analysis to acid rain data in Northern Italy to discriminate natural and man-made compounds

This paper presents the preliminary results of a study, the aim of which was to analyse the pluviometric and chemical rain data, recorded by a wet only network located in Northern Italy.More in detail, precipitations were collected on a weekly basis and chemical analysis was performed on pH, electric conductivity and Ca, Mg, Na, K, NH₄, NO₃, SO₄, Cl concentrations.The Principal Components Analysis pointed out that the first three components are enough to explain more than 90% of the variability of the parameters. Moreover each component may have a different physical interpretation, that is the first one is mainly related to the precipitation amount, while the second to the man made and natural sources and the last one to the sea/soil contribution.     

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.     

The hydrochemistry of groundwater in rural communities within the Tema District, Ghana

A detailed study has been carried out on groundwater in rural communities in the Tema District of the Greater Accra region of Ghana to establish the hydrochemistry and identify the various sources of contaminants as well assess the physical and chemical quality of the groundwater to ascertain their wholesomeness and the health impacts of the groundwater on the communities. The groundwater was found to vary considerably in terms of chemical and physical properties. Generally, the water was mildly acidic (pH 4.3–7.4), brackish to fresh, and undersaturated with respect to gypsum and halite. The majority of groundwater clustered toward Ca–Mg–SO₄ and Na–Cl facies. About 70% of boreholes sampled have elevated levels of NO₃ ^??–N, Cl^???, and SO₄ ^2? emanating from anthropogenic activities.     

The impact of ground-level fireworks (13?km long) display on the air quality during the traditional Yanshui Lantern Festival in Taiwan

In this study, the concentrations of CO, non-methane hydrocarbons, NO_X, SO₂, benzene, toluene, ethylbenzene, xylene (BTEX), PM₁₀, and PM_2.5 were continuously monitored before and after the fireworks display during the traditional Lantern Festival from March 2?C7, 2007 in Yanshui Town, Taiwan. Major roads in Yanshui Town were surrounded by fireworks 13 km in length, with the display lasting for 45 min. More than 200 small firecracker towers popped up randomly in town, resulting in exceedingly inhomogeneous air quality until the end of display at 03:00 the next day, March 5. During the fireworks display, the hourly concentration of PM₁₀ and PM_2.5 at Yanshui Primary School reached about 429 and 250 ??g m^???3, respectively, which is 10 times the normal level, and 6 s values even went as high as 1,046 and 842 ??g m^???3, respectively. Similarly, BTEX concentration went up to about five to 10 times its normal value during the fireworks display. As indicated by the distribution of submicron particle sizes, the number of particles with a diameter less than 100 nm increased abruptly during the event period. Metal components with concentrations of more than 10 times higher than the normal value at Yanshui Primary School were Sr, K, Ba, Pb, Al, Mg, and Cu, in sequence. Among water-soluble ions, the content of K^?+?, Mg^2?+?, and Cl^??? increased the most, all of which were related to the materials used in the fireworks. The results of this study indicate that fireworks can cause an abrupt increase in the concentration of trace substances in the air within a short period. Although the risks of these trace substances on public health remain to be further assessed, the study results can be utilized in the management of folk events.     

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.     

Monitoring of Fogwater Chemistry in the Gulf Coast Urban Industrial Corridor: Baton Rouge (Louisiana)

Seventeen fog events were sampled in Baton Rouge, Louisiana during 2002–2004 as part of characterizing wet deposition by fogwater in the heavily industrialized corridor along the Louisiana Gulf Coast in the United States. These samples were analyzed for chemical characteristics such as pH, conductivity, total organic and inorganic carbon, total metals and the principal ion concentrations. The dominant ionic species in all samples were NH₄⁺, NO₃⁻, Cl⁻ and SO₄²⁻. The pH of the fogwater sampled had a mean value of 6.7 with two cases of acidic pH of 4.7. Rainwater and fogwater pH were similar in this region. The acidity of fogwater was a result of NO₃⁻ but partly offset by high NH₄⁺. The measured gaseous SO₂ accounted for a small percentage of the observed sulfate concentration, indicating additional gas-to-particle conversion of SO₂ to sulfate in fogwater. The gaseous NO_x accounted for most of the dissolved nitrate and nitrite concentration in fogwater. The high chloride concentration was attributable to the degradation of chlorinated organics in the atmosphere. The metal composition was traced directly to soil-derived aerosol precursors in the air. The major metals observed in fogwater were Na, K, Ca, Fe, Al, Mg and Zn. Of these Na, K, Ca and Mg were predominant with mean concentrations > 100 μM. Al, Fe and Zn were present in the samples, at mean concentrations < 100 μM. Small concentrations of Mn (7.8 μM), Cu (2 μM), Pb (0.07 μM) and As (0.32 μM) were also observed in the fogwaters, and these were shown to result from particulates (PM_2.5) in the atmosphere. The contribution to both ions and metals from the marine sources in the Louisiana Gulf Coast was minimal. The concentrations of all principal ionic species and metals in fogwater were 1–2 orders of magnitude larger than in rainwater. Several linear alkane organic compounds were observed in the fogwater, representing the contributions from petroleum products at concentrations far exceeding their aqueous solubility. A pesticide (atrazine) was also observed in fogwater, representing the contribution from the agricultural activities nearby.     

Quality assessment of various bottled waters marketed in Lebanon

Thirty-two domestic bottled water brands were analyzed for various physico-chemical as well as bacterial water quality parameters. Recorded results were compared with the Lebanese Standards Institution standards of quality and standards of identity as well as various international water standards for bottled waters. Results showed a widespread in the characteristics of investigated bottled waters, yet the majority met the different bottled water standards for physico-chemical parameters except for pH (4 brands), hardness (2 brands), and calcium (2 brands). All samples showed negative growth for fecal coliforms, yet 18.8% (N = 6) and 59.4% (N = 19) of the samples revealed positive results for total coliforms and heterotrophic plate count at 37°C, respectively. Generated Piper diagrams revealed that the majority of investigated waters are of calcium?Cmagnesium bicarbonate type; some brands were rich in sodium?Cpotassium chloride, and few were of the mixed type. Comparison of the study results with reported label values indicated good agreement with stated pH values but considerable variation for dry residue, Mg, Na, K, Ca, Mg, HCO₃, Cl, and SO₄. Identification labels showed varying compliance with the Lebanese Standards Institution standards of identity.     

Effects of chronic ammonium sulfate treatment on the forest at the Bear Brook Watershed in Maine

At the Bear Brook Watershed in Maine (BBWM), the forest tree composition was characterized and the effects of the chronic ammonium sulfate ((NH₄)₂SO₄) treatment on basal area growth, foliar chemistry, and gas exchange were investigated on forest species. The BBWM is a paired watershed forest ecosystem study with one watershed, West Bear (WB), treated since 1989 with 26.6 kg N ha^???1 year^???1 and 30 kg S ha^???1 year^???1applied bimonthly as (NH₄)₂SO₄, while the other watershed, East Bear (EB), serves as a reference. Tree species richness, density, and mortality were found to be similar between watersheds. Basal area increment was estimated from red spruce and sugar maple, showing that, for the first 7 years of treatment, it was significantly higher for sugar maple growing in WB compared to EB, but no differences were observed for red spruce between watersheds. However, the initial higher sugar maple basal area growth in WB subsequently decreased after 8 years of treatment. Foliar chemical analysis performed in trees, saplings, and ground flora showed higher N concentrations in the treated WB compared to the reference EB. But, foliar cation concentrations, especially Ca and Mg, were significantly lower for most of the species growing in WB compared with those growing in EB. For sugar maple, foliar N was higher on WB, but there were no differences in foliar Ca and Mg concentrations between treated and reference watersheds. In addition, only sugar maple trees in the treated WB showed significantly higher photosynthetic rates compared to reference EB trees.     

Chemical Composition of Bottled Water in Saudi Arabia

Fourteen domestic and seven imported bottled water brands were analysed in Saudi Arabia for various physico-chemical water quality parameters. The results of the analysis were compared with the drinking water standards set by Saudi Arabia and World Health Organization. The levels of different physico-chemical parameters like TDS, Ca, Mg, Na, K, NO₃, Cl and SO₄ of all local and imported bottled water brands met the different drinking water standards. Fluoride was found below the Saudi Arabian Standard Organization recommended limits in two of the local brands whereas fluoride levels in all of the imported brands were below the recommended values. In one imported brand, pH was found not conforming to the recommended standards. The concentrations of trace metals in all brands were within the drinking water standards. Comparison of the study results with the reported label values indicated good agreement with stated pH values but considerable variation for Ca, Mg, and Na in the local brands and comparatively low variation in the imported brands. Low F and SO₄ variations were found in the local brands and comparatively high SO₄ variation in the imported brands.     

Precipitation Chemistry and Occurrence of Acid Rain Over Dhanbad, Coal City of India

The present study investigated the chemical composition of wet atmospheric precipitation over Dhanbad, coal city of India. The precipitation samples were collected on event basis for three years (July 2003 to October 2005) at Central Mining Research Institute. The precipitation samples were analyzed for pH, conductivity, major anions (F, Cl, NO₃, SO₄) and cations (Ca, Mg, Na, K, NH₄). The pH value varied from 4.01 to 6.92 (avg. 5.37) indicating acidic to alkaline nature of rainwater. The pH of the rainwater was found well above the reference pH (5.6), showing alkalinity during the non-monsoon and early phase of monsoon, but during the late phase of monsoon, pH tendency was towards acidity (<5.6~pH) indicating the non-availability of proper neutralizer for acidic ions. The observed acidic events at this site were 91, (n = 162) accounting 56% for the entire monitoring months. The (NO₃ + Cl)/SO₄ ratio in majority of samples was found below 1.0, indicating that the acidity is greatly influenced by SO₄. The calculated ratio of (Ca + NH₄)/(NO₃ + SO₄) ranges between 0.42–5.13 (average 1.14), however in most of the samples, the ratio is greater than unity (>1.0) indicating that Ca and NH₄ play an important role in neutralization of acidic ions in rainwater. Ca and SO₄ dominate the bulk ionic deposition and these two ions along with NH₄ accounts 63% of the annual ionic deposition.     

Major ion chemistry and weathering processes in the Midyan Basin, northwestern Saudi Arabia

Chemical characteristics of 72 groundwater samples collected from Midyan Basin have been studied to evaluate major ion chemistry together with the geochemical and weathering processes controlling the water composition. Water chemistry of the study area is mainly dominated by Na, Ca, SO₄, and Cl. The molar ratios of (Ca?+?Mg)/total cations, (Na?+?K)/total cations, (Ca?+?Mg)/(Na?+?K), (Ca?+?Mg)/(HCO₃?+?SO₄), (Ca?+?Mg)/HCO₃, and Na/Cl reveal that water chemistry of the Midyan Basin is controlled by evaporite dissolution (gypsum and/or anhydrite, and halite), silicate weathering, and minor contribution of carbonate weathering. The studied groundwater samples are largely undersaturated with respect to dolomite, gypsum, and anhydrite. These waters are capable of dissolving more of these minerals under suitable physicochemical conditions.     

Source evaluation of physicochemically contaminated groundwater of Dera Ismail Khan area, Pakistan

Groundwater samples collected from Dera Ismail Khan, Pakistan, in 15 different stations were analyzed to determine the status of concentration of different physicochemical parameters. The samples were collected around a sugar mill in the study area. Sample location was selected on the basis of the flow of sugar mill effluents and groundwater. The samples were collected at random intervals in different villages. The physicochemical parameters such as pH, electrical conductivity (EC), total dissolved salts (TDS), TH, HCO₃, NO₃, SO₄, PO₄, Na, K, Ca, Mg, Fe, F, and Pb have been analyzed. The results showed that values of the tested parameters for EC, TDS, TH, HCO₃, SO₄, and Na near the sugar mill were very high, which indicate the descent of standard norms of quality and protection procedures for the groundwater around this area.     

Fluctuations of Climatic Conditions, Elemental Cycling and Forest Growth at the Watershed Scale

The relationships between fluctuations in climatic conditions,forest productivity and elemental cycling were studied from 1994 to 1997 in a headwater catchment of the southern Laurentians dominated by sugar maple (Acer saccharumMarsh.) growing on podzolic soils. Annual budgets show that H⁺, K, and NO₃ were retained in the watershed whileCa, Mg and Na were lost. The magnitude of the net annual budget for Ca, Mg and Na was correlated to annual variationsin precipitation with the absolute budget value decreasing during dry years. Stemwood (r² = 0.85) and total tree biomass production (r² = 0.99) were correlated with mean annual temperature but fine roots and leaf litter werenot. During the growing season, the pH of the organic horizons(FH) decreased as the volumetric water content of soildecreased. A positive association was also found between airtemperature and H₂O-soluble (r² = 0.88) and PO₄-extractable (r² = 0.99) SO₄ in the upper B horizon. On a multi-year scale, we suspect that the decreasein the storage of inorganic SO₄ in the soil results from the cumulative effects of annual variations in climatic conditions superimposed on the long-term decrease in SO₄deposition from the atmosphere. These soil changes were reflected by a decline in SO₄, Ca and Mg concentrationsin the stream. The generalisation of the observed short-term patterns to longer time scales must be approached with caution. Yet, our results indicate that the associations between climatic variations and the biogeochemistry of the ecosystem occur at different spatial and temporal scales and integrate abroad range of chemical components and ecosystem compartments. This reflects the inherent complexity of natural systems and offers a vast palette of indicators of the response of terrestrial ecosystems to variations in the intensity of environmental factors such as climatic conditions.