Modeling the surface–atmosphere exchange of ammonia

New parameterizations for surface–atmosphere exchange of ammonia are presented for application in atmospheric transport models and compared with parameterizations of the literature. The new parameterizations are based on a combination of the results of three years of ammonia flux measurements over a grassland canopy (dominated by Lolium perenne and Poa trivialis) near Wageningen, the Netherlands and existing parameterizations from literature. First, a model for the surface–atmosphere exchange of ammonia that includes the concentration at the external leaf surface is derived and validated. Second, a parameterization for the stomatal compensation point (expressed as Γ_s, the ratio of [NH₄⁺]/[H⁺] in the leaf apoplast) that accounts for the observed seasonal variation is derived from the measurements. The new, temperature-dependent Γ_s describes the observed seasonal behavior very well. It is noted, however, that senescence of plants and field management practices will also influence the seasonal variation of Γ_s on a shorter timescale. Finally, a relation that links Γ_s to the atmospheric pollution level of the location through the ‘long-term’ NH₃ concentration in the air is proposed.     

Biogeochemical Control of the Coupled CO2–O2 System of the Baltic Sea: A Review of the Results of Baltic-C

Past, present, and possible future changes in the Baltic Sea acid–base and oxygen balances were studied using different numerical experiments and a catchment–sea model system in several scenarios including business as usual, medium scenario, and the Baltic Sea Action Plan. New CO₂ partial pressure data provided guidance for improving the marine biogeochemical model. Continuous CO₂ and nutrient measurements with high temporal resolution helped disentangle the biogeochemical processes. These data and modeling indicate that traditional understandings of the nutrient availability–organic matter production relationship do not necessarily apply to the Baltic Sea. Modeling indicates that increased nutrient loads will not inhibit future Baltic Sea acidification; instead, increased mineralization and biological production will amplify the seasonal surface pH cycle. The direction and magnitude of future pH changes are mainly controlled by atmospheric CO₂ concentration. Apart from decreasing pH, we project a decreasing calcium carbonate saturation state and increasing hypoxic area.     

Estimation of the exchange of sulphur pollution over the Balkan region in 1995–2000

The Bulgarian dispersion model 'Eulerian Model for Air Pollution' (EMAP) is used to estimate the sulphur pollution over the Balkan region for the period 1995–2000. A subdomain of the European Monitoring and Evaluation Programme (EMEP) grid is chosen containing 12 countries. The computational grid in this domain has a space step of 25 km, twice as fine as the EMEP grid. The former operational DWD 'Europa-Model' is used as meteorological driver. The source input is the official EMEP emission data. Monthly calculations are made having the last moment fields from the previous month as initial conditions for the next one. The boundary conditions are set to zero, so the influence of other European sources is not accounted for in this study. According to the EMEP methodology, multiple runs are made setting every time the sources of various countries to zero. The impact of every country in the pollution of all others is estimated.     

Reconstructing the Development of Baltic Sea Eutrophication 1850–2006

A comprehensive reconstruction of the Baltic Sea state from 1850 to 2006 is presented: driving forces are reconstructed and the evolution of the hydrography and biogeochemical cycles is simulated using the model BALTSEM. Driven by high resolution atmospheric forcing fields (HiResAFF), BALTSEM reproduces dynamics of salinity, temperature, and maximum ice extent. Nutrient loads have been increasing with a noteworthy acceleration from the 1950s until peak values around 1980 followed by a decrease continuing up to present. BALTSEM shows a delayed response to the massive load increase with most eutrophic conditions occurring only at the end of the simulation. This is accompanied by an intensification of the pelagic cycling driven by a shift from spring to summer primary production. The simulation indicates that no improvement in water quality of the Baltic Sea compared to its present state can be expected from the decrease in nutrient loads in recent decades.     

Difficulties inherent to the use of analytic solution of the condensation–evaporation equation for multicomponent aerosols

We present the analytic solution to the problem of multicomponent aerosol evolution due to condensation and/or evaporation of its components. We pose the general equation that governs the evolution of the particle size distributions of each species, and then solve it through the method of characteristic curves. The obtained solution is of interest because it permits an approximate analysis of cases of practical importance without numerical methods. Furthermore, the analytic solutions can be used to validate the numerical methods which, up to now, are only compared with mono-component cases. When all components condense, the obtained solution is valid for all time values. When some of the components evaporate the problem is more complex, due to the fact that no component exists in a negative amount. This suggests the formation of shock waves (high peaks in particle size distribution) and rare-faction waves, which are difficult to handle. Finally, we apply the method to several interesting cases.     

The assessment of the soil–plant-animal transport of the risk elements at the locations affected by brown coal mining

Environmental Science and Pollution Research - The North Bohemian Brown Coal Basin (Czech Republic) is suggested as a source of significant pollution in the surrounding environment with various...     

Review of advances in the thin layer chromatography of pesticides: 2008–2010

Techniques and applications of thin layer chromatography (planar chromatography) for the separation, detection, qualitative and quantitative determination, and preparative isolation of pesticides and their metabolites and other related compounds are reviewed for the period from November 1, 2008 to November 1, 2010. Analyses are described for a variety of samples types and pesticide classes. In addition to references on residue analysis, studies such as pesticide structure-retention relationships, identification and characterization of plant pesticides and synthesized pesticides, metabolism, degradation, mobility, identification of biomarkers for detection of herbicide effects in plants, and lipophilicity are covered.     

Review of advances in the thin layer chromatography of pesticides: 2004–2006

Applications of thin layer chromatography and high performance thin layer chromatography for the separation, detection, and qualitative and quantitative determination of pesticides, other agrochemicals, and related compounds are reviewed for the period from July 1, 2004 to November 1, 2006. Analyses are covered for a variety of samples, such as food, crops, biological, environmental, pharmaceuticals, and formulations, and for residues of pesticides of various types, including insecticides, herbicides, and fungicides, belonging to different chemical classes. In addition to references on residue analysis, studies such as pesticide-structure relationships, metabolism, degradation, and lipophilicity are covered, many of which make use of thin layer radiochromatography.     

Review of advances in the thin layer chromatography of pesticides: 2012–2014

Publications reporting techniques and applications of thin layer chromatography (planar chromatography) for the separation, detection, qualitative, and quantitative determination, and preparative isolation of pesticides and their metabolites are reviewed for the period from November 1, 2012 to November 1, 2014. Analyses are described for a variety of sample types and pesticide classes. In addition to references on residue analysis, studies such as pesticide structure – retention relationships, identification and characterization of natural and synthesized pesticides, metabolism, bioactivity, degradation, soil mobility, and lipophilicity are covered.     

Review of advances in the thin layer chromatography of pesticides: 2006–2008

Applications of thin layer chromatography and high performance thin layer chromatography for the separation, detection, qualitative and quantitative determination, and preparatire isolation of pesticides and their metabolites are reviewed for the period from July 1, 2006 to November 1, 2008. Analyses are described for a variety of sample types and pesticide classes. In addition to references on residue and formulation analysis, studies such as pesticide-structure relationships, identification and characterization of plant pesticides, metabolism, degradation, mobility, and lipophilicity are covered. Future prospects for pesticide thin layer chromatography are also considered.     

Plant–bacteria partnerships for the remediation of hydrocarbon contaminated soils

Plant–bacteria partnerships have been extensively studied and applied to improve crop yield. In addition to their application in agriculture, a promising field to exploit plant–bacteria partnerships is the remediation of soil and water polluted with hydrocarbons. Application of effective plant–bacteria partnerships for the remediation of hydrocarbons depend mainly on the presence and metabolic activities of plant associated rhizo- and endophytic bacteria possessing specific genes required for the degradation of hydrocarbon pollutants. Plants and their associated bacteria interact with each other whereby plant supplies the bacteria with a special carbon source that stimulates the bacteria to degrade organic contaminants in the soil. In return, plant associated-bacteria can support their host plant to overcome contaminated-induced stress responses, and improve plant growth and development. In addition, plants further get benefits from their associated-bacteria possessing hydrocarbon-degradation potential, leading to enhanced hydrocarbon mineralization and lowering of both phytotoxicity and evapotranspiration of volatile hydrocarbons. A better understanding of plant–bacteria partnerships could be exploited to enhance the remediation of hydrocarbon contaminated soils in conjunction with sustainable production of non-food crops for biomass and biofuel production.     

Space–time analysis of precipitation-weighted sulfate concentrations over the eastern US

This paper illustrates a simple technique of performing space–time analysis of precipitation-weighted SO₄²⁻ concentration data across the eastern US that were collected by the National atmospheric deposition program. Using a moving average filter and two-dimensional spatial data filtering algorithm on the time series of precipitation-weighted SO₄²⁻ concentrations, we show that decreases of about 50% have occurred in SO₄²⁻ concentrations in Minnesota, Wisconsin, and over the northeastern US between 1985 and 1998, generally consistent with SO₂ emissions’ reductions over this period. The decreases in SO₄²⁻ concentrations tended to be smaller in the midwest and south.     

Chemical composition of snowfall in the high Arctic: 1990–1994

From 1990 to 1994 at Alert, Nunavut, Canada, weekly snow samples were collected under low wind conditions to avoid contamination by blowing snow. They were analysed for major ions, Br⁻, and the organic ions methylsulphonate, formate, acetate and propionate. In the Arctic, where annual precipitation is low and blowing snow is common, these observations are unique. On an equivalent weight basis, acids and sea salt in snowfall are mixed approximately equally from December to January but from March to May acids dominate. The acidity of snowfall increases progressively throughout the winter to a May peak of ∼16 μeq l⁻¹. SO₄²⁻, Br⁻, and the organic acids acetate, and propionate peak in snowfall after polar sunrise indicate the influence of enhanced photochemical reactions. The greater enrichment of halides relative to sea salt Na⁺ in snow compared to aerosols indicates that gaseous uptake by snowflakes is important in the removal of these substances from the atmosphere and their deposition on to the Earth's surface. There is a marked difference between the seasonal variation of enrichment of Cl⁻ and Br⁻ in snow. The latter show a marked increase after polar sunrise while the former does not. These results provide valuable baseline information on the ionic content of fresh snowfall to be used in understanding the results of snowpack chemistry and post-depositional process studies conducted in the high Arctic.     

Evaluating the circular economy–based big data analytics capabilities of circular agri-food supply chains: the context of Turkey

Environmental Science and Pollution Research - Agri-food supply chains (AFSCs) are one of the significant building blocks of agricultural production, and their sustainability aims are advanced by...     

Current State of the Altai Glaciers (Russia) and Trends Over the Period of Instrumental Observations 1952–2008

Results of research into climate and glacier dynamics in the Altai Mountains (Russia) over the period of instrumental observations (1952–2008) are presented in this article. About 1030 glaciers with a total area of 805 km² and volume of 42.5 km³ have been recorded in the Altai Region. The average summer air temperature in different regions of the Altai has increased during the study period from about 0.2°C (Aktru) to 1.1°C (Akkem). The annual atmospheric precipitation rate has also increased, by 8–10%. Since 1952, the glacier area in different regions of the Altai has decreased by 9–27%, and volume by 12–24%. By 2008, as a result of degradation, the total number of glaciers was 953 with an area of 724 km² and volume of 38 km³.     

The key role of hydrophobicity in the determination of pharmaceuticals by liquid chromatography–electrospray ionization-mass spectrometry under the interference of natural organic matter

Environmental Science and Pollution Research - The determination of trace-level pharmaceuticals in water is generally performed using liquid chromatography combined with mass spectrometry, which is...     

Spatio-temporal trends of PCBs in the Swedish freshwater environment 1981–2012

Polychlorinated biphenyls (PCBs) have been monitored in perch (Perca fluviatilis), pike (Esox lucius), and Arctic char (Salvelinus alpinus) in reference lakes since the late 1960s. Temporal trends and spatial patterns are currently monitored in nine and 32 lakes, respectively. Overall, PCB concentrations are decreasing. However, this is not consistent for all congeners across all lakes and species. Perch has comparatively low PCB concentrations relative to suggested target levels, but individual congener concentrations in some lakes are concerningly high. No temporal trend is seen for CB-118 and CB-153 in perch, but significant decreasing trends exist for Arctic char and pike, for which monitoring started earlier than for perch. The lower/higher chlorinated congener ratio decreased over time in most lakes, indicating fewer new emissions. CB-118 and CB-153 concentrations in perch show spatial gradients across Sweden, with higher concentrations found near urban/industrial areas.     

Biosynthesized silver nanoparticles regulate the iron status in the spleen of Plasmodium chabaudi–infected mice

Environmental Science and Pollution Research - Malaria is a dangerous disease affecting millions around the globe. Biosynthesized nanoparticles are used against a variety of diseases including...     

Organic composition of fogwater in the Texas–Louisiana gulf coast corridor

Fogwater and air samples were collected in Baton Rouge between November 2004–February 2005 and during February 2006 at Houston. Organic compounds present in the fog samples were detected, quantified and then grouped into different compound classes based on molecular size, solubility and polarity using gas chromatography/mass spectrometry, high performance liquid chromatography with diode array detection and ion chromatography. Organic compounds were grouped as n-alkanes, aromatics and polycyclic aromatics, carbonyls, alcohols, amides and esters. Organic compounds in fog and air samples in Houston indicated clear urban/industrial anthropogenic origin, while compounds detected in Baton Rouge fog and air samples showed a mix of both agricultural and urban/industrial anthropogenic inputs. Among the various polycyclic aromatic compounds detected, the total concentration of naphthalene and its derivatives was 2.8 μg m^?3 in Houston and 0.08 μg m^?3 in Baton Rouge air. Analysis of concentrations of organic compounds pre- and post- fog revealed that compounds with low vapor pressure had higher scavenging efficiency in fog sampled at the two locations. Concentrations of organic compounds in fog samples were higher than those predicted by conventional air-water Henry's law equilibrium. Observed higher concentrations in the aqueous phase were modeled accounting for surface adsorption and accumulation of gas phase species and the presence of humic-like substances in fogwater.