Artificial-lawn mats were used as sediment traps in floodplains to measure sediment input and composition during flood events. To estimate the natural variability, 10 traps were installed during two flood waves at three different morphological units in a meander loop of the River Elbe. The geochemical composition of deposited and suspended matter was compared. The sediment input showed weak correlations with concentration and composition of river water. It also correlated poorly with flood duration and level as well as distance of trap position from the main river. This is due to the high variability of the inundation, different morphological conditions and the variability of sources. The composition of the deposits and the suspended matter in the river water was comparable. Hence, for the investigated river reach, the expected pollution of the floodplain sediments can be derived from the pollution of the suspended matter in the river during the flood wave. The deposition of polluted sediments on floodplains is characterised by a high local variability.

We attempted to elucidate seasonal variations in fossil-fuel-derived carbon (FC) and biomass-derived carbon (BC) in urban atmospheric aerosols. We undertook continuous measurements of the composition of fine particle (PM₂.₁) in central Tokyo, including the ¹⁴C/¹²C ratio. The percent modern carbon (pMC) contained in all samples averaged 43, and the highest was 54 in late December and the lowest was 31 in early August. From the observed carbonaceous component concentrations and the pMC we could calculate the content ratio of FC and BC in PM₂.₁ and investigate their seasonal variations. Although there was almost no seasonal variation in the ratio of FC, the ratio of BC was observed to rise in early winter. This indicates that FC is influenced by the emission sources without seasonal variations (such as automobiles driven in urban areas). Furthermore, there is significant correlation between BC and organic carbon (OC), and even for urban areas, it is considered that the contribution of biomass carbon to OC in PM₂.₁ is high.

The importance of the chemical composition in evaluating groundwater flow is discussed. Two different geological environments, a felsic volcanic region around San Luis Potosí (SLPB), Mexico, and a sedimentary basin, part of the Pannonian Basin (PB), in Hungary, were chosen to explore the effect of local, intermediate and regional groundwater flows on the chemical evolution of water in different geological circumstances. In the study areas contrasting stable isotopes and groundwater temperature values, as well as the chemical composition of groundwater were convenient tools to propose groundwater flow direction and to study contamination processes in the different groundwater flow systems. Results indicate that regardless of the geological framework variability of the chemical composition of the shallow (<100 m) groundwater is significant; at depth the chemical content of groundwater becomes homogeneous, and the concentrations are smaller than at shallow depths. The Cl- and NO- ₃ concentrations indicate mainly up- and downward vertical flow directions suggesting local flow systems in the shallow layers. The linear regression between Cl- and Na⁺ suggests that evaporation processes are the main control of the Cl- concentration. Deviations from the regression line suggest processes such as pollution at shallow depths in both study areas. Based on the distribution of Ca⁺², Mg⁺² and Na⁺, a lateral flow can be traced. The large dimensions of the geological units involved with the regional flow systems implies a long groundwater flow path, also these flows remain isolated from anthropogenic contamination, then groundwater has not been altered by human influence, although in the SLPB a communication between the local and intermediate flows has been found. Recharge areas of the local and intermediate flow systems are more vulnerable to contamination processes than the discharge areas, where the expected low dissolved oxygen content of ascending water could play a control. Differences in the lithology between the PB (sedimentary basin) and the SLPB (felsic volcanic basin) explain the contrasting saturation indices calculated for chalcedony and calcite and the lack of the expected development of HCO- ₃, SO-² ₄ Cl- facies and contrasting aerobic/oxidizing conditions.

Aerosol samples were collected during the wintertime from Nov. 24, 1998 to Feb. 12, 1999 in Beijing, China. Chemical composition was determined using several analytical techniques, including inductive coupled plasma atomic emission spectroscopy (ICP-AES), graphite furnace atomic absorption spectroscopy (GFAAS) and flame atomic absorption spectroscopy (FAAS) for trace elements, ion chromatography (IC) for water-soluble ions and CHN elemental analyzer for organic carbon (OC) and elemental carbon (EC). The average concentration of aerosol was 375 ± 169 μg m⁻³, ranging from 136 to 759 μg m⁻³. Multilinear regression (MLR) analysis was performed and crustal matter, secondary particles and organics were identified as three major components of aerosol in wintertime in Beijing, accounting for 57.3% ± 9.8%, 13.4% ± 8.0%, and 22.8% ± 5.9% of the total concentration, respectively. Based on performance evaluation, Al, SO₄ ²⁻ and OC were selected as tracers of the three components, with the regression coefficients of 23.5, 1.78 and 1.26, respectively. A regression constant of 19.6 was obtained, which accounts for other minor components in aerosol. On average 93.5% of the total aerosol concentration, ranging from 82% to 105%, was explained by crustal matter, secondary particle and organics. Meteorological conditions are important factors that can influence the concentration level and chemical composition of aerosols. Wind would be favorable for the pollutant dilution, leading to low aerosol levels, whereas too strong a wind may cause regional soil dust and local road dust to be resuspended resulting in a high contribution of crustal matter. Circuitous air movement, high RH% and low wind speed facilitated the secondary particle formation, not only inorganic salts, such as sulfate and nitrate, but also secondary organic carbon in a similar way.

Lygeum spartum, Zygophyllum fabago and Piptatherum miliaceum are typical plant species that grow in mine tailings in semiarid Mediterranean areas. The aim of this work was to investigate metal uptake of these species growing on neutral mine tailings under controlled conditions and their response to fertilizer additions. A neutral mine tailing (pH of soil solution of 7.1-7.2) with high total metal concentrations (9,100 and 5,200 mg kg-¹ Zn and Pb, respectively) from Southern Spain was used. Soluble Zn and Pb were low (0.5 and <0.1 mg l-¹, respectively) but the major cations and anions reached relatively high levels (e.g. 2,600 and 1,400 mg l-¹ Cl and Na). Fertilization caused a significant increase of the plant weight for the three species and decreased metal accumulation with the exception of Cd. Roots accumulated much higher metal concentrations for the three plants than shoots, except Cd in L. spartum. Shoot concentrations for the three plants were 3-14 mg kg-¹ Cd, 150-300 mg kg-¹ Zn, 4-11 mg kg-¹ Cu, and 1-10 mg kg-¹ As, and 6-110 mg kg-¹ Pb. The results indicate that neutral pH mine tailings present a suitable substrate for establishment of these native plants species and fertilizer favors this establishment. Metal accumulation in plants is relatively low despite high total soil concentrations.

The study of mineral components in respirable particles (particulate matter with diameter less than 10 μm, PM₁₀) in ambient air is important in understanding and improving air quality. In this study, PM₁₀ samples were collected in various areas around Beijing during 2002~2003, including an urban setting, a satellite city and a rural area. The mineralogical composition of these PM₁₀ samples was studied by X-ray diffraction (XRD), environmental scanning electron microscopy / and energy-dispersive X-ray analyzer (ESEM/EDX). The results indicated that mineral composition of PM₁₀ in different seasons and in different region varied significantly. Mineral mass concentration in Beijing PM₁₀ reached the highest percentage in the spring and fell to the lowest level in the autumn. The minerals in the spring PM₁₀ were dominated by clay minerals and quartz, followed by plagioclase, K-feldspar, calcite, dolomite, hematite, pyrite, magnesite, gypsum and laumontite as well as some unidentified materials. Fewer mineral types were collected in summer, however some new components, including K(NH₄)Ca(SO4)₂·H₂O, NH₄Cl and As₂O₃·SO₃ were noted to be present, suggesting that atmospheric chemical reaction in Beijing air were more active in summer than in other seasons. Mineral components in Beijing urban air were at a higher percentage with fewer phases than that in satellite city air. In conclusion, there was considerable variation in mineral components in PM₁₀ samples collected in different seasons and areas, which reflects the related air quality of sampling areas.

Sedimentprofiles of the last 4,000-14,000 years are presented from three dimictic lakes in Mecklenburg-Vorpommern (North-eastern Germany). Sedimentological composition, major trace elements and nutrients as well as parameter for core chronology (palynology, ¹⁴C-AMS) were investigated in order to reconstruct the historical development of the lakes during the Holocene. Palynological results reflect different human settlement phases and environmental changes from the late Pleistocene to the Subatlantic. Since the Middle Ages, a permanent settlement in the catchment area resulted in higher sedimentation rates in the three lakes. Variations in sediment composition like organic matter, carbonate and mineral content were caused by different land management techniques and natural changes in the catchment area. The phosphorus accumulation increased in the upper sediment layers, but the highest phosphorus accumulations were not found in the industrial phase, but in older sediments associated with human settlement activities in the catchment area. The heavy metals lead and zinc increase in the uppermost part of all three lakes reflecting the atmospheric anthropogenic input during the last 150-200 years.