Airborne trace element pollution in 11 European cities assessed by exposure of standardised ryegrass cultures

Within a European biomonitoring programme, Italian ryegrass (Lolium multiflorum Lam.) was employed as accumulative bioindicator of airborne trace elements (As, Cd, Cr, Cu, Fe, Ni, Pb, Sb, V, Zn) in urban agglomerations. Applying a highly standardised method, grass cultures were exposed for consecutive periods of four weeks each to ambient air at up to 100 sites in 11 cities during 2000–2002. Results of the 2001 exposure experiments revealed a clear differentiation of trace element pollution within and among local monitoring networks. Pollution was influenced particularly by traffic emissions. Especially Sb, Pb, Cr, Fe, and Cu exhibited a very uneven distribution within the municipal areas with strong accumulation in plants from traffic-exposed sites in the city centres and close to major roads, and moderate to low levels in plants exposed at suburban or rural sites. Accumulation of Ni and V was influenced by other emission sources. The biomonitoring sites located in Spanish city centres featured a much higher pollution load by trace elements than those in other cities of the network, confirming previously reported findings obtained by chemical analyses of dust deposition and aerosols. At some heavily-trafficked sites, legal thresholds for Cu, Pb, and V contents in foodstuff and animal feed were reached or even surpassed. The study confirmed that the standardised grass exposure is a useful and reliable tool to monitor and to assess environmental levels of potentially toxic compounds of particulate matter.     

Aryl hydrocarbon receptor-mediated activity of atmospheric particulate matter from an urban and a rural site in Switzerland

Atmospheric particulate matter (PM) is an air-suspended mixture of solid and liquid particles that vary in size, shape, and chemical composition. Long-term exposure to elevated concentrations of fine atmospheric particles is considered to pose a health threat to humans and animals. In this context, it has been hypothesized that toxic chemicals such as polycyclic aromatic hydrocarbons (PAHs) play an important role. Some PAHs are known to be carcinogenic and it has been shown that carcinogenic effects of PAHs are mediated by the aryl hydrocarbon receptor (AhR). In this study, PM1 was collected at a rural and an urban traffic site during an intense winter smog period, in which concentration of PM1 often exceeded 50 μg m^?3. We applied an in vitro reporter gene assay (DR-CALUX) to detect and quantify PM1-associated chemicals that induce AhR-mediated gene expression. This activity was expressed as CALUX equivalents of 2,3,7,8-tetrachlorodibenzodioxin (PM-TCDD-CEQs). In addition, concentrations of PAHs in the PM1 extracts were determined using gas chromatography/high-resolution mass spectrometry. Concentrations of PM-TCDD-CEQs ranged from 10 to 85 pg m^?3 and from 19 to 87 pg m^?3 at the urban and rural site, respectively. By the use of known relative potency factors, the measured concentration of a PAH was converted into a PAH-TCDD-CEQ concentration. ΣPAH-TCDD-CEQ and PM-TCDD-CEQ were highly correlated at both sites (r² = 0.90 and 0.69). The calculated ΣPAH-TCDD-CEQs explain between 2% and 20% of the measured PM-TCDD-CEQs. Benzo[k]fluoranthene was the most important PAH causing approximately 60% of the total ΣPAH-TCDD-CEQ activity. In contrast to NO, CO, PM10, and PM1, the concentration of PM-TCDD-CEQs showed no significant difference between the two sites. No indications were found that road traffic emissions caused elevated concentrations of PM-TCDD-CEQs at the urban traffic site.     

Desorption of arsenic from clay and humic acid-coated clay by dissolved phosphate and silicate

Arsenic (As) contaminated aquifers contain iron minerals and clays that strongly bind As at their surfaces. It was suggested that As mobilization is driven by natural organic matter (including fulvic acids (FA) and humic acids (HA)) present in the aquifers either via providing reducing equivalents for reductive dissolution of Fe(III) (hydr)oxides or via competitive desorption of As from the mineral surfaces. In the present study we quantified sorption of As(III) and As(V) to Ca(2+)-homoionized illite (IL) and to kaolinite (Kao) as well as to HA-coated clays, i.e., illite-HA (IL-HA) and kaolinite-HA (Kao-HA) at neutral pH. Clay-HA complexes sorbed 28-50% more As than clay-only systems upon addition of 100μM As(III)/As(V) to 0.5g of clay or HA-clay with Ca(2+) probably playing an important role for HA binding to the clay surface and As binding to the HA. When comparing sorption of As(V) and As(III) to clay and HA-clay complexes, As(V) sorption was generally higher by 15-32% than sorption of As(III) to the same complexes. IL and IL-HA sorbed 11-28% and 6-11% more As compared to Kao and Kao-HA, respectively. In a second step, we then followed desorption of As from Kao, Kao-HA, IL and IL-HA by 100 and 500μM phosphate or silicate both at high (0.41-0.77μmol As/g clay), and low (0.04 to 0.05μmol As/g clay) As loadings. Phosphate desorbed As to a larger extent than silicate regardless of the amount of As loaded to clay minerals, both in the presence and absence of HA, and both for illite and kaolinite. At high loadings of As, the desorption of both redox species of As from clay-HA complexes by phosphate/silicate ranged from 32 to 72% compared to 2-54% in clay only systems meaning that As was desorbed to a larger extent from HA-coated clays compared to clay only systems. When comparing As(III) desorption by phosphate/silicate to As(V) desorption in high As-loading systems, there was no clear trend for which As species is desorbed to a higher extent in the four clay systems meaning that both As species behave similarly regarding desorption from clay surfaces by phosphate/silicate. Similarly, no significant differences were found in high As-loading systems in the amount of As desorbed by phosphate/silicate when comparing Kao vs. IL and Kao-HA vs IL-HA systems meaning that both clay types behave similarly regarding desorption of As by phosphate/silicate. At low As loadings, up to 80% of As was desorbed by phosphate and silicate with no noticeable differences being observed between different As species, different types of clay, clay vs clay-HA or the type of desorbant (phosphate and silicate). The results of this study showed that HA sorption to Ca(2+)-homoionized clay minerals can increase As binding to the clay although the As sorbed to the clay-HA is also released to a greater extent by competing ions such as phosphate and silicate. Desorption of As depended on the initial loadings of As onto the clay/clay-HA. Based on our results, the effect of humic substances on sorption of As and on desorption of As by phosphate and silicate has to be considered in order to fully understand and evaluate the environmental behavior of As in natural environments.     

Formation of a ternary neptunyl(V) biscarbonato inner-sphere sorption complex inhibits calcite growth rate

Neptunyl, Np(V)O(2)(+), along with the other actinyl ions U(VI)O(2)(2+) and Pu(V,VI)O(2)((+,2+)), is considered to be highly mobile in the geosphere, while interaction with mineral surfaces (inner- or outer-sphere adsorption, ion-exchange, and coprecipitation/structural incorporation) may retard its migration. Detailed information about the exact interaction mechanisms including the structure and stoichiometry of the adsorption complexes is crucial to predict the retention behavior in diverse geochemical environments. Here, we investigated the structure of the neptunyl adsorption complex at the calcite-water interface at pH 8.3 in equilibrium with air by means of low-temperature (15K) EXAFS spectroscopy at the Np-L(III) edge. The coordination environment of neptunyl consists of two axial oxygen atoms at 1.87(±0.01)?, and an equatorial oxygen shell of six atoms at 2.51(±0.01)?. Two oxygen backscatterers at 3.50(±0.04)? along with calcium backscatterers at 3.95(±0.03)? suggest that neptunyl is linked to the calcite surface through two monodentate bonds towards carbonate groups of the calcite surface. Two additional carbon backscatterers at 2.94(±0.02)? are attributed to two carbonate ions in bidentate coordination. This structural environment is conclusively interpreted as a ternary surface complex, where a neptunyl biscarbonato complex sorbs through two monodentate carbonate bonds to steps at the calcite (104) face, while the two bidentately coordinated carbonate groups point away from the surface. This structural information is further supported by Mixed Flow Reactor (MFR) experiments. They show a significant decrease of the calcite growth rate in the presence of neptunyl(V), in line with blockage of the most active crystal growth sites, step and kink sites, by adsorption of neptunyl. Formation of this sorption complex constitutes an important retention mechanism for neptunyl in calcite-rich environments.     

Comparison of bioluminescence and nitrification inhibition methods for assessing toxicity to municipal activated sludge

The aim of this study was to compare two alternative toxicity assessment methods to determine wastewater toxicity and predict treatment plant process upsets. The toxicity of two synthetic organic compounds (triclosan and 4-n-nonylphenol), which are commonly detected in municipal wastewater, and municipal and industrial wastewaters with different heavy metals content were evaluated by the nitrification inhibition assay and bioluminescence toxicity test. Comparison between both assays confirmed that Vibrio fischeri is generally more sensitive than autotrophic bacteria, and, if not calibrated, the bioluminescence method tends to overestimate toxic effects on activated sludge biomass. The nitrification inhibition assay appears to predict plant process upsets more accurately. Both methods showed a significant toxicity decrease through treatment that could be partially attributed to the significant heavy metals removal obtained by primary and secondary treatment. A good correlation for the two assays was obtained, as indicated by a high correlation coefficient (r2 = 0.80).     

Variation in sensitivity to cadmium among genetically characterized laboratory strains of the midge Chironomus riparius

Estimating the extent of intraspecific variation in sensitivity to contaminant exposure is important in order to explain variation in the outcome of toxicity tests and to predict the effects of chemical stress on natural populations of plants and animals. However, only few studies provide evident data concerning intraspecific variation in life-history traits caused by a differential response to chemical stress. In this study, we compared the life-history response of six laboratory strains of the midge Chironomus riparius to cadmium exposure in a full life-cycle assay. In addition, the level of genetic variation in all strains was measured at five variable microsatellite loci. Several significant differences in life-history traits among the strains were observed in controls and cadmium treatments. The extent of variation among strains was largest at moderate cadmium concentration (0.42 mg Cd/kg dw). At increased Cd concentrations all strains showed similar levels of high mortality and reduced reproductive success. All strains exhibited considerable levels of genetic impoverishment compared to field populations. Strains with low genetic variation showed reduced fitness in the controls and were more susceptible to Cd exposure. For instance, no reproductive success in the lowest Cd treatment was observed for the strain with the lowest level of genetic diversity. In contrast, this Cd concentration had no negative effects on life-history traits of more variable strains. These results confirm recent findings, that inbreeding and reduced genetic variation influence the reaction of populations towards environmental stress. In addition, we show that the level of genetic variation and inbreeding directly influences the outcome of toxicity tests and contributes to the lack of reproducibility of test results among laboratories.     

Mortality of the scleractinian coral <Emphasis Type="Italic">Cladocora caespitosa</Emphasis> during a warming event in the Levantine Sea (Cyprus)

A mortality event of Cladocora caespitosa corals and the extent of bleaching, necrosis and pigmented areas in the colonies were studied at the southeastern coast of Cyprus during a prolonged period of higher than average sea temperature anomalies (summer/autumn 2012). With the use of scuba diving and image analysis software, we monitored the extent of mortality of 29 colonies of C. caespitosa by measuring and comparing the area percentage of healthy tissue, affected tissue (bleached, necrotic) and older mortality events (encrusted skeleton). In September 2012, on average, 24 % of the colonies surface area was affected (bleaching and/or necrosis). In October 2012, C. caespitosa showed on average 26.3 % of the colony surface area affected, evidence of continuing deterioration. At the same time, 10 % (3 of 29) of the colonies showed an increase in the pigmentation of previously bleached polyps in small and marginal areas (6–8 %). Irrespective of the amount, the regaining of pigments recorded is considered an important find. Corals and marine organisms in general in the Levantine Sea are affected greatly by warming events, to the extent where a very small percentage of polyps/colonies show resilience under thermal stress. Natural bleaching of C. caespitosa, even though limited to a few colonies and very small portions of tissue/polyps, was documented for the first time in the Levantine Sea. We conclude that temperature anomalies are associated with the mortality event. Whether prolonged higher temperature is the direct cause, or whether it acts synergistically with other factors should be the subject of further investigations.     

Assessment of bioclimatic conditions on Crete Island,Greece

The objective of this study was to assess and analyze the human bioclimatic conditions of Crete Island, by applying two human thermal indices: physiological equivalent temperature (PET), derived from the Munich Energy-balance Model for Individuals human energy balance model, and Universal Thermal Climate Index (UTCI), based on the Fiala multi-node model of human thermoregulation. Human bioclimatic studies provide a framework for considering the effects of climatic conditions on human beings and highlighting the social/economic factors that mitigate or amplify the consequences of environmental changes. In order to estimate the thermal effect of the environment on the human body, it has been considered that the total effects of all thermal components, not only of individual parameters, should be taken into account. The climatic data (air temperature, relative humidity, cloudiness, wind speed) used in this study were acquired from the archives of the Hellenic National Meteorological Service, regarding ten meteorological stations in Crete Island. These data, covering the 30-year period 1975–2004, were used for the calculation of PET and UTCI in order to assess thermo-physiological stress levels. The findings of this analysis, such as bioclimatic diagrams, temporal and spatial distributions of PET and UTCI as well as trends and variability, will help stake holders to understand and interpret the island’s current bioclimate, in order to make any necessary adaptations and become more resilient to the foreseen climate change.     

Thermal terrain modeling of spatial objects, a tool for environmental and climatic change assessment

The aim of the current research effort is to include biophysical multi-temporal data and more specifically land surface temperature (LST) in the terrain modeling process that traditionally was based only on digital elevation data processing. The terrain partition framework (spatial objects) is defined by the borderlines of prefecture authorities of Greece. Each object is represented by a set of attributes derived from the digital elevation data, and objects are organized into clusters on the basis of their terrain dependent representation. Finally, the terrain is segmented to regions on the basis of the multi-temporal LST data, each region presenting a different thermal signature. The thermal regions are used in the spatial objects parametric representation and a new index is devised (LST climatic index) expressing the biophysical suitability of spatial objects at moderate resolution scale.     

Influence of near-to-nature stormwater management on the local water balance using the example of an urban development area

Near-to-nature stormwater management aims at replicating the quasi-natural local water balance and preserving the ecosystem's integrity of affected waters. Surface waters in the urban areas of Trier-Petrisberg are managed by a separate sewer system in conjunction with a complex retention system. To investigate the effect of this alternative rainwater management practice on the local water balance, a differentiated discharge and groundwater monitoring network with a high spatio-temporal measurement resolution has been implemented within the watershed. Additional information regarding the proportion and spatial distribution of discharge-generating surfaces was provided through visual interpretation of aerial photographs. As a result of this analysis, groundwater levels were found to not be significantly affected by an increase of local sealed surfaces, and the ecologically-justifiable maximum discharge in the tributary was infrequently exceeded. Regarding further building development and climate change, the hydrological load capacity of the retention basins will provide effective rainwater management, even with respect to increasing precipitation intensities and frequencies.