Exploratory analysis of excitation-emission matrix fluorescence spectra with self-organizing maps as a basis for determination of organic matter removal efficiency at water treatment works

In the paper, the self-organizing map (SOM) was employed for the exploratory analysis of fluorescence excitation-emission data characterizing organic matter removal efficiency at 16 water treatment works in the UK. Fluorescence spectroscopy was used to assess organic matter removal efficiency between raw and partially treated (clarified) water to provide an indication of the potential for disinfection by-products formation. Fluorescence spectroscopy was utilized to evaluate quantitative and qualitative properties of organic matter removal. However, the substantial amount of fluorescence data generated impeded the interpretation process. Therefore a robust SOM technique was used to examine the fluorescence data and to reveal patterns in data distribution and correlations between organic matter properties and fluorescence variables. It was found that the SOM provided a good discrimination between water treatment sites on the base of spectral properties of organic matter. The distances between the units of the SOM map were indicative of the similarity of the fluorescence samples and thus demonstrated the relative changes in organic matter content between raw and clarified water. The higher efficiency of organic matter removal was demonstrated for the larger distances between raw and clarified samples on the map. It was also shown that organic matter removal was highly dependent on the raw water fluorescence properties, with higher efficiencies for higher emission wavelengths in visible and UV humic-like fluorescence centers

The association between organic matter and clay minerals in carbonaceous chondrites

There is an established relationship between organic matter content and aqueous alteration processes [1,2]. However, the relationship between meteoritic organic matter and individual aqueously generated mineral matrix phases is poorly understood. Meteoritic organic matter is primarily composed of C, H and N and therefore their bulk abundances in chondrites are strongly controlled by the organic matter content. Mössbauer Spectroscopy can characterise the ferric iron bearing matrix minerals associated with aqueous alteration, such as Fe- bearing clays and magnetite. A combination of these two parameters may indicate the presence of any organic-mineral interactions

Study of the effect of pH, salinity and DOC on fluorescence of synthetic mixtures of freshwater and marine salts

In order to provide support for the discussion of the fate of organic matter in estuaries, a laboratory simulation was performed by changing freshwater ionic strength, pH and organic matter content. The change in spectroscopic characteristics caused by variations in salinity, pH and organic matter concentration in the filtered samples was observed by UV-Vis and fluorescence spectroscopy. The increase in emission fluorescence intensity of dissolved organic matter (DOM) due to increasing salinity (in the range 0 to 5 g l−1) is affected by the pH of the samples. The emission fluorescence intensity at the three maxima observed in the fluorescence spectra, is linearly correlated with dissolved organic carbon (DOC) concentration at several salinity values in the same sample. The increase in organic matter concentration caused a shift in the emission peak wavelength at 410 nm for several salinity values.We concluded that it is necessary to take into account the influence of salinity and pH on emission fluorescence of dissolved organic matter if it is to be used as a tracer in estuarine or near shore areas

Evaluation of organic matter stability during the composting process of agroindustrial wastes.

Composting of wastes from citrus industrial processing (pastazzo and sludge) was studied in order to evaluate the evolution of organic matter during the process and to individuate chemical and/or biochemical techniques able to set the stability of the final product. Composts from two open-air piles of different composition were sampled every month during the whole period of composting (5 months) and the organic matter of each sample was characterised by chemical and biochemical techniques. Humification rate (HR%) and humification index (HI) were determined. Extracted organic matter of six samples collected for each compost was investigated by isoelectric-focusing technique (IEF). The biochemical analysis was based on the study of C-mineralisation after the addition of each collected sample to soil. Results obtained clearly demonstrated organic matter evolution during composting processes. Humification rates increased and humification indexes decreased over time, while extracted organic matter showed electrophoretic behaviour typical of stabilised organic compounds. Moreover, mineralisation patterns confirmed the increased level of organic matter stability during the composting process

Possible role of organic matter in radiocaesium adsorption in soils

The aim of this review is to examine the hypothesis that organic matter decreases the adsorption of radiocaesium on clay minerals. The factors that determine radiocaesium mobility and bioavailability in soil are briefly outlined to show why a relationship between soil organic matter content and enhanced Cs bioavailability is paradoxical. In all the investigations reviewed the ionic compositions of both the solid and the solution phases have been strictly controlled. We show that the addition of organic matter to reference clay minerals causes decreases of up to an order of magnitude in the distribution coefficient of radiocaesium. Similarly, the chemical removal of organic matter from the clay-sized fraction of soil usually leads to an increase in Cs adsorption. We suggest that the nature of the organic matter and its interaction with mineral surfaces are as important as the amount present

Climate change: carbon losses in the Alps

The response of the terrestrial carbon cycle to global change is one of the main uncertainties in current climate change predictions1. Most terrestrial carbon is held in soils as organic matter derived from the decay of plant material (Fig. 1). Soil organic matter accounts for roughly three times more carbon than living vegetation, and for more carbon than vegetation and the atmosphere combined. Because elevated atmospheric CO2 concentrations have a fertilizing effect on plant growth, anthropogenic CO2 emissions have triggered increases in the land carbon sink2. However, models predict that other factors — such as water and nutrients — will eventually become limiting to plant growth, and hence to the land carbon sink. In contrast, the turnover of soil organic matter producing CO2 is expected to increase as the Earth warms. As a result, simulations using coupled carbon–climate models predict that the land surface will become a net source of CO2 before the end of the century, leading to a feedback loop between climate and soil carbon losses: increased emissions of CO2 from soil organic matter will lead to enhanced warming, which may then feedback to cause further soil organic matter losses. Prietzel and colleagues3, writing in Nature Geoscience, now provide evidence that warming has already caused a decline in soil organic matter in the German Alps

The Potential for Abiotic Methane in Arctic Gas Hydrates

Most methane enclosed in gas hydrates is biotic in origin, formed by microbial degradation of sedimentary organic matter. Increasingly, there is evidence that substantial gas hydrate may also be sourced from thermogenic decomposition of organic matter and subsequent migration of this gas into the gas hydrate stability zone. In addition, there is a third potential source of methane that does not involve organic matter at all— abiotic methane, which can be generated by magmatic processes or gaswater- rock reactions in the crust and upper mantle

Influence of organic matter in road deposited particulates in heavy metal accumulation and transport

The research study discussed in the paper investigated the influence of organic matter on heavy metal adsorption for different particle size ranges of build-up solids. Samples collected from road surfaces were assessed for organic matter content, mineral composition, particle size distribution and effective cation exchange capacity. It was found that the organic matter plays a key role in >75µm particles in the adsorption of Zinc, Lead, Nickel and Copper, which are generated by traffic activities. Clay forming minerals and metal oxides of Iron, Aluminium and Manganese was found to be important for heavy metal adsorption to <75µm particles. It was also found that heavy metals adsorbed to organic matter are strongly bound to particles and these metal ions will not be bio-available if the chemical quality of the media remains stable