Analyses of organic and inorganic carbon are of great interest in the field of soil analyses. Soil samples from a national monitoring project were provided for this study, including more than 130 forest sites from Austria. We investigated the humus layers (if present undecomposed litter (L), of mixed samples of F- (intermediate decomposed organic matter) and H-(highly decomposed organic matter) (FH)) and upper mineral soil layers (0-5 and 5-10 cm) of the samples. Mid-infrared spectra were recorded and evaluated by their band areas; subsequently we calculated models with the partial least squares approach. This was done by correlating calculated data of the mid-infrared spectra with gas-volumetrically determined carbonate values and measurements of organic carbon from an elemental analyzer. For carbonate determination, this approach gave satisfying results. For measurements of organic carbon, it was necessary to discriminate into humus layers and mineral soils or even more groups to obtain satisfactory correlations between spectroscopically determined and conventionally measured values. These additional factors were the presence of carbonate, the forest type, and the dominant tree species. In mineral soils, fewer subdivisions were necessary to obtain useful results. In humus layers, groupings of sites with more similar characteristics had to be formed in order to obtain satisfying results. The conclusion is that the chemical background of soil organic matter leading to different proportions of functional groups, especially in the less humified organic matter of the humus layers, plays a key role in analyses with mid-infrared spectroscopy. Keeping this in mind, the present approach has a significant potential for the prediction of properties of forest soil layers, such as, e.g., carbonate and organic carbon contents.
We evaluated the effect of acidic deposition and nitrogen on Austrian forests soils. Until thirty years ago air pollution had led to soil acidification, and concerns on the future productivity of forests were raised. Elevated rates of nitrogen deposition were believed to cause nitrate leaching and imbalanced forest nutrition. We used data from a soil monitoring network to evaluate the trends and current status of the pH and the C : N ratio of Austrian forest soils. Deposition measurements and nitrogen contents of Norway spruce needles and mosses were used to assess the nitrogen supply. The pH values of soils have increased because of decreasing proton depositions caused by reduction of emissions. The C : N ratio of Austrian forest soils is widening. Despite high nitrogen deposition rates the increase in forest stand density and productivity has increased the nitrogen demand. The Austrian Bioindicator Grid shows that forest ecosystems are still deficient in nitrogen. Soils retain nitrogen efficiently, and nitrate leaching into the groundwater is presently not a large-scale problem. The decline of soil acidity and the deposition of nitrogen together with climate change effects will further increase the productivity of the forests until a limiting factor such as water scarcity becomes effective.
In the framework of this study, nitrogen fluxes on a limestone site are investigated. The major goals are the assessment of the nitrogen status, the estimation of the nitrogen budget and the evaluation of the nitrogen saturation. The investigation area, the intensive investigation plot and the research equipment are described.
Environmental contextAnalysis of soil organic matter is important for understanding turnover and stabilisation processes of organic carbon in soils. Capillary electrophoresis is used here to investigate humic acids from soils of diverse forest sites, and show that the patterns of signals are indicative of soil characteristics. The method provides useful information of soil types and complements the existing set of methods for humic acid characterisation.
AbstractAnalyses of humic substances provide very useful information about turnover characteristics and stabilisation processes of soil organic matter in environmental soil samples. The present study investigates 113 samples of forest soils from three different layers (undecomposed litter (L), if present, mixed samples of F (intermediate decomposed) and H (highly decomposed) organic matter (FH) and upper mineral soil layers (Ah horizon) from 0 to 5 cm) by extracting humic acids (HAs) and recording electropherograms. Five signals of these electropherograms were evaluated and correlated with basic parameters from soil (organic carbon, Corg, and total nitrogen, Nt, and extraction yields of HAs) and HAs (total carbon, Ct, and Nt), and with signals from photometry, mid-infrared and fluorescence spectroscopy. The developed method was able to separate HAs from different soil layers by calculating a discriminant function based on the five evaluated electrophoretic signals. The dataset of this work opened the opportunity to correlate the observed electrophoretic signals with the other determined soil parameters and spectroscopic signals. This can be seen as a very important step in the direction to assignments of the obtained electrophoretic signals. Soil characteristics were reflected quite well by this method and, combined with the other approaches, it is suitable for applications in further studies.
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