We studied forest monitoring data collected at permanent plots in Italy over the period [2000][2001][2002][2003][2004][2005][2006][2007][2008][2009]

Acid deposition arising from sulphur (S) and nitrogen (N) emissions from fossil fuel combustion and agriculture has contributed to the acidification of terrestrial ecosystems in many regions globally. However, in Europe and North America, S deposition has greatly decreased in recent decades due to emissions controls. In this study, we assessed the response of soil solution chemistry in mineral horizons of European forests to these changes. Trends in pH, acid neutralizing capacity (ANC), major ions, total aluminium (Al ) and dissolved organic carbon were determined for the period 1995-2012. Plots with at least 10 years of observations from the ICP Forests monitoring network were used. Trends were assessed for the upper mineral soil (10-20 cm, 104 plots) and subsoil (40-80 cm, 162 plots). There was a large decrease in the concentration of sulphate (SO42-) in soil solution; over a 10-year period (2000-2010), SO42- decreased by 52% at 10-20 cm and 40% at 40-80 cm. Nitrate was unchanged at 10-20 cm but decreased at 40-80 cm. The decrease in acid anions was accompanied by a large and significant decrease in the concentration of the nutrient base cations: calcium, magnesium and potassium (Bc = Ca + Mg + K ) and Al over the entire dataset. The response of soil solution acidity was nonuniform. At 10-20 cm, ANC increased in acid-sensitive soils (base saturation ≤10%) indicating a recovery, but ANC decreased in soils with base saturation >10%. At 40-80 cm, ANC remained unchanged in acid-sensitive soils (base saturation ≤20%, pHCaCl2 ≤ 4.5) and decreased in better-buffered soils (base saturation >20%, pHCaCl2 > 4.5). In addition, the molar ratio of Bc to Al either did not change or decreased. The results suggest a long-time lag between emission abatement and changes in soil solution acidity and underline the importance of long-term monitoring in evaluating ecosystem response to decreases in deposition.

Abstract--The clay fraction of a Spodosol and its parent rock in the Apennlne mountains of central Italy were studied by powder X-ray diffraction (XRD) and infrared (IR) spectroscopy, to evaluate the possibility of transformation of chlorite into low-charge expandable minerals. Results indicated that the main phyllosilicate in the rock was a slightly weathered trioctahedral chlorite, rich in both Mg and Fe. together with dioctahedral mica and minor amounts of kaolinite. In the BC horizon, chlorite has undergone partial transformation into 2 vermiculitic components, in 1 of which the interlayer could be removed by hot Na-citrate treatment: the presence of a regular interstratified mineral (high-charge corrensite) was also observed. Further changes in the structure of chlorite were detected in the Bsl horizon, becoming more evident towards the soil surface. The first stage of weathering of chlorite involved Fe oxidation and partial expulsion of Mg from the hydroxide sheet, followed by deposition of A1 in the interlayer space. Iron is also removed from the interlayer sheet, possibly remaining, in the oxidized state, in the 2:1 octahedral sheet, and so contributing to the lowering of layer charge and transformation to a dioctahedral structure. When approaching the surface, A1 removal from the interlayers is enhanced by complexing agents, and further charge reduction leads to the formation of 2:1 minerals with a smectite nature. Illite. because ot its low content in the soil clay fraction, contributes marginally to this weathering sequence, forming the high charged expandable component observed in the Bhs horizon. At the soil surface, a randomly interstratified vermiculite/illite was detected, which probably originated from K fixation by the higher-charged expandable minerals. This study of weathering in a natural soil strongly supports the hypothesis, previously ascertained by laboratory experiments, that chlorite can transform into a low-charge expandable mineral.

There is a growing interest in the links between humus forms and soil biota, and little is known about these links in Mediterranean ecosystems. Culture-independent techniques, such as DNA extraction followed by DGGE and enzyme activities, allowed us to compare microbial communities in two horizons of a forest soil in different seasonal conditions. Direct in situ lysis was applied for extraction of DNA from soil; intracellular DNA was separated from extracellular and used to represent the composition of microflora. The aims were to describe how biochemical and microbiological parameters correlate with topsoil properties in typical Mediterranean Moder humus. Changes in bacterial and fungal community composition were evident from DGGE profiles. Degrees of similarity and clustering correlation coefficients showed that the seasonal conditions may affect the composition and activity of bacterial and fungal communities in the OH horizon, while in the E horizon the two communities were hardly modified. In the same season, OH and E horizons showed a different composition of bacterial and fungal communities and different enzyme activities, suggesting similar behaviour of eubacteria and fungi relatively to all the variables analysed. Evidently, different organic carbon content in soil horizons influenced microflora composition and microbial activities involved in the P and N cycles.

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