Through litter decomposition enormous amounts of carbon is emitted to the atmosphere. Numerous large-scale decomposition experiments have been conducted focusing on this fundamental soil process in order to understand the controls on the terrestrial carbon transfer to the atmosphere. However, previous studies were mostly based on site-specific litter and methodologies, adding major uncertainty to syntheses, comparisons and meta-analyses across different experiments and sites. In the TeaComposition initiative, the potential litter decomposition is investigated by using standardized substrates (Rooibos and Green tea) for comparison of litter mass loss at 336 sites (ranging from -9 to +26 °C MAT and from 60 to 3113 mm MAP) across different ecosystems. In this study we tested the effect of climate (temperature and moisture), litter type and land-use on early stage decomposition (3 months) across nine biomes. We show that litter quality was the predominant controlling factor in early stage litter decomposition, which explained about 65% of the variability in litter decomposition at a global scale. The effect of climate, on the other hand, was not litter specific and explained <0.5% of the variation for Green tea and 5% for Rooibos tea, and was of significance only under unfavorable decomposition conditions (i.e. xeric versus mesic environments). When the data were aggregated at the biome scale, climate played a significant role on decomposition of both litter types (explaining 64% of the variation for Green tea and 72% for Rooibos tea). No significant effect of land-use on early stage litter decomposition was noted within the temperate biome. Our results indicate that multiple drivers are affecting early stage litter mass loss with litter quality being dominant. In order to be able to quantify the relative importance of the different drivers over time, long-term studies combined with experimental trials are needed.

Fluorescent tetracationic porphyrin (TMPyP) molecules have been incorporated into optically transparent TiO(2) thin films acting as a host material. The films, with a columnar structure and open pores, were prepared by electron evaporation at glancing angles (GAPVD). The open porosity of the films has been estimated by measuring a water adsorption isotherm with a quartz crystal monitor. TMPyP molecules were infiltrated in the host thin films by their immersion into water solutions at controlled values of pH. The state of the adsorbed molecules, the infiltration efficiency, and the adsorption kinetics were assessed by analyzing the optical response of the films by UV-vis absorption and fluorescence techniques. The infiltration efficiency was directly correlated with the acidity of the medium, increasing at basic pHs as expected from simple considerations based on the concepts of the point of zero charge (PZC) developed for colloidal oxides. By a quantitative evaluation based on the analysis of the UV spectra, the infiltration process has been described by a Langmuir type adsorption isotherm and an Elovich-like kinetics. The accessibility of the infiltrated molecules in the TMPyP/TiO(2) composite films is assessed by following the changes of their optical properties when exposed to the acid vapors and their subsequent recovery with time.

a b s t r a c tTetracationic porphyrin (TMPyP) molecules were incorporated into an optically transparent TiO 2 thin film, prepared by Glancing Angle Physical Vapour Deposition (GAPVD), by simple infiltration (at pH 6.4). The preparation of optically transparent TMPyP/TiO 2 composite thin films provides a method for the integration of the porphyrin molecules into photonic devices for direct monitoring of gases. Previously, UV-visible and fluorescence spectral techniques have been used to study the reversible protonation of TMPyP in aqueous solution. The optical spectrum of TMPyP shows an intense Soret band at 423 nm with a 22 nm red shift upon protonation by HCl. The experimental conditions for monitoring the concentration of HCl gas by absorption spectroscopy have been optimized. The maximum absorbance change was observed at the Soret band wavelength. A selected temperature of 80 • C and a 300 s recovery period were found to be the optimum operating parameters (response time t 50 = 16.8 ± 0.7 s). The composite with smaller surface concentration of TMPyP ( = 0.3 × 10 −9 mol cm −2 ) presented the best detection limit (0.1 ppm). The response of the composite sensor was highly stable for several months.