Photoactive titanium dioxide nanoparticles modify heterotrophic microbial functioning

Environmental Science and Pollution Research - Nanoparticulate titanium dioxide (nTiO2) is frequently applied, raising concerns about potential side effects on the environment. While various...     

Temperature sensitivity of the turnover times of soil organic matter in forests.

Soils represent the largest carbon pool in the terrestrial biosphere, and climate change might affect the main carbon fluxes associated with this pool. These fluxes are the production of aboveground litter and root litter, and decomposition of the soil organic matter (SOM) pool by soil microorganisms. Knowledge about the temperature sensitivity of the decomposition of different SOM fractions is crucial in order to understand how climate change might affect carbon storage in soils. In this study, the temperature sensitivity of the turnover times of three different SOM fractions (labile, intermediate, and stabilized) was investigated for 11 forest sites along a temperature gradient. Carbon-14 isotope analyses of the SOM fractions combined with a model provided estimates of their turnover times. The turnover times of the labile SOM fraction were not correlated with mean annual soil temperature. Therefore it was not possible to estimate temperature sensitivity for the labile SOM fraction. Given considerable evidence elsewhere for significant temperature sensitivities of labile SOM, lack of temperature sensitivity here most likely indicates limitations of the applied methodology for the labile SOM fraction. The turnover times of the intermediate and the stabilized SOM fractions were both correlated with mean annual soil temperatures. The temperature sensitivity of the stabilized SOM fraction was at least equal to that of the intermediate SOM fraction and possibly more than twice as high. A correction for confounding effects of soil acidity and clay content on the temperature sensitivities of the intermediate and stabilized SOM fractions was included in the analysis. The results as observed here for the three SOM fractions may have been influenced by (1) modeling assumptions for the estimation of SOM turnover times of leaf and needle longevities, constant annual carbon inputs, and steady-state SOM pools, (2) the occurrence of summer drought at some sites, (3) differences between sites in quality of the SOM fractions, or (4) the relatively small temperature range. Our results suggested that a 1 degree C increase in temperature could lead to decreases in turnover times of 4-11% and 8-16%, for the intermediate and stabilized SOM fractions, respectively.     

Phytoremediation and sequestration of soil metals using the CRISPR/Cas9 technology to modify plants: a review

Environmental Chemistry Letters - Soil contamination by toxic metals is a major health issue that could be partly solved by using genetically-modified plants. For that, the recently developed...     

Nitration and hydroxylation of benzene in the presence of nitrite/nitrous acid in aqueous solution

This paper studies the nitration and hydroxylation of benzene in the presence of nitrite/nitrous acid in aqueous solution, both in the dark upon addition of hydrogen peroxide and under 360 nm irradiation. In both cases the detected transformation intermediates were phenol (P), nitrobenzene (NB), 2-nitrophenol (2NP) and 4-nitrophenol (4NP). P and NB directly form from benzene, and the initial formation rate of P is at least an order of magnitude higher than that of NB. In our experiments nitrophenols arise from P nitration, as can be inferred by their time evolution and isomer ratio (2NP:4NP=60:40, 3NP below detection limit). Nitrophenols may also form upon hydroxylation of NB, but in a different ratio (2NP:3NP:4NP=45:30:25). The detection of 3NP is thus a marker for the hydroxylation of NB, since this isomer is not formed in P nitration processes. The formation rates of P and NB increase with decreasing pH, both in the presence of HNO₂ + H₂O₂ in the dark (which produce HOONO) and in the presence of NO₂⁻/HNO₂ under irradiation. In the former case the pH dependence reflects the formation rate of HOONO. In the case of the irradiation experiments the pH effect can be accounted for by the higher molar absorbivity and photolysis quantum yield of nitrous acid when compared with nitrite. Interestingly, benzene does not react with HNO₂ alone in the dark. An important feature of benzene nitration in the presence of NO₂⁻/HNO₂ under irradiation is that the process is not inhibited by the addition of hydroxyl scavengers, differently from the case of phenol nitration. This finding indicates that nitrite irradiation might lead to the nitration of certain aromatic compounds in natural waters even in the presence of natural hydroxyl scavenging agents, which are usually thought to limit the environmental role of many photochemical processes.     

Ecotoxicologial evaluation of wastewater ozonation based on detritus-detritivore interactions

Advanced oxidation technologies such as ozonation have been proposed to improve removal efficiency of micropollutants during wastewater treatment. In a meta-analysis of peer-reviewed literature, we found no ecotoxicological effects of wastewater ozonation on invertebrates (n = 82), but significant adverse effects on bacteria (n = 24) and fish (n = 5). As information on functional endpoints or trophic interactions is lacking, we applied a bioassay relating to leaf litter decomposition to fill this gap. Leaf discs exposed to ozone-treated wastewater with a high (1.04 mg O₃ (mg DOC)⁻¹, n = 49) ozone concentration were significantly preferred by an aquatic detritivore, Gammarus fossarum, over discs conditioned in wastewater not treated with ozone. This effect might have been mediated by reduced bacterial and elevated fungal biomass, and appears to be the first demonstration of wastewater ozonation impacts on invertebrates and an associated ecosystem process. In accordance with the food-choice trials, chemical analyses revealed significantly decreased concentrations of organic micropollutants in wastewater treated with ozone at high concentrations. Thus, food-choice trials as applied here hold promise to assess environmental effects of advanced oxidation technologies in wastewater treatment and appear to be a valuable complement to the ecotoxicological toolbox in general.     

Tracing the fate of PCBs in forest ecosystems

Forests were shown to play an important role in influencing atmospheric concentrations and transport of persistent organic pollutants (POPs) in the environment. World forests cover more than 4 billion hectares and contain up to 80% of the above ground organic carbon. Given the lipophilic nature of POPs, this suggests that forests can influence the environmental fate of POPs at a global scale. POP accumulation in forest canopies still presents points of concern given the complexity of these ecosystems. In particular, the role of ecological parameters such as LAI (leaf area index) and SLA (specific leaf area) and their dynamics during the growing season was not sufficiently investigated yet. This paper reviews, compares and interprets a unique case study in which air and leaf concentrations and deposition fluxes for selected polychlorinated biphenyls (PCBs) were measured in three different forest types exposed to the same air masses. In order to trace the air-leaf-soil path of these compounds, a dynamic model of POP accumulation into forest canopy was applied. The dynamics of the canopy biomass strongly affected the trend of leaf concentration with time. Growth dilution effect can prevent the more chlorinated compounds from reaching the partitioning equilibrium before litter fall, while the more volatile compounds can approach equilibrium in the range of few weeks. An amount of up to 60 ng of PCBs per square metre of ground surface was predicted to be stored in each of the selected forests at fully developed canopy. Dry gaseous deposition fluxes to forest canopy were estimated to reach a maximum value of about 0.5-1.5 ng m(-2) d(-1) during the spring period.     

Effects of nano-TiO(2) in combination with ambient UV-irradiation on a leaf shredding amphipod

Production and use of engineered nanoparticles, such as titanium dioxide nanoparticles (nTiO₂), is increasing worldwide, enhancing their probability to enter aquatic environments. However, direct effects of nTiO₂ as well as ecotoxicological consequences due to the interactions of nTiO₂ with environmental factors like ultraviolet (UV) irradiation on representatives of detrital food webs have not been assessed so far. Hence, the present study displayed for the first time adverse sublethal effects of nTiO₂ at concentrations as low as 0.2 mg L⁻¹ on the leaf shredding amphipod Gammarus fossarum both in presence and absence of ambient UV-irradiation following a 7-d exposure. In absence of UV-irradiation, however, the effects seemed to be driven by accumulation of nTiO₂ at the bottom of the test vessels to which the gammarids were potentially exposed. The adverse sublethal and lethal effects on gammarids caused by the combined application of nTiO₂ and ambient UV-irradiation are suggested to be driven by the formation of reactive oxygen species. In conclusion, both the accumulation of nTiO₂ at the bottom of the test vessel and the UV induced formation of reactive oxygen species clearly affected its ecotoxicity, which is recommended for consideration in the environmental risk assessment of nanoparticles.