The ecology and functional role of biological soil crusts (BSCs) in arid and semi-arid zones have been extremely well studied. However, little is known about the biochemical properties related to the number and activity of the microbiota that form the crusts, even though information about these properties is very important for understanding many of the processes that affect the formations. In this study, several properties related to the activity and number of microorganisms (biomass-C, basal respiration, dehydrogenase activity and nitrogen mineralization potential) were determined at different depths (crusts, 0-0.5 cm; middle, 0.5-3 cm and deep, 3-5 cm layers) in two types of crusts (predominated by cyanobacteria and by lichens) in the Tabernas desert (Almeria, SE Spain). The absolute values of the above-mentioned properties and the values expressed relative to the total organic carbon (TOC) content were both much higher in the crust layers than in the surface horizons of soils under Mediterranean or Atlantic climates. A large part of the TOC in the BSCs was contained in the microbiota and another large part was readily metabolized during incubation of the crusts for 10 days at 25 °C. The net nitrogen mineralization rate was also high, and ammonification predominated in the crust layers, whereas nitrification predominated in the middle and deep layers. In all types of BSCs, the microbiota colonized the deep layers, although with greater intensity in the lichen-dominated BSCs than in the cyanobacterial BSCs. The results also indicate that hydrolytic enzymes are not stabilized on soil colloids and their activity depends only on the active microbiota.
A laboratory experiment was performed to examine the medium-term influence of three tetracycline antibiotics (chlortetracycline, CTC; tetracycline, TC and oxytetracycline, OTC) at different concentrations in four agricultural soils with similar pH and different soil organic content. After a 42-days incubation period, three different soil enzymes (β-glucosidase, urease, and phosphomonoesterase) were estimated, as well as the phospholipid fatty acids (PLFAs). A residual effect was observed on all microbial parameters measured in the four soils affecting to the soil enzymes activity and soil microbial communities structure (PLFA pattern). A different microbial sensitivity to antibiotics was detected depending on both, soil type and the microbial property considered. Specifically, in general, no antibiotic effect or even a slight positive effect was observed for phosphomonoesterase and β-glucosidase enzyme activities, respectively, while a negative effect was detected for urease activity values, particularly at higher doses of the antibiotics in a soil with a low organic matter content. The principal component analysis performed with the PLFAs data obtained for all soil samples showed different microbial communities depending mainly on soil type, followed by the antibiotic added to the soil (CTC, TC or OTC) and, in a lesser extent, by its concentration. In general, the PLFA patterns showed similar microbial communities structure due to OTC and TC addition in comparison to the microbial communities structure of soil treated with CTC. These results could be environmentally relevant, especially as regards potential effects of antibiotics on the soil microbiome and hence on health risk assessment of these antibiotics in soils.
This work examines the results of a soil incubation experiment in the laboratory, under controlled conditions of humidity and temperature. The purpose was to determine the medium-term influence of the presence of antibiotics on the total and specific microbial biomass, determined by means of the phospholipid fatty acids (PLFAs) analysis (total microbial biomass, and specific fungal, bacterial, actinobacterial, Gram-negative bacterial and Gram-positive bacterial biomass), as well as the relationship between some of these groups (fungal biomass/bacterial biomass, Gram-negative-bacterial /Gram-positive bacterial). The experiment was performed with four different cultivated soils with a similar pH but different organic matter (OM) content, to which eight doses of three antibiotics of the tetracycline group (tetracycline, oxytetracycline and chlorotetracycline) were added. Microbial biomass measurements (total and specific groups) were performed after 42 days of incubation. As expected, the total and specific microbial biomass values were different in the four soils studied. Both the total and the specific microbial biomass showed a similar response to the presence of antibiotics, although in several cases the data were inconsistent and difficult to interpret. In general, in all soils the addition of chlorotetracycline and tetracycline slightly modified or increased, to a greater or lesser extent, the values of both total and specific microbial biomass, particularly at higher doses. However, in certain cases, biomass values decreased due to the addition of the highest dose of oxytetracycline. With regard to fungal/bacterial and Gram<sup>-</sup>bacteria/Gram<sup>+</sup> bacterial biomass ratios, values slightly changed after the addition of the antibiotics.
Afforestation of marginal land has been recommended by the Intergovernmental Panel on Climate Change (IPCC) as a means of enhancing the capacity of soil to act as a carbon (C) sink. However, the success of this practice is variable and depends on many factors, including the type of land management used. In this study, we quantified and compared the C stocks in two highly productive agricultural soils afforested with poplar 10 years before the study and in adjacent soils still used for agricultural purposes. One of the agricultural soils was sown with grass and maize in a crop rotation system and the other was alternately sown with maize (6 months) and left fallow (6 months). In all soils, we estimated the C pools associated with the live biomass (including the C extracted by harvesting in the cropped soils in the 10 years since afforestation), dead biomass, amount of fertiliser added (quantifying all inputs of C added as fertiliser in the cropped soils since the start of afforestation) and the soil organic matter (0–100 cm), to enable estimation of the total C stocks in the ecosystem. Afforestation had different effects on the various C pools. Thus, although afforestation enhanced the C sink capacity of the ecosystem when carried out on agricultural land, the degree to which this occurred varied according to previous land use. The increase in C stocks that occurred from afforestation was lower in the plots employing maize-grass rotation, compared to those with maize-fallow rotation. The ecosystem C balance was quite similar in both afforested plots (247.4 and 233.0 Mg C ha−1), while it was quite different in the cultivated plots (182.3 Mg C ha−1 in Laraño; 73.9 Mg C ha−1 in A Barca). Although at both sites the C balance was higher in the afforested plot than in the cultivated plot, the differences were much smaller in Laraño (65.1 Mg C ha−1 higher in the forested plot than in the cultivated plot) than in A Barca (159.1 Mg C ha−1 higher in the forested plot than in the cultivated plot). Our results from highly productive agricultural land are similar to previous findings on marginal land.
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