18 research outputs found
Iron flocculation stimulates biogas production in Microthrix parvicella-spiked wastewater sludge
Municipal wastewater sludge has been used for fertiliser and biogas production for several decades. Chemical compounds such as iron and aluminium are common coagulants used in wastewater treatment plants to remove suspended solids, phosphorus and micro-organisms. This laboratory study explores whether ferric chloride (FeCl3 as PIX-111) or aluminium chloride (AlCl3 as PAX-18) flocculation could stimulate biogas production in wastewater sludge contaminated with Microthrix parvicella. In a fermentation process run in three replicates, cumulative methane production was in average about 25 % higher using the iron flocculated sludge than using the aluminium flocculated sludge; this difference was statistically significant (P\0.05) in the subsequent runs of the semi-continuous process. In all runs, the iron flocculated sludge produced less (P\0.05) hydrogen sulphide in the biogas than the aluminium flocculated sludge. The numbers of M. parvicella stayed at the similar levels throughout the process. It is concluded that biogas production is higher and more stable with iron coagulant in comparison with aluminium coagulant, presumably due to the reduced formation of hydrogen sulphide. Thus, iron coagulants seem to be better than aluminium coagulants to stimulate the methane production process. Both coagulants significantly suppressed multiplication of M. parvicella in the biogas reactor, i.e. they did not evoke foaming in this experiment
Denitrification is the major nitrous acid production pathway in boreal agricultural soils
Abstract
Nitrous acid (HONO) photolysis produces hydroxyl radicals—a key atmospheric oxidant. Soils are strong HONO emitters, yet HONO production pathways in soils and their relative contributions are poorly constrained. Here, we conduct ¹⁵N tracer experiments and isotope pool dilution assays on two types of agricultural soils in Finland to determine HONO emission fluxes and pathways. We show that microbial processes are more important than abiotic processes for HONO emissions. Microbial nitrate reduction (denitrification) considerably exceeded ammonium oxidation as a source of nitrite—a central nitrogen pool connected with HONO emissions. Denitrification contributed 97% and 62% of total HONO fluxes in low and high organic matter soil, respectively. Microbial ammonium oxidation only produced HONO in high organic matter soil (10%). Our findings indicate that microbial nitrate reduction is an important HONO production pathway in aerobic soils, suggesting that terrestrial ecosystems favouring it could be HONO emission hotspots, thereby influencing atmospheric chemistry
A review of the importance of mineral nitrogen cycling in the plant-soil-microbe system of permafrost-affected soils-changing the paradigm.
The paradigm that permafrost-affected soils show restricted mineral nitrogen (N) cycling in favor of organic N compounds is based on the observation that net N mineralization rates in these cold climates are negligible. However, we find here that this perception is wrong. By synthesizing published data on N cycling in the plant-soil-microbe system of permafrost ecosystems we show that gross ammonification and nitrification rates in active layers were of similar magnitude and showed a similar dependence on soil organic carbon (C) and total N concentrations as observed in temperate and tropical systems. Moreover, high protein depolymerization rates and only marginal effects of C:N stoichiometry on gross N turnover provided little evidence for N limitation. Instead, the rather short period when soils are not frozen is the single main factor limiting N turnover. High gross rates of mineral N cycling are thus facilitated by released protection of organic matter in active layers with nitrification gaining particular importance in N-rich soils, such as organic soils without vegetation. Our finding that permafrost-affected soils show vigorous N cycling activity is confirmed by the rich functional microbial community which can be found both in active and permafrost layers. The high rates of N cycling and soil N availability are supported by biological N fixation, while atmospheric N deposition in the Arctic still is marginal except for fire-affected areas. In line with high soil mineral N production, recent plant physiological research indicates a higher importance of mineral plant N nutrition than previously thought. Our synthesis shows that mineral N production and turnover rates in active layers of permafrost-affected soils do not generally differ from those observed in temperate or tropical soils. We therefore suggest to adjust the permafrost N cycle paradigm, assigning a generally important role to mineral N cycling. This new paradigm suggests larger permafrost N climate feedbacks than assumed previously
Thawing Yedoma permafrost is a neglected nitrous oxide source
In contrast to the well-recognized permafrost carbon (C) feedback to climate change, the fate of permafrost nitrogen (N) after thaw is poorly understood. According to mounting evidence, part of the N liberated from permafrost may be released to the atmosphere as the strong greenhouse gas (GHG) nitrous oxide (N2O). Here, we report post-thaw N2O release from late Pleistocene permafrost deposits called Yedoma, which store a substantial part of permafrost C and N and are highly vulnerable to thaw. While freshly thawed, unvegetated Yedoma in disturbed areas emit little N2O, emissions increase within few years after stabilization, drying and revegetation with grasses to high rates (548 (133–6286) μg N m−2 day−1; median with (range)), exceeding by 1–2 orders of magnitude the typical rates from permafrost-affected soils. Using targeted metagenomics of key N cycling genes, we link the increase in in situ N2O emissions with structural changes of the microbial community responsible for N cycling. Our results highlight the importance of extra N availability from thawing Yedoma permafrost, causing a positive climate feedback from the Arctic in the form of N2O emissions