Thickness of peat influences the leaching of substances and greenhouse gas emissions from a cultivated organic soil.

The off-site effects of agricultural organic soils include the leaching of N, P, and organic carbon (OC) to watercourses and CO2, CH4, and N2O emissions into the atmosphere. The aim of this study was to quantify how the thickness of organic layers affects these loads. A 19.56-ha experimental field drained by subsurface pipes was established in Ruukki, northwestern Finland. Three plots had a 60-80 cm-thick sedge peat layer and three others had a thickness of 20 cm or less. The drainage pipes lie in mineral soil that, in this field, contains sulfidic material. This study documents the experimental settings and reports on the leaching of substances in the first two years, as well as CO2, CH4 and N2O emissions during eight weeks in one summer. Total N (TN) and OC loads were higher from the thicker peat plots. The mean TN loads during a hydrological year were 15.4 and 9.2 kg ha-1 from the thicker and thinner peat plots, respectively, with organic N representing 36% of TN load. Total P (TP) load averaged 0.27 kg ha-1 yr-1. Dissolved P load represented 63 and 36% of TP in the thicker peat area and only 23 and 13% in the thinner peat area, and was thus increased upon peat thickness. These N and P loads through the subsurface drainage system represented roughly 83% of TN and 64% of TP loads from this field. There were no clear differences in greenhouse gas emissions among the plots during the eight-week monitoring period. Slowly oxidizing sulfide in the subsoil resulted in annual leaching of 147 kg S ha-1, almost ten times that of non-sulfidic soils. Our first results emphasize the effect of the peat thickness on the leaching of substances and warn about considering all organic soils as a single group in environmental assessments.

Nitrogen stocks and flows in an acid sulfate soil.

Besides causing acidification, acid sulfate (AS) soils contain large nitrogen (N) stocks and are a potential source of N loading to waters and nitrous oxide (N2O) emissions. We quantified the stocks and flows of N, including crop yields, N leaching, and N2O emissions, in a cultivated AS soil in western Finland. We also investigated whether controlled drainage (CD) and sub-irrigation (CDI) to keep the sulfidic horizons inundated can alleviate N losses. Total N stock at 0-100 cm (19.5 Mg ha-1) was smaller than at 100-200 cm (26.6 Mg ha-1), and the mineral N stock was largest below 170 cm. Annual N leaching (31-91 kg N ha-1) plus N in harvested grain (74-122 kg N ha-1) was 148% (range 118-189%) of N applied in fertilizers (90-125 kg N ha-1) in 2011-2017, suggesting substantial N supply from soil reserves. Annual emissions of N2O measured during 2 years were 8-28 kg N ha-1. The most probable reasons for high N2O emission rates in AS soils are concomitant large mineral N pools with fluctuating redox conditions and low pH in the oxidized subsoil, all favoring formation of N2O in nitrification and denitrification. Although the groundwater level was higher in CD and CDI than in conventional drainage, N load and crop offtake did not differ between the drainage methods, but there were differences in emissions. Nitrogen flows to the atmosphere and drainage water were clearly larger than those in non-AS mineral soils indicating that AS soils are potential hotspots of environmental impacts.

A multi-scale comparison of dissolved Al, Fe and S in a boreal acid sulphate soil.

Acid sulphate (AS) soils are most prevalent in the tropics, but the acidic discharge from cultivated AS soils also threatens water bodies under boreal conditions. Feasible options to reduce the acid load are needed. In this study, the groundwater of an AS field was monitored for 3.5 years, and the efficiency of waterlogging in mitigating the environmental risks caused by acidic discharge was investigated in a 2.5-year experiment with 10 monolithic lysimeters taken from the same field. In order to unravel the transferability of the results from lysimeters to the field scale, the Al, Fe and S concentrations in discharge water from the lysimeters were compared with those in the groundwater of the AS field (pedon and field scale), and in pore water (pedon and horizon scale). In the waterlogged bare lysimeters (HWB), the Al, Fe and S concentrations in discharge waters were broadly similar to those measured in the groundwater and followed the changes in the pore water. In the waterlogged cropped (reed canary grass, Phalaris arundinacea) lysimeters (HWC), in contrast, the discharge waters were markedly higher in Fe and lower in Al than the groundwater in the field. This outcome was attributable to the reduction of Fe(3+) to the more soluble Fe(2+) and the reduction-induced increase in pH, which enhanced the formation of Al(3+) hydroxy species. Lowering of the water table (LWC) caused soil ripening, which resulted in increased saturated hydraulic conductivity and porosity and enhanced the oxidation of sulphidic materials and acid formation. The responses of Al, Fe and S in drainage waters from HWC and LWC lysimeters resembled previous findings in AS soils. Based on this and the similarity between dissolved element concentrations in the discharge water of HWB lysimeters and groundwater in the field, we conclude that our monolithic lysimeters yielded realistic results concerning the efficiency of various methods in mitigating environmental risks related to cultivated AS soils.

Response of pore water Al, Fe and S concentrations to waterlogging in a boreal acid sulphate soil.

Environmental hazards caused by acid sulphate (AS) soils are of worldwide concern. Among various mitigation measures, waterlogging has mainly been studied in subtropical and tropical conditions. To assess the environmental relevance of waterlogging as a mitigation option in boreal AS soils, we arranged a 2.5-year experiment with monolithic lysimeters to monitor changes in the soil redox potential, pH and the concentrations of aluminium (Al), iron (Fe) and sulphur (S) in pore water in response to low and high groundwater levels in four AS soil horizons. The monoliths consisted of acidic oxidized B horizons and a reduced C horizon containing sulphidic material. Eight lysimeters were cropped (reed canary grass, Phalaris arundinacea) and two were bare without a crop. Waterlogging was conducive to reduction reactions causing a slight rise in pH, a substantial increase in Fe (Fepw) and a decrease in Al (Alpw) in the pore water. The increase in Fepw was decisively higher in the cropped waterlogged lysimeters than in the bare ones, which was attributable to the microbiologically catalysed reductive dissolution of poorly ordered iron oxides and secondary minerals. In contrast to warmer climates, Fepw concentrations remained high throughout the experiment, indicating that the reduction was poised in the iron range, while sulphate was not reduced to sulphide. Therefore, the precipitation of iron sulphide was negligible in the environment with a low pH and abundant with poorly ordered Fe oxides. Increased Fe in pore water counteracts the positive effects of waterlogging, when water is flushed from fields to watercourses, where re-oxidation of Fe causes acidity and oxygen depletion. However, waterlogging prevented further oxidation of sulphidic materials and decreased Alpw to one-tenth of the initial concentrations, and even to one-hundredth of the levels in the low water table lysimeters.

The microbial communities and potential greenhouse gas production in boreal acid sulphate, non-acid sulphate, and reedy sulphidic soils.

Acid sulphate (AS) soils along the Baltic coasts contain significant amounts of organic carbon and nitrogen in their subsoils. The abundance, composition, and activity of microbial communities throughout the AS soil profile were analysed. The data from a drained AS soil were compared with those from a drained non-AS soil and a pristine wetland soil from the same region. Moreover, the potential production of methane, carbon dioxide, and nitrous oxide from the soils was determined under laboratory conditions. Direct microscopic counting, glucose-induced respiration (GIR), whole cell hybridisation, and extended phospholipid fatty acid (PLFA) analysis confirmed the presence of abundant microbial communities in the topsoil and also in the deepest Cg2 horizon of the AS soil. The patterns of microbial counts, biomass and activity in the profile of the AS soil and partly also in the non-AS soil therefore differed from the general tendency of gradual decreases in soil profiles. High respiration in the deepest Cg2 horizon of the AS soil (5.66 µg Cg(-1)h(-1), as compared to 2.71 µg Cg(-1)h(-1) in a top Ap horizon) is unusual but reasonable given the large amount of organic carbon in this horizon. Nitrous oxide production peaked in the BCgc horizon of the AS and in the BC horizon of the non-AS soil, but the peak value was ten-fold higher in the AS soil than in the non-AS soil (82.3 vs. 8.6 ng Ng(-1)d(-1)). The data suggest that boreal AS soils on the Baltic coast contain high microbial abundance and activity. This, together with the abundant carbon and total and mineral nitrogen in the deep layers of AS soils, may result in substantial gas production. Consequently, high GHG emissions could occur, for example, when the generally high water table is lowered because of arable farming.