Nitrogen removal from on-site treated anaerobic effluents using intermittently aerated moving bed biofilm reactors at low temperature.

On-site post-treatment of anaerobically pre-treated dairy parlour wastewater (DPWWe; 10 degrees C) and mixture of kitchen waste and black water (BWKWe; 20 degrees C) was studied in moving bed biofilm reactors (MBBR). The focus was on removal of nitrogen and of residual chemical oxygen demand (COD). Moreover, the effect of intermittent aeration and continuous vs. sequencing batch operation was studied. All MBBRs removed 50-60% of nitrogen and 40-70% of total COD (CODt). Complete nitrification was achieved, but denitrification was restricted by lack of carbon. Nitrogen removal was achieved in a single reactor by applying intermittent aeration. Continuous and sequencing batch operation provided similar nitrogen and COD removal, wherefore simpler continuous feeding may be preferred for on-site applications. Combination of pre-treating upflow anaerobic sludge blanket (UASB) -septic tank and MBBR removed over 92% of CODt, 99% of biological oxygen demand (BOD7), and 65-70% of nitrogen.

Loss of diversity in wood-inhabiting fungal communities affects decomposition activity in Norway spruce wood.

Hundreds of wood-inhabiting fungal species are now threatened, principally due to a lack of dead wood in intensively managed forests, but the consequences of reduced fungal diversity on ecosystem functioning are not known. Several experiments have shown that primary productivity is negatively affected by a loss of species, but the effects of microbial diversity on decomposition are less studied. We studied the relationship between fungal diversity and the in vitro decomposition rate of slightly, moderately and heavily decayed Picea abies wood with indigenous fungal communities that were diluted to examine the influence of diversity. Respiration rate, wood-degrading hydrolytic enzymes and fungal community structure were assessed during a 16-week incubation. The number of observed OTUs in DGGE was used as a measure of fungal diversity. Respiration rate increased between early- and late-decay stages. Reduced fungal diversity was associated with lower respiration rates during intermediate stages of decay, but no effects were detected at later stages. The activity of hydrolytic enzymes varied among decay stages and fungal dilutions. Our results suggest that functioning of highly diverse communities of the late-decay stage were more resistant to the loss of diversity than less diverse communities of early decomposers. This indicates the accumulation of functional redundancy during the succession of the fungal community in decomposing substrates.

Mycoremediation of wood and soil from an old sawmill area contaminated for decades.

We investigated the potential of white-rot and litter-decomposing fungi for the treatment of soil and wood from a sawmill area contaminated with aged chlorinated phenols, dibenzo-p-dioxins and furans (PCDD/F). Eight screening assays with emphasis on application of non-sterile conditions were carried out in order to select the strains with capability to withstand indigenous microbes and contamination. Nine fungi were then selected for degrading pentachlorophenol (PCP), and 2,3,4,6-tetrachlorophenol (2,3,4,6-TeCP) and mineralizing radiolabelled pentachlorophenol ((14)C-PCP) in non-sterile soil or wood during 15 weeks of incubation. Soil indigenous microbes and fungal inoculated soil (fungal inoculum+indigenous microbes) achieved similar degradation of PCP and 2,3,4,6-TeCP and mineralization of (14)C-PCP. However, the mineralization rate of (14)C-PCP by indigenous microbes was much slower than that boosted by fungal inoculum. The litter-decomposing fungus (LDF) Stropharia rugosoannulata proved to be a suitable fungus for soil treatment. This fungus mineralized 26% of (14)C-PCP and degraded 43% of 2,3,4,6-TeCP and 73% of PCP. Furthermore, S. rugosoannulata attained 13% degradation of PCDD/F (expressed as WHO-Toxic Equivalent). In wood, white-rot fungi grew and degraded chlorophenols better than LDF. No efficient indigenous degraders were present in wood. Interestingly, production of toxic chlorinated organic metabolites (anisoles and veratroles) by LDF in wood was negligible.

Scots pine (Pinus sylvestris) bark composition and degradation by fungi: potential substrate for bioremediation.

The composition of Scots pine bark, its degradation, and the production of hydrolytic and ligninolytic enzymes were evaluated during 90 days of incubation with Phanerochaete velutina and Stropharia rugosoannulata. The aim was to evaluate if pine bark can be a suitable fungal substrate for bioremediation applications. The original pine bark contained 45% lignin, 25% cellulose, and 15% hemicellulose. Resin acids were the most predominant lipophilic extractives, followed by sitosterol and unsaturated fatty acids, such as linoleic and oleic acids. Both fungi degraded all main components of bark, specially cellulose (79% loss by P. velutina). During cultivation on pine bark, fungi also degraded sitosterol, produced malic acid, and oxidated unsaturated fatty acids. The most predominant enzymes produced by both fungi were cellulase and manganese peroxidase. The results indicate that Scots pine bark supports enzyme production and provides nutrients to fungi, thus pine bark may be suitable fungal substrate for bioremediation.