Real-time quantification of mcrA, pmoA for methanogen, methanotroph estimations during composting

Composting is the controlled biological decomposition of organic matter by microorganisms during predominantly aerobic conditions. It is being increasingly adopted due to its benefits in nutrient recycling, soil reclamation, and urban land use. However, it poses an environmental concern related to its contribution to greenhouse gas production. During composting, activities of methanogenic and methanotrophic communities influence the net methane (CH4) release into the atmosphere. Using quantitative polymerase chain reaction (qPCR), this study was aimed at assessing the changes in the methyl-coenzyme M reductase (mcrA) and particulate methane monooxygenase (pmoA) copy numbers for estimation of methanogenic and methanotrophic communities, respectively. Open-windrow composting of beef cattle (Bos Taurus L.) manure with temperatures reaching > 55 degrees C was effective indegrading commensal Escherichia coli within the first week. Quantification of community DNA revealed significant differences in mcrA and pmoA copy numbers between top and middle sections. Consistent mcrA copy numbers (7.07 to 8.69 log copy number g(-1)) were detected throughout the 15-wk composting period. However, pmoA copy number varied significantly over time, with higher values during Week 0 and 1 (6.31 and 5.41 log copy number g(-1), respectively) and the lowest at Week 11 (1.6 log copy number g(-1)). Net surface CH4 emissions over the 15-wk period were correlated with higher mcrA copy number. Higher net ratio of mrA: pmoA copy numbers was observed when surface CH4 flux was high. Our results indicate that mcrA and pmoA copy numbers vary during composting and that methanogen and methanotroph populations need to be examined in conjunction with net CH4 emissions from open-windrow composting of cattle feedlot manure.     

Inactivation of Ascaris suum in a biodrying compost system

Pathogen contamination of waterways is a serious concern in dairy farming areas where livestock waste is applied to agricultural fields. As an alternative, a biodrying composting system dries collected livestock waste, reduces the strong odors, and has been proposed as a means of reducing, and even eliminating pathogens present in the waste. Therefore, the survival of pathogens in a biodrying composting system was investigated. Dairy farm livestock waste was piled in a biodrying storage shed where forced aeration and natural decomposition processes heated a major portion of the waste pile to temperatures exceeding 55 degrees C. Ascaris suum eggs were used as the surrogate species and inoculated into special chambers and placed at three different elevations at different intervals along the length of the pile. Control chambers were stored in water at 4 degrees C in the laboratory. Both compost and control chambers were removed at Day 4, 8, 12, 16, and 20. The eggs were extracted from the chamber medium and analyzed for viability. No viable eggs were recovered from any of the chambers removed from the compost pile, while >or=90% viability was observed in the control chambers. High temperatures and continued drying were the major contributing factors to the inactivation of the helminth eggs. The complete inactivation of A. suum eggs by the biodrying process encourages the storage and treatment of manure to high temperatures and reduced moisture conditions before field spreading to reduce the risk of harmful pathogens contaminating waterways and potential drinking water supplies.     

Carbon, nitrogen balances and greenhouse gas emission during cattle feedlot manure composting

Carbon and N losses reduce the agronomic value of compost and contribute to greenhouse gas (GHG) emissions. This study investigated GHG emissions during composting of straw-bedded manure (SBM) and wood chip-bedded manure (WBM). For SBM, dry matter (DM) loss was 301 kg Mg(-1), total carbon (TC) loss was 174 kg Mg(-1), and total nitrogen (TN) loss was 8.3 kg Mg(-1). These correspond to 30.1% of initial DM, 52.8% of initial TC, and 41.6% of initial TN. For WBM, DM loss was 268 kg Mg(-1), TC loss was 154 kg Mg(-1), and TN loss was 1.40 kg Mg(-1), corresponding to 26.5, 34.5, and 11.8% of initial amounts. Most C was lost as CO2 with CH4 accounting for <6%. However, the net contribution to greenhouse gas emissions was greater for CH4 since it is 21 times more effective at trapping heat than CO2. Nitrous oxide (N2O) emissions were 0.077 kg N Mg(-1) for SBM and 0.084 kg N Mg(-1) for WBM, accounting for 1 to 6% of total N loss. Total GHG emissions as CO2-C equivalent were not significantly different between SBM (368.4 +/- 18.5 kg Mg(-1)) and WBM (349.2 +/- 24.3 kg Mg(-1)). However, emission of 368.4 kg C Mg(-1) (CO2-C equivalent) was greater than the initial TC content (330.5 kg Mg(-1)) of SBM, raising the question of the net benefits of composting on C sequestration. Further study is needed to evaluate the impact of composting on overall GHG emissions and C sequestration and to fully investigate livestock manure management options.     

Veterinary antimicrobials in feedlot manure: dissipation during composting and effects on composting processes

Composting of manure may lead to the degradation of veterinary antimicrobials, but it is largely unknown if the presence of antimicrobials affects the composting process. Open-air windrow composting of manure from beef cattle (Bos taurus) administered chlortetracycline, sulfamethazine, and tylosin was investigated in a 2-yr study. At windrow construction, chlortetracycline had extensively isomerized to iso-chlortetracycline. Sulfamethazine, tylosin, and iso-chlortetracycline dissipated by first-order kinetics, whereas the dissipation of enol/keto-chlortetracycline was better described by exponential equations. At the end of the composting period, proportions of antimicrobials remaining were as follows: iso-chlortetracycline (< 1%), chlortetracycline (1 to 4.5%), tylosin (6.3%), and sulfamethazine (6.8% [2005], 41% [2006]). Times for 50% dissipation (DT50) decreased in the order: tylosin (20.3 to 43.5 d) > iso-chlortetracycline (13.5 to 26.5 d) > enol/keto-chlortetracycline (5.5 to 9.8 d). The DT50 values for sulfamethazine varied from 26.8 d in 2005 to 237 d in 2006. Treatments with chlortetracycline showed significantly reduced temperature rises (10.1 to 11.0 degrees C) between Days 21 to 28 in 2006 compared with rises of 26.6 to 31.0 degrees C for control and tylosin treatments, suggesting an inhibition of microbial activity. During composting in 2005, manure from cattle administered chlortetracycline at 44 mg kg(-1) of feed lost significantly less dry matter, carbon, and nitrogen than manure from cattle fed 11 mg chlortetracycline kg(-1) of feed, implying that the higher level of chlortetracycline inhibited microbial decomposition of organic matter. The study shows that while composting leads to dissipation of antimicrobials, the microbially driven composting process may be inhibited by their presence.     

Carbon monoxide from composting due to thermal oxidation of biomass

Emissions of carbon monoxide (CO) were observed from decomposing organic wastes and litter under laboratory, pilot composting plant, and natural conditions. Field studies included air from inside a compost heap of about 200 m3, emissions from composting of livestock wastes at a biologically operating farm, and leaf litter pile air samples. The concentration of CO was up to 120 micromol mol(-1) in the compost piles of green waste, and up to 10 micromol mol(-1) in flux chambers above livestock waste windrow composts. The mean CO flux rates were approximately 20 mg CO m(-2) h(-1) for compost heaps of green waste, and varied from 30 to 100 mg CO m(-2) h(-1) for fresh dung windrows. Laboratory studies using a temperature and ventilation-controlled substrate container were performed to elucidate the origin of CO, and included hay samples of fixed moisture content at temperatures between 5 and 65 degrees C, including nonsterilized as well as sterilized samples. The concentration of CO was up to 160 micromol mol(-1) in these experiments, and Arrhenius-type plot analyses resulted in activation energies of 65 kJ mol(-1) for thermochemically produced CO from the nonsterilized compost substrate. Sterilized samples showed dramatically reduced CO2 but virtually unchanged CO emissions, albeit at a slightly lower activation energy, likely a result of the high-temperature sterilization. Though globally and regionally these CO emissions are only a minor source, thermochemically produced CO emissions might affect local air quality in and near composting facilities.     

The effect of phosphogypsum on greenhouse gas emissions during cattle manure composting

Phosphogypsum (PG), a by-product of the phosphate fertilizer industry, reduces N losses when added to composting livestock manure, but its impact on greenhouse gas emissions is unclear. The objective of this research was to assess the effects of PG addition on greenhouse gas emissions during cattle feedlot manure composting. Sand was used as a filler material for comparison. The seven treatments were PG10, PG20, PG30, S10, S20, and S30, representing the rate of PG or sand addition at 10, 20, or 30% of manure dry weight and a check treatment (no PG or sand) with three replications. The manure treatments were composted in open windrows and turned five times during a 134-d period. Addition of PG significantly increased electrical conductivity (EC) and decreased pH in the final compost. Total carbon (TC), total nitrogen (TN), and mineral nitrogen contents in the final composted product were not affected by the addition of PG or sand. From 40 to 54% of initial TC was lost during composting, mostly as CO(2), with CH(4) accounting for <14%. The addition of PG significantly reduced CH(4) emissions, which decreased exponentially with the compost total sulfur (TS) content. The emission of N(2)O accounted for <0.2% of initial TN in the manure, increasing as compost pH decreased from alkaline to near neutral. Based on the total greenhouse gas budget, PG addition reduced greenhouse gas emissions (CO(2)-C equivalent) during composting of livestock manure by at least 58%, primarily due to reduced CH(4) emission.     

Environmental assessment of two home composts with high and low gaseous emissions of the composting process

A Life Cycle Assessment (LCA) of two home composts with low and high gaseous emissions of the composting process is presented. The study focused on the gaseous emissions of the composting process. Gaseous emissions of methane, nitrous oxides, ammonia and volatic organic compounds of the composting process were experimentally measured in field real trials. The results showed that the differences in gaseous emissions between the two home composts were 4.5, 5.8 and 52 for methane, nitrous oxides and ammonia, respectively. Higher emissions of nitrous oxides and methane affected significantly the category of global warming potential, while higher emissions of ammonia affected mainly the categories of acidification potential, eutrophication potential and photochemical oxidation. The differences found in the compost emissions were attributable to the composting production management (quality and composition of waste stream, frequency mixing of waste, humidity and temperature monitoring, among others) as well as weather conditions (temperature and humidity).     

Spectroscopic and wet chemical characterization of solid waste organic matter of different age in landfill sites, southern Germany

Landfill sites are potential sources of hazardous emissions by degradation and transformation processes of waste organic matter. Its chemical composition and microbial degradability are key factors for risk management, after-care, and estimation of potential emissions. The aim of the study is to provide information about composition and extent of transformation of waste organic matter in four landfill sites in Bavaria, Southern Germany by means of (13)C NMR spectroscopy, acid-hydrolyzable carbohydrates, chloroform-methanol extractable lipids, acid-hydrolyzable proteins, and lignin compounds after CuO oxidation. Ten samples of about 20 to 25 yr, 15 to 20 yr, and 5 to 10 yr of deposition each were taken at 2 m depth intervals by grab drilling till 10-m depth. Increasing temperatures from about 15 degrees C at 2-m depth to >40 degrees C at 10-m depth are found at some of the sites, representing optimum conditions for mesophile methane bacteria. Moisture contents of 160 to 310 g kg(-1) (oven dry), however, provide limiting conditions for anaerobic biodecay. Spectroscopic and chemical variables generally indicate a low extent of biodegradation and transformation at all sites despite a considerable heterogeneity of the samples. Independent of the time and depth of deposition more than 50% of the carbohydrate fraction of the waste organic matter provide a high potential for methane emissions and on-site energy production. There was no significant accumulation of long-chain organic and aromatic compounds, and of lignin degradation products even after more than 25 yr of rotting indicating higher extent of decomposition or stabilization of the waste organic matter. Installation of seepage water cleaning and recirculation systems are recommended to increase suboptimal moisture contents with respect to microbial methanogenesis, energy production, and long-term stabilization of municipal solid waste.     

不同菌剂处理下猪粪和牛粪堆肥前期性质变化

以猪粪和牛粪为堆肥原料,设计了人工接种MixF-3菌剂堆肥、添加灭活菌剂堆肥和自然堆肥3个处理进行堆肥前期实验,探讨堆肥9d过程中温度、水分、有机碳、全氮和微生物量碳等参数的变化。结果表明,按1L/t接种MixF-3混合菌剂堆肥温度升温快,猪粪堆肥第48h和第84h时温度分别达到66℃和71.5℃,牛粪堆肥第48h时温度达69℃,明显高于灭活菌剂处理组和CK对照组。随着堆肥的进行,各处理组水分含量缓慢下降,牛粪比猪粪含水量略高。人工接种菌剂的猪粪和牛粪堆肥处理组中pH变化幅度小,有机碳碳含量的下降幅度比灭活组和自然堆肥组大,分别下降15.64%和11.25%,全氮含量缓慢升高但变化不大,人工接种牛粪比猪粪处理组中堆肥全氮含量升幅高;在猪粪和牛粪堆肥中人工接种菌剂微生物量碳降幅最小,分别为9537μg/g和3212μg/g,表明在猪粪和牛粪堆肥原料中添加MixF-3复合菌剂有利于微生物繁殖生长,同时拓宽了菌剂使用的单一性,更具有普遍性意义。     

Biological degradation and greenhouse gas emissions during pre-storage of liquid animal manure

Storage of manure makes a significant contribution to global methane (CH4) emissions. Anaerobic digestion of pig and cattle manure in biogas reactors before outside storage might reduce the potential for CH4 emissions. However, manure pre-stored at 15 to 20 degrees C in buildings before anaerobic digestion may be a significant source of CH4 and could reduce the potential CH4 production in the biogas reactor. Degradation of energy-rich organic components in slurry and emissions of CH4 and carbon dioxide (CO2) from aerobic and anaerobic degradation processes during pre-storage were examined in the laboratory. Newly mixed slurry was added to vessels and stored at 15 and 20 degrees C for 100 to 220 d. During storage, CH4 and CO2 emissions were measured with a dynamic chamber technique. The ratio of decomposition in the subsurface to that at the surface indicated that the aerobic surface processes contributed significantly to CO2 emission. The measured CH4 emission was used to calculate the methane conversion factor (MCF) in relation to storage time and temperature, and the total carbon-C emission was used to calculate the decrease in potential CH4 production by anaerobic digestion following pre-storage. The results show substantial methane and carbon dioxide production from animal manure in an open fed-batch system kept at 15 to 20 degrees C, even for short storage times, but the influence of temperature was not significant at storage times of <30 d. During long-term storage (90 d), a strong influence of temperature on the MCF value, especially for pig manure, was observed.     

Effect of chemical and microbial amendments on ammonia volatilization from composting poultry litter

Research has shown that aluminum sulfate (alum) and phosphoric acid greatly reduce ammonia (NH3) volatilization from poultry litter; however, no studies have yet reported the effects of these amendments on field-scale composting of poultry litter. The objectives of this study were to (i) evaluate NH3 volatilization from composting litter by measuring both NH3 volatilization and changes in total nitrogen (N) in the litter and (ii) evaluate potential methods of reducing NH3 losses from composting poultry litter. Poultry litter was composted for 68 d the first year and 92 d the second year. Eleven treatments were screened in Year 1, which included an unamended control, a microbial mixture, a microbial mixture with 5% alum incorporated into the litter, 5 and 10% alum rates either surface-applied or incorporated, and 1 and 2% phosphoric acid rates either surface-applied or incorporated. Treatments in Year 2 included an unamended control, a microbial mixture, alum (7% by fresh wt.), and phosphoric acid (1.5% by fresh wt.). Alum and phosphoric acid reduced NH3 volatilization from composting poultry litter by as much as 76 and 54%, respectively. The highest NH3 emission rates were from microbial treatments each year. Compost treated with chemical amendments retained more initial N than all other treatments. Due to the cost and N loss associated with composting poultry litter, composting is not economical from an agronomic perspective compared with the use of fresh poultry litter.     

Monitoring and optimizing the co-composting of dewatered sludge: a mixture experimental design approach

The management of dewatered wastewater sludge is a major issue worldwide. Sludge disposal to landfills is not sustainable and thus alternative treatment techniques are being sought. The objective of this work was to determine optimal mixing ratios of dewatered sludge with other organic amendments in order to maximize the degradability of the mixtures during composting. This objective was achieved using mixture experimental design principles. An additional objective was to study the impact of the initial C/N ratio and moisture contents on the co-composting process of dewatered sludge. The composting process was monitored through measurements of O(2) uptake rates, CO(2) evolution, temperature profile and solids reduction. Eight (8) runs were performed in 100 L insulated air-tight bioreactors under a dynamic air flow regime. The initial mixtures were prepared using dewatered wastewater sludge, mixed paper wastes, food wastes, tree branches and sawdust at various initial C/N ratios and moisture contents. According to empirical modeling, mixtures of sludge and food waste mixtures at 1:1 ratio (ww, wet weight) maximize degradability. Structural amendments should be maintained below 30% to reach thermophilic temperatures. The initial C/N ratio and initial moisture content of the mixture were not found to influence the decomposition process. The bio C/bio N ratio started from around 10, for all runs, decreased during the middle of the process and increased to up to 20 at the end of the process. The solid carbon reduction of the mixtures without the branches ranged from 28% to 62%, whilst solid N reductions ranged from 30% to 63%. Respiratory quotients had a decreasing trend throughout the composting process.     

Weed seed viability in composted beef cattle feedlot manure

Manure composting has gained increased acceptance by the beef cattle (Bos taurus) feedlot industry in southern Alberta, Canada. Unlike fresh manure, compost is often promoted as being "weed-free." Studies were conducted with five weed species in 1997 and thirteen in 1999 to examine the effect of feedlot manure composting on weed seed viability. Weed seeds were buried in open-air compost windrows and recovered at various times during the thermophilic phase of composting. Windrow temperature and water contents were also measured. Germinability was zero for all composted weed seeds at all sampling times in 1997. However, some seeds remained viable (positive tetrazolium test denoting respiration) on Day 70. In 1999, only one of the thirteen species retained germinability on Day 21 and only two species had respiring seeds on Day 42. Time-viability relationships during composting were defined by exponential decay models. Lethal temperatures to eliminate viability was species-dependent. In 1999, four weed species were killed in the initial 7 d of composting at a lethal temperature of 39 degrees C while temperatures of > 60 degrees C were required for two species. Regression analysis on weed seed viability versus windrow temperature resulted in significant R2 values, which showed that only 17 to 29% of the variation in viability was accounted for by temperature. The lack of definitive relationships between temperature and weed seed viability demonstrated that factors other than temperature may play a role in eliminating weed seeds during composting.     

Spatial variation in 2-methyl-4-chlorophenoxyacetic acid mineralization and sorption in a sandy soil at field level

The phenoxyacetic acid herbicide MCPA (2-methyl-4-chlorophenoxyacetic acid) is frequently detected in groundwater beneath Danish agricultural fields. We investigated spatial variation in microbial MCPA mineralization potential in a flat agricultural field of fine sandy soil (USDA classification: Humic Dystrudept) located on the Yoldia plains of Northern Jutland, Denmark. Samples for determination of MCPA mineralization and sorption were collected from the Ap and Bs horizons at 51 sampling sites located in a 200 x 220 m grid. Spatial variation in sorption was low in both horizons (distribution coefficient, 0.36-4.16 L kg(-1)). Sorption correlated strongly with soil organic carbon content in both horizons (CV, 93 and 83%, respectively) and negatively with soil pH. [Ring-(14)C]-MCPA mineralized readily in the Ap horizon, with 49 to 62% of the (14)C-MCPA being converted to (14)CO(2) during the 67-d incubation period. With the subsoil, mineralization of (14)C-MCPA varied considerably between samples (0.5-72.8%). At neither depth was there correlation between (14)C-MCPA mineralization and sorption, soil pH, organic carbon content, clay content, number of colony-forming units (CFU), pseudomonad CFU, or any of the four microbial activity parameters measured. The presence of microbial genes encoding for the TfdA enzyme was quantified using real-time polymerase chain reaction. No correlation was found between MCPA mineralization potential and the natural background number of tfdA genes present in the soil samples. The degradation kinetics suggests that the high (14)C-MCPA mineralization rate detected in soil samples was linked to growth of the MCPA-degrading soil microbial community.     

Variation in and constraints upon the decomposition of woolscour sludge

The woolscouring (wool washing) industry has traditionally been viewed as highly polluting and, consequently, effluent treatment systems have been sought. The first stage in the current treatment system for woolscour wastewater, a chemical flocculation process (Sirolan CF), creates a sludge composed of soil and wool grease. We investigated the chemical and biological characteristics of this sludge. The sludge was found to be highly variable on a day to day basis in terms of its chemical composition and biodegradability; 0.8 to 27.8% of sludge total nitrogen was mineralized over 30 d at 37 degrees C. The grease component of sludge (14-40% on a dry weight basis) may retard the decomposition of the sludge but the polyacrylamide flocculant used in its production and its pesticide content had no effect on the rate of decomposition. Our results suggest that variability in substrate quality may translate into variability in treatment performance and have important implications for the biological treatment of industrial wastes, including composting.     

Soil electrical conductivity and water content affect nitrous oxide and carbon dioxide emissions in intensively managed soils

Accumulation of soluble salts resulting from fertilizer N may affect microbial production of N(2)O and CO(2) in soils. This study was conducted to determine the effects of electrical conductivity (EC) and water content on N(2)O and CO(2) production in five soils under intensive cropping. Surface soils from maize fields were washed, repacked and brought to 60% or 90% water-filled pore space (WFPS). Salt mixtures were added to achieve an initial in situ soil EC of 0.5, 1.0, 1.5 and 2.0 dS m(-1). The soil cores were incubated at 25 degrees C for 10 d. Average CO(2) production decreased with increasing EC at both soil water contents, indicating a general reduction in microbial respiration with increasing EC. Average cumulative N(2)O production at 60% WFPS decreased from 2.0 mg N(2)O-N m(-2) at an initial EC of 0.5 dS m(-1) to 0.86 mg N(2)O-N m(-2) at 2.0 dS m(-1). At 90% WFPS, N(2)O production was 2 to 40 times greater than that at 60% WFPS and maximum N(2)O losses occurred at the highest EC level of 2.0 dS m(-1). Differences in the magnitude of gas emissions at varying WFPS were due to available substrate N and the predominance of nitrification under aerobic conditions (60% WFPS) and denitrification when oxygen was limited (90% WFPS). Differences in gas emissions at varying soil EC may be due to changes in mechanisms of adjustment to salt stress and ion toxicities by microbial communities. Direct effects of EC on microbial respiration and N(2)O emissions need to be accounted for in ecosystems models for predicting soil greenhouse gas emissions.     

Decomposition and nitrogen mineralization from biosolids and other organic materials: relationship with initial chemistry

Biosolids are effective forest fertilizers. In order to facilitate their use it is important that one be able to predict the amount and rate of mineralization of nutrients, particularly nitrogen, and the relationship between substrate chemistry and N release. We examined the relationships between substrate quality and nitrogen release in a variety of organic materials. Rates of decomposition and net N mineralization from four biosolids, wheat straw, paper fines, and Douglas-fir [Pseudotsuga menziesii (Mirb.) Franco] needle litter were measured during 391-d incubations in a greenhouse, and at two field sites in wet coastal and dry interior forests. Decomposition rates were best predicted by a model incorporating the ratio of carbon to organic matter. The decomposition model extrapolated well to the field when site-specific correction factors were applied. There was a weak relationship between rates of decomposition and net N mineralization. Rates of net N mineralization were best predicted by a model incorporating the initial organic N concentration and the proportion of phenolic C determined from solid-state 13C nuclear magnetic resonance (NMR) spectroscopy. The mineralization model extrapolated less well to the field, but the effect of substrate chemistry was still apparent. Among the four biosolids there was a strong correlation between organic N concentration and indices or protein determined from 13C NMR, suggesting that these protein indices may be useful for predicting N mineralization from biosolids. There was some evidence that the protein content and N mineralization in biosolids may be predictable from the sewage treatment process employed.     

Greenhouse gas balance for composting operations

The greenhouse gas (GHG) impact of composting a range of potential feedstocks was evaluated through a review of the existing literature with a focus on methane (CH(4)) avoidance by composting and GHG emissions during composting. The primary carbon credits associated with composting are through CH(4) avoidance when feedstocks are composted instead of landfilled (municipal solid waste and biosolids) or lagooned (animal manures). Methane generation potential is given based on total volatile solids, expected volatile solids destruction, and CH(4) generation from lab and field incubations. For example, a facility that composts an equal mixture of manure, newsprint, and food waste could conserve the equivalent of 3.1 Mg CO(2) per 1 dry Mg of feedstocks composted if feedstocks were diverted from anaerobic storage lagoons and landfills with no gas collection mechanisms. The composting process is a source of GHG emissions from the use of electricity and fossil fuels and through GHG emissions during composting. Greenhouse gas emissions during composting are highest for high-nitrogen materials with high moisture contents. These debits are minimal in comparison to avoidance credits and can be further minimized through the use of higher carbon:nitrogen feedstock mixtures and lower-moisture-content mixtures. Compost end use has the potential to generate carbon credits through avoidance and sequestration of carbon; however, these are highly project specific and need to be quantified on an individual project basis.     

Temperature and microbial activity effects on trace element leaching from metalliferous peats

Due to geochemical processes, peat soils often have elevated concentrations of trace elements, which are gradually released following drainage for agriculture. Our objectives were to use incubation temperatures to vary microbial activity in two metalliferous peats (M7 acidic peat and M3 neutral peat) from the Elba, New York region, and to use periodic leaching to assess the extent of trace element release from these soils. Dried soils were mixed with glass beads to maintain aeration, moistened, and incubated at 4, 16, 28, and 37 degrees C in 10-cm-diameter x 8-cm-tall columns. Five incubation-leaching cycles were performed, each consisting of 7.3 d of incubation (28 d for the final cycle) followed by 16 h of leaching with synthetic acid rain at 2.5 mm h(-1). Microbial activity was determined initially and after the final leaching by measuring C mineralization following glucose stimulation. Cumulative respiration results were ranked 28 > 16 > 4 > 37 degrees C, with M7 acidic peat respiration values greater than M3 neutral peat at each temperature. Initial leachate pH levels were between 2 and 4, with acidification less pronounced and shorter-lived for the M3 peat. Leachate S, dissolved organic carbon (DOC), NO3-N, and trace elements declined with successive leachings (rebounding slightly in the final M3 leachate), with concentrations typically greater in the M7 leachate. Elemental losses followed the same general ranking (28 > 16 > 4 > 37 degrees C); losses at 28 degrees C were 15 to 22% for As, Cd, Ni, and Zn from the M7 peat; losses from M3 were comparable only for Cu (1%) and Ni (19%). The correlation of respiration with S, DOC, and trace elements losses indicates that microbial processes mediated the release of trace elements in both peat soils. Neutral M3 peat pH levels limited losses of most analytes.     

Evaluation of extracted organic carbon and microbial biomass as stability parameters in ligno-cellulosic waste composts

Extracted organic C and microbial biomass were evaluated as stability parameters in 3 different ligno-cellulosic waste composts. Organic C was extracted by both water and alkali and further separated in humic-like carbon (HLC) and nonhumic carbon (NHC). Conventional humification parameters, such as humification index and degree of humification were calculated from NHC and HLC. Microbial biomass carbon (B(C)) was determined as an indicator of the degree of biochemical transformation, whereas ninhydrin reactive N (B(NIN)) was measured to obtain the stability parameter B(NIN)/N(TOT) (N(TOT), total N). The water-extracted organic C did not provide reliable information on the transformations underwent by the ligno-cellulosic wastes during composting, since its content remained almost unaltered during the whole process. In contrast, parameters based on the alkali-extracted organic C and microbial biomass clearly reflected organic matter (OM) changes during the process. There was an increase in the net amount of HLC in the alkali extracts throughout composting, especially in the first 7 to 12 wk of the process, as well as a relative enrichment of HLC with respect to NHC. Values of humification index and degree of humification in end products were consistent with an adequate level of compost stability. The stability parameter B(NIN)/N(TOT) showed to be a reliable indicator of stability in ligno-cellulosic wastes. Parameters based on the alkali-extracted C and microbial biomass clearly reflected the transformation of the OM during composting and can be used as stability parameters in ligno-cellulosic waste composts.