Denitrification potential and organic matter as affected by vegetation community, wetland age, and plant introduction in created wetlands

Denitrification potential (DP) and organic matter (OM) in soils were compared in three different vegetation communities-emergent macrophyte, open water, and forested edge-in two 10-yr-old created riverine wetlands. Organic matter, cold water-extractable organic matter (CWEOM), anaerobic mineralizable carbon (AnMC), and DP varied significantly (P<0.05) among vegetation communities. The surface (0 to 9 cm) soils in the emergent macrophyte community (EMC) showed highest DP (0.07+/-0.01 mg N h-1 kg-1), OM (84.90+/-5.60 g kg-1), CWEOM (1.12+/-0.20 g kg-1), and AnMC (1.50+/-0.10 mg C h-1 kg-1). In the deeper layer (9 to 18 cm), DP and CWEOM (0.04+/-0.01 mg N h-1 kg-1 and 1.13+/-0.20 g kg-1, respectively) were significantly higher in the open water community (OWC) than in the emergent macrophyte and forested edge communities. Plant introduction did not affect DP or OM content and characteristics. After 10 yr of wetland development, mean DP increased 25-fold in the surface layer (from 0.002 to 0.053 mg N h-1 kg-1); OM content more than doubled to 90.80+/-19.22 g kg-1, and CWEOM and HWEOM increased 2.5 and 2.7 times respectively from 1993 (prewetland conditions) to 2004. Humic acids were the most abundant form of OM in 2004 and 1993 samples. Significant (P<0.05) positive relationships between DP and OM, CWEOM, and AnMC were found in the surface layer; in the 9- to 18-cm layer, significant positive relationships were found between DP and CWEOM and AnMC.     

Organic phosphorus fractions in organically amended paddy soils in continuously and intermittently flooded conditions

Soil organic phosphorus (SOP) can greatly contribute to plant-available P and P nutrition. The study was conducted to determine the effects of organic amendments on organic P fractions and microbiological activities in paddy soils. Samples were collected at the Changshu Agro-ecological Experiment Station in Tahu Lake Basin, China, from an experiment that has been performed from 1999 to 2004, on a paddy soil (Gleysols). Treatments consisted of swine manure (SM), wheat straw (WS), swine manure plus wheat straw (SM + WS), and a control (chemical fertilization alone). Organic amendments markedly increased soil total organic phosphorus (TOP) and total organic carbon (TOC), especially in continuously flooded conditions. Based on the fractionation of SOP, organic amendments significantly increased soil labile organic phosphorus (LOP), moderately labile organic phosphorus (MLOP), and moderately stable organic phosphorus (MSOP) compared with the control. For SM and SM + WS treatments, LOP in continuously flooded soils decreased by 30.1 and 36.4%, respectively, compared to intermittently flooded soils. In organically amended soils, continuous flooding showed significantly lower microbial biomass phosphorus (MBP) and alkaline phosphatase activities (APA) than intermittent flooding. In intermittently flooded conditions, incorporating organic amendments into soil resulted in greater P uptake and biomass yield of rice than the control. In the intermittently flooded soils, APA (P < 0.05) and MBP (P < 0.01) were significantly and positively related to TOP, LOP, MLOP, and MSOP, whereas in continuously flooded soils, there was a significant (P < 0.05) negative relationship between MBP, TOP, and MSOP. Based on soil organic P fractions and soil enzymatic and microbiological activities, continuous flooding applied to paddy soils should be avoided, especially when swine manure is incorporated into paddy soil.     

Evaluating stream water quality through land use analysis in two grassland catchments: impact of wetlands on stream nitrogen concentration

We evaluated the impacts of natural wetlands and various land uses on stream nitrogen concentration in two grassland-dominated catchments in eastern Hokkaido, Japan. Analyzing land use types in drainage basins, measuring denitrification potential of its soil, and water sampling in all seasons of 2003 were performed. Results showed a highly significant positive correlation between the concentration of stream NO3-N and the proportion of upland area in drainage basins in both catchments. The regression slope, which we assumed to reflect the impact on water quality, was 24% lower for the Akkeshi catchment (0.012 +/- 0.001) than for the Shibetsu catchment (0.016 +/- 0.001). In the Akkeshi catchment, there was a significant negative correlation between the proportion of wetlands in the drainage basins and stream NO3-N concentration. Stream dissolved organic nitrogen (DON) and carbon (DOC) concentrations were significantly higher in the Akkeshi catchment. Upland and urban land uses were strongly linked to increases in in-stream N concentrations in both catchments, whereas wetlands and forests tended to mitigate water quality degradation. The denitrification potential of the soils was highest in wetlands, medium in riparian forests, and lowest in grasslands; and was significant in wetlands and riparian forests in the Akkeshi catchment. The solubility of soil organic carbon (SOC) and soil moisture tended to determine the denitrification potential. These results indicate that the water environment within the catchments, which influences denitrification potential and soil organic matter content, could have caused the difference in stream water quality between the two catchments.     

Denitrification in alluvial wetlands in an urban landscape

Riparian wetlands have been shown to be effective "sinks" for nitrate N (NO3-), minimizing the downstream export of N to streams and coastal water bodies. However, the vast majority of riparian denitrification research has been in agricultural and forested watersheds, with relatively little work on riparian wetland function in urban watersheds. We investigated the variation and magnitude of denitrification in three constructed and two relict oxbow urban wetlands, and in two forested reference wetlands in the Baltimore metropolitan area. Denitrification rates in wetland sediments were measured with a 15N-enriched NO3- "push-pull" groundwater tracer method during the summer and winter of 2008. Mean denitrification rates did not differ among the wetland types and ranged from 147 +/- 29 microg N kg soil(-1) d(-1) in constructed stormwater wetlands to 100 +/- 11 microg N kg soil(-1) d(-1) in relict oxbows to 106 +/- 32 microg N kg soil(-1) d(-1) in forested reference wetlands. High denitrification rates were observed in both summer and winter, suggesting that these wetlands are sinks for NO3- year round. Comparison of denitrification rates with NO3- standing stocks in the wetland water column and stream NO3- loads indicated that mass removal of NO3- in urban wetland sediments by denitrification could be substantial. Our results suggest that urban wetlands have the potential to reduce NO3- in urban landscapes and should be considered as a means to manage N in urban watersheds.     

Soil organic carbon of degraded wetlands treated with freshwater in the Yellow River Delta, China

Supplying freshwater is one of the important methods to help restore degraded wetlands. Changes in soil properties and plant community biomass were evaluated by comparing sites with freshwater treatment versus reference sites following freshwater addition to wetlands of the Yellow River Delta for 7 years. The results indicated that soil organic carbon (SOC) was significantly increased in all wetland sites that were treated with freshwater compared to the reference sites. The treatment wetlands had greater total nitrogen (TN), lower pH and electrical conductivity and higher water content in the soil compared to the reference wetlands. In general, the upper soil layer (0-20 cm) had greater SOC than the lower soil layer (20-40 cm). The increase of SOC in the freshwater reintroduction wetlands was higher in the Suaeda salsa plant community (mean ± standard error) (6.89 ± 0.63 g/kg) and Phragmites communis plant community (4.11 ± 0.12 g/kg) than in the Tamarix chinensis plant community (1.40 ± 0.31 g/kg) in the upper soil layer. The differences were especially marked between the treated and reference wetlands for SOC and TN in the P. communis plant communities. The C:N ratio of the soil was significantly greater in the treated compared to the reference wetlands for the S. salsa plant community. Although the C: N ratios increased after treatment, they were all <25 suggesting that N availability was not limiting soil organic matter decomposition. Our results indicate that freshwater addition and the concomitant increase in soil moisture content enhances the accumulation of SOC in the Yellow River Delta.     

Ecotoxic effect of phenanthrene on nitrifying bacteria in soils of different properties

Information on ecotoxicity of organic contaminants, such as polycyclic aromatic hydrocarbons (PAHs), in terrestrial environment is needed for establishing soil quality criteria and for risk assessment purposes. An ecotoxic effect of a model PAH compound (phenanthrene) toward soils microorganisms (nitrifying bacteria) was evaluated in 50 different soils. The soil samples were collected from agricultural land in four regions of Poland with varying levels of industrialization (Slaskie, Dolnoslaskie, Podlaskie, and Lubelskie voievodeships). Soils were characterized for basic physicochemical properties (texture, organic matter content, pH(KCl), total nitrogen content, total sorption capacity) and the content of contaminants including PAHs (73-800 microg kg(-1)), Pb (6-720 mg kg(-1)), and Zn (9-667 mg kg(-1)). Ecotoxicity of phenanthrene (applied at 10, 100, 500, and 1000 mg kg(-1)) to soils microorganisms was evaluated in laboratory studies in control conditions (incubation of soils for 7 d at 20 +/- 2 degrees C). Nitrification potential was used as the ecotoxicity measurements end point. The EC50 values (146-1670 mg kg(-1)) calculated from the square root-X linear regression model differed significantly in various soils, although it was difficult to establish a causative relationship between soil physicochemical characteristic and phenanthrene toxicity. A significant factor in the assessment of soils vulnerability to the effect of phenanthrene was level of soil contamination, particularly with PAHs. Soils with previous contamination were more susceptible (mean EC50, 325 mg kg(-1)) than soils from uncontaminated, rural areas (mean EC50, 603 mg kg(-1)).     

Adsorption of cadmium on biosolids-amended soils

Debate exists over the biosolid phase (organic or inorganic) responsible for the reduction in phytoavailable Cd in soils amended with biosolids as compared with soils amended with inorganic salts. To test the importance of these two phases, adsorption isotherms were developed for soil samples (nine biosolids-amended soils and their five companion controls) and two biosolids samples from five experimental sites with documented histories of biosolids application. Subsamples were treated with 0.7 M NaClO to remove organic carbon. Cadmium nitrate was added to both moist soil samples and their soil inorganic fractions (SIF) in a 0.01 M Ca(NO3)2 solution at three pH levels (6.5, 5.5, and 4.5), and equilibrated at 22 +/- 1 degrees C for at least 48 h. Isotherms of Cd adsorption for biosolids-amended soil were intermediate to the control soil and biosolids. Decreasing pH did not remove the difference between these isotherms, although adsorption of Cd decreased with decreasing pH level. Organic matter removal reduced Cd adsorption on all soils but had little influence on the observed difference between biosolids-amended and control soils. Thus, increased adsorption associated with biosolids application was not limited to the organic matter addition from biosolids; rather, the biosolids application also altered the adsorptive properties of the SIF. The greater affinity of the inorganic fraction of biosolids-amended soils to adsorb Cd suggests that the increased retention of Cd on biosolids-amended soils is independent of the added organic matter and of a persistent nature.     

What is soil organic matter worth?

The conservation and restoration of soil organic matter are often advocated because of the generally beneficial effects on soil attributes for plant growth and crop production. More recently, organic matter has become important as a terrestrial sink and store for C and N. We have attempted to derive a monetary value of soil organic matter for crop production and storage functions in three contrasting New Zealand soil orders (Gley, Melanic, and Granular Soils). Soil chemical and physical characteristics of real-life examples of three pairs of matched soils with low organic matter contents (after long-term continuous cropping for vegetables or maize) or high organic matter content (continuous pasture) were used as input data for a pasture (grass-clover) production model. The differences in pasture dry matter yields (non-irrigated) were calculated for three climate scenarios (wet, dry, and average years) and the yields converted to an equivalent weight and financial value of milk solids. We also estimated the hypothetical value of the C and N sequestered during the recovery phase of the low organic matter content soils assuming trading with C and N credits. For all three soil orders, and for the three climate scenarios, pasture dry matter yields were decreased in the soils with lower organic matter contents. The extra organic matter in the high C soils was estimated to be worth NZ$27 to NZ$150 ha(-1) yr(-1) in terms of increased milk solids production. The decreased yields from the previously cropped soils were predicted to persist for 36 to 125 yr, but with declining effect as organic matter gradually recovered, giving an accumulated loss in pastoral production worth around NZ$518 to NZ$1239 ha(-1). This was 42 to 73 times lower than the hypothetical value of the organic matter as a sequestering agent for C and N, which varied between NZ$22,963 to NZ$90,849 depending on the soil, region, discount rates, and values used for carbon and nitrogen credits.     

Nitrate removal in a riparian wetland of the Appalachian Valley and Ridge physiographic province

Riparian zones within the Appalachian Valley and Ridge physiographic province are often characterized by localized variability in soil moisture and organic carbon content, as well as variability in the distribution of soils formed from alluvial and colluvial processes. These sources of variability may significantly influence denitrification rates. This investigation studied the attenuation of nitrate (NO3- -N) as wastewater effluent flowed through the shallow ground water of a forested headwater riparian zone within the Appalachian Valley and Ridge physiographic province. Ground water flow and NO3- -N measurements indicated that NO3- -N discharged to the riparian zone preferentially flowed through the A and B horizons of depressional wetlands located in relic meander scars, with NO3- -N decreasing from > 12 to < 0.5 mg L(-1). Denitrification enzyme activity (DEA) attributable to riparian zone location, soil horizon, and NO3- -N amendments was also determined. Mean DEA in saturated soils attained values as high as 210 microg N kg(-1) h(-1), and was significantly higher than in unsaturated soils, regardless of horizon (p < 0.001). Denitrification enzyme activity in the shallow A horizon of wetland soils was significantly higher (p < 0.001) than in deeper soils. Significant stimulation of DEA (p = 0.027) by N03- -N amendments occurred only in the meander scar soils receiving low NO3- -N (<3.6 mg L(-1)) concentrations. Significant denitrification of high NO3- -N ground water can occur in riparian wetland soils, but DEA is dependent upon localized differences in the degree of soil saturation and organic carbon content.     

Sorption and mobility of ivermectin in different soils

Avermectins are widely used to treat livestock for parasite infections. Ivermectin, which belongs to the group of avermectins, is particularly hazardous to the environment, especially to crustaceans and to soil-dwelling organisms. Sorption is one of the key factors controlling transport and bioavailability. Therefore, batch studies have been conducted to characterize the sorption and desorption behavior of ivermectin in three European soils (Madrid, York, and artificial soil). The solid-water distribution coefficient (K(d)) for ivermectin sorption to the tested soils were between 57 and 396 L kg(-1) (determined at 0.1 microg g(-1)), while the organic carbon-normalized sorption coefficients (K(oc)) ranged from 4.00 x 10(3) to 2.58 x 10(4) L kg(-1). The Freundlich sorption coefficient (K(F)) was 396 (after 48 h) for the artificial soil over a concentration range of 0.1 to 50 microg g(-1), with regression constants indicating a concentration-dependent sorption. The obtained data and data in the literature are inconclusive with regard to whether hydrophobic partitioning or more specific interactions are involved in sorption of avermectins. For abamectin, hydrophobic partitioning seems to be one of the dominant types of binding, while hydrophobicity is less important for ivermectin, which is probably due to the lower lipophilicity of the molecule. Furthermore, the presence of cations such as Ca(2+) leads to decreasing sorption. Thus, it is presumed that ivermectin binds to soil by formation of complexes with immobile, inorganic soil matter. In contrast to abamectin, hysteresis could be excluded for ivermectin in the studied soils for the evaluation of sorption and desorption. The sorption mechanism is highly dependent on physicochemical properties of the avermectin.     

The effect of river pulsing on sedimentation and nutrients in created riparian wetlands

Sedimentation under pulsed and steady-flow conditions was investigated in two created flow-through riparian wetlands in central Ohio over 2 yr. Hydrologic pulses of river water lasting for 6 to 8 d were imposed on each wetland from January through June during 2004. Mean inflow rates during pulses averaged 52 and 7 cm d(-1) between pulses. In 2005, the wetlands received a steady-flow regime of 11 cm d(-1) with no major hydrologic fluctuations. Thirty-two sediment traps were deployed and sampled once per month in April, May, June, and July for two consecutive years in each wetland. January through March were not sampled in either year due to frozen water surfaces in the wetlands. Gross sedimentation (sedimentation without normalizing for differences between years) was significantly greater in the pulsing study period (90 kg m(-2)) than in the steady-flow study period (64 kg m(-2)). When normalized for different hydrologic and total suspended solid inputs between years, sedimentation for April through July was not significantly different between pulsing and steady-flow study periods. Sedimentation for the 3 mo that received hydrologic pulses (April, May, and June) was significantly lower during pulsing months than in the corresponding steady-flow months. Large fractions of inorganic matter in collected sediments indicated that allochthonous inputs were the main contributor to sedimentation in these wetlands. Organic matter fractions of collected sediments were consistently greater in the steady-flow study period (1.8 g kg(-1)) than in the pulsed study period (1.5 g kg(-1)), consistent with greater primary productivity in the water column during steady-flow conditions.     

Dissolved organic carbon and disinfection by-product precursor release from managed peat soils

A wetland restoration demonstration project examined the effects of a permanently flooded wetland on subsidence of peat soils. The project, started in 1997, was done on Twitchell Island, in the Sacramento-San Joaquin Delta of California. Conversion of agricultural land to a wetland has changed many of the biogeochemical processes controlling dissolved organic carbon (DOC) release from the peat soils, relative to the previous land use. Dissolved organic C in delta waters is a concern because it reacts with chlorine, added as a disinfectant in municipal drinking waters, to form carcinogenic disinfection byproducts (DBPs), including trihalomethanes (THMs) and haloacetic acids (HAAs). This study explores the effects of peat soil biogeochemistry on DOC and DBP release under agricultural and wetland management. Results indicate that organic matter source, extent of soil organic matter decomposition, and decomposition pathways all are factors in THM formation. The results show that historical management practices dominate the release of DOC and THM precursors. However, within-site differences indicate that recent management decisions can contribute to changes in DOC quality and THM precursor formation. Not all aromatic forms of carbon are highly reactive and certain environmental conditions produce the specific carbon structures that form THMs. Both HAA and THM precursors are elevated in the DOC released under wetland conditions. The findings of this study emphasize the need to further investigate the roles of organic matter sources, microbial decomposition pathways, and decomposition status of soil organic matter in the release of DOC and DBP precursors from delta soils under varying land-use practices.     

Mercury speciation in highly contaminated soils from chlor-alkali plants using chemical extractions

A four-step novel sequential extraction procedure (SEP) was developed to assess Hg fractionation and mobility in three highly contaminated soils from chlor-alkali plants (CAPs). The SEP was validated using a certified reference material (CRM) and pure Hg compounds. Total, volatile, and methyl Hg concentrations were also determined using single extractions. Mercury was separated into four fractions defined as water-soluble (F1), exchangeable (F2) (0.5 M NH4Ac-EDTA and 1 M CaCl2 were tested), organic (F3) (successive extractions with 0.2 M NaOH and CH3COOH 4% [v/v]), and residual (F4) (HNO3 + H2SO4 + HClO4). The soil characterization revealed extremely contaminated (295 +/- 18 to 11 500 +/- 500 mg Hg kg(-1)) coarse-grained sandy soils having an alkaline pH (7.9-9.1), high chloride concentrations (5-35 mg kg(-1)), and very low organic carbon content (0.00-18.2 g kg(-1)). Methyl Hg concentrations were low (0.2-19.3 microg kg(-1)) in all soils. Sequential extractions indicated that the majority of the Hg was associated with the residual fraction (F4). In Soils 1 and 3, however, high percentages (88-98%) of the total Hg were present as volatile Hg. Therefore, in these two soils, a high proportion of volatile Hg was present in the residual fraction. The nonresidual fraction (F1 + F2 + F3) was most abundant in Soil 1 (14-42%), suggesting a higher availability of Hg in this soil. The developed and validated SEP was reproducible and efficient for highly contaminated samples. Recovery ranged between 93 and 98% for the CRM and 70 and 130% for the CAP-contaminated soils.     

Soil biogeochemical characteristics influenced by alum application in a municipal wastewater treatment wetland

Constructed treatment wetlands are a relatively low-cost alternative used for tertiary treatment of wastewater. Phosphorus (P) removal capacity of these wetlands may decline, however, as P is released from the accrued organic soils. Little research has been done on methods to restore the treatment capacity of aging constructed wetlands. One possibility is the seasonal addition of alum during periods of low productivity and nutrient removal. Our 3-mo mesocosm study investigated the effectiveness of alum in immobilizing P during periods of reduced treatment efficiency, as well as the effects on soil biogeochemistry. Eighteen mesocosms were established, triplicate experimental and control units for Typha sp., Schoenoplectus californicus, and submerged aquatic vegetation (SAV) (Najas guadalupensis dominated). Alum was slowly dripped to the water column of the experimental units at a rate of 0.91 g Al m(-2) d(-1) and water quality parameters were monitored. Soil cores were collected at experiment initiation and completion and sectioned into 0- to 5- and 5- to 10-cm intervals for characterization. The alum floc remained in the 0- to 5-cm surface soil, however, soil pH and microbial parameters were impacted throughout the upper 10 cm with the lowest pH found in the Typha treatment. Plant type did not impact most biogeochemical parameters; however, data were more variable in the SAV mesocosms. Amorphous Al was greater in the surface soil of alum-treated mesocosms, inversely correlated with soil pH and microbial biomass P in both soil layers. Microbial activity was also suppressed in the surface soil of alum-treated mesocosms. This research suggests alum may significantly affect the biogeochemistry of treatment wetlands and needs further investigation.     

Quantifying carbon dioxide and methane emissions and carbon dynamics from flooded boreal forest soil

The boreal forest is subject to natural and anthropogenic disturbances, but the production of greenhouse gases as a result of flooding for hydroelectric power generation has received little attention. It was hypothesized that flooded soil would result in greater CO(2) and CH(4) emissions and carbon (C) fractionation compared with non-flooded soil. To evaluate this hypothesis, soil C and nitrogen (N) dynamics, CO(2) and CH(4) mean production rates, and (13)C fractionation in laboratory incubations at 14 and 21 degrees C under non-flooded and flooded conditions and its effect on labile and recalcitrant C sources were determined. A ferro-humic Podzol was collected at three different sites at the Experimental Lakes Area, Canada, with a high (19,834 g C m(-2)), medium (18,066 g C m(-2)), and low (11,060 g C m(-2)) soil organic C (SOC) stock. Soil organic C and total N stocks (g m(-2)) and concentrations (g kg(-1)) were significantly different (p < 0.05) among soil horizons within each of the three sites. Stable isotope analysis showed a significant enrichment in delta(13)C and delta(15)N with depth and an enrichment in delta(13)C and delta(15)N with decreasing SOC and N concentration. The mean CO(2) and CH(4) production rates were greatest in soil horizons with the highest SOC stock and were significantly higher at 21 degrees C and in flooded treatments. The delta(13)C of the evolved CO(2) (delta(13)C-CO(2)) became significantly enriched with time during decomposition, and the greatest degree of fractionation occurred in the organic Litter, Fungal, and Humic forest soil horizons and in soil with a high SOC stock compared with the mineral horizon and soil with a lower SOC stock. The delta(13)C-CO(2) was significantly depleted in flooded treatments compared with non-flooded treatments.     

Mercury sequestration in forests and peatlands: a review

Nearly all Hg in vegetation is derived directly from the atmosphere. Mass of Hg in forest vegetation (roughly 0.1 mg m(-2)) is about an order of magnitude smaller than that in the forest floor (1 mg m(-2)) and two orders of magnitude smaller than that in the mineral soil (10 mg m(-2)). Mass of Hg in peat (20 mg m(-2)) is greater than the sum of that in mineral soil and the forest floor; wetlands usually sequester more Hg than associated uplands. The strong relationship of Hg to organic matter, associated with binding by reduced S groups, is fundamental to understanding Hg distribution and behavior in terrestrial systems. The stoichiometry of the Hg-C relationship varies; Hg-S relationships, though less variable, are not constant. Because of the Hg-organic matter link, landscape conditions that lead to differential soil organic matter accumulation are likely to lead to differential Hg accumulation. The ratio of methylmercury (MeHg) to total Hg is generally low in both vegetation (near 1.5%) and soil (<1%), but areas of poorly drained soils and wetlands are sites of MeHg production. The annual emission of anthropic Hg from the 48 contiguous states of the USA (144 Mg) is two orders of magnitude less than the pool of Hg in forests of those states (30,300 Mg). Peatlands, less than 2% of total land area, sequester more than 20 times annual emissions (2930 Mg). If global climate change affects C storage it will indirectly affect Hg storage, having a major effect on the balance between emissions and sequestration and on the global Hg cycle.     

Potential of carbon accumulation in no-till soils with intensive use and cover crops in southern Brazil

The area under no-till (NT) in Brazil reached 22 million ha in 2004-2005, of which approximately 45% was located in the southern states. From the 1970s to the mid-1980s, this region was a source of carbon dioxide to the atmosphere due to decrease of soil carbon (C) stocks and high consumption of fuel by intensive tillage. Since then, NT has partially restored the soil C lost and reduced the consumption of fossil fuels. To assess the potential of C accumulation in NT soils, four long-term experiments (7-19 yr) in subtropical soils (Paleudult, Paleudalf, and Hapludox) varying in soil texture (87-760 g kg(-1) of clay) in agroecologic southern Brazil zones (central region, northwest basaltic plateau in Rio Grande Sul, and west basaltic plateau in Santa Catarina) and with different cropping systems (soybean and maize) were investigated. The lability of soil organic matter (SOM) was calculated as the ratio of total organic carbon (TOC) to particulate organic carbon (POC), and the role of physical protection on stability of SOM was evaluated. In general, TOC and POC stocks in native grass correlated closely with clay content. Conversely, there was no clear effect of soil texture on C accumulation rates in NT soils, which ranged from 0.12 to 0.59 Mg ha(-1) yr(-1). The C accumulation was higher in NT than in conventional-till (CT) soils. The legume cover crops pigeon pea [Cajanus cajan (L.) Millsp] and velvet beans (Stizolobium cinereum Piper & Tracy) in NT maize cropping systems had the highest C accumulation rates (0.38-0.59 Mg ha(-1) yr(-1)). The intensive cropping systems also were effective in increasing the C accumulation rates in NT soils (0.25-0.34 Mg ha(-1) yr(-1)) when compared to the double-crop system used by farmers. These results stress the role of N fixation in improving the tropical and subtropical cropping systems. The physical protection of SOM within soil aggregates was an important mechanism of C accumulation in the sandy clay loam Paleudult under NT. The cropping system and NT effects on C stocks were attributed to an increase in the lability of SOM, as evidenced by the higher POC to TOC ratio, which is very important to C and energy flux through the soil.     

Visible-near infrared reflectance spectroscopy for rapid, nondestructive assessment of wetland soil quality

Recent evidence supports using visible-near infrared reflectance spectroscopy (VNIRS) for sensing soil quality; advantages include low-cost, nondestructive, rapid analysis that retains high analytical accuracy for numerous soil performance measures. Research has primarily targeted agricultural applications (precision agriculture, performance diagnostics), but implications for assessing ecological systems are equally significant. Our objective was to extend chemometrics for sensing soil quality to wetlands. Hydric soils posed two challenges. First, wetland soils exhibit a wider range of organic matter concentrations, particularly in riparian areas where levels range from <1% in sedimentation zones to >90% in backwater floodplains; this may mute spectral responses from other soil fractions. Second, spectral inference of cation concentrations in terrestrial soils is for oxidized species; under reducing conditions in wetlands, oxidation state variability is observed, which strongly affects chroma. Riparian soils (n = 273) from western Florida exhibiting substantial target parameter variability were compiled. After minimal pre-processing, soils were scanned under artificial illumination using a laboratory spectrometer. A multivariate data mining technique (regression trees) was used to relate post-processed reflectance spectra to laboratory observations (pH, organic content, cation concentrations, total N, C, and P, extracellular enzyme activity). High validation accuracy was generally observed (r2(validation) > 0.8, RPD > 2.0, where RPD is the ratio of the standard deviation of an attribute to the observed standard error of validation); where accuracy was lower, categorical models (classification trees) successfully screened samples based on diagnostic functional thresholds (validation odds ratio > 10). Graphical models verified significant association between predictions and observations for all parameters, conditioning on biogeochemical covariates. Visible-near infrared reflectance spectroscopy offers both cost and statistical power advantages; hydric conditions do not appear to constrain application.     

Stabilization of composted organic matter after application to a humus-free sandy mining soil

The use of mining substrates for recultivation purposes is limited due to their low organic matter (OM) contents. In a 1-yr laboratory experiment we evaluated the stabilization of biowaste compost added to a humus-free sandy mining soil to examine the suitability of compost amendment for the formation of stable soil organic matter (SOM). The stabilization process was characterized by measuring enrichment of OM and nitrogen in particle size fractions obtained after dispersion with different amounts of energy (ultrasonication and shaking in water), carbon mineralization, and amount of dissolved organic carbon (DOC). During the experiment, 17.1% of the organic carbon (OC) was mineralized. Organic carbon enrichment in the < 20-micron particle size fraction at the beginning of the experiment was in the range of natural soils with similar texture. Within 12 mo, a distinct OC redistribution from coarse into fine fractions was found with both dispersion methods. The accumulation of OC was more pronounced for the size separates obtained by ultrasonication, where the carbon distribution between 0.45- to 20-micron particle size fractions increased from 30% at the beginning to 71% at the end of the experiment. Dissolved organic carbon contents ranged between 50 and 68 g kg-1 OC and decreased during the incubation. In conclusion, the exponential decrease of carbon mineralization and the OC enrichment in the fine particle size fractions both indicated a distinct OM stabilization in the mining soil.     

Leaching of dissolved organic carbon and carbon dioxide emission after compost application to six nutrient-depleted forest soils

The objective of this study was to assess the effect of compost application on soil respiration and dissolved organic carbon (DOC) output of nutrient-depleted forest soils. An amount of 6.3 kg m(-2) mature compost was applied to the forest floor of European beech (Fagus sylvatica L.), Norway spruce (Picea abies Karst.), and Scots pine (Pinus sylvestris L.) stands at Soiling and Unterlüss, Germany. Cumulative soil respiration significantly increased by 499 g C m(-2) in the spruce stand at Unterlüss and by 274 g C m(-2) in the beech stand at Soiling following compost application whereas soil respiration of the other four stands was not affected. The increases in soil respiration of the two stands were explained by improved microbial decomposition of soil organic matter. The DOC concentrations and fluxes in throughfall and seepage water at 10- and 100-cm depths were determined from August 1997 to March 2000. In the control plots, cumulative DOC outputs at 10 cm ranged between 57 and 95 g C m(-2), with the highest rates in the pine stands. Compost treatment significantly increased cumulative DOC outputs by 31 to 69 g C m(-2) at 10 cm and by 0.3 to 6.6 g C m(-2) at 100 cm. The mineral soils between the 10- and 100-cm depths acted as significant sinks for DOC, as shown by much lower cumulative outputs at 100 cm of 3 to 11 g C m(-2) in the control and 6 to 16 g C m(-2) in the compost plots. Our results suggest that a single, moderate application of mature compost to nutrient-depleted forest soils has little effect on C losses to the atmosphere and ground water.