Effects of N-enriched sewage sludge on soil enzyme activities

Sewage sludge is increasingly used as an organic amendment to soil, especially to soil containing little organic matter. However, little is known about utility of this organic amendment with N-enriched or adjusted C:N ratios in soil. We studied the effects of adding of different doses (0, 100, 200 and 300 t ha⁻¹) and C:N ratios (3:1, 6:1 and 9:1) of sewage sludge on enzyme activities (β-glucosidase, alkaline phosphatase, arylsulphatase and urease) in a clay loam soil at 25 °C and 60% soil water holding capacity. Nitrogen was added in the form of (NH₄)₂ SO₄ solution to the sludge to reduce the C:N ratio from 9:1 to 6:1 and 3:1. The addition of different doses and C:N ratios of the sludge caused a rapid and significant in the enzymatic activities in soils, this increase was specially noticeable in soil treated with high doses of the sludge. In general, enzymatic activities in sludge-amended soils tended to decrease with the incubation time. All activities reached peak values at 30 days incubation and then gradually decreased up to 90 days of incubation. Sewage sludges also the increased available metal (Cu, Ni, Pb and Zn) contents in the soils. However, the presence of available soil metals due to the addition of the sludge at all doses and C:N ratios did negatively affect all enzymatic activities in the soils. This experiment indicated that all doses and C:N ratios of sewage sludge applied to soil would have harmful effects on enzymatic activity. Some heavy metals found in sewage sludge may negatively influence soil enzyme activities during the decomposition of the sludge.     

Distribution and dynamics of soil organic matter in an Antarctic dry valley

Terrestrial ecosystems in the Antarctic dry valleys function under extremely cold and dry climatic conditions that severely constrain C and N cycling and, like other polar regions, are likely to be sensitive to environmental change. To characterize the distribution and dynamics of soil organic C (SOC) and N in the various landscape elements of an Antarctic dry valley, we measured soil profile organic C and organic N stocks, inorganic N (NH₄-N and NO₃-N), soil CO₂ effluxes, water contents and soil temperatures in the Garwood Valley, a relatively small valley in southern Victoria Land. We also conducted laboratory measurements of basal respiration on soils collected from the Valley. SOC and respiration rates were low and SOC was highly stratified in the soil profile, with the largest values observed near the surface. Significant variations of SOC stocks and soil CO₂ effluxes were observed between landscape elements and spatial variability was closely related to the distance from the lake, the major site of primary production. The fastest rate of SOC turnover (residence time c. 30 years) was found in the soils at the lake edge, slower rates were found in landscape elements close to the lake (c. 52-67 years), and the slowest rates in other landscape elements (c. 84-123 years) further away. A mass balance of organic C indicates that the quantity of C fixed in the lake, accumulated on the lake edge, exposed and subsequently displaced on a 14-year basis can explain the near-surface SOC turnover within the entire valley. We conclude that the displacement of organic matter derived from the lake is an important external source for the microbial processes in these soils at a landscape scale. However, further investigations are needed in order to evaluate the importance of displaced C compared to other nutrients (e.g. N) on the spatial control of observed soil respiration rates.     

Determination of arylsulphatase and phosphatase enzyme activities in soil using screen-printed electrodes modified with multi-walled carbon nanotubes

Sustainability of agricultural systems has become an important issue all over the world. The activity of enzymes is potentially an important quality bioindicator in soils. The aim of the present study was to develop a simple and convenient assay to determine the activity of arylsulphatase (AS), acid (ACP) and alkaline phosphatase (ALP) in agricultural soil. The activities of these enzymes were detected using a non-electroactive substrate, which produces an electroactive product. To this end, p-aminophenyl phosphate (pAPP) was used as a substrate which is converted to p-aminophenol (pAP) after enzymatic dephosphorylation; and 4-nitrocatechol sulphate (4-NCS) was used as a substrate for AS activity based on its catalytic effect on the hydrolysis of 4-NCS into 4-nitrocatechol (4-NC). The products of both enzymatic reactions were quantified on carbon-based screen-printed electrodes (SPCEs) modified with carbon nanotubes (CNTs), using Osteryoung square-wave voltammetry (OSWV). The determination of the reaction products allowed more sensitive determination of ALP, ACP and AS activities in soil than that obtained with a spectrophotometric method. This assay also diminishes the generation of waste, which is desirable in green analytical chemistry. The optimization of the analytical procedure in terms of the nature of electrode type, applied potential, pH of solution, and precision of measurements is reported.     

Mobile and readily available C and N fractions and their relationship to microbial biomass and selected enzyme activities in a sandy soil under different management systems

Within different land‐use systems such as agriculture, forestry, and fallow, the different morphology and physiology of the plants, together with their specific management, lead to a system‐typical set of ecological conditions in the soil. The response of total, mobile, and easily available C and N fractions, microbial biomass, and enzyme activities involved in C and N cycling to different soil management was investigated in a sandy soil at a field study at Riesa, Northeastern Germany. The management systems included agricultural management (AM), succession fallow (SF), and forest management (FM). Samples of the mineral soil (0—5, 5—10, and 10—30 cm) were taken in spring 1999 and analyzed for their contents on organic C, total N, NH₄⁺‐N and NO₃^—‐N, KCl‐extractable organic C and N fractions (Corg_(KCl) and Norg_(KCl)), microbial biomass C and N, and activities of β‐glucosidase and L‐asparaginase. With the exception of Norg_(KCl), all investigated C and N pools showed a clear relationship to the land‐use system that was most pronounced in the 0—5 cm profile increment. SF resulted in greater contents of readily available C (Corg_(KCl)), NH₄⁺‐N, microbial biomass C and N, and enzyme activities in the uppermost 5 cm of the soil compared to all other systems studied. These differences were significant at P ≤ 0.05 to P ≤ 0.001. Comparably high C_mic:C_org ratios of 2.4 to 3.9 % in the SF plot imply a faster C and N turnover than in AM and FM plots. Forest management led to 1.5‐ to 2‐fold larger organic C contents compared to SF and AM plots, respectively. High organic C contents were coupled with low microbial biomass C (78 μg g^—1) and N contents (10.7 μg g^—1), extremely low C_mic : C_org ratios (0.2—0.6 %) and low β‐glucosidase (81 μg PN g^—1 h^—1) and L‐asparaginase (7.3 μg NH₄‐N g^—1 2 h^—1) activities. These results indicate a severe inhibition of mineralization processes in soils under locust stands. Under agricultural management, chemical and biological parameters expressed medium values with exception for NO₃^—‐N contents which were significantly higher than in SF and FM plots (P ≤ 0.005) and increased with increasing soil depth. Nevertheless, the depth gradient found for all studied parameters was most pronounced in soils under SF. Microbial biomass C and N were correlated to β‐glucosidase and L‐asparaginase activity (r ≥ 0.63; P ≤ 0.001). Furthermore, microbial biomass and enzyme activities were related to the amounts of readily mineralizable organic C (i.e. Corg_(KCl)) with r ≥ 0.41 (P ≤ 0.01), suggesting that (1) KCl‐extractable organic C compounds from field‐fresh prepared soils represent an important C source for soil microbial populations, and (2) that microbial biomass is an important source for enzymes in soil. The Norg_(KCl) pool is not necessarily related to the size of microbial biomass C and N and enzyme activities in soil.<?show $6#>     

Tillage impacts on soil biological activity and aggregation in a Brazilian Cerrado Oxisol

Mechanized agriculture is increasing rapidly in the Cerrado region of Brazil, causing concerns about water quality, off-site impacts, and sustainability. Our objective was to determine the impact of tillage on soil biological activity and aggregate stability in an Oxisol typical to the region. Three different tillage practices common to the Cerrado region (no-till, disk harrow, and disk plow) and an area under native vegetation were examined. Five different soil enzyme activities, C- and N-mineralization, organic C, total N, and aggregate distribution were determined. Total N, acid phosphatase, arylamidase, and C- and N-mineralization were the most sensitive to changes in tillage management. For each of these analyses, the no-till system had greater concentrations or activities (18–186%) than disk plow in the 0–5 cm layer. Significant differences observed in the 0–5 cm depth did not necessarily translate into total profile differences to a depth of 30 cm. No-till had significantly greater levels of total N, and C- and N-mineralization (20–127%) than the disk harrow system. Total N ranged from 1.8 to 2.2 kg m⁻³; C- and N-mineralization (24-day incubation) ranged from 2.8 to 6.8 and 0.04 to 0.10 kg m⁻³, respectively, among tillage systems and soil depths. Enzyme activities in all treatments were more strongly correlated with total soil N than with soil organic C (SOC), contrary to the norm in temperate soils where the stronger correlation is with SOC. Mean weight diameter of water stable aggregates was related to SOC (r = 0.73) and total N (r = 0.92), indicating that soil organic matter does play a significant role in stabilizing aggregates in Oxisols. Results indicated the importance of reducing tillage as a means of increasing soil biological activity of the topsoil in the Cerrado region of Brazil. By understanding the effects of tillage on soil biological properties, management systems can be implemented that improve natural nutrient cycling processes and soil structure, resulting in increased agricultural sustainability of tropical ecosystems.     

Twenty years of intensive fertilization and competing vegetation suppression in loblolly pine plantations: Impacts on soil C, N, and microbial biomass

Silvicultural treatments of fertilization (F) and competing vegetation suppression (H) have continued to increase as demands for forest products have grown. The effects of intensive annual F and H treatments on soil C, N, microbial biomass, and CO₂ efflux were examined in a two-way factorial experiment (control, F, H, FxH) in late-rotation (20+ years) loblolly pine stands. This study is unique in testing the cumulative effects of continual H and repeated F treatments for the first 20 years of stand growth, an uncommon operational practice, and in having treatments replicated upon four different soil types in the state of Georgia, USA. Annual fertilization included applications of N, P, K and periodic additions of micronutrients while competing vegetation suppression was maintained for all non-pine vegetation with herbicides throughout the rotation. Measurements included total O-horizon (forest floor) organic matter, C, and N, and 0-10 cm mineral soil pH, C, N, microbial biomass C and N, and surface CO₂ efflux. Sample collections and analyses were conducted seasonally for 1.5 yrs. Competing vegetation suppression was associated with a decrease of total soil C, soil microbial biomass C and N, and soil surface CO₂ efflux, while increasing O-horizon C:N. The fertilization treatment greatly reduced soil microbial biomass C and N, soil pH, and O-horizon C:N, while increasing O-horizon mass, N content, and soil carbon. No significant interactions between F and H were found. The combination of F and H treatments acted additively to achieve the greatest loss of soil microbial biomass, which may possibly have negative implications for long-term soil fertility.     

Root and rhizomicrobial respiration: A review of approaches to estimate respiration by autotrophic and heterotrophic organisms in soil

Partitioning the root‐derived CO₂ efflux from soil (frequently termed rhizosphere respiration) into actual root respiration (RR, respiration by autotrophs) and rhizomicrobial respiration (RMR, respiration by heterotrophs) is crucial in determining the carbon (C) and energy balance of plants and soils. It is also essential in quantifying C sources for rhizosphere microorganisms and in estimation of the C contributing to turnover of soil organic matter (SOM), as well as in linking net ecosystem production (NEP) and net ecosystem exchange (NEE). Artificial‐environment studies such as hydroponics or sterile soils yield unrealistic C‐partitioning values and are unsuitable for predicting C flows under natural conditions. To date, several methods have been suggested to separate RR and RMR in nonsterile soils: 1) component integration, 2) substrate‐induced respiration, 3) respiration by excised roots, 4) comparison of root‐derived ¹⁴CO₂ with rhizomicrobial ¹⁴CO₂ after continuous labeling, 5) isotope dilution, 6) model‐rhizodeposition technique, 7) modeling of ¹⁴CO₂ efflux dynamics, 8) exudate elution, and 9) δ¹³C of CO₂ and microbial biomass. This review describes the basic principles and assumptions of these methods and compares the results obtained in the original papers and in studies designed to compare the methods. The component‐integration method leads to strong disturbance and non‐proportional increase of CO₂ efflux from different sources. Four of the methods (5 to 8) are based on the pulse labeling of shoots in a ¹⁴CO₂ atmosphere and subsequent monitoring of ¹⁴CO₂ efflux from the soil. The model‐rhizodeposition technique and exudate‐elution procedure strongly overestimate RR and underestimate RMR. Despite alternative assumptions, isotope dilution and modeling of ¹⁴CO₂‐efflux dynamics yield similar results. In crops and grasses (wheat, ryegrass, barley, buckwheat, maize, meadow fescue, prairie grasses), RR amounts on average to 48±5% and RMR to 52±5% of root‐derived CO₂. The method based on the ¹³C isotopic signature of CO₂ and microbial biomass is the most promising approach, especially when the plants are continuously labeled in ¹³CO₂ or ¹⁴CO₂ atmosphere. The “difference” methods, i.e., trenching, tree girdling, root‐exclusion techniques, etc., are not suitable for separating the respiration by autotrophic and heterotrophic organisms because the difference methods neglect the importance of microbial respiration of rhizodeposits.     

Relationship between carbon and nitrogen availability and extracellular enzyme activities in soil

Microorganisms rely on extracellular enzymes to break down insoluble organic polymers such as cellulose, protein, and chitin into smaller units for uptake. Our objective was to investigate the factors affecting the relationship between soil extracellular enzyme activities and C and N turnover. Several aerobic incubations were carried out with ammonium (NH₄⁺) and proteins as N sources and cellulose as the main C source. Cellulase (exocellulase and β-glucosidase) activity was positively correlated with the amount of cellulose added, as well as with the availability of N. A decrease in the C to N ratio of the amendments from 40 to 10 resulted in an increase in exocellulase and β-glucosidase activity of 18% and 10%, respectively. Similarly, the activity of protease initially depended on the amount and kind of protein added; later, however, an increase in carbon availability resulted in an elevated protease activity. Initially, protease and cellulase activity were induced by their corresponding substrates and an increase in activity of both enzymes resulted in a proportional increase in carbon dioxide (CO₂) evolution. Over time, however, the level of enzyme activity became increasingly determined by factors other than substrate availability. In addition, N turnover, while initially determined by the amount and kind of N source added, became increasingly dominated by the C to N ratio of the substrates added. Our study showed that even though enzyme activities alone may not be sufficient to describe the decomposition process, they can yield valuable information about the availability of specific organic compounds and their degradation over time.     

Short‐term sequestration of slurry‐derived carbon and nitrogen in temperate grassland soil as assessed by 13C and 15N natural abundance measurements

Land application of animal wastes from intensive grassland farming has caused growing environmental problems during the last decade. This study aimed to elucidate the short‐term sequestration of slurry‐derived C and N in a temperate grassland soil (Southwest England) using natural abundance ¹³C and ¹⁵N stable isotope techniques. Slurry was collected from cows fed either on perennial ryegrass (C3) or maize (C4) silages. 50 m³ ha^—1 of each of the obtained C3 or C4 slurries (δ¹³C = —30.7 and —21.3‰, δ¹⁵N = +12.2 and + 13.8 ‰, respectively) were applied to a C₃ soil with δ¹³C and δ¹⁵N values of —30.0 ± 0.2‰ and + 4.9 ± 0.3‰, respectively. Triplicate soil samples were taken from 0—2, 2—7.5, and 7.5—15 cm soil depth 90 and 10 days before, at 2 and 12 h, as well as at 1, 2, 4, 7, and 14 days after slurry application and analyzed for total C, N, δ¹³C, and δ¹⁵N. No significant differences in soil C and N content were observed following slurry application using conventional C and N analysis techniques. However, natural abundance ¹³C and ¹⁵N isotope analysis allowed for a sensitive temporal quantification of the slurry‐derived C and N sequestration in the grassland soil. Our results showed that within 12 hours more than one‐third of the applied slurry C was found in the uppermost soil layer (0—2 cm), decreasing to 18% after 2 days, but subsequently increasing to 36% after 2 weeks. The tentative estimate of slurry‐derived N in the soil suggested a decrease from 50% 2 hours after slurry application to only 26% after 2 weeks, assuming that the increase in δ¹⁵N of the slurry plots compared to the control is proportional to the amount of slurry‐incorporated N. We conclude that the natural abundance tracer technique can provide a rapid new clue to the fate of slurry in agricultural C and N budgets, which is important for environmental impacts, farm waste management, and climate change studies.     

Fate of low molecular weight organic substances in an arable soil: From microbial uptake to utilisation and stabilisation

Microbial uptake and utilisation are the main transformation pathways of low molecular weight organic substances (LMWOS) in soil, but details on transformations are strongly limited. As various LMWOS classes enter biochemical cycles at different steps, we hypothesize that the percentage of their carbon (C) incorporation into microbial biomass and consequently stabilisation in soil are different.Representatives of the three main groups of LMWOS: amino acids (alanine, glutamate), sugars (glucose, ribose) and carboxylic acids (acetate, palmitate) – were applied at naturally-occurring concentrations into a loamy arable Luvisol in a field experiment. Incorporation of ¹³C from these LMWOS into extractable microbial biomass (EMB) and into phospholipid fatty acids (PLFAs) was investigated 3 d and 10 d after application. The microbial utilisation of LMWOS for cell membrane construction was estimated by replacement of PLFA-C with ¹³C.35–80% of initially applied LMWOS-¹³C was still present in the composition of soil organic matter after 10 days of experiment, with 10–24% of ¹³C incorporation into EMB at day three and 1–15% at day 10. Maximal incorporation of ¹³C into EMB was observed from sugars and the least from amino acids. Strong differences in microbial utilisation between LMWOS were observed mainly at day 10. Thus, despite similar initial rapid uptake by microorganisms, further metabolism within microbial cells accounts for the specific fate of C from various LMWOS in soils.¹³C from each LMWOS was incorporated into each PLFA. This reflects the ubiquitous utilisation of all LMWOS by all functional microbial groups. The preferential incorporation of palmitate into PLFAs reflects its role as a direct precursor for fatty acids. Higher ¹³C incorporation from alanine and glucose into specific PLFAs compared to glutamate, ribose and acetate reflects the preferential use of glycolysis-derived substances in the fatty acids synthesis.Gram-negative bacteria (16:1ω7c and 18:1ω7c) were the most abundant and active in LMWOS utilisation. Their high activity corresponds to a high demand for anabolic products, e.g. to dominance of pentose-phosphate pathway, i.e. incorporation of ribose-C into PLFAs. The ¹³C incorporation from sugars and amino acids into filamentous microorganisms was lower than into all prokaryotic groups. However, for carboxylic acids, the incorporation was in the same range (0.1–0.2% of the applied carboxylic acid ¹³C) as that of gram-positive bacteria. This may reflect the dominance of fungi and other filamentous microorganisms for utilisation of acidic and complex organics.Thus, we showed that despite similar initial uptake, C from individual LMWOS follows deviating metabolic pathways which accounts for the individual fate of LMWOS-C over 10 days. Consequently, stabilisation of C in soil is mainly connected with its incorporation into microbial compounds of various stability and not with its initial microbial uptake.     

Grasses, litter, and their interaction affect microbial biomass and soil enzyme activity

Plant effects on ecosystem processes are mediated through plant-microbial interactions belowground and soil enzyme assays are commonly used to directly relate microbial activity to ecosystem processes. Live plants influence microbial biomass and activity via differences in rhizosphere processes and detrital inputs. I utilized six grass species of varying litter chemistry in a factorial greenhouse experiment to evaluate the relative effect of live plants and detrital inputs on substrate-induced respiration (SIR, a measure of active microbial biomass), basal respiration, dissolved organic carbon (DOC), and the activities of β-glucosidase, β-glucosaminidase, and acid phosphatase. To minimize confounding variables, I used organic-free potting media, held soil moisture constant, and fertilized weekly. SIR and enzyme activities were 2-15 times greater in litter-addition than plant-addition treatments. Combining live plants with litter did not stimulate microbial biomass or activity above that in litter-only treatments, and β-glucosidase activity was significantly lower. Species-specific differences in litter N (%) and plant biomass were related to differences in β-glucosaminidase and acid phosphatase activity, respectively, but had no apparent effect on β-glucosidase, SIR, or basal respiration. DOC was negatively related to litter C:N, and positively related to plant biomass. Species identity and living plants were not as important as litter additions in stimulating microbial activity, suggesting that plant effects on soil enzymatic activity were driven primarily by detrital inputs, although the strength of litter effects may be moderated by the effect of growing plants.     

Linking dynamics of soil microbial phospholipid fatty acids to carbon mineralization in a C natural abundance experiment: Impact of heavy metals and acid rain

A ¹³C natural abundance experiment including GC-c-IRMS analysis of phospholipid fatty acids (PLFAs) was conducted to assess the temporal dynamics of the soil microbial community and carbon incorporation during the mineralization of plant residues under the impact of heavy metals and acid rain. Maize straw was incorporated into (i) control soil, (ii) soil irrigated with acid rain, (iii) soil amended with heavy metal-polluted filter dust and (iv) soil with both, heavy metal and acid rain treatment, over a period of 74 weeks. The mineralization of maize straw carbon was significantly reduced by heavy metal impact. Reduced mineralization rate of the added carbon likely resulted from a reduction of the microbial biomass due to heavy metal stress, while the efficiency of ¹³C incorporation into microbial PLFAs was hardly affected. Since acid rain did not significantly change soil pH, little impact on soil microorganisms and mineralization rate was found. Temporal dynamics of labelling of microbial PLFAs were different between bacterial and fungal PLFA biomarkers. Utilization of maize straw by bacterial PLFAs peaked immediately after the application (2 weeks), while labelling of the fungal biomarker 18:2ω6,9 was most pronounced 5 weeks after the application. In general, ¹³C labelling of microbial PLFAs was closely linked to the amounts of maize carbon present in the soil. The distinct higher labelling of microbial PLFAs in the heavy metal-polluted soils 74 weeks after application indicated a large fraction of available maize straw carbon still present in the soil.     

Organic C and N stabilization in a forest soil: Evidence from sequential density fractionation

In mineral soil, organic matter (OM) accumulates mainly on and around surfaces of silt- and clay-size particles. When fractionated according to particle density, C and N concentration (per g fraction) and C/N of these soil organo-mineral particles decrease with increasing particle density across soils of widely divergent texture, mineralogy, location, and management. The variation in particle density is explained potentially by two factors: (1) a decrease in the mass ratio of organic to mineral phase of these particles, and (2) variations in density of the mineral phase. The first explanation implies that the thickness of the organic accumulations decreases with increasing particle density. The decrease in C/N can be explained at least partially by especially stable sorption of nitrogenous N-containing compounds (amine, amide, and pyrrole) directly to mineral surfaces, a phenomenon well documented both empirically and theoretically. These peptidic compounds, along with ligand-exchanged carboxylic compounds, could then form a stable inner organic layer onto which other organics could sorb more readily than onto the unconditioned mineral surfaces (“onion” layering model).To explore mechanisms underlying this trend in C concentration and C/N with particle density, we sequentially density fractionated an Oregon andic soil at 1.65, 1.85, 2.00, 2.28, and 2.55 g cm⁻³ and analyzed the six fractions for measures of organic matter and mineral phase properties.All measures of OM composition showed either: (1) a monotonic change with density, or (2) a monotonic change across the lightest fractions, then little change over the heaviest fractions. Total C, N, and lignin phenol concentration all decreased monotonically with increasing density, and ¹⁴C mean residence time (MRT) increased with particle density from ca. 150 years to >980 years in the four organo-mineral fractions. In contrast, C/N, ¹³C and ¹⁵N concentration all showed the second pattern. All these data are consistent with a general pattern of an increase in extent of microbial processing with increasing organo-mineral particle density, and also with an “onion” layering model.X-ray diffraction before and after separation of magnetic materials showed that the sequential density fractionation (SDF) isolated pools of differing mineralogy, with layer-silicate clays dominating in two of the intermediate fractions and primary minerals in the heaviest two fractions. There was no indication that these differences in mineralogy controlled the differences in density of the organo-mineral particles in this soil. Thus, our data are consistent with the hypothesis that variation in particle density reflects variation in thickness of the organic accumulations and with an “onion” layering model for organic matter accumulation on mineral surfaces. However, the mineralogy differences among fractions made it difficult to test either the layer-thickness or “onion” layering models with this soil. Although SDF isolated pools of distinct mineralogy and organic-matter composition, more work will be needed to understand mechanisms relating the two factors.     

Sorption of tannin and related phenolic compounds and effects on soluble-N in soil

Some tannins, plant-derived polyphenolic compounds, can rapidly affix to soil and affect the solubility of labile soil-N but a more complete understanding of the nature and persistence of tannin-soil interactions is needed. Forest and pasture soils from two depths were treated for 1 h with cool (23 ^°C) water (Control) or solutions that added 10 mg g⁻¹ soil tannic acid (TA), an imprecisely defined mixture of galloyl esters, gallic acid (GA), a phenol, or β-1,2,3,4,6-penta-O-galloyl-d-glucose (PGG), a hydrolyzable tannin. Soluble-C and N, in treatment supernatants, was measured to uncover evidence for sorption of treatments or effects on extraction of soil-N. Significant amounts of soluble-C, added with treatments, were not recovered in supernatants indicating sorption of nearly 90% of the PGG-C, about 75% of the TA-C but less than 25% of the GA-C in surface soil. Disappearance of soluble-C from treatment supernatants was accompanied by a corresponding reduction of total phenolic content. Treatments added a negligible amount of N to soil; but while PGG and TA reduced soluble-N, in extracts from surface soil, GA had little effect. Soluble-N in extracts was composed mainly of organic-N. Effects of tannins persisted in surface soil through 12 washings with hot water (80 ^°C), suggesting the formation of stable complexes with soil. The proportion of initial soil-C and N remaining after all extractions was higher in samples treated with PGG or TA than either the Control or GA treatment. We conclude PGG readily sorbs to soil and reduces the solubility of soil organic-N unlike GA, its simple monomeric constituent. These differences could be especially important near the surface where quantities of soil organic matter and biological activity are comparatively large and most easily affected by management.