Effect of microbial nitrogen immobilization during the growth period on the availability of nitrogen fertilizer for winter cereals

 Pot and field experiments were conducted to determine microbial immobilization of N fertilizer during growth periods of winter wheat and winter barley. In a pot experiment with winter wheat, Ca(¹⁵NO₃)₂ was applied at tillering [Zadok's growth stage (GS) 25)], stem elongation (GS 31) and ear emergence (GS 49). Rates of 100 mg N pot^–1, 200 mg N pot^–1 or 300 mg N pot^–1 were applied at each N application date. At crop maturity, ¹⁵N-labelled fertilizer N immobilization was highest at the highest N rate (3×300 mg N pot^–1). For each N-rate treatment about 50% of the total immobilized fertilizer N was immobilized from the first N dressing, and 30% and 20% of the total ¹⁵N immobilized was derived from the second and third applications, respectively. In field trials with winter wheat (three sites) and winter barley (one site) N was applied at the same growth stages as for the pot trial. N was also applied to fallow plots, but only at GS 25. N which was not recovered (neither in crops nor in soil mineral N pools) was considered to represent net immobilized N. A clear effect of N rate (51–255 kg N ha^–1) on net N immobilization was not found. The highest net N immobilization was found for the period between GS 25 (March) and GS 31 (late April) which amounted to 54–97% of the total net N immobilized at harvest (July/August). At GS 31, non-recovered N was found to be of similar magnitude for cropped and fallow plots, indicating that C from roots did not affect net N immobilization. Microbial biomass N (N_mic) was determined for cropped plots at GS 31. Although N_mic tended to be higher in fertilized than in unfertilized plots, fertilizer-induced increases in N_mic and net N immobilization were poorly correlated. It can be concluded that microbial immobilization of fertilizer N is particularly high after the first N application when crop growth and N uptake are low. Received: 6 July 1999     

Phosphate additions have no effect on microbial biomass and activity in a northern hardwood forest

High rates of atmospheric nitrogen (N) deposition have raised questions about shifting patterns of nutrient limitation in northern hardwood forests. Of particular interest is the idea that increased supply of N may induce phosphorus (P) limitation of plant and microbial processes, especially in acid soils where P sorption by Al is high. In this study, we established field plots and plant-free laboratory mesocosms with P and Ca additions to test the hypotheses that 1) microbial biomass and activity are limited by P in the northern hardwood forest soils at the Hubbard Brook Experimental Forest in NH USA; 2) elevated Ca increases inherent P availability and therefore reduces any effects of added P and 3) P effects are more marked in the more carbon (C) rich Oie compared to the Oa horizon. Treatments included P addition (50 kg P ha⁻¹), Ca addition (850 kg Ca ha⁻¹) and Ca + P addition (850 kg Ca ha⁻¹ and 50 kg P ha⁻¹). The P treatments increased resin-available P levels and reduced phosphatase activity, but had no effect on microbial biomass C, microbial respiration, C metabolizing enzymes, potential net N mineralization and nitrification in the Oie or Oa horizon of either field plots or plant free mesocosms, in either the presence or absence of Ca. Total, prokaryote, and eukaryote PLFA were reduced by P addition, possibly due to reductions in mycorrhizal fungal biomass. These results suggest that increased N deposition and acidification have not created P limitation of microbial biomass and activity in these soils.     

Soil organic nitrogen composition in Pinus forest acid soils: variability and bioavailability

 The total N content in the acid forest soils studied ranged between 0.41% and 1.43%, and in more than 98% was composed of organic N. Total hydrolysable organic N, hydrolysable unknown N (HUN) and α-aminoacidic N represented around 70%, 34% and 20% of the organic N, respectively, and varied in wide ranges. The percentages of amidic N and of the organic N compounds solubilised to NH₄ ⁺ were approximately 6% and 5%, respectively, and ranged in narrow intervals. Aminoglucidic N reached a maximum of 3.8% of the organic N and was undetectable in some of the samples analysed. Most of the hydrolysable N, HUN and α-aminoacidic N was solubilised with 1 N and 3 N HCl, while a high amount of the compounds recovered as NH₄ ⁺ (60%) was obtained with 6 N HCl. The distribution of aminoglucidic N in the four fractions of increasing hydrolytic intensity was very irregular. The organic N composition in the 0 to 5-cm and 5 to 10-cm layers was not significantly different. The variation among samples was determined mainly by the organic N compounds less resistant to acid hydrolysis (hydrolysable N and HUN less resistant to acid hydrolysis, amidic N and labile ammoniacal N) and by all α-aminoacidic N fractions. Aminoacidic N was positively correlated with electrical conductivity and negatively correlated with exchangeable Al. The net N mineralisation over 10 weeks of incubation was positive in all the soil samples analysed. The inorganic N content after the incubation and the microbial N content were positively correlated with other variables – mainly with amidic N and α-aminoacidic N, as well as with HUN and the hydrolysable N less resistant to hydrolysis. Received: 13 July 1999     

Soil microbial biomass and mineralization of carbon and nitrogen in ecological, integrated and conventional forage and arable cropping systems

 In a cropping systems experiment in southeastern Norway, ecological (ECO), integrated (INT) and conventional (CON) forage (FORAGE) and arable (ARABLE) model farms were compared. After 5 experimental years, topsoil was sampled in spring from spring grain plots and incubated for 449 days at controlled temperature (15  °C) and moisture content (50% water-holding capacity). There were no detectable differences between model farms in terms of total soil C or N. For INT and CON, however, values of microbial biomass C and N, microbial quotient (C_mic/C_org), and C and N mineralization were, or tended to be, higher for FORAGE than for ARABLE. For the ECO treatment, values were similar for FORAGE and ARABLE and did not differ significantly from that of CON-FORAGE. For INT and CON, the metabolic quotient (qCO₂) was lower for FORAGE than for ARABLE. Again, for the ECO treatment, values were similar for FORAGE and ARABLE and did not differ significantly from that of CON-FORAGE. We estimated the sizes of conceptual soil organic matter pools by fitting a decomposition model to biomass and mineralization data. This resulted in a 48% larger estimate for CON-FORAGE than for CON-ARABLE of physically protected biomass C. For physically protected organic C the difference was 42%. Moreover, the stability of soil aggregates against artificial rainfall was substantially greater for CON-FORAGE than for CON-ARABLE. On this basis, we hypothesized that the lower qCO₂ values in the FORAGE soils were mainly caused by a smaller proportion of active biomass due to enclosure of microorganisms within aggregates. Altogether, our results indicated a poorer inherent soil fertility in ARABLE than in FORAGE rotations, but the difference was small or absent in the ECO system, probably owing to the use of animal and green manures and reduced tillage intensity in the ECO-ARABLE rotation. Received: 28 October 1998     

Soluble organic nitrogen in agricultural soils

 The existence of soluble organic forms of N in rain and drainage waters has been known for many years, but these have not been generally regarded as significant pools of N in agricultural soils. We review the size and function of both soluble organic N extracted from soils (SON) and dissolved organic N present in soil solution and drainage waters (DON) in arable agricultural soils. SON is of the same order of magnitude as mineral N and of equal size in many cases; 20–30 kg SON-N ha^–1 is present in a wide range of arable agricultural soils from England. Its dynamics are affected by mineralisation, immobilisation, leaching and plant uptake in the same way as those of mineral N, but its pool size is more constant than that of mineral N. DON can be sampled from soil solution using suction cups and collected in drainage waters. Significant amounts of DON are leached, but this comprises only about one-tenth of the SON extracted from the same soil. Leached DON may take with it nutrients, chelated or complexed metals and pesticides. SON/DON is clearly an important pool in N transformations and plant uptake, but there are still many gaps in our understanding. Received: 10 June 1999     

Gross nitrogen mineralization and nitrification rates and their relationships to enzyme activities and the soil microbial biomass in soils treated with dairy shed effluent and ammonium fertilizer at different water potentials

 Gross N mineralization and nitrification rates and their relationships to microbial biomass C and N and enzyme (protease, deaminase and urease) activities were determined in soils treated with dairy shed effluent (DSE) or NH₄ ⁺ fertilizer (NH₄Cl) at a rate equivalent to 200 kg N ha^–1 at three water potentials (0, –10 and –80 kPa) at 20  °C using a closed incubation technique. After 8, 16, 30, 45, 60 and 90 days of incubation, sub-samples of soil were removed to determine gross N mineralization and nitrification rates, enzyme activities, microbial biomass C and N, and NH₄ ⁺ and NO₃ ^– concentrations. The addition of DSE to the soil resulted in significantly higher gross N mineralization rates (7.0–1.7 μg N g^–1 soil day^–1) than in the control (3.8–1.2 μg N g^–1 soil day^–1), particularly during the first 16 days of incubation. This increase in gross mineralization rate occurred because of the presence of readily mineralizable organic substrates with low C : N ratios, and stimulated soil microbial and enzymatic activities by the organic C and nutrients in the DSE. The addition of NH₄Cl did not increase the gross N mineralization rate, probably because of the lack of readily available organic C and/or a possible adverse effect of the high NH₄ ⁺ concentration on microbial activity. However, nitrification rates were highest in the NH₄Cl-treated soil, followed by DSE-treated soil and then the control. Soil microbial biomass, protease, deaminase and urease activities were significantly increased immediately after the addition of DSE and then declined gradually with time. The increased soil microbial biomass was probably due to the increased available C substrate and nutrients stimulating soil microbial growth, and this in turn resulted in higher enzyme activities. NH₄Cl had a minimal impact on the soil microbial biomass and enzyme activities, possibly because of the lack of readily available C substrates. The optimum soil water potential for gross N mineralization and nitrification rates, microbial and enzyme activities was –10 kPa compared with –80 kPa and 0 kPa. Gross N mineralization rates were positively correlated with soil microbial biomass N and protease and urease activities in the DSE-treated soil, but no such correlations were found in the NH₄Cl-treated soil. The enzyme activities were also positively correlated with each other and with soil microbial biomass C and N. The forms of N and the different water potentials had a significant effect on the correlation coefficients. Stepwise regression analysis showed that protease was the variable that most frequently accounted for the variations of gross N mineralization rate when included in the equation, and has the potential to be used as one of the predictors for N mineralization. Received: 10 March 1998     

Short-term effects of nitrogen on methane oxidation in soils

 The short-term effects of N addition on CH₄ oxidation were studied in two soils. Both sites are unfertilized, one has been under long-term arable rotation, the other is a grassland that has been cut for hay for the past 125 years. The sites showed clear differences in their capacity to oxidise CH₄, the arable soil oxidised CH₄ at a rate of 0.013 μg CH₄ kg^–1 h^–1 and the grassland soil approximately an order of magnitude quicker. In both sites the addition of (NH₄)₂SO₄ caused an immediate reduction in the rate of atmospheric CH₄ oxidation approximately in inverse proportion to the amount of NH₄ ⁺ added. The addition of KNO₃ caused no change in the rate of CH₄ oxidation in the arable soil, but in the grassland soil after 9 days the rate of CH₄ oxidation had decreased from 0.22 μg CH₄ kg^–1 h^–1 to 0.13 μg CH₄ kg^–1 h^–1 in soil treated with the equivalent of 192 kg N ha^–1. A ¹⁵N isotopic dilution technique was used to investigate the role of nitrifiers in regulating CH₄ oxidation. The arable soil showed a low rate of gross N mineralisation (0.67 mg N kg^–1 day^–1), but a relatively high proportion of the mineralised N was nitrified. The grassland soil had a high rate of gross N mineralisation (18.28 mg N kg^–1 day^–1), but negligible nitrification activity. It is hypothesised that since there was virtually no nitrification in the grassland soil then CH₄ oxidation at this site must be methanotroph mediated. Received: 31 October 1997     

Soil organic carbon stocks, storage profile and microbial biomass under different crop management systems in a tropical agricultural ecosystem

 We investigated the soil organic C and N stocks, storage profiles and microbial biomass as influenced by different crop management systems in a tropical agricultural ecosystem. The different crop management systems significantly affected the C and N stocks and microbial biomass C and N at different soil depths. Amongst the systems evaluated, the rice-wheat system maintained a higher soil organic C content. Inclusion of legumes in the system improved the soil organic matter level and also soil microbial biomass activity, vital for the nutrient turnover and long-term productivity of the soil. Irrespective of the cropping system, approximately 58.4%, 25.7% and 15.9% of the C was distributed in 0–15, 15–30 and 30–60 cm depths, respectively. Received: 10 October 1999     

Carbon and nitrogen accretion and dynamics in volcanic ash deposits from different subarctic habitats

Summary C and N pool sizes and rates of mineralization were studied in volcanic-ash deposits found in different subarctic habitats in southwestern Alaska. Surface ash samples were taken from white-spruce, alder, and moist- and dry-tundra habitats and were analysed for total and microbial C and N. C and N dynamics were studied using a 28-day aerobic laboratory incubation, with weekly measurement of evolved CO₂ and determination of inorganic-N pools initially and after 10 and 28 days. Total and microbial C and N and cumulative respired CO₂ all followed a similar pattern among the different habitats, with the moist-tundra habitat having the highest values and the spruce site the lowest. The size of the microbial biomass C and N pool in the spruce habitat was among the lowest reported for any ecosystem. Little net N mineralization occurred in the spruce-forest and dry-tundra ash over 28 days. Ash from the moist-tundra habitat immobilized a significant amount of N during the first 10 days of incubation, yet showed a large net release of N after 28 days. In contrast, the ash from the alder site exhibited net mineralization after both periods, with N production after 28 days being about 3.5 times that after 10 days. In addition, the alder-habitat ash was the only soil that showed net nitrification. Rates of total C and N accretion in the tundra and alder habitats were rapid relative to rates found for primary successions. The results of this study show that habitat has a profound effect on C and N cycling in subarctic environments.     

Land use effects on labile N extracted with permanganate and the nitrogen management index in the Cerrado region of Brazil

 The effect of land use on the availability of nitrogen (N) was studied by separating total N into a labile and a stable fraction by oxidation and extraction of labile N with KMnO₄. The nitrogen management index (NMI) was calculated following the method of Blair et al. (1995) for the carbon management index. In all systems, labile N released by KMnO₄ was a better indicator of N availability than total and stable N. The NMI was a good indicator of N availability but gave no information about the total amount of N. In land use system analysis, total N and labile N can be used together as a simple and rapid way to evaluate the N status of the soil. Legume-based pastures specifically increased the amount of labile N. Although soybeans had a dominant role in the continuous cropping systems studied, the total N contents of these systems were lower than those of the natural Cerrado. The availability of N under legume-based pastures and legume-based pasture-crop rotations was higher than under the natural Cerrado and the continuous cropping systems. Received: 11 June 1997     

Carbon and nitrogen mineralization in subarctic agricultural and forest soils

Summary C and N mineralization potentials were determined, in a 12-week laboratory incubation study, on soil samples obtained from recently cleared land which had been cropped to barley for 4 years (field soils) and from nearby undisturbed taiga (forest soils). Treatments for the cropped soils were conventional and no-tillage with and without crop residues removed. An average of about 3% of the total C was evolved as CO₂ from the field soils compared with > 10% and 4% for the upper (Oie) and lower (Oa) forest-floor horizons, respectively. Significantly more C was mineralized from the Ap of the no-till treatment with residue left on the surface than from the other field Ap horizons. Both forest-floor horizons showed rather long lag periods for net mineralization compared with the field soils, but at the end of the incubation, more mineral N was recovered from the forest Oie despite a rather wide C:N ratio, than from the field soils. After 12 weeks about 115, 200 and 20 g mineral N/g soil were recovered from the field Ap, the forest Oie and the forest Oa horizons, respectively. Very little C or N was mineralized from the B horizon of the forest or the field soils. Nitrification was rapid and virtually complete for the field soils but was negligible for both forest-floor O horizons.Paper no J-188 of the Journal Series of the Alaska Agricultural and Forestry Experiment Station     

Response of protozoan and microbial communities in various coniferous forest soils after transfer to forests with different levels of atmospheric pollution

During recent decades, forest ecosystems have been exposed to high levels of atmospheric pollution, and it has been argued that this affects the composition and activity of decomposer communities and, subsequently, ecosystem functioning. To investigate the effects of atmospheric pollution on protozoa and microflora, a new experimental design was used. Undisturbed soil columns, originating from six coniferous forests across Europe and representing different stages of soil acidification, were transferred to two Scots pine forests (Fontainebleau and Wekerom) with different levels of N and S deposition (NH₄ ⁺-N=4.90 and 42.50?kg ha^–1 year^–1; SO₄ ^–S=10.90 and 30.40?kg ha^–1 year^–1, respectively). The number of protozoa, microbial biomass C and microbial activity were estimated in the organic layer (Of) of the transferred soils at the two host sites after 21 months of incubation. The experiment aimed at answering two questions: (1) Do changes in environmental conditions, studied by transferring soils from one site to another, affect protozoa and microbial communities and, if so, (2) how important are changes in both N and S deposition in explaining the effects of soil transfer on protozoa and microbial communities? The interaction between protozoa and microbial communities was addressed with regard to these changes in environmental conditions. No effect of enhanced N or S deposition on protozoan numbers and microbial biomass C, basal respiration and caloric quotient was revealed. Reciprocal transfer of various soil columns resulted in lower abundance and activity of protozoa and microbes. This reduction could not be explained by differences in N and S deposition, but by differences in microclimate and adaptation. In some cases, protozoa correlated with pH, C/N ratio, P and S content and leached mineral N.     

Release and consumption of nitrogen by snail feces in Negev Desert soils

Snail grazing and feces production have been shown to be major components of the nitrogen (N) budget of Negev Desert ecosystems. However, the movement of N from feces into soil N cycling processes has not been studied. In this study, we measured immediate N release from different types of snail feces following wetting of dry desert soils, and characterized potential net N mineralization and nitrification and soil respiration over a 12-day incubation under laboratory conditions. The dynamics of morganic N exhibited two distinct phases during the 12-day incubation: (1) immediate release of inorganic N following wetting of the soil and (2) decline of inorganic N from day 1 today 12 of the incubation. The immediate pulse of N release from this one wetting event (6–25 mg N m^-2) was larger than annual atmospheric inputs of N to Negev Desert ecosystems (<2 mg N m^-2); however, from 50 to 80% of the N released upon wetting was consumed by the end of the incubation. There were differences in inorganic N release and respiration from feces from different kinds of snails, and from feces from the same species of snail fed different plants. The results suggest that while snail feces contribute significant amounts of plant available N to Negev ecosystems, plants must compete with other sinks for this N.     

Interaction of biochemical quality and particle size of crop residues and its effect on the microbial biomass and nitrogen dynamics following incorporation into soil

 Mineralization of N from organic materials added to soil depends on the quality of the substrate as a carbon, energy and nutrient source for the saprophytic microflora. Quality reflects a combination of biochemical and physical attributes. We investigated how biochemical composition interacts with particle size to affect the soil microflora and N dynamics following incorporation of crop residues into soil. Four fresh shoot and root crop residues were cut into coarse and fine particle sizes, and incorporated into sandy-loam soil which was incubated under controlled environment conditions for 6 months. In the case of the highest biochemical quality material, potato shoot (C/N ratio of 10 : 1), particle size had no effect on microbial respiration or net N mineralization. For lower biochemical quality Brussels sprout shoot (C/N ratio of 15 : 1), reducing particle size caused microbial respiration to peak earlier and increased net mineralization of N during the early stages of decomposition, but reduced net N mineralization at later stages. However, for the lowest biochemical quality residues, rye grass roots (C/N ratio of 38 : 1) and straw (C/N ratio of 91 : 1) reducing particle size caused microbial respiration to peak later and increased net immobilization of N. For Brussels sprout shoot, reducing particle size decreased the C content and the C/N ratio of residue-derived light fraction organic matter (LFOM) 2 months following incorporation. However C and N content of LFOM derived from the other materials was not affected by particle size. For materials of all qualities, particle size had little effect on biomass N. We conclude that the impact of particle size on soil microbial activities, and the protection of senescent microbial tissues from microbial attack, is dependant on the biochemical quality of the substrate. Received: 3 July 1998     

Ratios between estimates of microbial biomass content and microbial activity in soils

The content levels and activities of the microbiota were estimated in topsoils and in one soil profile at agricultural and forest sites of the Bornhöved Lake district in northern Germany. Discrepancies between data achieved by fumigation-extraction (FE) and substrate-induced respiration (SIR), both used for the quantification of microbial biomass, were attributed to the composition of the microbial populations in the soils. In the topsoils, the active, glucose-responsive (SIR) versus the total, chloroform-sensitive microbial (FE) biomass decreased in the order; field maize monoculture (field-MM)>field crop rotation (field-CR) and dry grassland>beech forest. This ratio decreased within the soil profile of the beech forest from the litter horizon down to the topsoil. Differences between microbial biomass and activities suggested varying biomass-specific transformation intensities in the soils. The metabolic quotient (qCO₂), defined as the respiration rate per unit of biomass, indicates the efficiency in acquiring organic C and the intensity of C mineralization, while biomass-specific arginine-ammonification (arginine-ammonification rate related to microbial biomass content) seems to be dependent on N availability. The qCO₂, calculated on the basis of the total microbial biomass, decreased for the topsoils in the same order as did the ratio between the active, glucose-responsive microbial biomass to the total, chloroform-sensitive microbial biomass, in contrast to qCO₂ values based on the glucose-responsive microbial biomass, which did not. There was no difference between the levels of biomass-specific arginine-ammonification in topsoils of the fertilized field-CR, fertilized field-MM, fertilized dry grassland and eutric alder forest, but levels were lower in the beech forest, dystric alder forest, and unfertilized wet grassland topsoils. Ratios between values of different microbiological features are suggested to be more useful than microbiological features related to soil weight when evaluating microbial populations and microbially mediated processes in soils.     

The impact of a low humus level in arable soils on microbial properties, soil organic matter quality and crop yield

 In arable soils in Schleswig-Holstein (Northwest Germany) nearly 30% of the total organic C (TOC) stored in former times in the soil has been mineralized in the last 20 years. Microbial biomass, enzyme activities and the soil organic matter (SOM) composition were investigated in order to elucidate if a low TOC level affects microbial parameters, SOM quality and crop yield. Microbial biomass C (C_mic) and enzyme activities decreased in soils with a low TOC level compared to soils with a typical TOC level. The decrease in the C_mic/TOC ratio suggested low-level, steady-state microbial activity. The SOM quality changed with respect to an enrichment of initial litter compounds in the top soil layers with a low TOC level. Recent management of the soils had not maintained a desirable level of humic compounds. However, we found no significant decrease in crop yield. We suggest that microbial biomass and dehydrogenase and alkaline phosphatase activities are not necessarily indicators of soil fertility in soils with a high fertilization level without forage production and manure application. Received: 12 December 1997     

Carbon respiration and nitrogen dynamics in Corsican pine litter amended with aluminium and tannins

We investigated the carbon (C) mineralisation and nitrogen (N) dynamics in litter from a Corsican pine forest in response to individual and combined additions of aluminium (Al), condensed tannin (extracted from fresh Corsican pine needles) and hydrolysable tannin (commercial tannic acid). Production rates of CO₂, NH₄⁺ and NO₃⁻ concentrations, tannin concentrations and Al speciation were determined at various time intervals during a 28-day incubation experiment. The addition of Al decreased CO₂ production and shut down nitrification. Exchangeable NH₄⁺ strongly increased in the Al-amended litter, likely due to (i) decreased microbial uptake of NH₄⁺, (ii) the inhibition of nitrification and (iii) competition for soil organic matter (SOM) binding sites by Al. Both tannin species affected C mineralisation and/or N dynamics, be it in different ways. Addition of tannic acid led to a strong increase of the C mineralisation rate and microbial uptake of N, caused by rapid degradation of this labile tannin and subsequent increased microbial nutrient demand. Net immobilisation of N occurred as long as one week after addition. Condensed tannin was not consumed but probably strongly bound to (nitrogenous) SOM compounds, forming recalcitrant complexes and decreasing net N mineralisation. Complexation of Al by tannins in solution before addition to the litter mitigated the Al-induced release of exchangeable NH₄⁺. In the case of condensed tannin with complexed Al, this was due to detoxification of Al through complexation. Increased microbial demand for N likely played a major role in decreased NH₄⁺ accumulation in the samples to which tannic acid with complexed Al was added. Nitrification was shut down despite of the complexation of Al by either condensed tannin or tannic acid.     

Microbial degradation of hydrolysable and condensed tannin polyphenol-protein complexes in soils from different land-use histories

Polyphenols are capable of binding to proteins and form polyphenol-protein complexes thus reducing the release of N from decomposing plant materials. The objective of this work was to test if under polyphenol-rich vegetations adapted microbial communities had developed capable of breaking down recalcitrant polyphenol-protein complexes. Soils used for this investigation were from different 10-year-old tropical agricultural systems (maize, sugarcane plots and Gliricidia sepium or Peltophorum dasyrrachis woodlots) and natural systems (secondary forest and Imperata cylindrica grassland). TA (tannic acid, hydrolysable tannin), QUE (quebracho, condensed tannin), BSA (bovine serum albumin, protein) or TA/BSA and QUE/BSA polyphenol-protein complexes were incubated at 28 °C in these soils. CO₂-C and ¹³C evolution were periodically monitored and mineral N release, microbial biomass N and phospholipid fatty acid (PLFA) profiles measured at the end.QUE was able to bind about 25% more protein than TA. In all systems the individual uncomplexed substrates were more easily degraded than the complexes. On average, net cumulative CO₂-C evolution from TA/BSA complexes was more than 5 times higher than from QUE/BSA complexes, indicating higher C availability and/or lower protection capability of TA compared to QUE. However, net N release was higher from QUE/BSA than from TA/BSA probably due to their higher protein-binding capacity and associated larger degradation of partly unprotected protein as suggested by ¹³C-CO₂ signatures. Microbial respiration patterns indicated that polyphenol complexes were initially degraded more quickly in the maize cropping system than in soils from under polyphenol-rich communities (Peltophorum and natural forest) but this pattern reversed with time. Long-term incubation of QUE/BSA complexes even caused a negative effect on microbial respiration in agricultural soils with low polyphenol contents (e.g. maize and sugarcane).Incubation of polyphenol complexes in soil depressed microbial biomass N in maize, sugarcane, Imperata and forest systems and led to reduced soil pH. However, microbial biomass was increased under the polyphenol-rich vegetation of Peltophorum. The PLFA group 18:2w6,9 was highly enhanced by condensed tannin-protein complexes additions as compared to control and hydrolysable polyphenol-protein complexes in soils with high polyphenol contents. Polyphenol complexes increased the fungi:bacteria ratio in systems with a high polyphenol content, particularly with condensed tannin complexes. The results indicated that systems with a high polyphenol content favoured development of fungal communities that are highly adaptable to phenol-rich soil conditions and high acidity, particularly with regards to the more recalcitrant condensed tannin-protein complexes.     

Carbon and nitrogen dynamics in a phosphorus-deficient soil amended with organic residues and fertilizers in western Kenya

The contribution of organic resources to the restoration of soil fertility in smallholder farming systems in East Africa is being tested as an alternative to costly fertilizers. Organic inputs are expected to have advantages over fertilizers by affecting many biochemical properties controlling nutrient cycling. Our study examined changes in soil C and N, C and N mineralization, microbial biomass C (MBC) and N (MBN), and particulate organic matter (POM) in a P-limiting soil in western Kenya after applications of organic residues and fertilizers to overcome P limitation to crops. Leaf biomass from six different tree (shrub) species was incorporated into the soil at 5 Mg ha^–1 for five consecutive maize growing seasons, over 2.5 years. Triple superphosphate was applied separately at 0, 10, 25, 50, and 150 kg P ha^–1 in combination with 120 kg N ha^–1 as urea. Soil inorganic N, soil organic C, mineralizable N, and total C in all POM fractions and total N in the 53- to 250-m POM fraction increased following addition of all organic residues compared to the control. Whether there was an advantage of organic residue incorporation over inorganic fertilizer use depended on the soil parameter studied, the organic residue and the rate of fertilization. Most differences were found in N mineralization where 14.4–21.6 mg N kg^–1 was mineralized in fertilizer treatments compared to 25.2–30.5 mg N kg^–1 in organic residue treatments. C and N mineralization and the 53- to 250-m POM fractions were the most sensitive parameters, correlating with most of the studied parameters. Organic residues can contribute to improved soil nutrient cycling while the magnitude of their contribution depends on the biochemical properties of the residues.     

Long-term winter cover cropping effects on corn (Zea mays L.) production and soil nitrogen availability

 This study was conducted to determine effects of long-term winter cover cropping with hairy vetch, cereal rye and annual ryegrass on soil N availability and corn productivity. From 1987 to 1995, with the exception of the first year of the study, the cover crops were seeded each year in late September or early October after the corn harvest and incorporated into the soil in late April or early May. Corn was seeded 10 days to 2 weeks after the cover crop residues had been incorporated, and N fertilizer was applied as a side-dressing at rates of 0, 67, 134, or 201 kg N ha^–1 each year. While the average annual total N input from the above-ground biomass of the cover crops was highest for hairy vetch (72.4 kg N ha^–1), the average annual total C input was highest for cereal rye (1043 kg C ha^–1) compared with the other cover crops. Hairy vetch was the only cover crop that significantly increased pre-side-dressed NO₃ ^–-N (N_i) corn biomass and N uptake at 0 N. At an N fertilizer rate of 134 kg N ha^–1 or higher, the cover crops had a minimal effect on corn biomass. This indicated that even after 9 years of winter cover cropping, the effect of the cover crops on corn growth resulted primarily from their influence on soil N availability. The amount of available N estimated from the cover crops (N_ac) was significantly correlated with relative corn biomass production (r ²=0.707, P<0.001). The total amount of available N, comprising N_ac and N added from fertilizer (N_f), was strongly correlated (r ²=0.820, P<0.001)) with relative corn biomass production. The correlation was also high for the available N comprising N_i and N_f (r ²=0.775, P<0.001). Although cereal rye and annual ryegrass did not improve corn biomass production in the short term, they benefited soil organic N accumulation and gradually improved corn biomass production compared with the control over the long term. Received: 10 August 1999