Release of sulphate, potassium, calcium and magnesium from spent mushroom compost under laboratory conditions

The release of sulphate-sulphur (SO₄ ^2–-S), potassium (K), calcium (Ca) and magnesium (Mg) from soil amended with spent mushroom compost (SMC), a by-product of mushroom production, was measured for 16 weeks in an open laboratory incubation at 25°C. Rates of application were up to 80 t ha^–1 moist SMC (0.84% SMC dry weight) both with and without inorganic fertilizer. The rates of nutrient application in the inorganic fertilizer were: 338 kg ha^–1 N, 100 kg ha^–1 of both phosphorus and K, and 114 kg ha^–1 S. SMC contains 1.7% K, 6.5% Ca, 0.4% Mg and 1.2% S (of which 87% is inorganic), and has a carbon:sulphur ratio of 26. The release of SO₄ ^2–-S was rapid, and was described using either a first or mixed order exponential equation, or (underestimated) by the CENTURY model. The release of K, Ca and Mg was initially rapid (first order) and then declined to a constant rate (zero order). Their release was also described using first/first order or first order/parabolic diffusion equations. Model parameters indicated the relative sizes of both readily releasable and recalcitrant nutrient pools. The recovery of SMC-supplied nutrients in the absence of fertilizer was 75–83% of the S, 40–45% of the K, 14–20% of the Ca and 43–66% of the Mg. When fertilizer was applied 33–45% of the S, 22–36% of the K, 12–24% of the Ca and –4 to 20% of the Mg that were supplied by the SMC and fertilizer were recovered in the leachate. The generally lower nutrient recovery when fertilizer was applied could have resulted from the incomplete recovery of fertilizer S and K, from soil fixation of applied nutrients, and from the lower pH following fertilizer application. Received: 3 April 1997     

Nutrient balance in Scots pine (Pinus sylvestris L.) forest. 2. Effects of plant growth and N-deposition on soil solution and leachate chemistry in a lysimeter experiment

Three years of N application to a Cambic arenosol (Typic Udorthent) in two lysimeter series, one with and one without young saplings of Pinus sylvestris L. have produced significant changes in soil solution and leachate chemistry. An application of 30 kg N/ha^*yr^?1 significantly increased NO₃ ^? leaching from the soil. This N load was also sufficient to significantly increase the mobility of the phyto-toxic elements Al³⁺ and Mn²⁺, likewise to increase leaching of the important plant nutrients Ca²⁺, Mg²⁺ and K⁺. At a N load of 90 kg N/ha^*yr^?1 significant increase in NH₄ ⁺ leaching was observed, but total leaching of NH₄ ⁺ was still very low compared to NO₃ ^? leaching. No significant treatment effects were found for SO₄ ^2?, Fe²⁺ and Cl^? in the leachate. Trees grown in the lysimeters buffered the acidifying effect of N application and increased the leachate pH by 0.2 pH units compared to lysimeters without trees.     

Deposition and Leaching of Sulphate and Base Cations in a Mixed Boreal Forest in Eastern Finland

Monthly fluxes of sulphate (SO₄ ^2-) and base cations(Ca²⁺, Mg²⁺, K⁺) were studied from 1993 to 1996 as precipitation passed through forest vegetation and surfacesoil layers in an area receiving low and declining levels of atmospheric sulphate pollution. The canopy was dominated by mature Norway spruce (Picea abies Karsten) and the soilwas a podzol developed on glacial till material. The mean annual bulk deposition of SO₄ ^2- collected in the open was 136 mol_c ha^-1 and that of Ca²⁺, Mg²⁺ and K⁺ was 44, 11 and 25 mol_c ha^-1, respectively. The annual total throughfall deposition of SO₄ ^2- was 318 mol_c ha^-1 and that of Ca²⁺, Mg²⁺ and K⁺ was 151, 64 and 181 mol_cha^-1, respectively. Sulphate was the dominant anion accompanying the base cations leached from the canopy. More than half (58%) of the annual total throughfall deposition ofSO₄ ^2- was retained by the O-horizon and only 15% leached from below the B-horizon. The annual leaching of Ca²⁺, Mg²⁺ and K⁺ from below the B-horizon was14, 25 and 9% of the annual total throughfall deposition, respectively. The transport of base cations through the soil was predominantely countered by SO₄ ^2- anions.     

Critical sulphur concentration and sulphur requirement of microbial biomass in a glucose and cellulose-amended regosol

 The critical S concentration and S requirement of the soil microbial biomass of a granitic regosol was examined. S was applied at the rate of 0, 5, 10, 20, 30 and 50 μg S as MgSO₄·7H₂O, together with either 3000 μg glucose-C or 3333 μg cellulose-C, 400 μg N, and 200 μg P g ^–1 soil and 200 μg K g^–1 soil. Microbial biomass, inorganic SO₄ ^2–-S, and CO₂ emission were monitored over 30 days during incubation at 25  °C. Both glucose and cellulose decomposition rates responded positively to the S made available for microbial cell synthesis. The amounts of microbial biomass C and S increased with the level of applied S up to 10 μg S g^–1 soil and 30 μg S g^–1 soil in the glucose- and cellulose-amended soil, respectively, and then declined. Incorporated S was found to be concentrated within the microbial biomass or partially transformed into soil organic matter. The concentration of S in the microbial biomass was higher in the cellulose- (4.8–14.2 mg g^–1) than in the glucose-amended soil (3.7–10.9 mg g^–1). The microbial biomass C:S ratio was higher in the glucose- (46–142 : 1) than in the cellulose-amended soil (36–115 : 1). The critical S concentration in the microbial biomass (defined as that required to achieve 80% of the maximum synthesis of microbial biomass C) was estimated to be 5.1 mg g^–1 in the glucose- and 10.9 mg g^–1 in the cellulose-amended soil. The minimum requirement of SO₄ ^2–-S for microbial biomass formation was estimated to be 11 μg S g^–1 soil and 21 μg S g^–1 soil for glucose- and cellulose-amended soil, respectively. The highest levels of activity of the microbial biomass were observed at the SO₄ ^2–-S concentrations of 14 μg S g^–1 soil and 17 μg S g^–1 soil, for the glucose and cellulose amendments, respectively, and were approximately 31–54% higher during glucose than cellulose decomposition. Received: 20 October 1999     

Lysimeter study with a cambic arenosol exposed to artificial acid rain: II. Input-output budgets and soil chemical properties

The effects of artificial precipitation with different pH levels on soil chemical properties and element flux were studied in a lysimeter experiment. Cambic Arenosol (Typic Udipsamment) in monolith lysimeters was treated for 6 1/2 yr with 125 mm yr^?1 artificial rain in addition to natural precipitation. Artificial acid rain was produced from groundwater with H₂SO₄ added. pH levels of 6.1, 4 and 3 were used. ‘Rain’ acidity was buffered, mainly due to cation exchange with Ca²⁺ and Mg²⁺, which were increasingly leached due to the acid input. The H⁺ retention was not accompanied by a similar increase in the output of Al ions, but a slight increase in the leaching of Al ions was observed in the most acidic treatment. The net flux of SO₄ ^2? from the lysimeters increased with increasing input of H₂SO₄, but in the most acidified lysimeters significant sorption of SO₄ ^2? was observed. The sorption was, however, most likely a concentration effect. The ‘long-term’ acidification effects on soil were mainly seen in the upper O and Ah-horizons, where an impoverishment of exchangeable Ca²⁺ and Mg²⁺ was observed. An increased proportion of Al ions on exchange sites in the organic layer was observed in the pH 3-treated soil. By means of budget calculations the annual release of base cations due to weathering was estimated to be between 33 and 77 mmol_c m^?2.     

Influence of different agricultural practices (type of crop, form of N-fertilizer) on soil nitrous oxide emissions

 N₂O emissions were periodically measured using the static chamber method over a 1-year period in a cultivated field subjected to different agricultural practices including the type of N fertilizer (NH₄NO₃, (NH₄)₂SO₄, CO(NH₂)₂ or KNO₃ and the type of crop (rapeseed and winter wheat). N₂O emissions exhibited the same seasonal pattern whatever the treatment, with emissions between 1.5 and 15 g N ha^–1 day^–1 during the autumn, 16–56 g N ha^–1 day^–1 in winter after a lengthy period of freezing, 0.5–70 g N ha^–1 day^–1 during the spring and lower emissions during the summer. The type of crop had little impact on the level of N₂O emission. These emissions were a little higher under wheat during the autumn in relation to an higher soil NO₃ ^– content, but the level of emissions was similar over a 7-month period (2163 and 2093 g N ha^–1 for rape and wheat, respectively). The form of N fertilizer affected N₂O emissions during the month following fertilizer application, with higher emissions in the case of NH₄NO₃ and (NH₄)₂SO₄, and a different temporal pattern of emissions after CO(NH₂)₂ application. The proportion of applied N lost as N₂O varied from 0.42% to 0.55% with the form of N applied, suggesting that controlling this agricultural factor would not be an efficient way of limiting N₂O emissions under certain climatic and pedological situations. Received: 1 December 1997     

Niederschlags-Chemismus und atmosphärische Element-Deposition in einem an der Nordseeküste von Schleswig-Holstein gelegenen Agrarökosystem

Precipitation chemistry and atmospheric element-deposition in an agroecosystem at the North-Sea Coast of Schleswig-Holstein The objective of this study was to examine the chemistry of bulk precipitation and atmospheric element inputs in an arable soil near the North Sea coast of Schleswig-Holstein, North Germany. Bulk precipitation was collected at weekly intervals from November 1989 to October 1991. Precipitation amount, pH, electrical conductivity, and concentrations of Na⁺, K⁺, NH₄⁺, Mg²⁺, Ca²⁺, Cl^?, NO₃^?, and SO₄^2? were recorded. The average volume-weighted pH was 5.5 and the average EC was 92 μS cm^?1. Sodium and Cl^? were with 64% and 76% the dominant ions (equivalent concentration) in bulk precipitation indicating the influence of the North Sea. The contribution of marine alkalinity to neutralization reactions of bulk precipitation was negligible (1%). The neutralizing substances NH₃ (63%) and Carbonate (36%) were more important. Deposition rates were in 1990 and 1991 97.0 and 51.7 kg Na⁺ ha^?1, 6.2 and 4.0 kg K⁺ ha^?1, 15.0 and 8.4 kg Mg²⁺ ha^?1, 13.2 and 10.4 kg Ca²⁺ ha^?1, 12.3 and 9.5 kg NH₄⁺-N ha^?1, 8.0 and 5.9 kg NO₃^?-N ha^?1, 168 and 83.1 kg Cl^? ha^?1 and 19.1 and 12.7 kg SO₄^2?-S ha^?1. In 1990 both more westerly winds and stronger wind-forces occurred than in 1991 and resulted in higher inputs of marine origin. Calculated on Cl^? basis 93% of Na⁺, 55% of K⁺, 74% of Mg²⁺, 24% of Ca²⁺, and 36% of SO₄^2? were of marine origin. Atmospheric input of marine origin supplied 39–72% of Mg and 21–37% of S requirement for crop production. The North Sea is an important source providing significant amounts of these elements to agricultural crops.     

The effects of feeding byOniscus asellus (Isopoda) on nutrient cycling in an incubated hardwood forest soil

Summary Oniscus asellus produced changes in the nutrients leached from Oie and Oa horizons of a hardwood forest soil. Soil with isopods lost more K⁺ (54%) from the Oie horizon and more Ca²⁺ (25%), Mg²⁺ (40%), and water-extractable S (23%) from the Oa horizon than soil without isopods. In contrast, soils with isopods lost less Ca²⁺ (39076) from the Oie horizon and less dissolved C-bonded S (33%) from the Oa horizon than soil without isopods. In addition, the Oia and Oa horizons exhibited different nutrient dynamics. When isopods were present, the Oa horizon leachates accumulated more Na⁺ K⁺, Ca²⁺, Mg²⁺, NO₃ ^– , water-soluble SO₄ ^2–, and dissolved C-bonded S, and the Oie horizon retained more of these nutrients. The type of leaching solution also had a major effect on nutrients. Leaching with a simulated soil solution resulted in smaller nutrient losses for K⁺ and Mg²⁺ in both horizons and for Na⁺, Ca²⁺, and NO₃ ^– in the Oa horizon than leaching with distilled water.     

Chemical and biological characteristics of alkaline saline soils from the former Lake Texcoco as affected by artificial drainage

 Soils from the former Lake Texcoco are alkaline saline and were artificially drained and irrigated with sewage effluents since the late 1980s. Undrained soil and soil drained for 1, 5 and 8 years were sampled, characterized and incubated aerobically for 90 days at 22±1  °C while production of CO₂, available P and concentrations of NH₄ ⁺, NO₂ ^– and NO₃ ^– were monitored. Artificial drainage decreased pH_H2O, water holding capacity, organic C, total N, and Na⁺, K⁺, Mg²⁺, B, Cl^– and SO₄ ^2– concentrations, increased inorganic C and Ca²⁺ concentrations more than 5-fold while total P was not affected. Microbial biomass C decreased with increased length of drainage but bacteria, actinomycetes, denitrifiers and cellulose-utilizing bacteria tended to show opposite trends. CO₂ production was less in soils drained ≥5 years compared to undrained soil but more than in soils drained for 1 year. Emission of NH₃ was negligible and concentrations of NH₄ ⁺ remained constant over time in each soil. Nitrification, as witnessed by increases in NO₃ ^– concentrations, occurred in soil drained for 8 years. NO₂ ^– concentrations decreased in soils drained ≤1 year in the first 7 days of the incubation and remained constant thereafter. It was found that artificial drainage of soils from the former Lake Texcoco profoundly affected soil characteristics. Decreases in pH and Na⁺, K⁺, Cl^– and SO₄ ^2– concentrations made conditions more favourable for plant growth, although low concentrations of inorganic N and available P might be limiting factors. Received: 1 December 1999     

Utilization of waste office paper to reduce nitrate leaching into the Northern Guam aquifer

 Rapid nitrate leaching losses due to current agricultural N management practices under the humid tropical environmental conditions of the Pacific island of Guam may contaminate fresh and salt water resources. Potential environmental contamination of the Northern Guam aquifer, which is overlain by shallow limestone-derived soils, is a major public concern because the aquifer is the sole underground source of fresh water for the island. The objectives of this study were to examine the use of waste office paper as a possible management alternative for reducing nitrate leaching due to N fertilizer applications in northern Guam while also providing sufficient N for crop growth. In a laboratory study, increasing rates of waste paper application reduced NO₃ ^–-N leaching up to approximately 200 days after incorporation of N fertilizer and paper treatments. Subsequent mineralization of immobilized N from paper applications was also observed, although cumulative NO₃ ^–-N leaching at the highest rate of paper addition was lower than the control after 394 days of incubation. The effect of waste paper on N availability and NO₃ ^–-N leaching after application of N fertilizer at rates up to 500 kg N ha^–1 was also evaluated in two field experiments planted with sweet corn (Zea mays var. rugosa Bonaf.) during consecutive dry and wet periods. Leaching losses of NO₃ ^–-N were higher during the wet cropping season, leading to lower crop yields and crop N uptake. Combining paper with N fertilizer reduced NO₃ ^–-N leaching losses but also decreased crop ear yields up to N fertilizer application rates of 250 kg N ha^–1 during the dry cropping season and up to rates of 100 kg N ha^–1 during the wet period. Although combining waste paper with N fertilizer reduced NO₃ ^–-N leaching losses, no improvements in fertilizer N recovery were observed during the field experiments. This lack of crop response may be due to the importance of early season N availability for the short-season horticultural crops grown on Guam. We suggest that the application of waste paper may be a useful management practice to reduce NO₃ ^–-N leaching losses when high soil NO₃ ^–-N levels remain after cropping due either to crop failure or to over-application of N fertilizer. Received: 11 May 1999     

N<Subscript>2</Subscript> fixation by faba bean (<Emphasis Type="Italic">Vicia faba</Emphasis> L.) in a gypsum-amended sodic soil

The response of faba bean to the application of four rates of gypsum (0, 2.5, 5.0, 10.0 t ha⁻¹) to a non-saline, alkaline sodic soil was measured in terms of grain yield, dry matter (DM) production, N accumulation and the proportional dependence of the legume on symbiotic N₂ fixation (P _atm). A yield-independent, time-integrated ¹⁵N-dilution model was used to estimate symbiotic dependence. A significant decrease in the exchangeable sodium percentage and significant increases in exchangeable Ca⁺⁺ and the Ca⁺⁺:Mg⁺⁺ ratio in the 0–10-cm soil layer were measured 30 months after application of 10 t ha⁻¹ gypsum. Despite low and erratic rainfall during crop growth, faba bean DM and N uptake responded positively to gypsum application. The symbiotic dependence of the legume at physiological maturity was little affected by sodicity (P _atm = 0.74 at zero gypsum and 0.81–0.82 at 2.5–10 t ha⁻¹ gypsum). The increase in fixed N due to gypsum application was mainly due to increases in legume DM and total N uptake. At 10 t ha⁻¹ of gypsum, faba bean fixed more than 200 kg N ha⁻¹ in above-ground biomass.     

Lysimeter study with a cambic Arenosol exposed to artificial acid rain: I. Concentrations of ions in leachate

The effects of artificial acid rain on soil leachate composition were studied in a lysimeter experiment. Cambic Arenosol (Typic Udipsamment) in monolith lysimeters was treated for 6 1/2 yr with 125 mm yr^?1 artificial rain in addition to natural precipitation. Artificial acid rain was produced from groundwater with H₂SO₄ added. pH levels of 6.1, 4 and 3 were used. Increasing content of H₂SO₄ in the artificial rain increased the concentration of Ca²⁺ and Mg²⁺ in the leachate significantly. The pH of the leachate was slightly reduced only by the most acidic treatment (pH 3). The H^+? retention was not accompanied by a proportionate increase in the Al ion concentration. A slight increase in the Al ion concentration was only observed in the leachate from the pH 3-treated lysimeter. We conclud that cation exchange and/or weathering were the main buffer mechanisms in the soil. The study supports conclusions from other acidification studies, that acidic precipitation is likely to increase the leaching of Ca²⁺ and Mg²⁺ from soils.     

Ion leaching from a sugar maple forest in response to acidic deposition and nitrification

Year-to-year variation in acidic deposition within a mature sugar maple-dominated forest and in leaching of ions from the associated podzolic soil were examined at the Turkey Lakes Watershed between 1981 and 1986. Below-canopy inputs to the soil of SO₄ ^2? and NO₃ ^? in throughfall averaged 640 and 295 eq. ha^?1 yr^?1; the corresponding ranges were 493–917 and 261–443 eq. ha^?1 yr^?1. The contribution of atmospheric deposition to SO₄ ^2? NO₃ ^? and Ca²⁺ leaching decreased over the six years. During the study period, the mean annual volume-weighted NO₃ ^? concentration decreased in throughfall and forest-floor percolate and increased in the mineral-soil solution collected below the effective rooting zone. A substantial shift in the balance between SO₄ ^2? and NO₃ ^?leaching from the mineral soil was observed; leaching of SO₄ ^2?decreased and NO₃ ^? leaching increased with time. Leaching of Ca²⁺ and Mg²⁺ from the soil was increased as a result of excess NO₃ ^? production in the soil. The calculated output of NO₃ ^? from the soil, which averaged 1505 eq. ha^?1 yr^?1, considerably exceeded the atmospheric deposition of NO₃ ^?, whereas SO₄ ^2? outputs were only moderately greater than inputs.     

Acid deposition and ion leaching from a podzolic soil under hardwood forest

The contribution of atmospheric acids to cation leaching from a podzolic soil under mature maple-birch forest in central Ontario was examined during 1983. The movement of base cations was associated largely with NO₃ ^?, SO₄ ^2? and organic acid anions in surface soil horizons, with SO₄ ^2? and NO₃ ^? below the effective rooting zone, and SO₄ ^2? and HCO₃ ^? in streamflow. Mineral soil horizons could adsorb little additional SO₄ ^2? or associated cations at current soil solution SO₄ ^2? concentrations. Therefore it is concluded that the soil in situ lacks a strong affinity for SO₄ ^2?. Current annual inputs to the forest of SO₄ ^2? and NO₃ ^? in bulk precipitation (26.4 and 18.2 kg ha^?1, equivalent to 8.8 kg S and 4.1 kg N ha^?1 , respectively) contributed significantly to cation leaching from the soil. In order to maintain exchangeable cations in soil at current levels, a rate of weathering yielding 29.6, 5.0, 4.4 and 2.2 kg ha^?1 yr^?1 of Ca²⁺, Na⁺, Mg²⁺ and K⁺, respectively, would be required.     

Sulfate adsorption by variable charge soils: Effect of low-molecular-weight organic acids

Sulfate (SO₄ ^2–) movement and transport in soils has received considerable attention in recent years. In most soils, SO₄ ^2– coexists with a variety of natural organic compounds, especially organic acids. Studies were conducted to assess the effect of low-molecular-weight organic acids (eight aliphatic and five aromatic acids) on SO₄ ^2– adsorption by variable charge soils from Chile and Costa Rica. The effects of type of organic acid, pH, type of soil, and organic acid concentration were investigated. In one experiment, a 1.0 g soil sample was equilibrated with 25 ml 0, 0.5, 1.0, 2.0, 4.0, or 6.0 mM K₂SO₄ in 1 mM NaCl in the presence or absence of 5 mM citric acid. In the second set of experiments, the adsorption of 2 mM SO₄ ^2– in soils at pH 4 or pH 5 in the presence or absence of one of 13 organic acids at a concentration of 2 mM or 5 mM was studied. Results showed that citric acid significantly decreased SO₄ ^2– adsorption by the two soils. Sulfate adsorption decreased with increasing pH of the equilibrium solution. Aliphatic acids, with the exception of cis-aconitic acid, decreased the amount of SO₄ ^2– adsorbed by the two soils, with oxalic, tartaric, and citric acid showing the greatest effect. The differences in pH values of the equilibrium solutions in the presence and absence of organic acids were significantly, but negatively, correlated with the amount of SO₄ ^2– adsorbed, suggesting chemisorption of SO₄ ^2– and the release of hydroxide ions. The ionization fraction values of the organic acids at the equilibrium pH were correlated with the amounts of SO₄ ^2– adsorbed, suggesting that the protonation of surface hydroxyl groups of the mineral phase increased as the strength of the ionization of the acid increased, thus creating more positively charged surfaces. Received: 12 February 1997     

Denitrification and total fertilizer-N losses from an irrigated cotton field

 In a 2-year field study, denitrification loss was measured from an irrigated sandy-clay loam under cotton receiving urea-N at 158–173 kg ha^–1. An acetylene inhibition-soil core method was employed for the direct measurement of denitrification, considering also the N₂O entrapped in the soil. Taking into account the N₂O evolved from soil cores and that entrapped in the soil, a total of 65.7 kg N ha^–1 and 64.4 kg N ha^–1 was lost due to denitrification during the 1995 and 1996 cotton-growing seasons, respectively. Most (>70%) of the denitrification loss occurred during June–August, a period characterized by high soil temperatures and heavy monsoon rains. On average, 35% of the denitrification-N₂O was found entrapped in the soil and the amount of entrapped N₂O was significantly correlated with head space N₂O concentration and with water-filled pore space. ¹⁵N-balance during the 1996 growing season revealed a loss of 71.8 kg N ha^–1. It was concluded that a substantial proportion of the fertilizer-N applied to irrigated cotton is lost under the semiarid subtropical climatic conditions prevailing in the Central Punjab region of Pakistan and that denitrification is the major N loss process under irrigated cotton in this region. Received: 8 March 1999     

Biological nitrogen fixation in faba bean (Vicia faba L.) in the Ethiopian highlands as affected by P fertilization and inoculation

 N₂ fixation by leguminous crops is a relatively low-cost alternative to N fertilizer for small-holder farmers in developing countries. N₂ fixation in faba bean (Vicia faba L.) as affected by P fertilization (0 and 20 kg P ha^–1) and inoculation (uninoculated and inoculated) with Rhizobium leguminosarium biovar viciae (strain S-18) was studied using the ¹⁵N isotope dilution method in the southeastern Ethiopian highlands at three sites differing in soil conditions and length of growing period. Nodulation at the late flowering stage was significantly influenced by P and inoculation only at the location exhibiting the lowest soil P and pH levels. The percentage of N derived from the atmosphere ranged from 66 to 74%, 58 to 74% and 62 to 73% with a corresponding total amount of N₂ fixed ranging from 169 to 210 kg N ha^–1, 139 to 184 kg N ha^–1 and 147 to 174 kg N ha^–1 at Bekoji, Kulumsa and Asasa, respectively. The total N₂ fixed was not significantly affected by P fertilizer or inoculation across all locations, and there was no interaction between the factors. However, at all three locations, N₂ fixation was highly positively correlated with the dry matter production and total N yield of faba bean. Soil N balances after faba bean were positive (12–58 kg N ha^–1) relative to the highly negative N balances (–9–44 kg N ha^–1) following wheat (Triticum aestivum L.), highlighting the importance of rotation with faba bean in the cereal-based cropping systems of Ethiopia. Received: 13 January 2000     

Nitrogen and phosphorus management on Dutch dairy farms: legislation and strategies employed to meet the regulations

 The high input of nutrients through the use of fertilizers, manure and animal feed make it possible to reach high levels of agricultural production. However, high nutrient inputs may also result in large nutrient losses and thus have adverse effects on groundwater, surface water, and the atmosphere. To minimize nutrient emissions from agriculture, the Dutch government has introduced regulations on nutrient use. These include: (1) a ban on spreading animal manure on agricultural land during the winter, (2) the obligation to cover storage facilities for animal manure, (3) compulsory low-emission applications of animal manure to land, and (4) applying levies when the maximum permissible annual N and P surpluses for farms are exceeded. The nutrient surplus is the difference between nutrient input into the farm and nutrient output from the farm. The maximum permissible N surpluses for 2000 are 250 kg N ha^–1 year^–1 and 125 kg N ha^–1 year^–1 for grassland and arable land, respectively, and for P, 35 kg P₂O₅ ha^–1 year^–1 for both grassland and arable land. When the annual permissible levels are exceeded, farmers are charged with a levy. Results obtained at the experimental dairy farm "De Marke" showed that a reduction in nutrient inputs via fertilizers and purchased food, in combination with restricted grazing, reduced the N surplus in such a way that the NO₃ ^– concentration in the groundwater decreased to about the maximum permissible level of 50 mg NO₃ ^– l^–1. Since these results were obtained on a sandy soil that is very sensitive to NO₃ ^– leaching, it is suggested that all dairy farmers should be able to sufficiently reduce NO₃ ^– leaching by improving their farm management. Received: 13 July 1999     

Long-term development of element budgets in a Norway spruce (Picea abies (L.) Karst.) forest of the German solling area

To evaluate ecosystem response to changing atmospheric deposition, element budgets were established over the period from 1973 to 1991 for a Norway Spruce (Picea abies (L.) Karst.) site. Budgets for Na⁺, Cl^?, Ca²⁺, Mg²⁺, N, S and H⁺ were based on total deposition and seepage water fluxes. The deposition of Ca²⁺, Mg²⁺, particularly, of S and H⁺ decreased with time, while calculated N deposition remained constant at a high level. The decrease in Ca²⁺ deposition led to a reduction of Ca²⁺ fluxes with seepage water. The decrease of Mg²⁺ deposition did not have an effect on the output fluxes of Mg²⁺. The reversibility of soil and seepage water acidification by reduced S deposition was delayed by the release of previously accumulated soil SO ₄ ^2? . The highest NO ₃ ^? fluxes were observed during the period of 1986 to 1988; NO ₃ ^? fluxes in general demonstrated a considerable annual and periodic variation. Total N accumulation in the ecosystem amounted to nearly 590 kg ha^?1 yr^?1 during the observation period. The major sink of N in the spruce site is the aggrading humus layer. The results emphasize the need for measurements over several years to make conclusions regarding the function of ecosystems in response to atmospheric deposition.     

Land use affects the distribution of soil inorganic nitrogen in smallholder production systems in Kenya

 We hypothesized that the integration of trees and shrubs in agricultural landscapes can reduce NO₃ ^– leaching and increase utilization of subsoil N. A field survey was conducted on 14 farms on acid soils in the subhumid highlands of Kenya, where there is little use of fertilizers, to determine the effect of vegetation types (VT) on soil NH₄ ⁺ and NO₃ ^– to 4 m depth. The VT included maize (Zea mays) with poor growth and good growth, Markhamia lutea trees scattered in maize, natural weed fallow, banana (Musa spp.), hedgerow, and eucalyptus woodlot. The effect of VT on NH₄ ⁺ was small (<1 mg N kg^–1). NO₃ ^– within a VT was about constant with depth below 0.25 m, but subsoil NO₃ ^– varied greatly among VT. Mean NO₃ ^–-N concentrations at 0.5–4 m depth were low beneath hedgerow and woodlot (<0.2 mg kg^–1), intermediate beneath weed fallow (0.2–0.7 mg kg^–1), banana (0.5–1.0 mg kg^–1) and markhamia (0.5–1.6 mg kg^–1), and high beneath both poor (1.0–2.1 mg kg^–1) and good (1.9–3.1 mg kg^–1) maize. Subsoil NO₃ ^– (0.5–4 m) was agronomically significant after maize harvest with 37 kg N ha^–1 m^–1 depth of subsoil beneath good maize and 27 kg N ha^–1 m^–1 depth beneath poor maize. In contrast, subsoil NO₃ ^– was only 2 kg N ha^–1 m^–1 depth beneath woodlot and hedgerow. These results demonstrate that the integration of perennial vegetation and the rotation of annual and perennial crops can tighten N cycling in agricultural landscapes. Received: 8 July 1999