Cation distribution,cycling, and removal from mineral soil in Douglas-fir and red alder forests

Overstory species influence the distribution and dynamics of nutrients in forest ecosystems. Ecosystem-level estimates of Ca, Mg, and K pools and cycles in 50-year old Douglas-fir and red alder stands were used to determine the effect of overstory composition on net cation removal from the mineral soil, i.e. cation export from the soil in excess of additions. Net cation removal from Douglas-fir soil was 8 kg Ca ha^–1 yr^–1, 1 kg Mg ha^–1 yr^–1, and 0.3 kg K ha^–1 yr^–1. Annual cation export from soil by uptake and accumulation in live woody tissue and O horizon was of similar magnitude to leaching in soil solution. Atmospheric deposition partially off-set export by adding cations equivalent to 28–88% of cation export. Net cation removal from red alder soil was 58 kg Ca ha^–1 yr^–1, 9 kg Mg ha^–1 yr^–1, and 11 kg K ha^–1 yr^–1. Annual cation accumulation in live woody tissue and O horizon was three times greater than in Douglas-fir, while cation leaching in soil solution was five to eight times greater. The lack of excessive depletion of exchangeable cations in the red alder soil suggests that mineral weathering, rather than exchangeable cations, was the source of most of the removed cations. Nitric acid generated during nitrification in red alder soil led to high rates of weathering and NO₃-driven cation leaching.     

The response of field grownPhaseolus vulgaris to Rhizobium inoculation and the quantification of N2 fixation using15N

Summary A field experiment was performed to assess the effects of Rhizobium inoculation and nitrogen fertilizer (100 kg N ha^–1) on four cultivars of Phaseolus beans; Carioca, Negro Argel, Venezuela 350 and Rio Tibagi. In the inoculated treatment 2.5 kg N ha^–1 of¹⁵N labelled fertilizer was added in order to apply the isotope dilution technique to quantify the contribution of N₂ fixation to the nutrition of these cultivars.Nodulation of all cultivars in the uninoculated treatments was poor, but the cultivars Carioca and Negro Argel were well nodulated when inoculated. Even when inoculated, nodulation of the cultivars Venezuela 350 and Rio Tibagi was poor and these cultivars showed little response to inoculation in terms of nitrogen accumulation or grain yield. The estimates of the contribution of N₂ fixation estimated using the isotope dilution technique, for the Carioca and Negro Argel cultivars, amounted to 31.7 and 18.4 kg N ha^–1 respectively. These two cultivars produced 991 and 883 kg ha^–1 of grain, respectively, when inoculated and 663 and 620 kg ha^–1 with the addition of 100 kg N ha^–1 of N fertilizer. The response to nitrogen was particularly poor due to high leaching losses in the very sandy soil at the experimental site.The Venezuela 350 and Rio Tibagi cultivars only responded to N fertilizer and not to inoculation with Rhizobium which stresses the great importance of selecting plant cultivars for nitrogen fixation in the field.     

Persistence and competitiveness of threeBradyrhizobium japonicum inoculant strains in clay loam Nile valley soil

The nitrogen contribution from the shoot and root system of symbiotically grown leucaena was evaluated in a field experiment on an Alfisol at IITA in Southern Nigeria. Maize in plots that received prunings from inoculated leucaena contained more N and grain yield was increased by 1.9 t.ha.^–1. Large quantities of nitrogen were harvested with leucaena prunings (300 kg N ha^–1 in six months) but the efficiency of utilization of this nitrogen by maize was low compared to inorganic N fertilizer (ammonium sulphate) at 80 kg N ha^–1. Maize yield data indicated that nitrogen in leucaena prunigs was 34 and 45% as efficient as 80 kg N ha^–1 of (NH₄)₂SO₄ for uninoculated and inoculated plants with Rhizobium IRc 1045, respectively. In plots where the prunings were removed, the leaf litter and decaying roots and nodules contributed N equivalent of 32 kg ha^–1. Twenty-five kg ha^–1 was the inorganic N equivalent from nitrogen fixed symbiotically by leucaena when inoculated with Rhizobium strain IRc 1045. Application of prunings from inoculated leucaena resulted in higher soil ogranic C, total N, pH and available NO₃.     

Rate of accumulation and emission of N2, N2O and CH4 from a flooded rice soil

In a field experiment using microplots, a flooded Crowley silt loam (Typic Albaqualfs) rice soil was fertilized with ¹⁵N labelled (60–74 atom %) urea and KNO₃. Emission of N₂, N₂O and CH₄ and accumulation in soil were measured for 21 d after fertilizer application.Emission of ¹⁵N₂-N measured from the urea and KNO₃ treated plots ranged from <15 to 570 and from 330 to 3,420 g ha^–1 d^–1, respectively. Entrapped ¹⁵N₂-N in the urea treated microplots was significantly lower (<15 g to 2.1 kg ha^–1) on all sampling dates compared to the ¹⁵N₂-N gas accumulation in the KNO₃ treated plots (6.4 to 31.5 kg ha^–1). Emissions of N₂O-N were low and did not exceed 4 g ha^–1 d^–1. Fluxes of CH₄ from the fertilizer and control plots were low and never exceeded 33 g ha^–1 d^–1. Maximum accumulation of CH₄ in the flooded soil measured 460 and 195 g ha^–1 for the urea and KNO₃ treatments, respectively.     

Response of field-grown chickpea (Cicer arietinum L.) to phosphorus fertilization for yield and nitrogen fixation

Application of phosphorus at 40, 60, 80 and 100 kg P₂O₅ ha^–1 in the presence of a uniform dressing of nitrogen (N) and potash (K₂O) each applied at 20 and 24 kg ha^–1 to chickpea (CM-88) grown in sandy loam soil in a replicated field experiment improved the nodulation response of the crop, increased its grain yield (ka ha^–1) by 18, 59, 40 and 14 percent, biomass yield (ka ha^–1) by 32, 32, 54 and 14 percent, biomass N (kg ha^–1) by 31, 48, 49, 19 percent, and biomass P (kg ha^–1) by 26, 40, 41 and 11 percent, respectively. The effect of phosphorus on the nitrogenase activity of the excised roots of chickpea was, however, inconsistent.     

Responses of maize grain yield to changes in acid soil characteristics after soil amendments

An experiment was conducted from 1997 to 2000 on an acid soil in Cameroon to assess the effectiveness of cultivating acid tolerant maize (Zea mays L.) cultivar and the use of organic and inorganic fertilizers as options for the management of soil acidity. The factors investigated were: phosphorus (0 and 60 kg ha^?1), dolomitic lime (0 and 2 t ha^?1), organic manure (no manure, 4 t ha^?1 poultry manure, and 4 t ha^?1 of leaves of Senna spectabilis), and maize cultivars (ATP-SR-Y – an acid soil-tolerant, and Tuxpeño sequia – an acid susceptible). On acid soil, maize grain yield of ATP-SR-Y was 61% higher than the grain yield of Tuxpeño sequia. Continuous maize cultivation on acid soil further increased soil acidity, which was manifested by a decrease in pH (0.23 unit), exchangeable Ca (31%) and Mg (36%) and by an increase in exchangeable Al (20%). Yearly application of 60 kg ha^?1 of P for 3 years increased soil acidity through increases in exchangeable Al (8%) and H (16%) and a decrease in exchangeable Ca (30%), Mg (11%) and pH (0.07 unit). Lime application increased grain yield of the tolerant (82%) and susceptible (208%) cultivars. The grain yield increases were associated with a mean decrease of 43% in exchangeable Al, and 51% in H, a mean increase of 0.27 unit in pH, 5% in CEC, 154% in exchangeable Ca, and 481% in Mg contents of the soil. Poultry manure was more efficient than leaves of Senna producing 38% higher grain yield. This yield was associated with increases in pH, Ca, Mg and P, and a decrease in Al. The highest mean grain yields were obtained with lime added to poultry manure (4.70 t ha^?1) or leaves of Senna (4.72 t ha^?1). Grain yield increase was more related to the decrease in exchangeable Al (r = ?0.86 to ?0.95, P<0.01) and increase in Ca (r = 0.78–0.94, P<0.01), than to pH (r = ?0.57 (non-significant) to ?0.58 (P<0.05)). Exchangeable Al was the main factor determining pH (r = ?0.88 to ?0.92, P<0.01). The yield advantage of the acid tolerant cultivar was evident even after correcting for soil acidity. Acid soil-tolerant cultivars are capable of bringing unproductive acid soils into cultivation on the short run. The integration of soil amendments together with acid soil-tolerant cultivar offers a sustainable and comprehensive strategy for the management of acid soils in the tropics.     

Characterisation of soil potassium supply as derived from sorption–desorption experiments

PlantK uptake depends on soil K supply and this can be modelled using the K concentration in the soil solution (C _K), the soil K buffer power (S _K) and the effective K diffusion coefficient. With the appropriate sorption–desorption curve, the parameters C _K and S _K can be estimated from the equilibrium K concentration (C _K,0) and from the slope of the curve at C _K,0 (S _K,0). However, buffer power is frequently estimated by the ratio of the soil exchangeable K content (E _K) to C _K. Up to now, S _K,0 had not been compared with this ratio, nor had C _K,0 been compared with any C _K estimate from soil solution extract measurements. To address this question, we collected 45 soil samples from 15 K fertilisation trials in France. The soils differed widely in their physicochemical characteristics, soil solution K concentration and buffer power. For each soil sample, a sorption–desorption curve was established from 16-h experiments performed at the estimated Ca concentration of the soil solution. The C _K,0 estimates were compared with the K concentrations measured in the soil solution obtained either by direct centrifugation (^C C _K) or by centrifugation with 1,1,2-trichlorotrifluoroethane (^TFE C _K). On average, ^C C _K values were 16% higher than ^TFE C _K values, whereas C _K,0 values were intermediate between the two. The K buffer power increased when CEC increased and when C _K decreased. Multiple linear regressions using either CEC at the soil pH and ^TFE C _K ^–1 or E _K and ^TFE C _K ^–1 as independent variables accounted for more than 98 or 95% of the variability of S _K,0. The buffer power estimated by the ratio of E _K to ^TFE C _K overestimated by 100% the S _K,0 value obtained from the sorption–desorption curves.     

Effects of P,K, and liming on soil pH,Al, Mn,K, and forage barley dry matter yield and quality for a newly-cleared Cryorthod

Forage barley dry matter yield and quality, as well as soil pH, Al, and Mn were monitored in response to P, K, and lime application on a newly cleared Typic Cryorthod (Orthid Podzol). The overall yearly yield level was affected by precipitation. Without liming soil acidification occurred after three years of production. The liming rate of 2.2 Mg.ha⁻¹ was found optimal for maintaining initial pH levels (5.66) and increasing forage barley yields. It was also found optimum for K and P utilization for these first years of production. Soil pH dropped an average of 0.33 units over the three years on unlimed P plots and 0.46 units over 4 years on K plots. Phosphorus and K fertilization increased N utilization and resulted in decreased soil acidification. Phosphorus availability was greater in the first year of cropping than in subsequent years, this was likely due to the effects of higher available moisture, liming release of native P, and effects of initial fertilization. There was a 148% increase in total dry matter yield and an 85% increase in protein yield of forage barley with P application. Liming increased total forage barley yields an average of 69% and total protein yields 48%. Reduced barley yields in unlimed plots were due to low soil pH. After two years of cultivation, unlimed plots contained exchangeable Al and soluble Mn levels reported toxic for other soils. The higher liming rates of 4.4 and 6.6 Mg.ha⁻¹ reduced soluble Mn to near critically low levels. soil Al and Mn were highly correlated to pH. Soil exchangeable Al, Mn, and soluble Mn along with tissue Al were inversely correlated to percentage yield. The average yield respone to three levels of applied K, increased from zero initially to 67% by the fourth year. Total dry-matter production increased 32% and total protein yield increased an average of 32% and total protein yield increased an average of 15% with K fertilization over four years. About 60% of the yield response occurred between the 0 and 22kg K.ha⁻¹ rates. Initial soil exchangeable K levels were not maintained even at the highest 66kg K.ha⁻¹ treatment. Soil exchangeable Al and soluble Mn were elevated with dropping pH. Soil K reserves and resupply of exchangeable K in these soils over the long term will be an important factor in crop production.     

Differences among maize cultivars in the utilization of soil nitrate and the related losses of nitrate through leaching

In a 2-year field experiment conducted on a Gleyic Luvisol in Stuttgart-Hohenheim one experimental and nine commercial maize cultivars were compared for their ability to utilize soil nitrate and to reduce related losses of nitrate through leaching. Soil nitrate was monitored periodically in CaCl₂ extracts and in suction cup water. Nitrate concentrations in suction water were generally higher than in CaCl₂ extracts. Both methods revealed that all cultivars examined were able to extract nitrate down to a soil depth of at least 120 cm (1988 season) or 150 cm (1987 season). Significant differences among the cultivars existed in nitrate depletion particularly in the subsoil. At harvest, residual nitrate in the upper 150 cm of the profile ranged from 73–110 kg N ha^–1 in 1987 and from 59–119 kg N ha^–1 in 1988. Residual nitrate was closely correlated with nitrate losses by leaching because water infiltration at 120 cm soil depth started 4 weeks after harvest (1987) or immediately after harvest (1988) and continued until early summer of the following year. The calculated amount of nitrate lost by leaching was strongly influenced by the method of calculation. During the winter of 1987/88 nitrate leaching ranged from 57–84 kg N ha^–1 (suction cups) and 40–55 kg N ha^–1 (CaCl₂ extracts), respectively. The corresponding values for the winter of 1988/89 were 47–79 and 20–39 kg N ha^–1, respectively. ei]Section editor: B E Clothier     

Spatial variability of indigenous supplies for N,P and K and its impact on fertilizer strategies for irrigated rice in West Africa

Present nutrient management recommendations for irrigated rice in West Africa are typically uniform for large regions. Even with optimal crop management, spatial variability of indigenous nutrient supplies may cause low fertilizer efficiency, low productivity of expensive inputs and high losses to the environment. Substantial efficiency increases were achieved with site- and season-specific nutrient management approaches, but the relative importance of different components (site or season) or of the precision level used (field, scheme, or region) remained unclear. We conducted a field trial in the Senegal River valley to investigate short-range variability of indigenous nutrient supplies of N (INS), P (IPS), and K (IKS) on a three hectare farm, and subsequently used the field data and simulation tools to study the agro-economic effects of fertilizer management options with different precision levels.Spatial variability of soil characteristics and of indigenous nutrient supplies (IS) at field level was high and covered a large part of the variability reported in regional studies. INS ranged from 19 to 78 kg N ha^–1, IPS ranged from 11 to 39 kg P ha^{– 1}, and IKS ranged from 70 to 150 kg K ha^–1. Rice yield ranged from 2.2 to 6.0 Mg ha^–1 in N omission plots, from 4.1 to 9.8 Mg ha^–1 in P omission plots, and from 5.3 to 9.6 Mg ha^–1 in K omission plots. The highest yield in the fully fertilized treatment was 11.6 Mg ha^–1. Simulated potential yield was 11.8 Mg ha^–1. Field-specific fertilizer management and an economically optimal target yield resulted in an average yield of 9.6 Mg ha^–1 compared to 7.5 Mg ha^–1 for the existing uniform recommendation. Net benefit from fertilizer use dropped by 19% as a result of reduced precision. Non-season-specific recommendations accounted for 12% of net benefit loss, whereas lower spatial precision contributed 7% to the net benefit loss. We concluded that uniform domain-specific recommendations within agro-ecological zones (i.e. adjusted to the seasonal yield potential) modified by crop diagnostics offer the best opportunities to optimize fertilizer efficiency and net benefits of fertilizer use for intensive irrigated rice-based systems in West Africa.     

Effect of crop residues on root growth and phosphorus acquisition of pearl millet in an acid sandy soil in Niger

The effect of long-term (1983–1988) applications of crop residues (millet straw, 2–4 t ha^-1 yr^–1) and/or mineral fertilizer (30 kg N, 13 kg P and 25 kg K ha^-1 yr^-1) on uptake of phosphorus (P) and other nutrients, root growth and mycorrhizal colonization of pearl millet (Pennisetum glaucum L.) was examined for two seasons (1987 and 1988) on an acid sandy soil in Niger. Treatments of the long-term field experiment were: control (–CR–F), mineral fertilizer only (–CR+F), crop residues only (+CR–F), and crop residues plus mineral fertilizer (+CR+F).In both years, total P uptake was similar for +CR–F and –CR+F treatments (1.6–3.5 kg P ha^-1), although available soil P concentration (Bray I P) was considerably lower in +CR–F (3.2 mg P kg^-1 soil) than in –CR+F (7.4) soil. In the treatments with mineral fertilizers (–CR+F; +CR+F), crop residues increased available soil P concentrations (Bray I P) from 7.4 to 8.9 mg kg^-1 soil, while total P uptake increased from 3.6 to 10.6 kg P ha^-1. In 1987 (with 450 mm of rainfall), leaf P concentrations of 30-day-old millet plants were in the deficiency range, but highest in the +CR+F treatment. In 1988 (699 mm), leaf P concentrations were distinctly higher, and again highest in the +CR+F treatment. In the treatments without crop residues (–CR–F; –CR+F), potassium (K) concentrations in the leaves indicated K deficiency, while application of crop residues (+CR–F; +CR+F) substantially raised leaf K concentrations and total K uptake. Leaf concentrations of calcium (Ca) and magnesium (Mg) were hardly affected by the different treatments.In the topsoil (0–30 cm), root length density of millet plants was greater for +CR+F (6.5 cm cm^-3) than for +CR–F (4.5 cm cm^-3) and –CR+F (4.2 cm cm^-3) treatments. Below 30 cm soil depth, root length density of all treatments declined rapidly from about 0.6 cm cm^-3 (30–60 cm soil depth) to 0.2 cm cm^-3 (120–180 cm soil depth). During the period of high uptake rates of P (42–80 DAP), root colonization with vesicular-arbuscular mycorrhizal (VAM) fungi was low in 1987 (15–20%), but distinctly higher in 1988 (55–60%). Higher P uptake of +CR+F plants was related to a greater total root length in 0–30 cm and also to a higher P uptake rate per unit root length (P influx). Beneficial effects of crop residues on P uptake were primarily attributed to higher P mobility in the soil due to decreased concentrations of exchangeable Al, and enhancement of root growth. In contrast, the beneficial effect of crop residues on K uptake was caused by direct K supply with the millet straw.     

Liming and deep ripping responses for a range of field crops

Grain yields were measured over 2 seasons from a range of field crops following liming and deep ripping an acid and compacted soil in north-eastern Victoria. Lime (2.5 t ha^–1) substantially reduced the level of exchangeable Al and exchangeable Mn whilst raising soil pH by about 1.0 unit. The crops grown were 7 cultivars of wheat and one cultivar each of triticale, oats, barley, rapeseed, safflower, field pea, chick pea and lupins. With the exception of lupin, liming the soil increased (p=0.05) the grain yield of all crops and cultivars. With the wheat cultivars there were 2 distinct groups with different tolerance to soil acidity. Wheat, oats, triticale and lupins had higher absolute yields than the other crops. Safflower and chick pea had very low yields without soil amendment. The magnitude of the lime response did not differ between the wheat cultivars (17%) or between any of the crop species (range 9–29%). Deep ripping the soil to break a hard compacted layer resulted in more yield for all the cereals and safflower. The results demonstrate the importance of using crops with tolerance to acid soil conditions as well as gains that can be obtained with ameliorating identifiable soil problems.     

Denitrification and N2O emission from urine-affected grassland soil

Denitrification and N₂O emission rates were measured following two applications of artificial urine (40 g urine-N m^–2) to a perennial rye-grass sward on sandy soil. To distinguish between N₂O emission from denitrification or nitrification, urine was also applied with a nitrification inhibitor (dicyandiamide, DCD). During a 14 day period following each application, the soil was frequently sampled, and incubated with and without acetylene to measure denitrification and N₂O emission rates, respectively.Urine application significantly increased denitrification and N₂O emission rates up to 14 days after application, with rates amounting to 0.9 and 0.6 g N m^–2 day^–1 (9 and 6 kg N ha^–1 day^–1), respectively. When DCD was added to the urine, N₂O emission rates were significantly lower from 3 to 7 days after urine application onwards. Denitrification was the main source of N₂O immediately following each urine application. 14 days after the first application, when soil water contents dropped to 15% (v/v) N₂O mainly derived from nitrification.Total denitrification losses during the 14 day periods were 7 g N m^–2, or 18% of the urine-N applied. Total N₂O emission losses were 6.5 and 3 g N m^–2, or 16% and 8% of the urine-N applied for the two periods. The minimum estimations of denitrification and N₂O emission losses from urine-affected soil were 45 to 55 kg N ha^–1 year^–1, and 20 to 50 kg N ha^–1 year^–1, respectively.     

Effects of Different Potassium (K) Fertilizer Rates on Yield Formation and Lodging of Rice

As one of the most important nutrients for plants, potassium (K) has substantial effects on growth and development of crops. Present study was conducted in three different sites in South China in late season in 2019 with the objective to study the effects of different applied amounts of K fertilizer on yield formation and lodging of rice. Four K fertilizer treatments, K₀: 0 kg potassium oxide (K₂O) ha⁻¹ (control); K₁: 64.20 kg K₂O ha⁻¹ ; K₂: 128.55 kg K₂O ha⁻¹ and K₃ 153.90 kg K₂O ha⁻¹ were applied in the field experiment. The results showed that K₂ and K₃ treatments significantly increased panicle number per unit area, grain number per panicle, seed-setting rate and the grain yield of rice compared with K₀ treatment. Higher net photosynthetic rates were recorded in K₂ and K₃ treatments than K₀ treatment at tillering stage, heading stage and maturity stage. K fertilizer treatments also increased the chlorophyll content and dry matter accumulation by 6.16–23.52% and 21.32–64.59% compared with K₀ treatment, respectively. Moreover, the total N and K accumulation in the aboveground tissues of rice significantly increased under K₂ and K₃ treatments compared with K₀ treatment. Furthermore, compared with K₀ treatment, K fertilizer treatments significantly enhanced the breaking-resistant strength by 40.94–144.24% and reduced the lodging index of rice by 13.14–36.72%.     

Effects of CO2 and nitrogen fertilization on vegetation and soil nutrient content in juvenile ponderosa pine

This paper summarizes the data on nutrient uptake and soil responses in opentop chambers planted with ponderosa pine (Pinus ponderosa Laws.) treated with both N and CO₂. Based upon the literature, we hypothesized that 1) elevated CO₂ would cause increased growth and yield of biomass per unit uptake of N even if N is limiting, and 2) elevated CO₂ would cause increased biomass yield per unit uptake of other nutrients only by growth dilution and only if they are non-limiting. Hypothesis 1 was supported only in part: there were greater yields of biomass per unit N uptake in the first two years of growth but not in the third year. Hypothesis 2 was supported in many cases: elevated CO₂ caused growth dilution (decreased concentrations but not decreased uptake) of P, S, and Mg. Effects of elevated CO₂ on K, Ca, and B concentrations were smaller and mostly non-significant. There was no evidence that N responded in a unique manner to elevated CO₂, despite its unique role in rubisco. Simple growth dilution seemed to explain nutrient responses in almost all cases.There were significant declines in soil exchangeable K⁺, Ca²⁺, Mg²⁺ and extractable P over time which were attributed to disturbance effects associated with plowing. The only statistically significant treatment effects on soils were negative effects of elevated CO₂ on mineralizeable N and extractable P, and positive effects of both N fertilization and CO₂ on exchangeable Al³⁺. Soil exchangeable K⁺, Ca²⁺, and Mg²⁺ pools remained much higher than vegetation pools, but extractable P pools were lower than vegetation pools in the third year of growth. There were also large losses of both native soil N and fertilizer N over time. These soil N losses could account for the observed losses in exchangeable K⁺, Ca²⁺, Mg²⁺ if N was nitrified and leached as NO ₃ ^– .     

Effect of phosphorus,potassium and zinc fertilizers on iron toxicity in wetland rice (Oryza sativa L.)

During the period January–August 1996, an investigation was carried out in La Mata, Cotuí, Dominican Republic with the objective to study the effect of P, K and Zn fertilizers on Fe toxicity in the rice varieties JUMA-57 (sensitive to Fe toxicity), ISA-40 and PSQ-4 (both tolerant to Fe toxicity). The rate of fertilizer application was 22 and 62 kg P ha^–1; 58 and 116 kg K ha^–1; 3 and 7 kg Zn ha^–1 and a constant dose of 140 kg N ha^–1 and 40 kg S ha^–1 on all fertilized plots. The control received no fertilizer. JUMA-57 was the only variety that showed symptoms of Fe toxicity. The observed symptoms showed a yellow to orange colour. Symptoms of Fe toxicity appeared first one week after transplanting (WAT), decreased at the fourth WAT, but returned six WAT and continued until the end of the experiment. Fertilizer application reduced symptom intensity and increased grain yield in all varieties, but only JUMA-57 did not reach the maximum yield typical for that variety. Fertilizer application did not completely overcome the toxicity effect, i.e. in symptom intensity and grain yield. The positive effect of fertilizer application could not be attributed to a specific nutrient. Intensity of symptoms was not related to Fe concentration in the leaves. The average Fe concentration of 108 mg kg^–1 was not high enough to be considered toxic. Symptoms could not be explained through Mn toxicity (average Mn concentration in the leaves was 733 mg kg^–1) nor Zn deficiency (average Zn concentration in the leaves was 20 mg kg^–1). There was a clear relationship, though, between soil DTPA extractable Fe and symptom intensity or grain yield. The toxic effect was observed when the DTPA extractable Fe in the flooded soil was above 200 mg kg^–1. From these results, we concluded that the Fe toxicity resulted from high Fe in the root zone and not from high Fe concentrations in the leaves.     

Response to inoculation and N fertilization for increased yield and biological nitrogen fixation of common bean (Phaseolus vulgaris L.)

Common bean (Phaseolus vulgaris L.) is able to fix 20–60 kg N ha^–1 under tropical environments in Brazil, but these amounts are inadequate to meet the N requirement for economically attractive seed yields. When the plant is supplemented with N fertilizer, N₂ fixation by Rhizobium can be suppressed even at low rates of N. Using the ¹⁵N enriched method, two field experiments were conducted to compare the effect of foliar and soil applications of N-urea on N₂ fixation traits and seed yield. All treatments received a similar fertilization including 10 kg N ha^–1 at sowing. Increasing rates of N (10, 30 and 50 kg N ha^–1) were applied for both methods. Foliar application significantly enhanced nodulation, N₂ fixation (acetylene reduction activity) and yield at low N level (10 kg N ha^–1). Foliar nitrogen was less suppressive to nodulation, even at higher N levels, than soil N treatments. In the site where established Rhizobium was in low numbers, inoculation contributed substantially to increased N₂ fixation traits and yield. Both foliar and soil methods inhibited nodulation at high N rates and did not significantly increase bean yield, when comparing low (10 kg N ha^–1) and high (50 kg N ha^–1) rates applied after emergence. In both experiments, up to 30 kg N ha^–1 of biologically fixed N₂ were obtained when low rates of N were applied onto the leaves.     

The effect of cropping and fertiliser nitrogen rates on nitrogen balance in soil

Summary Fertilizer/soil N balance of cropped and fallow soil has been studied in a pot experiment carried out with grey forest soil (southern part of Moscow region) at increasing rates of¹⁵N labelled ammonium sulfate (0; 8; 16; 32 mg N/100 g of soil). The fertilizer¹⁵N balance has been shown to depend upon its application rate and the presence of growing plants. Fertilizer N uptake efficiency was maximum (72.5%) and gaseous losses-minimum (12.5%) at the application rate of 16 mg N/100 g of soil. Fertilizer N losses from the fallow soil were 130–220% versus those from the cropped soil. At the application of fertilizer N the plant uptake of soil N was 170–240% and the amount of soil N as N–NH₄ exchangeable + N–NO₃ in fallow was 350–440% as compared to the control treatment without nitrogen (PK).After cropping without or with N fertilizer application at the rates of 8 and 32 mg N/100 g of soil, a positive nitrogen balance has been found which is likely due to nonsymbiotic (associative) N-fixation. It has been shown that biologically fixed nitrogen contributes to plant nutrition.     

Effects of forest clear-cutting on the sulphur, phosphorus and base cations fluxes through podzolic soil horizons

Clear-cutting considerably alters the flow of nutrients through the forest ecosystem. These changes are reflected in soil solution concentrations and fluxes. The effects of clear-cutting (stems only) on the fluxes of water soluble phosphorus (P), sulphur (S) and base cations (Ca, Mg and K) through a podzolic soil were studied in a Norway spruce dominated mixed boreal forest in eastern Finland. Bulk deposition, total throughfall (throughfall + stemflow) and soil percolate from below the organic (O), eluvial (E) and illuvial (B) horizons were collected for 4 years before and for 3 years after cutting. Annual deposition loads (kg ha^–1) to the forest floor were less after clear-cutting, averaging 1.7 S, 0.84 Ca, 0.14 Mg, 0.64 K and 0.10 P. Before cutting, the loads were 4.6 S, 2.7 Ca, 0.70 Mg, 6.2 K and 0.20 P. Annual fluxes of total S and sulphate (SO ₄ ^2– ) from below the O-horizon were also lower (33%) after clear-cutting, total S averaging 2.0 kg ha^–1, the flux from below the B-horizon also diminished after clear-cutting. The flux of total P (mainly inorganic) from below the O-horizon increased threefold (6.9 kg ha^–1; sum over the 3-year period) compared to period before cutting. The fluxes of base cations from below the O-horizon increased twofold. The flux of K⁺ from below the O- and E-horizons was most strongly correlated with that of phosphate (PO ₄ ^3– ) and those of Ca²⁺ and Mg²⁺ with the DOC flux. Increased fluxes of P and base cations to the mineral soil generated only slightly increased fluxes from below the B-horizon. The retention of base cations and P in the mineral soil indicates there was little change in leaching to ground and surface waters after clear-cutting.     

Factors affecting soil acidification under legumes I. Effect of potassium supply

This study examined the effect of K (as K₂SO₄) supply on acid production under N₂-fixing plants of lupin (Lupinus angustifolius L. cv. Gungurru) and clover (Trifolium subterraneum L. cv. Dalkeith) grown in a K-deficient soil with a low pH buffer capacity for 55 days in the glasshouse at 20/12 °C (day/night). Increasing K supply up to 240 mg K kg^-1 soil markedly increased plant growth of both species but clover growth was more responsive than lupin. Growing plants for 55 days decreased soil pH by 0.65–0.85 units under lupin and 0.45–0.83 units under clover. The amounts of H⁺ produced per kg biomass (specific acid production) were the highest at the nil K supply, generally decreased with increasing K level up to 30 mg K kg^-1 under lupin and up to 120 mg K kg^-1 soil under clover and only slightly increased with further increasing K under lupin. Increasing K₂SO₄ supply proportionally increased plant uptake of K and SO ₄ ^2- but generally decreased concentrations of Ca, Mg, Na, P and Cl. Specific acid production correlated well with concentrations of excess cations and ash alkalinity, and total acid production was strongly correlated with total excess cations and total ash alkalinity in plants. These relationships were not affected by K treatment and species. Specific acid production also correlated with plant Ca concentration but not with K concentration. In addition, lupin and clover extruded similar amounts of H⁺ per kg biomass produced. It is suggested that application of K₂SO₄ does not have a significant impact on acid production by lupin and clover.