Nitrogen cycling in leucaena (Leucaena leucocephala) alley cropping in semi-arid tropics

The success of alley cropping depends to a large extent on the efficiency of transfer of nitrogen (N) from the legume hedgerow plants to the non-legume crop. Here the idea is examined that leucaena prunings (residues) can supply enough N to maize plants to significantly reduce the degree of N deficiency. Two experiments on decomposition of leucaena leaf, stem, and petiole and mineralization of N from leucaena residues were conducted in field microplots which received application of either¹⁵N-labelled leucaena materials or ammonium sulphate fertilizer. The microplots were installed in alleys formed by leucaena hedgerows spaced 4.5 metres apart and cropped with maize. The decomposition of leucaena leaves, stems and petioles was estimated by several methods. The decomposition ranged from 50–58% with leaves, 25–67% with stems and 38–51% with petioles 20 days after addition. More than 55% of the N was released in 52 days during decomposition of leucaena residues. By 20 days after application of¹⁵N-labelled leucaena 3.3–9.4% of the added¹⁵N was found in the maize plants, 32.7–49.0% was in the leucaena residues, 36.0–48.0% in the soil and 0.3–21.9% lost (deficit). By 52 days 4.8% of the¹⁵N applied in leucaena prunings was taken up by maize, 45.1% was detected in the residues, 24.9% in the soil and 25.2% lost. However, when N fertilizer was applied, 50.2% of the fertilizer N was recovered by maize, 35.5% was retained in the soil and 14.3% apparently lost. There was a marked increase in maize plant dry matter and N uptake in the microplots with addition of leucaena prunings compared with those in the microplots without leucaena added. Most of the¹⁵N remaining in the soil profile, derived from leucaena residues, was detected in the top 25 cm soil with less than 2% found below 25 cm. ei]H Lambers     

Alleu cropping sequentially cropped maize and cowpea with Leucaena on a sandy soil in Southern Nigeria

Summary The potential of alley cropping maize and cowpea with the giant Leucaena (Leucaena leucocephala (Lam) de Wit) cultivar K-28 was studied on an Entisol (Psammentic Ustorthent) in Southern Nigeria. In this trial the crops were grown in 4 m wide alleys formed by periodically pruned leucaena hedgerows. The effect of application of leucaena prunings, nitrogen fertilizer and tillage was studied.Despite the very intensive pruning regime (five prunings/year) for a six-year period, the leucaena hedgerows continue to produce substantial amounts of prunings, nitrogen yield and stakes. Application of nitrogen to the maize crop increased dry matter and nitrogen yield from the leucaena prunings. Although high nitrogen yield was obtained from the prunings, the application of low nitrogen rates was still needed for obtaining a high maize yield. Maize grain yield can be sustained at about 2.0 t/ha with continuous application of leucacna prunings only. Without application of leucaena prunings and nitrogen maize yield continued to decline with subsequent croppings. Cowpea grain yield was not affected either by leucaena prunings or by residual nitrogen. Tillage (rototilling) resulted in either higher or the same maize and cowpea yields as compared with no-tillage.Application of leucaena prunings resulted in higher soil moisture retention, organic matter, exchangeable K, Ca, Mg, and also nitrate levels in the soil solution. Leucaena and maize appear to extract soil moisture from different zones in the soil. Timely pruning of hedgerows is necessary to minimize shading.     

Management of biological N2 fixation in alley cropping systems: Estimation and contribution to N balance

Alley cropping is being widely tested in the tropics for its potential to sustain adequate food production with low agricultural inputs, while conserving the resource base. Fast growth and N yield of most trees used as hedgerows in alley cropping is due greatly to their ability to fix N₂ symbiotically with Rhizobium. Measurements of biological N₂ fixation (BNF) in alley cropping systems show that some tree species such as Leucaena leucocephala, Gliricidia sepium and Acacia mangium can derive between 100 and 300 kg N ha^-1 yr^–1 from atmospheric N₂, while species such as Faidherbia albida and Acacia senegal might fix less than 20 kg N ha^-1 yr^-1. Other tree species such as Senna siamea and S. spectabilis are also used in alley cropping, although they do not nodulate and therefore do not fix N₂. The long-term evaluation of the potential or actual amounts of N₂ fixed in trees however, poses problems that are associated with their perennial nature and massive size, the great difficulty in obtaining representative samples and applying reliable methodologies for measuring N₂ fixed. Strategies for obtaining representative samples (as against the whole tree or destructive plant sampling), the application of ¹⁵N procedures and the selection criteria for appropriate reference plants have been discussed.Little is known about the effect of environmental factors and management practices such as tree cutting or pruning and residue management on BNF and eventually their N contribution in alley cropping. Data using the ¹⁵N labelling techniques have indicated that up to 50% or more of the tree's N may be below ground after pruning. In this case, quantification of N₂ fixed that disregards roots, nodules and crowns would result in serious errors and the amount of N₂ fixed may be largely underestimated. Large quantities of N are harvested with hedgerow prunings (>300 kg N ha^-1 yr^-1) but N contribution to crops is commonly in the range of 40–70 kg N ha^-1 season. This represents about 30% of N applied as prunings; however, N recoveries as low as 5–10% have been reported. The low N recovery in maize (Zea mays) is partly caused by lack of synchronization between the hedgerow trees N release and the associated food crop N demand. The N not taken up by the associated crop can be immobilized in soil organic matter or assimilated by the hedgerow trees and thus remain in the system. This N can also be lost from the system through denitrification, volatilization or is leached beyond the rooting zone. Below ground contribution (from root turnover and nodule decay) to an associated food crop in alley cropping is estimated at about 25–102 kg N ha^-1 season^-1. Timing and severity of pruning may allow for some management of underground transfer of fixed N₂ to associated crops. However many aspects of root dynamics in alley cropping systems are poorly understood. Current research projects based on ¹⁵N labelling techniques or ¹⁵N natural abundance measurements are outlined. These would lead to estimates of N₂ fixation and N saving resulting from the management of N₂ fixation in alley cropping systems.     

The fate of residual 15N-labelled fertilizer in arable soils: its availability to subsequent crops and retention in soil

An earlier paper (Macdonald et al., 1997; J. Agric. Sci. (Cambridge) 129, 125) presented data from a series of field experiments in which ¹⁵N-labelled fertilizers were applied in spring to winter wheat, winter oilseed rape, potatoes, sugar beet and spring beans grown on four different soils in SE England. Part of this N was retained in the soil and some remained in crop residues on the soil surface when the crop was harvested. In all cases the majority of this labelled N remained in organic form. In the present paper we describe experiments designed to follow the fate of this `residual' <sup>15</sup>N over the next 2 years (termed the first and second residual years) and measure its value to subsequent cereal crops. Averaging over all of the initial crops and soils, 6.3% of this `residual' ¹⁵N was taken up during the first residual year when the following crop was winter wheat and significantly less (5.5%) if it was spring barley. In the second year after the original application, a further 2.1% was recovered, this time by winter barley. Labelled N remaining after potatoes and sugar beet was more available to the first residual crop than that remaining after oilseed rape or winter wheat. By the second residual year, this difference had almost disappeared. The availability to subsequent crops of the labelled N remaining in or on the soil at harvest of the application year decreased in the order: silty clay loam>sandy loam>chalky loam>heavy clay. In most cases, only a small proportion of the residual fertilizer N available for plant uptake was recovered by the subsequent crop, indicating poor synchrony between the mineralization of ¹⁵N-labelled organic residues and crop N uptake. Averaging over all soils and crops, 22% of the labelled N applied as fertilizer was lost (i.e., unaccounted for in harvested crop and soil to a depth of 100 cm) by harvest in the year of application, rising to 34% at harvest of the first residual year and to 35% in the second residual year. In the first residual year, losses of labelled N were much greater after spring beans than after any of the other crops.     

Dry season groundnut stover management practices determine nitrogen cycling efficiency and subsequent maize yields

It is generally thought that grain legume residues make a substantial net N contribution to soil fertility in crop rotation systems. However, most studies focus on effects of residues on crops immediately sown after the legume crop while in fact in many tropical countries with a prolonged dry season there is a large gap before planting the next crop with potential for nutrient losses. Thus the objectives of this study were* to improve the efficiency of groundnut (Arachis hypogaea L.) stover-N (100 kg N ha ^–1) recycling by evaluating the effect of dry season stover management, i.e. surface application and immediate incorporation after the legume crop or storage of residues until next cropping in the rainy season. N dynamics (litterbags, mineral N, microbial biomass N, N ₂O emissions) were monitored and ¹⁵N labelled residues were applied to assess the fate of residue N in the plant–soil (0–100 cm) system during two subsequent maize crops. Recycling groundnut stover improved yield of the subsequent maize (Zea mays L.) crop compared to treatment without stover. A higher N recycling efficiency was observed when residues were incorporated (i.e. 55% total ¹⁵N recovery after second maize crop) than when surface applied (43% recovery) at the beginning of the dry season. This was despite the faster nitrogen release of incorporated residues, which led to more mineral N movement to lower soil layers. It appears that a proportion of groundnut stover N released during the dry season was effectively captured by the natural weed population (54–70 kg N ha ^–1) and subsequently recycled particularly in the incorporation treatment. Despite the presence of weeds major leaching losses occurred during the onset of the rainy season while N ₂O emissions were relatively small. There was a good correlation between soil microbial biomass N and first crop maize yield. Incorporation of groundnut residues led to small increases in economic yield, i.e., 3120 versus 3528 kg ha ^–1 over two cropping cycles in the surface versus incorporation treatments respectively, with corresponding residue ¹⁵N uptakes of 4 and 8%, while ¹⁵N recovery in water stable aggregates (9–15%) was not significantly different. In contrast, when stover was removed and applied before the first crop, yield benefits were highest with cumulative maize yields of 4350 kg ha ^–1 and residue utilization of 12%. However, N recycling efficiency was not higher than in the early incorporation treatment due to an asynchrony of N release and maize N demand during the first crop.     

The contribution of nitrogen by promiscuous soybeans to maize based cropping the moist savanna of Nigeria

Agronomic results indicate that maize grain yields generally are higher when the crop is planted following soybean than in continuous maize cultivation in the moist savanna agroecological zones of West Africa. Many factors have been hypothesized to explain this phenomenon, including enhanced N availability and the so-called `rotational effect'. There is, however, hardly any quantitative information on the residual N benefits of promiscuous soybeans to subsequent cereal crops grown in rotation with soybean. Three IITA promiscuous soybean breeding lines and two Brazilian soybean lines were grown in 1994 and 1995 at Mokwa in the southern Guinea savanna, Nigeria, to quantify the nitrogen contribution by soybeans to a succeeding crop of maize grown in rotation with soybean for two consecutive years, 1996 and 1997 using two methods of introducing ¹⁵N into soil (fresh ¹⁵N labelling and its residual ¹⁵N) and three maize cultivars (including one cultivar with high N use efficiency) used as reference plants. The nodulating soybeans fixed between 44 and 103 kg N ha^–1 of their total N and had an estimated net N balance input from fixation following grain harvest ranging from –8 to 43 kg N ha^–1. Results in 1996 and in 1997 showed that maize growing after soybean had significantly higher grain yield (1.2 – 2.3-fold increase compared to maize control) except for maize cultivar Oba super 2 (8644-27) (a N-efficient hybrid). The ¹⁵N isotope dilution method was able to estimate N contribution by promiscuous soybeans to maize only in the first succeeding maize crop grown in 1996 but not in the second maize crop in 1997. The first crop of maize grown after soybean accumulated an average between 10 and 22 kg N ha^–1 from soybean residue, representing 17–33% of the soybean total N ha^–1. The percentage ¹⁵N derived from residue recovery in maize grown after maize was influenced by the maize cultivars. Maize crop grown after the N-efficient hybrid cultivar Oba Super 2 (844-27) had similar ¹⁵N values similar to maize grown after soybeans, confirming the ability of this cultivar to use N efficiently in low N soil due to an efficient N translocation ability. The maize crop in 1997 grown after maize had lower ¹⁵N enrichment than that grown in soybean plots, suggesting that soybean residues contributed a little to soil available N and to crop N uptake by the second maize crop. The differential mineralization and immobilization turnover of maize and soybean residues in these soils may be important and N contribution estimates in longer term rotation involving legumes and cereals may be difficult to quantify using the ¹⁵N labelling approaches. Therefore alternative methods are required to measure N release from organic residues in these cropping systems.     

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.     

Cultivar variation in the effect of chlorsulfuron in depressing the uptake of copper in wheat

The application of herbicides has induced symptoms of nutrient deficiencies under some circumstances. This glasshouse study examined the effect of chlorsulfuron on the uptake and utilization of copper (Cu) in four cultivars of wheat plants (Triticum aestivum L. cvs. Kulin, Cranbrook, Gamenya and Bodallin) on a Cu-responsive soil. Application of chlorsulfuron depressed the concentration of Cu in wheat plants receiving either inadequate or adequate Cu. In plants with inadequate Cu supply, chlorsulfuron increased the severity of Cu deficiency. Shoot weight was markedly decreased by chlorsulfuron at all levels of Cu, through decreasing the number of tillers and the elongation of leaves. This decreased growth of shoots occurred prior to the effect on Cu concentration in tissues. The retranslocation of Cu in old tissues over time was unaffected by chlorsulfuron. In all wheat cultivars, the decreased growth of shoots were correlated with the concentration of Cu in the youngest fully emerged leaf blade with critical levels of 1.6−1.7 at day 25 and 0.9−1.0 μg g⁻¹ d. wt. at day 60. The application of chlorsulfuron tended to increase the critical level at day 25 but not at day 60. In addition, Kulin seems to be most, and Cranbrook least, sensitive to chlorsulfuron. This sensitivity was associated with the sensitivity of the cultivars to Cu deficiency. It is suggested that chlorsulfuron application induces Cu deficiency in wheat plants mainly due to effects on the uptake of Cu. This revised version was published online in June 2006 with corrections to the Cover Date.     

减量施氮对玉米-大豆套作系统下作物氮素吸收和利用效率的影响

为探索玉米-大豆套作系统中作物对N素吸收的差异特性,揭示减量施N对玉米-大豆套作系统的N高效利用机理。利用15N同位素示踪技术,结合小区套微区多年定位试验,研究了玉米单作(MM)、大豆单作(SS)、玉米-大豆套作(IMS)及不施N(NN)、减量施N(RN:180 kg N/hm2)、常量施N(CN:240 kg N/hm2)下玉米、大豆的生物量、吸N量、N肥利用率及土壤N素含量变化。结果表明,与MM(SS)相比,IMS下玉米茎叶及籽粒的生物量、吸N量降低,15N%丰度及15N吸收量增加,大豆籽粒及植株的生物量、吸N量及15N吸收量显著提高;IMS下玉米、大豆植株的N肥利用率、土壤N贡献率、土壤15N%丰度降低,15N回收率显著增加。施N与不施N相比,显著提高了单、套作下玉米、大豆植株的生物量、吸N量、15N丰度及15N吸收量;RN与CN相比,IMS下,RN的玉米、大豆植株总吸N量提高13.4%和12.4%,N肥利用率提高213.0%和117.5%,土壤总N含量提高12.2%和11.6%,土壤N贡献率降低12.0%和11.2%,玉米植株15N吸收量与15N回收率提高14.4%和52.5%,大豆的则降低57.1%和42.8%,单作与套作的变化规律一致。玉米-大豆套作系统中作物对N素吸收存在数量及形态差异,减量施N有利于玉米-大豆套作系统对N肥的高效吸收与利用,实现作物持续增产与土壤培肥。     

Nitrogen management in `adequate' input maize-based agriculture in the derived savanna benchmark zone of Benin Republic

Although the West-African moist savanna zone has a high potential for crop production, yields on farmers' fields are, on average, far below this potential, mainly due to the low use of external sources of nutrients. Since the mid-1990s, it has become clear that in order to upgrade crop production to levels needed to sustain the growing population without further degrading the soil resource base, inorganic fertilizers are required. Due to the physico-chemical nature of these soils and the relatively high cost of inorganic fertilizers, a general consensus exists in the research and development community that these inorganic inputs need to be complemented with organic matter. Here, we explore options to produce organic matter in-situ and evaluate the impact of combining inorganic and organic sources of N on maize yields, focusing on the densely populated derived savanna (DS) benchmark of Benin Republic. Although most of the farmers (93%) in this benchmark use inorganic fertilizer, applications rates are low (on average, 27 kg N ha^–1). A significant response to N was observed for 96% of the studied farmers' fields.Grain and herbaceous legumes were observed to produce between 383 and 8700 kg dry matter ha^–1 in the benchmark area. Inoculation with Rhizobia and inorganic P additions were shown to significantly improve biomass production on sites with low contents of Rhizobia and P. Although maize grain yield was observed to increase significantly following a legume compared with following a maize crop or natural fallow, these increases were insufficient in the case of a cowpea crop or were obtained at the cost of leaving the field `idle' for a whole year in the case of a herbaceous Mucuna fallow. Topping up a cowpea haulms equivalent of 45 kg N ha^–1 with 45 kg urea–N ha^–1 was shown to give maize yields similar to the yields obtained after applying 90 kg urea–N ha^–1 on the poorest fields. Moreover, on these fields, a positive interaction between cowpea–N and urea–N sources of 200 kg grain ha^–1 was observed. On the richest fields, the effects of applied organic matter and fertilizer were additive.Agroforestry systems are alternative cropping systems that produce organic matter in-situ. As tree roots go down below the rooting depth of food crops, sub-soil fertility was observed to influence tree biomass production. Yield increases in tree-crop intercrop systems – such as alley cropping – in the absence of inorganic inputs are often reduced by the occurrence of tree-crop competition. In cut-and-carry systems, where tree prunings are harvested from a field adjacent to the crop land, increases in maize grain yield caused by addition of those prunings were observed to be on the low side. Mixing these residues with urea, however, was shown to lead to added benefits of about 500 kg grains ha^–1, relative to the treatments with sole inputs of organic matter or urea. Although residue quality was shown to affect maize N uptake in a pot trial, its impact under field conditions was minimal for the range of considered residue qualities. In an alley cropping trial, maize yield was shown to be sustained on a non-degraded site and enhanced on a degraded site, when a minimal amount of mineral fertilizer was added with the prunings, whereas fertilizer application alone failed to do so in both cases.     

Long-term integrated soil fertility management in South-western Nigeria: Crop performance and impact on the soil fertility status

Crop response, tree biomass production and changes in soil fertility characteristics were monitored in a long-term (1986–2002) alley-cropping trial in Ibadan, Nigeria. The systems included two alley cropping systems with Leucaena leucocephala and Senna siamea on the one hand and a control (no-trees) system on the other hand, all cropped annually with a maize–cowpea rotation. All systems had a plus and minus fertilizer treatment. Over the years, the annual biomass return through tree prunings declined steadily, but more drastically for Leucaena than for Senna. In 2002, the nitrogen contribution from Leucaena residues stabilized at about 200 kg N/ha/year, while the corresponding value for Senna was about 160 kg N/ha/year. On average, the four Leucaena prunings were more equal in biomass as well as in amounts of N, P and cations, while the first Sennapruning was always contributing up to 60% of the annual biomass or nutrient return. Maize crop yields declined steadily in all treatments, but the least so in the Senna + fertilizer treatment where in 2002 still 2.2 tonnes/ha of maize were obtained. Nitrogen fertilizer use efficiency was usually higher in the Senna treatment compared to the control or the Leucaena treatment. Added benefits due to the combined use of fertilizer N and organic matter additions were observed only for the Sennatreatment and only in the last 6 years. At all other times, they remained absent or were even negative in the Leucaenatreatments for the first 3 years. Most chemical soil fertility parameters decreased in all the treatments, but less so in the alley cropping systems. The presence of trees had a positive effect on remaining carbon stocks, while they were reduced compared to the 1986 data. Trees had a positive effect on the maintenance of exchangeable cations in the top soil. Exchangeable Ca, Mg and K – and hence ECEC – were only slightly reduced after 16 years of cropping in the tree-based systems, and even increased in the Senna treatments. In the control treatments, values for all these parameters reduced to 50% or less of the original values after 16 years. All the above points to the Senna-based alley system with fertilizers as the more resilient one. This is reflected in all soil fertility parameters, in added benefits due to the combined use of fertilizer nitrogen and organic residue application and in a more stable maize yield over the years, averaging 2.8 tonnes/ha with maximal deviations from the average not exceeding 21%.     

Authors index

In a runoff irrigation system in Northern Kenya, we studied the nutrient interactions of sole cropped and alley cropped Sorghum bicolor (L.) Moench and Acacia saligna (Labill.) H.L. Wendl. The trees were pruned once before the cropping season and the biomass was used as fodder for animals. The nutrient contents in leaf tissue, soil and soil solution were monitored and the uptake of applied tracers (¹⁵N, Sr) was followed. The grain yield of alley cropped sorghum was similar to or slightly higher than in monoculture and did not decrease near the tree-crop interface. Foliar N and Ca contents of the crop were higher in the agroforestry combination than in monoculture, corresponding to higher soil N and Ca contents. Soil solution and soil mineral N dynamics indicate an increase of N under the tree row and unused soil N at the topsoil in the alley of the sole cropped trees as well as below 60 cm depth in the crop monoculture. The N use efficiency of the tree+crop combination was higher than the sole cropped trees or crops. Competition was observed for Zn and Mn of both tree and crop whereas for Ca only the tree contents decreased. P, K, Mg and Fe dynamics were not affected by alley cropping at our site. The lower uptake of applied Sr by trees in alley cropping compared to those of the monoculture stand suggested a lower competitiveness of the acacia than sorghum, which did not show lower Sr contents when intercropped. The study showed the usefulness of combining soil and plant analyses together with tracer techniques identifying nutrient competition, nutrient transfer processes and the complementary use of soil nutrients, as the main features of the tree-crop combination. This revised version was published online in June 2006 with corrections to the Cover Date.     

Crop uptake and leaching of 15N applied in ruminant slurry with selectively labelled faeces and urine fractions

Two animal slurries either labelled with ¹⁵N in the urine or in the faeces fraction, were produced by feeding a sheep with unlabelled and ¹⁵N-labelled hay and collecting faeces and urine separately. The slurries were applied (12 g total N ^-2) to a coarse sand and a sandy loam soil confined in lysimeters and growing spring barley (Hordeum vulgare L). Reference lysimeters without slurry were supplied with¹⁵ NH₄ ¹⁵NO³ corresponding to the inorganic N applied with the slurries (6 g N m^-2). In the second year, all lysimeters received unlabelled mineral fertilizer (6 g N m^-2) and grew spring barley. N harvested in the two crops (grain + straw) and the loss of nitrate by leaching were determined. ¹⁵N in the urine fraction was less available for crop uptake than mineral fertilizer ¹⁵N. The first barley crop on the sandy loam removed 49% of the ¹⁵N applied in mineral fertilizer and 36% of that applied with urine. The availability of fertilizer ¹⁵N (36%) and urine¹⁵ N (32%) differed less on the coarse sand. Of the¹⁵ N added with the faeces fraction, 12–14% was taken up by the barley crop on the two soils. N mineralized from faeces compensated for the reduced availability of urine N providing a similar or higher crop N uptake in manured lysimeters compared with mineral fertilized ones.About half of the total N uptake in the first crop originated from the N applied either as slurry or mineral fertilizer. The remaining N was derived from the soil N pool. Substantially smaller but similar proportions of¹⁵ N from faeces, urine and fertilizer were found in the second crop. The similar recoveries indicated a slow mineralization rate of the residual faeces N since more faeces was left in the soil after the first crop.More N was lost by leaching from manured lysimeters but as a percentage of N applied, losses were similar to those from mineral fertilizer. During the first and second winter, 3–5% and 1–3%, respectively, of the ¹⁵N in slurry and mineral fertilizer was leached as nitrate. Thus slurry N applied in spring just before sowing did not appear to be more prone to loss by nitrate leaching than N given in mineral fertilizer. Slurry N accounted for a higher proportion of the N leached, however, because more N was added in this treatment.     

Tree species selection and soil tillage in alley cropping systems with Phaseolus vulgaris L. in a humid premontane climate: biomass production,nutrient cycling and crop responses

The development of alley cropping systems is based on the assumption that leguminous trees planted in hedgerows influence the yield of associated crops favourably by means of the additional nutrient pool applied to the soil through tree prunings. An on-station field study (split-plot design in a randomised block design) was conducted on an Eutric Cambisol under humid premontane climate conditions in Costa Rica in order to evaluate the ability of Erythrina poeppigiana, Calliandra calothyrsus and Gliricidia sepium to increase bean (Phaseolus vulgaris) yields compared to sole cropping. Soil tillage was applied as a sub-treatment in order to evaluate if soil preparation would additionally alter soil fertility and bean yield. After seven years with pruning twice per year, the size of both the total N and P pool in the pruned tree material was about three times higher for Erythrina prunings than for Calliandra and Gliricidia prunings. Two and five weeks after mulch application 50–150% higher inorganic N pools were measured in the soil from Erythrina plots, the bean shoot biomass at harvest was increased by 65–100% and the bean yield was 15–50% higher than in plots with beans alone. Hence, of the three tree species, Erythrina was the best choice for alley cropping systems in the pedoclimatic environment studied. Soil tillage reduced bean yield, soil organic matter, total soil N content and soil microbial biomass N in the top soil and is not recommended for similar soils in humid premontane climates.     

Estimates of the residual nitrogen benefit of groundnut to maize in Northeast Thailand

Four cultivars of groundnut were grown in upland soil in Northeast Thailand to study the residual benefit of the stover to a subsequent maize crop. An N-balance estimate of the total residual N in the maize supplied by the groundnut was made. In addition three independent estimates were made of the residual benefits to maize when the groundnut stover was returned to the land and incorporated. The first estimate (Estimate 1) was an N-balance estimate. A dual labelling approach was used where ¹⁵N-labelled stover was added to unlabelled microplots (Estimate 2) or unlabelled stover was added to ¹⁵N-labelled soil microplots (Estimate 3). The nodulating groundnut cultivars fixed between 59–64% of their nitrogen (as estimated by the ¹⁵N isotope dilution method using non-nodulating groundnut as a non-fixing reference) producing between 100 and 130 kg N ha^-1 in their stover. Although the following maize crop suffered from drought stress, maize grain N and dry weights were up to 80% and 65% greater respectively in the plots where the stover was returned as compared with the plots where the stover was removed. These benefits were comparable with applications of 75 kg N ha^-1 nitrogen in the form of urea. The total residual N estimates of the contribution of the nodulated groundnut to the maize ranged from 16.4–27.5 kg N ha^-1. Estimates of the residual N supplied by the stover and fallen leaves ranged from 11.9–21.3 kg N ha^-1 using the N-balance method (Estimate 1), from 6.3–9.6 kg N ha^-1 with the labelled stover method (Estimate 2) and from 0–11.4 kg N ha^-1 with the labelled soil method. There was closest agreement between the two ¹⁵N based estimates suggesting that apparent added nitrogen interactions in these soils may not be important and that N balance estimates can overestimate the residual N in crops following legumes, even in very poor soils. This work also indicates the considerable ability of local groundnut cultivars to fix atmospheric nitrogen and the potential benefits from returning and incorporating legume residues to the soil in the upland cropping systems of Northeast Thailand. The applicability of the ¹⁵N methodology used here and possible reasons for the discrepancies between estimates 1, 2 and 3 are discussed.     

Uptake of carbon and nitrogen derived from carbon-13 and nitrogen-15 dual-labeled maize residue compost applied to radish, komatsuna, and chingensai for three consecutive croppings

A pot experiment was conducted to determine the effects of the application of ¹³C (1.256 atom%) and ¹⁵N (1.098 atom%) dual-labeled maize residue compost (MRC) on the nitrogen and carbon uptake by radish, komatsuna, and chingensai as compared with the effect of inorganic fertilizer (IF). The vegetables were grown over three consecutive growing seasons over 4 months; compost was applied at the rate of 24 g kg^–1 soil. Nonlabeled nitrogen fertilizer was applied to the compost treatments in the second and third crops to compare the effects of blends of compost with N fertilizer to fertilizer alone. The N uptake and yield of vegetables were significantly higher with the recommended inorganic N treatment. The vegetables took up significantly (P < 0.05) lower amounts of N from MRC than from IFs during the three cultivations. The values of the N uptake derived by fertilizer application to the plant exhibited significant differences among different vegetables. Nitrogen recovered by komatsuna and chingensai from MRC was 7.3 (6.6%), 2.7 (1.8%), and 2.3, (1.7%) in the first, second, and third crops, respectively. Radish, komatsuna, and chingensai recovered significant amounts of C from MRC in the first and second crops, with negligible C recovery in the third crop. The initial loss of fertilizer C in soil at the first crop indicates that the microbial decomposition decoupled substantial amounts of ¹³C/¹⁵N-labeled compounds early in plant development, thus giving the microorganisms a preemptive competitive advantage in the acquisition of easily available ¹³C/¹⁵N-labeled substrates. It is concluded that a combination of compost and inorganic N did not supply sufficient plant-available N to increase vegetables yields or N uptake over those of fertilizer alone. The data suggested that higher productivity of vegetables might be achieved after the accumulation of a certain amount of residual compost N.     

Turnover of residual 15N-labelled fertilizer N in soil following harvest of oilseed rape (t Brassica napus L.)

We studied the fate of ¹⁵N-labelled fertilizer nitrogen in a sandy loam soil after harvest of winter oilseed rape (Brassica napus L. cv. Ceres) given 100 or 200 kg N ha^-1 in spring, with or without irrigation. Our main objective was to quantify the temporal variations of the soil mineral N, the extractable soil organic N and soil microbial biomass N, and fertilizer derived N in these pools during autumn and winter. Nitrogen use efficiency of the oilseed rape crop varied from 47% of applied N in the 100N, irrigated treatment to 34% in the 200N, non-irrigated treatment. However, only in the latter treatment did we find significantly higher fertilizer derived soil mineral N than in the three other treatments which all had low soil mineral N contents at the first sampling after harvest (8 days after stubble tillage). Between 31% and 42% of the applied N could not be accounted for in the harvested plants or 0-15 cm soil layer at this first sampling. Over the following autumn and winter none of the remaining fertilizer derived soil N was lost from the 0–5 cm depth, but from the 5–15 cm depth a marked proportion of N derived from fertilizer was lost, probably by leaching. Negligible amounts of fertilizer derived extractable soil organic and mineral N (<1 kg N ha^-1, 0-15 cm) were found in all treatments after the first sampling.Soil microbial biomass N was not significantly affected by treatments and showed only small temporal variability (±11% of the mean 76 kg N ha^-1, 0- 15 cm depth). Surprisingly, the average amount of soil microbial biomass N derived from fertilizer was significantly affected by the treatments, with the extremes being 5.5 and 3.1 kg N ha^-1 in the 200N, non-irrigated and 100N, irrigated treatments, respectively. Also, the estimated exponential decay rate of microbial biomass N derived from fertilizer, differed greatly (2 fold) between these two treatments, indicating highly different microbial turnover rates in spite of the similar total microbial biomass N values. In studies utilising ¹⁵N labelling to estimate turnover rates of different soil organic matter pools this finding is of great importance, because it may question the assumption that turnover rates are not affected by the insertion of the label.     

Nitrogen use efficiency of monoculture and hedgerow intercropping in the humid tropics

The design of productive and efficient intercropping systems depends on achieving complementarity between component species resource capture niches. Spatiotemporal patterns of capture and use of pruning and urea nitrogen (N) by trees and intercrops were elucidated by isotopic tracing, and consequences for nitrogen use efficiency were examined. During the first cropping season after applying urea–¹⁵N, maize accounted for most of the plant ¹⁵N recovery in Peltophorum dasyrrachis (33.5%) and Gliricidia sepium (22.3%) hedgerow intercropping systems. Maize yield was greatest in monoculture, and maize in monoculture also recovered a greater proportion of urea ¹⁵N (42%) than intercropped maize. Nitrogen recovery during active crop growth will not be increased by hedgerow intercropping if hedgerows adversely affect crop growth through competition for other resources. However, hedgerows recovered substantial amounts of ¹⁵N during both cropping cycles (e.g. a total of 13–22%), showing evidence of spatio-temporal complementarity with crops in the spatial distribution of roots and the temporal distribution of Nuptake. The degree of complementarity was species-specific, showing the importance of selecting appropriate trees for simultaneous agroforestry. After the first cropping season 17–34% of ¹⁵N applied was unaccounted for in the plant-soil system. Urea and prunings N were recovered by hedgerows in similar amounts. By the end of the second (groundnut) cropping cycle, total plant ¹⁵N recovery was similar in all cropping systems. Less N was taken up by the maize crop from applications of labelled prunings (5–7%) than from labelled urea (22–34%), but the second crop recovered similar amounts from these two sources, implying that prunings N is more persistent than urea N. More ¹⁵N was recovered by the downslope hedgerow than the upslope hedgerow, demonstrating the interception of laterally flowing N by hedgerows.     

Row spacing effects of N2-fixation,N-yield and soil N uptake of intercropped cowpea and maize

In the tropics, cowpea is often intercropped with maize. Little is known about the effect of the intercropped maize on N₂-fixation by cowpea or how intercropping affects nitrogen fertilizer use effiency or soil N-uptake of both crops. Cowpea and maize were grown as a monocrop at row spacings of 40, 50, 60, 80, and 120 cm and intercropped at row spacing of 40, 50, and 60 cm. Plots were fertilized with 50 kg N as (NH₄)₂SO₄; microplots within each plot received the same amount of¹⁵N-depleted (NH₄)₂SO₄. Using the¹⁵N-dilution method, the percentage of N derived from N₂-fixation by cowpea and the recovery of N-fertilizer and soil N-uptake was measured for both crops at 50 and 80 days after planting.Significant differences in yield and total N for cowpea and maize at both harvest periods were dependent on row spacing and cropping systems. Maize grown at the closer row spacing accumulated most of its N during the first 50 days after planting, whereas maize grown at the widest row spacing accumulated a significant portion of its N during the last 30 days before the final harvest, 80 days after planting.Overall, no significant differences in the percentage of N derived from N₂-fixation for monocropped or intercropped cowpea was observed and between 30 and 50% of its N was derived from N₂.At 50 DAP, fertilizer and soil N uptake was dependent on row spacing with maize grown at the narrowest row spacing having a higher fertilizer and soil N recovery than maize grown at wider spacings. At 50 and 80 DAP, intercropped maize/cowpea did not have a higher fertilizer and soil N uptake than monocropped cowpea or maize at the same row spacing. Monocropped maize and cowpea at the same row spacing took up about the same amount of fertilizer or soil N. When intercropped, maize took up twice as much soil and fertilizer N as cowpea. Apparently intercropped cowpea was not able to maintain its yield potential.Whereas significant differences in total N for maize was observed at 50 and 80 DAP, no significant differences in the atom %¹⁴N excess were observed. Therefore, in this study, the atom %¹⁴N excess of the reference crop was yield independent. Furthermore, the similarity in the atom %¹⁴N excess for intercropped and monocropped maize indicated that transfer of N from the legume to the non-legume was small or not detectable.     

Alley cropping with Senna siamea in South-western Nigeria: II. Dry matter,total N,and urea-derived N dynamics of the Senna and maize roots

Crop and tree roots are crucial in the nutrient recycling hypotheses related to alley cropping systems. At the same time, they are the least understood components of these systems. The biomass, total N content and urea-derived N content of the Senna and maize roots in a Senna-maize alley cropping system were followed for a period of 1.5 years (1 maize-cowpea rotation followed by 1 maize season) to a depth of 90 cm, after the application of ¹⁵N labeled urea. The highest maize root biomass was found in the 0–10 cm layer and this biomass peaked at 38 and 67 days after planting the 1994 maize (DAP) between the maize rows (112 kg ha^–1, on average) and at 38, 67 and 107 DAP under the maize plants (4101 kg ha^–1, on average). Almost no maize roots were found below 60 cm at any sampling date. Senna root biomass decreased with time in all soil layers (from 512 to 68 kg ha^–1 for the 0–10 cm layer between 0 and 480 DAP). Below 10 cm, at least 62% of the total root biomass consisted of Senna roots and this value increased to 87% between 60 and 90 cm. Although these observations support the existence of a Senna root `safety net' between the alleys which could reduce nutrient leaching losses, the depth of such a net may be limited as the root biomass of the Senna trees in the 60–90 cm layer was below 100 kg ha^–1, equivalent to a root length density of only < 0.05 cm cm^–3. The proportion of maize root N derived from the applied urea (%Ndfu) decreased significantly with time (from 21% at 21 DAP to 8% at 107 DAP), while %Ndfu of the maize roots at the second harvest (480 DAP) was only 0.6%. The %Ndfu of the Senna roots never exceeded 4% at any depth or sampling time, but decreased less rapidly compared to the %Ndfu of the maize roots. The higher %Ndfu of the maize roots indicates that maize is more efficient in retrieving urea-derived N. The differences in dynamics of the %Ndfu also indicate that the turnover of N through the maize roots is much faster than the turnover of N through the Senna roots. The recovery of applied urea-N by the maize roots was highest in the top 0–10 cm of soil and never exceeded 0.4% (at 38 DAP) between the rows and 7.1% (at 67 DAP) under the rows. Total urea N recovery by the maize roots increased from 1.8 to 3.2% during the 1994 maize season, while the Senna roots never recovered more than 0.8% of the applied urea-N at any time during the experimental period. These values are low and signify that the roots of both plants will only marginally affect the total recovery of the applied urea-N. Measurement of the dynamics of the biomass and N content of the maize and Senna roots helps to explain the observed recovery of applied urea-N in the aboveground compartments of the alley cropping system.