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.     

Manipulation of quality and mineralization of tropical legume tree prunings by varying nitrogen supply

The effect of N supply on the quality of Calliandra calothyrsus and Gliricidia sepium prunings was studied in a glasshouse over a 7-month growing period. Increasing the concentration of N supplied from 0.625 to 10.0 mM NO₃-N resulted in increased N concentration but decreased polyphenol concentration, protein-binding capacity and C:N ratio of prunings from both species. Lignin concentration was not consistently altered by the N treatment. Mineralization of N from the prunings was measured over a 14-week period under controlled leaching and non-leaching conditions. The results indicated a strong interaction between legume species and concentration of N supply in their influence on N mineralization of the prunings applied to the soil. Differences in the %N mineralized were dictated by the quality of the prunings. The (lignin + polyphenol):N ratio was the pruning quality factor which could be used most consistently and accurately to predict N mineralization of the legume prunings incubated under leaching conditions, and the relationship was best described by a linear regression. Under non-leaching conditions, however, the protein-binding capacity appeared to be the most important parameter in determining the patterns of N release from the prunings studied. The relationship between the N mineralization rate constant and the protein-binding capacity was best described by a negative exponential function, y=0.078 exp(–0.0083x). The present study also indicated that the release of N from legume prunings containing a relatively high amount of polyphenol could be enhanced by governing the N availability conditions under which the plant is grown, for example whether or not it is actively fixing nitrogen. Estimates of pruning N mineralization after 14 weeks with the difference method averaged 6% (leaching conditions) and 22% (nonleaching conditions) more than with the ¹⁵N method for all legume prunings studied. The recovery of pruning by maize (4–38%) was well correlated with the % pruning N mineralized suggesting that incubation data closely reflect the pruning N value for a given catch crop under non-leaching conditions.     

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

In an alley cropping system, prunings from the hedgerow legume are expected to supply nitrogen (N) to the associated cereal. However, this may not be sufficient to achieve maximum crop yield. Three field experiments with alley-cropped maize were conducted in a semi-arid environment in northern Australia to determine: (1) the effect of N fertilizer on maize growth in the presence of fresh leucaena prunings; (2) the effect of incorporation of leucaena and maize residues on maize yield and the fate of plant residue¹⁵N in the alley cropping system; and (3) the¹⁵N recovery by maize from¹⁵N-labelled leucaena, maize residues and ammonium sulphate fertilizer.Leucaena residues increased maize crop yield and N uptake although they did not entirely satisfy the N requirement of the alley crop. Additional N fertilizer further increased the maize yield and N uptake in the presence of leucaena residues. Placement of leucaena residues had little effect on the availability of N to maize plants over a 2 month period. The incorporation of leucaena residues in the soil did not increase the recovery of leucaena¹⁵N by maize compared with placement of the residues on the soil surface. After 2 months, similar proportions of the residue¹⁵N were recovered by maize from mulched leucaena (6.3%), incorporated leucaena (6.1%) and incorporated maize (7.6%). By the end of one cropping season (3 months after application) about 9% of the added¹⁵N was taken up by maize from either¹⁵N-labelled leucaena as mulch or¹⁵N-labelled maize residues applied together with unlabelled fresh leucaena prunings as mulch. The recovery of the added¹⁵N was much higher (42.7%) from the¹⁵N-labelled ammonium sulphate fertilizer at 40 kg N ha^-1 in the presence of unlabelled leucaena prunings. Most of the added¹⁵N recovered in the 200 cm soil profile was distributed in the top 25 cm soil with little leached below that. About 27–41% of the leucaena¹⁵N was apparently lost, largely through denitrification from the soil and plant system, in one cropping season. This compared with 35% of the fertilizer¹⁵N lost when the N fertilizer was applied in the presence of prunings. ei]H Lambers     

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.     

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.     

Application of 15N and xylem ureide methods for assessing N2 fixation of three shrub legumes periodically pruned for forage

The apparently diminished capacity for N₂ fixation by the shrub legume Calliandra calothyrsus (Calliandra) relative to other woody perennial legumes was investigated in a field experiment in northern Queensland, Australia. In this trial, (i) the proportion of plant nitrogen (N) derived from symbiotic N₂ fixation (%Pfix) and the amounts of N₂ fixed were compared in Calliandra, Gliricidia sepium (Gliricidia) and Codariocalyx gyroides (Codariocalyx), (ii) variations in N₂ fixation due to season or tree age were determined, (iii) estimates of Pfix derived with the ¹⁵N natural abundance technique were compared with values obtained from ¹⁵N enrichment or xylem sap ureide procedures to determine whether the previous conclusions about Calliandra's ability to fix N had resulted from specific problems with the natural abundance methodology used in the earlier studies.Inoculated seedlings of each of the three shrub legume species were planted in dense stands (1.5 m rows, 0.5 m between trees) in two randomised blocks. The northern block was used solely for natural abundance measurements, while ¹⁵N-enriched KNO₃ (10 atom % ¹⁵N excess) was applied four times over a 52 week period to plots in the southern block. The non-nodulating tree legume Senna spectabilis (formally Cassia spectabilis) was used as a non-N₂-fixing reference for the ¹⁵N-based procedures, with Guinea grass (Panicum maximum) included as an additional non-fixing check. Growth by the trees above 75 cm was first cut and removed after 22 weeks and regrowth was subsequently pruned periodically for another 95 weeks. Sampling for dry matter production, N yield and estimates of Pfix were restricted to the central four of the 32 plants which constituted each replicate plot. Information generated during the 117 week study indicated that estimates of Pfix by ¹⁵N natural abundance were closely similar to values derived with ¹⁵N-enrichment or sap ureides. The data indicated that Calliandra had a reduced reliance upon N₂ fixation relative to Gliricidia and Codariocalyx for the first 65 weeks after establishment. This appeared to be due to more prolifc root growth by Calliandra than either of the other N₂-fixing species and an ability to extract a greater proportion of its N requirements from soil mineral N. However, after week 65 and for the remainder of the experiment, estimates of Pfix for Calliandra were similar to the other shrub legumes. Over 117 weeks, prunings from Calliandra and Gliricidia had removed 52–58 t dry matter ha^-1, and between 1471 and 1678 kg N ha^-1, of which 1026–1063 kg N ha^-1 was estimated to have been derived from N₂ fixation. At the time of final harvest, 65–73% of the fixed N was present in shoot regrowth of the N₂ fixing shrubs, 9–18% in the roots, 15% in the trunk, and 2–6% in fallen leaves.     

The Effect of Mixing Prunings of Two Tropical Shrub Legumes (Calliandra Houstoniana and Indigofera zollingeriana) with Contrasting Quality on N Release in the Soil and Apparent N Degradation in the Rumen

Lack of synchronization between N released from prunings applied to the soil as green manures and crop uptake as well as optimization of protein digestibility for ruminants, remain major research objectives for the selection of multipurpose tree and shrub legumes (MPT) for mixed smallholder systems in the tropics. Prunings of the high tannin, low quality MPT Calliandra houstoniana CIAT 20400 (Calliandra) and the tannin free, high quality MPT Indigofera zollingeriana (Indigofera) were mixed in the proportions 100:0, 75:25, 50:50, 25:75, and 0:100 (w/w) in order to measure the aerobic rate and extent of N release in a leaching tube experiment, and the anaerobic extent of N degradation in an in vitro gas production experiment. Parameters measured in Calliandra:Indigofera mixtures were compared to theoretical values derived from single species plant material (i.e. 100:0 and 0:100). Aerobic N release and apparent anaerobic N degradation increased with increasing proportion of the high quality legume (Indigofera) in the mixture. While N release in the soil was lower than theoretical values in the mixture 50% Calliandra/50% Indigofera, this was not the case with apparent anaerobic N degradation with the same mixture. Aerobic N immobilization was more pronounced for the mixture 75% Calliandra/25% Indigofera than for 100% Calliandra and negative interaction was observed with apparent anaerobic N degradation in the mixture 75% Calliandra/25% Indigofera. Plant quality parameters that best correlated with aerobic N release and apparent anaerobic N degradation in the rumen were lignin + bound condensed tannins (r=−0.95 and −0.95 respectively, P<0.001). In addition, a positive correlation (r=0.89, P<0.001) was found between aerobic N release in the leaching tube experiment and apparent N degradation in the in vitro anaerobic gas production experiment. Results show that mixing prunings of MPT materials with contrasting quality is an effective way to modify aerobic N release pattern as well as apparent anaerobic N degradation and could possibly be applied to minimize N losses in the rumen and in the soil. In addition, apparent anaerobic N degradation was identified as good predictor of aerobic N release in the soil, which has resource saving implications when screening MTP to be used as green manures.     

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.     

Alternate nitrogen amendments for organic fertilizers

The use of compost or manure in agriculture as an organic source of nutrients is common in many tropical, developing countries like Nigeria. One of the drawbacks of such materials is their low nitrogen (N) content (=1% N). Farmers commonly use chemical N fertilizers such as urea, calcium ammonium nitrate (CAN), and NPK formulations to obtain better crop growth and yield. These chemical supplements may have a negative impact on the environment through nitrate leaching into water, leading to eutrophication of surface waters that can affect public health. Gliricidia sepium, a fast-growing, tropical, perennial hedge plant was tested as a source of N in organo-mineral fertilizer formulations. Average nutrient content of Gliricidia is 3.8% N, 0.32% P, 1.8% K, 0.8% Ca, and 0.2% Mg. Using a sand culture and Amaranthus caudatus as a test crop, it was shown that amending commercial composts with 30% Gliricidia prunings would benefit many small-scale farmers and control environmental pollution.     

Mulching effect of plant residues with chemically contrasting compositions on maize growth and nutrients accumulation

Effects of application of prunings of three woody species (Acioa barteri, Gliricidia sepium and Leucaena leucocephala), maize (Zea mays L.) stover and rice (Oryza sativa L.) straw as mulch on maize were studied on an Alfisol in southern Nigeria in 1990 and 1991. Maize dry matter and grain yield were higher with applications of plant residues and N fertilizer in both years. Addition of Leucaena prunings gave the highest maize grain yield in both years. Compared to the 1990 results, Acioa showed the least grain yield decline among the mulch treatments in 1991. Nutrient uptake was enhanced by applications of plant residues. Leucaena prunings had the highest effect in both years and increased the mean N, P, and Mg uptake by 96%, 84%, and 50%, respectively, over the control. Addition of Acioa prunings increased K and Ca uptake by 59% and 92%, respectively, over the control. High quality (low C/N ratio and lignin level) plant residues enhance crop performance through direct nutritional contributions, whereas low quality (high C/N ratio and lignin level) plant residues do so through mulching effects on the microclimate. Intermediate quality plant residues have no clear effects on crop performance.     

Root distributions partially explain 15N uptake patterns in Gliricidia and Peltophorum hedgerow intercropping systems

The relative distributions of tree and crop roots in agroforestry associations may affect the degree of complementarity which can be achieved in their capture of below ground resources. Trees which root more deeply than crops may intercept leaching nitrogen and thus improve nitrogen use efficiency. This hypothesis was tested by injection of small doses of (¹⁵NH₄)₂SO₄ at 21.8 atom% ¹⁵N at different soil depths within established hedgerow intercropping systems on an Ultisol in Lampung, Indonesia. In the top 10 cm of soil in intercrops of maize and trees, root length density (L_rv) of maize was greater than that of Gliricidia sepium trees, which had greater L_rv in this topsoil layer than Peltophorum dasyrrachis trees. Peltophorum trees had a greater proportion of their roots in deeper soil layers than Gliricidia or maize. These vertical root distributions were related to the pattern of recovery of ¹⁵N placed at different soil depths; more ¹⁵N was recovered by maize and Gliricidia from placements at 5 cm depth than from placements at 45 or 65 cm depth. Peltophorum recovered similar amounts of ¹⁵N from placements at each of these depths, and hence had a deeper N uptake distribution than Gliricidiaor maize. Differences in tree L_rv across the cropping alley were comparatively small, and there was no significant difference (P<0.05) in the uptake of ¹⁵N placed in topsoil at different distances from hedgerows. A greater proportion of the ¹⁵N recovered by maize was found in grain following ¹⁵N placement at 45 cm or 65 cm depth than following placement at 5 cm depth, reflecting the later arrival of maize roots in these deeper soil layers. Thus trees have an important role in preventing N leaching from subsoil during early crop establishment, although they themselves showed a lag phase in ¹⁵N uptake after pruning. Residual ¹⁵N enrichment in soil was strongly related to application depth even 406 days after ¹⁵N placement, demonstrating the validity of this approach to mapping root activity distributions.     

Investigations on decomposition of foliage of woody species using a perfusion method

The time for half of the total oxidizable carbon to be converted into CO₂ and other gaseous products (t_1/2) was studied for five tree species used in agroforestry. The study was conducted in a perfusion system with continuous aeration, and moisture content maintained at field capacity. This method was found to be suitable for studies of the initial stages of tree foliage decomposition. The overall rate was in the decreasing order: Leucaena>Calliandra>Gliricidia>Prosopis>Cassia. Decomposition started rapidly and then decreased rapidly for 2 to 3 weeks followed by a gradual decrease which continued for the remainder of the time.The time for 50 per cent of total oxidizable carbon to decompose was about 19 days for Leucaena, 30 days for Calliandra and Gliricidia, while Prosopis and Cassia took more than 30 days. Leucaena released the largest quantity of total N into the perfusing solution while Cassia gave the lowest amount.     

Effects of herbicide chlorsulfuron on growth and nutrient uptake parameters of wheat genotypes differing in Zn-efficiency

Prunings of Calliandra calothyrsus, Grevillea robusta, Leucaena diversifolia and farm yard manure were applied each cropping season at 3 and 6 t dry matter ha⁻¹ to an Oxisol in Burundi. The field plots also received basal applications of nitrogen (N), phosphorus (P) and potassium (K). Application of the tree prunings or farm yard manure decreased the concentration of monomeric inorganic aluminium (Al) in soil solution from 2.92 mg Al dm⁻³ in the control plots to 0.75 mg Al dm⁻³ in the plots receiving 6 t ha⁻¹ Calliandra prunings. The other organic materials also decreased the concentration of monomeric inorganic aluminium in the soil solution. The lowered Al concentration led to a corresponding decrease in the percentage Al saturation of the 0–10 cm soil layer from 80% to 68%. Grain yields of maize and beans were strongly inversely related to the percentage Al saturation of the soil. This confirms that soil acidity was the main constraint to maize and beans production. The yield improvement was mainly attributed to the ameliorating effects of the organic matter application on Al toxicity. The nutrient content had less effect presumably because of fertilizer use. In the best treatments, the yield of maize increased from 0.9 to 2.2 t ha⁻¹ and the corresponding beans yield increased from 0.2 to 1.2 t ha⁻¹. A C Borstlap Section editor     

Fate of 15N-labelled nitrogen fertilizer applied to kiwifruit (Actinidia deliciosa) vines

The fate of ¹⁵N-labelled ammonium fertilizer applied once to six-year-old field-grown kiwifruit (Actinidia deliciosa Hayward) vines was measured over three years. The three main treatments were nitrogen (N) applied singularly at 100 or 200 kg N ha^–1 in early spring (two weeks before bud burst) or split with 100 kg N ha^–1 (unlabelled) in early spring and 100 kg N ha^–1 (¹⁵N-labelled) ten weeks later. All N treatments were applied to vines with a history of either 50 or 200 kg N ha^–1 yr^–1. For three years after ¹⁵n application, components of the vines and soil (0–600 mm depth) were sampled at harvest in late autumn and the N and ¹⁵N contents determined.By the first harvest, all plant uptake of ¹⁵N had occurred and this represented 48–53% of the ¹⁵N applied. There was no significant effect of current N fertilizer treatment or of N history on ¹⁵N recovery by vines. Removal of ¹⁵N in harvested fruit was small at 5–6% in the first year and 8% over 3 years. After 2–3 years, most plant ¹⁵N occurred in the roots and this component declined only slowly over time. In contrast, there was a large temporal decline in ¹⁵N in above-ground plant components due to the annual removal in leaf fall and pruning. An associated experiment showed that when ¹⁵N-labelled prunings and leaves were mulched and returned to the soil, only about 9% was recovered by plants within 2 years. Almost all remaining mulched material had been immobilised into the soil organic N.In all treatments, about 20% of the added ¹⁵N remained in soil at the first harvest. This was almost entirely in organic fractions (<0.4% in inorganic N) and mostly in the surface 150-mm layer. The ¹⁵N content in soil changed little over time (from 20 to 17% between the first and third harvests respectively) and indicated that most of the N had been immobilised into stable humus forms.     

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     

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.     

Microbial colonisation of tannin-rich tropical plants: Interplay between degradability,methane production and tannin disappearance in the rumen

Condensed tannins in plants are found free and attached to protein and fibre but it is not known whether these fractions influence rumen degradation and microbial colonisation. This study explored the rumen degradation of tropical tannin-rich plants and the relationship between the disappearance of free and bound condensed tannin fractions and microbial communities colonising plant particles using in situ and in vitro experiments. Leaves from Calliandra calothyrsus, Gliricidia sepium, and Leucaena leucocephala, pods from Acacia nilotica and the leaves of two agricultural by-products: Manihot esculenta and Musa spp. were incubated in situ in the rumen of three dairy cows to determine their degradability for up to 96 h. Tannin disappearance was determined at 24 h of incubation, and adherent microbial communities were examined at 3 and 12 h of incubation using a metataxonomic approach. An in vitro approach was also used to assess the effects of these plants on rumen fermentation parameters. All plants contained more than 100 g/kg of condensed tannins with a large proportion (32–61%) bound to proteins. Calliandra calothyrsus had the highest concentration of condensed tannins at 361 g/kg, whereas Acacia nilotica was particularly rich in hydrolysable tannins (350 g/kg). Free condensed tannins from all plants completely disappeared after 24-h incubation in the rumen. Disappearance of protein-bound condensed tannins was variable with values ranging from 93% for Gliricidia sepium to 21% for Acacia nilotica. In contrast, fibre-bound condensed tannin disappearance averaged ～ 82% and did not vary between plants. Disappearance of bound fractions of condensed tannins was not associated with the degradability of plant fractions. The presence of tannins interfered with the microbial colonisation of plants. Each plant had distinct bacterial and archaeal communities after 3 and 12 h of incubation in the rumen and distinct protozoal communities at 3 h. Adherent communities in tannin-rich plants had a lower relative abundance of fibrolytic microbes, notably Fibrobacter spp. whereas, archaea diversity was reduced in high-tannin-containing Calliandra calothyrsus and Acacia nilotica at 12 h of incubation. Concurrently, in vitro methane production was lower for Calliandra calothyrsus, Acacia nilotica and Leucaena leucocephala although for the latter total volatile fatty acids production was not affected and was similar to control. Here, we show that the total amount of hydrolysable and condensed tannins contained in a plant govern the interaction with rumen microbes affecting degradability and fermentation. The effect of protein- and fibre-bound condensed tannins on degradability is less important.     

Modelling of reserve carbohydrate dynamics, regrowth and nodulation in a N2-fixing tree managed by periodic prunings

We used a modified transport resistance approach to model legume tree growth, nodulation and dynamics of reserve carbohydrates after pruning. The model distributes growth between roots and shoots applying the transport resistance approach. Within shoots, growth is divided into leaves, branches and stems applying the pipe model theory. The model also accounts for the metabolic differences of principal N sources, nitrate, ammonium and atmospheric dinitrogen, in a mechanistic way. We compared the simulation results with measured biomass dynamics of Gliricidia sepium (Jacq.) Walp. (Papilionaceae: Robinieae) under humid and subhumid tropical conditions. Comparison showed that the biomass production predicted by the model is close to measured values. Total N₂ fixation is also similar to measured values. Qualitatively the model increases the proportion of N₂ fixation if roots acquire less mineral N. In the present study, the general form of the model is discussed and compared with similar models. The results encourage the use of this approach for studying biomass dynamics of legume trees under the scheme of periodic prunings. Also, it shows that process‐based models have potential in the simulation of trees disturbed by prunings, herbivory or similar factors.     

Short-term immobilisation and crop uptake of fertiliser nitrogen applied to winter wheat: effect of date of application in spring

Previous studies on the fate of fertiliser nitrogen applied to winter wheat in temperate climates have shown that nitrogen (N) applied early, at tillering for wheat, was less efficiently taken up than N applied later in the growth cycle. We examined the extent to which the soil microbial N immobilisation varied during the wheat spring growth cycle and how microbial immobilisation and plant uptake competed for nitrogen. We set up a pulse-15N labelled field experiment in which N was applied at eight development stages from tillering (beginning of March) to anthesis (mid-June). Each application was 50 kg N ha-1 as 15N labelled urea except for the first application which was 25 kg N ha-1. The distribution of fertiliser 15N in shoots, roots, mineral and organic soil N was examined by destructive sampling 7 and 14 days after each 15N pulse. The inorganic 15N pool was almost depleted by day 14. The N uptake efficiency increased with later applications from 45% at tillering to 65% at flowering. N immobilisation was rather constant at 13–16% of N applied, whatever the date of application. The increase in plant 15N uptake resulted in an increase in the total 15N recovery in the plant-soil system (15N in soil +15N in plant), suggesting that gaseous losses were lower at the later application dates.