Growth,competition, yield advantage and economics in soybean/pigeonpea intercropping system in semi-arid tropics of India: I. Effect of subsoiling

Opinions differ on the necessity of deep tillage for sustaining crop productivity in the rainfed Vertisols of the semi-arid tropics of central India. We conducted a field experiment for 3 years (2000–2002) with a factorial combination of three cropping systems (sole soybean, sole pigeonpea and soybean/pigeonpea intercropping in 2:1 row ratio) and three tillage practices (conventional, conventional + subsoiling in alternate years and conventional + subsoiling every year). Objectives were (i) to examine the effect of subsoiling Vertisols on sustaining yield of soybean/pigeon pea intercropping, and (ii) to assess the frequency of subsoiling for realizing maximum yield and profit. Though there was a reduction in growth and yield of intercrops, higher soybean equivalent yield (SEY) and area-time equivalent ratio (ATER) value in soybean/pigeonpea intercropping system as compared to sole soybean had a yield advantage. The average yield advantage in intercropping system was 60% higher than that from sole soybean. The yield advantage of intercropping system in terms of ATER was 7% greater with subsoiling than conventional tillage. The yield response to subsoiling was consistent over the period and on an average, subsoiling increased yield by 20%. The effect was associated with improved water storage and root length density. However, with respect to energy use efficiency and profit, the effect of subsoiling was comparable to conventional tillage. The variation in net return and benefit:cost ratio in subsoiling every year and subsoiling in alternate years in sole soybean and soybean/pigeonpea intercropping was not significant. However, in sole pigeon pea subsoiling every year out-yielded subsoiling in alternate years. The interactive effect of subsoiling and intercropping increased the yield by 21–25%. Thus, under rainfed cropping where drought of unpredictable intensity and duration is a prevailing feature, soybean/pigeon pea intercropping could be a promising option, especially when combined with subsoiling in alternate years.     

Wheat/maize or wheat/soybean strip intercropping: II. Recovery or compensation of maize and soybean after wheat harvesting

While early-maturing crops benefit from intercropping, late-maturing crops usually suffer growth penalties during the intercropping phase. It is possible, however, that recovery or compensation of the late-maturing crops occurs after the harvest of the early-maturing crops. Three field experiments were conducted at Baiyun in 1997 and at Jingtan in 1997 and 1998 to test the hypothesis in wheat/maize and wheat/soybean intercropping. The biomass and nutrient accumulation in intercropped soybean were significantly smaller than in sole soybean before wheat harvest but thereafter increased sharply at Jingtan site in 1997. The rates of dry matter accumulation in the intercropped maize (10.0–20.1 g/m² per day) were significantly lower than those in the sole maize (17.1–34.8 g/m² per day) during the early stage from 7 May to 3 August, while mostly intercropped with wheat. After 3 August, however, the rates of intercropped maize, increasing to 58.9–69.9 g/m² per day, was significantly greater than in sole maize (22.7–51.8 g/m² per day) at Baiyun site in 1997 and nutrient acquisition showed the same trends as growth. At Jingtan site in 1998, the disadvantage of the border row of intercropped maize resulted from interspecific competition diminished after wheat harvest and disappeared at maize maturity. It was concluded that there was indeed recovery of growth after wheat harvesting in wheat/maize and wheat/soybean intercropping. However, the recovery was limited under N₀P₀ treatment. The interspecific competition, facilitation and recovery are together contributed to yield advantage of intercropping.     

Foliar sprays of concentrated urea at maturity of pigeonpea to induce defoliation and increase its residual benefit to wheat

The pigeonpea (Cajanus cajan (L.) Millsp.) crop retains appreciable amounts of green foliage even after reaching physiological maturity, which if allowed to defoliate, could augment the residual benefit of pigeonpea to the following wheat (Triticum aestivum L.) in a pigeonpea–wheat rotation. The effect of addition of leaves present on mature pigeonpea crop to the soil was examined on the following wheat during the 1999/2000 growing season at Patancheru (17°4′N, 78°2′E) and during the 2001–2003 growing seasons at Modipuram (29°4′N, 77°8′E). At Patancheru, an extra-short-duration pigeonpea cultivar ICPL 88039 was defoliated manually and using foliar sprays of 10% urea (30 kg/ha) and compared with a millet (Pennisetum glaucum (L.) R.Br.) crop, naturally senesced leaf residue and no-leaf residue controls. At Modipuram, the effect of 10% urea spray treatment on mature ICPL 88039 was compared with the unsprayed control. At both locations, the rainy season crops were followed by a wheat cultivar UP 2338 at four nitrogen levels applied in a split plot design, which at Patancheru were 0, 30, 90 and 120 kg N ha⁻¹ and at Modipuram 0, 60, 120 and 180 kg N ha⁻¹. At Patancheru, urea spray added 0.5 t ha⁻¹ of extra leaf litter to the soil within a week without significantly affecting pigeonpea yield. This treatment, however, increased mean wheat yield by 29% from 2.4 t ha⁻¹ in the no-leaf residue pigeonpea or pearl millet plots to 3.1 t ha⁻¹. At Modipuram, the foliar sprays of urea added more leaf litter to the soil than at Patancheru. Here, increase in subsequent wheat yield due to additional pigeonpea leaf litter was 7–8% and net profit 21% more than in the unsprayed control. The addition of pigeonpea leaf litter to the soil resulted in a saving of 40–60 kg N for the following wheat crops in both the environments. The results demonstrated that pigeonpea leaf litter could play an important role in the fertilizer N economy in wheat. The urea spray at maturity of the standing pigeonpea crop significantly improved this contribution in increasing wheat yield, the effect of which was additional to the amount of urea used for inducing defoliation. The practice, if adopted by farmers, may enhance sustainability of wheat production system in an environmentally friendly way, as it could reduce the amount of fertilizer N application to soil and enhance wheat yield.     

Evaluating pea and barley cultivars for complementarity in intercropping at different levels of soil N availability

Two field experiments were carried out on a temperate sandy loam using six pea (Pisum sativum L.) and five spring barley (Hordeum vulgare L.) cultivars to determine cultivar complementarity in the intercrop for grain yield, dry matter production and nitrogen (N) acquisition. Crops were grown with or without the supply of 40 or 50 kg N ha⁻¹ in the two experiments. Cultivars were grown as sole crops (SC) and as mixed intercrops (IC) using a replacement design (50:50). The land equivalent ratio (LER), which is defined as the relative land area under SC that is required to produce the yields achieved in intercropping, were used to compare cultivar performance in intercropping relative to sole cropping.Barley was the stronger competitor in the intercrops and as a result barley grain yield and nitrogen uptake in IC were similar to SC. The per plant pea grain production and aboveground N accumulation in IC were reduced to less than half compared to SC pea plants due to competitive interactions.Application of N caused a dynamic change in the intercrop composition. Competition from barley increased with N application and the pea contribution to the combined intercrop grain yield decreased. The LER values showed that in the intercrop plant growth resources were used on average 20% more efficient without N application and 5–10% more efficient with N application.The choice of pea cultivar in the intercrop influenced the intercrop performance to a larger degree than the choice of barley cultivar. Furthermore, pea cultivar×cropping systems interactions was observed, indicating that cultivars performed differently in sole and intercrops. An indeterminate pea cultivar competed strongly with barley causing a greater proportion of peas in the intercrop yield, but caused a reduced N uptake and yield of barley. Determinate peas with normal leaves caused the highest degree of complementary use of N sources by allowing barley to exploit the soil N sources efficiently, while they contribute with fixed N₂. However, difference in performance among cultivars was observed. Using the indeterminate pea cultivar combined IC grain yield was in general lower than the greatest sole crop yield and vice versa for the determinate pea cultivars. Up to 22% (LER=1.22) greater combined IC grain yield was observed in several mixtures using determinate pea cultivars.From the present study, it is was concluded that there is a need for breeding suitable pea cultivars for intercropping purposes, since cultivars bred for sole cropping may not be the types, which are the most suitable for intercropping. For optimized N-use in pea–barley intercrops it is concluded that important traits for the intercropped pea are: (1) determinate growth, (2) a medium competitive root system for soil inorganic N and other nutrients during early growth, (3) high light absorption capacity by peas growing underneath the canopy of the higher barley component and (4) early establishment of symbiotic N₂ fixation to support a high growth rate during early growth stages.Fertilized pea–barley intercrops gave a 15% higher net income than fertilized barley sole cropping and is regarded as a better safeguard for the farmer’s earnings compared to pea sole cropping known for variable yields and poor competitive ability towards weeds.     

Interspecific competition,N use and interference with weeds in pea–barley intercropping

Field pea (Pisum sativum L.) and spring barley (Hordeum vulgare L.) were intercropped and sole cropped to compare the effects of crop diversity on productivity and use of N sources on a soil with a high weed pressure. ¹⁵N enrichment techniques were used to determine the pea–barley–weed-N dynamics. The pea–barley intercrop yielded 4.6 t grain ha⁻¹, which was significantly greater than the yields of pea and barley in sole cropping. Calculation of land equivalent ratios showed that plant growth factors were used from 25 to 38% more efficiently by the intercrop than by the sole crops. Barley sole crops accumulated 65 kg soil N ha⁻¹ in aboveground plant parts, which was similar to 73 kg soil N ha⁻¹ in the pea–barley intercrop and significantly greater than 15 kg soil N ha⁻¹ in the pea sole crop. The weeds accumulated 57 kg soil N ha⁻¹ in aboveground plant parts during the growing season in the pea sole crops. Intercropped barley accumulated 71 kg N ha⁻¹. Pea relied on N₂ fixation with 90–95% of aboveground N accumulation derived from N₂ fixation independent of cropping system. Pea grown in intercrop with barley instead of sole crop had greater competitive ability towards weeds and soil inorganic N was consequently used for barley grain production instead of weed biomass. There was no indication of a greater inorganic N content after pea compared to barley or pea–barley. However, 46 days after emergence there was about 30 kg N ha⁻¹ inorganic N more under the pea sole crop than under the other two crops. Such greater inorganic N levels during early growth phases was assumed to induce aggressive weed populations and interspecific competition. Pea–barley intercropping seems to be a promising practice of protein production in cropping systems with high weed pressures and low levels of available N.     

Using legumes to enhance nitrogen fertility and improve soil condition in cotton cropping systems

Many Australian cotton growers now include legumes in their cropping system. Three experiments were conducted between 1994 and 1997 to evaluate the rotational effects of winter or summer legume crops grown either for grain or green manuring on following cotton (Gossypium hirsutum L.). Non-legume rotation crops, wheat (Triticum aestivum) and cotton, were included for comparison. Net nitrogen (N) balances, which included estimates of N associated with the nodulated roots, were calculated for the legume phase of each cropping sequence. Faba bean (Vicia faba — winter) fixed 135–244 kg N ha⁻¹ and soybean (Glycine max — summer) fixed 453–488 kg N ha⁻¹ and contributed up to 155 and 280 kg fixed N ha⁻¹, respectively, to the soil after seed harvest. Green-manured field pea (Pisum sativum — winter) and lablab (Lablab purpureus — summer) fixed 123–209 and 181–240 kg N ha⁻¹, respectively, before the crops were slashed and incorporated into the topsoil.In a separate experiment, the loss of N from ¹⁵N-labelled legume residues during the fallow between legume cropping and cotton sowing (5–6 months following summer crops and 9 months after winter crops) was between 9 and 40% of ¹⁵N added; in comparison, the loss of ¹⁵N fertilizer (urea) applied to the non-legume plots averaged 85% of ¹⁵N added. Little legume-derived ¹⁵N was lost from the system during the growth of the subsequent cotton crop.The improved N fertility of the legume-based systems was demonstrated by enhanced N uptake and lint yield of cotton. The economic optimum N fertilizer application rate was determined from the fitted N response curve observed following the application of N fertilizer at rates between 0 and 200 kg N ha⁻¹ (as anhydrous ammonia). Averaged over the three experiments, cotton following non-legume rotation crops required the application of 179 kg N ha⁻¹, whilst following the grain- and green-manured legume systems required only 90 and 52 kg N ha⁻¹, respectively.In addition to improvements in N availability, soil strength was generally lower following most legume crops than non-legume rotation crops. Penetrometer resistance during the growth of the subsequent cotton crop increased in the order faba bean, lablab, field pea, wheat, cotton, and soybean. It is speculated that reduced soil strength contributed to improvement in lint yields of the following cotton crops by facilitating the development of better root systems.     

Will nutrient-efficient genotypes mine the soil? Effects of genetic differences in root architecture in common bean (Phaseolus vulgaris L.) on soil phosphorus depletion in a low-input agro-ecosystem in Central America

Crop genotypes with root traits permitting increased nutrient acquisition would increase yields in low fertility soils but have uncertain effects on soil fertility in the long term because of competing effects on nutrient removal vs. the soil conserving effects of greater crop biomass. This study evaluated the relative importance of phosphorus loss in crop extraction vs. phosphorus loss in soil erosion as influenced by genetic differences in root shallowness and therefore phosphorus uptake in common bean (Phaseolus vulgaris L.). Six recombinant inbred lines of varying root architecture and two commercial genotypes of bean were grown in unfertilized, steeply sloped (32%), low phosphorus (5.8 mg kg^?1, Fe-strip) Udults in Costa Rica. Fertilized (60 kg total phosphorus ha^?1) plots of commercial genotypes were also included in the study. Runoff was monitored throughout the bean growing season in 2005 and 2006, and in 2006, monitoring continued through the maize growing season. Phosphorus removed in plant biomass at harvest through the 2006 bean–maize crop cycle averaged 7.3 kg ha^?1 year^?1, greatly exceeding phosphorus loss due to erosion (0.15–0.53 kg ha^?1 year^?1) in unfertilized plots. In fertilized bean plots, total biomass phosphorus averaged 6.32 kg ha^?1 year^?1 and total eroded phosphorus averaged 0.038 kg ha^?1 year^?1, indicating rapid sorption of fertilizer phosphorus. Shoot growth of several recombinant inbred lines under low phosphorus was comparable to that of fertilized commercial genotypes, illustrating the effectiveness of selection for root traits for improving plant growth in low-phosphorus soils. Genotypic differences in root architecture of recombinant inbred lines led to 20–50% variation in groundcover by shoots, which was associated with 50–80% reduction in sediment loss. This study demonstrates that root architecture traits can affect nutrient cycling at the agro-ecosystem level, and that integrated nutrient management strategies are necessary to avoid soil nutrient depletion.     

Site-specific nutrient management for intensive rice cropping systems in Asia

Irrigated rice (Oryza sativa L.) yield increases in Asia have slowed down in recent years. Further, yield increases are likely to occur in smaller increments through fine-tuning of crop management. On-farm experiments at 179 sites in eight key irrigated rice domains of Asia were conducted from 1997 to 1999 to evaluate a new approach for site-specific nutrient management (SSNM). Large variation in initial soil fertility characteristics and indigenous supply of N, P, and K was observed among the eight intensive rice domains as well as among farms within each domain. Field- and season-specific NPK applications were calculated by accounting for the indigenous nutrient supply, yield targets, and nutrient demand as a function of the interactions between N, P, and K. Nitrogen applications were fine-tuned based on season-specific rules and field-specific monitoring of crop N status. The performance of SSNM was tested for four successive rice crops. Average grain yield in the SSNM increased by 0.36 Mg ha⁻¹ (7%) compared to the current farmers’ fertilizer practice (FFP) measured in the same cropping seasons or 0.54 Mg ha⁻¹ (11%) compared to the baseline FFP yield before intervention. Average nutrient uptake under SSNM increased by about 10% in the same seasons or by 13% (N) and 21% (P, K) compared to the baseline data. Yield increases were associated with a 4% decrease in the average N rate, but larger amounts of fertilizer-K at sites where the previous K use was low. Average N use efficiencies increased by 30–40%, mainly through the use of improved in-season N management schemes. Across all sites and four successive rice crops, profitability increased by US$ 46 ha⁻¹ per crop or 12% of the total average net return. The performance of SSNM did not differ significantly between high-yielding and low-yielding climatic seasons, but improved over time with larger benefits observed in the second year. Average profitability increased from US$ 32 ha⁻¹ pre crop in the first year to US$ 61 ha⁻¹ pre crop in the second year due to improvements in the SSNM approach and re-capitalization of P and K applied in the first year. SSNM required little extra credit for financing, and remained profitable even if rice prices are somewhat lower than current levels. Further, scope for improvement exists at many sites by alleviating other crop management constraints to nutrient use efficiency. Profit increases ranged from US$ 4 to 82 ha⁻¹ per crop among eight rice domains. However, profit decreases occurred in about 25% of all cases, indicating that a certain minimum level of crop care is required for SSNM to be profitable. Yields at sites with labor-saving direct-seeding of larger fields were about 1 Mg ha⁻¹ lower than those achieved at sites with labor-intensive transplanting and good management, raising concern about future trends in rice production. SSNM has potential for improving yields and nutrient efficiency in irrigated rice to close existing yield gaps. The major challenge for SSNM will be to retain the success of the approach while reducing the complexity of the technology as it is disseminated to farmers. The nature of the approach will need to be tailored to specific circumstances in different countries. In some areas, SSNM may be field or farm specific, but in many areas it is likely to be just region and season-specific.     

Interactions between non-flooded mulching cultivation and varying nitrogen inputs in rice–wheat rotations

A 3-year field experiment examined the effects of non-flooded mulching cultivation and traditional flooding and four fertilizer N application rates (0, 75, 150 and 225 kg ha⁻¹ for rice and 0, 60,120, and 180 kg N ha⁻¹ for wheat) on grain yield, N uptake, residual soil N_min and the net N balance in a rice–wheat rotation on Chengdu flood plain, southwest China. There were significant grain yield responses to N fertilizer. Nitrogen applications of >150 kg ha⁻¹ for rice and >120 kg ha⁻¹ for wheat gave no increase in crop yield but increased crop N uptake and N balance surplus in both water regimes. Average rice grain yield increased by 14% with plastic film mulching and decreased by 16% with wheat straw mulching at lower N inputs compared with traditional flooding. Rice grain yields under SM were comparable to those under PM and TF at higher N inputs. Plastic film mulching of preceding rice did not affect the yield of succeeding wheat but straw mulching had a residual effect on succeeding wheat. As a result, there was 17–18% higher wheat yield under N0 in SM than those in PM and TF. Combined rice and wheat grain yields under plastic mulching was similar to that of flooding and higher than that of straw mulching across N treatments. Soil mineral N (top 60 cm) after the rice harvest ranged from 50 to 65 kg ha⁻¹ and was unaffected by non-flooded mulching cultivation and N rate. After the wheat harvest, soil N_min ranged from 66 to 88 kg N ha⁻¹ and increased with increasing fertilizer N rate. High N inputs led to a positive N balance (160–621 kg ha⁻¹), but low N inputs resulted in a negative balance (−85 to −360 kg ha⁻¹). Across N treatments, the net N balances of SM were highest among the three cultivations systems, resulting from additional applied wheat straw (79 kg ha⁻¹) as mulching materials. There was not clear trend found in net N balance between PM and TF. Results from this study indicate non-flooded mulching cultivation may be utilized as an alternative option for saving water, using efficiently straw and maintaining or improving crop yield in rice–wheat rotation systems. There is the need to evaluate the long-term environmental risks of non-flooded mulching cultivation and improve system productivity (especially with straw mulching) by integrated resource management.     

Effect of N fertilizer top-dressing at various reproductive stages on growth,N2 fixation and yield of three soybean (Glycine max (L.) Merr.) genotypes

Soybean (Glycine max (L.) Merr.) is one of the most important food and cash crops in China and a key protein source for the farmers in northern China. Previous experiments in both the field and greenhouse have shown that N₂ fixation alone cannot meet the N requirement for maximizing soybean yield, and that N top-dressing at the flowering stage was more efficient than N top-dressing at the vegetative stages. However, the effect of N fertilizer application at other reproductive stages of soybean is unknown. Thus, a field experiment was conducted to study the effects of N applications at various reproductive stages on growth, N₂ fixation and yield of three soybean genotypes. The results showed that starter N at 25 kg ha⁻¹ resulted in minimum yield, total N accumulation and total amount of N₂ fixed in all three genotypes. N top-dressing at 50 kg ha⁻¹ at either the V2 or R1 stages, significantly increased N accumulation, yield and total amount of N₂ fixed in all three genotypes. However, N top-dressing at the same rate at either the R3 or R5 stage did not show this positive effect in any of the three genotypes. Thus, the best timing for N top-dressing during reproduction is at the flowering stage, which increased seed yield by 21% for Wuyin 9, 27% for You 91-19, and 26% for Jufeng, respectively, compared to the treatment without N top-dressing.     

Identification of quantitative trait loci controlling nodulation and shoot mass in progenies from two Brazilian soybean cultivars

Nitrogen (N) demand of soybean [Glycine max (L.) Merrill] can be supplied via biological nitrogen fixation (BNF), however, higher yielding cultivars increase plant demand for N. Phenotypes differing for traits associated with biological nitrogen fixation result from the expression of the multiple genes of both the host plant and the microsymbiont, but limited studies have been done on the genetics of the soybean BNF. Integrated maps of soybean with simple sequence repeat (SSR) markers [Cregan, P.B., Jarvik, T., Bush, A.L., Shoemaker, R.C., Lark, K.G., Kahler, A.L., Kaya, N., Van Toai, T.T., Lohnes, D.G., Chung, J., Specht, J.E., 1999. An integrated genetic linkage map of the soybean genome. Crop Sci. 39, 1464–1491.] offer an excellent opportunity for the identification of traits related to BNF. This study aimed at the identification of quantitative trait loci (QTLs) controlling BNF and nodulation in an F₂ population of 160 plants derived from an intraspecific cross between two Brazilian cultivars, Embrapa 20 × BRS 133, previously identified as having good potential for mapping of QTLs [Nicolás, M.F., Arias, C.A.A., Hungria, M., 2002. Genetics of nodulation and nitrogen fixation in Brazilian soybean cultivars. Biol. Fertil. Soils 36, 109–117.]. From 252 SSR markers tested in the parental genotypes 45 were polymorphic with high heterozygotes resolution. Mapping was performed with those 45 SSR markers for nodulation [nodule number (NN) and nodule dry weight (NDW)] and plant growth [shoot dry weight (SDW)] phenotypes in F_2:3 lines. A total of 21 SSR loci were mapped with a likehood of odds (LOD) value of 3.0 and a maximum Haldane distance of 50 cM, and were distributed in nine linkage groups with coverage of 251.2 cM. The interval mapping analysis with Mapmaker/QTL revealed two genomic regions associated with NN and NDW, with a contribution of putative QTLs of 7.1 and 10%, respectively. The regression analysis identified 13 significant associations between the marker loci and QTLs due to additive effects, with some of them being significantly associated with more than one phenotypic trait. Effects were observed in all variables studied, ranging from 2 to 9%. A one-way analysis of variance (ANOVA) also detected 13 significant associations, related to dominance effects. A two-way-ANOVA showed six epistatic interactions among non-linked QTLs for SDW, NN and NDW, explaining up to 15% of the trait variation and increasing the phenotypic expression from 8 to 28%. The data obtained in this work establish the initial stage for additional studies of the QTLs controlling BNF and indicate that effective marker-assisted selection using SSR markers may be feasible for enhancing BFN traits in soybean breeding programs.     

Influence of sources and doses of N and K on herbage,oil yield and nutrient uptake of patchouli [Pogostemon cablin (Blanco) Benth.] in semi-arid tropics

Patchouli oil is one of the most important essential oils used in modern perfumery and cosmetic industries. There is hardly any preparation of oriental nature where patchouli oil is not used. It is used mainly because of fixative property as it gives tenacity to other perfumes. Field experiments were conducted at Bangalore, India, to study the influence of sources and doses of N and K on herbage, oil yield, nutrient uptake, nitrogen utilization efficiency and oil content of patchouli [Pogostemon cablin (Blanco) Benth.]. The results revealed that application of 200 kg N/ha and 41.5 kg K/ha produced significant higher patchouli herbage and oil yields compared with controls. Similarly, N and K uptake were also higher at 200 kg N and 41.5 kg K/(ha year) compared with controls. DCD-coated urea produced higher herbage, oil yield and N uptake and utilization efficiency compared with prilled urea. There was no effect of sources of K on the yield of patchouli. The oil content was not influenced by N, K doses or sources applied. N and K depletion were noticed in the soil.     

Differential accumulation of sulfur-rich and sulfur-poor wheat flour proteins is affected by temperature and mineral nutrition during grain development

Hard red spring wheat (Triticum aestivum cv Butte86) was grown under controlled environmental conditions and grain produced under 24/17 °C, 37/17 °C or 37/28 °C day/night regimens with or without post-anthesis N supplied as NPK. Flour proteins were analyzed and quantified by differential fractionation and RP-HPLC, and endosperm proteins were assessed by two-dimensional gel electrophoresis (2-DE). High temperature or NPK during grain fill increased protein percentage and altered the proportions of S-rich and S-poor proteins. Addition of NPK increased protein accumulation per grain under the 24/17 °C but not the 37/28 °C regimen. However, flour protein composition was similar for grain produced with NPK at 24/17 °C or 37/28 °C. 2-DE of gluten proteins during grain development revealed that NPK or high temperature increased the accumulation rate for S-poor proteins more than for S-rich proteins. Flour S content did not indicate S-deficiency, however, and addition of post-anthesis S had no effect on protein composition. Although, high-protein flour from grain produced under the 37/28 °C regimen with or without NPK had loaf volumes comparable to flour produced at 24/17 °C with NPK, mixing tolerance was decreased by the high temperature regimen.     

Large applications of fertilizer N at planting affects seed protein and oil concentration and yield in the Early Soybean Production System

An inverse relationship between soybean [Glycine max (L.) Merr.] seed protein and oil concentration is well documented in the literature. A negative correlation between protein and yield is also often reported. The objective of this study was to determine the effect of high rates of N applied at planting on seed protein and oil. Nitrogen was surface-applied at soybean emergence at rates of 290 kg ha⁻¹ in 2002, 310 kg ha⁻¹ in 2003, and 360 kg ha⁻¹ in 2004. Eight cultivars ranging from Maturity Group II–IV were evaluated under the Early Soybean Production System (ESPS). However, not all cultivars were evaluated in all 3 years. Glyphosate herbicide was used in all 3 years and a non-glyphosate herbicide treatment was applied in 2002. Cultivars grown in 2003 were also evaluated under an application of 21.3 kg ha⁻¹ of Mn. All cultivar, herbicide, and Mn treatments were evaluated in irrigated and non-irrigated environments with fertilizer N (PlusN treatment) or without fertilizer N (ZeroN treatment). When analyzed over all management practices (years, cultivars, herbicide, and Mn treatments), the PlusN treatment resulted in a significant decrease in protein concentration (2.7 and 1.9%), an increase in oil concentration (2.2 and 2.7%), and a decrease in the protein/oil ratio (4.7 and 4.6%) for the irrigated and non-irrigated environments, respectively. However, the overall protein and oil yield increased with the application of fertilizer N at planting (protein: 5.0% irrigated, 12.7% non-irrigated and oil: 9.9% irrigated and 18.9% non-irrigated). These increases were due to the increase in seed yield with the application of large amounts of fertilizer at planting. Additionally, a significant correlation (r = 0.45, P = 0.0001) was found between seed protein concentration and seed yield. No significant correlation was found between seed oil concentration and seed yield. The data demonstrate the inverse relationship between protein and oil and indicate that large amounts of N applied at planting do not change this relationship.     

Nutrient and assimilate partitioning in two tropical maize cultivars in relation to their tolerance to soil acidity

The use of Al-tolerant and P-efficient maize cultivars is an important component of a successful production system on tropical acid soils with limited lime and P inputs. Grain yield and secondary plant traits, including root and aboveground biomass, nutrient content and leaf development, were evaluated from 1996 to 2002 in field experiments on an Oxisol in order to identify maize characteristics useful in genetic improvement. Here we present the results of the 2002 trial and compare them with previous results. The aim of this experiment was to assess the effect of assimilate and nutrient partitioning on the growth and grain yield of two tropical cultivars having different Al tolerance (CMS36, tolerant, Spectral, moderately tolerant). The soil had an Al saturation of 36% in topsoil (pH 4.5) and >45% below 0.3 m depth (pH 4.2). Measurements made from emergence to grain filling included: root, stem and leaf biomass, P and N content, leaf area index (LAI), radiation use efficiency (RUE), soil available N and root profiles at anthesis. The experiments consisted of two P treatments, zero applied or 45 kg P ha⁻¹ (−P and +P). All the treatments received N and K fertilizers. In −P, root biomass and LAI at anthesis were twice as great in CMS36 as in Spectral. In +P the differences between cultivars were negligible. Roots were deeper in CMS36 due to its higher Al tolerance. Total biomass and grain yield were not strongly related to root biomass and LAI. Other factors such as the leaf biomass and the amount of nutrients per unit leaf area were highly correlated with RUE and biomass. In −P, Spectral had the same total biomass but a higher grain yield than CMS36 (2.1 Mg ha⁻¹ versus 1.5 Mg ha⁻¹). This was due to a higher leaf P content (+40%), a greater RUE (+74%), and a lower number of sterile plants. In +P, CMS36 had higher total biomass and grain yield (4.1 Mg ha⁻¹ versus 3.1 Mg ha⁻¹). This was due to its higher leaf P (+25%) and leaf N (+43%) contents, and an increased RUE (+130%) that were associated with higher P and N uptake. Our results indicated that although root tolerance to Al toxicity is necessary for good crop performance on acid soils, assimilate and nutrient partitioning in the aboveground organs play a major role in plant adaptation and may partially compensate for a lower root tolerance.     

Interannual variation in soybean yield: interaction among rainfall,soil depth and crop management

Using data from large, grower-managed fields we investigated the variation in yield of dryland soybean in an area with low and variable summer rainfall, and soils that are variable in depth and poor in phosphorus (P). First, using data from unfertilised, wide-row (0.7 m) crops grown under standard management between 1989 and 1992 (Series 1), we quantified the relationship between yield and W, a rainfall-based estimate of water availability during the period of pod and grain set. Separate functions were established for deep (depth ≥ 1 m) and shallow soils (0.75 m ≥ depth ≥ 0.5 m). Second, we partially tested these functions using two independent data sets (Series 2 and 3). Third, we evaluated the effects on yield of large (18 kg P ha⁻¹, Series 4) or moderate doses of P fertiliser (8–12 kg P ha⁻¹) in narrow-row crops (0.35 m, Series 5). To investigate water × management interaction we (i) calculated ΔY, the difference between actual yield in Series 4 and 5 and yield calculated with the functions derived from Series 1, and (ii) tested the association between ΔY and actual W. In a set of 24 crops (Series 1), yield varied between 2.1 and 3.1 t ha⁻¹ in deep soils and between 1.3 and 2.6 t ha⁻¹ in shallow soils; non-linear functions described fairly well, the response of yield to W. Fertilisation with 18 kg P ha⁻¹ increased yield by 0.6 t ha⁻¹ irrespective of water availability. The combination of narrow rows and a moderate dose of fertiliser increased yield in 73% of crops in deep soil but only in 53% of crops in shallow soil. There was a positive association between ΔY and W in deep soil but no relationship between these variables in shallow soil. Yield responses to management were thus differentially affected by rainfall in deep and shallow soils.     

Weed control in a pigeon pea–wheat cropping system

Pigeon pea (Cajanus cajan (L.) Millsp.) seedlings compete poorly against the rapid growth of warm-season annual weeds. Weed control is required before this heat and drought-tolerant legume can be reliably grown in the U.S. southern Great Plains as a potential source of livestock hay between annual plantings of winter wheat (Triticum aestivum L.). Currently, no herbicides are labeled for use on pigeon pea grown in the U.S. Three years of replicated field experiments were conducted to determine the effects of applications (1× and 2× rates) of herbicides (pre-emergence, sulfentrazone + chlorimuron and metribuzin; post-emergence, imazapic and sethoxydim) on weed suppression, pigeon pea dry matter, and carry-over effects on a winter wheat crop. The most abundant summer weeds were broadleaf, and all herbicide treatments, except sethoxydim (grass herbicide), reduced weed densities compared to untreated plots without adversely affecting pigeon pea stands. Imazapic treatments provided the most effective weed control. Overall average pigeon pea dry matter ranged from 75 to 256 g m⁻² with sethoxydim and the untreated control ≤ metribuzin ≤ sulfentrazone + chlorimuron ≤ hand weeded control ≤ imazapic. Compared to the hand-weeded control, imazapic treatments greatly reduced wheat dry matter (1×, 65% and 2×, 91%) and grain yield (1×, 59% and 2×, 93%). Imazapic should not be used unless nontransgenic imidazolinone herbicide tolerant wheat cultivars are planted. While the other herbicides decreased negative effects of weeds on pigeon pea dry matter without greatly affecting productivity of a following wheat crop, appropriate labels for each of these herbicides will be required prior to their use by southern Great Plains pigeon pea producers.     

A crop model component simulating N partitioning during seed filling in pea

Seed N concentration is one of the main quality parameters in grain legume crops. Since few studies have aimed at modelling both seed and vegetative parts N concentrations, our objective was to model N partitioning between vegetative parts and filling seeds for pea (Pisum sativum L.) in field situations where both N nutrition and the plant genotype varied. A crop model component predicting the time courses of vegetative and seed N concentrations was built using knowledge concerning N partitioning during the seed filling period, which include a previously demonstrated relationship between the rate of individual seed N accumulation and the N availability within plants. A greenhouse experiment where assimilate availability was non-limiting was conducted with two genotypes. This experiment demonstrated the genotypic variability of one of the crop model component parameters, the maximum rate of individual seed N accumulation (SNR_max), allowing introduction of this parameter in the crop model component for the studied genotypes. Field experiments spanning 3 years and comprising various crop N nutrition and four genotypes were conducted to evaluate the crop model component. Observed seed and vegetative parts N concentrations ranged at harvest from 19.3 to 39.1 mg g⁻¹ and from 3.6 to 18.4 mg g⁻¹, respectively. N partitioning was well-simulated by the crop model component except when crops had deficient N nutrition. These results suggest that the parameter “NC_n-remob” (proportion of N in vegetative parts which is not available for remobilization to filling seeds), which is taken as constant in the crop model component, could depend upon the crop nutrition level. A sensitivity analysis highlights the need for a precise calibration of the parameters “NC_n-remob” and “SNR_max”. When the crop N nutrition level and further genotypic variability of these parameters are incorporated in the proposed crop model component, it will become a useful part of a pea crop model predicting yield and seed N concentration.     

Methyl jasmonate,alone or in combination with genistein,and Bradyrhizobium japonicum increases soybean (Glycine max L.) plant dry matter production and grain yield under short season conditions

Jasmonic acid (JA) is a plant hormone produced via the octadecanoid pathway from its precursor, linolenic acid. Jasmonates are involved in plant wound responses and defense against insects and fungal elicitors. They can also act as signal molecules in the Bradyrhizobium-soybean symbiosis. Pre-incubation of Bradyrhizobium japonicum inocula with gensitein (Ge), an effective inducer of nodulation genes in this species enhances soybean nodulation, nitrogen fixation and yield under low spring soil temperature field conditions. Since jasmonates are also able to induce nodulation genes and cause the production of lipo-chitooligosaccharides (LCOs) by B. japonicum, we conducted two field experiments, in southwestern Quebec, Canada, to determine whether pre-incubation of B. japonicum with methyl jasmonate (MeJA) alone or in combination with genistein (Ge), prior to inoculation, increased soybean plant dry matter production and grain yield. Experiments at each site used a two factor randomized complete block design (RCBD) with four replicates. Two B. japonicum strains (USDA3 and 532C) and four inducer molecule treatments [control, Ge (20 μM), MeJA (50 μM), and Ge + MeJA (20 μM + 50 μM)] were used in the study. The bacterial cultures were induced for 24 h with the inducer molecules and then applied into the furrows at the time of planting. Both Ge and MeJA, alone or in combination, increased plant growth, dry matter accumulation, and grain yield. This study showed that MeJA, alone or in combination with Ge, can be used to promote soybean plant growth and grain yield under short season field conditions.     

Emissions of ammonia,nitrous oxide and carbon dioxide from urban gardens in Niamey,Niger

Urban and peri-urban agriculture (UPA) contributes significantly to meet increasing food demands of the rapidly growing urban population in West Africa. The intensive vegetable cultivation in UPA gardens with its high nutrient inputs is often reported to operate at large surpluses of nutrients and presumably high turnover rates of organic matter (OM) and nitrogen (N) losses via emanation and leaching. Many of these claims are lacking solid data which would allow suggesting mitigation strategies. Therefore, this study aimed at quantifying gaseous emissions of ammonia (NH₃), nitrous oxide (N₂O), and carbon dioxide (CO₂) in three representative urban gardens of Niamey, Niger using a closed chamber gas monitoring system. Mean annual N emissions (NH₃-N and N₂O-N) in two gardens using river water for irrigation reached 53 and 48 kg N ha^?1 yr^?1, respectively, while 25 and 20 Mg C ha^?1 yr^?1 was lost as CO₂-C. In the garden irrigated with sewage water from the city's main wadi, N₂O was the main contributor to N losses (68%) which together with NH₃ reached 92 kg N ha^?1 yr^?1, while CO₂-C emissions amounted to 26 Mg ha^?1 yr^?1. Our data indicate that 28% of the total gaseous C emissions and 30–40% of the N emissions occur during the hot dry season from March to May and another 20–25% and 10–20% during the early rainy season from June to July. Especially during these periods more effective nutrient management strategies in UPA vegetable gardens should be applied to increase the nutrient use efficiency in UPA vegetable gardens.