A fundamental shift has taken place in agricultural research and world food production. In the past, the principal driving force was to increase the yield potential of food crops and to maximize productivity. Today, the drive for productivity is increasingly combined with a desire for sustainability. For farming systems to remain productive, and to be sustainable in the long-term, it will be necessary to replenish the reserves of nutrients which are removed or lost from the soil. In the case of nitrogen (N), inputs into agricultural systems may be in the form of N-fertilizer, or be derived from atmospheric N2 via biological N2 fixation (BNF).

Biological nitrogen fixation: An efficient source of nitrogen for sustainable agricultural production?

Measuring plant-associated nitrogen fixation in agricultural systems

Agriculturally important grasses such as sugar cane (Saccharum sp.), rice (Oryza sativa), wheat (Triticum aestivum) sorghum (Sorghum bicolor), maize (Zea mays), Panicum maximum, Brachiaria spp., and Pennisetum purpureum contain numerous diazotrophic bacteria, such as, Acetobacter diazotrophicus, Herbaspirillum spp., Azospirillum spp. These bacteria do not usually cause disease symptoms in the plants with which they are associated and the more numerous of them, for example, Herbaspirillum spp. and A. diazotrophicus, are obligate or facultative endo-phytes that do not survive well (or at all) in native soil; these are thought to be spread from plant generation to plant generation via seeds, vegetative propagation, dead plant material, and possibly by insect sap feeders. By contrast, Azospirillum spp. are not wholly endophytic but are root-associated, soil-dwelling bacteria that are also often found within plants, probably entering host plants via seeds or via wounds/cracks at lateral root junctions. Endophy...

Infection and Colonization of Sugar Cane and Other Graminaceous Plants by Endophytic Diazotrophs

Inputs of biologically fixed N into agricultural systems may be derived from symbiotic relationships involving legumes and Rhizobium spp., partnerships between plants and Frankia spp. or cyanobacteria, or from non-symbiotic associations between free-living diazotrophs and plant roots. It is assumed that these N2-fixing systems will satisfy a large portion of their own N requirements from atmospheric N2, and that additional fixed N will be contributed to soil reserves for the benefit of other crops or forage species. This paper reviews the actual levels of N2 fixation attained by legume and non-legume associations and assesses their role as a source of N in tropical and sub-tropical agriculture. We discuss factors influencing N2 fixation and identify possible strategies for improving the amount of N2 fixed.

Biological nitrogen fixation: investments, expectations and actual contributions to agriculture

Building Soil Nitrogen Capital in Africa

The seasonal patterns of nodulation, acetylene reduction, nitrogen uptake and nitrogen fixation were studies for 11 pigeonpea cultivars belonging to different maturity groups grown on an Alfisol at ICRISAT Center, Patancheru, India. In all cultivars the nodule number and mass increased to a maximum around 60–80 days after sowing and then declined. The nodule number and mass of medium- and late-maturing cultivars was greater than that of early-maturing cultivars. The nitrogenase activity per plant increased to 60 days after sowing and declined thereafter, with little activity at 100 days when the crop was flowering. At later stages of plant growth nodules formed down to 90 cm below the soil surface but those at greater depth appeared less active than those near the surface.

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Nodulation, nitrogen fixation and nitrogen uptake in pigeonpea (Cajanus cajan (L.)) (Millsp) of different maturity groups

Factors affecting nitrogenase activity associated with sorghum and millet roots have been studied. Plants grown in iron cores in the field and then assayed had significantly higher activity than plants cored at the time of assay. Mechanical disturbance during transportation of the cores reduced the activity significantly. Any delay between cutting off the plant top and injecting C2H2 gas led to a reduction in the level of nitrogenase activity determined. Diurnal variation in nitrogenase activity was noted but was not correlated with soil temperature. Most activity occurred at the end of the photoperiod. Seasonal variation in nitrogenase activity of plants was observed and was correlated with the ontogenetic development of the host plant, being most at flowering. A low but significant correlation existed between soil moisture content and nitrogenase activity associated with the plant.

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Factors affecting nitrogenase activity (C2H2 reduction) associated with sorghum and millet estimated using the soil core assay

Six mycorrhizal fungi were tested as inoculants for pearl millet (Pennisetum americanum Leeke) grown in pots maintained in a greenhouse. VAM fungi varied in their ability to stimulate plant growth and phosphorus uptake. Inoculation withGigaspora margarita, G. calospora andGlomus fasciculatum increased shoot drymatter 1.3 fold over uninoculated control. In another pot trial, inoculation withGigaspora calospora andGlomus fasciculatum resulted in dry matter and phosphorus uptake equivalent to that produced by adding phosphorus at 8 kg/ha.

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Effect of mycorrhizal inoculation and soluble phosphorus fertilizer on growth and phosphorus uptake of pearl millet

A non destructive intact-plant assay for estimating nitrogenase activity (C2H2 reduction) of pot-grown sorghum and millet plants is described. Plants with intact shoots sustained more activity than plants whose tops were removed prior to the assay. With this technique individual plants can be assayed several times during their life cycle. The C2H2 reduction was linear up to 16h incubation in this assay procedure. More rapid diffusion of C2H2 was achieved by injection through a Suba seal in the bottom of the pot. The equlibration of injected C2H2 in the gas phase of the pots filled with sand and sand:FYM media was completed within 1 h. Significantly higher nitrogenase activity and better growth of sorghum and millet plants occurred when plants were grown in a mixture of sand and farmyard manure (FYM) than when plants were grown in vermiculite, soil, or sand + soil medium. Nitrogenase activity and plant growth were greater in a mixture of sand with 2 and 3% FYM than with 0.5 and 1% FYM. Activity was higher when the plants were incubated at 33°C and 40°C than at 27°C. Activity also increased with increasing soil moisture. There were significant differences amongst 15 sorghum cultivars screened for associated nitrogenase activity. This new technique has good prospects for screening cultivars of millet, sorghum and other grain crops for their nitrogen-fixing ability.

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P. J. Dart

Papers

Nodulation, nitrogen fixation and nitrogen uptake in pigeonpea (Cajanus cajan (L.)) (Millsp) of different maturity groups

Factors affecting nitrogenase activity (C2H2 reduction) associated with sorghum and millet estimated using the soil core assay

Effect of mycorrhizal inoculation and soluble phosphorus fertilizer on growth and phosphorus uptake of pearl millet

An intact plant assay for estimating nitrogenase activity (C2H2 reduction) of sorghum and millet plants grown in pots