“…As a result, inoculant rhizobia may only form 5-10% of the nodules produced in the first year, with the frequency with which they are found in nodules declining even further in subsequent crops. This has usually been perceived as a problem of competition between the inoculant rhizobia and those that are indigenous to the soil and has led to an intensive research effort emphasizing: (1) the selection of strains for competitive ability (Berg et ai., 1988;Caldwell, 1969;Johnson and Means, 1964;Klubek et al, 1988;Smith and Wollum, 1989), (2) the use oflarger than normal inoculation rates (Kapusta and Rouwenhoest, 1973;Weaver and Frederick, 1974a;, (3) development of improved inoculant carriers and delivery systems (Boonkerd et al, 1978;Kremer and Peterson, 1983;Stoddard, 1976;Wilson, 1975), (4) detailed ecological studies of the indigenous strains, and especially of those belonging to B. japonicum serogroup 123 Moawad et al, 1984;Sadowsky et al, 1987b;Viteri and Schmidt, 1987;, (5) studies on the molecular basis for competitive interaction, (6) repeated inoculation (Dunigan et al, 1984;Howieson, 1995;McLoughlin et al, 1990), and (7) host preference and restriction in nodulation (Cregan et al, 1986;Ferrey et al, 1994;Sadowsky et al, 1987b;Sadowsky et al, 1990;Sadowsky and Cregan, 1992). Strains of microorganisms which are stable members of the microbial community (members of the "local" microbial flora) appear to have a selective, competitive advantage in occupying available niches in that local environment (Atlas and Bartha 1993).…”