Severe drought conditions limited soybean production
(6.2% per acre yield decline from 2011) across much of the United States in
2012. Though 2012 will soon be behind us, the implications of the 2012 drought
may progress well into the 2013 growing season (Image 1). One area of concern
among growers is the impact of the drought on soil microbial populations; most
importantly Bradyrhizobium japonicum. Soybean
live in a symbiotic (mutually beneficial) relationship with B. japonicum.
The soybean plant provides nutrients and a protective growing environment for
the rhizobia. In turn, the rhizobia “fix” atmospheric nitrogen into ammonia
(NH3), which can then be used by the soybean plant. For this relationship to
exist and benefit the soybean plant, effective nitrogen-fixing bacteria must be
present in the soil in relatively high numbers at planting time (Conley and
Christmas, 2005).
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| Image 1. U.S. Drought Monitor Map for December 11, 2012. |
To date, little research has
been published that quantifies the impact of soil desiccation (e.g. drought) on
endemic B. japonicum populations.
Pena-Cabriales and Alexander (1979) reported a biphasic decline in Rhizobium
japonicum numbers in soils undergoing drying. The initial rapid phase of R.
japonicum loss coincided with major water loss (simulated drought)
whereas the secondary and subsequently slower decline in numbers was governed
by the soil water content of specific soils. Pena-Cabriales and Alexander
(1979) also noted that organic matter content provided little protection
against R. japonicum desiccation and loss. In a parallel study
Oso-Afiana and Alexander (1982) reported similar results when comparing strains
of R. japonicum and cowpea rhizobia under desiccation. As one
would expect, variation exists among Rhizobium spp. as well as
individual isolates within species in their response to soil desiccation,
though significant losses were evident regardless of species or isolate
(Foulds, 1971; Trotman and Weaver, 1995).
To further complicate the situation, most soybean
acres will be planted into corn ground that was subjected to severe drought
stress. This suggests that excess nitrogen may be present for the 2013 soybean
crop. In excess situations soybean will generally utilize the background nitrogen prior to
initiating maximum N fixation. This may lead to luxurious early season growth, which
in fields with a history of white mold, may cause problems if weather
conditions are conducive. High soil N reserves may also lead to increased
lodging. In either case, manage your soybean crop accordingly to minimize risk
of white mold or lodging. This can be accomplished through variety selection
(e.g. white mold tolerance, short statured soybean cultivars or good lodging
tolerance), decreasing seeding rates, and proper scouting to time fungicide
applications if needed.
I am not advocating that every soybean acre
automatically receive an inoculant treatment, however, the small amount of
research that is available on the topic does suggest that growers may expect
lowered B. japonicum populations going into the 2013 growing season.
Literature Cited.
Conley, S. P. and Christmas, E. P. 2005. Utilizing
Inoculants in a Corn-Soybean Rotation. Purdue Extension, SPS-100-W. 4 p.
Foulds, W. 1971. Effect of
drought on three species of rhizobium. Plant and Soil 35:665-667.
Furseth, B. J., Conley, S. P., and Ané, J.. 2010.
Enumeration of Soybean-Associated Rhizobia with Quantitative Real Time
Polymerase Chain Reaction. Crop Sci. 50: 2591-2596.
Osa-Afiana, L. O. and M.
Alexander. 1982. Clays anmd the survival of rhizobium in soils during
dessication. Soil. Sci. Soc. Am J. 46: 285-288.
Pena-Cabriales, J.J. and M.
Alexander. 1979. Soil. Sci. Soc. Am J. 43:962-966.
Trotman, A.P. and R. W.
Weaver. 1995. Tolerance of clover rhizobia to heat and desiccation stresses in
soil. Soil. Sci. Soc. Am J. 59:466-470.
