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Crop Rotation Strategies for the Management of herbicide-resistant Giant Ragweed
Jared Goplen
29 April 2013
Throughout the world, agricultural weeds have
historically been one of the most widespread and problematic
factors influencing agriculture. In the United States alone,
weeds annually cause a 12% overall reduction in yield,
equating to approximately $33 billion in lost crop production
(Pimentel et al. 2005). Weeds increase the cost of production
through reduced crop yield and quality, the increased
necessity of tillage, and require the added expense of
herbicides which cost an additional $8 billion annually
(Pimentel et al., 2005; USDA ERS, 2012). In addition to the
current cost of weeds, the development of herbicide
resistance adds additional economic and ecological concern.
Currently, there are 400 biotypes within 217 species of weeds known to have herbicide resistance
worldwide (Heap, 2013). In the Midwest alone, glyphosate resistant biotypes of common
waterhemp, horseweed, kochia, common ragweed and giant ragweed have been identified and are
becoming problematic (Heap, 2013). Several of these species, including giant ragweed (Ambrosia
trifida), have resistance to multiple herbicides. Weeds with multiple resistances reduce the
efficacy of existing and developing herbicide-resistant crop technologies, limit options for weed
control, and decrease profitability.
The use of weed control strategies that rely on weed emergence patterns and the seed-bank
represent ideal targets for integrated weed control. By using crop rotations that promote weed
seed-bank depletion via seed decay and predation, there is large potential to effectively manage
herbicide resistant weeds over the long term. Seed predation has been shown to remove as much
as 88% of giant ragweed seed over the course of one year in no-tillage corn (Harrison et al. 2003).
Higher levels of seed predation have also been shown to occur in small grain and alfalfa, since the
rate of seed predation tends to increase as the crop canopy develops (Westerman et al. 2005;
Hartzler et al. 2007). Crop rotations that vary in patterns of resource competition, soil disturbance
and mechanical damage also create environments hostile to any particular weed species, including
those with herbicide resistance (Liebman and Dyck, 1993).
Incorporating alfalfa into crop rotations not only limits soil erosion, but also reduces the
development and persistence of herbicide-resistant weed populations through frequent harvests,
which limit seed production of annual weeds adapted to corn-soybean systems (Olmstead &
Brummer, 2008). Wheat, on the other hand, breaks the cycle of adapted weeds since it is
established earlier than corn or soybean and is planted at higher densities in narrow rows, giving it
a competitive advantage over giant ragweed seedlings (Buhler, 2002). Herbicides with alternative
modes of action that are used in wheat also can be used to diversify weed control and control
resistant weeds. Wheat is harvested earlier than corn or soybean, which provides many chemical
or mechanical options for post-harvest weed control. Additionally, both wheat and alfalfa provide
a favorable habitat for a variety of insects, rodents, and fungi that prey on weed seeds within the
soil (Meiss et al. 2010a; Meiss et al. 2010b; Kaufman, and Kaufman, 1990; Hartzler et al. 2007).
Accurately predicting seedling emergence using emergence models allows growers to
optimize cultivation schedules, planting dates, and herbicide applications to target weeds when
they are most vulnerable, further enhancing weed control (Menalled & Schonbeck, 2011). Several
current giant ragweed emergence models are available. However, there is little information on
how different crops and rotations influence giant ragweed emergence. Different crops influence
the soil environment differently, specifically in the amount of light reaching the surface, soil
temperature, and soil moisture, which all can influence seedling emergence (Liebman and Dyck,
1993). Analyzing these factors in respect to existing giant ragweed emergence models will allow
the verification of previous models in addition to providing a new model specifically designed for
giant ragweed emergence in specific crops and rotations.
Our research includes a variety of crop rotations common to the Midwest, which
incorporate corn, soybean, wheat, and alfalfa. The depletion of giant ragweed seed in the seedbank will be monitored to determine how various crop rotations differentially affect seed-bank
depletion. Additionally, emergence will be monitored in each crop rotation over the course of the
growing season to confirm applicability of previous emergence models as well as to develop a
new model focusing on giant ragweed emergence in alternative crops. Understanding the rotation
effects on the weed seed bank and emergence patterns in addition to developing reliable weed
emergence models will provide growers with both proactive and reactive options to manage
herbicide-resistant weeds.
The increasing prevalence of herbicide-resistant weeds has resulted in the need for new
weed control technologies, including those which are nonchemical (Walsh et al, 2012). However,
many new weed control technologies require an increased understanding of basic weed biology
and ecology (Wyse, 1992). An additional study involves monitoring the seed-rain of giant
ragweed in a field setting over the course of the fall season to gain an understanding of basic giant
ragweed biology. This research used seed collection traps to monitor the seed rain of giant
ragweed at weekly intervals. Preliminary results show that giant ragweed seed tends to remain on
the plant well into the fall season, with 78% of the potentially viable seed remaining on the plant
through the month of October. Determining when giant ragweed drops seed provides insight into
what types of alternative weed management practices might be effective, including those relying
on capturing weed seed during crop harvest to prevent weeds like giant ragweed from replenishing
the seed-bank.
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