Field experiments were conducted in 2017 and 2018 at two locations in Indiana to evaluate the influence of cover crop species, termination timing, and herbicide treatment on winter and summer annual weed suppression and corn yield. Cereal rye and canola cover crops were terminated early or late (2 wk before or after corn planting) with a glyphosate- or glufosinate-based herbicide program. Canola and cereal rye reduced total weed biomass collected at termination by up to 74% and 91%, in comparison to fallow, respectively. Canola reduced horseweed density by up to 56% at termination and 57% at POST application compared to fallow. Cereal rye reduced horseweed density by up to 59% at termination and 87% at POST application compared to fallow. Canola did not reduce giant ragweed density at termination in comparison to fallow. Cereal rye reduced giant ragweed density by up to 66% at termination and 62% at POST application. Termination timing had little to no effect on weed biomass and density reduction in comparison to the effect of cover crop species. Cereal rye reduced corn grain yield at both locations in comparison to fallow, especially for the late-termination timing. Corn grain yield reduction up to 49% (4,770 kg ha–1) was recorded for cereal rye terminated late in comparison to fallow terminated late. Canola did not reduce corn grain yield in comparison to fallow within termination timing; however, late-terminated canola reduced corn grain yield by up to 21% (2,980 kg ha–1) in comparison to early-terminated fallow. Cereal rye can suppress giant ragweed emergence, whereas canola is not as effective at suppressing large-seeded broadleaves such as giant ragweed. These results also indicate that early-terminated cover crops can often result in higher corn grain yields than late-terminated cover crops in an integrated weed management program.

Field studies were conducted at Rosemount, MN, in 1992 and 1993 to quantify the demographic processes regulating the population dynamics of velvetleaf in soybean as part of a corn-soybean rotation. A consistent 6.8 ± 0.5% of the total velvetleaf seedbank emerged each year. Less than 21% of all velvetleaf seedlings survived each year in mixture with soybean, due in part to Verticillium spp wilt infection. The probability of seedling survival varied across time of emergence. Velvetleaf seed production in the absence of crop competition was 125 and 227 seeds plant−1 in 1992 and 1993, respectively. Velvetleaf plants that emerged early produced greater numbers of seed than later emerging plants. Velvetleaf survival and seed production were reduced up to 82% in the presence of crop competition. Soybean yield varied across soybean densities in both years, but was not reduced across velvetleaf densities.

In west central Minnesota the extent and duration of weed seed shed was measured for two years in corn that received cultivation but no herbicides. Percentage of seed production represented by viable (filled) seeds was about 79% for green foxtail, 68% for wild mustard, 49% for Pennsylvania smartweed, 48% for common lambsquarters, and 35% for redroot pigweed. Percentage viable seeds varied from 11% in 1993 to 59% in 1994 for redroot pigweed, but was more stable for other species. Seed shed commenced in late August in a cool year (1993) and early August in a warm year (1994). Average growing degree days (base 10 C) from corn planting until 25% seed shed was 983 for common lambsquarters, 984 for wild mustard, 1004 for Pennsylvania smartweed, and 1034 for both green foxtail and redroot pigweed. Brief weather events, such as wind storms, dispersed large percentages of total seed production within a single day. More than one-fifth of all viable seeds of green foxtail, redroot pigweed, and common lambsquarters were retained by the seedheads and dispersed by combines at harvest. In contrast, seeds of early-maturing species, such as wild mustard, were completely dispersed before corn harvest in the warmer year, but one-third of seeds were retained by seedheads at harvest in the cooler year. Measurement of seed shed was compared using five seed trap designs. The preferred design consisted of a 10-cm-diam plastic cup, whose bottom was replaced by a brass screen, and the entire unit attached to a small wooden stake for support. This design provided, on average, the highest estimates of seed production, least among-replication variability, highest correlation with weed population density and aboveground dry-weight, lowest assembly cost, and greatest ease for sample access and seed processing.

R230, an isolate of Rhizoctonia solani anastomosis group 5 from leafy spurge, caused root and crown rots on leafy spurge when inoculated via soil in greenhouse experiments. The fungus grew through soil over a wide range of matric potentials (–0.01 to −1 MPa). When applied to leafy spurge foliage, the fungus blighted young adventitious shoots, but not mature stems. Foliar infection required high relative humidity. Mycelial growth on plant surfaces stopped at below 92% relative humidity. Pathogenicity of R230 was not limited to leafy spurge. The fungus caused stem and foliar lesions on all crops tested (alfalfa, smooth bromegrass, corn, Kentucky bluegrass, soybean, tall fescue, and wheat) when plants were kept under high humidity. It reduced seedling emergence and survival in soybean, Kentucky bluegrass, and tall fescue. R230 also caused a foliar blight on spotted spurge. The potential for R230 to damage crops will limit application of the fungus to noncultivated areas and to sites where it is endemic.

Corn (maize) genotypes which varied in days to maturity were evaluated for level of Striga hermonthica parasitism in western Kenya during three seasons. Fifteen genotypes, with a wide range in days to maturity, were grown in fields heavily infested with S. hermonthica. Early and late-season Striga numbers and corn grain yield were used to evaluate Striga parasitism. There was considerable variation in the timing and amount of Striga attachment among seasons. Days to silking and late-season Striga numbers were correlated (P ≤ 0.05) in all experiments although only weakly in one of the experiments. Grain yield was negatively correlated with days to silking in two of three experiments as were yield and early season Striga numbers. Although earlier-flowering genotypes consistently supported less Striga, they did not always yield more than the later-maturing genotypes due to confounding effects of yield potential and adaptation. There was considerable variation in Striga parasitism among genotypes within maturity groups, and the relative response of genotypes varied between seasons. These data suggest that in some seasons early maturing genotypes have potential to reduce Striga attack in heavily infested areas and yield more than later-maturing genotypes.

Effects of wild proso millet interference with irrigated corn were evaluated in Nebraska and Colorado over a 2-yr period. Corn yield reductions ranged from 13 to 22% from a wild proso millet density of 10 plants m–2. As density increased, corn yield reduction could be predicted with a rectangular hyperbola regression model. Ten wild proso millet plants m–2 growing with corn produced 4200 to 6200 seed m–2. Corn yields were reduced 10% at one location if wild proso millet removal was delayed 2 weeks after corn planting. If removal was further delayed until 6 weeks after corn planting, corn yield reductions at the two locations ranged from 16 to 28%.

A simulation model was developed to predict the population dynamics and economics of velvetleaf control in a corn-soybean rotation. Data compiled from the literature were used to parameterize the model for two situations, one in which velvetleaf was infected by a Verticillium spp. wilt and one without infection. Verticillium was assumed to have no effect on corn or soybean yield. In the absence of control, simulated seedbank densities of a Verticillium-infected velvetleaf population were 5 to 50 times lower than for an uninfected velvetleaf population. The model was used to evaluate a threshold weed management strategy under the assumption that velvetleaf was the only weed and bentazon the only herbicide available for its control. In the absence of Verticillium, an economic optimum threshold of 2.5 seedlings 100 m−2 afforded the highest economic returns after 20 yr of simulation. Simulations in which velvetleaf was infected in 8 out of 20 randomly assigned years indicated a 6% increase in annualized net return and an 11 % reduction in the number of years that control was necessary. Sensitivity analysis indicated the parameter estimates having the greatest impact on economic optimum threshold were seedling emergence and survival, maximum seed production, and herbicide efficacy. Under an economic optimum threshold of 2.5 seedlings 100 m−2, management practices that manipulate the most sensitive demographic processes increased annualized net return by up to 13% and reduced long-term herbicide use by up to 26%. Results demonstrate that combining an economic optimum threshold with alternative weed management strategies may increase economic return and reduce herbicide use.

Consumption of weed seeds and waste grains by seed predators is an important ecosystem service that helps to regulate weed and volunteer crop populations in many agricultural systems. The prairie deer mouse is found in a variety of sparsely vegetated habitats throughout the central United States and is the dominant vertebrate seed predator in row-crop fields (corn and soybean) in this region. Evaluating the preferences of prairie deer mice for common agricultural weed seeds and waste grain is important to understand the potential ability of native mice to regulate volunteer crops and weed populations. We evaluated winter seed preference of deer mice using cafeteria-style feeding trials presented within row-crop fields in central Indiana and used compositional analysis to compare proportional consumption of seeds from five common agricultural weeds (common ragweed, common cocklebur, common lambsquarters, velvetleaf, and giant foxtail) and two grains (corn and soybean) during overnight feeding trials. Prairie deer mice significantly preferred corn to all other available seed types. Ragweed and soybean were also readily consumed and were preferred over seeds other than corn. Giant foxtail was intermediately preferred. Our results show that prairie deer mice have clear preferences for certain seeds commonly available in row-crop fields; mice likely contribute to reduction of waste grain and some weed seed populations.

The recent interest in cover crops as component of Midwest corn and soybean production systems has led to the need for additional research, including the effects of residual corn and soybean herbicide treatments on fall cover crop establishment. Field studies were conducted in 2013, 2014, and 2015 in Columbia, Missouri to investigate the effects of common residual herbicides applied in corn and soybean on establishment of winter wheat, tillage radish, cereal rye, crimson clover, winter oat, Austrian winter pea, Italian ryegrass, and hairy vetch. Cover crops were evaluated for stand and biomass reduction 28 d after emergence (DAE). Rainfall from herbicide application to cover crop seeding date was much greater in 2014 and 2015, which resulted in less carryover in these years compared to 2013. When averaged across all herbicides evaluated in these experiments, the general order of sensitivity of cover crops to herbicide carryover, from greatest to least was Austrian winter pea=crimson clover>oilseed radish>Italian ryegrass>hairy vetch>wheat >winter oat>cereal rye. Cereal rye had the fewest instances of biomass or stand reduction with only four out of the 27 herbicides adversely effecting establishment. Pyroxasulfone consistently reduced Italian ryegrass and winter oat biomass at least 67% in both the corn and soybean experiments. In the soybean experiment, imazethapyr- and fomesafen-containing products resulted in severe stand and biomass reduction in both years while flumetsulam-containing products resulted in the greatest carryover symptoms in the corn experiment. Results from these experiments suggest that several commonly used corn and soybean herbicides have the potential to hinder cover crop establishment, but the severity of damage will depend on weather, cover crop species, and the specific herbicide combination.

Goosegrass is a problematic summer annual weed in cotton, soybean, and corn production in the southern United States. Glyphosate is labeled for POST control of goosegrass in glyphosate-resistant (GR) cotton, soybean, and corn production. A population of goosegrass in west Tennessee not controlled by glyphosate was examined in greenhouse and laboratory studies. At 21 days after treatment (DAT), a glyphosate-susceptible (SS) biotype was controlled > 90% with glyphosate at rates greater than 210 g ae ha−1. Comparatively, the GR biotype was only controlled 12% at 210 g ae ha−1. Using goosegrass control data, I50 values for GR and SS biotypes were 868 and 117 g ae ha−1, susceptibility, resulting in a resistance factor (RF) of 7.4. Treatment with glyphosate at 210 g ae ha−1 reduced fresh weight biomass of the SS biotype to 5 g per pot compared to 36 g for the GR biotype. A total of 3,360 g ae ha−1 glyphosate was required to reduce fresh weights of the GR biotype to ∼5 g per pot. Using fresh and dry weight biomass data, I50 values for the GR biotype were 3 to 10 times greater than the SS biotype. On each date from 1 to 6 DAT the SS biotype accumulated higher concentrations of shikimate than the GR biotype. Future research should evaluate strategies for managing GR goosegrass with alternative modes of action. To prevent the spread of resistance, additional research evaluating programs for managing glyphosate-susceptible goosegrass in GR crops is also warranted.

Field trials were conducted in Virginia during 2000 and 2001 to evaluate long-term trumpetcreeper control in corn with dicamba, BAS 654 plus dicamba, 2,4-D, CGA 152005 plus primisulfuron, halosulfuron, primisulfuron, and mesotrione. Each of these herbicides was applied alone as a single postemergence (POST) treatment or as a component of a POST herbicide combination. Trumpetcreeper suppression ratings 3 mo after treatment (MAT) revealed a general trend toward higher levels of suppression with combinations of dicamba, BAS 654 plus dicamba, or 2,4-D with any of the sulfonylurea herbicides and lower levels of suppression with applications of any of the sulfonylurea herbicides alone. Combinations of dicamba, BAS 654 plus dicamba, or 2,4-D with mesotrione also provided some of the highest levels of trumpetcreeper suppression 3 MAT in both years. At 1 yr after treatment (YAT), 2,4-D alone, BAS 654 plus dicamba, CGA 152005 plus primisulfuron plus 280 g ai/ha dicamba, primisulfuron plus 280 g/ha dicamba, primisulfuron plus 2,4-D, mesotrione plus BAS 654 plus dicamba, and mesotrione plus 2,4-D reduced trumpetcreeper stem density by at least 52% when compared with that of the nontreated control. These herbicide treatments were the only ones that provided reductions in trumpetcreeper stem density 1 YAT when compared with that of the nontreated control. In 2000 and 2001, there were few differences in corn yield among the treatments evaluated in these trials, and no treatment resulted in corn yields that were lower than the nontreated control. Acceptable trumpetcreeper suppression may be achieved during the season of treatment with any of these herbicide combinations, but only a few treatments will provide long-term trumpetcreeper control.

A bioeconomic model is used to estimate how managing glyphosate resistance to horseweed affects short- and long-run profits in corn, soybean, and corn-soybean rotation systems. Model results found that resistance management reduces profits in the first year of implementation, but increases profits in the second and subsequent 18 yr. In all three systems, long run gains begin to outweigh short-run costs (and resistance management “pays for itself”) by the second year. Over a 20-yr horizon, the estimated annual average profit advantage from managing resistance exceeded $158 ha–1 ($64/acre) for corn, $137 ha–1 ($55/acre) for corn-soybean, and $55 ha–1 ($22/acre) for soybean. Seed immigration from a neighbor's field can reduce these gains, but this reduction is negligible if the neighbor also practices resistance management. If the neighbor did not manage resistance, however, the grower's estimated annual profit advantage fell to roughly $123 ha–1 ($50/acre) for corn, $60 ha–1 ($24/acre) for the corn-soybean rotation, and virtually zero for soybean. Methods applied in this study identify corn and corn-soybean rotations as cases where resistance management “pays for itself' quickly and significantly, even if the neighbor does not manage resistance. Continuous soybean presents a more challenging case that may require additional programs and incentives to encourage collective resistance management among growers. Even for continuous soybean, however, joint grower–neighbor resistance management can pay for itself within 2 yr.

Greenhouse studies were conducted to evaluate 14C-glufosinate absorption, translocation, and metabolism in glufosinate-resistant corn, goosegrass, large crabgrass, and sicklepod. Glufosinate-resistant corn plants were treated at the four-leaf stage, whereas goosegrass, large crabgrass, and sicklepod were treated at 5, 7.5, and 10 cm, respectively. All plants were harvested at 1, 6, 24, 48, and 72 h after treatment (HAT). Absorption was less than 20% at all harvest intervals for glufosinate-resistant corn, whereas absorption in goosegrass and large crabgrass increased from approximately 20% 1 HAT to 50 and 76%, respectively, 72 HAT. Absorption of 14C-glufosinate was greater than 90% 24 HAT in sicklepod. Significant levels of translocation were observed in glufosinate-resistant corn, with 14C-glufosinate translocated to the region above the treated leaf and the roots up to 41 and 27%, respectively. No significant translocation was detected in any of the weed species at any harvest timing. Metabolites of 14C-glufosinate were detected in glufosinate-resistant corn and all weed species. Seventy percent of 14C was attributed to glufosinate metabolites 72 HAT in large crabgrass. Less metabolism was observed for sicklepod, goosegrass, and glufosinate-resistant corn, with metabolites composing less than 45% of detectable radioactivity 72 HAT.

A field study was conducted on an s-triazine–adapted soil to determine the effects of s-triazine exclusion interval (1, 2, 3, or 4 yr), crop production system (continuous corn or continuous soybean), and rhizosphere proximity (bulk or rhizosphere soil) on atrazine degrader populations and activity. Atrazine degrader populations were quantified by a radiological Most Probable Number technique, while degrader activity was assessed via mineralization of ring-labeled 14C-atrazine. As the s-triazine exclusion interval increased, atrazine degrader populations declined exponentially, regardless of crop or rhizosphere proximity. Crop and exclusion interval interacted to affect degrader populations (P = 0.0043). Pooled over rhizosphere and bulk soil, degrader populations were 1.5-fold higher and declined 2.8-fold faster in soybean than corn. An interaction between rhizosphere proximity and exclusion interval was also noted (P = 0.0021), whereby degrader populations were 1.9-fold higher and declined 2.8-fold slower in rhizosphere compared with bulk soil, regardless of crop. The time required for 50% mineralization of ring-labeled 14C-atrazine (DT50) following exclusion of s-triazine herbicides increased linearly at a rate of 2.2 d yr−1. In contrast, the DT50 for this site prior to a known s-triazine application was 85 d and declined exponentially over 5 yr of successive atrazine applications: 24.5 d after 1 yr, 10.8 d after two successive years, and 3.8 d after five successive atrazine applications. Omitting s-triazines can reduce degrader populations and activity in adapted soils, but more than 4 yr is required to return mineralization kinetics to nonadapted levels, regardless of crop or rhizosphere proximity.

Atrazine is widely used to control broadleaf weeds and grasses in corn, sorghum, and sugarcane. Field persistence data published before 1995 showed that the average half-life of atrazine in soil was 66 d, and farmers expect to achieve weed control with a single application for the full season. However, reports of enhanced atrazine degradation in soil from fields that have a history of atrazine applications are increasing. A rapid laboratory assay was developed to screen soils for enhanced atrazine degradation. Soil (50 g) was placed in a 250 ml glass jar and treated with 7.5 ml of water containing atrazine (5 µg ai ml−1) and capped with a Teflon-lined lid. The assay was conducted at room temperature (25 C). Soil subsamples (1.5 to 3 g) were removed at 0, 1, 2, 4, 8, and 16 d after treatment and extracted with an equal weight of water (wt/vol). The atrazine in the water extract was assayed with high-pressure liquid chromatography (HPLC). The half-life of atrazine in soils with a history of use was ≤ 1.5 d, whereas the half-life in soils with no history of atrazine use was > 8 d. The advantages of this assay are (1) the ease of set up; (2) the rapidity of extraction, and (3) the simplicity of the quantification of the atrazine.

Certain winter annual weeds have been documented as alternative hosts to soybean cyst nematode (SCN), and infestations by such species are common in no-till production fields in the midwestern United States of Indiana, Ohio, and Illinois. The objective of this research was to determine the influence of crop rotation and winter annual weed management on winter weed growth, SCN population density, and crop yield. Two crop rotations (SS and soybean–corn rotation) and six winter annual weed-management systems (autumn-applied herbicide, spring-applied herbicide, autumn + spring applied herbicides, autumn-seeded Italian ryegrass, autumn-seeded wheat, and a nontreated check) were evaluated in long-term, no-tillage systems at West Lafayette, IN, and Vincennes, IN. In the fourth and fifth years of these experiments, the 2-yr corn–soybean rotation generally resulted in increased soybean yield, decreased winter annual weed growth, and reduced SCN population density compared with SS. Autumn or spring herbicide applications or both were a more effective option than cover crops at reducing winter annual weed density. Cover-crop systems generally did not differ from the nontreated check in winter weed density. Between years three and five, winter annual weed SCN hosts in nontreated check plots increased approximately threefold to levels as high as 102 and 245 plants m−2 at West Lafayette, IN, and Vincennes, IN, respectively, which are infestation levels at or above those commonly observed in production fields. However, controlling winter annual weeds did not influence crop yields or SCN population density. The results of these studies suggest that winter weed management, even at the high levels of weed infestation present in these studies, appears to have little value as a tool for SCN management in corn and soybean production systems in the midwestern United States.

Natural dissemination of johnsongrass seeds as well as the effect of combine harvesting on this process were studied in corn fields. The estimation of natural dispersal was carried out by two different methods, collecting seeds throughout the season using seed traps and sampling soil–surface seed abundance before harvest using a vacuum device. Both methods showed the same dispersal pattern. A minimum of 84.6% was dispersed in the first 2 m from the focus and a maximum of 1.6% was dispersed beyond the first 5 m. An average of 76.3% of these dispersed seeds were lost or buried after shedding but before harvest. Seed dispersal by the combine harvester was estimated from the difference between soil–surface seed abundance in the same sites pre and postharvest. Although the quantity of seeds dispersed by the combine was similar to those dispersed by natural factors, dispersal distances were significantly higher. Around 90% of the dispersed seeds were found in the first 5 m forward and backward of the combine direction from the infestation source, and 1.6% of the seeds were found beyond 22 m forward and 10 m backward of the combine direction from the infestation source. A large proportion of the seeds dispersed were dormant or not viable. It is concluded that the major role of sexual reproduction in johnsongrass population dynamics may be to spread the risks, promoting dispersal in time and space.

Seeds from natural populations of fierce thornapple and velvetleaf collected in a corn-growing area in central Spain were incubated at a range of constant temperatures and water potentials to model the progress of germination on the basis of the accumulation of hydrothermal time. Previous to the germination tests, the seeds were treated in two different ways: (1) dark storage under dry conditions (nonchilled seeds), and (2) burying in the original soil at 10-cm depth during 2 mo in winter (naturally chilled seeds). The results indicated different mechanisms inhibiting germination in both weed species. Whereas fierce thornapple displayed some type of embryo dormancy, the lack of germination in velvetleaf appeared to be entirely due to the seed coat. On the other hand, significant differences between nonchilled and naturally chilled seeds in fierce thornapple were observed, mainly due to the decrease in the mean base water potential of the 50th percentile in the latter, which indicated a loss of dormancy by exposure of the seeds to natural conditions. Hydrothermal time appears to be a good description of the germination patterns in both weed species, but in the case of fierce thornapple, only for naturally chilled seeds. Thus, the development of the hydrothermal model in fierce thornapple raises some questions for consideration concerning the influence of the type of seeds (conditions of storage, pretreatments of the seeds before germination tests) on its germination capacity.

Indirect effects of insect control strategies on weed populations are important to consider when developing robust integrated pest management strategies. Weed seed predation rates were investigated in corn managed under three contrasting treatments based on control practices for corn rootworm: (1) the transgenic crop Cry3Bb Bt corn, (2) the broad-spectrum insecticide tefluthrin, and (3) no insecticide control. This 2-yr field study conducted near Ithaca, NY, involved quantifying seed loss from velvetleaf, common lambsquarters, and giant foxtail in arenas with and without vertebrate exclosures. Velvetleaf and giant foxtail were unaffected by the insecticide treatment; however, average seed predation of common lambsquarters was lower in both the Bt corn (11.9%) and insecticide-treated plots (11.8%) compared with control plots (17.5%) that did not receive any insecticide. Seed predation of common lambsquarters was not affected by the vertebrate exclosure. Lower seed predation in the transgenic Bt corn and insecticide treatments was likely due to nontarget effects on carabids (Coleoptera: Carabidae). Although the reduction in seed predation was modest and limited to only one of the three weed species tested, our results highlight the need for greater risk assessment that includes the ecosystem service of weed seed predation when considering insect pest management options.

Weed-suppressive soils contain naturally occurring microorganisms that suppress a weed by inhibiting its growth, development, and reproductive potential. Increased knowledge of microbe–weed interactions in such soils could lead to the identification of management practices that create or enhance soil suppressiveness to weeds. Velvetleaf death and growth suppression was observed in a research field (fieldA) that was planted with high populations of velvetleaf, which may have developed via microbial mediated plant–soil feedback. Greenhouse studies were conducted with soil collected from fieldA (soilA) to determine if it was biologically suppressive to velvetleaf. In one study, mortality of velvetleaf grown for 8 wk in soilA was greatest (86%) and biomass was smallest (0.3 g plant−1) in comparison to soils collected from surrounding fields with similar structure and nutrient content, indicating that suppressiveness of soilA was not likely caused by physical or chemical factors. When soilA was autoclaved in another study, mortality of velvetleaf plants in the heat-treated soil was reduced to 4% compared to 55% for the untreated soil, thus suggesting that suppressiveness of soilA is biological in nature. A third set of experiments showed that suppressiveness to velvetleaf could be transferred to an autoclaved soil by amending the autoclaved soil with untreated soilA; this provided additional evidence for a biological basis for the effects of soilA. The suppressive condition in these greenhouse experiments was associated with high soil populations of fusaria. Fusarium lateritium was the most frequently isolated fungus from roots of diseased velvetleaf plants collected from fieldA, and also was the most virulent when inoculated onto velvetleaf seedlings. Results of this research indicate that velvetleaf suppression can occur naturally in the field and that F. lateritium is an important cause of velvetleaf mortality in fieldA.