Current recommendations for the control of glyphosate-resistant horseweed [Conyza canadensis (L.) Cronquist var. canadensis] in soybeans [Glycine max (L.) Merr.] consist of comprehensive herbicide programs, which often include herbicide applications outside the soybean growing season. Integration of cover crops with herbicides could potentially improve C. canadensis control and allow for a reduction in herbicide inputs. Two separate field studies were conducted from 2016 through 2018 with the objectives of: (1) determining the effect of planting date and seeding rate of a cereal rye (Secale cereale L.) cover crop on C. canadensis population density and control in the subsequent soybean crop; and (2) determining whether the cover crop could replace a fall herbicide treatment or allow for a reduction in the use of spring-applied residual herbicides. There was no effect of rye planting date, late September versus late October, on C. canadensis density in either study. In 2016 to 2017, C. canadensis density was greater in the absence of a rye cover crop in both studies, but otherwise not affected by seeding rates of 50 versus 100 kg ha−1. In the 2017 to 2018 season, the presence of rye resulted in an increased C. canadensis density in the spring residual herbicide study (Study I), and had no effect in the fall herbicide study (Study II). Conyza canadensis densities were lowest in the treatments where a comprehensive spring residual or fall herbicide treatment had been applied, averaged over rye planting date and seeding rate. Earlier-planted rye at a higher seeding rate produced the most biomass but did not result in lower C. canadensis densities. These results suggest that cereal rye planted at a density of 50 kg ha−1 as a cover crop before no-till soybeans may be sufficient to reduce glyphosate-resistant C. canadensis plant density, but cannot be relied upon to reduce the need for fall herbicide treatments and spring residual programs.

Tillage plus trifluralin (α,α,α-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine) and prometryn [2,4-bis (isopropylamino)-6-(methylthio)-s-triazine] and tillage plus trifluralin and fluometuron [1,1-dimethyl-3-(α,α,α-trifluoro-m-tolyl)urea] applied as soil-incorporated preplanting treatments were compared with tillage alone in cotton (Gossypium hirsutum L.) grown in 51-cm and 102-cm rows on fine sandy loam soil. Over 3 yr, cotton grown in 51-cm rows yielded 15% more than cotton grown in 102-cm rows. Final cotton emergence was not altered by weed-control treatment or by planting pattern. Weed-control treatments with herbicides provided essentially complete, season-long control of grass and broadleaf weeds. At cotton layby, more weeds were in no-herbicide plots with 51-cm rows compared with 102-cm rows, but at cotton harvest numbers of weeds in both row patterns were essentially equal.

Teliospores of Sphacelotheca holci Jack. [= S. cruenta (Kuhn.) Potter] infected johnsongrass [Sorghum halepense (L.) Pers. # SORHA) systemically after inoculation of cut stems in greenhouse studies. A preliminary host range test in the greenhouse revealed that no infection occurred on four varieties of sorghum (S. vulgare L.) and three cultivars of sudangrass (S. Sudanese L.). Infected johnsongrass plants grown in the greenhouse exhibited reduced vegetative growth and altered morphological characteristics compared to healthy johnsongrass plants. The aboveground biomass and lateral rhizome expansion of smutted johnsongrass field transplants were significantly lower than that of uninfected plants. Significant correlations between fraction of johnsongrass stems infected and plant weight, and basal area of plants were observed in field studies. Corn (Zea mays L.) and alfalfa (Medicago sativa L.) grown in competition with johnsongrass, and johnsongrass infected with S. holci reduced the aboveground biomass and rhizome length of johnsongrass plants significantly, compared to that of uninfected johnsongrass plants grown alone in greenhouse studies. Uninfected johnsongrass plants also exhibited higher plant weight than infected plants when both were grown in competition with alfalfa, regardless of the alfalfa planting density in the greenhouse or when measured after 3 months in field trials.

A three-year experiment was conducted near Scottsbluff, NE, to evaluate the selectivity of POST-applied imazethapyr for weed control in alfalfa, birdsfoot trefoil, cicer milkvetch, red clover, sainfoin, and yellow sweetclover. Imazethapyr injured all legumes 15 DAT. Imazethapyr also reduced the height of birdsfoot trefoil, cicer milkvetch, red clover, and yellow sweeclover 28 DAT. Legume first cutting yields were not reduced by imazethapyr and with alfalfa, birdsfoot trefoil, cicer milkvetch, and sainfoin, first cutting yields were increased by imazethapyr. Imazethapyr reduced weed biomass in all legume seedings. Weed biomass in new seedings of alfalfa was reduced more than that of the other legumes.

The growth of loblolly pine seedlings was reduced by interference from bermudagrass, tall fescue, and broomsedge. The order for treatment influence on pine seedling growth rate measurements was tall fescue > bermudagrass > broomsedge > weed free for the 2-yr study. The increase in height of seedlings for the weed free, broomsedge, bermudagrass, and tall fescue was 4.1, 2.9, 1.9, and 1.1 cm/month, respectively; and the average increase in seedling stem diameter was 1.3, 0.5, 0.4, and 0.2 mm/month, respectively.

The combined influence of plant competition and defoliation on development of Canada thistle was investigated in a 2-yr field study. Plant competition was induced by seeding tall fescue and crown vetch. Artificial defoliation was used to simulate various levels of leaf removal by insects. Both defoliation and induced competition reduced biomass of Canada thistle but their impact varied with environmental conditions. Defoliation had a greater detrimental influence than induced competition on thistle biomass in a dry year when growth of the plant competitors was suppressed. In a wet year, induced competition was more important in suppressing Canada thistle than defoliation, and moderate levels of defoliation (25%), applied once when the thistles were 12 to 15 cm in diam, stimulated root weight within the top 20 cm of soil. Reduction in thistle biomass increased with level of defoliation and was greatest when defoliation was applied repeatedly at 14-d intervals in the presence of induced competition. Crown vetch showed very little growth in one season and tall fescue was the primary source of competition for the thistles. The results confirm the hypothesis that combined stresses can substantially reduce biomass development of Canada thistle plants.

Long-term control of downy brome with an integrated approach is needed in order to sustain range productivity. Studies were conducted to study the effectiveness of a combination of downy brome control practices. In two studies, glyphosate and paraquat were evaluated at various rates for up to three successive years for control of downy brome in rangeland. A third study evaluated the competitiveness of perennial cool-season grasses against downy brome in the absence of herbicides. Glyphosate, at 0.55 kg/ha, and 0.6 kg/ha paraquat provided selective downy brome control on rangeland when applications were combined with intensive grazing. Downy brome control was greater than 90% following two sequential years of 0.6 kg/ha paraquat at either the two- to eight-leaf stage or bloom stage at both study locations. At one study location, 0.55 kg/ha glyphosate provided 97% control after the first application at both growth stages. In the second study, control averaged greater than 92% following three sequential applications of glyphosate. When perennial cool-season grasses were seeded in the spring following fall tillage (no herbicides) and allowed to establish for three growing seasons, three of the five species were effective in reducing the reestablishment of downy brome. ‘Luna’ pubescent wheatgrass, ‘Hycrest’ crested wheatgrass, ‘Sodar’ streambank wheatgrass, ‘Bozoisky’ Russian wildrye, and ‘Critana’ thickspike wheatgrass controlled 100, 91, 85, 45, and 32% of the downy brome, respectively. Yields of perennial grass dry matter were 1,714, 1,596, 1,135, 900, and 792 kg/ha. Replacing noncompetitive annual grasses with competitive cool-season perennials will provide a longer term solution to a downy brome problem than the use of herbicides alone or with intensive grazing.

Experiments were conducted near Scottsbluff, NE in 1991 and 1992 to evaluate the selectivity of imazethapyr for weed control in blue grama, intermediate wheatgrass, little bluestem, Russian wildrye, switchgrass, and western wheatgrass. Imazethapyr reduced weed biomass in all seedings and injured all perennial grasses 12 days after treatment (DAT). Imazethapyr reduced the height of intermediate wheatgrass, Russian wildrye, and switchgrass 35 DAT. Russian wildrye, and switchgrass biomass 50 DAT was reduced by imazethapyr. Weed biomass in new seedings of intermediate wheatgrass and western wheatgrass were reduced more than that of the other grasses.

Ecological restoration of shrub–steppe communities in the western United States is often hampered by invasion of exotic annual grasses during the process. An important question is how to create restored communities that can better resist reinvasion by these weeds. One hypothesis is that communities comprised of species that are functionally similar to the invader will best resist invasion, while an alternative hypothesis is that structurally more complex and diverse communities will result in more effective competitive exclusion. In this field experiment, we examined the effects of restored community structure on the invasion success of three annual grass weeds (downy brome, jointed goatgrass, and cereal rye). We created replicated community plots that varied in species composition, structural complexity and density, then seeded in annual grass weeds and measured their biomass and seed production the following year, and their cover after 1 and 3 yr. Annual grass weeds were not strongly suppressed by any of the restored communities, indicating that it was difficult for native species to completely capture available resources and exclude annual grass weeds in the first years after planting. Perennial grass monocultures, particularly of the early seral grass bottlebrush squirreltail, were the most highly invaded communities, while structurally complex and diverse mixtures of shrubs (big sagebrush, rubber rabbitbrush), perennial grasses (bluebunch wheatgrass and bottlebrush squirreltail) and forbs (Lewis flax, Utah sweetvetch, hairy golden aster, gooseberryleaf globemallow) were more resistant to invasion. These results suggest that restoration of sagebrush steppe communities resistant to annual grass invasion benefits from higher species diversity; significant reduction of weed propagule pressure prior to restoration may be required.

Jointed goatgrass is a problem weed in winter wheat production areas of the Great Plains. Winter wheat seeding rates are easily adjusted by the growers and influence competition by some weeds. Field experiments were initiated in Kansas, Nebraska, and Wyoming using winter wheat cultivars selected from leading adapted cultivars from each region to determine the effect of wheat plant density in the fall on jointed goatgrass competitiveness. Three winter wheat seeding rates (50, 67, and 84 kg seeds/ha) were used at Hays, KS, and Sidney, NE, and four seeding rates (33, 50, 67, and 101 kg seeds/ha) were used at Torrington and Archer, WY. An analysis of covariance model was fit with winter wheat fall plant density as the covariate. In 1996, winter wheat grain contamination (dockage) was reduced at the rate of about 6% for every 10 additional wheat plants/m2 above the threshold density of 70 plants/m2 at Archer, WY, and at the rate of about 0.5% for every 10 additional wheat plants/m2 above the threshold density of 110 plants/m2 at Hays, KS. At Hays the reduction occurred only with the semidwarf cultivar ‘Vista’. Increased wheat density reduced jointed goatgrass reproductive tillers in four out of six location–year combinations and biomass in two out of four location–year combinations. Despite the lack of a consistent reduction in jointed goatgrass competitiveness as the result of increased wheat density, increased seeding rates may be a good, low-cost, long-term investment as part of an integrated jointed goatgrass control program in winter wheat.

Wild oat, a troublesome weed in small grain cereals, infests about 11 million ha of cropland in the United States. Diversifying cereal production with alternative crops, such as yellow mustard and canola, provides flexible cropping systems, decreases production risks, and may allow more effective weed suppression. A greenhouse study was conducted to assess the competitive ability of yellow mustard and canola with wild oat in 1999 and 2000, using replacement series interference experiments to relate the results to plant development stages. Yellow mustard, regardless of its proportion in mixture, reduced aboveground biomass of wild oat 33 to 66%, leaf and tiller number 34 to 36%, and panicle production 58% compared with wild oat in monoculture. Canola did not affect wild oat biomass in mixtures. Yellow mustard per plant biomass in 2000 and inflorescence production in 1999 decreased 30 and 20% with increased density of yellow mustard in mixtures. Yellow mustard biomass was not affected by the addition of wild oat to the mixture, indicating the greater importance of intraspecific competition between yellow mustard relative to interspecific competition with wild oat. Canola per plant biomass was affected more by interspecific competition with wild oat than by intraspecific competition. A second greenhouse experiment was conducted to compare plant height and biomass accumulation by the three species over 7 wk. Yellow mustard had the greatest biomass accumulation and plant elongation rate, followed by canola and wild oat. The greater competitive ability of yellow mustard with wild oat, compared with canola, is likely associated with the rapid growth and canopy elevation of yellow mustard.

Greenhouse studies were conducted to evaluate the influence of wild radish–amended soil on tomato, bell pepper, and yellow nutsedge growth. In addition, yellow nutsedge interference with tomato and bell pepper was evaluated with and without the wild radish amendment. Leaf margins of tomato and bell pepper plants were necrotic for approximately 2 wk after transplanting into soil amended with 1% (wt/wt) wild radish biomass. Injury to both crops was transient, but bell pepper biomass through 9 wk after transplanting was negatively affected, whereas tomato was not. In a replacement series study, tomato was more competitive than yellow nutsedge in nonamended soil and the competitiveness of tomato further increased at the expense of reduced yellow nutsedge growth in wild radish–amended soil. Bell pepper was less competitive than yellow nutsedge in nonamended soil, but in wild radish–amended soil, bell pepper held a competitive advantage over yellow nutsedge. In addition, yellow nutsedge tuber production was reduced as much as 88% when soil was amended with wild radish, and tuber weight in nonamended soil was 0.32 g tuber−1 compared with 0.05 g tuber−1 in wild radish–amended soil. This research shows that competitiveness of tomato and bell pepper is increased over yellow nutsedge when soil is amended with wild radish, in addition to reducing yellow nutsedge tuber production and size.

Soil engineering by downy brome may be a facet of its competitiveness. Using rhizotrons in the greenhouse, we compared the growth and plant–soil relationships of downy brome grown in two field soil types: soil invaded for 12 yr by downy brome and a similar soil not yet invaded. For each soil type, downy brome was grown for two growth cycles. At harvest, root mass and soils were sampled at depths of 10, 40, and 80 cm (4, 16, and 32 in); aboveground biomass was also sampled. After the first growth cycle, downy brome grown in invaded soil had 250% greater aboveground biomass and nearly double the root mass per soil volume at 10 cm relative to downy brome grown in noninvaded soil; root mass per volume was similar at depths of 40 and 80 cm. For the second growth cycle, aboveground biomass declined, but was twice greater for downy brome grown in invaded soil; however, root mass per volume was similar between soil types for each depth. Soil attributes that positively related to aboveground biomass included bicarbonate-extractable P, DTPA (diethylentriamene pentaacetate)-extractable Mn, and solution-phase (80-cm depth). We conclude that the data support our hypothesis that downy brome has engineered the soil to increase its growth potential, but proof will require a more robust experimental design. Plant competition is affected by myriad interactions; however, a plant that can increase the availability of soil nutrients for itself and its growth potential, relative to competing plants, would appear to be at an advantage. The mechanistic underpinnings involved are inconclusive, but may involve increased availability of soil N, P, and Mn.

The common reed (Phragmites australis) is one of the most invasive vascular plants in northeastern North America. A competitive genotype from Eurasia has recently invaded road and agricultural ditches, which facilitate the dispersal of the plant over long distances. However, large tracts of roadsides—apparently propitious for the establishment of the plant—are not invaded by the grass. We hypothesized that the absence of the invader is associated with physical and biological characteristics of roadsides. To test this hypothesis, we collected field data and developed two statistical models to explain the presence or absence of the common reed along a highway of southern Quebec highly invaded by the plant but with contrasting patterns of common reed distribution. The models explained 23 to 30% of the total variance and correctly predicted the presence or absence of common reed 71% of the time. The models suggest that a dense woody plant cover over a drainage ditch limits the establishment and/or expansion of the common reed, probably by competition for light and space. Also, shaded ditches are not subjected to a frequent maintenance, and are therefore less disturbed, probably further reducing common reed invasion because the germination of their seeds is less likely without soil disturbance. This study yields insights on the potential of woody plants for controlling the expansion of invasive grasses, and could help to justify the preservation of dense shrubs and tree hedges along right-of-ways.

Biennial wormwood has been increasing in Manitoba, Canada, but information is limited on the potential of biennial wormwood to reduce crop yields. Field experiments were conducted over 5 site-yr throughout southern Manitoba in 2010 and 2011 to determine the effect of biennial wormwood density and relative time of biennial wormwood seedling recruitment on sunflower growth, development, yield, and seed quality. Biennial wormwood was broadcast on the soil surface at six densities into sunflowers planted in 75-cm rows, either at the same time the sunflower crop was planted (early weed seedling recruitment) or when the sunflowers were at about the four-leaf stage (late weed seedling recruitment). When biennial wormwood emerged at about the same time as the sunflowers, yield was reduced by up to 46%. Early-recruiting biennial wormwood had minimal effect on sunflower growth and development, but sunflower achene size and individual achene weight were reduced, even when no effect on sunflower yield was observed. Biennial wormwood plants that recruited after the four-leaf stage of the sunflower crop had no effect on sunflower yield or seed quality.

Kochia is a weed found in many sunflower fields across the Northern Great Plains. There is limited information about the ability of sunflower plants to compete with kochia, specifically when the weed grows both in the crop row and in the inter-row space, as in zero tillage systems that rely solely on herbicides to manage weeds. An experiment was conducted over seven site–yr, from 2009 to 2011, to determine the effect of kochia density and relative time of kochia seedling recruitment on sunflower growth and development, yield and seed quality. Kochia seed was broadcast on the soil surface at six densities, into sunflowers planted in 75-cm rows, either at the same time as the sunflower crop was planted (early weed seedling recruitment), or when the sunflowers were at the four-leaf stage (late weed seedling recruitment). When kochia plants emerged at the same time as the sunflowers, yield was reduced by up to 76% and sunflower head diam was reduced in four site–yr, stem diam was reduced in three site–yr, height was reduced in two site–yr and the number of leaves per sunflower plant was reduced in two site–yr The 5% action threshold for early emerging kochia was four kochia plants m−2 in the combined site–yr analysis. Additionally, early recruiting kochia seedlings reduced sunflower seed size and seed weight at two and three site–yr, respectively. Kochia plants that emerged after the four-leaf stage of the sunflower crop did not affect sunflower growth and development, yield, or seed quality. To reduce the potential for yield and seed quality losses, sunflower growers should be proactive with respect to managing kochia in sunflowers, particularly when the kochia plants emerge at about the same time as the sunflowers.

Predicting site vulnerability to nonnative plant establishment remains a difficult goal. Seedling survival is an important component of population dynamics and can affect the success of control strategies. Field manipulations allow potential causal mechanisms of site vulnerability to be evaluated under realistic environmental conditions. We conducted field studies to determine the effects of plant competition and differing precipitation regimes on spotted knapweed seedling survival. We also examined the effect of herbivory on rosette survival and growth. Seeds were sown into plots with vegetation intact or removed at three sites. Seeds were also sown into plots where plant competition and precipitation were manipulated in a factorial design at a single site. Field studies demonstrated that site accounted for much of the variation in emergence rate, while herbivory and plant competition affected seedling survival rates. We observed a wide range in emergence rates, with site averages ranging from 13.1 to 42.5%. Survival the following year ranged from 0.5 to 9.4% of sown seeds. Rosette survival was significantly higher when herbivores were excluded from plots. Below average precipitation reduced seedling survival; however, even with supplemental water, dry-down of exposed sites resulted in low seedling survival. Of the 8,000 seeds added to plots in one study, by autumn, only eight plants resulted, seven of which survived in watered plots with intact vegetation. Collectively, these results show that seedling survival is a critical phase in spotted knapweed population dynamics and can vary among habitats on the basis of plant competition and precipitation. Furthermore, herbivory affects all stages of the lifecycle from the seedling onward. The observed differences help explain the reported variability in seedling survival in the literature and inform efforts to control spotted knapweed using plant competition and biological controls.

Wild oat, a troublesome weed in cereals, infests about 11 million hectares of cropland in the United States. Diversifying cereal production with alternative crops, such as yellow mustard and canola, can provide flexibility in cropping systems, decrease production risks, and allow for effective weed suppression. The objective of the study was to quantify the competitive ability of yellow mustard and canola relative to wild oat in addition series field experiments, which were conducted in 1999 and 2000 near Genesee, ID. Biomass and seed production of wild oat were reduced 67 and 80%, respectively, in mixtures with yellow mustard, which was three to four times greater than the reduction in corresponding mixtures with canola. In addition, yellow mustard reduced the biomass and seed production of wild oat equally regardless of wild oat density. In contrast, the competitive effect of canola on wild oat biomass decreased 5 to 10 times when wild oat density increased from 100 to 200 plants m−2. Yellow mustard at all densities and at both biomass harvests suppressed wild oat biomass and seed production similarly. But suppression of wild oat by canola increased as canola density increased, and canola plants were more competitive at the flowering stage than at the rosette stage. Wild oat had little or no effect on yellow mustard seed yield but reduced canola seed yield 37%, when averaged over canola densities. Additionally, the oil content of canola seed was reduced 0.4% for every 1% of wild oat seed in the harvested seed. Models developed in this study accurately predicted plant populations of yellow mustard and canola that provided optimal weed suppression and crop yield for different wild oat populations.

Crop and weed competition studies rarely determine how plant-to-plant interactions alter the structure and physiology of crop roots. Soybean has the ability to detect neighboring weeds and to alter growth patterns including the allocation of resources to root growth. In this study, we hypothesized that low red : far red light ratio (R : FR) reflected from aboveground vegetative tissue of neighboring weeds would alter soybean root morphology and reduce root biomass and nodule number. All experiments were conducted under controlled conditions in which resources of light, water, and nutrients were nonlimiting. Low R : FR reflected from aboveground neighboring weeds reduced soybean seedling root length, surface area, and volume, including the number of nodules per plant. An accumulation of H2O2, an increase in malondialdehyde (MDA) content, a reduction in flavonoid content, and a decrease in 1,1-diphenyl-2-picrylhydrazyl (DPPH)–radicle scavenging activity were observed. The reduction in flavonoid content was accompanied by a decrease in the transcription of GmIFS and GmN93 and an increase in transcript levels of several antioxidant genes. These molecular and physiological changes may have a physiological cost to the soybean plant, which may limit the plant's ability to respond to subsequent abiotic and biotic stresses that will occur under field conditions.

Farmers typically use three applications of glyphosate to control weeds in no-till fallow. Some are now experimenting with an unconventional modification to this widely used approach. This modified approach is based on an intentional delay in the time of the first spraying. Farmers delay their first spraying because they want to rely on competition from winter annual grasses to suppress the growth of Russian thistle and eliminate the need for a third application. Optimism for this kind of weed-control program is tempered by concerns related to soil water storage. The objective of this research was to evaluate effects of delayed control of downy brome and volunteer winter wheat on the plant-available water content of, and loss of water from, no-till fallow. Treatments, applied to plots arranged in a randomized complete block design with four replications, were distinguished by the time of the initial glyphosate application. The initial early-season treatment was applied as soon as possible after emergence of downy brome and volunteer winter wheat. Initial mid-season and late-season treatments were applied 4 and 6 wk later, respectively. The amount of plant-available water in the soil profile ranged from 71.8 to 153.7 mm in May and 16.5 to 80.9 mm in September. Water loss was usually minimized in plots treated with the initial early-season treatment. An exception to this trend occurred at a site where the density of downy brome and volunteer winter wheat was greater than average. Abated water loss from the initial late-season treatment, at this site, may have been a consequence of reduced evaporation caused by a decrease in near-surface wind speed and deflection of solar radiation away from soil. Estimated impacts of water loss on grain yield of winter wheat, produced the year after fallow, range from 269 to 600 kg ha−1.