Competition between bluebunch wheatgrass and spotted knapweed was quantified using three addition series experiments in an environmental chamber. Using two density matrices, spotted knapweed plants were thinned by either 45 or 90% of their original densities 40 d after emergence. Another matrix of density combinations was not thinned. All plant material was harvested 90 d after thinning. Spotted knapweed was about four times more competitive than bluebunch wheatgrass. Reducing spotted knapweed by 45% did not alter the competitive relationship between the two species. We believe remaining knapweed individuals captured the majority of the newly available resources. Ninety percent reduction was necessary to shift the competitive relationship in favor of bluebunch wheatgrass. Successful integrated spotted knapweed management must exploit key mechanisms and processes directing plant community dynamics, in conjunction with weed density reduction, if communities are to be shifted toward those that are desired.

Dose-response studies estimating GR40 values indicated different levels of propanil resistance in junglerice populations from fields previously treated with propanil, compared to a check population collected where this herbicide had never been used. The GR40 for susceptible populations ranged from 0.36 to 0.50 kg ai ha−1 and for resistant populations ranged from 1.10 to 3.10 kg ai ha−1. Considerable variability in growth and morphology existed among populations. Variability in cumulative leaf area, aboveground biomass, mean relative growth rate, mean net assimilation rate, and mean leaf area ratio could not be related to propanil resistance. Competitiveness was not related to propanil resistance either. of several vegetative and reproductive parameters measured at maturity, only grain weight per plant and number of grains per plant were correlated with GR40 (r = −0.73, P = 0.06). This trend towards lower reproductive fitness in propanil-resistant junglerice plants may reduce its ecological success when growing with propanil-susceptible plants in the absence of this herbicide.

Three approaches to data analysis were compared to describe competitive interactions between wheat and Italian ryegrass. Replacement series were performed using the two species at total densities of 100, 200, and 400 plants/ m2, and separate monoculture experiments for each species at densities from 33 to 800 plants/m2. Approaches to data analysis included: 1) conventional analysis of replacement series experiments, 2) development of synthetic no-interaction responses from monoculture experiments for comparison with results from mixtures, and 3) responses of the reciprocal yield of individual plants to variation in densities of the two species. Wheat was the superior competitor to ryegrass; however, the three approaches varied in ability to quantify this competitive relationship. The conventional replacement series analysis was least sensitive in describing the influences of either density or proportion on the plant association. The synthetic no-interaction approach provided the most detailed analysis of the influence of proportion on the species interaction. The reciprocal yield approach provided the simplest and most sensitive analysis of the joint influences of density and proportion. The latter approach also provided the most quantitative analysis of the influence of density on the species interaction. Plant density and species proportion are important variables for interpreting the process of plant competition.

Experiments were conducted to determine the productivity and the competitive ability of a large crabgrass accession (PW2) resistant to acetyl-coenzyme A carboxylase (ACCase) inhibitors relative to a susceptible accession (A310). Under noncompetitive conditions in the field, shoot dry biomass and plant height over time were similar for the two accessions. Leaf area was slightly greater for A310 than for PW2. The instantaneous relative growth rate was similar for the accessions. The instantaneous net assimilation rate was slightly greater for A310 than for PW2; however, the instantaneous leaf area ratio was slightly greater for PW2 than for A310. At maturity, the seed yield was similar for the accessions. The inter-accession competitive ability of PW2 and A310 plants in the field was similar, based on shoot dry biomass or seed yield. In the greenhouse, interspecific competitive ability of the accessions with corn was similar, based on shoot dry biomass or seed yield. These results suggest that resistance to ACCase inhibitors is not associated with reduced fitness of the PW2 accession.

Greenhouse and field experiments were conducted to determine the effects of nitrogen (N) supply and purple nutsedge population densities on the yield of radish. In the greenhouse studies, additive series with purple nutsedge densities of 0, 50, 100, 200 or 350 plants m−2 were established. Nitrogen rates of 0, 110, 220, or 330 kg ha−1 were provided to the potting medium. A significant density by N interaction was found for radish fresh weight. Within a given nutsedge density, radish yield decreased as N rate increased. In field studies, additive series of 0, 50, 100, 150, or 200 nutsedge plants m−2 were established the same day radish was sown. Nitrogen rates were 100 or 200 kg ha−1. Marketable radish yield losses and nutsedge shoot dry weight and height were determined 30 d after seeding the crop. Nutsedge densities and N rates interactively influenced radish root yield. Radish yield loss reached 100% at nutsedge densities of 75 and 125 plants m−2 at 200 and 100 kg N ha−1, respectively. Purple nutsedge produced larger shoot biomass as N increased from 100 to 200 kg ha−1. Results of both greenhouse and field studies showed that as N increased, the negative effect of the weed on the crop was enhanced.

Density and spatial arrangement (rectangularity) effects on the competitive relationships, yield performance, and dynamics in canopy dominance of winter wheat and Italian ryegrass were evaluated using two addition series experiments. In experiment 1, combinations of six densities of each species formed the treatment matrix of addition series. In experiment 2, each species was tested at four densities and three rectangularities (RE) of winter wheat. In monocultures, crop density (plants per square meter) explained 82 to 85% of the total variation in the per-plant biomass of winter wheat in experiment 1. In mixtures of crop and weed, initial wheat density (N1) and initial ryegrass density (N2) and interaction of N1 and N2 explained 74 to 80% of the total variation in the per-plant biomass of winter wheat and 68 to 79% of Italian ryegrass in experiment 1. Intraspecific competition was apparent between 15 and 90 days after emergence (DAE) in winter wheat and between 90 and 170 DAE in Italian ryegrass. In mixtures, RE influenced plant size of Italian ryegrass up to 50 DAE only. Maximum winter wheat intraspecific competition occurred at 170 DAE, but maximum interspecific competition occurred during reproductive stages in mixtures. High RE increased seed yield, seed size, and harvest index of winter wheat and reduced biomass of Italian ryegrass. Grain yield of winter wheat was reduced up to 92% by competition from ryegrass. Even nine ryegrass plants in 100 winter wheat plants m−2 reduced winter wheat grain yield by 33%. However, the extent of loss in winter wheat grain yield was less in RE 16 (wider spacing) than in RE 1 (square planting) or 4 (close row spacing). Winter wheat was the stronger competitor during vegetative stages, but Italian ryegrass became the stronger competitor during the reproductive stages of development. Winter wheat leaves dominated at the top canopy during the vegetative stage, but ryegrass dominated at the top canopy during the reproductive stages. In the top canopy of mixtures at 200 DAE, the leaf area indices (LAI) of ryegrass was 6.6 times greater than winter wheat at RE 1 compared to only 1.6 times at RE 16. Greater LAI of Italian ryegrass in the top canopy reduced photosynthetically active radiation available to winter wheat by 68% at booting stage.

Effectiveness of the common soil fungus Sclerotinia sclerotiorum as a biological control for spotted knapweed and its effect on competitive interactions between spotted knapweed and bluebunch wheatgrass were evaluated in a growth chamber study using addition series methods. Total seeding densities ranged from 2000 to 60 000 seeds/m2. Mean bluebunch wheatgrass plant weight was 3.5 times greater than spotted knapweed weight per plant, respectively. Coefficient ratios estimating species interaction showed bluebunch wheatgrass density had a greater influence than spotted knapweed density on both bluebunch wheatgrass and spotted knapweed weights (2.11 and 0.51, respectively) when not under the influence of S. sclerotiorum. Niche differentiation ratios indicated a lack of resource partitioning between species (1.11). S. sclerotiorum reduced spotted knapweed density by 68 to 80% without reducing bluebunch wheatgrass density. Spotted knapweed weight per plant also was reduced by the addition of 5. sclerotiorum (1.4 to 1.2 mg) but there was not a corresponding increase in bluebunch wheatgrass weight. S. sclerotiorum decreased competition between spotted knapweed and bluebunch wheatgrass. This study provides evidence that establishment of bluebunch wheatgrass on spotted knapweed infested rangeland may be improved by combining S. sclerotiorum with high grass seeding rates.