Field studies using area-of-influence techniques were conducted in 1987 and 1988 to evaluate soybean growth and yield, and to predict soybean yield losses from photographs of jimsonweed and common cocklebur canopies. Differences in weed competitiveness within the 100-cm area of influence were induced by dates of soybean planting, locations, weed species, and years. Soybean yield losses within the first 20-cm interval from weeds correlated well with yield of all soybean plants within 100 cm of weeds (r2 = 0.86). Soybean growth responses as a function of distance from weeds were best described by complex polynomials, but simple linear functions, based on a data point from soybean plants nearest a weed and from the average of plants 60 to 100 cm from a weed, closely approximately actual yield losses (r2 = 0.96). Soybean yield losses were highly correlated (r2 = 0.84) with leaf area of weeds as viewed from directly above the weed-crop canopy. Weed canopy diameter, measured from overhead photographs 8 weeks after soybean emergence, also correlated well with soybean yield losses (r2= 0.82), but correlation with actual weed leaf area was not significant (r2 = 0.31).

Competitiveness of noogoora burr and fierce thornapple in irrigated cotton was assessed using area-of-influence methodology. Lint yields were regressed against distances from the weeds using spline regression. The resulting regression curves were used to estimate areas of influence and yield losses, which were further modeled as functions of weed size to understand weed competitiveness. Cotton lint yield reductions averaged 36 and 12%, with maximum distances of influence of 1.71 and 1.65 m for noogoora burr and fierce thornapple, respectively. Economic thresholds for control using hand hoeing were related to weed size. Thresholds for average-size weeds were one cocklebur in 195 m and one fierce thornapple in 73 m of cotton row.

Yield loss of hard red spring wheat due to competition from common milkweed was measured in grower fields in Minnesota. Wheat yield loss was measured using the area of influence and additive competitive methods. Simple linear regression of wheat yield and percentage wheat yield loss against distance from a common milkweed shoot gave r 2 values of 0.013 and 0.015, respectively, indicating limited value of the area of influence model for common milkweed in spring wheat. In an additive competition model, wheat yield was reduced 47% at the highest density of 12 common milkweed shoots m−2. Coefficients of determination for percentage yield loss regressed against common milkweed shoot density were 0.548, 0.547, and 0.529 for simple linear, nonlinear rectangular hyperbolic, and linear square root function models, respectively. Regression of percentage yield loss against common milkweed biomass resulted in r 2 values of 0.566, 0.645, and 0.658 for simple linear, nonlinear rectangular hyperbolic, and linear square root function models, respectively. Restrictions of common milkweed density due to factors other than competition limited yield loss response to the simple linear phase of both the nonlinear rectangular hyperbolic and the linear square root function models previously described.

In 1987 and 1988, effects of full-season interference of individual weeds on cotton yield were measured with area of influence procedures. In 1987, one spurred anoda, common cocklebur, large crabgrass, jimsonweed, common lambsquarters, redroot pigweed, common ragweed, or prickly sida plant per 3 m of row reduced cotton yield between 1% and 7%. Sicklepod did not cause a detectable yield loss. Redroot pigweed, common cocklebur and common ragweed caused 7%, 6% and 5% yield loss, respectively, in 1987. In row weed influence varied from 17 cm (large crabgrass interference) to 86 cm (common cocklebur interference). In 1988, yield losses by individual weeds ranged from 3% to 27%. Common cocklebur, jimsonweed, and common ragweed reduced cotton yields 28%, 15% and 12%, respectively. Spurred anoda and common cocklebur influenced 160 cm and 136 cm of cotton row, respectively. Sicklepod influenced only 47 cm of cotton row.

Intraspecific interference of sicklepod and interspecific interference between sicklepod and soybeans were investigated in field experiments in 1982 and 1983. Sicklepod growth and reproductive parameters were reduced as intraspecific spacing between plants decreased from 90 to 2.5 cm. Sicklepod plants growing intraspecifically were competing at spacings below 90 cm. Soybean plant heights were affected only slightly by sicklepod interference. Soybeans grew little in height from 35 to 84 days after emergence, while sicklepod plants continued to grow until they were 30 to 45 cm taller than the soybeans. Sicklepod plants spaced 10 and 30 cm apart in soybeans reduced soybean yield (25 to 35%) more than sicklepod spaced 90 cm apart. Sicklepod produced 900 to 2000 seeds per plant even when growth was restricted by interference from soybeans.

Volunteer corn (Zea mays L. # ZEAMX) is a troublesome weed in soybeans [Glycine max (L.) Merr.] grown in the Corn Belt. Field studies were conducted in 1983 and 1984 at Champaign, IL, to determine the soybean growth and yield parameters affected by volunteer corn interference. Soybean yield was inversely and linearly related to volunteer corn clump density, with yield losses reaching 25% at 5380 clumps/ha (10 plants/clump). Volunteer corn clumps of 1, 4, 7, and 10 plants reduced soybean yields by 6, 16, 21, and 22%, respectively, at a density of 5380 clumps/ha. Treatments of either the butyl ester of fluazifop {(±)-2-[4-[[5-(trifluoromethyl)-2-pyridinyl]oxy]phenoxy] propanoic acid} or glyphosate [N-(phosphonomethyl)glycine] were applied at various dates between 2 and 12 weeks after soybean emergence (WAE) to a volunteer corn infestation of 5380 clumps/ha (10 plants/clump). Volunteer corn caused soybean yield losses of 2, 6, 12, 19, and 27% when herbicides were applied at 2, 4, 6, 8, and 10 WAE, respectively. Volunteer corn interference reduced soybean seed yield, plant dry weight, pod number, seed number, leaf fresh weight, and leaf area index, within 40 cm of a clump of 10 volunteer corn plants. A clump of 10 volunteer corn plants reduced soybean pod number/plant within a radius of 86 cm.

Predicting crop yield reductions from weeds continues to challenge weed science. Useful methods based upon weed densities and upon area weeds influence have been developed. Results vary greatly from year to year and location to location for several reasons which are reviewed: 1) the shift in crop yield from a weed density-dependent to a weed density-independent relationship; 2) the effect of density on essential growth factor competed for; 3) differences among weed species in relative competitiveness for essential growth factors; 4) the differential effect of environmental conditions on the competitiveness of weed species; and 5) the effect of time of emergence on competition. To reduce the variability in prediction methods will necessitate developing a method based upon the factor(s) responsible for yield reduction.

Florida beggarweed seeds were collected in Georgia, Florida, and South Carolina from plants differing in morphological characteristics. Seedlings were transplanted into peanut rows in field studies at Tifton, GA, and Jay, FL, in 1986 and 1987, and frequent observations of vegetative and reproductive characteristics were made. The competitiveness of the Florida beggarweed selections was evaluated by comparing pod weights from peanut plants grown in rows adjacent to the individual weed selections with pod weights of weed-free peanuts. There were significant differences among selections of Florida beggarweed in days to maximum height, maximum node formation, maximum branching, and initial flowering and fruiting at both locations. Selection GA-1 generally reached these growth stages earliest, was shorter, narrower, had fewer nodes, and produced less dry matter and fewer seeds than GA-2, which was generally the latest maturing selection. GA-4 produced fewer branches and smaller seeds than the other selections. Peanut pod weights adjacent to Florida beggarweed plants were reduced 12 to 18% in 1986 and 10 to 24% in 1987 compared to weed-free checks. Florida beggarweed selection GA-2 was the most competitive and GA-4 was among the least competitive both years. The variation of measured parameters among Florida beggarweed selections in this study may contribute to the survival and adaptability of this weed with changing environmental conditions, cultural practices, and control measures.

Field studies were conducted in 1985 and 1986 to evaluate the stability of reciprocal interference relationships between common cocklebur and soybean under high and low soil moisture conditions. A significant soil moisture differential was established with portable rain exclusion shelters. Well-watered and drought-stressed common cocklebur reduced soybean yield 29 and 12%, respectively. Drought-stressed common cocklebur interfered with soybean over a shorter distance and the magnitude of the effect at a given distance was reduced. The reduced common cocklebur interference in drier soils was attributed to both common cocklebur and soybean growth responses to moisture stress. First, moisture stress caused greater reductions in common cocklebur canopy diameter, stem diameter, node number, and plant height than in soybean. Second, the soybean yield potential was reduced by moisture stress. The reduction in yield potential decreased the effect of the weed interference. Third, soybean canopy development was slowed, and canopy closure that occurred in about 12 weeks in well-watered soybeans never occurred in the moisture-stressed soybeans. This reduced the degree of light interference between both the common cocklebur and soybean and among the soybean plants. The results of this study indicate that the reciprocal interference relationships between common cocklebur and soybean are not stable across soil moisture conditions. The implications of unstable competitive parameters must be considered as threshold models are developed for various field crops.

A model of competition for light between peanut and three broadleaf weed species has been developed to run with the PNUTGRO model. The model simulates shading of the peanut canopy by reducing the total daily PAR received by the peanuts in a manner that realistically represents timing and quantity of light capture by the weeds. Data were collected in nursery plots of Florida beggarweed, sicklepod, and wild poinsettia in 1989, 1990, and 1991. These data provided the values for the critical parameters: maximum attenuation of PAR by the weed, time when the weed overtops the peanut canopy, time when maximum attenuation is reached, and the distance of influence of the weed. Florida beggarweed overtopped the peanut canopy 52 DAP, and reduced PAR reaching the peanuts 45% by 73 DAP. Sicklepod overtopped the peanut canopy 42 DAP and reached an attenuation of 41% 79 DAP. Wild poinsettia overtopped the peanut canopy 44 DAP, and had an attenuation value of 39% 85 DAP. The distances of influence were 162, 150, and 192 cm for Florida beggarweed, sicklepod, and wild poinsettia, respectively. Observed yield losses in the distance of influence were 26, 27, and 22%, respectively. The model predictions accounted for at least 90% of the yield losses observed in field studies. The model also proved capable of simulating competitive differences between morphologically and phenologically different populations of Florida beggarweed. Simulation models will play an important role in reducing the expenditure of time and resources required to document yield losses due to weeds in peanuts.

Field-studies were conducted over two years to determine the area of influence and duration of interference of wild poinsettia in soybean. Soybean canopy width averaged across years was reduced approximately 10% beginning at 6 wk of interference for both the 0- to 10-and 10-to 20-cm distances from the weed. Soybean dry weights decreased from 14 to 38% within 20 cm of the weed for 12 through 18 wk of interference. In 1990, soybean yield within 10 cm of wild poinsettia was similar to distances of 10 to 20 and 20 to 40 cm, but was less than that for distances greater than 40 cm from the weed. Weed interference resulted in a 9.5% yield reduction in the 0- to 10-cm distance when compared with the 80-to 100-cm distance. In contrast, yield of soybean in 1991 growing within 10 cm of the weed was less than at greater distances, corresponding to an 18% yield reduction when compared with 80 to 100 cm. Differences in wild poinsettia dry weights when growing alone and when growing within the soybean row occurred after 6 and 8 wk of interference in 1990 and 1991, respectively. In 1991 when rainfall during the growing season was twice that of the previous year, canopy width and dry weight of wild poinsettia growing within the soybean row were reduced an average of 57 and 82%, respectively, compared with weeds growing alone.

An area of influence method with biweekly destructive harvests 5 through 19 wk after planting (WAP) was used to monitor the reciprocal interference of common cocklebur and cotton in 1987 and 1988. Plant heights, leaf area, and leaf, stem, boll, fiber, and total plant biomass dry weights were measured in 15-cm increments away from common cocklebur or from a randomly selected cotton plant out to 105 cm. Data indicated that cotton less than 60 cm from common cocklebur was shorter, had less leaf area and lower leaf, stem, boll, and biomass dry weights than cotton beyond 60 cm from common cocklebur or cotton grown without common cocklebur interference. Differences in leaf area and biomass between cotton grown with and without common cocklebur interference were greater at and beyond 13 WAP sample dates than before 13 WAP. By 15 WAP, cotton leaf area and biomass were reduced an estimated 11% and 15%, respectively, averaged over the entire 105 cm of row. Cotton yield, harvested 27 WAP, was reduced an estimated 31% on plants grown with one common cocklebur plant per 2.1 m. Cotton yield was reduced on plants out to 99 cm from common cocklebur. Common cocklebur and cotton plants grown alone were taller, had greater leaf area, and greater leaf, stem, and biomass dry weight than those respective plants grown adjacent to cotton. Common cocklebur grown alone produced 67% more biomass than did cotton grown alone. Cotton plants grown adjacent to other cotton plants produced 89% and 96% less boll and fiber weight, respectively, than plants grown alone.

Density and spatial interference of barnyardgrass with ‘Lemont’ and ‘Newbonnet’ rice cultivars was investigated in 1987 and 1988. Barnyardgrass reduced grain yield of Lemont, a semidwarf cultivar, more than Newbonnet, a short-statured cultivar. Linear regression indicated that season-long interference of barnyardgrass at 1 to 20 plants m–2 reduced grain yields of Lemont and Newbonnet by 301 and 257 kg ha–1 per barnyardgrass plant, respectively. Grain yields of Lemont and Newbonnet were reduced by barnyardgrass densities to 40 plants m–2 but were not affected further at densities ≥40 plants m–2. Barnyardgrass reduced straw yield of Lemont more than of Newbonnet. Although barnyardgrass culms m–2 and straw yield increased as weed density increased, the weed produced more culms per plant at 2 and 5 m–2 than at 20 to 80 m–2. In a spatial interference experiment, Lemont grain yield reduction averaged 21% when plants were grown within 0 to 25 cm of a barnyardgrass plant group (group = 4 plants per 140 cm2). However, rice yields were not reduced when barnyardgrass plant groups were 25 to 50 or 50 to 100 cm away. Additional treatments included two barnyardgrass groups spaced 20, 40, 80, or 100 cm apart When Lemont grew between barnyardgrass groups spaced 20 or 40 cm apart, grain yields were reduced 40 and 27%, respectively, compared with weed-free rice. However, Lemont yield was not reduced when rice plants grew between weed plant groups spaced 100 cm apart.