Intensive surveys were conducted in 2 fields in eastern Nebraska to determine the spatial stability of common sunflower, velvetleaf, green and yellow foxtail, and hemp dogbane over 4 yr (1992 to 1995). The 1st field was planted to soybean in 1992 and corn in 1993, 1994, and 1995. The 2nd field was planted to corn in 1992 and 1994 and soybean in 1993 and 1995. Weed density was sampled prior to postemergence herbicide application at approximately 800 locations per year in each field on a regular 7 m grid. The same locations were sampled every year. Weed density at locations between the sample sites was determined by linear triangulation interpolation. Weed seedling distribution was significantly aggregated, with large weed-free areas in both fields. Common sunflower, velvetleaf, and hemp dogbane patches were very persistent in diameter in the east-west and north-south directions and in location and area over 4 yr in the 1st field. Foxtail distribution and density continuously increased in each of the 4 yr in the first field and decreased in the 2nd field. A geographic information system was used to overlay maps from each year for a species. This showed that 36% of the sampled area was continuously free of common sunflower, 62.5% was free of hemp dogbane, and 11.5% was free of velvetleaf in the 1st field, but only 1% was free of velvetleaf in the 2nd field. The persistence of broadleaf weed patches suggests that weed seedling distributions mapped in one year are good predictors of future seedling distributions. Improved and more efficient sampling methods are needed.

Hemp dogbane is sensitive to fluroxypyr and tolerant to clopyralid. Absorption, translocation, and metabolism of clopyralid and fluroxypyr were studied in hemp dogbane to determine if differences in these processes could be responsible for differential sensitivity. In addition, the effect of growth stage on herbicide absorption and translocation was evaluated. The 14C-herbicides were applied to the adaxial side of a single leaf located near the midpoint of hydroponically cultured plants. Uptake of fluroxypyr was more rapid than clopyralid. At 72 h after treatment (HAT), fluroxypyr and clopyralid absorption was 62 and 38%, respectively. Clopyralid was much more mobile than fluroxypyr, with 75% of the absorbed 14C from 14C-clopyralid recovered outside the treated leaf compared to only 45% for fluroxypyr 72 HAT. Relative to fluroxypyr, a higher percentage of 14C-clopyralid recovered outside the treated leaf translocated acropetally, especially when plants were treated during the vegetative stage. Treatment during the early reproductive stage increased basipetal and reduced acropetal translocation relative to the vegetative stage. Neither herbicide was metabolized rapidly. Approximately 60 and 90% of the recovered 14C was attributable to unaltered fluroxypyr and clopyralid, respectively, 72 HAT. Some differences in absorption, translocation, and metabolism between clopyralid and fluroxypyr exist, but they cannot fully account for differential sensitivity of hemp dogbane to these two herbicides. Differences in activity at the target site may be responsible for differential activity of these herbicides on hemp dogbane.

Field research was conducted to characterize hemp dogbane crown root carbohydrates, to quantify crown root lipids, and to determine seasonal fluctuation of each. The effect of day length on the release of hemp dogbane crown bud dormancy was studied in growth chambers. Total nonstructural carbohydrate (TNC) levels fluctuated with seasonal lows occurring during bud to mid-flowering and seasonal highs in fall predormancy periods. Starch was the primary storage carbohydrate, comprising up to 39.6% of crown root dry weight at the highest seasonal level. Ethanol soluble reducing sugar levels were negatively correlated with seasonal starch levels, and appeared to be maltose and glucose accumulated before conversion to sucrose for translocation. Most lipids were in ethanol soluble fractions and were inversely correlated with seasonal TNC patterns. The maximum level of total lipids in crown roots was 6%. Lipids appeared to be by-products of metabolism in nonarticulated lacticifers and not a significant carbon energy source. An 18-h day length resulted in a 10-fold increase in intact, 2-yr-old crown root dormancy release compared with 10- or 14-h day lengths in growth chamber studies. Seasonal carbohydrate fluctuations in hemp dogbane suggest the most effective control with mowing or tillage would occur when applied at mid- to full flower before root carbohydrates begin to recover. The most effective translocation of phloem mobile herbicides to crown roots would occur after mid- to late flower through leaf senescence when carbohydrates are being stored in the roots.

Control and regrowth of hemp dogbane, wild blackberry, and triazine-resistant common lambsquarters (TR-CHEAL) were studied in no-till corn from 1992 to 1994. Hemp dogbane, wild blackberry, and TR-CHEAL population increased 10, 123, and 177%, respectively, between 1992 and 1994 in plots treated with PRE applications of paraquat, atrazine, and metolachlor (weedy checks). POST applications of tank mixtures of 35 g ai/ha nicosulfuron or 20 g/ha primisulfuron with 280 g/ha 2,4-D or 140 g/ha dicamba, and 560 g/ha dicamba applied alone controlled hemp dogbane, wild blackberry, and TR-CHEAL 67 to 98%. These treatments reduced the population or prevented expansion of these weeds the year following treatment. In 1992, corn yield response to weed control was inconsistent. In 1993 and 1994, all plots treated with POST herbicides yielded higher than the weedy check. Corn yield of plots treated with combinations of nicosulfuron or primisulfuron with 2,4-D or dicamba and 560 g/ha dicamba applied alone were 102 to 149% and 124 to 153% higher than the weedy check in 1993 and 1994, respectively.

Management of perennial weeds is a major concern in reduced-tillage cropping systems. Field research was conducted at Nashua, IA, from 1977 through 1990 to evaluate the long-term impacts of tillage and cropping patterns on perennial weed populations in corn and soybean production. Continuous corn and a corn/soybean rotation were conducted utilizing moldboard plow, chisel plow, ridge tillage, and no-tillage systems. The research area was free of established perennial weed species at the initiation of the experiment in 1977. Hemp dogbane was observed by 1980, with the greatest densities in no-tillage. By 1990, continuous corn had greater hemp dogbane densities with no-tillage than other tillage system by crop rotation treatments. American germander densities were not affected by tillage systems in 1980 and 1981, but by 1990, corn/soybean rotations had greater densities in moldboard plow than other tillage systems. Field bindweed developed primarily in the corn/soybean rotations with the greatest densities occurring in no-tillage. Greater and more diverse populations of perennial weeds developed in reduced-tillage systems than in the moldboard plow system. However, practices used to control annual weeds and environmental factors interacted with tillage to regulate perennial weed populations.

Apocynum cannabinum is a native creeping perennial distributed throughout the U.S., with increasing importance in reduced tillage systems throughout the Midwest. Apocynum cannabinum has been shown to be a difficult species to control in field crops. Effective weed management is often a function of the timing of control practice. Knowledge of weed emergence patterns may be useful in predicting the optimum time of weed management. The objectives of these studies were to describe how temperature and moisture affect A. cannabinum seed germination and to describe the relationship between growing degree units (GDU) and A. cannabinum vegetative shoot emergence. At constant temperatures, seed germination was described as a sigmoidal function of temperature (r 2 = 0.83), with maximum germination (32%) from 26 to 34 C. Under alternating temperatures, seed germination increased in a linear relationship between mean temperatures of 15 and 34 C (r 2 = 0.85). Maximum seed germination (88%) occurred at a mean temperature of 34 C under alternating temperatures. The relationship between seed germination and osmotic potential between −1.0 and 0 MPa was described by a gompertz function (r 2 = 0.98). Germination at −1.0 MPa was 4% and increased in a near linear manner to the nontreated control (0 MPa), which had 80% germination. Vegetative shoot emergence in 1997 and 1998 had a sigmoidal relationship to GDU using a base temperature of 6 C (r 2 = 0.96). However, initial shoot appearance was not consistent over years, with first emergence recorded on May 21, 1997 (132 GDU), and May 5, 1998 (73 GDU). Approximately 50% of the shoots emerged before June 7, 1997 (282 GDU), and May 21, 1998 (285 GDU); therefore, optimal weed management programs will need to be initiated following this GDU accumulation.

Hemp dogbane and wild blackberry have become significant weed problems in no-tillage corn production in Maryland. Nicosulfuron (31 to 62 g ha−1) plus crop oil concentrate (COC) gave 67% or more hemp dogbane and wild blackberry control. There was no difference in hemp dogbane or wild blackberry control between 31 and 94 g ai ha−1 nicosulfuron. Tank mixtures of 2,4-D or dicamba with nicosulfuron gave 72 to 100% hemp dogbane and wild blackberry control. Hemp dogbane control following applications of 560 g ha−1 2,4-D was 97% in 1989 and 63% in 1990. Wild blackberry control with 2,4-D was 40% both years. Dicamba at 280 g ha−1 gave 70 and 55% control of hemp dogbane and 75 and 65% control of wild blackberry in 1989 and 1990, respectively. Triclopyr plus 2,4-D provided 72 to 98% hemp dogbane control and 92 to 98% wild blackberry control. However, triclopyr plus 2,4-D applied at 280 plus 560 g ha−1 injured corn, and corn yields were reduced compared with weedy controls in 1990.

Field studies were conducted to compare the short- and long-term control of hemp dogbane by POST applications of Dowco 433, clopyralid, and 2,4-D amine. Dowco 433 at 140 g ae ha–1 controlled 81 to 93% of weeds at 8 wk after treatment. Good control (79 to 89%) was also achieved with 560 g ae ha–1 2,4-D amine at 8 wk after treatment. Twelve months after treatment, control of hemp dogbane averaged 65 to 75% where Dowco 433 was applied at rates of 140 g ha–1 or higher. Similar results were obtained with 2,4-D amine at 560 g ha–1. Control with clopyralid was minimal. Weed height and dry weight were reduced with all treatments except clopyralid. The effect of early versus late application was also evaluated in two studies. In certain situations, control 8 wk after treatment was greater when application was made during the early reproductive growth stage as opposed to the vegetative growth stage.

Absorption and translocation of nicosulfuron and dicamba applied alone and combined was studied in 25-cm-high hemp dogbane originating from lateral roots that had overwintered. Absorption of 14C-nicosulfuron by hemp dogbane was not affected by applications of 70 g ai/ha unlabeled dicamba. Upward translocation of 14C-nicosulfuron in hemp dogbane was 86% greater 6 d after treatment (DAT) when dicamba was tank mixed with nicosulfuron, compared to nicosulfuron applied alone. Combinations of nicosulfuron plus dicamba increased translocation of nicosulfuron to hemp dogbane crown and roots 237 and 130%, 1 and 6 DAT, respectively, compared to nicosulfuron applied alone. Absorption of 14C-dicamba by hemp dogbane was not affected by the addition of 31 g ai/ha nicosulfuron. Upward translocation of dicamba in hemp dogbane was 42% greater 6 DAT for nicosulfuron plus dicamba compared to dicamba applied alone. Increased hemp dogbane control with nicosulfuron plus dicamba compared to either herbicide applied alone can be explained by enhanced translocation of both herbicides.

Recent interest in describing the spatial distribution of weeds and studying their association with site properties has increased the use of interpolation to estimate weed seedling density from spatially referenced data. In addition, farmers and consultants adopting elements of site-specific farming practices are using interpolation methods for mapping weed densities as well as soil properties. This study was conducted to compare the performance of four interpolation methods, namely inverse-distance weighting (IDW), ordinary point kriging (OPK), minimum surface curvature (MC), and multiquadric radial basis function (MUL), with respect to their ability to map weed-seedling densities. These methods were evaluated on data from four weed species, velvetleaf, hemp dogbane, common sunflower, and foxtail species, of contrasting biology and infestation levels in corn and soybean production fields in Nebraska. Mean absolute difference (MAD) and root mean square (RMS) between the observed point sample data and the estimated weed seedling density surfaces were used to evaluate the performance of the interpolation methods. Four neighborhood search types were compared within each interpolation method, and Search3 (12 to 16 neighboring locations) generated an interpolated surface with the smallest MAD and RMS indicating the highest precision. IDW with a power coefficient of p = 4 gave the smallest MAD and RMS, as did a test with an elliptical search and no anisotropy. The level of precision of all four interpolation methods was very poor for weed species with low infestation levels (> 75% of field weed-free; MAD ranged from 100 to 187% of the observed mean density), whereas precision was improved for weed species with high infestation levels (< 25% of field weed-free; MAD ranged from 45 to 85%). No single interpolator appears to be more precise than another. Implications of this study indicate that grid sample spacing and quadrat size are more important than the specific interpolation method chosen.

Field studies were conducted in three site-years to measure no-till Glycine max yield loss in relation to Apocynum cannabinum vegetative shoot density. Apocynum cannabinum densities of 28 to 40 shoots m−2 reduced predicted G. max yield 58 to 75% and 62 to 94% with the rectangular hyperbolic and linear regression models, respectively. Differences between locations were attributed to rainfall and temperatures, with delayed G. max canopy closure and higher yield loss where soil moisture remained high and temperatures were relatively cool. Application of these predictive G. max yield loss equations to field populations of A. cannabinum showed that between 19 and 36% and 20 and 29% G. max yield loss could be expected from within A. cannabinum patches for the rectangular hyperbolic and linear regression models, respectively. The rectangular hyperbolic regression model appeared to describe the relation between G. max yield loss and A. cannabinum density accurately; however, the model appeared to be dominated by the initial linear phase. This may indicate a lack of high levels of intraspecific competition among A. cannabinum shoots. The results of this study indicate that there is a strong linear relation between G. max yield loss and A. cannabinum shoot density. We conclude that the biological basis for the use of the rectangular hyperbolic model for creeping perennial weeds is questionable.

Identification of associations between site properties and weed species abundance led to the generation of hypotheses as to why weed populations occur where they do, or do not, in agricultural fields. The objective of this research was to use a multivariate statistical technique, canonical correlation analysis, to identify the associations. Two continuous Zea mays production fields under center-pivot irrigation in the central Platte River Valley of Nebraska were grid-sampled between 1994 and 1997 for nine site properties and six to seven weed species. Weed species were identified and counted just prior to postemergence weed control in two adjacent quadrats (1 by 0.38 m) at each grid sampling point. These quadrats represented untreated weed populations emerging between crop rows and treated populations that survived preemergence herbicide banded within the crop row. Canonical correlation analysis identified one to five significant correlations between linear combinations of site properties and weed species abundance depending on field site, years, and between- vs. on-crop row weed populations. The first pair of linear combinations consistently described an association that separated weed species across a gradient of topography and soil type. The second pair of linear combinations described associations between weed species and soil fertility. In all cases, it was hypothesized that management practices strongly interacted with site properties to create the observed associations with weed populations. Other hypothesized mechanisms for weed patchiness include patchiness in available soil moisture that would influence weed seed germination, emergence, and seedling growth. Additional variation in plant-available preemergence herbicide concentration across the field site would vary weed control efficacy. Another mechanism would be variation in soil fertility that affects the growth, reproduction, and competitive ability of both the crop and the weed.