Field experiments were conducted in Louisiana over 2 yr to evaluate the influence of full-season interference from johnsongrass, common cocklebur, or hemp sesbania at densities of 2.5, 0.5, and 2.0 plants m–1 of row, respectively, and simulated insect defoliation of soybean on weed and soybean growth. Defoliation at R2 (full bloom) and R5 (beginning seed development) soybean growth stages was accomplished by removal of zero, one, or two leaflets per soybean trifoliate, which approximated 0, 33, and 66% defoliation, respectively. Height and dry weight of all weeds were not affected by soybean defoliation level or defoliation stage. Soybean height 3 wk after defoliation at R5 was not influenced by weed interference, soybean defoliation level, or defoliation stage in either year. Averaged across soybean defoliation levels and stages in 1994, johnsongrass, common cocklebur, and hemp sesbania reduced soybean yields 30, 15, and 14%, respectively. In 1995, johnsongrass reduced soybean yield 35%. As soybean defoliation level increased, a linear decrease in soybean yield was observed. Averaged across weeds and soybean defoliation stages, 33 and 66% defoliation reduced soybean yield 6 and 20% in 1994 and 12 and 33% in 1995, respectively. Defoliation at R5 resulted in 10% lower yield than defoliation at R2 in one of two years. Yield reduction due to combinations of weeds and soybean defoliation was additive.

Two field experiments were conducted to examine the competitive effect of common cocklebur and sicklepod in soybean. Factors examined included sap flow of both the weed and the crop, as well as the traditional parameters of weed and crop growth and crop yield. The intent was to determine to what extent competitive effects could be attributed to differential water utilization. In the first study, soybean planted at 20 plants m−1 row was infested with either sicklepod at 10 plants m−1 row or common cocklebur at two plants m−1 row. Sicklepod reduced soybean sap flow and yield 53 and 49%, respectively. Common cocklebur reduced soybean sap flow and yield 31 and 38%, respectively. Within a weed species, weed-induced yield and sap flow reductions were comparable, indicating that water deprivation was the primary detriment that these weeds inflicted on soybean. Individual common cocklebur plants were 3.9 times more competitive than sicklepod with respect to reducing soybean yield. However, sap flow of individual common cocklebur plants was only 1.4 times more than that of sicklepod, indicating that water deprivation was not the only causal factor in weed-crop competition. In the second experiment, sicklepod was planted in soybean (fixed density) and clipped to either half the height, same height as soybean, or left unclipped, in an attempt to simulate herbicide-induced stunting. Clipping sicklepod had a positive effect on soybean sap flow and yield. Thus, the benefits of reduced weed competition were achieved without killing sicklepod.

Field studies were conducted to determine the effect of common cocklebur interference in early-maturing (maturity group IV) soybean planted in April, May, and July. Common cocklebur density and length of interference did not affect soybean height, canopy width, or node number at any planting date. Removal of common cocklebur 4 weeks after emergence (WAE) prevented reduction of soybean leaf area, stem dry weight, dry leaf weight, dry pod weight, and seed yield. Aboveground biomass for common cocklebur emerging in July was less than biomass of April or May plantings. Common cocklebur planted into soybean 2, 4, or 8 wk after soybean emergence did not reduce soybean yield. Under parameters of this study, planting date was not a significant factor in yield reduction. Interference from one common cocklebur plant per 1.8, 0.9, and 0.3 m of soybean row for 8 wk reduced yields 7, 14, and 30%, and full-season interference reduced yields 16, 33, and 65%, respectively. The Arkansas Weed Management Computer program closely predicted actual yield loss for early-maturing soybean.

Common cocklebur and sicklepod are troublesome weeds in soybean in the southern United States. A field experiment was conducted from 1991 through 1995 to determine (1) the influence of tillage (no-till and tilled after initial seed deposition) and intraspecific and interspecific interference on seed production potential, emergence pattern, and soil seedbank of common cocklebur and sicklepod, and (2) the dominant species after introduction into a weed-free field. Under intraspecific interference, 1,430 and 1,392 common cocklebur achenes m−2 and 1,827 and 5,435 sicklepod seed m−2 were deposited to the seedbank after 1 and 2 yr of seed production, respectively. For both species, approximately 11% of the initial seedbank emerged under tilled conditions the first year after deposition. Under no-till conditions, only 0.7% of common cocklebur and 1.6% of sicklepod emerged. The second year after deposition, common cocklebur emergence in no-till decreased to 0.25% of the initial seedbank, while sicklepod increased to 8% of the initial seedbank and remained higher than in tilled plots. Under tilled conditions, common cocklebur became the dominant species, and sicklepod became dominant under no-till conditions. Seedbank depletion was greater for both species under tillage. Three years after initial seed deposition, sicklepod seed was 100% viable but common cocklebur achenes were not viable. Under no-till conditions, common cocklebur was depleted in the seedbank but sicklepod was not. Thus, sicklepod poses a greater long-term weed problem than common cocklebur, especially under no-till conditions.

The objective of this research was to explore the influence that weed decision threshold (DT; expressed as plants m−2), weed spatial distribution patterns, and spatial resolution of sampling have on potential reduction in herbicide use under site-specific weed management. As a case study, a small plot located in a typical corn field in central Spain was used, constructing very precise distribution maps of the major weeds present. These initial maps were used to generate herbicide prescription maps for each weed species based on different DTs and sampling resolutions. The simulation of herbicide prescription maps consisted of on/off spraying decisions based on information from two different approaches for weed detection: ground-based vs. aerial sensors. In general, simulations based on ground sensors resulted in higher herbicide savings than those based on aerial sensors. The extent of herbicide reductions derived from patch spraying was directly related to the density and the spatial distribution of each weed species. Herbicide savings were potentially high (up to 66%) with relatively sparse patchy weed species (e.g., johnsongrass) but were only moderate (10 to 20%) with abundant and regularly distributed weed species (e.g., velvetleaf). However, DT has proven to be a key factor, with higher DTs resulting in reductions in herbicide use for all the weed species and all sampling procedures and resolutions. Moreover, increasing DT from 6 to 12 plants m−2 resulted in additional herbicide savings of up to 50% in the simulations for johnsongrass and up to 28% savings in the simulations for common cocklebur. Nonetheless, since DT determines the accuracy of patch spraying, the consequences of using higher DTs could be leaving areas unsprayed, which could adversely affect crop yields and future weed infestations, including herbicide-resistant weeds. Considering that the relationship between DT and accuracy of herbicide application depends on weed spatial pattern, this work has demonstrated the possibility of using higher DT values in weeds with a clear patchy distribution compared with weeds distributed regularly.

Five common cocklebur biotypes from southern Minnesota, central Iowa, southern Iowa, and Ohio were grown at the Iowa State University Curtiss Research Farm in 1995 and 1996 to examine intraspecific variations. Maximum plant heights were measured, and anthesis dates and day of bur set were recorded. At the end of the growing season, all plants were excised at the soil surface and weighed. Common cocklebur biotypes did not differ significantly in height. Flowering date was associated strongly with photoperiod and varied little between years within a biotype. But flowering date and bur set date differed among biotypes. The highest dry matter yields occurred in later flowering biotypes.

Field studies were conducted in 2002 and 2003 to determine whether canopy formation influences pitted morningglory, common cocklebur, and sicklepod emergence in surface-tilled soybean. Each weed species was broadcast seeded before planting soybean in 19- and 97-cm-wide rows. Weed emergence beneath soybean was monitored after soybean emergence and compared with weed emergence in the absence of soybean (bareground treatment). Magnitude of daily diurnal soil temperature fluctuations diminished after soybean canopy formation, and light interception by soybean was positively related to the reduction in soil temperature. Canopy formation (50% light interception) occurred 16 to 17 d later in wide compared with narrow rows in both years. The red/far-red ratio of light available to seed on or near the soil surface was reduced from as much as 1.2 in full sunlight to less than 0.1 in the presence of a dense soybean canopy. Pitted morningglory emergence was not influenced by soybean canopy formation, whereas common cocklebur and sicklepod emergence were reduced as much as 33 and 68%, respectively. Although common cocklebur and sicklepod emergence diminished after soybean canopy formation, a small portion of the seedbank of both species emerged beneath the canopy. This research indicates that in a tilled system, emergence of some weed species is diminished by presence of an overlying canopy, but emergence does not completely cease with canopy formation. Late-season emergence of sicklepod and common cocklebur beneath a soybean canopy may contribute to replenishment of the soil seedbank, especially if these late-emerging cohorts are capable of surviving until the light environment is favorable for seed production.

Greenhouse studies were conducted to examine the influence of temperature and relative humidity (RH) on the foliar activity of mesotrione on five weed species. Regression analysis was performed allowing for comparison of estimated GR50 (herbicide dose to inhibit growth by 50%) values for each weed response at either temperature (18 or 32 C) or RH level (30 or 85%). Temperature and relative humidity did not influence the response of ivyleaf morningglory, common cocklebur, and velvetleaf to mesotrione markedly. An increase in temperature or relative humidity increased the efficacy of mesotrione on common cocklebur and velvetleaf up to threefold. Conversely, common waterhemp and large crabgrass were six- and sevenfold more susceptible at 18 C than at 32 C, respectively. Common waterhemp and large crabgrass were four- and twofold more susceptible to mesotrione at 85% compared with 30% RH, respectively. The influence of temperature and RH on the efficacy of mesotrione in foliar applications is species dependent and may be an important consideration for field applications.

DNA fragment analysis, based on amplification of intersimple sequence repeats by the polymerase chain reaction (ISSR-PCR), was used to assess genetic relationships of 217 U.S. accessions of common cocklebur. Twenty-four polymorphic markers were generated from six primers. Analysis of genetic similarity by clustering procedures resulted in separation of the accessions into two main clusters. Accessions within these two clusters were designated as either northern or southern genotypes. Forty-four of 48 accessions analyzed from Washington, Michigan, Iowa, and Ohio were northern genotypes, whereas 67 of 68 accessions analyzed from Mississippi, Arkansas, South Carolina, and North Carolina were southern genotypes. Accessions from Kansas, Missouri, and Illinois included 40 and 56 northern and southern genotypes, respectively, indicating a transition zone. In Illinois, accessions collected from northern and southern counties tended to be northern and southern genotypes, respectively. We conclude that much of the genetic variation among U.S. common cocklebur accessions is distributed along a latitudinal gradient.

Common cocklebur is a new weed in irrigated maize grown for forage in the hot, dry region of northwest Pakistan. We conducted experiments in the Khyber Pakhtunkhwa Province, Peshawar, Pakistan, during 2006 and 2007 to evaluate the interaction of common cocklebur density and maize density on biomass, leaf area index (LAI), and plant height of forage maize. Seven common cocklebur densities (0, 2, 4, 6, 8, 10, and 12 plants m−2) in maize planted at four densities (5, 7.5, 10, and 12.5 plants m−2) were evaluated. An ANOVA for both years revealed significant main effects and interactions for all variables. Regression of measured variables against common cocklebur density showed that maize biomass declined linearly as common cocklebur density increased from 0 to 12 plants m−2, with an increasing rate of decline for high maize densities and low maize densities. Combined data for all maize densities revealed that the relationship between maize biomass and common cocklebur biomass fit a linear function, with 1.28 to 1.35 kg ha−1 loss in maize biomass for each kilogram per hectare increase in common cocklebur biomass from about 1,500 to 3,200 kg ha−1. Above 8 to 10 common cocklebur plants m−2, weed biomass declined, presumably due to intraspecific competition. An increase in common cocklebur density decreased maize LAI about 0.15 to 0.3 units for each additional common cocklebur plant per square meter in 2006, and 0.11 to 0.24 units in 2007. Common cocklebur LAI increased in a linear fashion as density of the weed increased. Results suggest that the effect of common cocklebur interference on maize biomass was associated with a change in allocation of resources, resulting in increased crop height growth at the expense of a reduction in LAI and presumably potential light interception by the crop as common cocklebur density increased.

A study was undertaken to determine whether the relative leaf stages of common annual weeds and crops could serve as a reliable indicator of the time of weed emergence. Ten annual broadleaved and grass weeds were sown at successive intervals in field corn and soybean at Harrow, ON, Canada, in 1997, 1998, and 1999. All weeds emerging at a particular crop leaf stage were assigned to a cohort. Leaf numbers of the crop and different weed cohorts were recorded at 2- to 3-d intervals up to the eight-leaf stage of corn and the fourth trifoliate of soybean. For each weed species, categorical data analysis revealed a high degree of association between the leaf stage of a crop and the leaf number expected for an individual weed of a given cohort. For example, by the third trifoliate of soybean, most of the weeds emerging with the crop (VE cohort) had 8 to 10 leaves, whereas weeds in the V1, V2, and V3 cohorts averaged about seven, four, and two leaves, respectively. Year to year variation in the correspondence between crop and weed leaf numbers generally was small once variation due to time of weed emergence was removed, with one exception. Dry surface soil conditions during emergence of the VE cohort in corn in 1999 resulted in delayed leaf appearance of many weeds with respect to the crop. The relationship between weed and crop leaf stages can provide information for management decisions in two ways: (1) it indicates the relative time of weed emergence in assessing the need for control, and (2) it indicates the crop stage at which scouting for particular weed leaf stages should occur.

Southern Root-Knot nematode and common cocklebur interfere with cotton growth and yield. A greater understanding of the interaction of these pests with cotton growth and yield is needed for effective integrated pest management (IPM). An additive design was used in outdoor microplots with five common cocklebur densities (0, 1, 2, 4, and 8 plants per plot) growing in competition with cotton, with and without the presence of southern Root-Knot nematode. Differences in cotton height could not be detected among common cocklebur densities or nematode presence at 3 wk after transplanting (WAT); however, differences in crop height were observed at 5 WAT between nematode treatments. In the absence of nematodes, the relationship between cotton yield loss and common cocklebur density was described by a rectangular hyperbolic regression model (P < 0.0001). Maximum yield loss from common cocklebur in the absence of nematodes exceeded 80%. In the presence of nematodes, there was a linear relationship between cotton yield loss and common cocklebur density (P = 0.0506). The presence of nematodes at each common cocklebur density increased cotton yield loss 15 to 35%. Common cocklebur plant biomass was 25% greater in nematode treatments, likely because of the reduced competitiveness of the cotton plants in these plots. This study demonstrates that multiple pests can interact to cause an additive reduction in crop yield.

The objective of this research was to develop a model to predict common cocklebur seedling emergence in spring tillage and no-spring-tillage systems in the presence and absence of a soybean canopy. A Weibull function was used to accumulate heat units (i.e., growing degree days) at a 2.5 cm soil depth on days when mean soil temperature, soil water potential, and soil thermal fluctuation were above established thresholds. The base temperature, soil water potential, and soil thermal fluctuation thresholds used for model development were 17 C, −100 kPa, and 7.5 C, respectively. A single function adequately described common cocklebur seedling emergence in the presence and absence of drill-seeded soybean from data combined over an artificial (2004) and natural seedbank (2005) (R2 = 0.986). Model parameterization differed between the artificial and natural seedbank in the absence of spring tillage, but emergence was adequately described, regardless of soybean presence. Separate parameter estimates for the artificial and natural seedbanks were needed to adequately describe emergence in the system without spring tillage (R2 = 0.975 to 0.984). The ability of the model to account for reduced emergence when soil moisture is limited or when daily thermal fluctuation requirements are not met could assist practitioners with assessments associated with field scouting for weeds as well as other management decisions.

A field experiment was conducted in Boone and Callaway counties in Missouri in 2010 and 2011 to investigate herbicide programs for the management of summer annual grass and broadleaf weeds in soybean resistant to 2,4-D and glufosinate. Results revealed that the addition of 0.56, 0.84, or 1.12 kg ha−1 2,4-D (amine) to either or both POST applications of glufosinate in a two-pass POST herbicide program increased control of common waterhemp compared to two POST applications of glufosinate alone. Similar levels of common cocklebur, giant foxtail, large crabgrass, and barnyardgrass control were achieved with any of the two-pass POST programs that contained 2,4-D compared to two-pass POST programs containing glufosinate alone. Similar control of these species was also achieved with the inclusion of 2,4-D in either the first or second pass of glufosinate. Two-pass programs resulted in the highest levels of weed control (90%). Annual grass and broadleaf weed control was as much as 59% lower when one-pass POST herbicide programs were compared to PRE followed by (fb) POST or two-pass POST programs. However, one-pass POST programs were sufficient to obtain exceptional control of common cocklebur and giant foxtail. Across all site years, soybean yields ranged from 2,680 to 3,100 kg ha−1 for all herbicide treatments, but did not differ statistically. Overall, results from these experiments indicate that compared to glufosinate alone, PRE fb POST or two-pass POST herbicide programs that incorporate 2,4-D amine with glufosinate in 2,4-D–resistant soybean enhance control of common waterhemp, while providing similar levels of control of other summer annual grass and broadleaf weeds.

Using climate-controlled glasshouses, the growth of grain sorghum was evaluated with and without the presence of common cocklebur at current and projected future atmospheric concentrations of carbon dioxide [CO2]. Single-leaf photosynthetic rates declined for both species in competition; however, elevated CO2 reduced the percentage decline in common cocklebur and increased it in sorghum by 35 d after sowing (DAS) relative to ambient CO2. In monoculture, elevated CO2 significantly stimulated leaf photosynthetic rate, leaf area, and aboveground dry weight of common cocklebur more than that of sorghum. However, the stimulation of aboveground biomass or leaf area for monocultures of sorghum and common cocklebur at elevated CO2 did not adequately predict the CO2 response of aboveground biomass or leaf area for sorghum and common cocklebur grown in competitive mixtures. Overall, by 41 DAS, plant relative yield (PRY), in terms of aboveground biomass and leaf area, increased significantly for common cocklebur and decreased significantly for sorghum in competitive mixtures at elevated CO2. Data from this study indicate that vegetative growth, competition, and potential yield of economically important C4 crops could be reduced by co-occurring C3 weeds as atmospheric carbon dioxide increases.

At the time of grain harvest, weed seeds can be classed into one of four pools on the basis of dispersal status and location: (1) undispersed, remaining on the mother plant; (2) dispersed in the current year, on the soil surface; (3) dispersed in the current year and collected by harvest machinery; and (4) dispersed in a previous year and persisting within the soil seed bank. Knowledge of the relative sizes of these seed pools for different weed species under different crop environments will be useful for determining the best way to reduce the size of inputs to the soil seed bank. In fall 2004 and fall 2005, four randomly selected commercially managed corn and soybean fields in east-central Illinois were sampled to quantify weed seed pools at time of crop harvest. Thirty randomly located 0.125-m2 quadrats were placed within each field, the four seed pools mentioned above were sampled for each quadrat, and the species composition and abundance of each seed pool was determined. The magnitude of the weed seed rain varied among species and between years and crops. Twenty-six weed species were found to contribute to at least one of the four seed pools. However, the weed seed pools were consistently dominated by six species: velvetleaf, Amaranthus complex (redroot pigweed and waterhemp), ivyleaf morningglory, giant foxtail, prickly sida, and common cocklebur. For each of these species, the ratio of undispersed seeds to seeds in the soil seed bank at harvest time was ≥ 1 in at least one crop during one of the two experimental years, indicating a potential for the soil seed bank to be completely replenished or augmented by that year's seed rain. This analysis demonstrates the urgent need for techniques to limit weed seed inputs to the soil seed bank at the end of the growing season.

Common ragweed and common cocklebur plants were collected at two sites each in Illinois, Minnesota, and Ohio to analyze intraspecific variability of the gene encoding acetolactate synthase (ALS). A 385-nucleotide fragment within the coding sequence of ALS was compared among 24 plants of each of these two species from the six locations. Common ragweed ALS was highly variable, with polymorphisms observed at 48 (12.5%) of the 385 nucleotides among the 24 plants. Despite the numerous nucleotide polymorphisms, only two inferred amino acid polymorphisms were identified. No apparent population structure was suggested by the ALS sequence data, indicating widespread gene flow consistent with the wind-pollinated nature of common ragweed. In contrast to common ragweed, no ALS polymorphisms were identified among the common cocklebur plants used in this study. As a basis for comparing the extremes observed between common ragweed and common cocklebur, ALS intraspecific variability also was investigated in 10 plants each of tall waterhemp and smooth pigweed. Normalized to the number of plants analyzed, the number of nucleotide polymorphisms for both tall waterhemp and smooth pigweed was greater than that in common cocklebur but less than that observed in common ragweed. Information on variability of herbicide target-site genes may be useful in predicting the likelihood for herbicide-resistance development. However, all four of the species investigated in this study have evolved resistance to ALS-inhibiting herbicides, despite the different levels of ALS variability observed.

The overall objective of this study was to identify common patterns in the spatial distribution of the major weed species present in the corn-growing region of central Spain, exploring the scale dependence of these patterns and the possible associations or dissociations between individual species. Weed density was assessed in 16 commercial fields using digital images acquired in a 9-m by 9-m sampling grid. A set of six species was found in all the fields: black nightshade, common cocklebur, fierce thornapple, johnsongrass, purple nutsedge, and velvetleaf. Spatial analysis by distance indices and inverse distance weighting interpolation methods were performed to create weed distribution maps. The results showed aggregated spatial distribution patterns for all individual species regardless their life cycle, annual or perennial. Some associations and dissociations among species were found in the analysis of interactions. Nevertheless, the spatial patterns of co-occurrence of weed species were field-specific and therefore cannot be considered general patterns of weed co-occurrence. In order to explore the scale dependence of these results, an additional study was conducted in an experimental field located in the same area using a 1.0-m by 0.75-m sampling grid. Although this resolution allowed for a better definition of the positions of the weed patches and weed-free gaps, the results obtained revealed similar patterns to those observed with a coarser sampling resolution.

Greenhouse studies were conducted in 2003 at the Stine–Haskell Research Center to determine whether herbicide inhibitors of six specific sites in the carotenoid biosynthesis pathway would elicit synergistic responses when applied postemergence (POST) in combination with the photosystem II (PSII) inhibitor atrazine. Based on data analysis with the Isobole method, synergistic responses were observed on red morningglory, common cocklebur, and giant foxtail when atrazine was applied in mixtures with the deoxy-D-xylulose-5-phosphate reductoisomerase (DOXP reductoisomerase) inhibitor fosmidomycin, the p-hydroxyphenylpyruvate dioxygenase (HPPD) inhibitor mesotrione, and the DuPont proprietary zeta-carotene desaturase (ZDS) inhibitor DFPC. Clomazone (its metabolite ketoclomazone is the actual enzyme inhibitor), an inhibitor of 1-deoxy-D-xylulose-5-phosphate synthatase (DOXP synthase), provided synergistic responses on red morningglory, but antagonistic responses on both common cocklebur and giant foxtail when applied in mixtures with atrazine. Combinations of the lycopene cyclase (LC) inhibitor, CPTA, with atrazine produced synergistic responses on both common cocklebur and giant foxtail but were antagonistic on red morningglory. Norflurazon, a phytoene desaturase (PDS) inhibitor, applied in mixtures with atrazine provided synergistic responses on red morningglory, antagonistic responses on giant foxtail, and independent responses on common cocklebur. Because carotenoids have been determined to play a key role in quenching singlet oxygen species in the chloroplast and also assist in the maintenance of the D1 protein in PSII, this might help explain the synergistic responses with atrazine observed in our studies.

Greenhouse experiments were conducted to determine the effect of salinity, imazethapyr, and chlorimuron on weed growth. Five species, barnyardgrass, common cocklebur, ivyleaf morningglory, common purslane, and yellow nutsedge, were grown in potting soil and irrigated with nonsaline (EC ∼ 2 dS m−1) or sulfate-dominated saline (EC ∼ 7 dS m−1) nutrient solution. Plants were treated after emergence with imazethapyr (Pursuit formulation) at 70 g ae ha−1 or chlorimuron ethyl (Classic formulation) at 8.8 g ai ha−1. Results indicated that irrigation with saline water had no overall effect on the growth or survival of most tested weed species. Growth of yellow nutsedge (maximum height and stem diameter) was reduced for plants irrigated with saline water. Observed growth and survival trends in saline and nonsaline treatments were consistent with information on the herbicide label. Complete control of common purslane was not achieved by either chlorimuron or imazethapyr. Growth and survival of ivyleaf morningglory and yellow nutsedge were greater when plants were treated with imazethapyr than when treated with chlorimuron, whereas for barnyardgrass, growth and survival were significantly greater when plants were treated with chlorimuron. Both herbicides affected common cocklebur growth and survival in a similar way. For all tested species, most surviving plants were not vigorous and would not be highly competitive with crop plants. The results of these experiments suggest that weed control information mentioned on the labels for these herbicide formulations will not require modification for moderately saline soils.