The acetolactate synthase-inhibiting herbicides chlorimuron and imazaquin, and the diphenylether herbicides acifluorfen and lactofen, were applied alone and in all possible combinations to the foliage of common cocklebur, pitted morningglory, and prickly sida to evaluate interacting effects on absorption and translocation. The addition of unlabeled acifluorfen to 14C-chlorimuron increased absorption in common cocklebur, pitted morningglory, and prickly sida. Lactofen also increased absorption of 14C-imazaquin in all species. Conversely, imazaquin reduced absorption or translocation of 14C-acifluorfen in common cocklebur or pitted morningglory, respectively. In all species, absorption was lower when unlabeled chlorimuron or imazaquin was combined with 14C-lactofen than when applied alone.

The interaction of reduced rates of bentazon, chlorimuron, imazaquin, and imazethapyr with cultivation for broadleaf weed control in soybeans was investigated in field experiments conducted at three sites in Missouri in 1987 and 1988. Single reduced-rate herbicide applications provided soybean yields equal to full rates although visual weed control was slightly lower. Sequential applications of all four herbicides at reduced rates provided weed control and soybean yields equal to full-rate applications. The number of velvetleaf plants m−2 and seeds plant−1 were not influenced by herbicide, herbicide rate, or application timing. Cultivation improved weed control and soybean yield and decreased late-season weed populations and seed production.

Photosynthesis and growth responses to irradiance level during growth were compared in soybean (Glycine max L. Merr. ‘Century’) and three broadleaf weeds to determine if these responses were associated with differences in shade tolerance among species. In response to reduced irradiance during growth, leaf thickness of all species decreased, while chlorophyll content per unit leaf volume and photosynthetic rate per unit leaf volume, measured at low irradiance, increased. Soybean and common cocklebur (Xanthium strumarium L. #3 XANST) also exhibited a decrease in soluble proteins on a leaf volume basis under reduced irradiance, and common cocklebur further exhibited a decrease in ribulose-1,5-bisphosphate carboxylase (RuBPcase) protein per unit leaf volume. Decreased irradiance during growth did not alter the content of RuBPcase or other soluble proteins per unit leaf volume in jimsonweed (Datura stramonium L. # DATST) or velvetleaf (Abutilon theophrasti Medic. # ABUTH). The superior shade tolerance of common cocklebur compared to the other species was attributed in part to the levels of RuBPcase and other photosynthetic proteins in leaves developed at low irradiance.

Field experiment were conducted to determine interactions of chlorimuron or imazaquin with fomesafen, lactofen, or acifluorfen on three-leaf and eight-leaf common cocklebur, hemp sesbania, pitted morningglory, and prickly sida. Antagonism was the most common interaction with common cocklebur, and was most severe with chlorimuron combined with fomesafen or acifluorfen, whereas lactofen did not antagonize common cocklebur control. Reductions in control were greater when low rates of chlorimuron were used. On three-leaf prickly sida, control synergistically increased when imazaquin was combined with fomesafen or acifluorfen, but the majority of these combinations were additive on eight-leaf prickly sida. Three-leaf pitted morningglory control synergistically increased when 36 g ai ha–1 imazaquin was combined with 210 g ai ha–1 fomesafen or 110 or 220 g ai ha–1 lactofen. With eight-leaf pitted morningglory, synergism occurred when 2 g ai ha–1 chlorimuron was combined with the high rate of any diphenylether herbicide tested, and when 36 g ha–1 imazaquin was combined with 110 g ha–1 lactofen or 210 g ai ha–1 acifluorfen; however, at higher rates of chlorimuron or imazaquin, several antagonistic interactions occurred. Hemp sesbania was controlled over 90% by all combinations, and no interactions occurred.

Common cocklebur is an adaptable species found in diverse environments. We grew 28 common cocklebur accessions from 14 states at Urbana, IL, to compare their growth, physiology, and morphology in a common environment to determine if regional control recommendations of specific biotypes might be practical. Accessions were evaluated for midseason and maximum heights and widths, flowering date, insect damage, and petiole color in 1998 and 1999. Weight of aboveground tissue, photosynthetic rate, stomatal conductance, chlorophyll content, and leaf and bur morphology descriptions were also taken in 1999. Midseason and maximum widths, midseason height, flowering date, and insect damage differed significantly based on the year of evaluation. The year by accession interaction was a significant source of variation for midseason and maximum heights and widths, flowering date, insect damage, and petiole color. Within each year, accessions differed significantly for all measured variables except maximum width in 1998 and stomatal conductance in 1999. Accessions from northern states usually flowered earlier, and flowering date was negatively correlated with latitude of origin (1998 r = −0.76; 1999 r = −0.60). Nevertheless, some of the earliest flowering accessions were from the southern states. Results from cluster analysis indicated that several accessions had phenotypes more similar to accessions from distant sites than to nearby accessions. We conclude that the accessions differ for traits that may affect weediness, but proximal accessions differ too frequently to recommend regional, biotype-specific control strategies.

Field experiments were conducted in Pendleton, SC, in 2004 and 2005, to determine the influence of tillage with or without soybean on common cocklebur emergence. Treatments included no-till/no soybean (NTNS), no-till plus soybean (NTS), tillage/no soybean (TNS), and tillage plus soybean (TS). Emergence was monitored from an artificial seed bank in 2004 and a natural seed bank in 2005. Overall, common cocklebur emerged from early May through late October and presented multiple emergence. In no-till plots with or without soybean, initial emergence was delayed 7 d in both years. In TNS plots, major emergence (daily emergence > mean emergence plus standard deviation) of common cocklebur occurred from early May to late July. In NTNS plots, major emergence occurred from late May through late August. No-till reduced total common cocklebur emergence by 59 to 69% compared with tillage. At the V5 to V6 soybean growth stage, the daily soil thermal fluctuation at 2.5 cm soil depth diminished from approximately 15 to 5 C and reduced common cocklebur emergence by 84 to 91% for the rest of the growing season. Common cocklebur emergence was higher when the mean soil temperature was > 15 C, and the daily thermal fluctuation was > 7.5 C. This study suggests that strategies that promote early crop canopy development and minimum tillage should reduce common cocklebur emergence.

Winter sowing of lentil results in higher yields than a spring-sown crop. However, when lentil is winter-sown, the critical period of weed control is extended and might require sequential herbicide management strategies to obtain maximum yields. The efficacy of POST alone or soil applied followed by (fb) POST herbicides or hand weeding were evaluated in 2002 and 2003. Trifluralin (PPI) or pendimethalin (PRE) were applied at planting, and pyridate or oxyfluorfen were applied POST at the three- to four-leaf stage of lentil. The lowest level of weed biomass was recorded with all treatments, except pyridate alone in both years, pendimethalin PRE fb pyridate in 2002, and oxyfluorfen in 2003. Application of pyridate or oxyfluorfen POST alone resulted in lower yields. In 2002, trifluralin PPI or pendimethalin PRE fb one hand weeding or pendimethalin fb pyridate resulted in yields similar to the weed-free treatment. In 2003, yields were similar to the weed-free treatment, except pyridate or oxyfluorfen alone and trifluralin PPI fb oxyfluorfen. Weed species observed in the present study required sequential management to achieve both effective control and maximum lentil yield.

Experiments were conducted in 2002 and 2003 to determine the influence of soil thermal amplitude on common cocklebur emergence. Additionally, common cocklebur achenes were collected in fall of 2003 and of 2004 to assess changes in light and temperature requirements for germination over a 12-mo period under field conditions. Common cocklebur germination in response to the light environment and to constant and fluctuating temperatures were evaluated under controlled conditions following achene retrieval from the field. There was a linear inverse relationship between shade intensity and soil thermal amplitude, which explained 77% of the variability in emergence in the field over 2 yr. Emergence decreased as soil thermal amplitude declined, with 95% shading resulting in a 72 to 88% reduction in emergence. Neither red nor far-red light had much effect on germination, and burial did not induce a light requirement. Germination of achenes retrieved from the soil surface or buried in soil generally was not affected by red or far-red light, and the achenes did not acquire a red-light requirement following burial. Daily exposure to natural greenhouse light at 24 to 30 C was essential for germination immediately following achene maturation, whereas no germination occurred in darkness. A thermal fluctuation of 15 C increased germination percentages over those at constant temperatures regardless of time after maturation or retrieval-depth of achenes. The mean fluctuating temperature over all sample dates that was generally optimal for germination was 25 C (17.5/32.5 C low/high temperatures; 15 C daily fluctuation) in April or May and July or August in both years. Germination was generally optimum at constant temperatures of 35 or 40 C. The higher mean temperature requirement for germination at constant temperatures than at fluctuating temperatures likely contributes to reduced emergence in spring and summer months, when earlier emerging weed species or crops have already become established, and the thermal fluctuation requirement for germination reduces the likelihood of emergence in an environment where light availability is diminished.