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.

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.