A field in which Brassica napus volunteers were not controlled by several applications of glyphosate was investigated in 1998. This field had been planted with glufosinate-resistant and imidazolinone-resistant B. napus in 1997 and was adjacent to a field that had grown glyphosate-resistant B. napus. Mature volunteer B. napus were collected on a 50- by 100-m grid in the field. Progeny from 34 volunteers were sprayed with glyphosate at 440 g ae ha−1, and the survivors were sprayed with either glufosinate or imazethapyr at 400 or 50 g ai ha−1, respectively. Where seed numbers permitted (14 volunteers), seedlings were also sprayed sequentially with glyphosate, glufosinate, and imazethapyr, at 440 g ae ha−1, 400 g ai ha−1, and 50 g ai ha−1, respectively. In total, 15 volunteers had progeny that were between 66 and 82% resistant to glyphosate, consistent with the predicted 3:1 resistant : susceptible ratio. Volunteer B. napus plants with glyphosate-resistant seedlings were most common close to the putative pollen source; however, a plant with glyphosate-resistant progeny was collected 500 m from the adjacent field edge. Seedlings from all nine volunteers collected from the glufosinate-resistant area showed multiple resistance to glyphosate and glufosinate, whereas seedlings from 10 of 20 volunteers collected from the imidazolinone-resistant area showed resistance to imazethapyr and glyphosate. DNA extraction and restriction fragment length polymorphism (RFLP) analysis of seedlings confirmed that mature B. napus volunteers were hybrids resulting from pollen transfer rather than inadvertent seed movement between fields. Two seedlings from the 924 screened were resistant to all three herbicides. Progeny from these self-pollinated individuals were resistant to glyphosate and glufosinate at the predicted 3:1 resistant : susceptible ratio and resistant to imazethapyr at the predicted 15:1 resistant : susceptible ratio. Sequential crossing of three herbicide-resistant varieties is the most likely explanation for the observed multiple herbicide resistance. Integrated management techniques, including suitable crop and herbicide rotations, herbicide mixtures, and nonchemical controls should be used to reduce the incidence and negative effect of B. napus volunteers with multiple herbicide resistance.

Red rice has long been a troublesome, conspecific weed of cultivated rice. Rice varieties carrying certain herbicide-resistant traits acquired through genetic modification (herbicide-resistant varieties) now offer new options for red rice control. In concert with this innovation is the risk of gene flow, which can result in the transfer of that specific herbicide resistance to red rice and thus render this weed control measure ineffective. Gene flow in concept is simple, however, the parameters that determine the establishment of a new trait in a weed population are complex. Cross-pollination to make hybrid seed and the subsequent fate of those hybrid families in the general weed population are some of the biological factors that influence gene flow between red rice and cultivated rice. Natural outcrossing among rice plants is generally low. Most of the pollen dispersal studies published to date indicated that rice × rice outcrossing rates were less than 1.0%. Numerous reports summarized in this study suggest that outcrossing rates between rice and red rice can be highly variable but usually are similar to or lower than this level. However, once hybrids form, they may introgress into a red rice population within only a few generations. If hybrid seed families are to persist and establish herbicide-resistant red rice populations, they must successfully compete in the crop–weed complex. The ability to survive a herbicide applied to a herbicide-resistant rice variety would be a strong selective advantage for these hybrid families. Thus, the well-established principles of weed resistance management appear to be relevant for herbicide-resistant crop systems and should be used in combination with practices to minimize coincident flowering to mitigate the potential impact of gene flow from herbicide-resistant rice into red rice. For the rice–red rice crop–weed complex, there are both biological factors and agricultural practices that can work together to preserve these new weed control options.

This study was conducted to ascertain movement potential of imazethapyr resistance and to measure the relative growth and productivity of imazethapyr-resistant (IR) and imazethapyr-susceptible (IS) biotypes of common sunflower under noncompetitive and competitive conditions. Susceptible biotypes of common sunflower were planted in the field in concentric circles at distances of 5.5, 8.0, 15.0, and 30.0 m around a center of densely planted IR biotypes in four locations in northeast Kansas in 1998 and 1999. Pollen movement was analyzed by sampling the IS progeny for the presence of imazethapyr resistance. The distance in which resistance is first detected from the IR pollen source, first unnatural resistant distance (FURD), ranged from 12.1 to 15.5 m. Wind direction was highly correlated with FURD; the north sections had larger FURD. Greenhouse studies were conducted to study growth of IR and IS biotypes under noncompetitive and competitive conditions. Under noncompetitive conditions, leaf area and dry weight were slightly greater for the IR than the IS biotype at early growth stages, but photosynthesis and height were similar. Under competitive conditions, photosynthesis, leaf area, height, and dry weight of IR and IS biotypes were similar. As a result, IR–IR and IS–IS intracompetition equaled IR–IS intercompetition. Gene flow from IR to IS biotypes occurred with movement up to 15.5 m. The lack of differences between growth of the IR and IS biotype at late growth stages in noncompetitive conditions and similar growth of IR and IS biotypes under competitive conditions indicated no competitive advantage from imazethapyr resistance.