Greenhouse and field experiments were conducted to confirm and quantify linuron resistance in common purslane (Portulaca oleracea) collected from a carrot (Daucus carota) field in Imlay City, MI. Preliminary evaluation was made using a flotation test kit to identify resistance to linuron and atrazine. Subsequent greenhouse experiments indicated that this common purslane was resistant to 11.2 kg/ha linuron and 179 kg/ha atrazine. The resistance ratio for linuron was > 300 and was > 400 for atrazine. The resistant common purslane was also highly resistant to diuron, cyanazine, and prometryn but had a low level of negative cross-resistance to bromoxynil. Both resistant and susceptible biotypes of common purslane were sensitive to hexazinone and bentazon.

As a follow-up to greenhouse studies, acetolactate synthase (ALS) (EC 4.1.3.18) was extracted from one imidazolinone (IMI)-susceptible (S) and three IMI-resistant (R1, R2, and R3) smooth pigweed populations, and activity was assayed in the presence of imazethapyr, chlorimuron, thifensulfuron, and pyrithiobac. ALS inhibitor concentrations, required to reduce enzyme activity by a specified percentage compared with the untreated control (I p), were determined for each herbicide using regression analysis, and resistance ratios were calculated from these values. An I 50 value of >35 μM imazethapyr was calculated for all R populations compared with a value of 3.4 μM for the S population. With chlorimuron, thifensulfuron, and pyrithiobac data sets, pairwise comparisons of regression coefficients were used to determine significant differences between regression lines. Using this technique, it was established that ALS from R3 was more sensitive than ALS from S to inhibition by chlorimuron and thifensulfuron. Also, ALS from R2 and R3 displayed increased sensitivity to pyrithiobac compared with ALS extracted from the S population. We have confirmed enzyme-level resistance to imazethapyr in all R populations and have documented negative cross-resistance in some R populations to ALS inhibitors other than imazethapyr.

Several populations of smooth pigweed with resistance to imidazolinone (IMI) herbicides have been identified in recent years. One IMI-resistant population (R2) was 10-fold more sensitive to cloransulam-methyl in the greenhouse when compared with a susceptible (S) population. Laboratory studies were conducted to determine if differences in the absorption, translocation, and metabolism of cloransulam-methyl existed between S and R2 populations and to determine if these differences could account for the whole-plant responses observed in the greenhouse. Enzyme assays were also conducted to determine if differences in acetolactate synthase (ALS) sensitivity to cloransulam-methyl existed between S and R2 populations. Absorption of foliar-applied cloransulam-methyl was rapid and similar in both populations of smooth pigweed. Translocation of the absorbed radioactivity out of the treated leaf was symplastic and generally similar in both populations. Translocated radioactivity was detected primarily in shoots above and below the treated leaf with little movement to the roots. 14C-cloransulam-methyl metabolism was also similar in S and R2 populations. Differential tolerance to cloransulam-methyl in S and R2 populations in the greenhouse cannot be explained by differences in the absorption, translocation, and metabolism of this herbicide. However, ALS from R2 was 25-fold more sensitive to inhibition by cloransulam-methyl than ALS from S.

Field and greenhouse studies were conducted to evaluate the responses of several imidazolinone (IMI)-resistant Amaranthus hybridus populations to various acetolactate synthase (EC 4.1.3.18)-inhibiting herbicides. In 1996 field studies, IMI resistance was confirmed in one A. hybridus population (R4) that was not cross-resistant to the sulfonylurea herbicides CGA-277476, chlorimuron, or thifensulfuron. Amaranthus hybridus control with triazolopyrimidine herbicides was ≤ 35%, but control with cloransulam-methyl or flumetsulam plus cloransulam-methyl was higher than with IMI herbicides. Follow-up greenhouse studies were conducted in 1997 and 1998 to investigate the response of one IMI-susceptible (S) A. hybridus population collected near Painter, VA, and four IMI-resistant A. hybridus populations (R1, R2, R3, R4) collected from fields in Somerset County, MD, to postemergence imazethapyr, chlorimuron, thifensulfuron, pyrithiobac, and cloransulam-methyl applications. Resistance to imazethapyr was confirmed in all R populations, and no practical level of cross-resistance to chlorimuron, thifensulfuron, pyrithiobac, or cloransulam-methyl was detected. Based on resistance ratios, R populations were slightly more tolerant to chlorimuron and slightly more sensitive to pyrithiobac, thifensulfuron, and cloransulam-methyl than the S population.