Experiments were conducted to evaluate a biotype of smooth pigweed that had survived applications of sulfonylurea (SU) and imidazolinone (IMI) herbicides in a single season. The source field had a history of repeated acetolactate synthase (ALS)-inhibiting herbicide use over several years. Whole-plant response experiments evaluated the resistant (R11) biotype and an ALS-inhibitor susceptible (S) smooth pigweed biotype to herbicides from the SU, IMI, pyrimidinylthiobenzoate (PTB), and triazolopyrimidine sulfonanilide (TP) chemical families. The R11 biotype exhibited 60- to 3,200-fold resistance to all four ALS-Inhibiting herbicide chemistries compared with the S biotype. Nucleotide sequence comparison ofALSgenes from R11 and S biotypes revealed a single nucleotide difference that resulted in R11 having an amino acid substitution of aspartate to glutamate at position 376, as numbered relative to the protein sequence of mouseearcress. This is the first report of an amino acid substitution at this position of anALSgene isolated from a field-selected weed biotype. To verify the role of this mutation in herbicide resistance, theALSgene was cloned and expressed inArabidopsis. TransgenicArabidopsisexpressing thisALSgene exhibited resistance to SU, IMI, PTB, TP, and sulfonylaminocarbonyltriazolinone ALS-Inhibiting herbicide classes.

Experiments were conducted to identify acetolactate synthase (ALS, EC 2.2.1.6 [formerly EC 4.1.3.18]) mutation sites in eight biotypes of smooth pigweed and correlate these mutations with patterns of herbicide cross-resistance. Four herbicide-resistant smooth pigweed biotypes (R5, R6, R7, R8) collected from fields in Virginia, Delaware, and Maryland, showed a similar response to postemergence applications of the ALS-inhibitors imazethapyr, pyrithiobac, chlorimuron, thifensulfuron, and cloransulam. These R biotypes ranged from 261- to 537-fold resistant to imazethapyr and 29- to 88-fold resistant to pyrithiobac. The biotypes also had reduced sensitivity to chlorimuron and thifensulfuron of 2- to 14-fold and 10- to 25-fold, respectively, relative to a susceptible smooth pigweed biotype (S). Biotypes R6, R7, and R8 had reduced sensitivity of 3- to 10-fold to cloransulam relative to the S biotype, whereas R5 had increased sensitivity. All of these biotypes were found to have a serine to asparagine substitution at amino acid position 653, as numbered relative to the protein sequence ofArabidopsis thaliana. This stands in contrast to four other imidazolinone (IMI)-resistant smooth pigweed biotypes (R1, R2, R3, R4) that were collected from fields in Somerset County, Maryland. These biotypes were found to have an alanine to threonine substitution at position 122 of the ALS enzyme and were previously characterized at the whole-plant level with high-level resistance to IMI herbicides, increased sensitivity to pyrimidinylthiobenzoate and triazolopyrimidine sulfonanilide herbicides, and low to no cross-resistance to sulfonylurea herbicides.

Field experiments were conducted in 2002 and 2003 to evaluate total POST weed control in corn with mixtures of mesotrione, atrazine, and the commercial mixture of nicosulfuron plus rimsulfuron plus atrazine at registered and reduced rates. Treatments were compared with nicosulfuron plus rimsulfuron plus atrazine POST, andS-metolachlor plus atrazine PRE alone and followed by (fb) nicosulfuron plus rimsulfuron plus atrazine POST. All treatments controlled common lambsquarters 8 wk after the postemergence treatments (WAPT). Common ragweed control with POST mesotrione plus nicosulfuron plus rimsulfuron plus atrazine combinations was greater than 89%. Mesotrione plus the registered rate of nicosulfuron plus rimsulfuron plus atrazine POST controlled common ragweed more effectively than the PRE treatment alone. Addition of atrazine to mesotrione improved common ragweed control by at least 38 percentage points over mesotrione alone. Nicosulfuron plus rimsulfuron plus atrazine at the registered rate and in mixtures with mesotrione controlled morningglory species (pitted and ivyleaf morningglory) 89 to 91%. Large crabgrass control varied between 2002 and 2003. In 2002, large crabgrass control was 58 to 76% with all POST treatments, but in 2003, nicosulfuron plus rimsulfuron plus atrazine POST alone controlled large crabgrass greater than 86%. Large crabgrass was more effectively controlled by treatments withS-metolachlor plus atrazine PRE than by the total POST treatments in 2002. Giant foxtail was controlled at least 97% with nicosulfuron plus rimsulfuron plus atrazine treatments.S-metolachlor plus atrazine PRE fb nicosulfuron plus rimsulfuron plus atrazine POST controlled all weed species greater than 85%. Corn yields by total POST treatment combinations of mesotrione plus either rate of nicosulfuron plus rimsulfuron plus atrazine were comparable toS-metolachlor plus atrazine PRE alone or fb nicosulfuron plus rimsulfuron plus atrazine POST.