Few options are available for controlling bermudagrass invasion of seashore paspalum. Bermudagrass and seashore paspalum tolerance to topramezone, triclopyr, or the combination of these two herbicides were evaluated in both greenhouse and field conditions. Field treatments included two sequential applications of topramezone (15.6 g ai ha−1) alone and five rates of topramezone + triclopyr (15.6 + 43.2, 15.6 + 86.3, 15.6 + 172.6, 15.6 + 345.2, or 15.6 g ai ha−1 + 690.4 g ae ha−1). Secondary greenhouse treatments included a single application of topramezone (20.8 g ha−1) or triclopyr (258.9 g ha−1) alone, or in combination at 20.8 + 258.9 or 20.8 + 517.8 g ha−1, respectively. Greenhouse and field results showed that topramezone applications in combination with triclopyr present opposite responses between bermudagrass and seashore paspalum. Topramezone increased bermudagrass injury and decreased seashore paspalum bleaching injury compared to topramezone alone. In field evaluations, topramezone + triclopyr at 15.6 + 690.4 g ha−1 used in sequential applications resulted in >90% injury to bermudagrass, however, injury decreased over time. Furthermore, sequential applications of topramezone + triclopyr at 15.6 + 690.4 g ha−1 resulted in >50% injury to seashore paspalum. Application programs including topramezone plus triclopyr should increase bermudagrass suppression and reduce seashore paspalum injury compared to topramezone alone. However, additional studies are needed because such practices will likely require manipulation of topramezone rate, application timing, application interval, and number of applications in order to maximize bermudagrass control and minimize seashore paspalum injury.

Experiments were conducted in order to establish the mechanism by which the synergist MZH 2091 increases metribuzin activity on ivyleaf morningglory. Herbicide absorption and metabolism were compared for plants treated either with 14C-metribuzin alone or with 14C-metribuzin plus nonlabeled MZH 2091. The compounds were applied via the roots for 3 h and the absorption was determined. After the pulse treatment, the plants were grown for additional 0, 3, 6, 9, 12, 21, 45, or 69 h in water, and the metribuzin metabolism was studied in the cotyledons. The synergist did not interfere with herbicide uptake but did strongly inhibit metribuzin metabolism. The pathway of metribuzin metabolism in ivyleaf morningglory is discussed as well as the way it is affected by the synergist MZH 2091.

The antidotes dichlormid, MON-4660, CGA-154281, R-29148, and MON-13900 were tested in the greenhouse to protect Zea mays L. (corn) against RPA 201772 injury. High rates of RPA 201772 injured four Z. mays hybrids > 30%. R-29148 and MON-13900 were the most effective of the five antidotes evaluated. R-29148 applied at rates ⩾ 45 g ha−1 provided excellent protection against RPA 201772 injury and also prevented injury to Z. mays from diketonitrile, the active metabolite of RPA 201772. In laboratory studies, R-29148 did not alter absorption of 14C-RPA 201772 from soil; however, R-29148 significantly enhanced the rate of RPA 201772 metabolism and inactivation in Z. mays. The mixed function oxidase inhibitor piperonyl butoxide (PBO) increased RPA 201772 injury on all hybrids. These results demonstrate that Z. mays tolerance to RPA 201772 can be enhanced with the use of antidotes such as R-29148 and MON-13900, that R-29148 protects Z. mays from RPA 201772 and diketonitrile by the enhancement of metabolism, and that oxidative reactions may be involved in the metabolism of RPA 201772 in Z. mays.

The effect of the organophosphate insecticide malathion on the response of resistant rigid ryegrass population SLR 31 to the herbicides trifluralin, pendimethalin, clomazone, and triallate was investigated. The insecticide and herbicides were soil-applied prior to emergence of plants grown under controlled conditions. In the absence of malathion, the resistant population exhibited significant resistance to the four herbicides compared with a susceptible population. Levels of resistance, as determined by comparison of herbicide rates required to inhibit growth by 50%, were 35, 11, 2.4, and 2.4 for pendimethalin, trifluralin, triallate, and clomazone, respectively. Malathion had a synergistic effect on pendimethalin in the resistant population but not in the susceptible population. Malathion had no synergistic effect on trifluralin, triallate and clomazone. Resistance to triallate and clomazone was found despite the fact that the resistant population had never before been selected with these herbicides. This resistance, selected by other herbicides, further indicates that the use of alternative herbicides to control multiple resistant weeds is unlikely to be a successful resistance management approach.

The efficacy of the safeners naphthalic anhydride (NA), R-29148, benoxacor, and dichlormid as protectants of corn against injury from the methyl ester of tribenuron was evaluated under greenhouse conditions. Tribenuron applied alone reduced the root length of both ‘Pioneer 3180’ and ‘Northrup-King 9283’ corn. The concentration of tribenuron causing 50% reduction of corn root length (GR50) was 1 μM. NA applied as a seed dressing at 0.5 and 1.0% (w/w) was the most effective of the four safeners tested and provided excellent protection to both corn hybrids against 1, 2, and 4 μM tribenuron. Soaking corn seeds in an aqueous solution of R-29148 containing 0.5,1, or 2 mM protected ‘Pioneer 3180’ against 1 μM of tribenuron. The safening efficacy of R-29148 against tribenuron injury to ‘Northrup-King 9283’ corn was limited. Dichlormid and benoxacor, were less effective as tribenuron safeners and offered partial protection to both corn hybrids. Individual applications of the synergist piperonyl butoxide (PBO) at 0.1 and 0.2 mM did not affect the growth of corn seedlings. PBO synergized the activity of all concentrations of tribenuron, but only on the ‘Northrup-King 9283’ hybrid. These results demonstrate that the tolerance of corn to tribenuron can be enhanced with the use of safeners such as NA and R-29148, and that oxidative reactions may be involved in the metabolism of tribenuron by corn.

Glasshouse research was conducted to investigate the efficacy of herbicide safeners for improving creeping bentgrass (CBG) tolerance to various herbicides. CBG injury from amicarbazone (150 g ha−1), bispyribac-sodium (110 g ha−1), fenoxaprop-p-ethyl (35 g ha−1), imazapic (45 g ha−1), quinclorac (1,050 g ha−1), or topramezone (37 g ha−1) applied in combination with the herbicide safeners naphthalic anhydride or isoxadifen-ethyl was evaluated. These safeners reduced CBG injury from topramezone only. Topramezone was then applied in combination with naphthalic anhydride, isoxadifen-ethyl, cloquintocet-mexyl (cloquintocet), fenchlorazole-ethyl, mefenpyr-diethyl, and benoxacor. These experiments determined that CBG injury was lowest from topramezone in combination with cloquintocet. Additional experiments evaluated topramezone (37 g ha−1) with several rates of cloquintocet and determined that applications at ≥ 28 g ha−1 reduced CBG injury similarly. Cloquintocet (28 g ha−1) increased topramezone I50 values against CBG, but not large crabgrass or goosegrass. The cytochrome P450 (cP450) inhibitor malathion (1000 g ha−1) reduced topramezone I50 values against CBG in one experimental run. Topramezone–cloquintocet combinations warrant further research in field settings.

Discrimination of conspecific and heterospecific signals is a key element in the evolution of specific mate recognition systems. Lepidopteran pheromone signals are typically composed of several compounds that synergize attraction of conspecific and inhibit attraction of heterospecific males. Blends convey specificity, but not their single components, that are typically shared by several species. Many sex pheromones are blends of geometric or positional isomers of straight-chain acetates, while species-specific blends of analogous alcohols have not been described. We have, therefore, studied the attraction of tortricid moths to the geometric isomers (E,E)-, (E,Z)-, (Z,E)- and (Z,Z)-8,10-dodecadien-1-ol. Only one species responding to these alcohols seemed to be attracted to a blend of two isomers, while most species are attracted to only one alcohol isomer. Lack of a pronounced synergist or antagonist effect of the other geometric isomers explains the lack of specific attraction to isomer blends and reduces accordingly the number of specific communication signals composed of these alcohols. In comparison, many more species respond to the analogous (E,E)-, (E,Z)-, (Z,E)- and (Z,Z)-8,10-dodecadienyl acetates and their binary blends. The acetate isomers all play a behavioural role, either as attractants, attraction synergists or antagonists, and thus promote specific communication with acetate blends. Male moths seem to discriminate the acetate isomers with greater precision than the analogous alcohols. It is proposed that discrimination is facilitated by steric differences between the four acetate isomers, as compared to the more uniform steric properties of the alcohols.

Laboratory strain-R of Tribolium castaneum, resistant to lindane and multi-resistant strain-L, having developed resistance to lindane and malathion under field conditions, were compared with the standard susceptible strain-S for the nature of resistance to different groups of insecticides. Lindane resistance in both the strains extended to aldrin, dieldrin, endrin and heptachlor. Unlike laboratory strain-R, resistance did not extend to endosulfan in the field strain-L. Both the strains were found susceptible to p, p′-DDT, methoxychlor and allethrin. Also, lindane resistance did not extend to organophosphorous insecticides, viz., malathion, fenitrothion and dichlorovos. Lindane resistance extended to carbaryl and carbofuran, and only slightly to propoxur in the laboratory strain-R, whereas field strain-L remained susceptible to this group of insecticides. Synergist piperonyl-butoxide was found to overcome cross-resistance to endosulfan and propoxur, but to carbaryl in the lindane resistant strain-R. It is, therefore, indicated that one of the three mechanisms responsible for lindane resistance in the laboratory strain of T. castaneum, was stable in the field strain. Thus, the other two mechanisms showing cross-resistance to endosulfan and carbamates were unstable.