Inheritance of glyphosate resistance in a Palmer amaranth biotype from North Carolina was studied. Glyphosate rates for 50% survival of glyphosate-resistant (GR) and glyphosate-susceptible (GS) biotypes were 1288 and 58 g ha⁻¹, respectively. These values for F1 progenies obtained from reciprocal crosses (GR×GSandGS×GRwere 794 and 501 g ha⁻¹, respectively. Dose response of F1 progenies indicated that resistance was not fully dominant over susceptibility. Lack of significant differences between dose responses for reciprocal F1 families suggested that genetic control of glyphosate resistance was governed by nuclear genome. Analysis of F1 backcross (BC1F1) families showed that 10 and 8 BC1F1 families out of 15 fitted monogenic inheritance at 2000 and 3000 g ha⁻¹glyphosate, respectively. These results indicate that inheritance of glyphosate resistance in this biotype is incompletely dominant, nuclear inherited, and might not be consistent with a single gene mechanism of inheritance. Relative 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) copy number varied from 22 to 63 across 10 individuals from resistant biotype. This suggested that variableEPSPScopy number in the parents might be influential in determining if inheritance of glyphosate resistance is monogenic or polygenic in this biotype.

Late and early leaf spot, respectively caused by Nothopassalora personata and Passalora arachidicola, are damaging diseases of peanut (Arachis hypogaea) capable of defoliating canopies and reducing yield. Although one of these diseases may be more predominant in a given area, both are important on a global scale. To assist informed management decisions and quantify relationships between end-of-season defoliation and yield loss, meta-analyses were conducted over 140 datasets meeting established criteria. Slopes of proportion yield loss with increasing defoliation were estimated separately for Virginia and runner market type cultivars. Yield loss for Virginia types was described by an exponential function over the range of defoliation levels, with a loss increase of 1.2 to 2.2% relative to current loss levels per additional percent defoliation. Results for runner market type cultivars showed yield loss to linearly increase 2.2 to 2.8% per 10% increase in defoliation for levels up to approximately 95% defoliation, after which the rate of yield loss was exponential. Defoliation thresholds to prevent economic yield loss for Virginia and runner types were estimated at 40 and 50%, respectively. Although numerous factors remain important in mitigating overall yield losses, the integration of these findings should aid recommendations about digging under varying defoliation intensities and peanut maturities to assist in minimizing yield losses.

Field experiments were conducted to evaluate possible interactions of clethodim with imazapic applied as mixtures or sequentially for control of broadleaf signalgrass, fall panicum, goosegrass, and large crabgrass. Imazapic at 70 g ai/ha alone controlled grass weeds inconsistently, whereas clethodim at 140 g ai/ha alone controlled the same weeds at least 99%. Imazapic did not affect broadleaf signalgrass control by clethodim. Reduced control of fall panicum, goosegrass, and large crabgrass was observed when clethodim and imazapic were applied in mixture. Antagonism of clethodim occurred when clethodim was applied 1 d before or up to 3 d after application of imazapic (fall panicum and large crabgrass). Antagonism of goosegrass control was noted when imazapic was applied 3 d before or up to 7 d after application of clethodim. In other experiments, large crabgrass and Texas panicum control by clethodim (70 and 140 g/ha) applied alone or with imazapic (70 g/ ha) or bentazon (1.1 kg ai/ha) plus 2,4-DB (0.28 kg ai/ha) either with or without ammonium sulfate (2.8 kg/ha) was evaluated. Texas panicum control by clethodim was reduced by imazapic regardless of the ammonium sulfate rate. However, large crabgrass control by imazapic was not affected in these experiments. Control of both grasses by clethodim was reduced substantially by bentazon plus 2,4-DB, although in some instances ammonium sulfate improved control when in mixture. Ammonium sulfate improved control by clethodim in some instances irrespective of the broadleaf–sedge herbicide treatments.Nomenclature: Bentazon; clethodim; 2,4-DB; imazapic; broadleaf signalgrass, Brachiaria platyphylla (Griseb) Nash #3 BRAPP; fall panicum, Panicum dichotomiflorum L. # PANDI; goosegrass, Eleusine indica L. Gaertn. # ELEIN; large crabgrass, Digitaria sanguinalis L. Scop. # DIGSA; Texas panicum, Panicum texanum Buckl. # PANTE.Additional index words: Ammonium sulfate, antagonism, herbicide compatibility, herbicide interaction, sequential application.

Experiments were conducted in 1993 and 1994 to determine if seed treated with disulfoton at 3, 6, or 12 g ai kg⁻¹ reduced bleaching of rice foliage caused by clomazone applied delayed preemergence at 0.56, 1.1, 1.7, or 2.2 kg ai ha⁻¹ on silt loam and silty clay soils. Clomazone injured rice more on silt loam soil than on silty clay soil. Disulfoton reduced bleaching caused by clomazone. In additional field experiments conducted during 1995 and 1996, clomazone at rates as high as 2.2 kg ha⁻¹ did not affect grain yield in seven of 10 experiments. Clomazone at rates below 1.7 kg ha⁻¹ did not reduce grain yield in any of the experiments.