Previous reports have underscored antagonism that may result from mixing glyphosate and glufosinate across a wide range of application rates and for various broadleaf and grass weed species, but no investigation has been conducted to characterize glyphosate absorption and translocation when combined with glufosinate. The objectives of this study were to evaluate herbicide efficacy and assess herbicide interaction and physiological response with combinations of glyphosate and glufosinate on common lambsquarters, velvetleaf, and giant foxtail. Greenhouse studies to determine interaction resulted in strong and persistent antagonism between glyphosate at 110 and 220 g ae ha−1and glufosinate at 20 or 40 g ae ha−1in giant foxtail, whereas only transient and reduced antagonism was noted for velvetleaf and common lambsquarters. Combining glyphosate and glufosinate increased the maximum absorption of glyphosate by 9% and 23% in velvetleaf and giant foxtail, respectively, compared with glyphosate alone. In velvetleaf, averaged over time, only 2.6% of the applied radioactivity translocated out of the treated leaf when glufosinate was mixed with glyphosate compared with 9.9% when glyphosate was applied alone. In giant foxtail, 21.6% of the [14C]glyphosate translocated out of the treated leaf when glufosinate was mixed with glyphosate compared with 52.4% when glyphosate was applied alone. Conversely, no change in the radioactive pattern of translocation was noted for common lambsquarters. These results suggest that reduced translocation of glyphosate is the physiological mechanism responsible for the antagonism observed between glyphosate and glufosinate in giant foxtail and, to a lesser extent, in velvetleaf.

Dicamba is a synthetic auxin herbicide that may be applied over the top of transgenic dicamba-tolerant crops. The increasing prevalence of herbicide-resistant weeds has resulted in increased reliance on dicamba-based herbicides in soybean production systems. Because of the high volatility of dicamba, it is prone to off-target movement, and therefore has been of increased concern regarding dicamba drift onto nearby specialty crops. The present study evaluates twelve mid-Atlantic vegetable crops species for sensitivity to sub-lethal rates of dicamba. Soybean, snap bean, lima bean, tomato, eggplant, bell pepper, cucumber, summer squash, watermelon, pumpkin, sweet basil, lettuce, and kale were grown in the greenhouse and exposed to dicamba at 0, 0.056, 0.11, 0.28, 0.56, 1.12, 2.24 g ae ha−1, which is respectively 0, 1/10,000, 1/5,000, 1/2,000, 1/1,000, 1/500, and 1/250 of the maximum recommended label rate for soybean application (560 g ae ha−1). Vegetable crop injury was evaluated 4 weeks after treatment using visual rating methods and leaf deformation index (LDI) measurements. Overall, snap bean was the most sensitive crop species with dicamba rates as low as 0.11 g ae ha−1 resulting in significantly higher leaf deformation levels compared to the nontreated control. Other Fabaceae and Solanaceae species also demonstrated high sensitivity to sub-lethal rates of dicamba with rates ranging 0.28 to 0.56 g ae ha−1 causing higher leaf deformation compared to the nontreated control. While cucumber, pumpkin, and summer squash were no or moderately sensitive to dicamba, watermelon showed greater sensitivity with unique symptoms at rates as low as 0.056 g ae ha−1 based on visual evaluation. Within the range of tested dicamba rates, sweet basil, lettuce and kale demonstrated tolerance to dicamba with no injury observed at the maximum rate of 2.24 g ae ha−1.

Weed control remains a major challenge for economically viable grain sorghum production in the southeastern United States due to crop sensitivity to weed competition during early growth stages. Field experiments were conducted in 2012 and 2013 to determine the effects of grain sorghum row spacing, population density, and herbicide programs on Palmer amaranth control, crop growth, and grain yield. Treatments included row spacings of 19, 38, and 76 cm; grain sorghum population densities of 99,000, 198,000, 297,000, and 396,000 plants ha−1; and three herbicide programs: (1) a nontreated control, (2)S-metolachlor at 1,410 g ai ha−1plus atrazine at 1,820 g ha−1PRE, and (3)S-metolachlor at 1,070 g ha−1plus atrazine at 1,380 g ha−1PRE followed by 2,4 D at 330 g ha−1POST. Palmer amaranth control benefited from the addition of a POST herbicide and from crop density ≥297,000 plants ha−1. Under weedy conditions, Palmer amaranth density was not affected by narrower row spacing or increased crop density, whereas its dry biomass was reduced by 33% with 19 and 38 compared to 76 cm rows, and by 43% with ≥297,000 vs 99,000 plants ha−1. Row spacing had no effect on light interception by the crop canopy. However, crop density influenced canopy closure with maximum light interception occurring one and a half weeks earlier for density ≥297,000 plants ha−1. Yield increased by 18% for 19 vs 38 and 76 cm rows, whereas grain crop density had no effect. Overall, these results indicate that the combination of row spacing≤30 cm and crop density ≥297,000 plants ha−1provided at least 97% Palmer amaranth control in the absence of POST application and reduced its biomass by 32% in nontreated plots compared to 76 cm row spacing and crop density≤198,000 plants ha−1.

No abstract

Carolina redroot [Lachnanthes caroliniana (Lam.) Dandy] is a frequent weed of New Jersey cranberry (Vaccinium macrocarpon Aiton) bogs that competes with the crop for nutritional resources. Studies were conducted in 2018 to determine the effects of planting depth, soil moisture, lighting conditions, rhizome water content, and duration of rhizome submersion under water on L. caroliniana shoot emergence, vegetative growth, and rhizome development. Only planting depth greater than 12 cm significantly reduced shoot emergence (54%), biomass shoot and root production (27% and 65%, respectively), and rhizome formation (65%) compared with a 2-cm depth. Complete inhibition of new rhizome production was observed when the rhizome water content dropped to 30%. Soil moisture ≤30% decreased shoot biomass by ≥53% compared to 60% soil moisture, but marginally affected root biomass and had no impact on rhizome formation. Rhizome submersion for at least 120 d had minor effect on shoot emergence but reduced plant biomass by ≥28% and completely inhibited the formation of rhizomes. Finally, shading did not influence emergence but had a more dramatic effect on root and shoot biomass, which were reduced by 53% and 75%, respectively, and prevented the development of new rhizomes. This study demonstrates the plasticity of L. caroliniana to drought stress or long-lasting flooding conditions, therefore preventing consideration of cranberry bed temporary flooding or limitation of irrigation volume and frequency as viable management options. Sanding would not provide a layer of material sufficiently thick for reducing L. caroliniana shoot emergence. Reducing the quantity of light reaching the soil with black tarps or promoting rapid crop canopy closure are options that can complement the use of mesotrione for controlling L. caroliniana. Future research should address the practicality of these options, especially in bogs with low L. caroliniana pressure when early-summer weed regrowth occurs following dissipation of PRE herbicide activity.