Absorption, Translocation, and Metabolism of Halosulfuron in Cucumber, Summer Squash, and Selected Weeds

Greenhouse studies were conducted to investigate the absorption, translocation, and metabolism of foliar-applied [14C]halosulfuron-methyl in cucumber, summer squash, pitted morningglory, and velvetleaf. Cucumber and summer squash were treated at the 4-leaf stage, whereas velvetleaf and pitted morningglory were treated at 10 cm. All plants were collected at 4, 24, 48, and 72 h after treatment (HAT) for absorption and translocation studies and an additional 96-HAT interval was included in the metabolism study. Absorption did not exceed 45% in summer squash, whereas it plateaued around 60% in velvetleaf and cucumber and reached 80% in pitted morningglory 72 HAT. None of the four species translocated more than 23% of absorbed halosulfuron out of the treated leaf. Translocation in cucumber and summer squash was predominantly basipetal, while acropetal movement prevailed in velvetleaf. No significant direction of movement was observed for pitted morningglory. Negligible translocation occurred toward the roots, regardless of plant species. Of the total amount of [14C]halosulfuron-methyl absorbed into the plants at 96 HAT, more than 80% remained in the form of the parent compound in velvetleaf, summer squash, and pitted morningglory, whereas less than 20% was detected in cucumber. Rapid and high herbicide metabolism may explain cucumber tolerance to halosulfuron-methyl, while lack of metabolism contributes to summer squash and velvetleaf susceptibility. Pitted morningglory tolerance may be due to limited translocation associated with some level of metabolism, but further research would be needed to investigate other potential causes. Nomenclature: Halosulfuron-methyl; cucumber, Cucumis sativus L.; field pumpkin, Cucurbita pepo L.; pitted morningglory, Ipomoea lacunosa L. IPOLA; velvetleaf, Abutilon theophrasti Medik. ABUTH.

[1]  P. Westra,et al.  Halosulfuron Absorption, Translocation, and Metabolism in White and Adzuki Bean , 2016, Weed Science.

[2]  W. Vencill,et al.  Herbicide Absorption and Translocation in Plants using Radioisotopes , 2015, Weed Science.

[3]  R Core Team,et al.  R: A language and environment for statistical computing. , 2014 .

[4]  Christian Ritz,et al.  Nonlinear Regression Analysis of Herbicide Absorption Studies , 2011, Weed Science.

[5]  H. P. Wilson,et al.  Control of Yellow Nutsedge (Cyperus esculentus) and Smooth Pigweed (Amaranthus hybridus) in Summer Squash with Halosulfuron , 2008, Weed Technology.

[6]  H. P. Wilson,et al.  Halosulfuron Helps Control Several Broadleaf Weeds in Cucumber And Pumpkin , 2007 .

[7]  D. W. Monks,et al.  Sweetpotato Tolerance to Halosulfuron Applied Postemergence , 2007, Weed Technology.

[8]  Yong-song Zhang,et al.  Action mechanisms of acetolactate synthase-inhibiting herbicides ☆ , 2007 .

[9]  J. Norsworthy,et al.  Tolerance Of Cantaloupe To Postemergence Applications Of Rimsulfuron And Halosulfuron , 2007, Weed Technology.

[10]  D. W. Monks,et al.  Response of Five Summer-Squash (Cucurbita pepo) Cultivars to Halosulfuron1 , 2006, Weed Technology.

[11]  A. Culpepper,et al.  Halosulfuron has a variable effect on cucurbit growth and yield , 2005 .

[12]  J. S. McElroy,et al.  Absorption, translocation, and metabolism of halosulfuron and trifloxysulfuron in green kyllinga (Kyllinga brevifolia) and false-green kyllinga (K. gracillima) , 2004, Weed Science.

[13]  S. Powles,et al.  Inheritance and mechanism of resistance to herbicides inhibiting acetolactate synthase in Sonchus oleraceus L. , 1995, Theoretical and Applied Genetics.

[14]  R. Richardson,et al.  Absorption, translocation, and metabolism of CGA 362622 in cotton and two weeds , 2003, Weed Science.

[15]  A. Culpepper,et al.  Response of Squash and Cucumber Cultivars to Halosulfuron1 , 2003, Weed Technology.

[16]  R. Harvey,et al.  Yellow Nutsedge (Cyperus esculentus) and Annual Weed Control in Glyphosate-Resistant Field Corn (Zea mays)1 , 2002, Weed Technology.

[17]  KAREN A. RENNER,et al.  Yellow Nutsedge (Cyperus esculentus) Control and Tuber Production with Glyphosate and ALS-Inhibiting Herbicides1 , 2002, Weed Technology.

[18]  E. Santen,et al.  Nontuberous Sedge and Kyllinga Species' Response to Herbicides1 , 2002 .

[19]  S. Askew,et al.  Absorption, translocation, and metabolism of foliar-applied CGA 362622 in cotton, peanut, and selected weeds , 2002, Weed Science.

[20]  J. Masiunas,et al.  Evaluation of Herbicides for Pumpkin (Cucurbita spp.)1 , 2002, Weed Technology.

[21]  F. Yelverton,et al.  Purple (Cyperus rotundus) and Yellow Nutsedge (C. esculentus) Control in Bermudagrass (Cynodon dactylon) Turf1 , 2000 .

[22]  S. E. Hart,et al.  Physiological response of soybean (Glycine max) and two weed species to thifensulfuron and bentazon combinations , 1999, Weed Science.

[23]  T. C. Mueller,et al.  Absorption, translocation, and metabolism of primisulfuron and nicosulfuron in broadleaf signalgrass (Brachiaria platyphylla) and corn , 1999, Weed Science.

[24]  H. Fujiwara,et al.  Metabolism of halosulfuron-methyl by corn and wheat , 1997 .

[25]  C. Mallory-Smith,et al.  Altered acetolactate synthase activity in ALS-inhibitor resistant prickly lettuce (Lactuca serriola) , 1997, Weed Science.

[26]  J. Carey,et al.  Physiological basis for nicosulfuron and primisulfuron selectivity in five plant species , 1997, Weed Science.

[27]  J. W. Wilcut,et al.  Effect of MON-12037 on Purple (Cyperus rotundus) and Yellow (Cyperus esculentus) Nutsedge , 1995, Weed Technology.

[28]  H. M. Brown,et al.  Basis for soybean tolerance to thifensulfuron methyl. , 1990 .

[29]  S. G. Carmer,et al.  Least significant differences for combined analyses of experiments with two- or three-factor treatment designs , 1989 .

[30]  M. Patterson,et al.  Absorption, Translocation, and Metabolism of Foliar-Applied Chlorimuron in Soybeans (Glycine max), Peanuts (Arachis hypogaea), and Selected Weeds , 1989, Weed Science.

[31]  J. Pelletier Chemical weed control in vegetable crops. , 1986 .