Effect of carrier volume and spray quality on glyphosate-resistant soybean response to sublethal dicamba exposure.

BACKGROUND: Field experiments were conducted across three sites in Mississippi in 2018 to evaluate carrier volume and spray quality effects on glyphosate-resistant soybean response to dicamba. Treatments consisted of dicamba (5.6 g a.e. ha-1 ) plus glyphosate (8.7 g a.e. ha-1 ) applied to soybean at R1 using 140, 105, 70, 35, 14, or 7 L ha-1 . Each carrier volume was applied with TT11002 and XR110015 nozzles which resulted in Fine and Coarse spray qualities, respectively. A colorimetric dye was included in spray solutions to quantify spray coverage of each treatment. RESULTS: Spray coverage decreased with carrier volume and ranged from 21% to 3%. Conversely, soybean injury increased as carrier volume decreased. Soybean height 14 days after treatment (DAT) was reduced 34% to 37% from carrier volumes of 70 to 140 L ha-1 ; however, carrier volumes of 14 and 7 L ha-1 resulted in 45% height reductions. By 28 DAT soybean height was similar among volumes of 35 to 140 L ha-1 (39% to 42% reduction); however, volumes of 14 and 7 L ha-1 resulted in 46% and 51% reductions, respectively. Grain yield was reduced 14% from treatment at 140 L ha-1 and reductions increased with decreased carrier volume to 41% loss at 7 L ha-1 . Averaged across carrier volumes, Fine and Coarse sprays caused 30% and 26% yield loss, respectively. CONCLUSION: These data suggest that carrier volume profoundly affects soybean response to dicamba. Therefore, soybean response to sublethal dicamba doses applied at a constant carrier volume may not reflect physical drift exposure. © 2021 Society of Chemical Industry.

Influence of flooding period and seed burial depth on Palmer amaranth (Amaranthus palmeri) seed germination.

BACKGROUND: Flooding throughout fall and winter months is an effective practice for rice (Oryza sativa L.) straw decomposition, soil seedbank depletion, and waterfowl habitat in Mississippi. Nevertheless, limited research is available regarding the effects of fall-winter flooding and seed burial depth on Palmer amaranth (Amaranthus palmeri S. Wats.) seed germination. The objective of this study was to evaluate the effect of flooding period and seed burial depth on A. palmeri seed damage and germination in three different soil textures in Mississippi. RESULTS: Amaranthus palmeri seed damage was greater when seeds were buried in sandy loam compared to silt loam soil textures. An interaction between flooding period and seed burial depth was present for A. palmeri seed germination. Flooding periods of 1-month (at 0 and 15 cm burial depth) and 2 months (at 0 cm burial depth) provided similar A. palmeri seed germination compared to no-flooding (at 0 cm burial depth). In addition, flooding periods of 3, 4, and 5 months reduced A. palmeri seed germination by 10, 10 and 14 percentage points at 0 cm burial depth, and 36, 40, and 41 percentage points when seeds were buried at 15 cm, respectively, across all soil textures. CONCLUSION: This research demonstrates that flooding for 3, 4, and 5-months throughout fall and winter is an effective cultural practice to increase soil seedbank depletion through reduced germination potential to help manage herbicide-resistant A. palmeri populations in sandy loam, silt, and silt loam soil textures. © 2020 Society of Chemical Industry.

Resistance to clethodim in Italian ryegrass (Lolium perenne ssp. multiflorum) from Mississippi and North Carolina.

BACKGROUND: Clethodim, an acetyl-CoA carboxylase (ACCase)-inhibiting herbicide, is one of the few postemergence chemical control options available to growers of Mississippi to manage glyphosate and/or other herbicide resistant Italian ryegrass populations. Recently, clethodim failed to adequately control Italian ryegrass populations across Mississippi. A sethoxydim, also an ACCase inhibitor, -resistant Italian ryegrass population from North Carolina was cross-resistant to clethodim. This research characterized the magnitude and mechanisms of clethodim resistance in the Mississippi and North Carolina Italian ryegrass populations via whole-plant herbicide dose response, cross resistance, and metabolism studies, and molecular analysis. RESULTS: Two clethodim-resistant biotypes from Mississippi, MS24 and MS37, were 10- and 4-fold resistant, respectively, relative to a susceptible (SUS1) biotype. A North Carolina biotype, NC21, was 40-fold resistant to clethodim compared to SUS1. Two additional biotypes from North Carolina, NC22 and NC 23, recorded shoot dry weight reduction of only 17-30% of nontreated at the highest clethodim dose of 2.17 kg ha-1 , (8×). The NC22 biotype was cross-resistant to sethoxydim, fluazifop, quizalofop, and pinoxaden. Metabolic inhibitors such as piperonyl butoxide and 4-chloro-7-nitrobenzofurazan did not affect resistance of MS37, MS51, and NC22 biotypes to fenoxaprop, clethodim, or pinoxaden. The MS37 biotype had three target site mutations, I2041N, C2088R, and G2096A. Another clethodim-resistant biotype from Mississippi, MS51, had only the C2088R substitution. The NC22 and NC23 biotypes had I1781L, I2041N, and D2078G replacements. CONCLUSION: This study shows that the mechanism of resistance to clethodim in Italian ryegrass from Mississippi and North Carolina is due to target site modifications in the ACCase gene leading to broad cross-resistance to other ACCase-inhibiting herbicides. Published 2019. This article is a U.S. Government work and is in the public domain in the USA.

Transcriptomic changes in Echinochloa colona in response to treatment with the herbicide imazamox.

MAIN CONCLUSION: Presented here is the first Echinochloa colona leaf transcriptome. Analysis of gene expression before and after herbicide treatment reveals that E. colona mounts a stress response upon exposure to herbicide. Herbicides are the most frequently used means of controlling weeds. For many herbicides, the target site is known; however, it is considerably less clear how plant gene expression changes in response to herbicide exposure. In this study, changes in gene expression in response to herbicide exposure in imazamox-sensitive (S) and- resistant (R) junglerice (Echinochloa colona L.) biotypes was examined. As no reference genome is available for this weed, a reference leaf transcriptome was generated. Messenger RNA was isolated from imazamox-treated- and untreated R and S plants and the resulting cDNA libraries were sequenced on an Illumina HiSeq2000. The transcriptome was assembled, annotated, and differential gene expression analysis was performed to identify transcripts that were upregulated or downregulated in response to herbicide exposure for both biotypes. Differentially expressed transcripts included transcription factors, protein-modifying enzymes, and enzymes involved in metabolism and signaling. A literature search revealed that members of the families represented in this analysis were known to be involved in abiotic stress response in other plants, suggesting that imazamox exposure induced a stress response. A time course study examining a subset of transcripts showed that expression peaked within 4-12 h and then returned to untreated levels within 48 h of exposure. Testing of plants from two additional biotypes showed a similar change in gene expression 4 h after herbicide exposure compared to the resistant and sensitive biotypes. This study shows that within 48 h junglerice mounts a stress response to imazamox exposure.

EPSPS amplification in glyphosate-resistant spiny amaranth (Amaranthus spinosus): a case of gene transfer via interspecific hybridization from glyphosate-resistant Palmer amaranth (Amaranthus palmeri).

BACKGROUND: Amaranthus spinosus, a common weed of pastures, is a close relative of Amaranthus palmeri, a problematic agricultural weed with widespread glyphosate resistance. These two species have been known to hybridize, allowing for transfer of glyphosate resistance. Glyphosate-resistant A. spinosus was recently suspected in a cotton field in Mississippi. RESULTS: Glyphosate-resistant A. spinosus biotypes exhibited a fivefold increase in resistance compared with a glyphosate-susceptible biotype. EPSPS was amplified 33-37 times and expressed 37 times more in glyphosate-resistant A. spinosus biotypes than in a susceptible biotype. The EPSPS sequence in resistant A. spinosus plants was identical to the EPSPS in glyphosate-resistant A. palmeri, but differed at 29 nucleotides from the EPSPS in susceptible A. spinosus plants. PCR analysis revealed similarities between the glyphosate-resistant A. palmeri amplicon and glyphosate-resistant A. spinosus. CONCLUSIONS: Glyphosate resistance in A. spinosus is caused by amplification of the EPSPS gene. Evidence suggests that part of the EPSPS amplicon from resistant A. palmeri is present in glyphosate-resistant A. spinosus. This is likely due to a hybridization event between A. spinosus and glyphosate-resistant A. palmeri somewhere in the lineage of the glyphosate-resistant A. spinosus plants. Published 2014. This article is a U.S. Government work and is in the public domain in the USA.

Physiological and molecular basis of acetolactate synthase-inhibiting herbicide resistance in barnyardgrass (Echinochloa crus-galli).

Barnyardgrass biotypes from Arkansas (AR1 and AR2) and Mississippi (MS1) have evolved cross-resistance to imazamox, imazethapyr, and penoxsulam. Additionally, AR1 and MS1 have evolved cross-resistance to bispyribac-sodium. Studies were conducted to determine if resistance to acetolactate synthase (ALS)-inhibiting herbicides in these biotypes is target-site or non-target-site based. Sequencing and analysis of a 1701 base pair ALS coding sequence revealed Ala122 to Val and Ala122 to Thr substitutions in AR1 and AR2, respectively. The imazamox concentrations required for 50% inhibition of ALS enzyme activity in vitro of AR1 and AR2 were 2.0 and 5.8 times, respectively, greater than the susceptible biotype. Absorption of ¹4C-bispyribac-sodium, -imazamox, and -penoxsulam was similar in all biotypes. ¹4C-Penoxsulam translocation out of the treated leaf (≤2%) was similar among all biotypes. ¹4C-Bispyribac-treated AR1 and MS1 translocated 31- 43% less radioactivity to aboveground tissue below the treated leaf compared to the susceptible biotype. ¹4C-Imazamox-treated AR1 plants translocated 39% less radioactivity above the treated leaf and aboveground tissue below the treated leaf, and MS1 translocated 54 and 18% less radioactivity to aboveground tissue above and below the treated leaf, respectively, compared to the susceptible biotype. Phosphorimaging results further corroborated the above results. This study shows that altered target site is a mechanism of resistance to imazamox in AR2 and probably in AR1. Additionally, reduced translocation, which may be a result of metabolism, could contribute to imazamox and bispyribac-sodium resistance in AR1 and MS1.