Source: UNIVERSITY OF ARKANSAS submitted to NRP
INTEGRATED WEED MANAGEMENT FOR COTTON: DEVELOPING NEW TOOLS TO COMPLEMENT THE OLD
Sponsoring Institution
National Institute of Food and Agriculture
Project Status
ACTIVE
Funding Source
Reporting Frequency
Annual
Accession No.
1031896
Grant No.
2024-67014-41945
Cumulative Award Amt.
$294,000.00
Proposal No.
2023-07686
Multistate No.
(N/A)
Project Start Date
Apr 1, 2024
Project End Date
Mar 31, 2026
Grant Year
2024
Program Code
[A1811]- AFRI Commodity Board Co-funding Topics
Recipient Organization
UNIVERSITY OF ARKANSAS
(N/A)
FAYETTEVILLE,AR 72703
Performing Department
(N/A)
Non Technical Summary
We aim to develop novel tools for integrated weed management strategies for cotton, targeting the most problematic and/or most common weed species. These tools will supplement cover crops, improve the efficacy of herbicides, and provide another non-chemical tool for weed management that could reduce weed seedbank and curb herbicide-resistant weed evolution. The objectives are to: 1) evaluate the effect of trinexapac-ethyl (TE) on herbicide activity, weed fecundity and germination; 2) extend the residual activity of herbicides using soil adjuvants; 3) define microwave specific energies capable of inactivating weed seeds in soil while maintaining soil health in terms of fertility and beneficial microbes. Microwave application has not been exhaustively explored for weed management before. Preliminary data show some excellent cobinations of TE x Herbicide to manage Palmer amaranth and common lambsquarters. We will test two doses of TE and seven herbicides on four broadleaf species and six herbicides on four grass species. Two soil adjuvants and 12 soil-applied herbicides will be tested in two soil types. Our preliminarytests showed that microwave application can kill weedy rice seeds up to 6 cm soil depth. Microwave application did not affect the soil nutrient profile nor the microbial population. We will test microwave efficacy on ten key weeds, representing a wide range of seed types. This proposal is submitted to the commodity board topic A1811: Develop advanced integrated pest management (IPM) technologies and/or techniques that will complement and preserve current crop protection technologies/products for weeds in cotton, while simultaneously reducing the reliance on conventional pesticides.
Animal Health Component
50%
Research Effort Categories
Basic
(N/A)
Applied
50%
Developmental
50%
Classification

Knowledge Area (KA)Subject of Investigation (SOI)Field of Science (FOS)Percent
21317191140100%
Knowledge Area
213 - Weeds Affecting Plants;

Subject Of Investigation
1719 - Cotton, other;

Field Of Science
1140 - Weed science;
Goals / Objectives
The project goal is to develop tools to bolster integrated weed management of cotton, specifically to improve herbicide efficacy while simultaneously reducing weed seed production, germination, and the weed seedbank size. With microwave technology, our overall goal is to understand the efficacy and commercial viability of using microwaves of 915 MHz frequency in cotton fields before planting cotton, which accords deeper soil penetration and to understand variability in efficacy due to soil and weed properties.are:1. Evaluate the effect of TE on herbicide efficacy, weed fecundity, and seed germination capacity of major broadleaf and grass weed species in cotton.Hypothesis: The PGR trinexapac-ethyl can increase the efficacy of some post-emergence herbicides (i.e., glyphosate, flumioxazin, mesotrione, etc.) and reduce fecundity and seed viability of target weeds.2. Test the effect of novel soil adjuvants on the longevity of soil-applied herbicides and evaluate residual activity on fall-planted cover crops.Hypothesis: An appropriate soil adjuvant can extend the effective weed control of some soil-applied herbicides.3. Define microwave specific energies capable of inactivating weed seeds in the soil while maintaining soil health.Hypothesis: Microwave energy can heat the soil to a level that could kill weed seeds in the plow layer (upper 3-10 inches of soil), thereby reducing weed seed germination and weed infestation.
Project Methods
1.Trinexapac-ethyl (TE) andherbicide efficacy onbroadleaf and grass weedsofcotton, weed seed production and germination (Greenhouse).A two-factor factorial experiment will be conducted atSAREC, Fayetteville, AR. Factor A is herbicide (9 levels) and factor B is TE rate (0, 0.3, and 0.6 kg/ha) in 4 replications. Herbicide treatments:glyphosate, glufosinate, mesotrione, topramezone, flumioxazin, prometryn, 2,4-D, dicamba, and no herbicide. The broadleaf species:prickly sida,ivyleaf morningglory,common ragweed,spurred anoda, and Palmer amaranth. For grass weeds, the herbicides will include:glyphosate, glufosinate, topramezone, flumioxazin, prometryn, and clethodim.Grass species:barnyardgrass, goosegrass,Texas panicum, andItalian ryegrass.Data: Weed control 3 wkafter treatment (WAT);number of seeds per plant;and seed germination capacity. Seeds will be collected from survivors oftreatmentsand from nontreated plants. Seeds will be after-ripened. Fifty seeds per treatment, 3 replications, will be placed in Petri dishes lined with filter paper and moistened with 4 mL distilled water. The plates will be sealed and incubated under optimum conditionsand the germinated seeds counted after 14 d. The viability of non-germinated seeds will be checked using tetrazolium test. The germination test will be conducted twice. Total seedsper plant will be weighed and 500 seeds will be weighed to estimate the total number of seeds per plant.2. Trinexapac-ethyl (TE) andherbicide efficacy onbroadleaf and grass weedsofcotton, weed seed production and seed germination (Field Study).Broadleaf weeds: Fieldtests will be conducted at SAREC,Fayetteville in year 1 andyear 2. The test species will include: Palmer amaranth, common lambsquarters, prickly sida, common ragweed, andspurred anoda. The test will be conducted in a field naturally infested with Palmer amaranth and common lambsquarters. The other species will beoverseeded. Seeds will be mixed and spread across the field after land preparation. Cotton resistantto glyphosate, glufosinate, 2,4-Dand HHPD inhibitor herbicides will be planted between mid-April and mid-May. Grass species will be removed by overspraying the field with clethodim.The same herbicides and TE treatments as in the greenhouse studywill be applied, at4 wkafter planting cotton and atlayby. Plots will consist of 4 cotton rows, 36 in apart , 10 ft long. The treatments will be applied at 20 gal/A with recommended adjuvants. Each growth stage will be a separate experiment; the experimental design will be a split-plot randomized complete block with herbicide as the main factor and TE rate as the sub-factor.Grass weed test. Fieldtests will be conducted at SAREC, Fayetteville, AR in year 1 and 2. Weedspecies will include: barnyardgrass, goosegrass, and large crabgrass. The test will be conducted in a field naturally infested with barnyardgrass. Goosegrass and large crabgrass will be overseeded. A herbicide-resistantcotton varietywill be planted between mid-April and mid-May. Broadleaf species will be removed by overspraying the whole field with 2,4-D. The same herbicides and TE treatments as ingreenhouse grass testwill be appliedat: 4 wkafter planting or at layby. Plot size, experimental design, and herbicide application parameters will be the same as inthe broadleaf test.Data: Weed control 3 WAT,number of survivors, andseed production by species; seed germination capacity; and 5) cotton yield. Seed production will be estimated by quantifying seed rain on a 0.5 cm x 0.25 cm area attwo sites per plotusing a drop cloth. Before desiccating cotton, the weed canopy above the drop cloth will be shaken, and the cloth removed to retrieve weed seeds. Twoplants/plot per specieswill be harvested to quantify seeds remaining on the plant. The seeds will be weighed and seed numbers calculated by species. Germination capacity and seed viability will be evaluated as described previously.3.Extending the longevity of soil-active herbicides, for cotton and potential rotational crops, with soil adjuvants.A split-plot experimentwith four replications will be conductedinKibler and Rohwer, ARwherePalmer amaranth andEchinochloaspp. are the predominant species. Morningglory, prickly sida, common ragweed, spurred anoda, barnyardgrass, and large crabgrass will be seeded. This isa non-crop field experiment. The mainplot will be herbicide (13 levels) and the subplot will be soil adjuvant (3 levels) (Table 1). Improved formulations of a soil adjuvant (Anomynous 2023) will be tested: 1) ORO-RZ (2 pt/A), 2) OR369A (2 pt/A), and 3) no soil adjuvant. The treatments will be applied at 20 gal/A. The field will be irrigated at 0.5 A-inch after land preparation and weed seeding. The treatments will be applied 24 hr later. Soil sample will be collected at the time of herbicide application to determine soil moisture. Soil sample will also be submitted to the Soil testing facility of the University of Arkansas for soil texture analysis. The plot size will be 20 ft x 5 ft. Vegetation in the whole field will be desiccatedafter each evaluation time and once monthly thereafter, until Fall. In October, thefield will be no-till planted with a paired strip of cereal rye and Austrian winterpea cover crops perpendicular to theplot orientation to evaluate residual effect of treatments on fall-planted cover crops.Table 1.Herbicides, for cotton and rotational crops, to be tested with soil adjuvants.Common nameRate, medium texture soil (kg ai/ha)Common nameRate, medium texture soil (kg ai/ha)prometryn0.840sulfentrazone0.225metribuzin0.560pendimethalin0.930fluridone0.168chlorimuron0.009mesotrione0.224imazethapyr0.071flumioxazin0.071pyroxasulfone1.430oxyfluorfen0.560acetochlor1.456no herbicideData:density of major weed species 3, 6, 9, and 12 WAT; control of major weed species and overall weed control 3, 6, 9, and 12 WAT; injury on rye and Austrian winter pea 4 wk from planting; and dry shoot biomass of cover crops 8 wkfrom planting. Weeds will be counted in a 0.25-m x 0.25-m quadrat. Shoots of cover crops will be cut at ground level from 0.25-m x 0.25-m quadrat, oven-dried, and weighed.4. Evaluation of microwave energy (MW) for killing weed seeds in soilTen weed specieswill be tested (Table 2). These species represent seeds of different types. MW will tested at different weed seed density and differentsoil depthand soil physicochemical properties. Field soil naturally infested withPalmer amaranth and barnyardgrass will be collected from Kibler and Rohwer. Soil (same weight; 40% moisture, wet basis) will be placed in 6-inch diameter, 8-inch deep pots. Seeds of other species will be placed at different depths and densities. Palmer amaranth and barnyardgrass will be seeded separately into non-infested soil from each location to assess MW efficacy on these species at various depths.After MW treatment, the treated soil will be transferred into rectangular trays, which will be kept in the greenhouse to evaluate weed seed germination. Emerged seedlings will be counted by species at 15 and 30 d after treatment. Seedlings will be removed after counting. The remaining weed seeds will be recovered by washing the soil through a series of sieves of decreasing size and tested for viability.Table 2. Microwave treatments to be conducted at room temperature (23-25 °C)FactorsLevelsSpeciesPalmer amaranth, common lambsquarters, ivyleaf morningglory, prickly sida, common ragweed, spurred anoda, barnyardgrass, goosegrass, Italian ryegrass, and Texas panicumWeed seed density (no. of viable seeds/m2soil up to 12 inch depth)Low (<1000), medium (1000-5000), high (>5000)Soil depth (inches)3, 6, 9, 12Soil properties (temperature, moisture, bulk density, soil type)combinations will be tested to cover the range of the physicochemical propertiesMicrowave power (kW)10, 20, 30Exposure duration (sec)30, 60, 90Replication3; conducted twice

Progress 04/01/24 to 03/31/25

Outputs
Target Audience:1. Organic crop production researchers and weed scientists who are looking for alternative methods for nonchemical weed control as it pertains to using microwave to kill weed seeds. 2. Colleagues and private agriculture machinery enterprise from Brazil who want to collaborate on developing a field prototype for microwave application. 3. Those who are in the professional weed science society circle - as it pertains to late-season weed control to reduce weed seed deposit. Changes/Problems:One change that we had to make was to conduct separate experiments to evaluate the cotton response from the weed response. In the proposal, cotton was to be planted in a field infested with various key weeds. It became apparent that conducting the test like this would compromise our ability to evaluate the treatment effects well. Therefore, in 2024, we conducted four weed tests without cotton (grass - early timing, grass late- timing, broadleaf - early timing, and broadleaf - late timing). This turned out to be a better approach. In 2025, the weed tests will be repeated and the cotton response tests will be conducted in a field maintained free of weeds. What opportunities for training and professional development has the project provided?The post-doctoral associate and graduate students attended professional conferences and presented posters of preliminary data. These personnel were trained on how to collect soil samples for this research, prepare samples for MW treatment, how to implement the treatments, and how to conduct seed germination test in the greenhouse. Personnel were also trained on how to identify the weed species present. During the process of planning the experiments and data analysis, research personnel were trained on experimental design and data analysis as it applies to this experiment. How have the results been disseminated to communities of interest?Preliminary results were shared to potential collaborators and current producer collaborators to strengthen awareness and encourage continued support for this project. What do you plan to do during the next reporting period to accomplish the goals?1.Objective 1: Repeat the field experiments on grass and broadleaf weeds. Evaluate seed production and conduct seed germination tests. In the fall, conduct the first batch of greenhouse experiment to evaluate the effect of herbicide x TE treatments on key weeds that did not establish at sufficient levels in the field. Among these are: barnyardgrass, large crabgrass, broadleaf signalgrass, hemp sesbania, common ragweed, and pale smartweed. This series of greenhouse experiments will start with hemp sesbania in the fall 2025. Two field experiments will be conducted on weed-free cotton to evaluate TE x herbicide combinations at two growth stages: 4-leaf and close to layby. 2. Objective 2: The first batch of soil adjuvant x residual herbicidetest will be conducted in the greenhouse in the fall 2025 using Palmer amaranth as bioassay species. 3. Objective 3: Microwave treatments will be evaluated on other target weed species, grass and broadleaf, representing different seed sizes and hardness of seed coat.

Impacts
What was accomplished under these goals? Objective 1:Assess the effect of trinexapac-ehtyl (TE) on the efficacy of multiple herbicides on yellow foxtail (YF, Setaria pumila), broadleaf signalgrass (BS, Brachiaria platyphylla), southwestern cupgrass (SC, Eriochloa acuminata) and barnyardgrass (BG, Echinochloa crus-galli). A field study was conducted in 2024 at SAREC, University of Arkansas, where grass species were sown in 120 ft2 plots. This experiment followed a split plot-design with four replications. The treatments included TE (0, 0.534 lb/A) in mixture with the following herbicides: glyphosate (0.5, 0.65 lb/A), glufosinate-ammonium (0.32, 0.64 lb/A), flumioxazin (0.031, 0.062 lb/A), topramezone (0.009, 0.018 lb/A), clethodim (0.125,0.25 lb/A), quizalofop (0.031, 0.063 lb/A) and prometryn (0.8,1.6 lb/A). Herbicides were sprayed at 12-inch weeds (Study 1) and near-reproductive stage (Study 2). Visible control (%) was evaluated at to 21 d after treatment (DAT). Optimum differentiation of treatments was obsereved at 21 DAT, TE did not increase the efficacy of clethodim. Glufosinate-ammonium and glyphosate controlled all species 100% at the rates used. Prometryn controlled grass species 5-25% without TE. The efficacy of prometryn on BG and FT increased by 30% points with the addition of TE and increased by 40-50% points on SC and BS. TE also increased the activity of quizalofop by 20-30% points on BG, YF, and SC and 15% points on BS. Grass control with topramezone increased 35-35% for BY, YF and SC and 40-50% for BS. the mixture of TE with flumioxazin was synergistic, showing 50 - 60% improved in control of all species 21 DAT. While only glyphosate and glufosinate had 100% grass control, the increased control levels with TE mixture would likely reduce seed input into the seedbank. These results suggest that trinexapac-ethyl improves the activity of flumioxazin, topramezone, quizalofop, and prometryn on grass weeds. Further studies will evaluate the profitability of these mixtures. Twnety-eight TE x herbicide combinations were also tested on braodleaf weed species. These included Palmer amaranth, velvetleaf, prickly sida, and hemp sesbania. Weeds were harvested from up to 10 plants per plot for Palmer amaranth and velvetleaf. The other two species did not have reproductive plants in the majority of plots. Seed germination tests are on-going. Objective 2. Evaluation of the interaction of soil conditioners with residual herbicides. This experiment will be conducted as soon as activities for objective 1 wind down. Objective 3. Evaluation of microwave energy to kill weed seeds. Soil sampling.Silt loam and clay loam soil were collected from the University of Arkansas Division of AgricultureVegetable Research Station at Kibler, AR and from a rice/cotton field in Marion, AR, respectively. The soil samples were placed in sealed containers, then conditioned to approximately 20-25% soil moisture content (wet basis) to mimic soil moisture in crop fields before sowing. Microwave treatment.The industrial MW dryer (Model No. AMT2448.05, Industrial Microwave Systems, AMTEK, Cedar Rapids, IA) was used. The unit was operated at a 915 MHz frequency and consisted of 75 kW generator, 48-inch (121.9 cm) length drying oven, and a console for its operation. Soil to be treated was transferred to a polypropylene tray and a 4 in by 8 in a desired soil depth before treatment. Before each treatment, 25 seeds of junglerice weed were placed uniformly on 0.5 in of soil before piling up to the 3-in (7.6 cm) of soil depth. The initial seed germination of junglerice was 88%. Soil surface temperature was measured immediately after microwave treatment. After treatment, soil was mixed using a spatula, allowed to cool for 2 min, placed in plastic bags, then placed in trays in the greenhouse to evaluate germination. Experimental design. Seven levels of microwave treatment (factor #1) were tested with 6 factorial combinations of 3 power levels and 2 treatment durations. Control sample with no microwave treatment was the the 7th treatment. Two soil types (factor #2), silt loam and clay loam were included in the experiments. Soil depth was fixed to 3 in (7.6 cm). Seed germination assay in the greenhouse. The treated and nontreated soil samples were placed in 2-inch-deep containers with drainage holes at the bottom. The soil in containers was soaked in water to full saturation and then drained to 'field water holding capacity'. Weed emergence was assessed over three weeks (21 days). Emerged weeds were counted on day 7, 14 and 21; seedlings were removed after each count and the soil in each container was thoroughly mixed on day 7 and 14 to facilitate germination of all viable, non-dormant seeds. All emerged species were identified visually and counted as germinated. After the final count of germination, the total number of germinated seeds was normalized to account for the variability in initial level of infestation in soil samples. This is because the field soil is expected to have some natural infestation of junglerice. The level of seedling emergence was compared by calculating the total germinability index (TGI) Data Analyses.Data were subjected to analysis of variance (ANOVA) using JMP Pro 18 statistical software (JMP Pro 18, SAS Institute, Cary, NC) using a 4-factor factorialcompletely randomization design. The normality of data and homogeneity of variance were examined. The ANOVA was conducted to test the effect of microwave treatment, depth of seed placement and soil type and their interactions on the total germinability index and soil surface temperature. Student's t-test was used to compare the levels of each factor at at a 95% confidence level. Results: The effect of microwave treatment on TGI and soil surface temperature (SST) was significant but soil type and the interaction of these factors were not significant. The microwave treatment 10 kW for 30 sec raised the SST of silt loam soil by around 60 C - 70 C relative to the nontreated.The heating of soil surface with the lowest microwave energy level approached that of higher-energy treatments when the duration of exposure was extended to 60 sec.The treatment using any power levels for 60 sec consistently demonstrated the lowest TGI significantly reduced weed seed germination compared to the other microwave treatment levels. This suggests that longer exposures even at lowest power level are more effective at inhibiting weed seed germination. The control group, which did not receive any microwave treatment, had the highest TGI. The soil type did not significantly alter the outcomes, indicating a broad applicability of this method across different soil conditions. Furthermore, the interaction between microwave treatment and soil type showed no significant impact on TGI and SST, underscoring the consistency of microwave treatment effectiveness irrespective of soil variance.

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