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Susceptibility of Arkansas Palmer amaranth accessions to common herbicide sites of action

Published online by Cambridge University Press:  26 May 2020

Fidel González-Torralva*
Affiliation:
Postdoctoral Fellow, Department of Crop, Soil, and Environmental Sciences, University of Arkansas, Fayetteville, AR, USA
Jason K. Norsworthy
Affiliation:
Distinguished Professor and Elms Farming Chair of Weed Science, Department of Crop, Soil, and Environmental Sciences, University of Arkansas, Fayetteville, AR, USA
Leonard B. Piveta
Affiliation:
Program Associate, Department of Crop, Soil, and Environmental Sciences, University of Arkansas, Fayetteville, AR, USA
Vijay K. Varanasi
Affiliation:
Former Postdoctoral Research Associate, Department of Crop, Soil, and Environmental Sciences, University of Arkansas, Fayetteville, AR, USA
Tom Barber
Affiliation:
Professor, Department of Crop, Soil, and Environmental Sciences, Lonoke Agricultural Center, University of Arkansas, Lonoke, AR, USA
Chad Brabham
Affiliation:
Former Postdoctoral Research Associate, Department of Crop, Soil, and Environmental Sciences, University of Arkansas, Fayetteville, AR, USA
*
Author for Correspondence: Fidel González-Torralva, Altheimer Laboratory, 1366 West Altheimer Drive, Fayetteville, AR72704. Email: [email protected]
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Abstract

Palmer amaranth is one of the most difficult-to-control weeds in row crop systems and has evolved resistance to several herbicide sites of action (SOAs). A late-season weed-escape survey had been conducted earlier to determine the distribution of protoporphyrinogen oxidase–inhibitor resistant Palmer Amaranth in Arkansas. The objective of this study was to evaluate the susceptibility of Arkansas Palmer amaranth accessions to commonly used herbicide SOAs. The SOAs evaluated were group 2 + 9, 3, 4, 5, 10, 14, 15, and 27, and the representative herbicide from each group was imazethapyr + glyphosate (79 + 860 g ha−1), trifluralin (1,120 g ha−1), dicamba (280 and 560 g ha−1), atrazine (560 g ha−1), glufosinate (594 g ha−1), fomesafen (395 g ha−1), S-metolachlor (1,064 g ha−1), and tembotrione (92 g ha−1), respectively. Palmer amaranth mortality varied among accessions across SOAs. Averaged across accessions, the mortality rates, by treatment in order from lowest to highest, were as follows: glyphosate + imazethapyr (16%), tembotrione (51%), dicamba at 280 g ha−1 (51%), fomesafen (76%), dicamba at 560 g ha−1 (82%), atrazine (85%), trifluralin (87%), S-metolachlor (96%), and glufosinate (99.5%). This study provides evidence that Palmer amaranth accessions with low susceptibility to glyphosate + imazethapyr, fomesafen, and tembotrione are widespread throughout Arkansas. Of the remaining SOAs, most Palmer amaranth accessions were sensitive; however, within each herbicide SOA, except glufosinate, control of some accessions was less than expected and resistance is suspected.

Type
Note
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
© Weed Science Society of America, 2020

Introduction

The evolution and spread of herbicide-resistant weeds are partially driven by herbicide use pattern (Kniss Reference Kniss2018). This can be exemplified by the change in soybean [Glycine max (L.) Merr.] herbicide use patterns in the southern United States for control of herbicide-resistant Palmer amaranth. Before the development of glyphosate-resistant crops, acetolactate synthase (ALS; Group 2) and microtubule polymerization-inhibiting (MT; Group 3) herbicides were the primary site of action (SOA) used to control Palmer amaranth (Gossett et al. Reference Gossett, Murdock and Toler1992; Kniss Reference Kniss2018; Webster and Coble Reference Webster and Coble1997). By 2000, glyphosate (Group 9) became the dominant herbicide used, mainly because of its simplicity and effectiveness in glyphosate-resistant crops and the prevalence of ALS- and MT-resistant Palmer amaranth (Dill et al. Reference Dill, CaJacob and Padgette2008). Glyphosate-resistant Palmer amaranth was initially confirmed in 2005, and by 2009, nearly all soybean-producing states in the southern United States were infested with glyphosate-resistant accessions (Heap Reference Heap2020). Subsequently, protoporphyrinogen oxidase (PPO)-inhibiting herbicides (Group 14) became a common PRE and POST option for Palmer amaranth control (Riar et al. Reference Riar, Norsworthy, Steckel, Stephenson, Eubank and Scott2013), which eventually lead to PPO resistance in Palmer amaranth being confirmed in the mid-southern United States (Copeland et al. Reference Copeland, Giacomini, Tranel, Montgomery and Steckel2018; Varanasi et al. Reference Varanasi, Brabham, Norsworthy, Nie, Young, Houston, Barber and Scott2018).

Herbicide resistance is often a chronic trait, even in the absence of selection; thus, it is not surprising that reports of Palmer amaranth resistant to multiple SOAs are frequent. In response, industry has developed new herbicide-resistant traits to enable the use of alternative SOAs for control of herbicide-resistant Palmer amaranth and other troublesome weeds. Enlist™ (Pioneer, Johnson, IA) and Xtend® (Asgrow, Monmouth, IL) soybean and cotton (Gossypium hirsutum L.) cultivars are now commercially available and are resistant to auxinic herbicides (Group 4) such as 2,4-D or dicamba (Behrens et al. Reference Behrens, Mutlu, Chakraborty, Dumitru, Jiang, LaVallee, Herman, Clemente and Weeks2007; Wright et al. Reference Wright, Shan, Walsh, Lira, Cui, Song, Zhuang, Arnold, Lin, Yau, Russell, Cicchillo, Peterson, Simpson, Zhou, Ponsamuel and Zhang2010). Unique traits that confer resistance to 4-hydroxyphenylpyruvate dioxygenase (HPPD)-inhibiting herbicides (Group 27) such as isoxaflutole are now available in soybean and will soon be available in cotton (Dreesen et al. Reference Dreesen, Capt, Oberdoerfer, Coats and Pallett2018; Hawkes et al. Reference Hawkes, Langford, Viner, Vernooij and Dale2010). In addition, with the evolution and widespread occurrence of glyphosate-resistant weeds in soybean-producing regions of the United States, the utility of glyphosate on weeds like Palmer amaranth is becoming limited. Thus, it would be expected that crop traits that allow for in-crop use of glufosinate (Group 10) will increase in coming years. In the coming decade, a combination of herbicide-resistant traits in cotton and soybean, all of which enable the use of glufosinate, will likely be commercialized to improve control of herbicide-resistant weed populations (Gage et al. Reference Gage, Krausz and Walters2019; Nandula Reference Nandula2019), albeit multiple herbicide resistance could jeopardize the utility of technologies involving multiple traits.

Herbicide resistance in Palmer amaranth is a significant issue and resistance surveys are commonly used to determine the geographic magnitude of resistance (Bagavathiannan and Norsworthy Reference Bagavathiannan and Norsworthy2016; Bond et al. Reference Bond, Oliver and Stephenson2006; Copeland et al. Reference Copeland, Giacomini, Tranel, Montgomery and Steckel2018; Garetson et al. Reference Garetson, Singh, Singh, Dotray and Bagavathiannan2019; Kumar et al. Reference Kumar, Liu and Stahlman2020; Singh et al. Reference Singh, Roma-Burgos, Singh, Alcober, Salas-Perez and Shivrain2018; Varanasi et al. Reference Varanasi, Brabham, Norsworthy, Nie, Young, Houston, Barber and Scott2018; Wise et al. Reference Wise, Grey, Prostko, Vencill and Webster2009). Alternatively, the efficacy of SOAs can be determined through resistance surveys, which can aid the development and evaluation of current weed management programs (Beckie et al. Reference Beckie, Heap, Smeda and Hall2000; Burgos et al. Reference Burgos, Tranel, Streibig, Davis, Shaner, Norsworthy and Ritz2013). Previous Palmer amaranth resistance surveys in Arkansas revealed widespread resistance to glyphosate, ALS-, and PPO-inhibiting herbicides (Bagavathiannan and Norsworthy Reference Bagavathiannan and Norsworthy2016; Singh et al. Reference Singh, Roma-Burgos, Singh, Alcober, Salas-Perez and Shivrain2018; Varanasi et al. Reference Varanasi, Brabham, Norsworthy, Nie, Young, Houston, Barber and Scott2018). The objective of the current study was to evaluate the susceptibility of different Palmer amaranth accessions to available SOAs in Arkansas row crops using many of the same accessions previously screened for fomesafen resistance (Varanasi et al. Reference Varanasi, Brabham, Norsworthy, Nie, Young, Houston, Barber and Scott2018).

Materials and Methods

Plant Materials

Palmer amaranth accessions from corn (Zea mays L.), cotton, soybean, and rice (Oryza sativa L.) fields in Arkansas were collected in the fall 2016. As stated in Varanasi et al. (Reference Varanasi, Brabham, Norsworthy, Nie, Young, Houston, Barber and Scott2018), growers, crop consultants, extension agents, and graduate students collected the majority of accessions from soybean fields. At least 10 inflorescences were collected from each field (considered one unique accession) and threshed to make a composite seed sample.

Herbicide Susceptibility Screening

Herbicide screenings were conducted under greenhouse conditions at the Altheimer Laboratory, University of Arkansas, Fayetteville, AR. The greenhouse was maintained at 35/25 C day/night temperature and a 16-h photoperiod supplemented with light-emitting diodes (a semiconductor light source). The herbicides used in this study are described in Table 1. Total number of Palmer amaranth accessions screened to a particular herbicide depended on seed availability; therefore, not every accession was evaluated for response to all tested herbicides. In all experiments, a susceptible accession collected in 2001 was included (Bond et al. Reference Bond, Oliver and Stephenson2006). Experiments were conducted from spring 2017 to fall 2019. For POST herbicide screening experiments, seeds from each accession were germinated in 50-cell plastic trays filled with potting mix (Sunshine Premix No. 1; Sun Gro Horticulture, Bellevue, WA), and seedlings were thinned to one plant in each cell. Once plants reached the 4- to 6-leaf stage (7- to 13-cm tall), they were sprayed with the respective POST herbicide (Table 1). Plant mortality rates were recorded at 14 d after treatment (DAT) for contact herbicides and 21 DAT for systemic herbicides. A plant was considered alive if a meristem was green. Each herbicide screen was repeated in time. Fomesafen-induced mortality rates and target-site resistance mechanisms of the accessions used in this study were previously determined by Varanasi et al. (Reference Varanasi, Brabham, Norsworthy, Nie, Young, Houston, Barber and Scott2018) and are included here for complementary reasons.

Table 1. Common name, trade name, rate, application timing, and manufacturer information of herbicides used to determine the susceptibility of Palmer amaranth accessions.

a A nonionic surfactant at 0.25% vol/vol was included with dicamba, fomesafen, and glyphosate + imazethapyr.

b A methylated seed oil at 1% vol/vol was used with tembotrione.

For S-metolachlor (PRE) and trifluralin (PPI) herbicides (Table 1), screens were conducted using 12.2- × 9.5- × 5.7-cm flats (Insert TO standard; Hummert International, Earth City, MO) filled with a sieved silt loam soil (pH of 6.6 and 2.4% organic matter). The soil was collected from the Milo J. Shult Agricultural Research and Extension Center in Fayetteville, AR. S-metolachlor screens were conducted following the methodology described by Brabham et al. (Reference Brabham, Norsworthy, Houston, Varanasi and Barber2019). For trifluralin screens, soil-containing flats were initially sprayed, and soil was subsequently emptied into a plastic container, capped, shaken to simulate herbicide incorporation, and poured back into flats. Afterward, 100 seeds were scattered over the soil surface, lightly covered with soil, and watered over the top until soil saturation. For each PRE and PPI herbicide treatment and the nontreated control, there were three replications of each accession, and the experiment was repeated in time. At 21 DAT, the total number of plants with at least one true leaf was recorded, and mortality percentage values were calculated relative to emerged plants in the nontreated control.

Herbicides were applied using a research-chamber track sprayer equipped with 1100067 nozzles calibrated to deliver 187 L ha−1 at 1.6 km h−1. Appropriate adjuvants were included with POST herbicides (Table 1). Percent mortality of all treatments in each accession was used to obtain descriptive statistics, using Statistix software (Analytical Software, Tallahassee, FL).

Results and Discussion

Response to Atrazine

The average mortality rate of accessions in response to atrazine applied POST at 560 g ha−1 was 85% at 14 DAT (Table 2). Of the 144 accessions screened, 89%, 69%, and 42% of the accessions had a mortality rate of at least 70%, 80%, and 90%, respectively. Although most accessions were sensitive to the atrazine rate tested, a few accessions had less than acceptable mortality values and require additional study. On the basis of these results, atrazine remains an effective herbicide on most Palmer amaranth accessions in Arkansas, which is likely a result of corn and grain sorghum [Sorghum bicolor (L.) Moench ssp. bicolor] not being widely grown in the state (USDA 2019).

Table 2. Susceptibility of Palmer amaranth accessions collected across Arkansas to different herbicide sites of action.a

a Descriptive statistics were generated from mortality rates.

b S-metolachlor and trifluralin are the only herbicides applied PRE and PPI, respectively.

c An in-depth analysis of fomesafen data is presented in Varanasi et al. (Reference Varanasi, Brabham, Norsworthy, Nie, Young, Houston, Barber and Scott2018).

Response to Dicamba

Palmer amaranth accessions were collected before dicamba-resistant crops were commercially available; therefore, dicamba-resistant Palmer amaranth was not expected. At 21 DAT, the average mortality rate of 134 accessions to an application of dicamba at half the labeled rate (280 g ha−1) was 51%, and the mortality rate never exceeded 80% (Table 2). Regrowth was evident in numerous plants from all accessions at 21 DAT (data not shown). Increasing the dicamba application rate from 280 g to 560 g ha−1 decreased the variability in mortality rates and increased the average mortality rate by 31 percentage points to 82%. Furthermore, 33% of the 127 accessions screened had a mortality rate of 63% to 80%, but some plants within these accessions were severely injured and apparent regrowth was not likely. Overall, the Palmer amaranth accessions in this study were sensitive to dicamba at 560 g ha−1 but not 280 g ha−1. The lack of control with dicamba at 280 g ha−1 is concerning because the ability to make timely applications in the field is sometimes difficult, resulting in treatment of larger-than-labeled weeds or weeds partially covered by the crop canopy. If the dicamba-resistant technology is not managed properly, the probability is high for shifting the sensitivity of an accession toward one that will be more difficult to control. In fact, a dicamba-resistant Palmer amaranth accession has been reported in Kansas (Peterson et al. Reference Peterson, Jugulam, Shyam and Borgato2019), and previous research has shown that low-dose selection for resistance to dicamba in Palmer amaranth can occur rapidly (Tehranchian et al. Reference Tehranchian, Norsworthy, Powles, Bararpour, Bagavathiannan, Barber and Scott2017).

Response to Glufosinate

All accessions used were susceptible to glufosinate (594 g ha−1). Of the 185 accessions screened, 93%, 98%, and 100% of the accessions had a mortality rate of at least 99%, 95%, and 90%, respectively (Table 2). Averaged across accessions, glufosinate killed 99.5% of the treated plants. Resistance to this SOA in Palmer amaranth has not yet been documented, and our findings indicate glufosinate remains an effective, viable option for the control of Palmer amaranth. Glufosinate use in glufosinate-resistant crops is currently an underused weed management system in Arkansas (Riar et al. Reference Riar, Norsworthy, Steckel, Stephenson, Eubank and Scott2013). In the coming decade, glufosinate use is expected to increase as crops with multiple herbicide-resistance traits, including glufosinate resistance, are introduced to the market. For glufosinate to remain an effective tool, growers need to take a proactive resistance-management approach by combining or rotating effective SOAs with glufosinate.

Response to Glyphosate plus Imazethapyr

In Arkansas, glyphosate and ALS-resistant Palmer amaranth are already widespread (Bond et al. Reference Bond, Oliver and Stephenson2006; Salas et al. Reference Salas, Burgos, Tranel, Singh, Glasgow, Scott and Nichols2016; Singh et al. Reference Singh, Roma-Burgos, Singh, Alcober, Salas-Perez and Shivrain2018). Here, we were interested in evaluating Palmer amaranth accessions for multiple-herbicide resistance to both glyphosate and imazethapyr. Thus, glyphosate at 860 g ha−1 was applied in combination with imazethapyr at 79 g ha−1 to plants at the 4- to 6-leaf stage. As expected, 98% of the 140 accessions screened at 21 DAT had less than 80% mortality (Table 2). Most accessions had mortality rates ranging from 6% to 22%, which highlight the severity of glyphosate and imazethapyr resistance in Palmer amaranth accessions in Arkansas. In addition, the ALS-inhibiting herbicides pyrithiobac and trifloxysulfuron are not reliable options for controlling glyphosate-resistant Palmer amaranth in Arkansas, meaning that multiple resistance to Group 2 and Group 9 herbicides is common (Norsworthy et al. Reference Norsworthy, Griffith, Scott, Smith and Oliver2008). Hence, that 209 of 215 Palmer amaranth accessions showed multiple resistance to glyphosate and pyrithiobac was not surprising, as has been reported in the Mississippi Delta region of eastern Arkansas (Bagavathiannan and Norsworthy Reference Bagavathiannan and Norsworthy2016).

Response to S-metolachlor

The average mortality rate of 121 accessions to S-metolachlor at 1,064 g ha−1 was 96%; 74% of these accessions had a mortality rate of at least 95% (Table 2). Palmer amaranth with a low level of metabolic resistance to S-metolachlor, but not other Group 15 herbicides, has been reported in Arkansas (Brabham et al. Reference Brabham, Norsworthy, Houston, Varanasi and Barber2019). Brabham et al. (Reference Brabham, Norsworthy, Houston, Varanasi and Barber2019) reported the average LD90 values for the two susceptible and two resistant accessions were 190 and 1,168 g ha−1, respectively. The two resistant accessions from Brabham et al. (Reference Brabham, Norsworthy, Houston, Varanasi and Barber2019) were used in the current study and had an average 91% mortality rate.

Worryingly, an additional 14 of the 121 accessions screened in the current study had mortality rates of not more than 91%, indicating the spread of S-metolachlor resistance is still in the early stages. In Arkansas, S-metolachlor and other Group 15 herbicides are heavily relied upon to obtain season-long control of Palmer amaranth. Our findings highlight the need for growers to reduce the exposure of Palmer amaranth accessions to S-metolachlor by mixing with other effective SOAs or at least alternating between Group 15 herbicides. In other experiments carried out in pecan [Carya illinoinensis (Wangenh.) K. Koch] orchards, the use of PRE S-metolachlor provided more than 99% control of glyphosate-resistant Palmer amaranth accessions (Mohseni-Moghadam et al. Reference Mohseni-Moghadam, Schroeder, Heerema and Ashigh2013). In North Carolina, S-metolachlor had better efficacy in controlling glyphosate-resistant Palmer amaranth accessions than did pendimethalin in soybean cropping systems (Whitaker et al. Reference Whitaker, York, Jordan and Culpepper2010). Those findings suggest S-metolachlor is still an effective chemical alternative for controlling Palmer amaranth and, likewise, remains an option for controlling Palmer amaranth in most fields throughout Arkansas.

Response to Tembotrione

Like atrazine, the selection pressure for resistance to HPPD-inhibiting herbicides in Arkansas is presumed to be low; nonetheless, resistance can be found in nearby states (Heap Reference Heap2020). Furthermore, HPPD-inhibitor resistance is often associated with atrazine resistance and is metabolic (Küpper et al. Reference Küpper, Peter, Zöllner, Lorentz, Tranel, Beffa and Gaines2018; Ma et al. Reference Ma, Kaundun, Tranel, Riggins, McGinness, Hager, Hawkes, McIndoe and Riechers2013; Nakka et al. Reference Nakka, Godar, Wani, Thompson, Peterson, Roelofs and Jugulam2017). Given that most Palmer amaranth accessions in this study were susceptible to atrazine, we expected effective Palmer amaranth control with tembotrione at 92 g ha−1. However, we observed inconsistent control of Palmer amaranth accessions at 21 DAT. The average mortality rate of 154 accessions was 51%, and 93% of these accessions had a mortality rate less than 80% (Table 2). The typical plant response to tembotrione within an accession varied greatly and mimicked a bell-shaped curve that ranged from healthy to dead plants (data not shown). Moreover, Singh et al. (Reference Singh, Roma-Burgos, Singh, Alcober, Salas-Perez and Shivrain2018) reported that 33% of the 172 Palmer amaranth accessions collected in Arkansas from 2008 to 2016 exhibited reduced sensitivity to mesotrione (105 g ha−1). The observed variability in mortality rates in the current study and as reported by Singh et al. (Reference Singh, Roma-Burgos, Singh, Alcober, Salas-Perez and Shivrain2018) indicates that difficult-to-control accessions with triketone herbicides already exist in Arkansas.

Response to Trifluralin

In Arkansas, before the advent of glyphosate-resistant crops, trifluralin was a commonly used herbicide for Palmer amaranth control, but it is no longer widely used (Gossett et al. Reference Gossett, Murdock and Toler1992; Kniss Reference Kniss2018; Webster and Coble Reference Webster and Coble1997). The average mortality rate of 119 accessions sprayed with trifluralin at 1,120 g ha−1 was 87%, with 41% of the accessions having a mortality rate of at least 95% (Table 2). However, the mortality rate of 22% of accessions was less than 80%, indicating accessions with reduced sensitivity to trifluralin can be found in Arkansas. The first confirmed case of trifluralin resistance in Arkansas was reported in an accession collected in 2016 (Heap Reference Heap2020). However, trifluralin resistance in Palmer amaranth was already believed to be prevalent in Arkansas (J.K. Norsworthy, personal communication) and was documented in 1998 in the neighboring state of Tennessee (Heap Reference Heap2020). Nevertheless, only a trifluralin-resistant Palmer amaranth accession with cross-resistance to benefin, isopropalin, pendimethalin, and ethalfluralin has been confirmed in South Carolina (Gossett et al. Reference Gossett, Murdock and Toler1992). Palmer amaranth resistance to trifluralin in Arkansas needs to be confirmed and characterized in the low-susceptibility accessions.

Prevalence of Difficult-to-Control Accessions

Based on our results, control of Palmer amaranth with commonly used SOAs is becoming increasingly difficult in Arkansas. Accessions with three-way resistance to glyphosate, ALS-, and PPO-inhibiting herbicides appear to be common (Bond et al. Reference Bond, Oliver and Stephenson2006; Salas et al. Reference Salas, Burgos, Tranel, Singh, Glasgow, Scott and Nichols2016; Singh et al. Reference Singh, Roma-Burgos, Singh, Alcober, Salas-Perez and Shivrain2018; Varanasi et al. Reference Varanasi, Brabham, Norsworthy, Nie, Young, Houston, Barber and Scott2018). For example, resistance of the accessions used in this study to fomesafen was previously determined by Varanasi et al. (Reference Varanasi, Brabham, Norsworthy, Nie, Young, Houston, Barber and Scott2018), who reported 141 accessions had a target-site mutation that conferred resistance to fomesafen. In our study, glyphosate + imazethapyr did not control any of these accessions (data not shown). In addition, tembotrione (average mortality rate, 51%) had poor efficacy on most of these accessions, and nearly one-fifth of the accessions have suspected resistance to trifluralin (Figure 1).

Figure 1. Mortality (%) heatmap of Palmer amaranth accessions screened for sensitivity to different herbicides. Accessions known to contain a target-site resistance mechanism to fomesafen were given a 0% mortality value on the basis of data from Varanasi et al. (Reference Varanasi, Brabham, Norsworthy, Nie, Young, Houston, Barber and Scott2018). Abbreviations: Dicamba (H): dicamba high rate; Dicamba (L): dicamba low rate; Gly + Ima; glyphosate + imazethapyr.

Of the remaining herbicide SOAs, most Palmer amaranth accessions were sensitive to glufosinate, atrazine, dicamba (high rate), and S-metolachlor (Figure 1). However, within each herbicide, except glufosinate, control of some accessions was less than expected. This highlights the need to use a multitactic approach for Palmer amaranth management to protect the efficacy of the remaining effective SOAs and to mitigate and delay the dispersion of accessions with reduced sensitivity to these SOAs.

Acknowledgments

This research received no specific grant. No conflicts of interest have been declared.

Footnotes

Associate Editor: Amit Jhala, University of Nebraska, Lincoln

References

Bagavathiannan, MV, Norsworthy, JK (2016) Multiple-herbicide resistance is widespread in roadside Palmer amaranth populations. PLoS One 11:e0148748 CrossRefGoogle Scholar
Beckie, HJ, Heap, IM, Smeda, RJ, Hall, LM (2000) Screening for herbicide resistance in weeds. Weed Technol 14:428445 CrossRefGoogle Scholar
Behrens, MR, Mutlu, N, Chakraborty, S, Dumitru, R, Jiang, WZ, LaVallee, BJ, Herman, PL, Clemente, TE, Weeks, DP (2007) Dicamba resistance: enlarging and preserving biotechnology-based weed management strategies. Science 316:11851188 CrossRefGoogle ScholarPubMed
Bond, JA, Oliver, LR, Stephenson, DO (2006) Response of Palmer amaranth (Amaranthus palmeri) accessions to glyphosate, fomesafen, and pyrithiobac. Weed Technol 20:885892 CrossRefGoogle Scholar
Brabham, C, Norsworthy, JK, Houston, MM, Varanasi, VK, Barber, T (2019) Confirmation of S-metolachlor resistance in Palmer amaranth (Amaranthus palmeri). Weed Technol 33:720726 CrossRefGoogle Scholar
Burgos, NR, Tranel, PJ, Streibig, JC, Davis, VM, Shaner, D, Norsworthy, JK, Ritz, C (2013) Review: confirmation of resistance to herbicides and evaluation of resistance levels. Weed Sci 61:420 CrossRefGoogle Scholar
Copeland, JD, Giacomini, DA, Tranel, PJ, Montgomery, GB, Steckel, LE (2018) Distribution of PPX2 mutations conferring PPO-inhibitor resistance in Palmer amaranth populations of Tennessee. Weed Technol 32:592596 Google Scholar
Dill, GM, CaJacob, CA, Padgette, SR (2008) Glyphosate-resistant crops: adoption, use and future considerations. Pest Manag Sci 64:326331 Google ScholarPubMed
Dreesen, R, Capt, A, Oberdoerfer, R, Coats, I, Pallett, KE (2018) Characterization and safety evaluation of HPPD W336, a modified 4-hydroxyphenylpyruvate dioxygenase protein, and the impact of its expression on plant metabolism in herbicide-tolerant MST-FGØ72-2 soybean. Regul Toxicol Pharmacol 97:170185 CrossRefGoogle ScholarPubMed
Gage, KL, Krausz, RF, Walters, SA (2019) Emerging challenges for weed management in herbicide-resistant crops. Agriculture 9:180 Google Scholar
Garetson, R, Singh, V, Singh, S, Dotray, P, Bagavathiannan, M (2019) Distribution of herbicide-resistant Palmer amaranth (Amaranthus palmeri) in row crop production systems in Texas. Weed Technol 33:355365 CrossRefGoogle Scholar
Gossett, BJ, Murdock, EC, Toler, JE (1992) Resistance of Palmer amaranth (Amaranthus palmeri) to the dinitroaniline herbicides. Weed Technol 6:587591 CrossRefGoogle Scholar
Hawkes, TR, Langford, MP, Viner, RC, Vernooij, BTM, Dale, R, inventors; Syngenta Participation AG (2010) Mutant hydroxyphenylpyruvate dioxygenase polypeptides and methods of use. US patent 9,388,393. http://patft.uspto.gov/netacgi/nph-Parser?Sect1=PTO2&Sect2=HITOFF&p=1&u=%2Fnetahtml%2FPTO%2Fsearch-bool.html&r=1&f=G&l=50&co1=AND&d=PTXT&s1=Hawkes.AANM.&s2=Langford.AANM.&OS=AANM/Hawkes+AND+AANM/Langford&RS=AANM/Hawkes+AND+AANM/Langford. Accessed: May 28, 2020Google Scholar
Heap, I (2020) International Herbicide-Resistant Weed Database. www.weedscience.org. Accessed: January 12, 2020Google Scholar
Kniss, AR (2018) Genetically engineered herbicide-resistant crops and herbicide-resistant weed evolution in the United States. Weed Sci 66:260273 CrossRefGoogle Scholar
Kumar, V, Liu, R, Stahlman, PW (2020) Differential sensitivity of Kansas Palmer amaranth populations to multiple herbicides [published online ahead of print February 2, 2020]. Agron J https://doi.org/10.1002/agj2.20178 CrossRefGoogle Scholar
Küpper, A, Peter, F, Zöllner, P, Lorentz, L, Tranel, PJ, Beffa, R, Gaines, TA (2018) Tembotrione detoxification in 4-hydroxyphenylpyruvate dioxygenase (HPPD) inhibitor-resistant Palmer amaranth (Amaranthus palmeri S. Wats.). Pest Manag Sci 74:23252334 CrossRefGoogle Scholar
Ma, R, Kaundun, SS, Tranel, PJ, Riggins, CW, McGinness, DL, Hager, AG, Hawkes, T, McIndoe, E, Riechers, DE (2013) Distinct detoxification mechanisms confer resistance to mesotrione and atrazine in a population of waterhemp. Plant Physiol 163:363377 CrossRefGoogle Scholar
Mohseni-Moghadam, M, Schroeder, J, Heerema, R, Ashigh, J (2013) Resistance to glyphosate in Palmer amaranth (Amaranthus palmeri) populations from New Mexico pecan orchards. Weed Technol 27:8591 CrossRefGoogle Scholar
Nakka, S, Godar, AS, Wani, PS, Thompson, CR, Peterson, DE, Roelofs, J, Jugulam, M (2017) Physiological and molecular characterization of hydroxyphenylpyruvate dioxygenase (HPPD)-inhibitor resistance in Palmer amaranth (Amaranthus palmeri S. Wats.). Front Plant Sci 8:555 CrossRefGoogle Scholar
Nandula, VK (2019) Herbicide resistance traits in maize and soybean: current status and future outlook. Plants 8:337 CrossRefGoogle ScholarPubMed
Norsworthy, JK, Griffith, GM, Scott, RC, Smith, KL, Oliver, LR (2008) Confirmation and control of glyphosate-resistant Palmer amaranth (Amaranthus palmeri) in Arkansas. Weed Technol 22:108113 CrossRefGoogle Scholar
Peterson, D, Jugulam, M, Shyam, C, Borgato, E (2019) Palmer amaranth resistance to 2,4-D and dicamba confirmed in Kansas. eUpdate 734. https://webapp.agron.ksu.edu/agr_social/eu_article.throck?article_id=2110. Accessed: May 29, 2020Google Scholar
Riar, DS, Norsworthy, JK, Steckel, LE, Stephenson, DO, Eubank, TW, Scott, RC (2013) Assessment of weed management practices and problem weeds in the Midsouth United States—soybean: a consultant’s perspective. Weed Technol 27:612622 CrossRefGoogle Scholar
Salas, RA, Burgos, NR, Tranel, PJ, Singh, S, Glasgow, L, Scott, RC, Nichols, RL (2016) Resistance to PPO-inhibiting herbicide in Palmer amaranth from Arkansas. Pest Manag Sci 72:864869 CrossRefGoogle Scholar
Singh, S, Roma-Burgos, N, Singh, V, Alcober, EAL, Salas-Perez, R, Shivrain, V (2018) Differential response of Arkansas Palmer amaranth (Amaranthus palmeri) to glyphosate and mesotrione. Weed Technol 32:579585 CrossRefGoogle Scholar
Tehranchian, P, Norsworthy, JK, Powles, S, Bararpour, MT, Bagavathiannan, MV, Barber, T, Scott, RC (2017) Recurrent sublethal-dose selection for reduced susceptibility of Palmer amaranth (Amaranthus palmeri) to dicamba. Weed Sci 65:206212 CrossRefGoogle Scholar
[USDA] US Department of Agriculture (2019) Acreage. ISSN: 1949-1522. https://www.nass.usda.gov/Publications/Todays_Reports/reports/acrg0619.pdf. Accessed: May 28, 2020Google Scholar
Varanasi, VK, Brabham, C, Norsworthy, JK, Nie, H, Young, BG, Houston, M, Barber, T, Scott, RC (2018) A statewide survey of PPO-inhibitor resistance and the prevalent target-site mechanisms in Palmer amaranth (Amaranthus palmeri) accessions from Arkansas. Weed Sci 66:149158 CrossRefGoogle Scholar
Webster, TM, Coble, HD (1997) Changes in the weed species composition of the Southern United States: 1974 to 1995. Weed Technol 11:308317 CrossRefGoogle Scholar
Whitaker, JR, York, AC, Jordan, DL, Culpepper, AS (2010) Palmer amaranth (Amaranthus palmeri) control in soybean with glyphosate and conventional herbicide systems. Weed Technol 24:403410 CrossRefGoogle Scholar
Wise, AM, Grey, TL, Prostko, EP, Vencill, WK, Webster, TM (2009) Establishing geographic distribution level of acetolactate synthase resistance of Palmer amaranth (Amaranthus palmeri) accessions in Georgia. Weed Technol 23:214220 CrossRefGoogle Scholar
Wright, TR, Shan, G, Walsh, TA, Lira, JM, Cui, C, Song, P, Zhuang, M, Arnold, NL, Lin, G, Yau, K, Russell, SM, Cicchillo, RM, Peterson, MA, Simpson, DM, Zhou, N, Ponsamuel, J, Zhang, Z (2010) Robust crop resistance to broadleaf and grass herbicides provided by aryloxyalkanoate dioxygenase transgenes. Proc Natl Acad Sci 107:2024020245 Google ScholarPubMed
Figure 0

Table 1. Common name, trade name, rate, application timing, and manufacturer information of herbicides used to determine the susceptibility of Palmer amaranth accessions.

Figure 1

Table 2. Susceptibility of Palmer amaranth accessions collected across Arkansas to different herbicide sites of action.a

Figure 2

Figure 1. Mortality (%) heatmap of Palmer amaranth accessions screened for sensitivity to different herbicides. Accessions known to contain a target-site resistance mechanism to fomesafen were given a 0% mortality value on the basis of data from Varanasi et al. (2018). Abbreviations: Dicamba (H): dicamba high rate; Dicamba (L): dicamba low rate; Gly + Ima; glyphosate + imazethapyr.