INTRODUCTION
Control of many broadleaf and annual grass weeds in peanut (Arachis hypogaea L.) can be challenging and requires the use of a preplant application of a dinitroaniline herbicide such as trifluralin (Treflan®), pendimethalin (Prowl® or Prowl H20®), or ethalfluralin (Sonalan®) (Wilcut et al., 1995). Weeds such as Texas millet [Urochloa texana (Buckl.)], Palmer amaranth (Amaranthus palmeri S. Wats), pitted morningglory (Ipomoea lacunosa L.), yellow nutsedge (Cyperus esculentus L.), purple nutsedge (Cyperus rotundus L.), and smellmelon (Cucumis melo L.) are a continuing problem in peanut growing areas of the southwestern U.S. (Grichar and Dotray, 2013; Baughman et al., 2018; Dotray et al., 2018; Grichar et al., 2019). These weeds can escape control due to extremely high weed populations, improper soil incorporation, large seed size, and/or an inadequate herbicide rate (Grichar and Colburn, 1996). Also, the dinitroaniline herbicides alone do not adequately control any of these weeds season-long (Wilcut et al., 1995; Grichar et al., 1999; Grichar and Dotray, 2013; Baughman et al., 2018; Dotray et al., 2018; Grichar et al., 2019).
Norflurazon [4-chloro-5-(methylamino)-2-(3-trifluoromethyl)phenyl-3-(2H)-pyridazinone] is registered for use on peanut only in Alabama, Florida, Georgia, Mississippi, North Carolina, New Mexico, Oklahoma, South Carolina, Texas, and Virginia (Anonymous, 2015a). Norflurazon is not registered for use on Spanish peanuts and is only available for use on certain runner or Virginia-type peanut cultivars including ‘Florunner’, ‘GK-7’, ‘GA Runner’, ‘Southern Runner’, ‘NC 7’, ‘VA 93B’, ‘NC 9’, ‘NC-V11’, ‘VA-C 92R’, ‘AgraTech VC-1’, and ‘NC 10C’ (Anonymous, 2015a). Most if not all these cultivars are no longer commercially available for production.
Norflurazon is a phytoene desaturase inhibitor which catalyzes a rate-limiting step in carotenoid biosynthesis (Manaa et al., 2019). Carotenoid deficiency causes oxidative stress due to significant increase in reactive oxygen species (ROS) formation (Jung et al., 2000). Therefore, carotenoids are not only accessory pigments in the photosynthesis process, they also act as photoprotective agents by absorbing excess energy of triplet excited states of chlorophyll and detoxifying of singlet oxygen (Shaner, 2014). Norflurazon also inhibits the unsaturation of chloroplast lipids (Abrous-Belbachir et al., 2009). Other modes of action ascribed to norflurazon are: a) inhibition of the Hill reaction (Eder, 1979), b) alteration of the ratio of linolenic/linoleic acid (St. John 1976; St. John and Hilton, 1976; Eder, 1979), and c) influence on the chloroplast ribosomes (Eder, 1979). Lack of translocation and the presence of lysigenous or pigment glands are two major factors responsible for its selectivity in cotton (Gossypium hirsutum L.) (Strang and Rogers, 1974; 1975).
Norflurazon controls broadleaf weeds including prickly sida (Sida spinosa L.), spurred anoda [Anoda cristata (L.) Schlecht.], tropic croton (Croton glandulosus var. septentrionalis Muell.-Arg.], common ragweed (Ambrosia artemissiifolia L.), and common lambsquarters (Chenopodium album L.) and some annual grasses such as barnyardgrass (Echinochloa crus-galli L.), crowfootgrass (Dactyloctenium aegyptium), crabgrass (Digitaria spp.), fall panicum (Panicum spp.), and Texas millet [Urochloa texana (Buckl.)] (Anonymous, 2015a). Norflurazon also can suppress nutsedge (Cyperus spp.) (Wilcut et al., 1995; Jordan et al., 1998).
Currently, many peanut growers in Texas and Oklahoma apply pendimethalin in combination with either S-metolachlor or flumioxazin preemegence (PRE) and follow that with postemergence (POST) applications of a graminicide or broadleaf herbicide to control any weed escapes (authors’ personal observations). Imazapic has been used to control broadleaf and nutsedge weed issues in peanut for the last thirty years (Grichar, 2008); however, some weed resistant issues have developed (possibly Amranthus palmeri) and growers are concerned about the lack of available herbicides for control of problem weeds. Norflurazon would provide Texas and Oklahoma growers with another tool to combat these weed issues. Little research could be found on norflurazon use in Texas or Oklahoma on peanut. Also, since the peanut varieties cleared for use with norflurazon are either no longer available or commercially limited (Anonymous, 2015a), it was decided to evaluate the newer released peanut cultivars for tolerance to norflurazon in the Texas and Oklahoma peanut growing areas.
Materials and Methods
Norflurazon tolerance studies were conducted at the Texas A&M AgriLife Research site in south Texas near Yoakum (29.0369o N, 97.2616o W) during the 2019 and 2020 growing seasons, in the Texas High Plains during the 2019 and 2020 season in a producer’s field in Gaines County near Seminole (32.7429o N, 102.8253o W). The study in Oklahoma was conducted only in 2020 at the Oklahoma State University Caddo Research Station near Ft. Cobb (35.091o N, 98.275oW). Weed efficacy studies were also conducted during the 2019 and 2020 growing season at the Texas A&M AgriLife Research site near Yoakum.
The soils at Yoakum were a Denhawken sandy clay loam (fine, smectitic, hyperthermic, Vertic Haplustepts) with less than 1.0 % organic matter and pH 7.6 while near Seminole the soils were a Patricia loamy fine sand (fine-loamy, mixed, superactive, thermic Aridic Paleustalfs) with 1.4% organic matter and a pH 7.9. Soils at Ft. Cobb were a Cobb fine sandy loam (fine-loamy, mixed, active, thermic Typic Haplustalfs) with less than 1% organic matter and a pH 7.3.
Treatments in the peanut tolerance study consisted of a factorial arrangement of two norflurazon rates (0.56 or 1.12 kg/ha) and two application timings [preemergence (PRE) or early postemergence (EPOST). The PRE applications were made within two days of peanut planting while the EPOST applications were applied 7 to 13 d after planting depending on location (V1 to V3) (Boote, 1982). Treatments in the weed efficacy trials included norflurazon alone at 0.56 and 1.12 kg ai/ha applied either preplant incorporated (PPI) or PRE after peanuts were planted, pendimethalin at 1.06 kg ai/ha plus norflurazon at either 0.56 or 1.12 kg ai/ha applied PRE, and ethalfluralin at 0.84 kg ai/ha applied PPI followed by (fb) norflurazon at either 0.56 or 1.12 kg ai/ha applied PRE. Pendimethalin at 1.06 kg ai/ha plus S-metolachlor at 1.42 kg ai/ha applied PRE was included as a standard. An untreated check was included in each study and each study was replicated three to four times depending on location. The PPI treatments were incorporated with a tractor-driven power tiller approximately 5 cm deep immediately after herbicide application. The PPI treatments were not included in the tolerance study since currently, very few, if any growers mechanically incorporate soil-applied herbicides (authors’ personal observations).
Herbicides were applied using water as a carrier with a CO2-pressurized backpack sprayer. Trial variables for each location are listed in Table 1. Georgia 09-B (Branch, 2010) was planted in all Texas trials. The Spanish cultivar OLe’ (Anonymous, 2015b) was planted at Ft. Cobb.
For studies at Yoakum, each plot consisted of two rows spaced 97 cm apart and 7.6 m long while at the High Plains locations plot size was 4 rows spaced 102 cm apart and 9.1 m long. The Oklahoma location consisted of 2 rows spaced 91 cm apart and 7.6 m long. Traditional production practices were used to maximize peanut growth, development, and yield. Plots in the peanut tolerance studies received either ethalfluralin or pendimethalin applied PPI to control early season weeds. In south Texas, clethodim and 2,4-DB were applied postemergence (POST) to control any late- season weed infestations. Hand-weeding as needed was used exclusively in Oklahoma and the High Plains locations. Insecticides were not needed at any location in any year.
In the weed efficacy trials at Yoakum no irrigation was applied while in the peanut tolerance trials supplemental irrigation was used at all locations. At Yoakum, lateral hand-moved irrigation lines were used and irrigation was applied as needed throughout the growing season. Center pivot systems were used to apply irrigation as needed at Seminole and Ft. Cobb.
Peanut emergence was obtained 30 d after planting (DAP) at Seminole and 13 DAP at Ft. Cobb by counting emerged peanut plants in 2 m of row. Emergence data were not obtained at Yoakum. Peanut injury and weed control were estimated visually on a scale of 0 to 100 (0 indicating no control or plant death and 100 indicating complete control or plant death) relative to the untreated check (Frans et al. 1986). Weed control was evaluated throughout the growing season but only the 2 and 12 wks after planting (WAP) evaluations are presented.
Peanut yield was obtained by digging the pods based on maturity of control plots, air-drying in the field for 6 to 10 d, and harvesting individual plots with a small-plot thresher. Yield samples were cleaned and adjusted to 10% moisture prior to weighing.
Data for percentage of peanut injury and weed control were transformed to the arcsine square root prior to analysis; however, non-transformed means are presented because arscine transformation did not affect interpretation of the data. Data were subjected to ANOVA and analyzed using the SAS PROC MIXED procedure 23 (SAS, 2019). Treatment means were separated using Fisher’s Protected LSD at P < 0.05.
Results and Discussion
Peanut tolerance studies
Injury from norflurazon consisted of foliar chlorosis and bleaching and was present for approximately 3 wks after peanut emergence. No injury was observed later in the growing season.
South Texas (Yoakum)
There was a norflurazon rate by application timing interaction at the Yoakum location for the 7 d after emergence (DAE) evaluation for both years (Table 2). In 2019 norflurazon at both rates resulted in greater injury than the untreated check while in 2020 only norflurazon at 1.12 kg ai/ha resulted in greater injury. The PRE application of norflurazon had no effect on peanut when evaluated 7 DAE in either year while the EPOST application resulted in 17 and 18% injury in 2019 and 2020, respectively (Table 2).
Yields were combined over years since there was no treatment by year interaction (Table 3). No differences in yield were noted between norflurazon rate or application timing and the untreated check.
High Plains (Seminole)
Plant stands were not affected by any treatment in either year (data not shown). There was a norflurazon rate by application timing interaction for peanut injury in 2019 (Table 2). When evaluated 14 DAE, norflurazon at 1.12 kg ai/ha resulted in 16% peanut injury compared with 4% injury for norflurazon at 0.56 kg ai/ha. No differences were noted in peanut injury when norflurazon was applied either PRE or EPOST. No peanut injury (22 DAE) was observed in 2020 with norflurazon (data not shown).
Norflurazon did not affect peanut yield in 2019 while in 2020 norflurazon at 1.12 kg ai/ha applied PRE reduced yield 25% compared to the untreated check (Table 3). Manaa et al. (2019) reported that peanut plants grown in norflurazon-contaminated soil were impaired in their photosynthesis and displayed a reduction in growth. This reduction in photosynthesis may be linked to a decrease in chlorophyll content in depigmented leaves of peanut (Dankov et al., 2009) and may have contributed to the yield reduction.
Oklahoma (Ft. Cobb)
No reduction in stand was observed with any norflurazon treatment (data not shown). When evaluated 21 DAE there was a norflurazon rate effect but not an application timing effect (Table 2). Norflurazon at 0.56 kg ai/ha resulted in peanut injury similar to the untreated check while norflurazon at 1.12 kg ai/ha resulted in 5% injury. There was no difference in yield between the untreated check and any norflurazon rate or application timing (Table 3).
Weed efficacy studies
Texas millet control
Data are presented separately since there was a treatment by year interaction for both the 2 and 12 WAP evaluations (Table 4). At the 2 WAP evaluation in 2019, herbicide treatments which included either pendimethalin or ethalfluralin provided 99 to 100% control while norflurazon alone applied PPI controlled 88 to 89% and norflurazon alone applied PRE provided 94 to 98% control. In 2020, pendimethalin or ethalfluralin treatments provided 89 to 98% control while norflurazon alone at either 0.56 or 1.12 kg ai/ha applied PPI and norflurazon at 1.12 kg ai/ha applied PRE controlled Texas millet at least 93%. Norflurazon at 0.56 kg ai/ha applied PRE only provided 73% control (Table 4). In 2019, 12.2 mm of rainfall was received within 7 d of herbicide application while in 2020, 34.5 mm of rainfall was received within 7 d of herbicide application.
In 2019 when evaluated 12 WAP, either pendimethalin or ethalfluralin in combination with norflurazon at 0.56 kg ai/ha controlled Texas millet 90 to 96% while combinations with norflurazon at 1.12 kg ai/ha controlled this weed 80 to 84%. Norflurazon alone applied PPI and norflurazon alone at 0.56 kg ai/ha applied PRE controlled Texas millet < 65% while norflurazon at 1.12 kg ai/ha applied PRE provided 88% control (Table 4). In 2020 at the 12 WAP evaluation, only the ethalfluralin applied PPI followed by (fb) norflurazon applied PRE treatments provided > 80% control. No other herbicide treatments provided acceptable control of Texas millet.
Little information is available on norflurazon control of annual grasses. However, Wilcut et al. (1995) mentions that it will control some annual grasses. The Solicam® DF label states that norflurazon at 0.56 to 2.8 kg ai/ha will control Texas millet (Anonymous, 2015a).
Palmer amaranth control
The 2 WAP evaluation was combined over years since there was no treatment by year interaction; however, the 12 WAP evaluations are presented separately by year due a treatment by year interaction. All herbicide treatments provided > 91% control 2 WAP (Table 5). In 2019 at the 12 WAP evaluation, all herbicide treatments with the exception of norflurazon alone applied PRE controlled Palmer amaranth > 90%. In 2020, only ethalfluralin applied PPI fb norflurazon at 1.12 kg ai/ha applied PRE and pendimethalin plus S-metolachlor applied PRE controlled Palmer amaranth > 82%. No other herbicide treatment provided > 74% control.
Gossett et al. (1992) reported that norflurazon at 0.84 and 1.68 kg ai/ha controlled susceptible and dinitroaniline resistant Palmer amaranth equally (> 97%). Preemergence applications of norflurazon have been reported to control other broadleaf weeds such as spurred anoda at least 93% 4 WAP (Solano et al., 1976).
Smellmelon control
As with the Palmer amaranth evaluation, the 2 WAP evaluation was combined over years since there was no treatment by year interaction; however, the 12 WAP evaluations are presented separately by year due a treatment by year interaction. At the 2 WAP evaluation, all herbicide treatments, with the exception of norflurazon alone at 0.56 kg ai/ha applied PRE controlled smellmelon at least 95% (Table 5). In 2019 at the 12 WAP evaluation, all herbicide treatments provided >75% control. Pendimethalin plus norflurazon at 1.12 kg ai/ha applied PRE and the standard treatment of pendimethalin plus S-metolachlor provided perfect control. In 2020 norflurazon alone at 0.56 kg ai/ha applied PPI provided the most effective control. Adding either pendimethalin or ethalfluralin to norflurazon did not improve smellmelon control over norflurazon alone.
Henedina et al., (2012) reported that in greenhouse studies norflurazon at 2.64 kg/ha controlled citron melon [Citrullus lanatus (Thunb.) Matsum and Nalai] 55% 7 d after treatment (DAT) and this increased to 91% control 21 DAT. Lo and Merkle (1984) reported that grain sorghum [Sorghum bicolor (L.) Moench.], wheat (Triticum aestivum L.), and sicklepod (Cassia obtusufolia L.) were some of the most susceptible plants to norflurazon while cotton was one of the most tolerant.
Peanut injury at all locations was rate dependent. Jordan et al. (1998) reported that norflurazon reduced peanut yield and gross returns in two of four experiments regardless of cultivar and suggested that norflurazon use on Virginia-type peanut should be avoided except for the control of specific problem weeds. Weed control with norflurazon was erratic when applied alone but was greatly improved with tank-mixes of either pendimethalin or ethalfluralin. Season-long control of both annual grasses and broadleaf weeds requires the use of both PRE and POST herbicides to provide effective season-long grass control. Although norflurazon caused early-season chlorosis and bleaching, this injury was transient and resulted in a reduction in yield at only one of five locations. Peanut injury was more severe in south Texas with the EPOST application but in the Texas High Plains and Oklahoma no differences in injury was noted between the PRE and EPOST applications.
Acknowledgements
The Oklahoma Peanut Commission and The Texas Peanut Producers Board provided funding for this research.
Literature Cited
Abrous-Belbachir O., De Paepe R., Tremolieres A., Mathieu C., Aid F., and Benhassaine-Kesri G.. 2009. Evidence that norflurazon affects chloroplast lipid unsaturation in soybean leaves (Glycine max L.). J. Agric. Food Chem. 57:11434-11440.
Anonymous. 2015a. Solicam® DF product label. 38 pp. Tessenderlo Kerley, Inc. Phoenix, AZ.
Anonymous. 2015b. OLe’: A new Spanish peanut high in oleic acid. USDA Agric. Res. 63(2). agresearchmag.ars.usda.gov/2015/feb/peanut/. Accessed: May 12, 2022.
Baughman T. A., Grichar W. J., and Dotray P. A.. 2018. Weed control and peanut tolerance using pyroxasulfone in Oklahoma. J. Exp. Agric. Internatl. 21(3):1-11. Article No. [: JEAI. 39881].
Boote K. J. 1982. Growth stages of peanut (Arachis hypogaea L.). Peanut Sci. 9:35-40.
Branch W. B. 2010. Registration peanut of ‘Georgia-09B’. J. Plant Registration. 4(3):175.
Dankov K., Busheva M., Stefanov D., and Apostolova E. L.. 2009. Relationship between the degree of carotenoid depletion and function of the photosynthetic apparatus. J. Photochem. Photobiol. B: Biology. 96:49-56.
Dotray P. A., Baughman T. A., Grichar W. J., and Woodward J. E.. 2018. Performance of pyroxasulfone to control Amaranthus palmeri and Salsola kali in peanut. J. Exp. Agric. Internatl. 23(2):1-10. Article No. [: JEAI. 41505].
Eder F. A. 1979. Pyridazinines, their influence on the biosynthesis of carotenoids and the metabolism of lipids in plants. Z. Naturforsch. 34C:1052-1054.
Frans R., Talbert R., Marx D., and Crowley H. 1986. Experimental design and techniques for measuring and analyzing plant responses to weed control practices. pp. 29-46. In: Camper, N. D. (ed.). Research Methods in Weed Science. 3rd ed. Champaign, IL: Southern Weed Science Society.
Gossett B. J., Murdock E. C., and Toler J. E.. 1992. Resistance of Palmer amaranth (Amaranthus palmeri) to the dinitroaniline herbicides. Weed Technol. 6:587-591.
Grichar W. J. 2008. Herbicide systems for control of horse purslane (Triantherma portulacastrum L.), smellmelon (Cucumis melo L.) and Palmer amaranth (Amaranthus palmeri S. Wats) in peanut. Peanut Sci. 35:38-42.
Grichar W. J. and Colburn A. E.. 1996. Flumioxazin for weed control in Texas peanuts (Arachis hypogaea L.). Peanut Sci. 23:30-36.
Grichar W. J., Dotray P. A., and Sestak D. C.. 1999. Diclosulam for weed control in Texas peanut. Peanut Sci. 26:23-28.
Grichar W. J. and Dotray P. A.. 2013. Smellmelon control and peanut response to flumioxazin and paraquat alone and in combination. Peanut Sci. 40:135-141.
Grichar W. J., Dotray P. A., and Baughman T. A.. 2019. Evaluation of weed control efficacy and peanut tolerance to pyroxasulfone herbicide in the south Texas peanut production area. J. Exp. Agric. Internatl. 29(2):1-10. Article No. [: JEAI. 45347]. doi: [: 10.9734/JEAI/2019/45347].
Henedina A., Ramirez M., Jhala A. J., and Singh M.. 2012. Efficacy of PRE and POST herbicides for control of citron melon (Citrullus lanatus var. citroides). Weed Technol. 26:783-788.
Jordan D. L., Culpepper A. S., Batts R. B., and York A. C.. 1998. Response of Virginia-type peanut to norflurazon. Peanut Sci. 25:4-7.
Jung S. Y., Kim J. S., Cho K. Y., Tae G. S., Kang B. G.. 2000. Antioxidant responses of cucumber (Cucumis sativus) to photoinhibition and oxidative stress induced by norflurazon under high and low PPFDs. Plant Sci. 153:145-154.
Lo Chi-Chu and Merkle M. G.. 1984. Factors affecting the phytotoxicity of norflurazon. Weed Sci. 32:279-283.
Manaa I., Djebbar R., and Abrous-Belbachir O.. 2019. Impact of exogenous alpha tocopherol on peanut seedlings (Arachis hypogaea L.) treated by norflurazon. Acta Biol. Szegediensis. 63:125-133.
SAS Institute. 2019. SAS® Enterprise Guide 8.2 User’s Guide. Cary, NC.
Shaner D.L. 2014. Herbicide Handbook. Weed Science of America. Lawrence, KS.
Solano F., Schrader J. W., and Coble H. D.. 1976. Control of spurred anoda in cotton. Weed Sci. 24:553-556.
St. John J. B. 1976. Manipulation of galactolipid fatty acid composition with substituted pyridazinones. Plant Physiol. 57:38-40.
St. John J. B. and Hilton J. L.. 1976. Structure versus activity of substituted pyridazinones as related to mechanism of action. Weed Sci. 24:579-582.
Strang R. H. and Rogers R. L.. 1974. Behavior and fate of two phenylpyridazinone herbicides in cotton, corn, and soybeans. J. Agric. Food Chem. 22:1119-1125.
Wilcut J. W., York A. C., Grichar W. J., and Wehtje G. R.. 1995. The biology and management of weeds in peanut (Arachis hypogaea). In Pattee H. E. and Stalker H. T. (eds.). Advances in Peanut Science Amer. Peanut Res. Educ. Soc., Inc., Stillwater, OK. pp. 207-244.
Notes
- First author: Texas A&M AgriLife Research, Corpus Christi, TX 78406; Second author, Former Graduate Research Assistant, Texas Tech University, Lubbock, TX 79409-2122; third author, Texas A&M AgriLife Research and Texas A&M AgriLife Extension Service, Lubbock, TX 79403; fourth author, Texas A&M AgriLife Research, Lubbock, TX 79403. [^] Corresponding author’s E-mail: james.grichar@ag.tamu.edu