Small-scale Primary Screening Method to Predict Impacts of the Herbicide Flumioxazin on Native and Invasive Emergent Plants

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Small-scale Primary Screening Method to Predict Impacts of the Herbicide Flumioxazin on Native and Invasive Emergent Plants by LeeAnn M. Glomski and Michael D. Netherland PURPOSE: The purpose of this work was to develop and utilize a rapid, small-scale primary screening method to evaluate the activity of a recently registered aquatic herbicide, flumioxazin, against 23 native emergent plant species and five invasive emergent species. BACKGROUND: In evaluating potential use patterns of new aquatic herbicides, it is important to determine concentrations that impact target as well as non-target vegetation. The recently registered aquatic herbicide flumioxazin is efficacious against the floating weeds water lettuce (Pistia stratiotes L.) and giant salvinia (Salvinia molesta Mitchell) (Richardson et al. 2008) as well as the submersed species hydrilla (Hydrilla verticillata (L.f.) Royle) (Mudge and Haller 2006) and Eurasian watermilfoil (Myriophyllum spicatum L.) (Getsinger et al. 2011). These species are often found in close proximity to or intermixed with native emergent vegetation and information on the impact of flumioxazin to most emergent plant species is limited. Information regarding the selectivity of flumioxazin (and other aquatic herbicides) will help resource managers decide which herbicides, use rates, and timing of application are most appropriate to reduce injury to the native emergent species present. This work has become increasingly relevant as research conducted last year demonstrated a potential selective use pattern for flumioxazin in areas where water lettuce is intermixed with emergent species (Netherland 2011). The endangered snail kite (Rosthramus sociabilis) is utilizing habitats in areas of large-scale floating plant control operations. Current operational use of the broad-spectrum herbicide diquat, while highly effective at controlling water lettuce, generally results in significant visual injury symptoms on numerous emergent plant species. Aquatic plant managers are under increasing pressure to reduce nontarget injury to plants such as bulrush (Schoenoplectus spp), spikerush (Eleocharis spp), cattail (Typha spp), and other emergent species. Operational treatments in 2011-2012 included expanding the use of flumioxazin for selective water lettuce control on Lake Okeechobee and the St. Johns River, Florida. Determining the response of native and invasive plants to the different use rates and timing of flumioxazin will help refine use patterns. Flumioxazin is a protox-inhibiting herbicide originally registered for broadleaf weed control in terrestrial systems (Senseman 2007); however, it has been approved for use in aquatic sites in recent years. Protox inhibitors disrupt chlorophyll synthesis by competing with protoporphyrinogen for binding sites on the protoporphyrinogen oxidase enzyme. Without available binding sites, protoporphyrinogen leaks into the cytoplasm and is converted to protoporphyrin IX when exposed to light. Protoporphyrin IX then reacts with oxygen to form singlet oxygen radicals that damage cell membranes causing them to leak (Hess 2000, Senseman 2007). This leakage of electrolytes has been measured and used to determine herbicide injury of membrane-disrupting and photosynthesis- Approved for public release; distribution is unlimited.

Report Documentation Page Form Approved OMB No. 0704-0188 Public reporting burden for the collection of information is estimated to average 1 hour per response, including the time for reviewing instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing the collection of information. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden, to Washington Headquarters Services, Directorate for Information Operations and Reports, 1215 Jefferson Davis Highway, Suite 1204, Arlington VA 22202-4302. Respondents should be aware that notwithstanding any other provision of law, no person shall be subject to a penalty for failing to comply with a collection of information if it does not display a currently valid OMB control number. 1. REPORT DATE MAR 2013 2. REPORT TYPE 3. DATES COVERED 00-00-2013 to 00-00-2013 4. TITLE AND SUBTITLE Small-scale Primary Screening Method to Predict Impacts of the Herbicide Flumioxazin on Native and Invasive Emergent Plants 5a. CONTRACT NUMBER 5b. GRANT NUMBER 5c. PROGRAM ELEMENT NUMBER 6. AUTHOR(S) 5d. PROJECT NUMBER 5e. TASK NUMBER 5f. WORK UNIT NUMBER 7. PERFORMING ORGANIZATION NAME(S) AND ADDRESS(ES) US Army Engineer Research and Development Center,Aquatic Plant Control Research Program (APCRP),3909 Halls Ferry Road,Vicksburg,MS,39180 8. PERFORMING ORGANIZATION REPORT NUMBER 9. SPONSORING/MONITORING AGENCY NAME(S) AND ADDRESS(ES) 10. SPONSOR/MONITOR S ACRONYM(S) 12. DISTRIBUTION/AVAILABILITY STATEMENT Approved for public release; distribution unlimited 13. SUPPLEMENTARY NOTES 14. ABSTRACT 11. SPONSOR/MONITOR S REPORT NUMBER(S) 15. SUBJECT TERMS 16. SECURITY CLASSIFICATION OF: 17. LIMITATION OF ABSTRACT a. REPORT unclassified b. ABSTRACT unclassified c. THIS PAGE unclassified Same as Report (SAR) 18. NUMBER OF PAGES 7 19a. NAME OF RESPONSIBLE PERSON Standard Form 298 (Rev. 8-98) Prescribed by ANSI Std Z39-18

inhibiting herbicides (Falk et al. 2006; Koo et al. 1994; Koschnick et al. 2006; Li et al. 2000; Vanstone and Stobbe 1977; Yanase et al. 1990), freezing resistance and frost tolerance (Nunes and Smith 2003; Sukumaran and Weiser 1972; Dexter et al. 1932) and seed vigor (Duke et al. 1983). More recently, it has been used to determine the impacts of flumioxazin and carfentrazone-ethyl on native and invasive submersed plants (Glomski and Netherland, in press). In addition to emergent spray applications, flumioxazin can be applied as a submersed treatment to control invasive species such as hydrilla, Eurasian watermilfoil, water lettuce, and giant salvinia (Valent USA Corporation 2011). Many times, these species are found in close proximity to or intermixed with native emergent vegetation. Past research has shown that submersed herbicide applications can cause unintended damage to some emergent species while leaving other species undamaged. For example, submersed applications of the auxin mimics 2,4-D and triclopyr when used to control Eurasian watermilfoil, can impact white waterlily (Nymphaea odorata Ait.), soft-stem bulrush (Schoenoplectus tabernaemontani (C.C. Gmel.) Palla) and hardstem bulrush (S. acutus Muhl. Ex Bigelow) whereas spatterdock (Nuphar lutea (L.) Sm.) and American bulrush (S. americanus Pers.) are not impacted (Glomski and Nelson 2008; Glomski et al. 2009; Glomski and Netherland 2012). Some research has been conducted to determine the selectivity of submersed applications of the ALSinhibiting herbicides bispyribac-sodium, imazamox, and penoxsulam on emergent vegetation (Glomski and Mudge 2009; Koschnick et al. 2007). To date, there has been no extensive species screening for flumioxazin activity following submersed and emergent use patterns. MATERIALS AND METHODS: To determine the effect of flumioxazin on emergent plants, smallscale assays were conducted in reach-in growth chambers at the U.S. Army Engineer Research and Development Center s Lewisville Aquatic Ecosystem Research Facility (LAERF), Lewisville, Texas. Studies were conducted using a Percival E-36L (Perry, IA) growth chamber set at 25 C and continuous light. Light intensity was 430 µmol photons m -2 s -1. An incubation medium of 1 mm 2- (morpholino) ethanesulfonic acid buffer (MES) and 2% (w/v) sucrose was prepared and ph of the medium was adjusted to 6.5 with 2.1 N NaOH (Duke and Kenyon 1993, Kenyon et al. 1985). Twenty ml of medium were added to 150-mL cups along with 0.25 g of fresh leaf tissue. Species tested are listed in Table 1. The more tissue per cup, the more sensitive the assay (Duke and Kenyon 1993) and the weight used in these assays was enough to cover the surface (for most species) without overpacking the cups. Treatments included 100, 200, and 400 µg ai L -1 flumioxazin (Clipper, Valent USA Corporation, Walnut Creek, California) and an untreated control. Conductivity readings were taken in each cup after 2 days of herbicide exposure using an Accumet AP85 ph/conductivity meter (Fisher Scientific, Pittsburgh, Pennsylvania). Cups were then exposed to two freeze-thaw cycles before final conductivity readings were taken to determine total electroconductivity of the tissue. Percent electrolyte leakage was calculated using the following equation similar to Falk et al. (2006): (Conductivity before freeze-thaw/conductivity after freeze-thaw) * 100 Treatments were replicated four times and assay data were subjected to one-way analysis of variance (ANOVA) with means compared via the Student-Newman-Keuls method (SNK; α=0.05). 2

Table 1. Common and scientific name of plants screened for sensitivity to flumioxazin. Common Name Scientific Name Native? Alligatorweed Alternanthera philoxeroides (Mart.) Griseb. N American bulrush Schoenoplectus americanus (Pers.) Volkart ex Schinz & R. Keller Y American lotus Nelumbo lutea Willd. Y Arrowhead Sagittaria latifolia Willd. Y Cattail Typha latifolia L. Y Cuban bulrush Oxycaryum cubense (Poepp. & Kunth) Lye Y Duck potato Sagittaria lancifolia L. Y Floating water primrose Ludwigia peploides (Kunth) P.H. Raven Y Giant bulrush Schoenoplectus californicus (C.A. Mey.) Palla Y Giant salvinia Salvinia molesta D.S. Mitchell N Gulf Coast spikerush Eleocharis cellulosa Torr. Y Hardstem bulrush Schoenoplectus acutus Muhl. Ex Bigelow A. Love & D. Love Y Horsetail Equisetum hyemale L. Y Knotgrass Paspalum distichum L. Y Large-flower primrose Ludwigia grandiflora (Michx.) Greuter & Burdet N Maidencane Panicum hemitomon Schult. Y Mexican waterlily Nymphaea mexicana Zucc. Y Pale spikerush Eleocharis macrostachya Britton Y Pennywort Hydrocotyle sp. Y Pickerelweed Pontederia cordata L. Y Slender spikerush Eleocharis acicularis (L.) Roem. & Schult. Y Soft-stem bulrush Schoenoplectus tabernaemontani (C.C. Gmel.) Palla Y Spatterdock Nuphar lutea (L.) Sm. Y Squarestem spikerush Eleocharis quadrangulata (Michx) Roem. & Schult. Y Water hyacinth Eichhornia crassipes (Mart.) Solms N Water lettuce Pistia stratiotes L. N Water paspalum Paspalum fluitans (Elliot) Kunth Y White waterlily Nymphaea odorata Aiton Y RESULTS AND DISCUSSION: Of the 28 species tested, 15 showed no change in electrolyte leakage when exposed to increasing rates of flumioxazin, whereas 13 species showed a significant change compared to untreated plants (Table 2). Species that did not show a change in electrolyte leakage were categorized as not sensitive and species that did show a change were designated as sensitive. All of the bulrush and spikerush species tested fell into the not sensitive category and all of the grass and lily species were sensitive. Other species could not be grouped as easily. For example, within the genus Sagittaria, duck potato was found to be sensitive to flumioxazin, whereas arrowhead was not. The same was also true for the two Ludwigia species; large-flower primrose was sensitive but floating water primrose was not. Of the invasive floating species tested, giant salvinia and water lettuce were sensitive but water hyacinth was not. The remaining four species included horsetail and pennywort, which were not sensitive and alligatorweed and cattail, which were sensitive. It is interesting to note that of the sensitive plants, only maidencane and large-flower primrose showed evidence of a rate response to increased flumioxazin concentrations (Table 2). In contrast, all of the other species denoted as sensitive showed a similar level of electrolyte leakage in response to increasing rates of flumioxazin. While cattail was denoted as sensitive, the magnitude of change in electrolyte leakage was quite low compared to the other plants that were denoted as sensitive (Table 2). 3

Table 2. Mean (± SE) percent electrolyte leakage of emergent plants exposed to flumioxazin for two days. Each mean represents the average of four replicate treatments. Means sharing the same letter in each row do not significantly differ from each other. Data were subjected to a one-way analysis of variance and means were separated using the Student-Newman-Keuls Method (SNK; α=0.05). Species Control 100 µg L -1 200 µg L -1 400 µg L -1 Not Sensitive American bulrush 26.6 ± 1.0 27.6 ± 0.4 32.4 ± 2.2 33.2 ± 2.5 Arrowhead 22.9 ± 1.6 21.0 ± 2.7 24.5 ± 3.2 22.9 ± 3.6 Cuban bulrush 73.4 ± 3.8 66.4 ± 4.5 74.0 ± 4.9 79.8 ± 2.5 Flatstem spikerush 73.5 ± 1.0 73.2 ± 1.1 73.0 ± 2.2 70.2 ± 0.3 Floating water primrose 51.3 ± 0.4 53.8 ± 2.3 58.2 ± 2.5 57.8 ± 1.9 Giant bulrush 66.8 ± 3.8 62.2 ± 1.7 61.1 ± 2.8 63.5 ± 1.0 Gulf Coast spikerush 64.6 ± 6.1 57.6 ± 7.0 55.6 ± 1.9 53.7 ± 6.2 Hardstem bulrush 53.8 ± 3.8 64.2 ± 2.4 68.4 ± 8.4 56.7 ± 6.1 Horsetail 50.3 ± 4.5 67.5 ± 3.8 64.6 ± 7.8 64.4 ± 6.4 Pennywort 59.2 ± 4.9 57.2 ± 7.6 52.9 ± 3.1 52.5 ± 3.9 Pickerelweed 33.4 ± 1.9 36.9 ± 2.3 27.8 ± 2.8 27.3 ± 2.4 Slender spikerush 60.5 ± 6.9 58.9 ± 3.4 59.2 ± 3.8 64.5 ± 3.0 Soft-stem bulrush 74.1 ± 3.2 67.0 ± 3.5 69.6 ± 5.5 71.7 ± 4.7 Squarestem spikerush 61.6 ± 1.5 57.5 ± 7.4 59.0 ± 4.1 59.1 ± 1.4 Water hyacinth 47.6 ± 6.8 42.9 ± 4.2 43.9 ± 4.6 40.3 ± 7.7 Sensitive Alligatorweed 57.4 ± 2.6 b 87.0 ± 2.5 a 85.6 ± 2.6 a 86.3 ± 1.2 a American lotus 45.4 ± 3.2 b 64.9 ± 1.8 a 57.7 ± 5.0 a 62.1 ± 2.2 a Cattail 38.0 ± 2.6 b 44.6 ± 1.9 a 46.4 ± 1.9 a 48.4 ± 2.2 a Duck potato 19.5 ± 1.3 b 35.2 ± 2.9 a 27.6 ± 3.8 a 31.9 ± 4.2 a Giant salvinia 50.9 ± 4.3 b 68.3 ± 6.6 a 79.3 ± 1.3 a 76.2 ± 5.3 a Knotgrass 64.3 ± 2.6 b 80.6 ± 3.4 a 85.8 ± 2.4 a 77.6 ± 1.5 a Large-flower primrose 58.1 ± 3.5 b 66.6 ± 4.0 b 79.1 ± 4.0 a 81.1 ± 3.2 a Maidencane 67.4 ± 1.2 c 66.9 ± 2.5 c 80.1 ± 1.7 b 88.6 ± 1.5 a Mexican waterlily 22.4 ± 2.0 b 71.4 ± 6.6 a 71.9 ± 6.5 a 77.6 ± 5.3 a Spatterdock 52.6 ± 3.1 b 89.6 ± 6.7 a 95.3 ± 4.0 a 75.0 ± 7.4 a Water lettuce 45.5 ± 4.7 b 71.5 ± 6.7 a 75.6 ± 2.8 a 83.7 ± 4.9 a Water paspalum 43.0 ± 7.9 b 73.0 ± 3.5 a 65.9 ± 5.1 a 61.5 ± 2.1 a White waterlily 24.2 ± 3.8 b 60.3 ± 5.1 a 61.0 ± 6.1 a 55.4 ± 1.5 a The assay results will ultimately require additional field and mesocosm corroboration and it is likely that species will be further categorized into sensitive, not sensitive, and rate-dependent sensitive categories. Similar to results from the small-scale cup assay, duck potato and maidencane were sensitive to flumioxazin in a large-scale mesocosm trial conducted by Mudge and Haller (in press), with EC 50 values of 15 and 259 µg ai L -1, respectively. Mudge and Haller (in press) also reported an EC 50 value of 894 µg ai L -1 for pickerelweed, which was not found to be sensitive in this assay. Several species observed as highly sensitive following various field applications (e.g. American lotus, Mexican waterlily, spatterdock, water lettuce, and white waterlily) 1 were also sensitive in this assay. While cattails have not been particularly sensitive to flumioxazin following field applications for water lettuce 1 Personal Observation. 2012. Dr. Mike Netherland, Research Biologist, US Army Engineer Research and Development Center, Vicksburg, MS. 4

control at lower use rates (140 to 420 g ha -1 ), increasing use rates to 560 to 1120 g ha -1 can significantly increase visual injury. Flumioxazin is generally not recognized as being phloem-mobile (Senseman 2007); therefore, it is likely that many emergent rooted plants denoted as sensitive to flumioxazin will initially display strong injury symptoms on the vegetation above the water line. This assay cannot predict whether a given species will ultimately be controlled by flumioxazin, but it should indicate if a given species is likely to be severely injured by flumioxazin. Primary screens that provide rapid data on the relative sensitivity of a species to a given herbicide can enhance the design of larger scale studies as well as predict the response of field populations. The utility for these small assays to provide information on threatened or rare plant species has not been explored, but with the limited tissue requirements, this would be a good first step for determining potential sensitivity. Given the high cost, extensive time requirements, and limited number of replicates available in the larger systems, methods that can be used to predict response and improve study design are of significant value. As further selectivity data for the protox inhibitors is developed, managers can use this information for site-specific treatment recommendations when selective control is considered a priority. FUTURE WORK: The results of these assays require additional confirmation with various mesocosm and field trials to determine if rate responses in the assays can be used to further refine field recommendations. Additional assay and mesocosm trials focusing on sensitive species may help determine which of these plants are highly sensitive versus species that are moderately sensitive. This would provide valuable information to managers who are under increasing pressure to provide selective control. Additional assay development with other active ingredients is planned, as this approach can represent a low-cost predictive tool that improves study design. ACKNOWLEDGMENTS: Support for this project was provided by the Aquatic Plant Control Research Program (APCRP), Dr. Linda Nelson, Program Manager. Permission to publish this information was granted by the Chief of Engineers. Citation of trade names does not constitute an official endorsement or approval of the use of such products. POINTS OF CONTACT: For additional information, contact the authors, LeeAnn M. Glomski (972) 436-2215, LeeAnn.M.Glomski@usace.army.mil, Michael D. Netherland (352) 392-0335, Michael.D. Netherland@usace.army.mil or the Manager of the Aquatic Plant Control Research Program, Linda S. Nelson (601) 634-2656, Linda.S.Nelson@usace.army.mil. This technical note should be cited as follows: Glomski, L. M., and M.D. Netherland. 2013. Small-scale primary screening method to predict impacts of the protox inhibiting herbicide flumioxazin on native and invasive emergent plants. APCRP Technical Notes Collection (ERDC/TN APCRP- CC-18). Vicksburg, MS: U.S. Army Engineer Research and Development Center, Vicksburg, MS. http://ed.erdc.usace.army.mil/aqua/ 5

REFERENCES: Dexter, S. T., W. E. Tottingham, and L. F. Graber. 1932. Investigations of the hardiness of plants by measurement of electrical conductivity. Plant Physiol. 7(1):63-78. Duke, S. H., G. Kakefuda, and T. M. Harvey. 1983. Differential leakage of intracellular substances from imbibing soybean seeds. Plant Physiol. 72:919-924. Duke, S. O., and W. H. Kenyon. 1993. Peroxidizing activity determined by cellular leakage. In: Target assays for modern herbicides and related phytotoxic compounds, ed. P. Boger and G. Sandman, 61-66. Boca Raton, FL: CRC Press. Falk, J. S, K. Al-Khatib, and D. E. Peterson. 2006. Rapid assay evaluation of plant response to protoporphyrinogen oxidase (protox)-inhibiting herbicides. Weed Tech. 20:104-112. Getsinger, K. D., A. G. Poovey, L. Glomski, J. G. Slade, and R. J. Richardson. 2011. Utilization of herbicide contentration/exposure time relationships for controlling invasive plants on Lake Gaston, Virginia/North Carolina. ERDC/EL TR-11-5. Vicksburg, MS: U.S. Army Engineer Research and Development Center. Glomski, L. M., and C. R. Mudge. 2009. Effect of submersed applications of bispyribac-sodium on non-target emergent vegetation. APCRP Technical Notes Collection. ERDC/TN APCRP-CC-12. Vicksburg, MS: U.S. Army Engineer Research and Development Center. http://el.erdc.usace.army.mil/aqua/ Glomski, L. M., and L. S. Nelson. 2008. Evaluation of 2,4-D ester and triclopyr amine against waterlily and spatterdock. APCRP Technical Notes Collection. ERDC/TN APCRP-CC-07. Vicksburg, MS: U.S. Army Engineer Research and Development Center. http://el.erdc.usace.army.mil/aqua/ Glomski, L. M., and M. D. Netherland. 2012. Evaluation of liquid and granular triclopyr against waterlily, spatterdock and hardstem bulrush. In Aquatic Plant Management Society Annual Meeting Abstracts, Salt Lake City, UT. http://apms.org/wp/wp content/uploads/2012/10/2012finalagenda.pdf. Accessed September 6, 2012. Glomski, L. M., and M. D. Netherland. Utilization of a small-scale primary screening method to predict impacts of flumioxazin and carfentrazone-ethyl on native and invasive submersed plants. J. Aquat. Plant Manage. In press. Glomski, L. M., M. D. Netherland, and L. S. Nelson. 2009. Potential impact of submersed 2,4-D and triclopyr applications on native emergent plants. APCRP Technical Notes Collection. ERDC/TN APCRP-CC-10. Vicksburg, MS: U.S. Army Engineer Research and Development Center. http://el.erdc.usace.army.mil/aqua/ Hess, F. D. 2000. Light-dependent herbicides: An overview. Weed Sci. 48(2):160-170. Kenyon, W. H., S. O. Duke, and K. C. Vaughn. 1985. Sequence of effects of acifluorfen on physiological and ultrastructural parameters in cucumber cotyledon discs. Pestic. Biochem. Physiol. 24:240-250. Koo, S. J., J. C. Neal, and J. M. DiTomaso. 1994. Quinclorac-induced electrolyte leakage in seedling grasses. Weed Sci. 42:1-7. Koschnick, T. J., M. D. Netherland, and W. T. Haller. 2007. Effects of three ALS-inhibitors on five emergent native plant species in Florida. J. Aquat. Plant Manage. 45:47-51. Koschnick, T. J., W. T. Haller, and L. Glasgow. 2006. Documentation of landoltia (Landoltia punctata) resistance to diquat. Weed Sci. 54:615-619. Li, Z., R. H. Walker, G. Wehtje, and H. G. Hancock. 2000. Using electrolyte leakage to detect soybean (Glycine max) cultivars sensitive to sulfentrazone. Weed Tech. 14:699-704. Mudge, C. R., and W. T. Haller. 2006. Flumioxazin: A new EUP for aquatic weed control. In Aquatic Plant Management Society Annual Meeting Abstracts, Portland, OR. http://apms.org/wp/wp-content/uploads/2012/10/2006 program.pdf. Accessed September 6, 2012. Mudge, C. R., and W. T. Haller. Response of target and non-target floating and emergent aquatic plants to flumioxazin. J. Aquat. Plant Manage. In press. Netherland, M. D. 2011. Selective control of water hyacinth and water lettuce growing among bulrush. Aquatic Plant Management Society Annual Meeting Abstracts, Baltimore, MD. http://apms.org/wp/wp-content/uploads/2012/10/2011 program.pdf. Accessed September 6, 2012. 6

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