Hostname: page-component-cd9895bd7-7cvxr Total loading time: 0 Render date: 2024-12-25T08:09:58.551Z Has data issue: false hasContentIssue false

Do applications of systemic herbicides when green fruit are present prevent seed production or viability of garlic mustard (Alliaria petiolata)?

Published online by Cambridge University Press:  05 March 2021

Leo Roth
Affiliation:
Associate Research Specialist, Agronomy Department, University of Wisconsin–Madison, Madison, WI, USA
José Luiz C. S. Dias
Affiliation:
Agronomy and Weed Management Advisor–Merced, San Joaquin and Stanislaus Counties, University of California Cooperative Extension, Merced, CA, USA
Christopher Evans
Affiliation:
Forestry Extension and Research Specialist, Department of Natural Resources and Environmental Sciences, University of Illinois, Urbana, IL, USA
Kevin Rohling
Affiliation:
Forestry Research Technician, Department of Natural Resources and Environmental Sciences, University of Illinois, Urbana, IL, USA
Mark Renz*
Affiliation:
Professor and Extension Weed Specialist, Agronomy Department, University of Wisconsin–Madison, Madison, WI, USA
*
Author for correspondence: Mark Renz, Moore Hall, 1575 Linden Drive, University of Wisconsin–Madison, Madison, WI53706. (Email: [email protected])
Rights & Permissions [Opens in a new window]

Abstract

Garlic mustard [Alliaria petiolata (M. Bieb.) Cavara & Grande] is a biennial invasive plant commonly found in the northeastern and midwestern United States. Although it is not recommended to apply herbicides after flowering, land managers frequently desire to conduct management during this timing. We applied glyphosate and triclopyr (3% v/v and 1% v/v using 31.8% and 39.8% acid equivalent formulations, respectively) POST to established, second-year A. petiolata populations at three locations when petals were dehiscing and evaluated control, seed production, and seed viability. POST glyphosate applications at this timing provided 100% control of A. petiolata by 4 wk after treatment at all locations, whereas triclopyr efficacy was variable, providing 38% to 62% control. Seed production was only reduced at one location, with similar results regardless of treatment. Percent seed viability was also reduced, and when combined with reductions in seed production, resulted in a 71% to 99% reduction in number of viable seeds produced per plant regardless of treatment. While applications did not eliminate viable seed production, our findings indicate that glyphosate and triclopyr applied while petals are dehiscing is a viable alternative to cutting or hand pulling at this timing, as it substantially decreased viable A. petiolata seed production.

Type
Research Article
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
© The Author(s), 2021. Published by Cambridge University Press on behalf of the Weed Science Society of America

Management Implications

Glyphosate and triclopyr POST applications to rosettes in the early spring are standard treatments used to manage Alliaria petiolata (garlic mustard). However, weather and other priorities limit the window for management, forcing field practitioners to utilize more labor-intensive methods such as hand pulling. It is not known how late in the development of A. petiolata these herbicides can be applied to prevent viable seed production. Because prevention of soil seedbank replenishment is a key management factor for effective long-term control of biennial invasive species, we hypothesized late spring foliar herbicide applications to second-year A. petiolata plants when flower petals were dehiscing could be an effective management tool if seed production or viability is eliminated. Our study indicated that glyphosate applications at this timing provided 100% control of A. petiolata plants by 4 wk after treatment at all locations, whereas triclopyr efficacy was inconsistent. Although both glyphosate and triclopyr decreased viable seed production to nearly zero at one of our three study locations, the same treatments produced significant amounts of viable seed at the other two locations. Our findings suggest late spring glyphosate and triclopyr applications should not be recommended over early spring applications to rosettes for A. petiolata management, as our late spring application timing did not prevent viable seed production, and may require multiple years of implementation to eradicate populations. Nonetheless, this application timing holds value in areas devoid of desirable understory vegetation compared with no management practices or mechanical management options, including hand pulling when fruit are present, as overall viable seed production was reduced to levels similar to those seen with these treatments.

Introduction

Garlic mustard [Alliaria petiolata (M. Bieb.) Cavara & Grande] is a biennial invasive forb originally from Europe (Nuzzo Reference Nuzzo2000). It was introduced into North America in the 1800s (Grieve Reference Grieve2013) and by 2000 had spread to 34 U.S. states and four Canadian provinces (Nuzzo Reference Nuzzo2000). The continued spread of A. petiolata is well documented, including more than 50,000 unique occurrences in the United States, with most occurring in the northeastern and midwestern United States (EDDMapS 2020). Although A. petiolata commonly infests forests in partial sunlight, it can also be present in a wide range of habitats, including railroad ballast, floodplains, and xeric ridgetops (Byers and Quinn Reference Byers and Quinn1998; Nuzzo Reference Nuzzo2000). Forest understories dominated by A. petiolata are associated with negative impacts to native ecosystems, including low richness and diversity of native herbaceous vegetation (Anderson et al. Reference Anderson, Dhillion and Kelley1996; Nuzzo Reference Nuzzo2000) and reduced growth of tree seedlings that depend on arbuscular mycorrhizal fungi (Burke Reference Burke2008; Stinson et al. Reference Stinson, Campbell, Powell, Wolfe, Callaway, Thelen, Hallett, Prati and Klironomos2006).

While a range of management activities are effective for A. petiolata, hand pulling is the most common method used to control adult (second-year) plants. Hand pulling is effective (Panke and Renz Reference Panke and Renz2012; Shartell et al. Reference Shartell, Nagel and Storer2012) and is typically conducted when plants are bolting to fruiting, but this technique requires more time and results in more soil disturbance compared with other control methods. Additionally, hand pulling requires annual efforts and multiple years to maintain high levels of control. Herbicides are also effective for controlling A. petiolata, with applications made to green rosettes during the fall, winter, or spring between seedling germination and flower stalk elongation providing high levels of control (Becker et al. Reference Becker, Gerber, Hinz, Katovich, Panke, Renz, Reardon and Van Riper2013; Frey et al. Reference Frey, Herms and Cardina2007; Nuzzo Reference Nuzzo2000). While research has shown the period between fall and spring to be the ideal time for control and the prevention of seed production (Shartell et al. Reference Shartell, Nagel and Storer2012), many obstacles prevent herbicide application during this time frame. Snow and excessive rain can limit site access, and cold temperatures can reduce effectiveness of herbicides (Bryson Reference Bryson1987, Reference Bryson1988; Reddy Reference Reddy2000; Roggenbuck et al. Reference Roggenbuck, Rowe, Penner, Petroff and Burow1990). Additionally, competing priorities, including brush removal in fall and winter and prescribed fire in spring, conflict with timely herbicide application between fall and spring. Applications later in A. petiolata’s development would provide additional time to manage populations when precipitation is less frequent, daytime maximum temperatures are optimal for uptake of systemic herbicides, and other land management priorities are reduced. If effective, this application timing could extend the management window for A. petiolata, but herbicide efficacy remains unknown, and production of viable seed is a concern when fruit are present during herbicide application.

We evaluated late spring herbicide applications when A. petiolata petals were dehiscing and green fruits were just beginning to develop. The objectives of this study were to evaluate the effectiveness of foliar glyphosate or triclopyr applications just after petal dehiscence to control A. petiolata and prevent viable seed production. Three field locations were established for 1 yr (two in Wisconsin and one in Illinois) in either 2017 or 2018 to evaluate the effectiveness of this timing on A. petiolata control, seed production, and seed viability.

Materials and Methods

Study Sites

The study was conducted at two different locations in Wisconsin (2017 and 2018) and at one location in Illinois (2018). The experiment conducted in 2017 was located near Prairie du Sac (Prairie), WI (43.352°N, 89.758°W), and the experiments conducted in 2018 were located near Fitchburg, WI (43.019°N, 89.454°W), and Dixon Springs, IL, at the Dixon Springs Agricultural Center (Dixon) (37.428°N, 88.664°W). All research sites consisted of forested areas with the understory having at least 75% cover of A. petiolata (Figure 1). Soil types were silt loams at both Wisconsin locations with 2% to 3% organic matter, whereas the Illinois site was a silt loam with 0.6% organic matter (USDA-NRCS 2020). Total rainfall at Prairie, Fitchburg, and Dixon during the experimental period (June and July at Prairie and Fitchburg; May and June at Dixon) was 46% to 75% above the 30-yr monthly average, among sites. However, monthly temperatures were similar to the 30-yr average during the experimental periods (Table 1).

Figure 1. Stage of Alliaria petiolata development during treatment application at all three sites. Petal dehiscence has initiated, and green fruit are present and developing.

Table 1. Average monthly temperatures and precipitation during the experimental period at each research site with 30-yr monthly averages shown for comparison. a

a Abbreviations: Prairie, Prairie du Sac; Dixon, Dixon Springs Agricultural Center; temp., temperature; precip., precipitation.

b Midwest Regional Climate Center (2020) 1987–2018 averages.

Experimental Design, Measurements, and Analysis

Herbicides were applied at Prairie on May 27, 2017, Fitchburg on May 31, 2018, and at Dixon on May 7, 2018. All herbicides were applied POST to A. petiolata plants with green fruit present and dehiscing petals (Figure 1). Two herbicide treatments and one nontreated control were established in 1.5 by 5 m plots (7.5 m2 plots) arranged in a randomized complete block design with three replications at Prairie and four replications at Fitchburg and Dixon. Herbicide treatments consisted of triclopyr (1% v/v of a 31.8% acid equivalent formulation; Garlon® 3A, Dow AgroSciences, 9330 Zionsville Road, Indianapolis, IN, USA) plus methylated seed oil (1% v/v) and glyphosate (3% v/v of a 39.8% acid equivalent formulation; Roundup PowerMax®, Monsanto Company, 800 N Lindbergh Boulevard, St Louis, MO, USA) plus ammonium sulfate (9.6 g L−1). All herbicide treatments were applied to the foliage of individual plants until just before the point of runoff. Treatments were applied with a CO2-pressurized backpack sprayer using a single-nozzle boom equipped with one TeeJet® 11002VS nozzle (TeeJet® Technologies, 200 W. North Ave, Glendale Heights, IL, USA) estimated to deliver 280 L of spray solution ha−1. While applications targeted second year A. petiolata plants, spray solution also contacted rosettes underneath treated plants.

Effectiveness of treatments was evaluated by visually estimating control of A. petiolata and measuring seed production and viability. Visual estimates of control were performed 2, 4, and 6 wk after treatment on a rating scale of 0% to 100%, with 0% equivalent to no control and 100% equivalent to complete plant death. When A. petiolata siliques matured on the plant but before dehiscence between 6 and 8 wk after treatment, three plants were harvested from each plot. All seeds were removed from siliques, air-dried, pooled, and counted. Seed viability was estimated by subjecting subsamples of 50 seeds from each plot to a tetrazolium test (Sosnoskie and Cardina Reference Sosnoskie and Cardina2009). Tetrazolium-tested seeds were then dissected and analyzed using a dissecting microscope and classified as viable or nonviable using AOSA/SCST guidelines (AOSA/SCST 2010). Absolute number of viable seeds produced was estimated by multiplying the percentage of viable seed by the average number of seeds produced per plant for each treatment.

Initial analyses found a site by treatment interaction, and therefore each site was analyzed separately using PROC MIXED in SAS (SAS release 9.3, SAS Institute, 100 SAS Campus Drive, Cary, NC, USA). Treatments were considered fixed effects, whereas block was considered random. Differences were declared when P < 0.05, and mean separation was based on the PDIFF option of LSMEANS in SAS. Total seed production and seed viability data were square-root transformed to meet the ANOVA assumptions of normality and homoscedasticity; however, untransformed means are presented.

Results and Discussion

Control differed with respect to herbicide treatments at all research sites and evaluation timings (Table 2). Although our main study goal is to quantify the impacts of herbicide treatments on A. petiolata seed production and viability, visual assessment of control on the target weed species was collected as it is useful information for land managers (Enloe et al. Reference Enloe, O’Sullivan, Loewenstein, Brantley and Lauer2016). At 2 and 4 wk after treatment, glyphosate provided A. petiolata control of 78% to 100% compared with triclopyr, which only provided 20% to 62% control at all locations (Table 2). By 6 wk after treatment, control was >90% with both treatments at Dixon; however, glyphosate maintained higher control than triclopyr at Prairie (100% vs. 73%, respectively) (Table 2). Others have found many active ingredients to be effective at controlling A. petiolata in addition to glyphosate and triclopyr, but applications are recommended during the rosette stage (Panke and Renz Reference Panke and Renz2012). The poor control of adult A. petiolata plants by triclopyr could be explained by the late A. petiolata development stage at application, which could have substantial management implications, as Pardini et al. (Reference Pardini, Drake, Chase and Knight2009) estimate that >85% control of adult plants is required annually to reduce or eliminate populations. Given that this relationship is density dependent (Pardini et al. Reference Pardini, Drake, Chase and Knight2009), more research is required to understand what threshold of control is required to obtain A. petiolata population reductions.

Table 2. Visual estimates of control and SE (in parentheses) at 2, 4, and 6 wk after treatment of Alliaria petiolata. a

a Abbreviations: Prairie, Prairie du Sac; Dixon, Dixon Springs Agricultural Center; WAT, weeks after treatment.

b Treatments were applied when green fruits were present and petals were dehiscing. Glyphosate and triclopyr applications were made using 39.8% and 31.8% acid equivalent formulations, respectively.

c 6 WAT control data were not collected at the Fitchburg site.

d Different lowercase letters within a column indicate differences in treatment LS means (P < 0.05, PDIFF method for multiple comparison).

Effective long-term weed management strategies require understanding how management practices impact weed seed production and viability, especially for species like A. petiolata that rely on seed production to sustain populations. In our study, herbicide treatment effects on A. petiolata seed production per plant were identified at Dixon (P < 0.01); however, no difference among treatments was detected at Fitchburg or Prairie (P ≥ 0.10) (Table 3). At Dixon, glyphosate and triclopyr treatments provided equivalent reductions in A. petiolata seed production (74% and 64%) compared with nontreated plants (540 seeds plant−1). These findings align with previous research that documents seed reductions when herbicides are applied to flowering weeds (Clay and Griffin Reference Clay and Griffin2000; Taylor and Oliver Reference Taylor and Oliver1997; Walker and Oliver Reference Walker and Oliver2008; Menalled et al. Reference Menalled, Davis and Mangold2018). However, at Prairie and Fitchburg, we did not detect a significant herbicide treatment effect compared with nontreated plants (Table 3; P > 0.05), suggesting reduction in seed production is highly variable. Other research has found that POST herbicide applications failed to reduce the number of seeds (Steckel et al. Reference Steckel, Defelice and Sims1990) or that seed production per plant was more affected by crop canopy than herbicide treatments (Mosqueda et al. Reference Mosqueda, Lim, Sbatella, Jha, Lawrence and Kniss2020). Thus, weed seed production responses to POST weed control strategies vary, as they can be impacted by different factors such as weed species, time of application, and other edaphoclimatic conditions.

Table 3. Total number of seeds produced per plant, percentage of viable seeds produced, and total number of viable seeds produced per plant of established Alliaria petiolata at 41–56 d after treatment. a

a Abbreviations; Prairie, Prairie du Sac; Dixon, Dixon Springs Agricultural Center.

b Treatments were applied when green fruit were present, and petals were dehiscing. Glyphosate and triclopyr were made using 39.8% and 31.8% acid equivalent formulations, respectively.

c Different lowercase letters within a column indicate differences in treatment LS means (P < 0.05, PDIFF method for multiple comparison).

d P-values listed as not significant if ≥0.10.

Although herbicide applications did not result in significantly lower A. petiolata seed production in two of our three research locations, glyphosate and triclopyr applications decreased the percent viability and number of viable seeds per plant compared with the untreated control at all locations (P < 0.01, P < 0.05, and P < 0.01 at Prairie, Fitchburg, and Dixon, respectively) (Table 3). The greatest reduction in seed viability occurred at Dixon, where a >95% reduction in seed viability was observed with glyphosate and triclopyr applications (Table 3). The percent of A. petiolata seed viability was highly variable, as it depended on the site and herbicide treatment (<1% to 46.5%). Despite this variability, the total number of viable seeds produced decreased similarly across glyphosate and triclopyr treatments at each location. Glyphosate or triclopyr applications reduced the number of viable seeds anywhere from 71% to 99.5% compared with untreated plants (P < 0.05) but never eliminated viable seed (Table 3). This clearly demonstrates that late spring POST applications of glyphosate and triclopyr can result in production of viable seed; therefore, land managers should consider this before selecting this approach over earlier timings that would prevent seed production.

These results are similar to those seen with hand pulling of A. petiolata plants. Shartell et al. (Reference Shartell, Nagel and Storer2012) found a 76% reduction in adult A. petiolata density 1 mo after treatment, but hand-pulled plants can produce viable seed (Chapman et al. Reference Chapman, Cantino and McCarthy2012). Despite similar results, hand pulling likely requires increased effort in moderate to large populations and has substantial soil disturbance that can increase the potential for establishment of A. petiolata seedlings compared with our approach. These differences in combination with the lack of control of seedling plants the following year (Shartell et al. Reference Shartell, Nagel and Storer2012) highlight the benefits of glyphosate or triclopyr applications in late spring over hand pulling. However, substantial risk to desirable understory vegetation growing among A. petiolata exists with this approach. If spray solution contacts these desirable plants’ leaves or stems, high levels of injury or even mortality may occur. This hazard may limit the benefit of this approach to areas devoid of desirable species in the forest understory at the time of application.

In summary, our findings indicate that even though late spring POST glyphosate and triclopyr applications decrease A. petiolata seed productivity and viability in the year of herbicide application, the later timing should not be recommended over early spring POST applications to rosettes, as the later timing did not completely prevent viable seed production. Glyphosate or triclopyr applied at this late stage of development is a suitable alternative to hand pulling, although both strategies require repeated implementation to reduce or eliminate A. petiolata populations. The value of this herbicide application timing may be particularly evident in large sites that have dense infestations of A. petiolata and lack desirable understory vegetation sensitive to glyphosate or triclopyr. In these areas, the increased efficiency of this herbicide application method relative to hand pulling could permit managers to manage more area in a given year.

Acknowledgments

The authors would like to thank Christopher Bloomingdale, Niels Jorgensen, Anne Pearce, and Chelsea Zegler for their support. This research received no specific grant from any funding agency or the commercial or not-for-profit sectors. No conflicts of interest have been declared.

Footnotes

Associate Editor: John Cardina, Ohio State University

References

Anderson, RC, Dhillion, SS, Kelley, TM (1996) Aspects of the ecology of an invasive plant, garlic mustard (Alliaria petiolata) in central Illinois. Restor Ecol 4:181191 CrossRefGoogle Scholar
[AOSA/SCST] Association of Official Seed Analysts/Society of Commercial Seed Technologists (2010) Tetrazolium Testing Handbook. Ithaca, NY:AOSA/SCST. 32 pGoogle Scholar
Becker, R, Gerber, E, Hinz, HL, Katovich, E, Panke, B, Renz, M, Reardon, R, Van Riper, L (2013) Biology and biological control of garlic mustard. Washington, DC: U.S. Department of Agriculture, Forest Service, Forest Health Technology Enterprise Team FHTET-2012-05. 76 pGoogle Scholar
Bryson, CT (1987) Effects of rainfall on foliar herbicides applied to rhizome johnsongrass. Weed Sci 35:115119 CrossRefGoogle Scholar
Bryson, CT (1988) Effects of rainfall on foliar herbicide applied to seedling johnsongrass (Sorghum halepense). Weed Technol 2:153158 CrossRefGoogle Scholar
Burke, DJ (2008) Effects of Alliaria petiolata (garlic mustard; Brassicaceae) on mycorrhizal colonization and community structure in three herbaceous plants in a mixed deciduous forest. Am J Bot 95:14161425 CrossRefGoogle Scholar
Byers, DL, Quinn, JA (1998) Demographic variation in Alliaria petiolata (Brassicaceae) in four contrasting habitats. J Torrey Bot Soc 125:138149 CrossRefGoogle Scholar
Chapman, JI, Cantino, PD, McCarthy, BC (2012) Seed production in garlic mustard (Alliaria petiolata) prevented by some methods of manual removal. Nat Area J 32:305315 CrossRefGoogle Scholar
Clay, PA, Griffin, JL (2000) Weed seed production and seedling emergence responses to late-season glyphosate applications. Weed Sci 48:481486 CrossRefGoogle Scholar
EDDMapS (2020) Early Detection & Distribution Mapping System. University of Georgia–Center for Invasive Species and Ecosystem Health. http://www.eddmaps.org. Accessed: March 25, 2020Google Scholar
Enloe, SF, O’Sullivan, SE, Loewenstein, NJ, Brantley, EF, Lauer, DK (2016) Triclopyr application timing and concentration influence low-volume basal bark efficacy on Chinese privet (Ligustrum sinense). Invasive Plant Sci Manag 9:235241 CrossRefGoogle Scholar
Frey, MN, Herms, CP, Cardina, J (2007) Cold weather application of glyphosate for garlic mustard (Alliaria petiolata) control. Weed Technol 21:656660 CrossRefGoogle Scholar
Grieve, M (2013) A Modern Herbal. Mineola, NY: Dover. 919 pGoogle Scholar
Menalled, UD, Davis, SC, Mangold, JM (2018) Effect of herbicide management practices used by invasive plant managers on Berteroa incana (hoary alyssum) seed biology and control. Invasive Plant Sci Manag 11:101106 CrossRefGoogle Scholar
Midwestern Regional Climate Center (2020) cli-MATE: MRCSS Application Tools Environment. https://mrcc.illinois.edu/CLIMATE. Accessed: March 26, 2020Google Scholar
Mosqueda, EG, Lim, CA, Sbatella, GM, Jha, P, Lawrence, NC, Kniss, AR (2020) Effect of crop canopy and herbicide application on kochia (Bassia scoparia) density and seed production. Weed Sci 68:278284 CrossRefGoogle Scholar
Nuzzo, V (2000) Element Stewardship Abstract for Alliaria petiolata (Alliaria officinalis) Garlic Mustard. Fairfax, VA: Nature Conservancy. 19 pGoogle Scholar
Panke, B, Renz, M (2012) Garlic Mustard (Alliaria petiolata). Management of Invasive Plants in Wisconsin. Madison: University of Wisconsin Extension A3924-07. 4 pGoogle Scholar
Pardini, EA, Drake, JM, Chase, JM, Knight, TM (2009) Complex population dynamics and control of the invasive biennial Alliaria petiolata (garlic mustard). Ecol Appl 19:387397 CrossRefGoogle Scholar
Reddy, KN (2000) Factors affecting toxicity, absorption, and translocation of glyphosate in redvine (Brunnichia ovata). Weed Technol 14:457462 CrossRefGoogle Scholar
Roggenbuck, FC, Rowe, L, Penner, D, Petroff, L, Burow, R (1990) Increasing postemergence herbicide efficacy and rainfastness with silicone adjuvants. Weed Technol 4:576580 CrossRefGoogle Scholar
Shartell, LM, Nagel, LM, Storer, AJ (2012) Efficacy of treatments against garlic mustard (Alliaria petiolata) and effects on forest understory plant diversity. Forests 3:605613 CrossRefGoogle Scholar
Sosnoskie, LM, Cardina, J (2009) Laboratory methods for breaking dormancy in garlic mustard (Alliaria petiolata) seeds. Invasive Plant Sci Manag 2:185189 CrossRefGoogle Scholar
Steckel, LE, Defelice, MS, Sims, BD (1990) Integrating reduced rates of postemergence herbicides and cultivation for broadleaf weed-control in soybeans (Glycine max). Weed Sci 38:541545 CrossRefGoogle Scholar
Stinson, KA, Campbell, SA, Powell, JR, Wolfe, BE, Callaway, RM, Thelen, GC, Hallett, SG, Prati, D, Klironomos, JN (2006) Invasive plant suppresses the growth of native tree seedlings by disrupting belowground mutualisms. PLoS Biol 4:07270731 CrossRefGoogle ScholarPubMed
Taylor, SE, Oliver, LR (1997) Sicklepod (Senna obtusifolia) seed production and viability as influenced by late-season postemergence herbicide applications. Weed Sci 45:497501 CrossRefGoogle Scholar
[USDA-NRCS] U.S. Department of Agriculture–Natural Resources Conservation Service (2020) Web Soil Survey. http://websoilsurvey.nrcs.usda.gov. Accessed: March 26, 2020Google Scholar
Walker, ER, Oliver, LR (2008) Weed seed production as influenced by glyphosate applications at flowering across a weed complex. Weed Technol 22:318325 CrossRefGoogle Scholar
Figure 0

Figure 1. Stage of Alliaria petiolata development during treatment application at all three sites. Petal dehiscence has initiated, and green fruit are present and developing.

Figure 1

Table 1. Average monthly temperatures and precipitation during the experimental period at each research site with 30-yr monthly averages shown for comparison.a

Figure 2

Table 2. Visual estimates of control and SE (in parentheses) at 2, 4, and 6 wk after treatment of Alliaria petiolata.a

Figure 3

Table 3. Total number of seeds produced per plant, percentage of viable seeds produced, and total number of viable seeds produced per plant of established Alliaria petiolata at 41–56 d after treatment.a