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Response of black swallowwort (Vincetoxicum nigrum) to herbicides plus mowing

Published online by Cambridge University Press:  20 December 2022

Lindsey R. Milbrath*
Affiliation:
Research Entomologist, USDA-ARS Robert W. Holley Center for Agriculture and Health, Ithaca, NY, USA
Jeromy Biazzo
Affiliation:
Biologist, USDA-ARS, Robert W. Holley Center for Agriculture and Health, Ithaca, NY, USA
Scott H. Morris
Affiliation:
Research Technician, Soil and Crop Sciences Section, School of Integrative Plant Science, Cornell University, Ithaca, NY, USA
Antonio DiTommaso
Affiliation:
Professor, Soil and Crop Sciences Section, School of Integrative Plant Science, Cornell University, Ithaca, NY, USA
*
Author for correspondence: Lindsey R. Milbrath, USDA-ARS Robert W. Holley Center for Agriculture and Health, 538 Tower Road, Ithaca, NY 14853. Email: lindsey.milbrath@usda.gov
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Abstract

The invasive vine black swallowwort [Vincetoxicum nigrum (L.) Moench = Cynanchum louiseae Kartesz & Gandhi, Apocynaceae] is difficult to control, and herbicide studies are lacking. This long-lived perennial species is primarily found in high-light environments in natural areas and perennial cropping systems in northeastern North America. We conducted a 3-yr herbicide efficacy study, with or without mowing, in an old-field site infested with V. nigrum in Dutchess County, NY, USA. Experimental plots were either herbicide treated in early July or mowed in early July and subsequently herbicide treated in late August for 2 yr with the potassium salt of glyphosate (2.02 kg ae ha−1), the isopropylamine salt of glyphosate (1.35 kg ae ha−1), or the butoxyethyl ester of triclopyr (1.79 kg ae ha−1). Both glyphosate formulations were effective in reducing V. nigrum aboveground biomass, although they were somewhat less effective in reducing cover or stem densities of V. nigrum plants >10-cm tall after 2 yr compared with untreated plots. Mowing did not always enhance the efficacy of foliar glyphosate applications. Triclopyr, with or without mowing, was generally not effective against V. nigrum in our study. The only significant effect of triclopyr was to increase the cover of grasses in the plots. While annual applications of glyphosate can be useful for management of V. nigrum infestations, higher rates and more frequent applications of triclopyr need to be investigated to determine its usefulness for V. nigrum control.

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BY
To the extent this is a work of the US Government, it is not subject to copyright protection within the United States. Published by Cambridge University Press on behalf of the Weed Science Society of America.
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, provided the original article is properly cited.
Copyright
© U.S. Department of Agriculture - Agricultural Research Service and the Author(s), 2022

Management Implications

Black swallowwort (Vincetoxicum nigrum) is a European twining vine that was introduced into eastern North America. Herbicidal control is a potentially effective management approach, but herbicide control studies have only been published for the related pale swallowwort (Vincetoxicum rossicum). We evaluated different herbicides, combined with mowing or not, applied over 2 yr to a moderate- to high-density population of V. nigrum in Dutchess County, NY, USA. Vincetoxicum nigrum in plots was either sprayed at flowering in early July or mowed in early July followed by a herbicide application in late August after plants had flowered again. We tested the potassium salt of glyphosate (2.02 kg ae ha−1), the isopropylamine salt of glyphosate (1.35 kg ae ha−1), and the butoxyethyl ester of triclopyr (1.79 kg ae ha−1). Both glyphosate formulations reduced V. nigrum aboveground biomass by 83% to 98% after 2 yr, although reductions in V. nigrum cover or stem densities of plants >10-cm tall were not as large relative to untreated plots. Mowing did not always enhance the efficacy of foliar glyphosate applications. In contrast, triclopyr, with or without mowing, was generally not effective against V. nigrum, although grass cover did increase. Repeated single applications of glyphosate can be useful for the management of V. nigrum, but higher rates and possibly more frequent applications of triclopyr will need to be assessed to determine if triclopyr can be used for the control of V. nigrum.

Introduction

Black swallowwort [Vincetoxicum nigrum (L.) Moench = Cynanchum louiseae Kartesz & Gandhi, Apocynaceae], a herbaceous viny perennial plant, was first introduced into North America in the mid-1800s (Sheeley and Raynal Reference Sheely and Raynal1996). Originating in southwestern Europe, V. nigrum is currently reported from 21 U.S. states and the Canadian provinces of Ontario and Quebec (USDA-NRCS 2022). Within the United States, the primary infestations occur in northeastern states, with increasing populations in some midwestern states (Alred et al. Reference Alred, Hufbauer and Szűcs2022). As previously noted, the one reported infestation of V. nigrum in California has likely disappeared (Milbrath and Biazzo Reference Milbrath and Biazzo2016). Along with its congener pale swallowwort [Vincetoxicum rossicum (Kleopow) Barb. = Cynanchum rossicum (Kleopow) Borhidi] from southeastern Europe, it has invaded a variety of habitats ranging from open field to forest, including both unmanaged and managed lands (DiTommaso et al. Reference DiTommaso, Lawlor and Darbyshire2005). Infestations of V. nigrum primarily occur in open-field habitats, whereas forest invasion is much less common for this species. Vincetoxicum nigrum spreads through its wind-dispersed seeds, and stem densities also increase over time via tillering from root crown buds (Averill et al. Reference Averill, DiTommaso, Mohler and Milbrath2011).

Mechanical control such as digging rootstocks may be suitable for small patches, but hand-pulling stems or mowing must be done repeatedly within a season to prevent seed production (Milbrath et al. Reference Milbrath, DiTommaso, Biazzo and Morris2016) and, in the case of V. rossicum, for several years to suppress populations (Biazzo and Milbrath Reference Biazzo and Milbrath2019). Long-term control with the biological control agent Hypena opulenta (Christoph) (Lepidoptera: Erebidae), the only agent released to date, is uncertain given the vigorous growth of Vincetoxicum species under full sun conditions and the preference of the moth for shaded environments (Livingstone et al. Reference Livingstone, Smith, Bourchier, Ryan, Roberto and Cadotte2020; Milbrath et al. Reference Milbrath, DiTommaso, Biazzo and Morris2016). At present, broad-spectrum herbicides remain the most effective control for Vincetoxicum species. Previously published herbicide studies have only involved V. rossicum. These studies have primarily focused on the systemic herbicides glyphosate and triclopyr, usually alone or in combination with some form of cutting (Averill et al. Reference Averill, DiTommaso and Morris2008; Cain and Irvine Reference Cain, Irvine and Lycan2011; Christensen Reference Christensen1998; DiTommaso et al. Reference DiTommaso, Milbrath, Bittner and Wesley2013; Lawlor and Raynal Reference Lawlor and Raynal2002; Mervosh and Boettner Reference Mervosh and Boettner2009; Mervosh and Gumbart Reference Mervosh and Gumbart2015). Results using various formulations and rates of glyphosate and triclopyr have varied from poor to excellent control of V. rossicum. In many cases, glyphosate provided higher control (e.g., Mervosh and Gumbart Reference Mervosh and Gumbart2015), although triclopyr has the advantage of selectively controlling dicot species, an important consideration if dealing with grass-dominated habitats. The cutting or mowing of plants several weeks before foliar herbicide applications is often done to reduce interfering vegetation, promote good regrowth of the targeted weed species with subsequent greater coverage by the herbicide, and potentially diminish carbohydrate reserves by forcing regrowth (Brandsaeter et al. Reference Brandsæter, Mangerud, Helgheim and Berge2017; Delabays et al. Reference Delabays, Bohren, Mermillod, Baker and Vertenten2008; DiTommaso et al. Reference DiTommaso, Milbrath, Bittner and Wesley2013; Håkansson Reference Håkansson2003; Hewett Reference Hewett1985; Ringselle et al. Reference Ringselle, Bergkvist, Aronsson and Andersson2015). Also, applying herbicides for at least 2 yr has usually been recommended to control escapes and seedlings (Averill et al. Reference Averill, DiTommaso and Morris2008; Cain and Irvine Reference Cain, Irvine and Lycan2011). The efficacy of herbicides for V. nigrum control has not yet been quantified and may differ from herbicide efficacy for its congener due to biological differences. For example, root-to-shoot ratios are much lower for V. nigrum (typically <1) compared with V. rossicum (1.4 or higher), potentially affecting the potential of regrowth (DiTommaso et al. Reference DiTommaso, Averill, Qin, Ho, Westbrook and Mohler2021; Milbrath Reference Milbrath2008).

The main objective of this study was to determine V. nigrum control efficacy of different herbicide treatments that were labeled for use against Vincetoxicum species in New York State, with or without a prior mowing, applied over two growing seasons. We hypothesized that (1) glyphosate would have more consistent and better efficacy than triclopyr and (2) a previous mowing would enhance the efficacy of foliar-applied herbicides relative to not mowing.

Materials and Methods

Field Site

The experiment was conducted on the grounds of the Cornell University Cooperative Extension Office, Millbrook, Dutchess County, NY, USA (41.7805°N, 73.7388°W). We did not have access to other large infestations of V. nigrum where herbicides were allowed. However, it is standard practice for land managers to reapply herbicides to the same area in subsequent years when managing invasive species, including Vincetoxicum. Our study therefore assessed annual repeated treatments. A 0.25-ha grassy area was used that had not been mown for 17 yr before our study. It included a moderate to high-density (65 to 150 stems m−2), open-field stand of V. nigrum still in early stages of succession to woody plant species. The soil was a Hoosic gravelly loam (sandy-skeletal, mixed, mesic Typic Dystrudepts). Common grass species were Kentucky bluegrass (Poa pratensis L.), smooth brome (Bromus inermis Leyss.), quackgrass [Elymus repens (L.) Gould], and orchardgrass (Dactylis glomerata L.). Common broadleaf species included smooth bedstraw (Galium mollugo L.), rough goldenrod (Solidago rugosa Mill.), common speedwell (Veronica officinalis L.), and yellow toadflax (Linaria vulgaris Mill.), whereas spotted St. Johnswort (Hypericum punctatum Lam.), rough fleabane (Erigeron strigosus Muhl. ex Willd.), and other species were much sparser. Woody species included common buckthorn (Rhamnus cathartica L.), Japanese zelkova [Zelkova serrata (Thunb.) Makino], and Morrow’s honeysuckle (Lonicera morrowii A. Gray).

Experimental Design and Treatments

The study was conducted from June 2018 to June 2020, with mowing and herbicide treatments applied in 2018 and 2019. Based on an initial assessment of V. nigrum stem densities and cover in June 2018, plots were arranged in a completely randomized design. The experiment included two factors in a repeated-measures design: seven management treatments in a one-way treatment structure with repeated measures on years. Each treatment was replicated seven times for a total of 49 experimental units measured up to three times. Treatments were applied to 4 by 1.9 m plots marked with labeled PVC pipes and separated by 2-m buffer zones and included an unmanaged control, three treatments involving herbicide applications at flowering (early July), and three treatments in which plants were cut at flowering (early July) followed by a herbicide application at reflowering (late August). Comparisons of herbicides alone to a single mowing alone (or other mechanical method of control) were not done, because pulling or cutting stems one to two times per year has not been shown to be effective for Vincetoxicum species (Averill et al. Reference Averill, DiTommaso and Morris2008; DiTommaso et al. Reference DiTommaso, Milbrath, Bittner and Wesley2013; Mervosh and Gumbart Reference Mervosh and Gumbart2015; Milbrath et al. Reference Milbrath, DiTommaso, Biazzo and Morris2016).

Herbicides were applied using a CO2-pressurized backpack sprayer (R & D Sprayers, Opelousas, LA) equipped with a four-nozzle boom (XR80015 TeeJet® nozzles, Glendale Heights, IL) to provide a 2-m-wide spray pattern. Nozzle pressure was 172 kPa (25 psi), and applications were timed to deliver an equivalent rate of 187 L ha−1 (20 gal ac−1). The herbicides used included the potassium salt of glyphosate (Roundup ProMax®, 48.7% ai, Monsanto, St Louis, MO), the isopropylamine salt of glyphosate (Ranger Pro®, 41.0% ai, Monsanto), and the butoxyethyl ester of triclopyr (Garlon 4 Ultra®, 60.45% ai, Corteva Agriscience, Johnston, IA). We used 2% solutions of the two glyphosate products based on specific Federal Insecticide, Fungicide, and Rodenticide Act 2(ee) supplemental label concentrations for V. nigrum in New York State that were available as of 2017 (NYS DEC 2017). We also chose to use a similar 2% solution of triclopyr (equivalent to 3.74 L ha−1 or 1.6 qt ac−1) that was within the 2(ee) label of 2.34 to 18.71 L ha−1 (1 to 8 qt ac−1) (NYS DEC 2017). A previous study with V. rossicum showed that a similar low dosage of triclopyr could be very effective (Averill et al. Reference Averill, DiTommaso and Morris2008). Glyphosate solutions included a 0.5% by volume of an organosilicone surfactant (Kinetic®, Helena Chemical, Collierville, TN) and the butoxyethyl ester of triclopyr included a 1.25% by volume of the surfactant (equivalent to 2.34 L ha−1 or 1 qt ac−1) based on specific label recommendations. Herbicide rates applied were glyphosate at 2.02 kg ae ha−1 (1.80 lb ae ac−1, Roundup ProMax®) and 1.35 kg ae ha−1 (1.20 lb ae ac−1, Ranger Pro®), and butoxyethyl ester of triclopyr at 1.79 kg ae ha−1 (1.60 lb ae ac−1).

Herbicide-only treatments were applied July 10, 2018, and July 9, 2019. Mowing-herbicide treatments included mowing on July 10, 2018, and July 9, 2019, with a rotary mower (Husqvarna HD 800HW, Husqvarna Professional Products, Charlotte, NC) throughout the entire plot to a height of 8 cm, which is a typical mowing height for land managers. Herbicides were then applied 7 wk later on August 28, 2018, and August 28, 2019, when plants were at flowering and early follicle production stages, that is, similar to when the first herbicide applications occurred in July.

Pre- and Posttreatment Data Collection

A pretreatment assessment of plant cover and V. nigrum stem densities was made on June 20, 2018. Two posttreatment assessments were made on June 26, 2019, and June 29, 2020, each approximately 1 yr after treatment. A 1 by 1 m quadrat was placed in the middle of each plot, and two opposite corners were permanently marked with PVC pipes. Percent cover of V. nigrum, grasses, other herbaceous dicots, woody species, and bare ground in each 1-m2 subplot was visually estimated by the same observer in all years. All V. nigrum stems >10-cm tall (consisting of larger vegetative juveniles and flowering plants) were counted in each 1-m2 subplot. Stems <10-cm tall (seedlings and young vegetative juveniles) were counted from two separate 0.0625-m2 quadrats placed at opposite corners of a 1-m2 subplot. After cover and density data collection in June 2020, V. nigrum aboveground dry biomass was determined by cutting plants in each subplot at soil level, oven-drying tissues at 70 C for 48 h, and weighing. We did not quantify seed output posttreatment, because our June data collection occurred before most follicle production had begun.

Statistical Analyses

A mixed model was used including a repeated-measures analysis with an autoregressive covariance structure (PROC MIXED, SAS v. 9.4, SAS Institute, Cary, NC) for the dependent variables stem density (<10-cm tall, average of two counts per subplot) and percent cover. Dependent variables were transformed using the logarithmic or logit transformations to fit the assumptions of the model. For the stem density (>10-cm tall) data, a generalized linear mixed model with a negative binomial distribution, a log link, and an error term for repeated measures was used (PROC GLIMMIX, SAS v. 9.4, SAS Institute). In all analyses, management treatment and year were fixed effects. Logarithmic-transformed biomass data were analyzed with a mixed model with management treatment as a fixed effect (PROC MIXED). Stepwise removal of nonsignificant interaction terms was done to determine the best model for each parameter. Preselected groups of means were compared using Fisher’s protected LSD test with the SLICE option and a modified Bonferroni correction (based on the actual number of comparisons being made for each parameter rather than all possible comparisons) (SAS v. 9.4, SAS Institute).

Results and Discussion

Pretreatment V. nigrum densities and percent cover of different plant groups (year 2018) did not differ among the various management treatment plots (Figures 1 and 2). Temperatures (lows and highs) did not vary substantially among the 3 yr of the study or from the 30-yr average at the site (data not shown; CLIMOD 2021). Precipitation was more variable, with a wetter than normal summer in 2018 and a dry spring in 2020.

Figure 1. Mean (+SE, back-transformed, n = 7) stem densities per square meter for Vincetoxicum nigrum >10-cm tall for seven treatments during a 3-yr study. Pretreatment values were in year 2018; values in 2019 and 2020 were 1-yr post first and second herbicide treatment, respectively. Bars within each year denoted by the same letter are not different (Fisher’s protected LSD test with Bonferroni correction, P > 0.05). “ns” indicates no significant differences.

Figure 2. Mean (+95% confidence interval, back-transformed, n = 7) percent cover of (A) Vincetoxicum nigrum, (B) other broadleaf plants, (C) grasses, and (D) bare ground in 1-m−2 subplots for seven treatments during a 3-yr study. Pretreatment values were in year 2018; values in 2019 and 2020 were 1-yr post first and second herbicide treatment, respectively. Bars within each year denoted by the same letter are not different (Fisher’s protected LSD test with Bonferroni correction, P > 0.05). “ns” indicates no significant differences.

Density, Cover, and Biomass of Vincetoxicum nigrum

Posttreatment stem densities of V. nigrum (>10-cm tall) varied to a limited degree among treatments over time (treatment by year interaction, F(12, 84) = 5.07, P < 0.001). None of the treatments differed from the unmanaged control at 1 yr after treatment (2019), although stem densities were significantly reduced (approximately 75%) for the mowing plus glyphosate-isopropylamine treatment (14 stems m−2) compared with glyphosate-isopropylamine alone (62 stems m−2; Figure 1). After two seasons of treatment (2020), most treatments again did not differ from the control plots (75 stems m−2; Figure 1), with the exception of the mowing plus glyphosate-isopropylamine treatment (12 stems m−2 or 84% reduction; Figure 1).

Changes in percent cover of V. nigrum also varied among years (treatment by year interaction: V. nigrum F(12, 89.7) = 4.81, P < 0.001) and were comparable to results for stem densities (>10-cm tall). Specifically, mowing plus either glyphosate formulation generally had the lowest percent cover in 2019 and 2020 with 85% reductions compared with the control plots (Figure 2A). Percent cover of V. nigrum after foliar sprays of glyphosate alone or triclopyr with or without mowing were not significantly less than cover in untreated plots, although trends toward lower percent cover were evident for some herbicide treatments after 2 yr (Figure 2A).

Significant reductions in aboveground dry mass per square meter of V. nigrum at 2 yr after treatment were present for several herbicide treatments (F(6, 42) = 20.11, P < 0.001). Specifically, dry mass of V. nigrum was reduced by 83% with foliar sprays of glyphosate and 93% to 98% with mowing plus glyphosate sprays (Figure 3). The two formulations of glyphosate gave similar levels of dry mass reduction, but the addition of mowing did not always enhance the efficacy of foliar applications alone. In contrast, triclopyr alone did not reduce the dry mass of V. nigrum, although a nonsignificant trend toward greater V. nigrum suppression was evident with the addition of mowing (Figure 3). As noted by Lawlor and Raynal (Reference Lawlor and Raynal2002) for V. rossicum, the stunting and proliferation of stems from herbicide damage can complicate stem density and percent cover measurements, whereas biomass can give a more accurate picture of herbicide impact. Our biomass results are somewhat similar to the stem density and percent cover results but clearly indicate strong efficacy for glyphosate and a lack of efficacy for triclopyr (Figures 1 and 2A). Our initial hypothesis that glyphosate would provide more consistent and better efficacy than triclopyr was met, although we had not necessarily expected such poor results with triclopyr.

Figure 3. Mean (+SE, back-transformed, n = 7) aboveground dry mass of Vincetoxicum nigrum from 1-m−2 subplots after 2 yr of seven treatments. Bars denoted by the same letter are not different (Fisher’s protected LSD test with Bonferroni correction, P > 0.05).

Our results differ substantially from DiTommaso et al. (Reference DiTommaso, Milbrath, Bittner and Wesley2013) in that all the different formulations and rates of glyphosate and triclopyr they used substantially reduced old-field V. rossicum stem density (>5 cm), cover, and dry mass by about 90% or more. However, they used 1.7 to 2.7 times higher herbicide rates than the present study. We used 2% solutions with resulting lower dosages because that was specifically indicated in the Section 2(ee) labels for New York State for both glyphosate products (NYS DEC 2017). Because we chose to keep a similar 2% solution for triclopyr, the amount of product applied was on the lower end allowed in the Section 2(ee) label for triclopyr (NYS DEC 2017). Other studies have also reported a consistently high efficacy of glyphosate against the congener V. rossicum, whereas the efficacy of triclopyr has been more variable. Mervosh and Boettner (Reference Mervosh and Boettner2009) reported similar reductions 1 yr later in seedpod mass (66% to 71%) and control ratings (7.0 to 7.8 out of 10) for single low rates of a triethylamine salt of triclopyr (1.26 kg ae ha−1) or an isopropylamine salt of glyphosate (1.12 kg ae ha−1). Lawlor and Raynal (Reference Lawlor and Raynal2002) reported similar efficacy among single foliar applications of the isopropylamine salt of glyphosate (3.1 or 7.8 kg ae ha−1) and the butoxyethyl ester of triclopyr (1.9 kg ae ha−1), with average reductions 1 yr later in V. rossicum stem density, percent cover, and aboveground biomass of 73%, 83%, and 83%, respectively, compared with untreated plots. Averill et al. (Reference Averill, DiTommaso and Morris2008) also reported excellent control of V. rossicum at 2 yr after a single application of butoxyethyl ester of triclopyr (1.9 kg ae ha−1). They observed a 74% reduction in cover and 44% and 84% reductions in stem densities of <10-cm- and >10-cm-tall V. rossicum, respectively. This treatment also prevented follicle production in V. rossicum. In the latter two examples, the rates of triclopyr were similar to the present study (1.79 kg ae ha−1).

In contrast, whereas foliar applications of isopropylamine glyphosate (2.2 kg ai ha−1) resulted in a 76% reduction in V. rossicum cover after 2 yr of treatment, no reductions occurred with a triethylamine salt of triclopyr (1.7 kg ai ha−1) (Mervosh and Gumbart Reference Mervosh and Gumbart2015). Cain and Irvine (Reference Cain, Irvine and Lycan2011) also reported as low as 30% control in one trial using the butoxyethyl ester of triclopyr. Mervosh and Gumbart (Reference Mervosh and Gumbart2015) suggested earlier-season applications of triclopyr might provide better control than they had observed, as was demonstrated by Averill et al. (Reference Averill, DiTommaso and Morris2008). DiTommaso et al. (Reference DiTommaso, Milbrath, Bittner and Wesley2013) showed excellent control also could be achieved with a late-season application of triclopyr. Some authors have noted that two to three applications per season gave much better and longer-lasting control of V. rossicum than single applications of either glyphosate or triclopyr, although repeat applications over more than 1 yr may still be needed (Cain and Irvine Reference Cain, Irvine and Lycan2011; Christensen Reference Christensen1998; Mervosh and Boettner Reference Mervosh and Boettner2009). This has not yet been studied for V. nigrum. Beyond Vincetoxicum species, glyphosate also seems to perform better than triclopyr in some, but not all, cases when used as a foliar application against other invasive or weedy plant species (Farooq et al. Reference Farooq, Zaman, Boyd and White2019; Knezevic et al. Reference Knezevic, Osipitan, Oliveira and Scott2018; Meighani et al. Reference Meighani, Karaminejad and Farrokhi2021; Roth et al. Reference Roth, Dias, Evans, Rohling and Renz2021).

Mowing in early summer followed 7 wk later by a foliar herbicide generally did not enhance reductions in V. nigrum stem densities, cover, or biomass compared with an early-summer herbicide application, contrary to our initial hypothesis. We chose to wait until substantial reflowering had occurred after mowing and before applying the herbicides, as was done by DiTommaso et al. (Reference DiTommaso, Milbrath, Bittner and Wesley2013), but shorter durations between mowing and herbicides could be examined. A comparison of herbicide efficacy with or without subsequent mowing has not been investigated for the related V. rossicum. However, Averill et al. (Reference Averill, DiTommaso and Morris2008) noted that cutting V. rossicum plants 4 wk after spraying triclopyr gave similar results to spraying only. Cut-stem treatments, that is, immediately applying herbicides to stems of plants after they are cut, have also been effective for control of V. rossicum. Lawlor and Raynal (Reference Lawlor and Raynal2002) reported comparable control with either an isopropylamine salt of glyphosate (3.1 kg ae ha−1) or a triethylamine salt of triclopyr (1.4 kg ae ha−1) cut-stem treatment. Results were also similar between the cut-stem and foliar applications of glyphosate but were less for the cut-stem compared with a butoxyethyl ester triclopyr foliar application (Lawlor and Raynal Reference Lawlor and Raynal2002). Mervosh and Gumbart (Reference Mervosh and Gumbart2015) also reported acceptable reductions in V. rossicum vigor and plot coverage with cut-stem applications of 50% solutions of an isopropylamine salt of glyphosate or triethylamine salt of triclopyr. Cut-stem treatments have not been evaluated for V. nigrum, and integration of mechanical, chemical, and potentially biological control should be investigated for enhancing the management of perennial plants such as V. nigrum (Lym and Nelson Reference Lym and Nelson2002; Miller Reference Miller2016; Tipping et al. Reference Tipping, Gettys, Minteer, Foley and Sardes2017).

Stem densities of small V. nigrum plants (<10-cm tall) significantly declined over each year independent of treatment (year effect, F(2, 81.5) = 43.77, P < 0.001). Densities (averaged over two 0.0625-m2 plots) were 55.0 ± 13.9 (2018), 6.7 ± 1.7 (2019), and 2.3 ± 0.6 (2020). The lack of treatment effects on seedlings and young juveniles may have been confounded by natural annual fluctuations in seedling recruitment (Biazzo and Milbrath Reference Biazzo and Milbrath2019; unpublished data) as well as the shielding of small V. nigrum plants from herbicide sprays by larger V. nigrum and other broadleaf species prevalent at the site, particularly G. mollugo. This interfering vegetation would have included regrown foliage in those plots that had been mown several weeks earlier. Vincetoxicum nigrum has a more sprawling and trailing vine growth habit than its congener V. rossicum, creating mats of vegetation (personal observation). Other researchers have reported variable herbicide efficacy on early-stage Vincetoxicum plants. Averill et al. (Reference Averill, DiTommaso and Morris2008) documented V. rossicum seedling reductions compared with unmanaged plots from the butoxyethyl ester of triclopyr within the same growing season but not after 1 yr. DiTommaso et al. (Reference DiTommaso, Milbrath, Bittner and Wesley2013) reported reductions in small V. rossicum (<5-cm tall) densities in an old field after 2 yr, but not after 1 yr, of various cutting plus herbicide treatments.

Cover of Other Plants

Percent cover varied over time for the different plant groups or bare ground relative to different herbicide treatments (treatment by year interaction: broadleaf F(12, 87.4) = 4.07, P < 0.001; grass F(12, 80) = 4.31, P < 0.001; bare ground F(12, 90.7) = 5.26, P < 0.001). Woody species only constituted <1% cover and are therefore not shown. Cover of other broadleaf species generally did not differ over the 3 yr, except for an apparent temporary increase in a few treatments in 2019 (Figure 2B). The most abundant species besides V. nigrum in and around the plots was G. mollugo. The application timing or rates may not have been ideal for control of G. mollugo; many plants were already producing seeds at the July application. This species is difficult to manage with herbicides (Mersereau and DiTommaso Reference Mersereau and DiTommaso2003). It is also possible that G. mollugo grew into the plots from outside the treated area. The cover of grasses was initially 4% to 23% (Figure 2C). After 2 yr of herbicide applications, grass cover was generally the greatest for both triclopyr treatments (41% to 64%), whereas grass cover was 0.5% to 2.0% in the glyphosate plots (Figure 2C). This is not surprising due to the selectivity of triclopyr for broadleaf plants; Mervosh and Boettner (Reference Mervosh and Boettner2009) and DiTommaso et al. (Reference DiTommaso, Milbrath, Bittner and Wesley2013) reported similar changes in vegetation when comparing glyphosate and triclopyr treatments against V. rossicum. As expected, bare ground increased substantially for all glyphosate treatments but only after two seasons of application (27% to 59%; Figure 2D). While glyphosate was very effective against V. nigrum, active restoration of treated areas would be needed to prevent undesirable vegetation growing into the bare areas produced by glyphosate. Assuming different dosages or frequencies of application could enhance the efficacy of triclopyr toward V. nigrum for preserving grass species, the grasses present at our site are widespread, naturalized Eurasian species. They can be considered invasive when trying to restore natural areas to native species (DiTommaso et al. Reference DiTommaso, Milbrath, Bittner and Wesley2013). This would not be an issue for many pasture systems.

In the present study we assessed two broad-spectrum herbicides for the control of an invasive species that is primarily found in open fields of natural areas. The efficacy of annual applications of two different glyphosate formulations toward V. nigrum was excellent; and mowing before spraying may improve efficacy. In contrast, we did not observe control with a low rate of triclopyr even after 2 yr of application, although other studies with the congener V. rossicum indicate higher control with this herbicide. In part, this may be due to higher planned application rates (DiTommaso et al. Reference DiTommaso, Milbrath, Bittner and Wesley2013). However, we speculate that the effective dose may also have been greater in some studies that used a similar planned rate to ours, because they applied the herbicide with spray bottles or single-nozzle wands until the foliage was wet (Averill et al. Reference Averill, DiTommaso and Morris2008; Lawlor and Raynal Reference Lawlor and Raynal2002). In contrast, results with timed sprays of triclopyr with multi-nozzle booms have ranged from poor (Mervosh and Gumbart [Reference Mervosh and Gumbart2015] with a triethylamine salt; present study with a butoxyethyl ester) to good (Mervosh and Boettner [Reference Mervosh and Boettner2009] with a triethylamine salt). The preservation of grasses is one advantage to using triclopyr over glyphosate, whether in natural areas or pasture systems. However, if triclopyr is to be a consistent tool for V. nigrum suppression, higher triclopyr rates, greater frequency of applications, and integration with other management tactics should be investigated for improved V. nigrum control.

Acknowledgments

This research was funded by the U.S. Department of Agriculture–Agricultural Research Service. No conflicts of interest have been declared. The authors would like to thank the Dutchess County Department of Public Works for allowing this field study and the anonymous reviewers for their comments, which improved this article. Mention of trade names or commercial products in this article is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the U.S. Department of Agriculture. USDA is an equal opportunity provider and employer.

Footnotes

Associate Editor: Stephen F. Enloe, University of Florida

References

Alred, B, Hufbauer, RA, Szűcs, M (2022) Potential impact and phenology of the biological control agent, Hypena opulenta on Vincetoxicum nigrum in Michigan. Biocontrol Sci Technol 32:671684 Google Scholar
Averill, KM, DiTommaso, A, Mohler, CL, Milbrath, LR (2011) Survival, growth, and fecundity of the invasive swallowworts (Vincetoxicum rossicum and V. nigrum) in New York State. Invasive Plant Sci Manag 4:196206 CrossRefGoogle Scholar
Averill, KM, DiTommaso, A, Morris, SH (2008) Response of pale swallow-wort (Vincetoxicum rossicum) to triclopyr application and clipping. Invasive Plant Sci Manag 1:196206 CrossRefGoogle Scholar
Biazzo, J, Milbrath, LR (2019) Response of pale swallowwort (Vincetoxicum rossicum) to multiple years of mowing. Invasive Plant Sci Manag 12:169175 CrossRefGoogle Scholar
Brandsæter, LO, Mangerud, K, Helgheim, M, Berge, TW (2017) Control of perennial weeds in spring cereals through stubble cultivation and mouldboard ploughing during autumn or spring. Crop Prot 98:1623 CrossRefGoogle Scholar
Cain, NP, Irvine, M (2011) Programs for swallow-wort (dog-strangling vine) control [abstract]. Pages 3839 in Lycan, DW, ed. Proceedings of the 65th Annual Meeting of the Northeastern Weed Science Society. Baltimore, MD: Northeastern Weed Science Society Google Scholar
Christensen, T (1998) Swallowworts: the ecology and control of Vincetoxicum spp. Wildflower 14:2125 Google Scholar
CLIMOD (2021) Northeast Regional Climate Center. http://climod2.nrcc.cornell.edu. Accessed: March 22, 2021Google Scholar
Delabays, N, Bohren, C, Mermillod, G, Baker, A, Vertenten, J (2008) Breaking the life cycle of common ragweed (Ambrosia artemisiifolia L.) to exhaust seed bank. I. Efficiency and optimization of various mowing schemes. Rev Suisse d’Agric 40:143149 Google Scholar
DiTommaso, A, Averill, KM, Qin, Z, Ho, M, Westbrook, AS, Mohler, CL (2021) Biomass allocation of Vincetoxicum rossicum and V. nigrum in contrasting competitive environments. Am J Bot 108:16461661 CrossRefGoogle ScholarPubMed
DiTommaso, A, Lawlor, FM, Darbyshire, SJ (2005) The biology of invasive alien plants in Canada. 2. Cynanchum rossicum (Kleopow) Borhidi [= Vincetoxicum rossicum (Kleopow) Barbar.] and Cynanchum louiseae (L.) Kartesz & Gandhi [= Vincetoxicum nigrum (L.) Moench]. Can J Plant Sci 85:243263 CrossRefGoogle Scholar
DiTommaso, A, Milbrath, LR, Bittner, T, Wesley, FR (2013) Pale swallowwort (Vincetoxicum rossicum) response to cutting and herbicides. Invasive Plant Sci Manag 6:381390 CrossRefGoogle Scholar
Farooq, MH, Zaman, QU, Boyd, NS, White, SN (2019) Evaluation of broadcast and spot herbicide applications for narrowleaf goldenrod [Euthamia graminifolia (L.) Nutt.] management in lowbush blueberry. Weed Technol 33:739747 CrossRefGoogle Scholar
Håkansson, S (2003) Weeds and Weed Management on Arable Land–An Ecological Approach. Wallingford, UK: CABI Publishing. 274 pCrossRefGoogle Scholar
Hewett, DG (1985) Grazing and mowing as management tools on dunes. Vegetatio 62:441447 CrossRefGoogle Scholar
Knezevic, SZ, Osipitan, A, Oliveira, MC, Scott, JE (2018) Lythrum salicaria (purple loosestrife) control with herbicides: multiyear applications. Invasive Plant Sci Manag 11:143154 CrossRefGoogle Scholar
Lawlor, FM, Raynal, DJ (2002) Response of swallow-wort to herbicides. Weed Sci 50:179185 CrossRefGoogle Scholar
Livingstone, SW, Smith, SM, Bourchier, RS, Ryan, K, Roberto, A, Cadotte, MW (2020) An experimental application of Hypena opulenta as a biocontrol agent for the invasive vine Vincetoxicum rossicum . Ecol Solut Evid 1:e12022 Google Scholar
Lym, RG, Nelson, JA (2002) Integration of Aphthona spp. flea beetles and herbicides for leafy spurge (Euphorbia esula) control. Weed Sci 50:812819 CrossRefGoogle Scholar
Meighani, F, Karaminejad, MR, Farrokhi, Z (2021) Invasive weed swallow-wort (Cynanchum acutum L.) response to chemical and mechanical practices. Weed Biol Manag 21:124132 CrossRefGoogle Scholar
Mersereau, D, DiTommaso, A (2003) The biology of Canadian weeds. 121. Galium mollugo L. Can J Plant Sci 83:453466 Google Scholar
Mervosh, TL, Boettner, C (2009) Impacts of several herbicides on pale swallow-wort (Cynanchum rossicum) and other vegetation. Abstract no. 185 in 2009 Weed Science Society of America Meeting Abstracts. Orlando, FL: Weed Science Society of AmericaGoogle Scholar
Mervosh, TL, Gumbart, D (2015) Cutting and herbicide treatments for control of Oriental bittersweet, pale swallow-wort and Morrow’s honeysuckle. Nat Areas J 35:256265 CrossRefGoogle Scholar
Milbrath, LR (2008) Growth and reproduction of invasive Vincetoxicum rossicum and V. nigrum under artificial defoliation and different light environments. Botany 86:12791290 CrossRefGoogle Scholar
Milbrath, LR, Biazzo, J (2016) Impact of the defoliating moth Hypena opulenta on invasive swallow-worts (Vincetoxicum species) under different light environments. Biol Control 97:112 Google Scholar
Milbrath, LR, DiTommaso, A, Biazzo, J, Morris, SH (2016) Tolerance of swallowworts (Vincetoxicum spp.) to multiple years of artificial defoliation and clipping. Invasive Plant Sci Manag 9:111 CrossRefGoogle Scholar
Miller, TW (2016) Integrated strategies for management of perennial weeds. Invasive Plant Sci Manag 9:148158 CrossRefGoogle Scholar
[NYS DEC] New York State Department of Environmental Conservation (2017) Bureau of Pesticides Management—Information Portal. https://www.dec.ny.gov/nyspad/products. Accessed March 22, 2017Google Scholar
Ringselle, B, Bergkvist, G, Aronsson, H, Andersson, L (2015) Under-sown cover crops and post-harvest mowing as measures to control Elymus repens . Weed Res 55:309319 CrossRefGoogle Scholar
Roth, L, Dias, JLCS, Evans, C, Rohling, K, Renz, M (2021) Do applications of systemic herbicides when green fruit are present prevent seed production or viability of garlic mustard (Alliaria petiolata)? Invasive Plant Sci Manag 14:101105 CrossRefGoogle Scholar
Sheely, SF, Raynal, DJ (1996) The distribution and status of Vincetoxicum in eastern North America. Bull Torrey Bot Club 123:148156 CrossRefGoogle Scholar
Tipping, PW, Gettys, LA, Minteer, CR, Foley, JR, Sardes, SN (2017) Herbivory by biological control agents improves herbicidal control of waterhyacinth (Eichhornia crassipes). Invasive Plant Sci Manag 10:271276 Google Scholar
[USDA-NRCS] U.S. Department of Agriculture–Natural Resources Conservation Service (2022) The PLANTS Database. https://plants.usda.gov. Accessed: April 19, 2022Google Scholar
Figure 0

Figure 1. Mean (+SE, back-transformed, n = 7) stem densities per square meter for Vincetoxicum nigrum >10-cm tall for seven treatments during a 3-yr study. Pretreatment values were in year 2018; values in 2019 and 2020 were 1-yr post first and second herbicide treatment, respectively. Bars within each year denoted by the same letter are not different (Fisher’s protected LSD test with Bonferroni correction, P > 0.05). “ns” indicates no significant differences.

Figure 1

Figure 2. Mean (+95% confidence interval, back-transformed, n = 7) percent cover of (A) Vincetoxicum nigrum, (B) other broadleaf plants, (C) grasses, and (D) bare ground in 1-m−2 subplots for seven treatments during a 3-yr study. Pretreatment values were in year 2018; values in 2019 and 2020 were 1-yr post first and second herbicide treatment, respectively. Bars within each year denoted by the same letter are not different (Fisher’s protected LSD test with Bonferroni correction, P > 0.05). “ns” indicates no significant differences.

Figure 2

Figure 3. Mean (+SE, back-transformed, n = 7) aboveground dry mass of Vincetoxicum nigrum from 1-m−2 subplots after 2 yr of seven treatments. Bars denoted by the same letter are not different (Fisher’s protected LSD test with Bonferroni correction, P > 0.05).