Abstract
Rumex obtusifolius is a troublesome weed especially in organically managed grasslands. Manual weeding is commonly used for R. obtusifolius control, but its effectiveness and effect on plant species composition in upland grassland has never been investigated. Therefore the aim of our study was to reveal the effect of manual weeding by digging out R. obtusifolius taproots to depths of 5 or 15 cm, either once or twice, in: (i) presence of R. obtusifolius plants; (ii) plant species composition. Additional treatments were grazed and unmanaged grassland (both without digging out R. obtusifolius taproot). Digging out taproots twice, to 15 cm, reduced the presence of R. obtusifolius significantly. Grazing without digging out taproots was the treatment that was most favourable for R. obtusifolius plants. Manual weeding had no significant effect on species richness. The empty spaces after plant removal were filled by nutrient-demanding species (Poa pratensis, Poa trivialis, Festuca pratensis and Lolium perenne, Trifolium repens and Taraxacum sp.). On unmanaged grassland the number of R. obtusifolius plants decreased, species richness was reduced, but this allowed the spread of other tall weedy species (Urtica dioica, Galium album and Elytrigia repens). Digging out taproots to a depth of 15 cm, performed twice, can be an effective method for R. obtusifolius control in organically managed grasslands, as this procedure eliminated the majority of R. obtusifolius plants. However, the use of this weeding method over large areas of grassland is limited due to time-consuming and hard physical work.
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Key message
-
Manual weeding can be effective in the eradication of Rumex obtusifolius.
-
The effectiveness of manual weeding together with its effect on plant species composition in upland grassland had not been investigated previously.
-
Empty spaces left after manual weeding were filled by nutrient-demanding grasses and forbs.
-
Digging out the taproots twice, to 15 cm depth, can be an effective method for R. obtusifolius control in permanent grasslands under the conditions of organic farming.
Introduction
Rumex obtusifolius L. (broad-leaved dock) is one of the most troublesome weed species in temperate grasslands and can also colonise permanent agricultural crops (Novák 1994; Brant et al. 2006), where they can survive for ten or more years (Martinková et al. 2009). It produces high plant biomass and large numbers of seeds, and is generally avoided by grazing livestock; these attributes combined with its perennial character, persistent soil seed bank and high ability to regenerate from fragmented underground organs (Cavers and Harper 1964; Zaller 2004) can lead it to becoming a persistent weed that reduces the quality of herbage for grazing or forage conservation. Its regeneration strategy includes its ability to regenerate from buds on the strong underground stem system above the root collar (Pino et al. 1995). In conventionally managed grasslands, R. obtusifolius can be controlled by selective herbicides (Hopkins and Johnson 2003), but chemical control requires very specific attention to detail in the timing of spraying. Factors such as the growth stage of docks at spraying (Brock 1972; Dimitrova and Marinov-Serafimov 2008; DiTomaso et al. 2013), the technique of application (Power et al. 2013; Jursík et al. 2008) and weather conditions (Pimentel 1995) can affect the success of herbicidal treatment.
Under organic farming, however, the use of herbicides is prohibited and only biological or mechanical methods of weed control are allowed. Biological methods that have been used or investigated for R. obtusifolius control include using specific insects, e.g. Gastrophysa viridula (Hatcher et al. 1997; Honěk and Martinková 2004), pathogenic fungi-like Uromyces rumicis (Keary and Hatcher 2004), or specific grazers such as goats (Hejcman et al. 2014). Nevertheless, the application of biological methods on farmland is still problematic. Cessation of management has also been shown to reduce the numbers of R. obtusifolius plants in grassland (Martinková et al. 2009; Hejcman et al. 2012). Mechanical methods that have been investigated include using different intensities of defoliation (Hopkins and Johnson 2002), heating of plants (Latsch et al. 2007, 2011), motorised milling of roots (Pötsch and Griesebner 2007) and manual digging of taproots (Strnad et al. 2010). In a study by Stilmant et al. (2010) frequent cutting of R. obtusifolius reduced the vigour of the aboveground organs, particularly decreasing the number of leaves, the size of the largest leaf and also the amount of herbage production contributed by Rumex. Plants of R. obtusifolius can, however, tolerate a high cutting frequency for several years, and three cuts per year may not be sufficient for its elimination from grassland (Niggli et al. 1993; Hopkins and Johnson 2002; Stilmant et al. 2010; Hann et al. 2012).
After plants of R. obtusifolius become established in grassland they develop deep taproots with a high storage capacity for assimilates and nutrients. Persistence is allowed by the high regeneration ability of the root collar after disturbance and by a high clonal reproduction potential (Pino et al. 1995; Strnad et al. 2010). Buds are common on dock root crowns in the upper 10 cm layer of the soil. Therefore digging plants out from <10 cm below the soil surface is not an effective method for R. obtusifolius control (Dierauer 1993; Bond et al. 2007; Strnad et al. 2010), at least in soils with high contents of plant-available nutrients, as in the cited studies. However, the effects of root digging to soil depths of 5 and 15 cm, performed once or twice, on the survival of R. obtusifolius in upland grasslands dominated by A. capillaris have never been investigated. Furthermore, there have been no studies of the effects on plant species composition and species richness of manual dock control in permanent grasslands.
The aim of our study was therefore to answer the following questions: (i) How effective is digging out R. obtusifolius taproots to 5 or 15 cm soil depth, performed once or twice, for its control in A. capillaris grassland, assessed over 5 years? (ii) Which plant species replace R. obtusifolius after its removal by digging? (iii) Is the absence of grassland management a less effective method of control than digging out R. obtusifolius taproots? and (iv) How do different weeding treatments affect the species richness of vascular plants?
Materials and methods
Study site
The experimental grassland was situated in Krásná Studánka, Liberec, Czech Republic (50°48′29.24″N, 15°2′17.56″E, 394 m.a.s.l.). The bedrock is biotite granite covered by Cambisol with a pH (KCl) value of 5.45 and an organic C concentration of 4.53 %. Contents of plant-available (Mehlich III; Mehlich 1984) P, K, Ca and Mg were 28, 67, 1728 and 58 mg kg−1, respectively. The mean annual temperature is 7.2 °C and the mean annual precipitation is 803 mm (Liberec meteorological station). The grassland was classified as upland hay mesophile meadow (alliance Arrhenatherion; Chytrý 2007). The dominant vascular plant species before the introduction of management treatments were A. capillaris (cover 64 %), Taraxacum sp. (14 %), Trifolium repens (14 %) and R. obtusifolius (7 %). At the beginning of the experiment, the mean density of R. obtusifolius was about two plants per square metre. The 8 ha experimental pasture was managed organically and rotationally stocked by Gasconne suckler cows with their calves during four grazing cycles per vegetation season. To reduce the number of inflorescences of R. obtusifolius plants, ungrazed sward patches were cut twice (after the second and fourth grazing cycles) per vegetation season.
Experimental design
The experiment was established in the centre of the 8 ha pasture in four complete randomised blocks with individual 3 m × 3 m plots. Six treatments were applied: (i) grazed, taproot of R. obtusifolius dug out to a depth of 15 cm below ground twice (GD15T); (ii) grazed, taproot of R. obtusifolius dug out to a depth of 15 cm once (GD15O); (iii) grazed, taproot of R. obtusifolius dug out to a depth of 5 cm below ground twice (GD5T); (iv) grazed, taproot of R. obtusifolius dug out to a depth of 5 cm below ground once (GD5O); (v) grazed, without digging out R. obtusifolius taproot (GND—the traditional farm management which was the control); (vi) no grassland management—unmanaged pasture without digging out R. obtusifolius taproot (UND). Digging of R. obtusifolius taproots was performed manually using two special narrow spade for each of the two depths (Fig. 1). The first weeding was performed on 14th August 2007 and the second on 20th May 2008. There was no weeding in the years 2009–2011.
Data collection
The percentage cover of vascular plant species and the numbers of broad-leaved dock plants were monitored in 2 m × 2 m plots located in the middle of each of the 3 × 3 m experimental plots from 2007 to 2011. The cover of all vascular plant species was assessed once in the spring (from the end of May to the beginning of June) and the numbers of R. obtusifolius plants were counted twice in spring (the end of May to beginning of June) and autumn (from end of October to beginning of November) during each of the 5 years of the experiment. One R. obtusifolius plant was defined as having all visible shoots growing from buds inside a circle of 30 cm diameter around the main shoot. Young seedlings were counted if the leaf length was at least 5 cm. The nomenclature of vascular plant species follows Kubát et al. (2002).
Statistical analyses
A one-way ANOVA was used to analyse the treatment effects on the number of R. obtusifolius plants (recalculated per square metre) in the spring and autumn sampling dates of a particular year. The effect of time, treatment and their interaction on the cover of dominant plant species and species richness was evaluated by a repeated ANOVA. The success rate of manual weeding was expressed as the ratio of the final (year 2011) to initial (year 2007) number of R. obtusifolius plants and it was tested by one-way ANOVA. Post hoc comparison using the Tukey HSD test was applied to identify significant differences between treatments on a particular sampling date. Ratio data were log transformed in order to meet the assumptions of ANOVA. All univariate analyses were performed using STATISTICA 12 software (StatSoft, Tulsa, USA). The community response was analysed using constrained ordinations. Redundancy analysis (RDA) in the CANOCO 5 programme (terBraak and Šmilauer 2012) was used to evaluate multivariate plant species composition data in particular years. The blocks were used as covariables in all analyses to restrict permutations to the blocks. Cover data in RDA were logarithmically transformed [y = log 10 (y + 1)] to down-weight dominant species and 999 permutations were used in all analyses. An ordination diagram, constructed by the CANOCO 5 programme, was used to visualise the results of the RDA analysis of data collected in 2011.
Results
There were no significant differences in R. obtusifolius numbers among treatments after the first weeding treatment in August 2007 (Fig. 2). The first significant differences in R. obtusifolius numbers among treatments appeared after the second digging in May 2008. After spring 2008, there were strong variations in R. obtusifolius numbers depending on the applied treatments. Generally, the lowest numbers of R. obtusifolius plants were recorded in treatments where manual weeding was applied twice (GD5T, GD15T). Only a slight reduction was recorded in treatments with one digging treatment and in UND treatment. Higher numbers of R. obtusifolius plants were usually recorded in the spring under UND treatment than under other treatments. In 2011, we recorded 3, 26, 28, 33, 34 and 77 % of the initial number of R. obtusifolius plants recorded in 2007 in the GD15T, GD15O, GD5O, UND, GD5T and GND treatments, respectively (Fig. 3). Although at the end of the experiment, a 23 % reduction in the number of R. obtusifolius plants was recorded in GND treatment, there was a high degree of variation caused by differences amongst individual plots. In several cases, the numbers of R. obtusifolius plants were even higher in 2010 than in 2007.
No significant effect of the treatments on plant species composition as calculated by RDA was recorded in 2007 (Table 1). The variability of plant species composition explained by the treatments was more than 50 % after 5 years of the experiment in 2011. Three groups of treatments with similar plant species composition were recognised on the ordination diagram based on RDA analysis of data collected in 2011 (Fig. 4): GD5T, GD15T and GD15O treatments form the first group, GND and GD5O treatments make up the second group and UND comprises the third group. The association of individual species with particular management treatments is clearly visible from the ordination diagram. GD5T, GD15T and GD15O treatments had low coverage of R. obtusifolius, which was replaced particularly by Poa pratensis. Tall weedy forbs Urtica dioica, Galium album and tall grasses Elytrigia repens and Dactylis glomerata were associated with UND treatment. The GND and GD5O treatments supported the productive grasses Poa trivialis, Festuca pratensis and Lolium perenne. All of the grazed treatments were favourable for the development of the prostrate forbs T. repens and Taraxacum sp. The majority of the most abundant plant species in the sward (Agrostis capillaris, D. glomerata, E. repens, F. pratensis, G. album, L. perenne, P. pratensis and Trifolium repens) were significantly affected by time and treatment but not by their interactions (Figs. 5, 6; Table 2). Rumex obtusifolius, Taraxacum sp. and U. dioica were the only three dominant species whose cover was affected not only by time and treatment but also by their interactions (Fig. 6; Table 2). No effect of time, treatment or their interaction was revealed for Veronica chamaedrys.
Species richness of vascular plants was significantly affected by time, treatment and their interaction (Table 2). Species richness was stable in all managed treatments, but it decreased from 15 to 9 species per 4 m2 in the UND treatment (Fig. 7).
Discussion
The main finding of this study was that all of the manual weeding treatments, as well as the treatment of no grassland management, resulted in a significantly reduced density of R. obtusifolius plants in A. capillaris-dominated grassland. The repeated digging to a depth of 15 cm was the most successful treatment for reducing R. obtusifolius as 97 % of plants were eradicated. This depth was also recommended by Pötsch and Griesebner (2007) who used an innovative motorised rotating milling cutter system for mechanical destruction of R. obtusifolius plants in Austrian alpine pastures. Likewise, Dierauer (1993) and Bond et al. (2007) concluded that, under conditions of organic farming, the only effective method for control of R. obtusifolius is to remove the entire root or to cut the root at least 10 cm below ground. This means that it is necessary to remove the majority of buds, which are responsible for the vegetative reproduction of R. obtusifolius (Pino et al. 1995). Manual weeding at a depth of 5 cm, however, could still result in a reduction in the number of R. obtusifolius plants, as also noted by Dierauer (1993). Nevertheless this reduction was not statistically significant due to high standard errors resulting from limited replication of the treatments. Conversely, Strnad et al. (2010) reported that manual weeding by digging of the plants to 5 cm below the ground is not sufficient for R. obtusifolius control even when applied eight times during three vegetation seasons. The differences in results between these studies were probably caused by the different content of plant-available nutrients in the soil. In the study of Strnad et al. (2010) there were N fertiliser applications and the soil had levels of plant-available P and K that were five and four times higher than that found in our study. It seems that manual weeding is much more efficient under conditions of lower soil nutrient availability (especially N, P and K), as low nutrient supply does not allow fast regrowth of R. obtusifolius plants after manual weeding. On the other hand, in soil with high Ca and Mg availability, the density of R. obtusifolius plants was weakly positively related to K availability but showed no relation to P availability (Hann et al. 2012).
Manual weeding of R. obtusifolius not only reduced its presence in the sward but also had a significant successional effect on the cover of the dominant vascular plant species in A. capillaris grassland. Plants of R. obtusifolius were mainly replaced by nutrient-demanding grasses (P. pratensis, P. trivialis, F. pratensis and L. perenne) and also by prostrate forbs (T. repens and Taraxacum sp.) which quickly colonised the gaps created by the manual removal of Rumex. These plant species are of relatively high value for grazing livestock because of their high forage value (Frame 1992). Manual weeding of R. obtusifolius had no substantial effect on species richness. Species richness was reduced in the treatment with no grassland management, a finding also observed previously in temperate grasslands (Pavlů et al. 2012). There was almost no regeneration of R. obtusifolius plants via seedlings in all of the managed treatments, based on personal observations (Vilém Pavlů) (data not presented). It is likely that repeated defoliation of ungrazed patches prevented seed production and generative reproduction of R. obtusifolius. Any young seedlings of R. obtusifolius are likely to have been grazed or damaged by cutting or by hooves of the cattle during the grazing. Similarly, Stilmant et al. (2010) recorded a reduction in the vigour of the aerial parts of R. obtusifolius under grazing treatment, associated with a reduction in the number of leaves, the size of the largest leaf and the herbage mass. In the spring we found a higher number of R. obtusifolius plants in the treatment with no grassland management due to the presence of seedlings close to mother plants (personal observation, Vilém Pavlů). These seedlings did not survive until the autumn of the same year, however, as they were suppressed by overgrowing tall grasses and forbs. This confirmed the low competitive ability of R. obtusifolius seedlings in closed grassland stands (Weaver and Cavers 1979). The low presence of R. obtusifolius plants in the treatment with no grassland management in the final year of the experiment is in accordance with previous studies (Pavlů et al. 2008; Martinková et al. 2009; Hejcman et al. 2012) in which high mortality of R. obtusifolius plants was recorded in unmanaged grassland after several years, probably due to the effects of competition from tall grasses and forbs. Under conditions of no grassland management, however, mature plants of R. obtusifolius can produce a large number of germinable seeds; these seeds may be able to survive in the soil seed bank for decades (Toole and Brown 1946). Additionally, unmanaged grassland supported tall weedy species with high nutrient requirements, such as U. dioica, G. album and E. repens; these are not considered desirable plant species in agricultural grasslands (Frame 1992).
Manual weeding of R. obtusifolius can be an effective method for its control in temperate grasslands. Manual digging of R. obtusifolius taproots is commonly made by farmers (Pötsch and Griesebner 2007) but has not been adequately tested under experimental conditions. In addition to being an appropriate technique for use in organic farming, this method of manual weeding of R. obtusifolius can also be used in grasslands managed according to agri-environment and conservation schemes, where the use of herbicides approved for dock control might present problems for other dicotyledons of conservation interest. It is also a weed-control method which is also suitable for conventional farmers who prefer not to use herbicides, including many horse keepers. However, the use of this weeding method over large areas of grassland is limited due to time-consuming and hard physical work.
Conclusion
Manual or mechanical weeding of R. obtusifolius by digging out the taproots can be an effective method for R. obtusifolius control in organically managed grasslands dominated by Agrostis capillaris. Digging of R. obtusifolius taproots to the depth of 15 cm, performed twice, was the most successful method as this procedure eliminated the majority of R. obtusifolius plants. Bare ground gaps created by digging are colonised by nutrient-demanding grasses and forbs with high forage value. Although removal of grassland management, thereby allowing the sward to grow unmown and ungrazed, can reduce the number of R. obtusifolius plants in the sward, the plants present can produce seeds which can contribute further to weed infestation of surrounding areas. Additionally, the absence of grassland management supports tall weedy species and considerably reduces the species richness of vascular plants.
Author contributions
VP, JG and LP conceived and designed the research. JG, VP, LP, VL and RH conducted the experiments. RH and VP analysed the data. VP, RH, LP and MH wrote the manuscript. All authors read and approved the manuscript.
References
Bond W, Davies G, Turner RJ (2007) The biology and non-chemical control of broad-leaved dock (Rumex obtusifolius L.) and curled dock (R. crispus L.). Garden organic web. http://www.gardenorganic.org.uk/sites/www.gardenorganic.org.uk/files/organic-weeds/dock-review.pdf. Accessed 25 Mar 2015
Brant V, Svobodová M, Šantrůček J, Hlavičková D (2006) The influence of plant covers of set-aside fields and their management on the weed spectrum. J Plant Dis Prot Spec Issue 20:941–947
Brock JL (1972) The control of broad-leaved dock (Rumex obtusifolius L.) in newly-sown red clover (Trifolium pratense L.) with trifluralin, carbetamide and asulam. Weed Res 12:310–315
Cavers PB, Harper JL (1964) Biological flora of the British Isles. Rumex obtusifolius L. and Rumex crispus L. J Ecol 52:737–766
Chytrý M (ed) (2007) Vegetace České republiky. 1. Travinná a keříčková vegetace (Vegetation of the Czech Republic. 1 Grassland and Heathland Vegetation). Academia, Prague
Dierauer HU (1993) Efficiency of different non-chemical methods of controlling broadleaf dock (Rumex obtusifolius). In: Proceedings of the 4th international conference I.F.O.A.M.—non chemical weed control, Dijon, pp 311–314
Dimitrova T, Marinov-Serafimov P (2008) Chemical control of curled dock (Rumex crispus L.) and other weeds in noncropped areas. Pestic Phytomed (Belgrade) 23:123–126
DiTomaso JM, Kyser GB, et al. (2013) Weed control in natural areas in the Western United States. Weed Research and Information Center, University of California Web. http://wric.ucdavis.edu/information/natural%20areas/wr_R/Rumex_crispus-obtusifolius.pdf. Accessed 27 April 2015
Frame J (1992) Improved grassland management. Farming Press Books, Ipswich
Hann P, Trska C, Kromp B (2012) Effects of management intensity and soil chemical properties on Rumex obtusifolius in cut grasslands in lower Austria. J Pest Sci 85:5–15
Hatcher PE, Paul ND, Ayres PG, Whittaker JB (1997) Added soil nitrogen does not allow Rumex obtusifolius to escape the effects of insect-fungus interactions. J Appl Ecol 34:88–100
Hejcman M, Strnad L, Hejcmanová P, Pavlů V (2012) Effects of nutrient availability on performance and mortality of Rumex obtusifolius and R. crispus in unmanaged grassland. J Pest Sci 85:191–198
Hejcman M, Strnad L, Hejcmanová P, Pavlů V (2014) Biological control of Rumex obtusifolius and Rumex crispus by goat grazing. Weed Biol Manag 14:115–120
Hoňek A, Martinková Z (2004) Gastrophysa viridula (Coleoptera: Chrysomelidae) and biocontrol of Rumex: a review. Plant Soil Environ 50:1–9
Hopkins A, Johnson RH (2002) Effect of different manuring and defoliation patterns on broad-leaved dock (Rumex obtusifolius) in grassland. Ann Appl Biol 140:255–262
Hopkins A, Johnson RH (2003) Impact of control of dock (Rumex obtusilfolius) on potential production from N-fertilised swards. Grassl Sci Eur 8:200–203
Jursík M, Holec J, Zatoriová B (2008) Biology and control of another important weeds of the Czech Republic: broad-leaved dock (Rumex obtusifolius) and curled dock (Rumex crispus). List Cukr Rep 124:215–219 (In Czech)
Keary IP, Hatcher PE (2004) Combining competition from Lolium perenne and an insect–fungus combination to control Rumex obtusifolius seedlings. Weed Res 44:33–41
Kubát K, Hrouda L, Chrtek J jun, Kaplan Z, Kirschner J, Štěpánek J (eds) (2002) Klíč ke květeně České republiky (Key to the flora of the Czech Republic). Academia, Prague (In Czech)
Latsch R, Sauter J, Hermle S, Dürr L, Anken T (2007) Control of Rumex obtusifolius L. in grassland using microwave technology. Tagung Landtechnik AgEng 2007. VDI-Verlag, Hanover, pp 501–506
Latsch R, Kaeser A, Kauter J (2011) Hot water steam in dock control. Landtechnik 66:170–172
Martinková Z, Honěk A, Pekár S, Štrobach J (2009) Survival of Rumex obtusifolius L. in unmanaged grassland. Plant Ecol 205:105–111
Mehlich A (1984) Mehlich no. 3 soil test extractant, a modification of Mehlich no. 2. Commun Soil Sci Plant Anal 15:1409–1416
Niggli U, Nösberger J, Lehmann J (1993) Effects of nitrogen fertilization and cutting frequency on the competitive ability and the regrowth capacity of Rumex obtusifolius L. in several grass swards. Weed Res 33:131–137
Novák J (1994) Botanical and production changes in ruderal grassland after non-tillage reseeding. Rostl Výr 40:1049–1056
Pavlů L, Pavlů V, Gaisler J, Hejcman M (2008) Effect of cessation of grazing management on dynamics of grassland weedy species. J Plant Dis Prot Spec Issue 21:581–586
Pavlů V, Gaisler J, Pavlů L, Hejcman M, Ludvíková V (2012) Effect of fertiliser application on plant species composition of Festuca rubra grassland under cutting management and its after effect under abandonment. Acta Oecol 45:42–49
Pimentel D (1995) Amounts of pesticides reaching target pests: environmental impacts and ethics. J Agric Environ Ethics 8:17–29
Pino J, Haggar RJ, Sans FX, Masalles RM, Sackville-Hamilton RN (1995) Clonal growth and fragment regeneration of Rumex obtusifolius L. Weed Res 35:141–148
Pötsch EM, Griesebner C (2007) Control of broad-leaved dock on organic grassland farms. Grassl Sci Eur 12:138–141
Power EF, Kelly DL, Stout JC (2013) The impacts of traditional and novel herbicide application methods on target plants, non-target plants and production in intensive grasslands. Weed Res 53:131–139
Stilmant D, Bodson B, Vrancken C, Losseau C (2010) Impact of cutting frequency on the vigour of Rumex obtusifolius. Grass Forage Sci 65:147–153
Strnad L, Hejcman M, Křišťálová V, Hejcmanová P, Pavlů V (2010) Mechanical weeding of Rumex obtusifolius L. under different N, P and K availabilities in permanent grassland. Plant Soil Environ 56:393–399
ter Braak CJF, Šmilauer P (2012) Canoco reference manual and user’s guide: software for ordination (version 5.0). Microcomputer Power, Ithaca
Toole E, Brown E (1946) Final results of the Duvel buried seed experiment. J Agric Res 72:201–210
Weaver SE, Cavers PB (1979) Dynamics of seed populations of Rumex crispus and R. obtusifolius (Polygonaceae) in disturbed and undisturbed soil. J Appl Ecol 16:909–917
Zaller JG (2004) Ecology and non-chemical control of Rumex crispus and R. obtusifolius (Polygonaceae): a review. Weed Res 44:414–432
Acknowledgments
This research was supported financially by National Agency for Agriculture Research (QH 72217), Czech University of Life Sciences (CIGA 20124208) and by ESF & MEYS (CZ.1.07/2.3.00/30.0040). We are grateful to Irena Jonášová, Věra Ismanická and Vlastislav Černý for their help with the fieldwork. The useful comments of three anonymous reviewers are gratefully acknowledged.
Author information
Authors and Affiliations
Corresponding author
Additional information
Communicated by M. Traugott.
Rights and permissions
About this article
Cite this article
Hujerová, R., Pavlů, L., Pavlů, V. et al. Manual weeding of Rumex obtusifolius and its effects on plant species composition in organically managed grassland. J Pest Sci 89, 257–266 (2016). https://doi.org/10.1007/s10340-015-0683-x
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10340-015-0683-x