Open Access
How to translate text using browser tools
30 September 2022 Seed germination responses of broomrape species (Phelipanche ramosa and Phelipanche aegyptiaca) to various sanitation chemicals
Pershang Hosseini, O. Adewale Osipitan, Mohsen B. Mesgaran
Author Affiliations +
Abstract

Branched broomrape, an obligate root parasitic weed, has recently re-emerged in tomato fields in several California counties. California produces more tomato than any other state, and the outbreak of this noxious weed could potentially wreak havoc on the industry's economy. Preventive measures must be taken to stop or reduce the spread of branched broomrape seeds to other areas. Branched broomrape can produce thousands of tiny seeds, which can easily spread with farm machinery over short and long distances. To prevent branched broomrape seed dispersal, sanitation and disinfection of farm equipment are necessary before entering a new farm. We tested the effectiveness of various ammonium compounds, including didecyl dimethyl ammonium chloride (DDAC), alkyl dimethyl benzyl ammonium chloride (ADBC), didecyl dimethyl ammonium bromide (DDAB), ammonium bromide (AB), and ammonium chloride (AC) on prevention of branched broomrape seed germination. Dose-response analysis showed that three chemical products, ADBC, DDAB, and DDAC, could completely inhibit branched broomrape seeds (potentially making them nonviable) at 1%, 1%, and 10% wt/vol concentrations, respectively. These three compounds were further tested in an exposure duration experiment that additionally included Egyptian broomrape. Only 10 min of exposure to these compounds was needed to prevent germination of both branched and Egyptian broomrape seeds at 1% (ADBC, DDAB) and 10% wt/vol (DDAC). Lower concentrations can provide similar inhibition effects when combined with longer exposure times. Egyptian broomrape seeds were more sensitive than branched broomrape seeds. Findings suggest that quaternary ammonium compounds could be used as potential sanitation agents to disinfect agriculture machinery from branched and Egyptian broomrape seeds.

Nomenclature: Branched broomrape, Phelipanche ramosa (L.) Pomel; Egyptian broomrape, Phelipanche aegyptiaca; tomato, Lycopersicon esculentum L.

Introduction

California is the largest producer of processing tomato, accounting for more than 90% of U.S. production (Winans et al. 2020). However, the profitability of the tomato industry in California is seriously threatened due to the presence of the parasitic weed branched broomrape. This parasitic weed was first reported on tomato in California in 1928 (Stout and Wagnon 1953, quoted in Musselman 1980) and became the target of an eradication effort about four decades ago (Osipitan et al. 2021). Branched broomrape is currently classified as an “A” pest in California. An “A” pest is a pest of known economic importance subject to state-enforced action involving “eradication, quarantine regulation, containment, rejection, or other holding action” (CDFA 2020). Detection of branched broomrape in a commercial tomato field leads to quarantine and crop destruction without harvest. Egyptian broomrape has also been reported in several tomato fields in California (Miyao 2017) but is currently assumed to be less of a threat than branched broomrape.

Broomrapes (Orobanche and Phelipanche spp.) have been known as the most destructive parasitic plants globally, and controlling them is a challenge. Branched broomrape is a holoparasitic weed that attaches to the host root and absorbs water, minerals, and carbohydrates from its host. It can severely damage the host by reducing the aerial biomass and leaf chlorophyll content (Mauromicale et al. 2008) with yield losses of up to 80% (Eizenberg and Goldwasser 2018). To germinate, seeds of branched broomrape need to be close to the host roots because the host root exudation triggers germination. Because seeds can maintain their viability in the seed bank for several decades (Joel 2013), eradication is difficult. Branched broomrape has many hosts besides tomato, including cabbage (Brassica oleracea), canola (B. napus), carrot (Daucus carota L.), celery (Apium graveolens L.), pepper (Capsicum fruitisence), potato (Solanum tuberosum L.), sunflower (Helianthus annuus L.), and lettuce (Lactuca sativa; Osipitan et al. 2021). The broad range of hosts can further complicate control and eradication plans. Moreover, branched broomrape has been noted to extend its host range to affect new species (Le Corre et al. 2014); for example, the seeds of a new race of sunflower broomrape (Orobanche cumana Wallr.) has expanded its host range to Solanaceae crops by parasitizing tomato and tobacco (Nicotiana tabacu L.; Dor et al. 2020).

Branched broomrape produces hundreds of thousands of tiny seeds (0.2 to 0.4 mm), which can be transported easily by humans, water, wind, and animals (Eizenberg et al. 2012; Ginman et al. 2015). Farm machinery (e.g., harvesters) is one of the most important ways of dispersal of broomrape seeds in tomato fields (Hershenhorn et al. 2009; Rubiales and Fernández-Aparicio 2012). Because cropping systems in California are highly mechanized, dispersal of broomrape seeds via farm machinery is particularly concerning. Movement of farm equipment between plots of the same farm or between farms is very common, which can facilitate both the short- and long-distance dispersal of broomrape seeds. To effectively contain branched broomrape, farming implements used in an infested field must be cleaned and sanitized before entering other fields or farms. The first step in equipment sanitation is removing all plant and soil residues. The next step involves using effective disinfecting chemicals to disinfect broomrape seeds left on the equipment (Osipitan et al. 2021).

Quaternary ammonium compounds are surface-active chemicals that are widely used as sanitation solutions in the food processing industry and in disinfectants, fabric softeners, and cosmetics (Martínez-Carballo et al. 2007). Initial research with some ammonium compounds as potential equipment disinfectants suggests that didecyl dimethyl ammonium chloride, alkyl dimethyl benzyl ammonium chloride, dioctyl dimethyl ammonium chloride, octyl decyl dimethyl ammonium chloride, and ammonium bromide can effectively prevent germination of Egyptian broomrape seeds (Hershenhorn et al. 2009). However, data on the effectiveness of sanitation methods for both branched broomrape and Egyptian broomrape is scarce. Thus the objective of this study was to test the ability of various quaternary ammonium compounds to prevent the germination of branched and Egyptian broomrape seeds with the goal of finding a material to disinfect farm machinery.

Materials and Methods

Collection of Broomrape Seeds

Soil samples were collected from preidentified branched broomrape–infested fields near Woodland, CA (38.7574°N, 121.7677° W) in 2019. The soil samples were transferred to the Contained Research Facility of the University of California, Davis. In this facility, 80 plastic pots (2.4 L) were filled with the collected soil, moistened, and placed in a growth chamber. The growth chamber was set at a 28/20 C (day/night) temperature regime for 2 wk to precondition the branched broomrape seeds that might occur in the collected soil (Murdoch and Kebreab 2013). Following this conditioning period, two beefsteak tomato seedlings (10 to 15 cm tall) were transplanted to each pot to stimulate the germination of the presumed broomrape seeds. About 100 d after planting, the emerged branched broomrape plants were mature and produced seeds. Capsules were collected from plants, crushed, and sieved to obtain clean seeds. The collected seeds (∼0.2 mm in size) were stored in darkness at a temperature of 4 C in the Contained Research Facility until use.

Evaluation of Quaternary Ammonium Compounds

We evaluated five quaternary ammonium compounds for their effectiveness in preventing the germination of branched broomrape seeds. These chemicals included ammonium bromide (AB), didecyl dimethyl ammonium bromide (DDAB), ammonium chloride (AC), alkyl dimethyl benzyl ammonium chloride (ADAC), and didecyl dimethyl ammonium chloride (DDAC). The compounds were supplied in technical form (≥90% concentration) by Sigma-Aldrich (St. Louis, MO). For AB, AC, DDAB, and DDAC we tested seven concentrations: 0% (distilled water), 0.01%, 0.05%, 0.125%, 0.2%, 0.5%, and 1% (wt/vol) of distilled water. For ADAC, the concentrations were 0%, 0.2%, 0.5%, 1%, 2.5%, 5%, and 10% (wt/vol) of distilled water.

Each solution (500 µl) was added to a 5-ml Eppendorf tube equipped with a paper filter, and about 100 seeds were placed in the Eppendorf tubes for 10 min and then centrifuged at 1,500 rpm for 2 min using Z206-A® compact centrifuge (Benchmark Scientific, Beachwood, OH). The centrifuge was used to drain the solutions from the seeds. Afterward, distilled water was added to the tubes to wash the seeds, and the water was drained by centrifuging for 2 min. Seeds were then extracted from the tubes, placed on filter papers (Whatman®; Global Life Sciences Solutions, Marlborough, MA) in 5-cm-diameter Petri dishes, moistened with distilled water, and kept at 25 C in darkness for 10 d within an incubator (Isotemp Incubator; Fisher Scientific) as the preconditioning period.

Following the preconditioning period, 1 ml of 10–5 M of a strigolactone analog (GR24) was added to the Petri dishes. GR24 is widely used to induce germination in seeds of broom-rapes in the absence of host (Fernández-Aparicio et al. 2011; Ibdah et al. 2014). Seeds were incubated (Isotemp Incubator; Fisher Scientific) at 25 C and kept in the dark for 14 d where germinated, and ungerminated seeds were counted 7 and 14 d after incubation using a stereomicroscope (Nikon SMZ 1500). Seeds were considered germinated when a protruded radicle was visible. The experiment was conducted with three replicates per concentration of each compound in April 2020 and was repeated in July 2020.

Effects of Exposure Duration

A second study was conducted to determine the impact of the exposure duration of the quaternary compounds on the germination of branched broomrape and Egyptian broomrape seeds. The exposure times tested were 10 minutes, 1 hour, and 24 hours including centrifuge time. In this study, three compounds, ADAC, DDAB, and DDAC were tested at seven concentrations of 0 (distilled water), 0.01, 0.05, 0.125, 0.2, 0.5, and 1% (wt/vol) of distilled water. Treatment application, seed conditioning, and germination test were as described above. All treatments were replicated three times in September 2020, and the experiment was repeated in October 2020.

Data analysis

Seed germination data (as a surrogate for seed viability) were subjected to dose-response analysis using the drc package (Ritz et al. 2015) in R software (R Core Team 2020) following the guideline provided by Keshtkar et al. (2021). For both studies, data from the two experimental runs were pooled because there was no difference between the full model (with the experimental run as a covariate) and the reduced model (without the experimental run), as detailed below. A three-parametric log-logistic function (Equation 1; Streibig et al. 1993) best described the seed germination of branched broomrape in relation to the concentration of ADAC, DDAB, DDAC, and AB:

e01_723.gif

where Y is broomrape total seed germination (percentage), e is the effective dose needed for a 50% response (ED50), u is the upper limit, and b is the relative slope around the inflection point (e). In the exposure duration experiment, the three-parametric log-logistic function (Equation 1) also showed the best fit for branched broomrape seed germination. However, for AC data, a four-parametric log-logistic function (Equation 2; (Streibig et al. 1993) was found to provide better fits:

e02_723.gif

with the addition parameter l indicating the lower limit of the curve. Note that in the above four-parameter model, parameter e shows the response halfway between the upper, u, and lower, l, limits and should not be used as the ED50 (Keshtkar et al. 2021). Germination data from all chemical compounds, except AC, were fitted to Equation 1 simultaneously. To test whether the parameters of the model differ between the chemical compounds, we compared the size of error between a full model and various reduced models (lacking 1 or 2 parameters). An F-test was conducted to compare the error across these two types of models using the “anova()” function of the MASS package in R. For example, to test the null hypothesis that parameter e (ED50) does not differ between ADAC, DDAB, DDAC, and AB compounds, we first fitted a (reduced) model that assumed a single e parameter across the dose-response curves of these four chemistries. A full model was then fitted to the same data using four individual e parameters for each chemistry. The latter more complex model (i.e., full) is justified, and hence the four curves differ in parameter e, if its size of model error is significantly smaller than that of the reduced model as indicated by the F-test. A similar test was performed for all other parameters of the models to test whether they differ across chemical compounds or exposure duration treatments.

Results and Discussion

Screening of Ammonium Compounds

All five quaternary ammonium compounds, except AC, were effective in preventing the germination of broomrape seeds (potentially making them nonviable), as shown by our dose-response analysis (Figure 1). Comparing various reduced models vs. the full model showed that both the upper limit, u, and slope, b, parameters can be fixed across curves of ADAC, DDAB, DDAC, and AB without significantly reducing the goodness of fit (Table 1);that is, these parameters did not vary between the tested compounds. As represented by parameter u, total seed germination in control was ∼70% (SE = 3.3). The effective dose for 50% reduction in germination (parameter e) varied significantly across the above four chemistries and ranged from 0.014 (SE = 0.016) in ADAC to 0.124 (SE = 0.033 (wt/vol) in AB (Table 1). A four-parameter logistic model with a lower limit l > 0 was used for AC, because branched broomrape germination never approached zero over the tested doses. For AC, the ED50 was not estimable because the lower limit of the model (∼39%) was greater than half the maximum response (i.e., 64.4% × 0.5 = 32.2%).

Germination responses of branched broomrape seeds to DDAB and DDAC, and to a lesser extent to AB, were similar: the decline occurred slowly, and complete prevention was achieved at the maximum concentration (i.e., 1%). However, the declining response to ADAC was more abrupt than that of other compounds (Figure 1), as shown by its very low ED50 value (Table 1). AC had a poor sanitation effect on branched broomrape seeds, and even at the highest concentration rate more than half the seeds were able to germinate (Figure 1). Two ammonium compounds, AB and AC, were eliminated for the exposure duration experiment.

Exposure Duration

A three-parameter log-logistic model was used to characterize the seed germination responses of both branched and Egyptian broomrape to different sanitation doses across three exposure durations of 10 min, 1 h, and 24 h (Figure 2 and Table 2). All three chemical compounds (ADAC, DDAB, and DDAC) displayed a significant effect on seed germination of both broomrape species seeds, and complete prevention was achieved with the three tested exposure durations when these chemicals were applied at the maximum rate (i.e., 1% wt/vol). However, ED50 values for all disinfectants decreased with increased exposure duration in both broomrape species. For ADAC, for example, a concentration of 0.216% (wt/vol) was required to provide a 50% reduction in branched broomrape seed germination when seeds were exposed to this chemical for 10 min. In contrast, only 0.0006% (wt/vol) was enough to give the same level of reduction in seed germination when exposure duration increased to 24 h. The same trend was observed with the two other products, DDAB and DDAC, across both broomrape species. A comparison of ED50 values between the two broomrape species indicated that these ammonium compounds could halt germination in Egyptian broomrape seeds at lower concentrations compared to branched broomrape seeds, suggesting greater sensitivity of Egyptian broomrape seeds to ammonium compounds (Table 2).

Sanitation of farm equipment before entering other farms can help reduce the introduction of broomrape seeds to non-infested fields. Quaternary ammonium compounds are widely used as disinfectants and have been found to be effective for broomrape seed eradication. As part of a national eradication program in southern Australia, a quaternary ammonium compound containing didecyl dimethyl ammonium chloride (DDAC; commercial name NiproQuat) was found to significantly render the branched broomrape seeds nonviable on farm machinery (Hershenhorn et al. 2009).

ADBC (alkyl dimethyl benzyl ammonium chloride), known commercially as Zoharquat 50, is a bactericidal, fungicidal, and algicidal agent that has provided promising results for sanitation of tomato harvesters contaminated with Egyptian broomrape seeds (Hershenhorn et al. 2009). At 1% (wt/vol) ADBC caused a 20% reduction in the germination of Egyptian broomrape seeds, but when the concentration increased to 10% (wt/vol), this product ultimately prevented the germination of all Egyptian broomrape seeds collected from the tomato harvester (Hershenhorn et al. 2009).

DDAB, with the commercial name Bromosept 50, is a disinfectant agent with effectiveness against bacterial, viral, and fungal pathogens. The sanitation effect of DDAB against Egyptian broomrape seeds was tested in the laboratory and a commercial disinfecting facility (Hershenhorn et al. 2009). This research concluded that soaking Egyptian broomrape seeds in DDAB at 0.1 % (wt/vol) for 5 min completely prevented the germination of seeds in a petri dish. DDAB sprayed at a higher rate of 1% (wt/vol) completely prevented the germination of Egyptian broomrape seeds attached to the sides of a commercial tomato harvester (Hershenhorn et al. 2009).

Table 1.

Estimated parameter values for the three-parameter (Equation 1) and four-parameter (Equation 2) log-logistic models were used to describe the branched broomrape seed germination responses to the increasing doses of different ammonium compounds.e,f

img-z4-2_723.gif

Figure 1.

Dose response curves of branched broomrape seed germination in response to doses of five different ammonium products. A three-parameter logistic model (Equation 1) was used for AB, ADAC, DDAC, and DDAB, whereas AC data were fitted to a four-parameter model (Equation 2). Lines are fitted values, and solid circles indicate observed germination averaged across two experimental runs with three replicates each (i.e., n = 6). Error bars indicate 95% confidence intervals. Model parameter estimates are shown in Table 1. Abbreviations: AB, ammonium bromide; AC, ammonium chloride; DDAC, didecyl dimethyl ammonium chloride; ADAC, alkyl dimethyl benzyl ammonium chloride; DDAB, didecyl dimethyl ammonium bromide.

img-z4-4_723.jpg

Several studies have noted that sanitation and prevention are integral parts of the noxious and quarantine plant eradication program (Panetta and Scanlan 1995; Quinn et al. 2013). Human activities and farm machinery are among the most effective agent of weed seed dispersal (Liebman et al. 2001). The spatial distribution pattern of Egyptian broomrape in a tomato field showed a strong link between some specific farm activities and the level of infestation: the container collection site and the washing site of combines had the highest level of Egyptian broomrape contamination (Eizenberg et al. 2012). Containers and farm equipment can collect broomrape seeds and transport them to another location, hence they should be disinfected and sanitized before exiting an infested field. Our study showed that most commercially available ammonium compounds are effective on broomrape seeds and can be used to sanitize farm equipment.

Table 2.

Estimated parameter values for the three-parameter (Equation 1) log-logistic models used to describe the branched broomrape and Egyptian broomrape seed germination responses to the increasing doses of ammonium compounds over various exposure durations.d,e

img-z5-2_723.gif

Figure 2.

Dose response curves of branched broomrape and Egyptian broomrape seed germination in response to doses of three different ammonium products under three exposure durations of 10 min, 1 h, and 24 h. A three-parameter logistic model (Equation 1) was fitted to germination data. Lines are fitted values, and solid circles indicate observed germination averaged across two experimental runs with three replicates each (i.e., n = 6). Error bars indicate 95% confidence intervals. Model parameter estimates are shown in Table 2. Abbreviations: DDAC, didecyl dimethyl ammonium chloride; ADAC, alkyl dimethyl benzyl ammonium chloride; DDAB, didecyl dimethyl ammonium bromide.

img-z5-4_723.jpg

Removing seeds from equipment before leaving an infested field should constitute a key component of any broomrape eradication program. Further research should be conducted to evaluate the efficacy of other sanitizer classes (e.g., peracetic acid, acid-anionic sanitizers, fatty acid sanitizers, biguanide, and peroxides), which are used in the food industry and have been found to be more effective than quaternary ammonium compounds in sterilizing surfaces (Bernardi et al. 2019). Furthermore, a shorter exposure time needs to be evaluated for equipment sanitation in further studies.

Acknowledgments.

This research was funded by the California Department of Food and Agriculture through Specialty Crop Block Grant Program 19-0001-043-SF. The authors declare no conflicts of interest.

References

1.

Bernardi AO, Garcia MV, Copetti MV (2019) Food industry spoilage fungi control through facility sanitization. Curr Opin Food Sci 29:28–34 Google Scholar

2.

[CDFA] California Department of Food and Agriculture (2020) California Pest Rating.  www.cdfa.ca.gov/plant/IPC/encycloweedia/winfo_weedratings.html. Accessed: July 12, 2022 Google Scholar

3.

Dor E, Plakhine D, Joel DM, Larose H, Westwood JH, Smirnov E, Ziadna H, Hershenhorn J (2020) A new race of sunflower broomrape (Orobanche cumana) with a wider host range due to changes in seed response to strigolactones. Weed Sci 68:134–142 Google Scholar

4.

Eizenberg H, Aly R, Cohen Y (2012) Technologies for smart chemical control of broomrape (Orobanche spp. and Phelipanche spp.). Weed Sci 60:316–323 Google Scholar

5.

Eizenberg H, Goldwasser Y (2018) Control of Egyptian broomrape in processing tomato: A summary of 20 years of research and successful implementation. Plant Dis 102:1477–1488 Google Scholar

6.

Fernández-Aparicio M, Yoneyama K, Rubiales D (2011) The role of strigolactones in host specificity of Orobanche and Phelipanche seed germination. Seed Sci Res 21:55–61 Google Scholar

7.

Ginman E, Prider J, Matthews J, Virtue J, Watling J (2015) Sheep as vectors for branched broomrape (Orobanche ramosa subsp. mutelii [F.W. Schultz] Cout.) seed dispersal. Weed Biol Manag 15:61–69 Google Scholar

8.

Hershenhorn J, Eizenberg H, Dor E, Kapulnik Y, Goldwasser Y (2009) Phelipanche aegyptiaca management in tomato. Weed Res 49:34–47 Google Scholar

9.

Ibdah M, Dubey NK, Eizenberg H, Dabour Z, Abu-Nassar J, Gal-On A, Aly R (2014) Cucumber mosaic virus as a carotenoid inhibitor reducing Phelipanche aegyptiaca infection in tobacco plants. Plant Signal Behav 9:e972146 Google Scholar

10.

Joel DM (2013) Seed production and dispersal in the Orobanchaceae. Pages 143–146 in DM Joel, J Gressel, LJ Musselman, eds. Parasitic Orobanchaceae: Parasitic mechanisms and control strategies. Berlin, Heidelberg: Springer Google Scholar

11.

Keshtkar E, Kudsk P, Mesgaran MB (2021) Perspective: common errors in dose–response analysis and how to avoid them. Pest Manag Sci 77: 2599–2608 Google Scholar

12.

Le Corre V, Reibel C, Gibot-Leclerc S (2014) Development of microsatellite markers in the branched broomrape Phelipanche ramosa L. (Pomel) and evidence for host-associated genetic divergence. Int J Mol Sci 15:994–1002 Google Scholar

13.

Liebman M, Mohler CL, Staver CP (2001) Ecological management of agricultural weeds. Cambridge, UK: Cambridge University Press. 546 p Google Scholar

14.

Martínez-Carballo E, Sitka A, González-Barreiro C, Kreuzinger N, Fürhacker M, Scharf S, Gans O (2007) Determination of selected quaternary ammonium compounds by liquid chromatography with mass spectrometry. Part I. Application to surface, waste and indirect discharge water samples in Austria. Environ Pollut 145:489–496 Google Scholar

15.

Mauromicale G, Monaco AL, Longo AM (2008) Effect of branched broomrape (Orobanche ramosa) infection on the growth and photosynthesis of tomato. Weed Sci 56:574–581 Google Scholar

16.

Miyao G (2017) Egyptian broomrape eradication effort in California: a progress report on the joint effort of regulators, university, tomato growers and processors. Acta Hortic:139–142 Google Scholar

17.

Murdoch AJ, Kebreab E (2013) Germination ecophysiology. Pages 195–219 in DM Joel, J Gressel, LJ Musselman, eds. Parasitic i: Parasitic mechanisms and control strategies. Berlin, Heidelberg: Springer Google Scholar

18.

Musselman LJ (1980) The biology of Striga, Orobanche, and other root-parasitic weeds. Annu Rev Phytopathol 18:463–489 Google Scholar

19.

Osipitan O, Hanson B, Goldwasser Y, Fatino M, Mesgaran MB (2021) The potential threat of branched broomrape for California processing tomato: A review. Calif Agric 75:64–73 Google Scholar

20.

Panetta FD, Scanlan JC (1995) Human involvement in the spread of noxious weeds: what plants should be declared and when should control be enforced? Plant Prot Q 10: 69–74 Google Scholar

21.

Quinn LD, Barney JN, McCubbins JS, Endres AB (2013) Navigating the “Noxious” and “Invasive” regulatory landscape: Suggestions for improved regulation. BioScience 63:124–131 Google Scholar

22.

R Core Team (2020) R: A language and environment for statistical computing. Vienna: R Foundation for Statistical Computing  https://www.R-project.org/. Accessed: February 14, 2019 Google Scholar

23.

Ritz C, Baty F, Streibig JC, Gerhard D (2015) Dose-Response Analysis Using R. PLOS ONE 10:e0146021 Google Scholar

24.

Rubiales D, Fernández-Aparicio M (2012) Innovations in parasitic weeds management in legume crops. A review. Agron Sustain Dev 32:433–449 Google Scholar

25.

Stout GL, Wagnon HK (1953) Branched broomrape, Orobanche ramosa L., a pest of tomato and certain other crops. Bull Calif Dep Agric 42:45–51 Google Scholar

26.

Streibig JC, Rudemo M, Jensen JE (1993) Dose-response curves and statistical models. Pages 29–55 in: Streibig JC, Kudsk P, eds. Herbicide Bioassays. Boca Raton, FL: CRC Press Google Scholar

27.

Winans K, Brodt S, Kendall A (2020) Life cycle assessment of California processing tomato: an evaluation of the effects of evolving practices and technologies over a 10-year (2005–2015) timeframe. Int J Life Cycle Assess 25:538–547 Google Scholar
© The Author(s), 2022. Published by Cambridge University Press on behalf of the Weed Science Society of America.
Pershang Hosseini, O. Adewale Osipitan, and Mohsen B. Mesgaran "Seed germination responses of broomrape species (Phelipanche ramosa and Phelipanche aegyptiaca) to various sanitation chemicals," Weed Technology 36(5), 723-728, (30 September 2022). https://doi.org/10.1017/wet.2022.74
Received: 1 July 2022; Accepted: 18 September 2022; Published: 30 September 2022
KEYWORDS
Ammonium compounds
broomrape seeds
disinfection
Dose-response
farm machinery
sanitation
seed dispersal
Back to Top