Hostname: page-component-8448b6f56d-c4f8m Total loading time: 0 Render date: 2024-04-25T06:48:27.778Z Has data issue: false hasContentIssue false

Identification of a Johnsongrass (Sorghum halepense) Biotype Resistant to ACCase-Inhibiting Herbicides in Northern Greece

Published online by Cambridge University Press:  20 January 2017

Nikolaos S. Kaloumenos
Affiliation:
Laboratory of Agronomy, School of Agriculture, Aristotle University of Thessaloniki, 541 24 Thessaloniki, Greece
Ilias G. Eleftherohorinos*
Affiliation:
Laboratory of Agronomy, School of Agriculture, Aristotle University of Thessaloniki, 541 24 Thessaloniki, Greece
*
Corresponding author's E-mail: eleftero@agro.auth.gr.

Abstract

A johnsongrass population from a cotton field in northern Greece along with a population from the university farm (“Control”) were evaluated for resistance to the herbicide quizalofop; cross-resistance to cycloxydim, propaquizafop, and fluazifop (acetyl coenzyme A [CoA] carboxylase [ACCase]-inhibiting herbicides), and multiple resistance to nicosulfuron (acetolactate synthase [ALS]-inhibiting herbicides). In greenhouse experiments, the application of four times the recommended rates of quizalofop and propaquizafop to suspected resistant rhizomatous plants resulted in 4 and 5% growth reduction, respectively. However, the growth of suspected resistant seedlings was reduced by 54 and 28% after the application of two times the recommended rate of the same herbicides. In contrast, the application of quizalofop and propaquizafop at recommended rates on rhizomatous plants and seedlings of the Control population reduced their growth by 97 to 100%. Also, the growth reduction of both populations by the application of cycloxydim, fluazifop, and nicosulfuron at recommended rates ranged from 93 to 100%. In the field experiment, quizalofop and propaquizafop applied at four times the recommended rate reduced growth of the suspected resistant population by 9 and 18%, respectively, whereas the recommended rate of fluazifop gave a 94% growth reduction of this weed. The herbicide rate required for 50% growth reduction (GR50) values for rhizomatous plants of the suspected resistant population were 0.90 and 2.465 kg ai/ha for quizalofop and propaquizafop, respectively, whereas the corresponding GR50 values for the seedlings were 0.074 and 0.185 kg ai/ha. These results indicate that a johnsongrass population developed cross-resistance to quizalofop and propaquizafop, but did not evolve cross-resistance to cycloxydim and fluazifop or multiple resistance to nicosulfuron.

Type
Weed Biology and Competition
Copyright
Copyright © Weed Science Society of America 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Literature Cited

Bradley, K. W. and Hagood, E. S. 2001. Identification of a johnsongrass (Sorghum halepense) biotype resistant to aryloxyphenoxypropionate and cyclohexandione herbicides in Virginia. Weed Technol 15:623627.CrossRefGoogle Scholar
Bradley, K. W., Wu, J. J., Hatzios, K. K., and Hagood, E. S. 2001. The mechanism of resistance to aryloxyphenoxypropionate and cyclohexanedione herbicides in a johnsongrass biotype. Weed Sci 49:477484.CrossRefGoogle Scholar
Bridges, D. C. and Chandler, J. M. 1987. Influence of johnsongrass (Sorghum halepense) density and period of competition on cotton yield. Weed Sci 35:6367.CrossRefGoogle Scholar
Burke, C. I., Wilcut, J. W., and Cranmer, J. 2006a. Cross-resistance of a johnsongrass (Sorghum halepense) biotype to aryloxyphenoxypropionate and cyclohexandione herbicides. Weed Technol 20:571575.CrossRefGoogle Scholar
Burke, C. I., Burton, J. D., York, A. C., Cranmer, J., and Wilcut, J. W. 2006b. Mechanism of resistance to clethodim in a johnsongrass (Sorghum halepense) biotype. Weed Sci 54:401406.CrossRefGoogle Scholar
Damanakis, M. E. 1983. Weed species in wheat fields of Greece—1982, 1983 survey. Zizaniologia 1:8590.Google Scholar
De Prado, R., González-Gutiérrez, J., Menéndez, J., Gasquez, J., Gronwald, J. W., and Giménez-Espinosa, R. 2000. Resistance to acetyl CoA carboxylase-inhibiting herbicides in Lolium multiflorum . Weed Sci 48:311318.CrossRefGoogle Scholar
Délye, C. 2005. Weed resistance to acetyl coenzyme A carboxylase inhibitors: an update. Weed Sci 53:728746.CrossRefGoogle Scholar
Devine, D. M. 1997. Mechanisms of resistance to acetyl-coenzyme A carboxylase inhibitors: a review. Pestic. Sci 51:259264.3.0.CO;2-S>CrossRefGoogle Scholar
Devine, M. D. and Shulka, A. 2000. Altered target as a mechanism of herbicide resistance. Crop Prot 19:881889.CrossRefGoogle Scholar
Eleftherohorinos, I. G. and Kotoula-Syka, E. 1995. Influence of herbicide application rate and timings for post-emergence control of Sorghum halepense (L.) Pers. in maize. Weed Res 35:99103.CrossRefGoogle Scholar
Haitas, V. C., Kotoula-Syka, E., and Eleftherohorinos, I. G. 1995. Influence of propaquizafop application rate and time on Sorghum halepense (L) Pers. control and cotton (Gossypium hirsutum) yield. Weed Res 35:16.CrossRefGoogle Scholar
Heap, I. 2009. The International Survey of Herbicide Resistant Weeds. www.weedscience.com. Accessed: April 15, 2009.Google Scholar
Heap, J. and Knight, R. 1982. A population of ryegrass tolerant to the herbicide diclofop-methyl. J. Aust. Inst. Agric. Sci 48:156157.Google Scholar
Holm, L. G., Plucknett, D. L., Pancho, J. V., and Herberger, J. P. 1977. The World's Worst Weeds: Distribution and Biology. Honolulu: University Press of Hawaii. 609.Google Scholar
McWhorter, C. G. 1972. Factors affecting johnsongrass rhizome production and germination. Weed. Sci 20:4145.CrossRefGoogle Scholar
McWhorter, C. G. 1989. History, biology, and control of johnsongrass. Rev. Weed Sci 4:85121.Google Scholar
McWhorter, C. G. and Anderson, J. M. 1993. Effects of johnsongrass (Sorghum halepense), hemp sesbania (Sesbania exltata), and delayed harvest on soybeans. Weed Technol 7:355360.CrossRefGoogle Scholar
Mitskas, B. M., Tsolis, C. E., Eleftherohorinos, I. G., and Damalas, C. A. 2003. Interference between corn and johnsongrass (Sorghum halepense) from seed or rhizomes. Weed Sci 51:540545.CrossRefGoogle Scholar
Preston, C. 2004. Herbicide resistance in weeds endowed by enhanced detoxification: compilations for management. Weed Sci 52:448453.CrossRefGoogle Scholar
Rentina, A. R., Craig-Kennard, A. C., Beaudoin, J. D., and Breen, M. K. 1990. Inhibition of acetyl-coenzyme A carboxylase by two classes of grass-selective herbicides. J. Agric. Food Chem 38:12821287.CrossRefGoogle Scholar
Seefeldt, S. S., Jensen, J. E., and Fuerst, E. P. 1995. Log-logistic analysis of herbicide dose-response relationships. Weed Technol 9:218227.CrossRefGoogle Scholar
Smeda, R. J., Snipes, C. E., and Barrentine, W. L. 1997. Identification of graminicide-resistant johnsongrass (Sorghum halepence). Weed Sci 45:132137.CrossRefGoogle Scholar
Vasilakoglou, I., Dhima, K., and Eleftherohorinos, I. 2005. Allelopathic potential of bermudagrass and johnsongrass and their interference with cotton and corn. Agron. J. 97:303313.CrossRefGoogle Scholar
Yu, Q., Collavo, A., Zheng, M. Q., Owen, M., Sattin, M., and Powles, S. B. 2007. Diversity of acetyl-coenzyme A carboxylase mutations in resistant Lolium populations: evaluation using clethodim. Plant Physiol 145:547558.CrossRefGoogle ScholarPubMed