Abstract
Chemical control is an efficient method and the most used in agriculture; however, resistant weeds have evolved worldwide due to the selection pressure caused by the repeated use of herbicides with the same mechanism of action. Some mechanisms of action have a greater disposition to evolve resistance, with the Acetolactate Synthase (ALS) and Photosystem II (PSII) inhibitors. Resistant biotypes seriously compromise agricultural crops, making management difficult and increasing control costs; therefore, management alternatives must be adopted to minimize the damage caused by resistant biotypes. For genetically modified varieties, such as glyphosate-resistant soybeans, other herbicides with different mechanisms of action are being included in management programs to control resistant biotypes. The use of herbicides with different mechanisms of action in annual rotations, tank mixes and sequential applications, can delay the evolution of resistance, minimizing the selection pressure imposed by a single specific mechanism of action. Integrated weed management combining different control methods is a viable alternative for controlling resistant biotypes. Thus, the chapter covers the evolution of resistance in the world and in Brazil, the different mechanisms of resistance to target and non-target site, methods of identification of resistant biotypes, and alternatives for integrated management of herbicide resistant weeds.
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References
Alcántara-de la Cruz R, Amaral GDS, Oliveira GM et al (2020a) Glyphosate resistance in Amaranthus viridis in Brazilian citrus orchards. Agriculture 10:304. https://doi.org/10.3390/agriculture10070304
Alcántara-de la Cruz R, Oliveira GM, Carvalho LB et al (2020b) Herbicide resistance in Brazil: status, impacts, and future challenges. In: Kontogiannatos D, Kourti A, Mendes KF (eds) Pests, weeds and diseases in agricultural crop and animal husbandry production. IntechOpen, London, pp 1–25
Alcántara-de la Cruz R, Silva AG, Mendes KF et al (2021) Absorption, translocation, and metabolism studies of herbicides in weeds and crops. In: Mendes KF (ed) Radioisotopes in weed research. CRC Press, Boca Raton, FL, pp 127–154
Anagnostopoulos C, Stasinopoulou P, Kanatas P, Travlos I (2020) Differences in metabolism of three Conyza species to herbicides glyphosate and triclopyr revealed by LC-MS/MS. Chil J Agric Res 80(1):100–107
Andres A, Concenço G, Schreiber F (2017) Predictions for weed resistance to herbicides in Brazil: a botanical approach. In: Pacanoski Z (ed) Herbicide resistance in weeds and crops. IntechOpen, London, pp 133–157
Anthony RG, Waldin TR, Ray JA et al (1998) Herbicide resistance caused by spontaneous mutation of the cytoskeletal protein tubulin. Nature 393(6682):260
Arora A, Sairam RK, Srivastava GC (2002) Oxidative stress and antioxidative system in plants. Curr Sci 82(10):1227–1238
Ashworth MB, Han H, Knell G, Powles SB (2016) Identification of triazine-resistant Vulpia bromoides. Weed Technol 30(2):456–463. https://doi.org/10.1614/WT-D-15-00127.1
Avila-García WV, Sanchez-Olguin E, Hulting AG, Mallory-Smith C et al (2012) Target-site mutation associated with glufosinate resistance in Italian ryegrass (Lolium perenne L. ssp. multiflorum). Pest Manag Sci 68(9):1248–1254. https://doi.org/10.1002/ps.3286
Baerson SR, Rodriguez DJ, Tran M et al (2002) Glyphosate-resistant goosegrass. Identification of a mutation in the target enzyme 5-enolpyruvylshikimate-3-phosphate synthase. Plant Physiol 129(3):1265–1275. https://doi.org/10.1104/pp.001560
Bass C, Field LM (2011) Gene amplification and insecticide resistance. Pest Manag Sci 67(8):886–890. https://doi.org/10.1002/ps.2189
Beckie HJ, Rebound X (2009) Selecting for weed resistance: Herbicide rotation and mixture. Weed Technol 23(3):363–370
Beckie HJ, Harker KN (2017) Our top 10 herbicide-resistant weed management practices. Pest Manag Sci 73:1045–1052. https://doi.org/10.1002/ps.4543
Beckie HJ, Tardif FJ (2012) Herbicide cross resistance in weeds. J Crop Prot 35:15–28. https://doi.org/10.1016/j.cropro.2011.12.018
Bogalin DC, Silveira OR, Gazziero DLP (2016) Amaranthus palmeri: Programa de erradicação da espécie no Estado de Mato Grosso. In: Meschede DK, Gazziero DLP (eds) A era glyphosate: agricultura, meio ambiente e homem. Midiograf, Londrina, pp 321–336
Bracamonte E, Fernández-Moreno PT, Barro F et al (2016) Glyphosate-resistant Parthenium hysterophorus in the Caribbean Islands: non target site resistance and target site resistance in relation to resistance levels. Front Plant Sci 7:1845. https://doi.org/10.3389/fpls.2016.01845
Bracamonte E, Silveira HMD, Alcántara-de la Cruz R et al (2018) From tolerance to resistance: mechanisms governing the differential response to glyphosate in Chloris barbata. Pest Manag Sci 74:1118–1124. https://doi.org/10.1002/ps.4874
Brown HM, Fuesler TP, Ray TB et al (1991) Role of plant metabolism in crop selectivity of herbicides. In: Frehse H (ed) Pesticide chemistry: advances in international research, development and legislation. Wiley-VCH, Reinheim, pp 257–266
Brunharo CACG, Takano HK, Mallory-Smith CA et al (2019) Role of Glutamine synthetase isogenes and herbicide metabolism in the mechanism of resistance to glufosinate in Lolium perenne L. spp. multiflorum biotypes from Oregon. J Agric Food Chem 67:8431–8440. https://doi.org/10.1021/acs.jafc.9b01392
Burgos NR, Tranel PJ, Streibig JC et al (2013) Confirmation of resistance to herbicides and evaluation of resistance levels. Weed Sci 61(1):4–20. https://doi.org/10.1614/WS-D-12-00032.1
Burnet MWM, Holtum JAM, Powles SB (1994) Resistance to nine herbicide classes in a Lolium rigidum biotype. Weed Sci 42:369–377
Busi R, Powles SB (2013) Cross-resistance to prosulfocarb and triallate in pyroxasulfone-resistant Lolium rigidum. Pest Manag Sci 69(12):1379–1384
Carvalho LB, Alves PLDCA, Gonzalez-Torralva F et al (2012) Pool of resistance mechanisms to glyphosate in Digitaria insularis. J Agric Food Chem 60(2):615–622. https://doi.org/10.1021/jf204089d
Casale FA, Giacomini DA, Tranel PJ (2019) Empirical investigation of mutation rate for herbicide resistance. Weed Sci 67(4):361–368. https://doi.org/10.1017/wsc.2019.19
Caverzan A, Piasecki C, Chavarria G et al (2019) Defenses against ROS in crops and weeds: the effects of interference and herbicides. Int J Mol Sci 20(5):1086. https://doi.org/10.3390/ijms20051086
Christoffoleti PJ, Nicolai M (2016) Aspectos de resistência de plantas daninhas à herbicidas, 4th edn. Associação Brasileira de Ação à Resistência de Plantas Daninhas ao Herbicidas (HRAC-BR), Piracicaba
Christoffoleti PJ, Victoria Filho R, Silva CB (1994) Resistência de plantas daninhas à herbicidas. Planta Daninha 12(1):13–20
Christoffoleti PJ, Westra P, Moore F III (1997) Growth analysis of sulfonylurea-resistant and-susceptible kochia (Kochia scoparia). Weed Sci 45(5):691–695
Christoffoleti PJ, Carvalho SJP, Nicolai M et al (2007) Prevention strategies in weed management. In: Upadhyaya MK, Blackshaw RE (eds) Non-chemical weed management: principles, concepts and technology. CABI, Oxfordshire, pp 1–16
Christoffoleti PJ, Nicolai M, López-Ovejero RF et al (2016) Resistência de plantas daninhas à herbicidas: termos e definições importantes. In: Christoffoleti PJ, Nicolai M (eds) Aspectos de Resistência de Plantas Daninhas à herbicidas, 4th edn. Associação Brasileira de Ação à Resistência de Plantas Daninhas ao Herbicidas (HRAC-BR), Piracicaba, pp 11–31
Christopher JT, Powles SB, Liljegren DR et al (1991) Cross resistance to herbicides in annual ryegrass (Lolium rigidum) chlorsulfuron resistance involves a wheat-like detoxification system. Plant Physiol 94(4):1036–1043
Collavo A, Sattin M (2014) First glyphosate-resistant Lolium spp. biotypes found in European annual arable cropping system also affected by ACCase and ALS resistance. Weed Sci 54:325–334. https://doi.org/10.1111/wre.12082
Comont D, Knight C, Crook L et al (2019) Alterations in life-history associated with non-target-site herbicide resistance in Alopecurus myosuroides. Front Plant Sci 10:837. https://doi.org/10.3389/fpls.2019.00837
Constantin J, Oliveira Junior RS, Oliveira Neto AM (2013) Buva: Fundamentos e recomendações para manejo, 1st edn. Omnipax, Curitiba
Cummins I, Wortley DJ, Sabbadin F et al (2013) Key role for a glutathione transferase in multiple-herbicide resistance in grass weeds. Proc Natl Acad Sci 110(15):5812–5817. https://doi.org/10.1073/pnas.1221179110
D’Avignon DA, Ge X (2018) In vivo NMR investigations of glyphosate influences on plant metabolism. J Magn Reson 292:59–72. https://doi.org/10.1016/j.jmr.2018.03.008
Dayan FE, Owens DK, Corniani N et al (2015) Biochemical markers and enzyme assays for herbicide mode of action and resistance studies. Weed Sci 63:23–63. https://doi.org/10.1614/WS-D-13-00063.1
De Prado JL, Osuna MD, Heredia A, De Prado R (2005) Lolium rigidum, a pool of resistance mechanisms to ACCase inhibitor herbicides. J Agric Food Chem 53(6):2185–2191. https://doi.org/10.1021/jf049481m
Délye C (2013) Unravelling the genetic bases of non-target-site-based resistance (NTSR) to herbicides: a major challenge for weed science in the forthcoming decade. Pest Manag Sci 69(2):176–187. https://doi.org/10.1002/ps.3318
Délye C, Matéjicek A, Michel S (2008) Cross-resistance patterns to ACCase-inhibiting herbicides conferred by mutant ACCase isoforms in Alopecurus myosuroides Huds. (black-grass) re-examined at the recommended herbicide field rate. Pest Manag Sci 64(11):1179–1186. https://doi.org/10.1002/ps.1614
Délye C, Deulvot C, Chauvel B (2013a) DNA analysis of herbarium specimens of the grass weed Alopecurus myosuroides reveals herbicide resistance pre-dated herbicides. PLoS One 8:75117. https://doi.org/10.1371/journal.pone.0075117
Délye C, Jasieniuk M, Le Corre V (2013b) Deciphering the evolution of herbicide resistance in weeds. Trends Genet 29(11):649–658. https://doi.org/10.1016/j.tig.2013.06.001
Délye C, Duhoux A, Pernin F et al (2015) Molecular mechanisms of herbicide resistance. Weed Sci 63:91–115. https://doi.org/10.1614/WS-D-13-00096.1
Dimaano NG, Yamaguchi T, Fukunishi K et al (2020) Functional characterization of cytochrome P450 CYP81A subfamily to disclose the pattern of cross-resistance in Echinochloa phyllopogon. Plant Mol Biol 102:403–416. https://doi.org/10.1007/s11103-019-00954-3
Duke SO (2011) Glyphosate degradation in glyphosate-resistant and -susceptible crops and weeds. J Agric Food Chem 59(11):5835–5841
Duke SO (2019) Enhanced metabolic degradation: the last evolved glyphosate resistance mechanism of weeds? Plant Physiol 181(4):1401–1403. https://doi.org/10.1104/pp.19.01245
Elstner EF, Wagner GA, Schutz W (1988) Activated oxygen in green plants in relation to stress situations. Pestic Biochem Physiol 7:159–187
Ferreira EA, Santos JB, Silva AA et al (2006) Translocação do glyphosate em biótipos de azevém (Lolium multiflorum). Planta Daninha 24(2):365–370. https://doi.org/10.1590/S0100-83582006000200021
Ferreira EA, Galon L, Aspiazú I et al (2008) Glyphosate translocation in hairy fleabane (Conyza bonariensis) biotypes. Planta Daninha 26(3):637–643. https://doi.org/10.1590/S0100-83582008000300020
Ferreira EA, Germani C, Vargas L et al (2009) Resistência de Lolium multiflorum ao Glyphosate. In: Agostinetto D, Vargas L (eds) Resistência de plantas daninhas no Brasil. Gráfica Berthier, Passo Fundo, pp 271–289
Figueiredo MRA, Leibhart LJ, Reicher ZJ et al (2018) Metabolism of 2,4-dichlorophenoxyacetic acid contributes to resistance in a common waterhemp (Amaranthus tuberculatus) population. Pest Manag Sci 74(10):2356–2362. https://doi.org/10.1002/ps.4811
Funke T, Yang Y, Han H et al (2009) Structural basis of glyphosate resistance resulting from the double mutation Thr(97) → Ile and Pro(101) → Ser in 5-enolpyruvylshikimate-3-phosphate synthase from Escherichia coli. J Biol Chem 284:9854–9860. https://doi.org/10.1074/jbc.M809771200
Gaines TA, Zhang W, Wang D et al (2010) Gene amplification confers glyphosate resistance in Amaranthus palmeri. Proc Natl Acad Sci U S A 107(3):1029–1034. https://doi.org/10.1073/pnas.0906649107
Gaines TA, Patterson EL, Neve P (2019) Molecular mechanisms of adaptive evolution revealed by global selection for glyphosate resistance. New Phytol 223(4):1770–1775. https://doi.org/10.1111/nph.15858
Gaines TA, Duke SO, Morran S et al (2020) Mechanisms of evolved herbicide resistance. J Biol Chem 295:10307–10330. https://doi.org/10.1074/jbc.REV120.013572
García MJ, Palma-Bautista C, Vazquez-Garcia JG et al (2020) Multiple mutations in the EPSPS and ALS genes of Amaranthus hybridus underlie resistance to glyphosate and ALS inhibitors. Sci Rep 10:17681. https://doi.org/10.1038/s41598-020-74430-0
Gazziero DL, Silva AF (2017) Characterization and management of Amaranthus palmeri. Embrapa Soja, Londrina
Ge X, D’Avignon DA, Ackerman J (2011) Rapid vacuolar sequestration: the horseweed glyphosate resistance mechanism. Pest Manag Sci 66:345–348. https://doi.org/10.1002/ps.1911
Ge X, D’Avignon DA, Ackerman JJ et al (2012) Vacuolar glyphosate-sequestration correlates with glyphosate resistance in ryegrass (Lolium spp.) from Australia, South America, and Europe: a 31P NMR investigation. J Agric Food Chem 60:12432–12450. https://doi.org/10.1021/jf203472s
Ghanizadeh H, Harrington KC (2017) Non-target site mechanisms of resistance to herbicides. Crit Rev Plant Sci 36:24–34. https://doi.org/10.1080/07352689.2017.1316134
Ghanizadeh H, Harrington KC (2020) Perspective: root exudation of herbicides as a novel mode of herbicide resistance in weeds. Pest Manag Sci 76(8):2543–2547. https://doi.org/10.1002/ps.5850
Goggin DE, Cawthray GR, Powles SB (2016) 2,4-D resistance in wild radish: reduced herbicide translocation via inhibition of cellular transport. J Exp Bot 67(11):3223–3235. https://doi.org/10.1093/jxb/erw120
Gronwald JW (1994) Resistance to photosystem II inhibiting herbicides. In: Powles SB, Holtum JAM (eds) Herbicide resistance in plants: biology and biochemistry. Lewis Publishers, Boca Raton, FL, pp 83–139
Guo F, Iwakami S, Yamaguchi T et al (2019) Role of CYP81A cytochrome P450s in clomazone metabolism in Echinochloa phyllopogon. Plant Sci 283:321–328. https://doi.org/10.1016/j.plantsci.2019.02.010
Guttieri MJ, Eberlein CV, Mallory-Smith CA et al (1992) DNA sequence variation in domain A of the acetolactate synthase genes of herbicide-resistant and -susceptible weed biotypes. Weed Sci 40:670–677
Han H, Yu Q, Purba E et al (2012) A novel amino acid substitution Ala-122-Tyr in ALS confers high-level and broad resistance across ALS-inhibiting herbicides. Pest Manag Sci 68(8):1164–1170. https://doi.org/10.1002/ps.3278
Hawkes TR (2014) Mechanisms of resistance to paraquat in plants. Pest Manag Sci 70(9):1316–1323. https://doi.org/10.1002/ps.3699
Healy-Fried ML, Funke T, Priestman MA et al (2007) Structural basis of glyphosate tolerance resulting from mutations of Pro101 in 5-enolpyruvylshikimate-3-phosphate synthase. J Biol Chem 282:32949–32955. https://doi.org/10.1074/jbc.M705624200
Heap IA (2014) Global perspective of herbicide-resistant weeds. Pest Manag Sci 70:1306–1315. https://doi.org/10.1002/ps.3696
Heap IA (2021) The international survey of herbicide resistant weeds. http://www.weedscience.org/Pages/filter.aspx. Accessed 27 Mar 2021
Herbicide Resistance Action Committee HRAC (2021a) Guideline to the management of herbicide resistance. http://ipmwww.ncsu.edu/orgs/hrac/guideline.html. Accessed 27 Mar 2021
Herbicide Resistance Action Committee HRAC (2021b) How to minimize resistance risks and how to respond to cases of suspected and confirmed resistance. http://ipmwww.ncsu.edu/orgs/hrac/hoetomil.html. Accessed 27 Mar 2021
Hirschberg J, Mcintosh L (1983) Molecular basis of herbicide resistance in Amaranthus hybridus. Science 222(4630):1346–1349
Ikeda FS, Avalieri S, Lima Junior FDM et al (2019) Estratégias de controle de Amaranthus palmeri resistente à herbicidas inibidores de EPSPS e ALS. Embrapa Agrossilvipastoril, Brasília
Jablonkai I (2015) Herbicide metabolism in weeds - selectivity and herbicide resistance. In: Price A, Kelton J, Sarunaite L (eds) Herbicides, physiology of action and safety. IntechOpen, London, pp 1609–2600
Jha P, Norsworthy JK, Riley MB, Bridges W (2010) Annual changes in temperature and light requirements for germination of palmer amaranth (Amaranthus palmeri) seeds retrieved from soil. Weed Sci 58(4):426–432. https://doi.org/10.1614/WS-D-09-00038.1
Jugulam M, Shyam C (2019) Non-target-site resistance to herbicides: recent developments. Plants 8(10):417. https://doi.org/10.3390/plants8100417
Jugulam M, DiMeo N, Veldhuis LJ et al (2013) Investigation of MCPA (4-chloro-2-ethylphenoxyacetate) resistance in wild radish (Raphanus raphanistrum L.). J Agric Food Chem 61:12516–12521. https://doi.org/10.1021/jf404095h
Kaundun SS, Hutchings SJ, Dale RP et al (2017) Mechanism of resistance to mesotrione in an Amaranthus tuberculatus population from Nebraska, USA. PLoS One 12(6):e0180095
Keith BK, Burns EE, Bothner B et al (2017) Intensive herbicide use has selected for constitutively elevated levels of stress-responsive mRNAs and proteins in multiple herbicide-resistant Avena fatua L. Pest Manag Sci 73(11):2267–2281. https://doi.org/10.1002/ps.4605
Kissmann KG (1996) Resistência de plantas à herbicidas. Basf Brasileira S.A, São Paulo
Krieger-Liszkay A (2005) Singlet oxygen production in photosynthesis. J Exp Bot 56(411):337–346. https://doi.org/10.1093/jxb/erh237
Kudsk P (2014) Reduced herbicide rates: present and future. Julius-Kühn-Archiv 443:37–44. https://doi.org/10.5073/jka.2014.443.003
Laforest M, Soufiane B, Simard MJ et al (2017) Acetyl-CoA carboxylase overexpression in herbicide resistant large crabgrass (Digitaria sanguinalis). Pest Manag Sci 73(11):2227–2235. https://doi.org/10.1002/ps.4675
Lamichhane JR, Devos Y, Beckie HJ et al (2017) Integrated weed management systems with herbicide-tolerant crops in the European Union: lessons learnt from home and abroad. Crit Rev Biotechnol 37:459–475. https://doi.org/10.1080/07388551.2016.1180588
Larran AS, Lorenzetti F, Tuesca D et al (2018) Molecular mechanisms endowing cross-resistance to ALS-inhibiting herbicides in Amaranthus hybridus from Argentina. Plant Mol Biol Rep 36:907–912. https://doi.org/10.1007/s11105-018-1122-y
Le Clere S, Wu C, Westra P, Sammons RD (2018) Cross-resistance to dicamba, 2,4-D, and fluroxypyr in Kochia scoparia is endowed by a mutation in an AUX/IAA gene. Proc Natl Acad Sci 115:2911–2920. https://doi.org/10.1073/pnas.1712372115
Li J, Li M, Gao X, Fang F (2017) A novel amino acid substitution Trp574Arg in acetolactate synthase (ALS) confers broad resistance to ALS-inhibiting herbicides in crabgrass (Digitaria sanguinalis). Pest Manag Sci 73:2538–2543. https://doi.org/10.1002/ps.4651
Livingston M, Fernandez-cornejo J, Frisvold GB (2016) Economic returns to herbicide resistance management in the short and long run: the role of neighbor effects. Weed Sci 64:595–608
Long W, Malone J, Boutsalis P, Preston C (2019) Diversity and extent of mutations endowing resistance to the acetolactate synthase (AHAS)-inhibiting herbicides in Indian hedge mustard (Sisymbrium orientale) populations in Australia. Pestic Biochem Physiol 157:53–59. https://doi.org/10.1016/j.pestbp.2019.03.004
Lorentz L, Gaines TA, Nissen SJ et al (2014) Characterization of glyphosate resistance in Amaranthus tuberculatus populations. J Agric Food Chem 62(32):8134–8142. https://doi.org/10.1021/jf501040x
Mao C, Xie H, Chen S et al (2016) Multiple mechanism confers natural tolerance of three lilyturf species to glyphosate. Planta 243:321–335. https://doi.org/10.1007/s00425-015-
Markus C, Barroso AAM, Dalazen G et al (2021) Resistência de plantas daninhas aos herbicidas. In: Barroso AAM, Murata AT (eds) Matologia: Estudos sobre plantas daninhas. Editora Fábrica da Palavra, Jaboticabal, pp 324–364
Marochi A, Ferreira A, Takano HK et al (2018) Managing glyphosate-resistant weeds with cover crop associated with herbicide rotation and mixture. Cienc Agrotec 42(4):381–394. https://doi.org/10.1590/1413-70542018424017918
Maroli AS, Nandula VK, Dayan FE et al (2015) Metabolic profiling and enzyme analyses indicate a potential role of antioxidant systems in complementing glyphosate resistance in an Amaranthus palmeri biotype. J Agric Food Chem 63(41):9199–9209. https://doi.org/10.1021/acs.jafc.5b04223
Martins JF, Barroso AAM, Carvalho LB et al (2016) Plant growth and genetic polymorphism in glyphosate-resistant sourgrass (Digitaria insularis L. Fedde). Aust. J Crop Sci 10(10):e1466. https://doi.org/10.21475/ajcs.2016.10.10.p7761
Maxwell BD, Mortimer AM (1994) Selection for resistance herbicide. In: Powles SB, Holtum JAM (eds) Herbicide resistance in plants: biology and biochemistry. Lewis Publishers, Boca Raton, FL, pp 1–25
Mcelroy JS, Hall ND (2020) Echinochloa colona with reported resistance to glyphosate conferred by aldo-keto reductase also contains a Pro-106-Thr EPSPS target site mutation. Plant Physiol 183(2):447–450. https://doi.org/10.1104/pp.20.00064
Mendes KF (2020) Plantas daninhas resistentes ao glyphosate no Brasil: biologia, mecanismo de resistência e manejo, 1st edn. Brazil Publishing, Curitiba
Mendes KF, Silveira RF, Inoue MH, Tornisielo VL (2017) Procedures for detection of resistant weeds using 14C-herbicide absorption, translocation, and metabolism. In: Pacanoski Z (ed) Herbicide resistance in weeds and crops. IntechOpen, London, pp 161–176
Mendes RR, Takano HK, Oliveira RS et al (2020a) A Trp574Leu target site mutation confers imazamox-resistance in multiple-resistant wild poinsettia populations from Brazil. Agronomy 10:1057
Mendes RR, Takano HK, Leal JF et al (2020b) Evolution of EPSPS double mutation imparting glyphosate resistance in wild poinsettia (Euphorbia heterophylla L.). PLoS One 15:e0238818. https://doi.org/10.1371/journal.pone.0238818
Mendes RR, Takano HK, Adegas FS et al (2020c) Target site mutation in PPO2 evolves in wild poinsettia (Euphorbia heterophylla) with cross-resistance to PPO-inhibiting herbicides. Weed Sci 68:437–444
Merotto Júnior A, Goulart IC, Nunes AL et al (2016) Evolutionary and social consequences of introgression of non-transgenic herbicide resistance from rice to weedy rice in Brazil. Evol Appl 9(7):837–846. https://doi.org/10.1111/eva.12387
Michel A, Arias RS, Scheffler BE et al (2004) Somatic mutation-mediated evolution of herbicide resistance in the nonindigenous invasive plant hydrilla (Hydrilla verticillata). Mol Ecol 13(10):3229–3237. https://doi.org/10.1111/j.1365-294X.2004.02280.x
Michitte P, De Prado R, Espinoza N et al (2007) Mechanisms of resistance to glyphosate in a ryegrass (Lolium multiflorum) biotype from Chile. Weed Sci 55(5):435–440. https://doi.org/10.1614/WS-06-167.1
Monquero PA, Christoffoleti PJ (2001) Manejo de populações de plantas daninhas resistentes à herbicidas inibidores da acetolactato sintase. Planta Daninha 19(1):67–74
Monquero PA, Christoffoleti PJ, Dias CTS (2000) Weed resistance to ALS-inhibiting herbicides in soybean (Glycine max) crop. Planta Daninha 8(3):419–425
Moretti ML, Van Horn CR, Robertson R et al (2017a) Glyphosate resistance in Ambrosia trifida. Part 2. Rapid response physiology and non-target-site resistance. Pest Manag Sci 74:1079–1088. https://doi.org/10.1002/ps.4569
Moretti ML, Alárcon-Reverte R, Pearce S et al (2017b) Transcription of putative tonoplast transporters in response to glyphosate and paraquat stress in Conyza bonariensis and Conyza canadensis and selection of reference genes for qRT-PCR. PLoS One 12(7):e0180794. https://doi.org/10.1371/journal.pone.0180794
Mortensen DA, Egan JF, Maxwell BD et al (2012) Navigating a critical juncture for sustainable weed management. Biosci J 62(1):75–84. https://doi.org/10.1525/bio.2012.62.1.12
Mortimer AM (1998) Review of graminicide resistance. http://ipmwww.ncsu.edu/orgs/hrac/monograph1.htm. Accessed 27 Mar 2021
Moss S (2017) Herbicide resistance weeds. In: Hatcher PE, Froud-Williams RJ (eds) Weed research: expanding horizons, 1st edn. John Wiley & Sons Ltd., London, pp 181–214
Moss S (2019) Integrated Weed Management (IWM): why are farmers reluctant to adopt non-chemical alternatives to herbicides? Pest Manag Sci 75:1205–1211. https://doi.org/10.1002/ps.5267
Murphy BP, Tranel PJ (2019) Target-site mutations conferring herbicide resistance. Plants 8(10):382. https://doi.org/10.3390/plants8100382
Nakka S, Godar AS, Wani PS et al (2017) Physiological and molecular characterization of hydroxyphenylpyruvate dioxygenase (HPPD)-inhibitor resistance in Palmer amaranth (Amaranthus palmeri S. Wats.). Front Plant Sci 8:555. https://doi.org/10.3389/fpls.2017.00555
Nandula VK, Ray JD, Ribeiro DN et al (2013) Glyphosate resistance in tall waterhemp (Amaranthus tuberculatus) from Mississippi is due to both altered target-site and nontarget-site mechanisms. Weed Sci 61(3):374–383. https://doi.org/10.1614/WS-D-12-00155.1
Nandula VK, Wright AA, Bond JA et al (2014) EPSPS amplification in glyphosate-resistant spiny amaranth (Amaranthus spinosus): a case of gene transfer via interspecific hybridization from glyphosate-resistant Palmer amaranth (Amaranthus palmeri). Pest Manag Sci 70(12):1902–1909. https://doi.org/10.1002/ps.3754
Nandula VK, Riechers DE, Ferhatoglu Y et al (2019) Herbicide metabolism: crop selectivity, bioactivation, weed resistance, and regulation. Weed Sci 67(2):149–175. https://doi.org/10.1017/wsc.2018.88
Ngo TD, Malone JM, Boutsalis P et al (2018) EPSPS gene amplification conferring resistance to glyphosate in windmill grass (Chloris truncata) in Australia. Pest Manag Sci 7(4):1101–1108. https://doi.org/10.1002/ps.4573
Norsworthy JK, Ward SM, Shaw DR et al (2012) Reducing the risks of herbicide resistance: best management practices and recommendations. Weed Sci 60(1):31–62. https://doi.org/10.1614/WS-D-11-00155.1
Oliveira MF, Brighenti AM (2018) Controle de Plantas Daninhas: Métodos físico, mecânico, cultural, biológico e alelopatia. Embrapa Milho e Sorgo, Sete Lagoas
Oliveira MC, Gaines TA, Dayan FE et al (2018) Reversing resistance to tembotrione in an Amaranthus tuberculatus (var. rudis) population from Nebraska, USA with cytochrome P450 inhibitors. Pest Manag Sci 74(10):2296–2305. https://doi.org/10.1002/ps.4697
Ovejero RFL, Takano HK, Nicolai M et al (2017) Frequency and dispersal of glyphosate-resistant sourgrass (Digitaria insularis) populations across Brazilian agricultural production areas. Weed Sci 65(2):285–294. https://doi.org/10.1017/wsc.2016.31
Palma-Bautista C, Rojano-Delgado AM, Vázquez-García JG et al (2020) Resistance to fomesafen, imazamox and glyphosate in Euphorbia heterophylla from Brazil. Agronomy 10:1573. https://doi.org/10.3390/agronomy10101573
Pan L, Yu Q, Han H et al (2019) Aldo-keto reductase metabolizes glyphosate and confers glyphosate resistance in Echinochloa colona. Plant Physiol 181(4):1519–1534. https://doi.org/10.1104/pp.19.00979
Pan L, Yu Q, Wang J et al (2021) An ABCC-type transporter endowing glyphosate resistance in plants. Proc Natl Acad Sci 118(16):e2100136118. https://doi.org/10.1073/pnas.2100136118
Pandhair V, Sekhon BS (2006) Reactive oxygen species and antioxidants in plants: an overview. J Plant Biochem Biotechnol 15(2):71–78. https://doi.org/10.1007/BF03321907
Patzoldt WL, Hager AG, McCormick JS et al (2006) A codon deletion confers resistance to herbicides inhibiting protoporphyrinogen oxidase. Proc Natl Acad Sci 103(33):12329–12334. https://doi.org/10.1073/pnas.0603137103
Perotti VE, Larran AS, Palmieri VE et al (2019) A novel triple amino acid substitution in the EPSPS found in a high-level glyphosate-resistant Amaranthus hybridus population from Argentina. Pest Manag Sci 75(5):1242–1251. https://doi.org/10.1002/ps.5303
Peterson MA, Collavo A, Ovejero R et al (2018) The challenge of herbicide resistance around the world: a current summary. Pest Manag Sci 74:2246–2259. https://doi.org/10.1002/ps.4821
Petter FA, Sulzbacher AM, Silva AF et al (2015) Use of cover crops as a tool in the management strategy of sourgrass. Rev Bras Herbicid 14(3):200–209
Pinho CF, Leal JFL, Santos SA et al (2019) First evidence of multiple resistance of Sumatran Fleabane (Conyza sumatrensis (Retz.) E. Walker) to five- mode-of-action herbicides. Aust J Crop Sci 13:1688–1697. https://doi.org/10.21475/ajcs.19.13.10.p1981
Powles SB, Preston C (2021) Herbicide cross resistance and multiple resistance in plants. http://ipmwww.ncsu.edu/orgs/hrac/mono2.htm. Accessed 27 Mar 2021
Powles SB, Yu K (2010) Evolution in action: plants resistant to herbicides. Annu Rev Plant Biol 61:317–347. https://doi.org/10.1146/annurev-arplant-042809-112119
Preston C, Mallory-Smith CA (2001) Biochemical mechanisms, inheritance, and molecular genetics of herbicide resistance in weeds. In: Powles SB, Shaner DL (eds) Herbicide resistance and world grains. CRC Press, New York, NY, pp 23–60
Preston C, Tardif FJ, Christopher JT, Powles SB (1996) Multiple resistance to dissimilar herbicide chemistries in a biotype of Lolium rigidum due to enhanced activity of several herbicide degrading enzymes. Pestic Biochem Physiol 54(2):123–134
Proskuryakov SY, Konoplyannikov AG, Gabai VL (2003) Necrosis: a specific form of programmed cell death? Exp Cell Res 283:1–16
Qasem JR (2013) Herbicide resistant weeds: the technology and weed management. In: Price A, Kelton J (eds) Herbicides-current research and case studies in use. IntechOpen, London, pp 445–471
Queiroz ARS, Delatorre CA, Lucio FR et al (2019) Rapid necrosis: a novel plant resistance mechanism to 2,4-D. Weed Sci 68(1):6–18. https://doi.org/10.1017/wsc.2019.65
Riar DS, Tehranchian P, Norsworthy JK et al (2015) Acetolactate synthase-inhibiting, herbicide-resistant rice flatsedge (Cyperus iria): cross-resistance and molecular mechanism of resistance. Weed Sci 63(4):748–757. https://doi.org/10.1614/WS-D-15-00014.1
Rojano-Delgado AM, Portugal JM, Palma-Bautista C et al (2019) Target site as the main mechanism of resistance to imazamox in a Euphorbia heterophylla biotype. Sci Rep 9:e15423. https://doi.org/10.1038/s41598-019-51682-z
Salas RA, Dayan FE, Pan Z et al (2012) EPSPS gene amplification in glyphosate-resistant Italian ryegrass (Lolium perenne ssp. multiflorum) from Arkansas. Pest Manag Sci 68(9):1223–1230. https://doi.org/10.1002/ps.3342
Sammons RD, Gaines TA (2014) Glyphosate resistance: state of knowledge. Pest Manag Sci 70(9):1367–1377. https://doi.org/10.1002/ps.3743
Scarabel L, Panozzo S, Loddo D et al (2020) Diversified resistance mechanisms in multi-resistant Lolium spp. in three European countries. Front Plant Sci 11:608845. https://doi.org/10.3389/fpls.2020.608845
Scherner A, Schreiber F, Andres A et al (2018) Rice crop rotation: a solution for weed management. In: Shah F, Khan ZH, Iqbal A (eds) Rice crop current developments. IntechOpen, London, pp 25–44
Silva AA, Vargas LL, Ferreira EA (2007) Herbicidas: Resistência de Plantas. In: Silva AA, Silva JF (eds) Tópicos em manejo de plantas daninhas. Editora UFV, Viçosa, pp 280–324
Svyantek A, Aldahir P, Chen S et al (2016) Target and nontarget resistance mechanisms induce annual bluegrass (Poa annua) resistance to atrazine, amicarbazone, and diuron. Weed Technol 30:773–782. https://doi.org/10.1614/WT-D-15-00173.1
Takano HK, Oliveira Júnior RS, Constantin J et al (2018) Spread of glyphosate-resistant sourgrass (Digitaria insularis): independent selections or merely propagule dissemination? Weed Biol Manag 18:50–59. https://doi.org/10.1111/wbm.12143
Torra J, Rojano-Delgado AM, Rey-Caballero J et al (2017) Enhanced 2,4-D metabolism in two resistant Papaver rhoeas populations from Spain. Front Plant Sci 8:1584. https://doi.org/10.3389/fpls.2017.01584
Tranel PJ (2017) Herbicide-resistance mechanisms: gene amplification is not just for glyphosate. Pest Manag Sci 73(11):2225–2226. https://doi.org/10.1002/ps.4679
Tranel PJ, Wright TR, Heap IM (2021) Mutations in herbicide-resistant weeds for herbicide inhibitors ALS. http://www.weedscience.com. Accessed 27 Mar 2021
Trezzi MM, Felippi CL, Mattei D et al (2005) Multiple resistance of acetolactate synthase and protoporphyrinogen oxidase inhibitors in Euphorbia heterophylla biotypes. J Environ Sci Health B 40(1):101–109. https://doi.org/10.1081/pfc-200034254
Trezzi MM, Vidal RA, Kruse ND et al (2009) Fomesafen absorption site as a mechanism of resistance in an Euphorbia heterophylla biotype resistant to PROTOX inhibitors. Planta Daninha 27(1):139–148. https://doi.org/10.1590/S0100-83582009000100018
Trezzi MM, Vidal RA, Kruse ND et al (2011) Eletrolite leakage as a technique to diagnose Euphorbia heterophylla biotypes resistant to PPO-inhibitors herbicides. Planta Daninha 29(3):655–662. https://doi.org/10.1590/S0100-83582011000300020
Vargas L, Silva AA, Borém A et al (1999) Resistência de plantas daninhas à herbicidas. JARD Prod. Gráficas, Viçosa
Vázquez-García JG, Alcántara-de la Cruz R, Palma-Bautista C et al (2020) Accumulation of target gene mutations confers multiple resistance to ALS, ACCase, and EPSPS inhibitors in Lolium species in Chile. Front Plant Sci 11:553948. https://doi.org/10.3389/fpls.2020.553948
Vencill WK, Nichols RL, Webster TM et al (2012) Herbicide resistance: toward an understanding of resistance development and the impact of herbicide-resistant crops. Weed Sci 60:2–30. https://doi.org/10.1614/WS-D-11-00206.1
Vidal RA, Fleck NG (1997) The risk of finding herbicide resistant weed biotypes. Planta Daninha 15(2):152–161. https://doi.org/10.1590/S0100-83581997000200008
Vila-Aiub MM (2019) Fitness of herbicide-resistant weeds: current knowledge and implications for management. Plants 8(11):469. https://doi.org/10.3390/plants8110469
Vila-Aiub MM, Balbi MC, Distéfano AJ et al (2012) Glyphosate resistance in perennial Sorghum halepense (Johnsongrass), endowed by reduced glyphosate translocation and leaf uptake. Pest Manag Sci 68(3):430–436. https://doi.org/10.1002/ps.2286
Vila-Aiub MM, Yu Q, Powles SB (2019) Do plants pay a fitness cost to be resistant to glyphosate? New Phytol 223(2):532–547. https://doi.org/10.1111/nph.15733
Vrbničanin S, Pavlović D, Božić D (2017) Weed resistance to herbicides. In: Pacanoski Z (ed) Herbicide resistance in weeds and crops. IntechOpen, London, pp 7–35
Wang H, Zhang L, Li W et al (2019) Isolation and expression of acetolactate synthase genes that have a rare mutation in shepherd’s purse (Capsella bursa-pastoris (L.) Medik.). Pestic Biochem Physiol 155:119–125. https://doi.org/10.1016/j.pestbp.2019.01.013
Webster TM, Scully BT, Grey TL, Culpepper AS (2013) Winter cover crops influence Amaranthus palmeri establishment. Crop Prot 52:130–135. https://doi.org/10.1016/j.cropro.2013.05.015
Weed Science Society of America (1998) Herbicide resistance and herbicide tolerance definitions. Weed Technol 12(4):789
White AD, Owen MD, Hartzler RG et al (2002) Common sunflower resistance to acetolactate synthase-inhibiting herbicides. Weed Sci 50:432–437. https://doi.org/10.1614/0043-1745(2002)050[0432:CSRTAS]2.0.CO;2
WSSA – Weed Science Society of America (1998) “Herbicide resistance” and “herbicide tolerance” defined. Weed Technol 12:789
Xu Y, Xu L, Shen J et al (2021) Effects of a novel combination of two mutated acetolactate synthase (ALS) isozymes on resistance to ALS-inhibiting herbicides in flixweed (Descurainia sophia). Weed Sci 69:430–438. https://doi.org/10.1017/wsc.2021.26
Yanniccari M, Gigón R, Larsen A (2020) Cytochrome P450 herbicide metabolism as the main mechanism of cross-resistance to ACCase- and ALS-inhibitors in Lolium spp. populations from Argentina: a molecular approach in characterization and detection. Front Plant Sci 11:600301. https://doi.org/10.3389/fpls.2020.600301
Yu Q, Powles SB (2014) Metabolism-based herbicide resistance and cross-resistance in crop weeds: a threat to herbicide sustainability and global crop production. Plant Physiol 166(3):1106–1118. https://doi.org/10.1104/pp.114.242750
Yu Q, Han H, Cawthray GR et al (2013) Enhanced rates of herbicide metabolism in low herbicide-dose selected resistant Lolium rigidum. Plant Cell Environ 36:818–827. https://doi.org/10.1111/pce.12017
Yuan JS, Tranel PJ, Stewart C Jr (2007) Non-target-site herbicide resistance: a family business. Trends Plant Sci 12(1):6–13
Zagnitko O, Jelenska J, Tevzadze G et al (2001) An isoleucine/leucine residue in the carboxyltransferase domain of acetyl-CoA carboxylase is critical for interaction with aryloxyphenoxypropionate and cyclohexanedione inhibitors. Proc Natl Acad Sci 98:6617–6622. https://doi.org/10.1073/pnas.121172798
Zhang C, Li FENG, He TT et al (2015) Investigating the mechanisms of glyphosate resistance in goosegrass (Eleusine indica) population from South China. J Integr Agric 14:909–918. https://doi.org/10.1016/S2095-3119(14)60890-X
Zhao N, Yan Y, Wang H et al (2018) Acetolactate synthase overexpression in mesosulfuron-methyl-resistant shortawn foxtail (Alopecurus aequalis Sobol.): reference gene selection and herbicide target gene expression analysis. J Agric Food Chem 66:9624–9634. https://doi.org/10.1021/acs.jafc.8b03054
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Mendes, K.F., Mielke, K.C., La Cruz, R.Ad., Alberto da Silva, A., Ferreira, E.A., Vargas, L. (2022). Evolution of Weed Resistance to Herbicides. In: Mendes, K.F., Alberto da Silva, A. (eds) Applied Weed and Herbicide Science. Springer, Cham. https://doi.org/10.1007/978-3-031-01938-8_7
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