This review summarizes what is currently known about herbicide resistance in Bromus spp. worldwide. Additional information on the biology and genetics of Bromus spp. is provided to further the understanding of resistance evolution and dispersal of the different species. Cases of herbicide resistance have been confirmed in Bromus catharticus Vahl., Bromus commutatus Schrad. (syn.: Bromus racemosus L.), Bromus diandrus Roth, Bromus japonicus Thunb. (syn.: Bromus arvensis L.), Bromus madritensis L., Bromus rigidus Roth (syn.: Bromus diandrus Roth ssp. diandrus), Bromus rubens L., Bromus secalinus L., Bromus sterilis L., and Bromus tectorum L. in 11 countries. Bromus spp. populations have evolved cross- and multiple resistance to six herbicide sites of action: acetyl-coenzyme A carboxylase, acetolactate synthase, photosystem II, very-long-chain fatty-acid, 5-enolpyruvylshikimate-3-phosphate synthase, and 4-hydroxyphenylpyruvate dioxygenase inhibitors. Resistance mechanisms varied from target-site to non–target site or a combination of both. Bromus spp. are generally highly self-pollinated, but outcrossing can occur at low levels in some species. Bromus spp. have different ploidy levels, ranging from diploid (2n = 2x = 14) to duodecaploid (2n = 12x = 84). Herbicide resistance in Bromus spp. is a global issue, and the spread of herbicide-resistance alleles primarily occurs via seed-mediated gene flow. However, the transfer of herbicide-resistance alleles via pollen-mediated gene flow is possible.

Italian ryegrass [Lolium perenne L. spp. multiflorum (Lam.) Husnot] is one of the most troublesome weeds worldwide. Lolium multiflorum is also a grass seed crop cultivated on 50,000 ha in Oregon, where both diploid and tetraploid cultivars are grown. For this work, we will refer to the species as L. multiflorum, since the common names annual ryegrass and Italian ryegrass both refer to the same species. A survey was conducted to understand the distribution and frequency of L. multiflorum and its susceptibility to selected herbicides used in its control. The herbicides selected were clethodim, glufosinate, glyphosate, mesosulfuron-methyl (mesosulfuron), paraquat, pinoxaden, pyroxsulam, quizalofop-P-ethyl (quizalofop), pronamide, flufenacet + metribuzin, and pyroxasulfone. The ploidy levels of the populations were also tested. A total of 150 fields were surveyed between 2017 and 2018, of which 75 (50%) had L. multiflorum present. Herbicide-resistant populations were documented in 88% of the 75 populations collected. The most frequent resistances were to acetyl-CoA carboxylase (ACCase), acetolactate synthase (ALS), 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) inhibitors, and combinations thereof. Multiple resistance and cross-resistance, found in 75% of the populations, were the most frequent patterns of resistance. Paraquat-resistant biotypes were confirmed in six orchard crop populations for the first time in Oregon. Herbicide resistance was spatially clustered, with most cases of resistance in the northern part of the surveyed area. Populations resistant to ALS and ACCase inhibitors were prevalent in wheat (Triticum aestivum L.) fields. Multiple resistance was positively correlated with plant density. Tetraploid feral populations were identified, but no cases of herbicide resistance were documented. This is the first survey of herbicide resistance and ploidy diversity in L. multiflorum in western Oregon. Resistant populations were present across the surveyed area, indicating that the problem is widespread.

Cytological understanding is an important parameter to understand the genetic architecture of yam bean. The ploidy level and genome size of two cultivated species of yam bean (Pachyrhizus erosus and P. tuberosus) were estimated using flow cytometric analysis of young leaf tissue, with propidium iodide as a fluorescent dye. Six genotypes of P. erosus and three genotypes of P. tuberosus were analysed. Rice (Oryza sativa cv. Nipponbare) and Mung bean (Vigna radiata cv Berken) were used as internal reference standards. Variation of 2C nuclear DNA content among the six P. erousus lines was 4.18%, ranging from 1.17 to 1.22 pg, whereas only 1.8% variation was observed among the three P. tuberosus lines, which ranged from 1.07 to 1.09 pg. Moreover, it was found that the nuclear DNA content of P. tuberosus was lower than that of P. erosus. The result of the flow cytometric analysis showed that all the species were diploid (2n = 2x) and coefficient of variation (CV%) of all the accessions of the two species was less than 3.5%. This is the first report of ploidy analysis and genome size estimation of the leguminous underutilized tuber crop yam bean using flow cytometry. This result will be helpful for yam bean genome sequencing and crop improvement programmes.