Palmer amaranth is native to the United States, but was discovered in 2015 in Brazil. Palmer amaranth populations in Brazil were very difficult to control using glyphosate, which resulted in many changes to standard weed management practices. A genotyping assay was used to confirm that the population detected in Mato Grosso State, Brazil, was correctly identified as Palmer amaranth and that it was not tall waterhemp. Greenhouse dose—response curves and shikimate accumulation assays showed that the Brazilian population was highly resistant to glyphosate, with an LD50 value (3,982 g glyphosate ha^-1) more than twice the typical use rates and very little shikimate accumulation at 1 mM glyphosate concentrations in a leaf-disk assay. The Brazilian population was also resistant to sulfonylurea and imidazolinone acetolactate synthase (ALS) inhibitor herbicides. The resistance mechanisms in the Brazilian population were identified as increased EPSPS gene copy number for glyphosate resistance (between 50- and 179-fold relative EPSPS gene copy number increase) and two different alleles for target-site mutations in the ALS gene (W574L and S653N). These results confirm the introduction of Palmer amaranth to Brazil using a genetic marker for species identification, as well as resistance to glyphosate and ALS inhibitors.

Nomenclature: Glyphosate; Palmer amaranth, Amaranthus palmeri S. Wats; tall waterhemp, Amaranthus tuberculatus (Moq.) Sauer.

The failure of PRE and POST applications of atrazine to control Palmer amaranth in recent field studies prompted further investigation to determine whether this population had evolved resistance to multiple herbicide sites of action, including glyphosate (Group 9), thifensulfuron (Group 2), and atrazine (Group 5). Greenhouse and laboratory experiments were conducted to: (1) confirm the presence of resistance to glyphosate, an ALS inhibitor (thifensulfuron), and atrazine in a single Palmer amaranth population; and (2) establish the molecular basis for resistance to these herbicide sites of action. In the greenhouse, glyphosate thifensulfuron atrazine at 1.26 kg ae ha^-1 0.0044 kg ai ha^-1 1.12 kg ai ha^-1 provided 55% control of the suspected multiply resistant (MR) Palmer amaranth population and 93% control of the known susceptible population (S). The decreased sensitivity of the MR population compared with the S population at labeled use rates of these herbicides indicated that this population was likely resistant to three different herbicide site of action groups. The RF values for POST applications of glyphosate, thifensulfuron, and atrazine were 12.2, 42.9, and 9.3 times, respectively, for the MR Palmer amaranth population relative to the S population. The RF value for atrazine PRE for the MR population was 112.2 times. Laboratory experiments confirmed that the mechanisms for resistance to ALS-inhibiting herbicides and glyphosate in the MR Palmer amaranth population were target-site based, via amino acid substitution and amplified EPSPS copy number, respectively. There was a Pro to Leu substitution at site 197 in the ALS inhibitor—resistant plants, and there was a greater than 50-fold increase in EPSPS copy number in the glyphosateresistant plants. There were no nucleotide changes in the psbA gene; therefore, atrazine resistance in this population was not target-site mediated. The evolution of this multiple herbicide-resistant Palmer amaranth population poses significant management challenges to Michigan farmers.

Nomenclature: Atrazine; glyphosate; thifensulfuron; Palmer amaranth; Amaranthus palmeri S. Wats.

Palmer amaranth's ability to evolve resistance to different herbicides has been studied extensively, but there is little information about how this weed species might be evolving other life-history traits that could potentially make it more aggressive and difficult to control. We characterized growth and morphological variation among 10 Palmer amaranth populations collected in Florida and Georgia from fields with different cropping histories, ranging from continuous short-statured crops (vegetables and peanut) to tall crops (corn and cotton) and from intensive herbicide use history to organic production. Palmer amaranth populations differed in multiple traits such as fresh and dry weight, days to flowering, plant height, and leaf and canopy shape. Differences between populations for these traits ranged from 36% up to 87%. Although glyphosate-resistant (GR) populations collected from cropping systems including GR crops exhibited higher values of the aforementioned variables than glyphosate-susceptible (GS) populations, variation in traits was not explained by glyphosate resistance or distance between populations. Cropping system components such as crop rotation and crop canopy structure better explained the differences among populations. The higher growth of GR populations compared with GS populations was likely the result of multiple selection forces present in the cropping systems in which they grow rather than a pleiotropic effect of the glyphosate resistance trait. Results suggest that Palmer amaranth can evolve life-history traits increasing its growth and reproduction potential in cropping systems, which explains its rapid spread throughout the United States. Furthermore, our findings highlight the need to consider the evolutionary consequences of crop rotation structure and the use of more competitive crops, which might promote the selection of more aggressive biotypes in weed species with high genetic variability.

Nomenclature: glyphosate; Palmer amaranth, Amaranthus palmeri S. Wats.; corn, Zea mays L.; cotton, Gossypium hirsutum L.; peanut, Arachis hypogaea L.

Italian ryegrass is a major weed problem in wheat production worldwide. Field studies were conducted at Fayetteville, AR, to assess morphological characteristics of ryegrass accessions from Arkansas and differences among other Lolium spp.: Italian, rigid, poison, and perennial ryegrass. Plant height, plant growth habit, plant stem color, and node color were recorded every 2 wk until maturity. The number of tillers per plant, spikes per plant, and seeds per plant were recorded at maturity. All ryegrass accessions from Arkansas were identified as Italian ryegrass, which had erect to prostrate growth habit, green to red stem color, green to red nodes, glume (10 mm) shorter than spikelet (19 mm), and medium seed size (5 to 7 mm) with 1 to 3mm awns. However, significant variability in morphological characteristics was found among Arkansas ryegrass accessions. When Lolium species at the seedling stage (1- to 2-wk-old plants) were compared, poison ryegrass was characterized as having a large main-stem diameter and wide droopy leaves, whereas perennial ryegrass exhibited a short and a very narrow leaf blade. These two can be distinguished from Italian and rigid ryegrass, which have leaf blades wider than perennial ryegrass but narrower than poison ryegrass. Italian and rigid ryegrass are difficult to distinguish at the seedling stage but are distinct at the reproductive stage. At maturity, Italian ryegrass and poison ryegrass seeds are awned, but perennial and rigid ryegrass seeds are awnless. Poison ryegrass awns were at least 4-fold longer than Italian ryegrass awns. Perennial ryegrass flowered 3 wk later than the other species. Poison ryegrass glumes were longer than the spikelets, whereas Italian ryegrass glumes were shorter than the spikelets. Morphological traits indicate that some Italian ryegrass populations are potentially more competitive and more fecund than others.

Nomenclature: Italian ryegrass, Lolium perenne L. ssp. multiflorum (Lam.) Husnot.; perennial ryegrass, Lolium perenne L.; poison ryegrass Lolium temulentum L.; rigid ryegrass, Lolium rigidum Gaudin; wheat, Triticum aestivum L.

Glyphosate-resistant (GR) kochia is an increasing concern for growers across the U.S. Great Plains and Canadian prairies. Integrated strategies to mitigate resistance will require an improved understanding of the seed germination dynamics of GR kochia populations. Experiments were conducted to characterize the germination of GR vs. glyphosate-susceptible (GS) kochia populations under different constant (5 to 35 C) and alternating (5/10 to 30/35 C) temperatures. Seven GR and two GS populations were collected from wheat—fallow fields in northern Montana. Selected lines of GR and GS were obtained after three generations of recurrent group selection in the greenhouse. The GR-selected lines had 4.1 to 10.8 average EPSPS copies compared with a single EPSPS gene copy for the GS selected lines. Four out of seven GR selected lines had lower final germination (d parameter) and took more time to complete 50% cumulative germination (I₅₀ values) under all constant and alternating temperatures, compared with the GS selected lines. Those GR selected lines also had a delayed germination initiation (I₁₀ values), particularly at lower temperatures (5 to 10 C constant or 5/10 C alternating). In contrast, the final germination (d) of the other three GR selected lines did not differ from GS lines at a majority of temperatures tested. The I₅₀ values of those GR lines were also comparable to GS lines under a majority of the temperatures. There was no significant correlation of observed percent cumulative germination and EPSPS gene copy number of selected kochia lines. The temperature-dependent dormancy and altered germination characteristics of the four GR kochia lines reflect the common selection of resistance and avoidance (glyphosate or other preseeding treatments) mechanisms. This is most likely attributed to long-term, intensive cropping practices and less diverse weed control methods, rather than a fitness cost or pleiotropic effect of multiple copies of the EPSPS gene.

Nomenclature: Glyphosate, kochia; Kochia scoparia (L.) Schrad.

Lack of understanding the effects of single- and multiple-weed interference on soybean yield has led to inadequate weed management in Primorsky Krai, resulting in much lower average yield than neighboring regions. A 2 yr field experiment was conducted in a soybean field located in Bogatyrka (43.82°N, 131.6°E), Primorsky Krai, Russia, in 2013 and 2014 to investigate the effects of single and multiple interference caused by naturally established weeds on soybean yield and to model these effects. Aboveground dry weight was negatively affected the most by weed interference, followed by number of pods and seeds. Soybean yield under single-weed interference was best demonstrated by a rectangular hyperbolic model, showing that common ragweed and barnyardgrass were the most competitive weed species, followed by annual sowthistle, American sloughgrass, and common lambsquarters. In the case of multiple-weed interference, soybean yield loss was accurately described by a multivariate rectangular hyperbolic model, with total density equivalent as the independent variable. Parameter estimates indicated that weed-free soybean yields were similar in 2013 and 2014, i.e., estimated as 1.72 t and 1.75 t ha^-1, respectively, and competitiveness of each weed species was not significantly different between the two years. Economic thresholds for single-weed interference were 0.74, 0.66, 1.15, 1.23, and 1.45 plants m^-2 for common ragweed, barnyardgrass, annual sowthistle, American sloughgrass, and common lambsquarters, respectively. The economic threshold for multiple-weed interference was 0.70 density equivalent m^-2. These results, including the model, thus can be applied to a decision support system for weed management in soybean cultivation under single and multiple-weed interference in Primorsky Krai and its neighboring regions of Russia.

Nomenclature: Common ragweed, Ambrosia artemisiifolia L.; barnyardgrass, Echinochloa crus-galli (L.) Beauv.; annual sowthistle, Sonchus oleraceus L.; common lambsquarters, Chenopodium album L.; American sloughgrass, Beckmannia syzigachne (Steud.) Fernald; soybean, Glycine max (L.) Merr.

Sown-grass margin strips, historically established to limit pesticide drift and soil erosion, are now also promoted for enhancing floral diversity and associated ecosystem services. To better understand weed community assembly in grass margin strips, we performed floral surveys in 75 sown-grass margin strips in two regions in France and characterized each species using information from trait databases. We hypothesized that traits of dominant species would differ between newly sown-grass margin strips and older strips. Weed species were separated into functional groups based on their traits using multiple correspondence analysis and hierarchical ascendant classification. Functional group trajectories were investigated in sown-grass margin strips that differed in age using a space-for-time substitution approach. We found that geophyte, competitor, and monocotyledon species were more frequent and abundant in grass margin strips than therophyte, ruderal, and dicotyledon species. Results also showed that floral diversity was greatest in grass margin strips of intermediate age. Our findings have implications for optimizing diversity and ecosystem services on land enrolled in conservation programs and suggest that mowing later in the season and periodic soil disturbance can increase floral diversity. The analytical framework that we introduced in this research can also be used to explore weed community assembly in other systems.

Windmillgrass is a major weed in agricultural systems in northern Australia, and it has now become more common in southern Australia. Because little information is available on the biology of this weed species in southern Australia, studies were conducted to investigate plant development and seed biology. Under irrigated field conditions in South Australia, windmillgrass required 748 to 786 growing degree days from emergence to mature seed production. Freshly harvested seed had low dormancy with 16% to 40% germination. Seeds required light exposure for germination and less than 2% germination was observed in complete darkness. Seed could germinate over a wide temperature range (10 to 40 C) with maximum germination at 20 to 25 C. At 25 to 30 C, 50% germination occurred within 27.3 to 45.5 h, and the predicted base temperature for germination of the two populations investigated ranged from 9.2 to 11.2 C. The sodium chloride concentration and osmotic potential required to inhibit germination by 50% were 51 to 73 mM and -0.27 MPa, respectively. Seedling emergence was completely inhibited by burial of seed, which is consistent with its absolute requirement for light exposure to begin germination. Under field conditions, there was no clear effect of burial depth on seed viability in the first 2 yr with average rainfall, and seeds were completely nonviable after 12 mo. However, in the third year, with low spring—summer rainfall, buried seeds (37% viability after 14 mo) persisted longer than those left on the soil surface (6% viability after 14 mo). This study provides important information on plant development and seed biology of windmillgrass that will contribute to the development of a management program for this weed species in southern Australia.

Nomenclature: Windmillgrass, Chloris truncata R. Br.

Consumption of weed seeds and waste grains by seed predators is an important ecosystem service that helps to regulate weed and volunteer crop populations in many agricultural systems. The prairie deer mouse is found in a variety of sparsely vegetated habitats throughout the central United States and is the dominant vertebrate seed predator in row-crop fields (corn and soybean) in this region. Evaluating the preferences of prairie deer mice for common agricultural weed seeds and waste grain is important to understand the potential ability of native mice to regulate volunteer crops and weed populations. We evaluated winter seed preference of deer mice using cafeteria-style feeding trials presented within row-crop fields in central Indiana and used compositional analysis to compare proportional consumption of seeds from five common agricultural weeds (common ragweed, common cocklebur, common lambsquarters, velvetleaf, and giant foxtail) and two grains (corn and soybean) during overnight feeding trials. Prairie deer mice significantly preferred corn to all other available seed types. Ragweed and soybean were also readily consumed and were preferred over seeds other than corn. Giant foxtail was intermediately preferred. Our results show that prairie deer mice have clear preferences for certain seeds commonly available in row-crop fields; mice likely contribute to reduction of waste grain and some weed seed populations.

Nomenclature: Common cocklebur, Xanthium strumarium L.; common ragweed, Ambrosia artemisiifolia L.; common lambsquarters, Chenopodium album L.; giant foxtail, Setaria faberi Herrm.; velvetleaf, Abutilon theophrasti Medik.; corn, Zea mays L.; soybean, Glycine max (L.) Merr.

Feather fingergrass is a major weed in agricultural systems in northern Australia and has now spread to southern Australia. To better understand the biology of this emerging weed species, its growth, development, and seed biology were examined. Under field conditions in South Australia, seedlings that emerged after summer rainfall events required 1,200 growing degree days from emergence to mature seed production and produced 700 g m^-2 shoot biomass. Plants produced up to 1,000 seeds panicle^-1 and more than 40,000 seeds plant^-1, with seed weight ranging from 0.36 to 0.46 mg. Harvested seeds were dormant for a period of about 2 mo and required 5 mo of after-ripening to reach 50% germination. Freshly harvested seed could be released from dormancy by pretreatment with 564mM sodium hypochlorite for 30 min. Light significantly increased germination. Seed could germinate over a wide temperature range (10 to 40 C), with maximum germination at 15 to 25 C. At 20 to 25 C, 50% germination was reached within 2.7 to 3.3 d, and the predicted base temperature to germinate was 2.1 to 3.0 C. The osmotic potential and NaCl concentration required to inhibit germination by 50% were -0.16 to -0.20 MPa and 90 to 124 mM, respectively. Seedling emergence was highest (76%) for seeds present on soil surface and was significantly reduced by burial at 1 (57%), 2 (49%), and 5 cm (9%). Under field conditions, seeds buried in the soil persisted longer than those left on the soil surface, and low spring—summer rainfall increased seed persistence. This study provides important information on growth, development, and seed biology of feather fingergrass that will contribute to the development of a more effective management program for this weed species in Australia.

Nomenclature: Feather fingergrass, Chloris virgata Sw.

Maximizing cereal rye biomass has been recommended for weed suppression in cover crop—based organic no-till planted soybean; however, achieving high biomass can be challenging, and thick mulch can interfere with soybean seed placement. An experiment was conducted from 2012 to 2014 in New York to test whether mixing barley and cereal rye would (1) increase weed suppression via enhanced shading prior to termination and (2) provide acceptable weed suppression at lower cover crop biomass levels compared with cereal rye alone. This experiment was also designed to assess high-residue cultivation as a supplemental weed management tool. Barley and cereal rye were seeded in a replacement series, and a split-block design with four replications was used with management treatments as main plots and cover crop seeding ratio treatments (barley:cereal rye, 0:100, 50:50, and 100:0) as subplots. Management treatments included high-residue cultivation and standard no-till management without high-residue cultivation. Despite wider leaves in barley, mixing the species did not increase shading, and cereal rye dominated cover crop biomass in the 50:50 mixtures in 2013 and 2014, representing 82 and 93% of the biomass, respectively. Across all treatments, average weed biomass (primarily common ragweed, giant foxtail, and yellow foxtail) in late summer ranged from 0.5 to 1.1Mg ha^-1 in 2013 and 0.6 to 1.3Mg ha^-1 in 2014, and weed biomass tended to decrease as the proportion of cereal rye, and thus total cover crop biomass, increased. However, soybean population also decreased by 29,100 plants ha^-1 for every 1Mg ha^-1 increase in cover crop biomass in 2013 (P = 0.05). There was no relationship between cover crop biomass and soybean population in 2014 (P = 0.35). Soybean yield under no-till management averaged 2.9Mg ha^-1 in 2013 and 2.6 Mg ha^-1 in 2014 and was not affected by cover crop ratio or management treatment. Partial correlation analyses demonstrated that shading from cover crops prior to termination explained more variation in weed biomass than cover crop biomass. Our results indicate that cover crop management practices that enhance shading at slightly lower cover crop biomass levels might reduce the challenges associated with excessive biomass production without sacrificing weed suppression in organic no-till planted soybean.

Nomenclature: common ragweed, Ambrosia artemisiifolia L.; giant foxtail, Setaria faberi Herrm.; yellow foxtail, Setaria pumila (Poir.) Roemer & J. A. Schultes; barley, Hordeum vulgare L.; cereal rye, Secale cereale L.; soybean, Glycine max (L.) Merr.

Bararpour MT, Norsworthy JK, Burgos NR, Korres NE, Gbur EE (2017) Identification and Biological Characteristics of Ryegrass (Lolium spp.) Accessions in Arkansas. Weed Sci 65(3). doi: 10.1017/wsc.20l6.28

Mohammad T. Bararpour's affiliation was incorrect in the original publication. The correct affiliation for this author is:

Assistant Professor, Delta Research and Extension Center, Mississippi State University, Stoneville, MS 38776.

We apologize for this error.