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Perhaps the incidence and impact of glyphosate-resistant weed species are now great enough that real solutions to glyphosate resistance can be discussed without much backlash. It is clear to most weed scientists who are involved in herbicide research, and even those who are not, that the best way to reduce selection pressure for herbicide resistance is to minimize herbicide use. However, the “solutions” that have emerged in most recent meetings on herbicide resistance have usually involved more herbicide use—herbicide rotation, tank-mixtures, PRE- followed by POST-herbicides, “right-rates,” etc. To an unbiased observer, it would appear that many weed emperors are wearing no clothes. Are we as a weed science discipline choosing to ignore true integrated solutions to the herbicide resistance problem?
Changes in the weed flora of cropping systems reflect the impacts of factors that create safe sites for weed establishment and facilitate the influx and losses to and from the soil seedbank. This analysis of the annual surveys of the Southern Weed Science Society documents changes in the weed flora of the 14 contiguous southern states since the advent of transgenic, herbicide-resistant crops. In 1994 and 2009, the top five weeds in corn were morningglories, Texas millet, broadleaf signalgrass, johnsongrass, and sicklepod; in this same period Palmer amaranth, smartweeds, and goosegrass had the greatest increases in importance in corn. In cotton, morningglories and nutsedges were among the top five most troublesome weeds in 1995 and 2009. Palmer amaranth, pigweeds, and Florida pusley were also among the five most troublesome species in 2009; the weeds with the largest increases in importance in cotton were common ragweed and two species with tolerance to glyphosate, Benghal dayflower and Florida pusley. In soybean, morningglories, nutsedges, and sicklepod were among the top five weed species in 1995 and 2009. Two species with glyphosate resistance, Palmer amaranth and horseweed, were the second and fourth most troublesome weeds of soybean in 2009. In wheat, the top four weeds in 2008 were the same as those in 1994 and included Italian ryegrass, wild garlic, wild radish, and henbit. Crop production in the southern region is a mosaic of various crop rotations, soil types, and types of tillage. During the interval between the surveys, the predominant change in weed management practices in the region and the nation was the onset and rapid dominance of the use of glyphosate in herbicide-resistant cultivars of corn, cotton, and soybean. Because of the correspondence between the effects of glyphosate on the respective weed species and the observed changes in the weed flora of the crops, it is likely the very broad use of glyphosate was a key component shaping the changes in weed flora. Only eight of the top 15 most troublesome weeds of cotton and soybean, the crops with the greatest use of glyphosate, were the same in 1995 and 2009. In contrast, in corn and wheat where adoption of glyphosate-resistant cultivars lags or is absent, 12 of the 15 most troublesome weeds were the same in 1994 and 2008. These findings show on a regional scale that weeds adapt to recurrent selection from herbicides, currently the predominant weed management tool. Future research should seek methods to hinder the rapid spread of herbicide-tolerant and evolution of herbicide-resistant weed species. As new tools are developed, research should focus on ways to preserve the efficacy of those tools through improved stewardship.
Nomenclature: annual bluegrass, Poa annua L. POAAN; Benghal dayflower, Commelina benghalensis L. COMBE; broadleaf signalgrass, Urochloa platyphylla (Nash) R.D. Webster BRAPP; common ragweed, Ambrosia artemisiifolia L. AMBEL; Florida pusley Richardia scabra L. RCHSC; goosegrass Eleusine indica (L.) Gaertn. ELEIN; groundcherries, Physalis spp.; henbit, Lamium amplexicaule L. LAMAM; horseweed, Conyza canadensis (L.) Cronq. ERICA; Italian ryegrass, Lolium perenne L. ssp. multiflorum (Lam.) Husnot LOLMU; johnsongrass, Sorghum halepense (L.) Pers. SORHA; morningglories, Ipomoea spp.; nutsedges, Cyperus spp.; Palmer amaranth, Amaranthus palmeri S. Wats. AMAPA; pigweed,
Weed interference with crop growth is often attributed to water, nutrient, or light competition; however, specific physiological responses to these stresses are not well described. This study's objective was to compare growth, yield, and gene expression responses of corn to nitrogen (N), low light (40% shade), and weed stresses. Corn vegetative parameters from V2 to V12 stages, yield parameters, and gene expression using transcriptome (2008) and quantitative polymerase chain reaction (qPCR) (2008/09) analyses at V8 were compared among the stresses and with nonstressed corn. N stress did not affect vegetative parameters, although grain yield was reduced by 40% compared with nonstressed plants. Shade, present until V2, reduced biomass and leaf area > 50% at V2, and recovering plants remained smaller than nonstressed plants at V12. However, grain yields of shade-stressed and nonstressed plants were similar, unless shade remained until V8. Weed stress reduced corn growth and yield in 2008 when weeds remained until V6. In 2009, weed stress until V2 reduced corn vegetative growth, but yield reductions occurred only if weed stress remained until V6 or later. Principle component analysis of differentially expressed genes indicated that shade and weed stress had more similar gene expression patterns to each other than they did to nonstressed or N-stressed tissues. However, corn grown in N-stressed conditions shared 252 differentially expressed genes with weed-stressed plants. Ontologies associated with light/photosynthesis, energy conversion, and signaling were down-regulated in response to all three stresses. Shade and weed stress clustered most tightly together, based on gene expression, but shared only three ontologies, O-METHYLTRANSFERASE activity (lignification processes), POLY(U)-BINDING activity (posttranscriptional gene regulation), and stomatal movement. Based on morphologic and genomic observations, weed stress to corn was not explained by individual effects of N or light stress. Therefore, we hypothesize that these stresses share limited signaling mechanisms.
Japanese foxtail is one of the most common and competitive annual grass weeds of wheat in China. Whole-plant dose-response experiments were conducted with fenoxaprop and pinoxaden to confirm and characterize resistant and susceptible Japanese foxtail populations and to elucidate the basis of resistance to these herbicides. The resistant Japanese foxtail population was 49-fold resistant to fenoxaprop and 16-fold (cross) resistant to pinoxaden relative to the susceptible population, which was susceptible to both fenoxaprop and pinoxaden herbicides. Molecular analysis of resistance confirmed that the Ile1781 to Leu mutation in the resistant population conferred resistance to both fenoxaprop and pinoxaden. This is the first report of cross resistance of Japanese foxtail to pinoxaden in the world and of a target site mutation that corresponded to resistance to both fenoxaprop and pinoxaden in Japanese foxtail. Prior selection pressure from fenoxaprop could result in evolution of resistance to fenoxaprop and cross resistance to pinoxaden in Japanese foxtail population.
Nomenclature: Fenoxaprop; pinoxaden; Japanese foxtail, Alopecurus japonicus Steud; Wheat, Triticum aestivum L.
Acetolactate Synthase- (ALS) inhibiting herbicides are important components for the control of ryegrass species infesting cereal-cropping systems worldwide. Although resistance to ALS herbicides in ryegrasses has evolved more than 25 yr ago, few studies have been dedicated to elucidate the molecular mechanisms involved. To this end, we have investigated the molecular basis of chlorsulfuron, sulfometuron-methyl, and imazapyr resistance in AUS5 and AUS23, two ryegrass populations from Australia. Comparison between whole-plant herbicide assays and DNA sequencing results showed that resistance to the nonmetabolizable herbicide sulfometuron-methyl was associated with four different proline mutations at ALS codon position 197 (P197) in AUS23. In addition to three P197 amino acid changes impacting on the efficacies of the two sulfonylurea herbicides, the tryptophan to leucine target-site mutation at ALS codon position 574 (W574L) was present in AUS5, conferring resistance to both sulfometuron-methyl and imazapyr. The samples were also characterized by non target-site-based resistance impacting on the metabolizable herbicide chlorsulfuron only. Interestingly, compound mutant heterozygotes threonine/serine at ALS position 197, and plants with double mutations at positions 197 and 574 were detected, thus reflecting the ability of this outcrossing species to accumulate mutant alleles. Whole-plant dose-response assays conducted on predetermined wild-type and mutant genotypes originating from the same populations allowed for a more precise estimation of the dominant and very high levels of resistance associated with the proline to serine target-site mutation at ALS codon position 197 (P197S) and W574L mutations. The two highly efficient polymerase chain reaction- (PCR) based derived cleaved amplified polymorphic sequence (dCAPS) markers developed here will allow for quick confirmation of 197 and 574 ALS target-site resistance in ryegrass species field samples and also contribute to identify populations characterized by other likely resistance mechanisms in this important weed species.
Greenhouse and laboratory studies were conducted to confirm and quantify glyphosate resistance, quantify pyrithiobac resistance, and investigate interaction between flumiclorac and glyphosate mixtures on control of Palmer amaranth from Mississippi. The GR50 (herbicide dose required to cause a 50% reduction in plant growth) values for two glyphosate-resistant biotypes, C1B1 and T4B1, and a glyphosate-susceptible (GS) biotype were 1.52, 1.3, and 0.09 kg ae ha−1 glyphosate, respectively. This indicated that the C1B1 and T4B1 biotypes were 17- and 14-fold resistant to glyphosate, respectively, compared with the GS biotype. The C1B1 and T4B1 biotypes were also resistant to pyrithiobac, an acetolactate synthase (ALS) inhibitor, with GR50 values of 0.06 and 0.07 kg ai ha−1, respectively. This indicated that the C1B1 and T4B1 biotypes were 7- and 8-fold, respectively, more resistant to pyrithiobac compared with the GS biotype, which had a GR50 value of 0.009 kg ha−1. Flumiclorac was antagonistic to glyphosate by reducing glyphosate translocation. The C1B1 and T4B1 absorbed less glyphosate 48 h after treatment (HAT) compared with the GS biotype. The majority of the translocated glyphosate accumulated in the shoot above the treated leaf (that contains the apical meristem) in the GS biotype and in the shoot below the treated leaf in the resistant biotypes, C1B1 and T4B1, by 48 HAT. The C1B1 biotype accumulated negligible shikimate levels, whereas the T4B1 and GS biotypes recorded elevated levels of shikimate. Metabolism of glyphosate to aminomethylphosphonic acid was not detected in either of the resistant biotypes or the susceptible GS biotype. The above results confirm multiple resistance to glyphosate and pyrithiobac in Palmer amaranth biotypes from Mississippi and indicate that resistance to glyphosate is partly due to reduced absorption and translocation of glyphosate.
Three herbicidal ionic liquids (HILs)—alkyldi(2-hydroxyethyl)methylammonium (2,4-dichlorophenoxy)acetate, dialkyldimethylammonium (2,4-dichlorophenoxy)acetate, and alkyltrimethylammonium (2,4-dichlorophenoxy)acetate—were synthesized and their activity against broad-leaved weeds was investigated under field conditions. HILs as [cation][2,4-D] used in winter wheat were much more active compared to 2,4-D-dimethylammonium salt and demonstrated efficacy similar to 2,4-D 2-ethylhexyl ester. HILs exhibited desirable surface properties such as low contact angle of droplets and low surface tension. Moreover, the HILs may be safer to operators and neighboring plants due to their nonvolatile nature. HILs at 450 g ha−1 of 2,4-D did not injure wheat.
Glyphosate-resistant (GR) volunteer corn has emerged as a problematic weed in corn∶soybean rotational systems, partly because of the rapid increase in adoption of corn hybrids that contain traits for both glyphosate and insect resistance. Volunteer GR corn can decrease soybean yields. The objectives of this study were to quantify the impact of volunteer corn on soybean growth and yield and determine how volunteer corn densities affect western corn rootworm (WCR) emergence. Volunteer corn seed was hand-planted at targeted densities of 0.5, 2, 4, 8, 12, and 16 seeds m−2 at soybean planting and 21 d after planting to evaluate both early- and late-emerging cohorts. WCR emergence was assessed with the use of field emergence traps placed over individual corn plants in the 0.5- and 16-plants-m−2 plots in 2008 and 2009. In 2010, WCR emergence traps were also placed over individual and clumped volunteer corn plants at densities of two and eight plants m−2. Soybean yield reductions ranged from 10 to 41% where early-emerging volunteer corn densities ranged from 0.5 to 16 plants m−2. No soybean yield loss occurred with the late-emerging cohort of volunteer corn. Twice as many adult WCRs emerged from a single volunteer corn plant growing at densities of 8 and 16 plants m−2, compared with plots containing 0.5 and 2 plants m−2. These results demonstrate that controlling volunteer corn will not only prevent soybean yield loss, but also may reduce the risk of WCR larval survival after exposure to Bt (Bacillus thuringiensis Berliner derived) corn.
Nomenclature: Glyphosate; western corn rootworm, Diabrotica virgifera virgifera LeConte;corn, Zea mays L.; soybean, Glycine max L. Merr.
Experiments were conducted in the laboratory and screenhouse to determine the effects of scarification; alternating day/night temperatures; light, salt, and water stress; seed burial depth; and rice residue on seed germination and seedling emergence of threelobe morningglory, and to evaluate the response of this weed to commonly available POST herbicides in the Philippines. Germination was stimulated by seed scarification, suggesting that inhibition of germination in this species is mainly due to the hard seed coat. Germination of the scarified seeds was not influenced by the tested temperatures (alternating day/night temperatures of 25/15, 30/20, and 35/25 C) and light. The concentrations of sodium chloride, ranging from 0 to 250 mM, did not influence germination of the scarified seeds of threelobe morningglory. The osmotic potential required for 50% inhibition of maximum germination was −0.35 MPa, although some seeds germinated at −0.6 MPa. Seedling emergence was greatest for the seeds placed on the soil surface (96%), and emergence declined with increased burial depth in soil. The burial depth required for 50% inhibition of maximum emergence was 2.8 cm. No seedlings emerged from a burial depth of 6 cm or greater. Residues of up to 6 Mg ha−1 on the soil surface did not influence seedling emergence of threelobe morningglory. The herbicide 2,4-D at 400 g ai ha−1 provided excellent control of threelobe morningglory when applied at the four-leaf (100%) and six-leaf (97%) stages. However, at the eight-leaf stage, percent control was reduced to 67% and herbicide rate had to be increased twofold to achieve 95% control. The information gained from this study could contribute to developing components of integrated weed management strategies for threelobe morningglory. Soil inversion by tillage to bury weed seeds below their maximum depth of emergence and early application of an effective POST herbicide could serve as important tools for managing threelobe morningglory.
Nomenclature: 2,4-D; glyphosate; metsulfuron chlorimuron; threelobe morningglory, Ipomoea triloba L. IPOTR; rice, Oryza sativa L.
Several volatile allelochemicals were identified and characterized from fresh leaf tissues of the invasive croftonweed. A simple bioassay was used to demonstrate the release of volatile allelochemicals from leaf tissues. The bioassays revealed that foliar volatile components of croftonweed exhibited significant effects on the seedling growth of upland rice. Peroxidase (POD) activity, superoxide dismutase (SOD) activity, and root oxidizability rose as the concentration of volatiles increased. Activity for both POD and SOD significantly increased with exposure to 15 g and 20 g of croftonweed leaf tissue for 5 d. Root activity was significant at 10 g compared to the control. The volatile components also stimulated the development of the aerenchyma tissue and inhibited lateral root formation. Leaf volatiles of croftonweed were identified by gas chromatography coupled with mass spectrometry (GC–MS). Some of the compounds identified included α-phellandrene, camphene, ρ-cymene, 2-carene, α-pinene, limonene, and (z)-3-hexen-1-ol. Bioassays showed that four of these compounds could account for the observed phytotoxicity imparted by total leaf volatiles. Limonene, 2-carene, α-pinene and camphene had no phytotoxic effect on shoot elongation. Phellandrene did cause inhibition in shoot growth at all concentrations. Both (z)-3-hexene-1-ol and ρ-cymene inhibited both shoot elongation and root elongation, but the effects of the two compounds on root length were more significant than on the shoot length.
Nomenclature: Croftonweed, Ageratina adenophora (Spreng.) King and H. E. Robins; upland rice, Oryza sativa L.
Cogongrass is a troublesome, invasive weedy species with reported allelopathic properties. The phytotoxicity of different constituents isolated from roots and aerial parts of this species was evaluated on garden lettuce and creeping bentgrass. No significant phytotoxic activity was detected in the methylene chloride, methanol, or water extracts when tested at 1.0 mg ml−1. However, the total essential oil extract of cogongrass aerial parts was active. Bioactivity-guided fractionation of this extract using silica gel column chromatography led to the identification of megastigmatrienone, 4-(2-butenylidene)-3,5,5-trimethyl-2-cyclohexen-1-one (also called tabanone), as a mixture of four stereoisomers responsible for most of the activity. Tabanone inhibited growth of frond area of lesser duckweed, root growth of garden onion, and fresh weight gain of garden lettuce with 50% inhibition values of 0.094, 3.6, and 6.5 mM, respectively. The target site of tabanone is not known, but its mode of action results in rapid loss of membrane integrity and subsequent reduction in the rate of photosynthetic electron flow.
Buffalobur is an invasive summer annual species in Xinjiang Province, China. Our purpose was to investigate certain aspects of the seed biology of this weedy species that might be useful in controlling it. In contrast to a previous report that fresh seeds have physical (water-impermeable seed coat) plus physiological (low growth potential of embryo) dormancy, our results, along with those of others, verify that the seeds have only physiological dormancy. The seed's coat is water-permeable, the embryo is fully developed at seed maturity, and dormancy can be broken by cold stratification in the field during winter and early spring. Fifty-five percent of seeds buried in the soil in autumn germinated in the soil the following May, and 53% of the remaining nongerminated seeds germinated when tested in light in the laboratory. Thus, about 20% of the seeds did not germinate but were viable, demonstrating that the species forms at least a short-lived persistent seed bank. This information will be useful in planning a management strategy for this highly invasive species in northwest China.
The physiological process underlying grain yield (GY) loss in maize as a result of weed competition is not understood clearly. We designed an experiment to test the hypotheses that early season stress caused by the presence of neighboring weeds will increase plant-to-plant variability (PPV) of individual plant dry matter (PDM) within the population. This increase in PPV will reduce GY through a reduction in harvest index (HI). Field experiments were conducted in 2008, 2009, and 2010. A glyphosate-resistant maize hybrid was cropped at a density of 7 plants m−2. As a model weed, winter wheat was seeded at the same time as maize and controlled with glyphosate at the 3rd or 10th to 12th leaf-tip stage of maize. Weed competition early in the development of maize decreased PDM and GY. This reduction in PDM, which occurred early in the development of maize, was attributed initially to a delay in rate of leaf appearance. Reductions in PDM were accompanied by an increase in PPV of PDM. This increase in PPV, however, did not reduce HI and did not contribute to the GY reductions created by weed competition, as hypothesized. As weed control was delayed, a reduction in fraction of photosynthetically active radiation (fIPAR) accounted for a further reduction in PDM and notably, a reduction in DMA from 17th leaf-tip stage through to maturity. The rapid loss of PDM and the subsequent inability to accumulate dry matter during maturation accounted for a rapid decline in kernel number (KN) and kernel weight (KW).
Nomenclature: Glyphosate; maize, Zea mays L. ZEAMX; winter wheat, Triticum aestivum L. TRZAW.
Perennial weeds constitute a serious problem in Greek cotton-growing areas, as they strongly competing against the crop and downgrade the final product. Monitoring weeds at a regional scale and relating their occurrence with abiotic factors will assist in the control of these species. Purple nutsedge, field bindweed, bermudagrass, and johnsongrass were studied in cotton crops for three consecutive growing seasons (2007 through 2009) in a large area of central Greece. Weed densities and uniformities per sampling site were assessed in relation to soil and climatic data. Abundance index (AI), which is highly dependent on abiotic factors, was also estimated, and revealed purple nutsedge to the most persistent and damaging species among the recorded weeds. Field bindweed showed the highest correlation with soil properties and especially with clay content. Furthermore, correlation analysis was used over the sampling years in order to assess the stability of weed occurrence in the sampling sites. Purple nutsedge, field bindweed, and bermudagrass proved to be stable in location and intensity. The weed density spatial distribution was evaluated by using local indicators of spatial autocorrelation (LISA) statistics, and was mapped by ordinary kriging and co-kriging interpolation methods. Only 1 to 3 spatial outliers were identified in each 1 of the 3 yr. Between the two interpolation methods co-kriging delivered better results for field bindweed and purple nutsedge, indicating that soil data could improve the estimation of weed occurrence. These co-kriging interpolated weed maps would be a very useful tool for decision makers in taking appropriate weed control measures.
Nomenclature: Purple nutsedge, Cyperus rotundus L. CYPRO; field bindweed, Convolvulus arvensis L. CONAR; bermudagrass, Cynodon dactylon (L.) Pers. CYNDA; johnsongrass, Sorghum halepense (L.) Pers. SORHA; cotton, Gossypium hirsutum L. GOSHI.
Effective in-season weed management options are limited for organic cereal farmers. Two alternatives to current farmer practices are improving efficacy of physical weed control through use of interrow cultivation or increasing the competitive ability of the crop through elevated seeding rates and more uniform spatial planting patterns. It is unknown how these two methods affect yield, quality, and economic returns. Field experiments were conducted in the northeast United States to determine whether the yield gain from increased weed control from these contrasting weed management strategies resulted in increased net returns and how these different systems affected grain quality. Wheat was planted at two seeding rates (400 and 600 plants m−2), in three row spacings (11, 18, and 23 cm). A fourth crop arrangement that approaches a more uniform spatial distribution through a combination of drilling and broadcasting seed was included. For weed control, treatments received tine harrowing. Wheat sown in wide rows also received interrow cultivation. Each system was sown in the presence and absence of condiment mustard, which was sown as a surrogate weed. Increased seeding rate reduced weed density 64% compared to a crop-free check and 30% compared to regional farmers' practices of 18-cm rows and 400 plants m−2. Increased seeding rates lowered grain protein 5% compared to standard seeding rates. Wide rows, in combination with interrow cultivation, reduced weed density 62%, increased yield 16%, and net returns 19% compared to regional organic practices. Significant increases in grain N were limited to weed-free plots. While increased seeding rates improved weed suppression, the high input cost of organic seed make this an unsatisfactory alternative to interrow cultivation and current farmer practices, as yield would need to be .15 t ha−1 higher at elevated density to offset the extra cost of seed.
Nomenclature: Wheat, Triticum aestivum L.; white mustard, Sinapis alba L.
A hydrothermal time model was developed to simulate field emergence for three weed species in maize (common lambsquarters, johnsongrass, and velvetleaf). Models predicting weed emergence facilitate well-timed and efficient POST weed control strategies (e.g., chemical and mechanical control methods). The model, called AlertInf, was created by monitoring seedling emergence from 2002 to 2008 in field experiments at three sites located in the Veneto region in northeastern Italy. Hydrothermal time was calculated using threshold parameters of temperature and water potential for germination estimated in previous laboratory studies with seeds of populations collected in Veneto. AlertInf was validated with datasets from independent field experiments conducted in Veneto and in Tuscany (west central Italy). Model validation resulted in both sites in efficiency index values ranging from 0.96 to 0.99. AlertInf, based on parameters estimated in a single region, was able to predict the timing of emergence in several sites located at the two extremes of the Italian maize growing area.
Nomenclature: common lambsquarters, Chenopodium album L.,CHEAL; johnsongrass, Sorghum halepense L. Pers, SORHA; velvetleaf, Abutilon theophrasti Medik., ABUTH.
Canada thistle is difficult to manage in organic farming systems and others with reduced reliance on herbicides. Previous field studies found that defoliation or sudangrass interference suppressed Canada thistle. Our objective was to understand the factors causing suppression of Canada thistle observed in the field. Three greenhouse studies were conducted utilizing frequency of defoliation, sudangrass interference and defoliation, and interspecific phytotoxicity to discern mechanisms of Canada thistle suppression. Increased defoliation frequency (up to four defoliations) decreased Canada thistle shoot height, shoot and root mass, and root-to-shoot ratio. Plants with larger root mass had greater shoot mass and number (r = 0.87 and 0.73, respectively), indicating a probable interdependence of root size (carbohydrate reserves), bud density, and subsequent shoot growth. In the sudangrass interference and defoliation study, Canada thistle shoot dry mass was 38.7, 2.76, and 0.39 g pot−1 in the defoliation only, sudangrass interference only, and defoliation interference surface mulch treatments, respectively. Sudangrass interference by itself was effective in suppressing thistle growth; combining interference with defoliation did not further reduce growth (2.76 and 2.83 g pot−1, respectively). In the experiment minimizing interspecific competition, we found no evidence of sudangrass having a phytotoxic effect on Canada thistle. Overall results indicate that sudangrass competition or frequent shoot removal suppresses growth of Canada thistle.
Nomenclature: Canada thistle, Cirsium arvense (L.) Scop.; sudangrass, Sorghum bicolor (L.) Moench spp. drummondii (Nees ex Steud.) de Wet and Harlan.
While witchweed is nearing eradication in the United States, it continues to thrive in other parts of the world, especially in Africa, together with other witchweed species. The continuing problems from witchweeds and other parasitic weeds, the broomrapes, dodders and mistletoes, are outlined, including their extent, the degrees of damage caused, and the difficulties in their control. While a small minority are being successfully controlled by the use of immune varieties, most are currently controlled by existing techniques only partially, or on a local basis, and they may even be spreading or intensifying. The challenges they present are emphasised.
Small broomrape is a federally listed noxious weed that was first identified in Oregon in 1923. Between 1923 and 1997, there were only six reports of the species in Oregon. Small broomrape is a holoparasitic weed that attaches to the root of its host and can lead to crop failure depending on the level of infestation. Small broomrape was identified in a red clover field in Oregon in 1998. In 2000 and 2001, the Oregon Department of Agriculture surveyed red and white clover fields in Oregon for the presence of small broomrape; 15 infested fields were identified in 2000 and 22 in 2001. The source of the small broomrape seed was not identified although there was speculation that small broomrape seed may have been contaminated clover seed stock. In 2000, a quarantine was established for small broomrape in red clover seed. Research identified effective, easy to implement management strategies for small broomrape including the use of false host crops and imazamox. In 2003, the ODA amended the quarantine to eliminate the mandatory seed sampling and testing and the requirement of reporting infested fields and seed lots. In 2011, there are still populations of small broomrape present in red clover fields in Oregon.
Nomenclature: Small broomrape, Orobanche minor Sm.; red clover, Trifolium pratense L.
Striga is a major constraint to food production in Africa. Most technologies developed for the eradication of Striga asiatica from the United States are not adaptable to Africa. Imazapyr and pyrithiobac coated imidazolinone-resistant (IR)-resistant maize seed prior to planting at rates of 30 to 45 g ha−1 provide near season long control of Striga and can increase maize yields three- to fourfold if supplied with fertilizer. Slow release seed coatings reduce maize injury when post-planting rains are sparse and improve Striga control when there is excessive rainfall early in the season. Models suggest that herbicide resistance may not be a significant threat in short season maize, but vigilance in removing flowering Striga plants that are not controlled is recommended due to the known risk of evolution of resistance to these herbicides. Stacking the IR gene with glyphosate resistance and using imazapyr treated seed and applying glyphosate mid-season would provide season long Striga control and delay the evolution of resistance to both herbicides. To date, adoption of this technology has been limited by a number of factors. However, it should be included as one component of a multi-factor approach to increasing maize productivity in areas of Africa where Striga is problematic.
Parasitic weeds such as Phelipanche and Orobanche are obligate holoparasites that attack roots of almost all economically important crops in semiarid regions of the world. A wide variety of parasitic weed control strategies (chemical, biological, cultural, and resistant crops) has been tried. Unfortunately, most are partially effective and have significant limitations. The current mini review will discuss the needs for alternative methods and will summarize current and new biotechnology-based approaches for broomrape control. At present, we have generated transgenic tobacco plants expressing a cecropin peptide (sarcotoxin IA), under the control of the inducible HMG2 promoter. Transgenic lines enhanced host resistance to the parasitic weed; transgenes showed higher numbers of aborted parasitization events, reduced Phelipanche biomass, and increased host biomass. Sarcotoxin IA had no obvious effect on growth and development of transgenic host plants. Mannitol content in the parasite is regulated by Mannose 6-Phosphate Reductase (M6PR) gene, an essential process to broomrape species for water and nutrient uptake from the host. In our study, we used the inverted repeat technique to silence the parasite target gene, M6PR. In this study it was shown that the endogenous M6PR mRNA from P. aegyptiaca tubercles or shoots grown on transgenic tomato plants harboring the M6PR silencing construct was reduced by 60 to 80%. The number of dead tubercles was also increased significantly on transgenic plants as compared with the control plants. The strategies presented here are potentially superior to other methods in that they are effective, have a low cost of implementation for producers, and are safe for the environment.
James H. Westwood, Claude W. dePamphilis, Malay Das, Mónica Fernández-Aparicio, Loren A. Honaas, Michael P. Timko, Eric K. Wafula, Norman J. Wickett, John I. Yoder
The Parasitic Plant Genome Project has sequenced transcripts from three parasitic species and a nonparasitic relative in the Orobanchaceae with the goal of understanding genetic changes associated with parasitism. The species studied span the trophic spectrum from free-living nonparasite to obligate holoparasite. Parasitic species used were Triphysaria versicolor, a photosynthetically competent species that opportunistically parasitizes roots of neighboring plants; Striga hermonthica, a hemiparasite that has an obligate need for a host; and Orobanche aegyptiaca, a holoparasite with absolute nutritional dependence on a host. Lindenbergia philippensis represents the closest nonparasite sister group to the parasitic Orobanchaceae and was included for comparative purposes. Tissues for transcriptome sequencing from each plant were gathered to identify expressed genes for key life stages from seed conditioning through anthesis. Two of the species studied, S. hermonthica and O. aegyptiaca, are economically important weeds and the data generated by this project are expected to aid in research and control of these species and their relatives. The sequences generated through this project will provide an abundant resource of molecular markers for understanding population dynamics, as well as provide insight into the biology of parasitism and advance progress toward understanding parasite virulence and host resistance mechanisms. In addition, the sequences provide important information on target sites for herbicide action or other novel control strategies such as trans-specific gene silencing.
The witchweeds, members of the genus Striga, are noxious and persistent pests in farmers' fields and serious constraints to crop productivity throughout Africa, India, and Southeast Asia. Among the primary hosts for Striga are the major cereals (maize, sorghum, rice, and millet) and grain legumes (cowpea) that are important food staples worldwide. The negative impact of parasitic plants on crop productivity increases globally each year, and their potential for affecting domestic agriculture looms larger as the movement of seed resources expands on a global scale. At the present time there is a limited understanding of how Striga and other parasitic plants select a suitable host and overcome the innate defense responses of the host in order to complete their life-cycle. In the grasses most reported resistance to Striga appears to be polygenic with a large genotype by environment interaction. In contrast, resistance to S. gesnerioides in cowpea is conferred by single dominant genes functioning in a race-specific manner suggesting that a gene-for-gene mechanism similar to effector-triggered immunity (ETI) described in other host–pathogen interactions is likely operating in these parasite-host associations. A hallmark of ETI is the direct or indirect recognition of parasite-derived avirulence (Avr) factors and other effectors that interfere with plant innate immunity by host sensors (or R proteins) leading to activation of defense responses. The recent cloning and functional characterization of a race-specific R gene from cowpea encoding a canonical coiled-coil (CC)-nucleotide binding site (NBS)-leucine-rich repeat (LRR) type R-protein opens the door for further exploration of the mechanism of host resistance and provides a focal point for studies aimed at uncovering the molecular and genetic factors underlying parasite virulence and host selection. The potential for the development of novel strategies for parasite control and eradication based on parasite virulence factors is discussed.
Broomrapes (Orobanche and Phelipanche spp.) are obligate root parasites that spend most of their life cycle in the soil subsurface, making them hard to detect. In these underground developmental stages, broomrapes are highly sensitive to herbicides, and therefore knowledge of the dynamics of their parasitism is essential to precisely apply herbicide for their control. To address these complexities, two approaches have been proposed: (1) estimating the temporal variation in parasitism dynamics and predicting broomrape parasitism on its host by thermal time; (2) characterizing the spatial variation in infestation within and between fields by using a geographical information system and a global positioning system. In addition, the use of molecular markers to identify broomrape infestation (species and amount) in the field can contribute to determining its spatial distribution, which can then be used for site-specific weed management. In this paper, we discuss how technology can be optimized for control of the root-parasitic broomrapes. Special attention is given to the development of integrative approaches. An example of a decision support system for the rational management of Egyptian broomrape in processing tomato is given.
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