<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">AS</journal-id><journal-title-group><journal-title>Agricultural Sciences</journal-title></journal-title-group><issn pub-type="epub">2156-8553</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/as.2012.38119</article-id><article-id pub-id-type="publisher-id">AS-25455</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject><subject> Earth&amp;Environmental Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Research on the allelopathic potential of wheat
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>au</surname><given-names>Lam</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Cho</surname><given-names>Wing Sze</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yao</surname><given-names>Tong</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Tzi</surname><given-names>Bun Ng</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Sydney</surname><given-names>Chi Wai Tang</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>James</surname><given-names>Chung Man Ho</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Qiaoqing</surname><given-names>Xiang</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Xiao</surname><given-names>Lin</given-names></name><xref ref-type="aff" rid="aff6"><sup>6</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yanbo</surname><given-names>Zhang</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff6"><addr-line>The Fuling Centre Hospital, Chong Qing, China</addr-line></aff><aff id="aff2"><addr-line>School of Chinese Medicine, The University of Hong Kong, Hong Kong, China</addr-line></aff><aff id="aff5"><addr-line>Department of pulmonary respiration, The Fuling Centre Hospital, Chong Qing, China</addr-line></aff><aff id="aff4"><addr-line>Department of Medicine, The University of Hong Kong, Hong Kong, China</addr-line></aff><aff id="aff3"><addr-line>The School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong, China</addr-line></aff><aff id="aff1"><addr-line>School of Chinese Medicine, The University of Hong Kong, Hong Kong, China;</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>ybzhang@hkucc.hku.hk(YZ)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>17</day><month>12</month><year>2012</year></pub-date><volume>03</volume><issue>08</issue><fpage>979</fpage><lpage>985</lpage><history><date date-type="received"><day>2</day>	<month>August</month>	<year>2012</year></date><date date-type="rev-recd"><day>16</day>	<month>September</month>	<year>2012</year>	</date><date date-type="accepted"><day>27</day>	<month>October</month>	<year>2012</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Objective: This paper mainly discusses the Allelopathic potential of Wheat. Methods: This paper is prepared by reviewing the latest academic literatures. Result: The green revolution in the 1960s caused an increase in the demand for food. The agricultural sector and farmers tended to spend more time on the agricultural work but the crop yield was suppressed by the weeds. Hence, the usage of herbicide insecticides, fungicides and others chemicals had been increased. Although herbicides are efficient for weed controls, the continuous uses had gradually stimulated the weeds developing an effecttive resistance to the chemicals. Wheat (
  Triticum aestivum L.) is known as allelopathic against crops and weeds. Allelopathy of wheat (
  Triticum aestivum L.) has been extensively examined for its potentials in weeds management. The allelopathic activity of wheat has been attributed to hydroxamic acids, the related compounds and phenolic acids. Therefore, it could effectively reduce herbicide uses in order to maintain an eco-friendly environment and a cost-effective weed control.
 
</p></abstract><kwd-group><kwd>Wheat; Allelopathic Effect; Allelopathic Crop; Straw; Stubble; Benzoxazinones; Phenolics</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. INTRODUCTION</title><p>The green revolution in the 1960s and increased demand for food. The agricultural sector and farmers also tend to spend more time outside agricultural work. But the weeds are a major constraint limiting crop yield in agricultural systems and in organic systems in particular [<xref ref-type="bibr" rid="scirp.25455-ref1">1</xref>]. Weeds reduce crop yield by 5% in the most highly developed countries, 10% in the less developed countries and 25% in the least developed countries. Hence, herbicide insecticides, fungicides and others use has been increased in the last few decades. A herbicide use has been increased many fold. According to the statistics of the total pesticides used worldwide, herbicides accounts for 37%, while 24%, 9% and 29% are insecticides, fungicides and others. In which 332 herbicide resistant biotypes including 189 species (113 broad-leaved and 76 grasses) have been reported in more than 0.30 million fields worldwide. Although herbicides are efficient for weed control, continuous use has caused the development of resistance in weeds against several herbicides [<xref ref-type="bibr" rid="scirp.25455-ref2">2</xref>]. Furthermore, herbicides also pollute the soil, water and aerial environments and herbicide residues in food have deteriorated food quality and enhanced the risk of disease [<xref ref-type="bibr" rid="scirp.25455-ref3">3</xref>]. Therefore, there is growing public as well as scientific concern about the use of herbicides.</p></sec><sec id="s2"><title>2. ALLELOPATHIC EFFECT OF WHEAT</title><p>Allelopathy is a phenomenon in which one plant inhibits growth of other plants through release of allelochemicals. It is a phenomenon in which the seconddary metabolites, produced by plants, microorganisms, viruses, and fungi stimulate or suppress the growth and development of agricultural and biological systems (excluding animals). The crops inhibit weeds—A very promising, it has emerged as an alternative to synthetic herbicides for weed management in field crops [4,5]. It can reduce herbicide use to obtain eco-friendly and costeffective weed control. Earlier, confirmed, a large number of crops and trees has been found to possess allelopathic potential [<xref ref-type="bibr" rid="scirp.25455-ref6">6</xref>]. International research on the allelopathy of wheat is active [<xref ref-type="bibr" rid="scirp.25455-ref7">7</xref>]. Research on wheat allelopathy has progressed rapidly from the initial phase of evaluation of wheat allelopathy to the identification of wheat allelochemicals, the degradation of these compounds andfurther, to the identification of genetic markers associated with wheat allelopathy [8,9].</p><sec id="s2_1"><title>2.1. Straw of Wheat</title><p>Wheat (Triticum aestivum L.) is known to be allelopathic against crops and weeds. Wheat straw reduced weed densities and biomass by an average of 90% compared with those plots without residues. Also, reported that wheat straw caused 16.8% reduction of broad-leaved weeds [<xref ref-type="bibr" rid="scirp.25455-ref10">10</xref>]. But aqueous leachate of wheat straw and the extract of decomposed wheat straw inhibit the growth of wheat. Display the aqueous extracts of wheat residues at 2 and 4 % concentration significantly inhibited germination and growth. Wheat straw was decomposed under laboratory conditions at pH = 5, 7 and 8 [<xref ref-type="bibr" rid="scirp.25455-ref11">11</xref>]. Study display that, pH = 7 showed very strong inhibition of wheat seed germination. Also, all acidic extracts can inhibit the growth of some plant growthand inhibited the germination and root growth of test species [<xref ref-type="bibr" rid="scirp.25455-ref12">12</xref>]. Chemical analysis indicated that syringoylglycerol 9-O-b-D-glucopyranoside inhibited the roots growth of lettuce and cress at concentrations greater than 0.1 and 10.0 lM, respectively. On the other hand, L-tryptophan inhibited the roots growth of lettuce and cress at concentrations greater than 0.1 and 1.0 lM, respectively. The content of syringoylglycerol 9-O-b-D-glucopyranoside and L-try-ptophan in the leachate of wheat straw (100 g eq./L) was 18.4 &#177; 0.7 and 6.2 &#177; 0.6 lM, respectively. Syringoylglycerol 9-O-b-D-glucopyranoside (18.4 lM) showed 21.5 and 13.5% inhibition in the lettuce and cress roots assay, respectively. On the other hand, 6.2 lM of L-tryptophan showed 47.5 and 35.0% inhibition in the lettuce and cress roots assay, respectively [<xref ref-type="bibr" rid="scirp.25455-ref13">13</xref>]. In which，phenolic acids and organic acids have a strong inhibition effect. Nitrogen (N)-containing chemicals had a weaker inhibition effect and, in some cases, a stimulation effect [<xref ref-type="bibr" rid="scirp.25455-ref14">14</xref>].</p></sec><sec id="s2_2"><title>2.2. Stubble of Wheat</title><p>Retention of crop stubbles is a key component of conservation farming systems, which are promoted worldwide [<xref ref-type="bibr" rid="scirp.25455-ref15">15</xref>]. Stubble mulching changes the conditions at the air and soil interface and influences the physical, chemical, and biological properties of the soil. Retained crop stubbles reduce soil evaporation, erosion and degradation, increase water availability to crops and maintain soil organic matter. In addition, stubble mulching efficiently controls weed propagation and enhances the capacity of crops to compete with weeds for growth resources. These changes have a large effect on the growth and development of crops. Thus, stubble mulching has ecological, social, and economic benefits and is important for the sustainable development of agriculture [16, 17]. Despite these benefits to production and sustainability, adoption has been slow in many areas of the world [<xref ref-type="bibr" rid="scirp.25455-ref18">18</xref>]. In the United States and Australia and show that retained crop stubbles can reduce the yield of crops [<xref ref-type="bibr" rid="scirp.25455-ref19">19</xref>]. Experiments demonstrate that poor growth of canola through surface-retained wheat stubble is primarily related to the physical effects of the stubble rather than biochemical effects related to stubble phytotoxicity or N —Immobilisation. Wheat stubble on canola of development was delayed, LAI and RMR were reduced, hypocotyls were longer, and SRL was increased. Fifty-two days after sowing, surface-mulch reduced total plant biomass through a reduction in both the number of plants per unit area as well as a reduction in individual plant size. Subsequent growth and final seed yield was also reduced to the same extent (26%) [<xref ref-type="bibr" rid="scirp.25455-ref20">20</xref>]. An accompanying paper focuses on more detailed investigations of the physical impacts of the stubble on canola growth, particularly the impact of reduced light penetration through stubble on growth of canola seedlings. This suggests that elongation of the hypocotyl in canola in response to reduced and/or altered quality and quantity of light during emergence and delayed development the growth reduction caused by the hypocotyls elongation in the 50 mm tubes was on average 57% [<xref ref-type="bibr" rid="scirp.25455-ref21">21</xref>].</p></sec></sec><sec id="s3"><title>3. AIIELOPATHIC SUBSTANCE OF WHEAT</title><p>Wheat (Triticum aestivum) has been extensively studied for its allelopathic potential. The common allelochemicals from crop plants are generally secondary metabolites. These include phenolics, terpenoids, alkaloids, coumarins, tannins, flavonoids, steroids and quinines. The allelopathic activity of wheat has been attributed to hydroxamic acids and related compounds and phenolic acids [<xref ref-type="bibr" rid="scirp.25455-ref22">22</xref>]. In general, the allelochemicals of plants to the environment is as follows: 1) exudation from roots, 2) leaching from plants by fog, mist and rain, 3) decomposition of residues [<xref ref-type="bibr" rid="scirp.25455-ref23">23</xref>]. In which, crop plant root exudation has been chemically investigated from as early as 1921 when Lyon and Wilson studied the liberation of organic substances through the roots of growing plants. Further suggest that organic substances can interfere with basic processes of receiver plants as photosynthesis, cell division, respiration and protein synthesis [<xref ref-type="bibr" rid="scirp.25455-ref24">24</xref>] and indirectly provoke other forms of stresses. Another important effect of these allelochemicals is the activation of cellular antioxidant system in response to uncontrolled production and accumulation of reactive oxygen species [<xref ref-type="bibr" rid="scirp.25455-ref25">25</xref>]. Rovira has written a review covering plant root exudation. Allelopathic secondary metabolites such as methoxyphenylacetic acid have been observed to move from one plant to another through their root systems and as one of the important world crops, the root exudates from wheat have become a focus of allelopathic study [26-29].</p><sec id="s3_1"><title>3.1. Benzoxazinones</title><p>Benzoxazinones present in exudates from Triticum aestivum pointed to the presence of such constituents as DIMBOA, 2,-dihydroxy-1,4 benzoxazin-3-one (DIBOA), 2-hydroxy-1,4-benzoxazin-3-one (HBOA), 2-hydroxy- 7-methoxy, 1, 4-benzoxazin-3-one (HMBOA), and 2,7- dihydroxy-1,4-benzoxazin-3-one (DHBOA). Of these benzoxazinones, only DIBOA and DIMBOA are hydroxamic acids (hydroxyl group on the nitrogen atom at position 4)<sup> </sup>[<xref ref-type="bibr" rid="scirp.25455-ref31">31</xref>]. In which, wheat with high concentrations of tramine or hydroxamic acids are very useful for a rotation in an area with high aphid populations. This is very profitable for the development of natural herbicides and resistances varieties [<xref ref-type="bibr" rid="scirp.25455-ref32">32</xref>].</p></sec><sec id="s3_2"><title>3.2. Phenolics</title><p>Phenolics are the most common water-soluble allelochemicals known to play a significant role in plant— Plant interactions, including allelopathy [33,34]. Several studies indicate that phenolics, upon entering the soil, are sorbed, detoxified or transformed to simpler forms, phenolics may markedly suppress weed growth in field when they influence nutrient uptake and may even serve as a carbon source for microbes [<xref ref-type="bibr" rid="scirp.25455-ref35">35</xref>].</p></sec></sec><sec id="s4"><title>4. GENETIC GENES</title><p>Allelopathy in wheat is complex and determined by many known, partially known, and unknown factors. It has been described as a dark grey system (grey theory) [<xref ref-type="bibr" rid="scirp.25455-ref36">36</xref>]. Allelopathic potential in wheat and genetic, chemical and ecological factors and a synergistic relationship.</p><p>Heritability and its degree of influence on yield were more evident in the vegetative growth stage compared to the reproductive stage. Research indicated that allelopathic effects exhibited high heritability (55% - 95%) throughout the life cycle of wheat. In which, Heritability was highest in the tillering stage and weakest in the seed filling stage [<xref ref-type="bibr" rid="scirp.25455-ref37">37</xref>]. Allelopathic potential varied and was discontinuous throughout the wheat life cycle. Implying that multiple genes participated in the expression of allelopathy. In addition, that genotype &#183; tillage interaction was reported in tests involving diverse genotypes. In a comparison of a conventional cultivar (Janz) and a novel experimental line (Vigor 18) bred for high leaf vigour, found that the latter grew best in unploughed soil. They suggested faster root growth, different exudates promoting more beneficial rhizosphere microflora, or modified shoot responses as possible mechanisms for the superior growth of Vigor 18. Hence, vigorous genotypes may present an opportunity for increased productivity under reduced tillage [<xref ref-type="bibr" rid="scirp.25455-ref38">38</xref>]. The genetic background for allelopathic potential in crops and the inner genetic mechanisms for allelopathic potential are gradually becoming known through the introduction of molecular biological techniques [<xref ref-type="bibr" rid="scirp.25455-ref39">39</xref>]. For example; Wheat-rye translocations involving 1 RS are also widely used in wheat breeding programmes [<xref ref-type="bibr" rid="scirp.25455-ref40">40</xref>] and have been shown to improve root characteristics, it to be used in breeding programmes to improve weed suppression ability of wheat. The most triticale cultivars, weed biomass could be reduced by 18% - 28%. If early vigour is also improved to the level of triticale, weed biomass could be reduced by 40% - 60%. In spring wheat, an improvement of PAAr by 20% resulted in an average reduction in weed biomass of four near isogenic breeding lines by 19% [<xref ref-type="bibr" rid="scirp.25455-ref41">41</xref>]. Some of the wheat-rye substitution lines showed a PAA value as high as 63%. Further screening it may be possible to find lines with perhaps 70% root inhibition or more. PAA values of that magnitude in new wheat cultivars could provide a viable alternative to the use of herbicides or at least allow reduced use of herbicides [<xref ref-type="bibr" rid="scirp.25455-ref42">42</xref>].</p></sec><sec id="s5"><title>5. TOXICITY OF WHEAT ALLELOPATHY</title><p>Autotoxicity is an intraspecific allelopathy occur when a plant species releases chemical substances that inhibit or delay germination and growth of the same plant species. Application of the concepts of allelopathy and autotoxicity in depicting the chemical interactions between varieties [<xref ref-type="bibr" rid="scirp.25455-ref43">43</xref>]. First appeared in an early report, who claimed that the roots of wheat, oats, and certain other crop plants exude chemicals inhibitory to their own seedlings. Since then, autotoxicity has been identified in many field crops, including alfalfa, rice, barley, wheat, asparagus and cucurbit crops [44,45]. Study display that, aqueous extract of wheat differed in varietal autotoxicity and varietal allelopathy, inhibiting wheat germination by 2% - 21%, radicle growth by 15% - 30%, and coleoptile growth by 5% - 20%. These results suggest that careful selection of suitable wheat varieties is necessary in a continuous cropping system in order to minimize the negative impacts of varietal allelopathy and varietal autotoxicity [<xref ref-type="bibr" rid="scirp.25455-ref46">46</xref>]. Confirmation under controlled environments showed that wheat residue water extracts were autotoxic to the germination and seedling growth of wheat. In solution culture, Protic, et al., found that wheat seedling root volume, total root area and active root area were decreased with an increase in the quantity of the wheat residue amended into the nutrient solution [47,48].</p></sec><sec id="s6"><title>6. ALLELOPATHIC CROP</title><p>Wheat has caused allelopathic inhibition to the growth and yield of crops such as rice, barley, rye (Secale cereale L.), cotton (Gossypium hirsutum L. Merr) and soybean (Glycine max L. Merr). Wheat straw was also allelopathic to a number of forage crops including sorghum (Sorghum bicolor L. Moench), sunflower, pearl millet (Pennisetum glaucum L.), clusterbean (Cyamopsis tetragonoloba L.), cowpeas (Vigna unguiculata L. Walp.) and mulberry [49,50].</p><sec id="s6_1"><title>6.1. Sorghum and Sunflower (Example)</title><p>Research indicates that, Sorghum and sunflower are well studied allelopathic crops [51,52]. Sorghum (Sorghum bicolor) is often chosen as a summer cover crop because of its rapid growth and ability to suppress weeds. Spring-planted sorghum residues provided up to 90% reductions in weed. Sorghum (Sorghum bicolor L.). It is the root hairs that are responsible for the exudation of the allelochemical. Contains gallic acid, protocateuic acid, syringic acid, vanillic acid, p-hydroxybenzoic acid, p-coumaric acid, benzoic acid, ferulic acid, m-coumaric acid, caffeic acids, p-hydroxybenzaldehyde and sorgoleone [53,54]. In which sorgoleone that the usefulness of early vigour and PAA to improve weed suppression is also dependent on the available genetic variation, heritability and whether the traits are correlated negatively or positively to yield. The usefulness of early vigour for breeding purposes is well documented, with high variation and heritability for 6this trait [<xref ref-type="bibr" rid="scirp.25455-ref55">55</xref>]. Other, sunflower (Helianthus annuus) shows strong weed suppression. Anaya reported that soil incorporation of sunflower residues markedly inhibited density of dicot weeds by 66% and controlled 85% of total weed growth. Sunflower possesses chlorogenic acid, isochlorogenic acid, α-naphthol, scopolin and annuionones [56-59].</p><p>The sorghum and sunflower of many allelochemicals responsible for inhibitory action of these two crops have been identified. For example, mung bean (Vigna radiata), cotton (Gossypium hirsutum), wild oat and canary grass et al. In which, the sorghum (Sorghum bicolor L. Moench) and sunflower (Helianthus annuus L.) extracts for wild oat and canary grass management in wheat (Triticum aestivum). The sorghum + sunflower extracts combined of label rates of herbicides inhibited dry matter production of wild oat by up to 89% and canary grass by up to 92% [60-62]. Also, herbicide use can be reduced by up to 50%. Further to explore the possibility of reducing herbicide use by 75% [<xref ref-type="bibr" rid="scirp.25455-ref63">63</xref>].</p></sec><sec id="s6_2"><title>6.2. Mulberry Allelopathy (Example)</title><p>The allelopathic effects of mulberry on weeds and crops have been reported [64,65]. Can reduced the density and dry weight of weeds, In which included Bermudagrass. Bermudagrass has been classified as a noxious and common weed in the most cultivated areas of Africa, Australia, southern Europe, and Asia. It is considered to be one of the ten worst weeds in the world [66,67]. The mulberry (Morus alba) leaf water extracts on bermudagrass (Cynodon dactylon) and wheat (Triticum aestivum) were investigated. Four concentrations of extract (25%, 50%, 75%, and 100%) were compared with a control (distilled water).The results revealed that the pregermination application of 100% mulberry leaf water extract resulted in the complete inhibition of bermudagrass and wheat germination. However, postemergence, two foliar sprays suppressed only the growth of bermudagrass and promoted wheat growth. Further study display that the mulberry leaf water can decreased the germination of wheat when applied pre-emergence in the laboratory bioassay. However, the postemergence application significantly promoted wheat growth. The 100% mulberry leaf water extract had maximum activity on wheat. The selective action of the mulberry extract may be used as a foliar spray (early postemergence) at 12 L ha-1 to increase the growth and yield of wheat [<xref ref-type="bibr" rid="scirp.25455-ref68">68</xref>].</p></sec></sec><sec id="s7"><title>7. CONCLUSION</title><p>Allelopathy has been a core theme of the agricultural research, it has been a complex and variable topic. The main reason for the variability of allelopathic crop materials involves effectiveness of cooperation and the antagonism mechanism. Modern agricultural research investigating it on the basis of genetic level mainly focusing on the relationship between each genetic factor which has achieved certain results, yet there still have been more potential problems to be further solved. Wheat is the stable food for the mankind, therefore, conducting more research on wheat allelopathy in regards to the effects to the yield and quality of crops is significant in order to contribute to the human life as a whole.</p></sec><sec id="s8"><title>8. ACKNOWLEDGEMENTS</title><p>This study was supported by Funding from Innovation and Technology Support Programme, the Government of the Hong Kong Special Administrative Region No. ITS/313/11 and Seed Funding Programme for Basic Research from The Hong Kong University No. 201111159043.</p></sec><sec id="s9"><title>REFERENCES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.25455-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Lemerle, D., Verbeek, B. and Orchard, B. (2001) Ranking the ability of wheat varieties to compete with Lolium rigidum. Weed Research, 41, 197-209.  
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