Morphological differences among Raphanus raphanistrum populations and their relationship to related crops

Wild radish (Raphanus raphanistrum) has developed introgressed populations after hybridization with its cultivated counterpart (R. sativus) in California. Hybridization with various Brassica and Sinapis species is also possible. To determine if hybridization is responsible of the genetic diversity of European populations, six wild radish populations with distinct morphological traits were sampled from geographically distant regions in Europe. Plants were cultivated in an oilseed rape field and in insect‐proof cages. Silique and flower morphology, growth, and reproductive traits were measured. The wild radish populations could be discriminated by the morphological traits, but not related to geographic regions. In particular, populations of one region showed wide variability in terms of silique shape and growth behaviour, and small‐sized flowers. Although the origin of morphological diversity in wild radish is unclear, i.e. native or due to gene flow from the cultivated radish or other Brassicaceae, significant morphological divergence was found that could have relevant effects on plant ecology and adaptation.     

Variation of prezygotic barriers in the interspecific hybridization between oilseed rape and wild radish

Escape of transgenes from genetically modified oilseed rape, Brassica napus, into wild radish, Raphanus raphanistrum, depends on sexual compatibility. The variation in prezygotic barriers of two different cultivars for interspecific hybridization with a population of wild radish was investigated by hand crossing and fluorescence microscopy of pistils. Significant differences were observed between oil seed rape cultivars in their ability to accept wild radish pollen germinating onto their stigma and the rate of fertilization of ovules. Some differences among the pollen donor plants were also detected. These results suggest that the rate of interspecific hybridization in the field would depend upon the oilseed rape cultivar and the genotype composition of the local wild populations. The implication of S-related genes, as revealed through identification by pistil tissue prints of class I and II S-types of SLG (S-Locus Glycoprotein) and SLR1 (S-Locus Related),and immuno-IEF, was not significant. This revised version was published online in August 2006 with corrections to the Cover Date.     

Inheritance of sethoxydim resistance in foxtail millet, Setaria italica (L.) Beauv.

Interspecific hybridization between foxtail millet cultivars (Setaria italica) and a green foxtail (S. viridis) resistant to the herbicide sethoxydim were undertaken to breed foxtail millet for improved herbicide resistance. Parents, reciprocal F₁ hybrids, F₂ selfed derived populations and BC₁ backcross progeny were produced and analysed for mortality and fresh weight over a range of dosages. All resistant progeny were 700 times more resistant than susceptible cultivars and was symptom free under current field dosages. Segregations of resistant and susceptible progeny (3:1 in F₂ and 1:1 in BC₁) were not dependent upon dosage. Heterozygous individuals displayed the same magnitude of resistance as homozygous plants at twelve times the recommended field dosage. Results suggested that sethoxydim resistance in foxtail millet was controlled by a single, completely dominant, nuclear gene. This revised version was published online in July 2006 with corrections to the Cover Date.     

Potential for Selection in the Progeny of an Interspecific Hybrid in Foxtail Millet

Genetic variation for morphology and grain yield components was studied in the F₂ and 14 F₃ families of an interspecific cross of Setaria italica (foxtail millet) with S. viridis s. s. (green foxtail). It appeared possible to recover the cultivated type using a simple selection procedure in F₂ and F₃. Comparison with a cross involving S. viridis var. major (giant green foxtail) is discussed.     

Dinitroaniline Herbicide Cross-Resistance in Resistant Setaria italica Lines Selected from Interspecific Cross with S. viridis

Breeding of herbicide-resistant foxtail millet (Setaria italica (L.) Beauv.) is desirable in modern agriculture because no selective herbicide is available for this crop. Trifluralin-resistant millet lines obtained from a interspecific cross between a resistant green foxtail (Setaria viridis (L.) Beauv.) and a foxtail millet cultivar were tested for response to five dinitroaniline herbicides in greenhouse and field experiments. The results in the greenhouse study showed that the resistant type was cross-resistant to all tested herbicides. ED₅₀ values indicated that the highest resistance was obtained with trifluralin, the resistant biotype being seven and 33 times more resistant than the parent cultivar at the emergence and seedling stages, respectively. However, the doses recommended for efficient weed control resulted in some detrimental effects on emergence and growth in the field. Strategies for use of this resistance to control weeds in millet fields are proposed. © 1997 SCI.     

Longevity,dormancy and germination of Cyanus segetum

Cyanus segetum is an iconic, colourful weed in arable fields that provides ecological and societal services. To understand better both the infestation dynamics of C. segetum as an abundant, harmful weed and maintain sustainable populations where it provides beneficial services, we compared information on seed dormancy, seed longevity and germination conditions in two populations. Persistence of seeds buried in the soil was low, with <10% viable after 3 years. Periodic dormancy cycling was observed over the 4 years in the soil, with a maximum of dormant seeds in the spring and a minimum in the autumn; however, 20% of the seeds were non‐dormant all the time. Seeds of C. segetum were positive photosensitive, but light requirement varied among populations. Base water potential for germination was ?1 MPa. Base temperature ranged from 1 to 2°C. Optimum temperature for germination was about 10 to 15°C, but the mean thermal time varied greatly between populations, from 80 to 134 day °C. Photoperiod and temperature combinations had no effect on germination percentage, but both reduced the germination rate. Burial deeper than 2 cm greatly reduced germination and seedling emergence strongly decreased at depths >0.5 cm. No seeds buried deeper than 8 cm emerged. Low seed longevity and a wide range of germination conditions could partly explain the rapid disappearance of C. segetum populations after herbicide application began in western Europe. However, yearly sowing in restoration areas does not seem to be essential.     

谷子抗除草剂基因从栽培种向其近缘野生种漂移的研究

作物同种及栽培种与近缘野生种之间的基因漂移(基因流)是防范作物品种生物学混杂及评估转基因新种质田间释放后所产生的生态学效应的重要基础参数.本研究以显性抗除草剂(拿捕净)谷子种质作为花粉供体材料,以青狗尾草作为花粉受体材料进行了栽培种向其主要近缘野生种基因漂移的检测研究.研究结果表明,尽管一般认为谷子及其近缘     

Crop and density effects on weed beet growth and reproduction

Weed beet populations growing in each crop of the arable rotation could be a relay for the gene flow from adjacent transgenic herbicide‐resistant sugarbeet. In this study, weed beet growth and reproduction were assessed under several conditions which could be found in the rotation: various weed beet densities (ranging from 1 to 120 plants m^?2) and various crops (winter wheat, spring barley, spring pea, sugarbeet, maize, ryegrass). Measurements were carried out both on life‐cycle dynamics (bolting time, time to flowering onset, dynamics of flower opening) and on other quantitative data (survival rate, bolting rate and pollen, flower and seed production). Increasing weed beet density resulted in decreases in bolting rate and flower and seed production per plant. In cereals, weed beet establishment and reproduction were strongly reduced, compared with bare ground as a control situation. In pea, there was no effect on establishment, but the early harvest limited seed set. In the other crops, flower and seed production were reduced to a lesser extent. Parameters of the fitted equations on the bolting and flowering progress were modified by the weed beet density and by the crop. Our data may be used in a model predicting weed beet demographic evolution according to cropping system, and in assessing gene flow.     

Rapid bidirectional allele-specific PCR identification for triazine resistance in higher plants

Triazine resistance is reported to be due to chloroplast herbicide target insensitivity in most species, and this is most often caused by a Ser(264)-Gly mutation at the D1 protein. In order to ascertain whether this mutation is really predominant amongst resistant plants, and also for gene flow studies, a rapid test is needed that allows the testing of large quantities of plants. Here a bidirectional allele-specific PCR (polymerase chain reaction) identification is proposed. The designed primers were shown to be universal in the three grass and three broadleaf species examined.     

Pleiotropic effects of herbicide‐resistance genes on crop yield: a review

The rapid adoption of genetically engineered herbicide‐resistant crop varieties (HRCVs)—encompassing 83% of all GM crops and nearly 8% of the worldwide arable area—is due to technical efficiency and higher returns. Other herbicide‐resistant varieties obtained from genetic resources and mutagenesis have also been successfully released. Although the benefit for weed control is the main criteria for choosing HRCVs, the pleiotropic costs of genes endowing resistance have rarely been investigated in crops. Here the available data of comparisons between isogenic resistant and susceptible varieties are reviewed. Pleiotropic harmful effects on yield are reported in half of the cases, mostly with resistance mechanisms that originate from genetic resources and mutagenesis (atrazine in oilseed rape and millet, trifluralin in millet, imazamox in cotton) rather than genetic engineering (chlorsulfuron and glufosinate in some oilseed rape varieties, glyphosate in soybean). No effect was found for sethoxydim and bromoxynil resistance. Variable minor effects were found for imazamox, chlorsulfuron, glufosinate and glyphosate resistance. The importance of the breeding plan and the genetic background on the emergence of these effects is pointed out. Breeders' efforts to produce better varieties could compensate for the yield loss, which eliminates any possibility of formulating generic conclusions on pleiotropic effects that can be applied to all resistant crops. © 2013 Society of Chemical Industry