- freely available
Agronomy 2013, 3(1), 13-27; doi:10.3390/agronomy3010013
Abstract: In this work, we evaluate the role of agronomic factors in the selection for herbicide resistance in Apera spica-venti L. Beauv. (silky windgrass). During a period of three years, populations were collected in more than 250 conventional fields across Europe and tested for resistance in the greenhouse. After recording the field history of locations, a geo-referenced database has been developed to map the distribution of herbicide-resistant A. spica-venti populations in Europe. A Logistic Regression Model was used to assess whether and to what extent agricultural and biological factors (crop rotation, soil tillage, sowing date, soil texture and weed density) affect the probability of resistance selection apart from the selection pressure due to herbicide application. Our results revealed that rotation management and soil tillage are the factors that have the greatest influence on the model. In addition, first order interactions between these two variables were highly significant. Under conventional tillage, a percentage of winter crops in the rotation exceeding 75% resulted in a 1280-times higher risk of resistance selection compared to rotations with less than 50% of winter crops. Under conservation tillage, the adoption of >75% of winter crops increased the risk of resistance 13-times compared to rotations with less than 50% of winter crops. Finally, early sowing and high weed density significantly increased the risk of resistance compared to the reference categories (later sowing and low weed density, respectively). Soil texture had no significant influence. The developed model can find application in management programs aimed at preventing the evolution and spread of herbicide resistance in weed populations.
Chemical weed control through the use of herbicides has gained an increasing popularity among farmers over the last six decades. Since their appearance on the market, herbicides revolutionized the traditional concept of plant protection by removing weeds selectively, while avoiding labor-intensive and time-consuming soil cultivation practices, which ultimately resulted in cost-effective, safe and profitable food production .
For these reasons, herbicides represent the most extensively used weed control measure, accounting for up to 50% of the global plant protection market . The high adaptability potential of weeds together with herbicide over-reliance have resulted in the selection for herbicide-resistant weed populations on a large scale . At present, 210 weed species (~58% dicotyles and ~42% monocotyles) worldwide have evolved resistance to different herbicide modes of action . Recommendations for delaying the evolution of herbicide resistance have been mainly focused on herbicide rotation and herbicide mixtures [5,6]. However, other factors are known to affect the evolution of herbicide resistance in weed populations.
The recent trend of increase in proportion of autumn-sown crops in the agricultural systems of Central and Eastern Europe has promoted the incidence of a specialized weed flora [1,7]. This ultimately led to significant income losses deriving from the increased costs for weed control , whose effectiveness and profitability can be jeopardized by herbicide resistance.
Soil tillage is another management measure that plays an important role in the spread of weed populations, potentially including resistant ones. In fact, although reduced (e.g., tine cultivation prior to drilling) and no-till methods are likely to have several benefits (e.g., conservation of soil moisture and structure, reduction of water and wind erosion, time optimization and lower work inputs), they can also promote the germination of certain weed species as a consequence of the permanence of their seeds in the upper soil layers . This eventually results in higher rates of seedling emergence and population density, faster spread throughout the fields and higher competition ability, which may increase the likelihood of resistance emerging.
Finally, sowing date and weed density have a relevant impact on weed seed production, selection and survival . In particular, early sowing and high weed density may enhance crop-weed competition, which eventually results in the short-term spread of weeds  and, therefore, in increased probability of resistance development.
Among the numerous weed species spread worldwide, Apera spica-venti L. Beauv. (silky windgrass) is one of the most abundant in the agricultural fields of Central and Eastern Europe. It is an annual grass weed that can be mostly found in winter crops, especially in winter cereals and winter oilseed rape (Brassica napus L.) [7,10]. The seeds exhibit short primary dormancy [11,12] and germinate in late summer and fall, mostly on light-textured, humid soils [13,14]. Nevertheless, during mild winters, the seeds may continue to germinate, eventually causing infestations also in spring-sown crops [7,15]. Despite the presence of A. spica-venti also in North America and Canada, its relevance is higher in the Central and Eastern part of Europe (Germany, Switzerland, Poland, the Czech Republic, Slovakia and Hungary) and more recently in Northern Europe (Denmark and Sweden) . The economic importance of this weed has been quantified in yield losses of up to 30% , and the economic threshold has been estimated at ~10–30 plants m−2 . As the weed overgrows the crop during the last phenological development stages (July), A. spica-venti strongly competes for light . During the last years, reports on herbicide-resistant A. spica-venti populations have accumulated .
In 1994, the first case of resistance to photosystem II (PSII)-inhibiting herbicides was reported in Switzerland . Since then, several cases have been documented. In 1997, the first case of PSII-resistance was reported in Germany ; in 2005, three cases of resistance to acetolactate synthase (ALS)-inhibiting herbicides were documented in Poland, the Czech Republic and Germany [20,21,22]; in 2006, the first case of resistance to ALS-inhibitors was confirmed in Switzerland ; and in 2009, the first case of multiple resistance to PSII-, ALS- and acetyl-CoA-carboxylase (ACCase)-inhibiting herbicides was reported in Germany .
The objectives of this study were: (1) to develop a GIS (geographic information system) database for mapping the spread of herbicide-resistant A. spica-venti populations across Europe; (2) to assess and quantify the relative influence of crop rotation, soil tillage, sowing date, soil texture and weed density on the likelihood of resistance emergence in A. spica-venti; and (3) to provide farmers and consultants with rational and practicable solutions at the agronomic level aimed at preventing the evolution and spread of herbicide resistance in European cereal production systems.
2. Results and Discussion
2.1. Logistic Regression Analysis
The results of the greenhouse screening revealed that 80% of populations (210) were resistant to herbicides (mainly ALS-inhibitors), whereas resistance could not be confirmed in 53 cases (~20%). A great part of the investigated fields (72%) was characterized by a high percentage of winter crops in the rotations (>75%), whereas the rest of the cases (50%–75% and <50%) had a smaller proportion. Early sowing was less represented than middle and late sowing, accounting for 30% of total observations. Finally, conventional/conservation soil tillage and low/high weed density had a similar proportion in their categories (Table 1).
|Yes (%)||No (%)|
|No (not verified)||20.2|
|Crop Rotation *|
|Sowing Date **|
|Soil Texture ***|
|Weed Density ****|
* % of winter crops in the rotation; ** (winter crops) Early: until October 05; Middle: until October 15; Late: after October 15; *** Light: sandy; Middle: sand-clay/silt; Heavy: clay/silt; **** Plants m−2 (Low: <10; Middle: 10–40; High: >40).
The developed LRM showed a good fitness, calibration and discrimination (Table 2). According to the Nagelkerke R2, the model could explain the 64% of total variability in selection for herbicide resistance. The discrimination capacity of the fitted model resulted in 90% of correctly classified cases, with greater sensitivity (it correctly classified 97% of resistant cases) than specificity (it correctly classified 64% of non-resistant cases). ROC analysis showed a good discrimination, with an AUC of 0.92 (95% CI: 0.88–0.97) (Figure 1).
|Statistical method||Value||Degrees of freedom||p-value|
|Goodness of fit|
|Log Likelihood (LL)||−64.10|
|DiscriminationPercentage of correct classification||90.1|
LRM for the predictors resulted in two predictors with greater relative influence on the model. All factors, except for soil texture (p = 0.614), were statistically significant at 95% (crop rotation, soil tillage, sowing date and the interaction between crop rotation and soil tillage) and 90% confidence level (weed density). Rotation management, soil tillage and their interactions were the most important predictor variables (Table 3).
According to the analyzed data, the highest risk of herbicide resistance occurred in the presence of a high proportion of winter crops in the rotations (>75%); in these cases, under conventional tillage, the probability of resistance selection showed to be 1274.82-times higher compared to <50% of winter crops. This probability decreased as the proportion of spring-sown crops in the rotation increased (50%–75% of winter crops under conventional tillage), reaching the limit of 21.13-times compared to <50% of winter crops. Finally, under conservation tillage, a high percentage of winter crops in the rotations (>75%) resulted in a 12.75-fold increase of resistance selection compared to <50% of winter crops.
|Factors a||ORb||ORc||Wald||95% CI||% d|
|Crop Rotation (ref. <50%)||36.69||53.38|
|Tillage (ref. Plow)||2.49||87.67 **||10.05||5.52–1393.08||14.62|
|Sowing Date (ref. Middle/Late)||2.44||4.65 **||6.91||1.48–14.61||10.05|
|Weed Density (ref. Low/Middle)||1.96||2.11 *||2.31||0.81–5.52||3.36|
|Rotation * Tillage (ref. <50% & Plow)||12.77||18.58|
|(50%–75%) & (Reduced/ No–Till)||0.04 **||4.61||0.00–0.75|
|(>75%–100%) & (Reduced/ No–Till)||0.01 **||12.13||0.00–0.09|
* Factor significant at 90% confidence level (p-value ≤ 0.100); ** Factor significant at 95% confidence level (p-value ≤ 0.050); a The displayed factors are maintained in the final model after the modeling process; b Crude Odds Ratio (OR); c Adjusted Odds Ratio (OR); d Relative contribution of predictors.
The rest of the agronomic factors also resulted in a potential risk of resistance emergence. Early sowing and high density of A. spica-venti (>40 plants m−2) increased the probability of resistance selection 4.65- and 2.11-times compared to later sowing and lower densities, respectively (Table 3). In conclusion, the predominant presence of winter crops (>75%) in the rotation systems, together with conservation tillage, early sowing and high population density lead to a higher chance of herbicide resistance in A. spica-venti (Figure 2). Also, the effect of soil tillage under crop rotation practices significantly affects the selection of resistance.
Our results underline the role of farm management in the development of herbicide resistance. In fact, most interviewed farmers had reported reduced herbicide performance in the last 1–3 years despite adoption of rational chemical weed control strategies (single herbicide applications at the recommended field rate, tank mixtures and/or rotation of active ingredients). Statistical analysis of the collected data revealed that each factor, with the exception of soil texture, significantly increased the likelihood of resistance development.
Rotation management proved the most significant factor influencing the probability of resistance selection in A. spica-venti. In particular, a proportion of winter crops in the rotations exceeding 75% greatly increases the risk of herbicide resistance compared to situations in which winter and summer crops are more evenly distributed over the years. This is in accordance with most existing literature and can be attributed to two main reasons: (1) continuous cropping tends to favor and select the species within the weed flora that have phenological and physiological similarities to the crop (e.g., grass weeds in cereals) [24,25]. This eventually results in the establishment of an adapted, resilient weed flora with more competition ability, as it would be in a more diverse cropping system [25,26]; and (2) in consequence of repeated use of the same cultural practices over several years, the tolerance of weeds to the direct control methods (e.g., chemical weed control) is likely to develop and spread more quickly .
Also, conservation tillage practices resulted in an increased risk of resistance development in A. spica-venti compared to conventional tillage situations (e.g., moldboard plowing). It has been widely documented that low soil disturbance systems can cause a shift of the weed flora towards a troublesome composition . In the case of winter cereal cropping systems, for example, minimum tillage practices can promote the dominance of grasses with low-dormant seeds (e.g., Alopecurus myosuroides, A. spica-venti, Bromus spp.) within only a few years . Consequently, annual grass weeds, especially those whose seed anatomy enables easy wind dispersion, are becoming more prevalent since the adoption of conservation tillage practices [26,27].
Nevertheless, the significant interactions between rotation management and soil tillage evidenced the importance of combining appropriate rotation systems (i.e., a higher proportion of summer crops) with conventional tillage to reduce the risk of resistance development in A. spica-venti. In fact, even where conventional tillage is used, agricultural systems tending to monoculture are still at risk of resistance. On the other hand, if a percentage of winter crops exceeding 75% is foreseen in the rotation, the adoption of conservation tillage will increase the risk of resistance compared to a situation in which less than 50% of winter crops are foreseen in the rotation.
Sowing date confirmed as well its influence on the likelihood of resistance selection in A. spica-venti populations. Results revealed that early sowing of the winter crop increased the risk of herbicide resistance when compared to later sowing dates. Studies have shown that weed species characterized by early germination are favored by early sowing. Hartzler (2000) , for example, documented the correlation between the increase in the selection of Ambrosia trifida L. (giant ragweed) in the cropping regions of the U.S.A. and the move to earlier sowing dates of maize and soybean; this was consequent to weed seedling emergence after planting, which results in reduced effectiveness of control measures in both pre- and post-emergence. As A. spica-venti is a weed notoriously characterized by a short dormancy period and early emergence, the anticipation of winter crop sowing dates can play a decisive role in promoting recurrence of infestations and, therefore, increasing the risk for selection of herbicide-resistant populations. This problem can be particularly relevant in years with favorable weather conditions, which promote high seed germination rates, high population densities and, ultimately, higher competition ability.
Finally, high A. spica-venti densities proved to increase the likelihood of resistance selection. In accordance with several sources, weed density can have a relevant influence on the rate of herbicide resistance development (e.g., higher weed competition ability, higher seed production and faster spread and reduced penetration of herbicides into the plant foliage) . Overall, this factor resulted in A. spica-venti being twice as prone to evolve resistance in high density patches as in areas with low weed density.
The role of soil texture in the probability of resistance selection in A. spica-venti could not be statistically confirmed. Although the preference of this weed for light-textured soils (i.e., sandy soils) has been widely documented, most infested fields were characterized by a middle soil texture. Light soils (i.e., sandy soils) and heavy soils (i.e., clay soils) were under-represented.
3. Experimental Section
3.1. Sampling Strategy
Harvesting of A. spica-venti seeds took place over a period of three years (from 2007 till 2010) at 263 conventional fields across Europe (Germany, Poland and the Czech Republic). The provenance of the populations was homogenously distributed across the three countries (40% from Germany, 30% from Poland and 30% from the Czech Republic). The winter cropping system mainly consisted of wheat, barley and oilseed rape. Most of the interviewed farmers had observed reduced herbicide performance (especially ALS-inhibitors) over a 1 to 3 year period. Weed control consisted mostly of single herbicide applications in the spring (March-April). Seed collection was performed randomly throughout the fields, in different patches across each field and from different plants (>60 panicles) shortly before winter crop harvest. Samples were taken at a distance of more than 4 m from the field borders. Finally, the seeds collected from each field were pooled together (i.e., mixed populations) and stored accordingly at 4 °C until ready for greenhouse screening.
3.2. Screening for Herbicide Resistance
3.2.1. Greenhouse Screening: Seed Germination Tests
Seed germination tests were performed after breaking of primary dormancy. One hundred ripe seeds per population (in six replicates) were sown in 6 by 6 cm paper pots (Jiffy® Pots, Jiffy Products Ltd., Winchester, UK). Each pot was filled with sterilized sandy loam soil (5.1% organic carbon content; pH 6.9) and kept well-watered. Growing conditions consisted of 20/15 °C (with a 12 h photoperiod) and a light intensity of 122 µmol m−2 s−1. After 7–10 days, emerged seedlings per pot were counted.
3.2.2. Greenhouse Screening: Whole-Plant Pot Assays
A variable amount of seeds for each collected population (depending on the germinative ability) was sown in 8 by 8 cm paper pots (Jiffy® Pots, Jiffy Products Ltd., Winchester, UK) (in three replicates, according to standard experimental design) to give at least 20 plants per pot. Growing conditions were the same as above. Plants were kept well-watered and fertilized twice a week until harvest (8-8-6 N-P-K) (Wuxal® Super, Horticentre Ltd., Drury, New Zealand).
Herbicide treatments were carried out at the 2–3 leaf stage (BBCH 12-13) using a precision spray chamber (Aro, Langenthal, Switzerland). The tested herbicides consisted of five ALS-inhibitors [Lexus® (flupyrsulfuron-methyl 50% w/w), DuPont de Nemours; Glean® (chlorsulfuron 75% w/w), DuPont de Nemours; Monitor® (sulfosulfuron 80% w/w), Monsanto; Atlantis® OD (mesosulfuron-iodosulfuron 1.24% w/v), Bayer CropScience; Oust® XP (sulfometuron-methyl 75% w/w), DuPont de Nemours], two ACCase-inhibitors [Ralon® Super (fenoxaprop-P-ethyl 6.9% w/v), DuPont de Nemours; Select® 240 EC (clethodim 24.1% w/v), Stähler] and one PSII-inhibitor [Arelon® flüssig (isoproturon 50% w/v), Stähler] (Table 4). The appropriate surfactants [Trend® 90 (isodecyl alcohol ethoxylate 90% w/v), DuPont de Nemours; MonFastTM (ethoxylated fatty alcohol 60% w/v), Monsanto; Parasommer® (paraffin oil 65.4% w/v), Stähler] were added when necessary according to suppliers’ recommendations. The delivery volume (8004 EVS, Teejet® spraying systems Co., Illinois, USA) was calibrated to spray 400 L ha−1. The velocity of the nozzle was set at 800 mm s−1, the distance from the sprayed surface at 500 mm and the spraying pressure at 300 kPa. All herbicides were tested at the recommended field rate (according to manufacturer`s instruction for the control of A. spica-venti) and the fourfold of it. The purpose of the fourfold application rate was to clearly discriminate target site resistant populations for further laboratory investigations (data not shown). Two reference standards (herbicide-susceptible and herbicide-resistant) were included in each assay. Both standards were chosen following previous greenhouse investigations (data not shown). Herbicide performance was evaluated 15 and 30 days after treatment (DAT) according to OEPP/EPPO (European and Mediterranean Plant Protection Organization) guidelines . Finally, resistance was classified into two main categories: resistant and non-resistant (susceptible).
|Trade nameSurfactant (%)||Active ingredient (a.i.)||Amount of active ingredient (g a.i./Kg-L)||Applied doses (g a.i./ha)|
|Lexus® Trend 90® * (0.1%)||flupyrsulfuron-methyl||500||15, 60|
|Glean® Trend 90® (0.1%)||chlorsulfuron||750||15, 60|
|Monitor® MonFastTM ** (0.1%)||sulfosulfuron||800||10, 40|
|Atlantis® OD||mesosulfuron iodosulfuron||10.44 2||7.4, 29.6|
|Oust® XP Trend 90® (0.1%)||sulfometuron-methyl||750||37.5, 150|
|Ralon® Super Trend 90® (0.1%)||fenoxaprop-P-ethyl||69||82.8, 331.2|
|Select® 240 EC Parasommer® *** (0.5%)||clethodim||241.9||241.9, 967.6|
|Arelon® flüssig||isoproturon||500||1500, 6000|
* active ingredient: isodecyl alcohol ethoxylate (DuPont de Nemours); ** active ingredient: fatty alcohol ethoxylate (Monsanto); *** active ingredient: paraffin oil (Stähler).
3.3. Field History
The field history of the samples was provided by the farmers, who were requested to complete questionnaires reporting the following information: (1) field location (GPS coordinates or address); (2) crop rotation of the last 5–7 years, (3) soil tillage, (4) soil texture, (5) sowing date of the winter crop and (6) weed density. Categories within each factor are shown in Table 1. The factors 2–6 functioned as explanatory variables for the developed model. The results of greenhouse assays for verification of actual resistance after herbicide treatment functioned as categorical response for the model, using “yes” (resistance confirmed) and “no” (resistance not confirmed).
3.4. Technical Features of the GIS Database “Weedscout”
The information obtained from the questionnaires (field history) and the results of greenhouse assays (resistant/non-resistant) was used to develop a database in which the distribution of herbicide-resistant A. spica-venti populations is mapped. Weedscout 2.0, provided by Proplanta (Proplanta GmbH & Co. KG, Stuttgart, Germany), is a geo-referenced database and role-based web application for the storage, management and spatial representation of weed species and other location-related parameters. The multilingual administration interface of the software is based on the HTML PUBLIC “-//W3C//DTD HTML 4.01 Transitional//EN”, which is CCS3-compliant and Crossbrowser compatible (IE 6.0+®, FF 2+®, Safari 3.0+®, Opera 9.0+®, Chrome®). The server-side scripting language is based on PHP® 5.2.10 and the web database on MySQL® 4.0.27-standard de-iso-8859-1.
The cartographic representation of the data (available in aerial and terrain view) is run by Google maps 2.0. Different zoom levels allow detailed view of target areas. An online form was created for the upload of raw data (questionnaires), with the geocoding (i.e., the conversion of addresses into geographic coordinates) being automatically carried out by Google GClientGeocoder (Google maps-API). If no exact address can be given, the GPS coordinates (i.e., longitude and latitude) of locations are obtained through the marker function of Google Maps and automatically transferred into the form. After the greenhouse assays for verification of herbicide resistance, each population was identified by a colored flag, which is red in the case of verified resistance, green in the case of unverified resistance and yellow in the case of suspected populations that could not be tested due to seed scarcity or inability to germinate (Figure 3). The search results can be modulated by several filters (e.g., country, populations of interest and weed species), and specific geo-tools allow the calculation of distances and surfaces. Finally, an export function enables the backup and processing of metadata in XLS format.
The advantages of developing a geo-referenced database of herbicide-resistant A. spica-venti populations across Europe are manifold: (1) easy and fast acquisition of data for different purposes (not limited to herbicide resistance); (2) easy and fast acquisition of spatiotemporal features (e.g., evolution and spread of herbicide-resistant populations); (3) easy access to other GIS sources, such as point locations, distances and further documentary data; and (4) the creation of a specific weed database with global coverage ability. Further benefits include: (1) online access, which enables users to work on their data safely and effectively (many users can work on their own data at the same time); (2) free scalability, which enables data analysis at different levels (global, national, regional and target-specific); and (3) multi-filtering features, which enable flexible access to the metadata through the selection of specific criteria (weed species, populations of interest, country of provenance, field history etc.).
Overall, the developed database represents a useful instrument for studies aimed at monitoring the evolution and spread of herbicide resistance in A. spica-venti populations over time and space, thus allowing precise identification of agricultural areas with a potential risk of resistance.
3.5. Presentation of the Model and Statistical Analyses of the Data
Statistical analyses of the collected data were performed with the software SPSS® 15.0 (SPSS Inc., Chicago, IL, USA). The relationships between variables were analyzed using Spearman correlations, multicollinearity detection and contingency tables. A Logistic Regression Model (LRM) was used to describe the relationships of the explanatory variables (crop rotation, soil tillage, soil texture, sowing date and weed density) and first order interactions with herbicide resistance.
Logistic regression is a statistical method that uses one or more explanatory variables to predict the probability of a categorical response [31,32,33]. The response variable in LRM is the log of the odds ratio (logit). The logit transforms a variable constrained between zero and one (p) into a continuous variable, which is linear with respect to the vector of the explanatory variables:
In the ROC (receiver operating characteristic) analysis, sensitivity (true positive rate) is plotted against 1-specificity (false positive rate) to show the relationship between true positives (i.e., resistant cases correctly classified by the model) and false positives (i.e., non-resistant cases wrongly classified by the model). The area enclosed under the curve (AUC) is a measure of the overall performance of the predictive model and is expressed as the average value of sensitivity for all possible values of specificity. The perfect classification corresponds to 100% sensitivity (no false negatives) and 100% specificity (no false positives), with AUC = 1. The differences between the log likelihood of the full model and the log likelihood of a model without each predictor variable were calculated. The relative contribution of a predictor variable was defined as the ratio of its log likelihood difference to the sum of the all log likelihood differences multiplied by 100 .
In conclusion, this study confirmed the significant role of rotation management, soil tillage, sowing date and weed density in the selection of herbicide resistance in A. spica-venti. According to these results, growers should focus more effort on preventing the evolution and spread of herbicide-resistant populations. The rotation of crops having different growing periods is a mandatory management measure for ‘breaking’ the regular life cycle of weeds and delaying the selection of resistant plants. This should be corroborated by the adoption of conventional tillage methods (i.e., plowing) to suppress seedling emergence from deep soil layers. In fact, the inversion of soil layers after the light induction of the seeds (which is necessary for germination) will result in impaired emergence of the deeply buried seedlings (“fatal germination”) and, therefore, in reduced weed density and more effective control . Further measures should include increased crop competitiveness (e.g., higher seed density) for keeping weed population density as low as possible. Finally, early sowing of winter crops should be avoided when dealing with A. spica-venti infestations, as delaying the sowing date would facilitate weed suppression by seedbed preparation prior to planting. These measures, adequately combined together, will provide growers with useful tools for preventing and containing the spread of A. spica-venti in arable lands and will result in the decreased likelihood of herbicide resistance. Strategies relying solely on rotation of herbicide modes of action, although undoubtedly effective, will not ultimately result in successful long-term management of A. spica-venti in intensive cropping systems.
This project was funded by the DFG (Deutsche Forschungsgemeinschaft) and the companies Bayer CropScience, DuPont de Nemours and Monsanto Agrar Deutschland.
- Melander, B. Impact of drilling date on Apera spica-venti L. and Alopecurus myosuroides Huds. in winter cereals. Weed Res. 1995, 35, 157–166. [Google Scholar] [CrossRef]
- Zwerger, P.; Ammon, H.U. Unkraut: Ökologie und Bekämpfung; Eugen Ulmer: Stuttgart, Germany, 2002. [Google Scholar]
- Owen, M.J.; Walsh, M.J.; Llewellyn, R.S.; Powles, S.B. Widespread occurrence of multiple herbicide resistance in Western Australian annual ryegrass (Lolium rigidum) populations. Aust. J. Exp. Agric. 2007, 58, 711–718. [Google Scholar]
- Heap, I.M. International Survey of Herbicide Resistant Weeds. Available online: http://www.weedscience.org (accessed on 5 December 2012).
- Hatzios, K.K.; Penner, D. Interaction of herbicides with other agricultural chemicals in higher plants. Weed Sci. 1985, 1, 1–64. [Google Scholar]
- Beckie, H.J.; Hall, L.M.; Meers, S.; Laslo, J.J.; Stevenson, F.C. Management Practices Influencing Herbicide Resistance in Wild Oat. Weed Technol. 2004, 18, 853–859. [Google Scholar] [CrossRef]
- Melander, B.; Holst, N.; Jensen, P.K.; Hansen, E.M.; Olesen, J.E. Apera spica-venti population dynamics and impact on crop yield as affected by tillage, crop station, location and herbicide programmes. Weed Res. 2008, 48, 48–57. [Google Scholar] [CrossRef]
- Murphy, C.; Lemerle, D. Continuous cropping systems and weed selection. Euphytica 2006, 148, 61–73. [Google Scholar] [CrossRef]
- Mohler, C.L. Ecological bases for the cultural control of annual weeds. J. Prod. Agric. 1996, 9, 468–474. [Google Scholar]
- Hurle, K. Integrated management of grass weeds in arable crops. In Proceedings of the Brighton Crop Protection Conference—Weeds, Brighton, UK, 22–25 November 1993; pp. 81–88.
- Koch, W.; Hurle, K. Grundlagen der Unkrautbekämpfung; UTB Verlag: Stuttgart, Germany, 1978. [Google Scholar]
- Wallgren, B.; Avholm, K. Dormancy and Germination of Apera spica-venti L. and Alopecurus myosuroides Huds Seeds. Swed. J. Agric. Res. 1978, 8, 11–15. [Google Scholar]
- Rola, J. Dynamik von Unkrautpopulationen auf leichten Böden in Polen. J. Plant Dis. Prot. 1990, Special Issue XII, 97–100. [Google Scholar]
- Northam, F.E.; Callihan, R.H. The windgrasses (Apera Adans., Poaceae) in North America. Weed Technol. 1992, 6, 445–450. [Google Scholar]
- Andreasen, C. The Occurrence of Weed Species in Danish Arable Fields. Ph.D. Thesis, Department of Agricultural Sciences, The Royal Veterinary and Agricultural University, Copenhagen, Denmark, 1990..
- Gehring, K.; Thyssen, S. Unkraut-Steckbrief, Windhalm. Bayerische Landesanstalt für Landwirtschaft, Institut für Pflanzenschutz. Available online: http://www.lfl.bayern.de (accessed on 4 September 2012).
- Kötter, U. Entwicklung und Konkurrenzverhalten von Windhalm (Apera spica-venti) in Winterweizen und Winterroggen. Gesunde Pflanzen 1991, 4, 184–189. [Google Scholar]
- Mayor, J.P.; Maillard, A. A wind bent grass biotype resistant to the herbicide isoproturon found in Changins. Suisse Agric. 1997, 29, 39–44. [Google Scholar]
- Niemann, P. Resistance of silky bentgrass (Apera spica-venti) against Isoproturon. Mitteilungen der Biologischen Bundesanstalt für Land- und Forstwirtschaft 2000, 376, 147–148. [Google Scholar]
- Marczewska, K.; Rola, H. Biotypes of Apera spica-venti and Centaurea cyanus resistant to chlorsulfuron in Poland. In Proceedings of the 13th EWRS Symposium, Bari, Italy, 19–23 June 2005.
- Novakova, K.; Soukup, J.; Wagner, J.; Hamouz, P.; Namestek, J. Chlorsulfuron resistance in silky bent-grass (Apera spica-venti L. Beauv.) in the Czech Republic. J. Plant Dis. Prot. 2006, Special issue XX, 139–146. [Google Scholar]
- Balgheim, N.; Wagner, J.; Gerhards, R. ALS-inhibitor resistant Apera spica-venti (L.) Beauv. due to target-site mutation. In Proceedings of the 14th European Weed Research Society Symposium, Hamar, Norway, 17–21 June 2007.
- Delabays, N.; Mermillod, C.; Bohren, C. First case of resistance to sulfonylurea herbicides reported in Switzerland: A biotype of loose silky-bent (Apera spica-venti (L.) Beauv.). J. Plant Dis. Prot. 2006, Special Issue XX, 139–146. [Google Scholar]
- Bárberi, P. Weed Management for Developing Countries, 120 Addendum, 1st; Labrada, R., Ed.; FAO (Food Agricultural Organization of the United Nations): Roma, Italy, 2003. [Google Scholar]
- Cardina, J.; Webster, T.M.; Herms, C.P. Long-term tillage and rotation effects on soil seedbank characteristics. Annals of Applied Biology. 1998, 5, 213–220. [Google Scholar]
- Froud-Williams, R.J.; Chancellor, R.J.; Drennan, D.S.H. Potential changes in weed floras associated with reduced-cultivation systems for cereal production in temperate regions. Weed Res. 1981, 21, 99. [Google Scholar] [CrossRef]
- Gill, G.S.; Poole, M.L.; Holmes, J.E. Competition between wheat and brome grass in Western Australia. Aust. J. Exp. Agric. 1987, 27, 291–294. [Google Scholar] [CrossRef]
- Hartzler, B. Weed population dynamics. In Proceedings of the 2000 Integrated Crop Management Conference, Ames, IA, USA, 20–29 November 2000.
- OEPP/EPPO. General introduction to the EPPO guidelines for efficacy evaluation of plant protection products. OEPP/EPPO Bull. 1989, 19, 183–195.
- Proplanta GmbH & Co. KG. Available online: http://www.proplanta.de (accessed on 19 December 2012).
- Peduzzi, P.; Concato, J.; Kemper, E.; Holford, T.R.; Feinstein, A.R. A simulation study of the number of events per variable in logistic regression analysis. J. Clin. Epidemiol. 1996, 49, 1373–1379. [Google Scholar] [CrossRef]
- Long, J.S. Regression models for categorical and limited dependent variables. Sage Publ. 1997, 7, 11–33. [Google Scholar]
- Pampel, F.C. Logistic regression: A primer. Sage University Papers Series on Quantitative Applications in the Social Sciences. Sage Publ. 2000, 7–132. [Google Scholar]
- Escobar, G.J.; Greene, J.D.; Scheirer, P.; Gardner, M.N.; Draper, D.; Kipnis, P. Risk-adjusting hospital inpatient mortality using automated inpatient, outpatient and laboratory databases. Medical care 2008, 46, 232–239. [Google Scholar] [CrossRef]
- Davis, A.S.; Renner, K.A. Influence of seed depth and pathogens on fatal germination on velvetleaf (Abutilon theophrasti) and giant foxtail (Setaria faberi). Weed Sci. 2007, 55, 30–35. [Google Scholar] [CrossRef]
© 2013 by the authors; licensee MDPI, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).