Like conventional crops, some GM cultivars may readily hybridize with their wild or weedy relatives. The progressive introgression of transgenes into wild or weedy populations thus appears inevitable, and we are now faced with the challenge of determining the possible evolutionary effects of these transgenes. The aim of this study was to gain insight into the impact of interspecific hybridization between transgenic plants and weedy relatives on the evolution of the weedy phenotype.
Experimental populations of weedy birdseed rape (Brassica rapa) and transgenic rapeseed (B. napus) were grown under glasshouse conditions. Hybridization opportunities with transgenic plants and phenotypic traits (including phenological, morphological and reproductive traits) were measured for each weedy individual. We show that weedy individuals that flowered later and for longer periods were more likely to receive transgenic pollen from crops and weed×crop hybrids. Because stem diameter is correlated with flowering time, plants with wider stems were also more likely to be pollinated by transgenic plants. We also show that the weedy plants with the highest probability of hybridization had the lowest fecundity.
Our results suggest that weeds flowering late and for long periods are less fit because they have a higher probability of hybridizing with crops or weed×crop hybrids. This may result in counter-selection against this subset of weed phenotypes, and a shorter earlier flowering period. It is noteworthy that this potential evolution in flowering time does not depend on the presence of the transgene in the crop. Evolution in flowering time may even be counter-balanced by positive selection acting on the transgene if the latter was positively associated with maternal genes promoting late flowering and long flowering periods. Unfortunately, we could not verify this association in the present experiment.
Citation: Vacher C, Kossler TM, Hochberg ME, Weis AE (2011) Impact of Interspecific Hybridization between Crops and Weedy Relatives on the Evolution of Flowering Time in Weedy Phenotypes. PLoS ONE 6(2): e14649. doi:10.1371/journal.pone.0014649
Editor: Hans Henrik Bruun, University Copenhagen, Denmark
Received: March 19, 2010; Accepted: January 3, 2011; Published: February 3, 2011
Copyright: © 2011 Vacher et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: Financial support came from the French Ministère de la Recherche et de l'Enseignement Supérieur (Program: Impact of Biotechnologies in Agro-Ecosystems), and grants from the United States National Science Foundation (Grant: DEB-034530) and the National Science and Engineering Research Council of Canada to AEW. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
When transgenic plants were initially developed, most plant evolutionary biologists and geneticists considered spontaneous hybridization between species to be rare and of little importance in terms of evolution. This view extended to both crops and their wild or weedy relatives , but has now radically changed. More than twenty years of gene-flow research has shown that interspecific hybridization is very common in some groups of vascular plants ,  and may be of considerable evolutionary significance. Hybridization may occasionally result in the extinction of a population , , may trigger the evolution of plant invasiveness , or initiate speciation , . A substantial body of evidence ,  has now accumulated, demonstrating the high potential for interspecific hybridization between agricultural crops and their wild or weedy relatives. Transgenic crops are no exception, and empirical studies have provided evidence of transgene dispersal from GM crops to their weedy relatives , , , , .
Many factors have been shown to influence the rate of hybrid formation between crops and their wild or weedy relatives. Population effects such as the local densities of the parental types and their relative frequencies, have been demonstrated in several cases , , , , , . Mating system differences at the individual level due to, for example, selfing rates and apomixis, have also been found to affect hybridization rates . Moreover, several studies have shown that overlap in the flowering periods of crop and weed plants affect opportunities for hybridization , .
The aim of this study is to gain insight into the impact of hybridization with transgenic crops on the evolution of the weedy relatives by (1) verifying that hybridization opportunities for weedy plants depend on their phenotypic traits (including flowering phenology), (2) measuring the relative fitness of hybridizing weeds, and (3) searching for associations between the transgenic trait and the phenotypic traits increasing hybridization opportunities in the offspring of weedy plants.
We studied hybridization opportunities, phenotypic traits (including phenological, morphological and reproductive traits) and offspring phenotype of weedy individuals (Table 1) in experimental plant populations cultivated under glasshouse conditions. Experimental populations were composed of weeds (birdseed rape, Brassica rapa L., AA, 2n = 20) and transgenic plants in a 1∶1 ratio. Transgenic plants were crop plants of the Brassica genus (rapeseed, Brassica napus L. ssp oleifera, AACC, 2n = 38), F1 hybrids between B. rapa and B. napus, or first-generation backcrosses. Crop plants were all homozygous for the Btcry1Ac transgene from Bacillus thuringiensis (Bt) , F1 hybrids were all hemizygous and first-generation backcrosses and consisted of an equal mixture of hemizygotes and null homozygotes. Hybridization opportunities for each weedy individual was calculated as the expected proportion of pollen received from transgenic plants (PPR) based on the observed flowering schedules.
This experimental system was ideal for addressing the question of interest in this study, for three reasons. First, despite barriers to interspecific mating such as apomixis  or preferential exclusion of hybrid zygotes , numerous studies  have shown that B. napus and B. rapa readily hybridize under controlled conditions, but also in the field. Spontaneous hybridization has, for instance, been reported in weedy populations of B. rapa growing in agricultural crops , ,  and in natural populations of B. rapa occurring near waterways . Second, flowering time has been extensively studied in B. rapa , , , and temporal clines in phenotypic traits have been observed. For example, time to first flowering has been shown to be positively correlated with stem height and stem diameter , , . Third, transgenic lines of B. napus containing a green fluorescent protein (GFP) gene associated with the Bt transgene have been constructed , . The presence of the Bt transgene in the offspring of weedy plants can therefore be inferred by exposing the plants to UV light , .
(1) Relationship between hybridization opportunities for weedy individuals, their flowering phenology, and their morphology
As expected from previous results , weeds flowered earlier than transgenic crops and hybrids (Fig. 1), with the F1 hybrids flowering the latest. Correspondingly, the expected proportion of crosses between weeds and F1 plants was lower than that for crop or backcross plants (Table 2A). Moreover, PPR (log transformed) increased with the time to first flower and the duration of flowering in weedy individuals (see overall slopes in Table 2B). The overall slope for the interaction between the two phenological traits (Table 2B) was close to zero and did not qualitatively modify these effects. However, significant interactions (Table 3) indicated that the effects of phenology of weedy plants on PPR depended on transgenic type (crop, F1 hybrid or first-generation backcross). The regression coefficients and their 95% confidence limits indicated that a longer time to flowering and a longer flowering duration increased PPR more for F1 hybrids than for crops or first-generation backcrosses (see within-type slopes in Table 2B). Thus, weedy individuals flowering later and for longer periods were more likely to receive transgenic pollen, particularly if the transgenic donors were first-generation crop x weed F1 hybrids.
Phenology of weedy plants (WT; hatched bars) and their Bt-transgenic relatives (CR, F1 or BC; white bars). For each combination, three mixed populations of 30 plants were monitored. Bars represent are the mean numbers of opened flowers per population for each day of observation, with standard errors. WT: weedy plants of B. rapa; CR: Bt-crop plants of B. napus; F1: F1 hybrids between WT and CR; BC: Bt-plants from the backcross of F1 on WT. Arrows indicate the date at which 50% of the flowers had been produced.
As expected from the results of previous studies , , we observed temporal clines in the morphological traits under study. Time to first flower was positively correlated with stem diameter (rs = 0.31, P<0.001) and stem height (rs = 0.18, P<0.05). These correlations indicate that the opportunity for hybridization may not be random, and may instead depend on the morphology of the weed. We found a significant, single effect of stem diameter on PPR (F1,105 = 5.0, P<0.05). The overall slope was positive and its 95% confidence interval did not include zero (slope = 0.05, CL = (0.01, 0.09)), indicating that plants with large stems on the day of the first flower were more likely to hybridize with transgenic plants. No such effect was detected for stem height, either as a single effect (F1,104 = 0.05, P = 0.82) or in interaction with transgenic type (F2,104 = 0.87, P = 0.42).
(2) Relative fitness of hybridizing weeds
For any given weedy plant in the experimental populations, the total number of filled seeds decreased significantly with PPR (see overall slopes in Table 4B and the significant effect of PPR in Table 5). We observed no significant interaction between PPR and transgenic type (Table 5), indicating that this decrease in fecundity with PPR was not dependant on transgenic type (crop, F1 hybrid or first-generation backcross). This decrease in fecundity was observed despite the positive correlation between PPR and total flower production within weedy plants (rs = 0.37, P<0.001). An alternative analysis (not shown), including transgenic type as fixed effect and phenological traits of weeds (time to first flower or flowering duration) as covariates also predicted the total number of filled seeds. We found a significant effect of the time to first flower on the number of seeds, in interaction with transgenic type (F2,107 = 3.66, P<0.05). However, all the 95% confidence intervals of the regression coefficients for each transgenic type included zero, making further interpretation impossible. Flowering duration was significant as a single effect (F1,105 = 37.4, P<0.001). The overall slope was negative and its 95% confidence interval did not include zero (slope = −21.3, CL = (−28.77, −14.51)), indicating that weedy plants with longer flowering times produced fewer seeds. Thus, the weedy plants with the highest probability of being pollinated by Bt-transgenic plants were those with the lowest fecundity (Fig. 2).
Total number of filled seeds (TNS) produced by weedy individuals as a function of the expected proportion of pollen (PPR) received from transgenic plants (CR: Bt-crop plants of B. napus; F1: F1 hybrids between weedy plants and CR; BC: Bt-plants from the backcross of F1 on weedy plants). The grey line corresponds to the regression line across all transgenic types (TNS = −303.15 PPR +272.69); its slope is the overall slope given in Table 5.
(3) Associations between the transgenic trait and the phenotypic traits increasing hybridization opportunities in the offspring of weedy individuals
An analysis of offspring phenotype showed that time to first flower in weedy mother plants had a significant effect on the average time to first flower of their offspring (F1,104 = 7.48, P<0.05). Transgenic type (crop, F1 hybrid or first-generation backcross) did not affect time to first flowering in the offspring, either as a main effect (F2,71.3 = 0.20, P = 0.82) or in interaction with maternal time to first flower (F2,97.4 = 0.40, P = 0.66). In contrast, offspring stem diameter was not affected by maternal diameter (F1,104 = 1.80, P = 0.18) or maternal time to first flower (F1,104 = 2.03, P = 0.15). These results confirm that late-flowering plants tend to produce late-flowering offspring . Because late-flowering plants were also more likely to receive transgenic pollen, we therefore expected to find more transgenic offspring in the offspring of late-flowering weedy mothers and an association between the transgenic trait and time to first flower in the offspring generation.
Contrary to expectation, we found no evidence to suggest that weedy individuals with higher PPR produced more transgenic offspring. A total of 1648 seedlings, obtained from 126 weedy plants, were scored under UV light for the Bt-GFP construct. Only 38 seedlings, produced by 17 weedy mothers, scored positively. None of them was sired by the pollen of F1 hybrids. The proportions of fluorescent seedlings were equal to 0.04±0.01 for populations with crop plants, 0.0±0.0 for populations with F1 hybrids and 0.02±0.01 for populations with first-generation backcrosses (χ2 = 17.55, df = 2, P<0.001). Significant differences were observed between replicates for the proportion of positive scores (χ2 = 15.76, df = 2, P<0.001). The proportion of Bt-GFP+ seedlings was not correlated with PPR in populations with crop plants (rs = −0.16, P = 0.33) nor with backcross plants (rs = 0.23, P = 0.17). Correlations with the proportion of Bt-GFP+ seedlings were also weak and non significant for all other maternal traits measured. Thus, variation in the probability of weedy mother plants being pollinated by transgenic donors did not translate into variation in the proportion of Bt-seedlings in their offspring.
Because of the very low proportions of Bt-GFP+ seedlings, we could not study the associations between the transgenic trait and the phenotypic traits increasing hybridization opportunities in the offspring of weedy plants. Among the 1654 seedlings scored under UV light, 1048 reached the first flower stage and were measured. Unfortunately, only nine of these plants were Bt-GFP+, and seven of these nine plants were half sibs (the nine plants were produced by only three weedy mothers). The 31 remaining Bt-GFP+ seedlings did not reach the first flower stage. There were, therefore, clearly too few Bt-GFP+ plants to compare the phenotypic characteristics of Bt-GFP+ and Bt-GFP- offspring.
The aim of our experiment was to assess the impact of interspecific hybridization between weedy B. rapa and transgenic B. napus on the evolution of the weedy phenotype. This was done by identifying the phenotypic traits increasing hybridization opportunities for weedy individuals, searching for associations between thesephenotypic traits and the transgenic trait in the offspring of weedy mothers and evaluating the relative fitness of hybridizing weeds. Our results show that weedy individuals that flowered later and for longer periods were more likely to receive transgenic pollen from crops and weed×crop hybrids. Because stem diameter is correlated with flowering time , , plants with wider stems were also more likely to be pollinated by transgenic plants. Our results suggest that the transgene and maternal genes promoting late flowering, long flowering periods and stem thickening may be preferentially associated in the offspring of weedy mothers. However, although time to first flower is a heritable trait in B. rapa , our experiment did not confirm the gametic association between the transgene and genes promoting late-flowering in the offspring of hybridized weedy plants. Indeed, given the very small numbers of Bt-GFP+ seedlings recovered from the experimental populations, we could not study the association between the transgenic trait and other phenotypic traits in weed plant offspring.
We also found that the weedy plants with the highest probability of hybridization produced fewer seeds, despite producing larger numbers of flowers. The most straightforward interpretation of this result is that fecundity was reduced by hybrid crosses. Controlled crosses between the weedy and transgenic plants used in the experiment (unpublished results) and several previous studies ,  have indeed shown that crops and weed×crop hybrids have lower siring success than do weeds. Therefore, our experiment suggests that maternal weeds that flowered late and for long periods are less fit, because they have a higher probability of hybridizing with GM crop plants or hybrids. This may result in counter-selection against this subset of weed phenotypes, and a shorter earlier flowering period. It is noteworthy that this potential evolution in flowering time does not depend on the presence of the Bt transgene in the crop, and may even be counter-balanced by positive selection acting on the transgene if the latter was positively associated with maternal genes promoting late flowering and long flowering periods. Recent experiments indeed indicate that the Bt transgene does not induce any fitness costs in hybrids between transgenic B. napus and weedy relatives , . It may therefore convey a selective advantage under insect herbivore pressure .
In conclusion, our analyses show that phenological differences between weedy birdseed rape and transgenic rapeseed are likely to alter the phenotypic structure of weed populations, by promoting interspecific hybridization in only a subset of weedy plants with specific phenotypes and by altering the fitness of hybridizing weeds. Unfortunately, we could not verify the non-random association between the transgenic trait and other phenotypic traits in the offspring of weedy populations because of the very low rate of transgene introgression.
Materials and Methods
Nine populations, each composed of 15 Brassica rapa plants and 15 of one of three types of transgenic plants (see below) were sown as seeds and then grown from germination until death in a glasshouse at the University of California, Irvine. The nine populations were divided into three blocks, with each transgenic type replicated once per block. Plants were grown in individual Conetainer® (3.8×21 cm) pots filled with a 75/25 mixture of potting soil and sand. Before planting, seeds were vernalized on wet filter paper at 4°C for 5 days. Pots were spaced 7.6 cm apart and were watered every day until 90% stopped producing flowers. An equal amount of 10∶10∶10 NKP liquid fertilizer was applied to each pot on the sowing date.
The three types of transgenic plants were: Bt-transgenic B. napus crop plants, Bt-transgenic B. napus × B. rapa F1 hybrids, and first-generation backcrosses (B. rapa ×F1 hybrids). Over 20 unique seed and 20 unique pollen parents were used to produce each of the three types. B. rapa plants served as seed parents for the F1 and backcross types. B. napus were all homozygous for the Bt-GFP insertion, whereas the F1 plants were all hemizygous. The backcross generation was expected to consist of an equal mixture of hemizygotes and null homozygotes for the insertion.
B. rapa seeds were obtained from over 400 mature plants in a population at Back Bay, near Irvine, California . Transgenic B. napus plants were derived from spring rapeseed lines (variety Westar, supplied by Dr. Neal Stewart, University of Tennessee). In addition to the Btcry1Ac gene from Bacillus thuringiensis (Bt) , these lines contained a green fluorescent protein (GFP) gene (mGFP5er) under the control of the cauliflower mosaic virus 35S promoter and a nopaline synthase terminator cassette , . The fate of the Bt transgene could therefore be inferred by exposing the offspring to UV light , .
Flowering schedules were constructed for each individual plant by recording the time to first flower (i.e., the number of days between sowing and the first observed flower) and the number of opened flowers on every fourth day until the end of the flowering period. The lifetime of a flower is about three days (Weis A., pers. obs.), so this procedure made it possible to estimate the total number of flowers produced by each plant over the flowering period. The length of the flowering period was defined as the number of scoring days on which the plant had opened flowers.
Every fourth day, all open flowers on all plants were hand pollinated in each of the nine experimental populations (there were no natural pollinators in the experimental glasshouse). Each experimental population was composed of 30 plants which were numbered from 1 to 30. On each pollination day, a random sequence of 30 numbers (without repetition) was generated for each population. For a given population, a pollination session consisted of brushing all the flowers of the first plant in the sequence, and then brushing all of the flowers of the next plant. This was continued until the brush from the 30th plant was used to transfer pollen to the first plant. Each plant was brushed up and down several times to deposit the pollen from the previous plant in the sequence and collect the maximum amount of pollen. A given plant was only brushed if it was alive and had one or more open flowers. Otherwise the next plant in the sequence was considered. Each of the nine populations had its own brush, and new brushes were used for each pollination session. This hand-pollination procedure was chosen to approximate the behaviour of a bumble bee in a patch of oilseed rape. Bumblebees tend to visit many plants successively and rarely revisit the plants . They deposit most of the pollen from a source plant on immediate neighbours .
We did not keep track of the random sequences of plants generated for each experimental population on each pollination day so we used observed flowering schedules to calculate the expected proportion of pollen received from transgenic plants (PPR) for each weedy plant. On each pollination day, the probability of a weedy plant receiving pollen from a transgenic plant was assumed to be proportional to the number of transgenic plants in flower in the experimental population. Over the entire flowering period:where PPRij is the expected proportion of flowers crossed with a transgenic plant for weedy plant i from population j, θijd is the proportion of flowers open on pollination day d for the weedy plant i from population j, and Χjd is the proportion of plants in flower that were of the transgenic type on pollination day d in population j. The proportion Χjd was calculated by excluding the focal plant i, since B. rapa is known to be largely self-incompatible .
In addition to phenological traits, several morphological and reproductive traits were assessed. On the day of first flower, we recorded basal stem diameter and stem height. Dry siliques were collected once the plants had died. The aggregate mass of filled seeds was determined for each plant by separating these seeds from the lighter, aborted seeds, using an air-flow system. We selected five seeds per plant at random and weighed them, to estimate the total number of seeds per plant. We confirmed the accuracy of these measures by counting and weighing all the seeds for 47 plants spanning the range of seed masses.
Finally, for each weedy plant of the nine experimental populations described above, 14 randomly chosen seeds were sown and grown until the day of the first flower. If a mother plant had less than 14 seeds in total, all were sown. Growing conditions were identical to those for the parental generation. Each seedling was scored for fluorescence under high-intensity UV light, at the four-leaf stage. At this stage, the petioles and main nerves of the leaves of transgenic plants displayed fluorescence . This made it possible to determine the proportion of Bt-GFP+ seedlings for each mother plant. To investigate the association between the transgenic trait and phenotypic traits in the offspring, time to first flower was recorded for each seedling and, on the day of the first flower, basal stem diameter was measured.
We performed all statistical analyses with SAS/STAT® software . Plants that died during the experiment were excluded from the analysis and the final data set contained 117 weedy plants.
We first investigated how phenological traits affected the chances of interspecific hybridization between Bt-trangenic plants and weeds. We used a mixed linear model (SAS, Procedure MIXED), with transgenic type (crop, F1 hybrid or first-generation backcross) as the fixed treatment effect, phenological traits of weeds (time to first flower, flowering duration and total number of flowers) as covariates, and block and treatment×block interaction as random effects. The response variable was the proportion of flowers receiving pollen from Bt-transgenic plants (PPR). The response variable was log-transformed to increase its normality (Kolmogorov-Smirnov goodness-of-fit; SAS, Procedure UNIVARIATE). If a factor was not significant as a single effect or in interaction with other factors, it was eliminated from the model and the analysis was rerun. We continued until there was no further improvement in residual maximum likelihood.
We then investigated how morphological traits affected the chances of hybridization. Temporal phenotypic clines were assessed by correlating morphological traits of weeds (with time to first flower (Spearman's rank correlation test; SAS, Procedure CORR). A mixed linear approach (SAS, Procedure MIXED) was then used to determine whether the morphological traits changing with time to first flower had a significant effect on PPR. As above, transgenic type (crop, F1 hybrid or first-generation backcross) was treated as a fixed treatment effect, morphological traits were covariates and block and treatment×block interaction were treated as random effects.
We used the mixed linear approach (SAS, Procedure MIXED) with block and treatment x block interactions as random effects, to investigate whether the phenological and morphological traits which were found to favour hybridization of weedy mothers were transmitted to their offspring. In this model, transgenic type (crop, F1 hybrid or first-generation backcross) was treated as a fixed effect, the maternal trait as a covariate and the average offspring phenotypic trait as the response variable. The normality of the response variables was checked (Kolmogorov-Smirnov goodness-of-fit; SAS, Procedure UNIVARIATE), and data was transformed as necessary.
Finally we investigated the relationship between opportunities for hybridization and fecundity in weeds. We used the mixed linear approach (SAS, Procedure MIXED) with transgenic type (crop, F1 hybrid or first-generation backcross) as the fixed treatment effect, PPR as the covariate and block and treatment×block interaction as random effects. The response variable was the total number of filled seeds. Its normality was checked with a Kolmogorov-Smirnov goodness-of-fit test (SAS, Procedure UNIVARIATE).
We then checked that the mother plants with the highest expected probability of receiving transgenic pollen (PPR) also had the highest proportion of Bt-GFP+ seedlings. The proportion of Bt-GFP+ seedlings did not follow a normal distribution (Kolmogorov-Smirnov goodness-of-fit; SAS, Procedure UNIVARIATE) and could not be transformed. We therefore checked the effects of transgenic type, PPR and block separately, in non parametric one-way ANOVAs (SAS, Proc NPAR1WAY, Kruskal-Wallis test). The correlation between PPR and the proportion of Bt-GFP+ seedlings was assessed using Spearman's rank correlation test (SAS, Proc CORR).
We thank Donald Hermann for carrying out the preliminary experiments for this study.
Conceived and designed the experiments: CV MH AEW. Performed the experiments: CV TMK AEW. Analyzed the data: CV AEW. Wrote the paper: CV TMK MH AEW.
- 1. Ellstrand NC (2003) Current knowledge of gene flow in plants: implications for transgene flow. Philosophical Transactions of the Royal Society of London Series B-Biological Sciences 358: 1163–1170.
- 2. Ellstrand NC, Whitkus R, Rieseberg LH (1996) Distribution of spontaneous plant hybrids. Proceedings of the National Academy of Sciences of the United States of America 93: 5090–5093.
- 3. Rieseberg LH, Carney SE (1998) Plant hybridization. New Phytologist 140: 599–624.
- 4. Hedge SG, Nason JD, Clegg JM, Ellstrand NC (2006) The evolution of California's wild radish has resulted in the extinction of its progenitors. Evolution 60: 1187–1197.
- 5. Ellstrand NC, Schierenbeck KA (2000) Hybridization as a stimulus for the evolution of invasiveness in plants? Proceedings of the National Academy of Sciences of the United States of America 97: 7043–7050.
- 6. Abbott RJ (1992) Plant Invasions, Interspecific Hybridization and the Evolution of New Plant Taxa. Trends in Ecology & Evolution 7: 401–405.
- 7. Rieseberg LH (1997) Hybrid origins of plant species. Annual Review of Ecology and Systematics 28: 359–389.
- 8. Ellstrand NC, Prentice HC, Hancock JF (1999) Gene flow and introgression from domesticated plants into their wild relatives. Annual Review of Ecology and Systematics 30: 539–563.
- 9. Stewart CN, Halfhill MD, Warwick SI (2003) Transgene introgression from genetically modified crops to their wild relatives. Nature Reviews Genetics 4: 806–817.
- 10. Hall L, Topinka K, Huffman J, Davis L, Good A (2000) Pollen flow between herbicide-resistant Brassica napus is the cause of multiple-resistant B-napus volunteers. Weed Science 48: 688–694.
- 11. Quist D, Chapela IH (2001) Transgenic DNA introgressed into traditional maize landraces in Oaxaca, Mexico. Nature 414: 541–543.
- 12. Simard MJ, Legere A, Warwick SI (2006) Transgenic Brassica napus fields and Brassica rapa weeds in Quebec: sympatry and weed-crop in situ hybridization. Canadian Journal of Botany-Revue Canadienne De Botanique 84: 1842–1851.
- 13. Snow A (2009) Unwanted Transgenes Re-Discovered in Oaxacan Maize. Molecular Ecology 18: 569–571.
- 14. Pineyro-Nelson A, Van Heerwaarden J, Perales HR, Serratos-Hernandez JA, Rangel A, et al. (2009) Transgenes in Mexican maize: molecular evidence and methodological considerations for GMO detection in landrace populations. Molecular Ecology 18: 750–761.
- 15. Johannessen MM, Andersen BA, Jorgensen RB (2006) Competition affects gene flow from oilseed rape (female) to Brassica rapa (male). Heredity 96: 360–367.
- 16. Johannessen MM, Damgaard C, Andersen BA, Jorgensen RB (2006) Competition affects the production of first backcross offspring on F-1-hybrids, Brassica napus x B-Rapa. Euphytica 150: 17–25.
- 17. Linder CR, Taha I, Seiler GJ, Snow AA, Rieseberg LH (1998) Long-term introgression of crop genes into wild sunflower populations. Theoretical and Applied Genetics 96: 339–347.
- 18. Pertl M, Hauser TP, Damgaard C, Jorgensen RB (2002) Male fitness of oilseed rape (Brassica napus), weedy B-rapa and their F-1 hybrids when pollinating B-rapa seeds. Heredity 89: 212–218.
- 19. Vacher C, Weis AE, Hermann D, Kossler T, Young C, et al. (2004) Impact of ecological factors on the initial invasion of Bt transgenes into wild populations of birdseed rape (Brassica rapa). Theoretical and Applied Genetics 109: 806–814.
- 20. Pallett DW, Huang L, Cooper JI, Wang H (2006) Within-population variation in hybridisation and transgene transfer between wild Brassica rapa and Brassica napus in the UK. Annals of Applied Biology 148: 147–155.
- 21. Cummings CL, Alexander HM, Snow AA, Rieseberg LH, Kim MJ, et al. (2002) Fecundity selection in a sunflower crop-wild study: Can ecological data predict crop allele changes? Ecological Applications 12: 1661–1671.
- 22. Maagd RA, Bravo A, Crickmore N (2001) How Bacillus thuringiensis has evolved specific toxins to colonize the insect world. Trends in Genetics 17: 193–199.
- 23. Hauser TP, Jorgensen RB, Ostergard H (1997) Preferential exclusion of hybrids in mixed pollinations between oilseed rape (Brassica napus) and weedy B-campestris (Brassicaceae). American Journal of Botany 84: 756–762.
- 24. FitzJohn RG, Armstrong TT, Newstrom-Lloyd LE, Wilton AD, Cochrane M (2007) Hybridisation within Brassica and allied genera: evaluation of potential for transgene escape. Euphytica 158: 209–230.
- 25. Warwick SI, Simard MJ, Legere A, Beckie HJ, Braun L, et al. (2003) Hybridization between transgenic Brassica napus L. and its wild relatives: Brassica rapa L., Raphanus raphanistrum L., Sinapis arvensis L., and Erucastrum gallicum (Willd.) OE Schulz. Theoretical and Applied Genetics 107: 528–539.
- 26. Warwick SI, Legere A, Simard MJ, James T (2008) Do escaped transgenes persist in nature? The case of an herbicide resistance transgene in a weedy Brassica rapa population. Molecular Ecology 17: 1387–1395.
- 27. Wilkinson MJ, Elliott LJ, Allainguillaume J, Shaw MW, Norris C, et al. (2003) Hybridization between Brassica napus and B-rapa on a national scale in the United Kingdom. Science 302: 457–459.
- 28. Weis AE, Kossler TM (2004) Genetic variation in flowering time induces phenological assortative mating: Quantitative genetic methods applied to Brassica rapa. American Journal of Botany 91: 825–836.
- 29. Weis AE, Winterer J, Vacher C, Kossler TM, Young CA, et al. (2005) Phenological assortative mating in flowering plants: the nature and consequences of its frequency dependence. Evolutionary Ecology Research 7: 161–181.
- 30. Dorn LA, Mitchell-Olds T (1991) Genetics of Brassica campestris. 1. Genetic constraints on evolution of life-history characters. Evolution 45: 371–379.
- 31. Franks SJ, Sim S, Weis AE (2007) Rapid evolution of flowering time by an annual plant in response to a climate fluctuation. Proceedings of the National Academy of Sciences of the United States of America 104: 1278–1282.
- 32. Harper BK, Mabon SA, Leffel SM, Halfhill MD, Richards HA, et al. (1999) Green fluorescent protein as a marker for expression of a second gene in transgenic plants. Nature Biotechnology 17: 1125–1129.
- 33. Haseloff J, Siemering KR, Prasher DC, Hodge S (1997) Removal of a cryptic intron and subcellular localization of green fluorescent protein are required to mark transgenic Arabidopsis plants brightly. Proceedings of the National Academy of Sciences of the United States of America 94: 2122–2127.
- 34. Halfhill MD, Richards HA, Mabon SA, Stewart CN (2001) Expression of GFP and Bt transgenes in Brassica napus and hybridization with Brassica rapa. Theoretical and Applied Genetics 103: 659–667.
- 35. Allainguillaume J, Alexander M, Bullock JM, Saunders M, Allender CJ, et al. (2006) Fitness of hybrids between rapeseed (Brassica napus) and wild Brassica rapa in natural habitats. Molecular Ecology 15: 1175–1184.
- 36. Hauser TP, Shaw RG, Ostergard H (1998) Fitness of F-1 hybrids between weedy Brassica rapa and oilseed rape (B-napus). Heredity 81: 429–435.
- 37. Halfhill MD, Sutherland JP, Moon HS, Poppy GM, Warwick SI, et al. (2005) Growth, productivity, and competitiveness of introgressed weedy Brassica rapa hybrids selected for the presence of Bt cry1Ac and gfp transgenes. Molecular Ecology 14: 3177–3189.
- 38. Kun DC, Neal Stewart J, Wei W, Bao-cheng S, Zhi-Xi T, et al. (2009) Fitness and maternal effects in hybrids formed between transgenic oilseed rape (Brassica napus L.) and wild brown mustard [B. juncea (L.) Czern et Coss.] in the field. Pest Management Science 65: 753–760.
- 39. Stewart CN, All JN, Raymer PL, Ramachandran S (1997) Increased fitness of transgenic insecticidal rapeseed under insect selection pressure. Molecular Ecology 6: 773–779.
- 40. Franke DM, Ellis AG, Dharjwa M, Freshwater M, Fujikawa M, et al. (2006) A steep cline in flowering time for Brassica rapa in southern California: Population-level variation in the field and the greenhouse. International Journal of Plant Sciences 167: 83–92.
- 41. Cresswell JE (2000) A comparison of bumblebees' movements in uniform and aggregated distributions of their forage plant. Ecological Entomology 25: 19–25.
- 42. Cresswell JE, Bassom AP, Bell SA, Collins SJ, Kelly TB (1995) Predicted pollen dispersal by honey-bees and three species of bumble-bees foraging on oil-seed rape: A comparison of three models. Functional Ecology 9: 829–841.
- 43. Ellstrand NC (2003) Dangerous liaisons? When cultivated plants mate with their wild relatives. Dangerous liaisons? When cultivated plants mate with their wild relatives.xx+244.
- 44. SAS (1999) SAS/STAT® software, Version 8 of the SAS System for Unix, Copyright © 1999–2000, SAS Institute Inc., Cary, (North Carolina)