UNIVERSITE DE BOURGOGNE THÈSE Yongbo LIU - Université de ...
UNIVERSITE DE BOURGOGNE THÈSE Yongbo LIU - Université de ...
UNIVERSITE DE BOURGOGNE THÈSE Yongbo LIU - Université de ...
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given f ield (sympatry) or a cross f ields t hrough l ong di stance di spersal of pol len can be<br />
transmitted either through pollens or seeds from crops to wild relatives.<br />
1.2.1 Seed dispersal<br />
Seed banks of transgenic crops with dormant seeds can build up na turally in the soil. Seed<br />
loss at harvest, shallow cultivation and ploughing timing have been i<strong>de</strong>ntified as key factors to<br />
prevent incorporation of seeds into the seedbank (Begg et al. 2006). Oilseed rape (B. napus)<br />
possesses c haracteristics t hat f avour t he f ormation a nd p ersistence of a seed ba nk, i .e. pod<br />
shattering and inducible secondary dormancy. Volunteer recruitment from oilseed rape field<br />
was observed, suggesting seeds could be dormant in tilled as well as no-tilled fields (Simard<br />
et a l. 2002) . B esi<strong>de</strong> t he actual pr oduction a rea o f t ransgenic c rops a nd t he l ocations w here<br />
crops gr own, hum ans c an a lso be a ve ctor f or unw anted gene flow dur ing t he t ransport,<br />
processing, and exchange of transgenic seeds. Several GM oilseed rape plants were <strong>de</strong>tected<br />
at major ports and along roadsi<strong>de</strong>s in Japan, and these plants probably resulted from imported<br />
GM oilseed rape seeds because these seeds was not commercially cultivated (Saji et al. 2005;<br />
Aono et al. 2006). S imilarly, in Korea, a feral plant of GM maize (Zea mays) was <strong>de</strong>tected<br />
along a roadsi<strong>de</strong> near a Korean seaport (Kim et al. 2006). Volunteers arise from the seed bank<br />
in subsequent years, which can serve as a source or bridge for pollen flow.<br />
1.2.2 Pollen dispersal<br />
Oilseed rape is self-fertile, with pollen movement by both wind and insects (Williams et al.<br />
1987). Interplant outcrossing rates range from 12 to 47% (Becker et al. 1992; Lavigne et al.<br />
1998). Pollen-mediated gene flow in oilseed rape is affected by a variety of factors, including<br />
flowering t ime, ge notypes, w ind s peed a nd di rection, di stance be tween donor a nd r ecipient<br />
populations. Pollens of oilseed rape were observed 1.5km from source field, and they were<br />
sufficient in number (22 pollens grains m3) to allow seed set (Timmoms et al. 1995). Gene<br />
flow for transgenic oilseed rape could occur at several kilometers from pollen resource (Table<br />
1.1; Rieger et al. 2002; Cai et al. 2008). However, approximately half of the pollen produced<br />
by an individual plant fell within 3 m , and dispersal from whole plots instead of individual<br />
plants would have un<strong>de</strong>restimated the proportion of pollen (Lavigne et al. 1998).<br />
However, the majority of GM crossing fertilization occurs less than 10m (Husken and<br />
Dietz-Pfeilstetter 2007), with a <strong>de</strong>cline over 50m. Generally, the <strong>de</strong>gree of gene flow between<br />
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