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Repartition by States (USA) of the 73 wild sunflower populations collected and used as female parents in this study

Repartition by States (USA) of the 73 wild sunflower populations collected and used as female parents in this study

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The genetic base of sunflower elite lines is very narrow, due to many years of selection and breeding. To broaden the genetic diversity of the cultivated sunflower, in 1995 73 wild sunflower populations were crossed with 3 cultivated lines (Testers), and 219 hybrid offspring’s were evaluated in the field. GCA and SCA effects were computed suggestin...

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... each accession (hereafter referred as ''#num- ber''), ten seeds were sown in 1997 in the nursery of the INRA station of Melgueil (Mauguio, France), in one row plots, 4 m long with 75 9 35 cm planting density and were manually crossed as females with the pollen of 3 cultivated lines (testers), to construct the first generation of intermixing (pseudo F1 hybrid) ( Table 1, Fig. 1). The 3 tester lines were 89HR 2 (T 1 -restorer), 90R 19 (T 2 -restorer), RT 1 B 11 (T 3 - maintainer), all developed by INRA. ...

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... The cross A-6 × A-9 (3.58) showed positive and significant SCA effects for the NLP, which is desirable (Rabia et al., 2015). The cross A-5 × A-9 (2.53) showed significantly positive SCA effects, which is desirable for HD (Nooryazdan et al., 2011). The maximum negative and significant SCA effects for PH were shown by A-6 × A-8 (-1.32), which is desirable as short-statured plants are required to overcome lodging (Rauf et al., 2012). ...
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... In species with SSI for a given pair either incompatible or compatible, a few pollen grains-onto a stigma interactions are sufficient to enable the diagnostic whether their reaction is compatible or incompatible, such as in guayule (Gerstel 1950), hazelnut (Mehlenbacher and Thompson 1988) and senecio (Hiscock et al. 2002), but not for the olive tree (Bradley and Griggs 1963;Villemur et al. 1984;Vuletin-Selak et al. 2011, 2014. However, these observations of pollen cannot be done easily in the field for tens of plants, as it is required for breeders to study plenty of progenies as in a sunflower pre-breeding program (Nooryazdan et al. 2010). Breeders have used paper bags that have been checked to be pollen-proof for the species, and seed setting is measured with an electronic or mechanical seed counter. ...
... Levin (1996) has proposed that pseudo self-fertility should be the result of modifier loci unlinked to the self-incompatibility locus, that affect the activity of genes present at the S-locus. However, such modifier genes have not been characterized and mapped in Asteraceae (Nooryazdan et al. 2010). Moreover, within the scope of this hypothesis all olive tree varieties that carry R5 or R1 would carry different modifier genes, because they have different origins in the Mediterranean basin, and the heterozygosity in the olive tree is very high by 0.76 to 0.84 (Besnard et al. 2001;Breton et al. 2006). ...
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Self-fertility is largely decreased and even prevented by various mechanisms because, broadly, it causes inbreeding depression, although some species have retained self-reproduction regimes. Species of plants that display the self-incompatible sporophytic type of self-incompatibility may rarely self-pollinate. It is only possible in the absence of foreign compatible pollen. In the olive tree with a sporophytic mechanism, we will show that three co-dominant S-alleles R1, R3 and R5 do not lead to the same level of self-fertility. All varieties that carry R1 are less self-fertile than those that carry R5, whatever the other S-alleles, while those carrying R3 are intermediate. S-allele pair-wise combinations that differ by two or three levels of dominance, and not the other combinations allow self-fertility, and moreover each S-allele R1, R3 and R5 decreases, maintains and enhances the self-fertility rate, respectively.
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PARÂMETROS GENÉTICOS ENTRE CARACTERES QUANTITATIVOS NO GIRASSOL COMO CRITÉRIO DE SELEÇÃO PARA PRODUTIVIDADE DE AQUÊNIOS