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Those factors that allowed for a fluid transition to introducing the next question were: maintenance, regular mowing, no weeds, only grass (Table 2).
Among the 80 bags spawned for the first supplemented trial on Pangola grass (Table 4), both treatments T12 and T13 had one bag contaminated with the mold Trichoderma sp. by the end of the colonization period.
First the L. monocytogenes suspension was applied to the forage equivalent to approx. 10 107 cfu/g grass (Table 2).
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Broom (Cytisus scoparius L ., gorse (Ulex europeaus L ., pine regeneration (Pinus radiata) and various species of grasses (Table 2) dominated the spectrum of key problematic weeds described by respondents.
Silica-dried leaf tissue was obtained from 25 species of pooid grasses (Table 2).
Several NTSR genes or candidate genes had previously been identified in grasses (Table 3).
The reaction of forbs to the thinning of C. mopane differed markedly from that of the grasses (Table 5).
Our TILLING population has higher frequency of mutation (1/104 kb) than the other diploid grasses (Table 1).
PCR products varied in size from 496 bp – 646 bp, and this length heterogeneity provided a useful character for discriminating Agrostis spp. from other grasses (Table 1).
> Over the previous 6 months (March September 2011), we had collected seeds of local provenance at each of the three sites (where possible) from four native perennial grasses and four exotic annual grasses (Table 2).
In tall fescue the amino acid glycine was seen to restore seedling development, but this was not seen in the other grasses (Tables 1– 3).
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