Apomixis in hawkweed: Mendel's experimental nemesis. (1/24)

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Isolation and characterization of microsatellite loci from apomictic Hypericum perforatum (Hypericaceae). (2/24)

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Chromosome numbers and meiotic analysis in the pre-breeding of Brachiaria decumbens (Poaceae). (3/24)

A total of 44 accessions of Brachiaria decumbens were analysed for chromosome count and meiotic behaviour in order to identify potential progenitors for crosses. Among them, 15 accessions presented 2n = 18; 27 accessions, 2n = 36; and 2 accessions, 2n = 45 chromosomes. Among the diploid accessions, the rate of meiotic abnormalities was low, ranging from 0.82% to 7.93%. In the 27 tetraploid accessions, the rate of meiotic abnormalities ranged from 18.41% to 65.83%. The most common meiotic abnormalities were related to irregular chromosome segregation, but chromosome stickiness and abnormal cytokinesis were observed in low frequency. All abnormalities can compromise pollen viability by generating unbalanced gametes. Based on the chromosome number and meiotic stability, the present study indicates the apomictic tetraploid accessions that can act as male genitor to produce interspecific hybrids with B. ruziziensis or intraspecific hybrids with recently artificially tetraploidized accessions.  (+info)

Chromosomes carrying meiotic avoidance loci in three apomictic eudicot Hieracium subgenus Pilosella species share structural features with two monocot apomicts. (4/24)

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Evolution of the apomixis transmitting chromosome in Pennisetum. (5/24)

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Sexual reproduction development in apomictic Eulaliopsis binata (Poaceae). (6/24)

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Boechera, a model system for ecological genomics. (7/24)

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Density-independent mortality and increasing plant diversity are associated with differentiation of Taraxacum officinale into r- and K-strategists. (8/24)

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