1962
DOI: 10.1007/bf00888790
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Zur Ursache Der Abortion Von Samenanlagen In Diploid-Polyploid-Kreuzungen

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Cited by 22 publications
(14 citation statements)
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“…The balance of 2M:1P genome copies in the endosperm is crucial for reproductive success. Deviation from this ratio in response to hybridizations of plants that differ in ploidy frequently leads to unviable seeds, a phenomenon referred to as triploid block (von Wangenheim 1962;Scott et al 1998;Leblanc et al 2002;Stoute et al 2012;Sekine et al 2013). Importantly, interploidy hybridizations affect endosperm cellularization: Although maternal excess crosses (4x × 2x; by convention the maternal parent is always mentioned first) shift the cellularization to earlier timepoints, paternal-excess hybridization (2x × 4x) causes a delay or complete failure of endosperm cellularization (Scott et al 1998;Lafon-Placette and Köhler 2016).…”
mentioning
confidence: 99%
“…The balance of 2M:1P genome copies in the endosperm is crucial for reproductive success. Deviation from this ratio in response to hybridizations of plants that differ in ploidy frequently leads to unviable seeds, a phenomenon referred to as triploid block (von Wangenheim 1962;Scott et al 1998;Leblanc et al 2002;Stoute et al 2012;Sekine et al 2013). Importantly, interploidy hybridizations affect endosperm cellularization: Although maternal excess crosses (4x × 2x; by convention the maternal parent is always mentioned first) shift the cellularization to earlier timepoints, paternal-excess hybridization (2x × 4x) causes a delay or complete failure of endosperm cellularization (Scott et al 1998;Lafon-Placette and Köhler 2016).…”
mentioning
confidence: 99%
“…Main hypotheses are as follows: 1) variation of genomes in embryo: endosperm: maternal tissues from the normal 2: 3:2 ratio (Muntzing 1930(Muntzing , 1933, or its modifications (Watkins 1927, 1932, Katayama 1933, Boyes and Thompson 1937; 2) variation in genetic ' strength' or genetic value in different species (Howard 1939, 1947, Stephens 1942, Valentine 1956, Valentine and Woodell 1963; 3) somatoplastic sterility (Brink andCooper 1939, 1940); 4) an inharmonious interaction between male and female gametes at double fertilization (Kihara and Nishiyama 1932); 5) disturbed ratios between the amount of cytoplasm (extrachromosomalen Bestandteil) and the number of chromosome sets in the endosperm (Wangenheim 1962(Wangenheim , 1967. However, none of these hypotheses explains all the observed cases of seed failure.…”
mentioning
confidence: 99%
“…However, it is noteworthy that the diploid Raphanus-Brassica hybrids produced tetraploid offspring from pollination among themselves, and triploid offspring when planted with (diploid) Raphanus sativus but not when planted with (diploid) Brassica oleracea. This asymmetric mating might possibly be an example of the triploid-block effect that is known in many flowering-plant families to destroy triploid embryos, particularly autotriploids (Brink and Cooper 1947a, b;Katsiosis et al 1995;Kermicle and Alleman 1990;Kihara and Nishiyama 1932;Lin 1984;Müntzing 1933;von Wangenheim 1961). Rutishauser (1967) noted incompatibilities in pseudogamous apomictic Ranunculus consistent with a triploid-block effect.…”
Section: Evolutionary Modelsmentioning
confidence: 84%
“…3). Many, and perhaps most, sexual angiosperms require this 2:1 ratio (Brink and Cooper 1947a, b;Katsiosis et al 1995;Kermicle and Alleman 1990;Lin 1984;Vinkenoog and Scott 2001;Vinkenoog et al 2003;von Wangenheim 1961), which relates to the triploid-block effect (above). Centrogamous apomicts (discussed above) require fertilization of the central cell to form the endosperm, as in sexual reproduction (Nogler 1984).…”
Section: Rosoideaementioning
confidence: 96%