Summary
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1.
The partial inhibitor, Fp, described in the present paper, is quite different in its behavior from Ff, discussed in a previous paper (1926). The factor Fp suppresses the complete development of the white margin in producing it in the “half”-“slight” degrees.
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2.
The dominance of Fp is almost perfect.
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3.
The manifestation of this partial inhibitor is subject to fluctuation, contrary to that of the other partial inhibitor (cf.Imai 1926).
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4.
A strong linkage occurs between the allelomorphic pairs of Fp and fp versus Di and di, the latter controlling the intensity of the flower color, the cross-over value being about 3%.
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5.
The non-willow-leaf segregates bore flowers with white margin of a high degree, the willow-leaf ones, on the other hand, almost invariably had flowers which were either self-colored or with white margin pattern in a very slight degree. This may be due to another linkage relation.
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6.
Quite unexpectedly the maple-leaf mutants, produced by mutation of m′→m, have always the white margin in a degree averaging that of the flowers of the cordate-leaf plants.
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7.
The flowers of disguise-willow, which appeared as a bud-sport on a willow-leaf plant, however, had the average degree of the latter type.
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References
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Hagiwara, T., 1926.—Genetic studies of corolla-pattern in the morning glory. II. On the six kinds of the corolla-pattern. Bot. Mag. (Tokyo), 40: 203–225. (In Japanese).
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Takezaki, Y., 1916.—Inheritance of the Japanese morning glory. Journ. of the Japanese Breeders' Association, 1–1: 12–12.
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Imai, Y. Further studies on the genetics of the white margined flower of the Japanese morning glory. Genetica 9, 101–115 (1927). https://doi.org/10.1007/BF01508745
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DOI: https://doi.org/10.1007/BF01508745