Íslenskar landbúnaðarrannsóknir - 01.03.1970, Qupperneq 103

Íslenskar landbúnaðarrannsóknir - 01.03.1970, Qupperneq 103
COLOUR INHERITANCE IN ICELANDIC SHEEP 101 sires in the present study which show segre- gation at two loci simultaneouslv, but where the origin ol the alleles is not known. The groups of progeny are too small, however, to be of much value in an attempt to establish presence or absence of linkage by tests of heterogenity. CHAPTER VIII Discussion of inheritance of colour in sheep In the following, earlier investigations on the inheritance of the colours encountered in the present study will be discussed, i.e. recessive black and brown pigment in non- white sheep, white colour with or without tan, the colour patterns grey, badgerface, mouflon, grey mouflon and no pattern, and the presence or absence of white mark- ings. In addition the relation of dominant black and brown to the above colours will be discussed. The literature on these aspects of colour inheritance in sheep has been re- viewecl by Rae (1956), Rendel (1957), Berge (1958, 1964 a), Ryder and Stephen- son (1968) and Searle (1968). A. RECESSIVE BLACK VS. RECES- SIVE BROWN PIGMENT Roberts and White (1930 a), studying the inheritance of recessive black and recessive brown in the Shetland and Soay sheep (as contrasted to white), came to the conclus- ion that the brown pigment was recessive (or hypostatic) to black. Zóphóníasson (1934) and Berge (1958) arrived at the same conclusion for Icelandic and Old Norweg- ian sheep, respectively. In all these cases, there was no difficulty in distinguishing between black and brown pigment. Serra on the other hand, postulated three allelic genes for brown pigment, all recessive or hypostatic to black. Vasin (1928) found a recessive dark brown colour, which he as- sumes to be diluted black, in both the northern shorttailed sheep of Russia and in nonwhite Merinos. It is not certain whether this is the same brown as found in the Shetland, Soay, Icelandic and Old Norwegian sheep. Robf.rts and White (1930 b) describe a recessive bleaching of clominant black to brown, but as this bleaching is not present at birth it is rnost likely different from Vasin’s (1928) brown. Roberts (1932), describing the colour of the wild Mouflon and its inheritance, con- cluded that the undercoat of the Mouflon was clearly a brown, but the wild Mouflon was shown to carry genes for black pig- ment, so the brown colouring of the under- coat of the wild Mouflon rnust be due to a dilution of black. Ewart (1919) crossed sheep from Russia, called Siberian Mou- flon, witli Cheviot. The Fx was white, and a backcross of brown F2 females to the Siberian Mouflon ram gave purebreeding brown. It seerns likely fronr Ewart’s experi- ments that the brown colour in these cross- es is the same as the recessive brown in the Shetland and Soay sheep. This would imply that the Cheviots used in the experinrent also carried tlre recessive brown. Roberts and White (1930 a) state that tlre exact genetic relationship between black and brown cannot be established, as long as genes lower in the series, i.e. reces- sive to brown, are not discovered. Berge (1964 a) on the other hand, assumes that brown is produced by a honrozygous reces- sive gene which converts black pigment in-
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