000 | 01773nab a22004697a 4500 | ||
---|---|---|---|
001 | G51228 | ||
003 | MX-TxCIM | ||
005 | 20211006075533.0 | ||
008 | 121211b |||p||p||||||| |z||| | | ||
022 | 0 | _a0394-9257 | |
040 | _aMX-TxCIM | ||
041 | 0 | _aEn | |
043 | _aIT | ||
072 | 0 | _aF30 | |
072 | 0 | _aF62 F03 | |
082 | 0 | 4 | _a93-095259 |
100 | 1 | _aWanjari, K.B. | |
245 | 0 | 0 | _aStudies on triticale-wheat crossability |
246 | 0 | 0 | _aStudi sulle possibilita' di incrocio triticale-grano |
260 | _c1992 | ||
340 | _aPrinted | ||
500 | _a4 tables; 11 ref. Summary (En) | ||
500 | _aPeer-review: No - Open Access: No | ||
520 | _aCrossability was studied among seven secondary triticales and six wheat genotypes. Wheat x triticale crosses showed hih percentages of seed setting but the seeds were illfilled and poor in germination, which was in contrast to their reciprocals. The reciprocal differences were attributed to selective elimination of abnormal gametes of triticale on male side only. Genotypic differences for crossability were seen in both wheats and triticales. The Kr gene system of Krolow was found to operate in the presence of a particular rye chromosome rather than against the whole rye genome | ||
546 | _aEnglish | ||
595 | _aAC | ||
650 | 1 | 0 | _aChromosomes |
650 | 1 | 0 | _aGametes |
650 | 1 | 0 | _aGenes |
650 | 1 | 0 | _aGermination |
650 | 1 | 0 | _aHybridization |
650 | 1 | 0 | _aSecale cereale |
650 | 1 | 0 | _aSeed |
650 | 1 | 0 | _aSelection |
650 | 1 | 0 |
_aTriticales _91294 |
650 | 1 | 7 |
_aTriticum _gAGROVOC _2 _91295 |
650 | 1 | 0 |
_91134 _aGenotypes _gAGROVOC |
700 | 1 |
_aChopra, V.L., _ecoaut. |
|
700 | 1 |
_aJoshi, M.G, _ecoaut. |
|
773 | 0 |
_tJournal of Genetics and Breeding _n93-095259 _gv. 46, no. 3, p. 279-282 |
|
942 | _cJA | ||
999 |
_c15909 _d15909 |