scholarly journals Ploidy Levels of Hardy Actinidia Accessions in the U.S. Determined by Flow Cytometry

HortScience ◽  
1997 ◽  
Vol 32 (3) ◽  
pp. 439D-439 ◽  
Author(s):  
Mary Ann Start ◽  
James Luby ◽  
Robert Guthrie ◽  
Debby Filler

The hardy Actinidia species represent a source of genetic diversity for improving A. deliciosa (kiwifruit) as well as for creating new economically important cultivars through intra- and interspecific crosses. Attempts at breeding in Actinidia have been complicated by the existence of intraspecific as well as interspecific variation in ploidy. The haploid chromosome number in Actinidia is 29 and diploid (2n=2x=58), tetraploid (2n=4x=116), and hexaploid (2n=6x=174) levels have been identified. Because of the problems encountered when crossing parents differing in ploidy level, it is desirable to know the ploidy levels of plants to be used in breeding. We determined the ploidy levels of 61 Actinidia accessions currently available in the U.S., including primarily accessions of relatively winter-hardy species. The 61 accessions, representing eight species and three interspecific hybrids, were screened for ploidy using flow cytometry. Mitotic root tip cells from one plant from each putative ploidy level were examined microscopically to confirm the ploidy level derived from flow cytometry. There were 17 diploids, 40 tetraploids, and 4 hexaploids. Intraspecific variation was not found among accessions of the species arguta, callosa, deliciosa, kolomikta, melanandra, polygama, or purpurea. All kolomikta and polygama accessions were diploid. All arguta, callosa, melanandra, and purpurea accessions were tetraploid. Actinidia deliciosa was hexaploid. One chinensis accession was tetraploid. Two accessions (NGPR 0021.14 and 0021.3), acquired as chinensis, were hexaploid and may, in fact, be A. deliciosa based on their morphology. `Issai' (arguta × polygama) was hexaploid and `Ken's Red' and `Red Princess' (both melanandra × arguta) were tetraploid.

1971 ◽  
Vol 13 (2) ◽  
pp. 292-297 ◽  
Author(s):  
R. A. Forsberg ◽  
S. Wang

Avena abyssinica (2n=28) × A. strigosa (2n=14) 6x amphiploids were crossed with 13 different A. sativa (2n=42) varieties or selections. There was considerable variation in chromosome number within and among F1 plants. The mode was 40 in root tip cells and 41 in pollen mother cells (PMC's). The number of univalents in PMC's ranged from 10 to 27 with a mean of 18.9. The average number of bivalents was 7.1, ranging from 2 to 13. Multiple associations were common. Only 10.8% of the pollen grains contained normally developed nuclei, i.e. one vegetative and two elongated sperm nuclei. Forty of 41 F1 plants were completely self-sterile and only one seed was obtained from 16,950 florets. Seed set in backcross pollinations with A. sativa was 1.25%, providing some opportunity for perpetuation of desirable genes from lower ploidy levels.


HortScience ◽  
2005 ◽  
Vol 40 (5) ◽  
pp. 1194-1195 ◽  
Author(s):  
Lei Jiajun ◽  
Li Yuhua ◽  
Du Guodong ◽  
Dai Hanping ◽  
Deng Mingqin

A natural strawberry genotype, `Jilin 4', was collected from the Changbai Mountains located in Gongzhuling Region, Jilin Province, Northeast China. It was identified as a pentaploid (2n = 5x = 35) by counting the chromosomes of the root-tip cells. Natural pentaploid strawberries have not been reported as originating in China or outside of California in the U.S. Jilin 4 was the most vigorous genotype among representatives of all 15 wild species of Fragaria and more than 60 cultivars of F. ×ananassa in a common garden. The size of its flowers and anthers were similar to those of cultivars and it produced abundant runners. The pollen was viable, but the pistils were sterile. It appeared to be drought and cold tolerant, but showed symptoms of local virus infection. There are three possible origins of Jilin 4, which are discussed in this report.


1974 ◽  
Vol 16 (1) ◽  
pp. 219-227 ◽  
Author(s):  
R. S. Sadasivaiah ◽  
K. Lesins

Cytological studies on progenies obtained from intercrosses between colchicine-induced octoploid (2n = 8x = 64) plants of alfalfa showed normal, haploid and aneuploid chromosome numbers in cells of the same root tip. Critical observations on cells at different divisional stages revealed the occurrence of meiosis-like mitotic divisions, resulting in a reduction of chromosome number. The frequency of cells showing reductional divisions appeared to vary with the ploidy level of the material. The possible significance of chromosome reduction in plant evolution is indicated.


2010 ◽  
Vol 73 (5) ◽  
pp. 949-954 ◽  
Author(s):  
W. Kwankua ◽  
S. Sengsai ◽  
C. Kuleung ◽  
N. Euawong

2007 ◽  
Vol 49 (4) ◽  
pp. 481-486 ◽  
Author(s):  
Jian-You Li ◽  
Ai-Liang Jiang ◽  
Wei Zhang

Genome ◽  
1988 ◽  
Vol 30 (1) ◽  
pp. 36-43 ◽  
Author(s):  
K. Kerby ◽  
J. Kuspira

To help elucidate the origin of the B genome in polyploid wheats, karyotypes of Triticum turgidum, Triticum monoccum, and all six purported B genome donors were compared. The analysis utilized a common cytological procedure that employed the most advanced equipment for the measurement of chromosome lengths at metaphase in root tip cells. A comparison of the karyotypes of T. turgidum and T. monococcum permitted the identification of B genome chromosomes of T. turgidum. These consist of two SAT pairs, one ST pair, three SM pairs, and one M pair of homologues. Comparisons of the chromosomes of the B genome of T. turgidum with the karyotypes of the six putative B genome donors showed that only the karyotype of Aegilops searsii was similar to the one deduced for the donor of the B genome in T. turgidum, suggesting that Ae. searsii is, therefore, the most likely donor of the B genome to the polyploid wheats. Support for this conclusion has been derived from geographic, DNA-hybridization, karyotype, morphological, and protein data reported since 1977. Reasons why the B genome donor has not been unequivocally identified are discussed.Key words: phylogeny, karyotypes, Triticum turgidum, Triticum monococcum, B genome, B genome donors.


Nature ◽  
1949 ◽  
Vol 164 (4178) ◽  
pp. 930-930 ◽  
Author(s):  
J. CHAYEN

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