scholarly journals Chromosome Numbers of Rubus Species at the National Clonal Germplasm Repository

HortScience ◽  
1995 ◽  
Vol 30 (7) ◽  
pp. 1447-1452 ◽  
Author(s):  
Maxine M. Thompson

The U.S. Dept. of Agriculture, Agricultural Research Service, National Clonal Germplasm Repository (NCGR), Corvallis, Ore., maintains Rubus germplasm representing worldwide diversity of the genus. Chromosome numbers were counted for 201 plants representing 124 taxa (species and varieties). There are new reports for 42 taxa, confirmation for 72 previously reported, and 10 counts for plants unidentified to species. The basic chromosome number was seven, and ploidy levels ranged from 2x to 12x.

HortScience ◽  
1995 ◽  
Vol 30 (7) ◽  
pp. 1453-1456 ◽  
Author(s):  
Maxine M. Thompson

Chromosome numbers were counted for 90 Rubus cultivars and selections maintained at the U.S. Dept. of Agriculture, Agricultural Research Service, National Clonal Germplasm Repository, Corvallis, Ore. To my knowledge, 37 of the counts are new, including five that are corrections of previously published counts, 30 that are confirmations of numbers that were previously published but assumed from their parentage rather than actually counted, and 23 that are confirmations of previous counts. The basic number was 7, and 2n numbers ranged from 2x to 14x, including odd-ploids and aneuploids.


Bothalia ◽  
1996 ◽  
Vol 26 (1) ◽  
pp. 53-61 ◽  
Author(s):  
J. J. Spies ◽  
S. K. Spies ◽  
S. M. C. Van Wyk ◽  
A. F. Malan ◽  
E. J. L. Liebenberg

This is a report on chromosome numbers for 14 species of the subtribe Aveninae. which is largely naturalized in South Africa. This is the first chromosome number report for Helictotrichon longifolium (Nees) Schweick. (n = 14). H. longum (Stapf)Schweick. (n = 14). H. namaquensis Schweick. (n = 14) and Lophochloa cristata (L.) Hyl. (n = 7, 21/2. 14). The subtribe has a basic chromosome number of seven, and fewer ploidy levels occur in the naturalized species in South Africa than in the same species in other parts of the world. All tetraploid specimens were alloploids.


HortScience ◽  
2007 ◽  
Vol 42 (1) ◽  
pp. 172-173 ◽  
Author(s):  
Mark K. Ehlenfeldt ◽  
Chad E. Finn

G-435 and ARS 96–138 are two pink-fruited blueberry selections developed by the Agricultural Research Service of the U.S. Department of Agriculture. G-435, a tetraploid, is predominantly Vaccinium corymbosum L. (highbush blueberry) with a mixture of other Vaccinium species germplasm in its ancestry. It has been evaluated in New Jersey and Michigan. ARS 96–138 is a hexaploid that is half V. ashei Reade (rabbiteye blueberry) and half synthetically derived, hexaploid, highbush-type germplasm. It has been evaluated in New Jersey and Oregon. ARS 96–138 was partially derived from a pink-fruited sibling of G-435; thus, the two selections are related, although they possess different ploidy levels. They are released as germplasm for further evaluation, breeding, and possible commercialization. They represent a novel fruit color in blueberry that is of interest to the landscape nursery business.


Bothalia ◽  
1989 ◽  
Vol 19 (1) ◽  
pp. 125-132 ◽  
Author(s):  
J. J. Spies ◽  
E. J. L. Saayman ◽  
S. P. Voges ◽  
G. Davidse

Cytogenetic studies of 53 specimens of 14 species of the genus  Ehrharta Thunb. confirmed a basic chromosome number of 12 for the genus. Chromosome numbers for 13 species are described for the first time. The highest ploidy level yet observed in the genus (2n = lOx = 120) is reported for E. villosa var.  villosa. B chromosomes were observed in several specimens of four different species.


1969 ◽  
Vol 20 (5) ◽  
pp. 883 ◽  
Author(s):  
AJ Pritchard

The chromosome numbers of 31 species of Trifolium are reported, 18 for the first time. A reduction in basic chromosome number has occurred only in the three most highly specialized subgenera, and polyploids occur mainly in one of the more primitive subgenera.


1991 ◽  
Vol 116 (2) ◽  
pp. 336-341 ◽  
Author(s):  
N. Vorsa ◽  
James R. Ballington

Eight highbush blueberry (V. corymbosum L.) triploids (2n = 3x = 36) were crossed with diploids (2n = 2x = 24), tetraploids (2n = 4x = 48), and hexaploids (2n = 6x = 72). No plants were recovered from 4021 3x × 2x crosses. One triploid was relatively fertile in 3x × 4x and 3x × 6x crosses, which is most likely attributable to 2n gamete production in the triploid. The lack of fertility of triploids, which do not produce 2n gametes, in crosses with diploids and tetraploids suggests that the production of gametes with numerically balanced (n = 12 or 24) chromosome numbers is extremely low. In addition, the inability to recover progeny from 3x × 2x crosses also suggests that aneuploid gametophytes and/or zygotes, including trisomics, are inviable in blueberry. Pollen stainability was also highly reduced in triploids. Frequency distributions of anaphase I pole chromosomal constitutions of three triploids were significantly different from one another. Two of the three distributions were shifted toward the basic chromosome number of 12, with one triploid having 25% poles with 12 chromosomes. However, the sterility of 3x × 2x and 2x × 3x crosses indicates that lagging chromosomes during meiotic anaphases are probably not excluded from gametes, resulting in unbalanced gametes in blueberry. Triploids can be used as a bridge to facilitate gene transfer from the diploid and tetraploid levels to the hexaploid level in blueberry.


2004 ◽  
Vol 52 (1) ◽  
pp. 13 ◽  
Author(s):  
Khidir W. Hilu

The wide range in basic chromosome number (x = 2–18) and prevalence of polyploidy and hybridisation have resulted in contrasting views on chromosomal evolution in Poaceae. This study uses information on grass chromosome number and a consensus phylogeny to determine patterns of chromosomal evolution in the family. A chromosomal parsimony hypothesis is proposed that underscores (1) the evolution of the Joinvilleaceae/Ecdeiocoleaceae/Poaceae lineage from Restionaceae ancestors with x = 9, (2) aneuploid origin of x�=�11 in Ecdeiocoleaceae and Poaceae (Streptochaeta, Anomochlooideae), (3) reduction to x = 9, followed by chromosome doubling within Anomochlooideae to generate the x = 18 in Anomochloa, and (4) aneuploid increase from the ancestral x = 11 to x = 12 in Pharoideae and Puelioideae, and further diversification in remaining taxa (Fig. 3b). Higher basic chromosome numbers are maintained in basal taxa of all grass subfamilies, whereas smaller numbers are found in terminal species. This finding refutes the 'secondary polyploidy hypothesis', but partially supports the 'reduction hypothesis' previously proposed for chromosomal evolution in the Poaceae.


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