key words flow cytometry
Recently Published Documents


TOTAL DOCUMENTS

2
(FIVE YEARS 0)

H-INDEX

2
(FIVE YEARS 0)

1998 ◽  
Vol 76 (1) ◽  
pp. 157-165 ◽  
Author(s):  
Jérôme Thibault

Flow cytometry (FCM) has been used to estimate the nuclear DNA content of 11 Salix species and 5 hybrids. One hundred and sixty nine individuals were studied including 159 individuals from a sequence of 32 communities along a stretch of river in France and 10 individuals from French and English collections for comparison. Isolated nuclei were stained with propidium iodide. FCM was a significantly more practical and rapid technique than that of establishing the karyotype to survey many samples of Salix for variation in ploidy. The 2C DNA amounts for diploid species ranged from 0.76 to 0.98 pg, and tetraploid values ranged from 1.62 to 1.80 pg. The DNA values were consistent with the known ploidy levels. With the exception of a doubtful Salix xquercifolia, ploidy levels and DNA amounts of hybrids were intermediate compared with those of their parents. Intraspecific variation of nuclear DNA values including instrumental variation was low (i.e., 6-11% at the same ploidy level). FCM appeared to be an accurate tool for determination of Salix triploid hybrids. However, it remains limited concerning hybrids from crosses between species of the same ploidy level. Results suggest that natural hybridization might not be frequent in the communities studied, although they have been subject to disturbance. Previous overestimates of hybridization frequency in willows were probably due to misinterpretation of the effects of the environment on Salix spp. morphology; however, the extent and mechanisms of introgression in the genus remain to be further investigated. Key words: flow cytometry, Salix, hybridization, nuclear DNA content, riparian vegetation, disturbance.



1992 ◽  
Vol 70 (4) ◽  
pp. 802-809 ◽  
Author(s):  
K. Fuchs ◽  
K. P. Pauls

Flow cytometry was found to be sensitive to change in the physical characteristics of developing Brassica napus microspores. By measuring forward angle (10° – 19°) light scatter (FALS) and log 90° light scatter (L90LS) several stages of microspore development were characterized in small (1.5 mm to 2.5 mm), medium (2.5 mm to 3.5 mm), and large (3.5 mm to 4.5 mm) buds. Cell sorting was used to identify the types of cells that made up the subpopulations in two parameter plots of FALS versus L90LS including tetrad, translucent, trilobate, round, and oval microspores. Microspore development was found to be synchronous in the variety that was studied (‘Topas’) since only a few stages were found in each bud-size category. The study defined the normal process of pollen ontogeny in terms of the changes in light scatter that the cells underwent and demonstrated that flow cytometry is a useful method for analyzing this process. Key words: flow cytometry, Brassica napus, microspores, pollen, light scatter.



Sign in / Sign up

Export Citation Format

Share Document