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  • Flagella  (2)
  • Crane-fly spermatocytes  (1)
  • 1
    ISSN: 1615-6102
    Keywords: Flagella ; Flagellar apparatus ; Epipyxis ; Chrysophyceae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Cells ofEpipyxis pulchra possess two heteromorphic flagella that differ markedly in function, particularly during motility and prey capture. Flagellar heterogeneity is achieved during the course of at least three cell cycles. Prior to cell division, cells produce two new long, hairy flagella while the parental long flagellum is transformed into a new short, smooth flagellum. The parental short flagellum remains a short flagellum for this and subsequent cell division cycles. Although flagellar transformation requires only two cell cycles, developmental differences exist between daughter cells and the maturation of a flagellum/basal body requires at least three cycles.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 176 (1993), S. 14-16 
    ISSN: 1615-6102
    Keywords: Axoneme ; Flagella ; Historical ; Microtubule
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary An early paper demonstrating the existence of fibrils (microtubules) within the flagellum is summarised. The paper appears the first to have demonstrated the existence of flagellar microtubules using electron microscopy, and it has been neglected in the literature.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1615-6102
    Keywords: Mitosis ; Ultraviolet microbeam ; Spindle fibres ; Microtubules ; Crane-fly spermatocytes ; Newt epithelial cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary In order to resolve apparent differences in reported experiments, we directly compared the effects of ultraviolet (UV) microbeam irradiations on the behaviour of spindle fibres in newt epithelial cells and crane-fly spermatocytes, using the same apparatus for both cell types. This work represents the first time that irradiated crane-fly spermatocytes have been followed using a high-NA objective and video-enhancement of images. In both cell types, irradiation of a kinetochore fibre in metaphase produced an area of reduced birefringence (ARB), known to be devoid of spindle microtubules (MTs). Subsequently the kinetochore-ward edge of the ARB moved poleward with average velocities of 0.5 μm/min (n=20) in spermatocytes and 1.1 μm/min (n=6) in epithelial cells. The poleward edge of the ARB rapidly disappeared when viewed using a ×100, high-NA objective but generally remained visible when viewed with a ×32, low-NA objective; this difference suggests that MTs poleward from the ARB disperse vertically out of the narrow depth of field of the ×100 objective but that many remain encompassed by that of the ×32 objective. The primary difference in response between the two cell types was in the behaviour of the spindle poles after an ARB formed. In spermatocytes the spindle maintained its original length whereas in epithelial cells the pole on the irradiated side very soon moved towards the chromosomes, after which the other pole did the same and a much shortened functional metaphase spindle was formed.
    Type of Medium: Electronic Resource
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