FURTHER OBSERVATIONS ON THE REDUCTION OF FUSIFORM CAMBIAL CELLS IN THUJA OCCIDENTALIS L.

1953 ◽  
Vol 31 (1) ◽  
pp. 63-74 ◽  
Author(s):  
M. W. Bannan
Keyword(s):  
Cell Division ◽  
Cell Volume ◽  
Cell Shape ◽  
Transitional Period ◽  
Radial Expansion ◽  
Cambial Cell ◽  
Thuja Occidentalis ◽  
Daughter Cells ◽  
Fusiform Initials ◽  
Cambial Cells

The multiplication of fusiform initials in the cambium is accompanied by extensive loss or transformation of these cells. A few of the failing cambial cells lapse into maturation quickly, but the majority are transversely subdivided with varying proportions of the segments surviving and undergoing ultimate conversion to ray initials. The loss or conversion is attended with reduction in cell size. Increase in cell volume lags behind cell division during the periclinal divisions of the transitional period. The tangential dimensions of the successively formed cells are continuously reduced, and sometimes radial expansion is also retarded, especially toward the cell tips. Simultaneous shortening of the cells is due to alteration in cell shape combined with asymmetry in periclinal division such that daughter cells of unequal lengths are produced. Repetition of the process, the smaller cell functioning as the initiating cambial cell in each instance, results in continued shortening.

RAY CONTACTS AND RATE OF ANTICLINAL DIVISION IN FUSIFORM CAMBIAL CELLS OF SOME PINACEAE

1965 ◽  
Vol 43 (5) ◽  
pp. 487-508 ◽  
Author(s):  
M. W. Bannan
Keyword(s):  
Cell Multiplication ◽  
Cambial Cell ◽  
Intrinsic Factors ◽  
Ray Parenchyma ◽  
Ray Cells ◽  
Anticlinal Division ◽  
Fusiform Initials ◽  
Ray Parenchyma Cells ◽  
Cambial Cells ◽  
Resin Canals

The frequency of pseudotransverse divisions involved in cambial cell multiplication was found to be slightly higher in fusiform initials bordering on fusiform rays than in other cambial cells. The extent of difference was greater in Pinus than in Pseudotsuga or Picea. Because of the larger size of fusiform rays as compared to uniseriate rays, cambial cells adjoining the former were in contact with more ray cells per millimeter of cell length than cambial cells touching only uniseriate rays. As with the frequency of pseudotransverse division, the margin of difference in extent of ray contact was greater in Pinus than in Pseudotsuga or Picea. The evidence therefore indicates that the higher rate of pseudotransverse division in cambial cells adjoining fusiform rays was correlated with the greater area of ray contact, or more specifically, the increased contact with ray parenchyma cells. The higher rate of anticlinal division was apparently the consequence of an increase in ratio of survival of daughter initials arising in pseudotransverse division, some of the smaller newly formed initials persisting in contrast to the usual failure of similar initials situated elsewhere in the cambium. Mean height of uniseriate rays tended to increase with widening of the annual rings, but the size of fusiform rays was influenced to a much smaller degree. The frequency of fusiform rays, and horizontal resin canals, showed no consistent relationship with growth rate, but appeared to be determined by intrinsic factors.

scholarly journals Combined effect of cell geometry and polarity domains determines the orientation of unequal division

eLife ◽  
2021 ◽  
Vol 10 ◽  
Author(s):  
Benoit G Godard ◽  
Remi Dumollard ◽  
Carl-Philipp Heisenberg ◽  
Alex McDougall
Keyword(s):  
Cell Division ◽  
Mitotic Spindle ◽  
Cell Shape ◽  
Daughter Cell ◽  
Cleavage Plane ◽  
Mitotic Cell ◽  
Cell Geometry ◽  
Daughter Cells ◽  
Ascidian Embryos ◽  
Spindle Position

Cell division orientation is thought to result from a competition between cell geometry and polarity domains controlling the position of the mitotic spindle during mitosis. Depending on the level of cell shape anisotropy or the strength of the polarity domain, one dominates the other and determines the orientation of the spindle. Whether and how such competition is also at work to determine unequal cell division (UCD), producing daughter cells of different size, remains unclear. Here, we show that cell geometry and polarity domains cooperate, rather than compete, in positioning the cleavage plane during UCDs in early ascidian embryos. We found that the UCDs and their orientation at the ascidian third cleavage rely on the spindle tilting in an anisotropic cell shape, and cortical polarity domains exerting different effects on spindle astral microtubules. By systematically varying mitotic cell shape, we could modulate the effect of attractive and repulsive polarity domains and consequently generate predicted daughter cell size asymmetries and position. We therefore propose that the spindle position during UCD is set by the combined activities of cell geometry and polarity domains, where cell geometry modulates the effect of cortical polarity domain(s).

Bud and cambial zone phenology of lateral branches from Douglas-fir (Pseudotsugamenziesii) seedlings

1994 ◽  
Vol 24 (2) ◽  
pp. 286-296 ◽  
Author(s):  
K.H. Rensing ◽  
J.N. Owens
Keyword(s):  
Cell Division ◽  
Secondary Growth ◽  
Morphological Characteristics ◽  
Wood Formation ◽  
Douglas Fir ◽  
Winter Period ◽  
Cambial Cell ◽  
Leaf Initiation ◽  
Cambial Zone ◽  
Cambial Cells

Bud and cambial zone phenologies of outdoor-grown, containerized seedlings of Pseudotsugamenziesii (Mirb.) Franco (Douglas-fir) were determined and compared. Morphological characteristics of the live primordial shoots were related to known stages of bud development, while cambial zone phenology was based on anatomical characteristics. Secondary growth in branches of P. menziesii seedlings was separated into six stages: (i) early wood formation; (ii) latewood formation; (iii) cessation of cambial cell division; (iv) dormancy; (v) cambial cell expansion; and (vi) resumption of cell division. Early wood formation by the cambial zone, and primary leaf initiation in the shoot tips occurred until July. During this time of maximal activity, differences in wall thickness and shape distinguished cambial cells from vascular cells in early differentiation stages. By late July, earlywood formation was changing to latewood formation and bud-scale initiation had begun. The transition to preformed leaf initiation in the buds occurred over a period of 1 month in August and September. Cambial cell division ceased in early September but tracheid differentiation continued until about the end of October. Preformed leaf initiation lasted until the buds became dormant in mid-November. The cambial zone was dormant from the end of November until the beginning of March, and in transverse section was characterized by a distinct boundary at the border of the xylem and regular, cigar-shaped cambial cells with thick radial walls. Resumption of cambial activity in the 1st week of April began with radial expansion, followed about 2 weeks later by cell division. Differentiation of earlywood tracheids and bud swelling began in early April. The majority of buds flushed in the 3rd week of April. Rays in the lateral shoots were composed of monoseriate files of radially elongated cells. Ray initials were not observed. Ultrastructural features indicated that the dictyosomes of the cambial cells were active during the winter period.

Relative daughter cell volume and position of the division furrow in Tetrahymena

1983 ◽  
Vol 61 (1) ◽  
pp. 273-287
Author(s):  
K.K. Hjelm
Keyword(s):  
Cell Division ◽  
Cell Surface ◽  
Cell Volume ◽  
Mother Cell ◽  
Daughter Cell ◽  
Tetrahymena Pyriformis ◽  
Posterior Pole ◽  
Live Cells ◽  
Final Position ◽  
Daughter Cells

The relative daughter cell volume (RDCV) values for Tetrahymena pyriformis were determined at division on live cells. It was found that the anterior cell is generally larger than the posterior cell, and that the RDCV values are distributed in groups 5–6% apart. The RDCV value was found to be independent of predivision cell volume, indicating that the mother cell is divided into proportional volumes. The cells seem, however, not to assess volume directly but rather a parameter related to the cell volume. Furthermore, the RDCV value was found to increase during cell division, so that the final value is not reached until actual separation of daughter cells. It is suggested that the division furrow is positioned so that the area of the cell surface lying between the old oral apparatus and the posterior pole of the cell is divided into equal parts. It is further suggested that several alternative values of the RDCV are possible, only one of which is expressed in each cell. The early division furrow is placed anteriorly to its final position, and its location is adjusted during cytokinesis.

Cell Volume and the Control of the Chlamydomonas Cell Cycle

1982 ◽  
Vol 54 (1) ◽  
pp. 173-191 ◽  
Author(s):  
R. A. CRAIGIE ◽  
T. CAVALIER-SMITH
Keyword(s):  
Cell Cycle ◽  
Cell Wall ◽  
Cell Division ◽  
Simple Model ◽  
Cell Volume ◽  
Mother Cell ◽  
Dark Period ◽  
Size Fractions ◽  
Daughter Cells ◽  
Mother Cell Wall

Chlamydomonas reinhardii divides by multiple fission to produce 2n daughter cells per division burst, where n is an integer. By separating predivision cells from synchronous cultures into fractions of differing mean cell volumes, and electronically measuring the numbers and volume distributions of the daughter cells produced by the subsequent division burst, we have shown that n is determined by the volume of the parent cell. Control of n can occur simply, if after every cell division the daughter cells monitor their volume and divide again if, and only if, their volume is greater than a fixed minimum value. In cultures synchronized by 12-h light/12-h dark cycles, the larger parent cells divide earlier in the dark period than do smaller cells. This has been shown by two independent methods: (1) by separating cells into different size fractions by Percoll density-gradient centrifugation and using the light microscope to see when they divide; and (2) by studying changes in the cell volume distribution of unfractioned cultures. Since daughter cells remain within the mother-cell wall for some hours after cell division, and cell division causes an overall swelling of the mother-cell wall, the timing of division can be determined electronically by measuring this increase in cell volume that occurs in the dark period in the absence of growth; we find that cells at the large end of the size distribution range undergo this swelling first, and are then followed by successively smaller size fractions. A simple model embodying a sizer followed by a timer gives a good quantitative fit to these data for 12-h light/12-h dark cycles if cell division occurs 12-h after attaining a critical volume of approximately 140 μm3. However, this simple model is called into question by our finding that alterations in the length of the light period alter the rate of progress towards division even of cells that have attained their critical volume. We discuss the relative roles of light and cell volume in the control of division timing in the Chlamydomonas cell cycle.

THE REDUCTION OF FUSIFORM CAMBIAL CELLS IN CHAMAECYPARIS AND THUJA

1951 ◽  
Vol 29 (1) ◽  
pp. 57-67 ◽  
Author(s):  
M. W. Bannan
Keyword(s):  
Frequent Occurrence ◽  
Daughter Cells ◽  
Fusiform Initials ◽  
Cambial Cells ◽  
Fusiform Initial ◽  
Ray Initials

The loss of fusiform initials from the cambium, which is of frequent occurrence in all parts of the tree, takes place in different ways. Some cambial cells seem gradually to fail and are shortly lost from the cambium by maturation into more or less imperfect xylem or phloem elements. The majority are transversely subdivided by one or a succession of anticlinal divisions which begin near the center of the fusiform initial and usually extend to the daughter cells. The resulting segments shorten through the following periclinal divisions, some disappearing during the process of shortening and others undergoing transformation to ray initials. Nearly all new rays in the secondary body originate in this manner.

CAMBIAL BEHAVIOR WITH REFERENCE TO CELL LENGTH AND RING WIDTH IN THUJA OCCIDENTALIS L.

1960 ◽  
Vol 38 (2) ◽  
pp. 177-183 ◽  
Author(s):  
M. W. Bannan
Keyword(s):  
Ring Width ◽  
Growth Patterns ◽  
Cell Length ◽  
Cell Multiplication ◽  
Radial Increment ◽  
Cambial Cell ◽  
Thuja Occidentalis ◽  
Profound Influence ◽  
Fusiform Initials ◽  
The Relationship

The relationship between ring width and length of wood cells was studied by reference to mature white cedar trees of various growth patterns. These included trees of similar diameter but diverse growth rates, trees with transition from wide to narrow rings or from narrow to wide rings in their peripheral growth, and trees with rings varying in width in different radii. Although much fluctuation occurred among individuals there was in general an inverse relationship between cell length and ring width. On the other hand, the variations in frequency of pseudotransverse divisions in the cambium, which might be expected to have a profound influence on cell length because of their involvement in cambial cell multiplication, were not obviously related to the growth rate. The frequency of pseudotransverse divisions in the fusiform initials apparently is geared neither to circumferential expansion nor to number of periclinal divisions in the cambium but rather seems to be related simply to linear radial increment.

Altered morphology produced by ftsZ expression in Corynebacterium glutamicum ATCC 13869

Microbiology ◽  
2005 ◽  
Vol 151 (8) ◽  
pp. 2563-2572 ◽  
Author(s):  
Angelina Ramos ◽  
Michal Letek ◽  
Ana Belén Campelo ◽  
José Vaquera ◽  
Luis M. Mateos ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Cell Division ◽  
Corynebacterium Glutamicum ◽  
Cell Shape ◽  
Immunofluorescence Microscopy ◽  
Positive Bacterium ◽  
Fluorescent Band ◽  
Cylindrical Cell ◽  
Daughter Cells ◽  
Fold Reduction

Corynebacterium glutamicum is a Gram-positive bacterium that lacks the cell division FtsA protein and actin-like MreB proteins responsible for determining cylindrical cell shape. When the cell division ftsZ gene from C. glutamicum (ftsZCg ) was cloned in different multicopy plasmids, the resulting constructions could not be introduced into C. glutamicum; it was assumed that elevated levels of FtsZ Cg result in lethality. The presence of a truncated ftsZCg and a complete ftsZCg under the control of Plac led to a fourfold reduction in the intracellular levels of FtsZ, generating aberrant cells displaying buds, branches and knots, but no filaments. A 20-fold reduction of the FtsZ level by transformation with a plasmid carrying the Escherichia coli lacI gene dramatically reduced the growth rate of C. glutamicum, and the cells were larger and club-shaped. Immunofluorescence microscopy of FtsZ Cg or visualization of FtsZ Cg –GFP in C. glutamicum revealed that most cells showed one fluorescent band, most likely a ring, at the mid-cell, and some cells showed two fluorescent bands (septa of future daughter cells). When FtsZ Cg –GFP was expressed from Plac, FtsZ rings at mid-cell, or spirals, were also clearly visible in the aberrant cells; however, this morphology was not entirely due to GFP but also to the reduced levels of FtsZ expressed from Plac. Localization of FtsZ at the septum is not negatively regulated by the nucleoid, and therefore the well-known occlusion mechanism seems not to operate in C. glutamicum.

RING WIDTH, TRACHEID SIZE, AND RAY VOLUME IN STEM WOOD OF THUJA OCCIDENTALIS L.

1954 ◽  
Vol 32 (3) ◽  
pp. 466-479 ◽  
Author(s):  
M. W. Bannan
Keyword(s):  
Ring Width ◽  
Cambial Activity ◽  
Thuja Occidentalis ◽  
Stem Wood ◽  
Rate Of Growth ◽  
Fusiform Initials ◽  
Similar Range ◽  
Cambial Cells ◽  
Rates Of Growth

The interrelations between varied growth rates and those phases of cambial activity involved in determination of tracheid size and ray volume were investigated in Thuja occidentalis. Length of tracheids at the time of pseudotransverse division of the initiating cambial cells was determined from the peripheral wood of stems which fell within a similar range of size but differed in their rates of growth. The circumstances which favored accelerated growth, as shown in more frequent periclinal divisions in the cambium, encouraged earlier pseudotransverse division of fusiform initials and hence the production of shorter tracheids. Among trees of similar size decline in growth rate was accompanied by lengthening of cambial cells to a maximum associated with annual radial increments of 0.7 to 0.8 mm. Tracheid diameter was only slightly influenced by the rate of growth. Tangential width underwent minor increase in suppressed trees and radial diameter was slightly augmented in fast-growing trees. A positive correlation was revealed between ray volume and rate of growth.

THE RATE OF ELONGATION OF FUSIFORM INITIALS IN THE CAMBIUM OF PINACEAE

1965 ◽  
Vol 43 (4) ◽  
pp. 429-435 ◽  
Author(s):  
M. W. Bannan
Keyword(s):  
Cell Elongation ◽  
Radial Growth ◽  
Ring Width ◽  
Total Width ◽  
Mature Trees ◽  
Cambial Cell ◽  
Anticlinal Division ◽  
Fusiform Initials ◽  
Wide Ring ◽  
Cambial Cells

This report deals with the rate and amount of elongation of fusiform initials in the cycle of cell elongation and multiplication by pseudotransverse division which accompanies circumferential expansion of the cambium. In the recent growth of mature trees the yearly amount of cambial cell elongation drops as ring width decreases, but not in proportion to the decline in ring width. The cumulative elongation through lineal series of cells, per centimeter of xylem increment, increases as ring width decreases. The amount of cell elongation during the production of several narrow rings greatly exceeds that through a single wide ring having the same total width. It seems clear that the time factor is important in the elongation of cambial cells, and to some extent the interrelated frequency of anticlinal division, particularly when radial growth declines.

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