Germination of Compound Pollen Grains

Grana ◽  
1972 ◽  
Vol 12 (2) ◽  
pp. 113-120 ◽  
Author(s):  
A. N. Rao ◽  
E. T. Ong
1997 ◽  
Vol 75 (9) ◽  
pp. 1448-1459 ◽  
Author(s):  
E. Pacini

The different types of tapetum found in the spermatophyta are described, along with associated characters. The characters (taken singly, pairwise, or in multiple combinations) are (i) tapetum types; (ii) cell walls, tapetum types, and loculus; (iii) tapetal cells individually, tapetum types, and loculus; (iv) number of pollen grains enveloped by tapetal cells and type of pollen dispersing unit; (v) cell types and tapetum types; (vi) number of nuclei per cell and tapetum type; (vii) cycles of hyperactivity; (viii) exine formation; (ix) orbicles; (x) peritapetal membrane; (xi) plastid differentiation; (xii) stage of pollen development in which tapetal cells degenerate and type of pollen coat; (xiii) storage vacuoles; (xiv) sporophytic proteins; and (xv) devices of tapetal origin responsible for compound pollen formation and pollination. Examples are given and an analytical key of structural and functional diversity is provided as a helpful approach to the study of the tapetum. Key words: tapetum types, activities, pollen dispersing units.


1965 ◽  
Vol 13 (3) ◽  
pp. 379 ◽  
Author(s):  
P Khanna

The stamens are whorled in Brasenia schreberei and spirally arranged in Nelumbo nucifera. The anther is tetrasporangiate. Parietal layers are five-celled in thickness in B. schreberei and six-celled in N. nucifera. Endothecial cells contain a tannin-like substance and develop fibrous thickenings in N. nucifera. The middle layers are persistent in N. nucifera and ephemeral in B. schreberei. The tapetal cells become multinucleate and the layer develops cutinization on its inner walls in N. nucifera. It is secretory. Micronuclei are formed at the meiosis in the microspore mother cells. These degenerate in B. schreberei and form micropollen grains in N. nucifera. Polysporads and compound pollen grains occur frequently in the latter. Pollen sterility is common. In B. schreberei the carpel is horseshoe-shaped, unites with its margins, and bears two to three pendulous ovules with lamina1 placentation. The carpel in N. nucifera, however, remains open in its early development, unites by the growth of the interlocking hairs, and contains a single ovule. A single parietal layer is present in B. schreberei, and four to five such layers in N. nucifera. A hypostase is formed in B. schreberei. The nucellus functions as perisperm in the latter and is consumed early in N. nucifera. A linear megaspore tetrad is formed in which the chalazal megaspore is functional. The embryo sac is of the Polygonum type. The antipodal cells are ephemeral in B. Schreberei and persistent with secondary multiplication in N. nucifera. In post-fertilized ovules one of the synergids is persistent. Fertilization is non-synchronous in N. nucifera and simultaneous in B. schreberei. In N. nucifera the antipodal cells become enlarged and multinucleate, and occupy the elongated tube formed by the downward penetration of the embryo sac. They degenerate at the early globular stage of the embryo and are not persistent when the embryo is pear-shaped. In B. schreberei a transverse cytokinesis follows division of the primary endosperm nucleus and two unequal cells are formed. The small chalazal endosperm cell penetrates the nucellus below and forms a long tube-like haustorium occupying three-quarters of the length of the nucellus. Its nucleus subsequently hypertrophies and degenerates completely at the globular stage of the embryo. Endosperm is ab initio cellular in B. schreberei and free nuclear in N. nucifera.


Author(s):  
John R. Rowley

The morphology of the exine of many pollen grains, at the time of flowering, is such that one can suppose that transport of substances through the exine occurred during pollen development. Holes or channels, microscopic to submicroscopic, are described for a large number of grains. An inner part of the exine of Epilobium angustifolium L. and E. montanum L., which may be referred to as the endexine, has irregularly shaped channels early in pollen development although by microspore mitosis there is no indication of such channeling in chemically fixed material. The nucleus in microspores used in the experiment reported here was in prophase of microspore mitosis and the endexine, while lamellated in untreated grains, did not contain irregularly shaped channels. Untreated material from the same part of the inflorescence as iron treated stamens was examined following fixation with 0.1M glutaraldehyde in cacodylate-HCl buffer at pH 6.9 (315 milliosmoles) for 24 hrs, 4% formaldehyde in phosphate buffer at pH 7.2 (1,300 milliosmoles) for 12 hrs, 1% glutaraldehyde mixed with 0.1% osmium tetroxide for 20 min, osmium tetroxide in deionized water for 2 hrs and 1% glutaraldehyde mixed with 4% formaldehyde in 0.1M cacodylate-HCl buffer at pH 6.9 for two hrs.


Author(s):  
Liza B. Martinez ◽  
Susan M. Wick

Rapid freezing and freeze-substitution have been employed as alternatives to chemical fixation because of the improved structural preservation obtained in various cell types. This has been attributed to biomolecular immobilization derived from the extremely rapid arrest of cell function. These methods allow the elimination of conventionally used fixatives, which may have denaturing or “masking” effects on proteins. Thus, this makes them ideal techniques for immunocytochemistry, in which preservation of both ultrastructure and antigenicity are important. These procedures are also compatible with cold embedding acrylic resins which are known to increase sensitivity in immunolabelling.This study reveals how rapid freezing and freeze-substitution may prove to be useful in the study of the mobile allergenic proteins of rye grass and ragweed. Most studies have relied on the use of osmium tetroxide to achieve the necessary ultrastructural detail in pollen whereas those that omitted it have had to contend with poor overall preservation.


2014 ◽  
Vol 27 (1) ◽  
pp. 245-253
Author(s):  
Muhannad R. J. Allamy ◽  
TTaha Y. Al-Edany
Keyword(s):  

2020 ◽  
Vol 62 (1-2) ◽  
pp. 151-161
Author(s):  
T. Shagholi ◽  
M. Keshavarzi ◽  
M. Sheidai

Tamarix L. (Tamaricaceae) is a halophytic shrub in different parts of Asia and North Africa. Taxonomy and species limitation of Tamarix is very complex. This genus has three sections as Tamarix, Oligadenia, and Polyadenia, which are mainly separated by petal length, the number of stamens, the shape of androecial disk and attachment of filament on the androecial disk. As there was no palynological data on pollen features of Tamarix species of Iran, in the present study 12 qualitative and quantitative pollen features were evaluated to find diagnostic ones. Pollen grains of 8 Tamarix species were collected from nature. Pollen grains were studied without any treatment. Measurements were based on at least 50 pollen grains per specimen. Light and scanning electron microscopes were used. Multivariate statistical methods were applied to clarify the species relationships based on pollen data. All species studied showed monad and tricolpate (except some individuals of T. androssowii). Some Tamarix species show a high level of variability, in response to ecological niches and phenotypic plasticity, which make Tamarix species separation much more difficult. Based on the results of the present study, pollen grains features are not in agreement with previous morphological and molecular genetics about the sectional distinction.


2020 ◽  
Vol 8 (14) ◽  
pp. 20-28
Author(s):  
Leonora Adamchuk ◽  
◽  
Vladyslav Sukhenko ◽  
Mykola Skoryk ◽  
◽  
...  

Palaeobotany ◽  
2012 ◽  
Vol 3 ◽  
pp. 5-11
Author(s):  
A. V. Gomankov ◽  
V. F. Tarasevich

Dispersed bisaccate pollen grains of Scutasporites nanuki were studied by means of LM, SEM and TEM. Sacci ultrastructure of these pollen grains was rather peculiar. Sacci were like a thin fi lmy fringe attached to the central body near the equator. They were fi lled with sporopollenin elements of irregular shape and various dimensions with equally various cavities between them. Such an ultrastructure is called as spongy. The morphology and ultrastructure of S. nanuki is discussed in the context of the evolution of early conifers.


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