Pollen Tube Pathway and Stimulation of Embryo Sac Development inPistacia vera(Anacardiaceae)

1997 ◽  
Vol 79 (4) ◽  
pp. 361-369 ◽  
Author(s):  
Y SHURAKI
1970 ◽  
Vol 48 (1) ◽  
pp. 27-41 ◽  
Author(s):  
Jack Maze ◽  
Lesly R. Bohm ◽  
Lyle E. Mehlenbacher Jr.

The ovules of Stipa tortilis and Oryzopsis miliacea are hemianatropous, bitegmetic, and pseudocrassinucellate (sensu Davis 1966). The hemianatropous shape of the ovule is the result of characteristic patterns of cell division and enlargement in the chalazal area and areas alongside the embryo sac. Embryo sac development in both is Polygonum-type and both have proliferating antipodals. Endosperm is nuclear, although in O. miliacea it is atypical in that nuclear division is synchronous within one portion of the embryo sac, e.g. micropylar, but not synchronous between different portions of the embryo sac, e.g., micropylar and chalazal. Differences in ovule initiation, persistence of the outer integument, fate of the inner integument, nature of the nucellus, shape of the embryo sac, nature of the synergids, cytoplasm of the egg, polar nuclei, and endosperm exist between these two taxa. Both synergids of O. miliacea undergo changes before fertilization and one degenerates before fertilization. The pollen tube enters the embryo sac at the base of the persistent synergid. There is presently insufficient embryological data to permit meaningful speculation on relationships between Stipa and Oryzopsis. Embryologically, Stipa and Oryzopsis are festucoid grasses, as much other evidence indicates. Embryo sac development in the Gramineae is more similar to that of the Restionaceae than to that of the Cyperaceae. This is in contradiction to recent speculations on the relationships of the Gramineae.


2019 ◽  
Vol 61 (4) ◽  
pp. 313-322
Author(s):  
Milena Đorđević ◽  
Radosav Cerović ◽  
Sanja Radičević ◽  
Dragan Nikolić ◽  
Nebojša Milošević ◽  
...  

2012 ◽  
Vol 30 (2) ◽  
pp. 188 ◽  
Author(s):  
Dong-Mei LI ◽  
Cheng-Hou WU ◽  
Xiu-Lin YE ◽  
Cheng-Ye LIANG

2021 ◽  
Vol 22 (5) ◽  
pp. 2603
Author(s):  
Ana Marta Pereira ◽  
Diana Moreira ◽  
Sílvia Coimbra ◽  
Simona Masiero

Angiosperm reproduction relies on the precise growth of the pollen tube through different pistil tissues carrying two sperm cells into the ovules’ embryo sac, where they fuse with the egg and the central cell to accomplish double fertilization and ultimately initiate seed development. A network of intrinsic and tightly regulated communication and signaling cascades, which mediate continuous interactions between the pollen tube and the sporophytic and gametophytic female tissues, ensures the fast and meticulous growth of pollen tubes along the pistil, until it reaches the ovule embryo sac. Most of the pollen tube growth occurs in a specialized tissue—the transmitting tract—connecting the stigma, the style, and the ovary. This tissue is composed of highly secretory cells responsible for producing an extensive extracellular matrix. This multifaceted matrix is proposed to support and provide nutrition and adhesion for pollen tube growth and guidance. Insights pertaining to the mechanisms that underlie these processes remain sparse due to the difficulty of accessing and manipulating the female sporophytic tissues enclosed in the pistil. Here, we summarize the current knowledge on this key step of reproduction in flowering plants with special emphasis on the female transmitting tract tissue.


1994 ◽  
Vol 91 (1) ◽  
pp. 37-44 ◽  
Author(s):  
Francisco R. Tadeo ◽  
Manuel Talon ◽  
Eric Germain ◽  
Francoise Dosba

1986 ◽  
Vol 34 (4) ◽  
pp. 413 ◽  
Author(s):  
EG Williams ◽  
V Kaul ◽  
JL Rouse ◽  
BF Palser

Frequent overgrowths of pollen tubes within the embryo sac are characteristic of a number of interspecific crosses in the genus Rhododendron (Ericaceae). The combined techniques of sectioning, squashing and whole-ovule clearing have confirmed that in ovules showing this phenomenon the pollen tube fails to terminate growth and release sperms on entry into a synergid; instead it continues to grow beyond the synergid and egg cell, often filling the main body of the embryo sac with a coiled and distorted mass. Such ovules fail to develop further. The occurrence and possible causes of this error syndrome are discussed.


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