In vivo pollen tube cell ofArabidopsis thaliana I. Tube cell cytoplasm and wall

PROTOPLASMA ◽  
2000 ◽  
Vol 214 (1-2) ◽  
pp. 45-56 ◽  
Author(s):  
K. A. Lennon ◽  
E. M. Lord
Keyword(s):  
Pollen Tube ◽  
Cell Cytoplasm ◽  
Ofarabidopsis Thaliana ◽  
Tube Cell

The development of the male gametophyte and spermatogenesis in Taxus baccata L

1986 ◽  
Vol 228 (1250) ◽  
pp. 85-96 ◽  
Keyword(s):  
Pollen Tube ◽  
De Novo ◽  
Male Gametophyte ◽  
Generative Cell ◽  
Equal Size ◽  
Taxus Baccata ◽  
Transverse Wall ◽  
Proximal Pole ◽  
Spermatogenous Cell ◽  
Tube Cell

The development of the male gametophyte of Taxus baccata has been studied over a period of 20 weeks, from germination of the microspore in February to spermatogenesis in July. A few days after germination the microspore nucleus divides and a transverse wall forms at the equator cutting off the small generative cell and a large tube cell. The latter immediately begins to expand to form the pollen tube. The first division thus establishes the polarity of the gametophyte and the generative cell is regarded as proximal. The transverse wall is ephemeral, and within six weeks it has disappeared. The nucleus of the generative cell divides while still at the proximal pole. The two daughter nuclei are unequal in size, but they remain associated and together move distally. The larger nucleus eventually becomes the nucleus of the spermatogenous cell, and the smaller the sterile nucleus. The spermatogenous cell acquires a distinctive cytoplasm and becomes surrounded by a wall which arises de novo . The nucleus of the spermatogenous cell enlarges, but always remains towards one side of the cell so that at mitosis the spindle is contained within one hemisphere. After division the wall of the spermatogenous cell is ruptured and the two sperms are released as naked nuclei of equal size. The cytoplasm of the spermatogenous cell degenerates as it enters the tube, but remains recognizable until fertilization.

Evidence against electrophoresis as the principal mode of protein transport in vitellogenic ovarian follicles of Drosophila

Development ◽  
1987 ◽  
Vol 101 (2) ◽  
pp. 279-288
Author(s):  
J. Bohrmann ◽  
H. Gutzeit
Keyword(s):  
Nurse Cell ◽  
Protein Transport ◽  
Exchange Chromatography ◽  
Heterologous Proteins ◽  
Nurse Cells ◽  
Cell Cytoplasm ◽  
Two Dimensional Gel Electrophoresis ◽  
Electrophoretic Transport ◽  
Indicator Dyes

Charged cell constituents in polytrophic insect follicles are thought to be transported in the nurse cell-oocyte syncytium by way of electrophoresis. This concept, proposed by Woodruff & Telfer (1980) was based on electrophysiological data and microinjection of heterologous proteins using Hyalophora follicles. By microinjecting fluorescently labelled acidic and basic proteins into the nurse cells or oocyte of vitellogenic Drosophila follicles, we failed to obtain evidence for charge-dependent migration of these molecules. We have also analyzed the proteins of nurse cells and oocyte on isoelectric focusing gels, by means of two-dimensional gel electrophoresis, and by ion exchange chromatography to see if basic or acidic proteins accumulate in vivo in nurse cells and oocyte, respectively. For the bulk of the follicular proteins we found no accumulation. Further evidence against an electrophoretic transport system in Drosophila was obtained by estimating the intracellular pH from the colour of indicator dyes microinjected into the follicles; the results indicate that the pH in the nurse cell cytoplasm is lower than that in the ooplasm. According to the model developed for Hyalophora, electrophoretic transport would be favoured by high pH in the nurse cell cytoplasm.

In Vitro Germination of Eucalyptus Pollen: Response to Variation in Boric Acid and Sucrose

1989 ◽  
Vol 37 (5) ◽  
pp. 429 ◽  
Author(s):  
BM Potts ◽  
JB Marsden-Smedley
Keyword(s):  
Pollen Tube ◽  
Boric Acid ◽  
Pollen Tube Growth ◽  
Pollen Germination ◽  
Sucrose Concentration ◽  
Response Surfaces ◽  
Tube Growth ◽  
Pollen Competition

The effect of boric acid (0-450 ppm) and sucrose (0-40%) on pollen germination and pollen tube growth in Eucalyptus globulus, E. morrisbyi, E. ovata and E. tirnigera was examined in vitro. Over the con- centrations tested, sucrose had by far the largest effect upon both pollen germination and tube lengths. The optimum sucrose concentration for pollen germination (30%) and pollen tube growth (20%) differed markedly with very little (<lo%) germination occurring in the absence of sucrose. The interaction of sucrose and boric acid was significant. However, in general both pollen germination and pollen tube growth were increased by the addition of up to 100 ppm boric acid, but above this level the response plateauxed. The four species differed significantly in their pattern of response to both boric acid and sucrose and the predicted optima derived from analysis of response surfaces differed between species. The predicted sucrose concentration for optimal germination and growth of E. urnigera pollen was consistently less than the other species and in terms of the optimal level of boric acid for pollen tube growth species can be ranked in the order E. globulus > E. ovata > E. morrisbyi = E. urnigera. Pollen germination and tube growth of all four species on a medium comprising 20% sucrose and 200 ppm boric acid would not differ significantly from the observed maximum response of each species and this could suffice as a generalised medium. However, if only percentage germination is to be assessed 30% sucrose would be preferable. It is argued that subtle interspecific differences in optimal in vitro con- ditions for pollen germination and pollen tube growth are likely to reflect differences in pollen physiology which in vivo may have important implications for the success of hybridisation where pollen competition occurs.

scholarly journals Effect of Genetically Diverse Pollen on Pollination, Pollen Tube Overgrow, Fruit Set and Morphology of Kiwiberry (Actinidia arguta)

Agronomy ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 1814
Author(s):  
Agnieszka Stasiak ◽  
Piotr Latocha ◽  
Monika Bieniasz
Keyword(s):  
Pollen Tube ◽  
Fruit Set ◽  
Fruit Weight ◽  
High Yield ◽  
Positive Interactions ◽  
Dioecious Plants ◽  
Pollen Quality ◽  
Pollination And Fertilization

Successful pollination and fertilization are crucial processes for obtaining a high yield, especially for dioecious plants such as A. arguta. Determination of pollen tube growth on stigma and fruit development parameters, which were investigated in this study, can enable the evaluation of male–female compatibility—one of the factors of successful pollination. Pollen quality and grain size were analysed for two years on six male cultivars of A. arguta and one of A. chinensis var. deliciosa. Results showed high pollen quality, both with parameters above 80%. Pollen germination in vivo showed differences in pollen–stigma interactions. The highest positive interactions were observed for all female cultivar crosses with male ‘Nostino’ and ‘Rubi’ and the lowest one for A. chinensis var. deliciosa ‘Tomuri’. However, fruit set and average fruit weight were equally high in most of the combinations (fruit set above 75% for the majority of combinations). Some differences were noticed in the average seed number per fruit and weight. All tested male cultivars were able to fertilize tested female cultivars, but taking into account other characteristics such as pollen efficiency, some male cultivars seemed to be more proper for commercial orchards. Using A. chinensis var. deliciosa pollen seems to be unreasonable in tested conditions.

Insemination of the archegonium and fertilization in Taxus baccata L

1988 ◽  
Vol 89 (4) ◽  
pp. 551-560
Author(s):  
ROGER I. PENNELL ◽  
PETER R. BELL
Keyword(s):  
Pollen Tube ◽  
Male Gametophyte ◽  
Sperm Nucleus ◽  
Taxus Baccata ◽  
Close Apposition ◽  
Cell Cytoplasm ◽  
Spermatogenous Cell ◽  
Tube Lumen ◽  
Sperm Nuclei ◽  
Progressive Enlargement

A study of fertilization in Taxus baccata in the electron microscope has revealed novel features. Insemination of the archegonium is facilitated by local perforation of the wall of the young pollen tube. Digestion of the wall begins before the pollen tube pierces the megaspore membrane but is not completed until its tip makes contact with the neck cells of the archegonium. As soon as a pore is formed a single sperm nucleus and some cytoplasm of the male gametophyte enter the archegonium. Which of the paired sperm nuclei move from the pollen tube into the archegonium appears to be a matter of chance. Close apposition of sperm nucleus and egg nucleus is followed by the formation of numerous points of contact between the two. The membranes fuse at these points and pores are rapidly formed. The progressive enlargement of these pores ultimately eliminates any partitions and yields the zygotic nucleus. There is a possibility that, as in some other gymnosperms, the plastids and mitochondria of the zygote come in part from the male gametophyte, but whether from the remains of the spermatogenous cell cytoplasm or from the. pollen tube lumen is not clear.

scholarly journals Laccase Expression in Murine Pulmonary Cryptococcus neoformans Infection

2005 ◽  
Vol 73 (5) ◽  
pp. 3124-3127 ◽  
Author(s):  
Javier Garcia-Rivera ◽  
Stephanie C. Tucker ◽  
Marta Feldmesser ◽  
Peter R. Williamson ◽  
Arturo Casadevall
Keyword(s):  
Electron Microscopy ◽  
Cell Wall ◽  
Cryptococcus Neoformans ◽  
Lung Tissue ◽  
Immunogold Electron Microscopy ◽  
Cell Cytoplasm ◽  
Fungal Cell ◽  
Time Of Infection

ABSTRACT Cryptococcus neoformans laccase expression during murine infection was investigated in lung tissue by immunohistochemistry and immunogold electron microscopy. Laccase was detected in the fungal cell cytoplasm, cell wall, and capsule in vivo. The amount of laccase found in different sites varied as a function of the time of infection.

Pollen–pistil interaction, pistil histology and seed production in A×B grain sorghum crosses under chilling field temperatures

2009 ◽  
Vol 148 (1) ◽  
pp. 73-82 ◽  
Author(s):  
M. E. CISNEROS-LÓPEZ ◽  
L. E. MENDOZA-ONOFRE ◽  
H. A. ZAVALETA-MANCERA ◽  
V. A. GONZÁLEZ-HERNÁNDEZ ◽  
G. MORA-AGUILERA ◽  
...  
Keyword(s):  
Pollen Tube ◽  
Seed Production ◽  
Pollen Tube Growth ◽  
Pollen Germination ◽  
Vascular Tissue ◽  
Pollen Viability ◽  
Tube Growth ◽  
Male Sterile ◽  
Pollen Diameter

SUMMARYSix pairs of isogenic lines of sorghum (Sorghum bicolor L. Moench) were sown in field plots in Montecillo, State of México (2240 m altitude), in 2005 and 2006. Crosses A (♀)×B (♂) were done in each pair. In A-lines, the length of pistil, stigma, style and ovary, as well as the ovary width, were measured. In B-lines, pollen diameter, viability (cytoplasm density) and production were evaluated. Pollen germination and pollen tube growth in the pistils of the A-lines, were quantified in vivo with aniline blue and epifluorescence 18 h after pollination (HAP), while fertilized pistils were counted at 96 HAP. Histological studies on both pollinated and non-pollinated pistils were performed in one male-sterile line. Seed yield, mean-seed weight, seeds per panicle and seed set (SS; seeds/flower/panicle) were determined at harvest. Pollen viability was the variable most related to pollen germination and pollen tube growth. Stigma receptivity was not associated with its morphology. Growth of the pollen tube in stigma, style and ovary was observed in the transmitting tissue 18 HAP, running parallel to the vascular tissue. Yield under chilling field temperatures (minimum average of 6 and 8°C) prevailing during flower development and pollination ranged from 7 to 12 g/panicle. The differences in seed production and SS among A×B crosses did not depend on the amount and viability of pollen.

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