Pollen germination of Larix sibirica (Siberian larch) in vitro

1970 ◽  
Vol 48 (2) ◽  
pp. 213-215 ◽  
Author(s):  
Ronghui Ho ◽  
Glenn E. Rouse
Keyword(s):  
Pollen Tube ◽  
Pollen Germination ◽  
Generative Cell ◽  
Siberian Larch ◽  
Pollen Grains ◽  
The Body ◽  
Stalk Cell ◽  
Body Cell

Mature pollen grains of Siberian larch were successfully germinated in vitro for the first time. Mature grains, containing two prothallial cells, a generative cell, and a tube cell, were incubated in stock solution B for periods up to 5 days. At the 2-day stage, the generative cell had divided into a stalk cell and body cell. In 5 days, the body nucleus had divided into two male nuclei contained within the body cell. Pollen germination was limited to elongation of the intine towards the distal pole, accompanied by a splitting of the exine, but without any suggestion of the formation of a pollen tube. This supports the suggestion of previous studies in vivo on other species of Larix pollen that a pollen tube does not form before the pollen grain reaches the nucellus of the ovule.

Pollen germination of Tsuga heterophylla in vitro

1971 ◽  
Vol 49 (1) ◽  
pp. 117-119 ◽  
Author(s):  
RongHui Ho ◽  
Oscar Sziklai
Keyword(s):  
Male Gametophyte ◽  
Generative Cell ◽  
Calcium Nitrate ◽  
Pollen Grains ◽  
Potassium Nitrate ◽  
Tsuga Heterophylla ◽  
The Body ◽  
Stalk Cell

The development of the male gametophyte from western hemlock (Tsuga heterophylla (Raf.) Sarg.) pollen was complete after 5 days of incubation. This normally takes at least 6 weeks in vivo. The pollen was cultured in a solution containing boron, calcium nitrate, magnesium sulfate, and potassium nitrate. In 2 days the generative cell divided into the body cell and the stalk cell and after a further 3 days the body nucleus divided into two sperm nuclei. Morphological descriptions and measurements of the germinating pollen grains were made.

Germination and Development of Lodgepole Pine Pollen inVitro

1971 ◽  
Vol 1 (1) ◽  
pp. 12-19 ◽  
Author(s):  
Rong Hui Ho ◽  
Oscar Sziklai
Keyword(s):  
Pollen Tube ◽  
Pollen Tube Growth ◽  
Pollen Germination ◽  
Lodgepole Pine ◽  
Generative Cell ◽  
Calcium Nitrate ◽  
The Body ◽  
Tube Growth ◽  
Abnormal Development ◽  
Stalk Cell

Mature pollen grains of lodgepole pine (Pinuscontorta Dougl.) were incubated in solutions of sucrose, indoleacetic acid (IAA), and stock solution A containing boric acid, calcium nitrate, magnesium sulfate, and potassium nitrate. Sucrose solution did not stimulate pollen germination but did inhibit pollen tube growth. A slight promotion of tube growth resulted from an IAA solution, but no increase was obtained in germination percentage. Stock solution B (diluted one-tenth of concentration of stock solution A) was optimum for pollen germination and pollen tube growth. Two basic types of pollen tube development and pollen tube branching occurred. An abnormal development of the pollen tube, protruding through the saccus, was recorded. After 5 days of incubation in stock solution B, the generative cell divided into the stalk cell and the body cell, and 2 days later the body nucleus divided to form two male nuclei of either equal or unequal sizes.

scholarly journals Pollen tube growth of Paeonia tenuifolia L. (Paeoniaceae) in vitro and in vivo

1970 ◽  
Vol 40 (1) ◽  
pp. 93-95 ◽  
Author(s):  
Feruzan Dane ◽  
Nuran Ekici
Keyword(s):  
Pollen Tube ◽  
Pollen Germination ◽  
Pollen Viability ◽  
Pollen Grains ◽  
Pollen Tubes ◽  
In Vivo Studies ◽  
In Vivo Growth ◽  
Paeonia Tenuifolia

In vitro and in vivo studies on pollen germination of Paeonia tenuifolia L. (Paeoniaceae) revealed that pollen grains are shed at two-celled stage. Normal and abnormal pollens were observed. Pollen viability was recorded between 55 and 75%. In vitro studies revealed 85% germination and usually the germination was monosphonic. Some pollen tubes with swollen tube tip and undulations were found. Styles and stigma were found to contain many pollen tubes 24 hrs after pollination. Key words: Paeonia tenuifolia; Pollen tube; In vitro growth; In vivo growth  DOI: http://dx.doi.org/10.3329/bjb.v40i1.8003 Bangladesh J. Bot. 40(1): 93-95, 2011 (June)

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 Tradescantia bracteata pollen in vitro: pollen tubes development and mitosis

2015 ◽  
Vol 46 (4) ◽  
pp. 587-598 ◽  
Author(s):  
E. Lewandowska ◽  
M. Charzyńska
Keyword(s):  
Pollen Tube ◽  
Generative Cell ◽  
Metaphase Plate ◽  
Pollen Grains ◽  
Neutral Red ◽  
Generative Nucleus ◽  
Mitotic Spindles ◽  
Germinating Pollen ◽  
Vacuolar System

About 90 per cent of <i>Tradescantia bracteata</i> pollen germinates <i>in vitro</i> after 15 min. Mitosis starts in the pollen tube after about 3 h. The mitotic trans-formations of chromosomes within the generative nucleus are not synchronized. They involve succesively the linearly arranged chromosomes in the elongated generative nucleus. In metaphase the chromosomes are arranged tandem-like linearly along the pollen tube. The chromatides translocate in anaphase from various distances to the poles in a plane parallel to the metaphase plate. This suggests that chromosomes have individual mitotic spindles and that coordination of the chromosome transformations in the generative cell is much less strict than in a typical somatic mitosis. Starch is the storage material of pollen grains. In the vegetative cytoplasm of mature pollen grains minute reddish-orange vesicular structures are visible after staining with neutral red. They do not fuse with the vacuoles proper arising in germinating pollen grains to form the vacuolar system of the pollen tube.

scholarly journals Impact of Manganese on Pollen Germination and Tube Growth in Lily

2021 ◽  
Vol 74 ◽  
Author(s):  
Thomas Sawidis ◽  
Gülriz Baycu ◽  
Elżbieta Weryszko-Chmielewska ◽  
Aneta Sulborska
Keyword(s):  
Pollen Tube ◽  
Pollen Germination ◽  
Surrounding Medium ◽  
Pollen Grains ◽  
Lilium Longiflorum ◽  
Tube Growth ◽  
Low Concentrations ◽  
Main Effect

Abstract In vitro culture of Lilium longiflorum pollen grains was carried out to determine the role of manganese in pollen germination and pollen tube growth. Pollen germination was adversely affected by the presence of manganese (>10 −8 M), whereas low concentrations (10 −12 –10 −10 M) stimulated the process. Manganese caused morphological anomalies during tube growth, characterized by irregular pollen tube thickening and swollen tips. The main effect was the anomalous cell wall formation at the tip, in which the presence of several organelles reduced the number of secretory vesicles. A loose network of fibrillar material and spherical aggregates, mostly in the tip region, was detected, and this material was progressively loosened into the surrounding medium. As a response to potential toxicity, the excess manganese was isolated in vacuoles, which formed an internal barrier against penetration of manganese to the tip area. Elevated manganese concentrations might affect plant reproduction, resulting in anomalies in gamete development. Consequently, the loss in genetic diversity and decreased fruit set ultimately lower yield.

scholarly journals In vitro germination and viability of pea pollen grains after application of organic nano-fertilizers

2017 ◽  
Vol 32 (1) ◽  
pp. 61-65 ◽  
Author(s):  
Natalia Georgieva ◽  
Ivelina Nikolova ◽  
Valentin Kosev ◽  
Yordanka Naydenova
Keyword(s):  
Pollen Tube ◽  
Pollen Germination ◽  
Culture Media ◽  
Pollen Viability ◽  
Pollen Grains ◽  
Pollen Grain ◽  
In Vitro Germination ◽  
Pisum Sativum L ◽  
Pollen Tube Elongation

The objective of this study was to evaluate the influence of two organic nanofertilizers, Lithovit and Nagro, on in vitro germination, pollen tube elongation and pollen grain viability of Pisum sativum L cv. Pleven 4. The effect of their application was high and exceeded data for the untreated control (44.2 and 47.23 % regarding pollen germination and pollen tube elongation, respectively), as well as the effect of the control organic algal fertilizer Biofa (17.5 and 27.9 %, respectively). Pollen grains were inoculated in four culture media. A medium containing 15% sucrose and 1% agar had the most stimulating impact on pea pollen grains. Pollen viability, evaluated by staining with 1% carmine, was within limits of 74.72-87.97%. The highest viability of pollen grains was demonstrated after the application of Nagro organic nano-fertlizer.

scholarly journals Investigations of suitable pollinator for 0900 Ziraat sweet cherry cv.: pollen performance tests, germination tests, germination procedures, in vitro and in vivo pollinations

2008 ◽  
Vol 34 (No. 2) ◽  
pp. 47-53 ◽  
Author(s):  
F. Tosun ◽  
F. Koyuncu
Keyword(s):  
Pollen Tube ◽  
Pollen Germination ◽  
Sweet Cherry ◽  
Fruit Set ◽  
Pollen Viability ◽  
Performance Tests ◽  
Pollen Performance ◽  
Growth Experiments

The objective of this study was to determine suitable cultivars to be used as pollinators for 0900 Ziraat. 0900 Ziraat was used as a female cultivar; Bigarreu Gaucher, Bing, Noble, Starks Gold, Stella, Van, and Vista were used for pollination in the experiments. Starks Gold had the highest values in terms of anther number, average number of pollens per anther, number of pollen per flower and the morphological homogeneity. The pollen viability rates showed significant differences according to stain tests. <i>In vitro</i> pollen germination in 0.5% agar + 15% sucrose + 5 ppm boric acid medium increased with increasing incubation period, and the highest germination was obtained after 48 hours for all cultivars. In orchard trials parallel to pollen tube growth experiments in the laboratory, 0900 Ziraat &times; Starks Gold combination gave the best fruit set results.

scholarly journals Pollen germination and pollen tube growth in ZP maize lines

Genetika ◽  
2014 ◽  
Vol 46 (3) ◽  
pp. 935-948 ◽  
Author(s):  
Radosav Cerovic ◽  
Zorica Pajic ◽  
Milomir Filipovic ◽  
Milica Fotiric-Aksic ◽  
Sanja Radicevic ◽  
...  
Keyword(s):  
Pollen Tube ◽  
Pollen Tube Growth ◽  
Pollen Germination ◽  
Growth Dynamics ◽  
Tube Growth ◽  
Open Pollination ◽  
Successful Management ◽  
Parental Lines

The study was conducted on the in vitro pollen germination at 26?, 28?, 32? and 35?C for 24h of male parental lines, pollen tube growth in vivo in cross pollination of female and male parental lines that make couples in four hybrids: ZP 504 su (? ZPPL 51 ? ? ZPPL 67); ZP 677 (? ZPPL 17 ? ? ZPPL 201); ZP 704 (? ZPPL 109 ? ? ZPPL 79), ZP 611 k (? ZPPL 126 ? ? ZPPL 105), and the open pollination of female parental lines of the above mentioned hybrids. Pollen germination in vitro and pollen tube growth dynamics in vivo showed different genotypic specificities with the tests applied. The obtained results were discussed in the context of reproductive biology of ZP maize lines and aimed to create the preconditions for successful management and direction of the process in practice - seed production in certain environmental conditions.

Generative cell mitosis in pollen tubes of Nicotiana tabacum: Ultrastructure and 3-D reconstruction

1992 ◽  
Vol 50 (1) ◽  
pp. 848-849
Author(s):  
Hong-Shi Yu ◽  
S. D. Russell
Keyword(s):  
Pollen Tube ◽  
Generative Cell ◽  
Three Dimensional ◽  
Metaphase Plate ◽  
Preprophase Band ◽  
Mitotic Division ◽  
Mitotic Apparatus ◽  
Cell Mitosis

In bicellular pollen, the two sperm cells are formed by mitotic division of the generative cell (GC) in the pollen tube. This division is characterized by several unique features, including: lack of a preprophase band (PPB), absence of a metaphase plate, absence of normal spindle formation, and irregular patterns of cytokinesis. Purportedly, this is the result of spatial constraints within the pollen tube, which in vivo may be as narrow as 3 μm (as in Nicotiana) and slightly wider in vitro.Immunofluorescence studies of GC mitosis have been published in the last five years2−7, but only one incomplete ultrastructural report on GC division in vitro is available. This study is the first using three-dimensional (3-D) techniques to reconstruct the mitotic apparatus of the GC in vivo.

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