scholarly journals Optimization of In Vitro Pecan Pollen Germination

HortScience ◽  
2011 ◽  
Vol 46 (4) ◽  
pp. 571-576 ◽  
Author(s):  
Patrick J. Conner
Keyword(s):  
Polyethylene Glycol ◽  
Pollen Germination ◽  
Pollen Grains ◽  
Solid Support ◽  
Carya Illinoinensis ◽  
Testing System ◽  
In Vitro Germination ◽  
Ethanesulfonic Acid ◽  
Made In

Storage of pollen from 1 year to the next is often needed to enable desired crosses to be made in a pecan [Carya illinoinensis (Wangenh.) K. Koch] breeding program. Stored pollen is usually tested for viability through the use of in vitro germination tests. An in vitro germination testing system was developed for this purpose using cellophane booklets to provide a solid support for the pollen grains. Optimized germination media contained 5% sucrose, 20% polyethylene glycol 8000, 0.05% Ca(NO3)2, 0.025% H3BO3, and 10 mm 2-(N-morpholino)ethanesulfonic acid pH 6.0. Pollen should be rehydrated for 2 to 4 h in a humidified chamber before germination testing. A germination time of 4 to 24 h produces similar final germination percentages. Testing of pollen samples stored at –80 °C indicates that pecan pollen can be stored for at least 8 years without a decrease in viability. Chemical names used: polyethylene glycol (PEG); 2-(N-morpholino)ethanesulfonic acid (MES).

scholarly journals Pecan Pollen Stored Over a Decade Retains Viability

HortScience ◽  
2002 ◽  
Vol 37 (1) ◽  
pp. 176-177 ◽  
Author(s):  
Darrell Sparks ◽  
I.E. Yates
Keyword(s):  
Liquid Nitrogen ◽  
Pollen Morphology ◽  
Germ Tube ◽  
Pollen Grains ◽  
Carya Illinoinensis ◽  
In Vitro Germination ◽  
Fresh Pollen

In vitro germination of freshly collected pollen and pollen stored 1, 10, 11, 12, and 13 years in liquid nitrogen was examined for `Desirable' pecan [Carya illinoinensis (Wangenh.) C. Koch]. Viability of pollen stored in liquid nitrogen for 1, 10, 11, 12, and 13 years was not diminished in comparison to that of fresh pollen. Morphology of stored pollen grains and the germ tube was normal. Thus, liquid nitrogen may offer a means of haploid preservation of pecan.

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 In vitro pollen germination and pollen viability in passion fruit (Passiflora spp.)

2013 ◽  
Vol 35 (4) ◽  
pp. 1116-1126 ◽  
Author(s):  
Taliane Leila Soares ◽  
Onildo Nunes de Jesus ◽  
Janay Almeida dos Santos-Serejo ◽  
Eder Jorge de Oliveira
Keyword(s):  
Pollen Germination ◽  
Culture Medium ◽  
Pollen Viability ◽  
Pollen Grains ◽  
In Vitro Germination ◽  
Triphenyltetrazolium Chloride ◽  
Histochemical Analysis ◽  
High Viability ◽  
Three Stages

The use of Passiflora species for ornamental purposes has been recently developed, but little is known about pollen viability and the potential for crossing different species. The objective of this study was to evaluate the pollen viability of six Passiflora species collected from different physiological stages of development through in vitro germination and histochemical analysis using dyes. The pollen was collected in three stages (pre-anthesis, anthesis and post-anthesis). Three compositions of culture medium were used to evaluate the in vitro germination, and two dyes (2,3,5-triphenyltetrazolium chloride, or TTC, and Lugol's solution) were used for the histochemical analysis. The culture medium containing 0.03% Ca(NO3) 4H2O, 0.02% of Mg(SO4 ).7H2O, 0.01% of KNO3, 0,01% of H3BO3, 15% sucrose, and 0.8% agar, pH 7.0, showed a higher percentage of pollen grains germinated. Anthesis is the best time to collect pollen because it promotes high viability and germination. The Lugol's solution and TTC dye overestimated the viability of pollen, as all accessions showed high viability indices when compared with the results obtained in vitro.

scholarly journals Horse chestnut pollen quality

Genetika ◽  
2017 ◽  
Vol 49 (1) ◽  
pp. 105-115 ◽  
Author(s):  
Dusica Calic ◽  
Ljiljana Radojevic
Keyword(s):  
Pollen Germination ◽  
Pollen Grains ◽  
Basic Medium ◽  
Horse Chestnut ◽  
In Vitro Germination ◽  
Pollen Quality ◽  
Pollen Productivity ◽  
Germination Tube

Pollen quality of horse chestnut, expressed as pollen productivity, viability and germination was studied. Anthers of horse chestnut genotypes had pollen production from 3.66 to 5.06 x 103 pollen grains per anther, depending of genotype. Also, pollen of horse chestnut Ah1-Ah4 genotypes showed different viability (from 56 to 68%), after staining with fluorescein diacetate. Pollen germination of Ah1-Ah4 genotypes varied from 50-66% on basic medium. Inclusion of polyethylene glycol-PEG from 10%, 15% and 20% v/w increased pollen germination. The best results were achieved on medium with the largest PEG concentration. On these medium 76-91% pollen grains were germinated, depending of genotype. The best pollen quality, for all tested parameters, had genotype Ah2. Knowledge about morphology, production, viability, in vitro germination, tube growth as well as pollen: ovule ratio can be of great importance for future pollen biology studies.

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 Effect of high temperature on the reproductive development of chickpea genotypes under controlled environments

2012 ◽  
Vol 39 (12) ◽  
pp. 1009 ◽  
Author(s):  
Viola Devasirvatham ◽  
Pooran M. Gaur ◽  
Nalini Mallikarjuna ◽  
Raju N. Tokachichu ◽  
Richard M. Trethowan ◽  
...  
Keyword(s):  
Heat Stress ◽  
High Temperature ◽  
Pollen Germination ◽  
Pollen Viability ◽  
Pollen Grains ◽  
High Temperature Stress ◽  
Pollen Production ◽  
Seed Number ◽  
Controlled Environments

High temperature during the reproductive stage in chickpea (Cicer arietinum L.) is a major cause of yield loss. The objective of this research was to determine whether that variation can be explained by differences in anther and pollen development under heat stress: the effect of high temperature during the pre- and post-anthesis periods on pollen viability, pollen germination in a medium, pollen germination on the stigma, pollen tube growth and pod set in a heat-tolerant (ICCV 92944) and a heat-sensitive (ICC 5912) genotype was studied. The plants were evaluated under heat stress and non-heat stress conditions in controlled environments. High temperature stress (29/16°C to 40/25°C) was gradually applied at flowering to study pollen viability and stigma receptivity including flower production, pod set and seed number. This was compared with a non-stress treatment (27/16°C). The high temperatures reduced pod set by reducing pollen viability and pollen production per flower. The ICCV 92944 pollen was viable at 35/20°C (41% fertile) and at 40/25°C (13% fertile), whereas ICC 5912 pollen was completely sterile at 35/20°C with no in vitro germination and no germination on the stigma. However, the stigma of ICC 5912 remained receptive at 35/20°C and non-stressed pollen (27/16°C) germinated on it during reciprocal crossing. These data indicate that pollen grains were more sensitive to high temperature than the stigma in chickpea. High temperature also reduced pollen production per flower, % pollen germination, pod set and seed number.

scholarly journals Effects of Sucrose, Boric Acid, pH, and Incubation Time on in Vitro Germination of Pollen and Tube Growth of Chinese fir (Cunnighamial lanceolata L.)

Forests ◽  
2019 ◽  
Vol 10 (2) ◽  
pp. 102 ◽  
Author(s):  
Seif Fragallah ◽  
Sizu Lin ◽  
Nuo Li ◽  
Elly Ligate ◽  
Yu Chen
Keyword(s):  
Boric Acid ◽  
Pollen Germination ◽  
Tree Breeding ◽  
Chinese Fir ◽  
Tube Growth ◽  
In Vitro Germination ◽  
Acid Ph ◽  
Novel Approach ◽  
The Media

In vitro pollen germination provides a novel approach and strategy to accelerate genetic improvement of tree breeding. Studies about pollen germination and tube growth of Chinese fir are limited. Therefore, this study aimed to investigate the effects of sucrose, boric acid, pH, and time of incubation on pollen germination and tube growth. Pollen from 9 clones were selected. In vitro germination was performed in basic media as control, and in different concentrations of sucrose (0, 10 and 15%), boric acid (0.01, 0.1 and 0.2%), and pH levels (4.5, 5 and 7). Pollen germination rates and tube growth were recorded periodically at 1, 12, 24, and 48 h. The results showed that sucrose imposes significant effects on pollen germination and tube growth. The effects are most obvious at concentration of 15%. Boric acid significantly promoted germination and tube growth. The promotion was most notable in lower concentration of 0.01%. The media adjusted to pH 7.0 boosted the germination and pollen tube growth. The optimum time of incubation was 24 and 48 h for pollen germination and tube growth, respectively. Sucrose, pH, and time of incubation were positively correlated, whereas boric acid negatively correlated with pollen germination and tube growth. This study provided experimental evidences for selecting viable pollens for Chinese fir breeding.

scholarly journals Pollen Germination of Rhizoma Peanut cv. Florigraze1

1992 ◽  
Vol 19 (2) ◽  
pp. 105-107 ◽  
Author(s):  
W. L. Niles ◽  
K. H. Quesenberry
Keyword(s):  
Seed Production ◽  
Pollen Germination ◽  
Sucrose Concentration ◽  
Growing Season ◽  
In Vitro Germination ◽  
Arachis Glabrata ◽  
Pollen Germinability ◽  
Poor Seed ◽  
Dry Conditions

Abstract Assessing pollen germination is fundamental to investigating infertility in plants. A potential cause of poor seed production in Florigraze (Arachis glabrata Benth.), rhizomatous peanut, was investigated by incubating pollen on in vitro germination media. The optimum sucrose and boron concentrations for pollen germination was delineated in a series of factorial experiments. Pollen germinability was assessed four times during the growing season. Flowers were collected at 2 h intervals spanning 30 h of development from bud to wilted flower. The optimum sucrose concentration was 100 g kg-1 but there were no differences in germination for B concentrations between 50 and 1,000 mg kg-1. Up to 78% pollen germination was obtained in a solution consisting of 100 g kg-1 sucrose, 100 mg kg-1 H3BO3, 250 mg kg-1 Ca(NO3)2·4H2O, 200 mg kg-1 MgSO4·7H2O and 100 mg kg-1 KNO3 in deionized water. Repeatable estimates of germinability were obtained in incubations of less than 30 min at 35 C. Florigraze pollen collected from developing buds as early as 2200 h the night before anthesis germinated in vitro. Peak germination extended from 2400 h to 1200 h the morning of anthesis. Under cool, dry conditions, the pollen collected 2 d after anthesis remained germinable. These results suggested poor pollen germinability was not the basis of low seed production in rhizomatous peanut. Pollen with high in vitro germination can dependably be collected from Florigraze flowers throughout the growing season during the first 6 h following anthesis, usually between sunrise to noon.

Viability and in Vitro Germination of Johnsongrass (Sorghum Halepense) Pollen

2007 ◽  
Vol 21 (1) ◽  
pp. 23-29 ◽  
Author(s):  
Ian C. Burke ◽  
John W. Wilcut ◽  
Nina S. Allen
Keyword(s):  
Suspension Culture ◽  
Boric Acid ◽  
Pollen Germination ◽  
Pollen Viability ◽  
Calcium Nitrate ◽  
Medium Composition ◽  
In Vitro Tests ◽  
In Vitro Germination ◽  
Agar Culture

A high proportion of viable pollen grains must germinate to study the physiology of pollen growth to reduce the confounding effects of environmental influences on pollen germination. The objectives of this study were to evaluate the nuclear state and develop a suitable medium and culture method for in vitro germination of johnsongrass pollen. Johnsongrass pollen was trinucleate, and in vitro tests for pollen viability using Alexander's stain and a fluorochromatic reaction method (FCR) indicated johnsongrass pollen was viable (92.6 to 98.4%). A factorial treatment arrangement of four concentrations of sucrose, two concentrations of boric acid, and two concentrations of calcium nitrate were used to determine the optimum pollen-germination medium composition in suspension culture, agar culture, and cellophane membrane culture. Germination was highest in a suspension culture with a medium containing 0.3 M sucrose, 2.4 mM boric acid, and 3 mM calcium nitrate. Pollen germination using this medium was 78.9% when anthers were harvested just before anthesis.

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