A semi in vivo pollination technique to assess the level of gametophytic self-incompatibility and pollen tube growth in pear (Pyrus communis L.)

2022 ◽  
Author(s):  
Hanne Claessen ◽  
Bram Van de Poel ◽  
Wannes Keulemans ◽  
Nico De Storme
Keyword(s):  
Pollen Tube ◽  
Pollen Tube Growth ◽  
Pyrus Communis ◽  
Tube Growth ◽  
Self Incompatibility ◽  
Pyrus Communis L

scholarly journals Testing of self-(in)compatibility in apricot cultivars from European breeding programmes

2013 ◽  
Vol 40 (No. 2) ◽  
pp. 65-71 ◽  
Author(s):  
D. Milatović ◽  
D. Nikolić ◽  
B. Krška
Keyword(s):  
Fluorescence Microscopy ◽  
Pollen Tube ◽  
Pollen Tube Growth ◽  
Reliable Method ◽  
Pollen Tubes ◽  
Tube Growth ◽  
Self Incompatibility ◽  
Breeding Programmes

Self-(in)compatibility was tested in 40 new apricot cultivars from European breeding programmes. Pollen-tube growth in pistils from laboratory pollinations was analysed using the fluorescence microscopy. Cultivars were considered self-compatible if at least one pollen tube reached the ovary in the majority of pistils. Cultivars were considered self- incompatible if the growth of pollen tubes in the style stopped along with formation of characteristic swellings. Of the examined cultivars, 18 were self-compatible and 22 were self-incompatible. Fluorescence microscopy provides a relatively rapid and reliable method to determine self-incompatibility in apricot cultivars.      

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.

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.

Cellular Mechanisms for Pollen Tube Growth Inhibition in Gametophytic Self-incompatibility

2006 ◽  
pp. 201-221 ◽  
Author(s):  
Barend H. J. de Graaf ◽  
Chris Lee ◽  
Bruce A. McClure ◽  
Noni (V. E.) Franklin-Tong
Keyword(s):  
Pollen Tube ◽  
Growth Inhibition ◽  
Pollen Tube Growth ◽  
Tube Growth ◽  
Self Incompatibility ◽  
Cellular Mechanisms

Pollen Tube Growth in vivo as a Measure of Pollen Viability

Science ◽  
1962 ◽  
Vol 138 (3538) ◽  
pp. 436-437 ◽  
Author(s):  
W. H. Dempsey
Keyword(s):  
Pollen Tube ◽  
Pollen Tube Growth ◽  
Pollen Viability ◽  
Tube Growth
Sign in / Sign up

Export Citation Format

Share Document