Features of the Manifestation of Morphological Traits of Tomato Vegetative and Generative Pollen Cell Nuclei in Lines and F1 Hybrids Under the Influence of High and Low Temperatures

International Journal of Agriculture & Environmental Science
© 2024 by SSRG - IJAES Journal
Volume 11 Issue 5
Year of Publication : 2024
Authors : Milania MAKOVEI
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How to Cite?

Milania MAKOVEI, "Features of the Manifestation of Morphological Traits of Tomato Vegetative and Generative Pollen Cell Nuclei in Lines and F1 Hybrids Under the Influence of High and Low Temperatures," SSRG International Journal of Agriculture & Environmental Science, vol. 11,  no. 5, pp. 21-28, 2024. Crossref, https://doi.org/10.14445/23942568/IJAES-V11I5P103

Abstract:

The paper presents the results of the studies on the manifestation and variability pattern of morphological traits (nucleus diameter, perimeter, area) of vegetative (V) and generative (G) tomato pollen cells in parent lines (P1 and P2) and their F1 hybrids under optimal (25 °C), high (45 °C) and low temperatures (+7 °C). It has been shown that the nuclei of V and G pollen cells of different genotypes reacted ambiguously to the action of high and low temperatures. The V pollen cell nuclei were morphologically more homogeneous in the F1 populations than in their parental forms. On the contrary, the G pollen cell nuclei in the F1 populations showed high heterogeneity, especially against the background of stresses. The degree of variability of the morphological traits of the nuclei of vegetative (V) and generative (G) pollen cells in F1 hybrids depends on both the genotype characteristics of their parental forms and the types of stress factors (45 °C and +7 °C). It was found that the indices of the traits of the nuclei of V cells of the pollen of F1 hybrids in all variants (25 ºС, 45 ºС, +7 ºС) were controlled by the influence of paternal components. While the G pollen cell nucleus traits in F1 were under the control of paternal forms in optimal conditions (25 ºС), the degree of expression traits nucleus diameter, perimeter and area was under the influence of maternal forms when exposed to high and low temperatures (45 ºС and +7 ºС.)

Keywords:

F1 hybrids and their parental lines, Pollen, Tomato, Temperature factors, Vegetative and generative cell nucleus, Variability.

References:

[1] Beny Aloni et al., “The Effect of High Temperature and High Atmospheric CO2 on Carbohydrate Changes in Bell Pepper (Capsicum Annuum) Pollen in Relation to its Germination,” Physiologia Plantarum, vol. 112, no. 4, pp. 505-512, 2001.
[CrossRef] [Google Scholar] [Publisher Link]
[2] S.B. Chikkodi, and R.L. Ravikumar, “Influence of Pollen Selection for Alternaria Helianthi Resistance on the Progeny Performance against Leaf Blight in Sunflower (Helianthus Annuus L.),” Sexual Plant Reproduction, vol. 12, pp. 222-226, 2000.
[CrossRef] [Google Scholar] [Publisher Link]
[3] P.L. Cratao et al., “Acquired Tolerance of Tomato (Lycopersicon Esculentum. CV. Micro-Tom) Plants to Cadmium Induced Stress,” Annals Applied Biology, vol. 153, no. 3, pp. 321-333, 2008.
[CrossRef] [Google Scholar] [Publisher Link]
[4] Monica David, “Pollen Grain Expression of Intrinsic and Osmolite Induct Osmotic Adjustment in a Set of Heat Cultivars,” Romaine Agricultural Research, no. 29, pp. 45-52, 2012.
[Google Scholar]
[5] Nico De Storme, and Danny Geelen, “The Impact of Environmental Stress on Male Reproductive Development in Plants: Biological Processes and Molecular Mechanisms,” Plant Cell and Environment, vol. 37, no. 1, pp. 1-18, 2014.
[CrossRef] [Google Scholar] [Publisher Link]
[6] Ya.N. Demurin, and O.A. Rubanova, “Pollen Plant Analysis of Different Sunflower Genotypes” Oilseed Crops, vol. 2, no. 186, pp. 10- 17, 2021.
[Google Scholar]
[7] Rudi Dolferus et al., “The Physiology of Reproductive-Stage Abiotic Stress Tolerance in Cereals,” Molecular Stress Physiology of Plants, pp. 193-216, 2013.
[CrossRef] [Google Scholar] [Publisher Link]
[8] Margaret H. Frank, and Micael J. Scanlon, “Transcriptomic Evidence for the Evolution of Shoot Meristem Function in Sporophyte-Dominant Land Plants through Concerted Selection of Ancestral Gametophytic and Sporophytic Genetic Programs,” Molecular Biology and Evolution, vol. 32, no. 2, pp. 355-367, 2014.
[CrossRef] [Google Scholar] [Publisher Link]
[9] C. Frova et al., “Sporophytic and Gametophytic Components of Thermotolerance Effected by Pollen Selection,” Journal of Heredity, vol. 86, no. 1, pp. 50-54. 1995.
[CrossRef] [Google Scholar] [Publisher Link]
[10] Humaira Gul, and Rafiq Ahmad, “Effect of Salinity on Pollen Viability of Different Canola (Brassica napus L.) Cultivars as Reflected by the Formation of Fruits and Seeds,” Pakistan Journal of Botany, vol. 38, no. 2, pp. 237-247, 2006.
[Google Scholar]
[11] Anatoly Nikolaevich Кravchenko, Features of the Formation of Genetic Variability in the Process of Sporogametophyto- and Embryogenesis in Plants. [Online]. Available: https://earthpapers.net/osobennosti-formirovaniya-geneticheskoy-izmenchivosti-v-protsesse-sporogametofito-i-embriogeneza-u-rasteniy
[12] Jane Larkindale, and Elizabeth Vierling, “Core Genome Responses Involved in Acclimation to High Temperature,” Plant Physiology, vol. 146, no. 2, pp. 748-761, 2008.
[CrossRef] [Google Scholar] [Publisher Link]
[13] Anida Mesihovic et al., “Heat Stress Regimes for the Investigation of Pollen Thermotolerance in Crop Plants,” Plant Reproduction, vol. 29, pp. 93–105, 2016.
[CrossRef] [Google Scholar] [Publisher Link]
[14] David L. Mulcahy, “A Correlation between Gametophytic and Sporophytic Characteristics in Zea Mays L.,” Science, vol. 171, no. 3976, pp. 1155-1156, 1971.
[CrossRef] [Google Scholar] [Publisher Link]
[15] B. Nandini et al., “Genetic Variability Analysis for Grain Yield and its Components Traits in Traditional Rice Varieties,” International Journal of Current Microbiology and Applied Sciences, vol. 6, no. 8, pp. 494-502, 2017.
[CrossRef] [Google Scholar] [Publisher Link]
[16] Ettore Pacini, and Rudi Dolferus, “The Trails and Tribulations of the Plant Male Gametophyte- Understanding Reproductive Stage Stress Tolerance,” Abiotic and Biotic Stress in Plants, 2016.
[CrossRef] [Google Scholar] [Publisher Link]
[17] Z.P. Pausheva, Workshop on Plant Cytology, Moscow, Sprint-Nauka, pp. 1-271, 1988.
[Google Scholar] [Publisher Link]
[18] Basavanagounda S. Patil, R.L. Ravicumar, and P.M. Salimath, “Effect of Pollen Selection for Moisture Stress Tolerance on Progeny Performance in Sorghum,” Journal of Food, Agriculture & Environment, vol. 4, no. 1, pp. 201-204, 2006.
[Google Scholar] [Publisher Link]
[19] P.L. Рfahler, “Comparative Effectiveness of Pollen Genotype Selection in Higher Plants,” Pollen: Biology and Implications for Plant Breeding, pp. 361-366. 1982.
[Google Scholar] [Publisher Link]
[20] Etan Pressman, Mary M. Peet, and D. Mason Pharr, “The Effect of Heat Stress on Tomato Pollen Characteristics is Associated with Changes in Carbohydrate Concentration in the Developing Anthers,” Annals of Botany, vol. 90, no. 5, pp. 631-636, 2002.
[CrossRef] [Google Scholar] [Publisher Link]
[21] V.V. Roschina, and E.V. Melnikova, “Chemosensitivity of Pollen to Ozone and Peroxides,” Russian Journal of Plant Physiology, vol. 48, pp. 74-83, 2001.
[CrossRef] [Google Scholar] [Publisher Link]
[22] M. Sari Gorla et al., “The Extent of Gametophytic-Sporophytic Gene Expression in Maize,” Theoretical and Applied Genetic, vol. 72, pp. 42-47, 1986.
[CrossRef] [Google Scholar] [Publisher Link]
[23] D. Zamir, and I. Gadish, “Pollen Selection for Low Temperature Adaptation in Tomato,” Theoretical and Applied Genetics, vol. 74, pp. 545-548, 1987.
[CrossRef] [Google Scholar] [Publisher Link]