Effects of soil early-spring temperature on the morphometric parameters of mitochondria in Galanthus nivalis L. leaves

Authors

  • O M Fediuk Department of Phytochemistry and Membranology, M.G. Kholodny Institute of Botany, Kyiv, Ukraine
  • N O Bilyavska Department of Phytochemistry and Membranology, M.G. Kholodny Institute of Botany, Kyiv, Ukraine
  • E K Zolotareva Department of Phytochemistry and Membranology, M.G. Kholodny Institute of Botany, Kyiv, Ukraine

DOI:

https://doi.org/10.14719/pst.2018.5.4.405

Keywords:

Galanthus nivalis L., leaf, mitochondria, electron microscopy, morphometry, thermometry

Abstract

In the natural conditions early-spring period development of Galanthus nivalis L., the leaves germination from bulbs was carried out in the soil surface layer, mainly, covered with snow, so the leaves were exposed to low soil temperatures. It was found, that at the leaf germination stage, when exposed to minus soil temperature, the mitochondria were predominantly elongated, that is, functionally active. Under the influence of positive temperature, the mitochondria form changed to a round one, which indicates their transition to low functional activity. A similar tendency was manifested even during the budding stage, in particular, when the soil temperature was lowered to an average of –3.47 °C, the mitochondria changed their form to an elongated one, that is, they passed into an active functional state. Wherein, the temperature of the leaves was higher by 3.84 °C compared to the soil. At the stages of germination and budding of G. nivalis under natural conditions, a direct correlation was found between the soil surface layer temperature and the leaves temperature, and at the flowering stage this relation was reverse. During the flowering stage, despite the influence of predominantly positive soil temperatures, leaves growth was significantly slowed, and their temperature was only slightly higher by 0.38 °C compared to the soil. At the same time, the mitochondria changed their shape to a round one. Thus, the increase in their long axis at different stages in spring development, are aimed at adapting to influence low temperatures of the soil surface layer.

Downloads

Download data is not yet available.

References

1. Stefanowska M, Kura? M, Kacperska A. Low Temperature-induced Modifications in Cell Ultrastructure and Localization of Phenolics in Winter Oilseed Rape (Brassica napus L. var. oleifera L.) Leaves. Ann Bot. 2002;90(5):637–45. https://doi.org/10.1093/aob/mcf241

2. Buchner O, Holzinger A, Lütz C. Effects of temperature and light on the formation of chloroplast protrusions in leaf mesophyll cells of high alpine plants. Plant, Cell Environ. 2007; 30(11): 1347–56. https://doi.org/10.1111/j.1365-3040.2007.01707.x

3. Du YY, Chen H, Zhong WL, Wu LY, Ye JH, Lin C, et al. Effect of temperature on accumulation of chlorophylls and leaf ultrastructure of low temperature induced albino tea plant. African J Biotechnol. 2008; 7(12):1881–5. https://doi.org/10.5897/AJB2008.000-5036

4. Gie?wanowska I, Pastorczyk M, Kellmann-Sopy?a W, Górniak D, Górecki RJ. Morphological and Ultrastructural Changes of Organelles in Leaf Mesophyll Cells of the Arctic and Antarctic Plants of Poaceae Family Under Cold Influence. Arctic, Antarct Alp Res. 2015; 47(1):17–25. http://dx.doi.org/10.1657/AAAR0014-019

5. Klymchuk DO, Kosakivska I V, Akimov YM, Shcherbatyuk MM, Vorobyova T V. Structure-functional Peculiarities of Brassica campestris and Amarantus caudathus leave cells under low positive temperature. Bull of Kharkiv National Agrarian Univ. Ser Biol. 2011;3(24):15–24.

6. Heidarvand L, Millar AH, Taylor NL. Responses of the Mitochondrial Respiratory System to Low Temperature in Plants. CRC Crit Rev Plant Sci. 2017;36(4):217–40. https://doi.org/10.1080/07352689.2017.1375836

7. Liu ZG, Sun WC, Zhao YN, Li XC, Fang Y, Wu JY, et al. Effects of Low Nocturnal Temperature on Photosynthetic Characteristics and Chloroplast Ultrastructure of Winter Rapeseed. Russ J Plant Physiol. 2016; 63(4):451–60. https://doi.org/10.1134/S1021443716040099

8. Strauss M, Hofhaus G, Schröder RR, Kühlbrandt W. Dimer ribbons of ATP synthase shape the inner mitochondrial membrane. EMBO J. 2008;27(7):1154–60. https://doi.org/10.1038/emboj.2008.35

9. Taylor NL, Day DA, Millar AH. Targets of stress-induced oxidative damage in plant mitochondria and their impact on cell carbon/nitrogen metabolism. J Exp Bot. 2004; 55(394):1–10. https://doi.org/10.1093/jxb/erh001

10. Lehninger AL. The Mitochondrion: Molecular Basis of Structure and Function [Internet]. New York?Amsterdam: Verlag W. A. Benjamin, Inc.; 1964. 316 p. https://onlinelibrary.wiley.com/doi/abs/10.1002/ange.19650770829

11. Yu J, Cang J, Zhou Z, Liu L. Anatomical Structure Comparison Between Leaves of Two Winter Wheat Cultivars with Different Cold/Freezing Tolerance Under Low Temperature Stress. J Northeast Agric Univ. 2011;18(3):1–6. https://doi.org/10.1016/S1006-8104(13)60091-4

12. Vella NGF, Joss T V, Roberts TH. Chilling-induced ultrastructural changes to mesophyll cells of Arabidopsis grown under short days are almost completely reversible by plant re-warming. Protoplasma. 2012; 249(4):1137–49. https://doi.org/10.1007/s00709-011-0363-5

13. Fediuk OM, Bilyavska NO, Zolotareva OK. Effects of sucrose on structure and functioning of photosynthetic apparatus of Galanthus nivalis L. leaves exposed to chilling stress. Ann RSCB. 2017;XXI(3):43–51. https://doi.org/10.ANN/RSCB-2018-0002:RSCB

14. Weryszko-Chmielewska E, Chwil M. Flowering biology and structure of floral nectaries in Galanthus nivalis L. Acta Soc. Bot. Pol. 2016;85(1):1–20. https://doi.org/10.5586/asbp.3486

15. Scepankova I, Hudák J. Leaf and tepal anatomy, plastid ultrastructure and chlorophyll content in Galanthus nivalis L. and Leucojum aestivum L. Plant Syst Evol. 2004 Jan 23; 243(3–4):211–9. https://doi.org/10.1007/s00606-003-0086-y

16. Seymour RS. Dynamics and precision of thermoregulatory responses of eastern skunk cabbage Symplocarpus foetidus. Plant, Cell Environ. 2004 Aug 1; 27(8):1014–22. http://doi.wiley.com/10.1111/j.1365-3040.2004.01206.x

17. Seymour RS, Gibernau M, Ito K. Thermogenesis and respiration of inflorescences of the dead horse arum Helicodiceros muscivorus, a pseudo-thermoregulatory aroid associated with fly pollination. Funct Ecol. 2003 Dec 1; 17(6):886–94. http://doi.wiley.com/10.1111/j.1365-2435.2003.00802.x

18. Fediuk OM, Bilyavska NO. Ultrastructural changes in Galanthus nivalis L. foliar mitochondria at vegetation in hypothermal conditions. Bull of Kharkiv National Agrarian Univ. Ser Biol. 2015;2(35):58–63.

19. Gie?wanowska I, Szczuka E, Bednara J, Górecki R. Anatomical features and ultrastructure of Deschampsia antarctica (Poaceae) leaves from different growing habitats. Ann Bot. 2005 Nov 1;96(6):1109–19. https://doi.org/10.1093/aob/mci262

20. Gielwanowska I, Szczuka E. New ultrastructural features of organelles in leaf cells of Deschampsia antarctica Desv. Polar Biol. 2005 Nov 1;28(12):951–5. https://doi.org/10.1007/s00300-005-0024-2

Downloads

Published

02-10-2018

How to Cite

1.
Fediuk OM, Bilyavska NO, Zolotareva EK. Effects of soil early-spring temperature on the morphometric parameters of mitochondria in Galanthus nivalis L. leaves. Plant Sci. Today [Internet]. 2018 Oct. 2 [cited 2024 Dec. 22];5(4):149-54. Available from: https://horizonepublishing.com/journals/index.php/PST/article/view/405

Issue

Section

Research Articles

Similar Articles

You may also start an advanced similarity search for this article.