The photosynthetic apparatus of the moss Hylocomium lucidum is resistant to low extreme temperatures

A. V. Chasov; Часов А. В.; F. V. Minibaeva; Минибаева Ф. В.

doi:10.31857/S0367059723060033

The photosynthetic apparatus of the moss Hylocomium lucidum is resistant to low extreme temperatures

作者: Chasov A.V.¹, Minibaeva F.V.¹
隶属关系:
1. Kazan Institute of Biochemistry and Biophysics is a separate structural unit of the Federal Research Center “Kazan Scientific Center RAS”
期: 编号 6 (2023)
页面: 435-445
栏目: Articles
URL: https://journals.rcsi.science/0367-0597/article/view/232839
DOI: https://doi.org/10.31857/S0367059723060033
EDN: https://elibrary.ru/BEOGAR
ID: 232839

如何引用文章

全文:

开放存取

##reader.subscriptionAccessGranted##
受限制的访问

订阅存取

详细
作者简介
参考
补充文件
统计

详细

The influence of positive and negative temperatures, as well as dehydration/rehydration on the maximum photochemical efficiency, the rate of electron transfer in photosystem II and non-photochemical quenching of the moss Hylocomium splendens, widespread in the boreal forests of the Northern Hemisphere, is shown. It was found that this moss is resistant to low negative (–20 and –80°C) temperatures and significant water losses. On the contrary, in the hydrated state it is unstable to prolonged exposure to positive temperatures (40°C). High resistance to low temperatures and dehydration allowed H. splendens to successfully adapt to growing in northern latitudes and occupy a wide range.

关键词

Hylocomium splendens, photosynthesis, temperature stress, dehydration, rehydration

作者简介

A. Chasov

Kazan Institute of Biochemistry and Biophysics is a separate structural unit of the Federal Research Center “Kazan Scientific Center RAS”

Email: chasov@kibb.knc.ru
Russia, Kazan

F. Minibaeva

Kazan Institute of Biochemistry and Biophysics is a separate structural unit of the Federal Research Center “Kazan Scientific Center RAS”

编辑信件的主要联系方式.
Email: chasov@kibb.knc.ru
Russia, Kazan

参考

Gerdol R., Bragazza L., Marchesini R. Element concentrations in the forest moss Hylocomium splendens: variation associated with altitude, net primary production and soil chemistry // Environ. Pollut. 2002. V. 116. № 1. P. 129–135.https://doi.org/10.1016/S0269-7491(01)00198-1
Cowden P., Aherne J. Interspecies comparison of three moss species (Hylocomium splendens, Pleurozium schreberi, and Isothecium stoloniferum) as biomonitors of trace element deposition // Environ. Monit. Assess. 2019. V. 191: 220.https://doi.org/10.1007/s10661-019-7354-y
Гольцев В.Н., Каладжи М.Х., Кузманова М.А., Аллахвердиев С.И. Переменная и замедленная флуоресценция хлорофилла a – теоретические основы и практическое приложение в исследовании растений. М.; Ижевск: Институт компьютерных исследований, 2014. 220 с.
Arróniz-Crespo M., Gwynn-Jones D., Callaghan T.V. et al. Impacts of long-term enhanced UV-B radiation on bryophytes in two sub-Arctic heathland sites of contrasting water availability // Ann. Bot. 2011. V. 108. № 3. P. 557–565.https://doi.org/10.1093/aob/mcr178
Glime J.M. Bryophyte Ecology. V. 1: Physiological Ecology. 2017. https://digitalcommons.mtu.edu/bryophyte-ecology1/ (Electronic resource).
Takezawa D. Mechanisms underlying freezing and desiccation tolerance in bryophytes // Survival Strategies in Extreme Cold and Desiccation. Advances in Experimental Medicine and Biology. Eds. Iwaya-Inoue M. Singapore: Springer, 2018. V. 1081. P. 167–187.https://doi.org/10.1007/978-981-13-1244-1_10
Zhuo L., Liang Y.Q., Yang H.L. et al. Thermal tolerance of dried shoots of the moss Bryum argenteum // J. Therm. Biol. 2020. V. 89: 102469.https://doi.org/10.1016/j.jtherbio.2019.102469
Barrs H.D., Weatherley P.E. A re-examination of the relative turgidity technique for estimating water deficits in leaves // Aust. J. Biol. Sci. 1962. V. 15. P. 413–428.
Roads E., Longton R.E., Convey P. Millennial timescale regeneration in a moss from Antarctica // Current Biol. 2014. V. 24. № 6. P. R222–R223.https://doi.org/10.1016/j.cub.2014.01.053
Hearnshaw G.F., Proctor M.C.F. The effect of temperature on the survival of dry bryophytes // New Phytol. 1982. V. 90. P. 221–228.https://doi.org/10.1111/j.1469-8137.1982.tb03254.x
Long S.P., Humphries S., Falkowski P.G. Photoinhibition of photosynthesis in nature // Annu. Rev. Plant Physiol. 1994. V. 45. P. 633–662.https://doi.org/10.1146/annurev.pp.45.060194.003221
Alboresi A., Gerotto C., Giacometti G.M. et al. Physcomitrella patens mutants affected on heat dissipation clarify the evolution of photoprotection mechanisms upon land colonization // PNAS. 2010. V. 107. № 24. P. 11 128–11 133.https://doi.org/10.1073/pnas.1002873107
Бардунов Л.В. Древнейшие на суше. М.: Наука, 1984. 160 с.
Xia H., Chen K., Liu L. et al. Photosynthetic regulation in fluctuating light under combined stresses of high temperature and dehydration in three contrasting mosses // Plant Sci. 2022. V. 323: 111379.https://doi.org/10.1016/j.plantsci.2022.111379
Björkman O., Demmig B. Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77 K among vascular plants of diverse origins // Planta. 1987. V. 170. P. 489–504.https://doi.org/10.1007/BF00402983
Haldimann P., Feller U. Inhibition of photosynthesis by high temperature in oak (Quercus pubescens L.) leaves grown under natural conditions closely correlates with a reversible heat-dependent reduction of the activation state of ribulose-1,5-bisphosphate carboxylase/oxygenase // Plant Cell Environ. 2004. V. 27. P. 1169–1183.https://doi.org/10.1111/j.1365-3040.2004.01222.x