Photosynthetic responses of Eulophia dentata, Bletilla formosana, and Saccharum spontaneum under various photosynthetic photon flux density conditions
Status PubMed-not-MEDLINE Language English Country Czech Republic Media electronic-ecollection
Document type Journal Article
PubMed
39649396
PubMed Central
PMC11558585
DOI
10.32615/ps.2022.050
PII: PS60539
Knihovny.cz E-resources
- Keywords
- Bletilla, Eulophia, Saccharum, chlorophyll fluorescence, light intensity, photoinhibition,
- Publication type
- Journal Article MeSH
This study aimed to determine the photosynthetic performance and differences in chlorophyll fluorescence (ChlF) parameters between Eulophia dentata and its companion species Bletilla formosana and Saccharum spontaneum when subjected to different photosynthetic photon flux density (PPFDs). Leaf surfaces were then illuminated with 50, 100 (low PPFDs), 300, 500, 800 (moderate PPFDs); 1,000; 1,500; and 2,000 (high PPFDs) μmol m-2·s-1, and the ChlF parameters were measured during the whole process. Increasing nonphotochemical quenching of ChlF and decreasing potential quantum efficiency of PSII, actual quantum efficiency of PSII, and quantum efficiency ratio of PSII in dark recovery from 0-60 min were observed in all leaves. A significant and negative relationship was detected between energy-dependent quenching (qE) and photoinhibition percent in three species under specific PPFD conditions, whereas a significant and positive relationship was detected between photoinhibitory quenching (qI) and photoinhibition percent. The qE and qI can be easily measured in the field and provide useful ecological indexes for E. dentata species restoration, habitat creation, and monitoring.
Department of Forestry National Chung Hsing University 40227 Taichung Taiwan
Department of Forestry National Pingtung University of Science and Technology 91201 Pingtung Taiwan
Department of Horticulture and Biotechnology Chinese Culture University 11114 Taipei Taiwan
See more in PubMed
Adams W.W. III, Zarter C.R., Ebbert V., Demmig-Adams V.: Photoprotective strategies of overwintering evergreens. – BioScience 54: 41-49, 2004. 10.1641/0006-3568(2004)054[0041:PSOOE]2.0.CO;2 DOI
Björkman O., Demmig-Adams B.: Regulation of photosynthetic light energy capture, conversion, and dissipation in leaves of higher plants. – In: Schulze E.D., Caldwell M.M. (ed.): Ecophysiology of Photosynthesis. Pp. 17-47. Springer, Berlin-Heidelberg: 1995. 10.1007/978-3-642-79354-7_2 DOI
Bussotti F., Gerosa G., Digrado A., Pollastrini M.: Selection of chlorophyll fluorescence parameters as indicators of photosynthetic efficiency in large scale plant ecological studies. – Ecol. Indic. 108: 105686, 2020. 10.1016/j.ecolind.2019.105686 DOI
Chang L.H., Liu C.H., Li. C.Y.: [Asymbiotic germination and plant regeneration of Eulophia dentate Ames, a critically endangered plant in Taiwan.] – Taiwan J. Biodivers. 16: 241-251, 2014.
Colom M.R., Pini Prato E., Giannini R.: Chlorophyll fluorescence and photosynthetic response to light in 1-year-old needles during spring and early summer in Pinus leucodermis. – Trees-Struct. Funct. 17: 207-210, 2003. https://www.airitilibrary.com/Publication/alDetailedMesh?docid=20766971-201407-201408290002-201408290002-241-251
Demmig-Adams B., Adams W.W. III, Barker D.H. et al.: Using chlorophyll fluorescence to assess the fraction of absorbed light allocated to thermal dissipation of excess excitation. – Physiol. Plantarum 98: 253-264, 1996. 10.1034/j.1399-3054.1996.980206.x DOI
Demmig-Adams B., Adams W.W. III, Mattoo A.K.: Photoprotection, Photoinhibition, Gene Regulation, and Environment. Pp. 382. Springer, Dordrech: 2006. 10.1007/1-4020-3579-9 DOI
Demmig-Adams B., Stewart J.J., López-Pozo M. et al.: Zeaxanthin, a molecule for photoprotection in many different environments. – Molecules 25: 5825, 2020. PubMed PMC
Dewir Y.H., El-Mahrouk M.E.S., Al-Shmgani H.S. et al.: Photosynthetic and biochemical characterization of in vitro-derived African violet (Saintpaulia ionantha H. Wendl) plants to ex vitro conditions. – J. Plant Interact. 10: 101-108, 2015. 10.1080/17429145.2015.1018967 DOI
Editorial Committee of the Red List of Taiwan Plants: The Red List of Vascular Plants of Taiwan, 2017. Pp. 198. Endemic Species Research Institute, Forestry Bureau, Council of Agriculture, Executive Yuan and Taiwan Society of Plant Systematics, 2017.
Giudici G.N.M.: Photoinhibition of primary photosynthetic processes in hydrated Polytrichum commune: analysis of non-photochemical quenching affecting species resistance. – Czech Polar Rep. 9: 160-169, 2019. 10.5817/CPR2019-2-14 DOI
Guidi L., Lo Piccolo E., Landi M.: Chlorophyll fluorescence, photoinhibition and abiotic stress: does it make any difference the fact to be a C3 or C4 species? – Front. Plant Sci. 10: 174, 2019. 10.3389/fpls.2019.00174 PubMed DOI PMC
Johnson M.P., Ruban A.V.: Restoration of rapidly reversible photoprotective energy dissipation in the absence of PsbS protein by enhanced ΔpH. – J. Biol. Chem. 286: 19973-19981, 2011. 10.1074/jbc.M111.237255 PubMed DOI PMC
Kalapchieva S., Topalova E., Petkova V.: Morphological, physiological and productivity response in garden pea genotypes during high temperature stress. – Genetika 51: 417-428, 2019. 10.2298/GENSR1902417K DOI
Kałużewicz A., Bączek-Kwinta R., Krzesiński W. et al.: Effect of biostimulants on chlorophyll fluorescence parameters of broccoli (Brassica oleracea var. italica) under drought stress and rewatering. – Acta Sci. Pol.-Hortoru. 17: 97-106, 2018. 10.24326/asphc.2018.1.9 DOI
Li Z., Wang G., Liu X. et al.: Genome-wide identification and expression profiling of DREB genes in Saccharum spontaneum. – BMC Genomics 22: 456, 2021. 10.1186/s12864-021-07799-5 PubMed DOI PMC
Lin C.W., Hwang T.L., Chen F.A. et al.: Chemical constituents of the rhizomes of Bletilla formosana and their potential anti-inflammatory activity. – J. Nat. Prod. 79: 1911-1921, 2016. 10.1021/acs.jnatprod.6b00118 PubMed DOI
Makarenko M.S., Kozel N.V., Usatov A.V. et al.: A state of PSI and PSII photochemistry of sunflower yellow-green plastome mutant. – J. Biol. Sci. 16: 193-198, 2016. 10.3844/ojbsci.2016.193.198 DOI
Malnoë A.: Photoinhibition or photoprotection of photosynthesis? Update on the (newly termed) sustained quenching component qH. – Environ. Exp. Bot. 154: 123-133, 2018.
Maxwell K., Johnson G.N.: Chlorophyll fluorescence – a practical guide. – J. Exp. Bot. 51: 659-668, 2000. 10.1093/jexbot/51.345.659 PubMed DOI
Moya I., Loayza H., López M.L. et al.: Canopy chlorophyll fluorescence applied to stress detection using an easy to build micro-lidar. – Photosynth. Res. 142: 1-15, 2019. 10.1007/s11120-019-00642-9 PubMed DOI PMC
Murchie E.H., Niyogi K.K.: Manipulation of photoprotection to improve plant photosynthesis. – Plant Physiol. 155: 86-92, 2011. 10.1104/pp.110.168831 PubMed DOI PMC
Müller P., Li X.P., Niyogi K.K.: Non-photochemical quenching. A response to excess light energy. – Plant. Physiol. 125: 1558-1566, 2001. 10.1104/pp.125.4.1558 PubMed DOI PMC
Nilkens M., Kress E., Lambrev P. et al.: Identification of a slowly inducible zeaxanthin-dependent component of non-photochemical quenching of chlorophyll fluorescence generated under steady-state conditions in Arabidopsis. – BBA-Biomembranes 1797: 466-475, 2010. 10.1016/j.bbabio.2010.01.001 PubMed DOI
Orekhova A., Barták M., Casanova-Katny A., Hájek J.: Resistance of Antarctic moss Sanionia uncinata to photoinhibition: chlorophyll fluorescence analysis of samples from the western and eastern coasts of the Antarctic Peninsula. – Plant Biol. 23: 653-663, 2021. 10.1111/plb.13270 PubMed DOI
Pandey V.C., Bajpai O., Pandey D.N., Singh N.: Saccharum spontaneum: an underutilized tall grass for revegetation and restoration programs. – Genet. Resour. Crop Evol. 62: 443-450, 2015. 10.1007/s10722-014-0208-0 DOI
Pandey V.C., Sahu N., Singh D.P.: Physiological profiling of invasive plant species for ecological restoration of fly ash deposits. – Urban For. Urban Gree. 54: 126773, 2020. 10.1016/j.ufug.2020.126773 DOI
Papageorgiou G.C., Govindjee: The non-photochemical quenching of the electronically excited state of chlorophyll a in plants: definitions, timelines, viewpoints, open questions. – In: Demmig-Adams B., Garab G., Adams W.W. III, Govindjee (ed.): Non-Photochemical Quenching and Energy Dissipation in Plants, Algae and Cyanobacteria. Pp. 1-44. Springer, Dordrecht: 2014. 10.1007/978-94-017-9032-1_1 DOI
Pastenes C., Horton P.: Effect of high temperature on photosynthesis in beans. (I. Oxygen evolution and chlorophyll fluorescence) – Plant Physiol. 112: 1245-1251, 1996. 10.1104/pp.112.3.1245 PubMed DOI PMC
Portela F.C.S., Macieira B.P.B., Zanetti L.V. et al.: How does Cariniana estrellensis respond to different irradiance levels? – J. Forestry Res. 30: 31-44, 2019. 10.1007/s11676-017-0578-1 DOI
Rosa-Manzano E., Andrade J.L., García-Mendoza E. et al.: Photoprotection related to xanthophyll cycle pigments in epiphytic orchids acclimated at different light microenvironments in two tropical dry forests of the Yucatan Peninsula, Mexico. – Planta 242: 1425-1438, 2015. 10.1007/s00425-015-2383-4 PubMed DOI
Souza C.S.C.R, Santos V.A.H.F., Ferreira M.J., Gonçalves J.F.C.: [Biomass, growth and ecophysiological responses of young plants of Bertholletia excelsa Bonpl. subjected to different levels of irradiance.] – Cienc. Florest. 27: 557-569, 2017. [In Portuguese] 10.5902/1980509827736 DOI
Tüffers A.V., Naid G., von Willert D.J.: The contribution of leaf angle to photoprotection in the mangroves Avicennia marina (FORSSK.) VIERH. and Bruguiera gymnorrhiza (L.) LAM. under field conditions in South Africa. – Flora 194: 267-275, 1999. 10.1016/S0367-2530(17)30912-X DOI
Vaid S., Sharma S., Bajaj B.K.: Chemo-enzymatic approaches for consolidated bioconversion of Saccharum spontaneum biomass to ethanol-biofuel. – Bioresource Technol. 329: 124898, 2021. 10.1016/j.biortech.2021.124898 PubMed DOI
Wang C.W., Wong S.L., Liao T.S. et al.: Photosynthesis in response to salinity and submergence in two Rhizophoraceae mangroves adapted to different tidal elevations. – Tree Physiol. 42: 1016-1028, 2022. 10.1093/treephys/tpab167 PubMed DOI
Weng J.H., Chen L.F., Jiang C.Y. et al.: A comparison between yellow-green and green cultivars of four vegetable species in pigments, ascorbate, photosynthesis, energy dissipation, and photoinhibition. – Photosynthetica 49: 361-370, 2011. 10.1007/s11099-011-0046-7 DOI
Wong S.L., Chen C.W., Huang H.W., Weng J.H.: Using combined measurements of gas exchange and chlorophyll fluorescence to investigate the photosynthetic light responses of plant species adapted to different light regimes. – Photosynthetica 50: 206-214, 2012. 10.1007/s11099-012-0027-5 DOI
Wu T.Y., Chen C.C., Lay H.L.: Study on the components and antioxidant activity of the Bletilla plant in Taiwan. – J. Food Drug Anal. 18: 279-289, 2010. 10.38212/2224-6614.2229 DOI
Zulfugarov I.S., Ham O.K., Mishra S.R. et al.: Dependence of reaction center-type energy-dependent quenching on photosystem II antenna size. – BBA-Bioenergetics 1767: 773-780, 2007. 10.1016/j.bbabio.2007.02.021 PubMed DOI