Ecotype effects on photosynthesis performance using A/PFFD among Pinus nigra Arn.
DOI:
https://doi.org/10.15835/nbha51312599Keywords:
lighy curves, net photosynthesis, P. nigra Arn, provenanceAbstract
This study aimed to provide insights on intraspecific variability of photosynthesis performance of 19 provenances of black pine planted in a common garden. The experiment was conducted in an experimental trial located at Souiniet (the southern limit of its range) Photosynthetic capacity characterized by light-saturated net photosynthetic rates, associated light compensation points and apparent quantum yield was monitored by measuring the response of leaf gas exchange to light levels. Amax was the highest in provenances Puget Theniers (nigra ssp), Saint-Guilhem (salzmanni ssp), Marghese and les barres (laricio ssp). The lowest value was recorded in Olette of the subspecies salzmanni. Needles from two provenances Crimea (pallasiana ssp) and Les Barres (ssp laricio) revealed the highest apparent quantum yield (ɸ), followed by Brougatlès Ales (salzmanni ssp), Trenta Coste (ssp laricio), Les barres and Puget Theniers (nigra ssp). The lowest apparent quantum Yield was recorded in Laricio subspecies (Cosenza; Les barres and Bois frerot). The highest value of dark respiration (Rd) was shown in provenance Les barres (laricio ssp), while Grancia and Tavola of the laricio subspecies reported the lowest one. Provenances Tavola (laricio ssp) and Puget Theniers (nigra ssp) exhibited the highest LCP. The provenance Crimée (pallasiana ssp) and Aspromonto (laricio ssp) recorded the lowest values. The maximum values of photosynthesis are positively correlated with the total chlorophyll contents and Leaf Mass area. Our study illustrates that Photosynthesis performance showed a difference between 19 provenances of black pine; it seems that black pine photosynthetic performance is eco-typical independent.
References
Balaguer L, Martinez-Ferri E, Valladares F, Perez-Corona ME, Baquedano FJ, Castillo FJ, Manrique E (2001). Population divergence in the plasticity of the response of Quercus coccifera to the light environment. Functional Ecology 15(1):124-135. https://doi.org/10.1046/j.1365-2435.2001.00505.x
Bassow S, Bazzaz F (1997). Intra- and inter-specific variation in canopy photosynthesis in a mixed deciduous forest. Oecologia 109:507-515. https://doi.org/10.1007/s004420050111
Bauerle WL, McCullough C, Iversen M, Hazlett M (2020). Leaf age and position effects on quantum yield and photosynthetic capacity in hemp crowns. Plants 9(2):271. https://doi.org/10.3390/plants9020271
Chazdon RL, Field CB (1987). Determinants of photosynthetic capacity in six rainforest piper species. Oecologia 73:222-230. https://doi.org/10.1007/BF00377511
Chen Y, Xu DQ (2006). Two patterns of leaf photosynthetic response to irradiance transition from saturating to limiting one in some plant species. New Phytologist 169:789-798. https://doi.org/10.1111/j.1469-8137.2005.01624.x
Cornic G, Le Gouallec JL, Briantais JM, Hodges M (1989). Effect of dehydration and high light on photosynthesis of two C3 plants {Phaseolus vulgaris L. and Elatostema repens (Lour.) Hall f.). Planta 111:84-90. https://doi.org/10.1007/BF00392157
Diamond SE, Martin RA (2021). Physiological adaptation to cities as a proxy to forecast global-scale responses to climate change. Journal of Experimental Biology. https://doi.org/10.1242/jeb.229336
Fkiri S, Rzigui T, Elkhorchani A, Hassine AB, Khaldi A, Khouja ML, Nasr Z (2020). Tree growth and leaf gas exchange variability of three Mediterranean Pinus spp. growing in a common garden in Northeastern Tunisia. Euro-Mediterranean Journal for Environmental Integration 5(1):1-9. https://doi.org/10.1007/s41207-019-0136-7
Fox RJ, Donelson JM, Schunter C, Ravasi T, Gaitán-Espitia JD (2019). Beyond buying time: the role of plasticity in phenotypic adaptation to rapid environmental change. Philosophical Transactions of the Royal Society B: 374(1768)20180174. https://doi.org/10.1098/rstb.2018.0174
Fu WG, Li PP, Bian XM, Wu YY, Cao QY (2006). Diurnal photosynthetic changes of Phragmites communis in the wetland lying in Beigushan mountain of Zhenjiang prefecture. Acta Botanica Boreali-Occidentalia Sinica 26:0496-0501. https://doi.org/10.1007/s11099-007-0110-5
Gao J, Meng P, Wu B, Zhang JS, Chu JM (2006). Photosynthesis and transpiration of Salvia miltiorrhiza in tree-herb system of Prunus dulcis and Salvia miltiorrhiza. Journal of Beijing Forest University 28:64-67.
Giovannelli G, Roig A, Spanu I, Vendramin GG, Fady B (2017). A new set of nuclear microsatellites for an ecologically and economically important conifer: the European black pine (Pinus nigra Arn.). Plant Molecular Biology Reporter 35:379-388. https://doi.org/10.1007/s11105-017-1029-z
Huang M Y, Wong SL, Weng JH (2021). Rapid light-response curve of chlorophyll fluorescence in terrestrial plants: Relationship to CO2 Exchange among five woody and four fern species adapted to different light and water regimes. Plants 10(3):445. https://doi.org/10.3390/plants10030445
Köse N, Akkemik Ü, Dalfes N, Özeren MS, Tolunay D (2012). Tree-ring growth of Pinus nigra Arn. subsp. pallasiana under different climate conditions throughout western Anatolia. Dendrochronologia: 30: 295–301. https://doi.org/10.1016/j.dendro.2012.04.003.
Kremer A, Kleinschmit J, Cottrell J, Cundall EP, Deans JD, Ducousso A, … Funk C (2018). Proteomic analysis of the phycobiliprotein antenna of the cryptophyte alga Guillardia theta cultured under different light intensities. Photosynthesis Research 135:149-163. https://doi.org/10.1007/s11120-017-0400-0
Kreyling J, Wiesenberg LB, Thiel G, Wohlfart D, Huber C, Walter G, … Beierkuhnlein M (2012). Cold hardiness of Pinus nigra Arnold as influenced by geographic origin, warming, and extreme summer drought. Environmental and Experiment Botany 78: 99-108. https://doi.org/10.1016/j.envexpbot.2011.12.026.
Kyei-Boahen S, Lada R, Astatkie T, Gordon R, Caldwell C (2003). Photosynthetic response of carrots to varying irradiances. Photosynthetica 41:301-305. https://doi.org/10.1023/B:PHOT.0000011967.74465.cc.
Lefèvre F, Fady B, Jean F, Davi H, Pichot C, Oddou-Muratorio S (2015). Les processus biologiques de réponse des arbres et forêts au changement climatique : adaptation et plasticité phénotypique. Innovations Agronomiques 47:63-79.
Levanic T, Popa I, Poljansek S, Nechita C (2013). A 323-year long reconstruction of drought for SW Romania based on black pine (Pinus nigra) tree-ring widths. International Journal of Biometeorology 57:703-714. https://doi.org/10.1007/s00484-012-0596-9
Liu YF, Xiao LT, Tong JH, Li XB, (2005). Primary application on the non-rectangular hyperbola model for photosynthetic light-response curve. Chinese Agriculture Sciences Bulletin 121:76-79.
Lowe AJ, Munro RC, Petit RJ, Stephan BR (2002). Is there a correlation between chloroplastic and nuclear divergence, or what are the roles of history and selection on genetic diversity in European oaks?. Forest Ecology and Management 156:75-87. https://doi.org/10.1016/S0378-1127(01)00635-1
Marschall M, Proctor CF, (2004). Are bryophytes shade plants? Photosynthetic light responses and proportions of chlorophyll a, chlorophyll b and total carotenoids. Annals of Botany 94:593-603. https://doi.org/10.1093/aob/mch178
McKown AD, Klápště J, Guy RD, Geraldes A, Porth I, Hannemann J, ... Douglas CJ (2014). Genome-wide association implicates numerous genes underlying ecological trait variation in natural populations of Populus trichocarpa. New Phytology 203:535-553. https://doi.org/10.1111/nph.12815
Nouvellon Y, Laclau JP, Epron D, Kinana A, Mabiala A, Roupsard O, Saint-André L (2010). Within-stand and seasonal variations of specific leaf area in a clonal eucalyptus plantation in the Republic of Congo. Forest of Ecology and Management 259(9):1796-1807. https://doi.org10.1016/j.foreco.2009.05.023
Ögren E (1993) Convexity of the photosynthetic light-response curve in relation to intensity and direction of light during growth. Plant Physiology 101:1013-1019. https:/doi.org/10.1104/pp.101.3.101
Schaberg P, DeHayes D, Hawley G, Nijensohn S (2008). Anthropogenic alterations of genetic diversity within tree populations: implications for forest ecosystem resilience. Forest Ecology Management 256:855-862. https://doi.org/10.1016/j.foreco.2008.06.038
Seho M, Kohnle U, Albrecht A, Lenk E (2010). Growth analyses of four provenances of European Black Pine (Pinus nigra) growing on dry sites in southwest Germany (Baden-Wuerttemberg). Allgemeine Forst und Jagdzeitung 181:104-116.
Shishkova V, Panayotov M (2013). Climate growth relationship of Pinus nigra tree-ring width chronology from the Rhodope Mountains, Bulgaria. Bulgarian Journal of Agricultural Sciences 19:9-90.
Sow MD, Allona I, Ambroise C, Conde D, Fichot R, Gribkova S, ..., Maury S (2018). Epigenetics in forest trees: state of the art and potential implications for breeding and management in a context of climate change. Advances in Botanical Research: 88:387-453. https://doi.org/10.1016/bs.abr.2018.09.003
Strumia G, Wimmer R, Grabner M (1997). Dendroclimatic sensitivity of Pinus nigra Arnold in Austria. Dendrochronologia 15:129-137. https://doi.org/10.3959/2011-7.1
Thiel D, Laura Nagy L, Beierkuhnlein C, Huber G, Jentsch A, Konnert M, Kreyling J (2012). Uniform drought and warming responses in Pinus nigra provenances despite specific overall performances. Forest of Ecology and Management 270:200-208. https://doi.org/10.1016/j.foreco.2012.01.034
Vogelmann TC (1989) Penetration of light into plants. Photochemistry and Photobiology 50:895-902. https://doi.org/10.1111/j.1751-1097.1989.tb02919.x
Wang HT, Meng YY, Cao XP, Ai JN, Zhou JN, Xue S, Wang W (2015). Coordinated response of photosynthesis, carbon assimilation, and triacylglycerol accumulation to nitrogen starvation in the marine microalgae Isochrysis zhangjiangensis (Haptophyta). Bioresources Technology 177:282-288. https://doi.org/10.1016/j.biortech.2014.11.028
Yang JT, Preiser AL, Li Z, Weise SE, Sharkey TD (2016). Triose phosphate use limitation of photosynthesis: short-term and long-term effects. Planta 243:687-698. https://doi.org/10.1007/s00425-015-2436-8
Ye ZP (2007) A new model for relationship between irradiance and the rate of photosynthesis in Oryza sativa. Photosynthetica 45:637-640. https://doi.org/10.1007/s11099-007-0110-5
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2023 Sondes FKIRI, Touhami RZIGUI, Hanene GHAZGHAZI, Larbi M. KOUJA, Abelhamid KHALDI, Frédéric GUIBAL, Zouheir NASR

This work is licensed under a Creative Commons Attribution 4.0 International License.
License:
Open Access Journal:
The journal allows the author(s) to retain publishing rights without restriction. Users are allowed to read, download, copy, distribute, print, search, or link to the full texts of the articles, or use them for any other lawful purpose, without asking prior permission from the publisher or the author.