Relative Growth Rate and Net Assimilation Rate of Black Afara (Terminalia ivorensis) Seedlings Grown with Arbuscular Mycorrhizal Fungi (AMF) under NaCl Stress in Calabar, Nigeria
Published: 2023-12-18
Page: 331-338
Issue: 2023 - Volume 6 [Issue 2]
Samuel Eguom Osim *
Department of Plant Science and Biotechnology, Faculty of Biological Sciences, University of Cross River State, Calabar, Nigeria.
*Author to whom correspondence should be addressed.
Abstract
Aim: To ascertain how four distinct arbuscular mycorrhizal fungi (AMF) species affect the relative growth rate (RGR) and net assimilation rate (NAR) of Terminalia ivorensis under NaCl stress.
Study Location and Length: Calabar is situated in southern Nigeria. The study was carried out from February to May, 2022
Methodology: The field procedure was a 9x3x6 completely randomized design with nine treatments and three duplicates, which were further replicated six (6) times, totaling 162 pots. The Terminalia ivorensis young plants were induced using four different AM fungi species (Glomus mossae, Glomus intraradices, Glomus occultum and Glomus etunicatum) and predisposed to 75mM of NaCl stress. At six sequential harvests of 2, 4, 8, 10 and 12 weeks after emergence (WAE), dry biomass and AMF colonization were determined. relative growth rate and net assimilation rate were calculated using the dry weight data obtained at harvest (4,6,8,10 and 12 WAE).
Results: All the NaCl stressed young plants indisputably showed higher colonization of AMF in their roots than their unstressed replica. Young plants inoculated using Glomus intraradices (Gi) in fusion with NaCl (GiNaCl) had the maximum AMF root colonization of 98.35%, while 31.78% was the least in plants treated with G.occultum(Go) at 12 and 8 WAE, respectively. Plants treated with Glomus occultum revealed 0.46gg-1wk-1 as the highest RGR value and 0.22gg-1wk-1 was recorded in Gm, GmNaCl and GoNaCl as the least value at 12WAE. Furthermore, Glomus etunicatum treated plants recorded the maximum significant (p≤0.05) NAR of 0.55gg-1wk-1 and the least was 0.31gg-1wk-1 in seedlings inoculated with G.occultum under salt stress at 12 WAE.
Conclusion: The regeneration of afforestation and vegetation in Nigeria's coastal areas can be facilitated by inoculating with the right AMF, which can also increase the biomass production and accumulation of Terminalia ivorensis seedlings.
Keywords: Arbuscular mycorrhizal fungi, black afara (Terminalia ivorensis), relative growth rate, net assimilation rate, NaCl stress
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Wang J, Fu Z, Ren Q, Zhu L, Lin J, Zhang J, Cheng X, Ma J, and Yue J. Effect of Arbscular mychorrhizal Fungi on Growth, Photosynthesis and Nutrient Uptake of Zelkovaserrata (Thunb) Makino Seedlings under salts stress. Forest. 2019;10(186): 1-16.
Iwena OA. Essential geography. Ibanda: Tonal Publishers; 2008.
Osim SE. Dry biomass accumulation of Terminalia ivorensis (A. Chev) seedlings inoculated with arbuscular mycorrhizal fungi under salt stress. Journal of Science, Engineering and Technology. 2021;8(1):10-17.
Abdel-Fattah GM, Rabie GH, Lamis DS, Ralab AM. The Impact of the Arbuscular mycorrhizal Fungi on growth and physiological parameters of cowpea plants grown under salt stress conditions. International Journal of Applied Sciences and Biotechnology. 2016;4(3):372-379.
Chandrasekaran, M. Boopathi, T and Manivannan, p. Comprehensive assessment of ameliorative effects of AMF in alleviating Abiotic stress in Tomato plants. Journal of Fungi. 2021;7:303.
Khaliq A, Perveen S, Alamer KH, Haq MZU, Rafique Z, alsudays IM, Althobaiti AT, Saleh MA, Hussain S, Attia H. Arbuscular mycorrhizal fungi symbiosis to enhance plant-soil interaction. Sustainability. 2022;14:7840.
Wadsworth, F.H. Forest Production for Tropical America, Agricultural Handbook 710. United States Department of Agriculture; 1997.
Lemmens RHMJ, Soerianegara I, Wong WC. Timber trees: Minor commercial timbers. Leiden: Backhuys Publishers; 1995.
Rabie GH, Almadini AM. Role of bio-inoculants in development of salt-tolerance of Viciafaba plants under salinity stress. King Faisal University, Saudi Arabia, African Journal of Biotechnology. 2005;25: 221-242.
Abbaspour H, Fallahyan F, Fahimi H. Effects of endo-mycorrhizal fungi and salt stress on nutrient acquisition and growth of Pistacia avera L. Asian Network. Pakistan Journal of Biotechnology Sciences. 2005;8(7):1006-1010.
Hunt R. Plant growth and Analysis Studies in Biology-Number 96. Edward Arnold publishing, London, UK; 1978.
Heilmeier H, Scholze ED, Whale DM. Carbon and Nitrogen Partitioning in the Biennial Monocarp Arctium tomentosum. Mill Oecologia. 1986;70:466-474.
Koske RE, Gemma JN. A modified procedure for staining roots to detect V. A. mycorrhizas. Mycology Research. 1989;(92):486-488.
Giovannetti M, Mosse. An evaluation of techniques for measuring vesicular Arbuscular mycorrhizal infection in roots. New Phtologist. 1980;84:489-500.
AOAC. Association of Official Analytical Chemist. Methods of Analyss, Washington, DC, USA; 2003.
Malhi GS, Kaur M, Kaushik P, Alyemeni, M. N., Alsahli, A.A. and Ahmad, P. Arbuscular mycorrhiza in combating abiotic stresses in vegetables: An ecofriendly approach. Saudi J. Bio. Sci. 2021;28:1465.
Chandrasekaran M. Arbuscular mycorrhizal fungi mediated enhanced biomass, root morphology traits and nutrient uptake under drought stress: A meta-analysis. Fungi, 2022;8;660.
Osim SE, Etukudo MM. Growth Response of Pterocarpus mildbraedii (Harms) seedlings inoculated with Arbuscular mycorrhizal fungi (AMF) under salt stress in Calabar, Nigeria. Asian Journal of Research in Botany. 2022;8(2):21-28.
Jahromi F, Aroca R, Porcel R, Ruizlozano J. M. Influence of salinity on the invitro development of Glomusintraradices and on the invivo physiological and molecular responses of mycorrhizal lettuce plants. Microbial Ecology. 2008;55:45-53.
Rajput A, Rajput SS, Jha G. Physiological parameters leaf area index, crop growth rate, relative growth rate and net assimilation rate of different varieties of rice grown under different planting geometries and depths in SRI. Int, J. Pure App. Biosci. 2017;5(1):362-367.
Fu H, Yuan G, Cao T, Ni L, Li W, Zhu G. Relationships between relative growth rate and its components across II submerged macrophytes. Journal of Freshwater Ecology. 2012;27(4),471-480.
Rees M, Osborne CP, Woodward FI, Hulme SP, Turnbull LA, Taylor SH. Partitioning the components of relative growth rate: How important is plant size variation? The American Naturalist. 2010;176:152-161.
Paine CET, Marthews TR, Vogt DR, Purves D, Rees M, Hector A, Turnbull LA. How to fit non-linear plant growth models and calculate growth rate: An update for ecologist. Methods in Ecology and Evolution. 2012;3(3):245.
Christopher D, Philipson S, Toby R, Marthew TR, Reuben N, Glen R, Lindsay A, Turnbull LA. and Hector A. Light based regeneration niches: Evidence from 21 Dipterocarp spp using size-specific relative growth rates. Biotropica. 2012;3(4):265.
Chango GMC, Velly PBE. Relationship of physiological characters to yield parameters in oil seed rape. Canadian Journal of Plant Science. 2001;81:1-6.
Downton WJS. Photosynthesis in salt stressed grapevines. Aust. J. Plant Physio. 1974;183-192.
Singh, M. and Singh, S. Net assimilation rate, relative growth rate and yield of pea genotypes under different NaHco3 concentrations. Biologia Plantarum. 1994;36(1):145-148.
Juniper S, Abbott LK. Soil salinity delays germination and limits growth of hyphae form propagules of Arbuscular mycorrhizal fungi. Mycorrhiza. 2006; 16:371-379.
Giri B, Mukerji KG Mycorrhizal inoculants alleviates salt stress in Sesbania aegyptiaca and Sesbania grandiflora under field conditions: Evidence for reduced sodium and improved magnesium uptake. Mycorrhizal. 2004;14:307-312.
Sheng M, Tang, M, Chan H, Yang B, Zhang F, Huang Y. Influence of Arbuscular mycorrhizae on photosynthesis and water status of maize plants under salt stress. Mycorrhiza. 2008;18:287-295.
Zuccarini P. Mycorrhizal infection ameliorates chlorophyll content and nutrient uptake of lettuce exposed to saline irrigation. Plant, Soil and Environment. 2007;53:283-289.