Assessment of Eco-Physiological Potential and Folia-Morpho-Anatomical Variation in Triplochiton Scleroxcylon K. Schum
Author Affiliations
- 1The Department of Forestry and Wood Technology, School of Agriculture and Agricultural Technology, Federal University of Technology, Akure, Ondo State, Nigeria
- 2The Department of Forestry and Wood Technology, School of Agriculture and Agricultural Technology, Federal University of Technology, Akure, Ondo State, Nigeria
Res. J. Agriculture & Forestry Sci., Volume 14, Issue (4), Pages 1-10, October,8 (2026)
Abstract
This study assessed the eco-physiological growth performance and foliar morpho-anatomical characteristics of T. scleroxylon wildlings across three ecological locations in Ondo State, Nigeria: Owo (RUGIPO), Akungba-Akoko (AAUA), and Akure (FUTA). Five families (F1–F5) from Queen’s plot, Akure Forest Reserve, were evaluated to determine variations in growth traits, leaf morphology, venation patterns, epidermal structure, and stomatal characteristics, as well as their relationships with climatic factors. Growth parameters measured included height, collar diameter, and number of leaves, while foliar traits included leaf area, venation density, epidermal cell density, and stomatal characteristics. Climatic variables (air temperature, rainfall, and relative humidity) were correlated with the growth variable. Wildlings at FUTA recorded the highest mean collar diameter (5.97 ± 0.05 cm), height (31.89 ± 0.16 cm), and number of leaves (14.0 ± 0.12), compared to wildlings from Owo (5.06 ± 1.20 cm, 24.95 ± 0.09 cm, and 12.18 ± 0.22) and Akungba-Akoko (4.22 ± 0.09 cm, 24.13 ± 0.22 cm, and 7.0 ± 0.24) respectively. Among families, Family 1 exhibited superior growth performance with the highest mean height (33.79 cm) and collar diameter (5.99 cm), while Family 2 recorded the highest mean leaf number (13). Strong positive correlation was recorded between height and air temperature (r = 0.93), height and rainfall (r = 0.85), and height and number of leaves (r = 0.97). Foliar analysis revealed significantly higher epidermal cell density and stomatal density in FUTA (ECD = 64.00 mm⁻²; SD = 27.50 mm⁻²). The study demonstrates that both ecological conditions significantly influence early growth and foliar characteristics of T. scleroxylon. The superior performance of wildlings from family 1 in FUTA and other locations highlights their suitability for conservation, domestication, and plantation establishment. These findings provide empirical support for the selection of site-specific, genetically superior planting materials for sustainable forest management and afforestation programs in Nigeria.
References
- Nicotra, A. B., Atkin, O. K., Bonser, S. P., Davidson, A. M., Finnegan, E. J., Mathesius, U., Poot P., Purugganan M.D., Richards C.L., Valladares F. & van Kleunen, M.∙ (2010)., Plant phenotypic plasticity in a changing climate., Trends in plant science, 15(12), 684-692.
- Auld, J. R., Agrawal, A. A., & Relyea, R. A. (2010)., Re-evaluating the costs and limits of adaptive phenotypic plasticity., Proceedings of the Royal Society B: Biological Sciences, 277(1681), 503-511.
- Lamarque, L. J., Porte, A. J., Eymeric, C., Lasnier, J. B., Lortie, C. J., & Delzon, S. (2013)., A test for pre-adapted phenotypic plasticity in the invasive tree Acer negundo L., PLoS one, 8(9), e74239.
- Dickison, W. C. (2000)., Integrative plant anatomy., Elsevier.
- Markesteijn, L., Poorter, L., & Bongers, F. (2007)., Light‐dependent leaf trait variation in 43 tropical dry forest tree species., American Journal of Botany, 94(4), 515-525.
- Akinnagbe, A., Gailing, O., Finkeldey, R., & Lawal, A. (2019)., Towards conservation of genetic variation of tropical tree species with differing successional status: The case of Mansonia altissima A. Chev and Triplochiton scleroxylon K. Schum., Tropical Conservation Science, 12.
- Wilkinson H. (1979)., The plant surface (mainly leaf)., In Metcalfe CR and Chalk L (eds) Anatomy of Dicotyledons. Oxford: Clarendon Press London, pp. 97–165.
- Saheed, S. A., & Illoh, H. C. (2010)., A taxonomic study of some species in Cassiinae (Leguminosae) using leaf epidermal characters., Notulae Botanicae Horti Agrobotanici Cluj-Napoca, 38(1), 21-27.
- Postma, J. A., & Lynch, J. P. (2012)., Complementarity in root architecture for nutrient uptake in ancient maize/bean and maize/bean/squash polycultures., Annals of botany, 110(2), 521-534.
- Violle, C., Thuiller, W., Mouquet, N., Munoz, F., Kraft, N. J., Cadotte, M. W., ... & Mouillot, D. (2017)., Functional rarity: the ecology of outliers., Trends in ecology & evolution, 32(5), 356-367.
- Ehlers, B. K., Damgaard, C. F. and Laroche, F. (2016)., Intraspecific genetic variation and species coexistence in plant communities., Biology letters, 12(1), 20150853.
- Umaña, M. N. and Swenson, N. G. (2019)., Intraspecific variation in traits and tree growth along an elevational gradient in a subtropical forest., Oecologia, 191(1), 153-164.
- Novikova, T. P., Tylek, P., Mastrangelo, C. B., Drapalyuk, M. V., Kharin, S. V. and Novikov, A. I. (2023)., The root collar diameter growth reveals a strong relationship with the height growth of juvenile Scots pine trees from seeds differentiated by spectrometric feature., Forests, 14(6), 1164.
- Robakowski, P., Pietrzak, T., Kowalkowski, W., & Małecki, G. (2021)., Survival, growth and photochemical efficiency of silver fir seedlings produced with different technologies., New Forests, 52(6), 1055-1077.
- Wright, I. J., Reich, P. B., Westoby, M., Ackerly, D. D., Baruch, Z., Bongers, F., ... & Villar, R. (2004)., The worldwide leaf economics spectrum., Nature, 428(6985), 821-827.
- Niinemets, Ü. (2010)., Responses of forest trees to single and multiple environmental stresses from seedlings to mature plants: past stress history, stress interactions, tolerance and acclimation., Forest Ecology and management, 260(10), 1623-1639.
- Bonan, G. (1945)., Ecological climatology., American history, 1861(1900).
- Falconer, D. S. (1996)., Introduction to quantitative genetics., Pearson Education India.
- Körner, C. (2003)., Carbon limitation in trees., Journal of ecology, 91(1), 4-17.
- Sack, L., Scoffoni, C., John, G. P., Poorter, H., Mason, C. M., Mendez-Alonzo, R., & Donovan, L. A. (2013)., How do leaf veins influence the worldwide leaf economic spectrum? Review and synthesis., Journal of experimental botany, 64(13), 4053-4080.
- Xu, J., Grumbine, R. E., Shrestha, A., Eriksson, M., Yang, X., Wang, Y. U. N., & Wilkes, A. (2009)., The melting Himalayas: cascading effects of climate change on water, biodiversity, and livelihoods., Conservation Biology, 23(3), 520-530.
- Cheng, X., Ping, T., Li, Z., Wang, T., Han, H., & Epstein, H. E. (2022)., Effects of environmental factors on plant functional traits across different plant life forms in a temperate forest ecosystem., New Forests, 53(1), 125-142.
- James, S. A., & Bell, D. T. (2000)., Leaf orientation, light interception and stomatal conductance of Eucalyptus globulus ssp. globulus leaves., Tree Physiology, 20(12), 815-823.
- Luomala, E. M., Laitinen, K., Sutinen, S., Kellomäki, S. & Vapaavuori, E. (2005)., Stomatal density, anatomy and nutrient concentrations of Scots pine needles are affected by elevated CO2 and temperature., Plant, Cell & Environment, 28(6), 733-749.
- Bertolino, L. T., Caine, R. S., & Gray, J. E. (2019)., Impact of stomatal density and morphology on water-use efficiency in a changing world., Frontiers in plant science, 10, 225.
