Functional Traits of Stem and Leaf of Wrightia candollei S. Vidal
Jonathan O. Hernandez1, Marilyn O. Quimado1, Edwino S. Fernando1,
Dennis E. Pulan2, Pastor L. Malabrigo Jr.1, and Lerma S.J. Maldia1
1Department of Forest Biological Sciences, College of Forestry and Natural Resources (CFNR)
University of the Philippines Los Baños (UPLB), College, Laguna 4031 Philippines
2College of Agriculture, Southern Luzon State University
Lucban, Quezon, Philippines
*Corresponding author: This email address is being protected from spambots. You need JavaScript enabled to view it.
ABSTRACT
Morpho-anatomical functional traits of native tree species are deemed important in forest restoration. Although much is known about morpho-anatomical traits of many terrestrial plants, such traits in Philippine native trees remain unclear. In this study, the stem and leaf morpho-anatomy of W. candollei S. Vidal was investigated to provide insights on its potential for restoration of dry, degraded lands. Results suggest that the morpho-anatomical structure of leaf and stem of W. candollei conforms to characteristics typical of plants adapted to dry areas and to species commonly used for restoration. The presence of trichomes, multiple layers of storage cells and mechanical cells, sclerenchymatic phloem cap, multiple vascular bundles, living xylem parenchyma, and steep leaf inclination were observed and interpreted as important leaf and stem structural traits of W. candollei. These morpho-anatomical traits are commonly associated with (1) solar radiation and water loss reduction; (2) tissue/organ mechanical reinforcement; and (3) water uptake and storage. Therefore, W. candollei – in association with the other native species – might be potentially useful for restoration of dry degraded lands in the Philippines. However, ecophysiological and phenological studies, as well as watering regime experiments, are recommended to better understand the actual habitat preference of the species.
INTRODUCTION
The restoration of heavily degraded areas has become one of the emerging research interests across tropical countries. In the Philippines, two of the important observations noted from restoration efforts are (1) the selection of appropriate forest tree species and (2) their suitability to open-field conditions (Chechina and Hamann 2015). The selection of species for restoration of degraded lands is considered a complex task. Forest ecologists recommend native species for forest restoration because it is the best way to restore dry degraded lands’ ecological integrity into its original state. Native tree species may also have morpho-anatomical functional and adaptive traits that exotic species widely used for restoration may also have, allowing them to adapt to dry degraded environment. These traits have long been studied for many plants from the tropics. However, because plant responses to environmental stress are complex, the functions of these morpho-anatomical traits are still unknown to Philippine native trees in the context of forest restoration. . . . . . read more
REFERENCES
ARENA C, VITALE L, SANTO AV. 2008. Paraheliotropism in Robinia pseudoacacia L.: An efficient strategy to optimize photosynthetic performance under natural environmental conditions. Plant Biology 10(2): 194–201. doi:10.1111/j.1438-8677.2008.00032.x
ARONNE G. 2001. Seasonal Dimorphism in the Mediterranean Cistus incanus L. subsp. incanus. Annals of Botany 87(6): 789–794. doi:10.1006/anbo.2001.1407
BANDYOPADHYAY T, GANGOPADHYAY G, PODDAR R, MUKHERJEE KK. 2004. Trichomes: Their Diversity, Distribution, and Density in Acclimatization of Teak (Tectona grandis L.) Plants Grown in vitro. Plant Cell, Tissue and Organ Culture 78(2): 113–121. doi:10.1023/b:ticu.0000022534.03276.c5
CARDOSO-GUSTAVSON P, CAMPBELL LM, MAZZONI-VIVEIROS SC, DE BARROS F. 2014. Floral colleters in Pleurothallidinae (Epidendroideae: Orchidaceae). American Journal of Botany 101: 587–597.
CARLAND FM. 1999. Genetic Regulation of Vascular Tissue Patterning in Arabidopsis. The Plant Cell Online 11(11): 2123–2138. doi:10.1105/tpc.11.11.2123
CHAVES MM, MAROCO JP, PEREIRA JS. 2003. Understanding plant responses to drought—from genes to the whole plant. Functional Plant Biology 30(3): 239. doi:10.1071/fp02076
CHECHINA M, HAMANN A. 2015. Choosing species for reforestation in diverse forest communities: Social preference versus ecological suitability. Ecosphere 6(11). doi:10.1890/es15-00131.1
DELOS REYES MT, MAGPANTAY GD, CAGALAWAN AJ, LAPIS AB, CALINAWAN NM. 2016. Assessment of Genetic Diversity of Narra (Pterocarpus indicus Willd.) Populations from Various Seed Sources in the Philippines using RAPD. Journal of Environmental Science and Management 19(2): 54–63.
DE MICCO VD, ARONNE G. 2012. Occurrence of Morphological and Anatomical Adaptive Traits in Young and Adult Plants of the Rare Mediterranean Cliff Species Primula palinuri Petagna. The Scientific World Journal. p. 1–10. doi:10.1100/2012/471814
EL-LAMEY TM. 2015. Morphological and Anatomical Responses of Leucaena leucocephala (Lam.) de Wit. and Prosopis chilensis (Molina) Stuntz to Ras Sudr Conditions. Journal of Applied Environmental and Biological Sciences 5(7): 43–51.
ESCH JJ, CHEN M. A, HILLESTAD M, MARKS MD. 2004. Comparison of TRY and the closely related At1g01380 gene in controlling Arabidopsis trichome patterning. The Plant Journal 40(6): 860–869. doi:10.1111/j.1365-313x.2004.02259.x
FINKELDEY R, GUZMAN ND, CHANGTRAGOON S. 1999. The Mating System of Pterocarpus indicus Willd. at Mt. Makiling, Philippines. Biotropica 31(3): 525-530. doi:10.1111/j.1744-7429.1999.tb00397.x
GARCIA JD, SCREMIN-DIAS E, SOFFIATTI P. 2012. Stem and root anatomy of two species of Echinopsis (Trichocereeae, Cactaceae). Revista Mexicana De Biodiversidad 83(4). doi:10.7550/rmb.28124
GIBSON AC. 1983. Anatomy of photosynthetic old stems of nonsucculent dicotyledons from North American deserts. Botanical Gazette 144: 347–363.
GRATANI L, BOMBELLI A. 2000. Correlation between leaf age and other leaf traits in three Mediterranean maquis shrub species: Quercus ilex, Phillyrea latifolia, and Cistus incanus. Environmental and Experimental Botany 43(2): 141–153. doi:10.1016/s0098-8472(99)00052-0
HAVAUX M, TARDY F. 1999. Loss of chlorophyll with limited reduction of photosynthesis as an adaptive response of Syrian barley landraces to high-light and heat stress. Functional Plant Biology 26(6): 569. doi:10.1071/pp99046
HERNANDEZ JO, MALABRIGO PL, QUIMADO MO, MALDIA LSJ, FERNANDO ES. 2016. Xerophytic characteristics of Tectona philippinensis Benth. & Hook.f. Philippine Journal of Science 145(3): 259–269.
ICHIE T, INOUE Y, TAKAHASHI N, KAMIYA K, KENZO T. 2016. Ecological distribution of leaf stomata and trichomes among tree species in a Malaysian lowland tropical rain forest. Journal of Plant Research 129(4): 625–635. doi:10.1007/s10265-016-0795-2
JANZ D, LAUTNER S, WILDHAGEN H, BEHNKE K, SCHNITZLER J, RENNENBERG H, POLLE A. 2012. Salt stress induces the formation of a novel type of ‘pressure wood’ in two Populus species. New Phytologist 194(1): 129–141. doi:10.1111/j.1469-8137.2011.03975.x
JOHANSEN DA. 1940. Plant Microtechnique. New York: McGraw-Hill Book Co. p. 126–156.
KRÖBER W, PLATH I, HEKLAU H, BRUELHEIDE H. 2015. Relating Stomatal Conductance to Leaf Functional Traits. Journal of Visualized Experiments No. 104. doi:10.3791/52738
MAXIMOV NA, YAPP RH. 1929. The plant in relation to water. London: George Allen & Unwin.
METCALFE CR, CHALK L. 1959. Anatomy of Dicotyledons – Leaves, Stem, and Wood in Relation to Taxonomy. Oxford: Clarendon Press.
MILAN P, HAYASHI AH, APPEZZATO-DA-GLÓRIA B. 2006. Comparative leaf morphology and anatomy of three Asteraceae species. Brazilian Archives of Biology and Technology 49(1): 1352015. Relating Stomatal Conductance to Leaf Functional Traits 144. doi:10.1590/s1516-89132006000100016
MOYA R, FO MT. 2006. Variation in the wood anatomical structure of Gmelina arborea (Verbenaceae) trees at different ecological conditions in Costa Rica. Revista De Biología Tropical 56(2): 689–704. doi:10.15517/rbt.v56i2.5617
NING P, WANG J, ZHOU Y, GAO L, WANG J, GONG C. 2016. Adaptional evolution of trichome in Caragana korshinskii to natural drought stress on the Loess Plateau, China. Ecology and Evolution 6(11): 3786–3795. doi:10.1002/ece3.2157
NIKOLOVA A, VASSILEV A. 2011. A Study on Tribulus terrestris L. Anatomy and Ecological Adaptation. Biotechnology & Biotechnological Equipment 25 (2): 2369–2372.
NOBEL PS. 2006. Parenchyma–chlorenchyma Water Movement during Drought for the Hemiepiphytic Cactus Hylocereus undatus. Annals of Botany 97(3): 469–474. doi:10.1093/aob/mcj054
OLIVEIRA G, PEÑUELAS J. 2002. Comparative protective strategies of Cistus albidus and Quercus ilex facing photoinhibitory winter conditions. Environmental and Experimental Botany 47(3): 281–289. doi:10.1016/s0098-8472(02)00003-5
ORWA C, MUTUA A, KINDT R, JAMNADASS R, ANTHONY S. 2009. Agroforestree Database: A tree reference and selection guide version 4.0. Retrieved from http://www.worldagroforestry.org/sites/treedbs/treedatabases.asp
PLOMION C, LEPROVOST G, STOKES A. 2001. Wood Formation in Trees. Physiology 127: 1513–1523.
POLLE A, CHEN S. 2014. On the salty side of life: Molecular, physiological and anatomical adaptation and acclimation of trees to extreme habitats. Plant, Cell & Environment 38(9): 1794–1816. doi:10.1111/pce.12440
RAVEN PH, EVERT RF, CURTIS H. 1976. Biology of Plants. New York: Worth Publishers.
RETAMALES HA, CABELLO A, SERRA MT, SCHARASCHKIN T. 2015. Leaf micromorphology and anatomy of Myrceugenia rufa (Myrtaceae). An endemic coastal shrub of north-central Chile. Gayana Botánica 72(1): 76–83. doi:10.4067/s0717-66432015000100010
ROSSATTO DR, KOLB RM. 2010. Gochnatia polymorpha (Less.) Cabrera (Asteraceae) changes in leaf structure due to differences in light and edaphic conditions. Acta Botanica Brasilica 24(3): 605–612. doi:10.1590/s0102-33062010000300002
SACK L, SCOFFONI C. 2013. Leaf venation: Structure, function, development, evolution, ecology, and applications in the past, present, and future. New Phytologist 198(4): 983–1000. doi:10.1111/nph.12253
SERNA, L, MARTIN C. 2006. Trichomes: Different regulatory networks lead to convergent structures. Trends in Plant Science 11(6): 274–280. doi:10.1016/j.tplants.2006.04.008
SHIELDS LM. 1950. Leaf xeromorphy as related to physiological and structural influences. The Botanical Review 16(8): 399–447. doi:10.1007/bf02869988
TRUONG SK, MCCORMICK R. F, ROONEY W.L, MULLET JE. 2015. Harnessing Genetic Variation in Leaf Angle to Increase Productivity of Sorghum bicolor. Genetics 201(3): 1229–1238. doi:10.1534/genetics.115.178608
VALLADARES F, PEARCY RW. 1998. The functional ecology of shoot architecture in some sun and shade plants of Heteromeles arbutifolia M. Roem., a California chaparral shrub. Oecologia 114: 1–10.
VILLANUEVA EL, BUOT JI. 2015. Threatened Plant Species of Mindoro, Philippines. IAMURE International Journal of Ecology and Conservation 14(1). doi:10.7718/ijec.v14i1.901
WERKER E. 2000. Trichome diversity and development. Advances in Botanical Research 31: 1–35.
XU Z, ZHOU G. 2008. Responses of leaf stomatal density to water status and its relationship with photosynthesis in a grass. Journal of Experimental Botany 59(12): 3317–3325. doi:10.1093/jxb/ern185
YADOLLAHI A, ARZANI K, EBADI A, WIRTHENSOHN M, KARIMI S. 2011. The response of different almond genotypes to moderate and severe water stress in order to screen for drought tolerance. Scientia Horticulturae 129(3): 403–413. doi:10.1016/j.scienta.2011.04.007
ZANTEN MV, PONS TL, JANSSEN JA, VOESENEK LA, PEETERS AJ. 2010. On the Relevance and Control of Leaf Angle. Critical Reviews in Plant Sciences 29(5): 300–316. doi:10.1080/07352689.2010.502086