Sciences in Cold and Arid Regions ›› 2015, Vol. 7 ›› Issue (3): 229-237.doi: 10.3724/SP.J.1226.2015.00229

• ARTICLES • Previous Articles    

Comparative studies on leaf epidermal micromorphology and mesophyll structure of Elaeagnus angustifolia L. in two different regions of desert habitat

MengMeng Li1,2,3, YuBing Liu1,2, MeiLing Liu1,2,3, Dan Liu1,2,3   

  1. 1. Key Laboratory of Stress Physiology and Ecology in Cold and Arid Regions of Gansu Province, Cold and Arid Regions Environmental and Engineering Research Institute, Chinese Academy of Sciences, Lanzhou, Gansu 730000, China;
    2. Shapotou Desert Research & Experiment Station, Cold and Arid Regions Environmental and Engineering Research Institute, Chinese Academy of Sciences, Lanzhou, Gansu 730000, China;
    3. University of Chinese Academy of Sciences, Beijing 100049, China
  • Received:2014-09-12 Revised:2015-01-20 Published:2018-11-23
  • Contact: YuBing Liu, ybliu13@163.com E-mail:ybliu13@163.com
  • Supported by:
    This work was financially supported by the National Natural Science Foundation of China (Grant No. 91125029) and the State Key Development Program for Basic Research of China (973 Program, Grant No. 2013CB429904).

Abstract: In order to obtain qualitative and quantitative characteristics of leaf epidermal micromorphology and mesophyll structure to evaluate the responses of Elaeagnus angustifolia L. to different environmental factors, epidermal micromorphology was observed by scanning electron microscopy (SEM), and mesophyll structure was studied by light microscopy (LM) and transmission electron microscopy (TEM). Materials were selected from Linze County, Gansu Province (material A) and Qitai County, Xinjiang Uygur Autonomous Region (material B) of China. Results show that lamina thickness was higher in material A, with one layer of epidermal cells in both adaxial and abaxial surfaces, and epidermal cell radial length was significantly longer in the adaxial surface. E. angustifolia leaves are typically bifacial, with a higher ratio of palisade to spongy tissue in material A. The thickness of trichome layer of epidermis was thicker in material A. In contrast, cell wall and cuticular wax of the epidermal cells were thinner in material A than in material B. Chloroplast ultrastructure was different with the approximate spherical chloroplast containing numerous starch grains and osmiophilic granules in material A, while only the spindly chloroplast contained starch grains in material B. Multiple layers of peltate or stellate-peltate trichomes occupied both leaf surfaces in material A and the abaxial surface in material B, while the adaxial surface of material B contained few trichomes. Stomata were not observed on the leaf surfaces in materials A and B by SEM because of trichome obstruction. Our results indicate that the leaf structure of E. angustifolia is closely correlated with environmental factors, and the combination of leaf epidermal micromorphology and mesophyll structure afford resistance to environmental stress.

Key words: Elaeagnus angustifolia L., epidermal micromorphology, mesophyll structure, chloroplast

Chartzoulakis K, Patakas A, Kofidis G, et al., 2002. Water stress affects leaf anatomy, gas exchange, water relations and growth of two avocado cultivars. Scientia Horticulturae, 95(1-2): 39-50. DOI: 10.1016/S0304-4238(02)00016-X.
Cui XP, Liu GH, Zhang RL, 2006. Comparison of leaf anatomical structure between Salix gordejevii growing under contrasting habitats of Otingdag Sandland and Salix microtachya var. bordensis growing on the lowlands of dunes. Acta Ecologica Sinica, 26(6): 1842-1847.
Dickison WC, 2000. Integrative Plant Anatomy. San Diego: Academic Press, pp. 186-195.
Ehleringer JR, Björkman O, Mooney HA, 1976. Leaf pubescence: effects on absorptance and photosynthesis in a desert shrub. Science, 192(4237): 376-377. DOI: 10.1126/science.192.4237.376.
Ehleringer JR, Mooney HA, 1978. Leaf hairs: effects on physiological activity and adaptive value to a desert shrub. Oecologia, 37: 183-200. DOI: 10.1007/BF00344990.
Fahn A, 1986. Structural and functional properties of trichomes of xeromorphic leaves. Annals of Botany, 57(5): 631-637.
Fei SL, Fang JY, Fan YJ, et al., 1998. Anatomical characteristics of leaves and woods of Fagus lucida and their relationship to ecological factors in Mountain Fanjingshan, Guizhou, China. Acta Botanica Sinica, 41(9): 1002-1009.
Huang J, Maimaitijiang, 2005. Study on the classification of Elaeagnus in Xinjiang. Bulletin of Botanical Research, 25: 268-271. DOI: 10.3969/j.issn.1673-5102.2005.03.006.
Huang J, Maimaitijiang, Yang C, et al., 2005. Present situation and prospect about the study of Elaeagnus angustifolia L.. Chinese Wild Plant Resources, 24(3): 26-33.
Ivanova LA, P'yankov VI, 2001. Structural adaptation of the leaf mesophyll to shading. Russian Journal of Plant Physiology, 49(3): 419-431. DOI: 10.1023/A:1015513607202.
Kenzo T, Yoneda R, Azani MA, et al., 2008. Changes in leaf water use after removal of leaf lower surface hairs on Mallotus macrostachyus (Euphorbiaceae) in a tropical secondary forest in Malaysia. Journal of Forest Research, 13(2): 137-142. DOI: 10.1007/s10310-008-0062-z.
Li FL, Bao WK, 2005. Responses of the morphological and anatomical structure of the plant leaf to environmental change. Chinese Bulletin of Botany, 22: 118-127.
Liu YB, Li XR, Liu ML, et al., 2012. Responses of three different ecotypes of reed (Phragmites communis Trin.) to their natural habitats: leaf surface micro-morphology, anatomy, chloroplast ultrastructure and physio-chemical characteristics. Plant Physiology and Biochemistry, 51: 159-167. DOI: 10.1016/j. plaphy.2011.11.002.
Ma JJ, Ji CJ, Han M, et al., 2012. Comparative analyses of leaf anatomy of dicotyledonous species in Tibetan and Inner Mongolian grasslands. Science China Life Sciences, 55(1): 68-79. DOI: 10.1007/s11427-012-4268-0.
P'yankov VI, Kondratchuk AV, Shipley B, 1999. Leaf structure and specific leaf mass: the alpine desert plants of the Eastern Pamirs, Tadjikistan. New Phytologist, 143(1): 131-142.
Rury P, Dickison W, 1984. Structural correlations among wood, leaves and plant habit. In: White RA, Dickison WC (eds.). Contemporary Problems in Plant Anatomy. Orlando: Academic Press, pp. 495-540.
Shepherd T, Griffiths DW, 2006. The effects of stress on plant cuticular waxes. New Phytologist, 171(3): 469-499. DOI: 10.1111/j.1469-8137.2006.01826.x.
Sun M, Lin Q, 2010. A revision of Elaeagnus L. (Elaeagnaceae) in mainland China. Journal of Systematics and Evolution, 48(5): 356-390. DOI: 10.1111/j.1759-6831.2010.00085.x.
Uphof JCT, Hummel K, 1962. Plant hairs. Encyclopedia of Plant Anatomy, 4(5): 1-292.
Wooley JT, 1970. Water relations of soybean leaf hairs. Agronomy Journal, 56(6): 569-571. DOI: 10.2134/agronj1964.0002196 2005600060014x.
Wuenscher JE, 1970. The effect of leaf hairs of Verbascum thapsus on leaf energy exchange. New Phytologist, 69(1): 65-73. DOI: 10.1111/j.1469-8137.1970.tb04050.x.
Zhang HX, Liu GH, Cui XP, 2005. Affection of aridity to anatomical structure of leave of Ulmus pumila L. var. sabulosa. Bulletin of Botanical Research, 25(1): 39-44.
Zhang ZX, Gao ZQ, Zhang Y, 1992. A SEM study on the morphology of foliar surface of seabuckthorn and Elaeagnus and their implication on taxonomy. 1. The morphology of foliar surface and their attachment. Bulletin of Botanical Research, 12(2): 169-176.
Zoric L, Merkulov L, Lukovic J, et al., 2009. Leaf epidermal characteristics of Trifolium L. species from Serbia and Montenegro. Flora-Morphology, Distribution, Functional Ecology of Plants, 204(3): 198-209. DOI: 10.1016/j.flora.2008.02.002.
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