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Journal of Arid Land  2012, Vol. 4 Issue (2): 171-179    DOI: 10.3724/SP.J.1227.2012.00171     CSTR: 32276.14.SP.J.1227.2012.00171
Research Articles     
Study of variegated and white flower petals of Capparis spinosa expanded at dusk in arid landscapes
Chrysanthi CHIMONA1, Avra STAMELLOU2, Apostolos ARGIROPOULOS1, Sophia RHIZOPOULOU1
1 Department of Botany, Faculty of Biology, National and Kapodistrian University of Athens, Athens 15781, Greece;
2 Department of Botany, School of Biology, Aristotelian University of Thessaloniki, Thessaloniki 54124, Greece
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Abstract   In this study, we provide the first evidence of two pairs of petals of the rapidly expanded and short-lived nocturnal flowers of Capparis spinosa L. (caper) during the prolonged drought period in Eastern Mediterranean region. The corolla of the winter-deciduous, perennial C. spinosa consists of two pairs of petals: a pair of white dis-tinct petals and a pair of connate variegated petals with green basal parts. The results indicated the presence of substantially different amounts of chlorophyll in the two pairs of petals, while their carbohydrates’ content is comparable with that of the green sepals. High resolution imaging of petal surfaces of short-lived flowers of C. spinosa, obtained by using scanning electron microscopy, revealed stomata on the adaxial epidermis on both the white and the green parts of the variegated petals; while dense hairs were found on the surface of the abaxial green parts of the variegated petals. Adaxial, epidermal cells of the variegated petals, viewed using atomic force microscopy, possess a submicron, cuticular microfolding that differs between the white and the green parts of the petals. It appears that microridges on the adaxial, white parts of petals of C. spinosa compensate for an increase in cell surface area of the short lived petals, while the roughness of the green parts of petals was found to be higher than that of the white parts. Thus, the micromorphology of surfaces of epidermal cells is expected to affect optical properties and wettability of the floral tissues. These findings may be particularly important for understanding the performance of the short-lived petals of C. spinosa, which are exposed to dryland environments.

Received: 23 November 2011      Published: 06 June 2012
Fund:  

The research grant PENED 03174, co-funded by the European Union (75%) and the Greek General Secretary of Research and Technology and Private Sectors (25%).

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Cite this article:

Chrysanthi CHIMONA, Avra STAMELLOU, Apostolos ARGIROPOULOS, Sophia RHIZOPOULOU. Study of variegated and white flower petals of Capparis spinosa expanded at dusk in arid landscapes. Journal of Arid Land, 2012, 4(2): 171-179.

URL:

http://jal.xjegi.com/10.3724/SP.J.1227.2012.00171     OR     http://jal.xjegi.com/Y2012/V4/I2/171

Argiropoulos A. 2009. Flower colour of Mediterranean plants. Ph.D. Thesis. Athens: University of Athens, 175–201.

Aschan G, Pfanz H. 2003. Non-foliar photosynthesis: a strategy of additional carbon acquisition. Flora, 198: 81–79.

Aytac Z, Kinaci G, Caylan A. 2009. Yield and some morphological characteristics of caper (Capparis spinosa L.) population cultivated at various slopes in Aegean ecological conditions. Pakistan Journal of Botany, 41: 591–596.

Bhushan B. 2009. Biomimetics: lessons from nature–an overview. Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences, 367: 1445–1486.

Cooremans B. 1999. An unexpected discovery in medieval Bruges (Flanders, Belgium): seeds of the caper (Capparis spinosa L.). En-vironmental Archaeology, 4: 97–101.

Dafni A, Eisikowitch D, Irvi Y. 1987. Nectar flow and pollinators’ efficiency in two co-occurring species of Capparis (Capparaceae) in Israel. Plant Systematics and Evolution, 157: 181–186.

Danin A. 2010. Capparis in the East Mediterranean countries. Flora Mediterranea, 20: 179–185.

Diamantoglou S, Rhizopoulou S. 1992. Free proline accumulation in sapwood, bark and leaves of three evergreen sclerophylls and a comparison with an evergreen conifer. Journal of Plant Physiology, 140: 361–365.

Eisikowitch D, Ivri Y, Dafni A. 1986. Reward partitioning in Capparis spp. along ecological gradient. Oecologia, 71: 47–50.

Evans R Y, Reid M S. 1986. Control of petal expansion during diurnal opening of roses. Acta Horticulturae, 181: 55–63.

Fahn A. 1979. Nectaries. In: Fahn A. Secretory Tissues of Plants. Lon-don: Academic Press, 51–111.

Gale R M O, Owens S J. 1983. Cell distribution and surface morphology in petals, androecia and styles of Commelinaceae. Botanical Journal of the Linnean Society, 87: 247–262.

Glover B J. 2007. Understanding flowers and flowering, an integrated approach. Oxford: Oxford University Press, 43–50.

Huang B, Wang Y, Huang S, et al. 2011. Guard cells on adaxial and abaxial epidermes of Erythrina corallodendron sepals. Biologia Plantarum, 55(4): 716–720.

Inocencio C, Alcaraz F, Calderón F, et al. 2002. The use of floral char-acters in Capparis sect. Capparis to determine the botanical and geographical origin of capers. European Food Research and Tech-nology, 214: 335–339.

Jiang H E, Li X, Ferguson D K, et al. 2007. The discovery of Capparis spinosa L. (Capparidaceae) in the Yanghai Tombs (2800 years b.p.), NW China, and its medicinal implications. Journal of Ethnophar-macology, 113: 409–420.

Koch K, Bhushan B, Barthlott W. 2009. Multifunctional surface struc-tures of plants: an inspiration for biomimetics. Progress in Materials Science, 54: 137–178.

Kutschera U. 2008. The growing of the outer epidermal wall: design and physiological role of a composite structure. Annals of Botany, 101: 615–621.

Levizou E, Drilias P, Kyparissis A. 2004. Exceptional photosynthetic performance of Capparis spinosa L. under adverse conditions of Mediterranean summer. Photosynthetica, 42: 229–235.

Özcan M. 2000. Pickling caper flower buds. Journal of Food Quality, 24: 261–269.

Pacini E, Nepi M. 2007. Nectar production and presentation. In: Nicolson S W, Nepi M, Pacini E. Nectaries and Nectar. The Nether-lands: Springer, 168–214.

Petanidou T, Van Laere A  J, Smets E. 1996. Change in floral nectar components from fresh to senescent flowers of Capparis spinosa (Capparidaceae), a nocturnally flowering Mediterranean shrub. Plant Systematics and Evolution, 199: 79–92.

Pfündel E E, Agati G, Zerovic Z G. 2006. Optical properties of plant surfaces. In: Riederer M, Muller C. Biology of the Plant Cuticle. Oxford: Blackwell, 216–247.

Polymeni R, Spanakis E, Argiropoulos A, et al. 2010. Aspects on the relief of living surfaces using atomic force microscopy allow “art” to imitate nature. Integrative Zoology, 5: 218–225.

Psaras G K, Diamantopoulos G S, Makrypoulias C. 1996. Chloroplast arrangement along intercellular spaces. Israel Journal of Plant Sci-ences, 44: 1–9.

Qian J, Chen F, Zhao X, et al. 2011. China rose petal as biotemplate to produce two-dimensional ceria nanosheets. Journal of Nanoparticle Research, 12: 7149–7158.

Rands S A, Glover B J, Whitney H M. 2011. Floral epidermal structure and flower orientation: getting to grips with awkward flowers. Ar-thropod-Plant Interactions, 5: 279–285.

Ren G, Healy R A, Klyne A M, et al. 2007. Transient starch metabolism in ornamental tobacco floral nectaries regulates nectar composition and release. Plant Science, 173: 277–290.

Rhizopoulou S. 1990. Physiological responses of Capparis spinosa L. to drought. Plant Physiology, 136: 341–348.

Rhizopoulou S, Diamantoglou S, Passiakou L. 1990. Free proline ac-cumulation in leaves, stems and roots of four Mediterranean native phrygana species. Acta Oecologica, 11: 585–593.

Rhizopoulou S, Meletiou-Christou M S, Diamantoglou S. 1991. Water relations for sun and shade leaves of four Mediterranean evergreen sclerophylls. Journal of Experimental Botany, 42: 627–635.

Rhizopoulou S, Heberlein K, Kassianou A. 1997. Field water relations of Capparis spinosa L. Journal of Arid Environments, 36: 237–248.

Rhizopoulou S, Psaras G. 2003. Development and structure of drought-tolerant leaves of the Mediterranean shrub Capparis spinosa L. Annals of Botany, 92: 377–383.

Rhizopoulou S, Ioannidi E, Alexandredes N, et al. 2006. A study on functional and structural traits of the nocturnal flowers of Capparis spinosa L. Journal of Arid Environments, 66: 635–647.

Rivera D, Inocencio C, Obon C, et al. 2002. Archaeobotany of capers (Capparis) (Capparaceae). Vegetation History and Archaeobotany, 11: 295–313.

Ryke K A, Page A M. 1998. Plastid ontogeny during petal development in Arabidopsis. Plant Physiology, 116: 797–803.

Sakcali M S, Bahadir H, Ozturk M. 2008. Ecophysiology of Capparis spinosa L.: a plant suitable for combating desertification. Pakistan Journal of Botany, 40: 1481–1486.

Sher H, Alyemeni M N. 2010. Ethnobotanical and pharmaceutical evaluation of Capparis spinosa L., validity of local folk and Unani system of medicine. Journal of Medicinal Plants Research, 4: 1751–1756.

Sibthorp J, Smith J E. 1825. Flora Graeca: Sive Plantarum Rariorum Historia, Quas in Provinciis Aut Insulis Graeciae. London: Richard Taylor, 70–71.

Sozzi G O. 2001. Caper bush: botany and horticulture. Horticultural Review, 27: 125–188.

Stoudt H N. 1941. The floral morphology of the Capparidaceae. American Journal of Botany, 28(8): 664–675.

Suleiman K M, Bhat N R, Abdal M S, et al. 2009. Growth of Capparis spinosa var. Inermis under different irrigation levels. Journal of Horticulture and Forestry, 1: 17–21.

Trili N, Nasri N, Saadaoui E, et al. 2009. Carotenoid and tocopherol composition of leaves, buds, and flowers of Capparis spinosa grown wild in Tunisia. Journal of Agricultural and Food Chemistry, 57: 5381–5385.

Vainstein A, Sharon R. 1993. Biogenesis of petunia and carnation co-rolla chloroplasts: changes in the abundance of nuclear and plas-tid-encoded photosynthesis specific gene products during flower development. Physiologia Plantarum, 89: 192–198.

van Doorn W G, Van Meeteren U. 2003. Flower opening and closing: a review. Journal of Experimental Botany, 54: 1801–1812.

van Doorn W G. 2004. Is petal senescence due to sugar starvation? Plant Physiology, 134: 35–42.

Wagner P R, Barthlott F W, Neinhuis C. 2003. Quantitative assessment to the structural basis of water repellency in natural and technical surfaces. Journal of Experimental Botany, 54: 1295–1303.

Weiss D, Shomer-Ilan A, Vainstein A, et al. 1990. Photosynthetic carbon fixation in the corolla of Fetunia hybrida. Physiologia Plantarum, 78: 345–350.

Zhang T, Tan D Y. 2009. An examination of the function of male flowers in an andromonoecious shrub Capparis spinosa. Journal of Integra-tive Plant Biology, 51: 316–324.

Zhang Y, Chen Y, Shi L, et al. 2012. Recent progress of dou-ble-structural and functional materials with special wettability. Journal of Materials Chemistry, 22: 799–815.

Zhuang Y L, Ratcliffe S. 2012. Relationship between dew presence and Bassia dasyphylla plant growth. Journal of Arid Land, 4(1): 11–18.
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