Eco-morphological traits of leaf of the Campanula L. species
DOI:
https://doi.org/10.14255/2308-9628/15.111/3Keywords:
adaptive traits, leaf, eco-morphological features, species of Campanula, climatic factors.Abstract
The functional features of leaf ecophysiology and ecomorphology of native and introduced of Campanula species in culture in the Ukraine steppe for the detection of their adaptive traits were studied. The study was performed with the use of modern methods, comparison parameters of leaf species groups conducted using test ANOVA. The influence of climatic factors of natural habitat of species on the functional ecomorphology of leaf and successful their introduction was revealed. Species of Campanula from warmer habitats are characterized greater the leaf width of both formations and the petiole length of rosette leaf. Species differ more in weight of rosette leaves from more humid regions, cauline leaf – from warmer regions with high evaporation. It was found that species from drier warmer regions with high evaporation of rainfall have low specific leaf area (SLA) and high values of m1/m of cauline leaf. The successful introduction of Campanula species in the Ukraine steppe increased in plants from arid habitats with high variation of evaporation, difference of precipitation and evaporation, duration of the period with temperatures above 10°C. Thus confirming the importance of eco-biological features of species in their adaptation to new environmental conditions. Compared with resistant species (group V) petrophytes of midland and subalpine zones (II), species of forests and meadows (III) and forests species (IV) have a smaller petiole diameter rosette leaves (dp), hence smaller hydraulic conductivity of leaf petiole, but in the conditions of introduction petrophytes accumulate despite this, more water through transpiration regulation, forest species – less. Petrophytes of midland and subalpine zones and species of forests and meadows are more specific leaf area (SLA) of cauline leaf, forests species – higher SLA of different formations. Species of these groups are adapted to arid conditions due to the high photosynthetic energy use efficiency (PEUE), water use efficiency (WUE) as their low. Species of forests and meadows compared with alpine and forest species accumulate large amounts of water in the rosette leaves, however, compared with the first to have lower efficiency of its use, as compared to the second more. Alpine species compared with petrophytes of midland and subalpine zones and species of forests and meadows characterized by high the maximum photosynthesis (Amax) and photosynthetic energy use efficiency (PEUE) cauline leaves; compared with the first have a greater hydraulic conductivity of leaf petiole and adapted to the new conditions of changes in epidermalstomatal complex of rosette leaves, which increases water use efficiency (WUE) in the spring.
References
AHROKLIMATICHESKII ATLAS MIRA (1972). M., L.: Hidrometeoizdat. 115 p. [АГРОКЛИМАТИЧЕСКИЙ АТЛАС МИРА (1972). М., Л.: Гидрометеоиздат. 115 с.]
ALCITEPE E.M., YILDIZ K. (2010). Taxonomy of Campanula tomentosa Lam. and C. vardariana Bocquet from Turkey. Turk J. Bot., (34): 191-200.
BRODRIBB T.J., JORDAN G.J., CARPENTER R.J. (2013).Unified changes in cell size permit coordinated leaf evolution. New Phytologist, (199): 559-570.
ECOFLORA Ukrainy (2000). Kyiv: Fitosotsiotsentr. 1: 284 p. [ЕКОФЛОРА України. (2000). Київ: Фітосоціоцентр. 1: 284 с.]
FRANKS P.J. BEERLING (2009). Maximum leaf conductance driven by CO2 effects on stomatal size and density over geologic time. Proceedings of the National Academy of Sciences, USA. (106): 10343-10347.
GALSTON A.W., DAVIS P.J., SATTER R.L. (1980). The Life of the Green Plant. 3rd ed. Prentice-Hall, Englewood Cliffs, N.J.: 552 p.
GOSTIN I.N. (2012). Analele Stiintifice ale Universitatii Al. I. Cuza Lase S. Biologil vegetala, 58: (2): 47-50.
GUPTA B. (1961). Correlation of tissues in leaves II. Absolute stomatal numbers. Annals of Botany, (25): 71-77.
GYORGY E. (2009). Anatomic аdaptive strategies of some Cormophytes with individuals growing in light and shaden conditions. Not. Bot. Hort. Agrоbot. Cluj-Napoca, 37: (2): 33-39.
HUI F., GUIXIANG Y., TE C., LEYI N., MENG ZH., SHENGRUI W. (2012). An alternative mechanism for shade adaptation: implication of allometric responses of three submersed macrophytes to water depth. Ecol. Res., (27): 1087-1094.
KROKHMAL I. (2013). Functional anatomy of leaf Campanula alliariifolia Willd. Not. Bot. Horti Agrobot., 41: (2): 388-395.
KROKHMAL I.I. (2014). Chernomors’k. bot. z., 10 (2): 167-178. [КРОХМАЛЬ И.И. (2014). Анатомо-физиологические особенности листа Campanula glomerata L. Черноморск. бот. ж., 10 (2): 167-178]
LAMMERS T.G. (2007). World checklist and bibliography of Campanulaceae. The Board of Trustees of the Royal Botanic Gardens. Kew: 675 p.
NETSVETOV M.V. (2012). Influence of wind onto the structure and biomechanics of leaves Corylus colurna (Betulaceae). Bot. magazine, 97: (2): 160-173.
NIKLAS K.I. (1994). Plant allometry: the scaling of form and process. University of Chicago Press, Chicago.
NIKOLAEVSKAIA E.V. (1990). Vest. LGU, 3, 4 (24): 33-34. [НИКОЛАЕВСКАЯ Е.В. (1990). Изменчивость морфолого-анатомических признаков строения листа разных экотипов Trifolium repens L. в связи с вертикальной зональностью. Вест. ЛГУ, 3, 4 (24): 33-34]
OSUNKOYA O.O., BOYNE R., SCHARASCHKIN T. (2014). Coordination and plasticity in leaf anatomical traits of invasive and native vine species. Am. J. Bot., 101 (9): 1423-1436.
POORTER H., REMKES C. (1990). Leaf area ratio and net assimilation rate of 24 wild species differing in relative growth rate. Oecologia, (83): 553-559.
ROSADO B.H.P., HOLDER C.D. (2013). The significance of leaf water repellency in ecohydrological research: A review. Ecohydrology, (6): 150-161.
ROY B.A., STANTON M.L., EPPLEY S.M. (1999). Effects of environmental stress on leaf hair density and consequences for selection. Journal of Evolutionary Biology, (12): 1089-103.
SACK L., COWAN P.D., JAIKUMAR N., HOLBROOK N.M. (2003). The ‘hydrology’ of leaves: Co-ordination of structure and function in temperate woody species. Plant, Cell & Environment, (26): 1343-1356.
SCHEEPENS J.F., FREY E.S., STOCKLIN J. (2010). Genotypic and environmental variation in specific leaf area in a widespread Alpine plant after transplantation to different altitudes. Oecologia, (164): 141-150.
SCHMIDT R. (2014). Leaf structures affect predatory mites (Acari: Phytoseiidae) and biological control: A review. Experimental & Applied Acarology, (62): 1-17.
SHIPLEY B. (2002). Trade-offs between net assimilation rate and specific leaf area in determining relative growth rate: relationship with daily irradiance. Functional Ecology, 16: (5): 682-689.
SHIPLEY B. (2006). Net assimilation rate, specific leaf area and leaf mass ratio: which is most closely correlated with relative growth rate? A meta-analysis. Functional Ecology, 20: (4): 565-574.
SHIPLEY B., VILE D., GAMIER E., WRIGHT I.J., POORTER H. (2005). Functional linkages between leaf traits and net photosynthetic rate: reconciling empirical and mechanistic models. Functional Ecology, 19: (4): 602-615.
TSIALTAS J.T., KASSIOUMI M., VERESOGLOU D.S. (2002). Leaf Construction Cost of the Most Abundant Species in an Upland Grassland Area of Northern Greece. Russian Journal of Plant Physiology, 49: (3): 360-363.
VENDRAMINI F., DIAZ S., GURVICH D.E., WILSON P.J., THOMPSON K., HODGSON J.G. (2002). Leaf traits as indicators of resource-use strategy in floras with succulent species. New Phytologist, 154: (1): 147-157.
VIKTOROV V.P. (2005). Kolokolchiki (rod Campanula L.) Rossii i sopredelnykh stran. M. 320 p. [ВИКТОРОВ В.П. (2005). Колокольчики (род Campanula L.) России и сопредельных стран. М.: 320 с.]
WRIGHT I.J., REICH P.B., WESTOBY M., ACKERLY D.D., BARUSH Z., BONGERS F., CAVENDER-BARES J. et al. (2004). The worldwide leaf economics spectrum. Nature, (428): 821-827.
ZHONGQIANG L., DAN Y. (2009). Factors affecting leaf morphology: a case study of Ranunculus natans C.A. Mey. (Ranunculaceae) in the arid zone of northwest China. Ecol. Res., (24): 1323-1333.