Seasonal Dimorphism in the Mediterranean Cistus incanus L. subsp. incanus

Abstract Mediterranean perennial species are described as being sclerophyllous, or summer deciduous, or seasonally dimorphic. Field observation in the coastal maquis of Castelvolturno Nature Reserve, southern Italy, showed that Cistus incanus L. subsp. incanus is a seasonally dimorphic species as it develops brachyblasts with small leaves in summer, and dolichoblasts with large leaves in winter. Field biometric data confirmed that winter shoots were 14-times longer than those developed in summer and had many more leaves. The area of single winter leaves was five-times that of summer leaves. Anatomical leaf structure also changed with the season: winter leaves were flat while summer leaves had a crimped lamina which was partially rolled to form crypts in the lower surface. Leaves were covered by considerably more trichomes in summer than in winter. Stomata were uniformly distributed along the lower epidermis of winter leaves but were only present in the crypts of summer leaves. In summer leaves, a palisade layer was often found on both sides of the lamina, the mesophyll cells were generally smaller and the intercellular spaces were reduced. Winter leaves had a dorsiventral structure and larger intercellular spaces. Seasonal dimorphism is generally reported to be an adaptation to summer drought. However, the morphology and anatomy of C. incanus L. subsp. incanus showed that the subspecies has not only developed a strategy to survive summer drought, but has evolved two different habits, one more xerophytic than the other, to optimize adaptation to the seasonal climatic changes occurring in Mediterranean environments.

[1]  C. Werner,et al.  Two different strategies of Mediterranean macchia plants to avoid photoinhibitory damage by excessive radiation levels during summer drought , 1999 .

[2]  Y. Manetas,et al.  The effects of seasons, exposure, enhanced UV-B radiation, and water stress on leaf epicuticular and internal UV-B absorbing capacity of Cistus creticus: a Mediterranean field study , 1997 .

[3]  A. Kyparissis,et al.  Leaf demography and photosynthesis as affected by the environment in the drought semi-deciduous Mediterranean shrub Phlomis fruticosa L. , 1997 .

[4]  Jie He,et al.  ‘Photoinhibition’ of Heliconia under natural tropical conditions: the importance of leaf orientation for light interception and leaf temperature , 1996 .

[5]  J. Curtis,et al.  Leaf Anatomy, Emphasizing Unusual 'Concertina' Mesophyll Cells, of Two East African Legumes (Caesalpinieae, Caesalpinioideae, Leguminosae) , 1996 .

[6]  Shlomo Nir,et al.  NATO ASI Series , 1995 .

[7]  A. Kyparissis,et al.  Autumn revival of summer leaves in the seasonal dimorphic, drought semi-deciduous Mediterranean shrub Phlomis fructicosa L. , 1993 .

[8]  Y. Manetas,et al.  Seasonal leaf dimorphism in a semi-deciduous Mediterranean shrub: ecophysiological comparisons between winter and summer leaves , 1993 .

[9]  G. Orshan,et al.  Plant Pheno-Morphological Studies in Mediterranean-Type Ecosystems. , 1990 .

[10]  N. Christodoulakis,et al.  Leaf Structural Peculiarities in Sarcopoterium spinosum, a Seasonally Dimorphic Subshrub , 1990 .

[11]  N. Christodoulakis An Anatomical Study of Seasonal Dimorphism in the Leaves of Phlomis fruticosa , 1989 .

[12]  R. Specht The effect of summer drought on vegetation structure in the mediterranean climate region of Australia , 1987 .

[13]  J. Ehleringer,et al.  Leaf absorptance and leaf angle: mechanisms for stress avoidance , 1987 .

[14]  W. Oechel,et al.  Plant Response to Stress , 1987, NATO ASI Series.

[15]  D. Vokou,et al.  Structural and physiological features of woody plants in phryganic ecosystems related to adaptive mechanisms , 1982 .

[16]  F. di Castri,et al.  Ecosystems of the world [Vol.] 11. Mediterranean-type shrublands. , 1981 .

[17]  N. Margaris Physiological and biochemical observations in seasonal dimorphic leaves of Sarcopoterium spinosum and Phlomis fruticosa , 1977 .

[18]  P. Miller Leaf temperatures, leaf orientation and energy exchange in Quaking Aspen (Populus tremuloides) and Gambell's Oak (Quercus gambellii [gambelii]) in central Colorado , 1967 .

[19]  A. Rutter,et al.  The water relations of plants , 1963 .

[20]  N. Maximov The Physiological Significance of the Xeromorphic Structure of Plants , 1931 .

[21]  W. T. Penfound,et al.  Ecological Anatomy of Siomne Deciduous Forest Plants , 1928 .

[22]  R. H. Yapp,et al.  Spiraea Ulmaria, L., and its Bearing on the Problem of Xeromorphy in Marsh Plants , 1912 .

[23]  K. M. Wiegand The Relation of Hairy and Cutinized Coverings to Transpiration , 1910, Botanical Gazette.