A Comparative Study of the Leaf Anatomy of the Grasses Andropogon ischaetnum and Chrysopogon gryllus

Summary The leaf anatomy of the grasses Andropogon ischaemum and Chrysopogon gryllus was studied at the level of light and electron microscopy. These species are dominating the foot-hill grassland of Northern Greece. The volume of the intercellular airspace system of their leaves was estimated as well. The observations show that both plants have a xeromorphic appearance and belong to the C4 photosynthetic species, because they bear all the characteristics of the Kranz syndrome. The leaves of A. ischaemum have a water storing parenchyma at the top side of the midrip which is absent in C. gryllus. The bundle sheath cell chloroplasts of A. ischaemum bear a great quantity of starch and entirely lack grana, while the corresponding chloroplasts of C. gryllus bear rudimentary grana, but their starch content is far smaller. The cells of the assimilative mesophyll are arranged around the vascular bundles. This arrangement in A. ischaemum is more regular, the cells are elongated and with relatively small intercellular spaces; on the contrary, in C. gryllus, the intersections of these cells are almost circular, resulting in wider intercellular spaces. The chloroplasts of the mesophyll cells in A. ischaemum have peripheral reticulum and better developed grana than in C. gryllus. All these differences indicate that A. ischaemum is better adapted to withstand adverse environmental conditions than G. gryllus.

[1]  G. Byott LEAF AIR SPACE SYSTEMS IN C3 AND C4 SPECIES , 1976 .

[2]  W. Laetsch The C4 Syndrome: A Structural Analysis , 1974 .

[3]  W. Brown,et al.  Grass leaf ultrastructural variations , 1973 .

[4]  Bruce N. Smith,et al.  THE KRANZ SYNDROME IN THE GRAMINEAE AS INDICATED BY CARBON ISOTOPIC RATIOS , 1973 .

[5]  Clanton C. Black,et al.  Photosynthetic Carbon Fixation in Relation to Net CO2 Uptake , 1973 .

[6]  S. E. Frederick,et al.  Ultrastructure and distribution of microbodies in leaves of grasses with and without CO2-photorespiration , 1971, Planta.

[7]  J. Berry,et al.  Some methods for studying the photosynthetic taxonomy of the angiosperms. , 1970 .

[8]  W. Laetsch CHLOROPLAST SPECIALIZATION IN DICOTYLEDONS POSSESSING THE C4‐DICARBOXYLIC ACID PATHWAY OF PHOTOSYNTHETIC CO2 FIXATION , 1968 .

[9]  E. B. Tregunna,et al.  Carbon dioxide compensation—its relation to photosynthetic carboxylation reactions, systematics of the Gramineae, and leaf anatomy , 1968 .

[10]  M. D. Hatch,et al.  Photosynthesis by sugar-cane leaves. A new carboxylation reaction and the pathway of sugar formation. , 1966, The Biochemical journal.

[11]  T. A. Pedersen,et al.  PHOTOSYNTHESIS OF CARBON COMPOUNDS , 1966 .

[12]  E. Reynolds THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPY , 1963, The Journal of cell biology.

[13]  R. H. Brown,et al.  Distribution of the Post‐illumination CO2 Burst Among Grasses1 , 1972 .

[14]  D. Carr,et al.  A suberized layer in the cell walls of the bundle sheath of grasses. , 1970 .

[15]  A. Spurr A low-viscosity epoxy resin embedding medium for electron microscopy. , 1969, Journal of ultrastructure research.

[16]  M. Karnovsky,et al.  A formaldehyde-glutaraldehyde fixative of high osmolality for use in electron-microscopy , 1965 .