Epidermal Structure and Stomatal Development in Some Malvaceae and Bombacaceae

Epidermal structure and development of stomata in 15 speciesof the Malvaceae and two of Bombacaceae are described. The cellsof the epidermis are polygonal, isodiametric, or elongated withthick, straight, arched, or sinuous anticlinal walls and containchloroplasts and abundant druses of calcium oxalate. Cuticularstriations radiating from the guard cells or hair bases arenoticed. Six types of glandular and non-glandular trichomesare seen. The mature stomata are anomocytic, anisocytic, andparacytic in the members investigated of both the families.The ontogeny of anisocytic and paracytic stomata is syndetochelicor mesogenous, while that of anomocytic is haplocheilic or perigenous.An abnormal stoma with a single guard cell is also observed.An increase in number of subsidiary cells in anisocytic stomatais due to the division of the subsidiary cells.     

Epidermal studies in some Indian cultivars of Bougainvilleas

Epidermal studies in fifteen Indian cultivars of Bougainvilleas are described. The epidermal cells are polygonal isodiametric, or elongated with thick straight arched or slightly sinuous walls. Parallel culticular striations are radiating from guard cells. The mature stomata are anomocytic, paracytic and with a single subsidiary cell. The abnormal types noticed are: single guard cells with or without pores, arrested development, variously oriented contiguous stomata, cytoplasmic connections between nearby stomata and epidermal or subsidiary cells, and persistent stomatal cells. The development of anomocytic stomata is perigenous while that of the other types is mesogenous. Fifteen cultivars of Bougainvilleas are separated on the basis of bract colour, stomatal frequency and index per unit area.     

Variation in the structure and development of foliar stomata in the Euphorbiaceae

The structure and ontogeny of foliar stomata were studied in 50 species of 28 genera belonging to 17 tribes of the family Euphorbiaceae. The epidermal cells are either polygonal, trapezoidal, or variously elongated in different directions and diffusely arranged. The epidermal anticlinal walls are either straight, arched or sinuous. The architecture of cuticular striations varies with species. The mature stomata are paracytic (most common), anisocytic, anomocytic and diacytic. Occasionally a stoma may be tetracytic, cyclocytic or with a single subsidiary cell. The ontogeny of paracytic stomata is mesogenous dolabrate or trilabrate, mesoperigenous dolabrate; that of diacytic stomata is mesogenous dolabrate, whereas that of anisocytic stomata is mesogenous trilabrate; rarely an anisocytic stoma may be mesoperigenous. Hemiparacytic stomata are mesoperigenous unilabrate; tetracytic stomata are mesoperigenous dolabrate and anomocytic stomata perigenous. Abnormalities encountered include four types of contiguous stomata, stomata with a single or both guard cells aborted and persistent stomatal initials. Cytoplasmic connections between the guard cells of two adjacent stomata or the guard cell of a stoma and an adjacent epidermal/subsidiary cell, or both types occurring in a species, were noticed. The stomatal development, distribution, diversity and basic stomatal type with reference to systematics are discussed.     

Effects of external potassium supply on stomatal closure induced by abscisic acid

Abstract Epidermal strips of Commelina communis with ‘isolated’ stomata were incubated on Trizma-maleate buffer containing 0-500 mM KCL, with or without 10^?4 M ABA, for 2.5 h. The resulting stomatal apertures indicate that there is no absolute requirement for live epidermal and subsidiary cells for ABA-mediated closure. This implies that ABA has a direct effect on influx or efflux of K⁺ into or out of the guard cells rather than on uptake of K⁺ by the subsidiary cells. The possible in vivo role of subsidiary cells in stomatal closure is discussed.     

Action of growth regulators on the cotyledonary stomata ofCucumis sativus L.: Structure and ontogeny

Anomocytic stomata and stomata with single subsidiary cells are commonly observed Sometimes a stoma appears anisocytic. Double cytoplasmic connections between nearby stomata and division of guard cells with persistent or degenerating nuclei are seen in GA. One or more divisions of guard cells, displaced guard cells and single guard cells with or without pore are noticed in SUC. Formation of single guard cells is a common feature in TIBA. Paracytic stomata, one and a half stomata and persistent stomatal initials are seen in SUL. COUM seems to be not inhibitory inCucumis sativus. In COL stomata with unequal guard cells, unequal stomatal cells with thickening in between but without intervening pore, stoma with double pores, persistent stomatal initials which may be solitary or in groups with varying shapes and with one or two nuclei of different shapes are noticed. The growth regulators affect the frequency of stomata, epidermal cells; stomatal index; size of guard and epidermal cells.     

On Cordaites neimengensis sp. nov from Lower Permian of Zhungeerqi,Inner Mongolia, China

The leaf cuticle of Cordaites neimengensis sp. nov was studied by light and scanning electron microscopy. The specimens were collected from kower Permian of Zhungeerqi, Inner Mongolia (Neimenggu), China. Comparing with other species of Cordaites, it was a new species of the genus, based on the structure of its epidermis. Cordaites neimengensis sp. nov (Pis. Ⅰ to Ⅲ; Text-fig.l,B) The specimen comprises two incomplete leaves over 16 cm in length. One is about 1.4 cm wide at the lower part and 0.3 cm wide at the upper part, with nearly 29 veins per cm and 3 to 5 interstitials. The width of the other leaf is about 7.5 cm at the lower part and 8.2 cm at the upper part with 25 veins per cm and 3 to 5 interstitials. Epidermis amphistomatic. Epidermal cells of upper cuticle aligned in longitudinal rows, nearly rectangular in shape, about 33.6 to 86.4 pm x 10.2 to 28. 8 pm in size. Stomatal apparatus consisting of 2 sunken guard cells surrounded by 2 lateral and 2 polar subsidiary cells. Stomata haplocheillic, about 56.2 pm x 45.5 pm in size, usually arranged in short chains, with one polar subsidiary cell (usually 23.1 to 25.4 pm wide, 34.1 to 39.2 pm long in size) shared with 2 consecutive stomata. The polar subsidiary cells round, oblong or rhomboid in shape. The guard cells reniform or bean-shaped, usually 9.7 to 11.6 pm wide, 23.4 to 29.1 pm long in size. Density and index of stomata about 18/mm2 and 3.2%, respectively. Epidermal cells of lower cuticle also nearly rectangular in shape, about 62.4 to 144 pm × 9.6 to 16.8 pm in size. Stomata on the lower cuticle, haplocheillic, 40.8 pm wide and 48 pm long in size, with a pair of sunken guard cells, which is bean-shaped and surrounded by 2 lateral and polar subsidiary cells. Stomata arranging in parallel bands, typically one, sometimes two. As for the latter, a single row of lateral subsidiary cells (9.2 to 14.4 pm wide, 33.6 to 62.4 pm long in size) is shared with 2 parallel rows of stomata and occasionally also in bands with two rows side by side. In view outside, small papillae on the outer periclinal wall as well as the lateral subsidiary cells. In view inside, some folds along the anticlinal wall but flat about the periclinal wall. Nonstomatic bands usually with 1 to 10 rectangular cell rows. Density and index of the stomata about 209/mm2 and 27.2 %, respectively. 1401%-type: 9342; locality: Heidaigou of Zhungeerqi; Inner Mongolia, North China; Age: Lower Pennian (Shanxi Formation).     

利用激光扫描共聚焦显微镜研究拟南芥气孔发生与发育

通过激光扫描共聚焦显微镜,利用不同种类(波长)的激光研究拟南芥叶片气孔发生与发育。结果表明,利用紫外激光(351nm)扫描可以清楚观察到拟南芥表皮各种细胞及其发生发育的形态变化,包括表皮毛细胞、副卫细胞、保卫细胞、铺垫表皮细胞等。气孔发生过程中,首先原表皮细胞不对称分裂产生拟分生组织和副卫细胞,接着分化出保卫细胞母细胞,进一步发育形成保卫细胞,最终形成气孔器。气孔分化完成后,保卫细胞在紫外激光下不产生荧光,但利用蓝光激发(488nm)辅助荧光素染色,可清晰地看到保卫细胞。结果表明,激光扫描共聚焦显微镜在拟南芥叶表皮细胞形态研究上有独特的功能。     

Direct Measurements of Turgor Pressure Potentials of Guard Cells, I.

Measurements were made of pressures applied in subsidiary andguard cells which caused closure and opening of stomatal pores.These pressures were lower than would be expected from plasmolyticallydetermined osmotic potentials of guard cell saps. The pressuresneeded in guard cells to open almost closed stomata were practicallythe same as those required to close open stomata when appliedin adjacent subsidiary cells. Completely closed stomata couldnot be opened by this technique. The implications for the understandingof the mechanism of guard cell deformation, the Spannungsphase,and the pressure potentials of guard cells are discussed.     

Epidermal Structure and Stomatal Ontogeny in Some Polygonales and Centrospermae

The epidermal structure and ontogeny of stomata in 19 speciesof Centrospermae and two of Polygonales are described. The cellsof the epidermis are polygonal, isodiametric, or elongated invarious directions and arranged irregularly. The anticlinalepidermal walls are thick, sinuous, straight, or arched. Eleventypes of glandular and eglandular trichomes have been observed.Six types of stomata: anomocytic, paracytic, stomata with asingle subsidiary cell, diacytic, anisocytic, and transitionalbetween diacytic and paracytic, have been noticed in the speciesinvestigated. The ontogeny of anomocytic stomata is haplocheilicor perigenous, while that of the other five types is syndetocheilicor mesogenous. Abnormal stomata with a single guard cell, unequalguard cells, aborted guard cells, and arrested development arecommon. Groups of stomata are also frequent but contiguous stomataare rather rare.     

Stomatal Features in the Leaf of Aganosma dichotoma (Roth) K. Schum

Paracytic and anisocytic types of mature stomata are found inthe leaf of Aganosma dichotoma. Stomata with one guard cell,stomata with degenerated guard cells, and contiguous stomataare common. Stomata with arrested pore development are alsofound in certain cases. A single guard cell without any porehas not been designated as a stoma with one guard cell in thepresent investigation. Ontogeny of contiguous stomata have beentraced. Subsidiary cells are, morphologically, just like theircontiguous guard cells. Subsidiary cells may retain their shapeand contents even when their contiguous stoma becomes mature,or may change their shape and lose their contents. They mayor may not divide. Subsidiary cells form a whorl of more thantwo subsidiary cells around a stoma by their divisions. Degenerationof guard cell(s)— their contents and nuclei—havebeen traced. In certain cases guard cells divide forming morethan two guard cells associated to a single pore. Cytoplasmicconnections are found between two guard cells of nearby stomata,and between a guard cell and an epidermal cell. Near the wound,the epidermal cells over the veins become meristermatic givingrise to new epidermal cells but no meristemoid.     

Stomatal development and patterning in Arabidopsis leaves

The functional unit for gas exchange between plants and the atmosphere is the stomatal complex, an epidermal structure composed of two guard cells, which delimit a stomatal pore, and their subsidiary cells. In the present work, we define the basic structural unit formed in Arabidopsis thaliana during leaf development, the anisocytic stomatal complex. We perform a cell lineage analysis by transposon excision founding that at least a small percentage of stomatal complexes are unequivocally non-clonal. We also describe the three-dimensional pattern of stomata in the Arabidopsis leaf. In the epidermal plane, subsidiary cells of most stomatal complexes contact the subsidiary cells of immediately adjacent complexes. This minimal distance between stomatal complexes allows each stoma to be circled by a full complement of subsidiary cells, with which guard cells can exchange water and ions in order to open or to close the pore. In the radial plane, stomata (and their precursors, the meristemoids) are located at the junctions of several mesophyll cells. This meristemoid patterning may be a consequence of signals that operate along the radial axis of the leaf, which establish meristemoid differentiation precisely at these places. Since stomatal development is basipetal, these radially propagated signals may be transmitted in the axial direction, thus guiding stomatal development through the basal end of the leaf.     

Morphogenetic effects of various growth substances on the cotyledonary stomata of brinjal and tomato

The effect of different growth substances on the development of normal and abnormal stomata are presented. Anomocytic, paracytic, anisocytic and stoma with a single subsidiary cell are observed. Abnormal developments like persistent stomatal cells, degeneration of guard cells, unusual thickening, unequal guard cells, single guard cells and size and shape of the pore are noticed in various growth substances. The growth substances also affect the stomatal frequency, stomatal index, epidermal frequency and size of guard and epidermal cells in both the plants. The highest meristematic activity is found in MOR 100 ppm in brinjal and in GA 25 ppm in tomato. The largest size of stomata is found in COL 25 ppm in brinjal and in MH 50 ppm in tomato. The same growth substance responds differently in the two plants.     

ACTION OF FUSICOCCIN ON THE POTASSIUM BALANCE OF GUARD CELLS OF PHASEOLUS VULGARIS

Fusicoccin induces stomatal opening in both the light and dark. The stomatal aperture and K content of guard cells was measured to determine whether the action of fusicoccin in inducing stomatal opening is directly related to the uptake of K by the guard cells. Both detached and attached epidermis was treated with fusicoccin and the K content was determined by staining with cobalt sodium nitrite or by electron probe microanalysis. The K content of guard cells in detached epidermal strips floated on 10 μm fusicoccin in 10 mm KCl and aqueous CH₃OH (0.02%, v/v) increased in the light and dark as the stomata opened. After exposure to fusicoccin for 6 hr in the light, however, the stomata were closed and no K could be detected in the guard cells. The K content of guard cells of attached epidermis painted with fusicoccin also increased as the stomata opened, but the concentration of K in the subsidiary cells was not significantly altered by fusicoccin-stimulated opening. Moreover, painting with fusicoccin did not significantly change the Ca and P content of the guard or subsidiary cells. Stomata of epidermal strips, opened to their maximum width by fusicoccin, showed only a small and temporary closure when transferred to a solution of 10 μm abscisic acid. The use of metabolic inhibitors suggested that energy for the uptake of the K may be provided by both photophosphorylation and oxidative phosphorylation.     

Structure,ontogeny and taxonomic significance of trichomes and stomata in some Capparidaceae

The present work embodies epidermal structure, structure and ontogeny of stomata in five genera embracing sixteen species of the Capparidaceae namely Cleome (8 species) Capparis (5 species), Cadaba (1 species), Crataeva (1 species) and Maerua (1 species). The epidermal cells are polygonal, isodiametric or elongated arranged irregularly, with evenly or unevenly thickened, sinuous, straight or arched anticlinal walls. Two main types of trichomes: glandular (four types) and eglandular (five types) are noticed. The stomatal types include cyclocytic, triacytic, staurocytic, tetracytic, anomocytic, anisocytic, paracytic and with a single subsidiary cell. The ontogeny of stomata with a single subsidiary cell is perigenous or mesoperigenous, of paracytic mesoperigenous or mesogenous, of anisocytic is mesoperigenous or mesogenous, while that of the other types is perigenous. Abnormalities observed are: single guard cell; aborted guard cells; complete or incomplete division of guard cells; contiguous stomata; giant stomata and cytoplasmic connections. The present observations do not support the separation of Cleomaceae from the Capparidaceae.     

The genus Eugenia L. (Myrtaceae) in southern Africa: the structure and taxonomic value of stomata

The mature stomatal morphology of 11 southern African species of Eugenia , and also of E. uniflora L. (naturalized) and E. incerta Diimmer (a garden plant of unknown origin) has been studied by light and scanning electron microscopy.
Leaves of all the species are hypostomatic and water-stomata are occasionally present. Two different stomatal types, X and Y, differing mainly in their cuticular ornamentation, were found in the southern African species. The grouping of species based on stomatal characters supports a previous grouping of species on the basis of periderm and seed characters.
Conspicuous lipid bodies, usually present in the subsidiary cells, are limited to the southern African species. Although the subsidiary cells do not differ in shape and size from adjacent epidermal cells, their contents often have a higher tannin content than ordinary epidermal cells. The variable patterns of arrangement of the three to five subsidiary cells makes it difficult to identify the stomata with existing classifications based on mature topography. Thus, a new term 'anomostaurocytic' is proposed for the stomatal type found in the southern African species.
Stomata of E. uniflora and E. incerta are paracytic and anomocytic respectively, and the cuticular ornamentation of their stomata differs from those of the southern African species. The view that E. incerta is not closely related to the southern African species is supported by differences in its cuticular ornamentation, lack of lipid bodies in the subsidiary cells, anomocytic stomata and prominent T-pieces at the guard cell poles.     

Structure and Development of Stomata in Some Labiatae

The structure and ontogeny of stomata have been studied in 33species of the Labiatae. The mature stomata are diacytic, transitionalbetween paracytic and diacytic, and anomocytic. The anomocyticstomata are haplocheilic or perigenous. The diacytic and thetransitional type of stomata are syndetocheilic or mesogenousas the two subsidiary cells and a pair of guard cells arisefrom the same meristemoid. The diacytic and the transitionalstomata are formed through three successive mitotic divisions.Abnormal stomata with single guard cells, arrested developments,and contiguous stomata have been observed. Contiguous stomataare formed either from two adjacently placed meristemoids orare the result of spatial readjustment during maturation ofthe leaf.     

The Stomata of Gnetum

In both Gnetum gnemon and G. ula the atomatal development inthe collars and axes of the male and female cones and the outertwo envelopes of the ovule is of the haplocheilic type. In theleaf some stomata do show parallel subsidiary cells, but theyarise from the surrounding epidermal cells and do not seem tohave a common origin with the guard cells. This conflicts withearlier accounts and is of interest in relation to the typesof stomata met with in other gymnosperms, living and fossil.     

ABNORMAL GUARD CELL DEVELOPMENT IN AN OLIVE NECROTIC MUTANT OF MAIZE

A study of a mutant variety of Zea mays (ON8147) revealed that the mutant plants, in contrast with normal maize plants, do not exhibit a light-induced increase in the rate of transpiration, and that the ontogeny of the stomatal complex is abnormal. In later stages of differentiation, the guard cells of mutant plants deteriorate, leaving the mature stomata with only the two subsidiary cells. The subsidiary cells in stomata of mutant leaves are similar to those of normal leaves with respect to their capacity to accumulate K⁺ in the dark, but they do not lose K⁺ in the light, as do subsidiary cells of stomata of nonmutant plants. It is suggested that impairment of guard cell function causes death of the mutant plant seedlings primarily by restricting CO₂ entry into the leaf.     

Epidermal Structure and Ontogeny of Stomata in some Verbenaceae

The present paper deals with epidermal structure and developmentof stomata in 14 species of Verbenaceae. The epidermal cellsare either polygonal, isodia-metric, or elongated in variousdirections, and irregularly arranged. The anticlinal walls arethick, mostly sinuous, occasionally arched or straight. Thesurface of the cuticle shows parallel, rarely corrugated, striations.Some 12 types of eglandular and glandular trichomes, and foliarnectaries are noticed. The mature stomata are diacytic, anisocytic,paracytic, with a single subsidiary cell, anomocytic and perigenous.The development of anomocytic stomata is perigenous, while thatof others is mesogenous or syndetocheilic type. Abnormalitiesnoticed here include contiguous stomata, stomata with a singleguard cell, and aborted guard cells.     

Structure and Ontogeny of Stomata in Some Polemoniales

The ontogeny and structure of stomata in 22 genera and 51 speciesof the Polemoniales are described. Five main types of stomatanoticed are: anisocytic, anomocytic, diacytic, paracytic, andstomata with a single subsidiary cell. Three modes of stomataldevelopment: syndetocheilic or mesogenous, haplocheilic or perigenous,and meso-perigenous or syndeto-haplocheilic are observed. Abnormalitiesseen are: stomata with single guard cells, arrested developmentand contiguous stomata variously oriented. Contiguous stomataresult from adjacently placed meristemoids or readjustment duringmaturation. Stomata with a single guard cell are formed as aresult of degeneration of one of the guard cells before or afterpore formation. The stomatal apparatus varies in different organsof a plant in form, number, orientation and arrangement of thesubsidiary and also the surrounding cells. Three lines leadingto Polemoniales, Boraginales, and Solanales are distinet.