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.     

Studies on the structural and developmental variation and distribution of stomata in the Rubiaceae

The structure and ontogeny of the stomata has been studied in 26 species of Rubiaceae, in relation to their organographic distribution. The stomata are mostly paracytic on the leaves, but vary on other parts, particularly on the floral disk, where they are exclusively anomocytic. The foliar stomata are mesogenous and paracytic, but may be either dolabrate or trilabrate in origin. The disk stomata are perigenous and are probably derived from the mesogenous paracytic ones by the loss of divisive potential of their meristemoid due to anthogenetic factors. They are regarded to be hydathodal in function. If the dendroid habit is regarded as primitive, in the family, trilabrate stomata were quite possibly derived from dolabrate ones, which are mostly associated with the dendroid habit. Evidence from stomatal ontogeny is shown to be taxonomically important in the Rubiaceae.     

Observations on the structure and ontogeny of stomata and trichomes on developing and mature pericarps ofCassia occidentalis L

Paracytic, anisocytic, anomocytic, transitional forms, tetracytic, cyclocytic stomata and partly and completely amphicyclic forms are found, often on the same surface, in nine combinations. The most frequent type is paracytic. A few morphological variations in the basic types and eight types of abnormalities in stomata are recorded. The stomatal ontogeny may be mesogenous, mesoperigenous or perigenous. Trichomes are multicellular glandular club-shaped and unicellular eglandular. The taxonomic significance of stomata is indicated.     

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.     

Observations on the cotyledonary and hypocotyledonary stomata and trichomes in some Caesalpiniaceae with a note on their taxonomic

The structure and ontogeny of stomata on cotyledons and hypocotyls and the trichomes on hypocotyl are accounted for in eighteen species of Caesalpiniaceae. Trichomes are eglandular, bi- rarely tri-celled, smooth walled or walls wavy with cuticular striations or tubercles. Anomocytic, haplocytic, paracytic, diacytic, transitional, tetracytic, tricytic and cyclocytic stomata occur in different combinations even on the same surface of the cotyledon. In all, there are fourteen combinations. Inspite of the diversity, the most frequent type is anomocytic in most of the species and paracytic in some species of Cassia and Delonix (abaxial) but rarely it is haplocytic or anisocytic. In hypocotyls it is anomocytic. Ontogenetically anomocytic, tetracytic and cyclocytic stomata are perigenous, whereas other types are mesogenous or mesoperigenous. There is an increase in the number of subsidiary cells by their division or the neighbouring perigenes assuming their shapes. About eight such types are described. A pair of stomata has a common subsidiary cell. Twelve types of guard cell and stomatal approximation abnormalities are described. A range in the number, size and shape of the nuclei in guard cell are recorded. Megastomata (giant stomata) are observed in Parkinsonia and Tamarindus. The taxonomic significance of the stomata is also discussed.     

Epidermal structure and development of stomata in vegetative and floral organs ofHybanthus enneaspermus (Linn.)F. Muell

The present paper deals with the epidermal structure and ontogeny of stomata in vegetative and floral organs ofHybanthus enneaspermus. The epidermal cells are either polygonal or elongated with straight, sinuous or arched thick anticlinal walls. The surface of the cuticle shows parallel striations radiating from the guard cells or hair bases. Unicellular and uniseriate bicellular trichomes with verrucose margins have been observed on all organs. The mature stomata are anisocytic, paracytic, anomocytic and transitional between anisocytic and paracytic. The ontogeny of anisocytic and paracytic stomata is syndetocheilic or mesogenous, anomocytic is haplocheilic or perigenous, while that of the transitional type is mesoperigenous. Four types of stomata have been observed on all the vegetative and floral organs and their ontogeny from organ to organ of this plant is constant. Stoma with a single guard cell is the result of disintegration of one of the guard cells before or after pore formation. Contiguous stomata are also occasionally noticed.     

Trichomes and stomata,and their taxonomic significance in theUrticales

Structure and ontogeny of stomata and trichomes have been studied in 23 species and 3 varieties of theUrticales. Stomata are anomocytic, more rarely paracytic; anisocytic and sometimes helicocytic and transitorial types are found inUrticaceae andDorstenia, rarely inArtocarpus. The ontogeny of anomocytic and actinocytic stomata is perigenous, of paracytic either mesogenous or perigenous, of anisocytic either mesogenous or mesoperigenous, and of helicocytic and transitional types mesogenous. Among trichomes eglandular unicellular (wide spread), bicellular or uniseriate filiform (Cannabis); glandular capitate with uni- or bicellular (Moraceae, Ulmaceae, Cannabaceae), uniseriate filiform (Ulmaceae) or multiseriate stalk (Cannabis); sunken glands (Artocarpus); uniseriate glandular with uniseriate stalk (Celtis), and stinging emergences (Urticaceae) have been observed. It is concluded that theUrticales represent a natural order with four families:Ulmaceae, Moraceae, Urticaceae andCannabaceae which are distinct but interrelated with each other.     

Observations on the effects of morphactin EMD 7301 and EMD 7311 on the number,size, morphology and ontogeny of cotyledonary stomata ofAbelmoschus esculentus moench

Stomata on the cotyledons of Morphactin EMD 7301 and EMD 7311 treated seedlings may be anisocytic, anomocytic, paracytic, diacytio, transitional forms and haplocytic. In spite of this diversity, the most frequent type is anisocytic on both surfaces. The stomatal ontogeny may bo perigenous, mesogenous and mesoperigenous. Morphactin EMD 7301 and EMD 7311 increase the size of cotyledons in all concentrations accompanied by an increase in the number of stomata on the adaxial surface in 100, 150, 250 ppm of EMD 7301. The effect of morphactin is promotive to the size of stomata in all concentrations, but it retards the stomatal density and number of epidermal cells. This may be due to an increase in the size of the epidermal cells. The substrates, however, have no effect on the morphology and ontogeny of the stomata; probably they are inherent chracters.     

Structure and Development of Stomata on the Vegetative and Floral Organs in Some Members of Caesalpiniaceae

The structure and development of stomata in 19 species of thefamily Caesalpiniaceae are described. The study is mostly confinedto the leaves, but observations have also been made on othervegetative and floral organs of some species Stomata may beparacytic, anisocytic, anomocytic, and with one subsidiary cell.Occasionally a stoma is diacytic, cyclocytic, or actinocytic.Different types occur individually or may be found side by sideeven on the same surface of an organ. The most prevalent typein all the genera is paracytic except in Caesalpima where itis anomocytic. The development of an anomocytic stoma is perigenous,but those with subsidiary cells are largely mesogenous; rarelyparacytic stomata are mesoperigenous. In spite of diversityof stomata, different types of stomata have similar patternsof development in different organs of the same plant. The presentinvestigation also indicates that the inconstancy of stomatain the family is due to (a) their diversity and (b) an increasein the number of subsidiary cells either by their division orby the neighbouring perigenes becoming subsidiary cell-like.     

A new stomatal type inChenopodiaceae

A new stomatal type—paracytic mesoperigenous—which has not been separated from the paracytic mesogenous type in previous studies of theChenopodiaceae, is described. The frequent occurrence of this previously unknown paracytic mesoperigenous type in this family is demonstrated. As a result a new phylogenetic pathway between anisocytic mesoperigenous and paracytic mesogenous types may be drawn.     

Development of Normal and Abnormal Stomata in some Araliaceae

The present investigation describes the ontogeny of normal andabnormal stomata for three species of the Araliaceae. The maturestomata are mostly anisocytic, occasionally paracytic, and rarelyanomocytic. Several aberrent patterns of stomatal developmenthave been noticed in anisocytic stomata and a few in paracyticones. The ontogeny of anisocytic and paracytic stomata conformsto the syndetocheilic or mesogenous type, while that of anomocyticis haplocheilic or perigenous.     

Structure,Delimitation,Nomenclature and Classification of Stomata

The paper reviews stomatal types observed in 500 species of angiosperms besides those described in the literature and deals with the problems of their structure, delimitation, nomenclature and classification. In view of the varied definitions available in the literature for subsidiaries, stomatal types and,the definition and delimitations being variously interpreted by different workers, a modified definition for the subsidiaries and stomata is presented. In accordance with the international code of nomenclature for plants, the names of the stomata widely in use are retained (rule of priority). They have been presently classified as pericytic, desmocytic, paracytic, diacytic, anisocytic, anisotricytic, isotricytic, tetracytic,staurocytic, anomocytic, cyclocytic and a good number of varieties under each type are presented. These stomatal types are recognised on the basis of their structure rather than its ontogenetic pathways.     

StomataStructure, Delimitation, Nomenclature and Classification of Stomata

The paper reviews stomatal types observed in 500 species of angiosperms besides thosedescribed in the literature and deals with the problems of their structure, delimitation, nomenclature andclassification. In view of the varied definitions available in the literature for subsidiaries, stomatal types and,the definition and delimitations being variously interpreted by different workers, a modified definition forthe subsidiaries and stomata is presented. In accordance with the international code of nomenclature forplants, the names of the stomata widely in use are retained (rule of priority). They have been presentlyclassified as pericytic, desmocytic, paracytic, diacytic, anisocytic, anisotricytic, isotricytic, tetracytic,staurocytic, anomocytic, cyclocytic and a good number of varieties under each type are presented. Thesestomatal types are recognised on the basis of their structure rather than its ontogenetic pathways.     

Structure, distribution and taxonomic importance of foliar stomata in some Indian Amaranthaceae

The structure, distribution and taxonomic importance of foliar stomata in 45 taxa belonging to 19 genera have been studied. In all, six stomatal types have been recognized viz., anomocytic, anisocytic, diacytic, paracytic, hemiparacytic and brachyparacytic. The majority of the taxa are amphistomatic whereas hypostomatic leaves are confined to only three taxa. Stomatal diversity is common but most of the taxa show either dominance or codominance. Stomatal distribution is helpful in distinguishing the three tribes of the Amaranthaceae. The tribe Celosieae shows exclusive presence of anomocytic and anisocytic stomata whereas Amarantheae and Gomphreneae show other stomatal types viz., paracytic and diacytic in addition to anomocytic and anisocytic stomata. Further, the latter two tribes are each distinguishable into two subtribes on the basis of stomata.     

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.     

Structure, Delimitation, Nomenclature and Classification of Stomata

The paper reviews stomatal types observed in 500 species of angiosperms besides those described in the literature and deals with the problems of their structure, delimitation, nomenclature and classification. In view of the varied definitions available in the literature for subsidiaries, stomatal types and, the definition and delimitations being variously interpreted by different workers, a modified definition for the subsidiaries and stomata is presented. In accordance with the international code of nomenclature for plants, the names of the stomata widely in use are retained (rule of priority). They have been presently classified as pericytic, desmocytic, paracytic, diacytic, anisocytic, anisotricytic, isotricytic, tetracytic, staurocytic, anomocytic, cyclocytic and a good number of varieties under each type are presented. These stomatal types are recognised on the basis of their structure rather than its ontogenetic pathways.     

Ontogeny of stomata in some Gentianaceae

The mature epidermis and development of stomata in some species of Gentianaceae, viz. Canscora deccusata, C.diffusa, Hoppea dichotoma, Enicostema littorale, Nymphoides cristatum and Gentiana pedicellata , are described. The stomatal development is shown to be trilabrate mesogenous in Canscora deccusata, C.diffusa, Enicostema littorale and Hoppea dichotoma , mesoperigenous in Gentiana and perigenous in Nymphoides. It is suggested that adoption of an aquatic habit by Nymphoides may have resulted in suppression of divisions in its perigenous stomata.     

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.     

Structure, distribution and taxonomic importance of stomata in some Indian Tephrosia Pers.(Fabaceae)

SUBBA RAO, J.V.& SHANMUKHA RAO, S. R.(1994).Structure, distribution and taxonomic importance of stomata in some Indian Tephrosia Pers.(Fabaceae).Structure, distribution and taxonomic importance of stomata in all the vegetative parts of 18 taxa of Indian Tephrosia including five species endemic to south India are described. The stomata are anisocytic, anomocytic or paracytic. In addition, brachyparacytic stomata have been recorded for the first time in this taxon. This is the first attempt to assess subgeneric treatment in the light of stomatal characteristics and it suggests certain realignments at the infrageneric level in Indian Tephrosia.     

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.