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.     

Stomatogenesis in the genus Portulaca L. (Portulacaceae)

The stomata in the six Indian species of Portulaca L. are paracytic and predominantly dicyclic, completely enclosed at their polar ends by the subsidiaries, and mesogenous dolabrate and basipetal in differentiation except in P. oleracea , where they are diffuse in origin. The subsidiaries of the outer cycle develop directly from the stomatal meristemoids. The leaves are amphistomatic except in P. quadrifida , where they are epistomatic. The stomata are mostly orientated at c. 90^o to the midrib of the leaf, but in P. oleracea they are irregularly orientated. The origin of the stomatal orientation appears to be genetically regulated rather than epigenetic. In Portulaca , as in some other angiosperms, the epidermal pattern of the costae is similar to that of the interstices, i.e. stomatiferous with nearly isodiametric cells. This is considered to be due to prevention by the thick chlorenchyma, characteristic of these plants, of the stomatal inhibitory stimuli originating in the vascular tissues from reaching the epidermis.     

Stomatogenesis in the genus Hibiscus L. (Malvaceae)

In Hibiscus , stomata are anisocytic, anomocytic, paracytic and tetracytic, the first type being the most frequent and occurring in all plant parts in the ten species studied, whereas the others are scarce and have a limited organographic distribution. The stem, petiole, pedicel, staminal tube, ovary and style are stomatiferous; the leaf-blade, stipule, bracteole and sepals are amphistomatic and petals hypostomatic in the species investigated.
The stomatal types are often homoplastic, the anisocytic being either mesogenous trilabrate or mesoperigenous dolabrate, the anomocytic, mesoperigenous dolabrate or mesogenous trilabrate, and the tetracytic, mesoperigenous dolabrate or mesoperigenous trilabrate. But the typical paracytic stomata (with the subsidiaries completely enclosing the poles) are constantly mesogenous dolabrate and therefore probably indicate mesogenous dolabrate development. Although several patterns of stomatogenesis are encountered in any specific organ, only one of them is found to be dominant. A new subcategory of stomatal ontogeny, mesoperigenous trilabrate, is proposed in Hibiscus. No significant stomatal variation involving reduction in the divisive capacity of the meristemoid has been observed from the vegetative to floral parts; and stomata functioning as hydathodes have not been noticed in the latter, thus indicating that florogenic factors have no effect on the stomata.     

The Cuticle, Epidermis and Stomatal Ontogeny of Casuarina equisetifolia Forst

The cuticle, epidermis and stomatal ontogeny of Casuarina equisetifoliaForst. is described. The cuticle shows well marked impressionsof the epidermal cells and stomata. The epidermis of leaf andstem shows transversely oriented, tetracytic, mesoperigenousstomata with two lateral mesogene subsidiaries and two polarperigene neighbouring cells. Although the epidermal structureof Casuarina shows a good deal of resemblance with that of theBennettitales, it may not indicate any phylogenetic relationshipssince there are important differences in the structure and reproductionof the plants of these two groups.     

Stomatal architecture and evolution in basal angiosperms

Stomatal architecture-the number, form, and arrangement of specialized epidermal cells associated with stomatal guard cells-of 46 species of basal angiosperms representing all ANITA grade families and Chloranthaceae was investigated. Leaf clearings and cuticular preparations were examined with light microscopy, and a sample of 100 stomata from each specimen was coded for stomatal type and five other characters contributing to stomatal architecture. New stomatal types were defined, and many species were examined and illustrated for the first time. Character evolution was examined in light of the ANITA hypothesis using MacClade software. Analysis of character evolution, along with other evidence from this study and evidence from the literature on fossil angiosperms and other seed plant lineages, suggests that the ancestral condition of angiosperms can be described as anomo-stephanocytic, a system in which complexes lacking subdidiaries (anomocytic) intergrade with those having weakly differentiated subsidiaries arranged in a rosette (stephanocytic). From this ancestral condition, tangential divisions of contact cells led to the profusion of different types seen in early fossil angiosperms and Amborellaceae, Austrobaileyales, and derived Chloranthaceae, while the state in Nymphaeales is little modified. Formation of new, derived types by tangential division appears to be a recurrent theme in seed plant evolution.     

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.     

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.     

The bHLH protein, MUTE, controls differentiation of stomata and the hydathode pore in Arabidopsis

Stomata are turgor-driven epidermal valves on the surface of plants that allow for efficient gas and water exchange between the plant and its environment. The Arabidopsis thaliana basic helix-loop-helix (bHLH) protein, MUTE, is a master regulator of stomatal differentiation where it is required for progression through the stomatal lineage and the differentiation of stomata. The genetic control of stomatal spacing across the epidermal surface is variable in different organs. For instance, a distinct suite of genes from those in leaves regulates stomatal patterning in hypocotyls. Here we report that regardless of organ type, MUTE controls downstream events directing stomatal differentiation, specifically the transition from meristemoid to guard mother cell. Ectopic MUTE expression is sufficient to over-ride cell fate specification in cell types that do not normally differentiate stomata. Furthermore, MUTE is required for the production of the structure evolutionarily related to stomata, the hydathode pore. Consistently, MUTE displays expression at the tip of cotyledons and leaves, thus co-localizing with the auxin maxima. However, MUTE itself was not regulated by the auxin, and the absence of hydathode pores in mute did not affect the auxin maxima. Surprisingly, our analysis revealed that the requirement for MUTE could be partially circumvented under conditions of compromised inhibitory signaling.     

Structure,Ontogeny and Taxonomic Significance of Stomata in Some Cucurbitaceae

Stomatal structure, ontogeny in vegetative and floral organs of 9 genera and 12 species of Cucurbitaceae are described. The stomatal types conform to aperigenous, monoperigenous, diperigenous, hemipara-mesoperigenous and para-mesoperigenous types of Fryns-Claessens & Van Cotthem (1973). Stomatal abnormalities such as contiguous stomata, single guard cells with or without pore, one and a half stomata, degeneration of one or both the guard cells, cytoplasmic connections between guard cells of neighbouring stomata and a guard cell of a stoma and an adjacent epidermal cell, and division of guard cells are described. Stomata index, frequency of stomata, epidermal cells, size of guard and epidermal cells and organwise distribution of stomata are given. Stomatal studies does not support the view that the Cucurbitaceae are related to the Passifloraceae. The inclusion of 9 genera and 12 species studied in the tribe Cucumerineae is justified.     

麦冬、土麦冬和阔叶土麦冬叶表皮形态结构的观察

用光镜和扫描电镜观察了麦冬（Ophiopogon japonicus（L．f）Ker—Gawl.]、土麦冬（Liriope spicata Lour．）和阔叶土麦冬（L．platyphylla Wanget Tang）叶表皮显微结构、亚显微结构和角质层内表面的形态结构。结果表明,气孔主要分布于麦冬、土麦冬和阔叶土麦冬叶片的下表皮,气孔密度分别为76．4、114．3和99．8个·mm^-2;仅阔叶土麦冬叶片上表皮有少量气孔分布。3种植物的气孔器均不具有副卫细胞,并在叶脉间形成纵向气孔带。表皮细胞长方形,气孔带与非气孔带处表皮细胞的形态和大小差异较明显。麦冬气孔周围的表皮细胞平周壁具明显瘤状突起,导致气孔下陷;土麦冬气孔周围的表皮细胞平周壁呈波浪状突起,使气孔相对下陷;阔叶土麦冬气孔周围的表皮细胞平周壁基本无突起,气孔不下陷。3种植物的叶表皮均有发达的角质层和丰富的蜡质,且蜡质主要分布于下表皮气孔带处。这些结构特征可能与它们所具有的喜阳、耐阴和耐旱等特性有一定的相关性。     

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.     

Terminology and classification of stomata and stomatal development—a critical survey

The literature on terminology of stomata and stomatal development is reviewed and the terminology rationalized. The classification of developmental types and of the developing cells should not be combined with the morphological classification of mature stomatal complexes. The cells involved in the development should be distinguished on the basis of their origin and position in the developing stomatal complex, and not on the basis of their future form and appearance. It is unsound to distinguish any kind of cell only on the basis of a presumed future division by which it is replaced by its two daughter cells. Development of stomata begins with the formation of a stomatal meristemoid by an unequal division of a protodermal cell. A meristemoid may divide unequally to produce a new meristemoid and a mesogene cell. Stomatal meristemoids eventually function as guard-cell mother-cells. The adjective perigene is restricted to those cells that have arisen by divisions of protodermal cells surrounding the future stoma. The undivided cells surrounding protodermal cells should be termed agene cells, and not neighbouring cells, a term which should be restricted to morphological terminology.     

Specialized structures in the leaf epidermis of basal angiosperms: morphology, distribution, and homology

The morphology of specialized structures in the leaf epidermis of 32 species of basal (ANITA: Amborella, Nymphaeales, Illiciales, Trimeniaceae, and Austrobaileyaceae) angiosperms, representing all seven families and 11 of 14 genera, was investigated using light and scanning electron microscopy. Distribution, density, and size of structures were also measured, and character evolution was analyzed. Hydropotes are a synapomorphy of Nymphaeales and ethereal oil cells are a synapomorphy of Austrobaileyales, but uniseriate nonglandular trichomes appear to have arisen independently several times. Specialized structures are frequently characterized by adjacent epidermal cells that have striking similarities in their form and arrangement (i.e., architecture) to subsidiary cells of certain types of stomatal complexes. Additionally, forms intermediate to oil cells and stomata, to trichomes and stomata, and to hydropotes and oil cells are present in some taxa. Thus, all of these specialized structures and their adjacent epidermal cells form complexes that may be homologous with, and evolutionarily derived from stomatal complexes, and the specialized structure, or portion thereof, may be homologous to the stoma or guard mother cell. Improved knowledge of the morphology and evolution of these structures in the earliest branching extant angiosperm lineages has a bearing on many diverse areas of botany.     

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.     

青藏高原和内蒙古高原典型草地植物叶片肾型和哑铃型气孔器气孔特征及其与环境的关系

该研究利用植物制片技术,以中国青藏高原和内蒙古高原典型草地常见种或优势种植物的叶片为研究对象,通过比较分析叶片哑铃型气孔器和肾型气孔器的特征及其与环境因子的关系,揭示植物叶片两类气孔器对环境因子的响应策略。结果表明:(1)叶片哑铃型气孔器气孔指标的变异系数小于肾型气孔器。(2)叶片哑铃型气孔器气孔指标与环境气候指标的关系弱于肾型气孔器。(3)叶片哑铃型气孔器气孔特征与环境关系在叶片上下表面之间存在显著差异,而肾型气孔器气孔特征与环境因子的关系在叶片上下表面之间无显著差异。(4)叶片哑铃型气孔器的气孔特征与降水关系密切,而肾型气孔器气孔特征与温度关系密切。(5)同一种气孔器的气孔特征在两个地区(青藏高原和内蒙古高原)间存在显著差异。研究认为,肾型气孔器和哑铃型气孔器的气孔特征及其与环境之间的关系存在差异,在分析气孔特征时有必要将肾形与哑铃形保卫细胞形成的气孔器加以区分,该研究结果有助于进一步理解中国草地植物叶气孔特征对气候变化的响应与适应策略。     

Regulation of jasmonate metabolism and activation of systemic signaling in Solanum nigrum: COI1 and JAR4 play overlapping yet distinct roles

? Understory plants are subjected to highly intermittent light availability and their leaf gas exchanges are mediated by delayed responses of stomata and leaf biochemistry to light fluctuations. In this article, the patterns in stomatal delays across biomes and plant functional types were studied and their effects on leaf carbon gains and water losses were quantified. ? A database of more than 60 published datasets on stomatal responses to light fluctuations was assembled. To interpret these experimental observations, a leaf gas exchange model was developed and coupled to a novel formulation of stomatal movement energetics. The model was used to test whether stomatal delays optimize light capture for photosynthesis, whilst limiting transpiration and carbon costs for stomatal movement. ? The data analysis showed that stomatal opening and closing delays occurred over a limited range of values and were strongly correlated. Plant functional type and climate were the most important drivers of stomatal delays, with faster responses in graminoids and species from dry climates. ? Although perfectly tracking stomata would maximize photosynthesis and minimize transpiration at the expense of large opening costs, the observed combinations of opening and closure times appeared to be consistent with a near-optimal balance of carbon gain, water loss and movement costs.     

Stomatal types ofCactaceae

The stomatal types (i.e. the arrangement of epidermal cells in the vicinity of a stomatal pore in superficial view) have been examined in more than 150 taxa ofCactaceae, mostly using documented material. Preparations have been made by mazerating pieces of tissue with modified Jeffrey's Solution and staining with chlore-zinc-jodine.—The examined members of the subfamilyCactoideae showed parallelocytic stomata with only minor deviations in a number of cases. Members of the subfamiliesPereskioideae andOpuntioideae show parallelocytic stomata on the leaves, but the stomatas of the stem represent a different type, which apparently is not yet described. It is termed opuntioid here. In most cases the stomata are superficial but a few taxa show markedly sunken or hidden stomata.—In taxa of the subfamiliesPereskioideae andOpuntioideae the stomata are generally oriented parallel to the stem axis with only minor deviations. The stomata of taxa of the subfamilyCactoideae do in general not show a particular orientation with the notable exception of a number of epiphytic genera from the tribeHylocereeae.—The results of these investigations in general coincide well with the generic classification of theCactaceae byHunt (1967). A few cases where stomatal characters suggest a differing classification merit further investigations.—Additionally, the possibilities to distinguish between paracytic and parallelocytic stomata are discussed and an amended definition for the latter is given.     

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.