Variable Development and Cellular Patterning in the Epidermis of Ruscus hypoglossum

The general problem was the meaning of the variability of cellulardevelopment of the stomata-bearing epidermis of Ruscus hypoglossumin which 'immature stomata' occur, i.e. cells that have gonethrough part but not the final stages of stomatal development.The development of the epidermis was followed in vivo, by makingrepeated replicas of the same developing tissues using dentalimpression material. The development of stomata occurred overthe entire surface of large phyllodes and was not synchronous.The early development of future and 'immature stomata' couldnot be distinguished, neither by the form of the cells nor bythe timing of the initial, unequal divisions. The process ofstomatal development did not stop at any one, characteristicsstage. Statistical analyses indicated that the pattern of functionalstomata would have been less orderly if all stomatal initialshad developed into mature structures. The results suggest thatin Ruscus epidermal patterning occurs during, rather than preceding,stomatal development: many stomata are initiated, but they followa labile developmental program and cellular interactions selectthose that reach the mature functional state.Copyright 1993,1999 Academic Press Cellular patterns, epigenetic selection, immature stomata, Ruscus hypoglossum, spacing patterns, stomata, subsidiary cells, unequal divisions     

Stomatal distribution patterns change according to leaf development and leaf water status in <Emphasis Type="Italic">Salix miyabeana</Emphasis>

Salix is a pioneer woody plant genus characterized by a strong plasticity in leaf morphology. The aims of this paper were to determine stomatal distribution (1) in mature leaves in response to environmental conditions, and (2) during leaf development. Stomata of abaxial and adaxial faces of mature leaves of Salix miyabeana SX67 (cultivated in short rotation coppice) were analyzed at the end of summer 2012 and 2013 at six locations in Quebec, Canada. Within each site and across the two growing seasons, stomatal density of abaxial faces was diluted by an increase in area of mature leaves due to higher rainfall. For shrubs with more than one growing season, stomatal density of abaxial faces was affected by annual rainfall, independently of site, whereas leaf area was predominantly influenced by site but was also modulated in part by rainfall. The number of stomata per leaf was site-specific, independently of rainfall. These leaves were mainly hypostomatic, although those collected on shrubs during their first growing season after coppicing (i.e. with a high root:shoot ratio) were amphistomatic. Similarly, at early development stages (surface area <2.8 cm²), leaves were amphistomatic, whereas stomata on adaxial faces of larger leaves were occluded. Nevertheless, stomatal conductance of abaxial faces increased with leaf area, whereas stomatal density was best described by a quadratic relationship. This strategy allows for a maximum uptake of carbon while limiting water loss during leaf development and to adapt the morphology of mature leaves depending on moisture and site conditions.     

盾叶秋海棠叶表皮气孔簇的发育及分布格局

气孔是植物控制气体交换和调节水分散失的门户。大部分高等植物气孔的分布格局是相邻气孔之间被一至多个表皮细胞所间隔。而在有限分布的几个科属的植物种中发现气孔成簇分布的现象 ,即由 2至多个紧密相邻的气孔器组成相对独立的单元 ,称为气孔簇 (stomatalcluster)。以中国原产的盾叶秋海棠 (BegoniapeltatifoliaLi)为研究对象 ,探讨了叶表皮气孔簇的发育机制及其分布格局。结果表明 :气孔发育初期 ,气孔拟分生组织的成簇 (相邻紧密 )排列可能是气孔簇形成的主要机制 ;气孔副卫细胞恢复分裂形成的卫星拟分生组织也对气孔簇的形成起一定的作用。把气孔簇和单个气孔视为一个气孔单元发现 ,盾叶秋海棠气孔单元密度 (单位面积中气孔单元数 )和气孔单元大小 (气孔单元所包含气孔数 )在叶片上呈有规律的分布 :前者由叶片中部向叶尖、叶缘逐圈增多 ,而后者逐圈减少。对这种分布格局的成因进行了讨论     

Changes in stomatal frequency, stomatal conductance and cuticle thickness during leaf expansion in the broad-leaved evergreen species, Eucalyptus regnans

Aspects of leaf anatomical and physiological development were investigated in the broad-leaved evergreen species, Eucalyptus regnans F.Muell. Newly emergent leaves were tagged in the field and measured for stomatal conductance while a subset was collected every 14 days for the measurement of stomata and cuticle over a 113-day period. Cuticle thickness increased during leaf expansion, the increase following a sigmoid curve. Stomatal frequency (no. mm⁻²) decreased from 56 to 113 days after leaf emergence. The frequency of both immature and intermediate developmental stages of stomata also decreased over this time, but the total number of stomata per leaf remained relatively constant. Stomatal conductance (g _s) of young expanding leaves increased during expansion, and was significantly linearly correlated with stomatal frequency (excluding immature stomata), and with cuticle thickness. The progressive increase in g _s in young developing leaves was contrary to the observed changes in structural characteristics (increased cuticle thickness and decreased stomatal frequency). This increase in g _s with development may be related to the progressive increase in number of mature stomata with larger apertures and, therefore, a higher total pore area in fully expanded leaves.     

Stomatal patterning in Tradescantia: an evaluation of the cell lineage theory.

The cell lineage theory, which explains stomatal patterning in monocot leaves as a consequence of orderly divisions, was studied in Tradescantia. Data were collected to test the theory at three levels of organization: the individual stoma; stomata distributed in one dimension, in linear fashion along cell files; and stomata apportioned in two dimensions, across the length and breadth of the leaf. In an attempt to watch the patterning process through regeneration, stomata in all visible stages of development were laser ablated. The results showed that the formation of stomatal initials was highly regular, and measurements of stomatal frequency and spacing showed that pattern was determined near the basal meristem when the stomatal initials arose. Following the origin of initials, the pattern was not readjusted by division of epidermal cells. Stomatal initials were not committed when first present and a small percentage of them arrested. The arrested cells, unlike stomata, were consistently positioned in cell files midway between a developed pair of stomata. At the one-dimensional level of pattern, stomata in longitudinal files were separated by a variable number of epidermal cells and the frequency of these separations was not random. The sequential spacing of stomata also was not random, and stomata separated by single epidermal cells were grouped into more short and long series than expected by chance. The stomatal pattern across the width of the leaf resulted from cell files free of stomata which alternated with cell files containing stomata, but not with a recurring periodicity. Files lacking stomata were found only over longitudinal vascular bundles. Laser ablations of developing stomata did not disrupt the pattern in nearby cells or result in stomatal regeneration. We conclude that the cell lineage theory explains pattern as an individual stomatal initial arises from its immediate precursor and satisfactorily accounts for the minimum spacing of stomata in a cell file, i.e., stoma-epidermal cell-stoma. However, the theory does not explain the collective stomatal pattern along the cell files, at the one-dimensional level of patterning. Nor does the theory account for the for the two-dimensional distribution of stomata in which regions devoid of stomata alternate with regions enriched with stomata, but not in a highly regular nor haphazard manner. We suggest that the grouping of epidermal cells and stomata separated by single epidermal cells in cell files may result from cell lineages at a specific position in the cell cycle as they traverse the zone where stomatal initials form.(ABSTRACT TRUNCATED AT 400 WORDS)     

Juvenile Rhus glabra leaves have higher temperatures and lower gas exchange rates than mature leaves when compared in the field during periods of high irradiance

We sought to test the hypothesis that stomatal development determines the timing of gas exchange competency, which then influences leaf temperature through transpirationally driven leaf cooling. To test this idea, daily patterns of gas exchange and leaflet temperature were obtained from leaves of two distinctively different developmental stages of smooth sumac (Rhus glabra) grown in its native habitat. Juvenile and mature leaves were also sampled for ultrastructural studies of stomatal development. When plants were sampled in May-June, the hypothesis was supported: juvenile leaflets were (for part of the day) from 1.4 to 6.0 degrees C warmer than mature leaflets and as much as 2.0 degrees C above ambient air temperature with lower stomatal conductance and photosynthetic rates than mature leaflets. When measurements were taken from July to October, no significant differences were observed, although mature leaflet gas exchange rates declined to the levels of the juvenile leaves. The gas exchange data were supported by the observations that juvenile leaves had approximately half the number of functional stomata on a leaf surface area basis as did mature leaves. It was concluded that leaf temperature and stage of leaf development in sumac are strongly linked with the higher surface temperatures observed in juvenile leaflets in the early spring possibly being involved in promoting photosynthesis and leaf expansion when air temperatures are cooler.     

The development of stomata and other epidermal cells on the rice leaves

In the leaves of rice (Oryza sativa), stomatal initials arose from two asymmetric cell divisions and a symmetric division. Guard mother cells (GMCs) and long cells in stomatal files (LCSs) were formed through the first asymmetric division of the precursor cell of GMCs. Subsidiary cells (SCs) were produced by the second asymmetric division of subsidiary mother cells or LCSs. Following SC formation, GMCs divided once symmetrically to generate guard cells and then differentiated terminally to form mature stomata. The developmental patterns of long cells, prickle hairs and short cells (phellem cells and silica cells) were also examined. Interestingly, we found that the different developmental stages of stomata and epidermal cells occurred in the similar location of immature leaves of the same phyllotaxis. In addition, two spacing patterns (“one stoma, one long cell” and “one short cell row”) probably exist in rice leaves.     

大花美人蕉花发育过程中气孔密度和气孔指数的动态变化

对大花美人蕉(Canna generalis Bailey)不同发育时期花瓣、苞片和花萼上气孔的分布情况、气孔密度和气孔指数的变化进行了研究。结果表明,花瓣、苞片和花萼上、下表皮均有气孔分布。花瓣、苞片和花萼上表皮的气孔密度和气孔指数均小于下表皮的。随着花的发育,花瓣、苞片和花萼上的气孔密度和气孔指数一般呈现先上升后下降的变化趋势。     

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.     

合意非洲铁羽片表皮及气孔器的发育研究

用光学显微镜和扫描电镜对合意非洲铁羽片表皮及气孔器的发育过程进行观察研究。结果显示,(1)在羽片发育过程中表皮细胞变化不明显,主要是细胞伸长和壁增厚的过程;表皮的角质层连续出现。(2)气孔器发育可大致分3个阶段:保卫细胞母细胞阶段、幼保卫细胞阶段和成熟保卫细胞阶段;气孔器发育方式为单唇型或周源型;成熟气孔器属单环型。(3)在羽片发育过程中,气孔密度起初很低,后急剧升高并达到峰值,之后逐渐下降并趋于稳定。(4)有早熟气孔器。(5)羽片表皮发育成熟的方式是由基部向顶部逐步推进。     

Peculiarities of the development of skeletal muscles in physiologically mature and immature mammals]

In one set of experiments, studies have been made on the time during which the membrane potential, action potential, total protein and the content of the dry substance of skeletal muscles of rats and dogs attain the values typical for adult animals. Chronologically, this time is 5-fold shorter in rats, than in dogs. In the other set of experiments, the same indices were studied in physiologically mature (with respect to calendar age) and immature rats and dogs. It was shown that in immature animals these indices are significantly lower than in mature ones. During natural development, physiologically immature organisms are the main objects of elimination at early postnatal stages via natural selection.     

Variable Cell Lineages form the Functional Pea Epidermis

Evidence was sought for cellular programs and cellular interactionsacting during the formation of stomatal spacing patterns. Dailyreplicas of the surfaces of Pisum sativum leaves were used toreconstruct the cellular development of specific regions ofthe epidermis. During the period studied small primordia becamemature leaves; this involved a 250-fold increase in area anda 20-fold increase in cell number. The earliest event correlatedwith the development of a stoma was an unequal division, andsuch divisions were common in neighbouring and even within thesame cells. A distinct cell lineage started with these unequaldivisions, forming both a stoma and most of the cells that separatedit from its neighbours. Both products of an unequal divisionbecame regular epidermal cells only where such development preventedthe formation of two stomata that would have been in directcontact with one another. Neighbouring stomata often developedand matured together, indicating that there was no mutual inhibitionbetween developing stomata that were more than one cell apart.It is concluded that stomata are products of an intracellularprogram which generates stomatal patterns during rather thanpreceding development. This program can be modified and evenstopped during its entire course, allowing for the correctionof local ‘mistakes’ of stomatal patterning. Cell lineages, cell determination, cellular interactions, epidermal development, garden peas, immature stomata, pattern formation, Pisum sativum, spacing patterns, stomata, unequal divisions     

Cellular Interactions in the Development of Stomatal Patterns in Vinca major L

The development of the leaf epidermis of Vinca major L. wasfollowed in situ by epi-illumination microscopy and evidencewas sought for cellular interactions. Stomata were often foundto be initiated in adjoining cells. The epidermal cells whichseparated such stomata when they had matured were formed fromthe same cells as the stomatal complexes themselves. The presenceof developing and mature stomata may influence only the orientationof divisions in neighbouring cells, and not the initiation andmaturation of stomata. There is great variability in the relativeorientation, timing and number of divisions which intervenebetween the first unequal division and the maturation of a stomaas well as the location of stomata relative to the spongy mesophylland minor veins. The results indicate that continuous short-rangeinteractions between the future guard cells and the adjoiningcells, rather than interactions between future stomata or afixed programme of development, are essential for the formationof the pattern of functional stomata in the mature leaf. Vinca major L., cell lineage, cellular interactions, development of stomata, epi-illumination microscopy, meristemoids, patterned differentiation, stomata     

Development of elastic fibers of nuchal ligament, aorta, and lung of fetal and postnatal sheep: an ultrastructural and electron microscopic immunohistochemical study

The morphogenesis of elastic fibers of the nuchal ligament, aorta, and lung of sheep was studied by light microscopy, transmission electron microscopy, and immunohistochemical methods for the detection of elastin. The degree of maturation of the amorphous materials of elastic fibers was assessed morphologically in preparations stained by the tannic acid and periodic acid methenamine-silver methods. With both of these methods, the amorphous components of mature fibers stained less intensely than did those of immature fibers. Elastic fibers in early stages of development consisted of many microfibrils and few, small, branching masses of immature amorphous material. Thicker fibers were formed by the coalescence of growing masses of amorphous materials. In late stages of formation of elastic fibers, the mature amorphous materials were associated with few microfibrils; and they were partially surrounded by immature amorphous materials associated with many microfibrils. Antielastin antibody reacted evenly with amorphous materials in very early stages of elastic-fiber development, but reacted only with the other zones of amorphous materials in later stages; it also reacted with the microfibrils in all stages. These findings were interpreted as indicating that the microfibrils were associated with small amounts of elastin on their surfaces. This conclusion is in agreement with ultrastructural observations showing 1) that development of microfibrils precedes that of the amorphous material and 2) that the microfibrils adjacent to the immature amorphous materials are covered with small amounts of tannic acid-positive amorphous materials. These observations suggest that microfibrils serve as sites for elastin deposition, both in early elastogenesis and in subsequent growth of elastic fibers. However, the nature of the interaction between elastin and microfibrils remains unknown.     

Developmental mechanism and distribution pattern of stomatal clusters in Cinnamomum camphora

We report the stomatal cluster development mechanism and distribution pattern in Cinnamomum camphora. The results indicated that the clustered arrangement of meristemoids at the juvenile stage of the leaf development contributed greatly to the pattern of stomatal clusters. Additionally, division of an epidermal cell (EC), which is between small stomata, and growth of small stomata to push the ECs aside to become directly contacting had an impact on the development as well as the pattern of stomatal clusters. The latter way may play a more important role in stomata clustering of the wide-type C. camphora. There are no significant difference in the stomatal index (the number of stomata per the sum of the number of epidermal cells and the number of stomata) among different part of leaves, while the stomatal cluster index (the number of stomata in stomatal clusters per the total number of stomata) was found to increase gradually from the apex to the base and from the middle part to the marginal part of the leaf. The possible reason of this pattern was discussed. Published in Russian in Fiziologiya Rastenii, 2006, Vol. 53, No. 3, pp. 348–353. The text was submitted by the authors in English.     

Changes in water status during water stress at different stages of development in wheat

The dynamics of stomatal resistance and osmotic adjustment in response to plant water deficits and stage of physiological development was studied in the leaves of spring wheat ( Triticum aestivum L., GWO 1809). Plants were germinated and grown in pots in a growth chamber at the Duke University Phytotron to four physiological stages of development (4th leaf, 7th leaf, anthesis, and soft dough), during which time stomatal resistance, total water potential and osmotic potential were measured on the last fully developed leaf of water stressed and non-stressed plants. Pressure potential was obtained by difference. Stomatal closure of the abaxial and adaxial surfaces were independent of each other, each having a different critical total water potential. The total water potential required to close the stomata on the last fully developed leaf were different at different stages of physiological development, decreasing as the plants grew older. The development of osmoregulation in wheat allows the closure of stomata during the vegetative stage at a high total water potential, but insures that stomata remain open from anthesis through the ear filling period to a lower total water potential.     

Innervation of developing intrafusal muscle fibers in the rat

The chronology of development of spindle neural elements was examined by electron microscopy in fetal and neonatal rats. The three types of intrafusal muscle fiber of spindles from the soleus muscle acquired sensory and motor innervation in the same sequence as they formed--bag2, bag1, and chain. Both the primary and secondary afferents contacted developing spindles before day 20 of gestation. Sensory endings were present on myoblasts, myotubes, and myofibers in all intrafusal bundles regardless of age. The basic features of the sensory innervation--first-order branching of the parent axon, separation of the primary and secondary sensory regions, and location of both primary and secondary endings beneath the basal lamina of the intrafusal fibers--were all established by the fourth postnatal day. Cross-terminals, sensory terminals shared by more than one intrafusal fiber, were more numerous at all developmental stages than in mature spindles. No afferents to immature spindles were supernumerary, and no sensory axons appeared to retract from terminations on intrafusal fibers. The earliest motor axons contacted spindles on the 20th day of gestation or shortly afterward. More motor axons supplied the immature spindles, and a greater number of axon terminals were visible at immature intrafusal motor endings than in adult spindles; hence, retraction of supernumerary motor axons accompanies maturation of the fusimotor system analogous to that observed during the maturation of the skeletomotor system. Motor endings were observed only on the relatively mature myofibers; intrafusal myoblasts and myotubes lacked motor innervation in all age groups. This independence of the early stages of intrafusal fiber assembly from motor innervation may reflect a special inherent myogenic potential of intrafusal myotubes or may stem from the innervation of spindles by sensory axons.     

The too many mouths and four lips mutations affect stomatal production in Arabidopsis

Stomata regulate gas exchange through the aerial plant epidermis by controlling the width of a pore bordered by two guard cells. Little is known about the genes that regulate stomatal development. We screened cotyledons from ethyl methanesulfonate-mutagenized seeds of Arabidopsis by light microscopy to identify mutants with altered stomatal morphology. Two mutants, designated too many mouths (tmm) and four lips (flp), were isolated with extra adjacent stomata. The tmm mutation results in stomatal clustering and increased precursor cell formation in cotyledons and a virtual absence of stomata in the inflorescence stem. The flp mutation results in many paired stomata and a small percentage of unpaired guard cells in cotyledons. The double mutant (tmm flp) exhibits aspects of both parental phenotypes. Both mutations appear to affect stomatal production more than patterning or differentiation. tmm regulates stomatal production by controlling the formation, and probably the activity, of the stomatal precursor cell.     

Stomatal response of hybrid poplar to incident light, sudden darkening and leaf excision

Responses of abaxial and adaxial stomata of Populus trichocarpa Torr. & Gray. × P. deltoides Bartr. (ex Marsh.) cv. Unal to incident light, sudden darkening and leaf excision in the light and in the dark were studied on 5-year-old trees in the field using diffusion porometry. Stomatal closure in the dark was found to be incomplete in most cases studies. Stomata closed after leaf excision in the dark within 90 min. Stomatal closure after darkening of an entire tree or an entire branch (white the rest of the tree was in the light) was slower, and complete stomatal closure was noticed only for adaxial stomata after 3 h. Adaxial stomata were more reactive and sensitive than abaxial stomata to sudden darkening and leaf excision in the light and the dark. In all treatments, stomatal response was more responsive in mature leaves than in young, still expanding leaves.