AN INVESTIGATION OF THE MORPHOGENETIC MECHANISMS WHICH CONTROL THE DEVELOPMENT OF ZONATION IN SEEDLING SHOOT APICAL MERISTEMS

The development of zonation in the shoot apical meristems of 28 species of cacti was examined. At germination the embryonic apex may have one of three types of organization: 1) tunica/corpus; 2) tunica/central mother cells/corpus; 3) tunica/central mother cells/peripheral zone/pith-rib meristem. Apices of the third type have complete zonation and undergo little or no further structural development. Both of the other types develop the missing zones. First, the apices become mitotically active, and peripheral zone characters develop in the outer corpus. Simultaneously, or slightly later, the central mother cells differentiate if they are not yet present. The final step is the formation of the pith-rib meristem. The sequence of appearance of the zones was constant throughout all species examined, but the time of appearance of only one zone could be correlated with any other morphogenetic process: the development of peripheral zone characteristics in the outer corpus occurs with or before the beginning of leaf production. The development of zonation appears to be independent of apical size, shape, or age, either real age or plastochron age. This has been interpreted to indicate that the metabolic mechanism controlling the development of zonation in shoot apical meristems is largely autonomous and independent of other aspects of morphogenesis occurring in the seedling. Also, the fact that leaf initiation and shoot axis production can both occur before the development of either the central mother cells or the pith-rib meristem indicates that neither of these zones is essential for these two apical morphogenetic activities.     

DEVELOPMENT OF VACUOLES AND LIPID BODIES IN APICAL MERISTEMS OF PINUS BANKSIANA

Shoot apical meristems of jack pine were examined weekly during the first 8 weeks post-germination with light and electron microscopy. Most of the storage lipids were utilized by the end of the 2nd week. A few lipid bodies, possibly high in phospholipid content, remained in the apical initials and central mother cells and, during the 3rd week, gave rise to vacuoles via lamellar or myelin-like structures which were first seen on their periphery. The inter-lamellar spaces enlarged and eventually a vacuole was formed. At 5 weeks, elongate and spherical osmiophilic inclusions, presumably lipid, were found in the endoplasmic reticulum. Lipid bodies, visible with light microscopy, began to accumulate in the apical initials and central mother cells in the 6th week.     

AN INVESTIGATION OF THE PHYLOGENETIC AND ONTOGENETIC VARIABILITY OF SHOOT APICAL MERISTEMS IN THE CACTACEAE

The sizes, shapes and zonations of the shoot apical meristems of 22 species of cacti were examined. This family was chosen because of its great diversity of habits; the more primitive members are nonsucculent. leafy trees and more advanced members are highly specialized “leaf-less” stem-succulents. By combining these measurements with those already in the literature, a sample of almost 70 species was obtained. Apical meristems range in size from only 80 μm in diam in some species to as much as 1.500 μm in diam in others. The shape ranges from being flat to almost hemispherical. Despite the great range in size and shape of the apical meristems, or the range in the morphologies of the leaves and stems which are produced by the meristems. all apices had the usual zonation: tunica, central mother cells, peripheral zone, and pith-rib meristem. The sizes of each of the zones. expressed either as the number of cells per zone or expressed as a percentage of the whole apex. were highly variable. The variation in apical dimensions and zone sizes occurred both phylogenetically and ontogenetically. and this has been interpreted to indicate that the morphogenetic mechanisms which control apical size and zonation are easily modified, both during the development of individual plants and during the evolution of new species.     

SHOOT APICAL MERISTEMS AND MUTATION: STRATIFIED MERISTEMS AND ANGIOSPERM EVOLUTION

Although apical meristems with a tunica-corpus organization occur in some gymnosperms and in practically all angiosperms, the adaptive significance of such meristems is unknown. Mathematical modeling and computer simulation studies have shown that such stratified meristems promote the long-term retention of many categories of somatic mutation (selectively advantageous, neutral, and disadvantageous). These mutations are maintained primarily as periclinal chimeras. The individual component meristems of a stratified apex have relatively small populations of apical initials. Thus, in long-lived genets, the individual component meristems of the stratified meristems of the ramets would be expected to accumulate mutations due to the operation of Muller's Ratchet. In angiosperms the accumulation of mutants and the associated loss in reproductive capacity (sexual) is compensated for by developmental selection that promotes the loss of defective genotypes without proportionate losses in reproductive capacity.     

A MORPHOMETRIC STUDY OF THE ULTRASTRUCTURE OF ECHINOCEREUS ENGELMANNII (CACTACEAE). I. SHOOT APICAL MERISTEMS AT GERMINATION

At germination the shoot apical meristems of Echinocereus engelmannii were discs with a volume of 666,000 μm³ and were composed of a unistratose tunica (volume: 260,000 μm³) and a corpus which was two cell-layers thick (volume: 406,000 μm³). Four days after germination the nucleus constituted 28.9% of the volume of the cell, and the vacuole constituted 24.5%. The mitochondria were 13.3% of the volume of the tunica cytoplasm, the chloroplasts 9.4%, and the dictyosomes only 1.2%. The endoplasmic reticulum was too sparse to be accurately measured. The organelles of the corpus were identical in size and shape to those of the tunica, but there were statistically significant differences in their cellular and cytoplasmic densities: the more distal corpus layer (C1) was less vacuolate (16.6% of the cell volume), and both corpus layers contained more chloroplasts, 12.0% of the cytoplasmic volume in C1 and 14.3% in the more proximal corpus layer (C2). During the first four days after germination there was a dramatic increase in the size of the central vacuole (e.g., from 15.4% to 24.5% in the tunica), and the mitochondria increased in density from 10.2% of the cytoplasmic volume to 13.3%. Chloroplast density also increased in all meristem layers, but the dictyosome density decreased, as much as a 30% loss in C2. There was also a highly significant reduction in the number of cisternae per dictyosome, from 5.47 to 4.77. Surprisingly, there was no change in heterochromatin: ca. 27% of the volume of the nuclei of all layers was heterochromatic at all stages studied. Thus, the organellar structure of corpus cells is distinctly different from that of tunica cells, and as the apical meristem becomes active after germination, the changes which occur are not uniform in the meristem but rather are zone-specific.     

SHOOT APICAL MERISTEMS AND MUTATION: FIXATION OF SELECTIVELY NEUTRAL CELL GENOTYPES

Shoot apical meristems are interpreted as either structured, that is having a permanent set of apical initials, or stochastic, having apical initials which represent “... momentary representatives of the continuous meristematic residue at the apex of the relevant layer or zone” (Newman, 1965). The two main parameters of stochastic growth are the average number of apical initials (α) and the number of mitotic cycles (r) of the initials and their daughter cells prior to the random selection of subsequent initials. Mathematical analysis and computer simulation studies of stochastic growth have shown that if one starts with 1 mutant initial and α-1 nonmutant initials, eventually a mosaic plant results. The frequency of shoot apices composed of mutant cells is 1/α and the frequency of shoot apices composed of only nonmutant cells is (1 – α)/α. These asymptotics are only attained after considerable growth, thus mericlinal chimeras can persist for many nodes and give the appearance that a permanent set of initials is present.     

PRIMORDIAL LEAF AND PHYTOHORMONE EFFECTS ON EXCISED SHOOT APICAL MERISTEMS OF COLEUS BLUMEI BENTH.

Coleus blumei Benth. apical meristems and apical meristems +1, +2, +3 primordial leaf pairs were cultured to examine phytohormone influences on development and correlative effects of developing primordial leaves on in vitro responses. The meristem with no phytohormones or low levels of IAA could not develop in vitro. At least 0.1 mg/l IAA and optimumly 1-2 mg/l IAA were required for development into complete plants. IAA from 0.1 to 3 mg/l also resulted in root development with no apparent leaf or shoot formation. Levels of IAA higher than 3 mg/l were inhibitory to development. Kinetin, as a substitute for naturally occurring cytokinins, alone (0.0003 to 3 mg/l) resulted in development of rosettes of leaves. In the presence of IAA (***1 mg/l) and kinetin (0.003 mg/l) plants, rosettes, individual leaves with roots, and roots developed from isolated meristems. Glutamine and adenine sulfate both appeared inhibitory to meristem development. With +1, +2, +3 developing primordial leaf pairs left attached to the apical dome, three pairs were required for plant formation in the absence of phytohormones. In the presence of IAA, two pairs of primordial leaves resulted in plant formation; whereas, with IAA and low levels of kinetin one pair of primordial leaves was enough. Higher levels of kinetin were inhibitory to plant development with primordial leaves present. ABA appeared to be inhibitory to development of meristems and meristems +1, +3 primordial leaves at low concentrations and resulted in death at ***1 mg/l. Developing primordial leaves appear to supply the apical meristem with a balance of phytohormones during growth. Meristem development into a plant first involved formation of leaf primordia. Establishment of a bipolar axis with root formation followed.     

IN VITRO DEVELOPMENT OF THE ISOLATED SHOOT APICAL MERISTEM OF ANGIOSPERMS

Development of complete plants was achieved from isolated shoot apical meristems of Nicotiana tabacum L., Daucus carota L., Nicotiana glauca Grah., Tropaeolum majus L., and Coleus blumei Benth. The explants consisted of only meristematic dome tissue with no visible leaf primordia. A simple nutrient medium composed of the Murashige and Skoog salt mixture, 100 mg/liter myo-inositol, 0.4 mg/liter thiamin-HCl, 1-2 mg/liter IAA, 30 g/liter sucrose, and 1% agar was adequate. Histologically there occurred principally tissue enlargement during the first 3-6 days, followed by appearance of bipolar organization in 6-9 days and formation of a well-defined root apex and initiation of first leaf primordium by 12 days.     

SIMULATIONS OF CELL DIMENSIONS IN SHOOT APICAL MERISTEMS: IMPLICATIONS CONCERNING ZONATE APICES

Surface areas, differential curvatures, volumes, and dimensions of cell-like units were described for various geometric shapes approaching the morphology of shoot apical meristems (SAM) in vascular plants. Geometric relationships are given in both graphic and dynamic simulations of shape. If the surface of the SAM is described by the revolution of a parabolic, hyperbolic, or circular function, then the greatest change in the surface areas or volumes of equally spaced transverse sections will occur in those regions showing the greatest differential in surface curvature. Subdivision of the SAM volume into cell-like units leads to quantitative expressions of changes in “cell” length to width and width to depth (aspect) ratios. Dependent upon the geometry of the SAM, differential expressions of aspect ratios may lead to a zonate pattern within the SAM corresponding to a central-mother-cell zone (CMC), a peripheral zone (PZ), and a pith-rib meristem (PRM). The boundary between the PRM and PZ, as seen in median longitudinal section, is a geometric consequence of the deployment of cells with aspect ratios best suited to occupy the entire SAM volume. The number of cell-like lineages, L, in the SAM may be expressed by the aspect ratio of cells in longitudinal section, n_x-y, such that for the PRM and PZ, L = k₁n_x-y^-5.38 and L = k₂n_x-y^3.18, respectively. Cellular patterns seen in the “corpus” of the SAM may not, therefore, be the a priori result of physiologically distinct populations of cells. Computer simulations are discussed within the data set derived from a study of the SAM of cacti.     

芸薹属植物发育过程中顶端结构的解剖学研究

本文采用解剖学方法研究花椰菜、青花菜、结球甘蓝和大白菜在生长发育过程中顶端分生组织结构的变化及之间存在的差异。结果显示它们的顶端分生组织结构都是由最初幼苗的原套-原体结构逐渐发育到过渡型分区结构、典型化五个分区结构,至开始进入生殖生长时期的四个分区结构(形成层状细胞区消失)。四种植物在进入生殖生长后,顶端分生组织细胞行为不同:大白菜和甘蓝顶端亚外套两侧细胞分裂分化形成顶生叶原基,在顶生叶原基内侧的细胞将进行分裂产生花序侧枝原基。花椰菜和青花菜顶端亚外套两侧细胞分裂形成花序分生组织,花序分生组织增生即为花球体;内部解剖结构表现为分生组织不断分裂增多的过程。这些结果为研究花序表型发生的解剖学本质及分子生物学研究分生组织发育方向奠定了基础。     

THE ROOT APICAL MERISTEM OF EQUISETUM DIFFUSUM: STRUCTURE AND DEVELOPMENT

The root apical meristem of Equisetum diffusum Don has a prominent four-sided pyramidal apical cell with its base (distal face) in contact with the root cap. Derivatives (merophytes) that contribute to the main body of the root are produced from the three proximal faces of the apical cell. The first division of a proximal merophyte is periclinal to the root surface separating a small inner cell from a larger outer cell. The inner cell is the precursor of the vascular cylinder. The larger outer cell is the precursor of the epidermis, cortex, endodermis, and pericycle. Radial sectors, established early in the development of the cortex, alternate with sectors in the vascular cylinder. These developmental steps show quite clearly that early root development in Equisetum is markedly different from that of most ferns.