TENDRILS OF PASSIFLORA FOETIDA: HISTOGENESIS AND MORPHOLOGY

Passiflora foetida bears an unbranched tendril, one or two laterally situated flowers, and one accessory vegetative bud in the axil of each leaf. The vegetative shoot apex has a single-layered tunica and an inner corpus. The degree of stratification in the peripheral meristem, the discreteness of the central meristem, and its centric and acentric position in the shoot apex are important plastochronic features. The procambium of the lateral leaf trace is close to the site of stipule initiation. The main axillary bud differentiates at the second node below the shoot apex. Adaxial to the bud 1–3 layers of cells form a shell-zone delimiting the bud meristem from the surrounding cells. A group of cells of the bud meristem adjacent to the axis later differentiates as an accessory bud. A second accessory bud also develops from the main bud opposite the previous one. A bud complex then consists of two laterally placed accessory bud primordia and a centrally-situated tendril bud primordium. The two accessory bud primordia differentiate into floral branches. During this development the initiation of a third vegetative accessory bud occurs on the axis just above the insertion of the tendril. This accessory bud develops into a vegetative branch and does not arise from the tissue of the tendril and adjacent two floral buds. The trace of the tendril bud consists of two procambial strands. There is a single strand for the floral branch trace. The tendril primordium grows by marked meristematic activity of its apical region and general intercalary growth.     

Ontogeny of Tendrils in Antigonon leptopus H. & Arn.

In Antigonon leptopus the main tendrillar and axillary branchis a modified inflorescence axis. It usually bears 6–7lateral bracts out of which 3–4 lower ones are small andleaf-like while the upper 2–3 are tendrillar; 2–3tendrils are also present at its terminal end. The vegetativeshoot apex shows a single layer of tunica and an inner massof corpus without any cytohistological zonation. The earliestaxillary bud or tendril meristem arises at the second node andit elongates due to rib meristem activity. The bract primordiaarise in an acropetal succession. The initiation of the bract-tendriland the leafy bract is similar. In the development of the bract-tendril,marginal meristem activity is absent or reduced and the differentiationof the apical and subapical initials is absent. The terminalbract-tendrils arise as lateral appendages and the residuumof the apical meristem of the main axillary tendril persistsfor some time. In the flowering period the floral buds arisein the axils of the bracts and bract-tendrils. No flowers arepresent in the axils of terminal bract-tendrils.     

SHOOT HISTOGENESIS: SUBAPICAL MERISTEMATIC ACTIVITY IN A CAULESCENT PLANT AND THE ACTION OF GIBBERELLIC ACID AND AMO-1618

Sachs , R. M., A. Lang , C. F. Bretz and Joan Roach . (U. California, Los Angeles.) Shoot histogenesis: subapical meristematic activity in a caulescent plant and the action of gibberellic acid and Amo—1618. Amer. Jour. Bot. 47(4): 260—266. Illus. 1960.–Studies on gibbereilininduced stem formation in rosette plants (Sachs et al., 1959) have shown that a zone of intensive meristematic activity, arising below the existing apical meristem, is almost solely responsible for stem histogenesis, i.e., the formation of the cells constituting the elongate stem. An extensive subapical zone of meristematic activity is also present in caulescent plants, such as Chrysanthemum morifolium, Amo-1618 ([4-hydroxy-5 isopropyl-2 methylphenyl] trimethylammonium chloride, 1-piperidine carboxylate) completely inhibits subapical meristematic activity in chrysanthemum, causing the plants to assume a dwarfed, rosette-like habit of growth. Gibberellic acid, applied either simultaneously, or following the Amo—1618 treatment, completely prevents or reverses the effect of Amo—1618, making the plants retain or resume their normal growth habit. Amo—1618 and gibberellic acid have relatively little effect upon the activity of the apical meristem of Chrysanthemum. Thus, while the apical meristem proper (eu- or promeristem) is the site of shoot organization and the ultimate source of the cells of the entire shoot, the subapical zone of division, termed the subapical meristem, is largely responsible for stem histogenesis in caulescent as well as in rosette plants. Gibberellins, or native, gibberellin-like substances appear to regulate the activity of the subapical meristem and thus to play an important role in shoot development. Amo—1618 and related compounds seem to exert their dwarfing effect in plants by acting as antagonists of gibberellins, at least with respect to the latters' function in regulating the subapical meristematic activity in the shoot.     

LEAF DEVELOPMENT IN DOXANTHA UNGUIS-CATI (BIGNONIACEAE)

Leaf structure in Doxantha unguis-cati is polymorphic. The usual mature compound leaf is composed of two lanceolate leaflets and a terminal tripartite spine-tendril. Leaf primordia are initiated simultaneously in pairs on opposite flanks of the shoot apical meristem by periclinal cell divisions in the third subsurface layer of the peripheral flank meristem. Two leaflet primordia are the first lateral appendages of the compound leaf. Initiation of these leaflet primordia occurs on the adaxial side of a compound leaf primordium 63–70 μm long. Lamina formation is initiated at the base of a leaflet primordium 70–90 μm long and continues acropetally. Mesophyll differentiation occurs in later stages of development of leaflets. The second pair of lateral appendages of the leaf primordium differentiate as prongs of the tendril. Initiation of the second pair of lateral appendages occurs on the adaxial side of a primordium approximately 168 μm long. Acropetal procambialization and vacuolation of cells extend to the apex of tendrils about 112 μm long, restricting the tendril meristem to the adaxial side of the primordium and resulting in curvature of the tendril. The tendril meristem is gradually limited to a more basipetal position as elongation of apical cells continues. Initiatory divisions and early ontogenetic stages of leaflets and tendrils are similar. Their ontogeny differs when the lateral primordia are approximately 70 μm long. Marginal and submarginal initials differentiate within leaflets but not in tendrils. Apical growth of tendrils ceases very early in ontogeny as compared with leaflets.     

The pleiotropic mutation dar1 affects plant architecture in Arabidopsis thaliana

Shoot architecture is shaped upon the organogenic activity of the shoot apical meristem (SAM). Such an activity relies on the balance between the maintenance of a population of undifferentiated cells in the centre of the SAM and the recruitment of organ founder cells at the periphery. A novel mutation in Arabidopsis thaliana, distorted architecture1 (dar1), is characterised by disturbed phyllotaxy of the inflorescence and consumption of the apical meristem late in development. SEM and light microscopy analyses of the dar1 SAM reveal an abnormal partitioning of meristematic domains, and mutations known to affect the SAM structure and function were found to interact with dar1. Moreover, the mutant shows an alteration of the root apical meristem (RAM) structure. Those observations support the hypothesis that DAR1 has a role in meristem maintenance and it is required for the normal development of Arabidopsis inflorescence during plant life.     

MORPHO-HISTOGENIC STUDIES ON TENDRILS OF VITACEAE

The origin and development of the tendrils were studied in 16 species of the Vitaceae: Ampelopsis (7 sp.), Parthenocissus (4 sp.), Vitis (3 sp.), and Tetrastigma (1 sp.). Two types of arrangement of leaf and tendril occur: (a) two successive nodes have leaf-opposed tendrils alternating with each other, followed by a third node, with a leaf unopposed by the tendril; (b) all the nodes have leaf-opposed tendrils. The tendril, like a leaf, is a lateral product of the apical meristem of the shoot. A leaf opposite a tendril is initiated earlier than the tendril. Anticlinal and periclinal divisions in the second and/or third layer of the peripheral meristem of the shoot apex initiate the tendril. The procambium of the tendril first appears towards its abaxial side. Vascularization of the tendril is independent of the axillary bud of the next node below. The positional relationship of the nodal plate vis-à-vis the leaf-opposed tendril shows that the tendril and the leaf belong to the same node. Histological evidence does not show the uplifting of the tendril to the next node above during internodal differentiation. Ontogenetic and morphologic correlation and homology between the inflorescence and the tendril do not substantiate that the tendril in the Vitaceae is an organ sui generis. All available evidence indicates that the tendril is an extra-axillary lateral branch.     

COMPARATIVE FOLIAR HISTOGENESIS IN ACORUS CALAMUS AND ITS BEARING ON THE PHYLLODE THEORY OF MONOCOTYLEDONOUS LEAVES

A comparative histogenetic investigation of the unifacial foliage leaves of Acorus calamus L. (Araceae; Pothoideae) was initiated for the purposes of: (1) re-evaluating the previous sympodial interpretation of unifacial leaf development; (2) comparing the mode of histogenesis with that of the phyllode of Acacia in a re-examination of the phyllode theory of monocotyledonous leaves; and (3) specifying the histogenetic mechanisms responsible for morphological divergence of the leaf of Acorus from dorsiventral leaves of other Araceae. Leaves in Acorus are initiated in an orthodistichous phyllotaxis from alternate positions on the bilaterally symmetrical apical meristem. During each plastochron the shoot apex proceeds through a regular rhythm of expansion and reduction related to leaf and axillary meristem initiation and regeneration. The shoot apex has a three- to four-layered tunica and subjacent corpus with a distinctive cytohistological zonation evident to varying degrees during all phases of the plastochron. Leaf initiation is by periclinal division in the second through fourth layers of the meristem. Following inception early growth of the leaf primordium is erect, involving apical and intercalary growth in length as well as marginal growth in circumference in the sheathing leaf base. Early maturation of the leaf apex into an attenuated tip marks the end of apical growth, and subsequent growth in length is largely basal and intercalary. Marked radial growth is evident early in development and initially is mediated by a very active adaxial meristem; the median flattening of this leaf is related to accentuated activity of this meristematic zone. Differentiation of the secondary midrib begins along the center of the leaf axis and proceeds in an acropetal direction. Correlated with this centralized zone of tissue specialization is the first appearance of procambium in the center of the leaf axis. Subsequent radial expansion of the flattened upper leaf zone is bidirectional, proceeding by intercalary meristematic activity at both sides of the central midrib. Procambial differentiation is continuous and acropetal, and provascular strands are initiated in pairs in both sides of the primordium from derivatives of intercalary meristems in the abaxial and adaxial wings of the leaf. Comparative investigation of foliar histogenesis in different populations of Acorus from Wisconsin and Iowa reveals different degrees of apical and adaxial meristematic activity in primordia of these two collections: leaves with marked adaxial growth exhibit delayed and reduced expression of apical growth, whereas primordia with marked apical growth show, correspondingly, reduced adaxial meristematic activity at equivalent stages of development. Such variations in leaf histogenesis are correlated with marked differences in adult leaf anatomy in the respective populations and explain the reasons for the sympodial interpretation of leaf morphogenesis in Acorus and unifacial organs of other genera by previous investigators. It is concluded that leaf development in Acorus resembles that of the Acacia phyllode, thereby confirming from a developmental viewpoint the homology of these organs. Comparison of development with leaves of other Araceae indicates that the modified form of the leaf of Acorus originates through the accentuation of adaxial and abaxial meristematic activity which is expressed only slightly in the more conventional dorsiventral leaf types in the family.     

A comparison of shoot-forming and non-shoot-forming somatic embryos of sweet potato [Ipomoea batatas (L.) Lam.] using computer vision and histological analyses

Diagnostic structural features for competence to form shoots were tested among sweet potato embryos by combining morphological image capture (using a computer vision system) with anatomical analyses (using light microscopy). Five major morphological variants (`perfect', `near perfect', `limited/no meristematic activity', `disrupted internal anatomy', and `proliferating') were identified among torpedo- and cotyledonary-stage embryos. Among these, only the first two were found to be competent for conversion into plantlets. Lack of organized shoot development in somatic embryos of sweet potato was associated with the following abnormalities: lack of an organized apical meristem, sparcity of dividing cells in the apical region, flattened apical meristem, and multiple meristemoids and/or diffuse meristematic activity throughout the embryo. Diagnostic separation of most shoot-forming and non-shoot-forming torpedo and cotyledonary embryo variants was achieved. Received: 27 January 1997 / Revision received: 28 January 1998 / Accepted: 12 February 1998     

A complex case of simple leaves: indeterminate leaves co-express ARP and KNOX1 genes

The mutually exclusive relationship between ARP and KNOX1 genes in the shoot apical meristem and leaf primordia in simple leaved plants such as Arabidopsis has been well characterized. Overlapping expression domains of these genes in leaf primordia have been described for many compound leaved plants such as Solanum lycopersicum and Cardamine hirsuta and are regarded as a characteristic of compound leaved plants. Here, we present several datasets illustrating the co-expression of ARP and KNOX1 genes in the shoot apical meristem, leaf primordia, and developing leaves in plants with simple leaves and simple primordia. Streptocarpus plants produce unequal cotyledons due to the continued activity of a basal meristem and produce foliar leaves termed “phyllomorphs” from the groove meristem in the acaulescent species Streptocarpus rexii and leaves from a shoot apical meristem in the caulescent Streptocarpus glandulosissimus. We demonstrate that the simple leaves in both species possess a greatly extended basal meristematic activity that persists over most of the leaf’s growth. The area of basal meristem activity coincides with the co-expression domain of ARP and KNOX1 genes. We suggest that the co-expression of ARP and KNOX1 genes is not exclusive to compound leaved plants but is associated with foci of meristematic activity in leaves.     

Effect of thidiazuron in germinating tamarind seedlings

Summary Tamarind, a multipurpose tropical tree species, is economically important for sustainable development of wasteland due to its hardy nature and adaptability to various agroclimatic ocnditions. Reports on in vitro morphogenesis in this species are limited, due to its recalcitrant and callogenic nature. To overcome these limitations, an attempt was made to induce meristematic activity in seedling explants. Seedlings were germinated in medium with or without thidiazuron (4.54, 9.08, 13.12, 18.16 μM). This growth regulator restricted the differentiation of the apical meristem to form shoots. It triggered proliferation of the meristematic tissue at the cotyledonary node and a large number of meristematic buds appeared in a ridial pattern around the node. The meristematic activity extended to the junction of the epicotyl and hypocotyl, giving rise to buds in the form of protuberances in all sides of the junction. These buds differentiated to form shoot primordia and subsequently to shoots in medium devoid of growth regulators. Plants developed by micrografting of these shoots on seedling-derived rootstocks survived in soil.     

Developmental analyses of the phyllomorph formation in the rosulate species Streptocarpus rexii (Gesneriaceae)

Although some species of Streptocarpus (Gesneriaceae) do not possess a layered shoot apical meristem (SAM), but three individual meristems, the basal meristem (BM), the petiolode meristem (PM) and the groove meristem (GM) on the petiolode from which additional phyllomorphs are formed. To gain insights into the processes involved, we examined the development of seedlings from germination to the formation of the primary phyllomorph in S. rexii, a rosulate species. Our specific focus was to examine the relationship between the functional activity of the GM and meristematic activity, which was assessed by a combined analysis of toluidine blue staining of histological sections and the incorporation of BrdU into meristematic tissues. The results were integrated into 3-D graphics, which suggests a complex spatial and temporal interaction within the GM. The significance of our observations is discussed and compared to the SAM observed in most other angiosperms.     

Hydathode anatomy in Potentilla palustris (Rosaceae)

Guttating leaf teeth of Potentilla palustris plants from Wisconsin, USA, were cleared or processed for plastic sectioning or scanning electron microscopy. Anatomical features include: 1) long slender hydathode area occupying most of the tooth, 2) adaxial pad of small, flat epidermal cells with 50 or more sunken water pores about the size of ordinary abaxial stomates, 3) three converged bundles that extend distally, where their tracheary files are separated by intervening files of xylem parenchyma cells with sinuous walls, 4) adaxial mass of small, loosely arranged epithem cells above the xylem, 5) one slender phloem strand that extends only about a third of the way into the hydathode, and 6) bundle sheath extending distally only abaxially and along the flanks of the hydathode. Potentilla hydathodes differ significantly from non-guttating ones described earlier in Physocarpus (Rosaceae).     

New methods of obtaining plantlets and tetraspores from fragments and cell aggregates of meristematic and submeristematic tissue of the red alga Palmaria palmata

Isolation of meristematic tissue of the red alga Palmaria palmata by a freezing-thawing method and further maintenance of the tissue in culture showed the existence of groups of meristematic cells in superficial cortical layers of thallus forming wart-like outgrowths. For the first time, proliferations (plantlets) were obtained from meristematic tissue of sporophytic and male gametophytic fronds and tetraspores from submeristematic tissue of sporophytic fronds within a short period (6 weeks). Tissue fragments (1 × 1 mm²) from upper margins of fresh thalli and cell aggregates (10−100,000 cells) from marginal meristem and meristematic warts of fresh thalli and thalli after the freezing-thawing procedure were cultured for getting plantlets. Tissue fragments (TF) and cell aggregates (CA) from submeristematic tissue of fresh thalli were cultured for obtaining tetraspores. For mass getting proliferations (plantlets) and tetraspores we recommend to use CA from marginal tissue of fresh fronds because of fast growth, high numbers of proliferations and simple techniques of the method. The freezing-thawing method allows also to identify meristematic tissue and to obtain plantlets of red algae with apical meristem (e.g., Gelidium spp.).     

Effect of boron on cell elongation and division in squash roots

This work establishes that cessation of root elongation of intact squash (Cucurbita pepo L.) plants is an early result of boron deficiency. Root elongation is slowed by 6 hours and is virtually stopped as early as 24 hours after boron is first withheld from the nutrient solution. As root elongation ceased, cell elongation progressed distally into the region normally occupied by the apical meristem and eventually the meristem became indistinguishable. Differentiation was determined by use of an elongation index in which cell length was compared to cell width. This index ranged from a low of 0.8 in boron-sufficient root meristems to a high of 3 in root meristems grown in a boron-deficient nutrient solution for 98 hours. It is concluded that a continuous supply of boron is not essential for cell elongation but is required for maintenance of meristematic activity. Boron may act as a regulator of cell division in this tissue.     

THE APICAL MERISTEM OF SPLACHNIDIUM RUGOSUM (PHAEOPHYTA)1

The meristem of Splachnidium rugosum consists of a central apical cell surrounded by a region of actively dividing cells, many of which bear hairs. Conceptacle initials are scattered throughout the surface layer of the meristematic region. Conceptacle initials and apical hairs differentiate adjacent to the apical cell. The apical cell and the conceptacle initials are distinctive, pear-shaped cells possessing similar cytological features that are consistent with significant metabolic activity. They have a nucleus surrounded by dictyosomes, a stellate chloroplast, mitochondria, and numerous vesicles and physodes. When the apical cell is damaged as a result of experimental manipulation, growth ceases. It is inferred that the apical cell controls cell division in the meristematic region and also the differentiation of conceptacle initials and apical hairs. The apical meristems of Splachnidium and species of the Fucales have several important features in common, including the growth-regulatory role of the apical cell and the process of conceptacle initiation. The taxa may possibly have a common evolutionary origin. The problematic and unresolved taxonomic status of Splachnidium is discussed.     

Marginal and laminar hydathode-like structures in the leaves of the desiccation-tolerant angiosperm Myrothamnus flabellifolius Welw.

The fan-shaped leaves of the resurrection plant Myrothamnus flabellifolius Welw. fold during episodes of drought and consequent desiccation of the tissue. The leaf teeth of M. flabellifolius have several features characteristic of hydathodes. Tracheary elements from the three vein endings that converge in each leaf tooth subtend and extend into a cluster of cells significantly smaller than those of the adjacent mesophyll. The stomata overlying this putative epithem are larger than the other stomata on the leaf surface. Crystal violet is absorbed via these stomata in non-transpiring leaves, suggesting that they are water pores. Two to four such water pores occur per hydathode and are readily distinguished in desiccated leaves. Laminar hydathodes apparently also occur in the leaves of M. flabellifolius. Branched vein endings that terminate in short, wide tracheary elements subtend the outer edges of the abaxial leaf ridge, which otherwise lack stomata, and coincide with regions of crystal violet uptake. Guttation could not be induced in M. flabellifolius. However, desiccated leaves readily absorb liquid water through the leaf surface. The use of Calcafluor White to trace the pathway of apoplastic water movement suggests a role for both types of hydathode in foliar water uptake during rehydration while the accumulation of Sulphorhodamine G (indicating solute retrieval from the apoplast) in the epithem of transpiring plants suggests the hydathodes may be a pathway of water loss in the desiccating leaf.     

Some Cytological Changes accompanying the Regeneration of Meristematic Activity at the Apex of Decapitated Roots of Vicia faba L.

The changes that took place in mitotic index (MI), labellingindex (LI) and the relative proportions of interphase nucleiwith different amounts of DNA have been investigated duringthe regeneration of meristematic activity at the apex of rootsof Vicia faba over the 144 h period following removal of thecap and apical mm of the meristem. Measurements were also madeof the corresponding changes that took place as cells were displacedbasally along the root from the apex over the experimental period.In both parts of the root, MI and the relative proportions ofnuclei with different DNA contents changed from levels similarto those at the apex of the controls at the start and end ofthe experiment to levels resembling those found in more matureparts of the root at 24 and 48 h. In contrast to these results,LI declined over the experimental period. These cytologicalchanges were aresult of the development of lateral root primordiain both the apical 2 mm of the decapitated roots and as cellswere displaced out of the meristem into more basal parts ofthe root. It was concluded that the events leading to the regenerationof meristematic activity at the apex of roots from which thecap and apical mm of the meristem were removed, are no differentfrom those which result in lateral formation as cells are displacedbasally along the primary root from the apex, and they takeplace over the same time interval in both systems.