COMPARATIVE FLOWER DEVELOPMENT IN THE CLEISTOGAMOUS SPECIES VIOLA ODORATA. I. A GROWTH RATE STUDY

In Viola odorata, chasmogamous (CH) or open flowers and small, short-petioled leaves are produced under 11 hr or less of daylight, cleistogamous (CL) or closed flowers and large, long-petioled leaves under 14 hr or more of daylight, and intermediate floral and leaf forms under transitional photoperiods. CL flowers are approximately four times smaller than CH flowers and differ morphologically in repressed growth of the anterior petal spur and staminal nectaries, and recurving of the style which remains enclosed within the cone formed by anther appendages. Both CH and CL shoot systems conform to a (2 + 3) phyllotaxis with minor differences in leaf divergence angles and phyllotactic indices. The larger CL leaf grows significantly faster than the CH leaf, and an increased rate of leaf initiation occurs in the CL apex represented by a plastochron of 3.4 days compared to 4.3 days in the CH apex. The plastochron index was used to indirectly age young floral primordia nondestructively until prophase of meiosis I within the anthers. This event occurs 8 days earlier in the CL than the CH flower. Time from meiosis until flower maturity, determined by direct observation, is about 14 days for the CL flower, versus 21 days for the CH flower.     

EARLY LEAF ONTOGENY AND SHOOT DEVELOPMENT IN BROWNEA ARIZA (LEGUMINOSAE)

Brownea ariza Benth. (Leguminosae: Caesalpinioideae) shows early shoot tip abortion and subsequent renewal growth from the pseudoterminal bud. This species is unusual in that the entire shoot system is formed before flushing from the bud occurs, shoot tip abortion occurs during flushing, and the aborting portion contains three to six leaves as well as primordial structures varying from hood to peg shape. This study focused on the morphological changes from initiation of scale and foliage leaf primordia in the “resting” renewal bud through bud elongation to flushing and bud abortion. Scanning electron microscopy revealed that embryonic scale leaves are hood-shaped while foliage leaf primordia show early segmentation into leaflets and stipules. No transitional stages were observed. Bud scales and foliage leaves show opposite developmental trends. In bud scales, length at maturity increases from first to last formed, while length decreases in sequentially formed foliage leaves. Early in leaf development the stipules keep pace with the elongation of the rachis. When the bud reaches about one half of its final length the leaf rachis begins to exceed the lengths of its stipules. This young rachis terminates in a distinct mucro that persists until maturity at which time it abscises. Growth patterns indicate that mucro and rachis are a single developmental unit. The early abortion of a shoot tip containing several leaves cannot be easily rationalized. Previous suggestions have involved maintenance of form and ecological adaptation. We add the possibility of elimination of cell progeny encumbered by mutations. From this and other studies of this group, it is clear that at maturity leaves of different species may look alike, e.g., Hymenaea and Colophospermum are bifoliolate; Brownea, Saraca, and others are multifoliolate. However, early stages of leaf ontogeny are quite diverse and may be of systematic value, since these early differences are lost or masked by later development.     

INDETERMINATE GROWTH OF LEAVES IN GUAREA (MELIACEAE): A TWIG ANALOGUE

Leaves of seed plants are generally characterized as organs of determinate growth. In this regard, Guarea and related genera seem unusual in that the pinnately compound leaves of these plants contain a bud at their tip from which new pinnae expand from time to time. Previous studies (based upon superficial examinations of leaf-tip buds) have produced contradictory conclusions regarding how long the leaf apex remains meristematic and produces new pinna primordia. In order to determine whether leaf development in Guarea is truly indeterminate, we microscopically examined leaf-tip buds of G. guidonia and G. glabra. In both species, the leaf apex remains meristematic and continues to produce new pinna primordia as the leaf ages. Unexpanded leaves of G. guidonia contained an average of 23 pinna primordia, while the oldest leaves we examined had initiated an average of 44 total pinnae. In G. glabra, unexpanded leaves contained 8 pinnae, whereas an average of 28 pinnae had been initiated on the oldest leaves. These results indicate that leaf development in Guarea is truly indeterminate. Periodic examination of individual intact leaves indicated that the leaves commonly continue their growth for 2 or more years (observed maximum = 51 months). As new leaflets are initiated at the shoot apex (and subsequently expand in rhythmic flushes), older (basal) leaflets may abscise. In addition, the petiole and rachis of the leaf thicken and become woody as a result of the activity of a vascular cambium. Guarea leaves therefore seem to function as the analogue of a typical twig (stem) in general habit as well as in their indeterminate apical growth and secondary thickening.     

VASCULARIZATION OF DEVELOPING LEAVES OF GLEDITSIA TRIACANTHOS L. I. THE NODE,RACHIS, AND RACHILLAE

Leaves of Gleditsia triacanthos L. are served by three leaf traces that subdivide in the node to produce subsidiary bundles. The subsidiary bundles differentiate basipetally in the stem and acropetally in the petiole using the original leaf trace bundles (those that developed acropetally) as templates for their development. Within the pulvinus, the acropetal bundle components merge to form the rachis vasculature consisting of a semicircular arc and a ventral chord; several small bundles diverge to form ventral ridge bundles. Mixing of bundles occurs during vascularization of the lateral rachillae axes. Each diverging rachilla axis receives bundles from the semicircular arc, the ventral chord, and a ridge bundle in a relatively reproducible and predictable pattern. During this process the main rachis vasculature is gradually depleted, but the ridge bundles are reconstituted following divergence of each rachilla pair. The distal rachilla pair is vascularized by a bilateral partitioning of the entire rachis vasculature; a remnant of the central leaf trace terminates in a subulate terminal appendage. Vascularization of the bipinnate G. triacanthos leaf is compared to that of the simple Populus deltoides leaf.     

Morphogenetic Studies on Osmunda cinnamomea L.: THE AUXIN RELATIONSHIPS OF EXPANDING FRONDS

Net production of diffusible auxin by fronds of O. cinnamomeahas been found to extend throughout the period of final expansion,with a maximum which occurs shortly after the rate of elongationhas reached its maximum and begun to decline. Auxin is apparentlyproduced only in the pinnae, and from these it enters the rachiswhere its movement is polar. Diffusible auxin moves throughthe rachis without significant loss except in the region ofextensive elongation where a certain amount disappears. No suchdisappearance was found in ether extraction studies. Moreover,in certain cases, ether-extractable auxin persists for as muchas 48 hours in the rachis after removal of the auxin source,although none can be obtained by diffusion under these conditions.It is concluded that diffusible auxin is more closely relatedto growth phenomena in the frond than is extractable auxin.In many cases, there is an apparent failure of transport inthe leaf base which reduces or eliminates expected auxin yieldsby diffusion at this level. Diffusible auxin is an essentialparticipant in three morphogenetic phenomena in the developingfrond: rachis elongation, crozier uncoiling, and final differentiationof xylem and hypodermal sclerenchyma. In none of these can itbe considered as a specific determining factor since the responseto auxin depends upon the physiological state of the reactingcells. In the intact frond diffusible auxin is present in excessof the minimum required for both rachis elongation and uncoiling.Several aspects of the relationship between auxin distributionand development in the frond are discussed.     

REGIONS OF CELL DIVISION AND ELONGATION DURING STEM GROWTH OF XANTHIUM

Regions of cell division and cell elongation were established during stem growth of Xanthium pensylvanicum (cocklebur). From percent mitosis it was determined that the region of cell division in a Xanthium stem of Plastochron Index (PI) 13.89 was 20 mm long, starting from the stem apex and proceeding in a basipetal direction. Measurements of cortical cell lengths demonstrated that mature cell length in the stem of the same plant was reached at about 55 mm distance from the stem apex. Between 20 and 55 mm distance from the apex, shoot growth occurred by cell elongation alone. The maximum rate of change in cell length (dC/dX) was at about 15 mm distance from the stem apex. The length of the apical growth region was a function of the age of the plants. The older the plant, the longer its apical region of elongation. Growth of Xanthium stems was due primarily to elongation of internodes; the nodal regions did not seem to elongate.     

慈姑匍匐茎的起源和球茎的膨大研究

匍匐茎的发生一般见于主茎倒二或倒三叶原基的叶腋部位。在匍匐茎发生区域的主茎一侧,匍匐茎原始细胞的基部形成壳状区;壳状区的形成对匍匐茎原基的外凸起一定作用。匍匐茎无居间分生组织;它的伸长依靠顶端分生组织细胞的横向分裂,使轴向细胞数目增多,并使细胞的轴向延伸。球茎的膨大是通过匍匐茎第8—10节基本分生组织的细胞有丝分裂,增加细胞数目,然后细胞体积的扩大来实现的。球茎中的淀粉一般为单粒淀粉;匍匐茎中的淀粉由单粒和复合两种淀粉粒组成。     

Vascular development of the grapevine (<Emphasis Type="Italic">Vitis vinifera</Emphasis> L.) inflorescence rachis in response to flower number,plant growth regulators and defoliation

The grapevine inflorescence is a determinate panicle and as buds emerge, shoot, flower and rachis development occur simultaneously. The growth and architecture of the rachis is determined by genetic and environmental factors but here we examined the role of flower and leaf number as well as hormones on its elongation and vascular development. The consequences of rachis morphology and vascular area on berry size and composition were also assessed. One week prior to anthesis, Merlot and Cabernet Sauvignon field vines were exposed to manual flower removal, exogenous plant growth regulators or pre-bloom leaf removal. Manual removal of half the flowers along the vertical axis of the inflorescence resulted in a shorter rachis in both cultivars. Conversely, inflorescences treated with gibberellic acid (GA₃) and the synthetic cytokinin, 6-benzylaminopurine (BAP) resulted in a longer rachis while pre-bloom removal of all leaves on the inflorescence-bearing shoot did not alter rachis length relative to untreated inflorescences. Across the treatments, the cross-sectional areas of the conducting xylem and phloem in the rachis were positively correlated to rachis girth, flower number at anthesis, bunch berry number, bunch berry fresh mass and bunch sugar content at harvest. Conversely, average berry size and sugar content were not linked to rachis vascular area. These data indicate that the morphological and vascular development of the rachis was more responsive to flower number and plant growth regulators than to leaf removal.     

EARLY HISTOGENESIS OF THE ADULT LEAVES OF DARLINGTONIA CALIFORNICA (SARRACENIACEAE) AND ITS BEARING ON THE NATURE OF EPIASCIDIATE FOLIAR APPENDAGES

In order to assess the validity of various interpretations of tubular leaves of angiosperms, a histogenetic study of the ontogeny of adult leaves of Darlingtonia californica was undertaken. The adult leaf of Darlingtonia is characterized by a sheathing leaf base, an elongate ascidium, an overarching hood, and two “fishtail” appendages which arise near the leaf apex. A keellike growth, with two rows of alternate vascular bundles, traverses the tube from base to mouth. Ontogenetic studies show that the primordium arises by a monopodial rather than a sympodial mode of growth as previously reported. After the formation of a small, erect primordium, a restricted adaxial meristem is initiated that expands both adaxially and upwards. This “querzone” serves, in effect, to congenitally combine the two primordial margins during its extension. Growth and maturation of the subjacent portions cause tubular elongation in the leaf. Primordial apical divisions are later replaced by more general intercalary growth with acropetal and centrifugal maturation. The hood and fishtails are established early in ontogeny by adaxial growth of the primordial apex and subsequent activation of juxtaposed localized meristems. Comparative morphology has established that the epiascidiate leaf is a foliar appendage that undergoes certain specific morphogenetic modifications. It has a structural relationship to ensiform appendages of Acacia and Acorus as well as to peltate foliar organs. The early ontogeny of Darlingtonia leaves is considered to be homologous with other epiascidiate foliar organs, including some supposedly primitive carpels.     

A CALAMITEAN SHOOT APEX FROM THE PENNSYLVANIAN OF IOWA

Melchior , Robert C., and John W. Hall . (U. Minnesota, Minneapolis.) A calamitean shoot apex from the Pennsylvanian of Iowa. Amer. Jour. Bot. 48(9): 811–815. Illus. 1961.—A shoot apex of a calamitean stem is described from the Des Moines Series, Middle Pennsylvanian. Internodal elongation of the 7 preserved internodes follows a sigmoid curve. A large apical cell has produced derivatives in a fashion apparently comparable to those in Equisetum arvense, except for the number of cells in the first leaf primordium ring and, possibly, the intercalary meristem. Pith meristem developed close to the apical cell. Data from internodal cell elongation of hypodermal cells of the cortex are presented which demonstrate intercalary internodal growth; no intercalary meristems are preserved and the existence of intercalary meristems which might have produced a jointed stem like that of Equisetum is only inferred.     

Testing the optimal defense hypothesis in Stryphnodendron adstringens (Fabaceae,Mimosoideae) leaves: the role of structure,number, position and nectar composition of extrafloral nectaries

Stryphnodendron adstringens is a common Cerrado tree that possesses extrafloral nectaries (EFNs) on its leaves, which are located at the base and apex of the rachis and along the secondary veins. The position of EFNs and their nectar production can be affected by defense strategies because plant organs possess different values and herbivory vulnerability. Here we aimed to elucidate anatomy, histochemistry, nectar composition and EFN number on leaves of S. adstringens in the light of the optimal defense hypothesis. We found a convergence on anatomy and histochemical characterization because the three studied types of EFNs have epidermis, secretory parenchyma and vascular tissue, showing phenolic compounds and polysaccharides in the secretory parenchyma cells. The nectar contained glucose, fructose and sucrose, which attract ants of the Camponotus and Cephalotes genus. We found differences in the number of EFNs along the secondary veins and in the nectar composition between EFNs located at the base and apex of the rachis of the leaf. The number of EFNs on the secondary veins increases from the base to the apex, suggesting a strategy to induce ant patrolling over the entire leaf region. EFNs at the base secreted more nectar, which should be related to the protection of the leaf base, which is the part most vulnerable to herbivore attack and the most valued organ. We concluded that EFNs of S. adstringens are anti‐herbivore defenses whose pattern matches the predictions of the optimal defense hypothesis.     

DEVELOPMENTAL ASPECTS OF THE SHOOT APEX,LEAF, AND BELTIAN BODIES OF ACACIA CORNIGERA

The final event of leaf ontogeny in Acacia cornigera is the production of a Beltian body at the tip of each rachis and pinnule. This structure serves as a food source for an ant, Pseudomyrmex ferruginea F. Smith, that lives in a mutualistic relationship with the plant. The mature Beltian body consists of an epidermis, hypodermis, cortex and central vascular bundle. Anatomical and cytohistological comparisons between the shoot apex and leaf ontogeny in A. cornigera and similar developmental aspects of the phyllode of A. longifolia Willd. and of the leaf of A. decurrens var. dealbata F.v.M. indicate that each type of photosynthetic organ is characterized by a different period of longevity of its group of sub-apical initials. The phylogenetic history of Beltian bodies is also discussed.     

THE SHOOT-GROWTH RHYTHM OF A TROPICAL TREE,THEOBROMA CACAO

The shoot-growth rhythm of tropical trees is a little understood phenomenon. Correlations of tree growth with environment, determined from field studies in the tropics, have been largely inconclusive, and few studies have been done under controlled environmental conditions. As an initial part of a project to study shoot-growth rhythms in tropical trees this paper describes the rhythm in Theobroma cacao L. An individual shoot passes through alternate periods of growth and dormancy. The growth period is characterized by the expansion of leaves and elongation of the shoot. During dormancy the length of the shoot remains constant, and no new leaves expand. Shoot-growth rhythm was divided into phases. Dissection of shoot tips from the various phases shows that the total number of leaves and leaf primordia in the shoot apex remains constant during the dormant period and does not increase until the onset of the growth period. This indicates that activity of the apical meristem as well as leaf expansion and shoot elongation are rhythmic. We found that the rhythm of shoot growth persists under controlled environmental conditions and that growth under these conditions is asynchronous, as it appears to be in the field. Our data strongly suggest endogeneity.     

THE GROWTH OF THE STEM TIP OF KALANCHOËU CV. ‘BRILLIANT STAR’

Stein , Diana B. and o . L. Stein . (Montana State U., Missoula.) The growth of the stem tip of Kalanchoë cv. ‘Brilliant Star.‘ Amer. Jour. Bot. 47 (2) : 132—140. Illus. I960.–The purposes of this investigation were (1) to define as clearly as possible the events in the shoot apex and its immediate derivatives during the ontogeny of the shoot; and (2) to determine the changes which occur during the transition from a vegetative to a reproductive meristem. Rate of leaf production in Kalanchoë is basically constant. The rate of leaf growth subsequent to the early primordial state is, however, dependent on the age of the plant and on the environment in which the plant is grown. By keeping these factors constant a correlation can be demonstrated between the size of the youngest visible leaf and the microscopic primordia. Throughout its ontogeny the general architecture of the shoot apex remains essentially the same. Two tunica layers cover the corpus in the vegetative shoot apex, and even in the flowering meristem these 2 layers can be detected. The apex is essentially flat and blends into the adjacent leaf primordia early in the plastochron. About 10 days after flower induction has been started the apex changes its form to a dome, primarily by increased cell division. At the same time the rate of elongation of the youngest internodes increases thus placing the flowering stem tip atop an elongated stem. Axillary development is ultimately responsible for the development of a dichasium.     

THE CUTICULAR ANATOMY OF FRENELOPSIS VARIANS FROM THE LOWER CRETACEOUS OF CENTRAL TEXAS

Stem fragments identified as Frenelopsis varions Fontaine have been found in the Lower Cretaceous (Albian) of central Texas. The cuticle is extremely thick and characterized by 5–6 subsidiary cells with papillae overarching the stomatal chamber. Guard cells are deeply sunken below the epidermis. Stomatal complexes are arranged in axial rows extending from the base of an internode to its apex. The rows of stomata continue into the sheathing leaf where the rows curve towards the leaf apex. The epidermis of F. varions was apparently long persistent and underwent prolonged growth. Axial rows of stomata are frequently disrupted resulting in a random pattern of stomata. A single, highly reduced, sheathing leaf is present at each node. The margin of the leaf has numerous unicellular trichomes and extends to form a slightly triangular blade.     

A SEASONAL STUDY OF THE VEGETATIVE SHOOT APEX AND THE PATTERN OF PITH DEVELOPMENT IN HIBISCUS SYRIACUS

Tolbert , Robert J. (West Virginia U., Morgantown.) A seasonal study of the vegetative shoot apex and the pattern of pith development in Hibiscus syriacus. Amer. Jour. Bot. 48(3): 249–255. Illus. 1961.—The shoot apex of Hibiscus syriacus L. is described as having a cytohistological zonation superimposed on a tunica-corpus configuration. The apex is flat-topped or may have a saddle-back or concave appearance as seen in median longitudinal section. The metrameristem, consisting of the tunica and corpus initials, is comprised of large, light-staining, vacuolate cells that have thick cell walls and exhibit much dark-staining intercellular substance. Surrounding the metrameristem is the flanking meristem, which is responsible for the outer layers of the shoot, and from which the leaf primordia arise. The pith rib meristem lies below the metrameristem and consists of files of cells that are responsible for the pith. There are no major seasonal changes in the structure of the apex during the yearly cycle. The pith displays a long-shoot type of development with the cells remaining in distinct files during the first flush of growth in the spring. As growth slows and internode elongation is gradually reduced, the pith displays the characteristic short-shoot type of development, consisting of a spongy tissue of rounded cells with many intercellular spaces and no distinct files of cells. A crown is differentiated across the top of the pith at the end of the growth period. This consists of a band of cells with thick, dark-staining cell walls, which separates by the apex from the last year's growth. In contrast to many gymnosperms, this crown is dispersed by renewed cell activity the following spring.     

TRANSLOCATION OF APPLIED GIBBERELLIN IN BEAN SEEDLINGS

The direction and extent of GA transport in Pinto beans has been studied. The increase in growth rate was used as a measure of the amount of GA which reached the stem apex. The evidence showed that a similar increase in stem growth occurred whether GA was applied to the first trifoliolate leaf or to the apex of the shoot, but considerably less elongation resulted when GA was applied to primary leaves. When leaves were treated with GA after remaining in darkness for extended times, no increase in stem elongation was observed; however, growth was promoted when the plants were returned to light. The time required for a sufficient amount of GA to be translocated from the leaf to increase stem growth is less than 1 hour. The maximum growth response was found when the treated leaf was left on the plant for 3 or more hours. A study of GA movement in two-branched plants was made. The untreated branch showed no growth response when GA was applied to the apex of the other branch, even if the dose of GA was 20 × greater than a saturating dose. Similar results were observed when GA was applied to the first trifoliolate leaf. Considerable GA moved from a mature leaf to the opposite shoot if this untreated branch had been defoliated. The pattern of GA movement to the opposite shoot was dependent on the position of the treated leaf on the shoot. It is concluded that the movement of applied GA is related to carbohydrate transport within the plant.     

Correlative inhibition of lateral bud growth in Phaseolus vulgaris L. timing of bud growth following decapitation

Summary On intact, 3-week-old plants of Phaseolus the larger bud in the axils of the primary leaves shows slow, continuous elongation growth. Release from correlative inhibition can be detected within 30 min following decapitation. When 0.1% indoleacetic acid in lanolin is applied to the decapitated stem stump, the lateral bud shows slow growth during the first 7 h, then stops completely for a further 15 h but after 2 days a further gradual increase in length is observed.The movement of ¹⁴C-labelled assimilates from the subtending primary leaf into the lateral bud increases following removal of the shoot apex. When indole acetic acid is applied to decapitated plants the ability of the buds to import ¹⁴C increases for 5–7 h and then declines to a negligible amount. Little or no radioactivity from tritiated indoleacetic acid is transported into the lateral buds of decapitated plants during the first 48 h following removal of the apex and it appears that rapid metabolism of the compound occurs in the stem tissues.     

Ethylene and auxin-induced cell growth in relation to auxin transport and metabolism and ethylene production in the semi-aquatic plant,Regnellidium diphyllum

Cell elongation in the rachis of the semiaquatic fern Regnellidium diphyllum is induced by the addition of ethylene or indoleacetic acid (IAA). Experiments with whole plants or rachis segments have shown that ethylene-induced growth requires the presence of auxin. Ethylene does not cause a modification in either endogenous auxin levels or in the extent of auxin metabolism but auxin transport is reduced. Rates of ethylene production in Regnellidium are not altered by either mechanical excitation or by the addition of auxin. A two-hormone control of cell expansion is proposed in which an initial, auxin-dependent growth event pre-conditions the cells to a further subsequent (or synchronous) ethylene-dependent growth event.Abbreviation IAA indole-3yl-acetic acid     

COMPARATIVE STUDY ON EARLY ONTOGENY OF COMPOUND LEAVES IN LARDIZABALACEAE

The early ontogeny of the pinnately, palmately, and ternately compound leaves in the Lardizabalaceae was studied by SEM. The leaf primordium of each of the three leaf types emerges as an identical short protrusion on the shoot apex; the leaf primordium produces the first leaflet initials laterally on its margin. Successive acropetal growth of the leaf axis and the following inception of the leaflet primordia are responsible for the pinnately compound leaf, whereas short basipetal growth accompanied with initiation of two or more pairs of leaflet initials results in a palmately compound leaf. If no elongation of the leaf axis nor additional inception of leaflet primordia occur during early ontogeny, a ternate leaf ensues.