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.     

Arrangement of cortical microtubules in the shoot apex of Vinca major L.

The arrangements of cortical microtubules (MTs) and of cellulose microfibrils in the median longitudinal cryosections of the vegetative shoot apex of Vinca major L., were examined by immunofluorescence microscopy and polarizing microscopy, respectively. The arrangement of MTs was different in the various regions of the apex: the MTs tended to be arranged anticlinally in tunica cells, randomly in corpus cells, and transversely in cells of the rib meristem. However, in the inner layers of the tunica in the flank region of the apex, cells with periclinal, oblique or random arrangements of MTs were also observed. In leaf primordia, MTs were arranged anticlinally in cells of the superficial layers and almost randomly in the inner cells. Polarizing microscopy of cell walls showed that the arrangement of cellulose microfibrils was anticlinal in tunica cells, random in corpus cells, and transverse in cells of the rib meristem; thus, the patterns of arrangement of microfibrils were the same as those of MTs in the respective regions. These results indicate that the different patterns of arrangement of MTs and microfibrils result in specific patterns of expansion in the three regions. These differences may be necessary to maintain the organization of the tissues in the shoot apex.Abbreviations MT(s) microtubule(s) - lp length of the youngest leaf primordium     

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.     

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.     

THE DEVELOPMENTAL ANATOMY OF LONG-BRANCH TERMINAL BUDS OF PINUS BANKSIANA

A study of the composition of long-branch terminal buds (LBTB) of Pinus banksiana Lamb. and the yearly periodicity associated with their formation, development, and elongation was undertaken. Each LBTB has lateral bud zones and zones of cataphylls lacking axillary buds. When present, staminate cone primordia differentiate from the lowest lateral buds in the lowest lateral bud zone of the LBTB. Ovulate cone primordia and lateral long-branch buds can differentiate from the upper lateral buds in any lateral bud zone. When both types of buds are present, lateral long-branch buds are uppermost. Dwarf-branch buds occur in all lateral bud zones. During spring LBTB internodes elongate, new cataphylls are initiated, dwarf branches elongate, needles form and elongate, pollen forms and is released, and ovulate cones are pollinated. During summer buds form in the axils of the newly formed cataphylls. By early fall the new LBTB are in overwintering condition and the four types of lateral buds are discernable. The cytohistological zonation of the LBTB shoot apex is similar to that of more than 20 other conifer species. Cells in shoot apices of pine are usually arranged in distinct zones: apical initials, subapical initials, central meristem, and peripheral meristem. Periclinal divisions occur in the surface cells of the apex; therefore no tunica is present. At any given time, shoot apex volume and shape vary among LBTB in various positions on a tree. In any one LBTB on a tree, shoot apex shape changes from a low dome during spring to a high dome during summer to an intermediate shape through fall and winter.     

LEAF DEVELOPMENT IN THE NORMAL AND SOLANIFOLIA MUTANT OF TOMATO (LYCOPERSICON ESCULENTUM)

Leaf development in the normal (lobed margin) and the solanifolia (sf/sf) mutant (entire margin) of tomato (Lycopersicon esculentum) was compared at the light and scanning electron microscope levels. The shoot apices of the mutant plants contained microbodies near the axil of the youngest leaf, which were absent in the normal plants. The structural and morphological events in the initiation of leaf primordia were similar in the two genotypes. The pattern of leaflet emergence was also similar in the two types of plants, but the timing of leaflet production was different. The first pair of leaflet primordia in the normal plants was produced on P₃, whereas in the mutant it was not produced until P₅. The adult leaves of sf/sf plants were larger than those of normal, and the greater leaf area in the mutant was associated with a greater adaxial epidermal cell and areole area. A continuous marginal fimbriate vein (MFV) was present along the margin of each of the normal leaflets. However, a continuous MFV was absent in the mutant leaflets. It is suggested that the absence of a continuous MFV in the mutant might alter the nutritional and hormonal supply to the leaf margin, which ultimately leads to a modified leaf, i.e., with an entire margin.     

Growth and Development of the Banana Plant: II. The Transition from the Vegetative to the Floral Shoot in Musa acuminata cv. Gros Michel

The changes that occur in the shoot apex of the banana, as itpasses from the vegetative to the flowering stage, are described.The crucial events occur well before floral primordia are evident,and they require a redistribution of activity in the variousgrowing regions. The vegetative shoot apex is in a central depressionin the rhizome; there is virtually no internodal growth in theaxis, the most active growth is in the leaf bases; vegetativebuds do not form in the leaf axils but only appear adventitiouslyfar from the tip of the shoot. With the onset of flowering thisis changed; growth in the axis itself, previously suppressed,occurs and flower buds arise as primordia in the axils of subtendingbracts. The bracts do not show the market growth in their baseswhich is so characteristic of leaves. Thus, the shoot apex risesto the level of the rhizome and then above it; as it does so,its tip changes in shape from a broad flattened some to a pointedcone. At the transitional stage, more activity occurs in thecells of the mantle, or tunica, which now consists of 3 to 4layers over the central dome. Below, in the central or mothercell zone of the corpus, which was quiescent in the vegetativeshoot, the cells spring into greater activity, becoming moreprotoplasmic and stain more deeply. Directly below this regionin the rib meristem, cells show transverse divisions. Bractprimordia occur high on the flanks of the apex, and, thoughthey originate in the manner of leaves, their subsequent growthis different. Flower primordia occur even in the axils of bractsclose to the shoot tip. Thus, the problem now is to designatethe source, nature, and mode of action of the stimuli whichinitiate and control this quite different distribution of growthin the floral, as contrasted with the vegetative, shoot. Thesignificance of the previously more quiescent central, or mothercell zone, of the apex as the source of such stimuli, is stressed.Thus, flowering first requires that the limiting controls whichapply to the vegetative shoot be released, and, secondly, thatthe apex of the shoot, rather than the leaf base, becomes themain centre of growth and development.     

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.     

EARLY LEAF ONTOGENY AND THE SHOOT APEX OF COLOPHOSPERMUM MOPANE (LEGUMINOSAE)

Shoot tips of Colophospermum mopane (Kirk ex Benth.) Kirk ex Léonard produce leaves which at maturity are bifoliate and devoid of stipules. Investigation of their early ontogeny, however, shows that these leaves begin as trifoliate structures partially enclosed by their stipules. The latter are fused along their mid regions, forming a tongue-like “connector.” The lower chamber of this stipule pair harbors the apical meristem while the upper compartment enfolds the two lateral leaflets. The terminal leaflet, histologically resembling the stipules, also fulfills a similar function by covering the top portion of its sister leaflets. Anatomically, the shoot apex displays a pendulum symmetry, with rather steep elevation of that internode portion which subtends the newly formed primordium. Some comparisons with the shoot apex of Hymenaea are drawn.     

STRUCTURAL AND HISTOLOGICAL STUDIES OF THE CAMBIUM AND SHOOT MERISTEMS OF SOYBEAN TREATED WITH 2,3,5-TRIIODOBENZOIC ACID

Flowering soybeans were sprayed at the tips with 50 ppm TIBA. Microscopic and macroscopic observations were made of the nodes, internodes, and shoot meristems every week for 4 wks after TIBA treatment. TIBA-treated plants produced open flowers at the upper nodes 1 week earlier than did control plants. Accompanying this early flower development, the following changes occurred in the upper internodes, as compared to controls: (a) increased activity of the procambium; (b) rapid development of thick-walled protophloem cells; (c) production of small vessels. Three weeks after treatment middle internodes of treated plants showed less cambial activity than did corresponding internodes of controls. The changes in the middle internodes of treated plants suggest a close correlation with increased flowering. Two weeks after treatment some lateral shoot apices at nodes nearest the main shoot apex exhibited the following changes, in contrast with controls: (a) development of conical apices with stack-of-brick-like peripheral cells; (b) shrinkage of protoplasmic contents in some rib meristem cells and young pith cells; (c) frequent thickening of primary walls in young pith cells. Three weeks after treatment cells of lateral shoot meristems with conical axillary buds showed a denser stain for protein than did cells of corresponding meristems of controls. Floral apices in these meristems also stained more densely for protein than did similar apices in control plants. Together with early flower production in the upper nodes of treated plants, less starch occurred 2–3 weeks after treatment than in corresponding nodes of controls. Two to three weeks after treatment lateral shoot apices of both treated and control plants had numerous, large starch grains in the rib meristem, young pith, leaf and bud primordia, and developing flowers but few starch grains appeared in the tunica, corpus, and procambium.     

ANATOMY AND ASPECTS OF DEVELOPMENT OF THE STAMINATE INFLORESCENCES AND FLORETS OF SEVEN SPECIES OF ALLOCASUARINA (CASUARINACEAE)

The morphology, ontogeny, and vascular anatomy of the staminate inflorescences and florets of seven species of Allocasuarina are described. The generally terminal but open-ended inflorescences occur on monoecious or staminate dioecious trees and consist of whorls of bracts, each subtending a sessile axillary floret. Each floret consists of one terminal stamen with a bilobed, tetrasporangiate anther enclosed typically by cuculliform appendages, commonly considered bracteoles, an inner median pair and an outer lateral pair. The mature stamen is exerted, the anther is basifixed and is extrorsely dehiscent. In early development of a male inflorescence very little internodal elongation occurs and enclosing cataphylls appear. The inflorescence apex is a low dome with a uniseriate tunica and a small group of central corpus cells. Bract primordia are initiated by periclinal divisions of C₁ followed by further divisions of the corpus and anticlinal divisions in the tunica. The bracts are epinastic and become gamophyllous except apically by cell divisions in both sides of each primordium. Stomata are restricted to the axis furrows and the abaxial tips of the bracts. The axillary florets arise in acropetal succession initiated by periclinal divisions in C₁ accompanied by anticlinal divisions in the tunica. The lateral floral appendages are also initiated by C₁ followed by anticlinal divisions in the tunica. They become adnate basally later with the subtending bract. The median sterile appendages are initiated in a manner similar to the initiation of the outer appendages. The stamen is initiated by divisions in the outer layers of the corpus and in the tunica, and then develops first by apical growth followed by intercalary growth. The vascular system of the inflorescence is identical to that of the vegetative stem. Each floret is supplied by a single bundle that has its source in a branch from each of the two traces supplying a bract. Six bundles arise from the floral bundle; four of these terminate in the base of the stamen and two form an amphicribal bundle that supplies the anther. Pollen is binucleate, 3- to 7-porate. The exine is tegillate.     

MORPHOLOGY AND VASCULATURE OF THE LEAF OF POTATO (SOLANUM TUBEROSUM)

The leaf and stem of the potato plant (Solanum tuberosum L. cv. Russet Burbank) were studied by light microscopy to determine their morphology and vasculature; scanning electron microscopy provided supplemental information on the leaf's morphology. The morphology of the basal leaves of the potato shoot is quite variable, ranging from simple to pinnately compound. The upper leaves of the shoot are more uniform, being odd pinnate with three major pairs of lateral leaflets and a number of folioles. The primary vascular system of the stem is comprised of six bundles, three large and three small ones. The three large bundles form a highly interconnected system through a repeated series of branchings and arch-producing mergers. Two of the three large bundles give rise to short, lateral leaf traces at each node. Each of the small bundles in the stem is actually a median leaf trace which extends three internodes before diverging into a leaf. The three leaf traces enter the petiole through a single gap; thus the nodel anatomy is three-trace unilacunar. Upon entering the petiole, each of the laterals splits into an upper and a lower lateral. Whereas the upper laterals diverge entirely into the first pair of leaflets, the lower laterals feed all of the lateral leaflets through a series of bifurcations. Prior to their entering the terminal leaflet, the lower laterals converge on the median bundle to form a single vascular crescent which progresses acropetally into the terminal leaflet as the midvein, or primary vein. In the midrib, portions of the midvein diverge outward and continue as secondaries to the margin on either side of the lamina. Near the tip of the terminal leaflet, the midvein consists of a single vascular bundle which is a continuation of the median bundle. Six to seven orders of veins occur in the terminal leaflet.     

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.     

Acropetal leaflet initiation of Eschscholzia californica is achieved by constant spacing of leaflets and differential growth of leaf

In compound leaves, leaflet primordia are initiated directionally along the lateral sides. Our understanding of the molecular basis of leaflet initiation has improved, but the regulatory mechanisms underlying spatio-temporal patterns remain unclear. In this study, we investigated the mechanisms of acropetal (from the base to the tip) progression of leaflet initiation in Eschscholzia californica. We established an ultraviolet-laser ablation system to manipulate compound-leaf development. Local ablation at the leaflet incipient site generated leaves with asymmetric morphology. In the majority of cases, leaflets that were initiated on the ablated sides shifted apically. Finite time-course observation revealed that the timing of leaflet initiation was delayed, but the distance from the leaf tip did not decrease. These results were suggestive of the local spacing mechanism in leaflet initiation, whereby the distance from the leaf tip and adjacent pre-existing leaflet determines the position of leaflet initiation. To understand how such a local patterning mechanism generates a global pattern of successive leaflet initiation, we assessed the growth rate gradient along the apical–basal axis. Our time-course analysis revealed differential growth rates along the apical–basal axis of the leaf, which can explain the acropetal progression of leaflet initiation. We propose that a leaflet is initiated at a site where the distances from pre-existing leaflets and the leaf tip are sufficient. Furthermore, the differential growth rate may be a developmental factor underlying the directionality of leaflet initiation.     

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.     

ONTOGENY OF THE INFLORESCENCE IN CHENOPODIUM ALBUM

Gifford , Ernest M., Jr ., and Herbert B. Tepper . (U. California, Davis.) Ontogeny of the inflorescence in Chenopodium album. Amer. Jour. Bot. 48(8): 657–667. Illus. 1961.—Chenopodium album, a short-day plant, was induced to flower by subjecting it to successive cycles of 7 hr light and 17 hr darkness. After 4 inductive days, the first macroscopic change is evident in the appearance of precocious axillary bud primordia. After 5–6 days, a primordial inflorescence is visible, and after 7–8 days a terminal flower appears on the main inflorescence axis. The vegetative apex has a biseriate tunica, the cells of which are larger than those of the corpus. The cells of the tunica stain lighter, possess larger nucleoli, and are more vacuolate than cells of the subjacent corpus. After photoinduction, the tunica-corpus organization is maintained, and after 4 short-days, the shoot apex possesses a mantle of 3–4 layers of cells because there are few periclinal divisions in the cells of the outer corpus. The cells of the mantle stain uniformly and are more chromatic than those of the underlying tissue. Mitotic activity was recorded in the upper 40-μ segment of the apex. In the vegetative apex, mitotic activity is greater in the lower portion of the segment. Following photoinduction, mitoses increase throughout the apex until a maximum is reached on the 4th day. Also, the plastochronic interval decreases after photoinduction. Nucleoli of cells of the corpus enlarge following induction until all nucleoli of the apex are nearly equal. Included in the paper are discussions of the general morphological differences between vegetative and flowering shoots.     

Shoot apex,leaf development and unifacial tip inAgave wightii drumm. et prain (agavaceae)

The shoot apex has one tunica layer enclosing a mass of corpus which is differentiated cytohistologically into central mother cell zone, flank zone, rib zone and a ‘cambium-like’ zone. Occurrence of ‘cambium-like’ zone during minimal phase is considered as an expression of nodal region. Agave wightii shows spirodistichous arrangement of leaves which have an expanded photosynthetic surface with a reduced unifacial tip. Leaves are initiated by periclinal divisions in the second layer. Vertical growth in the leaves is by subapical initials and lateral growth is by marginal and submarginal initials in their early stages of development. The unifacial tip is formed by the extension of adaxial meristematic activity. The derivatives thus formed are pushed to the abaxial side of the primordiuj. Hence the unifacial part of the leaf is regarded as equivalent to a phyllode.     

DOSAGE EFFECTS OF THE LANCEOLATE GENE IN TOMATO

In contrast to the odd-pinnately compound leaf of the normal (+/+) tomato plant (Lycopersicon esculentum), the single-gene mutant lanceolate (La/+) generally has a simple leaf. Lanceolate plants, also, have small fruits and flowers, weak apical dominance, and exhibit variation in the position and fusion of cotyledons. Homozygous mutants (La/La) appear in 3 different phenotypes, 1 of which, narrow, has narrow simple leaves, sterile inflorescences, and extremely weak apical dominance. The other 2, modified, and reduced, lack an organized shoot. After selfing La/ + plants for 9 generations, autotetraploids were produced with the aid of colchicine. In addition, several triploid plants arose spontaneously. The study of diploid, triploid, and tetraploid material with various proportions of the La allele revealed in many characters a graded series as a function of the La dosage. With increasing La dose, there was a gradual reduction in: (1) total leaf length; (2) the number and size of primary and secondary lateral leaflets; (3) the number and size of marginal lobes of the terminal leaflet, associated with an increase in the proportional length of the terminal leaflet. Many leaves were found with the basal lobes of the terminal leaflet resembling incompletely separated lateral leaflets. The differences in leaf shape between different genotypes came about before the leaf primordium was 3 mm long. There was a progressive delay in the initiation of lateral primordia with increasing La dosage. It is proposed that the gradual changes from compound to simple leaves with increasing La dosage are produced by successively greater restrictions of meristematic activity after the terminal leaflet is formed. With increasing proportion of La alleles, the reproductive structures showed: (1) a decrease in the number of flowers per inflorescence; (2) a decrease in the length of the sepals; (3) an increase in the proportion of flowers with dialytic anthers. Dialytic anthers had narrow adaxial lobes and were frequently twisted along their main axes. The common denominator for most trends affected by the La allele seems to be a general reduction of growth, but more so in lateral than in longitudinal growth. Histological data suggest that the reduction in lateral growth is mainly brought about by a reduction of cell division in lateral meristems.     

Some Aspects of Floral Histogenesis in Bajra (Pennisetum typhoides S. & H.)

The young reproductive apex in Bajra (Pennisetum typhoides S.& H.) possesses a biseriate tunica and a massive corpus.The cells of three or four peripheral layers and six to eightlayers at the summit of the apex are eumeristematic. The centralregion consists of elongated, highly vacuolated, and lightlystained cells arranged in files. The initiation of the spikeletbud is by periclinal divisions first in the corpus and laterin T₂ cells. Similarly the longer bristle or the extension ofthe fascicular axis develops from the corpus and T₂ cells. Theother bristles develop from the tunica layers. The chaff membersare initiated and develop like a leaf. The development of thestamen resembles that of a spikelet or an axillary bud. Thedevelopment of the carpel is similar to that of the leaf primordium.The origin and development of the male flower is like that ofan axillary bud.