Morphology and development of the primary and accessory buds of Eucalyptus regnans

1972 ◽  
Vol 20 (2) ◽  
pp. 175 ◽  
Author(s):  
KW Cremer

The vegetative axillary buds of Eucalyptus regnans F. Muell. at various ages were studied by light microscopy in serial sections and by direct observations in the field and glasshouse. All buds (except the very first apical bud) originated from axillary meristems, i.e. from generative tissue which arose in the axils of primordial leaves and survived in a meristematic condition for many years. Each axillary meristem normally produced one emergent primary bud and then an indefinite sequence of concealed accessory buds. The extensive dynamic shoot-system condensed within a primary bud comprised secondary as well as tertiary axes and their respective appendages. All parts were present throughout the year in a continuous sequence of maturation which extended also to the expanding shoot. During winter, development appeared to be merely slowed down or suspended. Primary buds which did not grow into shoots were shed after only a few weeks. The accessory buds were formed in a uniserial descending series at the base of and abaxial to each primary axillary bud. The first of the accessory buds was initiated within the primary bud, and the second within the expanding shoot. The first accessory bud resembled young primary buds in structure, but subsequent accessory buds were less and less complex. Keeping pace with the cambium, the axillary meristem formed a radial trace of thick-walled parenchyma in the wood and accessory buds embedded in a strand of thin-walled parenchyma in the bark. The distal portions of the bud strand and the buds embedded in it were shed progressively with the decorticating bark. Each of the bud strands which traversed the bark of 20-year-old E. viminalis Labill. was found to contain six to 12 radial strips of meristematic tissue. When epicormic growth was stimulated, several of these strips produced files of separate, new, condensed shoots. Of the scores of shoots thus initiated throughout the length of the bud strand, up to 10 or 20 of the distal ones emerged from the bark and grew into epicormic shoots. The buds of 20 other eucalypt species were examined by dissecting microscope only. It appeared that their bud systems were essentially similar to that of E. regnans. The widened concept of the axillary meristem shifts attention from individual buds to the continuous generative powers of the axillary meristem and helps to explain the outstanding capacity of the eucalypts to produce new shoots.

Development ◽  
2001 ◽  
Vol 128 (15) ◽  
pp. 2881-2891 ◽  
Author(s):  
Paula McSteen ◽  
Sarah Hake

Organogenesis in plants is controlled by meristems. Shoot apical meristems form at the apex of the plant and produce leaf primordia on their flanks. Axillary meristems, which form in the axils of leaf primordia, give rise to branches and flowers and therefore play a critical role in plant architecture and reproduction. To understand how axillary meristems are initiated and maintained, we characterized the barren inflorescence2 mutant, which affects axillary meristems in the maize inflorescence. Scanning electron microscopy, histology and RNA in situ hybridization using knotted1 as a marker for meristematic tissue show that barren inflorescence2 mutants make fewer branches owing to a defect in branch meristem initiation. The construction of the double mutant between barren inflorescence2 and tasselsheath reveals that the function of barren inflorescence2 is specific to the formation of branch meristems rather than bract leaf primordia. Normal maize inflorescences sequentially produce three types of axillary meristem: branch meristem, spikelet meristem and floral meristem. Introgression of the barren inflorescence2 mutant into genetic backgrounds in which the phenotype was weaker illustrates additional roles of barren inflorescence2 in these axillary meristems. Branch, spikelet and floral meristems that form in these lines are defective, resulting in the production of fewer floral structures. Because the defects involve the number of organs produced at each stage of development, we conclude that barren inflorescence2 is required for maintenance of all types of axillary meristem in the inflorescence. This defect allows us to infer the sequence of events that takes place during maize inflorescence development. Furthermore, the defect in branch meristem formation provides insight into the role of knotted1 and barren inflorescence2 in axillary meristem initiation.


2015 ◽  
Vol 7 (4) ◽  
pp. 471-474
Author(s):  
Owk ANIEL KUMAR ◽  
Songa RAMESH ◽  
Sape SUBBA TATA

An optimal plant propagation method of Physalis angulata L., a medicinally important herbaceous plant species has been developed using axillary meristem explants. Shoot bud proliferation was initiated from axillary meristem explants cultured on MS medium supplemented with various concentrations of 0.5-2.5mg/L/(BAP)/(Zeatin)/(KIN). The maximum in vitro response of shooting frequency of explants (88.1%) and shoots per explant (42) was achieved with medium containing 1.0mg/L BAP. Multiple shoot culture was established by repeated subculturing of the shoot buds of axillary meristems on shoot multiplication medium. Among the subculture media BAP in combination with 1.5mg/L (IAA)+0.25mg/L(GA3) produced maximum shoots per explant (128±0.29) after two weeks of culture. Effective in vitro shoot elongation and rooting was achieved on 1.0mg/L(GA3) and 1.0mg/L(IBA), respectively. Most of the generated shoots were successfully transferred to soil under field conditions. The survival percentage of the transferred plants on soil was found to be 90 per cent.  This protocol can be used for commercial propagation and for future genetic improvement studies.


Development ◽  
1996 ◽  
Vol 122 (5) ◽  
pp. 1535-1544 ◽  
Author(s):  
D. Bradley ◽  
C. Vincent ◽  
R. Carpenter ◽  
E. Coen

The presentation of flowers on a modified stem, the inflorescence, requires the integration of several aspects of meristem behaviour. In Antirrhinum, the inflorescence can be distinguished by its flowers, hairy stem, modified leaves, short internodes and spiral phyllotaxy. We show, by a combination of physiological, genetical and morphological analysis, that the various aspects of the inflorescence are controlled by three pathways. The first pathway, depends on expression of the floricaula gene, and is rapidly and discretely induced by exposure to long daylength. Activation of this pathway occurs in very young axillary meristems, resulting in a floral identity. In addition, the length of subtending leaves and hairiness of the stem are partially modified. The second pathway affects leaf size, internode length, and stem hairiness, but does not confer floral meristem identity. This pathway is induced by long daylength, but not as rapidly or discretely as the floricaula-dependent pathway. The third pathway controls the switch in phyllotaxy from decussate to spiral and is activated independently of daylength. The coordination of these three programmes ensures that apical and axillary meristem behaviour is integrated.


HortScience ◽  
2001 ◽  
Vol 36 (6) ◽  
pp. 1049-1052 ◽  
Author(s):  
Richard K. Schoellhorn ◽  
James E. Barrett ◽  
Carolyn A. Bartuska ◽  
Terril Nell

Effects of heat stress on viable and nonviable axillary meristem development and subsequent lateral branching in 'Improved Mefo' chrysanthemum [Dendranthema ×grandiflorum Ramat. (Kitamura)] were studied. Plants grown at 33 °C day/27 °C night produced more nonviable buds than did plants grown at 23 °C day/18 °C night. A negative linear relationship {y = 28.7 + [-0.66 (x days)], r2 = 0.70} between timing of exposure to high temperatures and the number of nonviable buds was observed. Histological examination 28 days after exposure to 33 °C/27 °C revealed that plants showed both normal and abnormal bud development. Abnormal bud development occurred as a consequence of premature differentiation of axillary meristematic tissue into nonmeristematic parenchyma tissue immediately after separation of axillary from apical meristems.


2020 ◽  
Author(s):  
Omid Karami ◽  
Arezoo Rahimi ◽  
Majid Khan ◽  
Marian Bemer ◽  
Rashmi R. Hazarika ◽  
...  

AbstractPost embryonic development and growth of flowering plants are for a large part determined by the activity and maturation state of stem cell niches formed in the axils of leaves, the so-called axillary meristems (AMs)1,2. Here we identify a new role for the Arabidopsis AT-HOOK MOTIF CONTAINING NUCLEAR LOCALIZED 15 (AHL15) gene as a suppressor of AM maturation. Loss of AHL15 function accelerates AM maturation, whereas ectopic expression of AHL15 suppresses AM maturation and promotes longevity in Arabidopsis and tobacco. Together our results indicate that AHL15 expression acts as a key molecular switch, directly downstream of flowering genes (SOC1, FUL) and upstream of GA biosynthesis, in extending the plant’s lifespan by suppressing AM maturation.


1986 ◽  
Vol 34 (4) ◽  
pp. 357 ◽  
Author(s):  
GE Burrows

The presence of axillary meristems in apparently blank leaf axils from the main stem of 2-year-old Araucaria cunninghamii is demonstrated. These meristems are groups of cells of meristematic appearance, which possess neither a bud-like organisation nor vascular or pro-vascular connections with the central vascular cylinder. They are first discernible in the axils of the recently initiated leaves, where each meristem is delimited from the vacuolating cortex by a shell zone. The axillary meristems then persist indefinitely in an inhibited, undifferentiated state, unless stimulated to bud formation by decapitation of the terminal shoot apex. They are exogenous in origin but are subsequently buried beneath the stem surface by the formation of localised periderms, the bark patches, and are not abscissed when extensive periderm formation begins. A. cunninghamii is apparently unique amongst conifers in possessing distinct, long-lived, exogenously initiated meristems or bud primordia in macroscopically blank leaf axils. The meristems are found in most leaf axils not occupied by branch buds. In this respect A. cunninghamii differs from most conifers and approaches the typical condition of angiosperms. The axillary meristems are inter- mediate in form between previously described vegetative axillary structures in gymnosperms and angiosperms.


2015 ◽  
Vol 112 (43) ◽  
pp. 13372-13377 ◽  
Author(s):  
Mary Galli ◽  
Qiujie Liu ◽  
Britney L. Moss ◽  
Simon Malcomber ◽  
Wei Li ◽  
...  

In plants, small groups of pluripotent stem cells called axillary meristems are required for the formation of the branches and flowers that eventually establish shoot architecture and drive reproductive success. To ensure the proper formation of new axillary meristems, the specification of boundary regions is required for coordinating their development. We have identified two maize genes, BARREN INFLORESCENCE1 and BARREN INFLORESCENCE4 (BIF1 and BIF4), that regulate the early steps required for inflorescence formation. BIF1 and BIF4 encode AUXIN/INDOLE-3-ACETIC ACID (Aux/IAA) proteins, which are key components of the auxin hormone signaling pathway that is essential for organogenesis. Here we show that BIF1 and BIF4 are integral to auxin signaling modules that dynamically regulate the expression of BARREN STALK1 (BA1), a basic helix-loop-helix (bHLH) transcriptional regulator necessary for axillary meristem formation that shows a striking boundary expression pattern. These findings suggest that auxin signaling directly controls boundary domains during axillary meristem formation and define a fundamental mechanism that regulates inflorescence architecture in one of the most widely grown crop species.


Author(s):  
J. F. DeNatale ◽  
D. G. Howitt

The electron irradiation of silicate glasses containing metal cations produces various types of phase separation and decomposition which includes oxygen bubble formation at intermediate temperatures figure I. The kinetics of bubble formation are too rapid to be accounted for by oxygen diffusion but the behavior is consistent with a cation diffusion mechanism if the amount of oxygen in the bubble is not significantly different from that in the same volume of silicate glass. The formation of oxygen bubbles is often accompanied by precipitation of crystalline phases and/or amorphous phase decomposition in the regions between the bubbles and the detection of differences in oxygen concentration between the bubble and matrix by electron energy loss spectroscopy cannot be discerned (figure 2) even when the bubble occupies the majority of the foil depth.The oxygen bubbles are stable, even in the thin foils, months after irradiation and if van der Waals behavior of the interior gas is assumed an oxygen pressure of about 4000 atmospheres must be sustained for a 100 bubble if the surface tension with the glass matrix is to balance against it at intermediate temperatures.


Author(s):  
Robert Glaeser ◽  
Thomas Bauer ◽  
David Grano

In transmission electron microscopy, the 3-dimensional structure of an object is usually obtained in one of two ways. For objects which can be included in one specimen, as for example with elements included in freeze- dried whole mounts and examined with a high voltage microscope, stereo pairs can be obtained which exhibit the 3-D structure of the element. For objects which can not be included in one specimen, the 3-D shape is obtained by reconstruction from serial sections. However, without stereo imagery, only detail which remains constant within the thickness of the section can be used in the reconstruction; consequently, the choice is between a low resolution reconstruction using a few thick sections and a better resolution reconstruction using many thin sections, generally a tedious chore. This paper describes an approach to 3-D reconstruction which uses stereo images of serial thick sections to reconstruct an object including detail which changes within the depth of an individual thick section.


Author(s):  
L.E. Murr

Ledges in grain boundaries can be identified by their characteristic contrast features (straight, black-white lines) distinct from those of lattice dislocations, for example1,2 [see Fig. 1(a) and (b)]. Simple contrast rules as pointed out by Murr and Venkatesh2, can be established so that ledges may be recognized with come confidence, and the number of ledges per unit length of grain boundary (referred to as the ledge density, m) measured by direct observations in the transmission electron microscope. Such measurements can then give rise to quantitative data which can be used to provide evidence for the influence of ledges on the physical and mechanical properties of materials.It has been shown that ledge density can be systematically altered in some metals by thermo-mechanical treatment3,4.


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