Patterns of vegetative growth and reproduction in relation to branch orders: the plant as a spatially structured population

The patterns of vegetative growth and reproduction in relation to orders of terminal branches were examined in the evergreen woody plant, Eurya japonica. The branch order number was determined centrifugally. The trunk was given order number 1; branches issuing directly from the trunk were order 2; branches growing on order 2 branches were order 3, and so on. The results of this study show the differential patterns of vegetative growth and reproduction in relation to the branch orders. Lower-order shoots of terminal branches grew more, but produced few flowers. On the other hand, for the higher-order terminal branches, shoot growth was very limited but flowering was more intense. The results show that a tree can be interpreted not as a mere population of equivalent modules but as a spatially structured population. Thus, it is essential to consider the position of modules within the branch system when patterns of vegetative growth and reproduction are examined. It is hypothesized that the difference in the opportunity cost in relation to the branch orders is the main cause of the spatial structure for patterns of vegetative growth and reproduction. Furthermore, for same-order terminal branches, current-year shoot elongation was independent of flowering intensity. These results suggest that this species only invests resources in reproduction that are surplus to its requirements for the functions associated with survival, such as growth and/or storage. Received: 22 July 1999 / Accepted: 12 January 2000     

A detached branch stops being recognized as self by other branches of a neuron

The multiple peripheral projections of a single leech mechanosensory neuron form individual arbors that do not overlap at all with each other, a phenomenon that has been termed “self-avoidance” (Yau, 1976; Kramer and Stent, 1985). This is in marked contrast to the peripheral arbors of adjacent segmental homologues, which partially overlap with each other at their boundaries in target areas of the body wall (Nicholls and Baylor, 1968; Gan and Macagno, 1995). How a neurite differentiates between sibling neurites of the same cell and those of a homologue is not known, but possible mechanisms include the recognition of surface markers of neuronal identity or the detection of cell-specific patterns of activity. In order to test whether this self-recognition requires a neurite to be in direct communication with its soma, we used a laser microbeam to sever a branch of a dye-filled pressure-sensitive (P) neuron in an intact leech embryo. Time-lapse observations of the P cell arbor in the living, unanesthetized, animal for up to 24 h following the surgery showed that the detached branch continued to show dynamic growth behavior throughout the period of observation. However, the detached branch ceased being avoided by the rest of the cell within a few hours, other, attached branches of the neuron overgrowing its territory and directly overlapping with it. Our experiments provide direct evidence for the existence of strong growth-inhibiting interactions between sibling processes, and indicate that self-avoidance by the growing neurites of a cell requires physical continuity between these neurites. © 1998 John Wiley & Sons, Inc. J Neurobiol 35: 53–64, 1998     

Regeneration of an identifiable motoneuron in the crayfish. II. Patterns of reconnection and synaptic strength established in the presence of an extra nerve

The regeneration of neuromuscular connections to the superficial flexor muscle system in the crayfish has been studied under a variety of experimental manipulations. These have provided insight into the factors that can influence the regeneration program of neurons. In this work the regeneration of the largest excitor motoneuron was studied under two different conditions: (1) when the original neuron and a transplanted neuron were growing simultaneously into a denervated target, and (2) when a transplanted neuron was growing into a target that had its original nerve supply intact. In condition 1 both the transplanted and the original neuron formed normal patterns of connectivity and synaptic strength in comparable periods of time. In condition 2 the rate of growth of the transplanted neuron is significantly reduced and does not extend into the lateral fibers of the muscle. It is concluded that the regeneration program of this neuron is not affected by the presence of other neurons growing at the same time into a denervated muscle. Since regeneration is seriously affected if growth occurs into a fully innervated target area, it is suggested that lack of growth stimuli from the target or competitive interactions between established and growing synaptic terminals could influence the regeneration program of this neuron.     

Distribution of Cell Adhesion Molecules (CAM) along the Branching Neurite Surface: Model-Inherited Effects of the Branch Diameters and Mode of CAM Transport

In many cases, an increase in the surface density of cell adhesion molecules (CAM) in the distal parts of a growing neurite is favorable for the neurite elongation. This increase is attained by exocytotic insertion of CAM-containing vesicles into the growth cones with subsequent redistribution of CAM along the cell surface due to lateral diffusion and endocytosis. Using a mathematical model describing these processes, we quantitatively describe conditions providing two qualitatively different profiles in a branching neurite: (i) the CAM surface density increases along both daughter branches, which would be in favor of further outgrowth of both branches, i.e., successful branching, or (ii) the CAM surface density increases along one daughter branch and decreases along another branch, which could lead to the retraction of the latter. The geometric factors and mechanisms underlying the intracellular CAM transport to the daughter growth cones were proved to determine the profile of CAM surface density. A similarity in the diameters of daughter branches, their short lengths, a high value of the lateral transfer constant, and partitioning of CAM transport at the branching point proportionally to the surface areas of daughter branches are in favor of an increase in the CAM surface density along both daughter branches. Asymmetric branching can lead to a decrease in the CAM surface density along the thinner or thicker daughter branch, if CAM trafficking was equally partitioned or was proportional to the branch cross-sectional areas, respectively. The proposed model helps to understand possible relationships between the intracellular CAM trafficking, CAM surface distribution, and geometry of branching of the neurites.     

Disruption of peripheral target contact influences the development of identified central dendritic branches in a leech motor neuron in vivo

Retrograde signaling from target tissues has been shown to influence many aspects of neuronal development in a number of developmental systems. In these experiments using embryonic leeches (Hirudo medicinalis), we examined how depriving a neuron of contact with its peripheral target affects the development of the cell's central arborization. We focused our attention on the motor neuron cell 3, which normally stimulates dorsal longitudinal muscle fibers to contract. At different locations in the periphery and in embryos of several different stages, we cut the nerve containing the growing axon of cell 3. This surgery led to dramatic overgrowth of cell 3's central dendritic branches, which normally accept synaptic contacts from other neurons, including the inhibitory motor neuron cell 1. When cell 3's peripheral axon was cut relatively early in development, its overgrown central branches eventually retracted. However, cells that were disrupted later in development retained their overextended branches into adulthood. In addition, if the axon was cut close to the ganglion early in development, depriving the cell of contact with any dorsal tissues, the central branches failed to retract and were instead retained into adulthood. Unlike cell 3, the central branches of cell 1, which has the same peripheral target muscles as cell 3, remained unchanged following all axotomy protocols. These results suggest that in at least some neurons contact with peripheral targets can influence development of the central processes that normally mediate synaptic contacts.     

Stages in axon formation: observations of growth of Aplysia axons in culture using video-enhanced contrast-differential interference contrast microscopy

The regenerative growth in culture of the axons of two giant identified neurons from the central nervous system of Aplysia californica was observed using video-enhanced contrast-differential interference contrast microscopy. This technique allowed the visualization in living cells of the membranous organelles of the growth cone. Elongation of axonal branches always occurred through the same sequence of events: A flat organelle-free veil protruded from the front of the growth cone, gradually filled with vesicles that entered by fast axonal transport and Brownian motion from the main body of the growth cone, became more voluminous and engorged with organelles (vesicles, mitochondria, and one or two large, irregular, refractile bodies), and, finally, assumed the cylindrical shape of the axon branch with the organelles predominantly moving by bidirectional fast axonal transport. The veil is thus the nascent axon. Because veils appear to be initially free of membranous organelles, addition of membrane to the plasmalemma by exocytosis is likely to occur in the main body of the growth cone rather than at the leading edge. Veils almost always formed with filopodial borders, protruding between either fully extended or growing filopodia. Therefore, one function of the filopodia is to direct elongation by demarcating the pathway along which axolemma flows. Models of axon growth in which the body of the growth cone is pulled forward, or in which advance of the leading edge is achieved by filopodial shortening or contraction against an adhesion to the substrate, are inconsistent with our observations. We suggest that, during the elongation phase of growth, filopodia may act as structural supports.     

Developmental responses of individual Onobrychis plants to spatial heterogeneity

An experimental study was undertaken to assess the extent to which better-situated branches correlatively inhibit other branches on the same plant which are growing in relatively inferior conditions. The experiments were carried out on naturally-grown Onobrychis squarrosa L. (Papilionaceae), a dominant annual plant of the Mediterranean region of Israel. Treatments were carried out (i) on young plants that only had a seminal shoot, and (ii) on plants after lateral branches had started growing. Differential shade conditions were achieved by the repeated removal of neighbours on one side of the plants. The plants were either left intact or damaged by removing different parts of their branch system. In intact plants, growth responses to the differential light conditions which were expressed by the number of branches, leaves and fruits showed some evidence for support of the shaded branches by the exposed branches on the same plant. In contrast, heterogeneous treatments of both shade and branch damaging led to development that reflected marked correlative inhibition of the shaded parts of the plant. The results show that a latent potential for correlative inhibition between branches exists throughout plant development and that in Onobrychis it can be readily realised when plants are damaged. This could depend on known traits of auxin acting as a correlative signal of growing branches. The observed responses of Onobrychis can be understood as an adaptive strategy which reflects the low reliability of environmental signals and the high cost of changing the course of development, especially in short-lived annual plants.     

Bathymetric adaptations of reef-building corals at davies reef,great barrier reef,Australia. I. Long-term growth responses of Acropora formosa (Dana 1846)

In situ rates of linear growth (branch extension) were measured for Acropora formosa (Dana) at depths of 5, 10, and 15 m. Estimates of radial branch growth and internal accretion were made at the shallowest and deepest sites. In addition, reciprocal transplant experiments between these two sites were conducted using branches of different lengths. The in situ results showed that individual branches at the deep site extended twice as fast, and deposited more calcium carbonate than branches at the shallow site. Branch initiation, however, was more rapid at the shallow site. Thus, if the extension of new lateral branches were included to obtain a measure of overall growth, rates were highest at the shallow site. The initial length of the transplanted branches significantly affected growth rates. Longer branches showed greater overall growth within all treatments. Branch extension rates, however, increased with initial branch length at the deep site, while tending to remain constant at the shallow site. This result is interpreted as evidence that the extension of each branch tip at the deep site was supported by translocated metabolites derived from a greater volume of zooxanthellae-bearing tissue than at the shallow site. A. formosa exhibits different growth patterns at different depths. At the deep site, extension is favoured over branch initiation. Consequently, translocation from a greater volume of tissue is presumably available to sustain the higher extension rate at each tip. At the shallow site, where extension is less rapid but branch initiation is more rapid, each tip probably receives translocate from a smaller volume of tissue. These mechanisms result in different growth forms at the two sites and are apparently adaptations to different environmental conditions. Light or water motion, or a combination of the two are proposed as probable controlling factors.     

Wind-acclimated thallus morphogenesis in a lichen (Evernia prunastri, Parmeliaceae) probably favored by grazing

How does the morphogenesis of a widespread epiphytic lichen interact with the environment, leading to amazingly polymorphic and wind-tolerant fruticose thalli? A series of photographs showed that the normal branches were basically even and flat with isotomic-dichotomous branchings. Numerous deviations from this basic regular pattern were found and traced back to their origins in the asymmetry of the branches’ cross sections. This was observed quantitatively (statistically testable) in the field, while the thalli were growing. This large variability in growth of single branches was a prerequisite for the polymorphism seen in complete thallus growth forms. The structure and distribution of the mentioned important asymmetries in branch cross sections can best be explained by the effect of grazing on cortex and phycobiont layer. Very small-scale growth observations and experimental simulation confirmed this. In thalli with many such small-scale variations in branch growth the overall thallus growth form became wind acclimated as a result of the selective effect of wind exposure on the thallus phenotype: branches growing windwardly grew more slowly. Such thalli were well protected from being dislodged by wind, and they desiccate slowly as demonstrated by a previous study.     

Apical control of branch growth and angle in woody plants

Apical control is the inhibition of a lateral branch growth by shoots above it (distal shoots). If the distal shoots are cut off to remove apical control, the lateral branch can grow larger and may bend upwards. Apical control starts when new lateral buds grow after passing through a period of dormancy. Buds initially break and produce leaves, then apical control is exerted and the lower (proximal) laterals stop growing. Apical control also inhibits growth of large, old branches. Gravimorphism and restricted water and nutrient transport can inhibit branch growth, but they are not primary mechanisms of apical control. Apical control may reduce branch photosynthesis. Under apical control allocation of branch-produced assimilate to the stem is relatively high, so low assimilates in the branch may limit branch growth even though hormone levels are adequate for growth. Hormones appear to be involved in apical control, but it is not known how. One role of hormones may be to maintain the strength of the stem sink for branch-produced assimilate. Upward bending of a woody branch after release from apical control requires both new wood production and production of wood cells that can generate an upward bending moment. Apical control inhibits radial growth of branches and, in some species, may regulate the production of wood with an upward bending moment.     

Size structure of current-year shoots in mature crowns

Characteristics of current-year shoot populations were examined for three mature trees of each of three deciduous broad-leaved species. For first-order branches (branches emerging from the vertical trunk) of the trees examined, lengths or diameters of all current-year shoots were measured. Total leaf mass and total current-year stem mass of first-order branches were estimated using an allometric relationship between leaf or stem mass and length or diameter of current-year stems. For each tree, the number of current-year shoots on a first-order branch was proportional to the basal stem cross-sectional area of the branch. On the other hand, first-order branches had shoot populations with size structures similar to each other. As a result, the leaf mass of a first-order branch was proportional to the basal stem cross-sectional area of the branch, being compatible with the pipe-model relationship. All current-year shoot populations had positively skewed size structures. Because small shoots have a larger ratio of leaf mass to stem mass than large shoots, first-order branches had an extremely large ratio of leaf mass to current-year stem mass. This biased mass allocation will reduce costs for current stem production, respiration and future radial growth, and is beneficial to mature trees with a huge accumulation of non- photosynthetic organs. The allometric relationships between leaf mass and basal stem diameter and that between leaf mass and current-year stem mass of first-order branches were each similar across the trees examined. Characteristics of shoot populations tended to offset inter-species diversity of shoot allometry so that branch allometry shows inter-species convergence.     

Branch development in Lupinus angustifolius L.#II. Relationship with endogenous ABA, IAA and cytokinins in axillary and main stem buds

The concentrations of indole-3-acetic acid (IAA), cytokinins (CK) and abscisic acid (ABA) were measured in buds of different regions (main stem and lateral branches) of Lupinus angustifolius L. (cv. Merrit) and at different stages in the development of branches. In lupin, branching patterns are the result of discrete regions of axillary branches (upper, middle and basal) which elongate at much different rates. Early in development only the main shoot elongates, followed usually by basal branch growth and then rapid upper branch growth. Branches in the middle of the main stem grow only weakly or fail to develop. Levels of IAA were generally high in the apical buds of slowly growing branches and low in buds from strongly growing branches, whereas CK levels showed the opposite relationship. CK:IAA ratio showed a closer relationship with the rate of growth of a particular branch better than the levels of either CK or IAA alone. During early stages of growth ABA concentration did not follow the rate of branch growth. However, later in development, where growth did not closely match the ratio of CK:IAA, ABA level showed a strong negative relationship with growth. A significant decrease in ABA was associated with continued strong growth of the main stem apex following a decline in CK:IAA ratio. Overall, the best relationship between the level of growth factors in apical buds and branching pattern in lupin was the ratio of CK:IAA, implying that high CK:IAA at a given bud would promote growth. ABA level appeared to play a secondary role, as a growth inhibitor.     

Embryonic development of the innervation of the locust extensor tibiae muscle by identified neurons: formation and elimination of inappropriate axon branches

Intracellular dye fills have been used to reveal the pattern of embryonic growth of each of the four neurons which innervate the extensor tibiae muscle (ETi) of the hind leg of the locust. The growth cone of the slow extensor tibiae motoneuron (SETi), the first of the four neurons to leave the central nervous system, pioneers nerve 3 (N3). The fast extensor motoneuron (FETi), the next neuron to grow out, follows earlier outgrowing motoneurons into the periphery in nerve 5 (N5) and then rejoins SETi in N3. As it transfers from N5 to N3, it is transiently dye-coupled to the Tr1 pioneer neuron which spans the gap between the two nerves. It then follows SETi onto the ETi muscle in the femur. The common inhibitory neuron and the dorsal unpaired median neuron (DUMETi) follow SETi and FETi in nerves 3B2 and 5B1, respectively. SETi's growth cone requires almost twice as long to reach ETi as those of the three later motoneurons, all of which follow preexisting neural pathways. At least three of the four developing motoneurons form one or more axon branches not found in the adult. These branches may occur (1) at segmental boundaries; (2) where the nerve, which the growth cone is following, itself branches or the growth cone encounters another nerve; or (3) when the axon continues to grow beyond its target muscle. These findings contrast with the apparent absence of inappropriate axon branches in another developing locust neuromuscular system and during the innervation of zebrafish myotomes, but resemble in some ways the transient production of inappropriate axonal branches reported for embryonic leech motoneurons.     

Heat Stress Induces Changes in Protein Synthesis and Fast Axonal Transport in Bullfrog Sensory Neurons

The effects of heat stress on protein synthesis and fast axonal transport were examined in an in vitro bullfrog primary afferent neuron preparation. The magnitude of effect was determined for individual [35S]methionine-labelled protein species separated via two-dimensional gel electrophoresis. Elevation of temperature of the preparation from 18 degrees C to 33 degrees C caused a transient inhibition of synthesis of non-heat-shock proteins, whereas the synthesis of a 74,000-dalton protein increased to 927% of controls after 4 h. Similar prolonged stress conditions had no effect on the relative abundance of 36 individual, newly synthesized proteins undergoing fast axonal transport. A dramatic exception was represented by a 55,000-dalton glycoprotein whose fast transport was increased to 291% of control. The increase in transport of this protein during a time when synthesis and transport of other non-heat-shock proteins were not enhanced suggests that it may play a unique role in the early cellular events that mediate survival or thermotolerance in the neuron.     

BRANCHING PATTERNS OF INDIVIDUAL SYMPATHETIC NEURONS IN CULTURE

The growth of single sympathetic neurons in tissue culture was examined with particular regard to the way in which the patterns of axonal or dendritic processes (here called nerve fibers), were formed. The tips of the fibers were seen to advance in straight lines and to grow at rates that did not vary appreciably with time, with their position in the cell outgrowth, or with the fiber diameter. Most of the branch points were formed by the bifurcation of a fiber tip (growth cone), apparently at random, and thereafter remained at about the same distance from the cell body. It seemed that the final shape of a neuron was the result of the reiterated and largely autonomous activities of the growth cones. The other parts of the cell played a supportive role but, apart from this, had no obvious influence on the final pattern of branches formed.     

Direct evidence for Ca2+ regulation of hyphal branch induction

Grinberg, A., and Heath, I. B. 1997. Direct evidence for Ca2+ regulation of hyphal branch induction. 22, 127-139. Irradiation of growing hyphae of Saprolegnia ferax with microbeams of UV (300-380 and 385-450 nm) light induced an increase in cytoplasmic [Ca2+] followed by precocious formation of one or more branches within about 4 min. The distribution of branches was strongly skewed toward the subapical side of the irradiation site, but otherwise was apparantly random. Apical (10-&mgr;m) irradiations were more effective than subapical (50-&mgr;m) ones in that they induced branches at comparable frequencies but with lower doses, consistent with higher concentrations of putative target intracellular Ca2+ storage structures in this region. Once formed, induced adjacent branches seem to compete for "resources," with those closer than approximately 50 &mgr;m inhibiting each other. The results are most consistent with Ca2+-induced accumulation of branch initiating factors being the cause, not the consequence, of branch formation, thus supporting a primary role for Ca2+ in regulation of hyphal tip growth. Copyright 1997 Academic Press. Copyright 1997 Academic Press     

Target Regulation of Axotomy-Sensitive Proteins

Large changes in the production of certain proteins often follow axotomy. How the cell body is signaled to make these changes, or terminate them after regeneration is finished, is unclear. This issue was addressed by studying an axotomized giant identified neuron, the giant cerebral neuron of the sea slug Aplysia, both in vivo and in culture. One week after axon crush in vivo, there were increases of 1.5-18-fold in the 5-h incorporation of [35S]methionine into seven proteins identified by two-dimensional gel electrophoresis. There were decreases of five- to 28-fold in the labeling of four other proteins. An axotomized giant cerebral neuron grows vigorously when placed in culture and forms chemical synapses with appropriate target cells while continuing unabated growth. The labeling of two of the proteins that up-regulate after axotomy in vivo was suppressed by the presence of target cells in culture. For one of the proteins, this effect was also produced by membranes of target cells, but not by medium conditioned by exposure to target cells. These results are consistent with the idea that loss of membrane-membrane contact with target cells (or its restoration) is involved in the initiation (or termination) of the up-regulation of certain proteins after axotomy.     

Responses of crown architecture in Betula pendula to competition are dependent on the species of neighbouring trees

We measured the growth responses of individual shoots and branches of Betula pendula when growing next to trees of the same species or Pinus sylvestris, Larix sibirica or Alnus glutinosa. We used the three-dimensionally digitized response variables and the size and distance of trees growing within a 5-m radius of the study trees to establish a relationship between tree performance and the effect of competing neighbouring tree species on crown architecture. B. pendula was able to modify its crown architecture and thus alter its strategy to compete with different neighbours. Trees of B. pendula growing beside species counterparts had the highest growth of new long shoots in relation to the already existing branch length [growth vigour (GV)], while GV was the lowest next to L. sibirica. With B. pendula or P. sylvestris as its main neighbour, B. pendula invested in short shoots by growing them rather densely in short branches with limited numbers, whereas with L. sibirica the number, length and angle of the branches were high. The competitive response was also strongly dependent on tree ontogeny and the shoot and branch characteristics were significantly affected by their location inside the crown. B. pendula was able to respond to the challenges posed by its neighbours, which was also reflected in the GV. The ability to maintain steady growth with alternative crown designs in different neighbourhoods reflects plasticity in the crown responses.     

Experimental studies of the capacity of ants for the addition and subtraction of small numbers]

In the laboratory experiments Formica polyctena ants had to transmit the information about the position of a "branch" situated on a long "trunk". Each branch ended in an empty trough, save one filled with syrup. The food was placed on different branches with different frequencies; on the preliminary chosen special branches the troughs were filled substantially more frequently than on the others. For example, in 1993 we chose two special branches, nos. 10 and 20, on which the food was placed with a probability of 1/3, while for any of the other 28 branches the probability was 1/84. When the ants had learnt this, they changed the way of information transmission about the coordinates of the branch containing food and spent less time to transmit the messages about branches nos. 10 or 20. Careful analysis of time required for transmitting messages about trough coordinates suggests that ants "present" the number of a branch in a way similar to that for the Roman figures, and the "special" numbers (10 and 20 in the case) have the same significance as the basic Roman figures V, X, L, etc. Thus, the ants seem to be able, first, to put the duration of a message into agreement with its frequency and, second, to add and subtract small numbers, as people do when use the Roman figures.     

The Paxillin-like protein AgPxl1 is required for apical branching and maximal hyphal growth in A.gossypii

The development from young, slowly growing hyphae to fast growing hyphae in filamentous fungi is referred to as hyphal maturation. We have identified the Paxillin-like protein AgPxl1 in Ashbyagossypii as a developmental protein that is specifically required for hyphal maturation. The early development of A.gossypii strains lacking AgPxl1 is indistinguishable from wild-type. However, at later developmental stages the maximal hyphal extension rate is less than half compared to wild-type and apical branching is affected. Apical branching is characterised as the symmetric division of fast growing hyphal tips resulting in two sister hyphae. In Agpxl1Delta strains two thirds of the apical branching events lead to asymmetric sister hyphae where growth of one branch is either completely aborted or slowed down while extension of the other branch is not affected. This suggests that AgPxl1 plays a role in the organisation of growth and efficient division of growth upon apical branching in mature mycelia. The conserved C-terminal LIM domains are necessary for AgPxl1 function and also contribute to tip localisation. AgCLA4, a PAK-like kinase, is epistatic to AgPXL1 and robust localisation of AgPxl1 depends on AgCla4. This suggests that AgCla4 acts upstream of AgPxl1.