Mother trees, altruistic fungi, and the perils of plant personification.

There are growing doubts about the true role of the common mycorrhizal networks (CMN or wood wide web) connecting the roots of trees in forests. We question the claims of a substantial carbon transfer from 'mother trees' to their offspring and nearby seedlings through the CMN. Recent reviews show that evidence for the 'mother tree concept' is inconclusive or absent. The origin of this concept seems to stem from a desire to humanize plant life but can lead to misunderstandings and false interpretations and may eventually harm rather than help the commendable cause of preserving forests. Two recent books serve as examples: The Hidden Life of Trees and Finding the Mother Tree.

Wall architecture with high porosity is established at the tip and maintained in growing pollen tubes of Nicotiana tabacum.

A major question in pollen tube growth in planta remains: do the pollen tube walls form a barrier to interaction with the environment? Using cryo-FESEM, we directly assessed the 3D construction and porosity of tobacco pollen tube walls. Fractured mature primary walls showed a 40-50 nm spaced lattice of continuous fibers interconnected by short rods in the primary wall. These observations agree with TEM observations of sectioned walls. In the secondary callose wall, for which no structure is visible using TEM, cryo-FESEM also revealed a 50 nm lattice consisting of longer fibers, approximately 10-15 nm wide, with rod-like, thinner interconnections at angles of approximately 90° with the longer fibers. Such architecture may reflect functional needs with respect to porosity and mechanical strength. The wall does not form a mechanical barrier to interaction with the environment and is gained at low cost. Cryo-FESEM additionally revealed another special feature of the wall: the tubes were tiled with scales or rings that were highly conspicuous after pectin extraction with EDTA. These rings cause the typical banding patterns of pectin that are commonly seen in pollen tubes during oscillatory growth, as confirmed by staining with toluidine blue as well as by DIC microscopy. Growth analysis by VEC-LM showed that the ring- or scale-like structures of the primary wall consist of material deposited prior to the growth pulses. The alternating band pattern seen in the callose wall is probably imposed by constrictions resulting from the rings of the primary wall.

Calcium Control of Pollen Tube Tip Growth.

The role of calcium in pollen tube tip growth is reviewed. Calcium ions are essential for growth, but are inhibitory at high concentrations (above c. 10-2 M). Calcium intake is limited to the growing tip, and the inward flux of calcium appears to establish an ionic current within the surrounding medium. Cellular transport of calcium is reviewed against a background of the functional requirements for calcium ions. It is concluded that calcium-induced polarized tip growth depends on a dual control system; (1) intake through spatially localized calcium ion channels coupled with (2) cytoplasmic sequestration and transport from the tip region in organelles. This system maintains conditions appropriate for directed activity of the cytoskeleton and subsequent vesicle fusion at the growing tip.

Pollen tube tip growth.

This review considers pollen tube growth with regard to current information on pollen tube cytoplasm, wall structure and calcium ion interactions with pollen tubes. Pollen tubes have a marked cytoplasmic Polarity with a number of distinct zones along the tube, each with a characteristic complement of cytoplasmic and nuclear structures. The cytoplasmic structures are characteristic of secretory cells with extensive endoplasmic reticulum cisternae and numerous dictyosomes. The dictyosomes produce secretory vesicles that are mainly directed to the extending tip of the tube, where they provide new plasma membrane and wall components. The rates of secretory vesicle production and delivery have been estimated, allowing quantitative assessments of the rate of delivery of materials to the tip. Pollen tubes contain cytoskeletal components, with microtubules and microfilament strands lying axially in the main tube and diffuse microfilament strands at the tip. The tube wall consists of an outer fibrous layer containing pectins and an inner, more homogeneous layer containing callose and cellulose-like microfibrils, possessing both ß-1,4 and ß-1,3 linkages. Protein is also present in the wall. The tube tip lacks the inner callosic wall. This type of structure is considered to be different from that of elongating sporophyte tissue cells which are enclosed by a wall containing layers of cellulose microfibrils. Calcium ions are required for pollen tube growth and, in at least some species, act as a chemotropic agent. High concentrations of calcium ions in the external medium inhibit growth. Pollen tubes contain some calcium ions bound to the cell wall and larger amounts located intracellularly, which enter the tube at the tip. This intracellular calcium is present as ions that exist freely within the cytoplasmic Matrix and as ions bound to membrane systems. The highest concentrations in both of these pools are found at the tip and in both they decline towards the base. The structure of the tip and the activity involved in providing components for plasma membrane and Wall assembly provide a basis for considering possible mechanisms of tip growth. Two hypotheses to account for the regulation of tip extension are considered, cell wall control and cytoskeletal control. In the cell wall hypothesis, control depends on an interaction between internal turgor pressure and a plastic cell wall. The mechanical properties of the wall are assumed to be partly dependent on the availability of external calcium ions to crosslink acidic pectin chains. According to this hypothesis, high external calcium ion concentrations cause cessation of tip growth due to increased mechanical resistance of the tip wall. Various observations on plant cell-wall interactions with calcium ions and on experimentally-treated pollen tubes provide evidence that does not support this hypothesis. The cytoskeletal control hypothesis of tip growth depends on the internal tip cytoskeleton to contain the tube tip cytoplasm against the internal turgor pressure during cell wall assembly. The activities and mechanical properties of the cytoskeleton are assumed to depend on the availability of external calcium ions. High external concentrations are believed to cause a state of rigor in the cytoskeleton and hence a cessation of tip growth. Some experimental evidence is presented which suggests that the effects of excess calcium ions are on intracellular processes, and not extracellular ones. The mitochondrial zone behind the tip is believed to maintain the tip calcium ion concentration at an optimal level for growth. Some comparisons are made between tip growth in pollen tubes and that in other tip growing cells. CONTENTS Summary 323 I. Introduction 324 II. Cytoplasm 326 III. Wall structure 332 IV. Calcium 335 V. Tip growth 339 VI. Conclusions 350 References 351.