Budgeting for the wood-wide web

How appropriate that at the turn of a century that has overseen a second industrial revolution in agriculture, there is an increasing appreciation of the central role played by the mycorrhizal symbiosis, first described in the latter part of the nineteenth century (Frank, 1885). Simply stated, nearly all families of plants form root symbiotic organs, termed mycorrhizas, with soil fungi belonging to all the main phyla, namely Zygomycotina, Ascomycotina, Basidiomycotina and the Fungi Imperfecti (Harley & Harley, 1987). The importance of this symbiosis in controlling plant nutrient status and growth is well established (Smith & Read, 1997), but a report in this issue now provides, long awaited, nitrogen and phosphorus budgets for mycorrhizal trees (Perez-Moreno & Read, pp. 301–309).     

Monstrous plant architecture

Monstera acuminata is a plant with a problem – it attains a large body size, yet has no secondary growth. For many years, observers have noted the differences in architecture between monocots and woody dicots, particularly in terms of overall size and comparisons of tree-like forms. However, very little is known about the functional morphology of smaller-bodied and ecologically significant climbing and hemiepiphytic monocots, of which M. acuminata is one. In its wider context, the diversity of plant growth forms contributes to the complex structure of many terrestrial ecosystems, where herbs, trees, shrubs, vines, lianas, root-climbers, epiphytes and hemiepiphytes may be said to comprise the 'skeleton' of the ecosystem (Speck & Rowe, 1999). This is seen readily, for example, in the humid tropics, which arguably possess the highest taxonomic and structural diversity that has ever been formed by plants on earth. In this issue, López-Portillo et al . (pp. 289–299) investigate the development of plant architecture in Monstera , and demonstrate a range of novel hydraulic parameters.     

Corrigendum

New Phytologist 144 (1999), 195–202
In the October 1999 issue of New Phytologist , we published the research paper entitled 'Identification and expression analysis of two fungal cDNAs regulated by ectomycorrhiza and fruit body formation' by Uwe Nehls et al . ( New Phytol . (1999) 144 , 195–202). Since its publication, the authors have identified an important error in Fig. 4: the labels SC13 and SC25 are in incorrect positions and should be transposed.
We apologise to our readers for this mistake.     

Apoplastic barriers to radial oxygen loss and solute penetration: a chemical and functional comparison of the exodermis of two wetland species, Phragmites australis and Glyceria maxima

Few studies have examined exodermal development in relation to the formation of barriers to both radial oxygen loss (ROL) and solute penetration along growing roots. Here, we report on the structural development, chemical composition and functional properties of the exodermis in two diverse wetland grasses, Glyceria maxima and Phragmites australis. Anatomical features, development, the biochemical composition of exodermal suberin and the penetration of apoplastic tracers and oxygen were examined. Striking interspecific differences in exodermal structure, suberin composition and quantity per unit surface area, and developmental changes along the roots were recorded. Towards the root base, ROL and periodic acid (H(5)IO(6)) penetration were virtually stopped in P. australis; in G. maxima, a tight ROL barrier restricted but did not stop H(5)IO(6) penetration and the exodermis failed to stain with lipidic dyes. Cultivation in stagnant deep hypoxia conditions or oxygenated circulating solution affected the longitudinal pattern of ROL profiles in G. maxima but statistically significant changes in exodermal suberin composition or content were not detected. Interspecific differences in barrier performance were found to be related to hypodermal structure and probably to qualitative as well as quantitative variations in suberin composition and distribution within exodermal cell walls. Implications for root system function are discussed, and it is emphasized that sufficient spatial resolution to identify the effects of developmental changes along roots is crucial for realistic evaluation of exodermal barrier properties.     

Hypaphorine, an indole-3-acetic acid antagonist delivered by the ectomycorrhizal fungus Pisolithus tinctorius, induces reorganisation of actin and the microtubule cytoskeleton in Eucalyptus globulus ssp bicostata root hairs

Hypaphorine, an indole alkaloid from the ectomycorrhizal fungus Pisolithus tinctorius Coker & Couch., counteracts indole-3-acetic acid (IAA) activity and controls the rate of root hair elongation in Eucalyptus globulus ssp. bicostata. The present investigation shows that hypaphorine changes cytoskeletal organisation in elongating root hairs of the host. The actin cytoskeleton was investigated by two different fixation and labelling procedures, which gave similar results. In control root hairs, actin organisation was characterised by (i) an actin cap at the very tip region, (ii) a subapical region with reduced labelling and containing fine actin filaments, and (iii) axial bundles of actin filaments running from the subapical part to the base of the root hair. In the hypaphorine-treated root hairs no actin cap was distinguished. The fine actin filaments occurring in the subapical region were replaced by a few thick actin filament bundles that extended from the subapical region toward the root hair tip. In the hypaphorine-treated hairs the total number of actin filament bundles along most of the root hair length was significantly reduced, presumably due to aggregation of pre-existing actin filaments. The first signs of alteration to the cytoskeleton could be detected as soon as 15 min after hypaphorine treatment. In hypaphorine-treated, but not in control root hairs, a patch of aggregated microtubules regularly occurred at a distance of approximately 10 m from the tip, possibly as a consequence of changes induced by hypaphorine in the actin cytoskeleton. The hypaphorine-induced aggregations in the actin and microtubule cytoskeletons could stabilise the structure of cytoskeletal elements, which in turn could hinder the vesicle delivery at the tip necessary for elongation. Such cytoskeletal alterations may be a consequence of the antagonism between IAA and hypaphorine. The latter view was supported by restoration of the actin cytoskeleton in hypaphorine-treated root hairs by IAA application.     

Root Browning in Pinus banksiana Lamb. and Eucalyptus pilularis Sm. 1. Anatomy and Permeability of the White and Tannin Zones

Growing tree roots are characteristically brown with white tips. The browning process, which occurs as the white region matures, has often been attributed to the deposition of suberin in various tissues. However, in pouch-grown tree seedlings of jack pine (Pinus banksiana Lamb.) and eucalyptus (Eucalyptus pilularis Sm.), browning was not linked to suberization but was caused by the deposition of condensed tannins in the walls of all cells external to the stele. Therefore, we propose using the term “tannin zone” to refer to this region of the root. Vitality tests indicated that the cells of the epidermis and cortex were alive in white regions but were dead in brown regions. Following sequential treatment with berberine hemisulfate and potassium thiocyanate, the cortical walls external to the endodermal Casparian band were full of berberine thiocyanate crystals, indicating that they were permeable to berberine. These walls should also be permeable to water and ions, which have smaller molecular dimensions than the tracer dye. Based on the anatomy and permeability of the tannin zone, we predict that its capacity for ion uptake would be reduced compared to the white zone because of a reduced absorptive plasmalemma surface area. In jack pine, some uptake could be effected by the passage cells of the endodermis. The tannin zone should be even less absorptive in eucalyptus because the exodermis remains an apoplastic barrier and the endodermis lacks passage cells. It is difficult to predict the difference between the tannin and white zones with respect to water uptake. Death of the cells external to the endodermis would reduce the resistance of the root to water movement, but deposition of tannins would increase it. The deposition of suberin lamellae in increasing numbers of endodermal cells may also retard water flow. The anatomy and physiological properties of the tannin zone are unique from those of the distal, white zone and the proximal, cork-clad zone.     

Enzymes in the exsheathing fluid of nematodes and their biological significance

Rogers W. P. 1982. Enzymes in the exsheathing fluid of nematodes and their biological significance. International Journal for Parasitology12: 495–502. The characteristics of an enzyme which hydrolysed denatured collagen and a lipase in exsheathing (ecdysal) fluid are described. A highly purified collagenase from Clostridium histolytica attacked isolated sheaths and reacted to additives in the same way as exsheathing fluid. However, relative to their activities with Azocoll or $\text{p-}\text{phenylazobenzyloxycarbonyl}\text{-}\text{L}\text{-}\text{Pro}\text{-}\text{L}\text{-}\text{Leu}\text{-}\text{Gly}\text{-}\text{L}\text{-}\text{Pro}\text{-}\text{D}\text{-}\text{Arg}$ as substrates, the enzyme of exsheathing fluid was >400 times as active as the bacterial collagenase in its action on isolated sheaths.It is suggested that the lipase in exsheathing and hatching fluids may, in association with the pseudocollagenase (and sometimes with chitinase also) have a function in the hatching of eggs. The pseudocollagenase alone may serve as the exsheathing enzyme. The leucine aminopeptidase in hatching and exsheathing fluids may be concerned in the breakdown of the excretory cell and the release of the fluids.     

Extracellular complexation of Cd in the Hartig net and cytosolic Zn sequestration in the fungal mantle of Picea abies – Hebeloma crustuliniforme ectomycorrhizas

Compartmentation of heavy metals on or within mycorrhizal fungi may serve as a protective function for the roots of forest trees growing in soils containing elevated concentrations of metals such as Cd and Zn. In this paper we present the first quantitative measurements by X‐ray microanalysis of heavy metals in high‐pressure frozen and cryosectioned ectomycorrhizal fungal hyphae. We used this technique to analyse the main sites of Cd and Zn in fungal cells of mantle and Hartig net hyphae and in cortical root cells of symbiotic Picea abies – Hebeloma crustuliniforme associations to gain new insights into the mechanisms of detoxification of these two metals in Norway spruce seedlings. The mycorrhizal seedlings were exposed in growth pouches to either 1 mM Cd or 2 mM Zn for 5 weeks. The microanalytical data revealed that two distinct Cd‐ and Zn‐binding mechanisms are involved in cellular compartmentation of Cd and Zn in the mycobiont. Whereas extracellular complexation of Cd occurred predominantly in the Hartig net hyphae, both extracellular complexation and cytosolic sequestration of Zn occurred in the fungal tissue. The vacuoles were presumed not to be a significant pool for Cd and Zn storage. Cadmium was almost exclusively localized in the cell walls of the Hartig net (up to 161 mmol kg ^{? 1} DW) compared with significantly lower concentrations in the cell walls of mantle hyphae (22 mmol kg ^{? 1} DW) and in the cell walls of cortical cells (15 mmol kg ^{? 1} DW). This suggests that the apoplast of the Hartig net is a primary accumulation site for Cd. Zinc accumulated mainly in the cell walls of the mantle hyphae (111 mmol kg ^{? 1} DW), the Hartig net hyphae (130 mmol kg ^{? 1} DW) and the cortical cells (152 mmol kg ^{? 1} DW). In addition, Zn occurred in high concentrations in the cytoplasm of the fungal mantle hyphae (up to 164 mmol kg ^{? 1} DW) suggesting that both the cell walls and the cytoplasm of fungal tissue are the main accumulation sites for Zn in P. abies resulting in decreased Zn transfer from the fungus to the root.     

Age and growth analysis of the shortfin mako, <Emphasis Type="Italic">Isurus oxyrinchus</Emphasis>, in the western and central North Pacific Ocean

We determined the age and growth rates of male and female shortfin makos, (Isurus oxyrinchus), from the western and central North Pacific Ocean. Growth band pairs were counted on half-cut vertebral centra using a shadowing method. In this method, we focused on the ridges on the surface of the centra, consisting of a convex and concave structure. After comparing four enhancing methods, we decided on the use of shadowing method for aging. Vertebrae from 128 males and 147 females were examined. The centrum edge analysis suggested annual band pair formation. Von Bertalanffy growth curves were fitted separately to the length-at-age data for males and females with birth length fixed. Until approximately 7 years of age, both sexes showed similar growth rates; thereafter, males showed a significantly slower growth rate compared to females. It was suggested males and females mature at approximately 6 years and 16 years, respectively. These life-history characteristics suggest relatively low productivity for this species, which agrees with reports on populations in other geographic regions.