Overview of the LiMB database.

The rapidly increasing number of databases relevant to molecular biology has given rise to a need for a coordinated effort to identify, characterize, and link them. The LiMB database, which contains information about molecular biology and related databases, is a step in that direction. It serves molecular biologists seeking data sets containing information relevant to their research, and is also intended to anticipate the needs of database designers and managers building software links for related data sets. We present an abbreviated version of the database here; the full database is available free of charge as described below.

An investigation of the fixation and staining of lipids by a combination of malachite green or other triphenylmethane dyes with glutaraldehyde.

Mixtures of the monocationic triphenylmethane dyes, malachite green or crystal violet, with glutaraldehyde, retained and stained phospholipid droplets in chloroplasts of leaves of Lolium multiflorum Lam. These dyes also stained trilinolenin; phosphatidic acid dioleoyl, dipalmitoyl; phosphatidylcholine dioleoyl, dilinoleoyl; and phosphatidylethanolamine dioleoyl on filter paper models. In this model system the dipalmitoyl derivatives of phosphatidylcholine and phosphatidylethanolamine did not stain well, if at all. Washing of the dyed samples with 0.5 M sodium chloride solution did not remove the colour, suggesting that the interaction is unlikely to be purely ionic. Except with trilinolenin, the colour and possibly the lipid samples were removed from the filter paper model system on washing with 100% ethyl alcohol. Other triphenylmethane dyes (methyl green, light green and fast green FCF) did not retain phospholipid droplets in tissue. Fast green did, however, stain phospholipids in the model system. Two quinone-imine dyes, neutral red and toluidine blue O, while staining phospholipids in the model system did not retain droplets on the chloroplasts but did assist in the retention and staining of cell membranes. The basis of the reaction between lipid and dye is discussed in relation to the structural formulae of the dyes and model lipids. It is possible that there is an interaction between the hydrophobic fatty acid ester side chains of the lipid and the dyes. Neither the phosphate nor the polyhydric alcohol moieties of the lipid seem to be essential for staining or retention of lipid.

Ultrastructure of the salt glands of the mangrove, Avicennia marina (Forssk.) Vierh., as indicated by the use of selective membrane staining.

Each salt-excreting gland of the mangrove Avicennia marina (Forsskål) Vierh. consists of two to four collecting cells, one stalk cell, and eight to twelve excretory cells. Differential membrane staining by zinc iodide-osmium tetroxide (as a post-fixative) or phosphotungstic acid (as a section-stain) was used to characterise the ultrastructure of the glands. A large amount of tubular endoplasmic reticulum was found in the stalk and excretory cells of the gland, but not in the collecting cells. The ultrastructural arrangement of the endoplasmic reticulum indicates that salt is loaded from the apoplasm into the endoplasmic reticulum of the symplasm at the base of the stalk cell, traverses both cell types in the endoplasmic reticulum, and is excreted at the outer edge of the gland by an eccrine-type mechanism. Increasing development of the tubular endoplasmic reticulum accompanied differentiation of the gland cells.

The effect of caffeine, different fixation regimes and low temperature on microtubules in the cells of higher plants : Evidence for diversity in their response to chemical and physical treatments.

Caffeine, (1:3:7-tri-methyl-xanthine), either as a prefixation treatment or included with glutaralde-hyde as the primary fixative, destroys or disorganises the microtubules associated with the formation of secondary walls in fibres from the flowering stem of the grass Lolium temulentum L. There is no observable effect of caffeine treatment on the microtubules associated with primary wall formation in collenchyma and young fibres from L. temulentum or in root cap cells of Zea mays L. and Phaseolus vulgaris L. The microtubules associated with primary wall formation are destroyed by cold treatment but not those associated with secondary wall formation. Tannic acid included in the fixative shows the microtubules associated with secondary wall formation in fibres of L. temulentum to be composed of 13 subunits. Treatment with lanthanum hydroxide does not stain the core or the halo of the microtubules.

APICAL INTRUSIVE GROWTH OF FIBRES FROM THE FLOWERING STEM OF LOLIUM TEMULENTUM L.

Extension of the internode below the point of insertion of the flag leaf of Lolium temulentum L. takes place in the lower 10 to 15 mm. Extension of the long epidermal cells also takes place in this region. However, fibre cells show little extension in the lower 10 mm and maximum extension occurs at about 30 mm above the node. Thus, there is extension of fibre cells within that portion of the internode which has ceased extension and is bounded by an epidermis, the cells of which have also ceased elongation. This suggests the occurrence of intrusive growth of the fibres and evidence for this is shown from the measurement of macerated fibres and from electron micrographs. The walls of fibre cells measured in internodes of different lengths and ages thicken only very slightly in the lower 30 mm and most cell wall thickening occurs between 45 and 90 mm above the node. Thus most cell wall thickening occurs after the fibre cells have ceased to elongate.

The proportion of sieve elements in the phloem of some tropical trees.

Measurements have been made of the proportion of the area of sieve elements in the cross-sectional area of the secondary phloem of trees of two tropical genera in which the presence of storied sieve plates makes the recognition of sieve elements particularly easy. This proportion, often accepted as one fifth in the literature on phloem and translocation, rises as high as three quarters in one of the trees measured.