Germination ecology of six shrubs in fire-prone Cape fynbos

To explain the recruitment and coexistence of species which establish after fire, this study predicted that each species would have different germination cues as a component of different regeneration niches. Furthermore, for species subject to natural fire frequencies of 10–20 years, fire-related cues, seed dormancy, extended longevity and fire-related germination cues might be predicted. However, results indicated broadly similar germination requirements. Seeds subjected to two heat treatments and a charcoal extract failed to show significantly enhanced germination. Instead, highest germination successes were achieved under alternating diurnal temperatures which implied an indirect fire cue, viz. the removal of insulating vegetation. Leachate solution inhibited germination in two species suggesting allelopathic effects during inter-fire periods. Only two species showed dormancy and three species did not have extended longevity but showed declining germinability after three years. Finally, in order to determine the potential germination from a soil-stored seed bank, data analysis simulated a seed bank comprising three years' accumulation of seeds. In each species the proportion of germinable seeds varied each year over the three years. Also, the germinability in response to ageing varied for each year's seed production. This would explain the variation in densities of the six species after different fire events, and hence offers a better explanation for species' coexistence.     

The activity of Triton X-100 soluble chlorophyllase in liposomes

Chlorophyllase (chlorophyll-chlorophyllidohydrolase, EC 3.1.1.14) was isolated and purified from Phaseolus vulgaris L. chloroplasts and etioplasts dissolved in 1% Triton X-100 and 10% glycerol. A 100 and 40-fold purification, respectively, was achieved. Enzyme preparations from both sources had similar affinities for chlorophyll a when assayed in a Triton X-100 medium. When electrophoresed in sodium dodecyl sulphate polyacrylamide gels the major band in both preparations migrated as a peptide of 30,000 daltons. Chlorophyll containing liposomes were also used as a substrate for chlorophyllase. The rate of hydrolysis did not follow Michaelis-Menten kinetics. When chlorophyllide a or methyl chlorophyllide a was incorporated in the liposomes, then in the presence of phytol dissolved in methanol, methylchlorophyllide a and chlorophyll a were shown to be synthesized. Apparently the purified enzyme in the presence of lipids, is endowed with both synthetic and hydrolytic activity.Abbreviations DEAE diethylaminoethyl - MeOH methanol - SDS sodium dodecyl sulphate     

Use of [14C]lysine to detect microbial contamination in liquid foods.

A radiometric method for microbiological control in food industries is suggested. This method, based on the labeling of cells by [14C]lysine, was tested by using nine species of yeast and two species of bacteria.     

Metabolism of exogenous arachidonic acid by mouse peritoneal macrophages

On incubation of resident mouse peritoneal macrophages with arachidonic acid several hydroxyacyl derivatives detectable in cellular supernatants are formed. As main products monohydroxyarachidonic acids (monoHETE's) were identified. In addition, smaller amounts of dihydroxyarachidonic acids (diHETE's) supernatants by reversed phase HPLC, normal phase HPLC in combination with UV-spectroscopy and combined gas-chromatography / masspectrometry revealed the presence of 5-, 8-, 12- and 15 - mono-HETE's, two distinct 5, 12-diHETE's, several 8, 15-diHETE's and 14, 15-diHETE. Among the 5, 12-diHETE's, only small amounts of a compound with the characteristics of LTB, were detected. Under the conditions employed, the cycloxygenase products PGE₂ and PGI₂ (as 6-keto-PGF_1g) were only minor metabolites. In contrast, when macrophage cultures were stimulated with the phagocytic stimulus zymosan, PGI₂, PGE₂ and LTC₄ were found as the major conversion products of arachidonic acid, whereas mono- and diHETE's were not formed in detectable amounts.     

Retrospective monitoring of rangeland vegetation change: ecohistory from deposits of sheep dung associated with shearing sheds

This paper explores the potential of a new method of reconstructing historical vegetation change in the Australian rangelands. Historical monitoring of rangeland vegetation has been so deficient that it is not possible to determine whether a long‐term trend toward degradation has occurred (as is often assumed) or, indeed, if it is continuing to occur. Because long‐term records are unavailable any attempt to monitor vegetation retrospectively must be based on proxy measures rather than direct observation. Where historical data are lacking an integration of palaeoecological, archaeological and ecological methods is required to reconstruct the past. Our research is based on a detailed analysis of sheep faeces deposited near a shearing shed in the semiarid rangelands of south‐west Queensland between the late 1930s and the mid‐1990s. The faeces in these deposits represent the diet of sheep in the days leading up to the property’s annual shearing and as such are a potentially useful index to changes in vegetation. Results indicate significant changes in the diet of sheep since the late 1940s. The potential of this method, and its limitations, are discussed. Long‐term records are critical in understanding issues of sustainability in land management and it is intended that this paper will stimulate further research into historical vegetation change in rangelands.     

Autosomal dominant polycystic kidney disease--in vitro culture of cyst-lining epithelial cells.

The major form of autosomal dominant polycystic kidney disease (ADPKD) in humans is linked to the PKD1 gene on chromosome 16p. The identity of the gene and the underlying pathogenetic mechanisms are not yet defined. Cyst-lining epithelial cells derived from a polycystic kidney were successfully grown in culture and designated MZ-PKD-1 cells. By linkage analysis, the related pedigree of the nephrectomized patient could be linked to the PKD1 gene on chromosome 16p. Thus, these cells exhibit the genotype of a mutated PKD1 gene and represent an in vitro culture model for ADPKD involving chromosome 16p. The antigenic phenotype was characterized immunohistologically by epithelial differentiation antigens and markers of individual nephron segments. An essentially identical antigenic pattern of proximal tubular cells was observed both in vitro and in fresh frozen tissue. Electron microscopy showed the formation of a microvillous-like coating. During growth phases in vitro successive changes in the cell shape were observed. MZ-PKD-1 cells exhibited a limited lifespan ending in replicative senescence. Northern blot analysis of kidney-growth-related genes, c-myc, TGF-alpha, TGF-beta 1, and EGF receptor revealed abundant expression of all of these genes in MZ-PKD-1 cells.