Harvesting of Aloeferox was estimated (in 1996) to bring in an annual income ofR4 million per year to rural communities alone - a vital source of income for full-time tappers who rely solely on Aloe ferox as their only form of financial survival. They are joined on occasion by casual-tappers who rely on tapping to supplement their incomes in times of hardship (Newton and Vaughan 1996). Landowner's also benefit by allowing harvesting on their land in exchange for a percentage of the harvest (Newton and Vaughan 1996). Trade in bitters sap or gel far outweighs that of other plant parts so care is taken by harvesters to keep the plants alive for future tapping. Leaves from only the lower third of the leaf rosette ( 10 - 15 leaves) are harvested, and 2 - 4 cm at the base of the leaves are left to prevent damage to vascular tissues (Newton and Vaughan 1996, Mac Farlane 2004). Populations are only harvested every 18 - 36 months allowing plants to recover from the loss of leaf material. Plants suffering from insect-infestation or disease are not harvested to avoid weakening the plant further and possibly causing death (Newton and Vaughan 1996). Effort is also made by landowners to relocate plants growing in areas they plan to transform and to monitor harvesting activities on their properties (Newton and Vaughan 1996). The vested interest in keeping the plants alive has inadvertently assured the preservation of populations at past harvesting levels although no formal conservation or resource management policy presently exists for A. ferox (Newton and Vaughan 1996). Effects of harvesting, which are not limited to the direct effect of leaf removal on the plant but include indirect effects - such as reduced reproductive output, reduced sap production and even trampling of recruits - have nonetheless raised concern for the long-term survival of populations (Newton and Vaughan 1996). This study addressed some of the indirect effects of harvesting on Aloe ferox on both population and individual plants levels. On the population level plant density, mortality, susceptibility to disease and sizeclass structure was compared between unharvested and harvested populations. On the individual plant level vegetative traits, flower production and sap production were compared between unharvested and harvested plants. One of few other studies on ecology of A. ferox by Hoffman (1988) assessed some of these characteristics for a population in Port Elizabeth, South Africa.

No description available.

This report investigates the potential for the culture of G. gracilis, an indigenous red alga, into the west coast mariculture farm Jacobs Bay Sea Products Pty. Various methods for cultivating Gracilaria as well as environmental parameters, which influence growth of Gracilaria, are disltussed below. From these optimal conditions for the polycultivation of G. gracilis are determined. Cultivation can take place either, in open waters, or on land. Open water systems are generally less intensive than land based operations. Open water systems can be either bottom planted or suspended. Suspended cultivation has the advantage of maintaining the plant thalli in optimal light intensities. Land based systems can make use of ponds, raceways or tanks. Tanks and raceways are more productive than ponds, but require higher flow rates and regulated nutrient regimes.

The cosmopolitan Asteraceae tribe Gnaphalieae, or paper daisies or everlastings, form a significant component of both the dry and cool temperate floras of southern Africa. Within this tribe exists a small Afrotemperate genus, Macowania, endemic to the grassland biome of South Africa and occurring almost exclusively within the Drakensberg region, apart from two disjunct species in North Africa. The age, relationships and geographic origin of Macowania is investigated in order to provide insight into the factors affecting speciation, especially uplift events, on this small Afrotemperate genus. A well-supported phylogenetic hypothesis based on both nuclear and chloroplast genes suggests that Macowania is sister to a clade corresponding to the Relhania clade s.s., and that these are in turn sister to a clade containing the genera Athrixia and Pentatrichia. Macowania is monophyletic only with the inclusion of the enigmatic monotypic genus Arrowsmithia, resulting in the future synonymy of Macowania with Arrowsmithia. The anomalous species M. pinifolia, previously part of the genus Athrixia, is placed in a polytomy with the Relhania s.s. clade and the remaining species of Macowania and Arrowsmithia. DNA sequence data could not be obtained for several Macowania species, including the taxa from North Africa. The placement of these species within Macowania is confirmed by means of a parsimony analysis of morphological characters against a molecular backbone constraint tree. One species, M. tenuifolia, is well-supported in two different placements within Macowania by chloroplast and nuclear DNA sequence data. The best position of this species is inferred by incongruence decomposition analysis and morphological affinities. Bayesian relaxed clock methods and ancestral area reconstruction using maximum likelihood and squared change parsimony estimate the age and ancestral area of the genus, and determine the timing and route of colonisation of the Drakensberg. Diversification within Macowania is consistent in timing with the uplift events during the Miocene and Pliocene that resulted in significant vertical movement in eastern South Africa, suggesting that colonisation of the high-elevation Drakensberg grassland by Macowania was promoted by uplift. The topographic heterogeneity and increased river action resulting from the uplift may also have promoted evolution into new habitats and potentially mediated the movement of the ancestor of Macowania into the Drakensberg region via riparian habitats.

No description available.

The perennation of orchids is poorly understood, in particular that of the Orchidoidae. The understanding of perennation in the Orchidoidae is important because the root-stem tuberoid is used as the one character defining the Orchidoidae as a monophyletic group. The root-stem tuberoid has never been examined for variation before. This project focuses on perennial growth in the Diseae in order to study the structure and function of the root stem tuberoid in relation to other organs and to contribute to the understanding of Orchidoid phylogeny.

The hybrid zone between Calendulauda albescens and C. barlowi, located near the Orange River, contains a wide range of phenotypically intermediate individuals. This study examines the mitochondrial DNA of some of these individuals to determine if possible introgression is occuring from C. albescens to C. barlowi. Mitochondrial DNA from 13 lark individuals found in the C. albescens/C. barlowi hybrid zone was analysed. A 358 base pair cytochrome-b sequence was obtained. The neighbour-joining phylogenetic tree obtained revealed two distinct clades, a C. albescens and C. barlowi clade. The C. barlowi clade was supported with a bootstrap value of 100. The C. albescens clade contained individuals of intermediate morphology, as represented by their hybrid index scores, indicating that intermediates between the two species contain the mitochondrial DNA of only one species, C. albescens. These results point at introgression from C. albescens to C. barlowi, with female C. albescens choosing to mate with male C. barlowi.

No description available.

The presence of the sporophytic 'Falkenbergia rufolanosa' phase of the invasive algal species Asparagopsis armata was first recorded in South Africa 57 years ago. The introduction of this highly invasive alga, of Australian/New Zealand origins, to Europe in the 1920's has since led to a number of recorded invasions by the gametophytic Asparagopsis phase in both the Mediterranean and Atlantic oceans. Recently however, a number of commercial uses for both phases of A. armata have been identified, which have given rise to industrial interest in the species as a candidate for commercial cultivation. Previous studies on European strains of F. rufolanosa and A. armata have identified a number of life history traits, which not only increase A. armata 's invasive ability, but also make it a useful species for commercial tank cultivation. However, different strains are known to have different environmental parameters which regulate their survival, growth and reproduction capabilities. This study investigated the growth of the South African strain of F. rufolanosa in culture, in response to different environmental variables, as well as the conditions necessary for tetrasporogenesis to occur, in order to assess its potential impacts, both as an invasive threat and as a species for commercial cultivation in South Africa.

Different histories for forests in Southern Africa have been hypothesized from vegetation biogeography and pollen analysis. However, the history of forests is still controversial. Phylogeography uses gene genealogies to infer history of distributions. Two forest endemic moss species were sampled: Leptodon smithii; and Neckera valentiniana. Two gene regions were used, trnLF (chloroplast genome) and ITS1 (nuclear genome). Neckera valentiniana showed no variation from the populations sampled. Results from Leptodon smithii based on the trn and ITS region suggest that forests once were widespread, but then became fragmented. Dispersal corridors still exist between Southern Cape populations and Western Cape populations.