A prevailing view exists in the literature which suggests that macroalgae growing in slow-flow environments (<4 cm s⁻�) are less productive because of "mass-transfer" limitation compared to fast-flow environments. Macroalgae in slow-flow environments are thought to have thicker diffusion boundary-layers which limit the flux of essential molecules to and from the algal thallus. However nutrient demand of a macroalga can also influence nutrient flux. The main objective of this research was to determine the relative importance of physical (mainstream velocity) and physiological (nutrient demand) factors influencing the growth rate of Adamsiella chauvinii, a small (<20 cm) red algal species, that grows within the benthic boundary-layer in a soft sediment habitat. To establish the influence of water velocity, the growth rate of A. chauvinii was measured in situ each month (March 2003 to March 2004) at three sites with varying degrees of water velocity (slow, intermediate and fast) at which all other environmental parameters (photon flux density, seawater temperature and nutrients) were similar. To determine the metabolic demand and nutrient uptake rate of A. chauvinii, the internal nutrient status (C:N, soluble tissue nitrate, ammonium and phosphate), uptake kinetics (V[max] and K[s]) and nutrient uptake rate at a range of mainstream velocities were also determined on a seasonal basis. The hydrodynamic environment around A. chauvinii canopies was characterised in situ and compared with controlled laboratory experiments. Growth rates of Adamsiella chauvinii thalli at the slow-flow site were significantly lower in winter (June) to summer (February) than the intermediate- and fast-flow sites, while in autumn growth rates were similar between sites. However, A. chauvinii at the slow-flow site had similar or higher tissue N content compared to thalli at the other two sites during winter, spring and summer suggesting that growth rates of A. chauvinii were not mass-transfer limited. Nitrogen uptake rates of A. chauvinii were similar between sites in summer and winter, however uptake rates were lower in summer compared to winter even though thalli were nitrogen limited in summer. Water velocity had no effect on nitrate uptake in either summer or winter and uptake of ammonium increased with increasing water velocity during summer only. Two hydrodynamically different environments were distinguished over a canopy of A. chauvinii, with both the laboratory and field velocity profiles in good agreement with each other. In the top half of the canopy, the Turbulent Kinetic Energy (TKE) and Reynolds stresses were greatest while in the bottom half of the canopy flow rates were less than 90 % of mainstream velocity (< 1 cm s⁻�). When considered together, the influence of water velocity on the growth rates of A. chauvinii was not completely clear. Results suggest that mainstream velocity had little influence on nutrient availability to A. chauvinii because of the unique hydrodynamic environment created by the canopy. Nutrients, especially ammonium and phosphate, derived from the sediment and invertebrates, may provide enough nitrogen and phosphate to saturate the metabolic demand of Adamsiella chauvinii, consequently, A. chauvinii is well adapted to this soft-sediment environment.

I investigated the ecological functions of halogenated secondary metabolites from the red alga Asparagopsis armata, their localisation in specialised cells and also their cost of production. A. armata produces large amounts of halogenated metabolites ( &lt 20 ??g / mg dry weight) that are sequestered in gland cells, as was demonstrated with light, epifluorescence and transmission electron microscopy. Cellular structures were identified that likely assist the release of metabolites from the gland cells to the algal surface. The halogenated metabolites of A. armata have multiple ecological roles, functioning as both inhibitors of bacterial fouling and as herbivore deterrents. Their activity against bacteria and herbivores was measured by a novel test in which the metabolites were manipulated in A. armata by omitting bromide ions from the culture media. This technique prevented the production of halogenated metabolites, but did not impact on other aspects of algal biology. Algae lacking halogenated metabolites (bromide [-] algae) had higher densities of epiphytic bacteria than those that continued to produce metabolites (bromide [+] algae). Bioassays with pure compounds against individual bacterial isolates further supported an inhibitory role for the halogenated metabolites against epiphytic bacteria, and also indicated an affect on bacterial community structure as well as abundance. Bromide (+) A. armata produced halogenated metabolites that also deterred feeding by two herbivores (an amphipod and an abalone), but not a third (an opisthobranch mollusc). A novel outcome from these feeding assays was the demonstration of a relationship between herbivore size and consumption of the chemically defended A. armata by the abalone Haliotis rubra. In addition to the fitness benefits gained from chemical defence, there were also costs for allocating resources to secondary metabolites. These costs were only detected under limiting light resources, consistent with predictions of the plant defence models. The integration of chemical analyses and cellular measures of chemical defence proved essential in elucidating resource allocation to chemical defence in the filamentous stage of A. armata. This thesis highlights that the simple relationships between growth and defence in filamentous algae can provide an excellent model for studies of the ecology and evolution of chemical defences in marine algae.

The largest of the 80 families in the division Rhodophyta is the Rhodomelaceae. A great many genera and species are restricted to Australasia, which is the major centre of diversity and distribution. Perhaps as a consequence, the Rhodomelaceae has remained relatively unstudied compared with most other red algal families even at the morphological/anatomical level. Within the confines of a PhD program it would not be possible to study all of the 125 genera credited to the Rhodomelaceae. The focus of this thesis has, therefore, been narrowed down to selected tribes and genera, all of which have a strong Australasian component. Anatomical and molecular analyses have been undertaken on members of the tribes Amansieae, Pleurostichidieae, Streblocladieae and Sonderelleae and the genus Halydictyon. The results of these analyses have led to the description of two new genera, three new species, and one new tribe as well as the resurrection of two genera and the recombination of ten species. The taxonomic position and validity of the studies tribes and genera has also been established.

The medicinal chemistry of selected marine algae indigenous to South Africa was investigated. Following the isolation and characterisation of a number of new and known compounds, the associated in vitro cytotoxic profiles of these new compounds was investigated. Plocamium maxillosum yielded two new cyclic polyhalogenated monoterpenes which were characterised as 2E-chloromethine-4E-chlorovinyl-4-methyl-5-cyclohexen-1-one (2.1) and 2Z-chloromethine-4E-chlorovinyl-4-methyl-5-cyclohexen-1-one (2.2) on the basis of one and two dimensional NMR spectroscopic data and MS analysis. These compounds were also found to have good cytotoxic activity against breast cancer cell lines. Although these compounds are based on a regular monoterpene skeleton, they represent an uncommon feature not often seen in cyclic halogenated monoterpenes from marine algae. Plocamium robertiae yielded one new cyclic polyhalogenated monoterpene identified as 4,5- dibromo-5-chloromethyl-1-chlorovinyl-2-chloro-methylcyclohexane (2.6) and one known compound called 2,4-dichloro-1-chlorovinyl-1-methylcyclohexane-5-ene or Plocamene D (2.9). Portieria hornemannii was collected from Port Edward in Natal and yielded three new compounds, namely; 3Z-1,6-dibromo-3-(bromomethylidene)-2,7-dichloro-7-methyloctane (3.1), 1E,3Z-1,6-dibromo-3-(bromomethylidene)-7-chloro-7-methyloct-1-ene (3.2), 1Z,3Z- 1,6-dibromo-3-(bromomethylidene)-7-chloro-7-methyloct-1-ene (3.3), and one known compound, namely; 3S,6R-6-bromo-3-(bromomethyl)-3,7-dichloro-7-methyloct-1-ene (3.4). Compounds 3.1 and 3.2 showed no cytotoxic activity against breast cancer cells. Another Portieria hornemannii sample was collected from Noordhoek in the Eastern Cape, it yielded one known compound referred to as 3Z-6-bromo-3-(bromomethylidene)-2,7- dichloro-7-methyloct-1-ene (3.5), as well as one new compound called portieric acid A (3.6) or 5-bromo-2-(bromomethylidene)-6-chloro-6-methylheptanoic acid. Portieric acid A showed slight cytotoxic activity and also represents a new class of compound within the genus Portieria. The isolation of secondary metabolites from the South African red alga, Laurencia glomerata, yielded two known compounds; 7-hydroxylaurene (4.9) and cis-neolaurencenyne (4.12), as well as one chamigrane related compound (4.11). Laurencia flexuosa yielded one known compound called 3Z-bromofucin (4.13). Using 1H NMR, GC and molecular systematics, a novel method for identifying different species of Laurencia was also investigated.

Doctor Scientiae (Biodiversity and Conservation Biology) / The purpose of this thesis was to provide a revision and characterization of the species of nongeniculate coralline algae previously ascribed to the now defunct genus Porolithon; to provide a modern account of selected taxa from the genus Hydrolithon and descriptions of taxa found to conform the generic delimitation of Hydrolithon and to use a phenetic cluster analysis to determine the taxonomic relationships between the various taxa ascribed to the genera Polorithon and Hydrolithon. / South Africa

The rhodophytes or red seaweeds are an ancient group of organisms that are related to plants. Like terrestrial plants, they use secondary compounds to protect themselves from microbial infection and grazing by herbivores. However, unlike terrestrial plants, they produce mostly halogenated secondary compounds and rarely alkaloids. Osmundaria serrata (Rhodophyta) is found along the eastern South African coast and the Maldive Islands. Its descriptive common name is “red spirals” and the species is adapted to live in habitats with high wave action. Extracts from this seaweed had previously shown to have antimicrobial activity, but ecologically irrelevant microbes were used to test the extracts. In this study, ten bacteria were isolated from the surface of O. serrata and its habitat, and identified. Mostly aerobic and Gram-negative bacteria were isolated (Halomonas and Pseudomonas species) along with facultatively anaerobic forms (Vibrio spp.) and a Gram-positive (Marinococcus sp.). These were used in bioassays to compare the activity of extracts made from O. serrata and other seaweeds that occur in the same habitat. Marine bacteria are the initial colonizers in biofilm formation and subsequent fouling of surfaces in marine environments. The study of these bacteria in relation to their macroalgal hosts may help to control biofouling of surfaces that cause economic losses worldwide. A comparison was made between using agar dilution and microtitre methods for testing the antibacterial activity of an O. serrata extract. The microtitre method was found to be more sensitive than the agar dilution method. Possibly because e some of the bacteria on the petri plates (in the agar dilution method) were not in direct contact with the toxicant in the growth medium, but were in direct contact in the liquid medium of the wells in the microtitre plates. The extract from 0. serrata was the most active of the thirteen species of macroalgae collected from the same habitat and tested for antibacterial activity. Deformities in bacteria were observed in response to the 0. serrata extract. Increased capsule production and blebbing of the outer membranes were observed by transmission electron microscopy (negative staining). Lanosol diethyl ether was isolated from 0. serrata and tested for antibacterial activity. Lanosol is produced mainly by the rhodophytes, but it is also found in other macroalgae and fungi in lower concentrations. The compound inhibited the test bacteria with average MIC's of 0.27 ± 0.07 mg.mr1 (bacteriostatic) and 0.69 ± 0.15 mg.mr1 (bactericidal). Different forms of biofilm were observed by scanning electron microscopy on the thirteen species of macroalgae. These ranged from a very little biofilm covering on the calcified reds to complex communities on the other macroalgae. The treatment with OS04 vapour before fixation in glutaraldehyde preserved the biofilm structure better than no treatment and indicated that lipids are important in maintaining biofilm structure. Since a complex biofilm community was seen on the surface of 0. serrata, it is unlikely that lanosol functions as an antifouling agent. This chemical seems to multifunctional with antimicrobial and feeding deterrent activities. / Thesis (PhD (Botany))--University of Pretoria, 2006. / Plant Science / unrestricted

A preliminary electrophoretic study on Bangia vermicularis Harvey (Rhodophyta) along the coast of British Columbia was undertaken to determine whether enzyme banding patterns could be used to identify the relatedness of the populations which varied in chromosome number (3, 6 or 4) and life history (asexual or sexual). Material from nineteen sites was tested for seven enzymes: glutamate dehydrogenase (GDH); malate dehydrogenase (MDH); lactate dehydrogenase (LDH); superoxide dismutase (SOD), glucose 6-phosphate dehydrogenase (G6PDH); phosphoglucoisomerase (PGI); and phosphoglucomutase (PGM). Unlike higher plants, some of the banding patterns obtained in Bangia could only be explained if the enzymes SOD, GDH, LDH and PGI are monomers and the enzymes PGM, SOD, GDH, PGI, and G6PDH have only one cellular location. Generally, with the exception of two enzymes, PGI and G6PDH, which were highly polymorphic, only one to three bands were evident. Considerable amounts of variation in the mobility of the isoenzymes were detected between populations independent of chromosome number or sexuality. Contrary to expectations, often populations with three chromosomes or six ' chromosomes had the same number of loci and many of the three chromosome populations had some banding patterns indicative of diploids. Consequently, if there had been a polyploid origin of the six chromosome populations then there must also have been many gene duplications in the three chromosome populations. Alternatively, if the three chromosome populations arose by aneuploid reduction within a six chromosome population then there must also have been gene silencing and/or the formation of null alleles. Populations that were very close geographically differed to a large extent suggesting that there may be little gene flow between populations. The variability between populations could be explained by isolation over long periods of time during which changes could have occurred in the structure and regulation of the enzymes tested. / Science, Faculty of / Botany, Department of / Graduate

No description available.

No description available.

A study of the red algal order Gelidiales in British Columbia and northern Washington was conducted. Gelidiales are represented in the study area by four species, Gelidium coulteri, G. purpurascens, G. vagum and Pterocladia caloglossoides, and a key to identify the taxa is provided. Earlier reports of G. crinale, G. pusillum, G. robustum and G. sinicola from British Columbia and northern Washington have been shown to be misidentifications of the other taxa and are excluded from the flora. The occurrence of G. vagum in the British Columbian flora is significant because it appears to have been introduced from the northwest Pacific and now has a disjunct distribution, occurring in Japan and China and on two islands in the Strait of Georgia, British Columbia. Gelidium vagum and the Gulf of California species, G. johnstonii, are considered to be sister species. They share the unique character of monoecy (i.e. unique in the genus) and a morphological resemblance, but differ in several other characters, including arrangement of cortical cells, shape and flattening of tetrasporangial stichidia, shape of stichidial apices and position of the apical initial with respect to the adjacent cortex, presence/absence of an apical furrow and sterile margin in tetrasporangial stichidia and presence/absence of intact third order filaments in mature cystocarps. The life history of Gelidium vagum was completed in culture, only the second Gelidium species for which this has been accomplished. Gelidium vagum has a triphasic Polysiphonia-type life history with isomorphic (monoecious) gametophytes and tetrasporophytes, and carposporophytes growing on gametophytes. The rare occurrence (G. purpurascens, G. coulteri) or absence (Pterocladia caloglossoid.gametophytes in the field and the lack of successful completion of a life history in culture suggests that, whereas these species may occasionally complete a Polysiphonia-type life history in situ, vegetative or apomictic mechanisms are more important in maintaining field populations. Chromosome counts of n = 14 - 15 were made on undivided tetrasporangia of G. vagum. The pattern of spore germination in Gelidium coulteri, G. purpurascens and G. vagum is similar for carpospores and tetraspores. A single germ tube grows from the spore, the entire cytoplasmic contents of the spore evacuate into the germ tube and a wall cuts the germ tube off from the empty spore. The germ tube divides unequally to form a concave and a fusiform cell. The primary attachment rhizoid forms from a derivative of the concave cell and the sporeling apical cell forms from a fusion cell derivative. As apical organization is established, the subapical cell produces two lateral periaxial cells. Carpogonium and carposporophj'te development was followed in Gelidium purpurascens and G. vagum. The functional carpogonium is intercalary. Non-functional carpogonia divide transversely with a concave wall and become sessile and degenerate. The fertilized carpogonium consistenty forms a fusion cell by fusing with adjacent cortical cells. Fusion cell lobes cut off gonimoblast filaments that send out processes that fuse with haploid gametophyte cells of nutritive chains. Carposporangia are produced terminally and laterally by gonimoblast cells and protrude into two locules that have formed as the cortex is pushed away from the plate of second order filaments. Carpospores are released through a single ostiole in each locule. Spermatogenesis, tetrasporogenesis and rhizine morphology were studied ultrastructurally for the first time in Gelidiales. In spermatangial development, apical chloroplasts in the spermatangial mother cell are cut off by a furrow, a mechanism previously not reported in red algae for exclusion of chloroplasts from spermatangia. As the spermatangium matures, spermatangial vacuoles form from the coalescence of vesiculated endoplasmic reticulum and dictyosome-derived vesicles. Spermatangial vacuoles are discharged from the spermatangium just prior to the release of the spermatium. Stages of tetrasporangium development are marked by wall development. Prior to karyokinesis, the young tetrasporangium is dominated by a large nucleus. Following karyokinesis, chloroplasts, starch grains and dictyosomes increase in abundance, a wall layer is deposited, and dictyosomes undergo a series of morphological changes from small and flat, to large and flat producing fibrillar vesicles, to hemispherical and producing cored vesicles. At cytokinesis an electron dense wall layer is deposited around the tetrasporangium and in the cleavage furrow, and cored vesicles secrete a mucilage-like material inside this wall layer. / Science, Faculty of / Botany, Department of / Graduate