The intertidal red alga, Gracilaria chilensis Bird, McLachlan et Oliveira (Rhodophyta, Gracilariales), lives in an environment in which light is highly variable in terms of both amplitude and duration. A laboratory investigation of the photophysiology of G. chilensis was conducted to assess the response of the photosynthetic apparatus to light variability characteristic of the natural environment. Freshly collected Gracilaria chilensis was found to exhibit an endogenous rhythm of photosynthesis in conditions of constant limiting light and temperature. However, such a phenomenon was not observed in saturating light. Rhythms of phycobiliprotein concentration and dark respiration were also observed but were not as well-defined and could nor account for the photosynthetic rhythm. The photosynthetic response of G. chilensis to light fluctuations of various durations (0.25 to 900 seconds) and light levels was compared to that in static light. G. chilensis was able to utilise rapidly fluctuating light (< 1 second) more efficiently than fluctuations of longer duration (60-900 second). Mean photosynthetic rates were enhanced by up to l50% in fluctuating light of less than 60 sec duration over that predicted from steady-state. The photosynthetic apparatus of freshly collected G. chilensis was found to have many low-light "shade" acclimation characteristics. These included a low compensation point (5 µmolm-2 s-l) and onset of saturation (80 µmolm-2 s-l) suggesting sensitivity to photoinhibition. However, (laboratory) low-light acclimated G. chilensis was able to tolerate periods of constant high light (2000 µmolm-2 s-l)for periods of six hours without detectable detrimental effect on photosynthetic capacity, although photosynthetic efficiency was significantly inhibited after two hours of this treatment. The time course and characteristics of photoacclimation were determined by culturing G. chilensis in low- (15 µmol m-2 s-l) and high- (180 µmol m-2 s-l) light and high- and low-nitrogen regimes. The observed change in photosynthetic characteristics and pigment concentration indicated that acclimation began after a time lag of l-2 days, was complete after approximately a week and was reversible. Acclimation to growth light included changes in growth rate, P-I response curves, pigment concentration and composition and other biochemical components (e.g. carbon/nitrogen ratio). The nitrogen regime significantly affected pigment concentration in the high-light grown plants and the response suggests pigments play a role in nitrogen storage as well as light harvesting. These various physiological characteristics described above were interpreted as important mechanisms that enable G. chilensis to optimise photosynthetic response in the highly dynamic and stressful zone of the intertidal environment.

Persistence of Colletotrichum acutatum Simmonds f.sp. pinea Dingley & Gilmour in pine nursery soils and its infectivity of Pinus radiata D. Don seedlings were studied. Sampling procedures were compared in the search of soils for fungal propagules. Those most frequently used were soil dilution plate method, surface-soil dilution plate technique, and plating of debris picked from soil. A selective medium for direct isolation from soil was prepared comprising potato dextrose agar as the basal medium and incorporating benomyl (50 ppm), quintozene (7.5 or 75 ppm), streptomycin sulfate (100 ppm), chloramphenicol (100 ppm) and chlortetracycline HCl (100 ppm). Studies in plots at Auckland, Tokoroa and Rotorua indicated that fungal structures within P. radiata debris persisted for long periods; up to 25 months in the Auckland plots. In vitro, the viability of conidia in natural soil declined very rapidly; more than 50% of conidia were non-viable within 4 weeks of their introduction into soil incubated at 15 and 25 C. Similar experiments conducted at different matric potentials indicated that drier soils (-0.3 or -0.4 bar) had higher levels of viable conidia over periods of time compared to wetter soils of -0.1 bar or at saturation. Segments of pine seedlings introduced to soils into which various concentrations of conidia were previously incorporated showed increasing colonization with increasing conidial concentration at both 15 and 25 C after 4 days. Maximum colonization of segments occurred at conidial concentrations 106 ml-1 to 107 ml-1. Artificially-inoculated segments of pine seedlings were introduced into soil and then these were recovered at different time periods. After two months in soil 100% recovery of the fungus was obtained from all leaf, stem and root segments plated. Recovery levels from all the plated stem and root segments after 8.5 months were never lower than 68%. Recovery levels from leaf segments were lower because many of these had decomposed leaving only the central xylem strands. Conidia-laden membrane filters were introduced into soil. A method of microscopic study used after removal of these from soil enabled easy observation of resultant structures. Appressoria were formed while the fungus was in soil. Other potential survival propagules were thick-walled, darkly-pigmented, short hyphae within pine debris. It is considered that the short individual cells of such hyphae could survive as chlamydospores, and these are believed to be the prime means of long-term survival in soil. Several fumigants were tested for effectiveness in eradication of the fungus from soil. All chemicals tested, namely chloropicrin, methyl bromide, "Di-Trapex" and dazomet significantly reduced viability of conidia and the fungus in pine debris. Weeds from a pine nursery were inoculated with conidia; of these, only Epilobium ciliatum Raf. became infected. Infection of healthy parts was infrequent but saprophytic growth in older parts frequently killed the plant. This species is therefore a potential alternative host, although its importance as an inoculum source for infection of pine seedlings is unknown. Experimentally it was shown that infection could occur by rain splash of conidia onto healthy plants. Infection of P. radiata seedlings was studied at several constant and alternating temperatures. Initial infection was greatest at higher temperatures (ca 24 C); while full symptoms of the disease were best expressed at lower temperatures (12 to 18 C). Inoculated seedlings had significantly reduced shoot and root development at 12, 15, 18 C, but not at 6, 9, 23, 24, 27 C, after 53 days. Increase in height of healthy seedlings was significantly greater than that of inoculated seedlings, after 52 days at 18 C. Pathogenicity on P. radiata seedlings of an isolate of C. acutatum f.sp. pinea isolated from soil, "whitish isolate", was comparable to the normal "coloured isolate". / Whole document restricted, but available by request, use the feedback form to request access.

The flowering plant family Alseuosmiaceae comprises three genera of shrubs: Alseuosmia A. Cunn. from New Zealand; Memecylanthus Gilg and Schltr. and Periomphale Baill. (=Pachydiscus Gilg and Schltr.) from New Caledonia. These genera are readily excluded from their traditional position in the Caprifoliaceae by virtue of their alternate leaves, valvate corolla lobes and their southern hemisphere distribution. Four species of Alseuosmia, including one hitherto undescribed species, are accepted here. The New Caledonian genera are poorly represented in herbaria; they may each be monotypic. Condensed tannin (leucocyanidin) and ellagitannin are abundant in all Alseuosmia tissues. Other simple phenolic compounds here (as detected in acid hydrolysates) include quercetin, kaempferol, caffeic acid and p-coumaric acid. Triterpenoid saponins are abundant in leaf tissue; alkaloids and probably iridoid compounds too, are absent. Tannin is found throughout the ovary tissue of Alseuosmia and in the inner and outer epidermises of the ovular integument. The floral vascular anatomy is detailed for the Alseuosmiaceae and reviewed for eight allied families. No features of the vascular system imply particular affinity of the Alseuosmiaceae with any of these allies. Within this family the association of different morphological and anatomical floral features supports the contention that primitive characters tend to be associated with one another in their distribution throughout the members of a taxon. The primary vascular pattern in the stem of Alseuosmia is of an open (sympodial) nature. The mature nodal anatomy is 3-trace trilacunar. All genera have a stem endodermis with prominent Casparian banding, and in Alseuosmia at least this endodermis passes through the secondary and quaternary stages (lignification-suberisation of walls; accumulation of phenolic compounds) as found in a typical root endodermis. All species of Alseuosmia lack rays in the secondary wood, whereas memecylanthus and Periomphale have extremely tall (indefinitely-prolonged?) rays. The vessels of these genera are relatively primitive (end-plate angle c.10-19°, no bars per scalariform plate c.16-37), and thus are comparable to vessels of the Escalloniaceae and Caprifoliaceae. The root periderm has a cortical origin in Alseuosmia and the root pith is persistent. Multicellular uniseriate hairs are found in the leaf axils in all Alseuosmiaceae. Hairs with similar structure and development are found in some genera of Pittosporaceae but not, so far as is known, in other related groups. Within Pittosporum, these uniseriate hairs appear to be homologous with the T-hairs many species have. The chromosome number of 2n=18 probably characterises all the species of Alseuosmia. A. macrophylla A. Cunn. is an obligate outbreeder with an incompatibility mechanism operating at the stylar level, while A. pusilla is self-compatible. Pollinating agents for the species are unknown. No internal barriers to hybridism exist between A. macrophylla and A. banksii A. Cunn. and the hybrid swarm between these species is recognised here as A. X quercifolia A. Cunn. Neither do internal barriers exist between A. macrophylla and A. pusilla, but differences in flowering time and mode of breeding help to keep these species separate in the field. Mature pollen of Alseuosmia is trinucleate: the ovule is uni-tegmic-tenuinucellate. The distinctness of the Alseuosmiaceae is upheld and its affinities are suggested to be with the Escalloniaceae, and to a lesser extent, with the Pittosporaceae.

This thesis demonstrates some of the potential of Phyllocladus trichomanoides D. Don (tanekaha) for dendrochronological research, especially dendroclimatology. The type of vegetation associated with sites producing a chronology showed no obvious pattern. The resulting non-specific range of suitable sites for dendrochronological sampling was thought to be a favorable species characteristic. Standardization of tree-ring series using a 50-year Gaussian filter resulted in 28% improvement of retained common variance above that obtained from using conventional polynomial filters. The problem of autocorrelation was investigated. Tanekaha had a consistent autocorrelation pattern through both space (i.e. latitudinal and altitudinal ranges) and time (preserved forest and contemporary stands). P. glaucus (toatoa) also showed a spatially consistent yet distinctive pattern. These different diagnostic patterns implied a non-climatic cause (i.e. physiological), illustrating the need to ensure their removal before species chronologies are compared or used for climate modelling. Low order autoregressive models (ARMA(p,0)) were used to filter out the significant levels of autocorrelation. Subsequent comparison of the chronologies showed a consistent and highly significantly correlated pattern between both sites and species. The paucity of information about the physiology of Phyllocladus spp. led to the testing of several climatic variables in response function analyses. The "best" variables (based on only statistical evidence) were minimum monthly temperature, monthly total raindays and an optimal 12 month span of August (t) to July (t+1). Preliminary attempts with response functions using different combinations of predictor (climate variables) and predictand (chronologies) data sets generally failed to verify. Neither the extent of time from which the response functions were based (no analogue situation) nor a supposed "physiological shock" period (poor growth period) were the causes for non-verification. Further investigation showed that, for both the individual and combined chronologies, the temperature response was similar but rainfall varied. The instability through time of the rainfall response was particularly disconcerting since it broke one of the fundamental assumptions used in dendroclimatology. It was therefore concluded that climatic reconstruction could be attempted only on the temperature data. The temperature data of three seasons (spring, summer and autumn) were tried with transfer function models. Of these the summer season explained the most variance and had the highest reduction of error(RE) values. The selected model used the period 1918 to 1982 for calibration and 1853 to 1917 for verification. Summer temperatures from 1982 to 1750 were reconstructed. The reconstruction modeled only c.30% of the variance but was highly correlated to the summer temperature series developed by Norton (1983). This was interpreted as further independent verification of the reconstructed series. The summer temperatures reconstructed from 1982 to 1750 were concluded to have been similar to the recorded pattern from 1853. The same regressors were applied to the buried forest chronology and the summer temperatures reconstructed from 105 BC to AD 175. Because of the non-continuous tree-ring record no comment can be made of actual ambient conditions in comparison to those of today. However, the reconstructed pre-Taupo summer series did show increased variation towards the time of the eruption and more pronounced cool summers than hot ones. Another applied use of a tanekaha chronology was demonstrated with 14C dating. A statistically significant fit of 14C ages was obtained between twelve contiguous decades from the buried forest tanekaha chronology with that from a Northern hemisphere decadal calibration curve based on Sequioadendron giganteum(Stuiver & Becker 1986). This "wiggle-matching" to the calibration curve places the year of the Taupo eruption as AD 177±18 10. An Independent check of the "new" date was conducted using the most reliable data of Healy et al. (1964) with the same calibration series as described above. A date of AD177±4 44 was obtained which supports the wiggle-matched date. The confidence interval of the wiggle-matched date also coincides with the date proposed by Wilson et al. (1980) of AD186 (based purely on ancient written records).

A total of six hundred and sixteen fungal and two hundred and thirty two bacterial isolates were obtained either from the sapwood of Pinus radiata or from other sources, including UV mutagenesis. All isolates were screened on Pinus radiata wood chips for their survival and colonisation attributes. Of these isolates, two hundred and eighty two failed to grow or caused permanent deep seated discolourations or decay and were eliminated from the study. The remaining five hundred and sixty six isolates were assessed for their antagonistic ability against sapstain. In a dual screen on Pinus radiata wood chips, one hundred and twelve fungal and four bacterial isolates inhibited the growth of the known sapstain fungus, Ophiostoma piceae. In a second biological control screen, on Pinus radiata wood blocks, isolates of Gliocladium viride, Gliocladium roseum, Trichoderma hamatum, Trichoderma harzianum, Trichoderma sp., Trichothecium roseum and an isolate of the Thelephoraceae proved inhibitory to the sapstain isolates Ophiostoma piceae and Sphaeropsis sapinea providing between 94 and 100% control. These isolates were considered for further examination in the field. The remaining isolates provided poor or inconsistent inhibition or were mould fungi and, therefore, not suitable for direct application. All fungal and bacterial isolates that had shown inhibitory ability in the initial biological control screen and the remaining non-staining bacteria were examined for their ability to produce non-volatile metabolites that were inhibitory to sapstain. The bacterial isolates were examined in a preliminary dual plate screen in which 91 isolates were identified as producing inhibitory compounds. The best of these bacterial isolates were screened, with the fungal isolates, in a non-volatile metabolite trial utilising filter sterilised culture filtrates. Isolates of Bacillus sp., Fusarium solani, Gliocladium roseum, Gliocladium virens, Trichoderma harzianum, Trichoderma sp., Trichoderma viride and Trichothecium roseum were found to be significantly inhibitory to the growth of Ophiostoma piceae at concentrations of 50% or less. However, the filtrates did not provide adequate sapstain control, when tested on Pinus radiata wood block, to prompt consideration for further examination in the field. Studies are currently examining several of these isolates for the production of biologically active compounds. The six most promising isolates, from the wood chip and wood block trials, were tested in the field for their ability to control sapstain on unseasoned Pinus radiata sapwood and/or peeled logs. These were Gliocladium viride (FK75), Trichoderma hamantum (FK561), Trichoderma harzianum (FK228), Trichoderma sp. (FK247), Trichothecium roseum (FK238) and an isolate of the Thelephoraceae (FK33). The fungi were prepared as mycelial/spore homogenates. For application to the timber, the homogenates were mixed with 0.2% Alcosorb gel, producing 108 cfu/ml suspensions, these suspensions were applied by dipping. Diluted homogenates, 108 cfu/ml, were applied as spray treatments to the logs. All of the biological control agent treatments reduced the level of sapstain on either the logs or timber with Trichoderma harzianum (FK228), Trichoderma sp. (FK247) and Trichothecium roseum (FK238) providing control equivalent to that of the fungicides NP-1 and Diffusol for portions of the trial. Trichoderma sp. (FK247) and Trichothecium roseum (FK238) gave sapstain control in excess of 90% for the first 30 days of the timber trial equalling the control provided by NP-1 and Diffusol. In another trial, Trichoderma harzianum (FK228) was more effective than NP-1, providing 60% sapstain control, after six months, on the internal tissue of Pinus radiata logs. The six isolates selected for the field trials were examined in additional studies. In a dual inoculation study, Trichoderma sp. (FK247) exhibited localised antibiotic ability causing the lysis of mycelium of sapstain fungi. There was no evidence of mycoparasitic action by any of the six isolates. Trichoderma harzianum (FK228), Trichoderma sp. (FK247) and Trichothecium roseum (FK238) were observed to degrade cellulose. However, neither these nor the other isolates caused a significant change in the mechanical properties of Pinus radiata timber when compared to untreated controls. Decreasing pH or the addition of nitrate were identified as having potential for the promotion of biological control agent growth. The potential of mixed biological control agent inoculations was also examined. While these results are preliminary, they are extremely encouraging and provide a basis from which future studies can develop.

Aquatic macrophytes possess an internal lacunar system of proliferated intercellular airspaces. Lacunar gas exchange processes were investigated in Egeria densa Planch., a submerged freshwater angiosperm. Investigations of oxygen exchange between Egeria shoot segments and the water revealed that up to 17% of the photosynthetically-produced oxygen is retained within the lacunae. A consequence of this partitioning, which results from the relatively low solubility of oxygen in water, is the development of internal lacunar pressures up to 20 kPa above atmospheric pressure. This storage of oxygen in Egeria casts doubts on oxygen-based measurements of productivity in aquatic macrophytes, unless both internal and external sinks are monitored. Pressurisation also revealed that storage is greater in static water than in flowing water, suggesting that boundary layer limitations to oxygen transfer can also affect partitioning. Pressures fall to sub-atmospheric values in the dark, due to respiratory consumption of the internal oxygen. The Egeria respiratory gas exchanges in the dark demonstrated a steady concentration gradient between plant and water within an hour of darkening. However, the material steadily consumes approximately 30% of its respired oxygen from the lacunae, rather than the water. This oxygen supply is again due to the low oxygen solubility. The lacunae also assist the radial oxygen supply into the respiring tissue; it was found that the Michaelis-Menten constant for the respiratory response to oxygen tension in Egeria was some two to three times greater in material with infiltrated lacunae than in uninfiltrated material. Oxygen storage in the stem lacunae resulted in a longitudinal (shoot to root) movement of this gas, which was monitored using a bicompartment apparatus. The root oxygen release rate varied with light intensity and water flow rate in a similar manner to the internal pressure changes. Further experiments, involving measurements of the oxygen flux rates in the Egeria rhizosphere, demonstrated that this root oxygen loss is capable of effecting substantial diurnal oxygen fluctuations in the surrounding sediment. These processes may be interrupted by natural infiltration of the airspaces, but the factors involved here remain uncertain. The mean internal oxygen transport rate in Egeria (6.28 μ102 h-1) was consistent with estimates of lacunar oxygen concentration gradients calculated from Fick's Law, suggesting that diffusion is the oxygen transport mechanism in Egeria. However, by connecting shoots into manometers, internal pressure gradients of some 0.9 kPa m-1 were detected. These gradients were 103 -fold greater than the pressure gradient required to account for oxygen transport in Egeria, but were transient features, as the pressure equilibrated throughout the lacunar system 20 - 30 minutes after a dark/light change. Mass flow was therefore proposed as a transitory, but potentially significant, contribution to oxygen transport. Root to shoot carbon dioxide transport was measured using 14CO2 tracing. The CO2 uptake (mean internal transport = 4.96 μ1CO2 h-1) represented <10% of the total carbon fixed; the concentration of root-derived carbon in shoot tissue declined rapidly from the root insertion point. These results are compared with those of previous studies, and the significance of the Egeria lacunar system assessed.

Two Coelomycete genera, Ascochytula Died. and Ascochytella Tassi, were studied in order to determine their generic affinities, especially with Ascochyta. Ascochytula obiones (Jaap) Died., the type species of Ascochytula, is considered to be congeneric with Ascochyta pisi Lib., the type species of the earlier genus, Ascochyta Lib. Ascochytula is thus reduced to synonymy with Ascochyta. Of the thirty-six species and two varieties named in, or directly associated with, Ascochytula, twenty are herein described as species of Ascochyta and four are excluded from Ascochyta. The remaining species were either not examined, or are nomina dubia. The following names are proposed: Ascochyta asparagina (Petrak) comb. nov., A. deformis (P. Karsten) comb. nov., A. dorycnii (Petrak) comb. nov., A. ludwigiana (Petrak) comb. nov., A. moravica (Petrak) comb. nov., A. obiones (Jaap) comb. nov., A. phlomidicola nom. nov., and A. ulicis (Grove) comb. nov. Ascochytella Tassi, which has often been confused with Ascochytula, is also synonymised with Ascochyta. The original thirteen species in Ascochytella were examined, and A. vicina (Sacc.) Tassi chosen as the lecto-type species. Most of the thirteen species are regarded as being either misplaced in Ascochytella, or nomina dubia, and only four, including the lectotype, are accepted as species of Ascochyta. The name, Placodiplodia canthiifolia (Cooke & Massee) comb. nov. is proposed. The type species of Ascochyta, and of six related genera, Ascochytulina Petrak, Coniothyrium Corda. Diplodina Westend., Pseudodiplodia (P. Karsten) Sacc., Scolecosporiella Petrak, and Stagonospora (Sacc.) Sacc. were studied to determine the distinctions between these six genera and Ascochyta. Microdiplodia Allescher and Diplodia Fr. are also discussed, in relationt to Ascochyta. Ascochyta paspali (H. Sydow) Punith. (≡ Ascochytula paspali H. Sydow), which causes a leaf stripe disease of Paspalum dilatatum Poir., an important perennial grass of northern North Island pastures, was examined in detail. At some temperatures, under controlled climate conditions, the fungus significantly reduced the yield of P. dilatatum. A. paspali was found to grow systemically, as mycelium within the xylem vessels, and was able to infect all parts of the plant, including the roots and seeds. Green leaves sometimes became infected systemically without production of visual symptoms. Infected seed is suggested as a means for disease spread. No teleomorph for A. paspali was found, and the fungus is thought to over-winter in the dormant grass. The seasonal fluctuation in levels of P. dilatatum and of the disease was studied in two Northland pastures with paspalum as a component. One pasture was studied for fourteen months, and the other for four months. Disease levels, and paspalum levels, were determined by point quadrat analysis and by sorting of randomly cut samples. Levels of both the host and of the disease peaked in summer, while both were at low levels, or apparently absent, over the winter months.

No description available.

Botrytis cinerea and Sclerotinia sclerotiorum are the two most serious pathogens on kiwifruit in New Zealand. Because of the pesticide regulations in some of the countries to which New Zealand exports fruit, total protection from Botrytis stem end rot with current dicarboximide fungicides is not possible. The aim of this thesis was to investigate biological control measures for Botrytis stem end rot and Sclerotinia diseases of kiwifruit. More than 1000 microorganisms, isolated from the leaves and flowers of kiwifruit during spring and autumn, and selected from BCAs reported to be effective against B. cinerea and./or S. sclerotiorum, were tested in vitro for their antagonistic ability against B. cinerea and S. sclerotiorum. Successful antagonists were those that, in dual culture on agar plates, produced a zone of inhibition, an area of browning of the pathogens, or grew rapidly over the pathogens and inhibited their growth. The fifty most promising isolates from the initial screen were tested on fruit for their ability to reduce Botrytis and Sclerotinia fruit rots. Mature kiwifruit were artificallv wounded and dual inoculated with a spore suspension of one of the fifty test organisms and either a conidial suspension of B. cinerea or a mycelial suspension of S. sclerotiorum. Following 8-12 weeks incubation in a cool store, fruit were assessed for Botrytis or Sclerotinia induced rot. Isolates of Bacillus spp., Epicoccum purpurascens, Pseudomonas sp. and Trichoderma. spp. reduced, Botrytis fruit rot from 92% (inoculated control) to 0%.Isolates of Alternaria spp., pestalotia sp. and a non-sporulating isolate also reduced the number of fruit rotting to some extent. Similarly, isolates of Bacillus spp., E purpurascens and Trichoderma spp. reduce d Sclerotinia fruit rot from 100% (inoculated control) to 0%. Isolates of Alternaria spp., Myrothecium verrucaria and Pestalotia sp. were also successful at reducing the level of Sclerotinia fruit rot. It was considered undesirable if potential biological control agents (BCAs) were able to colonize kiwifruit that were to be marketed for human consumption. In order to determine if microorganisms, shown to be effective in preventing Botrytis or Sclerotinia fruit rot, were capable of themselves colonizing fruit, isolations were made from fruit dual inoculated with B. cinerea, S. sclerotiorum and/or one of several BCAs. Strains of the BCAs Bacillus spp., Pseudomonas sp. and E. purpurascens were not found to be saprophytic on fruit. Isolates of Alternaria sp., Bacillus sp., E purpurascens, pestalotia sp., Pseudomonas sp. and T. harzianum significantly inhibited germination and germ tube elongation of B. cinerea conidia in vitro in a nutrient solution, over a 24 h period. For example, the presence of Alternaria alternata A6 spores in a nutrient solution reduced germination of B. cinerea conidia from 100% to 20%. The presence of E purpurascens A77 spores inhibited B. cinerea conidial germ tube elongation from >840 pm (in control conidia) to 27 µm. The presence of any one of the BCAs tested prevented germination of B. cinerea conidia in a non-nutrient water solution, in comparision to germination of up to 86% in controls. A spore or cell suspension of each of the isolates Bacillus sp.M60, E. purpurascens A77 and T. harzianum C65 were spray inoculated onto kiwifruit blossoms produced in vivo in the glasshouse, immediately prior to inoculation of the blossoms with a condial suspension of B. cinerea. Application of the BCAs were completely effective in preventing colonization of blossoms by B- cinerea conidia. The effectiveness of each of the isolates E. purpurascens A77,T. harzianum C65 and either Bacillus sp.M60 or M53 to reduce the viability of sclerotia of B. cinerea and S. sclerotiorum was tested in soil punnets. A spore or cell suspension of each respective BCA was applied to the surface of replicated punnets that were seeded with either B. cinerea or S. sclerotiorum. Following 8 weeks incubation, punnets were harvested and viability of sclerotia assessed. T. harzianum C65 and Bacillus sp. M60 significantly reduced the viability of B. cinerea sclerotia from 8 sclerotia/punnet (control) to 4 sclerotia/punnet. T. harzianum C65 and E. purpurascens A77 caused a significant reduction in apothecia production of S. sclerotiorum, from 2.7 apothecia/punnet (control) to 0.7 apothecia/punnet. Bacillus sp.M8 and E purpurascens A77 were tested for their ability to reduce Botrytis stem end rot and Sclerotinia field rot in a kiwifruit orchard. The isolates tested did not successfully reduce either disease. Possible explanations for this are discussed. In order to monitor the survival of particular isolates of BCAs in the field, a technique was developed to distinguish between individual strains of a BCA species. The polymerase chain reaction (PCR) was utilized to identify DNA polymorphisms within the genome of T. harzianum C65, in comparison with other strains of Trichoderma spp.. A sequence of polymorphic DNA was cloned, sequenced and used as a hybridization probe in southern blotting to enable T. harzianum c65 to be distinguished from other strains of Trichoderma spp.. From the results obtained in this study, it was considered that Bacillus M60, E purpurascens 477 and Pseudomonas M30 were the best isolates for the biological control of Botrytis stem end rot on kiwifruit. Further work to enable application of these isolates as postharvest BCAs is discussed. Of the isolates tested in this study, T. harzianum C65 was considered the best isolate for use against Sclerotinia diseases on kiwifruit. Methods of selecting more effective BCAs against S. sclerotiorum are discussed.

Summary: 1. A Study was made of some aspects of the utilization by Spirodela oligorrhiza of ammonium, nitrate, nitride, and organis nitrogenous compounds as sole sources of nitrogen. 2. S. oligorrhiza was grown in axenci culture under carefully defined conditions, and the only factor to be consciously varied were those relating to the nitrogen source. 3. Ammonium, or some product of assimilation, inhibited the utilization of nitrate by inhibiting, at least partially, the uptake of nitrate, and by inhibiting almost completely the reduction of nitrate to nitrite. 4. Nitrite also inhibited the utilization of nitrate. 5. Ammonium and nitrite were taken up and assimilated simultaneously when they were supplied together in the medium. 6. Nitrate reductase and nitrite reductase were found to be adaptive enzymes, being present in S. ologorrhiza only when it was supplied with nitrate or nitrite. There was good correlation between the concentration of nitrate in plants and the level of nitrate reduction that they contained...