School of Agriculture, Food and Ecosystem Sciences - Theses
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ItemThe occurrence of brittleheart in Eucalyptus regnans and its effect on various wood properties( 1990)This project is mainly concerned with a description of anatomical and ultrastructural characteristics of cell wall deformations in brittleheart of E. regnans, development of methodology for quantification of percentage of broken fibre pieces (PBFP) in E. regnans, and physical and anatomical properties of E. regnans in relation to the occurrence of brittleheart. Two 1939 regrowth E. regnans butt logs and one mature growth E. regnans butt log removed from a tree approximately 120 years old were used in the study. The anatomical and ultrastructural characteristics of cell wall deformations were examined with bright field, polarized light, and scanning electron microscopy. The microscopic compression lines were found to consist of slip planes, minute compression failures, corrugations, and buckles. The width of microscopic compression lines along the longitudinal fibre axis ranged from one single fold in the cell wall up to 7 times the average fibre width. The length of the microscopic compression lines ranged from ones which only crossed a few fibres to ones which crossed up to 200 fibres. The severity of microscopic compression lines appeared to be dependent on the type of cell wall deformations and degree of compaction in the deformed zone. In the methodology studies it was found that for a pulp sample prepared from a 2 mm by 2 mm by 15 mm wood chip approximately 400 cellular elements in 8 out of 16 areas on a slide needed to be counted in order to obtain PBFP with less than 10% error. For macerated thin sections, all the cellular elements on 2 slides each carrying about 600 fibres and fibre pieces needed to be counted. A highly significant correlation was found between the length of microscopic compression lines per unit area and the microscopically determined PBFP. A highly significant correlation was found between the theoretical PBFP and the microscopically determined PBFP. These findings confirm that maceration of wood containing cell wall deformations results in broken fibres and verifies the validity of the maceration technique for quantifying the amount of microscopic compression lines. PBFP was found to increase with macerating time. A maceration time around 10 hours appears sufficient to cause fibres having cell wall deformations to break but longer times cause fibres without cell wall deformations to also break due to overmaceration. A significant relationship was found between PBFP determined after 5 hours and after 10 hours of maceration at the same temperature. It was found that parameters extracted or derived from cell length distributions produced by the Kajaani FS-200 may be used to determine the amount of fibre fragments in pulp samples. These parameters were the high peak, the length weighted average, and the mass weighted average of the cell length distributions for pulps which had PBFP greater than 10. Based on the maceration technique, brittleheart was detected in both the mature and the 1939 regrowth logs. Brittleheart was more severe and occupied a larger area in the mature growth than in the regrowth wood. The PBFP was found to be mostly below 5 in the regrowth wood although relatively high PBFP values of 21 and 30 were observed. PBFP values as high as 85 was found in the mature growth wood. In general, PBFP was found to be higher nearer the pith, decreasing toward the bark, and dropping to zero before reaching the two-thirds theoretical point where the stress is assumed to be 0. A large circumferential variation in PBFP was observed in four adjacent growth rings of the mature log. A large variation in PBFP was also found within a volume of 1000 mm^3 for both the mature and the 1939 regrowth wood. The earlywood PBFP was found to be significantly higher than the latewood PBFP for the mature and regrowth logs. A total of 72 green and 132 12% MC Izod specimens were prepared from the two 1939 regrowth logs and tested for impact strength. The mean Izod value was found to be 9.9 ft.lb for the 132 12% MC Izod specimens and 9.2 ft.lb for the 72 green Izod specimens. For side-matched Izod specimens, the mean Izod value was found to be 9.2 ft.lb at green and 9.7 ft.lb at 12% MC and the mean for the 12% MC specimens did not reflect the expected increase in strength with moisture loss. Excessively low Izod values (eg. 1.8 ft.Ib) were found in the 12% MC Izod specimens located near the pith. For 76 12% MC Izod specimens, their PBFP, fibre length, and specific gravity were also measured. Significant relationships (p=0.01) were found between Izod values and specific gravity, PBFP, and fibre length for these 76 12% MC Izod specimens. Specific gravity and fibre length positively contribute to the impact strength whereas PBFP negatively affects the impact strength. Brash-break specimens showed a low mean Izod value, a low mean specific gravity, the presence of brittleheart, and a short mean fibre length.
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ItemA study on damping-off in a regeneration mixed eucalypt forest( 1986)Although damping-off is known to cause considerable loss before and after emergence of seedlings in forest nurseries, little is known of its role in seedling mortality after direct seeding in artificial regeneration of mixed eucalypt forests. Findings reported in this thesis are the result of a survey for the presence of damping-off fungi in soils and dying seedlings, and tests of their pathogenicity to a range of eucalypts found in the Wombat State Forest of Victoria. This study was carried out in conjunction with a research programme established by the Victorian Department of Conservation, Forests and Lands to determine which factors govern the successful establishment of E. obliqua and E. radiata in three seed-bed types under five levels of overwood. Propagule counts for Pythiaceous fungi in burnt and unburnt soils from field experiment, plots prior to sowing indicated that the inoculum level was low and differed with levels of overwood retained following site preparation in summer (Chapter 2). Baiting the soils with E. sieberi cotyledons, apples or directly sowing E. sieberi seed in samples of the field soil showed that both burnt and unburnt soils were variably infested with Pythium spp., Fusarium spp., and Cylindrocarpon destructans. A small portion of the seed to be sawn in the field plots without any fungicidal pre-treatment was found to harbour a range of fungi, sane of which had the potential to inhibit germination of the eucalypts sown on the plots (Chapter 3). The fungi having this ability were however not isolated from damped off seedlings in the experimental plots. Field studies showed that the proportion of germinated seedlings killed as a result of damping-off was lower than that attributable to frost heave, droughting following freezing and insect damage (Chapter 4). Damping-off was found to be widespread over the entire study site and the rate of damping-off to differ with seed-bed type. Overwood density did not affect the disease level. Although Pythium spp. were responsible for most deaths, Cylindrocarpon destructans and Fusarium spp. also caused some mortality. Pathogenicity tests (Chapter 5) confirmed that the fungi associated with seedling mortality in the field can cause significant pre- and post-emergence damping-off in a range of eucalypts found at the study site. The fungi differed in their pathogenicity to the eucalypts and sane induced feeder root necrosis after the two leaf stage of seedling development. No differences in susceptibility to post-emergence damping-off were found between the tree species sown on the plots and others of economic importance in the forest. The overall findings and their implications for direct sowing as a management option in future field regenerations are discussed in Chapter 6.