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Strategies for the control of the foliar diseases of oats in South Australia / by Andrew R. Barr.Barr, Andrew Robert January 1994 (has links)
Bibliography: p. 410-429. / 429 p., [20] leaves of plates : ill. (some col.), map ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Thesis (Ph.D.)--University of Adelaide, Dept. of Plant Science, 1995?
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Phytophthora root rot of chestnutChambers, Susan M., 1967- January 1993 (has links) (PDF)
Bibliography: leaves 158-189.
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Strategies for the control of the foliar diseases of oats in South AustraliaBarr, Andrew R. (Andrew Robert) January 1994 (has links) (PDF)
Bibliography: p. 410-429.
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Feeding determinants in aphids with special reference to the Rose Aphid Macrosiphum rosae (L.)Peng, Zhongkui. January 1991 (has links) (PDF)
Bibliography: leaves 170-189. This thesis looks at aphid feeding determinants by type and location. It examines the role of leaf surface chemicals in the discrimination of host plants and the deterrent effect of catechin and its oxidative condensation products.
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Pathology and molecular comparison of a range of pea seed-borne mosaic virus isolatesAli, Akhtar. January 1999 (has links) (PDF)
Copies of author's previously published articles inserted. Bibliography: leaves 128-143. This thesis describes the development of serological and nucleic acid based diagnostic methods for pea-seed borne mosaic virus (PSbMV), the isolation of specific effects on infected pea plants, the collection and biological comparison of new PSbMV isolates from Pakistan, the cloning and sequencing of specific parts of the genome of selected isolates, nucleotide and amino acid sequence comparisons between selected isolates, and the development of a ribonuclease protection assay (RPA) for identifying genomic differences among the PSbMV isolates. It is the first comparison of a range of geographically different isolates of PSbMV on the basis of both biological and molecular properties.
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Molecular characterization of criniviruses and ilarviruses infecting strawberryTzanetakis, Ioannis E. 19 March 2004 (has links)
Pallidosis is a disease of strawberry identified in 1957 with an unknown etiology.
Two previously uncharacterized viruses in strawberry, Strawberry pallidosis associated
virus (SPaV) and Beet pseudo-yellows virus (BPYV), have been found associated with
disease symptoms. The complete nucleotide sequence of both viruses was determined and
molecular detection protocols developed. In addition, an immunological tissue blot assay
was developed for SPaV. Phylogenetic analysis of SPaV placed it in the genus
Crinivirus, family Closteroviridae, along with BPYV. Transmission studies identified
Trialeuroides vaporariorum, the greenhouse whitefly, as a vector of SPaV, while the virus
was not transmitted by pollen or seed. The geographic distribution of both SPaY and
BPYV in the United States was examined.
Two ilarviruses of strawberry were investigated. Tobacco streak virus (TSV) is
the type member of the genus Ilarvirus, family Bromoviridae, and can cause severe yield
losses in small fruit crops. Sequence and phylogenetic analysis of 15 "TSV" isolates from
Fragaria and Rubus revealed that they are homogeneous and represent a new virus
species designated as Strawberry necrotic shock virus (SNSV). Nucleic acid-based
protocols failed to identify any plants of the study infected with TSV an indication that
the virus may not be a pathogen of Fragaria and Rubus.
Fragaria chiloensis latent virus (FC1LV) is the second member of the genus
Ilarvirus that infects strawberry. Previously, the virus had been found only in Chile and
although many plants have been tested in North America using a serological test, none
was found infected with the virus. A molecular test has been developed and used to
confirm the presence of the virus in strawberries along the west coast of North America.
Phylogenetic analysis of the coat protein gene of the virus place it in subgroup 4 of the
genus along Prune dwarf virus, while it was previously thought to be related most closely
to Lilac ring mottle virus and Asparagus virus-2.
The role of the newly identified viruses and other viruses infecting strawberry is
discussed in association with the strawberry decline disease found to cause severe
symptoms and yield losses in both California and British Columbia, Canada.
The significance of the work presented in this publication includes: the
identification of two viruses associated with strawberry pallidosis disease; the complete
nucleotide sequence of two criniviruses, an emerging group of plant viruses adds to the
limited knowledge we have about this diverse virus genus; the identification of FC1LV in
North America; the identification of SNSV as a distinct virus species which demonstrates
the need of further studies on TSV, a virus species that infect a wide range of plant
species and may actually be a cluster of diverse species. The high incidence of the
pallidosis associated viruses points to the significance of the disease and their role in
strawberry decline. The development of fast, sensitive and reliable tests for four
strawberry viruses will have an impact to the strawberry industry, since the need for high
quality, virus-free plants is essential for a crop that is asexually propagated. / Graduation date: 2004
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Sequence determination and regional epidemiology of raspberry bushy dwarf virus (RBDV)Taylor, Susannah M. 08 July 1999 (has links)
Raspberry bushy dwarf virus (RBDV) is the sole member of the idaeovirus genus
of plant viruses. It is a pollen-borne virus that economically impacts both red and black
raspberries worldwide. Three strains of the bipartite RBDV have been reported. The
common strain found in North America, South America, Australia, New Zealand and
Europe and the resistance breaking strain found only in Europe are serologically
indistinguishable while the black raspberry strain from North America is distinct.
Resistance to RBDV is conferred by a single dominant gene, Bu. The resistance
breaking strain is able to infect all raspberry cultivars containing the Bu loci. The
sequence of a full-length clone of the common strain was determined and compared to
the previously published sequence of the resistance breaking strain. Nucleotide
homology between the two isolates was 97.6% for RNA 1 and 97.6% for RNA 2.
Comparison of the predicted RNA 1 protein product of the two strains showed 97.9%
homology. The predicted amino acid sequence of the movement protein and the coat
protein from RNA 2 demonstrated 98.6% and 98.5% identity respectively.
The differential rate of virus spread under field conditions in the Pacific
Northwest was also investigated. The possibility of higher temperatures inhibiting virus infected
pollen was explored by using in vitro germination and enzymatic staining
procedures. Results from a two year study of virus-infected and virus-free raspberry
pollen viability from both the Oregon and southern Washington region and the northern
Washington and southern British Columbia region suggest temperature does not affect
pollen germination or viability.
Further studies were conducted to determine if a virus-degrading agent could be
present on bee-stored raspberry pollen that becomes active only at higher temperatures.
RBDV infected pollen from hives in northern Washington was collected and tested by
ELISA after receiving either no heating or 32 hours of heating at 20, 30 or 40 C.
Preliminary results indicate no such agent exists in red raspberry pollen from hives in the
Pacific Northwest. / Graduation date: 2000
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Biology and control of Fusarium spp. on Douglas-fir (Pseudotsuga menziesii)Hoefnagels, Mari��lle Henriette, 1965- 02 December 1996 (has links)
Fusarium spp. are among the most important pathogens of Douglas-fir
(Pseudotsuga menziesii) seedlings in bareroot nurseries. Currently the most effective
disease control method is soil fumigation with methyl bromide. As methyl bromide is
phased out, however, other disease management strategies may become more important.
We explored two alternative approaches to management of Fusarium diseases in
Douglas-fir seedlings. The first approach was to transfer certain components of conifer
forest soil, where Fusarium usually does not occur, to nursery soil, where Fusarium is
often abundant. Specifically, we tested two hypotheses: (1) conifer forest soil contains a
greater proportion of bacteria antagonistic in vitro to Fusarium than does nursery soil,
and (2) pine needles, humic acid, ectomycorrhizal fungi, or bacteria obtained from forest
soil will protect Douglas-fir seedlings against disease caused by soilborne Fusarium spp.
if added to nursery soil. We did not find conclusive evidence to support either
hypothesis. The second approach was to investigate the potential for biological control
of seedborne Fusarium. Previous workers have shown, and we have confirmed in our
studies, that Fusarium present on a small percentage of Douglas-fir seeds before cold
stratification may spread during stratification; we recovered Fusarium from nearly all
stratified seeds, representing three seedlots, plated on three culture media. When these
seeds were planted in pasteurized soil, however, seedborne Fusarium did not cause
significant disease in seedlings. Biological control of seedborne Fusarium during
stratification may be important both to reduce the contribution of seedborne Fusarium to
nursery soil and to protect germinants from soilborne Fusarium. We hypothesized that
Pseudomonas chlororaphis isolate RD31-3A, a fluorescent pseudomonad previously
shown to control Fusarium on Douglas-fir, would reduce the spread of Fusarium during
stratification and protect seedlings from damping-off when seeds were planted into soil
infested with pathogenic F. oxysporum. High populations of RD31-3A were recovered
from seeds after stratification, and bacterial treatment reduced the spread of Fusarium
without affecting seed germination or subsequent seedling dry weights. RD31-3A did
not, however, protect seedlings from soilborne F. oxysporum. Nevertheless, seed
treatment with bacteria during stratification may be an efficient way to deliver biological
control agents to conifer seeds. / Graduation date: 1997
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Pathogenic variability and adaptation of Septoria tritici to different wheat cultivarsAhmed, Hafiz Uddin 01 November 1993 (has links)
Experiments were done to determine pathogenic variability
and pathogenic adaptation of Septoria tritici to different
wheat cultivars. Fifteen S. tritici isolates from
California, Oregon, and Texas were evaluated on seedlings of
two sets of geographically diverse wheat cultivars under
greenhouse conditions. Significant isolate effects, cultivar
effects, and isolate X cultivar interactions were found,
though the interaction terms were very small compared to the
main effects of isolate and cultivar. All except one isolate
were virulent to two sets of cultivars, and the virulence
patterns varied among the isolate-cultivar combinations.
Variability in virulence among the S. tritici isolates
within and between locations also was observed. The isolates
were usually more virulent to the cultivars of the same
geographic origin than cultivars of other locations, and
this demonstrates location-specific adaptation of S.
tritici.
Four populations of S. tritici, secured from four
winter wheat cultivars grown in a field experiment, were
evaluated on seedlings of the same wheat cultivars under
greenhouse conditions. Significant spore population
differences, cultivar differences, and spore population X
cultivar interactions were obtained. The interaction term
was fairly large compared to the main effect of spore
population, and it is likely that the significant
interaction was due to increased virulence of S. tritici to
its own cultivar of origin. The "own" spore population
(inoculation with spore population obtained from the same
cultivar) produced significantly larger area under disease
progress curve on the cultivar of origin than the "others"
(inoculation with spore populations obtained from other
cultivars), suggesting cultivar-specific adaptation of S.
tritici. Spore populations obtained from the two susceptible
cultivars indicated general adaptation to all of the test
cultivars, whereas, the spore population secured from the
most resistant cultivar showed specific adaptation to its
cultivar of origin. Consequences of pathogenic variability,
increased virulence, and adaptation of S. tritici to wheat
cultivars are discussed. / Graduation date: 1994
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Insects and InsecticidesToumey, J. W. 11 1900 (has links)
This item was digitized as part of the Million Books Project led by Carnegie Mellon University and supported by grants from the National Science Foundation (NSF). Cornell University coordinated the participation of land-grant and agricultural libraries in providing historical agricultural information for the digitization project; the University of Arizona Libraries, the College of Agriculture and Life Sciences, and the Office of Arid Lands Studies collaborated in the selection and provision of material for the digitization project.
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