Includes an article co-authored by the author during preparation of this thesis. / Bibliography: leaves 111-131. / xi, 131 leaves : ill. (some col.) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / This study aimed to develop a range of tissue culture techniques that could by utilised in the improvement of Prunus dulcis Mill., with the primary focus being on the development of a genetic transformation system. The two key requirements for such a system, an in vitro shoot regeneration procedure and methodology for foreign DNA introduction, formed the basis of this research. (abstract) / Thesis (Ph.D.)--Adelaide University, Dept. of Horticulture, Viticulture and Oenology, 2001

Thesis (M.S.)--Florida State University, 2004. / Advisor: Dr. Shridhar K. Sathe, Florida State University, College of Human Sciences, Dept. of Nutrition, Food and Exercise Sciences. Title and description from dissertation home page (viewed June 15, 2004). Includes bibliographical references.

Thesis (Ph. D.)--University of Adelaide, Dept. of Horticulture, Viticulture and Oenology, 1995? / Includes bibliographical references (leaves 186-209).

Bibliography: leaves 186-209.

Bibliography: leaves 186-209. / xiii, 209 leaves : ill. (some col.) ; 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 Horticulture, Viticulture and Oenology, 1995

Thesis (M. Ag. Sci)--University of Adelaide, 1987. / Includes bibliographical references (leaves 256-323).

Thesis (Ph. D.)--Ohio State University, 2006. / Title from first page of PDF file. Includes bibliographical references (p. 160-175).

Title page, table of contents and abstract only. The complete thesis in print form is available from the University of Adelaide Library. / The Australian almond improvement program was initiated in 1997 to develop improved cultivars that are adapted to local conditions and consumer demands. The program combines molecular techniques along with the traditional approach of controlled hybridisation with mass selection. This research project was carried out to assist the Australian almond improvement program in the areas of micropropagation, cryopreservation, and rapid identification of self-incompatibility genotypes of almond. Micropropagation was accomplished successfully for two commercially important almond cultivars ('Nonpareil' 15-1 and 'Ne Plus Ultra') and an almond/peach hybrid rootstock by culturing shoot tips, about 0.7 cm long with 3 - 5 leaves, on appropriate shoot multiplication media. For 'Nonpareil' 15-1, AP medium with 0.049 uM IBA, 3 uM BAP, 0.058 M sucrose, and 0.7% agar at pH 5.7 was effective. MS medium with 0.049 uM IBA, 5 uM BAP, 0.088 M sucrose, and 0.7% agar at pH 5.7 was suitable for 'Ne Plus Ultra'. For the almond/peach hybrid rootstock, MS medium supplemented with 10 uM BAP, 0.088 M sucrose, and 0.7% agar provided the best shoot proliferation. Shoots of the rootstock, about two cm long, readily produced roots after one week in the dark and two weeks in the light on half strength MS medium supplemented with 2.4 uM IBA, 0.088 M sucrose and 0.7% agar at pH 5.7, with 88.0% rooting efficiency. The two almond cultivars did not readily produce roots, but, at about 1.5 cm long, were micrografted successfully onto the rootstock. These micrografted plantlets were acclimatised and transferred to potting mix with 92% survival. Shoot tips of the two almond cultivars and the almond/peach hybrid rootstock were cryopreserved successfully using a one-step vitrification technique. Three-week-old in vitro cultures were cold-hardened at 4°C on multiplication media (Murashige and Skoog for 'Ne Plus Ultra' and the hybrid rootstock; Almehdi and Parfitt for 'Nonpareil' 15-1) for three weeks. Shoot tips, 2 - 2.5 mm long, were excised and precultured for one day at 4°C on the same basal medium, without plant growth regulators, supplemented with 0.7 M sucrose. After the preculture, the shoot tips were incubated in vitrification solution at 25°C for 45 min for the almond cultivars and 60 min for the almond/peach hybrid rootstock, and then stored under liquid nitrogen (LN) for up to 24 months. After rapid thawing at 30°C, the shoot tips were washed with the appropriate liquid basal medium containing 1.0 M sucrose and then cultured on the same basal medium, solidified with agar, but excluding NH₄N0₃ or (NH₄)₂S0₄. Shoot regeneration was usually observed within 2 - 3 weeks. Survival of shoots after thawing varied from 56-80% for 'Ne Plus Ultra', 35-53% for 'Nonpareil' 15-1, and 62 - 82% for the almond/peach hybrid rootstock. Non-vitrified shoots that were stored on basal medium at 3.5-5°C showed good survival up to six months, but thereafter survival decreased rapidly. Cryopreservation has considerable potential for long-term storage of almond germplasm, but future research should be aimed at improving the regeneration of 'Nonpareil' 15-1, the most important commercial cultivar grown in Australia. The genetic stability of almond DNA to both in vitro culture and the cryopreservation process was evaluated by comparing the fingerprints of the DNA from the original orchard trees, from the in vitro cultures before and after cryopreservation for up to 24 months, and from plants regenerated from in vitro cultures. The fingerprints were prepared by initially digesting the DNA with two isoschizomer pairs of restriction enzymes, one of each pair being 'methylation sensitive' and the other 'methylation insensitive', followed by amplification of the digested products using randomly amplified polymorphic DNA (RAPD) with six different 10-mer primers. Changes in methylation were found between the original orchard trees and in vitro cultures, and there was also the possibility that some structural changes may have occurred. However, no methylation or structural changes could be attributed to the cryopreservation procedure. Plants regenerated from the in vitro cultures before and after cryopreservation should be monitored carefully in the future for changes in morphology compared to the original trees. Partial genomic and cDNA sequences of the self-incompatibility alleles S1, S2, S7, S8, S9, S10, S23, and Sf were obtained from Prunus dulcis cvs 'Anxaneta' (S2S9), 'Cristomorto' (S1S2), 'Ferragnes' (S1S3), 'Gabaix' (S5S10), 'Ne Plus ultra' (S/S7), 'Nonpareil' 15-1 (S7S8), 'Primorskiy'(S5S9), 'Ramilette' (S6S23), and IRTA Selection 12-2 (SfSf). Total DNA was extracted from leaves, and cDNA was prepared from total RNA extracted from styles. The partial cDNA sequences of the S1 allele from 'Ferragnes', and the S7 and S8 alleles from 'Nonpareil' 15-1 matched those reported in the literature for the alleles Sb, Sc, and Sd respectively. The sequences of the S1, S2, S7, S8, S9, S10, S23, and Sf alleles found in genomic DNA contained introns of 562, 253, 1,530, 2,208, 1,343, 710, 494, and 662 bp respectively, and partial exons of 510, 537, 489, 498, 486, 495, 489, and 543 bp respectively. In addition, one allele of the Australian cultivars, 'Johnston's Prolific' and 'Pierce', was identified and found to have the same sequence as S23 in 'Ramilette', suggesting that this cultivar may have been an early introduction to Australia from Spain. The exon/intron splice junction sites of all alleles followed the GT / AG consensus sequence rule, and the sequences were found to be highly conserved. Both the length and the sequence of each intron was unique, and a technique of identifying the S-alleles of almond was developed based on primers that targetted the intron sequences. The use of these primers has increased the speed, precision, and efficiency with which the incompatilibity genotypes of almond cultivars can be detected, compared to other published techniques. The primers confirmed the S-allele specificities for 26 out of 30 cultivars for which published information is available, and are currently in use in the Australian almond improvement program to identify incompatibility groups in the breeding progeny. Future work should be directed towards obtaining the sequences of the introns for the remaining known S-alleles, S3 to S6, and S11 to S22. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1051244 / Thesis (Ph.D.) -- University of Adelaide, Dept. of Horticulture, 2002

Title page, table of contents and abstract only. The complete thesis in print form is available from the University of Adelaide Library. / The Australian almond improvement program was initiated in 1997 to develop improved cultivars that are adapted to local conditions and consumer demands. The program combines molecular techniques along with the traditional approach of controlled hybridisation with mass selection. This research project was carried out to assist the Australian almond improvement program in the areas of micropropagation, cryopreservation, and rapid identification of self-incompatibility genotypes of almond. Micropropagation was accomplished successfully for two commercially important almond cultivars ('Nonpareil' 15-1 and 'Ne Plus Ultra') and an almond/peach hybrid rootstock by culturing shoot tips, about 0.7 cm long with 3 - 5 leaves, on appropriate shoot multiplication media. For 'Nonpareil' 15-1, AP medium with 0.049 uM IBA, 3 uM BAP, 0.058 M sucrose, and 0.7% agar at pH 5.7 was effective. MS medium with 0.049 uM IBA, 5 uM BAP, 0.088 M sucrose, and 0.7% agar at pH 5.7 was suitable for 'Ne Plus Ultra'. For the almond/peach hybrid rootstock, MS medium supplemented with 10 uM BAP, 0.088 M sucrose, and 0.7% agar provided the best shoot proliferation. Shoots of the rootstock, about two cm long, readily produced roots after one week in the dark and two weeks in the light on half strength MS medium supplemented with 2.4 uM IBA, 0.088 M sucrose and 0.7% agar at pH 5.7, with 88.0% rooting efficiency. The two almond cultivars did not readily produce roots, but, at about 1.5 cm long, were micrografted successfully onto the rootstock. These micrografted plantlets were acclimatised and transferred to potting mix with 92% survival. Shoot tips of the two almond cultivars and the almond/peach hybrid rootstock were cryopreserved successfully using a one-step vitrification technique. Three-week-old in vitro cultures were cold-hardened at 4°C on multiplication media (Murashige and Skoog for 'Ne Plus Ultra' and the hybrid rootstock; Almehdi and Parfitt for 'Nonpareil' 15-1) for three weeks. Shoot tips, 2 - 2.5 mm long, were excised and precultured for one day at 4°C on the same basal medium, without plant growth regulators, supplemented with 0.7 M sucrose. After the preculture, the shoot tips were incubated in vitrification solution at 25°C for 45 min for the almond cultivars and 60 min for the almond/peach hybrid rootstock, and then stored under liquid nitrogen (LN) for up to 24 months. After rapid thawing at 30°C, the shoot tips were washed with the appropriate liquid basal medium containing 1.0 M sucrose and then cultured on the same basal medium, solidified with agar, but excluding NH₄N0₃ or (NH₄)₂S0₄. Shoot regeneration was usually observed within 2 - 3 weeks. Survival of shoots after thawing varied from 56-80% for 'Ne Plus Ultra', 35-53% for 'Nonpareil' 15-1, and 62 - 82% for the almond/peach hybrid rootstock. Non-vitrified shoots that were stored on basal medium at 3.5-5°C showed good survival up to six months, but thereafter survival decreased rapidly. Cryopreservation has considerable potential for long-term storage of almond germplasm, but future research should be aimed at improving the regeneration of 'Nonpareil' 15-1, the most important commercial cultivar grown in Australia. The genetic stability of almond DNA to both in vitro culture and the cryopreservation process was evaluated by comparing the fingerprints of the DNA from the original orchard trees, from the in vitro cultures before and after cryopreservation for up to 24 months, and from plants regenerated from in vitro cultures. The fingerprints were prepared by initially digesting the DNA with two isoschizomer pairs of restriction enzymes, one of each pair being 'methylation sensitive' and the other 'methylation insensitive', followed by amplification of the digested products using randomly amplified polymorphic DNA (RAPD) with six different 10-mer primers. Changes in methylation were found between the original orchard trees and in vitro cultures, and there was also the possibility that some structural changes may have occurred. However, no methylation or structural changes could be attributed to the cryopreservation procedure. Plants regenerated from the in vitro cultures before and after cryopreservation should be monitored carefully in the future for changes in morphology compared to the original trees. Partial genomic and cDNA sequences of the self-incompatibility alleles S1, S2, S7, S8, S9, S10, S23, and Sf were obtained from Prunus dulcis cvs 'Anxaneta' (S2S9), 'Cristomorto' (S1S2), 'Ferragnes' (S1S3), 'Gabaix' (S5S10), 'Ne Plus ultra' (S/S7), 'Nonpareil' 15-1 (S7S8), 'Primorskiy'(S5S9), 'Ramilette' (S6S23), and IRTA Selection 12-2 (SfSf). Total DNA was extracted from leaves, and cDNA was prepared from total RNA extracted from styles. The partial cDNA sequences of the S1 allele from 'Ferragnes', and the S7 and S8 alleles from 'Nonpareil' 15-1 matched those reported in the literature for the alleles Sb, Sc, and Sd respectively. The sequences of the S1, S2, S7, S8, S9, S10, S23, and Sf alleles found in genomic DNA contained introns of 562, 253, 1,530, 2,208, 1,343, 710, 494, and 662 bp respectively, and partial exons of 510, 537, 489, 498, 486, 495, 489, and 543 bp respectively. In addition, one allele of the Australian cultivars, 'Johnston's Prolific' and 'Pierce', was identified and found to have the same sequence as S23 in 'Ramilette', suggesting that this cultivar may have been an early introduction to Australia from Spain. The exon/intron splice junction sites of all alleles followed the GT / AG consensus sequence rule, and the sequences were found to be highly conserved. Both the length and the sequence of each intron was unique, and a technique of identifying the S-alleles of almond was developed based on primers that targetted the intron sequences. The use of these primers has increased the speed, precision, and efficiency with which the incompatilibity genotypes of almond cultivars can be detected, compared to other published techniques. The primers confirmed the S-allele specificities for 26 out of 30 cultivars for which published information is available, and are currently in use in the Australian almond improvement program to identify incompatibility groups in the breeding progeny. Future work should be directed towards obtaining the sequences of the introns for the remaining known S-alleles, S3 to S6, and S11 to S22. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1051244 / Thesis (Ph.D.) -- University of Adelaide, Dept. of Horticulture, 2002

Thesis (Ph. D.)--University of California, (Davis), 1952. / Degree granted in Plant Pathology. Includes bibliographical references (leaves 69-71). Also available via the World Wide Web. (Restricted to UC campuses).