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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 57 (1985), S. 2526-2533 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @photogrammetric record 12 (1986), S. 0 
    ISSN: 1477-9730
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Architecture, Civil Engineering, Surveying
    Notes: Over the past decade, photogrammetry has been increasingly applied as a precise three dimensional measuring tool in industrial and engineering works. Analytical photogrammetry is now routinely employed in tasks of measurement as diverse as machine tool inspection and fixture checking, structural deformation monitoring, the provision of control databases to guide industrial robots and the measurement of structures in earth orbit. Traditional photogrammetric techniques and instrumentation are usually inappropriate for industrial work and the development of complete, fully integrated close range photogrammetric systems has recently gained considerable impetus. This paper details some of the significant new developments in industrial photogrammetry, with particular reference to technological advances in the Simultaneous Triangulation and Resection System (STARS) designed by Geodetic Services, Inc. for industrial photograininetry. Practical aspects of industrial measurement are also presented in a review of some of the varying tasks that GSI has carried out in recent years. Emphasis is placed on demonstrating the flexibility, accuracy, reliability and economy of photogrammetry, as well as the progress made in automating this measurement technique.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant breeding 101 (1988), S. 0 
    ISSN: 1439-0523
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: To develop a system of clectrofusion for the genus Medicago, protoplast yields from 2 genotypes of M, sativa and 7 wild type1 accessions were determined. Protoplast extraction protocols from mesophyll cells, from suspension culture and from calls were evaluated. An alternating current of 10 volts an a frequency of 150 mhz was applied to tht1 protoplasts Ho align them in a pearl chain formation. A direct current pulse of 150 volts applied for 0.25 usec gave the highest number of protoplast fusions for material from mesophyll cells and suspension culture for both M. sativa and wild species. Over 20% of the protoplasts which occupied places in the “pearl chains” yielded fusion products. An average of 25% of the protoplasts treated with an electrical fusion pulse survived, started, to regenerate cell walls and to divide after a 12 days interval. This system can be used to produce new hybrids which, previously, could not be made in the genus Medicago.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    World journal of microbiology and biotechnology 11 (1995), S. 409-415 
    ISSN: 1573-0972
    Keywords: Breeding ; embryo culture ; haploids ; micropropagation ; protoplasts ; synthetic seed ; transformation ; wide hybridization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Plant tissue culture comprises a set of in vitro techniques, methods and strategies that are part of the group of technologies called plant biotechnology. Tissue culture has been exploited to create genetic variability from which crop plants can be improved, to improve the state of health of the planted material and to increase the number of desirable germplasms available to the plant breeder. Tissue-culture protocols are available for most crop species, although continued optimization is still required for many crops, especially cereals and woody plants. Tissueculture techniques, in combination with molecular techniques, have been successfully used to incorporate specific traits through gene transfer. In vitro techniques for the culture of protoplasts, anthers, microspores, ovules and embryos have been used to create new genetic variation in the breeding lines, often via haploid production. Cell culture has also produced somaclonal and gametoclonal variants with crop-improvement potential. The culture of single cells and meristems can be effectively used to eradicate pathogens from planting material and thereby dramatically improve the yield of established cultivars. Large-scale micropropagation laboratories are providing millions of plants for the commercial ornamental market and the agricultural, clonally-propagated crop market. With selected laboratory material typically taking one or two decades to reach the commercial market through plant breeding, this technology can be expected to have an ever increasing impact on crop improvement as we approach the new millenium.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell reports 4 (1985), S. 15-18 
    ISSN: 1432-203X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The effects of ABA, 2,4-D, kinetin and cold exposure on the cold hardiness of Medicago sativa L. cell suspensions were investigated. Cultures treated with 5×10−5 M ABA at 2°C for 4 weeks in the absence of kinetin showed a 50% survival after freezing to −12.5°C, whereas cultures grown at 25°C under normal conditions tolerated freezing to only −3°C. The optimum ABA treatment of 5×10−5 M for 4 weeks was effective only in combination with cold exposure. Of six cell lines tested, all showed different degrees of induced cold hardiness. The results suggest that ABA alone cannot induce freezing tolerance on alfalfa cell suspension cultures and that the deletion of kinetin and combination of low temperature and ABA is critical for the induction of cold hardiness in alfalfa cell suspension cultures.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-2048
    Keywords: Brassica (microspore embryogenesis) ; Embryogenesis (induction in microspores) ; Microspore embryogenesis ; mRNA in microspore embryogenesis ; Protein in microspore embryogenesis ; Stress and microspore embryogenesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Brassica napus L. microspores at the late uninucleate to early binucleate stage of development can be induced in vitro to alter their development from pollen to embryo formation. High temperatures or other stress treatments are required to initiate this redirection process. The critical period for induction of microspore embryogenesis is within the first 8 h of temperature-stress imposition. During this period, which precedes the first embryogenic nuclear division, the process regulating the induction and sustainment of microspore embryogenesis is activated. A number of mRNAs and proteins, some of them possibly heat-shock proteins, appear in microspores during the commitment phase of the induction process.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-2048
    Keywords: Brassica (microspore embryogenesis) ; Embryogenesis (induction in microspores) ; Microspore embryogenesis ; mRNA in microspore embryogenesis ; Protein in microspore embryogenesis ; Stress and microspore embryogenesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Brassica napus L. microspores at the late uninucleate to early binucleate stage of development can be induced in vitro to alter their development from pollen to embryo formation. High temperatures or other stress treatments are required to initiate this redirection process. The critical period for induction of microspore embryogenesis is within the first 8 h of temperature-stress imposition. During this period, which precedes the first embryogenic nuclear division, the process regulating the induction and sustainment of microspore embryogenesis is activated. A number of mRNAs and proteins, some of them possibly heat-shock proteins, appear in microspores during the commitment phase of the induction process.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell reports 5 (1986), S. 468-470 
    ISSN: 1432-203X
    Keywords: alfalfa ; embryogenesis ; electrical field ; polarity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Mesophyll protoplasts of Medicago sativa were exposed to low voltage electrical fields immediately following isolation. Several exposure times and voltages were utilized. At the lower doses, protoplast aggregation and subsequent embryogenesis were stimulated. A clone of ‘Rangelander’, which was directly-embryogenic (i.e. embryos were derived from single mesophyll protoplasts without an intervening callus phase), was induced to form embryos in all samples exposed to the lowest level electrical fields, while unexposed controls formed few or no embryos. A clone of ‘Regen S’, which was previously not directly-embryogenic, was induced to follow the ‘Rangelander’ pattern of development and to produce early globular embryos.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1573-5060
    Keywords: Brassica napus ; donor plant age ; embryogenesis ; haploid ; microspore culture ; microspore stage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Effect of age of donor plants and age of inflorescence on embryogenesis in microspore culture of B. napus was examined. Microspores isolated from buds of older plants had a higher embryo yield than those of younger ones. The effect of the age of inflorescence showed a different pattern. In older plants, a higher embryogenesis response was observed in microspores isolated from buds of new inflorescences, while in young plants, microspores isolated from buds of old inflorescences showed high embryo yield. These different responses were considered to be attributable to a difference in the developmental stage of pollen at the time of microspore isolation. Our results indicated that microspores collected from older inflorescences and older plants have sufficient embryogenic potential when the optimum developmental stage of pollen was used. Frequency of embryo to plant conversion was influenced by the size of embryos subcultured, but not by donor plant age or the age of the inflorescence.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell, tissue and organ culture 35 (1993), S. 121-129 
    ISSN: 1573-5044
    Keywords: abscisic acid ; Brassica oleracea ; embryogenesis ; microspore culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Desiccation tolerance of broccoli microspore-derived embryos was induced by exogenous application of abscisic acid (ABA). Embryos, which were desiccated to about 10% water content, were estimated for viability after rehydration. Survival was dependent on the ABA concentration and the development stage of embryo, but not on the length of exposure period to ABA or genotype. Cotyledonary stage embryos acquired the highest desiccation tolerance when treated with 1×10-4M ABA. Under this condition, on average 27–48% of the desiccated embryos could convert into plants. Embryos treated with 1×10-6M ABA or no ABA or earlier development-staged embryos, such as globular and heart stages, lost viability after desiccation. A one day exposure to ABA had the similar effect on the induction of desiccation tolerance as a 7-day treatment. The dried embryos maintained their ability of plant conversion after three months of storage under room conditions. The plants derived from the desiccated embryos were not different in the morphology or ploidy level from those from non-desiccated ones.
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