Gotowe bibliografie tematyczne / Brassica – Breeding

Gotowa bibliografia na temat „Brassica – Breeding”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 19 lutego 2022

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Artykuły w czasopismach na temat "Brassica – Breeding"

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Czajka, Agnieszka, Monika Markiewicz, Beata Kowalska i Urszula Smolińska. "Reaction of clubroot-resistant genotypes of Brassica rapa, Brassica napus and Brassica oleracea to Polish Plasmodiophora brassicae pathotypes in laboratory tests". European Journal of Plant Pathology 158, nr 2 (26.08.2020): 533–44. http://dx.doi.org/10.1007/s10658-020-02100-y.

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Abstract The Brassica genotypes selected for the experiments were previously found to be resistant to various Plasmodiophora brassicae pathotypes (Pb). Their interaction with pathotypes Pb2, Pb3 and Pb9 isolated in Poland was studied, using macroscopic observation for the presence of root galls, microscopic observations of P. brassicae plasmodia in the root hairs and quantitative PCR for determination of the pathogen’s quantity in plant roots and growing media. Of the Brassica genotypes studied, only B. rapa var. capitata line AABBcc was fully resistant to all the Polish pathotypes of P. brassicae. Some of the other “clubroot-resistant” genotypes tested were resistant to selected pathotypes, e.g. Brassica napus var. rapifera ‘Wilhelmsburger’ to Pb 2 and Pb3, Brassica oleracea var. capitata ‘Kilaton F1’ to Pb2 and Brassica rapa subsp. pekinensis ‘Bilko F1’ to Pb3, but were susceptible to others. B. oleracea var. capitata ‘Bindsachsener’, B. oleracea var. acephala subvar. lacinata ‘Verheul’ and B. napus var. napus ‘Mendel F1’ were moderately to highly susceptible to all Polish P. brassicae pathotypes. These results show that the classification of virulence of P. brassicae pathotypes selected in various areas differs significantly toward the same Brasssica genotypes and puts in question the practical value of pathotype classification determined with differential sets for farmers and plant breeders. Our results showed that B. rapa var. capitata AABBcc line, B. napus var. rapifera ‘Wilhelmsburger’, B. oleracea var. capitata ‘Kilaton F1’, B. rapa subsp. pekinensis ‘Bilko F1’ could be considered in Brassica breeding programmes as a source of resistance to Polish P. brassicae isolates.
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Hasan, Jakir, Swati Megha i Habibur Rahman. "Clubroot in Brassica: recent advances in genomics, breeding, and disease management". Genome 64, nr 8 (sierpień 2021): 735–60. http://dx.doi.org/10.1139/gen-2020-0089.

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Clubroot disease, caused by Plasmodiophora brassicae, affects Brassica oilseed and vegetable production worldwide. This review is focused on various aspects of clubroot disease and its management, including understanding the pathogen and resistance in the host plants. Advances in genetics, molecular biology techniques, and omics research have helped to identify several major loci, QTL, and genes from the Brassica genomes involved in the control of clubroot resistance. Transcriptomic studies have helped to extend our understanding of the mechanism of infection by the pathogen and the molecular basis of resistance/susceptibility in the host plants. A comprehensive understanding of the clubroot disease and host resistance would allow developing a better strategy by integrating the genetic resistance with cultural practices to manage this disease from a long-term perspective.
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Chahil, Gurminder Singh, i Jagdev Singh Kular. "Biology of Pieris Brassicae (Linn.) on Different Brassica Species in the Plains of Punjab". Journal of Plant Protection Research 53, nr 1 (1.01.2013): 53–59. http://dx.doi.org/10.2478/jppr-2013-0008.

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Abstract Biology of Pieris brassicae reared on Brassica napus, B. juncea, B. rapa, and B. carinata was studied. Adult butterflies, collected in November from the plains of Punjab, India, were sexed, paired, and released onto the four Brassica spp. in a greenhouse. In a multigeneration study (Parental, F1, and F2), the effect of the four Brassica spp. on the egg laying, incubation period and hatching percentage was assessed in a greenhouse study. Hatched larvae were collected, reared on fresh leaves of respective Brassica spp, in laboratory conditions. Data collected on larval stadia, pre-pupal and pupal durations, adult longevity, and sex ratio were assessed to understand the effects of these four species. Of the four species, B. carinata, with a shorter incubation period, higher hatching percentage, and shorter developmental periods was most susceptible. In this study, B. rapa was the most resistant species and may be recommended for further breeding programs in order to reduce the economic damage caused by P. brassicae.
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Stringam, G. R., V. K. Bansal, M. R. Thiagarajah, D. F. Degenhardt i J. P. Tewari. "Development of an agronomically superior blackleg resistant canola cultivar in Brassica napus L. using doubled haploidy". Canadian Journal of Plant Science 75, nr 2 (1.04.1995): 437–39. http://dx.doi.org/10.4141/cjps95-072.

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The doubled haploid breeding method and greenhouse screening using cotyledon bio-assay were successfully applied to transfer blackleg resistance from the Australian cultivar Maluka (Brassicas napus), into susceptible advanced B. napus lines from the University of Alberta. This approach for blackleg resistance breeding was effective and efficient as several superior blackleg resistant breeding lines were identified within 4 yr from the initial cross. One of these lines (91–21864NA) was entered in the 1993 trials of the Western Canada Canola/Rapeseed Recommending Committee. Key words: Blackleg resistance, Leptosphaeria maculans, doubled haploid, Brassica napus
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Raijiciv, T. S., M. Ivancevic, D. Stevanovic i D. Vinterhalter. "BREEDING BRASSICA VEGETABLE CROPS IN YUGOSLAVIA". Acta Horticulturae, nr 539 (październik 2000): 123–27. http://dx.doi.org/10.17660/actahortic.2000.539.15.

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NWANKITI, OGUGUA. "Cytogenetic and breeding studies with Brassica". Hereditas 66, nr 1 (2.09.2009): 109–26. http://dx.doi.org/10.1111/j.1601-5223.1970.tb02338.x.

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Gabrielson, R. L., i Józef Robak. "Temperature sensitivity of resistance to two pathotypes of Plasmodiophora brassicae in Brassica oleracea". Acta Agrobotanica 41, nr 2 (2013): 237–43. http://dx.doi.org/10.5586/aa.1988.013.

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Several methods were evaluated in an attempt to develop a greenhouse screening procedure that would predict field resistance of brassica breeding lines to clubroot disease caused by <i>Plasmodiophora brassicae</i>. Several <i>Brassica oleracea</i> cultivars and breeding lines bred for resistance to <i>Plasmodiophora brassicae</i> and a susceptible Chinese cabbage cultivar were exposed to high levels of inoculum of both pathotypes PB 6, PB 7 at 12, 15, 20, 25 and 30°C. No infection occurred on any host at 12°C. Chinese cabbage was heavily diseased from 15-30°C. Bagder Shipper cabbage, a cauliflower deriving resistance from this variety, and Oregon CR-1 broccoli were resistant to pathotype PB 6 at 15 and 20°C and partially resistant at 25 and 30°C. They were resistant to pathotype PB 7 and 15°C and almost totally susceptible at 20, 25° and 30°C. Oregon cabbage line OR 123 was resistant to pathotype PB 6 at 15°C at almost completely susceptible at 20, 25 and 30°C. It was resistant to pathotype PB 7 at all temperatures. Temperature sensitivity of resistance can partially explain why breeding lines are resistant in field trials and susceptible in greenhouse tests.
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Jakir Hasan, Muhammad, Stephen E. Strelkov, Ronald J. Howard i Habibur Rahman. "Screening of Brassica germplasm for resistance to Plasmodiophora brassicae pathotypes prevalent in Canada for broadening diversity in clubroot resistance". Canadian Journal of Plant Science 92, nr 3 (maj 2012): 501–15. http://dx.doi.org/10.4141/cjps2010-006.

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Hasan, M. J., Strelkov, S. E., Howard, R. J. and Rahman, H. 2012. Screening of Brassica germplasm for resistance to Plasmodiophora brassicae pathotypes prevalent in Canada for broadening diversity in clubroot resistance. Can. J. Plant Sci. 92: 501–515. Clubroot disease of crucifers, caused by Plasmodiophora brassicae, poses a threat to the Canadian canola industry, and the development of resistant cultivars is urgently needed. Germplasm resistant to local pathotype(s) is the prime requirement for breeding clubroot-resistant cultivars. The objective of this study was to identify Brassica germplasm possessing resistance to P. brassicae pathotypes prevalent in Alberta. Pathotype-specific resistance was identified in the diploid species Brassica rapa (AA) and B. oleracea (CC), and in the amphidiploid B. napus (AACC). Among B. rapa genotypes, turnip was the most resistant, followed by winter type and spring type oilseed rape. The rutabaga group of B. napus, on the other hand, was homogeneous for resistance to Canadian P. brassicae pathotypes. The diploid species B. nigra (BB) also showed pathotype-specific resistance. However, the two amphidiploids carrying the B. nigra genome, B. juncea (AABB) and B. carinata (BBCC) were completely susceptible to clubroot.
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Farid, Mehdi, Rong-Cai Yang, Berisso Kebede i Habibur Rahman. "Evaluation of Brassica oleracea accessions for resistance to Plasmodiophora brassicae and identification of genomic regions associated with resistance". Genome 63, nr 2 (luty 2020): 91–101. http://dx.doi.org/10.1139/gen-2019-0098.

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Clubroot disease caused by Plasmodiophora brassicae is a challenge to Brassica crop production. Breakdown of resistance controlled by major genes of the Brassica A genome has been reported. Therefore, identification of resistance in the Brassica C genome is needed to broaden the genetic base of resistance in Brassica napus canola. In this study, we evaluated 135 Brassica oleracea accessions, belonging to eight variants of this species to identify resistant accessions as well as to identify the genomic regions associated with resistance to two recently evolved P. brassicae pathotypes, F3-14 (3A) and F-359-13 (5X L-G2). Resistance to these pathotypes was observed more frequently in var. acephala (kale) followed by var. capitata (cabbage); few accessions also carried resistance to both pathotypes. Association mapping using single nucleotide polymorphism (SNP) markers developed through genotyping by sequencing technique identified 10 quantitative trait loci (QTL) from six C-genome chromosomes to be associated with resistance to these pathotypes; among these, two QTL associated with resistance to 3A and one QTL associated with resistance to 5X L-G2 carried ≥3 SNP markers. The 10 QTL identified in this study individually accounted for 8%–18% of the total phenotypic variance. Thus, the results from this study can be used in molecular breeding of Brassica crops for resistance to this disease.
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De Jong, Van, B. E. Braithwaite, T. L. Roush, A. Stewart i J. G. Hampton. "Opportunities for developing value-added brassica seed". NZGA: Research and Practice Series 14 (1.01.2010): 139–46. http://dx.doi.org/10.33584/rps.14.2008.3174.

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New Zealand produces approximately 5,500 tonnes of brassica seed per year, two thirds of which, valued at $13M, is exported. Black rot caused by Xanthomonas campestris pv. campestris is a common disease of brassicas, and while crop losses are not extensive in New Zealand, internationally total crop losses have been reported. Seeds are the primary source of inoculum and the ease with which this inoculum spreads means that even small traces can cause severe epidemics. Genetic resistance to black rot is a complex trait which makes breeding for resistance in brassicas challenging. The effectiveness of chemical and cultural practices is variable. Biological control with natural antagonistic microbes may provide a more effective means of controlling black rot and other pests and diseases, and create opportunities for increasing the export value of brassica seed. Current cultural practices and the potential for biological control for the management of black rot are reviewed. Keywords: biocontrol, Brassicaceae, crucifer
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Rozprawy doktorskie na temat "Brassica – Breeding"

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Sharpe, Andrew Glenn. "Marker-assisted breeding in oilseed rape (Brassica napus)". Thesis, University of East Anglia, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.361724.

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Majer, Dorothea. "Genetic variation in Pyrenopeziza brassicae and its interaction with its host Brassica napus ssp. oleifera". Thesis, University of East Anglia, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.338299.

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Snowdon, Rodney John [Verfasser]. "Genome analysis and molecular breeding of Brassica oilseed crops / Rodney John Snowdon". Gießen : Universitätsbibliothek, 2011. http://d-nb.info/1061195929/34.

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Snowdon, Rod [Verfasser]. "Genome analysis and molecular breeding of Brassica oilseed crops / Rodney John Snowdon". Gießen : Universitätsbibliothek, 2011. http://nbn-resolving.de/urn:nbn:de:hebis:26-opus-80641.

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Schelfhout, Christopher James. "DNA marker assisted breeding in interspecific crosses to improve canola (Brassica napus L.)". University of Western Australia. School of Plant Biology, 2008. http://theses.library.uwa.edu.au/adt-WU2008.0167.

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[Truncated abstract] In order to expand the gene pool of canola-quality rapeseed (Brassica napus) reciprocal interspecific crosses were made between B. napus cv. Mystic and near canola-quality B. juncea breeding line JN29. F1 progeny from these crosses were used to make backcrosses to both parents in all possible combinations and directions, and were selfed to form F2-derived lines. The highest frequencies of viable F2 and BC1 progeny were obtained when B. napus was the maternal parent of the interspecific hybrid. BC1 and F2 progeny (and subsequent generations) were grown under field conditions to identify agronomic improvements over the parents. Transgressive segregation was observed in F2 and BC1 and in subsequent generations for agronomic traits (seed yield under high or low rainfall conditions, plant biomass, harvest index, height, branching and days to anthesis) and seed quality traits (oil, protein, glucosinolates, oleic acid). The majority of progeny conformed to B. napus morphology, and a minority segregated to B. juncea morphology in subsequent generations. Some of the B. juncea morphotypes had lower glucosinolates and higher oleic acid than the parent JN29, with no detectable erucic acid, and thereby conformed to canola quality. Methods were developed for tracing B-genome in interspecific progeny. A repetitive DNA sequence pBNBH35 from B. nigra (genome BB, 2n = 16) was used to identify B-genome chromosomes and introgressions in interspecific progeny. Specific primers were designed for pBNBH35 in order to amplify the repetitive sequence by PCR. A cloned sub-fragment of 329 bp was confirmed by sequencing as part of pBNBH35. PCR and hybridisation techniques were used on an array of Brassica species to confirm that the pBNBH35 subfragment was Brassica B-genome specific. Fluorescence in situ hybridisation (FISH) in B nigra, B. juncea (AABB, 2n=36) and B. napus (AACC, 2n=38) showed that the pBNBH35 sub-fragment was present on all eight Brassica Bgenome chromosomes and absent from A- and C-genome chromosomes. The pBNBH35 repeat was localised to the centromeric region of each B-genome chromosome. FISH clearly distinguished the B-genome chromosomes from the A-genome chromosomes in the amphidiploid species B. juncea. This is the first known report of a B-genome repetitive marker that is present on all Brassica Bgenome chromosomes. ... The results suggest that novel B. napus genotypes have been generated containing introgressions of B-genome chromatin from B. juncea chromosomes. B. juncea morphology occurred in interspecific progeny with a chromosome complement similar to B. napus (2n = 38) and without the entire Bgenome present. It also is highly likely that recombination has occurred between the A-genome of the two Brassica species. This research has demonstrated that the secondary gene pool of B. napus may be accessed by selfing interspecific hybrids, and without sacrificing canola quality, if the B. juncea parent is near canola-quality. Interspecific progeny may be screened to enhance the proportion with B-genome positive signals. Some progeny with B. junceatype morphology had improved seed quality over the JN29 parent.
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Coventry, Jane. "Development of S allele diagnostics for a hybrid canola (Brassica napus L.) breeding program". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/MQ61886.pdf.

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Kieffer, Martin Louis. "The in vitro manipulation of cauliflower (Brassica oleracea L. convar. botrytis (L.) Alef. var. botrytis L.) meristematic tissues for utilisation in genetic improvement programmes". Thesis, University of Plymouth, 1996. http://hdl.handle.net/10026.1/2557.

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Cauliflower curd meristem activity (organogenic, plastochronic, phyllotactic) was analysed biometrically and confirmed that the curd is the product of a constant process of meristem production and branch ramification with little if any dominance between branch apices. A growth model based on curd branching pattern was developed and its mathematical expression enabled the estimation of the number of meristems carried by a curd at maturity to be over ten million which was previously widely underestimated. Analysis of the response to the in vitro culture of this meristematic tissues revealed that meristems are not predetermined to produce flower and that their shoot regeneration capacity is under several levels of control, the most important being explant physical property (size) and the culture system (nutrient supply). Optimisation of these parameters enabled the development of a low cost, semi-automated protocol for mass production of cauliflower propagules at an unprecedented scale with over 10000 propagules produced per curd. Micropropagules a few millimetres in length were produced, encapsulated in calcium alginate hydrogel, stored at 4°C for several months and used as an 'artificial seed' system of cauliflower propagation. The response to the procedure of micropropagule production is genotype-dependent with summer heading varieties being less reactive than winter heading varieties, this phenomenon was also associated with plasmalemma instability at the cellular (protoplast) level. Furthermore, this material was successfully cryopreserved in liquid nitrogen using a dehydration / vitrification method. The micropropagation protocol is of great interest when used as a regeneration system for experiments involving genetic manipulation such as genetic transformation. A preliminary study of genetic transformation by microprojectile bombardment, using the gus reporter gene, allowed transient expression in curd meristematic tissue. The fundamental and industrial implications for cauliflower breeding of the different protocols developed in this thesis are discussed.
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Wang, Tina Y. "Determining the Fate of Hybridized Genomes in the Allopolyploid Brassica napus". DigitalCommons@CalPoly, 2010. https://digitalcommons.calpoly.edu/theses/358.

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Polyploidy is widely acknowledged as a widespread mechanism in the evolution and speciation of the majority of flowering plants. Allopolyploid forms through interspecific hybridization and whole genome duplication. While allopolyploids may display increased vigor relative to their progenitors, they can also face challenges to fertility following hybridization. Genetic changes in allopolyploids result from recombination between the hybridized subgenomes, which can influence phenotype and ultimately determine fitness of future generations. To study dynamic changes that follow allopolyploid formation, Brassica napus lineages were derived by hybridizing Brassica oleracea and Brassica rapa. Two lineages of B. napus were analyzed for genetic and phenotypic changes in the S2, S7, and S12 generations. Although these lineages were genetically identical at the time of hybridization, divergence was apparent by the S2 generation. There was a significant increase in sequence loss across generations within both lineages. Four of six generations from both lineages displayed no significant differences to each other in sequence loss relative to the parental generation. In both lineages, there was a bias towards losing sequences from the B. olereacea subgenome. Some individual plants showed novel phenotypes; however, there was no correlation between the examined genetic changes and selected phenotypes.
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Pontoppidan, Mia. "Modified fatty acid composition in Brassica napus using transformation and somatic hybridisation /". Uppsala : Swedish Univ. of Agricultural Sciences (Sveriges lantbruksuniv.), 1999. http://epsilon.slu.se/avh/1999/91-576-5461-1.pdf.

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Leeks, C. R. F. "Determining seed vigour in selected Brassica species". Lincoln University, 2006. http://hdl.handle.net/10182/1274.

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Variables for the accelerated ageing (AA) test, methods for reducing fungal contamination during the AA test, using the conductivity test as a vigour test, the effect of seed size on seed vigour and the relationship between laboratory test results and field perfonnance in selected Brassica spp were investigated. In the first experiment, three seed lots of turnip rape hybrid (B. rapa x campestris), turnip (B. campestris) and forage rape (B. napus); and seven seed lots of Asian rape (B. napus), six seed lots of Asian kale (B. oleraceae var. alboglabra L.) and five seed lots of choisum (B. rapa var. pekinensis) with germinations above 90% were aged at two different temperatures (41 and 42°C ± 0.3°C) and three ageing times (24, 48 and 72 ± 15 minutes). The second experiment was divided into three sections. In the first, the same seed lots and species were aged at one temperature (41°C) and time (72 h), but either 40 ml of saturated salts; KCl (83%RH), NaCl (76%RH), NaBr (55%RH); or distilled water (96%RH) were used as the ageing solutions. In the second, one turnip rape hyprid seed lot was aged at three temperatures (41, 42 and 45°C) and two times (72 and 96h), again using the three saturated salts and distilled water as ageing solutions. In the third, three turnip rape hybrid seed lots and three Asian kale seed lots were surface sterilised (1 % sodium hypochlorite) prior to ageing at one temperature (41°C) and time (72 h). In the third experiment, the same species and seed lots used in experiment one at their original seed moisture content (SMC) were tested for conductivity after soaking in deionised water for 4, 8, 12, 16, 20 and 24 h. They were then re-tested after the SMC had been adjusted to 8.5%. In the fourth experiment, three seed lots of forage rape and three seed lots of Asian kale were graded into three seed size categories; large (retained on a 2.0 mm screen), medium (retained on a 1.7 mm screen) and small (passed through a 1.7 mm screen). Graded seeds were then tested for standard germination, AA (41°C/48 h) and conductivity (measured at 16 and 24 h). In the final experiment, the relationships between laboratory tests for the six species (each consisting of three seed lots), field emergence from three sowings, and cold room emergence were evaluated. Both time and temperature influenced post-AA germination. Increasing the ageing period from 48 to 72 hours at 41°C, and 24 to 48 hours at 42°C resulted in decreased mean germination percentage for all species but not always clear separation of seed lots. While there were sometimes few differences between ageing at 41°C and 42°C, the former is preferred because it is already the temperature used for other species. For Asian rape, choisum and turnip, the previously recommended testing conditions of 41°C/72 h provided good seed lot separation, but for Asian kale and turnip rape hybrid, AA testing at 41°C/48 h provided better results. Seed moisture content after ageing ranged from 29-37% depending on species. Fungal growth on seeds during the ageing period appeared to reduce post-ageing germination in some seed lots . Substituting saturated salts for distilled water did not stress seed lots in the AA test, due to the lowered RH%, the exception being seed lots 1210 and 1296. For forage and Asian species, seed lot germination mostly remained above 90% when aged for 72 h at lowered RH%. Increasing the ageing duration from 72 to 96 hours resulted in some decreases in post-AA germination but no clear separation of seed lots. Surface sterilising the seeds prior to the AA test resulted in a lower incidence of contaminant fungi which was associated with a lower percentage of abnormal seedlings. The conductivity test was mostly able to identify vigour differences among forage and Asian vegetable brassica seed lots. Differences in conductivity readings were observed among seed lots in all species. Increasing the period of imbibition resulted in increased conductivity from most seed lots but radicle emergence occurred after 16-20 h of imbibition. Variation was observed in the time to reach 95% maximum of the imbibition curve for most species. Conductivity readings at 16 h would avoid possible influences of radicle emergence on results. Adjusting the SMC to 8.5% resulted in reduced variation in conductivity among replicates of seed lots, due to a reduction in imbibition damage. Seed size had a significant effect on both post-AA germination and conductivity results. In forage rape, large size seeds had higher post-AA germination cf. medium cf. small size seeds. In Asian kale, large size seeds had higher post-AA germination compared with small size seeds. For both forage rape and Asian kale, large size seeds had lower conductivity readings cf. small size seeds. The correlation analyses demonstrated significant relationships between AA testing and field emergence parameters (percentage emergence, emergence index and emergence rate). Significant relationships were also observed between conductivity testing and these field emergence parameters. Based on the correlation analysis, AA testing at 41°C/48 hand/or 42°C/48 h could be recommended to be used as an AA test for turnip and Asian rape; and 41°C/48 hand/or 41°C/72 h for Asian kale and choisum. Based on the correlation analysis, conductivity testing at 16 h can be used to predict the field emergence potential of forage and Asian vegetable seed lots. Vigour tests were consistently able to provide better indicators of field perfonnance than the standard germination test, although these relationships did vary with the different field sowings.
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Książki na temat "Brassica – Breeding"

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Kumar, A., S. S. Banga, P. D. Meena i P. R. Kumar, red. Brassica oilseeds: breeding and management. Wallingford: CABI, 2015. http://dx.doi.org/10.1079/9781780644837.0000.

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Kole, Chittaranjan, i Jan Sadowski. Genetics, genomics and breeding of vegetable Brassicas. Enfield, N.H: Science Publishers, 2011.

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Myers, James Robert. Outcrossing potential for Brassica species and implications for vegetable crucifer seed crops of growing oilseed Brassicas in the Willamette Valley. [Corvallis, Or.]: Oregon State University, Extension Service, 2006.

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Edwards, David. Genetics, genomics and breeding of oilseed Brassicas. Enfield, N.H: Science Publishers, 2011.

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Chen, Bao-Yuan. Resynthesized Brassica napus L.: A potential in breeding and research. Svalo v, Sweden: Dept. of Crop Genetics and Breeding, Swedish University of Agricultural Sciences, 1989.

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Weerakoon, Shyama Ranjani. Mustard (Brassica juncea [L.] Czern & Cross) germplasm in Sri Lanka and its potential uses. [Nugegoda]: The Open University of Sri Lanka, 2010.

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Wahiduzzaman, Md. Potentials for species introgression in Brassica napus with special reference to earliness and seed colour. Uppsala: Institutionen för växtförädling, Sveriges lantbruksuniversitet, 1987.

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Kang, Tal-sun. Kyŏngnam chiyŏk paio tijel wŏllyoyong yuchʻae silchŭng chaebae yŏnʼgu =: Studies on empirical culture of rape (Brassica campestris M.) for production of bio-diesel fuel in Kyeongnam province. [Seoul]: Nongchʻon Chinhŭngchʻŏng, 2008.

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Kang, Tal-sun. Kyŏngnam chiyŏk paio tijel wŏllyoyong yuchʻae silchŭng chaebae yŏnʼgu =: Studies on empirical culture of rape (Brassica campestris M.) for production of bio-diesel fuel in Kyeongnam province. [Seoul]: Nongchʻon Chinhŭngchʻŏng, 2008.

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Asfaw, Nigussie Alemayehu. Germplasm diversity and genetics of quality and agronomic traits in Ethiopian mustard (Brassica carinata A. Braun). Göttingen: Cuvillier, 2001.

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Części książek na temat "Brassica – Breeding"

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Branca, Ferdinando, i Elena Cartea. "Brassica". W Wild Crop Relatives: Genomic and Breeding Resources, 17–36. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-14871-2_2.

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Lakshmikumaran, M., T. Mohapatra, V. S. Gupta i P. K. Ranjekar. "Molecular Markers in Improvement of Wheat and Brassica". W Plant Breeding, 229–55. Dordrecht: Springer Netherlands, 2004. http://dx.doi.org/10.1007/978-94-007-1040-5_10.

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Velasco, Pablo, Víctor Manuel Rodríguez, Marta Francisco, María Elena Cartea i Pilar Soengas. "Genetics and Breeding of Brassica Crops". W Reference Series in Phytochemistry, 61–86. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-25462-3_2.

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Velasco, Pablo, Víctor Manuel Rodríguez, Marta Francisco, María Elena Cartea i Pilar Soengas. "Genetics and Breeding of Brassica Crops". W Glucosinolates, 1–26. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-26479-0_2-1.

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Renard, M., R. Delourme, J. Mesquida, G. Pelletier, C. Primard, L. Boulidard, C. Dore, V. Ruffio, Y. Herve i J. Morice. "Male Sterilities and F1 Hybrids in Brassica". W Reproductive Biology and Plant Breeding, 107–19. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-76998-6_11.

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Lühs, W. W., A. Voss, J. Han, A. Gräfin zu Münster, D. Weier, F. P. Wolter, M. Frentzen i W. Friedt. "Genetic modification of erucic acid biosynthesis in Brassica napus". W Developments in Plant Breeding, 323–30. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4475-9_36.

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Abdel-Razzak, Hesham S. "Turnip (Brassica rapa var. rapa L.) Breeding". W Advances in Plant Breeding Strategies: Vegetable Crops, 345–405. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-66965-2_9.

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Li, Genyi, i Peter B. E. McVetty. "Genetics and Gene Mapping of Disease Resistance in Brassica". W Translational Genomics for Crop Breeding, 327–44. Chichester, UK: John Wiley & Sons Ltd, 2013. http://dx.doi.org/10.1002/9781118728475.ch16.

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Voss, A., W. W. Lühs, R. J. Snowdon i W. Friedt. "Development and molecular characterisation of nematode-resistant rapeseed (Brassica napus L.)". W Developments in Plant Breeding, 195–202. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4475-9_22.

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Barsby, Tina L., Roger J. Kemble i Stephen A. Yarrow. "Brassica Cybrids and Their Utility in Plant Breeding". W Plant Molecular Biology, 223–34. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4615-7598-6_21.

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Streszczenia konferencji na temat "Brassica – Breeding"

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Gladkaya, А. S. "RAPESEED (BRASSICA NAPUS Z.) AS A PROMISING FORAGE CROP". W «Breeding, seed production, cultivation technology and processing of agricultural crops». Federal State Budgetary Scientific Institution Federal Scientific Rice Centre, 2021. http://dx.doi.org/10.33775/conf-2021-284-287.

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Volovik, V. T., S. E. Sergeeva, T. V. Leonidova i L. M. Korovina. "Direction of the breeding of surpits in Federal Scientific Center for Forage Production and Agroecology named after V.R.Williams". W Растениеводство и луговодство. Тимирязевская сельскохозяйственная академия, 2020. http://dx.doi.org/10.26897/978-5-9675-1762-4-2020-114.

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Streszczenie:
As a result of breeding work in FWTC FPA created by varieties of spring (Svetlana, Nadezhda) and winter Brassica rapa (Sarja) with a fiber content of between 6.4 and 7.3%, fat content of 43.2-46.7% protein 23.5-24.5 cm%, a growing period of 76-88 days, seed yield between 2.5 (spring) to 3.5 t/ha (winter). The low content of glucosinolates and fiber in seeds allows the use of cake and meal in the diets of animals and poultry in high standards. The created varieties are in demand by production.
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