Gotowe bibliografie tematyczne / Lupines – Genetics

Gotowa bibliografia na temat „Lupines – Genetics”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 5 lutego 2022

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Artykuły w czasopismach na temat "Lupines – Genetics"

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Bielski, Wojciech, Michał Książkiewicz, Denisa Šimoníková, Eva Hřibová, Karolina Susek i Barbara Naganowska. "The Puzzling Fate of a Lupin Chromosome Revealed by Reciprocal Oligo-FISH and BAC-FISH Mapping". Genes 11, nr 12 (10.12.2020): 1489. http://dx.doi.org/10.3390/genes11121489.

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Old World lupins constitute an interesting model for evolutionary research due to diversity in genome size and chromosome number, indicating evolutionary genome reorganization. It has been hypothesized that the polyploidization event which occurred in the common ancestor of the Fabaceae family was followed by a lineage-specific whole genome triplication (WGT) in the lupin clade, driving chromosome rearrangements. In this study, chromosome-specific markers were used as probes for heterologous fluorescence in situ hybridization (FISH) to identify and characterize structural chromosome changes among the smooth-seeded (Lupinus angustifolius L., Lupinus cryptanthus Shuttlew., Lupinus micranthus Guss.) and rough-seeded (Lupinus cosentinii Guss. and Lupinus pilosus Murr.) lupin species. Comparative cytogenetic mapping was done using FISH with oligonucleotide probes and previously published chromosome-specific bacterial artificial chromosome (BAC) clones. Oligonucleotide probes were designed to cover both arms of chromosome Lang06 of the L. angustifolius reference genome separately. The chromosome was chosen for the in-depth study due to observed structural variability among wild lupin species revealed by BAC-FISH and supplemented by in silico mapping of recently released lupin genome assemblies. The results highlighted changes in synteny within the Lang06 region between the lupin species, including putative translocations, inversions, and/or non-allelic homologous recombination, which would have accompanied the evolution and speciation.
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Lambers, Hans, Jon C. Clements i Matthew N. Nelson. "How a phosphorus-acquisition strategy based on carboxylate exudation powers the success and agronomic potential of lupines (Lupinus, Fabaceae)". American Journal of Botany 100, nr 2 (luty 2013): 263–88. http://dx.doi.org/10.3732/ajb.1200474.

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Susek, Karolina, Wojciech Bielski, Katarzyna B. Czyż, Robert Hasterok, Scott A. Jackson, Bogdan Wolko i Barbara Naganowska. "Impact of Chromosomal Rearrangements on the Interpretation of Lupin Karyotype Evolution". Genes 10, nr 4 (1.04.2019): 259. http://dx.doi.org/10.3390/genes10040259.

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Plant genome evolution can be very complex and challenging to describe, even within a genus. Mechanisms that underlie genome variation are complex and can include whole-genome duplications, gene duplication and/or loss, and, importantly, multiple chromosomal rearrangements. Lupins (Lupinus) diverged from other legumes approximately 60 mya. In contrast to New World lupins, Old World lupins show high variability not only for chromosome numbers (2n = 32–52), but also for the basic chromosome number (x = 5–9, 13) and genome size. The evolutionary basis that underlies the karyotype evolution in lupins remains unknown, as it has so far been impossible to identify individual chromosomes. To shed light on chromosome changes and evolution, we used comparative chromosome mapping among 11 Old World lupins, with Lupinus angustifolius as the reference species. We applied set of L. angustifolius-derived bacterial artificial chromosome clones for fluorescence in situ hybridization. We demonstrate that chromosome variations in the species analyzed might have arisen from multiple changes in chromosome structure and number. We hypothesize about lupin karyotype evolution through polyploidy and subsequent aneuploidy. Additionally, we have established a cytogenomic map of L. angustifolius along with chromosome markers that can be used for related species to further improve comparative studies of crops and wild lupins.
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Wright, K. L., D. E. Otterby, J. G. Linn, M. D. Stern, G. D. Marx i D. G. Johnson. "Evaluation of White Lupines and Triticale in Calf Starter Diets". Journal of Dairy Science 72, nr 4 (kwiecień 1989): 1002–11. http://dx.doi.org/10.3168/jds.s0022-0302(89)79195-5.

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Talhinhas, Pedro, S. Sreenivasaprasad, João Neves-Martins i Helena Oliveira. "Genetic and Morphological Characterization of Colletotrichum acutatum Causing Anthracnose of Lupins". Phytopathology® 92, nr 9 (wrzesień 2002): 986–96. http://dx.doi.org/10.1094/phyto.2002.92.9.986.

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Anthracnose, caused by Colletotrichum sp., is a serious problem of lupins (Lupinus spp.) worldwide. Morphological characters and molecular markers were used to characterize 43 Colletotrichum isolates from lupins, 8 isolates from other hosts, and 18 reference isolates representing related Colletotrichum spp., to assess the pathogen diversity and resolve its taxonomy. All lupin Colletotrichum isolates tested positive with C. acutatum-specific polymerase chain reaction (PCR) and did not test positive with C. gloeosporioides-specific PCR. Spore shape and colony diameter as well as insensitivity to benomyl grouped the lupin anthracnose isolates closer to C. acutatum than to C. gloeosporioides. Analysis of internal transcribed spacer (ITS) sequences of 57 Colletotrichum isolates grouped all lupin isolates with C. acutatum and distinct from C. gloeosporioides. Further, tub2 and his4 sequences revealed groups concordant with ITS, reducing the excessive dependence on the latter. Arbitrarily primed-PCR and amplified fragment length polymorphism analyses revealed intraspecific subgroups, but neither was useful to decipher species level relationships. ITS, tub2, and his4 results strongly support designating lupin anthracnose pathogen as C. acutatum or its subspecies. Most Colletotrichum isolates from lupins from worldwide locations are genetically homogeneous and form a distinct subgroup within C. acutatum. Present results also underline the potential of the C. acutatum-specific PCR for routine pathogen diagnosis.
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Deckert, J., J. Jeleńska, Z. Zaborowska i A. B. Legocki. "Isolation and classification of a family of cyclin gene homologues in Lupinus luteus." Acta Biochimica Polonica 44, nr 1 (31.03.1997): 37–42. http://dx.doi.org/10.18388/abp.1997_4437.

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The lupine (Lupinus luteus cv. Ventus) cDNA clones encoding homologues of cyclin (CycB1;2, CycB1;3, CycB1;4) have been isolated from cDNA library prepared from roots inoculated with Bradyrhizobium lupini. Comparison of the deduced amino-acid sequences of CycB1;2, CycB1;3, CycB1;4 and previously described CycB1;1 (Deckert et al. 1996, Biochimie 78, 90-94) showed that they share 46-65% of identical amino acids. The presence of conserved residues (Renaudin et. al., in The Plant Cell Cycle, in the press; Renaudin et al., Plant Mol. Biol, in the press) along with phylogenetic analysis of known plant cyclins revealed that the four lupine sequences belong to subgroup 1 of B-like mitotic cyclins.
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Dubrulle, Guillaume, Flora Pensec, Adeline Picot, Karim Rigalma, Audrey Pawtowski, Sophie Nicolleau, Nathalie Harzic, Patrice Nodet, Riccardo Baroncelli i Gaétan Le Floch. "Phylogenetic Diversity and Effect of Temperature on Pathogenicity of Colletotrichum lupini". Plant Disease 104, nr 3 (marzec 2020): 938–50. http://dx.doi.org/10.1094/pdis-02-19-0273-re.

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Although lupin anthracnose caused by Colletotrichum lupini is a significant threat for spring and winter lupin crops, it has been poorly studied so far. This study aimed at characterizing the (i) phylogenetic, (ii) morphological, and (iii) physiological diversity of collected isolates from anthracnose-affected lupins. The genetic identification of representative isolates (n = 71) revealed that they were all C. lupini species, further confirming that lupin anthracnose is caused by this species. However, multilocus sequencing on these isolates and 16 additional reference strains of C. lupini revealed a separation into two distinct genetic groups, both of them characterized by a very low genetic diversity. The diversity of morphological characteristics of a selected subset of C. lupini isolates was further evaluated. To the best of our knowledge, microsclerotia production observed for some isolates has never been reported so far within the Colletotrichum acutatum species complex. Finally, the modeling of growth responses of a subset of C. lupini strains revealed the capacity of some strains to grow in vitro at 5°C. This ability was also evidenced in planta, because C. lupini DNA was detectable in plants from 14 days postinoculation at 5°C onward, whereas symptoms began to appear a week later, although at a very low level. Since lupin crops are planted during winter or early spring, growth studies in vitro and in planta demonstrated the capability of the species to grow at temperatures ranging from 5 to 30°C, with an optimum close to 25°C. In this study, C. lupini-specific primers were also designed for real-time quantitative PCR on fungal DNA and allowed the detection of C. lupini in asymptomatic field samples. These results open perspectives to detect earlier and limit the development of this pathogen in lupin crops.
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Lee, S. T., K. E. Panter, J. A. Pfister, D. R. Gardner i K. D. Welch. "The effect of body condition on serum concentrations of two teratogenic alkaloids (anagyrine and ammodendrine) from lupines (Lupinus species) that cause crooked calf disease1". Journal of Animal Science 86, nr 10 (1.10.2008): 2771–78. http://dx.doi.org/10.2527/jas.2007-0610.

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Ramírez-Betancourt, Astrid, Arianna Michelle Hernández-Sánchez, Guadalupe Salcedo-Morales, Elsa Ventura-Zapata, Norma Robledo, Michael Wink i Kalina Bermúdez-Torres. "Unraveling the Biosynthesis of Quinolizidine Alkaloids Using the Genetic and Chemical Diversity of Mexican Lupins". Diversity 13, nr 8 (14.08.2021): 375. http://dx.doi.org/10.3390/d13080375.

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Quinolizidine alkaloids (QAs) are synthesized by the genus Lupinus as a defense against herbivores. Synthesis of QAs in lupins is species- and organ-specific. Knowledge about their biosynthesis and their corresponding pathways are still fragmentary, in part because lupins of commercial importance were mainly investigated, representing a small sample of the chemodiversity of the genus. Here, we explore the use of three Mexican lupins: Lupinus aschenbornii, Lupinus montanus, and Lupinus bilineatus as a model to study the physiology of QA biosynthesis. The corresponding QA patterns cover widely and narrowly distributed tetracyclic QAs. Quinolizidine alkaloid patterns of seeds and plantlets at different developmental stages were determined by GLC–MS and compared to identify the onset of de novo QA synthesis and to gain insight into specific and common biosynthesis trends. Onset of de novo QA biosynthesis occurred after the metabolization of seed QA during germination and was species-specific, as expected. A common QA pattern, from which the diversity of QA observed in these species is generated, was not found; however, lupanine and 3β-lupanine were found in the three specieswhile sparteine was not found in Lupinus bilineatus, suggesting that this simplest tetracyclic QA is not the precursor of more complex QAs. Similar patterns of metabolization and biosynthesis of structurally related QAs were observed, suggesting a common regulation.
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Guilengue, Norberto, João Neves-Martins i Pedro Talhinhas. "Response to Anthracnose in a Tarwi (Lupinus mutabilis) Collection Is Influenced by Anthocyanin Pigmentation". Plants 9, nr 5 (2.05.2020): 583. http://dx.doi.org/10.3390/plants9050583.

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Anthracnose, caused by Colletotrichum lupini, is a major limiting factor for lupin production. Tarwi or Andean Lupin (Lupinus mutabilis) is generally regarded as susceptible to anthracnose, but the high protein and oil content of its seeds raise interest in promoting its cultivation in Europe. In this study we evaluated the response to anthracnose of 10 tarwi accessions contrasting in anthocyanin pigmentation, by comparison to white lupin (Lupinus albus), using a contemporary Portuguese fungal isolate. A severity rating scale was optimized, including weighted parameters considering the type of symptoms and organs affected. All tarwi accessions were classified as susceptible, exhibiting sporulating necroses on the main stem from seven days after inoculation. Anthracnose severity was lower on anthocyanin-rich tarwi plants, with accession LM34 standing out as the less susceptible. Accession I82 better combines anthracnose response and yield. In global terms, disease severity was lower on white lupin than on tarwi. Although based on a limited collection, the results of the study show the existence of genetic variability among L. mutabilis towards anthracnose response relatable with anthocyanin pigmentation, providing insights for more detailed and thorough characterization of tarwi resistance to anthracnose.
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Rozprawy doktorskie na temat "Lupines – Genetics"

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Boersma, Jeffrey George. "Contributions to the molecular genetics of the Narrow-leaf Lupin (Lupinus augustifolius L.) : mapping, marker development and QTL analysis". University of Western Australia. School of Earth and Geographical Sciences, 2007. http://theses.library.uwa.edu.au/adt-WU2008.0001.

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[Truncated abstract] Narrow-leaf lupin (Lupinus angustifolius L.) was first recorded as having been introduced into Germany during the mid-19th century for use as green manuring and as fodder crops. However, it was not until post World-War I that there was any serious attempt to domesticate the species. Since that time several key domestication genes have been incorporated to enable the species to be grown as a crop over a range of climates, harvested as a bulk commodity and, the seed used for both animal and human consumption. However, the recent domestication of this species has seen a rather limited use of wild germplasm largely as a result of the difficulty in retaining these key domestication genes. To make the task of retaining these genes manageable, it was decided to resort to molecular technology. A mapping population of F8 derived recombinant inbred lines (RILs) has previously been established by the Department of Agriculture and Food, Western Australia, from a cross between a domesticated breeding line 83A:476 and a wild type P27255 in narrow-leaf lupin. The parents together with 89 RILs (of a population of 115) were subjected to DNA fingerprinting using microsatelliteanchored fragment length polymorphism (MFLP) to rapidly generate DNA markers for construction of a linkage map. Five hundred and twenty two unique markers of which 21% were co-dominant, were generated and mapped. Phenotypic data for the domestication traits: mollis (soft seeds), leucospermus (white flower and seed colour); Lentus (reduced pod-shattering), iucundis (low alkaloid), Ku (early flowering) and moustache pattern on seed coats; were included. Three to 7 molecular markers were identified within 5 cM of each of these domestication genes. The anthracnose resistance gene Lanr1 was also mapped. Linkage groups were constructed using MapManager version QTXb20, resulting in 21 linkage groups consisting of 8 or more markers. ... Five pairs of QTLs were found to be involved in epistasis, 2 of these having an effect on early vigour and another 3 influencing the time to opening of the first florets. Variation explained for each trait ranged from 28% for seed size, to 88% for days to flowering. We showed that it was possible to use this data to predict genotypes of superior progeny for these traits under Mediterranean conditions. QTL regions were compared on a second published linkage map and regions of conserved synteny with the model legume Medicago truncatula high-lighted. The work presented in this thesis demonstrates the importance of tight linkage between markers and genes of interest. It is especially important when dealing with genetically diverse material as found in the wild. One of the main problems faced by molecular scientists is the phenomenon known as linkage disequilibrium in marker populations caused by either small population size or 4 insufficient opportunity for recombination. This frequently results in the development of markers with little or no application outside of the population in which it was developed. Although the relatively small size of the population used in this study exposes it to such constraints, in this case excellent and valuable results were achieved in developing useful markers to at least 3 of the domestication traits within a relatively short time period of less then 4 years.
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Weitemier, Kevin Allen. "Phylogeographic Patterns and Intervarietal Relationships within Lupinus lepidus: Morphological Differences, Genetic Similarities". PDXScholar, 2010. https://pdxscholar.library.pdx.edu/open_access_etds/919.

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Lupinus lepidus (Fabaceae) contains many morphologically divergent varieties and was restricted in its range during the last period of glaciation. A combination of phylogenetic (with the trnDT and LEGCYC1A loci) and population genetics approaches (with microsatellites and LEGCYC1A are used here to characterize intervarietal relationships and examine hypotheses of recolonization of areas in the Pacific Northwest affected by glaciation. Sequenced loci are not found to form a clade exclusive to L. lepidus, nor are any of the varieties found to form clades. Population genetics analyses reveal only negligible genetic structure within L. lepidus, with the majority of variation being found within populations. Isolation-by-distance analysis reveals some correlation between population genetic distances and geographic distance. Microsatellite and sequence results are consistent with a scenario whereby the Oregon and Washington regions were rapidly colonized from the south, with independent invasions along the eastern and western sides of the Cascade Mountains. A predicted disjunction between northern and southern populations is found within the microsatellite data but not the sequence data, suggesting that northern populations were recolonized via a process involving the spread of novel microsatellite mutations, perhaps through the persistence of a glacial refuge isolated from southern populations. Varieties are not shown to be genetically isolated, and are interpreted as representing ecotypes, with local selection outpacing the effects of migration.
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Geering, Andrew D. W. "The epidemiology of cucumber mosaic virus in narrow-leafed lupins (Lupinus angustifolius) in South Australia". Title page, table of contents and summary only, 1992. http://web4.library.adelaide.edu.au/theses/09PH/09phg298.pdf.

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Suso, Henri-Pierre. "Development of a system for the genetic transformation of white lupin (Lupinus albus)". Thesis, University of Reading, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.271196.

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Babaoglu, Mehmet. "Genetic manipulation of lupins". Thesis, University of Nottingham, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.320790.

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Wijayanto, Teguh. "Genetic manipulation of programmed cell death (PCD) for reduced susceptibility to necrotrophic fungi in narrow-leafed lupin (Lupinus angustifolius) /". Connect to this title, 2006. http://theses.library.uwa.edu.au/adt-WU2007.0206.

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Wilson, Rachel Erin. "The Genetic Basis for Seed Coat Polymorphisms In Lupinus Perennis". Bowling Green State University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1566754995812035.

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Bishop, John G. "Demographic and population genetic variation during colonization by the herb Lupinus lepidus on Mount St. Helens /". Thesis, Connect to this title online; UW restricted, 1996. http://hdl.handle.net/1773/5177.

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Julier, Bernadette. "Etude génétique et physiologique de l'architecture déterminée chez le lupin blanc d'hiver. Conséquences agronomiques et en sélection". Phd thesis, ENSA de Rennes, 1994. http://tel.archives-ouvertes.fr/tel-00676075.

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Comme chez de nombreux protéagineux, l'architecture déterminée a semblé une voie prometteuse pour réduire le développement végétatif et améliorer le rendement et la stabilité du rendement du lupin blanc d'hiver (Lupinus albus L.). Une étude à la fois génétique et physiologique de ce type architecturale et de ses conséquences sur le développement et la mise en place du rendement a donc été entreprise. L'hérédité du caractère d'architecture déterminée est monogénique récessive, ce qui permet une utilisation simple en sélection. Le développement végétatif est réduit car tous les bourgeons passent à l'état floral précocément dans le cycle. Les ramifications portent chacune moins de feuilles que chez les indéterminés, et le nombre de niveaux végétatifs est réduit. La distribution des feuilles sur les ramifications suit un profil caractéristique en forme de cloche. La structure des ramifications a pu être modélisée. Il existe une grande variabilité génétique pour l'architecture, bien que la relation positive entre tardiveté de floraison et développement végétatif soit forte. L'interception de la lumière par le couvert en fonction du temps est similaire chez les déterminés et les indéterminés. Cependant, les déterminés atteignent une interception maximale moins importante en raison de leur développement végétatif restreint. La proportion de lumière qui parvient jusqu'aux feuilles de la tige principale est accrue. Le rendement des génotypes déterminés semble compétitif avec celui des génotypes indéterminés. La production de matière sèche est plus faible mais l'indice de récolte est supérieur. La date de maturité est sensiblement avancée, surtout sous des climats frais et humides, et la stabilité du rendement est plus grande. Ces caractéristiques sont liées à la réduction du développement végétatif, et à une compétition entre développement végétatif et développement reproducteur plus faible que celle observée chez les indéterminés. Le rendement est produit essentiellement sur la tige principale et le premier niveau de ramifications, et ces sites sont moins sujets à des aléas climatiques que les niveaux supérieurs. La variabilité génétique pour les composantes du rendement est large. On met en évidence des relations entre certains caractères d'architecture et les potentialités de rendement. Un développement végétatif trop restreint aussi bien qu'un développement excessif nuisent au rendement. Les caractères de développement des ramifications (nombre de feuilles et nombre de niveaux végétatifs) sont des critères de sélection pertinents chez les lupins déterminés.
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Książki na temat "Lupines – Genetics"

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Lupins: Geography, classification, genetic resources, and breeding. St. Petersburg: Pub. House "Intan", 2002.

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americano, Istituto italo-latino, i Fundación "Pro Bolivia ", red. Investigaciones sobre el mejoramiento genético y cultural de trigo duro, girasol, maíz, fríjol, lupino y haba en Bolivia. Roma: IILA, 1987.

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Części książek na temat "Lupines – Genetics"

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Cowling, Wallace. "Lupins (Lupinus L.)". W Plant Genetic Resources of Legumes in the Mediterranean, 191–206. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-015-9823-1_11.

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Legocki, A. B., J. Biesiadka, W. Golinowski, J. Kopcinska, B. Lotocka, A. Rudzinska, M. Sikorski, T. Stepkowski i P. Strozycki. "Molecular Genetics of a Model Plant: Lupinus luteus". W Biological Nitrogen Fixation for the 21st Century, 309–10. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5159-7_174.

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Shahidul, Islam, Huaan Yang i Guijun Yan. "Molecular Markers for Genetics and Plant Breeding: The MFLP Marker System and Its Application in Narrow-Leafed Lupin (Lupinus angustifolius)". W Legume Genomics, 179–201. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-613-9_13.

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Seliga, Henryka. "The role of copper in nitrogen fixation in Lupinus luteus L." W Plant Nutrition — from Genetic Engineering to Field Practice, 459–62. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1880-4_96.

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Tang, C., B. T. Cobley, S. Mokhtara, C. E. Wilson i H. Greenway. "High pH in the nutrient solution impairs water uptake in lupinus angustifolius L." W Plant Nutrition — from Genetic Engineering to Field Practice, 763–65. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1880-4_169.

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Sikorski, M., U. Szybiak-Stróżycka, P. Stróżycki, B. Golińska, C. J. Madrzak, R. Kamp, B. Wittmann-Liebold i A. B. Legocki. "Coordinated Expression of Nodule-Specific and Root Genes in Yellow Lupin". W Molecular genetics of plant-microbe interactions, 127–29. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-4482-4_28.

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Crosbie, Julie, Nancy Longnecker, Fleur Davies i Alan Robson. "Effects of Seed Manganese Concentration on Lupin Emergence". W Plant Nutrition — from Genetic Engineering to Field Practice, 665–68. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1880-4_145.

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Tang, C., A. D. Robson, N. E. Longnecker i H. Greenway. "Physiological responses of lupin roots to high pH". W Plant Nutrition — from Genetic Engineering to Field Practice, 755–58. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1880-4_167.

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Taylor, Candy M., Lars G. Kamphuis, Wallace A. Cowling, Matthew N. Nelson i Jens D. Berger. "Ecophysiology and Phenology: Genetic Resources for Genetic/Genomic Improvement of Narrow-Leafed Lupin". W Compendium of Plant Genomes, 19–30. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-21270-4_2.

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Cowling, Wallace A. "Genetic Diversity in Narrow-Leafed Lupin Breeding After the Domestication Bottleneck". W Compendium of Plant Genomes, 1–17. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-21270-4_1.

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Streszczenia konferencji na temat "Lupines – Genetics"

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Novik, N. V., A. A. Lebedev i I. A. Yakub. "Genetic sources of economically valuable characteristics for breeding yellow lupine". W Растениеводство и луговодство. Тимирязевская сельскохозяйственная академия, 2020. http://dx.doi.org/10.26897/978-5-9675-1762-4-2020-126.

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Streszczenie:
Screening of world gene bank is carried out to develop initial material for yellow lupin breeding. During 2018-2020 the following genetic sources have been selected: the Polish variety Parus (k-3371) as a semi-early ripened source for plant tallness, high growth tempo and high green mass productivity; the variety Puissant (k-2170) as a source for plant tallness, high seed productivity and seed protein content; the variety SV 01060 (k-2193) as a source for plant tallness, moderate period of ripening, high green mass productivity, seed protein content and their size; the lines Tromusillo-2 (k-3276), W 72 (k-2936), W 105 (k-2933), No. 1004 (k-3913) and the breeding line 07-20-240-2384-3 as sources for tolerance to virus diseases; the breeding line 11-11-02-2-4-3 as a source for high seed and green mass productivity; the hybrid Borluta x Zhitomirskii (k-3592) as a source for plant tallness and moderate period of ripening; k-3915 as a source for moderate period of ripening and high seed productivity.
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"Differential gene expression in roots of yellow lupin sprouts under Fusarium treatment". W Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, 2019. http://dx.doi.org/10.18699/plantgen2019-188.

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Raporty organizacyjne na temat "Lupines – Genetics"

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Weitemier, Kevin. Phylogeographic Patterns and Intervarietal Relationships within Lupinus lepidus: Morphological Differences, Genetic Similarities. Portland State University Library, styczeń 2000. http://dx.doi.org/10.15760/etd.919.

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