scholarly journals Mediterranean White Lupin Landraces as a Valuable Genetic Reserve for Breeding

Plants ◽  
2021 ◽  
Vol 10 (11) ◽  
pp. 2403
Author(s):  
Ioannis Zafeiriou ◽  
Alexios N. Polidoros ◽  
Eirini Baira ◽  
Konstantinos M. Kasiotis ◽  
Kyriaki Machera ◽  
...  

Legumes crops are important for sustainable agriculture and global food security. Among them white lupin (Lupinus albus L.), is characterized by exceptional protein content of high nutritional value, competitive to that of soybean (Glycine max) and is well adapted to rainfed agriculture. However, its high seed-quinolizidine alkaloid (QA) content impedes its direct integration to human diet and animal feed. Additionally, its cultivation is not yet intensive, remains confined to local communities and marginal lands in Mediterranean agriculture, while adaptation to local microclimates restrains its cultivation from expanding globally. Hence, modern white lupin breeding aims to exploit genetic resources for the development of “sweet” elite cultivars, resilient to biotic adversities and well adapted for cultivation on a global level. Towards this aim, we evaluated white lupin local landrace germplasm from Greece, since the country is considered a center of white lupin diversity, along with cultivars and breeding lines for comparison. Seed morphological diversity and molecular genetic relationships were investigated. Most of the landraces were distinct from cultivars, indicating the uniqueness of their genetic make-up. The presence of pauper “sweet” marker allele linked to low seed QA content in some varieties was detected in one landrace, two breeding lines, and the cultivars. However, QA content in the examined genotypes did not relate with the marker profile, indicating that the marker’s predictive power is limited in this material. Marker alleles for vernalization unresponsiveness were detected in eight landraces and alleles for anthracnose resistance were found in two landraces, pointing to the presence of promising germplasm for utilization in white lupin breeding. The rich lupin local germplasm genetic diversity and the distinct genotypic composition compared to elite cultivars, highlights its potential use as a source of important agronomic traits to support current breeding efforts and assist its integration to modern sustainable agriculture.

1995 ◽  
Vol 75 (4) ◽  
pp. 841-849 ◽  
Author(s):  
S. Brebaum ◽  
G. J. Boland

Sweet white lupin (Lupinus albus) is an emerging crop in Ontario and, in 1993, up to 600 ha acres of lupin were planted. This crop is adapted to cool and moderately warm climates, is frost-resistant to −2 °C, requires sandy to loamy soils, requires inoculation with Bradyrhizobium sp. to achieve high yields, and improves soil structure and nutrients when included in a crop rotation. The crop requires 119–135 d to mature and is thermosensitive; both traits can reduce yield in seasons with unfavourable environments. The crop is not particularly competitive with weeds and effective weed control is a critical factor in crop production. Lupin is attacked by several pathogens and insects but knowledge on appropriate pest management practices needs to be improved. The harvested seed of sweet white lupin is primarily used as an on-farm source of protein. Seeds do not require heat treatment prior to being used as animal feed and can be included as a part of the protein component in the diets of ruminants, swine and poultry. High protein digestibility and high fibre content of lupin seeds can limit incorporation into the diets of ruminants and swine, respectively. Lupin can be beneficial in human diets because milk from lupin-fed animals contains more unsaturated fatty acids and less saturated fatty acids than milk from animals fed soybean meal. Sweet white lupin has several advantages and disadvantages as an emerging crop in Ontario, but additional research and development are needed. Key words: Lupin (sweet white), Lupinus albus


1998 ◽  
Vol 96 (6-7) ◽  
pp. 878-885 ◽  
Author(s):  
E. Garcia ◽  
M. Jamilena ◽  
J. I. Alvarez ◽  
T. Arnedo ◽  
J. L. Oliver ◽  
...  

2000 ◽  
Vol 1 (1) ◽  
pp. 26
Author(s):  
A. Trapero-Casas ◽  
A. Rodríguez-Tello ◽  
W. J. Kaiser

Several lupin (Lupinus) species are native to southern Spain. The white lupin, Lupinus albus L., is the most important crop, and its seeds are used for human consumption and animal feed. Posted 9 June 2000.


Plant Disease ◽  
2000 ◽  
Vol 84 (4) ◽  
pp. 488-488 ◽  
Author(s):  
A. Trapero-Casas ◽  
A. Rodríguez-Tello ◽  
W. J. Kaiser

Several lupin (Lupinus) species are native to southern Spain (2). The white lupin, Lupinus albus L., is the most important crop, and its seeds are used for human consumption and animal feed. Accessions of three indigenous species, L. albus, L. angustifolius L., and L. luteus L., and an introduced species from South America, L. mutabilis Sweet, were planted during October in replicated yield trials in acidic soils (pH 6.5) in the Sierra Morena Mountains (elevation 350 m) north of Córdoba. Root and crown rot disease was widespread and very serious on the indigenous lupins, particularly in several patches of white lupin cultivars. Infected plants were devoid of feeder rootlets, and the tap roots, crowns, and lower stems were necrotic and turned dark brown to black. Rotted roots were colonized heavily by fungal oospores. Many affected plants wilted and died before flowering. A Phytophthora sp. was isolated consistently from the necrotic roots and crowns of symptomatic white lupins. The same fungus also was isolated from the necrotic root tissues of the other indigenous lupin species. Isolates of the fungus from diseased white lupins were homothallic and produced oospores rapidly and abundantly on corn meal and V8 agars. Antheridia were amphigynous, and aplerotic oospores ranged from 22 to 32 μm (average 27 μm). Nonpapillate, ovoidobpyriform sporangia were produced only in water on simple sympodial sporangiophores. Cultures on V8 agar grew at 5 to 30°C (optimum ≈25°C). The species was identified as Phytophthora erythroseptica Pethybr. based on morphology of oospores, sporangia, and other cultural characteristics (1). Koch's postulates were fulfilled by planting seeds of white lupin cv. Multulupa in sterile potting soil infested with a blended culture on V8 agar from a white lupin isolate of P. erythroseptica and reisolating the fungus after 28 days from lesions that developed on the roots and crowns of inoculated plants incubated in a greenhouse at 16 to 26°C. The fungus was not isolated from white lupins seeded in potting soil inoculated with sterile V8 agar. In pathogenicity tests, two isolates of P. erythroseptica from white lupins caused severe symptoms on the roots and crowns of inoculated white lupin cv. Multulupa similar to those observed on white lupins naturally infected in field trials. These isolates also caused root and crown rots on inoculated L. luteus and L. angustifolius. The fungus did not infect the roots or crowns of tarwi (L. mutabilis cv. SCG 20), alfalfa (Medicago sativa cv. Moapa), bean (Phaseolus vulgaris cv. Contender), chickpea (Cicer arietinum cv. Blanco Lechoso), faba bean (Vicia faba cv. Arboleda), lentil (Lens culinaris cv. local), pea (Pisum sativum cv. Lancet), soybean (Glycine max cv. Akashi), or subterranean clover (Trifolium subterraneum cv. Seaton-park). The tests were repeated, and the results were similar. This is the first report of P. erythroseptica infecting Lupinus spp. References: (1) D. C. Erwin and O. K. Ribeiro. 1996. Phytophthora Diseases Worldwide. The American Phytopathological Society, St. Paul, MN. (2) B. Valdés et al. 1987. Flora Vascular de Andalucía Occidental. Ketres, Barcelona, Spain.


2016 ◽  
Vol 8 (7) ◽  
pp. 23 ◽  
Author(s):  
Natalia Anastasova Georgieva ◽  
Valentin Ivanov Kosev

<p>An evaluation of the agronomic performance of two lupin species (<em>Lupinus albus</em> and <em>Lupinus luteus</em>) was conducted at the Institute of Forage Crops (Bulgaria) during 2012-2014. The hightest positive correlations among the agronomic traits in white lupin were between number of pods per plant and seed weight per plant (r = 0.956); plant height with pod stem length (r = 0.935) and pod length (r = 0.934); seed weight per plant and number of pods per plant (r = 0.956). In yellow lupin relatively high phenotypic correlations were detected between number of pods per plant and seed weight per plant (r = 0.956); seed weight per plant and number of pods (r = 0.875) and number of seeds per plant (r = 0.927). Collecting data on the mutual relationships among individual yield components and their effect on the yield remains crucial for their optimisation and development of improved lupin genotypes with high quality and stable yields. Based on the trait associations it can be concluded that lupin breeders should pay attention to the traits such as pod length, number of seeds per plant and 1000 seeds mass when selecting high-yielding genotypes.</p>


2021 ◽  
Vol 22 (8) ◽  
pp. 3856
Author(s):  
Sandra Rychel-Bielska ◽  
Anna Surma ◽  
Wojciech Bielski ◽  
Bartosz Kozak ◽  
Renata Galek ◽  
...  

White lupin (Lupinus albus L.) is a pulse annual plant cultivated from the tropics to temperate regions for its high-protein grain as well as a cover crop or green manure. Wild populations are typically late flowering and have high vernalization requirements. Nevertheless, some early flowering and thermoneutral accessions were found in the Mediterranean basin. Recently, quantitative trait loci (QTLs) explaining flowering time variance were identified in bi-parental population mapping, however, phenotypic and genotypic diversity in the world collection has not been addressed yet. In this study, a diverse set of white lupin accessions (n = 160) was phenotyped for time to flowering in a controlled environment and genotyped with PCR-based markers (n = 50) tagging major QTLs and selected homologs of photoperiod and vernalization pathway genes. This survey highlighted quantitative control of flowering time in white lupin, providing statistically significant associations for all major QTLs and numerous regulatory genes, including white lupin homologs of CONSTANS, FLOWERING LOCUS T, FY, MOTHER OF FT AND TFL1, PHYTOCHROME INTERACTING FACTOR 4, SKI-INTERACTING PROTEIN 1, and VERNALIZATION INDEPENDENCE 3. This revealed the complexity of flowering control in white lupin, dispersed among numerous loci localized on several chromosomes, provided economic justification for future genome-wide association studies or genomic selection rather than relying on simple marker-assisted selection.


1998 ◽  
Vol 8 (4) ◽  
pp. 415-422 ◽  
Author(s):  
Brenda Winkel Shirley

AbstractFlavonoids are secondary metabolites that are present at high levels in most plant seeds and grains. These compounds appear to play vital roles in defence against pathogens and predators and contribute to physiological functions such as seed maturation and dormancy. At the same time, particular subclasses of flavonoids, such as the proanthocyanidins (condensed tannins), negatively impact the use of seeds and grains in animal feed and can add undesirable qualities to food products for human consumption. This article presents an overview of investigations into the physiological and agronomic aspects of seed and grain flavonoids as well as a review of molecular genetic studies, particularly in maize,Arabidopsisand soybean, where mutants deficient in flavonoid biosynthesis provide useful tools for stydying the metabolic machinery underlying the accumulation of these compounds in reproductive structures.


2002 ◽  
Vol 85 (3) ◽  
pp. 762-767 ◽  
Author(s):  
Graham Brookes

Abstract The use of the technology of genetic modification (GM) in European agriculture and the food supply chain is currently controversial. Because of strong anti-GM technology sentiments, the use of ingredients derived from plants containing GM have largely been eliminated from foods manufactured for direct human consumption by the food supply chain in much of the European Union (EU). During the past year, the attention of those opposed to the technology has turned to the use of GM ingredients in livestock production systems by incorporation of GM soy and maize in animal feed. A discussion is presented of the key issues relating to this subject, focusing on how supplies of GM or non-GM products are segregated or how their identities are preserved. The discussion is centered on GM maize and soybeans into which agronomic traits, such as herbicide tolerance and/or insect resistance, have been incorporated. These are currently the only crops into which some varieties containing GM have been approved for use in the EU.


Author(s):  
Thien Minh Nguyen ◽  
Tien Thi My Pham

The agronomic values of this population have been evaluated in the field experiments based on their phenotypic performance of agronomic traits, but the genetic variability of this population needs to be evaluated via techniques based on genetic material - DNA. In this study, the genetic variability in the investigated population of 71 hybrids and their parents was evaluated by RAPD technique, using eight selected arbitrarily primers; Genetic parameters and dendrogram expressing the genetic relationships among the investigated population were analyzed by GenALEx 6.1, Popgene 1.31 and NTSYSpc 2.1 softwares. Eight primers were used to generate the amplify products on each individual in the investigated population. From 74 genotypes, a total of 109 fragments were generated, among which, there were 89 polymorphic bands representing 81.65% with an average of 11 polymorphic bands/primer. Genetic similarity coefficient among the investigated population, based on DICE coefficient, ranged from 0.560 (LH05/0822 and PB260) to 0.991 (LH05/0781 and LH05/0841) with an average of 0,796, meaning that the genetic distance among ranged from 0.009 to 0.440 with an average of 0.231. The Shannon index and mean heterozygosity values were 0.328 and 0,176, respectively. This indicated that the progenies of the two investigated crosses possessed a relatively high range of genetic variability. The analysis of molecular variance (AMOVA) showed that genetic variation within population represented 62%, while genetic variation among two different crosses contributes 38% to the total genetic variability. Dendrogram based on DICE’s genetic similarity using UPGMA method showed that the hybrids divide into two major genetic groups (0.75), but the crosses were scattered independently of the hybrid.


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