scholarly journals Inheritance and cytogenetics of sterility in yellow lupin (Lupinus luteus L.)

2015 ◽  
Vol 45 (3) ◽  
pp. 207-223
Author(s):  
T. Kazimierski ◽  
E. Kazimierska
Keyword(s):  
Lupinus Luteus ◽  
Crossing Over ◽  
Yellow Lupin ◽  
Hybrid Combination ◽  
Primitive Forms ◽  
Prophase Of Meiosis

Amon g the hybrids of the cultivated form named 'Batavo', originating from Holland, and 6 primitive forms of the yellow lupin was one hybrid combination found (Batavo X primitive No. 5), which in F<sub>2</sub> and F<sub>3</sub> gives fertile and sterile plants with the ratio 3 : 1. The gene causing sterility was appeased as a result of crossing over at the time of prophase of meiosis in the sporogenic cells of F<sub>1</sub> plants. This gene in homozygotic condition in F<sub>2</sub> and F<sub>3</sub> plants causes the coalescence of chromosomes, disturbances in the process of meiosis and microsporogenesis what leads to forms with non viable microspores. The sterile plants blossom abundantly but they give not pods and seeds.

Localization of Flavonoids in the Yellow Lupin Seedlings and Their UV-B-absorbing Potential

2002 ◽  
Vol 57 (9-10) ◽  
pp. 811-816 ◽  
Author(s):  
Yasufumi Katagiri ◽  
Yasuyuki Hashidoko ◽  
Satoshi Tahara
Keyword(s):  
Lupinus Luteus ◽  
Yellow Lupin ◽  
External Stresses

Quantification of the flavonoids in yellow lupin (Lupinus luteus; Leguminosae) seedlings revealed that a flavone glucoside, 7-O-β-(2-O-β-rhamnosyl)glucosyl-4′,5,7-trihydroxyflavone (apigenine 7-O-β-neohesperidoside), is rich in the epicotyl and cotyledon. In hypocotyls and roots, 8-C-β-glucosyl-4′,5,7-trihydroxyisoflavone (genistein 8-C-β-glucoside) was a predominant flavonoid constituent. The roles of the localized flavonoids are briefly discussed relating to defense against biotic and abiotic external stresses.

Yellow lupin (Lupinus luteus) tolerates waterlogging better than narrow-leafed lupin (L. angustifolius) I. Shoot and root growth in a controlled environment

2000 ◽  
Vol 51 (6) ◽  
pp. 701 ◽  
Author(s):  
C. L. Davies ◽  
D. W. Turner ◽  
M. Dracup
Keyword(s):  
Root Growth ◽  
Western Australia ◽  
Shoot Growth ◽  
Dry Weight ◽  
Lupinus Luteus ◽  
Controlled Environment ◽  
Yellow Lupin ◽  
Legume Crop ◽  
Leaf Dry Weight ◽  
Better Than

We studied the adaptation of narrow-leafed lupin (Lupinus angustifolius) and yellow lupin (L. luteus) to waterlogging because yellow lupin may have potential as a new legume crop for coarse-textured, acidic, waterlogging-prone areas in Western Australia. In a controlled environment, plants were waterlogged for 14 days at 28 or 56 days after sowing (DAS). Plants were more sensitive when waterlogged from 56 to 70 DAS than from 28 to 42 DAS, root growth was more sensitive than shoot growth, and leaf expansion was more sensitive than leaf dry weight accumulation. Waterlogging reduced the growth of narrow-leafed lupin (60–81%) more than that of yellow lupin (25–56%) and the response was more pronounced 2 weeks after waterlogging ceased than at the end of waterlogging. Waterlogging arrested net root growth in narrow-leafed lupin but not in yellow lupin, so that after 2 weeks of recovery the root dry weight of yellow lupin was the same as that of the control plants but in narrow-leafed lupin it was 62% less than the corresponding control plants. Both species produced equal amounts of hypocotyl root when waterlogged from 28 to 42 DAS but yellow lupin produced much greater amounts than narrow-leafed lupin when waterlogged from 56 to 70 DAS.

Root growth of lupins is more sensitive to waterlogging than wheat

2011 ◽  
Vol 38 (11) ◽  
pp. 910 ◽  
Author(s):  
Helen Bramley ◽  
Stephen D. Tyerman ◽  
David W. Turner ◽  
Neil C. Turner
Keyword(s):  
Root Growth ◽  
Oxygen Deficiency ◽  
Triticum Aestivum L ◽  
Wheat Root ◽  
Lupinus Luteus ◽  
Apical Region ◽  
Basal Region ◽  
Yellow Lupin ◽  
Wheat Roots ◽  
Root Death

In south-west Australia, winter grown crops such as wheat and lupin often experience transient waterlogging during periods of high rainfall. Wheat is believed to be more tolerant to waterlogging than lupins, but until now no direct comparisons have been made. The effects of waterlogging on root growth and anatomy were compared in wheat (Triticum aestivum L.), narrow-leafed lupin (Lupinus angustifolius L.) and yellow lupin (Lupinus luteus L.) using 1 m deep root observation chambers. Seven days of waterlogging stopped root growth in all species, except some nodal root development in wheat. Roots of both lupin species died back progressively from the tips while waterlogged. After draining the chambers, wheat root growth resumed in the apical region at a faster rate than well-drained plants, so that total root length was similar in waterlogged and well-drained plants at the end of the experiment. Root growth in yellow lupin resumed in the basal region, but was insufficient to compensate for root death during waterlogging. Narrow-leafed lupin roots did not recover; they continued to deteriorate. The survival and recovery of roots in response to waterlogging was related to anatomical features that influence internal oxygen deficiency and root hydraulic properties.

Nodulation of lime pelleted lupins and serradella when inoculated with peat and agar cultures

1967 ◽  
Vol 7 (26) ◽  
pp. 259 ◽  
Author(s):  
QA Shipton ◽  
CA Parker
Keyword(s):  
Adverse Effect ◽  
Adverse Effects ◽  
Rock Phosphate ◽  
The Other ◽  
Lupinus Luteus ◽  
Yellow Lupin ◽  
Other Hand

Lime coating yellow lupin (Lupinus luteus L.) seed, when inoculated with bacteria from agar slopes, reduced nodulation substantially. By contrast, when peat cultures were used there was no adverse effect of lime coating on nodulation, even when inoculated seeds were stored for 61 days at 75�F, before planting. In two experiments the nodulation of unhulled serradella (Omithopus comljressus L.) was generally unaffected by lime coating when either agar or peat cultures were used. In a third experiment nodulation was significantly reduced with both agar and peat cultures on unhulled and hulled seed. This adverse effect was greater with agar cultures than with peat cultures. It is concluded that peat, and possibly the serradella seed pod, protects the bacteria from the effects of lime. The practice of lime coating lupin and serradella seed, when inoculated with peat cultures, is a useful technique, particularly when the seed is sown in contact with acid superphosphate. On the other hand, some adverse effects of lime on the nodulation of serradella when a peat culture was used suggest that other workers should test the suitability of the lime pelleting method under their own conditions. Rock phosphate and bentonite were also investigated as pelleting agents, but neither seemed to offer any advantages over lime.

Transgenic yellow lupin ( Lupinus luteus )

2000 ◽  
Vol 19 (6) ◽  
pp. 634-637 ◽  
Author(s):  
H. Li ◽  
S. J. Wylie ◽  
M. G. K. Jones
Keyword(s):  
Lupinus Luteus ◽  
Yellow Lupin

Polyamines in yellow lupin (Lupinus luteus L.) tolerance to soil drought

2017 ◽  
Vol 39 (9) ◽  
Author(s):  
Katarzyna Juzoń ◽  
Ilona Czyczyło-Mysza ◽  
Izabela Marcińska ◽  
Michał Dziurka ◽  
Piotr Waligórski ◽  
...  
Keyword(s):  
Lupinus Luteus ◽  
Soil Drought ◽  
Yellow Lupin

The role of alkaloids in conferring aphid resistance in yellow lupin (Lupinus luteus L.)

2012 ◽  
Vol 63 (5) ◽  
pp. 444 ◽  
Author(s):  
Kedar Nath Adhikari ◽  
Owain Rhys Edwards ◽  
Shaofang Wang ◽  
Thomas James Ridsdill-Smith ◽  
Bevan Buirchell
Keyword(s):  
Total Alkaloid ◽  
Resistance Breeding ◽  
Aphid Resistance ◽  
Lupinus Luteus ◽  
Human Consumption ◽  
Yellow Lupin ◽  
F2 Population ◽  
Legume Crop ◽  
Total Seed ◽  
Aphid Tolerance

A key goal in the breeding for aphid resistance of cultivated lupins is to manipulate the levels and distributions of alkaloids. Lupin alkaloids are known to be responsible for resistance to herbivorous insects, but the total seed alkaloid level must remain under 0.02% for animal and human consumption. Yellow lupin (Lupinus luteus L.) is being investigated as a new legume crop for Western Australia (WA), but most lines produced to date have been very susceptible to aphids. In contrast, breeders in WA have had ongoing success releasing narrow-leafed lupin (L. angustifolius L.) cultivars with adequate resistance to aphids. In this study, aphid performance was evaluated on yellow lupin plants in the glasshouse from an F2 population derived from a cross between Teo, a yellow lupin cultivar resistant to aphids and with high total alkaloid levels, and Wodjil, a single plant selection from Teo that is susceptible to aphids and has low total alkaloid levels, and their parents. Resistance in Teo and the F2 progeny was strongly associated with the alkaloids gramine and a gramine analogue. The absence of plants with intermediate levels of these alkaloids in progeny of this cross makes it unlikely that aphid-resistant lines can be generated using Teo as the resistance source. On the other hand, different alkaloids were correlated with aphid resistance in the narrow-leafed lupin cultivar Kalya, and aphid resistance was more evenly distributed among progeny of a cross of the resistant cultivar Kalya with the susceptible cultivar Tallerack. For this reason, additional yellow lupin lines with a more diverse alkaloid profile were selected for further study from the Australian lupin breeding program. A wide variation in the aphid tolerance among lines was observed and aphid tolerance was positively correlated with alkaloid content. However, four lines were identified with moderate levels of aphid resistance in a low alkaloid background. These lines had varying alkaloid profiles, but as expected none were dominated by gramine and its analogues. We believe these lines offer a greater opportunity for aphid resistance breeding in yellow lupins.

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