Resistance to wheat midge (Diptera: Cecidomyiidae) in winter wheat and the origins of resistance in spring wheat (Poaceae)

2015 ◽  
Vol 148 (2) ◽  
pp. 229-238 ◽  
Author(s):  
R.J. Lamb ◽  
M.A.H. Smith ◽  
I.L. Wise ◽  
R.I.H. McKenzie

AbstractNine winter wheat cultivars (Triticum aestivum Linnaeus) (Poaceae) were the source of the Sm1 gene for resistance to wheat midge, Sitodiplosis mosellana (Géhin) (Diptera: Cecidomyiidae), in spring wheat. All nine showed antibiosis characteristic of Sm1, as expected. They also showed oviposition deterrence and reduced hatch, which contributed to overall resistance. The overall level of resistance of the nine winter wheat cultivars was usually lower than that of resistant spring wheat lines in laboratory trials, but equally high in a field trial. Five of seven other North American winter wheat cultivars also showed resistance. Three of these were grown in the 1920s and earlier, before wheat varieties were officially registered. One of these, “Mediterranean”, came from Europe in the 1880s and may be the origin of Sm1 in North America. Two of 11 Chinese winter wheat lines showed resistance to wheat midge but at a lower level than that characteristic of Sm1. Widespread resistance in North American winter wheat cultivars was unexpected because wheat midge has not been a pest of winter wheat for many decades. North American winter wheat cultivars can provide sources of resistance to wheat midge, particularly high levels of oviposition deterrence as exhibited by “Goens” and “Rawhide”.

1996 ◽  
Vol 76 (4) ◽  
pp. 689-695 ◽  
Author(s):  
P. S. Barker ◽  
R. I. H. McKenzie

The objective of this study was to find resistance in wheat cultivars to the wheat midge (Sitodiplosis mosellana [Géhin]). A total of 61 spring and 61 winter wheats were assayed in 1992 to 1994. Thirteen selected cultivars were planted in 1994. Three kinds of apparent response to midge infestation were found. Eight winter wheat cultivars suffered neither the usual typical kind nor high numbers of shrivelling of the seeds often attributed to the midge, but produced instead small numbers of shorter and more rounded (tubby) seeds which could be due to midge activity. Cultivar RL5708 differed from all other cultivars in that it showed low proportions of damaged seeds, which were often associated with dead midge larvae. The third group included lines and cultivars showing the typical shrivelling of the seeds due to the wheat midge. In 1993 most late-planted spring wheat cultivars were less affected by the midge than the same cultivars planted earlier probably because of asynchrony between times of wheat flowering and midge opposition. The incorporation of resistance to the wheat midge into hard red spring wheats should contribute to a reduction of wheat losses in years when wheat midge are abundant. Key words: Winter wheat, spring wheat, wheat midge, Sitodiplosis mosellana, resistance


1970 ◽  
Vol 50 (2) ◽  
pp. 137-140 ◽  
Author(s):  
M. N. GRANT ◽  
HUGH McKENZIE

Significant levels of heterosis were demonstrated in F1 yield trials from crosses between three spring and three winter wheats (T. aestivum L.): Thatcher × Winalta, Cypress × Kharkov 22 MC, and Lee × Cheyenne. Yields up to 40% higher than those of the spring wheat parent were attributed to heterosis resulting from hybridization of genetically diverse spring and winter types. To our knowledge this is the first published report of heterosis for yield in F1 hybrids between spring and winter wheat cultivars. This information has significance in both hybrid wheat and conventional breeding programs.


2005 ◽  
Vol 19 (3) ◽  
pp. 539-548 ◽  
Author(s):  
Curtis R. Rainbolt ◽  
Donald C. Thill ◽  
Robert S. Zemetra ◽  
Dale L. Shaner

Several experiments were conducted to evaluate the utility of an in vivo acetolactate synthase (ALS) assay for comparing sensitivity to imazamox among imidazolinone-resistant wheat cultivars/lines. Ten single-gene imidazolinone-resistant winter wheat cultivars/lines, one two-gene and four single-gene imidazolinone-resistant spring wheat cultivars/lines, and three pairs of heterozygous and homozygous imidazolinone-resistant winter wheat lines were evaluated in the assay experiments. Additionally, a dose-response assay was conducted to evaluate the tolerance of several imidazolinone-resistant wheat cultivars to imazamox on a whole plant level. The I50value (i.e., the imazamox dose that inhibited ALS activity by 50%) of the winter wheat cultivar ‘Above’ was 54 to 84% higher than the I50values of 99-420, 99-433, and CV-9804. However, based on the results of this study, it is unclear whether genetic background or market class (hard red winter vs. soft white winter) influences the level of ALS inhibition by imazamox. Teal 15A, the two-gene imidazolinone-resistant spring wheat cultivar, had an I50value that was two to three times greater than the I50value of the single-gene imidazolinone-resistant spring wheat cultivars/lines. The heterozygous imidazolinone-resistant wheat lines had I50values that were 69 to 81% less than the I50values of the homozygous lines. In the whole plant dose response, theR50values (i.e., the imazamox dose that reduced biomass by 50%) of the susceptible cultivars Brundage 96 and Conan were 15 to 17 times less than the homozygous single-gene imidazolinone-resistant winter and spring cultivars/lines, whoseR50values were about 1.7 times less than theR50value of the two-gene imidazolinone-resistant spring wheat line, Teal 15A. The results of the in vivo ALS imazamox assays and the whole plant imazamox dose-response assay were similar, indicating that the in vivo assay can be used to accurately and quickly compare resistance between imidazolinone-resistant wheat cultivars/lines.


1975 ◽  
Vol 53 (19) ◽  
pp. 2198-2201 ◽  
Author(s):  
D. G. Green ◽  
C. D. Ratzlaff

Soluble carbohydrate patterns of two hardy winter wheat cultivars and two less hardy cultivars were compared during the cold-hardening process. Soluble carbohydrates increased in concentration as the seedlings developed and the cold-hardening process occurred. The largest soluble carbohydrate differentials between the hardy and less hardy winter wheat cultivars occurred in the sucrose and raffinose fractions. The accumulation of sucrose and raffinose in wheat growing at 7.2 °C–0.5 °C day–night was greater in the two less hardy winter wheat cultivars. An inverse relationship existed between soluble sugars and cold hardiness in the four cultivars studied.


1998 ◽  
Vol 78 (2) ◽  
pp. 239-244 ◽  
Author(s):  
B. Bizimungu ◽  
J. Collin ◽  
A. Comeau ◽  
C.-A. St-Pierre

An interspecific wheat × triticale hybridization program was initiated with the scope of widening and improving the winter wheat gene pool. However, progress was hampered by severe necrosis that caused the death of F1 hybrids from crosses between the most winterhardy wheat and triticale cultivars. This paper describes hybrid necrosis as the main barrier to gene transfer between winter wheat cultivars Borden, Augusta and Ruby, and hexaploid winter triticales OAC Wintri and K9-6. Crosses with tester lines revealed that the three winter wheats were carriers of the necrotic Ne2 allele. High temperature (30 °C) treatment until heading stage permitted to only partially circumvent the problem. A study of cross direction effects at the backcross level showed that the conventional method (F1 × wheat) was more efficient for plant recovery, but plants produced by the alternative backcross system (wheat × F1) were more self-fertile. Within the most winterhardy germplasm, hybrid necrosis is a major problem for transferring genes between winter wheat and triticale. The use of non-necrotic winter wheat lines such as MC11N, a local winter wheat selection, may have a special value as a bridge to circumvent the necrosis problem. Key words: Hybrid necrosis, Ne genes, wheat × triticale hybrids, cross direction


1985 ◽  
Vol 57 (4) ◽  
pp. 271-277
Author(s):  
Tuula Sontag ◽  
Hannu Salovaara

The polyacrylamide gel electrophoretic (PAGE) patterns of gliadins of 9 spring wheat cultivars (Apu, Drabant, Taava, Tapio, Ulla, Kadett, Luja, Ruso and Tähti) and of 5 winter wheat cultivars (Aura, Ilves, Linna, Nisu and Vakka) were determined. Most of the samples studied had specific gliadin PAGE patterns, indicating that electrophoregrams obtained with the procedure employed here can be used for identifying wheat cultivars grown in Finland. Only two cultivars, Taava and Ruso, which are close relatives, possessed similar PAGE patterns. The procedure uses a commercial vertical electrophoresis apparatus and thin gels. Up to 28 samples could be electrophoresed in three hours and analyzed after staining. The procedure can be applied in the identification of wheat cultivars currently grown in Finland.


2006 ◽  
Vol 96 (9) ◽  
pp. 951-961 ◽  
Author(s):  
P. A. Paul ◽  
P. E. Lipps ◽  
L. V. Madden

A total of 126 field studies reporting deoxynivalenol (DON; ppm) content of harvested wheat grain and Fusarium head blight index (IND; field or plot-level disease severity) were analyzed to determine the overall mean regression slope and intercept for the relationship between DON and IND, and the influence of study-specific variables on the slope and intercept. A separate linear regression analysis was performed to determine the slope and intercept for each study followed by a meta-analysis of the regression coefficients from all studies. Between-study variances were significantly (P < 0.05) greater than 0, indicating substantial variation in the relationship between the variables. Regression slopes and intercepts were between -0.27 and 1.48 ppm per unit IND and -10.55 to 32.75 ppm, respectively. The overall mean regression slope and intercept, 0.22 ppm per unit IND and 2.94 ppm, respectively, were significantly different from zero (P < 0.001), and the width of the 95% confidence interval was 0.07 ppm per unit IND for slope and 1.44 ppm for intercept. Both slope and intercept were significantly affected by wheat type (P < 0.05); the overall mean intercept was significantly higher in studies conducted using winter wheat cultivars than in studies conducted using spring wheat cultivars, whereas the overall mean slope was significantly higher in studies conducted using spring wheat cultivars than in winter wheat cultivars. Study location had a significant effect on the intercept (P < 0.05), with studies from U.S. winter wheat-growing region having the highest overall mean intercept followed by studies from Canadian wheat-growing regions and U.S. spring wheat-growing regions. The study-wide magnitude of DON and IND had significant effects on one or both of the regression coefficients, resulting in considerable reduction in between-study variances. This indicates that, at least indirectly, environment affected the relationship between DON and IND.


2021 ◽  
Author(s):  
I.R. Manukyan ◽  
N.N. Dogusova

The main problem of wheat immunity to leaf rust is the loss of efficiency of most Lrgenes. The decrease in efficiency is associated with microevolutionary processes within the population and the emergence of new virulent phytopathogen races that can overcome previously efficient resistance genes. The article presents the results of the phytopathological test and marker analysis of the selected material of winter wheat for resistance to the leaf rust pathogen (Puccinia recondita Rob.ex Desm f. sp. tritici.). The object of the research was 20 cultivar samples of various ecological and geographical origins. DNA was isolated from the leaves of 10-day-old wheat germs. Molecular markers were used for the following genes: Lr9 (SCS5), Lr10 (Fi.2245/Lr10-6/r2), Lr19/Sr25 (SCS265), Lr20/Sr15 (STS638), Lr24/Sr24 (Sr24#12), Lr34/Sr57 (csLV34), Lr37/Sr38/Yr17/Pch2/Cre5 (Ventriup/LN2), Lr41 (GDM35), Lr47 (PS10). Using molecular markers, the studied wheat varieties did not reveal the highly and partially effective genes Lr9, Lr19/Sr25, Lr24/Sr24, Lr41, and Lr47 in Russia, and the ineffective gene Lr20/Sr1. As a result of molecular screening, it was found that the List 25 variety had Lr37 genes; the Mif variety had Lr10 genes; the Eltan variety had Lr10 genes; the Markola variety had Lr34 genes; the Malvina variety had Lr26 genes; the Tvorets variety had Lr10 genes; the DB 1/05 variety had Lr10 genes; the Evklid variety had Lr10 genes; the Sumai aut variety had Lr34 genes; the Lebidka odes'ka variety had Lr34 genes; the Solara variety – Lr34; the Zhiva variety – Lr10, Lr34. When comparing the results of marker analysis with field resistance to leaf rust, the resistant type of reaction to infection (R) was shown by the cultivars: Battum, Eltan, Evklid, Areal, and Solara; the susceptible type of reaction (S) was noted in the cultivars Markola and Mallyska; the medium susceptible type of reaction (MS) – in the cultivars Lebidka odes'ka and Tvorets.


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