DISTRIBUTION AND SEASONAL ABUNDANCE OF SITODIPLOSIS MOSELLANA (DIPTERA: CECIDOMYIIDAE) IN SPRING WHEAT

1999 ◽  
Vol 131 (3) ◽  
pp. 387-397 ◽  
Author(s):  
R.J. Lamb ◽  
I.L. Wise ◽  
O.O. Olfert ◽  
J. Gavloski ◽  
P.S. Barker

AbstractThe wheat midge Sitodiplosis mosellana (Géhin) occurred in all wheat-growing areas of Manitoba during 1993–1997, with 95% of spring wheat fields having some seeds infested by larvae. The level of infestation varied, but each year in excess of 20% of seeds were infested in some fields. Infestation levels in adjacent fields were more similar than in fields separated by a few kilometres. Within fields, the infestation was similar at the edge and near the centre. Wheat midge larvae also overwintered in, and adults emerged from, fields in all wheat-growing areas of Manitoba. Adults emerged from the end of June to the end of July most years, and the peak period for adult flight was mid-July, about 1 month later than in parts of Europe where winter wheat predominates. The timing of the emergence was similar from place to place and year to year. Females constituted 95% of insects caught in a flight trap. The first 10% and 50% of the flight occurred on 9 and 16 July, respectively, and the timing of the flight was not related to growing degree-days. In early August, mature larvae began dropping from wheat heads. The timing of infestation of spring wheat was variable among years because of differences in timing between midge flights and the susceptible heading stage of the crop. Nevertheless, the wheat midge flight usually coincided with the susceptible stage of the spring wheat crop.

1985 ◽  
Vol 117 (5) ◽  
pp. 593-598 ◽  
Author(s):  
O.O. Olfert ◽  
M.K. Mukerji ◽  
J.F. Doane

AbstractLosses in yield of spring wheat due to infestations of Sitodiplosis mosellana (Géhin) were determined for 700 000 ha of arable land in northeast Saskatchewan, Canada in 1983. The proportion of kernels infested (y) was a power function of the number of wheat-midge larvae (x) (y = 35.3x0.725). One, 2, 3, and 4 larvae per kernel resulted in a level of infestation of 38, 58, 78, and 96%, respectively. There was no significant difference between infestation levels from fields sampled at the heading stage of crop growth and the estimates of infestation levels for these fields at harvest time. Yield of grain (y) was negatively exponential to an increase in level of infestation (x) (ln y = 5.7−0.017x). Infestations of 30, 60, and 90% reduced yields of spring wheat by 40, 65, and 79%, respectively. The average decrease in crop yield in the study area was about 30%, which resulted in estimated losses in total gross revenue of about $30 million.


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


2020 ◽  
Vol 112 (1) ◽  
pp. 537-549 ◽  
Author(s):  
Jagmandeep S. Dhillon ◽  
Bruno M. Figueiredo ◽  
Elizabeth M. Eickhoff ◽  
William R. Raun

Agriculture ◽  
2016 ◽  
Vol 6 (3) ◽  
pp. 47 ◽  
Author(s):  
Natalie Ruiz Castillo ◽  
Carlos Gaitán Ospina

2014 ◽  
Vol 67 (2) ◽  
pp. 117-122 ◽  
Author(s):  
Tomasz R. Sekutowski ◽  
Janusz Smagacz

An experiment, conducted over the period 2008–2010, evaluated the effect of tillage system on the occurrence and species composition of anthropophytes in winter wheat, maize and spring wheat. Regardless of crop plant and tillage system, anthropophytes (73.9%), represented by archaeophytes and kenophytes, were the main component of the flora in the crops studied, whereas apophytes accounted for the remaining 26.1%. Most archaeophytes (13 species) were found in the spring wheat crop under no-tillage, while their lowest number (6 species) occurred in the spring wheat crop under conventional tillage. The only kenophyte, <em>Conyza canadensis</em>, was found to occur in the spring wheat and maize crops in the no-tillage system. The following taxa were dominant species among archeophytes: <em>Geranium pusillum</em>, <em>Anthemis arvensis, </em>and <em>Viola arvensis </em>(regardless of tillage system and crop plant), <em>Anthemis arvensis </em>(in spring wheat – conventional tillage), <em>Echinochloa crus-galli </em>and <em>Setaria glauca </em>(in maize – reduced tillage and no-tillage), <em>Chenopodium album </em>(in maize – no-tillage) as well as <em>Apera spica-venti</em>, <em>Anthemis arvensis </em>and <em>Papaver rhoeas </em>(in winter wheat – no-tillage).


2001 ◽  
Vol 81 (2) ◽  
pp. 273-276 ◽  
Author(s):  
Joanne R. Thiessen Martens ◽  
Martin H. Entz

Long-term weather data for 21 sites across Manitoba, Saskatchewan and Alberta were analyzed to evaluate the availability of late-season heat and water resources between time of winter wheat maturity and freeze-up. Thermal time during this period ranged from 159 to 754 growing degree days; precipitation ranged from 42 to 152 mm. Southern Manitoba appears to be best suited to relay and double cropping. Southern Saskatchewan receives significant thermal energy; however, lack of precipitation may limit late season plant growth. Key words: Legumes, no-till, cropping system intensity


1996 ◽  
Vol 128 (3) ◽  
pp. 367-375 ◽  
Author(s):  
R.H. Elliott ◽  
L.W. Mann

AbstractIn a 3-year field study, potted plants of ‘Katepwa’ wheat, Triticum aestivum L., were exposed to ovipositing wheat midge. Sitodiplosis mosellana (Géhin), to determine when spikes are most susceptible to damage. After exposure, plants were maintained under controlled conditions for 4 weeks and examined for wheal midge larvae and damaged kernels, ‘Katepwa’ wheat became susceptible to wheat midge damage shortly after spikes emerged from the boot leaf. Location of larvae and damaged kernels within spikes was influenced by the duration spikelets were exposed to oviposition and pattern of anthesis within spikes. In 1992, frequencies of larvae and damaged kernels were 60–90 times higher in spikes exposed to oviposition during advanced heading (stages 57–59, Zadoks’ code) than in those exposed during flowering (stages 61–69). Kernel damage in spikes exposed to oviposition during stages 57–59, 61–65, and 65–70 was 48.5, 3.2, and 0.2%, respectively, in 1993 and 21.2, 1.0, and 0.6%, respectively, in 1994. Data indicated that susceptibility to midge damage declined 15- to 25-fold between heading and early anthesis and 35- to 240-fold between heading and advanced anthesis. Potential factors contributing to these declines and concomitant reductions in larval frequencies are discussed.Commercial fields of ‘Katepwa’ wheat should be monitored for ovipositing wheat midge throughout heading (stages 51–59) when spikes are most vulnerable to damage. Larval survival and kernel damage were so low after stage 61 that monitoring during anthesis should be unnecessary. Intensive inspection of fields throughout heading would ensure that chemical treatments are applied when they are necessary and most effective.


Author(s):  
Maryse Bourgault ◽  
Samuel A. Wyffels ◽  
Julia M. Dafoe ◽  
Peggy F. Lamb ◽  
Darrin L. Boss

Abstract The introduction of cover crops as fallow replacement in the traditional cereal-based cropping system of the Northern Great Plains has the potential to decrease soil erosion, increase water infiltration, reduce weed pressure and improve soil health. However, there are concerns this might come at the cost of reduced production in the subsequent wheat crop due to soil water use by the cover crops. To determine this risk, a phased 2-year rotation of 15 different cover crop mixtures and winter wheat/spring wheat was established at the Northern Agricultural Research Center near Havre, MT from 2012 to 2020, or four rotation cycles. Controls included fallow–wheat and barley–wheat sequences. Cover crops and barley were terminated early July by haying, grazing or herbicide application. Yields were significantly decreased in wheat following cover crops in 3 out of 8 years, up to maximum of 1.4 t ha−1 (or 60%) for winter wheat following cool-season cover crop mixtures. However, cover crops also unexpectedly increased following wheat yields in 2018, possibly due in part to residual fertilizer. Within cool-, mid- and warm-season cover crop groups, individual mixtures did not show significant differences impact on following grain yields. Similarly, cover crop termination methods had no impact on spring or winter wheat grain yields in any of the 8 years considered. Wheat grain protein concentration was not affected by cover crop mixtures or termination treatments but was decreased in winter wheat following barley. Differences in soil water content across cover crop groups were only evident at the beginning of the third cycle in one field, but important reductions were observed below 15 cm in the last rotation cycle. In-season rainfall explained 43 and 13% of the variability in winter and spring wheat yields, respectively, compared to 2 and 1% for the previous year cover crop biomass. Further economic analyses are required to determine if the integration of livestock is necessary to mitigate the risks associated with the introduction of cover crops in replacement of fallow in the Northern Great Plains.


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