WHEAT MIDGE INFESTATION OF SPRING CEREALS IN NORTHEASTERN SASKATCHEWAN

1987 ◽  
Vol 67 (1) ◽  
pp. 117-120 ◽  
Author(s):  
A. T. WRIGHT ◽  
J. DOANE

Annual canarygrass and oats were found to be free of natural infestations of wheat midge (Sitodiplosis mosellana Géhin) in northeastern Saskatchewan. Six-row barley cultivars had low infestations and triticale, rye, wheat and durum wheat, high levels of infestation. Differences among susceptible cultivars were frequently due to asynchrony of plant susceptibility and midge oviposition.Key words: Sitodiplosis mosellana Géhin, wheat midge, cereals, cultivars

2002 ◽  
Vol 134 (6) ◽  
pp. 851-854 ◽  
Author(s):  
R.J. Lamb ◽  
I.L. Wise ◽  
J.E. Gavloski ◽  
L.A. Kaminski ◽  
O.O. Olfert

Wheat midge larvae, Sitodiplosis mosellana (Géhin), attack developing seeds and cause losses of common wheat, Triticum aestivum L., and durum wheat, Triticum durum Desf. (Olfert et al. 1985; Lamb et al. 1999). Insecticide applied as the crop flowers can reduce damage (Elliott 1988). The economic threshold varies from 4 to 7% of common wheat seeds infested by larvae, depending upon grade of wheat and cost of insecticidal control (Lamb et al. 2000). To make control decisions, farmers count adults at sunset during the period from heading to flowering (Elliott and Mann 1996), and apply insecticide if densities reach a nominal threshold of one adult per four or five wheat spikes (Anonymous 1993). Decisions must be made although no relationship has been detected between the number of adults in the crop and subsequent densities of damaging larvae (Oakley et al. 1998), and farmers have little confidence in their counts. The pest is difficult to sample because adults are small, short-lived, crepuscular, and are usually hidden in the crop canopy (Pivnick and Labbé 1993); eggs are microscopic (Mukerji et al. 1988); larvae feed inside florets (Lamb et al. 2000); and mature larvae and pupae are in the soil (Lamb et al. 1999). Sticky traps have been used to sample midges in sorghum (Merchant and Teetes 1992) and in wheat (Oakley et al. 1998), with mixed results. Our objective was to determine if catches of wheat midge adults on sticky traps can effectively guide farmers in making control decisions.


2002 ◽  
Vol 134 (2) ◽  
pp. 193-203 ◽  
Author(s):  
I.L. Wise ◽  
R.J. Lamb ◽  
M.A.H. Smith

AbstractModern hulless wheats, Triticum aestivum L., are more susceptible to the wheat midge, Sitodiplosis mosellana (Géhin), than the hulled, wild, ancestral species. Hulless cultivars of barley, Hordeum vulgare L., are becoming more widely grown in western Canada than in the past. Hulled and hulless cultivars of two-rowed and six-rowed barleys were tested for their susceptibility to wheat midge, to determine if this midge might become a serious pest of barley and to assess which plant traits might affect host suitability. In the field, larval populations on 10 barley cultivars were much lower than on wheat. In the laboratory, when the flag leaf sheath was peeled back to expose preflowering spikes, female midges readily oviposited on spikes of barley, although less so on younger spikes. Few larvae were able to develop on barley when eggs were laid after spikes had flowered. All barleys completed flowering, or nearly so, before spikes emerged from the flag leaf sheath, with two-rowed cultivars flowering earlier than six-rowed barleys. No differences in larval densities were found between hulless and hulled barleys, and therefore, factors other than the hulled trait must account for reduced susceptibility of barley. Because barley flowers within the flag leaf sheath, its period of susceptibility to infestation is much shorter than for wheat, as evidenced by reduced infestation of earlier-flowering two-rowed cultivars compared with later-flowering six-rowed cultivars. Also, the tight closure of the leaf-like glumes that form the florets of barley probably makes access to young seeds more difficult for newly hatched larvae than is the case for wheat. At comparable crop growth stages, larval densities on all the barleys were < 10% of those on spring wheat. The introduction of hulless barley for production in Canada is unlikely to increase wheat midge damage on barley to an economic level.


2001 ◽  
Vol 133 (4) ◽  
pp. 579-591 ◽  
Author(s):  
R.J. Lamb ◽  
M.A.H. Smith ◽  
I.L. Wise ◽  
P. Clarke ◽  
J. Clarke

AbstractOver 250 durum wheats, Triticum durum Desf., and close relatives were screened for resistance to the wheat midge, Sitodiplosis mosellana (Géhin). Less than 2% showed consistently reduced egg and larval densities in field and laboratory trials. Two related accessions named ’Kahla’ had stable, low larval infestation levels, which were about 30% of those in commercial durum wheat cultivars. No antibiosis was detected in durum wheats. The reduction in infestation by larvae was associated with a similar reduction in oviposition. The resistance reduced egg densities by 80% or more in choice and no-choice laboratory tests and by about 70% in the field. Egg group size was not affected, and therefore reduced oviposition must have resulted from the number of egg groups deposited by females. The resistance was not associated with any of 12 morphological traits that were quantified for spikes. ’Kahla’ is the first durum wheat identified to have resistance against the wheat midge.


2000 ◽  
Vol 132 (5) ◽  
pp. 607-625 ◽  
Author(s):  
R.J. Lamb ◽  
J.R. Tucker ◽  
I.L. Wise ◽  
M.A.H. Smith

AbstractLarvae of the wheat midge, Sitodiplosis mosellana (Géhin), feed on developing seeds of common and durum wheats, Triticum aestivum L. and Triticum durum L. (Graminae). The trophic relationships between insect and plant were quantified as biomass gains or losses using plants infested artificially in the laboratory and naturally in plots and commercial fields. The biomass of seeds from different parts of a wheat spike varied, but seeds in all parts of a spike were infested, independently of their potential biomass. Most infested seeds had 1–3 larvae, but at least 11 larvae could mature on a single seed without reducing larval biomass. When larvae finished feeding and seeds attained about one third of their biomass, specific impact varied from 4.1 to 8.5 mg of seed biomass lost for each milligram of biomass gained by a larva, with the impact declining as the number of larvae per seed increased. Specific impact rose to 100 mg/mg as seeds of T. aestivum and a primitive wheat, Triticum monococcum L., matured, and higher still for T. durum. Wheat plants did not compensate for wheat midge damage, and no indirect damage to uninfested seeds was detected. The distribution of biomass for infested seeds was bimodal, with over 40% less than 8 mg when hand harvested, whereas infested seeds harvested mechanically had a unimodal distribution, with nearly all of the most severely damaged seeds removed during harvest. A visual rating system of six damage categories was related to the biomass of the seeds. The germination and early growth rate of infested seeds were reduced compared with those of uninfested seeds. Based on the biomass relationships for the insect–plant interaction and the visual rating of damage, high-protein number 1 grade common and durum wheat and number 1 grade durum wheat can tolerate up to 6% of the seeds being infested by larvae, before downgrading is likely. For other grades, the economic threshold is 10% of the seeds infested, based on yield loss. Seed growers can adopt the threshold for number 1 wheat (6% infestation) to prevent downgrading, which would also reduce the effects of infestation on seed germination to an acceptable level.


2016 ◽  
Vol 148 (5) ◽  
pp. 616-618 ◽  
Author(s):  
E.R. Echegaray ◽  
R.N. Stougaard ◽  
B. Bohannon

AbstractEuxestonotus error (Fitch) (Hymenoptera: Platygastridae) is considered part of the natural enemy complex of the wheat midge Sitodiplosis mosellana (Géhin) (Diptera: Cecidomyiidae). Although previously reported in the United States of America, there is no record for this species outside the state of New York since 1865. A survey conducted in the summer of 2015 revealed that E. error is present in northwestern Montana and is likely playing a role in the suppression of wheat midge populations.


2014 ◽  
Vol 146 (3) ◽  
pp. 335-346 ◽  
Author(s):  
M.A.H. Smith ◽  
I.L. Wise ◽  
S.L. Fox ◽  
C.L. Vera ◽  
R.M. DePauw ◽  
...  

AbstractSpring wheat varieties with the Sm1 gene for resistance to wheat midge, Sitodiplosis mosellana (Géhin) (Diptera: Cecidomyiidae), were compared with susceptible wheat (Triticum Linnaeus; Poaceae) with respect to sources of yield loss and reduction in market value from wheat midge feeding damage. Four resistant varietal blends (90% Sm1 wheat plus 10% susceptible refuge) and four susceptible cultivars were grown in replicated experiments at eight locations in western Canada. Frequencies and 1000-kernel weights of undamaged and midge-damaged seeds were assessed before harvest by dissecting samples of ripe spikes, and after harvest in samples of cleaned grain. Spike data were used to estimate yield losses from reduced weight of damaged seeds and loss of severely damaged seeds (⩽8 mg) at harvest. Among midge-damaged seeds in spikes, few were severely damaged in resistant varietal blends, whereas most were severely damaged in susceptible cultivars. Cleaned, harvested grain of resistant varietal blends and susceptible cultivars had similar frequencies of midge damage and were assessed similar market grades. The primary benefit of midge-resistant wheat was reduced yield loss due to seed damage by wheat midge larvae. Resistant wheat did not protect against loss of market grade, but market value could increase due to larger yields.


2006 ◽  
Vol 138 (2) ◽  
pp. 138-146 ◽  
Author(s):  
O. Mittapalli ◽  
R.H. Shukle ◽  
I.L. Wise

AbstractMariner-like element sequences were recovered from the genome of the orange wheat midge, Sitodiplosis mosellana (Géhin), with degenerate PCR primers designed to conserved regions of mariner transposases. The deduced amino acid sequences of the mariner-like transposases from S. mosellana showed 67% to 78% identity with the peptide sequences of other mariner transposases. A phylogenetic analysis revealed that the mariner-like elements from S. mosellana grouped in the mauritiana subfamily of mariner transposons. Results from Southern blot analysis suggest mariner-like elements are at a moderate copy number in the genome of S. mosellana.


1999 ◽  
Vol 131 (4) ◽  
pp. 475-481 ◽  
Author(s):  
H. Ding ◽  
R.J. Lamb

AbstractThe wheat midge, Sitodiplosis mosellana (Géhin), infests wheat, Triticum aestivum L., heads only up to anthesis when pollination occurs. The termination of infestation might be due to a deterrence of oviposition or to a suppression of larval growth on developing seeds. These hypotheses were tested in the laboratory by measuring oviposition preference, larval development, and larval preference for plants at different growth stages. Females showed no preference for ovipositing on heads at any stage from the onset of heading up to and including anthesis, and continued to lay eggs at a reduced rate 10 days after anthesis. Survival of newly hatched larvae was reduced on seeds 3–1 days after anthesis and survival and development was greatly reduced on seeds 5 or 6 days after anthesis. Larvae moved away from older seeds and fed on younger seeds in a choice test. Given a hatching time of 5–6 days, a failure to infest wheat after anthesis is not due to oviposition deterrence at anthesis, but to suppression of larval growth and development which begins soon after anthesis.


2021 ◽  
pp. 1-15
Author(s):  
Amanda Jorgensen ◽  
Maya L. Evenden ◽  
Owen Olfert ◽  
Jennifer Otani

Abstract Wheat midge, Sitodiplosis mosellana Géhin (Diptera: Cecidomyiidae), is an invasive pest of wheat, Triticum spp. (Poaceae), in North America and is found in all wheat-growing regions of the world. Wheat midge biology, particularly post-diapause emergence of adults, varies with geographic region. The biology of wheat midge has not previously been examined in the northernmost area of its range in Canada – the Peace River region of Alberta. Wheat midge adult emergence was compared in situ to two phenological models of wheat midge emergence developed in other geographic regions. In-field adult emergence did not match the published phenological models. In the Peace River region, adults emerged later than are predicted by both models and precision for both models was low. With the Saskatchewan model, accumulated rainfall that was more than 110 mm in May and early June delayed emergence, whereas accumulated rainfall that was less than 43 mm during that period caused earlier than predicted emergence. Multiple peaks of wheat midge emergence, up to 20 days apart, were observed at some sites, supporting the Jacquemin model depicting “waves” of emergence. Including differences in soil temperature accumulation related to precipitation and optimising the model temperature thresholds would improve accuracy of the current Canadian phenological model in the Peace River region.


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