SEASONAL ACTIVITY OF THE NATIVE ELM BARK BEETLE, HYLURGOPINUS RUFIPES, IN CENTRAL ONTARIO (COLEOPTERA: SCOLYTIDAE)

1981 ◽  
Vol 113 (4) ◽  
pp. 341-348 ◽  
Author(s):  
L. M. Gardiner

AbstractDaily trapping of native elm bark beetles, Hylurgopinus rufipes (Eichh.), in central Ontario showed that the population is divided into fairly discrete overwintering adult and larval groups. Group proportions depend on the stage of development of the local beetle infestation and disease infection. Both beetles and disease are spread by mass movement of beetles, in late summer and fall, in search of living elm trees in which to feed and overwinter.

2008 ◽  
Vol 34 (2) ◽  
pp. 116-122
Author(s):  
Irene Pines ◽  
Richard Westwood

Six mark-recapture experiments were conducted in Manitoba, Canada, to determine the effectiveness of fluorescent powder to mark emerging native elm bark beetle adults, Hylurgopinus rufipes (Eichoff) (Coleoptera: Scolytidae), the vector of Dutch elm disease, Ophiostoma novo-ulmi (Brazier), after departure from overwintering sites in spring and emergence from broodwood in summer. Native elm bark beetles marked themselves on emergence from overwintering sites and summer trap logs. The spring and summer periods of flight activity for unmarked and marked beetles were similar. Marked beetles were captured over 1 month after peak emergence in the spring and 2 months after emergence from trap logs in the summer. Marked beetles were captured up to 1 km (0.6 mi) from release sites. Where integrated Dutch elm disease management activities are implemented in buffer zones to minimize the number of elm bark beetles entering community urban forests, buffer zones should be a minimum of 1 km (0.6 mi) in width.


1989 ◽  
Vol 121 (3) ◽  
pp. 245-252 ◽  
Author(s):  
Paul D. Swedenborg ◽  
Richard L. Jones ◽  
Lee C. Ryker

AbstractMale native elm bark beetles, Hylurgopinus rufipes (Eichhoff), had distinctive simple multipulse stress and rivalry chirps, and a bimodally patterned premating stridulation at the gallery site. Males were strongly arrested at attractive female galleries. Not all female galleries were attractive to males. For a short period after the arrival of the first (resident) male, conspecific males often contested the resident male. Stridulation by females was not detected.


1996 ◽  
Vol 128 (3) ◽  
pp. 435-441 ◽  
Author(s):  
I.L. Pines ◽  
A.R. Westwood

AbstractThe native elm bark beetle, Hylurgopinus rufipes (Eichhoff), is the major vector of Dutch elm disease, Ophiostoma ulmi (Buisman) Nannf., in Manitoba. The herbicide Glowon™, monosodium methane arsenate (MSMA), was applied to a chainsaw cut in American elm, Ulmus americana L., tree stems to determine if the treated elms would become effective trap trees for H. rufipes. Three treatments were compared: treated with herbicide and girdled, girdled, and control. All herbicide-treated elms died within 18 days after application. Significantly higher numbers (P < 0.01) of native elm bark beetles were attracted to the herbicided elms, compared with the other treatments. Beetles bred only in the elms treated with herbicide. Of the total brood galleries constructed, 72% had no egg hatch while the remaining 28% had larval tunnels. Progeny adults emerged from less than 1% of the larval tunnels. MSMA application could supplement the Dutch elm disease management program in Manitoba.


1981 ◽  
Vol 113 (3) ◽  
pp. 263-264 ◽  
Author(s):  
J. L. Buth ◽  
R. A. Ellis

The first outbreak of Dutch elm disease in Manitoba was recorded in 1975 in Brandon, Selkirk, and Winnipeg (Hildahl 1977). The primary vector of the disease in Canada is the native elm bark beetle, Hylurgopinus rufipes (Eichh.). The smaller European elm bark beetle, Scolytus multistriatus (Marsh.), is considered the primary vector in most of the United States. In Canada, the latter species occurs throughout most of southern Ontario, parts of south-central Quebec, and has been recorded in New Bmnswick (Sterner et al. 1976).


1988 ◽  
Vol 120 (12) ◽  
pp. 1041-1050 ◽  
Author(s):  
Paul D. Swedenborg ◽  
Richard L. Jones ◽  
Mark E. Ascerno ◽  
Val R. Landwehr

AbstractField tests, using bolts of American elm trees either uninfested or infested with laboratory-reared or feral Hylurgopinus rufipes (Eichhoff), the native elm bark beetle, were conducted to evaluate colonization behavior of the beetle. The data confirm that (1) colonization of elm by H. rufipes can be accounted for by host attractants alone; (2) overwintered adult H. rufipes are attracted to broodwood (moribund or recently cut elm) in the spring, but summer-emergent adults are attracted to healthy elm; and (3) H. rufipes attacks broodwood primarily during evening beetle flights, and females initiate the gallery. A beetle-produced sex pheromone may be involved in the male–female pairing on broodwood.


Author(s):  

Abstract A new distribution map is provided for Hylurgopinus rufipes (Eichh.) (Hylastes rufipes[Hylurgopinus rufipes] Eichh.) (Col., Scolytidae) (Native Elm Bark Beetle). Host Plants: Ulmus spp. (A vector of Dutch Elm Disease) Information is given on the geographical distribution in NORTH AMERICA, Canada, U.S.A.


2008 ◽  
Vol 140 (5) ◽  
pp. 527-538 ◽  
Author(s):  
Patricia L. Johnson ◽  
Jane L. Hayes ◽  
John Rinehart ◽  
Walter S. Sheppard ◽  
Steven E. Smith

AbstractScolytus schevyrewi Semenov, the banded elm bark beetle, and S. multistriatus Marsham, the smaller European elm bark beetle, are morphologically similar. Reliance on adult external morphological characters for identification can be problematic because of wide within-species variability and the need for good-quality specimens. The inability to identify developmental stages can also hamper early-detection programs. Using two character identification systems, genitalic (aedeagus) morphology, and DNA markers (random amplified polymorphic DNA polymerase chain reaction (RAPD-PCR)) to distinguish S. schevyrewi from S. multistriatus, we examined specimens from geographically distinct populations of both species collected from infested host trees or semiochemical-baited funnel traps. We found that aedeagus morphology can be used to identify the two species. The use of two oligonucleotide primers in the RAPD-PCR analysis yielded distinct DNA banding patterns for the two species. Species identification using RAPD-PCR analysis was validated by a blind test and used to make species identifications of larval specimens. These tools improve the ability to differentiate between S. schevyrewi and S. multistriatus at immature and adult stages, and could be developed and used for other scolytines as well.


1930 ◽  
Vol 8 (4) ◽  
pp. 239-248 ◽  
Author(s):  
J. N. Oldham

Of the insects responsible directly or indirectly for losses in plant industry the Scolytidæ or bark-beetles are well known, particularly to those associated with the practice of forestry, in Europe and America through the effects of their outbreaks. Bark-beetle attacks have resulted in serious damage in many parts of the world although in Britain their depredations have been less severe probably owing to the limited extent of forest lands.


1979 ◽  
Vol 57 (4) ◽  
pp. 353-359 ◽  
Author(s):  
S. Takai ◽  
E. S. Kondo ◽  
J. B. Thomas

Adults of the North American native elm bark beetle, Hylurgopinus rufipes, naturally infested with Dutch elm disease fungus, Ceratocystis ulmi, were caged on trunks of white elms (Ulmus americana) so that infection could be studied. In surveys made in 1971, expression of external symptoms of Dutch elm disease was observed on elms which had been caged with beetles during the period May 26 to July 9, 1971. Vascular discoloration (internal symptom expression), fungus spread, fungus contamination of beetles, and transmission of fungus to the host by beetles were pronounced on elms caged with beetles from June 3 to July 2. Ceratocystis ulmi was recovered from leaves of trees caged during the period May 26 to July 2. Until May 31, 1972, dieback and death resulting from infection were restricted to trees caged with beetles during June. Corresponding development of vascular discoloration and fungus spread in the host also occurred, mostly during the caging period in June. There was no appreciable change in beetle activity in xylem tissue during the period of experiment. These results suggest that the period of highest susceptibility of white elm to Dutch elm disease in 1971 in central Ontario was June 3 to July 2.Inoculation through feeding by caged beetles carrying C. ulmi is probably the method that most closely approximates natural infection.


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