PRIMARY ATTRACTION OF MOUNTAIN PINE BEETLE, DENDROCTONUS PONDEROSAE HOPK. (COLEOPTERA: SCOLYTIDAE), TO BOLTS OF LODGEPOLE PINE

1991 ◽  
Vol 123 (2) ◽  
pp. 299-304 ◽  
Author(s):  
Henry A. Moeck ◽  
Clarence S. Simmons

AbstractThree field tests were conducted in which fresh lodgepole pine (Pinus contorta Douglas var. latifolia Engl.) material, namely bolts with and without bark, bark only, and freshly tapped resin, were placed in beetle-excluding “greenhouse” cages; empty cages served as controls. Two “window” flight traps per cage, at right angles to each other, caught mountain pine beetles (Dendroctonus ponderosae Hopkins) arriving at the cages. Significantly more mountain pine beetles were trapped at cages baited with bolts and wood only than at empty control cages. Primary attraction in the mountain pine beetle is thus established, in the absence of pheromones and normal visual cues (tree stem silhouette). More beetles were trapped at cages baited with bark only and with resin than at empty control cages, but differences were not significant at p = 0.05. The sex ratio of trapped beetles (4.83 females: 1 male) was more than twice as high as the reported sex ratios of free-flying and emerging beetles.

1985 ◽  
Vol 117 (3) ◽  
pp. 267-275 ◽  
Author(s):  
L. Safranyik ◽  
D.A. Linton

AbstractThe relationship between the density of insect holes in the bark (X1) and the density of emerged mountain pine beetles (Y) was investigated in naturally infested lodgepole pine in south-central British Columbia. The density of exit and ventilation holes (Ho) that were present in the bark prior to emergence by mountain pine beetle averaged 10% of all holes present following the emergence period. There was a weak but significant inverse relationship between Ho and both phloem thickness and density of emerged mountain pine beetles. Painting the bark with light-color latex paint did not affect survival or the temporal pattern of emergence by mountain pine beetle but ensured identification and greatly enhanced counting of fresh exit holes. Of the several regression models investigated, the relation between Y and both X1 and X2 (= X1 – Ho) was best fitted by a log-log linear model. A method is suggested for setting limits on the size of exit holes cut by mountain pine beetle in order to exclude from X2 much of the variation caused by exit holes cut by associated insects. A simple mathematical model was developed of the relationship between mean density of exit holes and the density of emerged mountain pine beetles.


1989 ◽  
Vol 19 (1) ◽  
pp. 60-64 ◽  
Author(s):  
Gene D. Amman ◽  
Ralph W. Thier ◽  
Mark D. McGregor ◽  
Richard F. Schmitz

Verbenone, a bark beetle antiaggregative pheromone, was deployed in lodgepole pine (Pinuscontorta Dougl. var. latifolia Engelm.) stands in the Sawtooth National Forest, Idaho, U.S.A., to test its efficacy in reducing tree losses to mountain pine beetle (Dendroctonusponderosae Hopkins). Treatments tested were verbenone, mountain pine beetle tree bait, verbenone plus mountain pine beetle tree bait, and a control. Each treatment was applied individually to 1-ha blocks and replicated four times. Treatment effects were measured by percentage of infested (i.e., mass-attacked) lodgepole pine. ANOVA showed a significant treatment effect (P < 0.005). Blocks treated with mountain pine beetle tree baits had significantly (P < 0.002) higher average percentages of infested trees (24.4%), whereas no significant difference occurred in percentages of infested trees among the other three treatments. Average percentages of infested trees were 0.9% for verbenone, 7.4% for verbenone plus mountain pine beetle tree bait, and 3.3% for the control. A 2.3-fold reduction in infested trees occurred when verbenone was applied to blocks treated with mountain pine beetle tree baits.


2008 ◽  
Vol 38 (8) ◽  
pp. 2313-2327 ◽  
Author(s):  
Peter L. Jackson ◽  
Dennis Straussfogel ◽  
B. Staffan Lindgren ◽  
Selina Mitchell ◽  
Brendan Murphy

An outbreak of the mountain pine beetle ( Dendroctonus ponderosae Hopk.) in central British Columbia, Canada, has reached an unprecedented size and intensity and has been spreading. The 2005 emergence and subsequent flight of mountain pine beetle was studied using direct observation of emergence, weather radar imagery, and aerial capture. To verify that the daytime, clear-air radar returns seen during this period were indeed generated by airborne mountain pine beetles, aerial sampling in the area covered by the radar was performed using a drogue capture net towed by a single-engine light aircraft. Results verify that airborne mountain pine beetles are being detected by the weather radar and that, during the emergence period, significant numbers of mountain pine beetles can be found at altitudes up to more than 800 m above the forest canopy. An estimate of transport distance indicates that mountain pine beetles in flight above the forest canopy may move 30–110 km·day–1. An estimate of the instantaneous density of mountain pine beetles in flight above the canopy on flight days in 2005 indicate a mean (maximum) density of 4950 (18 600) beetles·ha–1.


2000 ◽  
Vol 132 (6) ◽  
pp. 799-810 ◽  
Author(s):  
L. Safranyik ◽  
D.A. Linton ◽  
T.L. Shore

AbstractBark beetles were trapped for two summers in a mature stand of lodgepole pine, Pinus contorta var. latifolia Engelmann (Pinaceae), infested by mountain pine beetle, Dendroctonus ponderosae Hopkins, near Princeton, British Columbia. Columns of flight-barrier traps were suspended next to uninfested live trees and from dead brood trees containing new adult beetles. The brood trees had been treated in the previous year with mountain pine beetle pheromone bait alone or in combination with Ips pini Say (Coleoptera: Scolytidae) pheromone bait and subsequently killed by mountain pine beetles. A total of 3376 individuals from 30 species of Scolytidae were captured in the traps. Most of the species for which lodgepole pine is a nonhost or occasional host were captured in low numbers (one or two specimens). The most abundant species (> 30 individuals) were D. ponderosae, I. pini, Hylurgops porosus LeConte, Pityogenes knechteli Swaine, and Trypodendron lineatum Olivier. The treatments affected captures of mountain pine beetles and I. pini but only in the year when trees were either unbaited or baited simultaneously for mountain pine beetle and I. pini. There were significant differences among the five most abundant species in the mean heights and mean Julian dates of capture. In addition to host condition requirements, these differences reflected partitioning of the food and habitat resource and competitive interactions among species. There was no interaction between treatment and trap height, indicating that treatment did not affect the height distribution of flying beetles.


2014 ◽  
Vol 147 (1) ◽  
pp. 39-45 ◽  
Author(s):  
Fraser R. McKee ◽  
Dezene P.W. Huber ◽  
B. Staffan Lindgren ◽  
Robert S. Hodgkinson ◽  
Brian H. Aukema

AbstractThe mountain pine beetle, Dendroctonus ponderosae Hopkins (Coleoptera: Curculionidae), outbreak in British Columbia and Alberta, Canada, currently extends over 18.3 million ha of pine forest. The principal host of the insect is lodgepole pine, Pinus contorta var. latifolia Englemann (Pineaceae) although it is a generalist herbivore on pines. Mountain pine beetles do not typically colonise spruce. However, during the current outbreak, several instances of mountain pine beetle attack on interior hybrid spruce, Picea glauca (Moench) Voss×Picea engelmannii Parry ex. Engelmann (Pinaceae) have been noted in areas where severe lodgepole pine mortality has occurred. Occasionally, beetle reproduction within spruce has been successful. Reproductive behaviours of mountain pine beetles reared from pine and spruce, such as female host acceptance and male joining behaviour, were studied on bolts of pine and spruce in laboratory bioassays. Females more readily accepted spruce host material relative to pine. Females that developed in spruce had higher rates of host acceptance of both pine and spruce host material than females that had developed in pine. We interpret these latter results with caution, however, as inference is partially restricted by sourcing viable insects from one spruce in this study. Implications of these findings to the concepts of host adaptation and population dynamics of this eruptive herbivore are discussed.


Insects ◽  
2020 ◽  
Vol 11 (2) ◽  
pp. 112 ◽  
Author(s):  
José F. Negrón

The mountain pine beetle (MPB) (Dendroctonus ponderosae) is a bark beetle that attacks and kills ponderosa pine (Pinus ponderosa), among other pine species throughout the western conifer forests of the United States and Canada, particularly in dense stands comprising large trees. There is information on the stand conditions that the insect prefers. However, there is a paucity of information on how small-scale variation in stand conditions influences the distribution of tree mortality within a stand. I examined the small-scale distribution of ponderosa pine basal area pre- and post a mountain pine beetle infestation, and used geostatistical modeling to relate the spatial distribution of the host to subsequent MPB-caused tree mortality. Results indicated increased mortality in the denser parts of the stand. Previous land management has changed historically open low-elevation ponderosa pine stands with aggregated tree distribution into dense stands that are susceptible to mountain pine beetles and intense fires. Current restoration efforts are aimed at reducing tree density and leaving clumps of trees, which are more similar to historical conditions. The residual clumps, however, may be susceptible to mountain pine beetle populations. Land managers will want to be cognizant of how mountain pine beetles will respond to restoration treatments, so as to prevent and mitigate tree mortality that could negate restoration efforts.


1989 ◽  
Vol 121 (6) ◽  
pp. 521-523 ◽  
Author(s):  
A.J. Stock ◽  
R.A. Gorley

The mountain pine beetle, Dendroctonus ponderosae Hopk., causes extensive mortality of lodgepole pine, Pinus contorta var. latifolia Engelm., throughout western North America (Van Sickle 1982). The Prince Rupert Forest Region, in the northwest of British Columbia, initiated an aggressive beetle management program in 1981. Logging of infested stands, and winter felling and burning of individual infested trees are the most common direct control techniques.The “Bristol Lake” infestation developed in the Bulkley Forest District, approximately 55 km northwest of Smithers, B.C., on a steep rocky ridge within the valley of Harold Price Creek. The area contained large volumes of mature lodgepole pine, and control of the infestation was therefore considered critical to the local beetle management plan, but the size (50 ha) and rough topography of the infested area precluded normal direct control measures.


1980 ◽  
Vol 112 (2) ◽  
pp. 185-191 ◽  
Author(s):  
Barry G. Hynum ◽  
Alan A. Berryman

AbstractLanding rates as monitored by landing traps indicate that the mountain pine beetle, Dendroctonus ponderosae Hopkins, is not attracted to lodgepole pine, Pinus contorta Dougl., prior to the first gallery start. Bark terpene odors and DBH were not correlated with beetle landing rates, with the exception of beta-phellandrene which accounted for a statistically significant 18% of the variation in landing rates. Beetles were unable to distinguish between hosts, dead hosts and nonhosts during landing. The elderberry pith bioassay indicated the presence of a gallery initiation stimulant in the bark.


2003 ◽  
Vol 33 (7) ◽  
pp. 1331-1334 ◽  
Author(s):  
Diana L Six

Two ophiostomatoid fungi, Ophiostoma clavigerum (Robinson-Jeffrey & Davidson) Harrington and Ophiostoma montium (Rumbold) von Arx, are known to be associated with the mycangia of the mountain pine beetle, Dendroctonus ponderosae Hopkins. However, virtually nothing is known regarding the phoretic fungi carried on the external surface of the exoskeleton of this beetle. In this study, I compared the phoretic fungi of individual D. ponderosae with the fungi carried in their mycangia. As many beetles carried ophiostomatoid fungi on the exoskeleton as in the mycangia; however, the species of ophiostomatoid fungus carried phoretically on an individual beetle was not always the same as was carried in its mycangia. Ophiostoma montium was isolated more often from exoskeletal surfaces than from mycangia, while the reverse was true for O. clavigerum. It appears that O. clavigerum is highly adapted for mycangial dissemination, while O. montium is adapted to phoretic as well as mycangial dissemination. Ophiostoma ips (Rumbold) Nannf. was phoretic on two beetles, indicating that cross-contamination with fungi from cohabiting Ips spp. may sometimes occur. Several non-ophiostomatoid fungi were isolated from exoskeletal surfaces, but none consistently so. All non-ophiostomatoid fungi isolated were common saprophytes often found in beetle-killed trees. Yeasts were also common and were isolated more often from the exoskeleton than from mycangia.


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