Isolation of Fomitopsis pinicola from in-flight bark beetles (Coleoptera: Scolytidae)

1986 ◽  
Vol 64 (7) ◽  
pp. 1507-1509 ◽  
Author(s):  
Thomas M. Pettey ◽  
Charles Gardner Shaw

Isolations of Hymenomycetes on a preferential medium were attempted from preflight pine engraver beetles, Ips pini, and the following in-flight bark beetles: pine engraver beetle, I. pini; western pine beetle, Dendroctonus brevicomis; mountain pine beetle, Dendroctonus ponderosae; and red turpentine beetle, Dendroctonus valens. Thirty pine engraver beetles removed from ponderosa pine slash (preflight) yielded no hymenomycete. However, Hymenomycetes were isolated from 50 of 114 beetles (all species) trapped in flight; Fomitopsis pinicola from 44, and other unidentified suspected Hymenomycetes, from 6. Cryptoporus volvatus was not isolated from any of the in-flight beetles. Since most of these isolates were without clamps (monokaryotic), the beetles may acquire basidiospores after emergence from beetle galleries in coniferous trees as hypothesized previously for the Douglas-fir beetle, Dendroctonus pseudotsugae. The isolation of F. pinicola from all species of in-flight bark beetles indicates that these beetles may be important in the dissemination of this hymenomycete.

1958 ◽  
Vol 90 (10) ◽  
pp. 582-584 ◽  
Author(s):  
R. L. Lyon

The sex of the western pine beetle (Dendroctonus brevicomis Lec.) and the mountain pine beetle (Dendroctonus monticolae Hopk.) can be ascertained easily and with 100 percent accuracy by means of a secondary sex character on the seventh abdominal tergite of the male. This character can probably be used with equal accuracy to identify sex in all species of the genus Dendroctonus.The need to distinguish between the sexes of adult bark beetles often arises in studies of biology, behavior, or response. The sexing procedure is laborious when large numbers of beetles are involved and external markings of sex are not known. It is then necessary to dissect each beetle to check the genitalia. Dissection is impossible when iniury to the insect must be avoided.


2012 ◽  
Vol 42 (12) ◽  
pp. 2022-2036 ◽  
Author(s):  
Ryan S. Davis ◽  
Sharon Hood ◽  
Barbara J. Bentz

Bark beetles can cause substantial mortality of trees that would otherwise survive fire injuries. Resin response of fire-injured northern Rocky Mountain ponderosa pine ( Pinus ponderosa Douglas ex P. Lawson & C. Lawson) and specific injuries that contribute to increased bark beetle attack susceptibility and brood production are unknown. We monitored ponderosa pine mortality and resin flow and bark beetle colonization and reproduction following a prescribed fire in Idaho and a wildfire in Montana. The level of fire-caused tree injury differed between the two sites, and the level of tree injury most susceptible to bark beetle attack and colonization also differed. Strip-attacked trees alive 3 years post-fire had lower levels of bole and crown injury than trees mass attacked and killed by bark beetles, suggesting that fire-injured trees were less well defended. Brood production of western pine beetle ( Dendroctonus brevicomis LeConte) did not differ between fire-injured and uninjured trees, although mountain pine beetle ( Dendroctonus ponderosae Hopkins) brood production was low in both tree types, potentially due to competition with faster developing bark beetle species that also colonized trees. Despite a large number of live trees remaining at both sites, bark beetle response to fire-injured trees pulsed and receded within 2 years post-fire, potentially due to a limited number of trees that could be easily colonized.


2003 ◽  
Vol 38 (4) ◽  
pp. 602-611 ◽  
Author(s):  
Daniel R. Miller ◽  
John H. Borden

We conducted seven experiments in stands of mature lodgepole pine in southern British Columbia to elucidate the role of host volatiles in the semiochemical ecology of the pine engraver, Ips pini (Say) (Coleoptera: Scolytidae), with particular reference to the behavioral responses of predators and competing species of bark beetles. Our results demonstrated that the attraction of Ips pini and the bark beetle predators Lasconotus complex LeConte (Colydiidae), Thanasimus undatulus (Say) (Cleridae) and a Corticeus sp. (Tenebrionidae) were increased by 3-carene. In contrast, attraction of the bark beetle Pityogenes knechteli Swaine (Scolytidae) to ipsdienol was interrupted by 3-carene and α-pinene. Attraction of L. complex to ipsdienol was increased by γ-terpinene, a compound attractive to the mountain pine beetle, Dendroctonus ponderosae Hopkins (Scolytidae). Terpinolene interrupted the attraction of I. pini to ipsdienol.


2010 ◽  
Vol 25 (4) ◽  
pp. 181-185 ◽  
Author(s):  
Donald M. Grosman ◽  
Christopher J. Fettig ◽  
Carl L. Jorgensen ◽  
A. Steven Munson

Abstract Bark beetles (Coleoptera: Curculionidae, Scolytinae) are important tree mortality agents in western coniferous forests. Protection of individual trees from bark beetle attack has historically involved applications of liquid formulations of contact insecticides to the tree bole using hydraulic sprayers. More recently, researchers looking for more portable and environmentally safe alternatives have examined the effectiveness of injecting small quantities of systemic insecticides directly into trees. In this study, we evaluated trunk injections of experimental formulations of emamectin benzoate and fipronil for preventing tree mortality due to attack by western pine beetle (Dendroctonus brevicomis LeConte) on ponderosa pine (Pinus ponderosa Dougl. ex Laws.) in California, mountain pine beetle (Dendroctonus ponderosae Hopkins) on lodgepole pine (Pinus contorta Dougl. ex Loud.) in Idaho, and spruce beetle (D. rufipennis [Kirby]) on Engelmann spruce (Picea engelmannii Parry ex Engelm.) in Utah. Fipronil appeared ineffective for protecting P. ponderosa from mortality due to D. brevicomis over the 3 years in California because of insufficient mortality of untreated, baited control trees the first 2 years and high mortality of the fipronil-treated trees in the third year. Emamectin benzoate was effective in providing protection of P. ponderosa from D. brevicomis during the third year following a single application. To our knowledge, this is the first demonstration of the successful application of a systemic insecticide for protecting individual conifers from mortality due to bark beetle attack in the western United States. Estimates of efficacy could not be made during both field seasons in P. contorta because of insufficient mortality in control trees. Both emamectin benzoate and fipronil were ineffective for protecting P. engelmannii from D. rufipennis. Lower ambient and soil temperatures and soil moisture may have limited chemical movement and thus efficacy at the Idaho and Utah sites.


1972 ◽  
Vol 50 (9) ◽  
pp. 1943-1945 ◽  
Author(s):  
H. S. Whitney ◽  
F. W. Cobb Jr.

Three fungi—Ceratocystis nigrocarpa Davidson, an unidentified hyphomycete, and an unidentified basidiomycete—were isolated from extensive non-stained areas of sapwood of ponderosa pine infested with western pine beetle, Dendroctonus brevicomis Lec., in California. The two unidentified fungi were also present in the thoracic mycangium of the female beetle while C. nigrocarpa was found only externally on the beetle. The mycangium and its contents are illustrated. Ceratocystis minor (Hedgc.) Hunt, which was also found externally on the beetle but not in the mycangium, was isolated only from scattered patches of blue-stained sapwood. It is suggested that non-staining fungi play a role in causing the death of ponderosa pine trees attacked by D. brevicomis.


2005 ◽  
Vol 137 (3) ◽  
pp. 367-375 ◽  
Author(s):  
Donald R. Owen ◽  
David L. Wood ◽  
John R. Parmeter

AbstractThe host-colonization behavior of the red turpentine beetle, Dendroctonus valens LeConte (Coleoptera: Scolytidae), was investigated in stands of ponderosa pine, Pinus ponderosa P. & C. Lawson (Pinaceae), with black stain root disease in the central Sierra Nevada of California. By felling live trees, we found that trees with pitch tubes produced during the initiation of tunneling by D. valens had a significantly higher incidence of black stain root disease, caused by Leptographium wageneri var. ponderosum (Harrington et Cobb), than trees without pitch tubes. Trees with the most D. valens pitch tubes had the greatest likelihood of being diseased. Additionally, observations over a 3-year period revealed that trees with D. valens pitch tubes had a significantly higher mortality rate than trees without pitch tubes. Infection by L. wageneri was confirmed for most of the trees that died, and death typically did not occur without mass attacks by the western pine beetle, D. brevicomis LeConte, and (or) the mountain pine beetle, D. ponderosae Hopkins. Trees with the most D. valens pitch tubes had the highest mortality rate. An experiment was conducted to compare the attraction of D. valens and other insects to wounded-diseased, wounded-symptomless, and unwounded trees. More D. valens, Spondylis upiformis Mannerheim (Coleoptera: Cerambycidae), and Hylastes spp. (Coleoptera: Scolytidae) were attracted to wounded trees than to unwounded trees. Catches of these beetles on wounded-diseased trees were not significantly different from catches on wounded-symptomless trees.


Forests ◽  
2021 ◽  
Vol 12 (12) ◽  
pp. 1677
Author(s):  
Christopher J. Fettig ◽  
Leif A. Mortenson ◽  
Jackson P. Audley

We examined causes and levels of tree mortality one year after thinning and prescribed burning was completed in ponderosa pine (Pinus ponderosa Dougl. ex Laws.) forests at Pringle Falls Experimental Forest, Oregon, U.S. Four blocks of five experimental units (N = 20) were established. One of each of five treatments was assigned to each experimental unit in each block. Treatments included thinning from below to the upper management zone (UMZ) for the dominant plant association based on stand density index values for ponderosa pine followed by mastication and prescribed burning: (1) 50% UMZ (low density stand), (2) 75% UMZ (medium density stand), (3) 75% UMZ Gap, which involved a regeneration cut, (4) 100% UMZ (high density stand), and (5) an untreated control (high density stand). Experimental units were thinned in 2011 (block 4), 2012 (block 2), and 2013 (blocks 1 and 3); masticated within one year; and prescribed burned two years after thinning (2013–2015). A total of 395,053 trees was inventoried, of which 1.1% (4436) died. Significantly higher levels of tree mortality occurred on 100 UMZ (3.1%) than the untreated control (0.05%). Mortality was attributed to prescribed fire (2706), several species of bark beetles (Coleoptera: Curculionidae) (1592), unknown factors (136), windfall (1 tree), and western gall rust (1 tree). Among bark beetles, tree mortality was attributed to western pine beetle (Dendroctonus brevicomis LeConte) (881 trees), pine engraver (Ips pini (Say)) (385 trees), fir engraver (Scolytus ventralis LeConte) (304 trees), mountain pine beetle (D. ponderosae Hopkins) (20 trees), Ips emarginatus (LeConte) (1 tree), and Pityogenes spp. (1 tree).


1971 ◽  
Vol 103 (9) ◽  
pp. 1291-1313 ◽  
Author(s):  
Cornell O. Dudley

AbstractThe distributions of attack, gallery length, eggs, and first instar larvae of an endemic population of the western pine beetle in ponderosa pine are described.Mean gallery length (GL) and larval (L) densities of mature populations are significantly correlated with attack (A) density. The associations are adequately described by the simple linear regressionsThe ratios E/GL and L/GL are stable over a wide range of gallery length densities and consequently egg-gallery length and larval-gallery length correlations are highly significant. The regression equations areAll four equations predict values within 10% of observed values.An 88 cm2 sampling unit is satisfactory for sampling either egg or first instar larval populations. Taking four paired sampling units, evenly spaced along the infested bole, from each of four trees per generation, provided a sampling precision of 15%. Increasing the number of paired units to 10 and the number of trees sampled per generation to 9 improved the precision to 10%. If the trees are sampled before oviposition is complete, the number of sampled trees per generation should be increased by 1 for each level of precision.


1984 ◽  
Vol 62 (3) ◽  
pp. 551-555 ◽  
Author(s):  
T. D. Paine

The hypersensitive response obtained by inoculating the two mycangial fungi of the western pine beetle, Dendroctonus brevicomis LeC, and the blue-stain fungus, Ceratocystis minor Hedge, into ponderosa pine was measured during three different seasons in the same 12-month period. The lesions were produced faster and were significantly longer in the fall than in the summer. Similarly, lesions were longer and were produced faster when inoculations made in the summer were compared with spring inoculations. However, the response to a nonpathogenic fungus, a Penicillium sp., was not different from the response to mycangial fungi, suggesting that lesion production is a generalized response to infection that isolates fungus-colonized tissue from the rest of the tree. Ethanol extracts of hypersensitive-response lesions produced during the spring did not reduce growth of the mycangial fungi or C. minor when bioassayed at concentrations similar to those found in host tissue. This is different from other bark beetle–host tree systems that have been investigated.


1964 ◽  
Vol 96 (6) ◽  
pp. 883-888 ◽  
Author(s):  
A. A. Berryman

AbstractA guide to interpretation of X-rays of bark samples infested with the western pine beetle and its principal predators and parasites is presented. Illustrations of the radiographic images are given to enable analysts to gain experience more rapidly.


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