scholarly journals Changes in a Primary Resistance Parameter of Lodgepole Pine to Bark Beetle Attack One Year Following Fertilization and Thinning

Forests ◽  
2015 ◽  
Vol 6 (12) ◽  
pp. 280-292 ◽  
Author(s):  
Stephen Cook ◽  
Amy Carroll ◽  
Mark Kimsey ◽  
Terry Shaw
Keyword(s):  
Bark Beetle ◽  
Lodgepole Pine ◽  
Primary Resistance ◽  
Resistance Parameter ◽  
One Year

scholarly journals Riparian zones attenuate nitrogen loss following bark beetle-induced lodgepole pine mortality

2016 ◽  
Vol 121 (3) ◽  
pp. 933-948 ◽  
Author(s):  
Joel A. Biederman ◽  
Thomas Meixner ◽  
Adrian A. Harpold ◽  
David E. Reed ◽  
Ethan D. Gutmann ◽  
...  
Keyword(s):  
Bark Beetle ◽  
Lodgepole Pine ◽  
Nitrogen Loss ◽  
Riparian Zones

Bark beetle (Coleoptera: Scolytidae) diversity in spaced and unmanaged mature lodgepole pine (Pinaceae) in southeastern British Columbia

2004 ◽  
Vol 200 (1-3) ◽  
pp. 23-38 ◽  
Author(s):  
L. Safranyik ◽  
T.L. Shore ◽  
A.L. Carroll ◽  
D.A. Linton
Keyword(s):  
British Columbia ◽  
Bark Beetle ◽  
Lodgepole Pine

Bark beetle infestations of Lodgepole pine following a fire in South Central Oregon1

2009 ◽  
Vol 98 (1-5) ◽  
pp. 389-394 ◽  
Author(s):  
D. R. Geiszler ◽  
R. I. Gara ◽  
W. R. Littke
Keyword(s):  
Bark Beetle ◽  
Lodgepole Pine ◽  
South Central

scholarly journals MOISTURE CHANGES IN LODGEPOLE PINE BEFORE AND AFTER ATTACK BY THE MOUNTAIN PINE BEETLE

1961 ◽  
Vol 37 (4) ◽  
pp. 368-375 ◽  
Author(s):  
R. W. Reid
Keyword(s):  
Moisture Content ◽  
Mountain Pine Beetle ◽  
Lodgepole Pine ◽  
Dry Weight ◽  
Moisture Loss ◽  
Mountain Pine ◽  
Pine Beetle ◽  
Before And After ◽  
Blue Stain ◽  
One Year

The moisture content of the outer sapwood of non-infested lodgepole pine is normally about 85 to 165 per cent of oven dry weight. In trees that have been infested by the mountain pine beetle for one year, the sapwood moisture content can be as low as 16 per cent. There is a steep moisture gradient from about 160 per cent in the outer sapwood to about 30 per cent in the heart-wood. The moisture content in the centre is slightly higher than in the adjacent wood. In infested trees the sapwood moisture is greatly reduced within a year after the attack but moisture in the heartwood is not altered appreciably. Trees infested early in the season drop to a lower moisture content by fall than trees infested later in the season. In non-infested trees there is a diurnal and a seasonal moisture march; these do not occur in infested trees. The rapid moisture loss in the sapwood of infested trees is associated with blue-stain infection and successful establishment of bark-beetle broods

scholarly journals Soil Fungal Community in Norway Spruce Forests under Bark Beetle Attack

Forests ◽  
2019 ◽  
Vol 10 (2) ◽  
pp. 109 ◽  
Author(s):  
Petra Veselá ◽  
Martina Vašutová ◽  
Magda Edwards-Jonášová ◽  
Pavel Cudlín
Keyword(s):  
Bark Beetle ◽  
Fungal Community ◽  
Forest Ecosystems ◽  
Fungal Species ◽  
Thelephora Terrestris ◽  
Mature Forest ◽  
Soil Fungal Community ◽  
Ecm Fungi ◽  
Widespread Phenomenon ◽  
One Year

Bark beetle infestation is a widespread phenomenon in temperate forests, which are facing significant weather fluctuations accompanying climate change. Fungi play key roles in forest ecosystems as symbionts of ectomycorrhizal trees, decomposers, or parasites, but the effect of severe disturbances on their communities is largely unknown. The responses of soil fungal communities following bark beetle attack were determined using Illumina sequencing of soil samples from 10 microsites in a mature forest not attacked by bark beetle, a forest attacked by bark beetle, a forest destroyed by bark beetle, and a stand where all trees were removed after a windstorm. The proportion of ITS2 sequences assigned to mycorrhizal fungal species decreased with increased intensity of bark beetle attack (from 70 to 15%), whereas the proportion of saprotrophs increased (from 29 to 77%). Differences in the ectomycorrhizal (ECM) fungal community was further characterized by a decrease in the sequence proportion of Elaphomyces sp. and Russula sp. and an increase in Piloderma sp., Wilcoxina sp., and Thelephora terrestris. Interestingly, the species composition of the ECM fungal community in the forest one year after removing the windstorm-damaged trees was similar to that of the mature forest, despite the sequence proportion attributed to ECM fungi decreased.

Entomocorticium dendroctoni gen. et sp. nov. (Basidiomycotina), a possible nutritional symbiote of the mountain pine beetle in lodgepole pine in British Columbia

1987 ◽  
Vol 65 (1) ◽  
pp. 95-102 ◽  
Author(s):  
H. S. Whitney ◽  
R. J. Bandoni ◽  
F. Oberwinkler
Keyword(s):  
British Columbia ◽  
Bark Beetle ◽  
Pinus Contorta ◽  
Mountain Pine Beetle ◽  
Lodgepole Pine ◽  
Pine Bark ◽  
Mountain Pine ◽  
Pine Beetle ◽  
Blue Stain Fungi ◽  
Blue Stain

A new basidiomycete, Entomocorticium dendroctoni Whitn., Band. & Oberw., gen. et sp. nov., is described and illustrated. This cryptic fungus intermingles with blue stain fungi and produces abundant essentially sessile basidiospores in the galleries and pupal chambers of the mountain pine bark beetle (Dendroctonus ponderosae Hopkins Coleoptera: Scolytidae) in lodgepole pine (Pinus contorta Dougl. var. latifolia Engelm.). The insect apparently disseminates the fungus. Experimentally, young partially insectary reared adult beetles fed E. dendroctoni produced 19% more eggs than beetles fed the blue stain fungi.

ATTACK BY BARK BEETLES (COLEOPTERA: SCOLYTIDAE) FOLLOWING SPACING OF MATURE LODGEPOLE PINE (PINACEAE) STANDS

1999 ◽  
Vol 131 (5) ◽  
pp. 671-685 ◽  
Author(s):  
L. Safranyik ◽  
T.L. Shore ◽  
D.A. Linton
Keyword(s):  
Bark Beetle ◽  
Bark Beetles ◽  
Dominant Species ◽  
Management Practices ◽  
Lodgepole Pine ◽  
Species Accumulation Curves ◽  
The Third ◽  
Significant Difference ◽  
Accumulation Curves ◽  
Stick Model

AbstractVariation in bark beetle attack following spacing of mature lodgepole pine stands in the East Kootenays of British Columbia was analyzed in relation to stand location (site), spacing treatment, and harvesting injury. Observations were made on three sites, each having three treatments: 4 × 4 m spacing, 5 × 5 m spacing, and untreated control. There was no statistically significant difference in the numbers of attacked trees among sites or treatments. However, in the spaced plots 94.3% of the attacked trees sustained harvesting injury or were located adjacent to skid trails. Dendroctonus valens LeConte was the dominant species attacking trees on the two drier sites, and Dendroctonus murrayanae Hopkins was the dominant species on the third site. There was no statistically significant variation in the percentage of attacked stumps among sites or spacing treatments. On average, 80.7% of the stumps were attacked; attacked stumps had larger diameters than unattacked stumps. Thirteen species of bark beetles were found attacking stumps. Hylurgops porosus LeConte was the most numerous species at all three sites. Based on the fit of the Michaelis–Menten equations to species accumulation curves, an estimated 76–90% of the number of species attacking stumps at the three sites were observed in bark samples. Margalef’s index of diversity for the two drier sites (Cranbrook = 1.15, Parson = 1.13) was nearly identical and higher than at the moist site (Elkford = 0.89). Pairs of sites had five to six species in common, and the Sorensen coefficient of similarity ranged from 0.52 to 0.71, indicating moderate similarity in species composition. The abundance versus species rank relationship was fitted by three models: the MacArthur broken stick model, the geometric series, and the Zeta distribution. The latter gave good fit to data from two sites, but none of the fitted models gave satisfactory fit to data from the third site, mainly because of the high abundance of the second ranked species (Orthotomicus caelatus Eichhoff). Our results indicated that stand characteristics affected species assemblages and abundances of bark beetle species that attacked stumps. Management practices that minimize injury to trees during the spacing operations are emphasized to reduce attack by bark beetles.

scholarly journals Numerical Simulation of Crown Fire Hazard Immediately after Bark Beetle-Caused Mortality in Lodgepole Pine Forests

2012 ◽  
Vol 58 (2) ◽  
pp. 178-188 ◽  
Author(s):  
Chad Hoffman ◽  
Penelope Morgan ◽  
William Mell ◽  
Russell Parsons ◽  
Eva K. Strand ◽  
...  
Keyword(s):  
Numerical Simulation ◽  
Bark Beetle ◽  
Lodgepole Pine ◽  
Fire Hazard ◽  
Pine Forests ◽  
Crown Fire

scholarly journals Life history of a secondary bark beetle, Pseudips mexicanus (Coleoptera: Curculionidae: Scolytinae), in lodgepole pine in British Columbia

2009 ◽  
Vol 141 (1) ◽  
pp. 56-69 ◽  
Author(s):  
G.D. Smith ◽  
A.L. Carroll ◽  
B.S. Lindgren
Keyword(s):  
Life History ◽  
Bark Beetle ◽  
Pinus Contorta ◽  
Life History Traits ◽  
Lodgepole Pine ◽  
Degree Days ◽  
Northern Portion ◽  
History Of ◽  
Bark Beetle Associates

AbstractPseudips mexicanus (Hopkins) is a secondary bark beetle native to western North and Central America that attacks most species of pine (Pinus L. (Pinaceae)) within its range. A pair of life-history studies examined P. mexicanus in other host species, but until now, no work has been conducted on lodgepole pine (Pinus contorta Douglas ex Louden var. latifolia Engelm. ex S. Watson). Pseudips mexicanus in lodgepole pine was found to be polygynous. Galleries were shorter, offspring smaller, and the eggs laid per niche and the potential progeny fewer than in populations from California and Guatemala. Development from the time of female attack to emergence of adult offspring took less than 50 days at 26.5 °C, and the accumulated heat required to complete the life cycle was determined to be 889.2 degree days above 8.5 °C, indicating that in the northern portion of its range P. mexicanus is univoltine. Determination of these life-history traits will facilitate study of interactions between P. mexicanus and other bark beetle associates in lodgepole pine.

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