Distribution of Attacks by Dendroctonus ponderosae Hopk. on Pinus contorta Dougl. var. latifolia Engelm.

1965 ◽  
Vol 97 (2) ◽  
pp. 207-215 ◽  
Author(s):  
R. F. Shepherd

AbstractThe incidence of attacks by Dendroctonus ponderosae Hopk. (= monticolae) was recorded by square-foot quadrats from the total bark surface of 60 lodgepole pine trees, Pinus contorta Dougl. var. latifolia Engelm., according to location on the tree, proximity to branches, and degree of bark roughness. The frequency distribution of attack density was bimodal, but the bimodality was an artifact of sampling from a population having a varying mean density. A log (x + 1) transformation of the data permits the use of parametric tests. Alternative non-area sampling techniques showed that the spatial distribution of attacks within a small area tended toward regularity, probably following the distribution of bark niches. The greatest variance in attack density was associated with height, followed by areas, trees, diameters and aspects. Bark roughness was an important influence of distribution but number of branches was not.


2010 ◽  
Vol 40 (10) ◽  
pp. 2049-2058 ◽  
Author(s):  
Amanda F. Linnell Nemec ◽  
James W. Goudie ◽  
Roberta Parish

The aim of this work was to model the vertical location and number of branch primordia (buds) on the leader of lodgepole pine ( Pinus contorta Doug. ex Loud.) trees in central British Columbia. For species such as lodgepole pine, where branches occur in clusters rather than individually, the Gamma-Poisson model provides a natural framework for describing and simulating the distribution of buds on the annual shoot. Parameters in the model are identifiable with measurable attributes, that is, the average number of clusters per unit length of the annual shoot and the average number of buds per cluster, and can be related to explanatory variables via a log link. Applicability of the Gamma-Poisson model was demonstrated for a sample of 58 lodgepole pine trees ranging in age from 29 to 103 years old. The agreement between observed and expected cluster counts and spacing, cluster sizes, and total number of branches was good. Height to crown base and length of the annual shoot were selected as the best predictors of the number of clusters and number of buds per cluster, respectively, although other single variables were also identified as having significant predictive value.



2006 ◽  
Vol 8 (3) ◽  
pp. 243-251 ◽  
Author(s):  
Nancy E. Gillette ◽  
John D. Stein ◽  
Donald R. Owen ◽  
Jeffrey N. Webster ◽  
Gary O. Fiddler ◽  
...  


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.



2006 ◽  
Vol 82 (4) ◽  
pp. 579-590 ◽  
Author(s):  
John H Borden ◽  
Anna L Birmingham ◽  
Jennifer S Burleigh

Experiments were conducted near Williams Lake and Quesnel, BC in 2003 to evaluate the effectiveness of the anti-aggregation pheromone verbenone and a three-component non-host volatile (NHV) blend (E-2- and Z-3-hexen-1-ol and benzyl alcohol) in deterring attack of lodgepole pines, Pinus contorta var. latifolia Engelmann, by the mountain pine beetle, Dendroctonus ponderosae Hopkins. In 0.16-ha square plots, with a pheromone-baited tree in the centre and 16 release points at 10-m centres, either verbenone (in a polyurethane gel inside plastic membrane pouches, released at ca. 100 mg/day) or the NHVs (released from separate bubble caps at ca. 1.2 mg/day) deterred attack, but efficacy was not increased by combining them. When deployed from 25 release points at 10-m centres in 0.25-ha square plots, verbenone plus NHVs were effective in deterring attack in some (but not all) cases, when compared to attack in a 25-m wide band around the treated zone. In a test of the push-pull tactic, verbenone plus the NHV blend were tested in a 10-replicate experiment with 100, 44.4 or 25 release points/ha at 10-, 15- or 20-m centres, respectively, in a 1-ha square central zone surrounded by a 3-ha, 50-m-wide band containing 12 pheromone-baited lodgepole pines 50 m apart. Other treatments were pheromonebaited trees alone, and an untreated control. In the three push-pull treatments (but not the bait only or control treatments), 28 of 30 replicates had significantly more mass-attacked trees in the pheromone-baited outer 3 ha than in the inner ha treated with verbenone plus NHVs. The percentage of available trees ≥ 17.5 cm diameter at breast height (dbh) that were mass-attacked was < 10% in 5, 4 and 3 of 10 replicates when verbenone plus NHVs were deployed at 10-, 15- and 20-m centres, respectively, and was < 10% in two each of the bait only and control replicates. The mean ratios of newly-attacked green trees in 2003 to red trees killed in 2002 were significantly lower in the inner ha of the 10-m and 15-m centre treatments (2.6 and 2.7, respectively) than 5.9 in the untreated control. Also the pooled percentages of attacked trees that were not mass-attacked were significantly higher in the inner ha of the treatments with centres at 15 m (24.7%) and 10 m (17.6%) than in the other three treatments (all between 12% and 13%). Despite the apparent efficacy in 10-m and 15-m centre treatments, some replicates failed spectacularly. Failure was not significantly related to the incidence of red trees, but was negatively related to density/ha of available trees and positively related to mean dbh. We recommend operational implementation of the push-pull tactic at 10-m or 15-m centres when the density of available lodgepole pines is > 400/ha, the mean dbh is ≤ 25 cm, current attack is ≤ 15%, and the tactic is part of an integrated pest management program that includes sanitation harvesting. Using verbenone alone at 15-m centres would cost $380/ha (CAD), excluding labour. Key words: mountain pine beetle, Dendroctonus ponderosae, lodgepole pine, Pinus contorta var. latifolia, pheromones, semiochemicals, pest management



2015 ◽  
Vol 108 (1) ◽  
pp. 173-182 ◽  
Author(s):  
C. J. Fettig ◽  
A. S. Munson ◽  
M. Reinke ◽  
A. Mafra-Neto


2014 ◽  
Vol 44 (11) ◽  
pp. 1312-1319 ◽  
Author(s):  
Eleanor C. Lahr ◽  
Anna Sala

Stored resources in trees reflect physiological and environmental variables and affect life history traits, including growth, reproduction, resistance to abiotic stress, and defense. However, less attention has been paid to the fact that stored resources also determine tissue nutritional quality and may have direct consequences for the success of herbivores and pathogens. Here, we investigated whether stored resources differed between two hosts of the mountain pine beetle (Dendroctonus ponderosae Hopkins, 1902): lodgepole pine (Pinus contorta Douglas ex. Loudon), a common host, and whitebark pine (Pinus albicaulis Engelmann), a more naïve host that grows at higher altitudes. Phloem and sapwood were sampled in small- and large-diameter trees at two elevations, and nitrogen, phosphorus, nonstructural carbohydrates, and lipids were measured. We found that concentrations of stored resources increased with elevation and tree diameter for both species and that whitebark pine had thicker phloem than lodgepole pine. Overall, stored resources were higher in whitebark pine such that small-diameter whitebark pine trees often had resource concentrations higher than large-diameter lodgepole pines. These results suggest that whitebark pine is of higher nutritional quality than lodgepole pine, which could have implications for the current expansion of mountain pine beetles into higher altitude and latitude forests in response to climate warming.



1971 ◽  
Vol 103 (11) ◽  
pp. 1495-1503 ◽  
Author(s):  
H. S. Whitney

AbstractThe physical association between Dendroctonus ponderosae Hopk. and its associated blue stain fungi Ceratocystis montia Rumb. and Europhium clavigerum Robinson and Davidson and the yeasts Pichia pini (Holst) Phaff, Hansenula capsulata Wickerham, and H. holstii Wickerham is described in single broods reared in bolts of lodgepole pine, Pinus contorta Dougl. var. latifolia Engelm. Eggs just prior to hatch and first-instar larvae were always in contact with the microorganisms whereas newly laid eggs, second-, third-, and fourth-instar larvae were not. During pupation, blue stain fungi and yeasts colonized pupal chamber walls. Transfer of these microorganisms to the new generation of insects was ensured when tenerals contacted the microorganisms lining the pupal chamber. Ensured physical contact between these organisms supports the hypothesis of a symbiosis between them.



1998 ◽  
Vol 76 (2) ◽  
pp. 218-227 ◽  
Author(s):  
S M Bradbury ◽  
R M Danielson ◽  
S Visser

The ectomycorrhizal community associated with regenerating lodgepole pine (Pinus contorta Loud.) after clear-cutting in southwestern Alberta was investigated in 6-, 10-, and 19-year-old cut blocks and their adjacent 90-year-old undisturbed control stands. Twenty different mycorrhizal taxa were found in the 90-year-old undisturbed stands. Of these 20, 13 mycorrhizal taxa were found in the 6-year-old cut blocks, and 15 mycorrhizal taxa were found in both the 10- and 19-year-old cut blocks. The most common associate of all stand ages was Mycelium radicis atrovirens Melin (MRA), which overall colonized 29% (weighted average) of the root tips. Species or groups accounting for greater than 10% of the mycorrhizas in one or more age classes included Piloderma fallax (Karst.) Jül. (15% overall), Piloderma byssinum (Karst.) Jül. (11%), Cenococcum geophilum L. (8%), Russula-like (8%), Suillus brevipes (Pk.) Kuntze (5%), Suillus tomentosus (Kauff.) Sing., Snell & Dick (5%), and Lactarius deliciosus (L.:Fr.) S.F. Gray (2%). Although several mycorrhizal fungi exhibited significant differences in percent relative abundance of root tips colonized, when comparing cut blocks to their controls, there was no evidence to suggest that the suite of mycorrhizal fungi colonizing roots of young lodgepole pine trees was replaced by a different suite of mycorrhizal fungi in mature stands. Extensive fruit body collections, totalling 43 species of ectomycorrhizal fungi, throughout the study sites support this contention.Key words: Pinus contorta ectomycorrhizas, clear-cutting, second-rotation forests, succession.



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