Ten-year tree mortality following a jack pine budworm outbreak in Saskatchewan

1998 ◽  
Vol 28 (12) ◽  
pp. 1784-1793 ◽  
Author(s):  
W Jan A Volney

The fate of jack pine (Pinus banksiana Lamb.) trees growing in a variety of stand conditions was assessed annually for a decade following an outbreak of jack pine budworm (Choristoneura pinus Freeman) in central Saskatchewan. Mortality was clearly associated with the severity and damage sustained by the trees during the second year of the defoliation episode. The pattern of mortality was remarkably similar among stands that originated in decades that spanned 60 years. Mortality rates were highest in stands that originated in the 1890s and were lowest in stands of the most recent origin (1940s). Defoliation severity, the length of dead top, diameter at breast height, and relative tree height expressed as a standard normal variable accounted for 94% of the variability in survival time. A nonparametric proportional hazards model was developed to evaluate the relative risk of individual trees dying. Defoliation is an important process in determining stand density, basal area, and volume after juvenile stand development is complete. The results presented suggest a novel method to determine the hazard of trees in stands and thus assess the vulnerability of stands to future budworm attack.

1996 ◽  
Vol 26 (12) ◽  
pp. 2180-2190 ◽  
Author(s):  
Deborah G. McCullough ◽  
Lyle J. Buss ◽  
Larry D. Marshall ◽  
Jari Kouki

Stand-level mortality and top kill from a 1991–1993 jack pine budworm (Choristoneurapinuspinus Freeman) outbreak were surveyed annually in the Raco Plains area of the Hiawatha National Forest in Michigan's Upper Peninsula from 1992 to 1994. Defoliation was visually estimated and percentage of trees killed or top killed was determined in 104 stands. In 1994, tree mortality attributable to the outbreak averaged 8% and 17% of trees had dead tops. Current stand inventory data, including age, site index, basal area, and size, were acquired from the Hiawatha Forest. Stands were grouped on the basis of inventory variables used for jack pine management in the Lake States region of the United States. Differences in tree mortality and top kill between groups, and associations between tree mortality and inventory variables, were evaluated. Tree mortality was greater in overmature stands and in overstocked stands, but stand size had little effect. Contrary to expectations, mortality was lower on poor sites with low site index values than on better sites with higher site index values. Mortality was not related to abundance of open-grown, full-canopied wolf trees or to abundance of trees infected with pine gall rust (Endocronartiumharknessii (J.P. Moore) Y. Hiratsuka (=Peridermiumharknessii J.P. Moore)). Amount of top kill was related to defoliation severity and was higher in overmature and understocked stands. Top kill was not strongly associated with amount of tree mortality or with inventory variables.


1964 ◽  
Vol 40 (4) ◽  
pp. 474-481 ◽  
Author(s):  
P. E. Vezina

The concept of stand density in relation to thinning is examined and its development over the years is discussed. Present difficulties of objectively measuring stand density are recognized and probable future trends towards the development of better formulae to express stand density are outlined. Researchers should continue to collect information on interrelationships among stand variables. Certain merits accrue from description of stand density in terms of variables, such as crown closure, that can be measured with some precision from aerial photographs. Conversely, valid estimates of crown closure which are often difficult to obtain by means of devices from the ground, could be predicted from stand density. Three stand variables, used as expressions of stand density, were tested in crown closure simple regressions in even-aged, unmanaged stands of balsam fir (Abies balsamea (L.) Mill.) and jack pine (Pinus banksiana Lamb.). These are: total number of trees, number of trees 4 inches and up, and basal area per acre. The strongest relationship found was the one where crown closure is compared with basal area; it was stronger for jack pine than for balsam fir. This was explained by differences in tolerance among the two species. The significance of these relationships for the stand development, and the feasibility of using height-and diameter-based indices as measures of growing stock in studies of yield are discussed.


1995 ◽  
Vol 25 (3) ◽  
pp. 413-424 ◽  
Author(s):  
R.L. Korol ◽  
S.W. Running ◽  
K.S. Milner

Current research suggests that projected climate change may influence the growth of individual trees. Therefore, growth and yield models that can respond to potential changes in climate must be developed, TREE-BGC, a variant of the ecosystem process model FOREST-BGC, calculates the cycling of carbon, water, and nitrogen in and through forested ecosystems. TREE-BGC allocates stand-level estimates of photosynthesis to "each tree using a competition algorithm that incorporates tree height, relative radiation-use efficiency, and absorbed photosynthetically active radiation, TREE-BGC simulated the growth of trees grown in a dense and an open stand of interior Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) near Kamloops, B.C. The competition algorithm dynamically allocated stand estimates of photosynthesis to individual trees, and the trees were grown using an allometric relationship between biomass increment and height and diameter increment. Asymptotic height growth and the changes in the height–diameter relationship with competition were also incorporated in the model algorithms. Sapwood and phloem volume were used to calculate maintenance respiration. Predicted reductions in diameter growth with stand density were similar to those observed in the study stands. Although the carbon balance of individual trees was not tested, simulated tree diameter increments and height increments were correlated with the actual measurements of tree diameter increment (r2 = 0.89) and tree height increment (r2 = 0.78) for the 5-year period (n = 352). Although the model did not work well with trees that had diameters <5 cm, the model would be appropriate for a user who required an accuracy of ± 0.03 m3•ha−1 for volume, ± 0.02 m2•ha−1 for basal area, or ± 0.4 m for tree height over a 5-year period.


2008 ◽  
Vol 38 (10) ◽  
pp. 2566-2578 ◽  
Author(s):  
Robert Schneider ◽  
Frank Berninger ◽  
Chhun-Huor Ung ◽  
Pierre Y. Bernier ◽  
D. Edwin Swift ◽  
...  

Allometric equations for estimating foliage biomass, sapwood area, and branch basal area from tree diameters and crown lengths for jack pine ( Pinus banksiana Lamb.) in eastern Canada were calibrated using mixed models. A first model is presented that relates branch foliage biomass to branch diameter and relative position within the crown. These results show that a branch’s foliage biomass is inversely proportional to its depth within the crown. At the tree level, foliage biomass was found to be proportional to crown length and to vary with stem age and slenderness. Pipe model parameters (sapwood area and branch basal area to foliage biomass) were also calculated. The sapwood area to foliage biomass parameter is proportional to stand density, whereas branch basal area to foliage biomass is constant. The tree-level allometeric models were calibrated using a mixed-effects seemingly unrelated regression to account for between-model correlations.


1999 ◽  
Vol 16 (3) ◽  
pp. 138-143 ◽  
Author(s):  
W. T. Zakrzewski

Abstract A new model was derived to describe the inside bark cross-sectional area of tree stems. It is a rational function. The inputs required by the model are outside bark tree diameter at breast height (DBH) and total tree height (H). Knowledge of a species-specific bark thickness at 1.3 m expressed in terms of input variables is also needed. Defining the model involves estimating two regression coefficients using either nonlinear or linear regression (after linearization of the model). The formula is analytically integrable and thus provides analytical inside bark volume estimates for any stem section defined by height limits. The model is analytically solvable for a stem height location at any given inside bark diameter, so that stem sections can be defined by the required inside bark diameter limits. The new model can be calibrated using either section diameter or section volume data. It is suggested that involving the ratio H/DBH in the model accounts for the influence of stand density on stem profile. The formula was calibrated for jack pine (Pinus banksiana Lamb.) in Ontario. Wider applicability of the model is supported by results obtained for sugar maple (Acer saccharum Marsh.) in Ontario and Scots pine (Pinus silvestris L.) in Finland. Comparing volume estimates from the new model with those generated by Honer's formula confirms the advantages of the new model. North. J. Appl. For. 16(3):138-143.


1999 ◽  
Vol 29 (3) ◽  
pp. 382-392 ◽  
Author(s):  
Bradley E Conway ◽  
Larry A Leefers ◽  
Deborah G McCullough

Stand-level merchantable volume and financial losses resulting from a 1991-1993 jack pine budworm (Choristoneura pinus pinus Freeman) outbreak were quantified for 99 jack pine (Pinus banksiana Lamb.) stands in the Raco Plains area of the Hiawatha National Forest. Associations between standing value loss and stand inventory variables were evaluated. Stands were stratified into management groups based on age, site index, and stocking. Differences in standing value loss among groups were examined. Total standing merchantable volume loss and gross value loss were estimated to be 19 500 m3 and $289 800, respectively, for the 1480-ha sample area. Standing merchantable volume loss averaged 13.3 m3/ha or 14% of standing volume. Standing value loss within stands averaged $194/ha. Losses were concentrated in only a few stands with eight stands accounting for over half the total standing value loss. Standing value loss was positively associated with stand age and basal area and negatively associated with the proportion of open-grown, full-canopied "wolf" trees in the stand. A significant interaction in standing value loss was observed between age-class and site index class. No significant differences in standing value loss were observed among stocking classes. Results confirm overstocked stands over 50 years of age should be prioritized for harvest.


1999 ◽  
Vol 29 (10) ◽  
pp. 1510-1517 ◽  
Author(s):  
Bradley E Conway ◽  
Deborah G McCullough ◽  
Larry A Leefers

Growth of jack pine (Pinus banksiana Lamb.) trees from the Raco Plains area in the Upper Peninsula of Michigan was examined over an 18-year period (1978-1995) that included two jack pine budworm (Choristoneura pinus pinus Freeman) outbreaks. Specific volume increments were calculated for 84 trees grouped into three classes based on their status in 1996; 36 trees were undamaged, 24 trees had been recently top-killed, and 24 trees had been recently killed. Average growth was converted to proportion of previous years' growth for three periods: before the 1983-1985 outbreak, between the 1983-1985 and 1991-1993 outbreak, and after the onset of the 1991-1993 outbreak. Differences in growth over these periods among undamaged, recently top-killed, and recently killed trees were evaluated. Growth did not differ among the three groups before the 1983-1985 outbreak. From 1983-1990, undamaged and recently top-killed trees grew significantly more than recently killed trees. There was no difference in average growth from 1983 to 1990 between undamaged and recently top-killed trees. Growth of undamaged trees was significantly greater than growth of recently top-killed trees following the onset of defoliation from the 1991-1993 outbreak. Patterns of growth loss suggest that a history of defoliation stress from multiple budworm outbreaks was an important determinant of tree mortality.


2021 ◽  
Vol 13 (12) ◽  
pp. 2297
Author(s):  
Jonathon J. Donager ◽  
Andrew J. Sánchez Meador ◽  
Ryan C. Blackburn

Applications of lidar in ecosystem conservation and management continue to expand as technology has rapidly evolved. An accounting of relative accuracy and errors among lidar platforms within a range of forest types and structural configurations was needed. Within a ponderosa pine forest in northern Arizona, we compare vegetation attributes at the tree-, plot-, and stand-scales derived from three lidar platforms: fixed-wing airborne (ALS), fixed-location terrestrial (TLS), and hand-held mobile laser scanning (MLS). We present a methodology to segment individual trees from TLS and MLS datasets, incorporating eigen-value and density metrics to locate trees, then assigning point returns to trees using a graph-theory shortest-path approach. Overall, we found MLS consistently provided more accurate structural metrics at the tree- (e.g., mean absolute error for DBH in cm was 4.8, 5.0, and 9.1 for MLS, TLS and ALS, respectively) and plot-scale (e.g., R2 for field observed and lidar-derived basal area, m2 ha−1, was 0.986, 0.974, and 0.851 for MLS, TLS, and ALS, respectively) as compared to ALS and TLS. While TLS data produced estimates similar to MLS, attributes derived from TLS often underpredicted structural values due to occlusion. Additionally, ALS data provided accurate estimates of tree height for larger trees, yet consistently missed and underpredicted small trees (≤35 cm). MLS produced accurate estimates of canopy cover and landscape metrics up to 50 m from plot center. TLS tended to underpredict both canopy cover and patch metrics with constant bias due to occlusion. Taking full advantage of minimal occlusion effects, MLS data consistently provided the best individual tree and plot-based metrics, with ALS providing the best estimates for volume, biomass, and canopy cover. Overall, we found MLS data logistically simple, quickly acquirable, and accurate for small area inventories, assessments, and monitoring activities. We suggest further work exploring the active use of MLS for forest monitoring and inventory.


2010 ◽  
Vol 86 (6) ◽  
pp. 775-779 ◽  
Author(s):  
Alice Verrez ◽  
Dan Quiring ◽  
Thibaut Leinekugel Le Cocq ◽  
Greg Adams ◽  
Yill Sung Park

White pine weevil (Pissodes strobi Peck) damage was evaluated in one white pine (Pinus strobus L.) and four jack pine(Pinus banksiana Lamb) half-sib family test sites to determine the role of tree genotype in resistance to the weevil. Halfsibfamily explained a significant proportion of the variation in weevil attack at all sites. Estimates of family (0.16-0.54)and individual (0.09-0.24) heritabilities of jack pine resistance to white pine weevil were moderate. Estimates of family(0.37) and individual (0.22) heritability of resistance of white pine to the weevil were also moderate when the percentageof test trees damaged by the weevil was relatively low, but were insignificant four years later when more than three-quartersof trees were damaged. Significant positive correlations between mean tree height and mean incidence of trees damagedby the weevil were observed for four of seven site-years but relationships were weak, suggesting that any cost, withrespect to height growth, to breeding weevil resistant trees may be small.Key words: Pinus, Pissodes strobi, trade-offs, tree improvement, tree resistance, white pine weevil.


2004 ◽  
Vol 118 (4) ◽  
pp. 595 ◽  
Author(s):  
Brock Epp ◽  
Jacques C. Tardif

The Lodgepole Pine Dwarf Mistletoe (Arceuthobium americanum Nutt. ex Engelm.) is an important pathogen of Jack Pine (Pinus banksiana Lamb.). Dwarf Mistletoe alters tree form, suppresses growth, and reduces volume and overall wood quality of its host. Stem analysis and a 3-parameter logistic regression model were used to compare the growth of heavily and lightly to non infected Jack Pine trees. At the time of sampling, no significant reduction in diameter at breast height and basal area were observed in heavily infected trees. However, a significant reduction in height and volume and an increase in taper were observed in heavily infected trees. Growth models predicted a 21.1% lower basal area, 23.4% lower height and 42.1% lower volume by age 60 for the high infection group.


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