scholarly journals A Retrospective Assessment of Partial Cutting to Reduce Spruce Beetle-Caused Mortality in the Southern Rocky Mountains

2010 ◽  
Vol 25 (2) ◽  
pp. 81-87 ◽  
Author(s):  
E. Matthew Hansen ◽  
José F. Negron ◽  
A. Steven Munson ◽  
John A. Anhold

Abstract Tree susceptibility to bark beetle-caused mortality has been linked to stand characteristics such as basal area (BA) and average tree size, factors that can be manipulated through partial cutting. There is no experimental evidence, however, demonstrating the efficacy of partial cutting in spruce type. Such experiments are very difficult to complete because of the inability to manipulate bark beetle populations needed to challenge treated stands. To circumvent this difficulty, we identified spruce stands that were partially cut (for nonexperimental reasons) in advance ofbeetle activity and compared beetle-caused mortality to that in nearby spruce stands that were not treated. Treated stands had fewer infested stems and less infested BA than untreated stands, as well as smaller proportions of infested stems and BA. Untreated stands, however, had more residualspruce stems and BA than treated stands. Most of this difference was among stems 3–11 in. dbh with little difference in survivorship among larger stems. Spruce regeneration was not significantly different among treated and untreated stands. Spruce stand density index, spruce BA, and the number of spruce stems >11 in. dbh were the stand variables most strongly correlated with host mortality measurements. Insect population pressure appears to influence the degree of protection to residual spruce following partial cutting.

2003 ◽  
Vol 18 (4) ◽  
pp. 259-266 ◽  
Author(s):  
Joel D. McMillin ◽  
Kurt K. Allen ◽  
Daniel F. Long ◽  
Jeri Lyn Harris ◽  
José F. Negrón

Abstract Western balsam bark beetle, Dryocoetes confusus (Coleoptera: Scolytidae), has caused widespread mortality of subalpine fir (Abies lasiocarpa) in western North America throughout the past decade. The objectives of this study were to document the effects of this mortality, relate mortality to pre-existing stand conditions, and investigate the role of storm-damaged fir in beetle population dynamics in north-central Wyoming. Transect cruise lines and pairs of infested and uninfested plots were installed to detect changes in the forest overstory and understory and to determine associations between stand conditions and beetle-caused fir mortality. On average, beetles killed more than 70 trees/ac over the last several years. This mortality resulted in significant decreases in: subalpine fir basal area, trees per acre, stand density index, and the percentage of subalpine fir stems in the overstory. Small, but significant increases were detected in the understory; herbaceous plant abundance increased in the infested plots compared with the noninfested plots. Moreover, significant positive linear relationships were found between the amount of fir mortality and the percentage of subalpine fir trees in a stand, subalpine fir basal area, and subalpine fir stand density index. In addition, a significant positive linear relationship was found between the percentage of wind-caused downed fir logs in an area and the percentage of logs utilized by western balsam bark beetle. The blowdown events that occurred in the mid-1990s in combination with a high percentage of fir component has provided ideal conditions for continued beetle expansion. West. J. Appl. For. 18(4):259–266.


2007 ◽  
Vol 22 (2) ◽  
pp. 99-104 ◽  
Author(s):  
Nathan J. Poage ◽  
David D. Marshall ◽  
Michael H. McClellan

Abstract Reineke's (1933) maximum stand-density index (SDImax) was determined for 40 unthinned, fully stocked, even-aged, hemlock-spruce stands in southeast Alaska. A nonlinear model was used to identify objectively the linear portions of the stands' self-thinning trajectories for analysis. The objectives of the present study were (1) to use the modeled slopes and intercepts to determine the mean SDImax of the stands and (2) to identify stand and site factors associated with the variability observed in SDImax. The mean SDImax of the 40 hemlock-spruce stands in southeast Alaska was 619. Individually, none of the stand or site factors examined accounted for >30% of the variability observed in SDImax when all 40 stands were analyzed together. Although the spruce proportion of total stand basal area of most stands increased over time and the hemlock proportion of total stand basal area of most stands decreased over time, SDImax was not related to species proportion or changes in species proportion over time.


2019 ◽  
Vol 65 (6) ◽  
pp. 776-783 ◽  
Author(s):  
Xiongqing Zhang ◽  
Quang V Cao ◽  
Lele Lu ◽  
Hanchen Wang ◽  
Aiguo Duan ◽  
...  

Abstract Stand density index (SDI) has played an important role in controlling stand stocking and modeling stand development in forest stands. Reineke’s SDI (SDI_R) is based on a constant slope of –1.605 for the self-thinning line. For Chinese fir plantations, however, it has been reported that the self-thinning slope varied with site and climate, rendering SDI_R questionable. Remeasured data from 48 plots distributed in Fujian, Jiangxi, Guangxi, and Sichuan provinces were used to develop models for prediction of stand survival and basal area, with SDI_R incorporated as a predictor variable. Also included in the evaluation were growth models based on self-thinning slopes estimated from two groups of sites (SDI_S) or from climate variables (SDI_C). Results indicated that models with climate-sensitive SDI (SDI_C) performed best, followed by SDI_S and SDI_R. The control models without SDI received the worst overall rank. Inclusion of climate-sensitive SDI in growth and survival models can therefore facilitate modeling of the relation between stand density and growth/survival under future climate-change conditions.


2011 ◽  
Vol 28 (2) ◽  
pp. 61-65 ◽  
Author(s):  
Mark J. Ducey ◽  
John A. Kershaw

Abstract Vertical point sampling has seen relatively little use in practical forestry, in part because existing field techniques are difficult. We show how vertical point sampling can be implemented quickly and easily using a camera. We give tables and equations for calculating the height-squared factor, which plays a role similar to that of the basal area factor in horizontal point sampling. Some suggestions for choosing a height-squared factor are discussed, along with potential applications for further exploration. We illustrate the technique using a case study in southern Maine. Direct estimates with no statistically detectable bias were obtained using height-squared factors greater than 3. The results also suggested that the technique could be used as a correlate in double sampling for variables such as cubic volume, stand density index, and biomass, and possibly board foot volume as well.


2010 ◽  
Vol 2010 ◽  
pp. 1-8
Author(s):  
M. J. Ducey ◽  
R. A. Knapp

Basal area has shortcomings as a measure of stand density, but it is often preferred for operational assessments because it is easy to measure. Previous work has demonstrated that an additive version of Reineke's stand density index can be estimated by a simple tree count using a modified horizontal point sampling technique. We show that this technique can be extended further to estimate a mixed-species density measure that has been developed for complex stands in the northeastern United States, using wood specific gravity to harmonize the density contributions of different species. The sampling technique provides design-unbiased estimates of stand density from a weighted tree count, where the weights depend on specific gravity but not on diameter. Rounding the specific gravity values for different species in the calculation of estimates introduces a trivial amount of bias but streamlines the procedure for rapid use in the field.


Author(s):  
Micky Allen ◽  
Andreas Brunner ◽  
Clara Antón-Fernández ◽  
Rasmus Astrup

Abstract An understanding of the relationship between volume increment and stand density (basal area, stand density index, etc.) is of utmost importance for properly managing stand density to achieve specific management objectives. There are two main approaches to analyse growth–density relationships. The first relates volume increment to stand density through a basic relationship, which can vary with site productivity, age, and potentially incorporates treatment effects. The second is to relate the volume increment and density of thinned experimental plots relative to that of an unthinned experimental plot on the same site. Using a dataset of 229 thinned and unthinned experimental plots of Norway spruce, a growth model is developed describing the relationship between gross or net volume increment and basal area. The models indicate that gross volume increases with increasing basal area up to 50 m2 and thereafter becomes constant out to the maximum basal area. Alternatively, net volume increment was maximized at a basal area of 43 m2 and decreased with further increases in basal area. However, the models indicated a wide range where net volume increment was essentially constant, varying by less than 1 m3 ha−1 year−1. An analysis of different thinning scenarios indicated that the relative relationship between volume increment and stand density was dynamic and changed over the course of a rotation.


1994 ◽  
Vol 4 (1) ◽  
pp. 3 ◽  
Author(s):  
PZ Fule ◽  
WW Covington

Stand and natural fuel conditions were sampled in ponderosa pine forests in northern and central Arizona to develop predictive fuel depth and loading equations. Litter and duff depths can be estimated from measurements of stand density (basal area, stand density index). Although woody fuel loading did not correlate well with stand variables, correlations were found among loadings of different woody fuel size classes, so that results from a planar intersect tally of certain single woody fuel size classes may be used to predict the loadings in certain other size classes. The relatively low precision of estimates from these predictive equations can be substantially increased by applying them in a double sampling scheme. Making use of these predictive relationships, managers can devise simple, rapid, arid cost-effective fuel inventories that focus on the fuel category of interest. Fuel loads can be estimated at a desired precision with reduced investment of time and funds compared to a more comprehensive direct fuel inventory.


1996 ◽  
Vol 20 (2) ◽  
pp. 110-113 ◽  
Author(s):  
Roger A. Williams

Abstract Stand Density Index (SDI) equations and diagrams were developed and presented for loblolly pine (Pinus taeda L.) plantations in north Louisiana. Two different SDI diagrams are presented—one that utilizes the number of trees per acre and average stand diameter, and a second that uses the number of trees per acre and the basal (ft²) per acre. Basal area is presented as a second alternative to average stand diameter since many practicing foresters commonly use basal area for density management. South. J. Appl. For. 20(2):110-113.


1976 ◽  
Vol 6 (3) ◽  
pp. 357-367 ◽  
Author(s):  
Rene Doucet ◽  
John V. Berglund ◽  
C. Eugene Farnsworth

Dry matter production data were obtained for jack pine (Pinusbanksiana Lamb.) stands growing at three density levels on two sites. Regression equations relating tree weight to diameter and height were calculated for stem wood, stem bark, branches, needles, cones, and total aboveground biomass, as well as for periodic net annual increment of these components. Different sets of equations were needed to evaluate biomass on each site, but density levels within sites could be grouped. Total net periodic annual weight increment was linearly related to foliage weight and basal area, but a levelling-off at higher densities was evident when basal area was replaced by stand density index or bole area equivalent as the measure of density.


2009 ◽  
Vol 24 (2) ◽  
pp. 88-94 ◽  
Author(s):  
Gregory M. Filip ◽  
Stephen A. Fitzgerald ◽  
Kristen L. Chadwick ◽  
Timothy A. Max

Abstract Portions of a 30-year-old stand of ponderosa pine were precommercially thinned in 1966 and commercially thinned in 2000 at age 64 years to determine the effects of thinning from below on tree growth and mortality caused by Armillaria root disease in central Oregon. Thirty years after precommercial thinning, leave-tree mortality was significantly less in thinned plots than in unthinned plots, but leave-treeߝdiameter growth was not significantly increased by thinning. Leave-tree basal area (BA) per acre growth, however, was significantly greater in thinned plots.In 2007 at age 71 years, 7 years after commercial thinning of the same plots that were precommercially thinned in 1966, leave-tree mortality was less in thinned plots than in unthinned plots, but more time probably is necessary to adequately assess Armillaria-caused mortality after commercial thinning. Both tree diameter and BA growth were significantly increased by commercial thinning. Hypotheses on fungal-host dynamics are discussed, and recommendations for multiple thinning based on stand density index are given.


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