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J. C. Tappeiner

Publications and source records attributed to J. C. Tappeiner.

15 recordsLinked to original sources
USGS2005

Tree species and size structure of old-growth Douglas-fir forests in central western Oregon, USA

We characterized the structure of 91 old-growth forests dominated by Douglas-fir ( Pseudotsuga menziesii (Mirb.) Franco), using inventory data from recent (1985–1991) old-growth timber sales in western Oregon. The data were complete counts (i.e., censuses) of all live trees >20 cm diameter at breast height (dbh, measured at 1.4 m above the ground) over a mean area of 17.1 ha at each site. Across all sites, Douglas-fir accounted for 79% of the total basal area (m 2 /ha) of all species. The average density of trees >100 cm dbh was 19 trees/ha and 90% of these trees were Douglas-fir. Species other than Douglas-fir constituted only about 20% of the total basal area at each old-growth site, on average, but largely accounted for the structural variation between sites. We used multivariate techniques such as cluster analysis, indicator species analysis, and ordination with non-metric multidimensional scaling (NMS) to identify and characterize six structural groups in terms of basal area in different species–diameter classes. Almost 97% of the structural information was captured by the first ( r 2 = 0.841) and second ( r 2 = 0.128) NMS ordination axis. Geographic information systems (GIS) analysis and NMS indicated that the structural differences among groups of sites were associated with moisture, temperature, and elevation gradients within the study area. This type of analysis can be used to help define differences among old-growth forests and to set local structural goals for growing forests with old-growth characteristics.

Oregon↗
USGS2004

Seed and vegetative production of shrubs and growth of understory conifer regeneration

We observed flower and fruit production for nine understory shrub species in western Washington and Oregon and examined the relationships between shrub reproductive output and plant size, plant age, site factors, and overstory density to determine the factors that control flowering or fruiting in understory shrubs. In Washington, 50 or more shrubs or microplots (for rhizomatous species) were sampled for each of eight species. The variables examined were more useful for explaining abundance of flowers or fruit on shrubs than they were for explaining the probability that a shrub would produce flowers or fruit. Plant size was consistently the most useful predictor of flower/fruit abundance in all species; plant age was also a good predictor of abundance and was strongly correlated with plant size. Site variables (e.g., slope) and overstory competition variables (e.g., presence/absence of a canopy gap) also helped explain flower/fruit abundance for some species. At two Oregon sites, the responses of five species to four levels of thinning were observed for 2-4 yr (15 shrubs or microplots per treatment per year). Thinning increased the probability and abundance of flowering/fruiting for two species, had no effect on one species, and responses for two other species were positive but inconsistent between sites or from year to year. We believe reducing overstory density or creating canopy gaps may be useful tools for enhancing shrub size and vigor, thus, increasing the probability and abundance of fruiting in some understory shrub species.

Northwest Science↗
USGS2002

The effects of partial cutting on stand structure and growth of western hemlock-Sitka spruce stands in southeast Alaska

The effects of partial cutting on species composition, new and residual-tree cohorts, tree size distribution, and tree growth was evaluated on 73 plots in 18 stands throughout southeast Alaska. These partially cut stands were harvested 12-96 years ago, when 16-96% of the former stand basal area was removed. Partial cutting maintained stand structures similar to uncut old-growth stands, and the cutting had no significant effects on tree species composition. The establishment of new-tree cohorts was positively related to the proportion of basal-area cut. The current stand basal area, tree species composition, and stand growth were significantly related to trees left after harvest (p < 0.001). Trees that were 20-80 cm dbh at the time of cutting had the greatest tree-diameter and basal-area growth and contributed the most to stand growth. Diameter growth of Sitka spruce and western hemlock was similar, and the proportion of stand basal-area growth between species was consistent for different cutting intensities. Concerns about changing tree species composition, lack of spruce regeneration, and greatly reduced stand growth and vigor with partial cuts were largely unsubstantiated. Silvicultural systems based on partial cutting can provide rapidly growing trees for timber production while maintaining complex stand structures with mixtures of spruce and hemlock trees similar to oldgrowth stands.

Forest Ecology and Management↗
USGS2002

Long-term patterns of diameter and basal area growth of old-growth Douglas-fir trees in western Oregon

Diameter growth and age data collected from stumps of 505 recently cut old-growth Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) trees at 28 sample locations in western Oregon (U.S.A.) indicated that rapid early and sustained growth of old Douglas-fir trees were extremely important in terms of attaining large diameters at ages 100a??300 years. The diameters of the trees at ages 100a??300 years (D100a??D300) were strongly, positively, and linearly related to their diameters and basal area growth rates at age 50 years. Average periodic basal area increments (PAIBA) of all trees increased for the first 30a??40 years and then plateaued, remaining relatively high and constant from age 50 to 300 years. Average PAIBA of the largest trees at ages 100a??300 years were significantly greater by age 20 years than were those of smaller trees at ages 100a??300 years. The site factors province, site class, slope, aspect, elevation, and establishment year accounted for little of the variation observed in basal area growth at age 50 years and D100a??D300. The mean age range for old-growth Douglas-fir at the sample locations was wide (174 years). The hypothesis that large-diameter old-growth Douglas-fir developed at low stand densities was supported by these observations.

Canadian Journal of Forest Research↗
USGS2001

Salmonberry and salal annual aerial stem production: The maintenance of shrub cover in forest stands

Annual sprouting of aerial stems and ramets enables populations of salmonberry (Rubus spectabilis Pursh), salal (Gaultheria shallon Pursh), and probably other forest shrubs to maintain dense covers (>20 000 stems/ha). We studied annual stem production of salmonberry on cut (all stems cut within 15 cm of the ground) and uncut (stems were not treated) plots for 8 years and salal for 5 years in the understories of Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco), alder, and riparian stands, as well as clearcuts, which are all common stand types in western Oregon. Mean salmonberry stem production on uncut plots ranged from 4.7 stemsA?ma??2A?yeara??1 (95% CI 2.9a??7.4) in alder stands and clearcuts to 1.6 stemsA?ma??2A?yeara??1 (95% CI 1.0a??2.6) in conifer stands. Mean salal production was greater, ranging from 58 stemsA?ma??2A?yeara??1 (95% CI 25a??135) to 8.6 stemsA?ma??2A?yeara??1 (95% CI 3.7a??20.1) on uncut plots in clearcuts and unthinned Douglas-fir stands, respectively. Annual production of both species was somewhat greater on cut plots. Most stems produced in early spring die by December, but enough are recruited to replace mortality of older stems. Stem density was maintained for 8 years for salmonberry and 5 years for salal on both cut and uncut plots. Based on length of rhizomes and bud density we estimate that only 1a??5% of the buds in the rhizomes are needed to support this annual stem production. Although these species sprout vigorously after their aerial stems are killed, disturbance is not necessary for maintaining a dense cover. It appears that, once established, salal, salmonberry, and probably other clonal forest shrubs can maintain a dense cover that can interfere with establishment of trees and other shrubs in canopy gaps or other openings.

Canadian Journal of Forest Research↗
USGS1999

CFIRP: What we learned in the first ten years

In response to public dissatisfaction with forest management methods, we initiated the College of Forestry Integrated Research Project (CFIRP) to test alternative silvicultural systems in Douglas-fir (Pseudotsuga menziesii stands in western Oregon. We compared costs and biological and human responses among a control and three replicated silvicultural alternatives to clearcutting that retained structural features found in old Douglas-fir forests. Treatments were applied within 8- to 15-ha stands and attempted to mimic crown fires (modified clearcut), windthrow (green tree retention), and small-scale impacts such as root rot diseases (small patch group selection). We also compared costs in three unreplicated treatments (large patch group selection, wedge cut, and strip cut). Each treatment included differences in the pattern of retained dead trees (snags), as either scattered individuals or as clumps. Good communication among researchers and managers, a long-term commitment to the project, and careful documentation of research sites and data are important to the success of long-term silvicultural research projects. To date, over 30 publications have resulted from the project.

Conference Paper↗
USGS1998

Understory vegetation in old and young Douglas-fir forests of western Oregon

We studied understory composition in thinned and unthinned Douglas-fir ( Pseudotsuga menziesii (Mirb.) Franco)/western hemlock ( Tsuga heterophylla (Raf.) Sarg.) stands on 28 sites in western Oregon. These stands had regenerated naturally after timber harvest, 40–70 years before thinning. Commercial thinning had occurred 10–24 years previously, with 8–60% of the volume removed from below with the intent to homogenize spacing among trees. Undisturbed old-growth Douglas-fir stands were present for comparison on 18 of these sites. Total herbaceous cover was greater in thinned (25% cover) stands than in unthinned (13% cover) or old-growth (15% cover) stands. Species richness was also greater in thinned (137) than in unthinned (114) and old-growth (91) stands ( P =0.05). Part of the increased richness was caused by the presence of exotic species in thinned stands, but there were also more native grass and nitrogen-fixing species in thinned stands than in unthinned or old-growth stands. Groups of species differed among stand-types. For example, the frequency of tall cordate-leaved species was greater in old-growth stands ( P =0.009), but their relative cover was different only between old-growth and unthinned stands ( P =0.08). Both the cover and frequency of grasses and sedges in thinned stands were greater than in unthinned or old-growth stands ( P ≤0.002). Ordination of shrub cover showed differences among old-growth and unthinned stands compared to thinned stands, mainly because of the amount of Gaultheria shallon Pursh and Polystichum munitum (Kaulf.) Presl in heavily thinned stands. Ordination of herbaceous community data showed that there were much stronger differences among sites than among stand-types. The lack of difference among stand-types demonstrates the resiliency of herbaceous communities to disturbance associated with past and current forest management.

Oregon↗
USGS1998

Impact of alternative regeneration methods on genetic diversity in coastal Douglas-fir

Genetic implications of natural and artificial regeneration following three regeneration methods (group selection, shelterwood, and clearcut) were investigated in coastal Douglas-fir ( Pseudotsuga menziesii var. menziesii [Mirb.] Franco) using genetic markers (17 allozyme loci). In general, harvesting followed by either natural or artificial regeneration resulted in offspring populations little altered from those in the previous generation. Cutting the smallest trees to form shelterwoods, however, resulted in the removal of rare, presumably deleterious, alleles, such that slightly fewer alleles per locus were observed among residual trees (2.76) and natural regeneration (2.75) than found in uncut (control) stands (2.86). Thus, although the shelterwood regime appears quite compatible with gene conservation, it would be best to leave parent trees of a range of sizes in shelterwoods designated as gene conservation reserves, in order to maximize the number of alleles (regardless of current adaptive value) in naturally regenerated offspring. Seedling stocks used for artificial regeneration in clearcut, shelterwood, and group selection stands (7 total) had significantly greater levels of genetic diversity, on average, than found in natural regeneration. This is probably because the seeds used in artificial seedling stocks came from many wild stands and thus, sampled more diversity than found in single populations. For. Sci. 44(3): 390-396.

Forest Science↗
USGS1997

Use of artificially created Douglas-fir snags by cavity-nesting birds

In western Oregon, we created snags by sawing tops off live Douglas-fir ( Pseudotsuga menziesii ) (n = 821) trees and monitored their condition and use by cavity-nesting birds. We created snags in three silvicultural treatments: modified clearcut stands, two-story stands, and small-patch group-selection stands. We used two snag patterns: clumped and scattered. Created snags averaged 3.8/ha in density, 17 m in height, and 75 cm in diameter. Chainsaw-topped snags were used by cavity nesters within 5 yr of creation. Abundance of excavated cavities increased in all silvicultural treatments (P = 0.0001) and was higher in two-story and clearcut stands than in small-patch stands (P ≤ 0.0004). We did not, however, find that snag pattern (clumped v. scattered) affected use by cavity-nesting birds based on abundance of excavated cavities (P > 0.6). We observed excavated cavities in five hardwood species indicating that hardwoods represented an important resource for cavity-nesting birds. Creating conifer snags by topping and retaining hardwoods may retain or increase populations of cavity nesters in areas with low natural snag density.

Oregon↗
USGS1997

Density, ages, and growth rates in old-growth and young-growth forests in coastal Oregon

We studied the ages and diameter growth rates of trees in former Douglas-fir (Pseudotsuga menziesii (Mirb.)Franco) old-growth stands on 10 sites and compared them with young-growth stands (50-70 years old, regenerated after timber harvest) in the Coast Range of western Oregon. The diameters and diameter growth rates for the first 100 years of trees in the old-growth stands were significantly greater than those in the young-growth stands. Growth rates in the old stands were comparable with those from long-term studies of young stands in which density is about 100-120 trees/ha; often young-growth stand density is well over 500 trees/ha. Ages of large trees in the old stands ranged from 100 to 420 years; ages in young stands varied by only about 5 to 10 years. Apparently, regeneration of old-growth stands on these sites occurred over a prolonged period, and trees grew at low density with little self-thinning; in contrast, after timber harvest, young stands may develop with high density of trees with similar ages and considerable self-thinning. The results suggest that thinning may be needed in dense young stands where the management objective is to speed development of old-growth characteristics.

Canadian Journal of Forest Research↗
USGS1997

Methods for evaluating crown area profiles of forest stands

Canopy architectures of five structurally complex forest stands and three structurally simple forest stands in southwest Oregon and the Willamette Valley, Oregon, were evaluated and quantified through crown area profiles. Mixed conifer and mixed conifer hardwood stands across a range of sites were sampled for crown widths and heights. Crown width and shape equations were derived and used to quantify the stand crown area at incremental heights above the forest floor. Crown area profiles describe the spatial arrangement of aboveground forest vegetation and the total pore spaces between crowns. Plot by plot profiles were combined to produce vertical and horizontal displays of the stand crown area distribution. In complex stands, the forest space was moderately occupied by crowns from the forest floor up to heights over 30 m, producing uniform distributions of between-crown porosity. The structurally complex stands had between-crown porosity values of 70% to 90% for more than 23 vertical metres of canopy, and they had total between-crown porosities of 86% to 91%. The structurally simple stands had between-crown porosity values of 70% to 90% for less than 8 vertical metres of canopy, and they had total between-crown porosities of 69% to 85%. Variances in crown area indicate that variation in horizontal crown area (within heights) was larger in complex stands than in simple stands, but vertical crown areas (between heights) varied less in complex stands. The study provides a basis for discriminating between canopy architectures and for quantifying the porosity of forest canopies.

Canadian Journal of Forest Research↗