Experiments for alternative management of forest reserves: effects of partial cutting on stem growth and mortality of large oaks

2009 ◽  
Vol 39 (7) ◽  
pp. 1322-1330 ◽  
Author(s):  
Frank Götmark

Although protected forests are usually kept as free of human disturbance as possible, careful cutting may favour biodiversity in such areas. However, the use of heavy machinery during cutting operations may have a negative impact on protected forests. The large oaks ( Quercus spp.) found in many temperate nature reserves have a rich associated biodiversity. In 25 conservation forests in Sweden, the basal area growth and mortality of 250 large oaks (31–110 cm DBH) were compared between plots that were partially cut to promote the growth and survival of oaks and undisturbed plots. Each forest had one treatment plot (1 ha) and one undisturbed reference plot (1 ha) with similar levels of canopy cover. In 2002–2003, about 25% of the basal area was harvested in treatment plots, thereby increasing canopy openness from 14% to 33%. Cutting increased the mean relative basal area growth of large oaks (49% by plot, 22% by tree) after four seasons (P = 0.026). However, in nine forests, the growth rate was not higher in the treated plot than in the reference plot. Mortality, apparently due to cutting, was recorded only in one forest, where 18 large oaks died. Tree condition (percentage of dead large branches in crown) was the best (negative) predictor of growth rate, and openness around oak crown was also a (positive) predictor. Partial cutting favoured the growth of oaks and may be recommended, but a “hands-off” policy is also effective for these conservation forests.

2006 ◽  
Vol 36 (4) ◽  
pp. 961-971 ◽  
Author(s):  
Veronica I Emhart ◽  
Timothy A Martin ◽  
Timothy L White ◽  
Dudley A Huber

We quantified basal area increment phenology over a 2-year period in one loblolly pine (Pinus taeda L.) and four slash pine (Pinus elliottii Engelm. var. elliottii) full-sib families propagated as rooting cuttings. In 2002, basal area growth started in March and stopped in October for both species, while in 2003, initiation and cessation occurred 2 weeks earlier for all families. In both years, peaks in basal area increment occurred in short (2–3 week) periods in the early spring for all families, followed by linear basal area growth until cessation. While there were significant size differences among taxa (species and families) at age 6 and 7 years, genetic differences in basal area growth rate were only expressed during short, discrete time periods primarily in the spring and fall. Basal area growth rate increased during periods when water soil availability increased (up to 300 mm), but an excess in water availability in the soil had a negative impact on growth. Within-family individual-tree broad-sense heritabilities ranged from 0.01 to 0.37 for all traits. In general, heritabilities were higher for growth traits than for phenological traits for all families. Both the strength and direction of correlation estimates of phenological traits with growth rate varied across families and years.


2001 ◽  
Vol 77 (4) ◽  
pp. 685-695 ◽  
Author(s):  
Richard Zarnovican ◽  
Jean-Martin Lussier ◽  
Claude Laberge

Balsam fir basal area growth was studied 5 years after the preparatory cut in the context of natural regeneration by the shelterwood system. The study was carried out in a 60-year-old second-growth balsam fir-yellow birch stand. The felling trials were realized in 16 plots and consisted of control and three felling regimes (15, 30 and 45% of removed basal area). The periodic (5 years) mean growth rate on dbh of trees in plots varies between 6 and 12% in response to felling intensity. The basal area of plots presents a mean periodic growth rate of 7.4% independently of felling intensity. There are highly significant correlations between the live crown characteristics and periodic basal area growth. This growth is highly correlated with inital diameter and intensity of felling. The trees of higher relative size are more productive than the others and the impact of felling on periodic basal area growth is significant when the intensity of felling is greater than 30%. Conversely, the ratio between periodic basal area growth after treatment and periodic basal area growth before treatment is correlated only with the intensity of felling. Finally, intensity of felling had no effect on periodic basal area growth per square meter of crown projected area. Key words: preparatory felling, basal area growth, balsam fir


1988 ◽  
Vol 5 (3) ◽  
pp. 221-222
Author(s):  
Arlyn W. Perkey ◽  
Kenneth L. Carvell

1973 ◽  
Vol 3 (4) ◽  
pp. 495-500 ◽  
Author(s):  
James A. Moore ◽  
Carl A. Budelsky ◽  
Richard C. Schlesinger

A new competition index, modified Area Potentially Available (APA), was tested in a complex unevenaged stand composed of 19 different hardwood species. APA considers tree size, spatial distribution, and distance relationships in quantifying intertree competition and exhibits a strong correlation with individual tree basal area growth. The most important characteristic of APA is its potential for evaluating silvicultural practices.


Forests ◽  
2020 ◽  
Vol 11 (4) ◽  
pp. 409
Author(s):  
Gheorghe Marin ◽  
Vlad C. Strimbu ◽  
Ioan V. Abrudan ◽  
Bogdan M. Strimbu

In many countries, National Forest Inventory (NFI) data is used to assess the variability of forest growth across the country. The identification of areas with similar growths provides the foundation for development of regional models. The objective of the present study is to identify areas with similar diameter and basal area growth using increment cores acquired by the NFI for the three main Romanian species: Norway spruce (Picea abies L. Karst), European beech (Fagus sylvatica L.), and Sessile oak (Quercus petraea (Matt.) Liebl.). We used 6536 increment cores with ages less than 100 years, a total of 427,635 rings. The country was divided in 21 non-overlapping ecoregions based on geomorphology, soil, geology and spatial contiguousness. Mixed models and multivariate analyses were used to assess the differences in annual dimeter at breast height and basal area growth among ecoregions. Irrespective of the species, the mixed models analysis revealed significant differences in growth between the ecoregions. However, some ecoregions were similar in terms of growth and could be aggregated. Multivariate analysis reinforced the difference between ecoregions and showed no temporal grouping for spruce and beech. Sessile oak growth was separated not only by ecoregions, but also by time, with some ecoregions being more prone to draught. Our study showed that countries of median size, such as Romania, could exhibit significant spatial differences in forest growth. Therefore, countrywide growth models incorporate too much variability to be considered operationally feasible. Furthermore, it is difficult to justify the current growth and yield models as a legal binding planning tool.


2000 ◽  
Vol 24 (2) ◽  
pp. 112-120 ◽  
Author(s):  
Michael M. Huebschmann ◽  
Lawrence R. Gering ◽  
Thomas B. Lynch ◽  
Onesphore Bitoki ◽  
Paul A. Murphy

Abstract A system of equations modeling the growth and development of uneven-aged shortleaf pine (Pinus echinata Mill.) stands is described. The prediction system consists of two main components: (1) a distance-independent, individual-tree simulator containing equations that forecast ingrowth, basal-area growth, probability of survival, total and merchantable heights, and total and merchantable volumes and weights of shortleaf pine trees; and (2) stand-level equations that predict hardwood ingrowth, basal-area growth, and mortality. These equations were combined into a computer simulation program that forecasts future states of uneven-aged shortleaf pine stands. Based on comparisons of observed and predicted stand conditions in shortleaf pine permanent forest inventory plots and examination of the growth patterns of hypothetical stands, the simulator makes acceptable forecasts of stand attributes. South. J. Appl. For. 24(2):112-120.


2002 ◽  
Vol 32 (7) ◽  
pp. 1232-1243 ◽  
Author(s):  
Nathan J Poage ◽  
John C Tappeiner, II

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 100–300 years. The diameters of the trees at ages 100–300 years (D100–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 30–40 years and then plateaued, remaining relatively high and constant from age 50 to 300 years. Average PAIBA of the largest trees at ages 100–300 years were significantly greater by age 20 years than were those of smaller trees at ages 100–300 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 D100–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.


2004 ◽  
Vol 80 (3) ◽  
pp. 366-374 ◽  
Author(s):  
Lianjun Zhang ◽  
Changhui Peng ◽  
Qinglai Dang

Individual-tree models of five-year basal area growth were developed for jack pine (Pinus banksiana Lamb.) and black spruce (Picea mariana (Mill.) BSP) in northern Ontario. Tree growth data were collected from long-term permanent plots of pure and mixed stands of the two species. The models were fitted using mixed model methods due to correlated remeasurements of tree growth over time. Since the data covered a wide range of stand ages, stand conditions and tree sizes, serious heterogeneous variances existed in the data. Therefore, the coefficients of the final models were obtained using weighted regression techniques. The models for the two species were evaluated across 4-cm diameter classes using independent data. The results indicated (1) the models of jack pine and black spruce produced similar prediction errors and biases for intermediate-sized trees (12–28 cm in tree diameter), (2) both models yielded relatively large errors and biases for larger trees (> 28 cm) than those for smaller trees, and (3) the jack pine model produced much larger errors and biases for small-sized trees (< 12 cm) than did the black spruce model. Key words: mixed models, repeated measures, model validation


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