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Optymalizacja rozkladu piersnic w lesie przerebowym

86%
Sylwan
|
2005
|
tom 149
|
nr 02
12-24
Assuming multilayer structure as optimal for silver fir stands, we attempted to answer the following questions: 1) how to describe such structure, 2) to what extent does the structure of a particular stand differ from the optimal one, and 3) how to obtain the optimal structure. The study was based on the material collected in 12 stands in the Nawojowa Forest District (S Poland). Three to five 0.04 hectare circular plots were established in each stand, and diameters at breast height (d) of all trees with d > 7 cm were measured. Height (h) was measured for 25 trees selected within the stand. The top height determined for each stand enabled to classify trees into two layers: higher (group I) or lower (group II) than ⅔ of top height. Trees with d<7 cm were divided into 3 layers according to the height: III – h>2 m (higher upgrowth), IV – h between 0.5 and 2 m (lower upgrowth), and V – h<0.5 m (seedlings). Trees in layer V were counted on a 0.005 ha plot, while trees in layers IV and III on a 0.04 ha plot. The selected fir stands revealed high diversity in basic characteristics (tab. 1 and 2). The number of trees in layer III was higher than in layer II only in one stand, and was larger than the number of trees in layer I. Moreover, the variation in tree height formed a vertical canopy closure. The stand was considered to be a model one, and used to develop diameter distribution according to the BDq method. Most stands characterized a smaller number of trees in lower and larger in higher diameter classes compared to the model distribution. It seems that large number of thick trees prevent satisfactory growth of thinner trees. Fir stands proved to have a mosaic vertical structure. In some fragments, eight classes can be distinguished including one layer only: 1) upper (I), 2) middle (II), 3) upgrowth (III), combination of layers: 4) I and II, 5) I and III, 6) II and III, 7) I, II and III, and 8) gaps. The multi−layer structure of fir stands can be maintained only in the form of such a mosaic, but single−layer fragments are also needed to enhance the natural regeneration. We could select a stand with a close−to−optimal multilayer structure, which was considered as a model one and its diameter distribution was used in the BDq method. A comparison of the model curve with the empirical distribution of diameters at breast height for the stand under consideration allows determining diameter classes with an excess of trees that can be harvested without the fear of losing the multilayer structure of the stand. Whether a given tree has to be cut should depend on the vertical differentiation of trees in a particular fragment of the stand. In further studies, measurements in multilayer fir stands should be conducted to verify the model distribution.
7
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Zmienność proweniencyjna olszy czarnej w Polsce

72%
European black alder (Alnus glutinosa (L.) Gaertn.) is a widespread tree species associated with wetlands and riparian ecosystems, thus it plays an important ecological role. Due to its fast growth and favorable wood properties it also has a potential to satisfy a growing demand for wood and fiber. However, its growth potential is not fully realized in Poland. In this study we investigated variation in growth traits, productivity, and stem straightness among 11 populations of European black alder originating from the lowland distribution of the species in Poland. The common−garden experiment located in 1968 in Kórnik (mid−western Poland) has been so far the only provenance experiment with this species in our country. We measured height and diameter of all trees at the site, assessed stem straightness in a 5−step scale (1−crooked; 5−straight), and calculated productivity at age of 50 years, which should be considered close to the rotation age. We found significant variation among populations in all investigated traits. The difference in productivity between the best and the worst provenance reached 75%. Using published and unpublished data from previous measurements at this site we also analyzed a trend in provenance ranking through time. The best and worst provenance could be identified at age 16 years, but many ranking shifts took place afterwards at the intermediate rank positions. We conclude that growth, productivity and stem quality of black alder could be improved through selection of favorable provenances within the species. Selection decisions can be made at the age below the half the rotation age, although decisions at ¾ of rotation age would be more precise.
The research was conducted in three old−growth forests consisted of silver fir Abies alba Mill., European beech Fagus sylvatica L., and Norway spruce Picea abies Karst. located in the southern part of Poland (Żarnówka and Oszast) and the south−eastern Bosnia and Hercegovina (Perućica). The aim of the study was to compare basic stand characteristics and spatial heterogeneity in terms of variation in stand basal area and vertical structure. In each research area, small sample plots (0.015 ha) were localised in a regular 20×20 m grid covering approximately 10 ha. In each sample plot the diameter at breast height (d1.3 ≥ 7 cm) and species of all live trees were recorded. For each plot the basal area of live trees and an index of structural diversification were determined. As a measure of structural diversification, the simple variance in tree height was computed and scaled through comparison with a hypothetical variance of the uniform distribution. The spatial patterns of basal area and structural diversification were tested with paired−plot approach. In addition, simulation techniques were used to model variation in the basal area of live trees dependent on spatial scale. The Carpathian and Dinaric stands considerably differed in basal area (ranging from 36.1 to 65.2 m²/ha) and volume (varying from 522 to 1176 m³/ha), but all of them had diameter distributions proximate to a negative exponential model. The basal area recorded on the 0.015 ha plots had a very similar pattern of variation, which could be generalised as a truncated normal distribution. The distribution of the structural diversification index was different and resembled an uniform (Perućica) or a bimodal distribution with modal values at its extremes (Oszast and Żarnówka). However, in the spatial scales above 1,000 m² the index distribution become similar to a normal (Oszast) or a truncated normal (Perućica and Żarnówka) ones with high mean values, indicating the predominance of complex vertical structures. In general, the spatial variability in basal area and structural diversification of live trees tended to be random. These results suggest that the patch−mosaic assumption being fundamental for the developmental cycle hypothesis is inapplicable to the studied primeval forests. Regardless of differences in geographic location and site conditions, the studied stands show a similar spatial pattern of structural heterogeneity, suggesting a close resemblance of disturbance regimes driving its dynamics.
The aim of this study was to characterize the texture of a primeval forest composed of Fagus sylvatica (L.), Abies alba (Mill.) and Picea abies ((L.) H. Karst). Empirical data were collected in the Babia Góra National Park (southern Poland) in the stand being under strict protection since 1934. 259 circular plots with a radius of 7.0 m and an area of 154 m2 each were established in nodes of 20×20 m grid. For individual plots and blocks of the combined plots representing gradient of spatial scales between 0.015 and 0.640 ha, the number of trees, diameter at breast height (dbh) distributions, basal areas and the values of structural diversity indices of Gini (GI), Shannon (SH) and Staudhammer−LeMay (STVI) were determined. The indices were also calculated for several types of theoretical distributions. Based on the values obtained for the theoretical distributions, the individual plots and the blocks of the combined plots were classified as representing simple (GI0.30; STVI0.10), moderately diversified (0.30GI0.45 and 0.10 STVI0.30) or complex (GI0.45; STVI0.30) dbh structure. For all the spatial scales analyzed the average values of GI and STVI indices reached the level typical for populations of a high structural diversity (i.e. exceeded the values of 0.45 and 0.30 respectively). According to the GI and STVI values, the portion of stand patches with complex dbh structure ranged from 70.9% and 68.2% at the individual plots scale, respectively, up to 100% in the blocks of 16 plots (4×4). In general, in all the spatial scales analyzed the spatial diversification of the dbh distributions and basal area levels was higher than in managed selection forests and much higher than in managed single−storied stands. The dominant frequency of highly diversified dbh distributions found in the analysed stand was not concordant with the predictions of the forest dynamics theory based on developmental stages, according to which in primeval forests with a significant partition of Abies alba and Picea abies should prevail stand patches of rather simple dbh structure, characteristic for the long−lasting optimum stage.
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