Site carrying capacity of Norway spruce and Scots pine stands has increased in Germany and northern Europe (original) (raw)
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Canadian Journal of Forest Research, 2015
We examined the relationship between thinning intensity and volume increment predicted by four commonly used individual-tree growth models in Central Europe (i.e., BWIN, Moses, Prognaus, and Silva). We replicated conditions of older growth and yield experiments by selecting 34 young, dense plots of Norway spruce (Picea abies (L.) Karst.), Scots pine (Pinus sylvestris L.), and European beech (Fagus sylvatica L.). At these plots, we simulated growth, with mortality only, to obtain the maximum basal area. Maximum basal area was then decreased by 5% or 10% steps using thinning from below. Maximum density varied considerably between simulators; it was mostly in a reasonable range but partly exceeded the maximum basal area observed by the Austrian National Forest Inventory or the self-thinning line. In almost all cases, simulated volume increment was highest at maximum basal area and then decreased with decreasing basal area. Critical basal area, at which 95% of maximum volume increment c...
A density management diagram for Norway spruce in the temperate European montane region
Norway spruce is one of the most important conifer tree species in Europe, paramount for timber provision, habitat, recreation, and protection of mountain roads and settlements from natural hazards. Although natural Norway spruce forests exhibit diverse structures, even-aged stands can arise after disturbance or as the result of common silvicultural practice, including off-site afforestation. Many even-aged Norway spruce forests face issues such as senescence, insufficient regeneration, mechanical stability, sensitivity to biotic disturbances, and restoration. We propose the use of Density Management Diagrams (DMD), stand-scale graphical models designed to project growth and yield of even-aged forests, as a heuristic tool for assessing the structure and development of even-aged Norway spruce stands. DMDs are predicated on basic tree allometry and the assumption that self-thinning occurs predictably in forest stands. We designed a DMD for Norway spruce in temperate Europe based on wide-ranging forest inventory data. Quantitative relationships between tree- and stand-level variables that describe resistance to selected natural disturbances were superimposed on the DMD. These susceptibility zones were used to demonstrate assessment and possible management actions related to, for example, windfirmness and effectiveness of the protective function against rockfall or avalanches. The Norway spruce DMD provides forest managers and silviculturists a simple, easy-to-use, tool for evaluating stand dynamics and scheduling needed density management actions.
Growth Trends in European Forests
1996
Annual ring data collected from strict nature reserves and long-term permanent plots of the Finnish Forest Research Institute (ME1LA) did not reveal any longterm trend in the radial increment of Scots pine (Pinus sylvestris) in the southern part of Finland during the last 100 years. This result was supported by the analysis of stand wise increment data from permanent thinning experiments. The height development of dominant sample trees had been faster than that of previous site index curves. This was supposed to be mainly due to differences in the data of this study and of the index curves. According to our investigations, there were some indications of increasing productivity on some sample plots in the southernmost part of the country during the last 40 years. Possible reasons for non-existing growth trends are as follows: 1. The wide climatic variation of tree growth in northern latitudes could conceal the possible trend. The years 1961-1990 were slightly cooler than the years 19...
SSRN Electronic Journal
Heterogeneity of structure can increase mechanical stability, stress resistance and resilience, biodiversity and many other functions and services of forest stands. That is why many silvicultural measures aim at enhancing structural diversity. However, the effectiveness and potential of structuring may depend on the site conditions. Here, we revealed how the stand structure is determined by site quality and results from site-dependent partitioning of growth and mortality among the trees. We based our study on 90 mature, even-aged, fully stocked monocultures of Scots pine (Pinus sylvestris L.) sampled in 21 countries along a productivity gradient across Europe. A mini-simulation study further analyzed the site-dependency of the interplay between growth and mortality and the resulting stand structure. The overarching hypothesis was that the stand structure changes with site quality and results from the site-dependent asymmetry of competition and mortality. First, we show that Scots pine stands structure across Europe become more homogeneous with increasing site quality. The coefficient of variation and Gini coefficient of stem diameter and tree height continuously decreased, whereas Stand Density Index and stand basal area increased with site index. Second, we reveal a site-dependency of the growth distribution among the trees and the mortality. With increasing site index, the asymmetry of both competition and growth distribution increased and suggested, at first glance, an increase in stand heterogeneity. However, with increasing site index, mortality eliminates mainly small instead of all-sized trees, cancels the size variation and reduces the structural heterogeneity. Third, we modelled the site-dependent interplay between growth partitioning and mortality. By scenario runs for different site conditions, we can show how the site-dependent structure at the stand level emerges from the asymmetric competition and mortality at the tree level and how the interplay changes with increasing site quality across Europe. Our most interesting finding was that the growth partitioning became more asymmetric and structuring with increasing site quality, but that the mortality eliminated predominantly small trees, reduced their size variation and thus reversed the impact of site quality on the structure. Finally, the reverse effects of mode of growth partitioning and mortality on the stand structure resulted in the highest size variation on poor sites and decreased structural heterogeneity with increasing site quality. Since our results indicate where heterogeneous structures need silviculture interventions and where they emerge naturally, we conclude that these findings may improve system understanding and modelling and guide forest management aiming at structurally rich forests.
Forest stand growth dynamics in Central Europe have accelerated since 1870
Forest ecosystems have been exposed to climate change for more than 100 years, whereas the consequences on forest growth remain elusive. Based on the oldest existing experimental forest plots in Central Europe, we show that, currently, the dominant tree species Norway spruce and European beech exhibit significantly faster tree growth (þ32 to 77%), stand volume growth (þ10 to 30%) and standing stock accumulation (þ6 to 7%) than in 1960. Stands still follow similar general allometric rules, but proceed more rapidly through usual trajectories. As forest stands develop faster, tree numbers are currently 17–20% lower than in past same-aged stands. Self-thinning lines remain constant, while growth rates increase indicating the stock of resources have not changed, while growth velocity and turnover have altered. Statistical analyses of the experimental plots, and application of an ecophysiological model, suggest that mainly the rise in temperature and extended growing seasons contribute to increased growth acceleration, particularly on fertile sites
Mixing of complementary tree species may increase stand productivity, mitigate the effects of drought and other risks, and pave the way to forest production systems which may be more resource-use efficient and stable in the face of climate change. However, systematic empirical studies on mixing effects are still missing for many commercially important and widespread species combinations. Here we studied the growth of Scots pine (Pinus sylvestris L.) and European beech (Fagus sylvativa L.) in mixed versus pure stands on 32 triplets located along a productivity gradient through Europe, reaching from Sweden to Bulgaria and Spain to the Ukraine. Stand inventory and increment coring on the mainly 60-80 year-old trees and 0.02-1.55 ha sized, fully stocked plots provided insight how species mixing modifies the structure, dynamics and productivity compared with neighbouring pure stands. In mixture standing volume (+12 %), stand density (+20 %), basal area growth (+12 %), and stand volume growth (+8 %) were higher than the weighted mean of the neighbouring pure stands. Scots pine and European beech contributed rather equally to the overyielding and overdensity. In mixed stands mean diameter (+20 %) and height (+6 %) of Scots pine was ahead while both diameter and height growth of European beech were behind (-8 %). The overyielding and overdensity were independent of the site index, the stand growth and yield, and climatic variables despite the wide variation in precipitation (520-1,175 mm yr-1), mean annual temperature (6-10.5 °C), and the index de Martonne (28-61 mm °C-1) on the sites. Therefore this species combination is potentially useful for increasing productivity across a wide range of site and climatic conditions. Given the significant overyielding of stand basal area growth but the absence of any relationship with site index and climatic variables we hypothesize that the overyielding and overdensity results from several different types of interactions (light-, water-, and nutrient-related) that are all important in different circumstances. We discuss the relevance of the results for ecological theory and for the ongoing silvicultural transition from pure to mixed stands and their adaptation to climate change.
Mixing of complementary tree species may increase stand productivity, mitigate the effects of drought and other risks, and pave the way to forest production systems which may be more resource-use efficient and stable in the face of climate change. However, systematic empirical studies on mixing effects are still missing for many commercially important and widespread species combinations. Here we studied the growth of Scots pine (Pinus sylvestris L.) and European beech (Fagus sylvatica L.) in mixed versus pure stands on 32 triplets located along a productivity gradient through Europe, reaching from Sweden to Bulgaria and from Spain to the Ukraine. Stand inventory and taking increment cores on the mainly 60–80 year-old trees and 0.02–1.55 ha sized, fully stocked plots provided insight how species mixing modifies the structure, dynamics and productivity compared with neighbouring pure stands. In mixture standing volume (+12 %), stand density (+20 %), basal area growth (+12 %), and stand volume growth (+8 %) were higher than the weighted mean of the neighbouring pure stands. Scots pine and European beech contributed rather equally to the overyielding and overdensity. In mixed stands mean diameter (+20 %) and height (+6 %) of Scots pine was ahead, while both diameter and height growth of European beech were behind (-8 %). The overyielding and overdensity were independent of the site index, the stand growth and yield, and climatic variables despite the wide variation in precipitation (520–1175 mm year-1), mean annual temperature (6–10.5 0C), and the drought index by de Martonne (28–61 mm 0C-1) on the sites. Therefore, this species combination is potentially useful for increasing productivity across a wide range of site and climatic conditions. Given the significant overyielding of stand basal area growth but the absence of any relationship with site index and climatic variables, we hypothesize that the overyielding and overdensity results from several different types of interactions (light-, water-, and nutrient-related) that are all important in different circumstances. We discuss the relevance of the results for ecological theory and for the ongoing silvicultural transition from pure to mixed stands and their adaptation to climate change.
2012
ŠteFančík, i., StrMeň, S., podráZSký, S., Vacek, S. 2012. Growth responses of a Norway spruce (Picea abies [L.] Karst.) small pole-stage stand in a region exhibiting extensive decline of allochthonous spruce forests to differentiated thinning. Folia oecol., 39: 77–87. The paper deals with assessment of the growth responses of a 26-year old Norway spruce (Picea abies [L.] Karst.) small pole-stage stand, situated in a region affected by mass dying of spruce monocultures, dependent on the different treatment intensity. The intervention was realized at a stand age of 22 years – in order to decrease its density to 1,600 and 1,100 individuals per hectare. Characteristics of quantitative production (number of trees, basal area, stand volume, diameter increment) were analysed and compared among the presented variants of treatment. The special attention was paid to the assessment of target trees (400 individuals per hectare). The results have confirmed correctness of heavy treatments in spru...
In a forest stand, competition plays a central role, affecting individual growth. The size–growth relationship (SGR) indicates whether large trees grow proportionally more than (asymmetric SGR), equal to (symmetric), or less than (inversely asymmetric) smaller trees. SGR is thus an indicator of the growth partitioning and competition intensity within a stand. Using tree-ring analysis, we investigated long-term trends and interannual variability of SGR in several Norway spruce (Picea abies (L.) Karst.) stands in the Paneveggio Forest (eastern Italian Alps) over a 100-year period. The study plots were characterized by different stand structures (one multilayered and two monolayered) and disturbance histories (different dates of logging). Logging conducted until the 1940s induced an inversely asymmetric SGR in all the plots. During the successive five decades, in the monolayered plots, it shifted to direct asymmetric (plot 1) and to symmetric (plot 2). In the multilayered plot (plot 3), SGR remained inversely asymmetric. A direct effect of climate on SGR interannual variability was not found. However, fast-growing trees had a stronger climatic signal than slow-growing trees, indicating that growth rate affects tree response to climate. Moreover, we observed that sensitivity to climate was reduced in the monolayered plots over the study period, possibly as a consequence of increased competition.