Jerzy Skrzyszewski

Species proportions by area in mixtures of Scots pine (Pinus sylvestris L.) and European beech (Fagus sylvatica L.)

Scots pine (Pinus sylvestris L.) and European beech (Fagus sylvatica L.) dominate many of the European forest stands. Also, mixtures of European beech and Scots pine more or less occur over all European countries, but have been scarcely investigated. The area occupied by each species is of high relevance, especially for growth evaluation and comparison of different species in mixed and monospecific stands. Thus, we studied different methods to describe species proportions and their definition as proportion by area. 25 triplets consisting of mixed and monospecific stands were established across Europe ranging from Lithuania to Spain in northern to southern direction and from Bulgaria to Belgium in eastern to western direction. On stand level, the conclusive method for estimating the species proportion as a fraction of the stand area relates the observed density (tree number or basal area) to its potential. This stand-level estimation makes use of the potential from comparable neighboring monospecific stands or from maximum density lines derived from other data, e.g. forest inventories or permanent observations plots. At tree level, the fraction of the stand area occupied by a species can be derived from the proportions of their crown projection area or of their leaf area. The estimates of the potentials obtained from neighboring monospecific stands, especially in older stands, were poorer than those from the maximum density line depending on the Martonne aridity index. Therefore, the stand-level method in combination with the Martonne aridity index for potential densities can be highly recommended. The species’ proportions estimated with this method are best approximated by the proportions of the species’ leaf areas. In forest practice, the most commonly applied method is an ocular estimation of the proportions by crown projection area. Even though the proportions of pine were calculated here by measuring crown projection areas in the field, we found this method to underestimate the proportion by 25% compared to the stand-level approach.

EuMIXFOR empirical forest mensuration and ring width data from pure and mixed stands of Scots pine (Pinus sylvestris L.) and European beech (Fagus sylvatica L.) through Europe

Key messageThis data set provides unique empirical data from triplets of Scots pine (Pinus sylvestrisL.) and European beech (Fagus sylvaticaL.) across Europe. Dendrometric variables are provided for 32 triplets, 96 plots, 7555 treesand 4695 core samples. These data contribute to our understanding of mixed stand dynamics.Dataset access athttp://dx.doi.org/10.5061/dryad.8v04m. Associated metadata available athttps://metadata-afs.nancy.inra.fr/geonetwork/apps/georchestra/?uuid=b3e098ca-e681-4910-9099-0e25d3b4cd52&hl=eng.

Crookedness of pedunculate oak (Quercus robur L.) growing under a canopy of Scots pine (Pinus sylvestris L.)

Natural regeneration of pedunculate oak growing under a canopy of Scots may be used for conversion into a mixed or predominantly broadleaved forest. From an economic perspective it is desirable that the oaks have straight stems. In this paper we present a case study for analysing oak stem curvature and its causes. The study was conducted in a mature pine stand with understorey oaks of age ca. 60 years in Poland. The oaks were classified into two main groups as either straight or crooked. The following variables were measured or assessed for the oaks: (1) stem curvature (crookedness), total tree height, diameter at breast height (DBH) and some tree crown characteristics, (2) the growth of DBH and height in each year of the life of each tree and (3) the competitive pressure of surrounding trees. Durable stem curvatures were formed at the culmination of the height increment. The first 20 years of the life of the oak were crucial in terms of stem quality. The annual height increment was larger in the years when the curvature was formed than in adjacent years. The factors that caused crooked stems were the same for straight and crooked oaks, but the magnitude of the response was different. When planning the conversion of Scots pine into oak, full overhead light should be provided as early as possible, but not later than 20 years since the establishment of the regeneration.

Regeneration patterns of the late-successional Abies alba Mill.: inhibition in monospecific stands and colonization in mixed stands

Key messageInAbies albaMill. stands and mixed stands ofA. albaandPicea abiesL. (H. Karst), microsites neighbouring the trunks of adult trees were more conducive toA. albaregeneration. Although at the stand level, the effect ofFagus sylvaticaL. was positive; the local effect of the adultF. sylvaticaneighbourhood was insignificant. Hence, forming mixed stands with a fine-grained mosaic of admixed species might better facilitate natural regeneration ofA. albathan monospecific stands.ContextThe establishment of natural regeneration in Abies alba Mill. stands is a slow, spatially heterogeneous and stochastic process. Recent studies based on inventory data indicate that A. alba more readily regenerates in mixed stands than in monospecific stands.AimsThe objective was to examine how this positive association evidenced at the stand level operates on the scale of microsites with contrasting local species composition and stand density.MethodsIn 8 monospecific and 22 mixed stands with Fagus sylvatica L. or Picea abies L. (H. Karst), microsites with a contrasting density of A. alba seedlings were selected and compared in terms of local species composition, stand density, canopy characteristics and topsoil properties.ResultsIn A. alba stands, seedling density was positively associated with the proximity of adult trees. In mixed stands of A. alba and P. abies, adult trees of both species exerted a positive effect on A. alba regeneration, but the P. abies neighbourhood influenced regeneration occurrence more strongly than the A. abies neighbourhood. In mixtures with F. sylvatica, however, the effect of local stand density and local species composition was not evidenced at all.ConclusionAlthough at the stand level, P. abies and F. sylvatica exert a positive effect on A. alba regeneration, on the microsite scale, their influences differ. In stands with a dominance of A. alba, the hampered seedling establishment in gaps may be considered an inhibitive effect that facilitates the emergence of other species.

Acer Pseudoplatanus L., Tilia Cordata Mill. and Pinus Sylvestris L. as Valuable Tree Species in the Carpathian Forests

Sycamore maple, little-leaf linden, and Scots pine occurring in unique mixed stands, such as beech and sycamore maple in the Bieszczady Mountains, linden forest in the Obrozyska Reserve (the Beskid Sądecki Mountains), and scattered Carpathian pine forests, were the subject of this study. It was found that sycamore maple can be a highly productive admixture and a co-dominant or even dominant species in beech forests as a protective species of the upper timberline at altitudes between 930 and 1,160 m. Little-leaf linden in stands where site conditions meet its requirements, especially in the lower part of the lower mountain zone at altitudes up to 600–700 m, is a suitable admixture or even co-dominant species that increases productivity. In the Polish Carpathian forests three pine population groups were distinguished on the basis of morphological (cone) traits—lowland, foothill, and mountain group—which also varied according to timber quality, stem, and crown traits, as well as copper (Cu), iron (Fe), and potassium (K) content in needles. Pine is a very good nursing tree species that enables other tree species, especially fir, to occur among pine trees or underneath their canopies.