Current issue: 55(3)
Under compilation: 55(4)
Fresh and herb-rich upland forest sites in the north-western part of the central boreal vegetation zone in Finland were studied with respect to vegetation structure and vegetation-environment relationships (soil, stand characteristics). Two fresh heath vegetation data sets, one from the northern boreal zone and the other from the central boreal zone, were compared with the data of this study using multivariate methods.
The variation in heath forest vegetation within the climatically uniform area was mainly determined by the fertility of the soil (primarily Ca and Mg) and the stage of stand development. N, P and K content of the humus layer varied little between the vegetation classes. Fertile site types occurred, in general, on coarse-textured soils than infertile site types, may be due to the fact that the sample plots were located in various bedrock and glacial till areas, i.e. to sampling effects.
The place of the vegetational units of the study area in the Finnish forest site type system is discussed. The vegetation of the area has features in common with the northern boreal zone as well as the southern part of the central boreal vegetation zone. The results lend some support to the occurrence of a northern Myrtillus type or at least that intermediate form of fresh and herb-rich mineral soil sites commonly occur in the studied area. It is argued that the older name Dryopteris-Myrtillus type is more suitable than Geranium-Oxalis-Myrtillus type for herb-rich heath sites in the study area.
The article is a lectio praecursoria held on May 18, 1968 at the University of Helsinki. It deals with some aspects connected with the adaptation of mathematic-statistical methods and in particular with multivariate methods. Among these regression, factor, and principal-component analysis are mostly used by the Finnish forest economists.
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Biogeographical patterns of the Scolytidae in Fennoscandia and Denmark, based on species incidence data from the approximately 70 km x 70 km quadrats (n = 221) used by Lekander et al. (1977), were classified to environmental variables using multivariate methods (two-way indicator species analysis, detrended correspondence analysis, canonical correspondence analysis).
The distributional patterns of scolytid species composition showed similar features to earlier presented zonations based on vegetation composition. One major difference, however, was that the region was more clearly divided in an east-west direction. Temperature variables associated with the location of the quadrat had the highest canonical coefficient values on the first axis of the CCA. Although these variables were the most important determinants of the biogeographical variation in the beetle species assemblages, annual precipitation and the distribution of Picea abies also improved the fit of the species data.
Samples with the most deviant rarity and typicality indices for the scolytid species assempblages in each quadrat were concentrated in several southern Scandinavian quadrats, in some quadrats in northern Sweden, and especially on the Swedish islands (Öland, Gotland, Gotska Sandön) in the Baltic Sea. The use of rarity indices which do not take the number of species per quadrat, also resulted high values for areas near Stockholm and Helsinki with well-known faunas. Methodological tests in which the real changes in the distribution of Ips acuminatus and I. amitinus were used as indicators showed that the currently available multivariate methods are sensitive to small faunal shifts even, and thus permit analysis of the fauna in relation to environmental changes. However, this requires more detailed monitoring of the species’ distributions over longer time spans.
Distribution of seven species (Scolytus intricatus, S. laevis, Hylurgops glabratus, Crypturgus cinereus, Pityogenes salasi, Ips typographus, and Cyleborus dispar) were predicted by logistic regression models using climatic variables. In spite of the deficiencies in the data and the environmental variables selected, the models were relatively good for several but not for all species. The potential effects of climate change on bark beetles are discussed.
The PDF includes a summary in Finnish.
Multivariate methods are used to classify pine mires on the basis of edaphic properties into fertility groups in order to estimate the effect of fertilization in relation to site fertility. The data is based on two field inventories of NPK fertilization experiment in which 2,624 sample trees on 164 sample plots from 19 experimental fields were measured on Scots pine (Pinus sylvestris L.) dominated stands. The edaphic properties (total contents of nutrients and related properties) are based on 1,350 volumetric sub-samples of fertilized and non-fertilized control plots.
In a DECORANA ordination, based on standardised volumetric soil variables N-P and acid-base gradients jointly describing trophic status were distinguished. Mainly on the basis of these two gradients a TWINSPAN analysis divided the material into five edaphic groups. To independently allocate sample plots into fertility groups, discriminating multiple regressions were formed using the TS edaphic groups as class variable.
The effect of N, P, K, NP, NK, PK, and NPK treatments on tree growth was estimated on the basis of change in relative basal area increment during two growth periods. During five-year period immediately after fertilization N and P treatments evoked the strongest increase in growth. On the nutrient poor sites, the effect was almost double that on the fertile sites. The effect of N was short lasting while the P treatment still affected growth after 5–11 years. Although K treatment had little influence on tree growth needle samples collected 11 years after fertilization indicated increased K uptake on fertilized plots.
Generally, the effect of fertilization on absolute stand volume growth was small. During the 11-year study period the total increase in growth gained with NPK was some 3–4 m3/ha. Despite strong relative response of individual sample trees, due to low stand volume fertilization (and drainage) had practically no effect on volume growth on the sites of lowest fertility.
The PDF includes a summary in Finnish.