Petteri Muukkonen

Indirect methods of large-scale forest biomass estimation

Forest biomass and its change over time have been measured at both local and large scales, an example for the latter being forest greenhouse gas inventories. Currently used methodologies to obtain stock change estimates for large forest areas are mostly based on forest inventory information as well as various factors, referred to as biomass factors, or biomass equations, which transform diameter, height or volume data into biomass estimates. However, while forest inventories usually apply statistically sound sampling and can provide representative estimates for large forest areas, the biomass factors or equations used are, in most cases, not representative, because they are based on local studies. Moreover, their application is controversial due to the inconsistent or inappropriate use of definitions involved. There is no standardized terminology of the various factors, and the use of terms and definitions is often confusing. The present contribution aims at systematically summarizing the main types of biomass factors (BF) and biomass equations (BE) and providing guidance on how to proceed when selecting, developing and applying proper factors or equations to be used in forest biomass estimation. The contribution builds on the guidance given by the IPCC (Good practice guidance for land use, land-use change and forestry, 2003) and suggests that proper application and reporting of biomass factors and equations and transparent and consistent reporting of forest carbon inventories are needed in both scientific literature and the greenhouse gas inventory reports of countries.

Generalized allometric volume and biomass equations for some tree species in Europe

Since biomass is one of the key variables in ecosystem studies, widespread effort has aimed to facilitating its estimation. Numerous stand-specific volume and biomass equations are available, but these cannot be used for scaling up biomass to the regional level where several age-classes and structural types of stands coexist. Therefore simplified generalized volume and biomass equations are needed. In the present study, generalized biomass and volume regression equations were developed for the main tree species in Europe. These equations were based on data compiled from several published studies and are syntheses of the published equations. The results show that these generalized equations explain 64–99% of the variation in values predicted by the original published equations, with higher values for stem than for crown components.

Calibrated pollen accumulation rates as a basis for quantitative tree biomass reconstructions

Recent investigations show that the pollen accumulation rate (PAR) of the common tree taxa is directly related to the biomass and, by inference, to the population size of the taxa around the study site. Fossil PAR records preserved in lakes provide therefore a potential proxy for quantitative biomass and population reconstructions. We use the high-resolution PAR records obtained from two accurately dated lake sediment cores in Finland to generate quantitative Holocene biomass records for Pinus, Picea and Betula, the most common tree taxa of the European Boreal forest. PAR values were calibrated to biomass values by comparing the modern PAR values with the modern biomass values and assuming a linear relationship between the past PAR and biomass values. The obtained PAR and biomass values and trends are remarkably coherent between the two records. Pinus has a stable Holocene biomass size and its modern biomass, about 20 t/ha, corresponds with the natural Pinus biomass in the study regions. In contrast, Picea immigrated from the East during the mid Holocene, had a maximum biomass, 50—60 t/ha, at 3500—1000 cal. yr BP, and declined strongly during the last 1500—1000 years as a result of increased human activity and related rise of fire frequency. Thus, the modern Picea biomass in the study regions, about 22 t/ha, is only 35—40% of the natural Picea biomass. The results of this pilot study demonstrate the potential of the calibrated PAR data in quantitative biomass and population reconstructions. Such reconstructions can provide fresh insights into the structure of past plant communities and, when combined with records reflecting palaeoclimates, natural disturbances, and human activity, can help to disentangle the long-term importance of different enviromental drivers to changes in plants populations and ecosystems.

Needle biomass turnover rates of Scots pine (Pinus sylvestris L.) derived from the needle-shed dynamics

To understand carbon cycle and flows of forests, accurate information on tree-component-specific litter production of trees is needed. In the ecosystem models, the litterfall of living trees is usually predicted by the biomass component by average amounts corresponding to site conditions or by multiplying the biomass of the growing stock by the component-specific biomass turnover rate. In this study, the rates of needle biomass turnover of Scots pine (Pinus sylvestris L.) were derived from the needle-shed dynamics. When the rates for needle litter production were modelled, the weighting and yellowing effects were taken into account. The annual biomass turnover rates of needles for southern and northern Finland are 0.21 and 0.10, respectively. Species-specific estimation of litter production is essential for understanding the carbon cycle and flows of forests. Biomass turnover rates can provide useful litter production estimates for large areas with average biomass values as a source of data.

Differences in the forest landscape structure along the Finnish–Russian border in southern Karelia

Abstract This study describes forest landscape fragmentation and connectivity along the Finnish–Russian border near the Karelian Isthmus. The landscape pattern was analysed using classification data based on Landsat ETM+ and Landsat TM images in combination with systematic surveys in Finland (Finnish National Forest Inventory) (n=546) and the authors’ own fieldwork data in Russia (n=101). On the Finnish side the forest patches are significantly smaller than on the Russian side. In addition, the Finnish forests landscape is more scattered and distances between patches of the same forest type are longer. The Russian side is more dominated by broadleaved and mixed forest stands. The disparities are due to differences in forestry policy and traditions of forest practices. The growing conditions of the areas are similar. The habitat fragmentation and habitat connectivity are important issues because the Karelian Isthmus is one of three main corridors and migrating routes connecting large Russian boreal taiga forests and their fauna and flora with Finnish isolated boreal forests.