Biomass equations for sessile oak (Quercus petraea (Matt.) Liebl.) and hornbeam (Carpinus betulus L.) in aged coppiced forests in southwest Germany
Highlights
► Biomass equations for Quercus petraea, Carpinus betulus from coppice were developed. ► Power functions were used to estimate total aboveground woody biomass. ► Simplicity of biomass equations facilitate a wide-spread application. ► For accurate biomass estimations coppice specific equations are needed. ► Comparative calculations show that coppice functions can be used site independent.
Introduction
Coppicing is a traditional silvicultural management system applied all over the world. It is mostly used for the production of firewood and various non-timber forest products [1], [2], [3] whereas short rotation coppice systems are specifically employed to produce woody biomass for energy purposes only [4]. In many European countries, this practice was abandoned in the first half of the last century due to socio-economic changes [4], [5]. Managed coppiced forests (i.e. younger than 40 years) cover only 750 km² of Germany which represents 0.7% of the total forest area [6]. However, the area of abandoned, older coppice forests is assumed to amount to several thousand km². Because most privately owned forests are not inventoried, the actual area is not certain. These aged oak coppice forests represent a potential biomass source of unknown magnitude.
In rural environments, coppice stands often represent important elements of the cultural landscapes until today. The abandonment of periodic coppicing leads to a process of transformation during which the stands lose their typical coppice characteristics like multiple stem structure and increasingly resemble high forests in which individual trees have originated from seed. Subsequently, the specific ecological value of coppice forests [7], [8], [9] decreases and an important element of the cultural landscape gradually disappears. One way of preserving the ecological, cultural and historical value of aged coppice forests would be to resume coppicing, which would additionally benefit light and warmth demanding species and can increase biodiversity [7], [9]. Hence, the reintroduction of coppice management may also be motivated by concerns about biodiversity and landscape values [9].
Ongoing initiatives by the European Union (EU) call for a substantial increase in the use of renewable energy sources. It is aimed that by 2020 one fifth of the European energy consumption will be from renewable sources (European Parliament 2009: directive 2009/28/EG [10]). Of all renewable energy currently consumed in the EU, 47% is generated from forest biomass (i.e. wood and wood waste [11]). The resulting demand for biomass as an energy source has stimulated interest to resume coppicing of forests that had undergone this management in the past [12], [13]. However, aged coppice forests have often not been properly inventoried, particularly not on private land, and hence their potential contribution to biomass supply is difficult to quantify. One problem associated with the inventory of biomass in this type of forests is the lack of suitable biomass equations.
Based on strong relationships between tree weight and dendrometric values, like diameter at breast height (dbh), tree height or green crown height, biomass equations have been developed for many tree species around the world e.g. [14], [15], [16], [17]. However, only very few equations exist for trees originating from coppice. These trees differ from those managed in high forests in terms of crown size and stem form [18]. Owing to the origin of stems and since coppice forests are commonly not thinned, many trees have small crowns and multiple stems [19]. Accordingly, to calculate biomass of coppice trees, equations developed for trees grown in high forests may be less accurate.
There are no published biomass equations for aged oak coppice stands in Central Europe. It is also questionable, if biomass equations for younger coppice forests or those from other European regions [20], [21], [22], [23] could be used instead. Extrapolation of biomass equations to other regions may lead to inaccurate predictions (e.g. [24]). These differences can be explained by a number of factors, like e.g. silvicultutral practices, genetic differences and the influence of different site conditions.
The objective of this study was to develop easily applicable equations for the calculation of single tree biomass of the most common coppice forest species in south-western Germany, namely sessile oak (Quercus petraea) and hornbeam (Carpinus betulus). To facilitate the assessment of biomass removal by different harvesting intensities, separate equations were developed for different tree compartments such as for example stem with and without bark, stem and branches with a diameter larger than 7 cm and the whole tree (without leaves). In addition, we compared the allometric equations for oak from this study with equations from the literature to assess how these might differ between regions and silvicultural systems and how large the error for biomass estimates might be, if equations from the literature are applied.
Section snippets
Study sites
In the federal state of Rhineland-Palatinate (south-west Germany), aged coppice forests are very common. In this federal state, the forest area originating from coppice is assumed to cover 1600 km² (19.8% of the federal states total forest area [25]). From the landscapes characterized by aged coppice forests, two representative stands were selected.
Selection criteria for experimental stands were stand age (stands were representative of the dominant age class of the states aged coppice forests)
Biomass equations
For total tree dry mass, no significant differences (p > 0.05) were found between the two study sites for both tree species. Therefore, allometric equations were calculated after pooling of the species specific data of both sites.
Power models were found to be most suitable for the prediction of tree compartment dry mass as a function of dbh (with the exception of the hornbeam compartment “small wood”; Table 3). Strong relations (adjusted R² > 0.8) were found for oak between biomass of stem
Biomass equations
The power functions using solely dbh were able to explain 97% and 92% of the variability in the observed “total aboveground woody biomass” of oak and hornbeam, respectively. The equations for the oak compartments “heartwood” and “bark” had similarly good fits. With a few exceptions (T, S, BW, BW7) all remaining equations accounted for a minimum 70% of the variation among trees and were at least significant at the 0.01% level (Table 3).
These findings are in accordance with Zianis & Mecuccini [14]
Conclusions
In this study, power functions were developed to estimate total aboveground woody biomass of trees or tree compartments using only dbh as an easily measurable input variable. This simplicity of biomass equations might facilitate a more wide-spread application by forest practitioners to estimate biomass of different tree compartments (e.g. stem, stem bark, branchwood, small wood, twigs) rather than only stem volume.
Application of biomass equations developed for other coppice forest resulted in
Acknowledgments
The authors are grateful to the Deutsche Bundesstiftung Umwelt (DBU) for funding this project (file reference 25954-33/0). Special thanks go to Dr. Herbert Kraft and Ralf Dübbers (forest administration Baumholder) and to Ludwig Walter, Susanne Gühne and Rainer Mohr (forest administration Nastätten) for their substantial support during the field work. We also gratefully acknowledge statistical advice from Markus Lingenfelder, Stefanie Gärtner, Timo Kahl and Thomas Smaltschinski. Bernhard Thiel
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Both authors contributed equally to this work.