Bark Thickness and Heights of the Bark Transition Area of Scots Pine

Forests ◽  
2021 ◽  
Vol 12 (10) ◽  
pp. 1386
Author(s):  
Florian Wilms ◽  
Nils Duppel ◽  
Tobias Cremer ◽  
Ferréol Berendt

The estimation of forest biomass is gaining interest not only for calculating harvesting volumes but also for carbon storage estimation. However, bark (and carbon) compounds are not distributed equally along the stem. Particularly when looking at Scots pine, a radical change in the structure of the bark along the stem can be noted. At the bark transition area, the bark changes from thick and rough to thin and smooth. The aim of our study was (1) to analyze the height of the bark transition area where the bark structure changes and (2) to analyze the effect of cardinal direction on the bark thickness. Regression analyses and forward selection were performed including measured tree height, DBH, bark thickness, crown base height and upper and lower heights of the bark transition areas of 375 trees. While the cardinal direction had no effect on bark thickness, DBH was found to have a significant effect on the heights of the bark transition areas, with stand density and tree height having a minor additional effect. These variables can be used to estimate timber volume (without bark) with higher accuracy and to predict the carbon storage potential of forest biomass according to different tree compartments and compounds.

2012 ◽  
Vol 9 (8) ◽  
pp. 3381-3403 ◽  
Author(s):  
T. R. Feldpausch ◽  
J. Lloyd ◽  
S. L. Lewis ◽  
R. J. W. Brienen ◽  
M. Gloor ◽  
...  

Abstract. Aboveground tropical tree biomass and carbon storage estimates commonly ignore tree height (H). We estimate the effect of incorporating H on tropics-wide forest biomass estimates in 327 plots across four continents using 42 656 H and diameter measurements and harvested trees from 20 sites to answer the following questions: 1. What is the best H-model form and geographic unit to include in biomass models to minimise site-level uncertainty in estimates of destructive biomass? 2. To what extent does including H estimates derived in (1) reduce uncertainty in biomass estimates across all 327 plots? 3. What effect does accounting for H have on plot- and continental-scale forest biomass estimates? The mean relative error in biomass estimates of destructively harvested trees when including H (mean 0.06), was half that when excluding H (mean 0.13). Power- and Weibull-H models provided the greatest reduction in uncertainty, with regional Weibull-H models preferred because they reduce uncertainty in smaller-diameter classes (≤40 cm D) that store about one-third of biomass per hectare in most forests. Propagating the relationships from destructively harvested tree biomass to each of the 327 plots from across the tropics shows that including H reduces errors from 41.8 Mg ha−1 (range 6.6 to 112.4) to 8.0 Mg ha−1 (−2.5 to 23.0). For all plots, aboveground live biomass was −52.2 Mg ha−1 (−82.0 to −20.3 bootstrapped 95% CI), or 13%, lower when including H estimates, with the greatest relative reductions in estimated biomass in forests of the Brazilian Shield, east Africa, and Australia, and relatively little change in the Guiana Shield, central Africa and southeast Asia. Appreciably different stand structure was observed among regions across the tropical continents, with some storing significantly more biomass in small diameter stems, which affects selection of the best height models to reduce uncertainty and biomass reductions due to H. After accounting for variation in H, total biomass per hectare is greatest in Australia, the Guiana Shield, Asia, central and east Africa, and lowest in east-central Amazonia, W. Africa, W. Amazonia, and the Brazilian Shield (descending order). Thus, if tropical forests span 1668 million km2 and store 285 Pg C (estimate including H), then applying our regional relationships implies that carbon storage is overestimated by 35 Pg C (31–39 bootstrapped 95% CI) if H is ignored, assuming that the sampled plots are an unbiased statistical representation of all tropical forest in terms of biomass and height factors. Our results show that tree H is an important allometric factor that needs to be included in future forest biomass estimates to reduce error in estimates of tropical carbon stocks and emissions due to deforestation.


Author(s):  
Ferréol Berendt ◽  
Erik Pegel ◽  
Lubomir Blasko ◽  
Tobias Cremer

AbstractBark characteristics are not only used in the forest-wood supply chain, for example to calculate standing volumes, but also to transform wood volumes and masses. In this study, bark thickness, bark volume and bark mass were analyzed on the basis of 150 Scots pine discs, with a mean diameter of 13 cm. The mean double bark thickness was 3.02 mm, the mean bark volume proportion was 5.6% and mean bark mass proportion was 3.3%. Bark proportions were significantly affected by the log-specific variables ‘diameter over bark’, ‘proportion of bark damage’ and ‘double bark thickness’.


2020 ◽  
Vol 3 (1) ◽  
pp. 66
Author(s):  
Ferréol Berendt ◽  
Erik Pegel ◽  
Lubomir Blasko ◽  
Tobias Cremer

The wood of Scots pine (Pinus sylvestris L.) shows good properties as building and construction timber but also as furniture or pulp and paper, and thus, is one of the most commercially important European tree species. Scots pine are mostly harvested and processed with a high degree of mechanization. In Northeast Germany (federal states of Brandenburg and Berlin), 36% of harvested Scots pine have a diameter at breast height (DBH) between 7 and 19.9 cm. As a typical industrial wood assortment, a large proportion of the resulting small-sized logs are used in the wood industry to produce boards. Although bark is considered a by-product or waste product of the industry, no actual study has quantified the bark thickness, bark volume, bark mass and bark damage of such Scots pine logs. Therefore, the bark characteristics from 50 logs from 10 different piles were analyzed. Bark volume was quantified using the water displacement method, bark mass by weighing, bark thickness with a precision caliper and bark damage by tape measurements. The diameters of the analyzed 150 log discs were normally distributed and the mean value was 12.9 cm. The results showed average bark damages from 12.0%, which were mostly caused during the felling and processing of logs with the harvester. No significant correlation was found between double bark thickness (mean: 3.0 mm) and the diameter; whereas fresh bark volume (mean: 5.6%) and dry bark mass (mean: 3.3%) were significantly affected by the diameter. As shown for spruce by other authors, bark characteristics may change over time and therefore, should be measured regularly. Moreover, it was shown that bark parameters are site dependent. Thus, quantifying bark characteristics for economically important tree species at both the local and national scale is of great relevance. More detailed analyzes are described by Berendt et al. (2021) [1].


IAWA Journal ◽  
2000 ◽  
Vol 21 (1) ◽  
pp. 31-40 ◽  
Author(s):  
Teresa Quilhó ◽  
Helena Pereira ◽  
Hans Georg Richter

The axial variation of bark thickness and quantitative anatomical features of Eucalyptus globulus bark were analysed for one site based on individual measurements of ten 15-year-old trees at six height levels (DBH, 5%, 15%, 35%, 55% and 75% of total tree height). The parameters studied were: length, tangential diameter and percentage of sieve tubes; length, width, cell wall thickness and percentage of fibres; height and percentage of rays; percentage of sclereids in the secondary phloem. Bark thickness decreases from base to top of the tree. Fibre width and wall thickness decrease from base upwards. No distinct axial patterns of variation were observed for the other biometric variables studied. Parenchyma is the main cell type of the bark (50%) followed by fibres (27.9%), rays (12.1%), sieve tubes (2.7%), and sclereids (7.3%). The cell type proportions vary significantly within the tree, i.e., parenchyma, ray and sclereid proportions decrease, fibre and sieve tube proportions increase towards the top of the tree.


2021 ◽  
Vol 771 ◽  
pp. 144834
Author(s):  
Michał H. Węgrzyn ◽  
Patrycja Fałowska ◽  
Joanna Kołodziejczyk ◽  
Karima Alzayany ◽  
Piotr Wężyk ◽  
...  

2017 ◽  
Vol 07 (02) ◽  
pp. 255-269 ◽  
Author(s):  
Faith Kagwiria Mutwiri ◽  
Patroba Achola Odera ◽  
Mwangi James Kinyanjui

Forests ◽  
2020 ◽  
Vol 11 (4) ◽  
pp. 443 ◽  
Author(s):  
Lu Liu ◽  
Fuping Zeng ◽  
Tongqing Song ◽  
Kelin Wang ◽  
Hu Du

Understanding the driving factors of forest biomass are critical for further understanding the forest carbon cycle and carbon storage management in karst forests. This study aimed to investigate the distribution of forest aboveground biomass (AGB) and the effects of stand structural and abiotic factors on AGB in karst forests in Southwest China. We established a 25 ha plot and sampled all trees (≥1 cm diameter) in a subtropical mixed evergreen–deciduous broadleaf forest. We mapped the forest biomass distribution and applied a variation of partitioning analysis to examine the topographic, stand structural, and spatial factors. Furthermore, we used structural equation models (SEM) to test how these variables directly and/or indirectly affect AGB. The average AGB of the 25 ha plot was 73.92 Mg/ha, but that varied from 3.22 to 198.11 Mg/ha in the 20 m × 20 m quadrats. Topographic, stand structural, and spatial factors together explained 67.7% of the variation in AGB distribution. The structural variables (including tree density and the diameter at breast height (DBH) diversity) and topographic factors (including elevation, VDCN (vertical distance to channel network), convexity, and slope) were the most crucial driving factors of AGB in the karst forests. Structural equation models indicated that elevation, tree density, and DBH diversity directly affected AGB, and elevation also indirectly affected AGB through tree density and DBH diversity. Meanwhile, AGB was indirectly influenced by VDCN, convexity, and slope. The evaluation of stand structural and abiotic drivers of AGB provides better insights into the mechanisms that play a role in carbon storage in karst forests, which may assist in improving forest carbon management.


Forests ◽  
2020 ◽  
Vol 11 (12) ◽  
pp. 1316
Author(s):  
Luka Krajnc ◽  
Jožica Gričar

The research study examined the effect of tree properties (crown social class, diameter at breast height (DBH), and tree height) on bark thickness (BT) and sapwood moisture content (SMC) in Norway spruce (Picea abies (L.) H. Karst.). Both examined variables were shown to be positively affected by DBH and tree height. The relationship between DBH and SMC varied among crown social classes, while the relationship between DBH and BT was relatively constant across crown social classes. Crown social class had a relatively small effect on BT and SMC, having a more pronounced effect on SMC than on BT. The relationship between tree height and BT did not vary across crown social classes, while the relationship between SMC and tree height was found to change slightly across crown social classes. Measurements of BT and SMC in the field are affordable, fast, and easy to use. Both variables could potentially be used to improve predictions of bark beetle attacks, as they reflect the physiological state of an individual tree.


1983 ◽  
Vol 13 (3) ◽  
pp. 372-383 ◽  
Author(s):  
W. Carter Johnson ◽  
David M. Sharpe

Records of merchantable forest volumes can be used to estimate rates of carbon storage or depletion using a ratio to convert merchantable weights to total forest biomass (T/M ratio). We present evidence that the T/M ratio used to estimate carbon storage in midlatitude forests has been seriously underestimated by neglecting carbon in trees of unmerchantable size and quality and in coarse and fine litter. Ratios for forest types and size classes in Virginia based on detailed plot-level analysis ranged from 2.1 to 5.0; the mean weighted ratio of 2.7 was 55% greater than a ratio currently in use. More general analysis indicated that the T/M ratio for Virginia was representative of forests of the East; forests of the western United States were comparable to those of the East when woody debris was included in the estimate of total biomass. Application of the weighted ratio to growth of United States forests during 1952–1977 yielded a per-annum accretion of carbon in biomass (excluding soil carbon) of 0.15 Gt C•year−1, about 10% of the 1.6–1.9 Gt C•year−1 computed for midlatitude forests. More complete studies of counterbalancing carbon losses from forests, particularly losses in litter and soils after forest harvest and conversion to agriculture, are needed before the source or sink nature of midlatitude forests can be determined with confidence.


2017 ◽  
Vol 2017 ◽  
pp. 1-7 ◽  
Author(s):  
Süleyman Gülcü ◽  
Nebi Bilir

Tree height, basal diameter, and survival were examined in thirteen-year-old provenance test established by 30 seed sources of Scots pine (Pinus sylvestrisL.) at two exotic sites of the species in Southern part of Turkey. Variations within provenance and among provenances and relations among the traits were estimated to compare Scots pine provenance and two other native species. Averages of tree height and basal diameter were 350 cm and 52.7 mm in Aydogmus site and 385 cm and 51.2 mm in Kemer site, respectively. There were large differences within and among provenances for the characters. Sites were similar (p>0.05) for the characters, while there were significant differences (p≤0.05) among provenances within site according to results of variance analysis (ANOVA). Scots pine provenances were higher and had more thickness than that of black pine (Pinus nigraArnold) and Taurus cedar (Cedrus libaniA. Rich.) which were natural species of the region. There were positive and significant (p<0.05) correlations between height and basal diameter in the species. Average survivals were 56% and 35% of the provenances in the sites. They were 71% and 11% in black pine and 53% in Taurus cedar for the sites respectively.


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