Estimations of total ecosystem carbon pools distribution and carbon biomass current annual increment of a moist tropical forest

With increasing CO₂ in the atmosphere, there is an urgent need of reliable estimates of biomass and carbon pools in tropical forests, most especially in Africa where there is a serious lack of data. Information on current annual increment (CAI) of carbon biomass resulting from direct field measurements is crucial in this context, to know how forest ecosystems will affect the carbon cycle and also to validate eddy covariance flux measurements. Biomass data were collected from 25 plots of 13 ha spread over the different vegetation types and land uses of a moist evergreen forest of 772,066 ha in Cameroon. With site-specific allometric equations, we estimated biomass and aboveground and belowground carbon pools. We used GIS technology to develop a carbon biomass map of our study area. The CAI was estimated using the growth rates obtained from tree rings analysis. The carbon biomass was on average 264 ± 48 Mg ha⁻¹. This estimate includes aboveground carbon, root carbon and soil organic carbon down to 30 cm depth. This value varied from 231 ± 45 Mg ha⁻¹ of carbon in Agro-Forests to 283 ± 51 Mg ha⁻¹ of carbon in Managed Forests and to 278 ± 56 Mg ha⁻¹ of carbon in National Park. The carbon CAI varied from 2.54 ± 0.65 Mg ha⁻¹ year⁻¹ in Agro-Forests to 2.79 ± 0.72 Mg ha⁻¹ year⁻¹ in Managed Forests and to 2.85 ± 0.72 Mg ha⁻¹ year⁻¹ in National Park. This study provides estimates of biomass, carbon pools and CAI of carbon biomass from a forest landscape in Cameroon as well as an appropriate methodology to estimate these components and the related uncertainty.     

Influences of forest tending works on carbon distribution and cycling in a Pinus densiflora S. et Z. stand in Korea

This study was conducted to determine carbon (C) dynamics following forest tending works (FTW) which are one of the most important forest management activities conducted by Korean forest police and managers. We measured organic C storage (above- and below-ground biomass C, forest floor C, and soil C at 50 cm depth), soil environmental factors (soil CO₂ efflux, soil temperature, soil water content, soil pH, and soil organic C concentration), and organic C input and output (litterfall and litter decomposition rates) for one year in FTW and non-FTW (control) stands of approximately 40-year-old red pine (Pinus densiflora S. et Z.) forests in the Hwangmaesan Soopkakkugi model forest in Sancheonggun, Gyeongsangnam-do, Korea. This forest was thinned in 2005 as a representative FTW practice. The total C stored in tree biomass was significantly lower (P < 0.05) in the FTW stand (40.17 Mg C ha⁻¹) than in the control stand (64.52 Mg C ha⁻¹). However, C storage of forest floor and soil layers measured at four different depths was not changed by FTW, except for that at the surface soil depth (0–10 cm). The organic C input due to litterfall and output due to needle litter decomposition were both significantly lower in the FTW stand than in the control stand (2.02 Mg C ha⁻¹ year⁻¹ vs. 2.80 Mg C ha⁻¹ year⁻¹ and 308 g C kg⁻¹ year⁻¹ vs. 364 g C kg⁻¹ year⁻¹, respectively, both P < 0.05). Soil environmental factors were significantly affected (P < 0.05) by FTW, except for soil CO₂ efflux rates and organic C concentration at soil depth of 0–20 cm. The mean annual soil CO₂ efflux rates were the same in the FTW (0.24 g CO₂ m⁻² h⁻¹) and control (0.24 g CO₂ m⁻² h⁻¹) stands despite monthly variations of soil CO₂ efflux over the one-year study period. The mean soil organic C concentration at a soil depth of 0–20 cm was lower in the FTW stand (81.3 g kg⁻¹) than in the control stand (86.4 g kg⁻¹) but the difference was not significant (P > 0.05). In contrast, the mean soil temperature was significantly higher, the mean soil water content was significantly lower, and the soil pH was significantly higher in the FTW stand than in the control stand (10.34 °C vs. 8.98 °C, 48.2% vs. 56.4%, and pH 4.83 vs. pH 4.60, respectively, all P < 0.05). These results indicated that FTW can influence tree biomass C dynamics, organic C input and output, and soil environmental factors such as soil temperature, soil water content and soil pH, while soil C dynamics such as soil CO₂ efflux rates and soil organic C concentration were little affected by FTW in a red pine stand.     

Tree height in Brazil's ‘arc of deforestation’: Shorter trees in south and southwest Amazonia imply lower biomass

This paper estimates the difference in stand biomass due to shorter and lighter trees in southwest (SW) and southern Amazonia (SA) compared to trees in dense forests in central Amazonia (CA). Forest biomass values used to estimate carbon emissions from deforestation throughout, Brazilian Amazonia will be affected by any differences between CA forests and those in the “arc of deforestation” where clearing activity is concentrated along the southern edge of the Amazon forest. At 12 sites (in the Brazilian states of Amazonas, Acre, Mato Grosso and Pará) 763 trees were felled and measurements were made of total height and of stem diameter. In CA dense forest, trees are taller at any given diameter than those in SW bamboo-dominated open, SW bamboo-free dense forest and SA open forests. Compared to CA, the three forest types in the arc of deforestation occur on more fertile soils, experience a longer dry season and/or are disturbed by climbing bamboos that cause frequent crown damage. Observed relationships between diameter and height were consistent with the argument that allometric scaling exponents vary in forests on different substrates or with different levels of natural disturbance. Using biomass equations based only on diameter, the reductions in stand biomass due to shorter tree height alone were 11.0, 6.2 and 3.6%, respectively, in the three forest types in the arc of deforestation. A prior study had shown these forest types to have less dense wood than CA dense forest. When tree height and wood density effects were considered jointly, total downward corrections to estimates of stand biomass were 39, 22 and 16%, respectively. Downward corrections to biomass in these forests were 76 Mg ha⁻¹ (∼21.5 Mg ha⁻¹ from the height effect alone), 65 Mg ha⁻¹ (18.5 Mg ha⁻¹ from height), and 45 Mg. ha⁻¹ (10.3 Mg ha⁻¹ from height). Hence, biomass stock and carbon emissions are overestimated when allometric relationships from dense forest are applied to SW or SA forest types. Biomass and emissions estimates in Brazil's National Communication under the United Nations Framework Convention on Climate Change require downward corrections for both wood density and tree height.     

Carbon pools and productivity in a 1-km heterogeneous forest and peatland mosaic in Minnesota,USA

Determining the magnitude of carbon (C) storage in forests and peatlands is an important step towards predicting how regional carbon balance will respond to climate change. However, spatial heterogeneity of dominant forest and peatland cover types can inhibit accurate C storage estimates. We evaluated ecosystem C pools and productivity in the Marcell Experimental Forest (MEF), in northern Minnesota, USA, using a network of plots that were evenly spaced across a heterogeneous 1-km² mosaic composed of a mix of upland forests and peatlands. Using a nested plot design, we estimated the standing C stock of vegetation, coarse detrital wood and soil pools. We also estimated aboveground net primary production (ANPP) as well as coarse root production. Additionally we evaluated how vegetation cover types within the study area differed in C storage. The total ecosystem C pool did not vary significantly among upland areas dominated by aspen (160 ± 13 Mg C ha⁻¹), mixed hardwoods (153 ± 19 Mg C ha⁻¹), and conifers (197 ± 23 Mg C ha⁻¹). Live vegetation accounted for approximately 50% of the total ecosystem C pool in these upland areas, and soil (including forest floor) accounted for another 35–40%, with remaining C stored as detrital wood. Compared to upland areas, total C stored in peatlands was much greater, 1286 ± 125 Mg C ha⁻¹, with 90–99% of that C found in peat soils that ranged from 1 to 5 m in depth. Forested areas ranged from 2.6 to 2.9 Mg C ha⁻¹ in ANPP, which was highest in conifer-dominated upland areas. In alder-dominated and black spruce-dominated peatland areas, ANPP averaged 2.8 Mg C ha⁻¹, and in open peatlands, ANPP averaged 1.5 Mg C ha⁻¹. In treed areas of forest and peatlands, our estimates of coarse root production ranged from 0.1 to 0.2 Mg C ha⁻¹. Despite the lower production in open peatlands, all peatlands have acted as long-term C sinks over hundreds to thousands of years and store significantly more C per unit area than is stored in uplands. Despite occupying only 13% of our study area, peatlands store almost 50% of the C contained within it. Because C storage in peatlands depends largely on climatic drivers, the impact of climate changes on peatlands may have important ramifications for C budgets of the western Great Lakes region.     

Estimating state-wide biomass carbon stocks for a REDD plan in Acre, Brazil

As in many other developing countries, the state government of Acre, Brazil, is developing a program for compensating forest holders (such as communities of rubber tappers and indigenous peoples as well as small, medium and large private land holders) reducing their emission of atmospheric heat-trapping gases by not deforesting. We describe and then apply to Acre a method for estimating carbon stocks by land cover type. We then compare the results of our simple method, which is based on vegetation mapping and ground-based samples, with other more technically demanding methods based on remote sensing. We estimated total biomass carbon stocks by multiplying the measured above-ground biomass of trees >10 cm DBH in each of 18 forest types and published estimates for non-forest areas, as determined by measurement of 44 plots throughout the state (ranging from 1 to 10 ha each), by land-cover area estimated using a geographical information system. State-wide, we estimated average above-ground biomass in forested areas to be 246 ± 90 Mg ha⁻¹; dense forest showed highest (322 ± 20 Mg ha⁻¹) and oligotrophic dwarf forest (campinarana) the lowest biomass (20 ± 30 Mg ha⁻¹). The two most widespread forest types in Acre, open canopy forests dominated by either palms and bamboo (for which ground-based data are scant), support an estimated 246 ± 44 and 224 ± 50 Mg ha⁻¹ of above-ground biomass, respectively. We calculate the total above-ground biomass of the 163,000 km² State of Acre to be 3.6 ± 0.8 Pg (non-forest biomass included). This estimate is very similar to two others generated using much more technologically demanding methods, but all three methods, regardless of sophistication, suffer from lack of field data.     

Derivation of a spatially explicit 86-year retrospective carbon budget for a landscape undergoing conversion from old-growth to managed forests on Vancouver Island,BC

To understand the influence of disturbance, age–class structure, and land use on landscape-level carbon (C) budgets during conversion of old-growth forests to managed forests, a spatially explicit, retrospective C budget from 1920 through 2005 was developed for the 2500 ha Oyster River area of Fluxnet-Canada's coastal BC Station. We used the Carbon Budget Model of the Canadian Forest Sector (CBM-CFS3), an inventory-based model, to simulate forest C dynamics. A current (circa 1999) forest inventory for the area was compiled, then overlaid with digitized historic disturbance maps, a 1919 timber cruise map, and a series of historic orthophotographs to generate a GIS coverage of forest cover polygons with unique disturbance histories dating back to 1920. We used the combined data from the historic and current inventory and forest change data to first estimate initial ecosystem C stocks and then to simulate forest dynamics and C budgets for the 86-year period. In 1920, old-growth forest dominated the area and the long-term landscape-level net ecosystem C balance (net biome productivity, NBP) was a small sink (NBP 0.2 Mg C ha⁻¹ year⁻¹). From 1930 to 1945 fires, logging, and slash burning resulted in large losses of biomass C, emissions of C to the atmosphere, and transfers of C from biomass to detritus and wood products (NBP ranged from −3 to −56 Mg C ha⁻¹ year⁻¹). Live biomass C stocks slowly recovered following this period of high disturbance but the area remained a C source until the mid 1950s. From 1960 to 1987 disturbance was minimal and the area was a C sink (NBP ranged from 3 to 6 Mg C ha⁻¹ year⁻¹). As harvest of second-growth forest began in late 1980s, disturbances again dominated the area's C budget, partially offset by ongoing C uptake by biomass in recovering young forests such that the C balance varied from positive to negative depending upon the area disturbed that year (NBP from 6 to −15 Mg C ha⁻¹ year⁻¹). Despite their high productivity, the area's forests are not likely to attain C densities of the landscape prior to industrial logging because the stands will not reach pre-logging ages. Additional work is underway to examine the relative role historic climate variability has had on the landscape-level C budget.     

Recovery process of a mountain forest after shifting cultivation in Northwestern Vietnam

The recovery process of fallow stands in the mountainous region of Northwestern Vietnam was studied, based on a chronosequence of 1–26-year-old secondary forests after intensive shifting cultivation. The number of species present in a 26-year-old secondary forest attained 49% of the 72 species present in an old-growth forest. Total stem density decreased gradually from 172,500 ha⁻¹ in a 3-year-old forest to 24,600 ha⁻¹ in the 26-year-old stand, but stem density of larger trees (diameter at breast height (D) ≥ 5 cm) increased from 60 ha⁻¹ in a 7-year-old to 960 ha⁻¹ in the 26-year-old forests, which was similar to that of an old-growth forest. Annual biomass increment of the 26-year-old stand was 4.2 Mg ha⁻¹ year⁻¹. A saturation curve was fitted to biomass accumulation in secondary forests. After an estimated time of 60 years, a secondary forest can achieve 80% of the biomass of old-growth forests (240 Mg ha⁻¹). Species diversity expressed by Shannon Index shows that it takes 60 years for a secondary forest in fallow to achieve a plant species diversity similar to that of old-growth forests.     

Above-ground biomass dynamics after reduced-impact logging in the Eastern Amazon

Changes in above-ground biomass (AGB) of 17 1 ha logged plots of terra firme rain forest in the eastern Amazon (Brazil, Paragominas) were monitored for four years (2004–2008) after reduced-impact logging. Over the same time period, we also monitored two 0.5 ha plots in adjacent unlogged forest. While AGB in the control plots changed little over the observation period (increased on average 1.4 Mg ha⁻¹), logging resulted in immediate reductions in ABG that averaged 94.5 Mg ha⁻¹ (±42.0), which represented 23% of the 410 Mg ha⁻¹ (±64.9) present just prior to harvesting. Felled trees (dbh > 55 cm) accounted for 73% (±15) of these immediate losses but only 18.9 Mg ha⁻¹ (±8.1) of biomass was removed in the extracted logs. During the first year after logging, the annual AGB balance (annual AGB gain by recruitment and growth − annual AGB loss by mortality) remained negative (−31.1 Mg ha⁻¹ year⁻¹; ±16.7), mainly due to continued high mortality rates of damaged trees. During the following three years (2005–2008), average net AGB accumulation in the logged plots was 2.6 Mg ha⁻¹ year⁻¹ (±4.6). Post-logging biomass recovery was mostly through growth (4.3 ± 1.5 Mg ha⁻¹ year⁻¹ for 2004–2005 and 6.8 ± 0.9 Mg ha⁻¹ year⁻¹ for 2005–2008), particularly of large trees. In contrast, tree recruitment contributed little to the observed increases in AGB (1.1 ± 0.6 Mg ha⁻¹ year⁻¹ for 2004–2005 and 3.1 ± 1.3 Mg ha⁻¹ year⁻¹ for 2005–2008). Plots with the lowest residual basal area after logging generally continued to lose more large trees (dbh ≥70 cm), and consequently showed the greatest AGB losses and the slowest overall AGB gains. If 100% AGB recovery is desired and the 30-year minimum cutting cycle defined by Brazilian law is adhered to, current logging intensities (6 trees ha⁻¹) need to be reduced by 40–50%. Such a reduction in logging intensity will reduce financial incomes to loggers, but might be compensated for by the payment of environmental services through the proposed REDD (reduced emissions from deforestation and forest degradation) mechanism of the United Nations Framework Convention on Climate Change.     

Estimation of biomass and carbon stocks in plants,soil and forest floor in different tropical forests

An accurate characterization of tree carbon (TC), forest floor carbon (FFC) and soil organic carbon (SOC) in tropical forest plantations is important to estimate their contribution to global carbon stocks. This information, however, is poor and fragmented. Carbon contents were assessed in patula pine (Pinus patula) and teak (Tectona grandis) stands in tropical forest plantations of different development stages in combination with inventory assessments and soil survey information. Growth models were used to associate TOC to tree normal diameter (D) with average basal area and total tree height (H_T), with D and H_T parameters that can be used in 6–26 years old patula pine and teak in commercial tropical forests as indicators of carbon stocks. The information was obtained from individual trees in different development stages in 54 patula pine plots and 42 teak plots. The obtained TC was 99.6 Mg ha⁻¹ in patula pine and 85.7 Mg ha⁻¹ in teak forests. FFC was 2.3 and 1.2 Mg ha⁻¹, SOC in the surface layer (0–25 cm) was 92.6 and 35.8 Mg ha⁻¹, 76.1 and 19 Mg ha⁻¹ in deep layers (25–50 cm) in patula pine and teak, respectively. Carbon storage in trees was similar between patula pine and teak plantations, but patula pine had higher levels of forest floor carbon and soil organic carbon. Carbon storage in trees represents 37 and 60% of the total carbon content in patula pine and teak plantations, respectively. Even so, the remaining percentage corresponds to SOC, whereas FFC content is less than 1%. In summary, differences in carbon stocks between patula pine and teak trees were not significant, but the distribution of carbon differed between the plantation types. The low FFC does not explain the SOC stocks; however, current variability of SOC stocks could be related to variation in land use history.     

Carbon sequestration by forests and soils on mined land in the Midwestern and Appalachian coalfields of the U.S.

Carbon (C) accreditation of forest development projects is one approach for sequestering atmospheric CO₂, under the provisions of the Kyoto protocol. The C sequestration potential of reforested mined land is not well known. The purpose of this work was to estimate and compare the ecosystem C content in forests established on surface, coal-mined and non-mined land. We used existing tree, litter, and soil C data for fourteen mined and eight adjacent, non-mined forests in the Midwestern and Appalachian coalfields to determine the C sequestration potential of mined land reclaimed prior to the passage of the Surface Mining Control and Reclamation Act (1977). We developed statistically significant and biologically reasonable models for ecosystem C across the spectrum of site quality and stand age. On average, the highest amount of ecosystem C on mined land was sequestered in pine stands (148 Mg ha⁻¹), followed by hardwood (130 Mg ha⁻¹) and mixed stands (118 Mg ha⁻¹). Non-mined hardwood stands sequestered 210 Mg C ha⁻¹, which was about 62% higher than the average of all mined stands. Our mined land response surface models of C sequestration as a function of site quality and age explained 59, 39, and 36% of the variation of ecosystem C in mixed, pine, and hardwood stands, respectively. In pine and mixed stands, ecosystem C increased exponentially with the increase of site quality, but decreased with age. In mined hardwood stands, ecosystem C increased asymptotically with age, but it was not affected by site quality. At rotation age (60 yr), ecosystem C in mined hardwood stands was less on high quality sites, but similar for low quality sites compared to non-mined hardwood stands. The overall results indicated that the higher the original forest site quality, the less likely C sequestration potential was restored, and the greater the disparity between pre- and post-mining C sequestration stocks.     

Forest regeneration in artificial gaps twelve years after canopy opening in Acre State Western Amazon

The main objectives were to study the effect of gap size and canopy openness on the natural regeneration dynamics considering the parameters of sapling growth, recruitment, mortality, density, species composition and above-ground biomass accumulation. The study was carried out in 32 artificial gaps with sizes varying from 100 to 1200 m² and canopy openness from 10 to 45%, from the second to the twelfth year after gap creation. The gap size was measured using the vertical projection of the tree crowns on the ground (Brokaw's definition), and the canopy openness measurement by hemispherical photography. In the first five years, mean sapling growth (0.54 cm year⁻¹), mortality (3.9% year⁻¹) and AGB (26.2 Mg ha⁻¹ or 8.7 Mg ha⁻¹ year⁻¹) were significantly higher in the gaps than in the forest understorey (0.17 cm year⁻¹, 1.5% year⁻¹ and −0.59 Mg ha⁻¹ year⁻¹ respectively) and positively correlated with gap size and canopy openness. In the same period, recruitment was also significantly higher in the gaps (5.8% year⁻¹) than in the forest understorey (0.4% year⁻¹) but decreased with gap size and negatively correlated with canopy openness. In the first five years, the relative density of pioneer species was higher in the gaps but not significantly correlated with gap size or canopy openness. AGB increased linearly since canopy opening, and twelve years after gap creation it was still higher in larger (121.2 Mg ha⁻¹ or 10.1 Mg ha⁻¹ year⁻¹) rather than smaller (62.5 ha⁻¹ or 5.2 ha⁻¹ year⁻¹) gaps. Twelve years after gap creation there were no significant differences in the parameters of sapling growth, recruitment, and mortality which could be attributed to the original gap size and canopy openness.     

Effects of wood-ash application on potential carbon and nitrogen mineralisation at two forest sites with different tree species,climate and N status

In the future it may become common practice to return wood-ash to forest ecosystems in order to replenish nutrients removed when brash has been extracted as a source of bioenergy. Wood-ash contains most of the nutrients that are present in the brash before its removal and burning, with the important exception of nitrogen (N). In the present paper we report measurements of CO₂ emissions and net N mineralisation in the humus layer and the upper 5 cm of mineral soil 12 years after the application of wood-ash to two study sites, representing different tree species, climatic conditions and N deposition histories. We hypothesized that application of wood-ash would increase both carbon (C) and net N mineralisation rates at Torup, an N-rich site with Norway spruce (Picea abies (L.) Karst.) in the south, whereas the net N mineralisation rates would not be affected at Vindeln, an N-poor site with Scots pine (Pinus sylvestris L.) in the north, where a possible N-limitation would restrict any N mineralisation. The treatments, comprising additions of 0, 1, 3 or 6 Mg of granulated wood-ash ha⁻¹, were applied in a randomised block design, replicated three times. Wood-ash from the same batch was used for all treatments at both sites. All factors were measured under laboratory conditions with controlled temperature and moisture levels. The potential CO₂ emissions (kg ha⁻¹ year⁻¹ of CO₂–C) at Torup were significantly higher in the 3 and 6 Mg ha⁻¹ treatments than in the control treatment, and the highest application resulted in an extra loss of 0.5 Mg ha⁻¹ of soil C annually as compared to the control. No such differences were detected at Vindeln. The results suggest that wood-ash application can deplete soil organic C at locations with similar characteristics (N-rich soil, spruce dominated, warm climate) as at Torup in this study.     

Tree diversity and carbon stocks of some major forest types of Garhwal Himalaya,India

Four forest stands each of twenty major forest types in sub-tropical to temperate zones (350 m asl–3100 m asl) of Garhwal Himalaya were studied. The aim of the study was to assess the stem density, tree diversity, biomass and carbon stocks in these forests and make recommendations for forest management based on priorities for biodiversity protection and carbon sequestration. Stem density ranged between 295 and 850 N ha⁻¹, while total biomass ranged from 129 to 533 Mg ha⁻¹. Total carbon storage ranged between 59 and 245 Mg ha⁻¹. The range of Shannon–Wiener diversity index was between 0.28 and 1.75. Most of the conifer-dominated forest types had higher carbon storage than broadleaf-dominated forest types. Protecting conifer-dominated stands, especially those dominated by Abies pindrow and Cedrus deodara, would have the largest impact, per unit area, on reducing carbon emissions from deforestation.     

Below- and above-ground biomass and net primary production in a paleotropical natural forest (Sulawesi,Indonesia) as compared to neotropical forests

Data on the biomass and productivity of southeast Asian tropical forests are rare, making it difficult to evaluate the role of these forest ecosystems in the global carbon cycle and the effects of increasing deforestation rates in this region. In particular, more precise information on size and dynamics of the root system is needed. In six natural forest stands at pre-montane elevation (c. 1000 m a.s.l.) on Sulawesi (Indonesia), we determined above-ground biomass and the distribution of fine (d < 2 mm) and coarse roots (d > 2 mm), estimated above- and below-ground net production, and compared the results to literature data from other pre-montane paleo- and neotropical forests. The mean total biomass of the stands was 303 Mg ha⁻¹ (or 128 Mg C ha⁻¹), with the largest biomass fraction being recorded for the above-ground components (286 Mg ha⁻¹) and 11.2 and 5.6 Mg ha⁻¹ of coarse and fine root biomass (down to 300 cm in the soil profile), resulting in a remarkably high shoot:root ratio of c. 17. Fine root density in the soil profile showed an exponential decrease with soil depth that was closely related to the concentrations of base cations, soil pH and in particular of total P and N. The above-ground biomass of these stands was found to be much higher than that of pre-montane forests in the Neotropics, on average, but lower compared to other pre-montane forests in the Paleotropics, in particular when compared with dipterocarp forests in Malesia. The total above- and below-ground net primary production was estimated at 15.2 Mg ha⁻¹ yr⁻¹ (or 6.7 Mg C ha⁻¹ yr⁻¹) with 14% of this stand total being invested below-ground and 86% representing above-ground net primary production. Leaf production was found to exceed net primary production of stem wood. The estimated above-ground production was high in relation to the mean calculated for pre-montane forests on a global scale, but it was markedly lower compared to data on dipterocarp forests in South-east Asia. We conclude that the studied forest plots on Sulawesi follow the general trend of higher biomasses and productivity found for paleotropical pre-montane forest compared to neotropical ones. However, biomass stocks and productivity appear to be lower in these Fagaceae-rich forests on Sulawesi than in dipterocarp forests of Malesia.     

Timber mobilization and habitat tree retention in low-elevation mixed forests in Switzerland: an inventory-based scenario analysis of opportunities and constraints

Timber use in central Europe is expected to increase in the future, in line with forest policy goals to strengthen local wood supply for CO₂-neutral energy production, construction and other uses. Growing stocks in low-elevation forests in Switzerland are currently high as exemplified by the Swiss canton of Aargau, for which an average volume of 346 ± 16 m³ ha⁻¹ was measured in the 3rd Swiss National forest inventory (NFI) in 2004–2006. While this may justify a reduction of growing stocks through increased timber harvesting, we asked whether such a strategy may conflict with the sustainability of timber production and conservation goals. We evaluated a range of operationally relevant forest management scenarios that varied with respect to rotation length, growing stock targets and the promotion of conifers in the regeneration. The scenarios aimed at increased production of softwood, energy wood, the retention of potential habitat trees (PHTs) and the conversion to a continuous cover management system. They were used to drive the inventory-based forest simulator MASSIMO for 100 years starting in 2007 using the NFI sampling plots in Aargau. We analyzed model outputs with respect to projected future growing stock, growth, timber and energy yield and harvesting costs. We found growing stock to drop to 192 m³ ha⁻¹ in 2106 if business-as-usual (BAU as observed between the 2nd and 3rd NFI) timber volumes were set as harvesting targets for the whole simulation period. The promotion of conifers and a reduction of rotation lengths in a softwood scenario yielded 25% more timber over the whole simulation period than BAU. An energy wood scenario that reduced growing stock to 200 m³ ha⁻¹ by 2056 and promoted the natural broadleaved regeneration yielded 9% more timber than BAU before 2056 and 30% less thereafter due to decreasing increments. The softwood scenario resulted in higher energy yield than the energy wood scenario despite the lower energy content of softwood. Retaining PHT resulted in a reduction of timber harvest (0.055 m³ ha⁻¹ yr⁻¹ per habitat tree) and higher harvesting costs. Continuous cover management yielded moderate timber amounts throughout the simulation period, yet sustainably. Considering climate change, we discuss the risks associated with favoring drought- and disturbance-susceptible conifers at low elevations and emphasize that continuous cover management must allow for the regeneration of drought-adapted tree species. In conclusion, our simulations show potential for short-term increases in timber mobilization but also that such increases need to be carefully balanced with future forest productivity and other forest ecosystem services.

     

Carbon accumulation in the biomass and soil of different aged secondary forests in the humid tropics of Costa Rica

Efforts are needed in order to increase confidence for carbon accounts in the land use sector, especially in tropical forest ecosystems that often need to turn to default values given the lack of precise and reliable site specific data to quantify their carbon sequestration and storage capacity. The aim of this study was then to estimate biomass and carbon accumulation in young secondary forests, from 4 and up to 20 years of age, as well as its distribution among the different pools (tree including roots, herbaceous understory, dead wood, litter and soil), in humid tropical forests of Costa Rica. Carbon fraction for the different pools and tree components (stem, branches, leaves and roots) was estimated and varies between 37.3% (±3.3) and 50.3% (±2.9). Average carbon content in the soil was 4.1% (±2.1). Average forest plant biomass was 82.2 (±47.9) Mg ha⁻¹ and the mean annual increment for carbon in the biomass was 4.2 Mg ha⁻¹ yr⁻¹. Approximately 65.2% of total biomass was found in the aboveground tree components, while 14.2% was found in structural roots and the rest in the herbaceous vegetation and necromass. Carbon in the soil increased by 1.1 Mg ha⁻¹ yr⁻¹. Total stored carbon in the forest was 180.4 Mg ha⁻¹ at the age of 20 years. In these forests, most of the carbon (51-83%) was stored in the soil. Models selected to estimate biomass and carbon in trees as predicted by basal area had R² adjustments above 95%. Results from this study were then compared with those obtained for a variety of secondary and primary forests in different Latin-American tropical ecosystems and in tree plantations in the same study area.     

Estimating forest data for analyses of forest production and utilization possibilities at local level by means of multi-source National Forest Inventory

The sample plot data of National Forest Inventories (NFI) are widely used in the analysis of forest production and utilization possibilities to support national and regional forest policy. However, there is an increasing interest for similar impact and scenario analyses for strategic planning at the local level. As the fairly sparse network of field plots only provides calculations for large areas, satellite image data have been applied to produce forest information for smaller areas. The aim of this study was to test the feasibility of generating forest data for a Finnish forest analysis tool, the MELA system, by means of the Landsat satellite imagery and the NFI sample plot data. The study was part of the preparation of a local forestry programme, where a strategic scenario analysis for the forest area of two villages (ca 8000 ha) was carried out. Management units that approximate forest stands were delineated by image segmentation. Stand volume and other parameters for each forest segment were estimated from weighted means of the NFI sample plots, where the individual sample plot weights were estimated by the k nearest neighbour (kNN) method. Two different spectral features were tested: single pixel values and average pixel values within a segment. The estimated forest data were compared with the forest data based on independent stand-level field assessments in two subareas, a national park and an area of forest managed for timber production.In the national park, the estimated mean volume of the growing stock from both spectral feature sets (about 160 m³ ha⁻¹) was clearly lower than that obtained from stand-level field assessment (186 m³ ha⁻¹). Using average pixel values within a segment resulted in a higher proportion of pine and a lower proportion of spruce volume than using single pixel values. It also resulted in an estimated felling potential nearly 10% higher over the first 10-year period in the scenario analysis of the area dedicated to timber production. However, the maximum long-term sustainable removal was at the same level (about 30,000 m³ year⁻¹) for both feature sets over the simulated 30-year period. The resulting annual felling area in the first 10-year period was 12% lower when the segment averages were applied, but the difference subsequently levelled off. The kNN approach in estimating initial forest data for scenario analyses at the local level was found promising.     

Estimating the net carbon balance of boreal open woodland afforestation: A case-study in Québec’s closed-crown boreal forest

Black spruce (Picea mariana (Mill.) B.S.P.) is the dominant tree species in the Canadian province of Québec’s boreal ecosystem, particularly in the black spruce-feathermoss (BSFM) domain (between the 49th and the 52nd parallels). While black spruce is generally well adapted to regenerate after wildfires, regeneration failure can sometimes occur, resulting in the irreversible conversion of closed-crown BSFM to open black spruce-lichen woodlands (OW). With OWs representing approximately 7% (1.6 M ha) of Québec’s BSFM domain, the afforestation of OWs carries significant theoretical potential for carbon (C) sequestration, which has not yet been evaluated. The main objectives of the study were then: (i) to estimate the theoretical C balance of OW afforestation within the closed-crown BSFM domain in Québec’s boreal forest; (ii) to calculate, using the life cycle analysis (LCA) method, all the GHG emissions related to black spruce OW afforestation in the closed-crown BSFM domain of Québec. The CO2FIX v. 3.1 model was used to calculate the biological C balance between the baseline (natural OW of site index 9 at age 50) and afforestation (black spruce plantation of site index 6 at age 25) scenarios, using the best estimates available for all five recommended C compartments (aboveground biomass, belowground biomass, litter, deadwood, and soil). The simulation revealed a biological C balance of 77.0 t C ha⁻¹, 70 years following afforestation, for an average net sequestration rate of 1.1 t C ha⁻¹ year⁻¹. Biological C balance only turns positive after 27 years. When integrating the uncertainties related to both the plantation growth yield and the wildfire disturbance, the average sequestration rate varies between 0.2 and 1.9 t C ha⁻¹ year⁻¹. GHG emissions are 1.3 t CO₂ equiv. ha⁻¹ for all afforestation-related operations, which is less than 0.5% of the biological C balance after 70 years. Thus, GHG emissions do not significantly affect the net C balance of the afforestation project simulated. Several recommendations are made, mostly centered on the factors influencing the growth rate of carbon stocks and the impact of natural disturbances, to minimize the range of uncertainties associated to the sequestration potential and maximize the mitigation benefits of an OW afforestation project.     

A comparison of carbon assessment methods for optimizing timber production and carbon sequestration in Scots pine stands

Projected changes in forest carbon stocks and carbon balance differ according to the choice of estimation methods and the carbon pools considered. Here, we compared three carbon assessment methods for optimizing timber production and carbon sequestration in six example Scots pine (Pinus sylvestris L.) stands in Finland. The forest carbon stock was assessed, with three methods: stem carbon, biomass expansion factors (BEFs), and a process-based model. Given a carbon price of 40 € t⁻¹ (equivalent to 10.9 € t⁻¹ CO₂) and a 3% discount rate, the highest average carbon stock and mean annual increment (MAI) were obtained with the BEF method. Increasing the carbon price from 0 to 200 € t⁻¹ resulted in longer optimal rotations and higher MAI, and increased the average carbon stock, especially when carbon was assessed by the BEF method. Comparison of these carbon assessment methods, using economic sensitivity analyses, indicated that optimal thinning regimes and average carbon stocks are strongly dependent on the assessment method. The process-based method led to less frequent thinnings and shorter rotations than the BEF method, due to different predictions of biomass production. As a cost-effective option, optimal thinning regimes play a very important role in timber production and carbon sequestration.     

Formulating allometric equations for estimating biomass and carbon stock in small diameter trees

Biomass and carbon sequestration rate of a young (four year old) mixed plantation of Dalbergia sissoo Roxb., Acacia catechu Willd., and Albizia lebbeck Benth. growing in Terai region (a level area of superabundant water) of central Himalaya was estimated. The plantation is seed sown in the rainy season of year 2004 and spread over an area of 44 ha. Allometric equations for both above and below ground components were developed for three tree species. The density of trees in the plantation was 1322 trees ha⁻¹ The diameters of trees were below 10 cm. Five diameter classes were defined for D. sissoo and A. catechu and 3 for A. lebbeck. 5 trees were harvested in each diameter class. Individual tree allometry was exercised for developing the allometric equations relating tree component (low and above ground) biomass to d.b.h. Post analysis equations were highly significant (P > 0.001) for each component of all species. In the plantation Holoptelia integrifolia Roxb. (Family Ulmaceae) has been reduced to shrub form because of frost. Only the aboveground biomass of H. integrifolia and other shrubs were estimated by destructive harvesting method. Herbaceous forest floor biomass and leaf litter fall were also estimated. The total forest vegetation biomass was 10.86 Mg ha⁻¹ in 2008 which increased to 19.49 Mg ha⁻¹ in 2009. The forest is sequestering carbon at the rate of 4.32 Mg ha⁻¹ yr⁻¹.