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.     

Retrieval of forest attributes in complex successional forests of Central Indonesia: Modeling and estimation of bitemporal data

Quantification of forest parameters in different successional stages is required because of its importance as a source of global emissions and ecosystem changes. This study focuses on a successional tropical forest under logging practices in East Kalimantan province, Indonesia. We modeled the forest attributes using both a parametric multiple linear regression analysis and neural networks approach, with Landsat ETM data acquired in 2000 (ETM00). We compiled sample plot data using forest inventory data collected from 1997 to 1998. A total of 226 plots were used to train the models and 112 plots were used for the validation. The remote sensing data (spectral values, vegetation indices, texture, etc.) coupled with digital elevation model (DEM) were experimented with and selectively used to model basal area, stem volume and above ground biomass (AGB). We investigated the possibility to estimate the forest attributes from bitemporal ETM data by calibrating radiometric properties of the ETM image from 2003 (ETM03) using the multivariate alteration detection method. The Pearson correlations showed that the mean texture index is strongly correlated with the forest attributes. We show that neural networks resulted in a higher coefficient of determination (r²) and lower RMSE than multiple regressions for predicting the forest attributes. The estimated forest properties increased with the forest succession advancement (i.e. from the open forest to advanced secondary forest classes). The modeled basal area, stem volume and AGB varied from 10.7–15.1 m² ha⁻¹, 123.2–181.9 m³ ha⁻¹, and 132.7–185.3 Mg ha⁻¹, respectively. The RMSE_r values of model fitting ranged from 11.2% to 13.3%, and the test dataset estimated slightly higher RMSE_r which varied from 12% to 14.1%. The ETM03 forest attributes revealed favorable estimates, showing considerably higher estimates than the ETM00. The estimation of forest properties using neural networks makes Landsat data a valuable source of information for forest management, mainly with the recent free access to its historical dataset.     

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.     

Uncertainty of 21st century growing stocks and GHG balance of forests in British Columbia, Canada resulting from potential climate change impacts on ecosystem processes

Over the coming decades, climate change will increasingly affect forest ecosystem processes, but the future magnitude and direction of these responses is uncertain. We designed 12 scenarios combining possible changes in tree growth rates, decay rates, and area burned by wildfire with forecasts of future harvest to quantify the uncertainty of future (2010-2080), timber growing stock, ecosystem C stock, and greenhouse gas (GHG) balance for 67 million ha of forest in British Columbia, Canada. Each scenario was simulated 100 times with the Carbon Budget Model of the Canadian Forest Sector (CBM-CFS3). Depending on the scenario, timber growing stock over the entire land-base may increase by 14% or decrease by 9% by 2080 (a range of 2.8 billion m³), relative to 2010. However, timber growing stock available for harvest was forecast to decline in all scenarios by 26-62% relative to 2010 (a range of 1.2 billion m³). Forests were an annual GHG source in 2010 due to an ongoing insect outbreak. If half of the C in harvested wood was assumed to be immediately emitted, then 0-95% of simulations returned to annual net sinks by 2040, depending on scenario, and the cumulative (2010-2080) GHG balance ranged from a sink of −4.5 Pg CO₂e (−67 Mg CO₂e ha⁻¹) for the most optimistic scenario, to a source of 4.5 Pg CO₂e (67 Mg CO₂e ha⁻¹) for the most pessimistic. The difference in total ecosystem carbon stocks between the most optimistic and pessimistic scenarios in 2080 was 2.4 Pg C (36 Mg C ha⁻¹), an average difference of 126 Tg CO₂e yr⁻¹ (2 Mg CO₂e yr⁻¹ ha⁻¹) over the 70-year simulation period, approximately double the total reported anthropogenic GHG emissions in British Columbia in 2008. Forests risk having reduced growing stock and being GHG sources under many foreseeable scenarios, thus providing further feedback to climate change. These results indicate the need for continued monitoring of forest responses to climatic and global change, the development of mitigation and adaptation strategies by forest managers, and global efforts to minimize climate change impacts on forests.     

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.     

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.     

Ecosystem carbon stocks and distribution under different land-uses in north central Alberta,Canada

Land-use and land cover strongly influence carbon (C) storage and distribution within ecosystems. We studied the effects of land-use on: (i) above- and belowground biomass C, (ii) soil organic C (SOC) in bulk soil, coarse- (250–2000 μm), medium- (53–250 μm) and fine-size fractions (<53 μm), and (iii) ¹³C and ¹⁵N abundance in plant litter, bulk soil, coarse-, and medium- and fine-size fractions in the 0–50 cm soil layer in Linaria AB, Canada between May and October of 2006. Five adjacent land-uses were sampled: (i) agriculture since 1930s, (ii) 2-year-old hybrid poplar (Populusdeltoides × Populus × petrowskyana var. Walker) plantation, (iii) 9-year-old Walker hybrid poplar plantation, (iv) grassland since 1997, and (v) an 80-year-old native aspen (Populus tremuloides Michx.) stand. Total ecosystem C stock in the native aspen stand (223 Mg C ha⁻¹) was similar to that of the 9-year-old hybrid poplar plantation (174 Mg C ha⁻¹) but was significantly greater than in the agriculture (132 Mg C ha⁻¹), 2-year-old hybrid poplar plantation (110 Mg C ha⁻¹), and grassland (121 Mg C ha⁻¹). Differences in ecosystem C stocks between the land-uses were primarily the result of different plant biomass as SOC in the 0–50 cm soil layer was unaffected by land-use change. The general trend for C stocks in soil particle-size fractions decreased in the order of: fine > medium > coarse for all land-uses, except in the native aspen stand where C was uniformly distributed among soil particle-size fractions. The C stock in the coarse-size fraction was most affected by land-use change whilst the fine fractions the least. Enrichment of the natural abundances of ¹³C and ¹⁵N across the land-uses since time of disturbance, i.e., from agriculture to 2- and then 9-year-old hybrid poplar plantations or to grassland, suggests shifts from more labile forms of C to more humified forms of C following those land-use changes.     

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.     

Forest structure and live aboveground biomass variation along an elevational gradient of tropical Atlantic moist forest (Brazil)

Live aboveground biomass (AGB) is an important source of uncertainty in the carbon balance from the tropical regions in part due scarcity of reliable estimates of live AGB and its variation across landscapes and forest types. Studies of forest structure and biomass stocks of Neotropical forests are biased toward Amazonian and Central American sites. In particular, standardized estimates of aboveground biomass stocks for the Brazilian Atlantic forest are rarely available. Notwithstanding the role of environmental variables that control the distribution and abundance of biomass in tropical lowland forests has been the subject of considerable research, the effect of short, steep elevational gradients on tropical forest structure and carbon dynamics is not well known. In order to evaluate forest structure and live AGB variation along an elevational gradient (0–1100 m a.s.l.) of coastal Atlantic Forest in SE Brazil, we carried out a standard census of woody stems ≥4.8 cm dbh in 13 1-ha permanent plots established on four different sites in 2006–2007. Live AGB ranged from 166.3 Mg ha⁻¹ (bootstrapped 95% CI: 144.4,187.0) to 283.2 Mg ha⁻¹ (bootstrapped 95% CI: 253.0,325.2) and increased with elevation. We found that local-scale topographic variation associated with elevation influences the distribution of trees >50 cm dbh and total live AGB. Across all elevations, we found more stems (64–75%) with limited crown illumination but the largest proportion of the live AGB (68–85%) was stored in stems with highly illuminated or fully exposed crowns. Topography, disturbance and associated changes in light and nutrient supply probably control biomass distribution along this short but representative elevational gradient. Our findings also showed that intact Atlantic forest sites stored substantial amounts of carbon aboveground. The live tree AGB of the stands was found to be lower than Central Amazonian forests, but within the range of Neotropical forests, in particular when compared to Central American forests. Our comparative data suggests that differences in live tree AGB among Neotropical forests are probably related to the heterogeneous distribution of large and medium-sized diameter trees within forests and how the live biomass is partitioned among those size classes, in accordance with general trends found by previous studies. In addition, the elevational variation in live AGB stocks suggests a large spatial variability over coastal Atlantic forests in Brazil, clearly indicating that it is important to consider regional differences in biomass stocks for evaluating the role of this threatened tropical biome in the global carbon cycle.     

Effects of disturbance history and environmental factors on the diversity and productivity of understory vegetation in a cool-temperate forest in Japan

We assessed the species richness and aboveground productivity of understory plants in nine types of forest stand (116 plots in total) that had different disturbance histories that were combinations of the frequency of plantation (clear-cutting, site preparation, planting), typhoon damage, and selective cutting. We established two 1 m × 1 m quadrats to measure species richness and productivity and one 1 m × 30 m belt to measure species richness in each plot. Canopy leaf area index (LAI), soil NH₄⁺, soil C/N ratio, slope angle, and slope aspect were measured as current environmental factors affecting each plot. The variance in species richness was better explained by disturbance history (69% in quadrats; 86% in the belt) than by current environmental factors. Species richness and the Simpson index decreased as the frequency of plantation increased. In contrast, the variance in productivity was better explained by current environmental factors (82%), especially canopy LAI (45%), than by disturbance history. The relations of species presence and productivity to the explanatory variables differed among species, although there were some common responses within life forms. The effects of disturbance on species diversity remained for 20–80 years. Forest management should therefore take into account the long-term effects of disturbance history to maintain understory plant diversity.     

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 carbon sequestration changes in response to timber harvest

Forest succession contributes to the global terrestrial carbon (C) sink, but changes in C sequestration in response to varied harvest intensities have been debated. The forests of the Central Appalachian region have been aggrading over the past 100 years following widespread clear-cutting that occurred in the early 1900s and these forests are now valuable timberlands. This study compared the history of ecosystem C storage in four watersheds that have been harvested at different frequencies and intensities since 1958. We compared NPP, NEP, and component ecosystem C fluxes (g C m⁻² year⁻¹) in response to the four different harvest histories (no harvest, clear-cutting, single tree selection cutting, and 43 cm diameter-limit cutting). Clear-cutting had short-term negative effects on NEP but harvest did not significantly impact long-term average annual C sequestration rates. Average plant C (g C m⁻²) since 1950 was about 33% lower in response to a clear-cut event than plant C in an un-harvested forest, suggesting that the C sequestration associated with clear-cutting practices would decline over time and result in lower C storage than diameter-limit cut, selective cut, or un-harvested forests. Total C stored over a 55-year period was stimulated ∼37% with diameter-limit cutting and selective cutting relative to un-harvested forests.     

Hurricane Katrina impacts on forest trees of Louisiana's Pearl River basin

Hurricane disturbance has the potential to markedly affect coastal forest structure and ecosystem processes. This study focused on the impacts of Hurricane Katrina in Louisiana's Pearl River basin, which lies just west of Katrina's final landfall at the Louisiana–Mississippi border. Prior to landfall, composition and structure of bottomland hardwood forests in this region were studied with permanent forest inventory plots sampled in 1989, 1998, 2005 and following the storm in 2006. This enabled a direct comparison of forest structure and dynamics before and after the disturbance, including species-specific tree mortality and damage rates, biomass production, and differences among forest types having varied hydrologic regimes. Background tree mortality rate before Hurricane Katrina was 1.9%, while average annual mortality was 20.5% for the census interval including the disturbance. Change in live tree biomass estimated from allometric models demonstrated a shift from an average annual production of 3.5 Mg ha⁻¹ before the disturbance, to an average loss of 77.6 Mg ha⁻¹ from the storm. Damage associated with Hurricane Katrina varied significantly with tree species but not tree size. Flooded cypress-tupelo swamp forests sustained the least damage and frequently flooded bottomland hardwood forests sustained the highest damage. Hurricane disturbance influenced the structure and composition of these coastal forests through species-specific differences in damage and mortality rates, and varied impacts dependent on forest flooding regime.     

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.     

Effects of winter selective tree harvest on soil microclimate and surface CO2 flux of a northern hardwood forest

Soil surface CO₂ flux (S_flux) is the second largest terrestrial ecosystem carbon flux, and may be affected by forest harvest. The effects of clearcutting on S_flux have been studied, but little is known about the effect of alternative harvesting methods such as selective tree harvest on S_flux. We measured S_flux before and after (i) the creation of forest canopy gaps (simulating group tree selection harvests) and (ii) mechanized winter harvest but no tree removal (simulating ground disturbance associated with logging). The experiment was carried out in a sugar maple dominated forest in the Flambeau River State Forest, Wisconsin. Pre-treatment measurements of soil moisture, temperature and S_flux were measured throughout the growing season of 2006. In January–February 2007, a harvester created the canopy gaps (200–380 m²). The mechanization treatment consisted of the harvester traveling through the plots for a similar amount of time as the gap plots, but no trees were cut. Soil moisture and temperature and S_flux were measured throughout the growing season for 1 year prior to harvest and for 2 years after harvest. Soil moisture and temperature were significantly greater in the gap than mechanized and control treatments. Instantaneous S_flux was positively correlated to soil moisture and soil temperature at 2 and 10 cm, but temperature at 10 cm was the single best predictor. Annual S_flux was not significantly different among treatments prior to winter 2007 harvest, and was not significantly different among treatments after harvest. Annual (+1 std. err.) S_flux averaged 967 + 72, 1011 + 72, and 1012 + 72 g C m⁻² year⁻¹ in the control, mechanized and gap treatments, respectively, for the 2-year post-treatment period. The results from this study suggest selective group tree harvest significantly increases soil moisture and temperature but does not significantly influence S_flux.     

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.     

Carbon storage in old-growth and second growth fire-dependent western larch (Larix occidentalis Nutt.) forests of the Inland Northwest,USA

There is limited understanding of the carbon (C) storage capacity and overall ecological structure of old-growth forests of western Montana, leaving little ability to evaluate the role of old-growth forests in regional C cycles and ecosystem level C storage capacity. To investigate the difference in C storage between equivalent stands of contrasting age classes and management histories, we surveyed paired old-growth and second growth western larch (Larix occidentalis Nutt)–Douglas-fir (Pseudostuga menziesii var. glauca) stands in northwestern Montana. The specific objectives of this study were to: (1) estimate ecosystem C of old-growth and second growth western larch stands; (2) compare C storage of paired old-growth–second growth stands; and (3) assess differences in ecosystem function and structure between the two age classes, specifically measuring C associated with mineral soil, forest floor, coarse woody debris (CWD), understory, and overstory, as well as overall structure of vegetation. Stands were surveyed using a modified USFS FIA protocol, focusing on ecological components related to soil, forest floor, and overstory C. All downed wood, forest floor, and soil samples were then analyzed for total C and total nitrogen (N). Total ecosystem C in the old-growth forests was significantly greater than that in second growth forests, storing over 3 times the C. Average total mineral soil C was not significantly different in second growth stands compared to old-growth stands; however, total C of the forest floor was significantly greater in old-growth (23.8 Mg ha⁻¹) compared to second growth stands (4.9 Mg ha⁻¹). Overstory and coarse root biomass held the greatest differences in ecosystem C between the two stand types (old-growth, second growth), with nearly 7 times more C in old-growth trees than trees found on second growth stands (144.2 Mg ha⁻¹ vs. 23.8 Mg ha⁻¹). Total CWD on old-growth stands accounted for almost 19 times more C than CWD found in second growth stands. Soil bulk density was also significantly higher on second growth stands some 30+ years after harvest, demonstrating long-term impacts of harvest on soil. Results suggest ecological components specific to old-growth western larch forests, such as coarse root biomass, large amounts of CWD, and a thick forest floor layer are important contributors to long-term C storage within these ecosystems. This, combined with functional implications of contrasts in C distribution and dynamics, suggest that old-growth western larch/Douglas-fir forests are both functionally and structurally distinctive from their second growth counterparts.     

Transpiration along an age series of Eucalyptus globulus plantations in southeastern Australia

Many of the world's Eucalyptus plantations are grown on short rotations of 15 years or less, which often covers the most rapid phase of stand development and peaks in growth rates and leaf areas. Since transpiration is related to stand leaf area these short rotations that make use of rapid early growth rates, may also maximise plantation water use, which has implications for predicting their water requirements and impacts on catchment hydrology. This study examined the transpiration, leaf area and growth rates of Eucalyptus globulus Labill. plantations aged 2–8 years. Transpiration (E), estimated using the heat pulse technique, increased from 0.4 mm day⁻¹ at age 2 years to a peak of about 1.6–1.9 mm day⁻¹ in stands aged 5–7 years. This was associated with similar trends for stand leaf area index (LAI) and periodic annual increments of aboveground biomass, which both peaked at about age 4–6 years resulting in a linear relationship between E and LAI. While stand sapwood areas were continuing to increase at age 8 years, E was already declining due to reductions in sap velocity, from 13.5 cm h⁻¹ at age 2 years to 6.3 cm h⁻¹ at age 8 years and reduced sapwood area growth rates. Trees compensated for this reduction in sap velocity with declines in the leaf area (A_L) to sapwood area (A_S) relationship (A_L:A_S) with age. There was also a reduction in growth efficiency (aboveground biomass increment per LAI) with age. However, reductions in WUE were small after age 4 years, which explained the linear relationship between E and LAI. If E continues to decline successive short rotation lengths may not only make use of rapid early growth rates but could also increase plantation water use compared to longer rotations over the same period of time.     

An ecosystem approach to biodiversity effects: Carbon pools in a tropical tree plantation

This paper presents a synthesis of experiments conducted in a tropical tree plantation established in 2001 and consisting of 22 plots of 45 m × 45 m with either one, three or six native tree species. We examined the changes in carbon (C) pools (trees, herbaceous vegetation, litter, coarse woody debris (CWD), and mineral topsoil at 0-10 cm depth) and fluxes (decomposition of CWD and litter, as well as soil respiration) both through time and among diversity levels. Between 2001 and 2009 the aboveground C pools increased, driven by trees. Across diversity levels, the mean observed aboveground C pool was 7.9 ± 2.5 Mg ha⁻¹ in 2006 and 20.4 ± 7.4 Mg ha⁻¹ in 2009, a 158% increase. There was no significant diversity effect on the observed aboveground C pool, but we found a significant decrease in the topsoil C pool, with a mean value of 34.5 ± 2.4 Mg ha⁻¹ in 2001 and of 25.7 ± 5.7 Mg ha⁻¹ in 2009 (F_1,36 = 52.12, p < 0.001). Assuming that the biomass C pool in 2001 was negligible (<1 Mg ha⁻¹), then the plantation gained in C, on average, ∼20 and lost ∼9 Mg ha⁻¹ in biomass and soil respectively, for an overall gain of ∼11 Mg ha⁻¹ over 8 years. Across the entire data set, we uncovered significant effects of diversity on CWD decomposition (diversity: F_2,393 = 15.93, p < 0.001) and soil respiration (monocultures vs mixtures: t = 15.35, df = 11, p < 0.05) and a marginally significant time × diversity interaction on the loss of total C from the mineral topsoil pool (see above). Monthly CWD decomposition was significantly faster in monocultures (35.0 ± 24.1%) compared with triplets (31.3 ± 21.0%) and six-species mixtures (31.9 ± 26.8%), while soil respiration was higher in monocultures than in mixtures (t = 15.35, df = 11, p < 0.001). Path analyses showed that, as diversity increases, the links among the C pools and fluxes strengthen significantly. Our results demonstrate that tree diversity influences the processes governing the changes in C pools and fluxes following establishment of a tree plantation on a former pasture. We conclude that the choice of tree mixtures for afforestation in the tropics can have a marked influence on C pools and dynamics.