Comparing aboveground carbon sequestration between moso bamboo (Phyllostachys heterocycla) and China fir (Cunninghamia lanceolata) forests based on the allometric model

The purpose of this study was to compare carbon sequestration between moso bamboo (Phyllostachys heterocycla) and China fir (Cunninghamia lanceolata) forests. The study site was located in the lower mountain area of central Taiwan, where both moso bamboo and China fir were rich. In addition, moso bamboo and China fir forests were surveyed on 12 and 19 plantations, respectively. We predicted carbon sequestration based on the allometric model for moso bamboo and China fir forests and compared the relationships between characteristics of bamboo forests and elevation. The results showed that mean diameter at breast height (DBH), culms per hectare and aboveground biomass were not clearly affected by elevation, whereas a negative correlation (R = −0.600, p = 0.039) between mean DBH and stand density was found for moso bamboo forests. Moreover, the aboveground carbon storage was higher for China fir forests than for moso bamboo (99.5 vs. 40.6 Mg ha⁻¹). However, moso bamboo is an uneven-aged stand which is only composed of 1-5-year-old culms, while China fir is an even-aged stand and the age range is from 15 to 54 years, such that, per year, the mean aboveground carbon sequestration is 8.13 ± 2.15 and 3.35 ± 2.02 Mg ha⁻¹ for moso bamboo and China fir, respectively. On the other hand, the mean carbon sequestration of China fir decreases with increasing the age class. Furthermore, the ratio of moso bamboo to China fir is 2.39 and a T-test showed that the aboveground carbon levels were significantly different between these two species; thus, moso bamboo is a species with high potential for carbon sequestration.     

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.     

Carbon pools and temporal dynamics along a rotation period in Quercus dominated high forest and coppice with standards stands

Carbon pools in two Quercus petraea (sessile oak) dominated chronosequences under different forest management (high forest and coppice with standards) were investigated. The objective was to study temporal carbon dynamics, in particular carbon sequestration in the soil and woody biomass production, in common forest management systems in eastern Austria along with stand development. The chronosequence approach was used to substitute time-for-space to enable coverage of a full rotation period in each system. Carbon content was determined in the following compartments: aboveground biomass, litter, soil to a depth of 50 cm, living root biomass and decomposing residues in the mineral soil horizons. Biomass carbon pools, except fine roots and residues, were estimated using species-specific allometric functions. Total carbon pools were on average 143 Mg ha⁻¹ in the high forest stand (HF) and 213 Mg ha⁻¹ in the coppice with standards stand (CS). The mean share of the total organic carbon pool (TOC) which is soil organic carbon (SOC) differs only marginally between HF (43.4%) and CS (42.1%), indicating the dominance of site factors, particularly climate, in controlling this ratio. While there was no significant change in O-layer and SOC stores over stand development, we found clear relationships between living biomass (aboveground and belowground) pools and C:N ratio in topsoil horizons with stand age. SOC pools seem to be very stable and an impact of silvicultural interventions was not detected with the applied method. Rapid decomposition and mineralization of litter, indicated by low O-horizon pools with wide C:N ratios of residual woody debris at the end of the vegetation period, suggests high rates of turnover in this fraction. CS, in contrast to HF benefits from rapid resprouting after coppicing and hence seems less vulnerable to conditions of low rainfall and drying topsoil.     

Predicting growth and sequestration of carbon by plantations growing in regions of low-rainfall in southern Australia

In regions of Australia of low–medium rainfall (500–800 mm/year), there is growing community and land-owner support for re-planting trees to achieve multiple environmental objectives, particularly amelioration of soil salinity. Sequestration of carbon by newly established trees is not only another important environmental benefit, but also a potential commercial benefit. To obtain estimates of carbon sequestered by species of commercial potential in such regions, we calibrated the carbon (C) accounting model FullCAM to Eucalyptus cladocalyx and Corymbia maculata plantations. This was achieved by harvesting trees of a range in sizes to determine the allometric relationships that most accurately predict biomass and stem density from measures of stem diameter. Predictions of stem diameter were obtained from a forest growth model (3-PG) previously calibrated for these two species. By applying these predictions of changes in stem diameter as the stand matures in our allometric relationships, we estimated changes in partitioning of biomass (between stem, branches, bark, foliage and roots) and stem wood density as the stand matures under scenarios of 500, 600 and 750 mm mean annual rainfall. We found that for both species, regardless of annual rainfall, throughout the rotation 37–50% of carbon sequestered in the total tree biomass was in the stem, 18–27% in both branches and roots, and the remainder in foliage or bark. However, rate of accumulation of carbon was dependent on annual rainfall, with average annual rate of sequestration of carbon in tree biomass and litter during the first rotation of E. cladocalyx (or C. maculata) increasing from 3.68 (or 4.17) to 4.72 (or 4.86) Mg C ha⁻¹ yr⁻¹ as annual rainfall increased from about 500 to 750 mm. Although it was predicted that decomposition negated any accumulation of debris between successive rotations, carbon was predicted to accumulate in sawlog products, given that assumed rates of product decomposition were slightly less than their rate of accumulation. This resulted in a slight increase (<8 Mg C ha⁻¹) in predicted total sequestration of carbon between successive rotations.     

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.     

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.     

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.     

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.     

Forest structure,habitat and carbon benefits from thinning floodplain forests: Managing early stand density makes a difference

Forest ecosystems are increasingly expected to produce multiple goods and services, such as timber, biodiversity, water flows, and sequestered carbon. While many of these are not mutually exclusive, they cannot all be simultaneously maximised so that management compromise is inevitable. We used a 42-year dataset from a naturally regenerating floodplain forest of the river red gum (Eucalyptus camaldulensis) to investigate the effects of pre-commercial thinning on long-term patterns in habitat quality, forest structure and rates of carbon storage (i.e. standing aboveground carbon). Estimates of habitat quality were based on the density of hollow-bearing trees because hollows are ecologically important to many species of vertebrates and invertebrates in these forests. Thinning improved habitat value by producing 20 (±8) hollow-bearing trees per ha after 42 years, while the unthinned treatment produced none. Unthinned (highest density) stands were dominated by many slender trees, mostly <25 cm in diameter, whereas thinned stands produced negatively skewed size distributions with higher median and maximum stem diameters. Moderately thinned stands (560 trees ha⁻¹) had the highest aboveground carbon storage rate (4.1 t C year⁻¹) and the highest aboveground carbon stocks (200.2 ± 9.6 t C ha⁻¹) after 42 years, while the unthinned treatment had the lowest carbon storage rate (1.6 t C year⁻¹) and an intermediate level of aboveground standing carbon (165.1 ± 31.1 t C ha⁻¹). Our results highlight the importance of early stand density as a determinant of long-term forest structure, habitat quality and carbon storage rates. We recommend that thinning be considered as one component of a broader strategy for enhancing the structure, habitat value and aboveground carbon storage of developing floodplain forests.     

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.     

Radiation use efficiency in adjacent hardwood and pine forests in the southern Appalachians

The efficiency with which trees convert photosynthetically active radiation (PAR) to biomass has been shown to be consistent within stands of an individual species, which is useful for estimating biomass production and carbon accumulation. However, radiation use efficiency (?) has rarely been measured in mixed-species forests, and it is unclear how species diversity may affect the consistency of ?, particularly across environmental gradients. We compared aboveground net primary productivity (ANPP), intercepted photosynthetically active solar radiation (IPAR), and radiation use efficiency (? = ANPP/IPAR) between a mixed deciduous forest and a 50-year-old white pine (Pinus strobus L.) plantation in the southern Appalachian Mountains. Average ANPP was similar in the deciduous forest (11.5 Mg ha⁻¹ y⁻¹) and pine plantation (10.2 Mg ha⁻¹ y⁻¹), while ? was significantly greater in the deciduous forest (1.25 g MJ⁻¹) than in the white pine plantation (0.63 g MJ⁻¹). Our results demonstrate that late-secondary hardwood forests can attain similar ANPP as mature P. strobus plantations in the southern Appalachians, despite substantially less annual IPAR and mineral-nitrogen availability, suggesting greater resource-use efficiency and potential for long-term carbon accumulation in biomass. Along a 260 m elevation gradient within each forest there was not significant variation in ?. Radiation use efficiency may be stable for specific forest types across a range of environmental conditions in the southern Appalachian Mountains, and thus useful for generating estimates of ANPP at the scale of individual watersheds.     

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.     

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.     

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.     

The effect of land use type on net nitrogen mineralization on abandoned agricultural land: Silver birch stand versus grassland

The effect of land use type on the dynamics and annual rate of net nitrogen mineralization (NNM) in a naturally generated silver birch stand and in a grassland, both on abandoned agricultural land, was assessed in situ in the upper 0–20 cm soil layer using the method of buried polyethylene bags. Annual NNM rate in the birch stand (156 kg N ha⁻¹ year⁻¹) was higher than in the grassland (102 kg N ha⁻¹ year⁻¹); in both cases NNM covered a major part of the plants annual nitrogen demand. The rate of NNM in the upper 0–10 cm soil layer in the birch stand (99 kg N ha⁻¹ year⁻¹) exceeded the respective rate of NNM in the grassland (51 kg N ha⁻¹ year⁻¹) roughly two times. In the grassland the rates of NNM in the 0–10 and 10–20 cm layers were equal; in the birch stand NNM in the 0–10 cm layer was 1.7 times higher than in deeper 10–20 cm layer. The intensity of daily NNM in the upper 0–10 cm soil layer in the birch stand was the highest in June and in the grassland in May, 776 and 528 mg kg⁻¹ N day⁻¹, respectively. In our study no significant correlation was found between NNM and the environmental factors monthly mean soil temperature, soil moisture content and pH.     

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.     

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.     

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.     

Above- and belowground nutrients storage and biomass accumulation in marginal Nothofagus antarctica forests in Southern Patagonia

The above- and belowground biomass and nutrient content (N, P, K, Ca, S and Mg) of pure deciduous Nothofagus antarctica (Forster f.) Oersted stands grown in a marginal site and aged from 8 to 180 years were measured in Southern Patagonia. The total biomass accumulated ranged from 60.8 to 70.8 Mg ha⁻¹ for regeneration and final growth stand, respectively. The proportions of belowground components were 51.6, 47.2, 43.9 and 46.7% for regeneration, initial growth, final growth and mature stand, respectively. Also, crown classes affected the biomass accumulation where dominant trees had 38.4 Mg ha⁻¹ and suppressed trees 2.6 Mg ha⁻¹ to the stand biomass in mature stand. Nutrient concentrations varied according to tree component, crown class and stand age. Total nutrient concentration graded in the fallowing order: leaves > bark > middle roots > small branches > fine roots > sapwood > coarse roots > heartwood. While N and K concentrations increased with age in leaves and fine roots, concentration of Ca increased with stand age in all components. Dominant trees had higher N, K and Ca concentrations in leaves, and higher P, K and S concentrations in roots, compared with suppressed trees. Although the stands had similar biomass at different ages, there were important differences in nutrient accumulation per hectare from 979.8 kg ha⁻¹ at the initial growth phase to 665.5 kg ha⁻¹ at mature stands. Nutrient storage for mature and final growth stands was in the order Ca > N > K > P > Mg > S, and for regeneration stand was Ca > N > K > Mg > P > S. Belowground biomass represented an important budget of all nutrients. At early ages, N, K, S, Ca and Mg were about 50% in the belowground components. However, P was 60% in belowground biomass and then increased to 70% in mature stands. These data can assist to quantify the impact of different silviculture practices which should aim to leave material (mainly leaves, small branches and bark) on the site to ameliorate nutrient removal and to avoid a decline of long-term yields.     

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.