Modelling soil carbon sequestration of intensively monitored forest plots in Europe by three different approaches

Information on soil carbon sequestration and its interaction with nitrogen availability is rather limited, since soil processes account for the most significant unknowns in the C and N cycles. In this paper we compare three completely different approaches to calculate carbon sequestration in forest soils. The first approach is the limit-value concept, in which the soil carbon accumulation is estimated by multiplying the annual litter fall with the recalcitrant fraction of the decomposing plant litter, which depends on the nitrogen and calcium content in the litter. The second approach is the N-balance method, where carbon sequestration is calculated from the nitrogen retention in the soil multiplied with the present soil C/N ratio in organic layer and mineral topsoil. The third approach is the dynamic SMART2 model in combination with an empirical approach to assess litter fall inputs. The comparison is done by first validating the methods at three chronosequences with measured C pools, two in Denmark and one in Sweden, and then application on 192 intensive monitoring plots located in the Northern and Western part of Europe. Considering all three chronosequences, the N-balance method was generally most in accordance with the C pool measurements, although the SMART2 model was also quite consistent with the measurements at two chronosequences. The limit-value approach generally overestimated the soil carbon sequestration. At the intensive monitoring plots, the limit-value concept calculated the highest carbon sequestration, ranging from 160 to 978 kg ha⁻¹ year⁻¹, followed by the N-balance method which ranged from 0 to 535 kg ha⁻¹ year⁻¹. With SMART2 we calculated the lowest carbon sequestration from −30 to 254 kg ha⁻¹ year⁻¹. All the three approaches found lower carbon sequestration at a latitude from 60 to 70° compared to latitudes from 40 to 50 and from 50 to 60. Considering the validation of the three approaches, the range in results from both the N-balance method and SMART2 model seems most appropriate.     

Gradual forest edges can mitigate edge effects on throughfall deposition if their size and shape are well considered

For the protection and promotion of biodiversity in forest edges and interiors, forest edge management practices are put forward like the creation of gradual forest edges (i.e., edges with a gradual increase of vegetation height from open area to forest, e.g., by means of a fringe, a belt, and a mantle). In this study, we tested the mitigating effect of gradual forest edges on the atmospheric deposition of inorganic nitrogen (N) and the potentially acidifying pollutants SO₄²⁻, NO₃⁻, and NH₄⁺ (N + S). We conducted field experiments at three exposed forest edges in Flanders and the Netherlands and compared throughfall deposition at steep edges (i.e., edges with an abrupt transition from open area to forest) and at adjacent gradual edges. Along transects perpendicular to the edges, during three months in both winter and summer, throughfall deposition of Cl⁻, SO₄²⁻, NO₃⁻, and NH₄⁺ was monitored in the forest between 0 and 64 m from the edges and in the gradual edge vegetation. At the smoothest and best fitting gradual edge, the extra N + S throughfall deposition the forest received due to edge effects was lower than at the adjacent steep edge, with on average 80 and 100% in winter and summer, respectively. This was due to a halving of the depth of edge influence and an almost full reduction of the magnitude of edge influence. This decrease in throughfall deposition in the forest was not compensated by the additional throughfall deposition on the gradual edge vegetation itself, resulting in a final decrease in throughfall deposition in the forest edge by 60% in winter and 74% in summer. While this result confirms that gradual edges can mitigate edge effects on atmospheric deposition, the results of the other sites indicate the importance of size and shape of the gradual edge vegetation in mitigating edge effects on deposition: due to insufficient height (‘size’) or inadequate shape of the gradual edge vegetation, only small or insignificant decreases in throughfall deposition were observed. Hence, for mitigating edge effects on N + S and N deposition, our results support the recommendation of creating gradual edges at forests with poorly developed, abrupt edges, but it stresses the importance of a thorough consideration of the shape and size of the gradual edge vegetation in the design and management of gradual forest edges.     

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.     

Carbon sequestration and biodiversity of re-growing miombo woodlands in Mozambique

Land management in tropical woodlands is being used to sequester carbon (C), alleviate poverty and protect biodiversity, among other benefits. Our objective was to determine how slash-and-burn agriculture affected vegetation and soil C stocks and biodiversity on an area of miombo woodland in Mozambique, and how C stocks and biodiversity responded once agriculture was abandoned. We sampled twenty-eight 0.125 ha plots that had previously been cleared for subsistence agriculture and had been left to re-grow for 2 to ∼25 years, and fourteen 0.25 ha plots of protected woodlands, recording stem diameter distributions and species, collecting wood for density determination, and soil from 0 to 0.3 m for determination of %C and bulk density. Clearance for agriculture reduced stem wood C stocks by 19.0 t C ha⁻¹. There were significant relationships between period of re-growth and basal area, stem numbers and stem biomass. During re-growth, wood C stocks accumulated at 0.7 t C ha⁻¹ year⁻¹. There was no significant difference in stem C stocks on woodlands and on abandoned farmland 20–30 years old. Soil C stocks in the top 0.3 m on abandoned land had a narrower range (21–74 t C ha⁻¹) than stocks in woodland soils (18–140 t C ha⁻¹). There was no discernible increase in soil C stocks with period of re-growth, suggesting that the rate of accumulation of organic matter in these soils was very slow. The re-growing plots did not contain the defining miombo species, and total stem numbers were significantly greater than in woodland plots, but species richness and diversity were similar in older abandonments and miombo woodlands. Wood C stocks on abandoned farmland were capable of recovery within 2–3 decades, but soil C stocks did not change on this time-scale. Woodland soils were capable of storing >100 t C ha⁻¹, whereas no soil on a re-growing area exceeded 74 t C ha⁻¹, so there is a potential for C sequestration in soils on abandoned farmland. Management should focus on identifying C-rich soils, conserving remaining woodlands to protect soil C and preserve defining miombo species, and on investigating whether fire control on recovering woodland can stimulate accumulation of soil C and greater tree biomass, and restore defining miombo species.     

Carbon density and accumulation in woody species of tropical dry forest in India

We studied the carbon density and accumulation in trees at five sites in a tropical dry forest (TDF) to address the questions: how is the TDF structured in terms of tree and carbon density in different DBH (diameter at breast height) classes? What are the levels of carbon density and accumulation in the woody species of TDF? Is the vegetation carbon density evenly distributed across the forest? Does carbon stored in the soil reflect the pattern of aboveground vegetation carbon density? Which species in the forest have a high potential for carbon accumulation? The WSG among species ranged from 0.39 to 0.78 g cm⁻³. Our study indicated that most of the carbon resides in the old-growth (high DBH) trees; 88-97% carbon occurred in individuals ?19.1 cm DBH, and therefore extra care is required to protect such trees in the dry forest. Acacia catechu, Buchanania lanzan, Hardwickia binata, Shorea robusta and Terminalia tomentosa accounted for more than 10 t ha⁻¹ carbon density, warranting extra efforts for their protection. Species also differed in their capacity to accumulate carbon indicating variable suitability for afforestation. Annually, the forest accumulated 5.3 t-C ha⁻¹ yr⁻¹ on the most productive, wettest Hathinala site to 0.05 t-C ha⁻¹ yr⁻¹ on the least productive, driest Kotwa site. This study indicated a marked patchy distribution of carbon density (151 t-C ha⁻¹ on the Hathinala site to 15.6 t-C ha⁻¹ on the Kotwa site); the maximum value was more than nine times the minimum value. These findings suggest that there is a substantial scope to increase the carbon density and accumulation in this forest through management strategies focused on the protection, from deforestation and fire, of the high carbon density sites and the old-growth trees, and increasing the stocking density of the forest by planting species with high potential for carbon accumulation.     

Recovery of carbon and nutrient pools in a northern forested wetland 11 years after harvesting and site preparation

We measured the change in above- and below-ground carbon and nutrient pools 11 years after the harvesting and site preparation of a histic-mineral soil wetland forest in the Upper Peninsula of Michigan. The original stand of black spruce (Picea mariana), jack pine (Pinus banksiana) and tamarack (Larix laricina) was whole-tree harvested, and three post-harvest treatments (disk trenching, bedding, and none) were randomly assigned to three Latin square blocks (n = 9). Nine control plots were also established in an adjoining uncut stand. Carbon and nutrients were measured in three strata of above-ground vegetation, woody debris, roots, forest floor, and mineral soil to a depth of 1.5 m. Eleven years following harvesting, soil C, N, Ca, Mg, and K pools were similar among the three site preparation treatments and the uncut stand. However, there were differences in ecosystem-level nutrient pools because of differences in live biomass. Coarse roots comprised approximately 30% of the tree biomass C in the regenerated stands and 18% in the uncut stand. Nutrient sequestration, in the vegetation since harvesting yielded an average net ecosystem gain of 332 kg N ha⁻¹, 110 kg Ca ha⁻¹, 18 kg Mg ha⁻¹, and 65 kg K ha⁻¹. The likely source for the cations and N is uptake from shallow groundwater, but N additions could also come from non-symbiotic N-fixation and N deposition. These are the only reported findings on long-term effects of harvesting and site preparation on a histic-mineral soil wetland and the results illustrate the importance of understanding the ecohydrology and nutrient dynamics of the wetland forest. This wetland type appears less sensitive to disturbance than upland sites, and is capable of sustained productivity under these silvicultural treatments.     

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.     

Soil carbon dynamics under young tropical secondary forests on former pastures—A case study from Panama

Secondary forests are gaining increased importance in tropical landscapes and have recently been reported to act as potential belowground carbon sinks. While economic interest in the management of secondary forests to mitigate carbon emissions is rising, the dynamics of soil carbon stocks under these ecosystems remain poorly understood. Recent studies report conflicting results concerning soil carbon trends as well as multiple confounding factors (e.g. soil type, topography and land-use history) affecting these trends. In this study, organic carbon stocks were measured in the mineral soil up to 20 cm depth of at 24 active pastures, 5-8-year-old, and 12-15-year-old secondary forest sites on former pastures. Additionally, we estimated carbon stocks under a 100-year-old secondary forest and compared them to those of nearby mature forests. Abiotic conditions in the study area were homogenous, enabling us to isolate the effect of land-use change on soil organic carbon stocks. Contrary to our expectations, soil carbon stocks in the top 10 cm did not change with young secondary forest development. Pasture soils stored 24.8 ± 2.9 Mg ha⁻¹ carbon (mean ± standard error) in the top 10 cm, and no accumulation of soil carbon was apparent during the first 15 years of secondary succession. Soil carbon stocks under 100-year-old secondary forests, averaging 43.0 ± 7.9 Mg ha⁻¹ (mean ± standard error), were clearly higher than those recorded at younger sites and approached levels of soil carbon stocks under mature forests. These data indicate that soil carbon stocks in this region of Panama are not affected by the land-use transition from pasture to young secondary regrowth. However, an increase of soil carbon storage might be possible over a longer period of time. Our results support trends observed in other tropical areas and highlight the importance of environmental conditions such as soil properties rather than land-use transitions on soil carbon dynamics. While our understanding of organic carbon dynamics in tropical soils remains limited, these results underscore the challenges of undertaking short-term reforestation projects with the expectation of increasing soil carbon sequestration.     

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.     

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 impact of atmospheric deposition and climate on forest growth in European monitoring plots: An individual tree growth model

In the climate change discussion, the possibility of carbon sequestration of forests plays an important role. Therefore, research on the effects of environmental changes on net primary productivity is interesting. In this study we investigated the influence of changing temperature, precipitation and deposition of sulphur and nitrogen compounds on forest growth. The database consisted of 654 plots of the European intensive monitoring program (Level II plots) with 5-year growth data for the period 1994–1999. Among these 654 plots only 382 plots in 18 European countries met the requirements necessary to be used in our analysis. Our analysis was done for common beech (Fagus sylvatica), oak (Quercus petraea and Q. robur), Scots pine (Pinus sylvestris) and Norway spruce (Picea abies). We developed an individual tree growth model with measured basal area increment of each individual tree as responding growth factor and tree size (diameter at breast height), tree competition (basal area of larger trees and stand density index), site factors (soil C/N ratio, temperature), and environmental factors (temperature change compared to long-term average, nitrogen and sulphur deposition) as influencing parameters. Using a mixed model approach, all models for the tree species show a high goodness of fit with Pseudo-R² between 0.33 and 0.44. Diameter at breast height and basal area of larger trees were highly influential variables in all models. Increasing temperature shows a positive effect on growth for all species except Norway spruce. Nitrogen deposition shows a positive impact on growth for all four species. This influence was significant with p < 0.05 for all species except common beech. For beech the effect was nearly significant (p = 0.077). An increase of 1 kg N ha⁻¹ yr⁻¹ corresponds to an increase in basal area increment between 1.20% and 1.49% depending on species. Considering an average total carbon uptake for European forests near 1730 kg per hectare and year, this implies an estimated sequestration of approximately 21–26 kg carbon per kg nitrogen deposition.     

The impact of nitrogen deposition on carbon sequestration by European forests and heathlands

In this study, we present estimated ranges in carbon (C) sequestration per kg nitrogen (N) addition in above-ground biomass and in soil organic matter for forests and heathlands, based on: (i) empirical relations between spatial patterns of carbon uptake and influencing environmental factors including nitrogen deposition (forests only), (ii) ¹⁵N field experiments, (iii) long-term low-dose N fertilizer experiments and (iv) results from ecosystem models. The results of the various studies are in close agreement and show that above-ground accumulation of carbon in forests is generally within the range 15–40 kg C/kg N. For heathlands, a range of 5–15 kg C/kg N has been observed based on low-dose N fertilizer experiments. The uncertainty in C sequestration per kg N addition in soils is larger than for above-ground biomass and varies on average between 5 and 35 kg C/kg N for both forests and heathlands. All together these data indicate a total carbon sequestration range of 5–75 kg C/kg N deposition for forest and heathlands, with a most common range of 20–40 kg C/kg N. Results cannot be extrapolated to systems with very high N inputs, nor to other ecosystems, such as peatlands, where the impact of N is much more variable, and may range from C sequestration to C losses.     

氮沉降对森林碳汇功能影响的研究进展

氮沉降增加对森林碳汇功能的大小和稳定性具有重要影响。文中介绍了森林碳汇对氮沉降增加响应的研究进展,概述了同位素技术在该研究领域的应用前景,指出在沉降增加条件下森林光合产物分配和土壤碳周转速率变化将是未来森林碳循环研究的热点。     

Controls of litter quality on the carbon sink in soils through partitioning the products of decomposing litter in a forest succession series in South China

Through the long-term measurement and development of a method for partitioning the products of decomposing litter, the impact of chemical components of forest debris on soil organic carbon (SOC) accumulation was studied in a forest succession series in South China. We quantified how litter quality is strongly correlated with the partitioning of respiration, dissolved organic carbon (DOC) and fragments of decomposing litter. In the succession sequence of 60-year-old pine forest (PF), to 80-year-old mixed pine and evergreen broadleaved forest (MF) to more than 400-year-old monsoon evergreen broadleaved forest (MEBF), the litter C/N ratios and lignin contents were gradually decreasing, which in turn were correlated with increasing litter decomposition constants (k-values), gradually shortening residence times of standing litter pool. And, 53.5%, 65.6% and 76.2% of the gravimetric litter mass losses were going belowground through both DOC and fragmentation. Correspondingly, the SOC accumulation rates in the top 20 cm of mineral soils for the three forests from 1978 to 2008 were 26 ± 4, 33 ± 5 and 67 ± 5 g C m⁻² yr⁻¹, respectively. Results of the study support the idea that in order to increase carbon sequestration in soils and long-term functional ability of forest ecosystems to act as carbon sinks, “Kyoto Forests” should be designed and reconstructed with a high diversity of broadleaved species, especially containing nitrogen-fixing trees.     

Reduced soil respiration in gaps in logged lowland dipterocarp forests

We studied the effects of forest composition and structure, and related biotic and abiotic factors on soil respiration rates in a tropical logged forest in Malaysian Borneo. Forest stands were classified into gap, pioneer, non-pioneer and mixed (pioneer, non-pioneer and unclassified trees) based on the species composition of trees >10 cm diameter breast height. Soil respiration rates did not differ significantly between non-gap sites (1290 ± 210 mg CO₂ m⁻² h⁻¹) but were double those in gap sites (640 ± 130 mg CO₂ m⁻² h⁻¹). Post hoc analyses found that an increase in soil temperature and a decrease in litterfall and fine root biomass explained 72% of the difference between gap and non-gap sites. The significant decrease of soil respiration rates in gaps, irrespective of day or night time, suggests that autotrophic respiration may be an important contributor to total soil respiration in logged forests. We conclude that biosphere-atmosphere carbon exchange models in tropical systems should incorporate gap frequency and that future research in tropical forest should emphasize the contribution of autotrophic respiration to total soil respiration.     

Ecosystem carbon storage and partitioning in a tropical seasonal forest in Southwestern China

Tropical forests play an important role in the global carbon cycle. Despite an increasing number of studies have addressed carbon storage in tropical forests, the regional variation in such storage remains poorly understood. Uncertainty about how much carbon is stored in tropical forests is an important limitation for regional-scale estimates of carbon fluxes and improving these estimates requires extensive field studies of both above- and belowground stocks. In order to assess the carbon pools of a tropical seasonal forest in Asia, total ecosystem carbon storage was investigated in Xishuangbanna, SW China. Averaged across three 1 ha plots, the total carbon stock of the forest ecosystem was 303 t C ha⁻¹. Living tree carbon stocks (both above- and belowground) ranged from 163 to 258 t C ha⁻¹. The aboveground biomass C pool is comparable to the Dipterocarp forests in Sumatra but lower than those in Malaysia. The variation of C storage in the tree layer among different plots was mainly due to different densities of large trees (DBH > 70 cm). The contributions of the shrub layer, herb layer, woody lianas, and fine litter each accounted for 1–2 t C ha⁻¹ to the total carbon stock. The mineral soil C pools (top 100 cm) ranged from 84 to 102 t C ha⁻¹ and the C in woody debris from 5.6 to 12.5 t C ha⁻¹, representing the second and third largest C component in this ecosystem. Our results reveal that a high percentage (70%) of C is stored in biomass and less in soil in this tropical seasonal forest. This study provides an accurate estimate of the carbon pool and the partitioning of C among major components in tropical seasonal rain forest of northern tropical Asia. Results from this study will enhance our ability to evaluate the role of these forests in regional C cycles and have great implications for conservation planning.     

Research Advances in Effect of Nitrogen Deposition on Forest Carbon Sequestration

Nitrogen deposition imposes important impact on the function and the stability of forest carbon sequestration.This paper reviewed the research advances in the increasing response of forest carbon sequestration to nitiogen deposition, described the application prospects of stable carbon isotope technique in the research field.And finally this paper pointed out that,on the condition that nitrogen deposition rises,on the allocation of forest photosynthetic products and the change in soil carbon turnover rate are the two hotspots in the future carbon cycling research.     

Impacts of selective logging on above-ground forest biomass in the Monts de Cristal in Gabon

Selective logging is an important socio-economic activity in the Congo Basin but one with associated environmental costs, some of which are avoidable through the use of reduced-impact logging (RIL) practices. With increased global concerns about biodiversity losses and emissions of carbon from forest in the region, more information is needed about the effects of logging on forest structure, composition, and carbon balance. We assessed the consequences of low-intensity RIL on above-ground biomass and tree species richness in a 50 ha area in northwestern Gabon. We assessed logging impacts principally in 10 randomly located 1-ha plots in which all trees ?10 cm dbh were measured, identified to species, marked, and tagged prior to harvesting. After logging, damage to these trees was recorded as being due to felling or skidding (i.e., log yarding) and skid trails were mapped in the entire 50-ha study area. Allometric equations based on tree diameter and wood density were used to transform tree diameter into biomass.Logging was light with only 0.82 trees (8.11 m³) per hectare extracted. For each tree felled, an average of 11 trees ?10 cm dbh suffered crown, bole, or root damage. Skid trails covered 2.8% of the soil surface and skidding logs to the roadside caused damage to an average of 15.6 trees ?10 cm dbh per hectare. No effect of logging was observed on tree species richness and pre-logging above-ground forest biomass (420.4 Mg ha⁻¹) declined by only 8.1% (34.2 Mg ha⁻¹). We conclude from these data that with harvest planning, worker training in RIL techniques, and low logging intensities, substantial carbon stocks and tree species richness were retained in this selectively logged forest in Gabon.     

Dissolved Al reduces Mg uptake in Norway spruce forest: Results from a long-term field manipulation experiment in Norway

Dissolved aluminium (Al) in soils, mobilized by acid deposition, is considered a threat to forest health through hampering root growth and nutrient uptake. Since the end of the 1980s dissolved Al in forest soil water plays a key role in the assessment of critical loads of acid deposition. So far, most evidence for toxicity of dissolved Al in forest soil water is based on nutrient solution studies and pot experiments. Here, we present results from one of the few in situ ecosystem-scale forest manipulation experiments to study the effect of Al on mature forest trees. A plotwise addition of dilute AlCl₃ was conducted during seven years in an even-aged spruce forest (Picea abies) in an area in Norway with low acid deposition. Soil solution concentrations of Al were increased to potentially toxic levels (up to 500 μmol L⁻¹) and base cation (Ca + Mg + K) to inorganic Al ratios in the soil solution in the root zone were mostly below 1 in the Al-addition treatments. In the control treatment (only water addition) Al concentrations did not exceed 15 μmol L⁻¹ and base cation to inorganic Al ratios were above 1. The toxic effects of Al on fine root growth and plant growth found in hydroponic studies and pot trials are not confirmed by this field manipulation. However, magnesium (Mg) contents in needles decreased significantly and persistently in plots with elevated Al concentrations, whereas the needle Ca content did not respond. The depletion of the Mg content in needles is suggested to be due to antagonistic effects of high Al concentrations at the root surface, consistent with observed reductions in Mg to Al ratio of inner bark. This study clearly supports a role for Al in critical load functions for forests as dissolved Al causes a decrease in uptake of Mg. However, other signs of reduced forest vitality were not observed. Soil base cation status may need to be included in risk evaluations of forest health under acid deposition.