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.     

Estimates of forest biomass in the Brazilian Amazon: New allometric equations and adjustments to biomass from wood-volume inventories

Uncertainties in biomass estimates in Amazonian forests result in a broad range of possible magnitude for the emissions of carbon from deforestation and other land-use changes. This paper presents biomass equations developed from trees directly weighed in open forest on fertile soils in the southern Amazon (SA) and allometric equations for bole-volume estimates of trees in both dense and open forests. The equations were used to improve the commonly used biomass models based on large-scale wood-volume inventories carried out in Amazonian forest. The biomass estimates from the SA allometric equation indicate that equations developed in forests on infertile soils in central Amazonia (CA) result in overestimates if applied to trees in the open forests of SA. All aboveground components of 267 trees in open forests of SA were cut and weighed, and the proportion of the biomass stored in the crowns of trees in open forest was found to be higher than in dense forest. In the case of inventoried wood volume, corrections were applied for indentations and hollow trunks and it was determined that no adjustment is needed for the form factor used in the RadamBrasil volume formula. New values are suggested for use in models to convert wood volume to biomass estimates. A biomass map for Brazilian Amazonia was produced from 2702 plots inventoried by the RadamBrasil Project incorporating all corrections for wood density and wood volume and in factors used to add the bole volume of small trees and the crown biomass. Considering all adjustments, the biomass map indicates total biomass of 123.1 Gt (1 Gt = 1 billion tons) dry weight (aboveground + belowground) for originally forested areas in 1976 in the Brazilian Legal Amazon as a whole (102.3 Gt for aboveground only) at the time of the RadamBrasil inventories, which were carried out before intensive deforestation had occurred in the region. Excluded from this estimate are 529,000 km² of forest lacking sufficient RadamBrasil inventory data. After forest losses of 676,000 km² by 2006 – not counting 175,000 km² of this deforested area lacking RadamBrasil data – the estimated dry biomass stock was reduced to 105.4 and 87.6 Gt (aboveground + belowground and only above-ground). Thus, in 2006 the carbon storage in forested areas in Brazilian Amazonia as a whole will be around 51.1 Gt (assuming 1 Mg dry biomass = 0.485 Mg C). Biomass estimates by forest type (aggregated into 12 vegetation classes) are provided for each state in the Brazilian Legal Amazon.     

Normalization of wood density in biomass estimates of Amazon forests

Wood density is an important variable in estimates of biomass and carbon flux in tropical regions. However, the Amazon region lacks large-scale wood-density datasets that employ a sampling methodology adequate for use in estimates of biomass and carbon emissions. Normalization of the available datasets is needed to avoid bias in estimates that combine previous studies of wood density that used wood sampling at diverse positions in the bole or with various methods of density determination. This paper examines the question of whether regressions for radial variation and for variation in wood density along the bole, both developed in dense forest in central Amazonia (CA), are suitable for the open forests in southern Amazonia (SA) that are currently the target of most of Amazonia's deforestation activity. The wood density of the heartwood and density of full disks or slices (bark, sapwood and heartwood) in each tree were measured to assess the radial variation. For variation along the length of the bole, wood densities at breast height and at the top of the bole were used. Moisture content of the bole was measured in SA and compared with values reported by studies from CA in similar dense forest. Comparing regressions that predict full-disk density from heartwood density, the pattern of radial variation differs slightly and significantly between the two forest types (ANCOVA p = 0.006); the slopes have similar values but the intercepts differ. Variation along the bole in the two forest types does not differ significantly (p = 0.144), so the CA model for predicting mean bole density from the density of a slice at breast height gives an unbiased estimate of the mean bole density when applied to SA trees. In SA the mean moisture content of the bole was 0.416 (±0.068 S.D.; n = 223 trees). Moisture content of the bole had a strong inverse relationship with basic wood density (r = −0.77), which explains the lower moisture content in the trees in CA relative to SA. A much weaker inverse relationship was found between moisture content and green wood density (r = −0.292). The relationship between wood basic density and green (‘fresh’) density presented in this study provides an alternative means of obtaining basic wood density directly in the field when oven drying of samples is not possible.     

Biomass and greenhouse-gas emissions from land-use change in Brazil's Amazonian “arc of deforestation”: The states of Mato Grosso and Rondônia

We calculate greenhouse-gas emissions from land-use change in Mato Grosso and Rondônia, two states that are responsible for more than half of the deforestation in Brazilian Amazonia. In addition to deforestation (clearing of forest), we also estimate clearing rates and emissions for savannas (especially the cerrado, or central Brazilian savanna), which have not been included in Brazil's monitoring of deforestation. The rate of clearing of savannas was much more rapid in the 1980s and 1990s than in recent years. Over the 2006–2007 period (one year) 204 × 10³ ha of forest and 30 × 10³ ha of savanna were cleared in Mato Grosso, representing a gross loss of biomass carbon (above + belowground) of 66.0 and 1.8 × 10⁶ MgC, respectively. In the same year in Rondônia, 130 × 10³ ha of forest was cleared, representing gross losses of biomass of 40.4 × 10⁶ MgC. Data on clearing of savanna in Rondônia are unavailable, but the rate is believed to be small in the year in question. Net losses of carbon stock for Mato Grosso forest, Mato Grosso savanna and Rondônia forest were 29.0, 0.5 and 18.5 × 10⁶ MgC, respectively. Including soil carbon loss and the effects of trace-gas emissions (using global warming potentials for CH₄ and N₂O from the IPCC's 2007 Fourth Assessment Report), the impact of these emission sources totaled 30.9, 0.6 and 25.4 × 10⁶ Mg CO₂-equivalent C, respectively. These impacts approximate the combined effect of logging and clearing because the forest biomasses used are based on surveys conducted before many forests were exposed to logging. The total emission from Mato Grosso and Rondônia of 56.9 × 10⁶ Mg CO₂-equivalent C can be compared with Brazil's annual emission of approximately 80 × 10⁶ MgC from fossil–fuel combustion.     

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

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

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.     

Implications of fires on carbon budgets in Andean cloud montane forest: The importance of peat soils and tree resprouting

Fire in tropical montane cloud forests (TMCFs) is not as rare as once believed. Andean TMCFs sit immediately below highly flammable, high-altitude grasslands (Puna/Páramo) that suffer from recurrent anthropogenic fire. This treeline is a zone of climatic tension where substantial future warming is likely to force upward tree migrations, while increased fire presence and fire impacts are likely to force it downwards. TMCFs contain large carbon stocks in their peat soils and their loss through fire is a currently unaccounted for regional source of CO₂. This study, conducted in the southern Peruvian Andes (>2800 m), documents differences in live tree biomass, fine root biomass, fallen and standing dead wood, and soil organic carbon in 4 paired-sample plots (burned versus control) following the severe ground fires that occurred during the 2005 Andean drought. Peat soils contributed the most to biomass burning emissions, with lower values corresponding to an 89% mean stock difference compared to the controls (mean ± SE) (54.1 ± 22.3 vs. 5.8 ± 5.3 MgC ha⁻¹). Contrastingly, carbon stocks from live standing trees differed by a non-significant 37% lower value in the burned plots compared to the controls, largely compensated by vigorous resprouting (45.5 ± 17.4 vs. 69.2 ± 13.4 MgC ha⁻¹). Both standing dead trees and fallen dead wood were significantly higher in the burned plots with a three-fold difference from the controls: dead Trees 45.2 ± 9.4 vs. 16.4 ± 4.4 MgC ha⁻¹, and ca. a 2 fold difference for the fallen dead wood: 11.2 ± 5 vs. 6.7 ± 3.2 MgC ha⁻¹ for the burned plots versus their controls. A preliminary estimate of the regional contribution of biomass burning emissions from Andean TMCFs for the period 2000-2008, resulted in mean carbon emission rates of 1.3 TgC yr⁻¹ (max-min: 1.8-0.8 TgC yr⁻¹). This value is in the same order of magnitude than South American annual fire emissions (300 TgC yr⁻¹) suggesting the need for further research on Andean forest fires. On-going projects on the region are working on the promotion of landowner participation in TMCFs conservation through REDD+ mechanism. The heart of the proposed initiative is reforestation of degraded lands with green fire breaks enriched with economically valuable Andean plant species. The cultivation of these species may contribute to reduce deforestation pressure on the Amazonian cloud forest by providing an alternative income to local communities, at the same time that they prevent the spread of fire into Manu National Park and adjacent community-held forests, protecting forest and reducing CO₂ emissions.     

Future quantities and spatial distribution of harvesting residue and dead wood from natural disturbances in Canada

Interest in the use of bioenergy is increasing because of the need to mitigate climate change, the increasing costs and finite supply of fossil fuels, and the declining price of lumber and paper. Sound bioenergy policies must be informed by accurate estimates of potential feedstock production, rights to the production, social values and economics. Two of the main sources of bioenergy feedstock from forests are (i) harvesting residue and (ii) dead wood resulting from natural disturbances (i.e. standing dead timber). We modeled the production of bioenergy feedstock from these two sources from 2005 to 2020 for Canada's managed forest south of 60° N so that this information can be used in provincial and national strategic planning. Published estimates of harvesting residue vary widely, and our objective was to provide more precise estimates based on new forest inventory data and regional modeling. Natural disturbances result in very large quantities of dead wood on the landscape, but estimates of future stocks and annual production have not previously been made. Our estimates included a 50% discount factor to net-down theoretically available quantities to a more realistic estimate of potential ecologically sustainable bioenergy feedstock. The total future annual production averaged 51 ± 17 Tg year⁻¹ from natural disturbances and 20 ± 0.6 Tg year⁻¹ from clearcut harvesting residues. Harvesting residue for the area logged varied spatially from a low of 1.0 ± 0.77 kg m⁻² year⁻¹ to a high of 6.7 ± 0.1 kg m⁻² year⁻¹. Dead wood production due to insects was forecast to peak in the Montane Cordillera of British Columbia (BC) at 16.7 Tg year⁻¹ due to the current mountain pine beetle outbreak. Total dead wood production due to fire was highest in the western portion of the boreal forest (3.6 Tg year⁻¹ in the Boreal Shield of Saskatchewan), in part due to the high frequency of fires in these ecosystems and the large area of western boreal forest, but the highest density production was in BC: >9 kg m⁻² year⁻¹ in the burned area. Our results showed that the dead wood stocks of 331 Tg oven-dry matter potentially available for bioenergy in 2020 are much smaller than the 3100 ± 84 Tg of dead wood stocks estimated based on ecosystem dynamics. While bioenergy use will accelerate the release of greenhouse gases compared to on-site decay, the energy is renewable and can be used as a substitute for fossil fuels. The net benefit to the atmosphere of forest bioenergy use is affected by many factors, and future research should further assess which sustainable wood-based bioenergy strategies yield the greatest net greenhouse gas benefits over the different time scales needed for post-disturbance forest recovery.     

Above- and belowground biomass in a Brazilian Cerrado

Cerrado is a biome that occupies about 25% of the Brazilian territory and is characterized by a gradient of grassland to savanna and forest formations and by high species richness. It has been severely affected by degradation and deforestation and has been heavily fragmented over the past 4-5 decades. Despite the recognized overall ecological importance of the Cerrado, there are only few studies focusing on the quantification of biomass in this biome. We conducted such a case study in the South-East of Brazil in a cerrado sensu stricto (cerrado s.s.) with the goal to produce estimates of above- and belowground biomass and to develop allometric equations. A number of 120 trees from 18 species were destructively sampled and partitioned into the components: leaves, branches and bole. Five models with DBH (D), height (H), D²H and wood density (WD) as independent variables were tested for the development of allometric models for individual tree aboveground biomass (leaves + branches + bole). One model based on basal area (BA) as a stand parameter was also tested as an alternative approach for predicting aboveground biomass in the stand level. Belowground biomass was estimated by subsampling on 10 sample plots. Mean aboveground tree biomass (bole, branches and leaves) was estimated to be 62,965.5 kg ha⁻¹(SE = 14.6%) and belowground biomass accounted for 37,501.8 kg ha⁻¹ (SE = 23%). The best-fit equation for the estimation of individual tree aboveground biomass include DBH and wood density as explanatory variables (R² = 0.898; SEE = 0.371) and is applicable for the diameter range of this study (5.0-27.6 cm) and in environments with similar conditions of the cerrado s.s. sampled. In the stand level, the model tested presented a higher goodness of fit than the single tree models (R² = 0.934; SEE = 0.224). Our estimates of aboveground biomass are higher than reported by other studies developed in the same physiognomy, but the estimates of belowground biomass are within the range of values reported in other studies from sites in cerrado s.s. Both biomass estimates, however, exhibit relatively large standard errors. The root-to-shoot ratio of the sample trees is in the magnitude of reported values for savanna ecosystems, but smaller than estimated from other studies in the cerrado s.s.     

Growth and population structure of the tree species Malouetia tamaquarina (Aubl.) (Apocynaceae) in the central Amazonian floodplain forests and their implication for management

The long-term success of forest management depends primarily on the sustainability of timber production. In this study we analyse the population structure, tree age and wood increment of Malouetia tamaquarina (Aubl.) (Apocynaceae) to define a species-specific minimum logging diameter (MLD) and felling cycle by modelling volume growth. Contrary to other timber species in the nutrient-rich white-water floodplains forests (várzea), M. tamaquarina grows in the subcanopy of old-growth várzea forests. The wood of this species is utilized by local inhabitants in the floodplains for handicraft. In 35 plots of 25 m × 50 m we measured diameter at breast height (DBH) and tree height of all trees taller than 150 cm height. From 37 individuals with DBH > 15 cm we sampled two cores by increment borers to determine the wood density, tree age and diameter increment rates. In the management area of a várzea settlement with about 150 ha recently harvested trees of M. tamaquarina have been recorded and DBH was measured. The species presents an inverse J-shaped diameter distribution indicating that the species is obviously regenerating in the old-growth forests. Tree-ring analysis indicates a mean age of 74.5 years for a DBH of 22.7 cm for a studied population comprising 37 trees with maximum ages of up to 141 years for an individual with a DBH of 45.7 cm. The tree species has low annual diameter increment rates (3.16 ± 0.6 mm) despite a low wood density (0.36 ± 0.05 g cm⁻³). The volume growth model indicates a MLD of 25 cm and a felling cycle of 32.4 years. In the management area 35 trees with a mean DBH of 24 cm were recorded, similar to the defined MLD. The abundance of trees above the MLD is 2.7 trees ha⁻¹, or 405 trees, when extrapolated to the whole management area. Considering a felling cycle of 32.4 years (annual production unit of 4.63 ha) this results in total of 12.5 harvestable trees, almost three times less than actually harvested. The actual practice of harvesting M. tamaquarina risks the overexploitation of this slow-growing species.     

Past,present and future land-use in Xishuangbanna,China and the implications for carbon dynamics

Land use/land cover change is an important driver of global change and changes in carbon stocks. Estimating the changes in carbon stocks due to tropical deforestation has been difficult, mainly because of uncertainties in estimating deforestation rates and the biomass in the forest that have been cut. In this study, we combined detailed land-use change over a 27-year period based on satellite images and forest inventory data to estimate changes in biomass carbon stocks in the Xishuangbanna prefecture (1.9 million ha) of China. Xishuangbanna is located in southwestern China in the upper watershed of the Mekong River, and the major forest types are tropical seasonal rain forest, mountain rain forest, and subtropical evergreen broadleaf forest. In the past when the region was completely forested the total biomass carbon would have been approximately 212.65 ± 8.75 Tg C. By 1976 forest cover had been reduced to 70%, and in addition many forests had been degraded resulting in a large decrease in the total biomass carbon stocks (86.97 ± 3.70 Tg C). From 1976 to 2003, the mean deforestation rate was 13 722 ha year⁻¹ (1.12%), and this resulted in the loss of 370,494 ha of forest, and by 2003 total biomass carbon stocks had been reduced to 80.85 ± 2.64 Tg C. The annual carbon emissions due to land-use change, mainly forest conversion to agriculture and rubber plantations, were 0.37 ± 0.03 Tg C year⁻¹ between 1976 and 1988 and 0.13 ± 0.04 Tg C year⁻¹ between 1988 and 2003. During the next 20 years, if rubber plantations expand into forests outside of reserves, shrublands, grasslands, and shifting cultivation below 1500 m the total biomass carbon stocks of Xishuangbanna will decrease to 76.45 ± 1.49 Tg C in 2023. This would reflect a loss of 4.13 ± 1.14 Tg C between 2003 and 2023, or an annual loss of 0.21 ± 0.06 Tg C year⁻¹. Alternatively, if rubber plantations only expand into areas of shifting cultivation below 1500 m, and all areas presently in shrublands and grasslands are allowed to recover into secondary forests, total biomass carbon stock of the region would increase to 92.65 ± 3.80 Tg C in 2023. Under this scenario, the growth of existing forests and the expansion of new forests would result in a net sequestration of 0.60 ± 0.06 Tg C year⁻¹. This study demonstrates that the uncertainty of biomass estimates can be greatly reduced if detailed land-use analyses are combined with forest inventory data, and that slight changes in future land-use practices can have large implications for carbon fluxes.     

Factors causing variation in fine root biomass in forest ecosystems

Fine roots form one of the most significant components contributing to carbon cycling in forest ecosystems. We study here the effect of variation in root diameter classes, sampling depth and the inclusion of understorey vegetation root biomass in fine root biomass (FRB) estimates. The FRB estimates for different forest biomes are updated using a database of 512 forest stands compiled from the literature. We also investigate the relationships between environmental or forest stand variables and fine root biomass (≤2 mm in diameter) at the stand (g m⁻²) and tree level (g tree⁻¹). The FRB estimates extrapolated for the whole rooting depth were 526 ± 321 g m⁻², 775 ± 474 g m⁻² and 776 ± 518 g m⁻² for boreal, temperate and tropical forests, respectively, and were 26-67% higher than those based on the original sampling depths used. We found significant positive correlations between ≤1 and ≤2 mm diameter roots and between ≤2 and ≤5 mm roots. The FRB estimates, standardized to the ≤2 mm diameter class, were 34-60% higher and 25-29% smaller than those standardized to the ≤1 mm and ≤5 mm diameter classes, respectively. The FRB of the understorey vegetation accounted for 31% of the total FRB in boreal forests and 20% in temperate forests. The results indicate that environmental factors (latitude, mean annual precipitation, elevation, temperature) or forest stand factors (life form, age, basal area, density) can not explain a significant amount of the variation in the total FRB and a maximum of 30% that in the FRB of trees at the stand level, whereas the mean basal area of the forest stand can explain 49% of the total FRB and 79% of the FRB of trees at the tree level.     

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.     

Short-term community-level response of arthropods to group selection with seed-tree retention in a northern hardwood forest

We examined the short-term effects of group-selection harvesting with seed-tree retention on ground-dwelling and bark-dwelling arthropod communities in a northern hardwood forest in the Upper Peninsula of Michigan. Arthropods were sampled in 16 group-selection openings and 8 closed canopy reference plots. Two opening sizes were examined—radii of 0.5 (320 ± 27 m², n = 8) and 1.0 (1217 ± 62 m², n = 8) times the mean canopy height (22 m). Each opening and reference plot was centered on a single Betula alleghaniensis Britt. (yellow birch). Ground-dwelling arthropods were sampled using pitfall traps that were opened for two 1-week periods (rounds 1 and 2), and bark-dwelling arthropods were sampled with sticky traps attached to the centrally located B. alleghaniensis trees. Family-level diversity of ground-dwelling arthropods was lower in reference plots than in the openings, but the only significant difference occurred during round 2, between the matrix and large openings (P < 0.01). During both sampling periods, the ground-dwelling community exhibited a distinct clustering of family-level composition along environmental gradients such as opening size. Families such as Staphylinidae (rove beetles) and Trombidiidae (red velvet mites) were not favored by higher canopy openness while families such as Acrididae (grasshoppers) and Lycosidae (wolf spiders) were captured more in openings than in the forest matrix. Landing rates of wood-boring insects such as Buprestidae (metallic wood-boring beetles) and Xiphydriidae (wood wasps) were significantly higher on seed trees in group-selection openings than in reference plots (P < 0.05). Our results suggest that integrating group-selection openings within northern hardwood forests can lead to an increase in the family-level diversity of ground-dwelling arthropods, at least in the short term. Furthermore, seed trees left in such openings may be more attractive to bark- and wood-boring insects, which warrants further investigation into the susceptibility of these seed trees to damage by certain insect pests.     

Post-fire soil respiration in relation to burnt wood management in a Mediterranean mountain ecosystem

After a wildfire, the management of burnt wood may determine microclimatic conditions and microbiological activity with the potential to affect soil respiration. To experimentally analyze the effect on soil respiration, we manipulated a recently burned pine forest in a Mediterranean mountain (Sierra Nevada National and Natural Park, SE Spain). Three representative treatments of post-fire burnt wood management were established at two elevations: (1) “salvage logging” (SL), where all trees were cut, trunks removed, and branches chipped; (2) “non-intervention” (NI), leaving all burnt trees standing; and (3) “cut plus lopping” (CL), a treatment where burnt trees were felled, with the main branches lopped off, but left in situ partially covering the ground surface. Seasonal measurements were carried out over the course of two years. In addition, we performed continuous diurnal campaigns and an irrigation experiment to ascertain the roles of soil temperature and moisture in determining CO₂ fluxes across treatments. Soil CO₂ fluxes were highest in CL (average of 3.34 ± 0.19 μmol m⁻² s⁻¹) and the lowest in SL (2.21 ± 0.11 μmol m⁻² s⁻¹). Across seasons, basal values were registered during summer (average of 1.46 ± 0.04 μmol m⁻² s⁻¹), but increased during the humid seasons (up to 10.07 ± 1.08 μmol m⁻² s⁻¹ in spring in CL). Seasonal and treatment patterns were consistent at the two elevations (1477 and 2317 m a.s.l.), although respiration was half as high at the higher altitude.Respiration was mainly controlled by soil moisture. Watering during the summer drought boosted CO₂ effluxes (up to 37 ± 6 μmol m⁻² s⁻¹ just after water addition), which then decreased to basal values as the soil dried. About 64% of CO₂ emissions during the first 24 h could be attributed to the degasification of soil pores, with the rest likely related to biological processes. The patterns of CO₂ effluxes under experimental watering were similar to the seasonal tendencies, with the highest pulse in CL. Temperature, however, had a weak effect on soil respiration, with Q₁₀ values of ca. 1 across seasons and soil moisture conditions. These results represent a first step towards illustrating the effects of post-fire burnt wood management on soil respiration, and eventually carbon sequestration.     

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.     

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.     

Transpiration and hydraulic traits of old and regrowth eucalypt forest in southwestern Australia

We tested the hypothesis that overstorey of eucalypt forest dominated by tall, large diameter trees uses less water than regrowth stands in the high rainfall zone (>1100 mm year⁻¹) of the northern jarrah (Eucalyptus marginata) forest in southwestern Australia. We measured leaf area, cover, sapwood area and sapwood density at three paired old and regrowth stands. We also measured sapflow velocity at one paired stand (Dwellingup) from June 2007 to October 2008. Old stands had more basal area but less foliage cover, less leaf area and slightly thinner sapwood. The ratio of sapwood area to basal area decreased markedly as tree size increased. Sapwood area of the regrowth forest stands (6.6 ± 0.30 m² ha⁻¹) was nearly double that of the old stands (3.4 ± 0.17 m² ha⁻¹), despite larger basal area at the old stands. Leaf area index of the regrowth stands (2.1 ± 0.26) was only one-third larger than that at the old stands (1.5 ± 0.15); hence, the ratio of leaf area to sapwood area was larger in old stands than in regrowth stands (0.45 ± 0.022 m² cm⁻² versus 0.32 ± 0.045 m² cm⁻²). Our results are consistent with theories that trees have evolved to optimize carbon gain rather than maintain stomatal conductance. Neither sapwood density (540–650 kg m⁻³) nor sap velocity differed greatly between regrowth and old stands. At the old forest site, daily transpiration rose from 0.5 mm day⁻¹ in winter to 0.9 mm day⁻¹ in spring–summer, compared to 0.9 mm day⁻¹ and 1.8 mm day⁻¹ at the regrowth site. Annual water use by the overstorey trees was estimated to be ∼230 mm year⁻¹ for the old stand and ∼500 mm year⁻¹ at the regrowth stand, or 20% and 44% of annual rainfall. The overwhelming role of stand sapwood area in determining stand water use, combined with the marked changes in the ratio of sapwood area to basal area with tree age and size, suggest that stand overstorey structure can be managed to alter overstorey water use and catchment water yield. Silviculture to promote old-forest-like attributes may be a viable means of delivering multiple water and conservation benefits.     

Biomass burning in Brazil's Amazonian “arc of deforestation”: Burning efficiency and charcoal formation in a fire after mechanized clearing at Feliz Natal, Mato Grosso

Estimates of greenhouse-gas emissions from deforestation are highly uncertain because of high variability in key parameters and because of the limited number of studies providing field measurements of these parameters. One such parameter is burning efficiency, which determines how much of the original forest's aboveground carbon stock will be released in the burn, as well as how much will later be released by decay and how much will remain as charcoal. In this paper we examined the fate of biomass from a semideciduous tropical forest in the “arc of deforestation,” where clearing activity is concentrated along the southern edge of the Amazon forest. We estimated carbon content, charcoal formation and burning efficiency by direct measurements (cutting and weighing) and by line-intersect sampling (LIS) done along the axis of each plot before and after burning of felled vegetation. The total aboveground dry biomass found here (219.3 Mg ha⁻¹) is lower than the values found in studies that have been done in other parts of the Amazon region. Values for burning efficiency (65%) and charcoal formation (6.0%, or 5.98 Mg C ha⁻¹) were much higher than those found in past studies in tropical areas. The percentage of trunk biomass lost in burning (49%) was substantially higher than has been found in previous studies. This difference may be explained by the concentration of more stems in the smaller diameter classes and the low humidity of the fuel (the dry season was unusually long in 2007, the year of the burn). This study provides the first measurements of forest burning parameters for a group of forest types that is now undergoing rapid deforestation. The burning parameters estimated here indicate substantially higher burning efficiency than has been found in other Amazonian forest types. Quantification of burning efficiency is critical to estimates of trace-gas emissions from deforestation.     

Effect of habitat and grazing on the regeneration of wild Agave cupreata in Guerrero, Mexico

Agave cupreata is harvested from tropical dry forests, oak forests, and other habitats by rural communities in the Chilapa region of Guerrero, Mexico to make mescal, a traditional and culturally important liquor. Local management systems use various techniques to regulate Agave harvest and encourage regeneration, including the exclusion of cattle. This study examines the impacts of cattle exclusion and of the different habitat types on the population structure and density of A. cupreata. Sampling was conducted in pastures, oak forest, tropical dry forest, and mixed oak-tropical dry forest using 54 transects of 1000 m², where Agave was counted by size-class and measurements were taken of the vegetation and physical environment. Transects were divided between areas with cattle present and cattle excluded in all four habitats except for oak forest, where all areas were open to cattle. Agave density per 1000 m² was highest in pasture (148 ± 5, mean ± SE), followed by oak forest (100 ± 4), tropical dry forest (88 ± 5) and mixed oak-dry forest (81 ± 2). The size-class structures of Agave populations were also significantly different between vegetation types, with oak forest supporting higher seedling densities but lower numbers of juveniles. A regression subset selection algorithm showed that one of the most important factors influencing Agave populations was the presence of cattle, which can reduce densities by trampling and grazing on seedlings and floral stalks. Cattle presence significantly lowered Agave densities in the smaller size classes in all vegetation types but did not significantly alter size-class structure. Total Agave density per 1000 m² was significantly higher in transects where cattle were absent (148 ± 4) than where cattle were present (81 ± 1). In all areas sampled, the high number of juveniles relative to other size-classes suggests that Agave populations are successfully regenerating in the Chilapa region, and the higher Agave densities in fenced areas suggest that local management techniques are effectively increasing Agave yields. These results highlight the potential for sustainable management of Agave to conserve forest habitats while also providing important income from mescal to local communities in the region.