Size, species, and fire behavior predict tree and liana mortality from experimental burns in the Brazilian Amazon

Anthropogenic understory fires have affected large areas of tropical forest in recent decades, particularly during severe droughts. Yet, the mechanisms that control fire-induced mortality of tropical trees and lianas remain ambiguous due to the challenges associated with documenting mortality given variation in fire behavior and forest heterogeneity. In a seasonally dry Amazon forest, we conducted a burn experiment to quantify how increasing understory fires alter patterns of stem mortality. From 2004 to 2007, tree and liana mortality was measured in adjacent 50-ha plots that were intact (B0 - control), burned once (B1), and burned annually for 3 years (B3). After 3 years, cumulative tree and liana mortality (≥1 cm dbh) in the B1 (5.8% yr⁻¹) and B3 (7.0% yr⁻¹) plots significantly exceeded mortality in the control (3.2% yr⁻¹). However, these fire-induced mortality rates are substantially lower than those reported from more humid Amazonian forests. Small stems were highly vulnerable to fire-induced death, contrasting with drought-induced mortality (measured in other studies) that increases with tree size. For example, one low-intensity burn killed >50% of stems <10 cm within a year. Independent of stem size, species-specific mortality rates varied substantially from 0% to 17% yr⁻¹ in the control, 0% to 26% yr⁻¹ in B1, and 1% to 23% yr⁻¹ in B3, with several species displaying high variation in their vulnerability to fire-induced mortality. Protium guianense (Burseraceae) exhibited the highest fire-induced mortality rates in B1 and B3, which were 10- and 9-fold greater than the baseline rate. In contrast, Aspidosperma excelsum (Apocynaceae), appeared relatively unaffected by fire (0.3% to 1.0% mortality yr⁻¹ across plots), which may be explained by fenestration that protects the inner concave trunk portions from fire. For stems ≥10 cm, both char height (approximating fire intensity) and number of successive burns were significant predictors of fire-induced mortality, whereas only the number of consecutive annual burns was a strong predictor for stems <10 cm. Three years after the initial burn, 62 ± 26 Mg ha⁻¹ (s.e.) of live biomass, predominantly stems <30 cm, was transferred to the dead biomass pool, compared with 8 ± 3 Mg ha⁻¹ in the control. This biomass loss from fire represents ∼30% of this forest's aboveground live biomass (192 (±3) Mg ha⁻¹; >1 cm DBH). Although forest transition to savanna has been predicted based on future climate scenarios, our results indicate that wildfires from agricultural expansion pose a more immediate threat to the current carbon stocks in Amazonian forests.     

Prescribed fire,snag population dynamics,and avian nest site selection

Snags are an important resource for a wide variety of organisms, including cavity-nesting birds. We documented snag attributes in a mixed-conifer forest dominated by ponderosa pine in the Sierra Nevada, California where fire is being applied during spring. A total of 328 snags were monitored before and after fire on plots burned once, burned twice, or left unburned to assess the effects of prescribed fire on snag populations. The greatest loss of snags (7.1 snags ha⁻¹ or 43%) followed the first introduction of fire after a long fire-free period. On plots burned a second time 21% of snags (3.6 snags ha⁻¹) were lost, whereas 8% (1.4 snags ha⁻¹) were lost on unburned control plots in the same time period. New snags replaced many of those lost reducing the net snag losses to 12% (2.0 ha⁻¹) for plots burned once, and 3% (0.5 ha⁻¹) for plots burned twice and unburned plots. We also examined snags used by cavity-nesting birds. Snags preferred for nesting were generally ponderosa pine (Pinus ponderosa), larger diameter, and moderately decayed as compared to available snags. For monitored snags that met the preferred criteria, there was a net loss (1.7 snag ha⁻¹ or 34%) after the first burn, while the loss of useable snags was less than 1 snag ha⁻¹ following the second burn (15%) or on unburned controls (8%). We recommend protection of preferred snags, in particular large ponderosa pines, especially during primary fire applications on fire-suppressed landscapes.     

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.     

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.     

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.     

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

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

Carbon 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.     

The Brazil Eucalyptus Potential Productivity Project: Influence of water,nutrients and stand uniformity on wood production

We examined the potential growth of clonal Eucalyptus plantations at eight locations across a 1000+ km gradient in Brazil by manipulating the supplies of nutrients and water, and altering the uniformity of tree sizes within plots. With no fertilization or irrigation, mean annual increments of stem wood were about 28% lower (16.2 Mg ha⁻¹ yr⁻¹, about 33 m³ ha⁻¹ yr⁻¹) than yields achieved with current operational rates of fertilization (22.6 Mg ha⁻¹ yr⁻¹, about 46 m³ ha⁻¹ yr⁻¹). Fertilization beyond current operational rates did not increase growth, whereas irrigation raised growth by about 30% (to 30.6 Mg ha⁻¹ yr⁻¹, about 62 m³ ha⁻¹ yr⁻¹). The potential biological productivity (current annual increment) of the plantations was about one-third greater than these values, if based only on the period after achieving full canopies. The biological potential productivity was even greater if based only on the full-canopy period during the wet season, indicating that the maximum biological productivity across the sites (with irrigation, during the wet season) would be about 42 Mg ha⁻¹ yr⁻¹ (83 m³ ha⁻¹ yr⁻¹). Stands with uniform structure (trees in plots planted in a single day) showed 13% greater growth than stands with higher heterogeneity of tree sizes (owing to a staggered planting time of up to 80 days). Higher water supply increased growth and also delayed by about 1 year the point where current annual increment and mean annual increment intersected, indicating opportunities for lengthening rotations for more productive treatments as well as the influence of year-to-year climate variations on optimal rotations periods. The growth response to treatments after canopy closure (mid-rotation) related well with full-rotation responses, offering an early opportunity for estimating whole-rotation yields. These results underscore the importance of resource supply, the efficiency of resource use, and stand uniformity in setting the bounds for productivity, and provide a baseline for evaluating the productivity achieved in operational plantations. The BEPP Project showed that water supply is the key resource determining levels of plantation productivity in Brazil. Future collaboration between scientists working on silviculture and genetics should lead to new insights on the mechanisms connecting water and growth, leading to improved matching of sites, clones, and silviculture.     

Nitrogen leaching in response to increased nitrogen inputs in subtropical monsoon forests in southern China

Dissolved inorganic nitrogen (DIN) (as ammonium nitrate) was applied monthly onto the forest floor of one old-growth forest (>400 years old, at levels of 50, 100 and 150 kg N ha⁻¹ yr⁻¹) and two young forests (both about 70 years old, at levels of 50 and 100 kg N ha⁻¹ yr⁻¹) over 3 years (2004–2006), to investigate how nitrogen (N) input influenced N leaching output, and if there were differences in N retention between the old-growth and the young forests in the subtropical monsoon region of southern China. The ambient throughfall inputs were 23–27 kg N ha⁻¹ yr⁻¹ in the young forests and 29–35 kg N ha⁻¹ yr⁻¹ in the old-growth forest. In the control plots without experimental N addition, a net N retention was observed in the young forests (on average 6–11 kg N ha⁻¹ yr⁻¹), but a net N loss occurred in the old-growth forest (−13 kg N ha⁻¹ yr⁻¹). Experimental N addition immediately increased DIN leaching in all three forests, with 25–66% of added N leached over the 3-year experiment. At the lowest level of N addition (50 kg N ha⁻¹ yr⁻¹), the percentage N loss was higher in the old-growth forest (66% of added N) than in the two young forests (38% and 26%). However, at higher levels of N addition (100 and 150 kg N ha⁻¹ yr⁻¹), the old-growth forest exhibited similar N losses (25–43%) to those in the young forests (28–43%). These results indicate that N retention is largely determined by the forest successional stages and the levels of N addition. Compared to most temperate forests studied in Europe and North America, N leaching loss in these seasonal monsoon subtropical forests occurred mainly in the rainy growing season, with measured N loss in leaching substantially higher under both ambient deposition and experimental N additions.     

Accumulation of dead wood in abandoned beech (Fagus sylvatica L.) forests in northwestern Germany

Currently, there is much debate about what strategy is most suitable for increasing old-growth attributes in forests that have been managed intensively for wood production in the past. Passive restoration, i.e. cessation of forestry interventions, should be considered when the old-growth attributes desired can be restored within a feasible period of time.Our study focuses on standing and lying coarse dead wood (≥20 cm diameter) in beech-dominated forests in northwestern Germany. We analyzed monitoring data of 545 sample plots (sized 500-1000 m²) from 12 strict forest reserves (SFRs). The SFRs had been without forestry intervention for up to 28 years.Both, number of dead objects and volume of dead wood (m³ ha⁻¹) increased significantly with ongoing time since abandonment from forestry interventions. The mean amount doubled from 9 to 18 m³ ha⁻¹ within 10 years. The proportion of standing dead wood was about 40% of the total dead wood pool ≥20 cm diameter.With mixed linear modeling we showed that dead wood increased by a mean net rate of about 1 m³ ha⁻¹ a⁻¹. Therefore, after three decades critical values for restoring the dead wood pool could be reached. We hypothesized that the rate of dead wood input is mainly determined by disturbance driven tree mortality such as oak decline, bark beetle infestations and storms.A comparison with primeval forests or reserves abandoned more than 100 years ago showed that the SFRs studied are at the beginning of a long process of dead wood accumulation.Based on our results, the abandonment of forest activities in harvestable pure and mixed beech stands is an effective strategy for restoring the dead wood pool.     

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

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

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.     

Dynamics of large woody debris in small streams disturbed by the 2001 Dogrib fire in the Alberta foothills

We investigated the temporal dynamics of large woody debris (LWD) in five headwater streams before and after the 2001 Dogrib fire in the foothills of Alberta. The density of LWD varied from 5 to 41 logs per 50 m of stream reach and accounted for 19.4 ± 5.1 m³ ha⁻¹ (mean ± standard error) of wood in the riparian zones and 114.1 ± 30.1 m³ ha⁻¹ of wood in the bankfull margins of the stream channel. Individual logs averaged 18.9 ± 1.15 cm in diameter, 5.5 ± 0.7 m in length, and 0.2 ± 0.02 m³ in volume. Logs became significantly shorter in decay classes II–IV. Bridges were longer than partial bridges, which were longer than loose and buried LWD. Individual log volume was greatest for bridges, but not significantly different among other position classes. Bridges and loose LWD contributed little to stream morphology and function; however, 55% of partial bridges and all buried logs contributed to sediment storage, channel armouring, or riffles and pools in the stream channel.     

Short- and long-term effects of thinning and prescribed fire on carbon stocks in ponderosa pine stands in northern Arizona

Euro-American logging practices, intensive grazing, and fire suppression have increased the amount of carbon that is stored in ponderosa pine (Pinus ponderosa Dougl. Ex Laws) forests in the southwestern United States. Current stand conditions leave these forests prone to high-intensity wildfire, which releases a pulse of carbon emissions and shifts carbon storage from live trees to standing dead trees and woody debris. Thinning and prescribed burning are commonly used to reduce the risk of intense wildfire, but also reduce on-site carbon stocks and release carbon to the atmosphere. This study quantified the impact of thinning on the carbon budgets of five ponderosa pine stands in northern Arizona, including the fossil fuels consumed during logging operations. We used the pre- and post-treatment data on carbon stocks and the Fire and Fuels Extension to the Forest Vegetation Simulator (FEE-FVS) to simulate the long-term effects of intense wildfire, thinning, and repeated prescribed burning on stand carbon storage.The mean total pre-treatment carbon stock, including above-ground live and dead trees, below-ground live and dead trees, and surface fuels across five sites was 74.58 Mg C ha⁻¹ and the post-treatment mean was 50.65 Mg C ha⁻¹ in the first post-treatment year. The mean total carbon release from slash burning, fossil fuels, and logs removed was 21.92 Mg C ha⁻¹. FEE-FVS simulations showed that thinning increased the mean canopy base height, decreased the mean crown bulk density, and increased the mean crowning index, and thus reduced the risk of high-intensity wildfire at all sites. Untreated stands that incurred wildfire once within the next 100 years or once within the next 50 years had greater mean net carbon storage after 100 years compared to treated stands that experienced prescribed fire every 10 years or every 20 years. Treated stands released greater amounts of carbon overall due to repeated prescribed fires, slash burning, and 100% of harvested logs being counted as carbon emissions because they were used for short-lived products. However, after 100 years treated stands stored more carbon in live trees and less carbon in dead trees and surface fuels than untreated stands burned by intense wildfire. The long-term net carbon storage of treated stands was similar or greater than untreated wildfire-burned stands only when a distinction was made between carbon stored in live and dead trees, carbon in logs was stored in long-lived products, and energy in logging slash substituted for fossil fuels.     

High-severity wildfire effects on carbon stocks and emissions in fuels treated and untreated forest

Forests contain the world's largest terrestrial carbon stocks, but in seasonally dry environments stock stability can be compromised if burned by wildfire, emitting carbon back to the atmosphere. Treatments to reduce wildfire severity can reduce emissions, but with an immediate cost of reducing carbon stocks. In this study we examine the tradeoffs in carbon stock reduction and wildfire emissions in 19 fuels-treated and -untreated forests burned in twelve wildfires. The fuels treatment, a commonly used thinning ‘from below’ and removal of activity fuels, removed an average of 50.3 Mg C ha⁻¹ or 34% of live tree carbon stocks. Wildfire emissions averaged 29.7 and 67.8 Mg C ha⁻¹ in fuels treated and untreated forests, respectively. The total carbon (fuels treatment plus wildfire emission) removed from treated sites was 119% of the carbon emitted from the untreated/burned sites. However, with only 3% tree survival following wildfire, untreated forests averaged only 7.8 Mg C ha⁻¹ in live trees with an average quadratic mean tree diameter of 21 cm. In contrast, treated forest averaged 100.5 Mg C ha⁻¹ with a live tree quadratic mean diameter of 44 cm. In untreated forests 70% of the remaining total ecosystem carbon shifted to decomposing stocks after the wildfire, compared to 19% in the fuels-treated forest. In wildfire burned forest, fuels treatments have a higher immediate carbon ‘cost’, but in the long-term may benefit from lower decomposition emissions and higher carbon storage.     

Forest dynamics after selective timber harvesting in Papua New Guinea

Forest dynamics after timber harvesting is a major issue for tropical forest managers and communities. Timber harvesting provides income to communities and governments and resources to industry but it has also been identified as a potential contributor to deforestation and degradation of tropical forests. In Papua New Guinea (PNG) harvesting is primarily occurring in accessible primary forests however, the fate of these forests under current harvesting practices is poorly understood.In this study we investigated the impacts of selective harvesting on stand structure, growth and dynamics, recovery and degradation, and species diversity. We also assessed the impacts of forest fire after the 1997-98 El Nino on basal area (BA) growth and mortality rates of natural tropical forests in PNG. For this study we used data from 118 (105 in selectively harvested and 13 in un-harvested forest), one-hectare permanent sample plots distributed across the country and measured for over 15 years by the PNG Forest Research Institute (PNGFRI). We analysed data from 84 of these plots in harvested forest to examine temporal trends in stand condition following harvesting. Mortality rates were investigated in 10 of the 21 plots in harvested forest that were burned during the 1997-98 El Nino drought with sufficient data for analyses. We tested a model developed in Queensland tropical forests to determine whether or not a critical threshold residual BA existed for the recovery of harvested tropical forests in PNG. Results from a logarithmic regression analysis of the relationship between starting BA (BA at first census) and stand BA increment after selective harvesting showed a positive increase in BA growth (r² = 0.74, p < 0.05). However, there was no critical threshold in residual BA that determined whether a harvested forest was likely to degrade or recover BA growth after harvesting. Our analyses suggested that the response to harvesting was variable, with the majority of un-burned plots (75%) showing an increase in BA and remainder a decrease. Average BA of selectively-harvested tropical forests was about 17 m² ha⁻¹ ± 4.17 (SD). Average annual increment in BA across the 84 un-burned plots was 0.17 m² ha⁻¹ year⁻¹ ± 0.62 (SD). Thus these forests generally show capacity to recover after selective harvesting even when the residual BA is low. A proportion of the BA increment is made up of non-commercial pioneer species that originate in significant gaps after harvesting. On burned plots, BA is affected by high mortality rates. The fate of these forests will depend on the degree of future harvesting, potential conversion to agriculture and the impact of fire and other disturbances.     

Willow biomass production under conditions of low-input agriculture on marginal soils

In this study, the biomass yield and morphological traits of plants were reported from an experiment involving six genotypes of willow in northern Poland. Willow was planted using a pole cutting system, which we designated Eco-Salix, on sites that were unsuitable for food crops. The results presented here are from the first rotation of a four-year cutting cycle. In the field trial, the average willow biomass yield of oven-dry matter was 7.87 Mg ha⁻¹ year⁻¹. Willow plants that were planted as pole cuttings after four growing seasons reached a height of 6.64 m and a stem diameter of 50.5 mm. Clone UWM 043 produced higher yields and more favourable morphological traits when compared to registered Polish cultivars. The willow biomass yield obtained on peaty muck soil was significantly higher than from willow that was grown on heavy textured silt soil. The biomass harvested from plots planted at a density of 5,200 plants ha⁻¹ was 14% lower than plots that had a density of 7,400 plants ha⁻¹.     

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.     

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

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