Emissions of carbon from forestry and land-use change in tropical Asia

The net emissions of carbon from forestry and changes in land use in south and southeast Asia were calculated here with a book-keeping model that used rates of land-use change and associated per hectare changes in vegetation and soil to calculate changes in the amount of carbon held in terrestrial ecosystems and wood products. The total release of carbon to the atmosphere over the period 1850–1995 was 43.5 PgC. The clearing of forests for permanent croplands released 33.5 PgC, about 75% of the total. The reduction of biomass in the remaining forests, as a result of shifting cultivation, logging, fuelwood extraction, and associated regrowth, was responsible for a net loss of 11.5 PgC, and the establishment of plantations withdrew from the atmosphere 1.5 PgC, most of it since 1980. Based on comparisons with other estimates, the uncertainty of this long-term flux is estimated to be within ±30%. Reducing this uncertainty will be difficult because of the difficulty of documenting the biomass of forests in existence >40 years ago. For the 15-y period 1981–1995, annual emissions averaged 1.07 PgC y^–1, about 50% higher than reported for the 1980s in an earlier study. The uncertainty of recent emissions is probably within ± 50% but could be reduced significantly with systematic use of satellite data on changes in forest area. In tropical Asia, the emissions of carbon from land-use change in the 1980s accounted for approximately 75% of the region’s total carbon emissions. Since 1990 rates of deforestation and their associated emissions have declined, while emissions of carbon from combustion of fossil fuels have increased. The net effect has been a reduction in emissions of CO₂ from this region since 1990.     

Biomass,Carbon, and Nitrogen Pools in Mexican Tropical Dry Forest Landscapes

Tropical dry forest is the most widely distributed land-cover type in the tropics. As the rate of land-use/land-cover change from forest to pasture or agriculture accelerates worldwide, it is becoming increasingly important to quantify the ecosystem biomass and carbon (C) and nitrogen (N) pools of both intact forests and converted sites. In the central coastal region of México, we sampled total aboveground biomass (TAGB), and the N and C pools of two floodplain forests, three upland dry forests, and four pastures converted from dry forest. We also sampled belowground biomass and soil C and N pools in two sites of each land-cover type. The TAGB of floodplain forests was as high as 416 Mg ha^–1, whereas the TAGB of the dry forest ranged from 94 to 126 Mg ha^–1. The TAGB of pastures derived from dry forest ranged from 20 to 34 Mg ha^–1. Dead wood (standing and downed combined) comprised 27%–29% of the TABG of dry forest but only about 10% in floodplain forest. Root biomass averaged 32.0 Mg ha^–1 in floodplain forest, 17.1 Mg ha^–1 in dry forest, and 5.8 Mg ha^–1 in pasture. Although total root biomass was similar between sites within land-cover types, root distribution varied by depth and by size class. The highest proportion of root biomass occurred in the top 20 cm of soil in all sites. Total aboveground and root C pools, respectively, were 12 and 2.2 Mg ha^–1 in pasture and reached 180 and 12.9 Mg ha^–1 in floodplain forest. Total aboveground and root pools, respectively, were 149 and 47 kg ha^–1 in pasture and reached 2623 and 264 kg ha^–1 in floodplain forest. Soil organic C pools were greater in pastures than in dry forest, but soil N pools were similar when calculated for the same soil depths. Total ecosystem C pools were 306. The Mg ha^–1 in floodplain forest, 141 Mg ha^–1 in dry forest, and 124 Mg ha^–1 in pasture. Soil C comprised 37%–90% of the total ecosystem C, whereas soil N comprised 85%–98% of the total. The N pools lack of a consistent decrease in soil pools caused by land-use change suggests that C and N losses result from the burning of aboveground biomass. We estimate that in México, dry forest landscapes store approximately 2.3 Pg C, which is about equal to the C stored by the evergreen forests of that country (approximately 2.4 Pg C). Potential C emissions to the atmosphere from the burning of biomass in the dry tropical landscapes of México may amount to 708 Tg C, as compared with 569 Tg C from evergreen forests.     

Maximum impacts of future reforestation or deforestation on atmospheric CO2

There is scope for land‐use changes to increase or decrease CO₂ concentrations in the atmosphere over the next century. Here we make simple but robust calculations of the maximum impact of such changes. Historical land‐use changes (mostly deforestation) and fossil fuel emissions have caused an increase in atmospheric concentration of CO₂ of 90 ppm between the pre‐industrial era and year 2000. The projected range of CO₂ concentrations in 2100, under a range of emissions scenarios developed for the IPCC, is 170–600 ppm above 2000 levels. This range is mostly due to different assumptions regarding fossil fuel emissions. If all of the carbon so far released by land‐use changes could be restored to the terrestrial biosphere, atmospheric CO₂ concentration at the end of the century would be about 40–70 ppm less than it would be if no such intervention had occurred. Conversely, complete global deforestation over the same time frame would increase atmospheric concentrations by about 130–290 ppm. These are extreme assumptions; the maximum feasible reforestation and afforestation activities over the next 50 years would result in a reduction in CO₂ concentration of about 15–30 ppm by the end of the century. Thus the time course of fossil fuel emissions will be the major factor in determining atmospheric CO₂ concentrations for the foreseeable future.     

Effects of grazing intensity on soil carbon stocks following deforestation of a Hawaiian dry tropical forest

The effects of forest-to-pasture conversion on soil carbon (C) stocks depend on a combination of climatic and management factors, but factors that relate to grazing intensity are perhaps the least understood. To understand the long-term impact of grazing in converted pastures, methods are needed that accurately measure the impact of grazing on recent plant inputs to soil C in a variety of pasture management and climate settings. Here, we present an analysis from Hawai'i of changes in vegetation structure and soil organic carbon (SOC) along gradients of grazing intensity and elevation in pastures converted from dry tropical forest 100 years ago. We used hyperspectral remote sensing of photosynthetic vegetation, nonphotosynthetic vegetation (NPV) and exposed substrate to understand the effects of grazing on plant litter cover, thus, estimating recent plant inputs to soils (the NPV component). Forest-to-pasture conversion caused a shift from C3 to C4 plant physiology, thus the δ ¹³C method was used in soil cores to measure the fraction of SOC accumulated from pasture vegetation sources following land conversion. SOC decreased in pasture by 5–9 kg C m⁻², depending upon grazing intensity. SOC derived from C3 (forest) sources was constant across the grazing gradient, indicating that the observed variation in SOC was attributable to changes in C inputs following deforestation. Soil C stocks were also reduced in pastures relative to forest soils. We found that long-term grazing lowers SOC following Hawaiian forest-to-pasture conversion, and that these changes are larger in magnitude that those occurring with elevation (climate). Further we demonstrate a relationship between remotely sensed measurements of surface litter and field SOC measurements, allowing for regional analysis of pasture condition and C storage where limited field data are available.     

Substantial labile carbon stocks and microbial activity in deeply weathered soils below a tropical wet forest

Contrary to large areas in Amazonia of tropical moist forests with a pronounced dry season, tropical wet forests in Costa Rica do not depend on deep roots to maintain an evergreen forest canopy through the year. At our Costa Rican tropical wet forest sites, we found a large carbon stock in the subsoil of deeply weathered Oxisols, even though only 0.04–0.2% of the measured root biomass (>2 mm diameter) to 3 m depth was below 2 m. In addition, we demonstrate that 20% or more of this deep soil carbon (depending on soil type) can be mobilized after forest clearing for pasture establishment. Microbial activity between 0.3 and 3 m depth contributed about 50% to the microbial activity in these soils, confirming the importance of the subsoil in C cycling. Depending on soil type, forest clearing for pasture establishment led from no change to a slight addition of carbon in the topsoil (0–0.3 m depth). However, this effect was countered by a substantial loss of C stocks in the subsoil (1–3 m depth). Our results show that large stocks of relatively labile carbon are not limited to areas with a prolonged dry season, but can also be found in deeply weathered soils below tropical wet forests. Forest clearing in such areas may produce unexpectedly high C losses from the subsoil.     

Challenges to estimating carbon emissions from tropical deforestation

An accurate estimate of carbon fluxes associated with tropical deforestation from the last two decades is needed to balance the global carbon budget. Several studies have already estimated carbon emissions from tropical deforestation, but the estimates vary greatly and are difficult to compare due to differences in data sources, assumptions, and methodologies. In this paper, we review the different estimates and datasets, and the various challenges associated with comparing them and with accurately estimating carbon emissions from deforestation. We performed a simulation study over legal Amazonia to illustrate some of these major issues. Our analysis demonstrates the importance of considering land-cover dynamics following deforestation, including the fluxes from reclearing of secondary vegetation, the decay of product and slash pools, and the fluxes from regrowing forest. It also suggests that accurate carbon-flux estimates will need to consider historical land-cover changes for at least the previous 20 years. However, this result is highly sensitive to estimates of the partitioning of cleared carbon into instantaneous burning vs. long-timescale slash pools. We also show that carbon flux estimates based on 'committed flux' calculations, as used by a few studies, are not comparable with the 'annual balance' calculation method used by other studies.     

The potential ecological costs and cobenefits of REDD: a critical review and case study from the Amazon region

The United Nations climate treaty may soon include a mechanism for compensating tropical nations that succeed in reducing carbon emissions from deforestation and forest degradation, source of nearly one fifth of global carbon emissions. We review the potential for this mechanism [reducing emissions from deforestation and degradation (REDD)] to provoke ecological damages and promote ecological cobenefits. Nations could potentially participate in REDD by slowing clear‐cutting of mature tropical forest, slowing or decreasing the impact of selective logging, promoting forest regeneration and restoration, and expanding tree plantations. REDD could also foster efforts to reduce the incidence of forest fire. Potential ecological costs include the accelerated loss (through displaced agricultural expansion) of low‐biomass, high‐conservation‐value ecosystems, and substitution of low‐biomass vegetation by monoculture tree plantations. These costs could be avoided through measures that protect low‐biomass native ecosystems. Substantial ecological cobenefits should be conferred under most circumstances, and include the maintenance or restoration of (1) watershed functions, (2) local and regional climate regimes, (3) soils and biogeochemical processes, (4) water quality and aquatic habitat, and (5) terrestrial habitat. Some tools already being developed to monitor, report and verify (MRV) carbon emissions performance can also be used to measure other elements of ecosystem function, making development of MRV systems for ecological cobenefits a concrete possibility. Analysis of possible REDD program interventions in a large‐scale Amazon landscape indicates that even modest flows of forest carbon funding can provide substantial cobenefits for aquatic ecosystems, but that the functional integrity of the landscape's myriad small watersheds would be best protected under a more even spatial distribution of forests. Because of its focus on an ecosystem service with global benefits, REDD could access a large pool of global stakeholders willing to pay to maintain carbon in forests, thereby providing a potential cascade of ecosystem services to local stakeholders who would otherwise be unable to afford them.     

Forest carbon budgets in Southeast Asia following harvesting and land cover change

Terrestrial ecosystems play an important role in the global carbon (C)cycle. Tropical forests in Southeast Asia are constantly changing as a result of harvesting and conversion to other land cover. As a result of these changes, research on C budgets of forest ecosystems has intensified in the region over thelast few years. This paper reviews and synthesizes the available information. Natural forests in SE Asia typically contain a high C density (up to 500 Mg/ha). Logging activities are responsible for at least 50% decline in forest C density.Complete deforestation (conversion from forest to grassland or annual crops) results in C density of less than 40 Mg/ha. Conversion to tree plantations and other woody perennial crops also reduces C density to less than 50% of the originalC forest stocks. While much information has been generated recently, there are still large gaps of information on C budgets of tropical forests and its conversion to other land uses in SE Asia. There is therefore a need to intensify research in this area.     

Changes in Soil Carbon and Nitrogen after Contrasting Land-use Transitions in Northeastern Costa Rica

Northeastern Costa Rica is a mosaic of primary and secondary forests, tree plantations, pastures, and cash crops. Many studies have quantified the effects of one type of land-use transition (for example, deforestation or reforestation) on soil properties such as organic carbon (C) storage, but few have compared different land-use transitions simultaneously. We can best understand the effects of land-use change on regional and global ecosystem processes by considering all of the land-use transitions that occur in a landscape. In this study, I examined the changes in total soil C and nitrogen (N) pools (to 0.3 m) that have accompanied different land-use transitions in a 140,000-ha region in northeastern Costa Rica. I paired sites that had similar topography and soils but differed in recent land-use history. The following land-use transitions were represented: 12 conversions of primary forests to banana plantations, 15 conversions of pastures to cash crops, and four conversions of pastures to Vochysia guatemalensis tree plantations. The conversion of forests to bananas decreased soil C concentrations and inventories (Mg C ha^–1) in the surface soil by 37% and 16.5%, respectively. The conversion of pastures to cash crops reduced soil C concentrations and inventories to the same extent that forest-to-banana cropping did. Furthermore, young Vochysia plantations do not appear to increase soil C storage, at least over the 1st decade. When data from all land-use transitions were pooled, the difference in root biomass and leaf litter pools between land-use pairs explained 50% of the differences in soil C concentrations and 36% of the differences in soil C inventories. Thus, reduced productivity or C inputs to the soil is one mechanism that could explain the losses in soil C pools with land-use change. In this landscape, losses of soil C due to cultivation are rapid, whereas re- accumulation rates are slow. Total soil N pools (0–10 cm) were also reduced after the conversion of forests to banana plantations or the conversion of pastures to crops, despite fertilization of the cropped soils. This suggests that the added N fertilizer is not retained but instead is exported via produce, N gas emissions, and hydrologic processes.     

Historical Land-cover Conversion (1665–1820) in the Choptank Watershed,Eastern United States

Land-cover changes in the Choptank basin were estimated for 1665–1820 by using historical socioeconomic data and crop-rotation models. Socioeconomic data (human population, output per laborer, and crop yields) were obtained from the literature, whereas crop-rotation models, based on historical records, represented how agriculture was practiced. Model parameters and output were validated with export records, census data, and other historical records, and model errors were estimated to be approximately 5%. This approach indicated a sigmoidal pattern for conversion of primary forest to agricultural land by 1800. The initial time period, 1665–1720, was characterized by low-intensity tobacco and corn cultivation. Due to long fallows, the models indicated that there was little land in crops (approximately 5% of the region), but larger areas of secondary forest occurred on former cropland (approximately 15%). Although primary forest decreased, the initial result in the first 55 years was a low net rate of deforestation and occupation by low-intensity farms. However, after 1720, cropland expanded rapidly due to the use of wheat as a cash crop. From 1720 to 1775, primary and secondary forest rapidly disappeared, increasing agricultural land to 60% of the region. By 1800, approximately 80% was estimated to be converted to agriculture, and little primary forest remained. After 1800, the land needed for crops decreased due to improved management practices and crop yields, and some secondary forest on formerly cleared agricultural sites may have reappeared. We estimate that less than 150 years of European colonization resulted in virtually complete agriculturalization of a primarily forested landscape.