Impact of tropical land‐use change on soil organic carbon stocks – a meta‐analysis

Land‐use changes are the second largest source of human‐induced greenhouse gas emission, mainly due to deforestation in the tropics and subtropics. CO₂ emissions result from biomass and soil organic carbon (SOC) losses and may be offset with afforestation programs. However, the effect of land‐use changes on SOC is poorly quantified due to insufficient data quality (only SOC concentrations and no SOC stocks, shallow sampling depth) and representativeness. In a global meta‐analysis, 385 studies on land‐use change in the tropics were explored to estimate the SOC stock changes for all major land‐use change types. The highest SOC losses were caused by conversion of primary forest into cropland (?25%) and perennial crops (?30%) but forest conversion into grassland also reduced SOC stocks by 12%. Secondary forests stored less SOC than primary forests (?9%) underlining the importance of primary forests for C stores. SOC losses are partly reversible if agricultural land is afforested (+29%) or under cropland fallow (+32%) and with cropland conversion into grassland (+26%). Data on soil bulk density are critical in order to estimate SOC stock changes because (i) the bulk density changes with land‐use and needs to be accounted for when calculating SOC stocks and (ii) soil sample mass has to be corrected for bulk density changes in order to compare land‐use types on the same basis of soil mass. Without soil mass correction, land‐use change effects would have been underestimated by 28%. Land‐use change impact on SOC was not restricted to the surface soil, but relative changes were equally high in the subsoil, stressing the importance of sufficiently deep sampling.     

Temporal response of soil organic carbon after grassland‐related land‐use change

The net flux of CO₂ exchanged with the atmosphere following grassland‐related land‐use change (LUC) depends on the subsequent temporal dynamics of soil organic carbon (SOC). Yet, the magnitude and timing of these dynamics are still unclear. We compiled a global data set of 836 paired‐sites to quantify temporal SOC changes after grassland‐related LUC. In order to discriminate between SOC losses from the initial ecosystem and gains from the secondary one, the post‐LUC time series of SOC data was combined with satellite‐based net primary production observations as a proxy of carbon input to the soil. Globally, land conversion from either cropland or forest into grassland leads to SOC accumulation; the reverse shows net SOC loss. The SOC response curves vary between different regions. Conversion of cropland to managed grassland results in more SOC accumulation than natural grassland recovery from abandoned cropland. We did not consider the biophysical variables (e.g., climate conditions and soil properties) when fitting the SOC turnover rate into the observation data but analyzed the relationships between the fitted turnover rate and these variables. The SOC turnover rate is significantly correlated with temperature and precipitation (p < 0.05), but not with the clay fraction of soils (p > 0.05). Comparing our results with predictions from bookkeeping models, we found that bookkeeping models overestimate by 56% of the long‐term (100 years horizon) cumulative SOC emissions for grassland‐related LUC types in tropical and temperate regions since 2000. We also tested the spatial representativeness of our data set and calculated SOC response curves using the representative subset of sites in each region. Our study provides new insight into the impact grassland‐related LUC on the global carbon budget and sheds light on the potential of grassland conservation for climate mitigation.     

Hotspots of uncertainty in land‐use and land‐cover change projections: a global‐scale model comparison

Model‐based global projections of future land‐use and land‐cover (LULC) change are frequently used in environmental assessments to study the impact of LULC change on environmental services and to provide decision support for policy. These projections are characterized by a high uncertainty in terms of quantity and allocation of projected changes, which can severely impact the results of environmental assessments. In this study, we identify hotspots of uncertainty, based on 43 simulations from 11 global‐scale LULC change models representing a wide range of assumptions of future biophysical and socioeconomic conditions. We attribute components of uncertainty to input data, model structure, scenario storyline and a residual term, based on a regression analysis and analysis of variance. From this diverse set of models and scenarios, we find that the uncertainty varies, depending on the region and the LULC type under consideration. Hotspots of uncertainty appear mainly at the edges of globally important biomes (e.g., boreal and tropical forests). Our results indicate that an important source of uncertainty in forest and pasture areas originates from different input data applied in the models. Cropland, in contrast, is more consistent among the starting conditions, while variation in the projections gradually increases over time due to diverse scenario assumptions and different modeling approaches. Comparisons at the grid cell level indicate that disagreement is mainly related to LULC type definitions and the individual model allocation schemes. We conclude that improving the quality and consistency of observational data utilized in the modeling process and improving the allocation mechanisms of LULC change models remain important challenges. Current LULC representation in environmental assessments might miss the uncertainty arising from the diversity of LULC change modeling approaches, and many studies ignore the uncertainty in LULC projections in assessments of LULC change impacts on climate, water resources or biodiversity.     

Soil carbon stock change following afforestation in Northern Europe: a meta‐analysis

Northern Europe supports large soil organic carbon (SOC) pools and has been subjected to high frequency of land‐use changes during the past decades. However, this region has not been well represented in previous large‐scale syntheses of land‐use change effects on SOC, especially regarding effects of afforestation. Therefore, we conducted a meta‐analysis of SOC stock change following afforestation in Northern Europe. Response ratios were calculated for forest floors and mineral soils (0–10 cm and 0–20/30 cm layers) based on paired control (former land use) and afforested plots. We analyzed the influence of forest age, former land‐use, forest type, and soil textural class. Three major improvements were incorporated in the meta‐analysis: analysis of major interaction groups, evaluation of the influence of nonindependence between samples according to study design, and mass correction. Former land use was a major factor contributing to changes in SOC after afforestation. In former croplands, SOC change differed between soil layers and was significantly positive (20%) in the 0–10 cm layer. Afforestation of former grasslands had a small negative (nonsignificant) effect indicating limited SOC change following this land‐use change within the region. Forest floors enhanced the positive effects of afforestation on SOC, especially with conifers. Meta‐estimates calculated for the periods <30 years and >30 years since afforestation revealed a shift from initial loss to later gain of SOC. The interaction group analysis indicated that meta‐estimates in former land‐use, forest type, and soil textural class alone were either offset or enhanced when confounding effects among variable classes were considered. Furthermore, effect sizes were slightly overestimated if sample dependence was not accounted for and if no mass correction was performed. We conclude that significant SOC sequestration in Northern Europe occurs after afforestation of croplands and not grasslands, and changes are small within a 30‐year perspective.     

Initial soil C and land‐use history determine soil C sequestration under perennial bioenergy crops

In the UK and other temperate regions, short rotation coppice (SRC) and Miscanthus x giganteus (Miscanthus) are two of the leading ‘second‐generation’ bioenergy crops. Grown specifically as a low‐carbon (C) fossil fuel replacement, calculations of the climate mitigation provided by these bioenergy crops rely on accurate data. There are concerns that uncertainty about impacts on soil C stocks of transitions from current agricultural land use to these bioenergy crops could lead to either an under‐ or overestimate of their climate mitigation potential. Here, for locations across mainland Great Britain (GB), a paired‐site approach and a combination of 30‐cm‐ and 1‐m‐deep soil sampling were used to quantify impacts of bioenergy land‐use transitions on soil C stocks in 41 commercial land‐use transitions; 12 arable to SRC, 9 grasslands to SRC, 11 arable to Miscanthus and 9 grasslands to Miscanthus. Mean soil C stocks were lower under both bioenergy crops than under the grassland controls but only significant at 0–30 cm. Mean soil C stocks at 0–30 cm were 33.55 ± 7.52 Mg C ha^?1 and 26.83 ± 8.08 Mg C ha^?1 lower under SRC (P = 0.004) and Miscanthus plantations (P = 0.001), respectively. Differences between bioenergy crops and arable controls were not significant in either the 30‐cm or 1‐m soil cores and smaller than for transitions from grassland. No correlation was detected between change in soil C stock and bioenergy crop age (time since establishment) or soil texture. Change in soil C stock was, however, negatively correlated with the soil C stock in the original land use. We suggest, therefore, that selection of sites for bioenergy crop establishment with lower soil C stocks, most often under arable land use, is the most likely to result in increased soil C stocks.     

Agricultural intensification in Brazil and its effects on land‐use patterns: an analysis of the 1975–2006 period

Does agricultural intensification reduce the area used for agricultural production in Brazil? Census and other data for time periods 1975–1996 and 1996–2006 were processed and analyzed using Geographic Information System and statistical tools to investigate whether and if so, how, changes in yield and stocking rate coincide with changes in cropland and pasture area. Complementary medium‐resolution data on total farmland area changes were used in a spatially explicit assessment of the land‐use transitions that occurred in Brazil during 1960–2006. The analyses show that in agriculturally consolidated areas (mainly southern and southeastern Brazil), land‐use intensification (both on cropland and pastures) coincided with either contraction of both cropland and pasture areas, or cropland expansion at the expense of pastures, both cases resulting in farmland stability or contraction. In contrast, in agricultural frontier areas (i.e., the deforestation zones in central and northern Brazil), land‐use intensification coincided with expansion of agricultural lands. These observations provide support for the thesis that (i) technological improvements create incentives for expansion in agricultural frontier areas; and (ii) farmers are likely to reduce their managed acreage only if land becomes a scarce resource. The spatially explicit examination of land‐use transitions since 1960 reveals an expansion and gradual movement of the agricultural frontier toward the interior (center‐western Cerrado) of Brazil. It also indicates a possible initiation of a reversed trend in line with the forest transition theory, i.e., agricultural contraction and recurring forests in marginally suitable areas in southeastern Brazil, mainly within the Atlantic Forest biome. The significant reduction in deforestation that has taken place in recent years, despite rising food commodity prices, indicates that policies put in place to curb conversion of native vegetation to agriculture land might be effective. This can improve the prospects for protecting native vegetation by investing in agricultural intensification.     

Global environmental change effects on ecosystems: the importance of land‐use legacies

One of the major challenges in ecology is to predict how multiple global environmental changes will affect future ecosystem patterns (e.g. plant community composition) and processes (e.g. nutrient cycling). Here, we highlight arguments for the necessary inclusion of land‐use legacies in this endeavour. Alterations in resources and conditions engendered by previous land use, together with influences on plant community processes such as dispersal, selection, drift and speciation, have steered communities and ecosystem functions onto trajectories of change. These trajectories may be modulated by contemporary environmental changes such as climate warming and nitrogen deposition. We performed a literature review which suggests that these potential interactions have rarely been investigated. This crucial oversight is potentially due to an assumption that knowledge of the contemporary state allows accurate projection into the future. Lessons from other complex dynamic systems, and the recent recognition of the importance of previous conditions in explaining contemporary and future ecosystem properties, demand the testing of this assumption. Vegetation resurvey databases across gradients of land use and environmental change, complemented by rigorous experiments, offer a means to test for interactions between land‐use legacies and multiple environmental changes. Implementing these tests in the context of a trait‐based framework will allow biologists to synthesize compositional and functional ecosystem responses. This will further our understanding of the importance of land‐use legacies in determining future ecosystem properties, and soundly inform conservation and restoration management actions.     

Conversion of coastal wetlands,riparian wetlands,and peatlands increases greenhouse gas emissions: A global meta‐analysis

Land‐use/land‐cover change (LULCC) often results in degradation of natural wetlands and affects the dynamics of greenhouse gases (GHGs). However, the magnitude of changes in GHG emissions from wetlands undergoing various LULCC types remains unclear. We conducted a global meta‐analysis with a database of 209 sites to examine the effects of LULCC types of constructed wetlands (CWs), croplands (CLs), aquaculture ponds (APs), drained wetlands (DWs), and pastures (PASs) on the variability in CO₂, CH₄, and N₂O emissions from the natural coastal wetlands, riparian wetlands, and peatlands. Our results showed that the natural wetlands were net sinks of atmospheric CO₂ and net sources of CH₄ and N₂O, exhibiting the capacity to mitigate greenhouse effects due to negative comprehensive global warming potentials (GWPs; ?0.9 to ?8.7 t CO₂‐eq ha^?1 year^?1). Relative to the natural wetlands, all LULCC types (except CWs from coastal wetlands) decreased the net CO₂ uptake by 69.7%?456.6%, due to a higher increase in ecosystem respiration relative to slight changes in gross primary production. The CWs and APs significantly increased the CH₄ emissions compared to those of the coastal wetlands. All LULCC types associated with the riparian wetlands significantly decreased the CH₄ emissions. When the peatlands were converted to the PASs, the CH₄ emissions significantly increased. The CLs, as well as DWs from peatlands, significantly increased the N₂O emissions in the natural wetlands. As a result, all LULCC types (except PASs from riparian wetlands) led to remarkably higher GWPs by 65.4%?2,948.8%, compared to those of the natural wetlands. The variability in GHG fluxes with LULCC was mainly sensitive to changes in soil water content, water table, salinity, soil nitrogen content, soil pH, and bulk density. This study highlights the significant role of LULCC in increasing comprehensive GHG emissions from global natural wetlands, and our results are useful for improving future models and manipulative experiments.     

Animal manure application and soil organic carbon stocks: a meta‐analysis

The impact of animal manure application on soil organic carbon (SOC) stock changes is of interest for both agronomic and environmental purposes. There is a specific need to quantify SOC change for use in national greenhouse gas (GHG) emission inventories. We quantified the response of SOC stocks to manure application from a large worldwide pool of individual studies and determined the impact of explanatory factors such as climate, soil properties, land use and manure characteristics. Our study is based on a meta‐analysis of 42 research articles totaling 49 sites and 130 observations in the world. A dominant effect of cumulative manure‐C input on SOC response was observed as this factor explained at least 53% of the variability in SOC stock differences compared to mineral fertilized or unfertilized reference treatments. However, the effects of other determining factors were not evident from our data set. From the linear regression relating cumulative C inputs and SOC stock difference, a global manure‐C retention coefficient of 12% ± 4 (95% Confidence Interval, CI) could be estimated for an average study duration of 18 years. Following an approach comparable to the Intergovernmental Panel on Climate Change, we estimated a relative SOC change factor of 1.26 ± 0.14 (95% CI) which was also related to cumulative manure‐C input. Our results offer some scope for the refinement of manure retention coefficients used in crop management guidelines and for the improvement of SOC change factors for national GHG inventories by taking into account manure‐C input. Finally, this study emphasizes the need to further document the long‐term impact of manure characteristics such as animal species, especially pig and poultry, and manure management systems, in particular liquid vs. solid storage.     

云南保山西庄山地流域土地利用方式与土壤肥力关系研究

以云南省保山地区西庄流域为例,研究了自然因素及人为活动对土壤性质的影响。该流域的土壤通常pH较低,缺乏有效磷和交换性阳离子。仅发育于石灰岩的土壤具适宜的pH和交换性阳离子量。海拔对土壤有机碳含量具显著影响。文中详细讨论了海拔、母质和土地利用方式等对土壤肥力及土壤侵蚀的影响。     

Quantifying global greenhouse gas emissions from land‐use change for crop production

Many assessments of product carbon footprint (PCF) for agricultural products omit emissions arising from land‐use change (LUC). In this study, we developed a framework based on IPCC national greenhouse gas inventory methodologies to assess the impacts of LUC from crop production using oil palm, soybean and oilseed rape as examples. Using ecological zone, climate and soil types from the top 20 producing countries, calculated emissions for transitions from natural vegetation to cropland on mineral soils under typical management ranged from ?4.5 to 29.4 t CO₂‐eq ha^?1 yr^?1 over 20 years for oil palm and 1.2–47.5 t CO₂‐eq ha^?1 yr^?1 over 20 years for soybeans. Oilseed rape showed similar results to soybeans, but with lower maximum values because it is mainly grown in areas with lower C stocks. GHG emissions from other land‐use transitions were between 62% and 95% lower than those from natural vegetation for the arable crops, while conversions to oil palm were a sink for C. LUC emissions were considered on a national basis and also expressed per‐tonne‐of‐oil‐produced. Weighted global averages indicate that, depending on the land‐use transition, oil crop production on newly converted land contributes between ?3.1 and 7.0 t CO₂‐eq t oil production^?1 yr^?1 for palm oil, 11.9–50.6 t CO₂‐eq t oil production^?1 yr^?1 for soybean oil, and 7.7–31.4 t CO₂‐eq t oil production^?1 yr^?1 for rapeseed oil. Assumptions made about crop and LUC distribution within countries contributed up to 66% error around the global averages for natural vegetation conversions. Uncertainty around biomass and soil C stocks were also examined. Finer resolution data and information (particularly on land management and yield) could improve reliability of the estimates but the framework can be used in all global regions and represents an important step forward for including LUC emissions in PCFs.     

A global meta‐analysis of soil organic carbon response to corn stover removal

Corn (Zea mays L.) stover is a global resource used for livestock, fuel, and bioenergy feedstock, but excessive stover removal can decrease soil organic C (SOC) stocks and deteriorate soil health. Many site‐specific stover removal experiments report accrual rates and SOC stock effects, but a quantitative, global synthesis is needed to provide a scientific base for long‐term energy policy decisions. We used 409 data points from 74 stover harvest experiments conducted around the world for a meta‐analysis and meta‐regression to quantify removal rate, tillage, soil texture, and soil sampling depth effects on SOC. Changes were quantified by: (a) comparing final SOC stock differences after at least 3 years with and without stover removal and (b) calculating SOC accrual rates for both treatments. Stover removal generally reduced final SOC stocks by 8% in the upper 0–15 or 0–30 cm, compared to stover retained, irrespective of soil properties and tillage practices. A more sensitive meta‐regression analysis showed that retention increased SOC stocks within the 30–150 cm depth by another 5%. Compared to baseline values, stover retention increased average SOC stocks temporally at a rate of 0.41 Mg C ha^?1 year^?1 (statistically significant at p < 0.01 when averaged across all soil layers). Although SOC sequestration rates were lower with stover removal, with moderate (<50%) removal they can be positive, thus emphasizing the importance of site‐specific management. Our results also showed that tillage effects on SOC stocks were inconsistent due to the high variability in practices used among the experimental sites. Finally, we conclude that research and technological efforts should continue to be given high priority because of the importance in providing science‐based policy recommendations for long‐term global carbon management.     

Soil carbon sequestration and land‐use change: processes and potential

When agricultural land is no longer used for cultivation and allowed to revert to natural vegetation or replanted to perennial vegetation, soil organic carbon can accumulate. This accumulation process essentially reverses some of the effects responsible for soil organic carbon losses from when the land was converted from perennial vegetation. We discuss the essential elements of what is known about soil organic matter dynamics that may result in enhanced soil carbon sequestration with changes in land‐use and soil management. We review literature that reports changes in soil organic carbon after changes in land‐use that favour carbon accumulation. This data summary provides a guide to approximate rates of SOC sequestration that are possible with management, and indicates the relative importance of some factors that influence the rates of organic carbon sequestration in soil. There is a large variation in the length of time for and the rate at which carbon may accumulate in soil, related to the productivity of the recovering vegetation, physical and biological conditions in the soil, and the past history of soil organic carbon inputs and physical disturbance. Maximum rates of C accumulation during the early aggrading stage of perennial vegetation growth, while substantial, are usually much less than 100 g C m^?2 y^?1. Average rates of accumulation are similar for forest or grassland establishment: 33.8 g C m^?2 y^?1 and 33.2 g C m^?2 y^?1, respectively. These observed rates of soil organic C accumulation, when combined with the small amount of land area involved, are insufficient to account for a significant fraction of the missing C in the global carbon cycle as accumulating in the soils of formerly agricultural land.     

Projecting impacts of global climate and land‐use scenarios on plant biodiversity using compositional‐turnover modelling

Nations have committed to ambitious conservation targets in response to accelerating rates of global biodiversity loss. Anticipating future impacts is essential to inform policy decisions for achieving these targets, but predictions need to be of sufficiently high spatial resolution to forecast the local effects of global change. As part of the intercomparison of biodiversity and ecosystem services models of the Intergovernmental Science‐Policy Platform on Biodiversity and Ecosystem Services, we present a fine‐resolution assessment of trends in the persistence of global plant biodiversity. We coupled generalized dissimilarity models, fitted to >52 million records of >254 thousand plant species, with the species–area relationship, to estimate the effect of land‐use and climate change on global biodiversity persistence. We estimated that the number of plant species committed to extinction over the long term has increased by 60% globally between 1900 and 2015 (from ~10,000 to ~16,000). This number is projected to decrease slightly by 2050 under the most optimistic scenario of land‐use change and to substantially increase (to ~18,000) under the most pessimistic scenario. This means that, in the absence of climate change, scenarios of sustainable socio‐economic development can potentially bring extinction risk back to pre‐2000 levels. Alarmingly, under all scenarios, the additional impact from climate change might largely surpass that of land‐use change. In this case, the estimated number of species committed to extinction increases by 3.7–4.5 times compared to land‐use‐only projections. African regions (especially central and southern) are expected to suffer some of the highest impacts into the future, while biodiversity decline in Southeast Asia (which has previously been among the highest globally) is projected to slow down. Our results suggest that environmentally sustainable land‐use planning alone might not be sufficient to prevent potentially dramatic biodiversity loss, unless a stabilization of climate to pre‐industrial times is observed.     

Synergistic effects of climate and land‐use change influence broad‐scale avian population declines

Climate and land‐use changes are expected to be the primary drivers of future global biodiversity loss. Although theory suggests that these factors impact species synergistically, past studies have either focused on only one in isolation or have substituted space for time, which often results in confounding between drivers. Tests of synergistic effects require congruent time series on animal populations, climate change and land‐use change replicated across landscapes that span the gradient of correlations between the drivers of change. Using a unique time series of high‐resolution climate (measured as temperature and precipitation) and land‐use change (measured as forest change) data, we show that these drivers of global change act synergistically to influence forest bird population declines over 29 years in the Pacific Northwest of the United States. Nearly half of the species examined had declined over this time. Populations declined most in response to loss of early seral and mature forest, with responses to loss of early seral forest amplified in landscapes that had warmed over time. In addition, birds declined more in response to loss of mature forest in areas that had dried over time. Climate change did not appear to impact populations in landscapes with limited habitat loss, except when those landscapes were initially warmer than the average landscape. Our results provide some of the first empirical evidence of synergistic effects of climate and land‐use change on animal population dynamics, suggesting accelerated loss of biodiversity in areas under pressure from multiple global change drivers. Furthermore, our findings suggest strong spatial variability in the impacts of climate change and highlight the need for future studies to evaluate multiple drivers simultaneously to avoid potential misattribution of effects.     

Effect of land‐use and land‐cover change on mangrove blue carbon: A systematic review

Mangroves shift from carbon sinks to sources when affected by anthropogenic land‐use and land‐cover change (LULCC). Yet, the magnitude and temporal scale of these impacts are largely unknown. We undertook a systematic review to examine the influence of LULCC on mangrove carbon stocks and soil greenhouse gas (GHG) effluxes. A search of 478 data points from the peer‐reviewed literature revealed a substantial reduction of biomass (82% ± 35%) and soil (54% ± 13%) carbon stocks due to LULCC. The relative loss depended on LULCC type, time since LULCC and geographical and climatic conditions of sites. We also observed that the loss of soil carbon stocks was linked to the decreased soil carbon content and increased soil bulk density over the first 100 cm depth. We found no significant effect of LULCC on soil GHG effluxes. Regeneration efforts (i.e. restoration, rehabilitation and afforestation) led to biomass recovery after ~40 years. However, we found no clear patterns of mangrove soil carbon stock re‐establishment following biomass recovery. Our findings suggest that regeneration may help restore carbon stocks back to pre‐disturbed levels over decadal to century time scales only, with a faster rate for biomass recovery than for soil carbon stocks. Therefore, improved mangrove ecosystem management by preventing further LULCC and promoting rehabilitation is fundamental for effective climate change mitigation policy.