Carbon cycling and sequestration in a Japanese red pine (Pinus densiflora) forest on lava flow of Mt. Fuji

Biometric-based carbon flux measurements were conducted in a pine forest on lava flow of Mt. Fuji, Japan, in order to estimate carbon cycling and sequestration. The forest consists mainly of Japanese red pine (Pinus densiflora) in a canopy layer and Japanese holly (Ilex pedunculosa) in a subtree layer. The lava remains exposed on the ground surface, and the soil on the lava flow is still immature with no mineral soil layer. The results showed that the net primary production (NPP) of the forest was 7.3 ± 0.7 t C ha^?1 year^?1, of which 1.4 ± 0.4 t C ha^?1 year^?1 was partitioned to biomass increment, 3.2 ± 0.5 t C ha^?1 year^?1 to above-ground fine litter production, 1.9 t C ha^?1 year^?1 to fine root production, and 0.8 ± 0.2 t C ha^?1 year^?1 to coarse woody debris. The total amount of annual soil surface CO₂ efflux was estimated as 6.1 ± 2.9 t C ha^?1 year^?1, using a closed chamber method. The estimated decomposition rate of soil organic matter, which subtracted annual root respiration from soil respiration, was 4.2 ± 3.1 t C ha^?1 year^?1. Biometric-based net ecosystem production (NEP) in the pine forest was estimated at 2.9 ± 3.2 t C ha^?1 year^?1, with high uncertainty due mainly to the model estimation error of annual soil respiration and root respiration. The sequestered carbon being allocated in roughly equal amounts to living biomass (1.4 t C ha^?1 year^?1) and the non-living C pool (1.5 t C ha^?1 year^?1). Our estimate of biometric-based NEP was 25 % lower than the eddy covariance-based NEP in this pine forest, due partly to the underestimation of NPP and difficulty of estimation of soil and root respiration in the pine forest on lava flows that have large heterogeneity of soil depth. However, our results indicate that the mature pine forest acted as a significant carbon sink even when established on lava flow with low nutrient content in immature soils, and that sequestration strength, both in biomass and in soil organic matter, is large.     

High heterotrophic CO<Subscript>2</Subscript> emissions from a Malaysian oil palm plantations during dry-season

Tropical peatlands are currently being rapidly cleared and drained for the establishment of oil palm plantations, which threatens their globally significant carbon sequestration capacity. Large-scale land conversion of tropical peatlands is important in the context of greenhouse gas emission factors and sustainable land management. At present, quantification of carbon dioxide losses from tropical peatlands is limited by our understanding of the relative contribution of heterotrophic and autotrophic respiration to net peat surface CO₂ emissions. In this study we separated heterotrophic and autotrophic components of peat CO₂ losses from two oil palm plantations (one established in ‘2000’ and the other in 1978, then replanted in ‘2006’) using chamber-based emissions sampling along a transect from the rooting to non-rooting zones on a peatland in Selangor, Peninsular Malaysia over the course of 3 months (June–August, 2014). Collar CO₂ measurements were compared with soil temperature and moisture at site and also accompanied by depth profiles assessing peat C and bulk density. The soil respiration decreased exponentially with distance from the palm trunks with the sharpest decline found for the plantation with the younger palms with overall fluxes of 1341 and 988 mg CO₂ m^?2 h^?1, respectively, at the 2000 and 2006 plantations, respectively. The mean heterotrophic flux was 909 ± SE 136 and 716 ± SE 201 mg m^?2 h^?1 at the 2000 and 2006 plantations, respectively. Autotrophic emissions adjacent to the palm trunks were 845 ± SE 135 and 1558 ± SE 341 mg m^?2 h^?1 at the 2000 and 2006 plantations, respectively. Heterotrophic CO₂ flux was positively related to peat soil moisture, but not temperature. Total peat C stocks were 60 kg m^?2 (down to 1 m depth) and did not vary among plantations of different ages but SOC concentrations declined significantly with depth at both plantations but the decline was sharper in the second generation 2006 plantation. The CO₂ flux values reported in this study suggest a potential for very high carbon (C) loss from drained tropical peats during the dry season. This is particularly concerning given that more intense dry periods related to climate change are predicted for SE Asia. Taken together, this study highlights the need for careful management of tropical peatlands, and the vulnerability of their carbon storage capability under conditions of drainage.     

Carbon cycling and net ecosystem production at an early stage of secondary succession in an abandoned coppice forest

Secondary mixed forests are one of the dominant forest cover types in human-dominated temperate regions. However, our understanding of how secondary succession affects carbon cycling and carbon sequestration in these ecosystems is limited. We studied carbon cycling and net ecosystem production (NEP) over 4 years (2004–2008) in a cool-temperate deciduous forest at an early stage of secondary succession (18 years after clear-cutting). Net primary production of the 18-year-old forest in this study was 5.2 tC ha^?1 year^?1, including below-ground coarse roots; this was partitioned into 2.5 tC ha^?1 year^?1 biomass increment, 1.6 tC ha^?1 year^?1 foliage litter, and 1.0 tC ha^?1 year^?1 other woody detritus. The total amount of annual soil surface CO₂ efflux was 6.8 tC ha^?1 year^?1, which included root respiration (1.9 tC ha^?1 year^?1) and heterotrophic respiration (RH) from soils (4.9 tC ha^?1 year^?1). The 18-year forest at this study site exhibited a great increase in biomass pool as a result of considerable total tree growth and low mortality of tree stems. In contrast, the soil organic matter (SOM) pool decreased markedly (?1.6 tC ha^?1 year^?1), although further study of below-ground detritus production and RH of SOM decomposition is needed. This young 18-year forest was a weak carbon sink (0.9 tC ha^?1 year^?1) at this stage of secondary succession. The NEP of this 18-year forest is likely to increase gradually because biomass increases with tree growth and with the improvement of the SOM pool through increasing litter and dead wood production with stand development.     

Litter dynamics and fine root production in Schizolobium parahyba var. amazonicum plantations and regrowth forest in Eastern Amazon

Forest plantations and agroforestry systems with Schizolobium parahyba var. amazonicum have greatly expanded in the Brazilian Amazon, generally as an alternative for reforesting degraded areas. To our knowledge there are no reports of above- and below-ground production in these forest systems. We quantified litter and fine root production in 6-yr old Schizolobium-based plantation forests (monospecific: MON, mixture: MIX, and agroforestry system: AFS) and in ~25-yr old regrowth forest (REG) over 8–12 months. We used litter traps and ingrowth cores to quantify litter and fine root production, respectively. Annual litter production was significantly lower in Schizolobium-based plantations (mean ± standard error, MON?=?5.92?±?0.15, MIX?=?6.08?±?0.13, AFS?=?6.63?±?0.13 Mg ha^?1 year^?1) than in regrowth forest (8.64?±?0.08 Mg ha^?1 year^?1). Schizolobium-based plantations showed significantly higher litter stock (MON?=?7.7?±?1.0, MIX?=?7.4?±?0.1 Mg ha^?1) than REG (5.9?±?1.3 Mg ha^?1). Total fine root production over an 8-month period was significantly higher in Schizolobium-based plantations (MON?=?3.8?±?0.2, MIX?=?3.4?±?0.2, AFS?=?2.7?±?0.1 Mg ha^?1) than in REG (1.1?±?0.03 Mg ha^?1). Six-yr old Schizolobium-based plantations and ~25-yr old regrowth forests showed comparable rates of litter + fine root production, suggesting that young forest plantations may be an interesting alternative to restore degraded areas due to early reestablishment of organic matter cycling under the studied conditions.     

Experimental Manipulation of Forest Structure: Near-Term Effects on Gap and Stand Scale C Dynamics

Canopy gaps and coarse woody debris are two forest structural features that are more abundant in old-growth forests than in second-growth, even-aged stands. These features directly influence the carbon balance of the ecosystem, yet few studies have quantified their interactive effects. We experimentally manipulated the forest structure of a second-growth northern hardwood forest in north-central Wisconsin (USA) and measured the shift of C between pools of the ecosystem components. Here, we question the longevity of the changes to the aboveground pools and address their implications for total ecosystem C (TEC) and net ecosystem production (NEP) at both the gap and stand scale. At the scale of the gap, the harvest and removal of trees significantly reduced NEP (?3.2 to ?3.5 Mg C ha^?1 for gaps vs 2.2 to 2.5 Mg C ha^?1 for reference conditions), but did not alter heterotrophic respiration. The addition of woody debris without harvest significantly increased heterotrophic respiration, decreasing soil C storage of the gap area (?0.5 to ?1.1 Mg C ha^?1). The combined treatment of gap creation and woody debris addition made the gap area a significant C source to the atmosphere for the 3 years of the study (?4.9 to ?5.1 Mg C ha^?1). We also estimated how these structural features would affect C dynamics at a broader scale. The conversion of 10% of the stand canopy to gap conditions caused only a brief decrease in the stand NEP with the C balance returning to reference conditions by the third year following tree harvest. The woody debris additions caused an increase in both TEC and heterotrophic respiration. When combined the addition of canopy gaps and woody debris caused plots to initially become significant C sources, relative to undisturbed locations that were consistently accumulating C, with an annual NEP ranging from 2.1 to 2.8 Mg C ha^?1 y^?1. Understanding the effects of these structural features on forest C dynamics is highly relevant as the maturing forests of the region transition to more structurally complex forests and the demand for managing ecosystems for long-term C sequestration increases.     

Short-term simulated nitrogen deposition increases carbon sequestration in a Pleioblastus amarus plantation

In order to understand the influence of nitrogen (N) deposition on the key processes relevant to the carbon (C) balance in a bamboo plantation, a two-year field experiment involving the simulated deposition of N in a Pleioblastus amarus plantation was conducted in the rainy region of SW China. Four levels of N treatments: control (no N added), low-N (50 kg N ha^?1 year^?1), medium-N (150 kg N ha^?1 year^?1), and high-N (300 kg N ha^?1 year^?1) were set in the present study. The results showed that soil respiration followed a clear seasonal pattern, with the maximum rates in mid-summer and the minimum in late winter. The annual cumulative soil respiration was 585?±?43 g CO₂-C m^?2 year^?1 in the control plots. Simulated N deposition significantly increased the mean annual soil respiration rate, fine root biomass, soil microbial biomass C (MBC), and N concentration in fine roots and fresh leaf litter. Soil respirations exhibited a positive exponential relationship with soil temperature, and a linear relationship with MBC. The net primary production (NPP) ranged from 10.95 to 15.01 Mg C ha^?1 year^?1 and was higher than the annual soil respiration (5.85 to 7.62 Mg C ha^?1 year^?1) in all treatments. Simulated N deposition increased the net ecosystem production (NEP), and there was a significant difference between the control and high N treatment NEP, whereas, the difference of NEP among control, low-N, and medium-N was not significant. Results suggest that N controlled the primary production in this bamboo plantation ecosystem. Simulated N deposition increased the C sequestration of the P. amarus plantation ecosystem through increasing the plant C pool, though CO₂ emission through soil respiration was also enhanced.     

Heterotrophic soil respiration and soil carbon dynamics in the deciduous Hainich forest obtained by three approaches

Three different approaches were used to calculate heterotrophic soil respiration (Rh) and soil carbon dynamics in an old-growth deciduous forest in central Germany. A root and mycorrhiza exclosure experiment in the field separated auto- and heterotrophic soil respiration. It was compared to modeled heterotrophic respiration resulting from two different approaches: a modular component model of soil respiration calculated autotrophic and heterotrophic soil respiration with litter, climate and canopy photosynthesis as input variables. It was calibrated by independent soil respiration measurements in the field. A second model was calibrated by incubation of soil samples from different soil layers in the laboratory. In this case, the annual sum of Rh was calculated by an empirical model including response curves to temperature and a soil moisture. The three approaches showed good accordance during spring and summer and when the annual sums of Rh calculated by the two models were compared. Average Rh for the years 2002–2006 were 436 g C m^?2 year^?1 (field model) and 417 g C m^?2 year^?1 (lab-model), respectively. Differences between the approaches revealed specific limitations of each method. The average carbon balance of the Hainich forest soil was estimated to be between 1 and 35 g C m^?2 year^?1 depending on the model used and the averaging period. A comparison with nighttime data from eddy covariance (EC) showed that EC data were lower than modelled soil respiration in many situations. We conclude that better filter methods for EC nighttime data have to be developed.     

Nitrogen deposition promotes ecosystem carbon accumulation by reducing soil carbon emission in a subtropical forest

Background and aims

Tropical and subtropical forests are experiencing high levels of atmospheric nitrogen (N) deposition, but the responses of such forests ecosystems to N deposition remain poorly understood.

Methods

We conducted an 8-year field experiment examining the effect of experimental N deposition on plant growth, soil carbon dioxide efflux, and net ecosystem production (NEP) in a subtropical Chinese fir forest. The quantities of N added were 0 (control), 60, 120, and 240 kg ha^?1 year^?1.

Results

NEP was lowest under ambient conditions and highest with 240 kg of N ha^?1 year^?1 treatment. The net increase in ecosystem carbon (C) storage ranged from 9.2 to 16.4 kg C per kg N added in comparison with control. In addition, N deposition treatments significantly decreased heterotrophic respiration (by 0.69–1.85 t C ha^?1 year^?1) and did not affect plant biomass. The nitrogen concentrations were higher in needles than that in fine roots.

Conclusions

Our findings suggest that the young Chinese fir forest is carbon source and N deposition would sequester additional atmospheric CO₂ at high levels N input, mainly due to reduced soil CO₂ emission rather than increased plant growth, and the amount of sequestered C depended on the rate of N deposition.     

Will CO<Subscript>2</Subscript> Emissions from Drained Tropical Peatlands Decline Over Time? Links Between Soil Organic Matter Quality,Nutrients, and C Mineralization Rates

Conversion, drainage, and cultivation of tropical peatlands can change soil conditions, shifting the C balance of these systems, which is important for the global C cycle. We examined the effect of soil organic matter (SOM) quality and nutrients on CO₂ production from peat decomposition using laboratory incubations of Indonesian peat soils from undrained forest in Kalimantan and drained oil palm plantations in Kalimantan and Sumatra. We found that oil palm soils had higher C/N and lower SOM quality than forest soils. Higher substrate quality and nutrient availability, particularly lower ratios of aromatic/aliphatic carbon and C/N, rather than total SOM or carbon, explained the higher rate of CO₂ production by forest soils (10.80 ± 0.23 µg CO₂–C g C h^?1) compared to oil palm soils (5.34 ± 0.26 µg CO₂–C g C h^?1) from Kalimantan. These factors also explained lower rates in Sumatran oil palm (3.90 ± 0.25 µg CO₂–C g C h^?1). We amended peat with nitrogen (N), phosphorus (P), and glucose to further investigate observed substrate and nutrient constraints across the range of observed peat quality. Available N limited CO₂ production, in unamended and amended soils. P addition raised CO₂ production when substrate quality was high and initial P state was low. Glucose addition raised CO₂ production in the presence of added N and P. Our results suggest that decline in SOM quality and nutrients associated with conversion may decrease substrate-driven rates of CO₂ production from peat decomposition over time.     

Carbon allocation in a Bornean tropical rainforest without dry seasons

To clarify characteristics of carbon (C) allocation in a Bornean tropical rainforest without dry seasons, gross primary production (GPP) and C allocation, i.e., above-ground net primary production (ANPP), aboveground plant respiration (APR), and total below-ground carbon flux (TBCF) for the forest were examined and compared with those from Amazonian tropical rainforests with dry seasons. GPP (30.61 MgC ha^?1 year^?1, eddy covariance measurements; 34.40 MgC ha^?1 year^?1, biometric measurements) was comparable to those for Amazonian rainforests. ANPP (6.76 MgC ha^?1 year^?1) was comparable to, and APR (8.01 MgC ha^?1 year^?1) was slightly lower than, their respective values for Amazonian rainforests, even though aboveground biomass was greater at our site. TBCF (19.63 MgC ha^?1 year^?1) was higher than those for Amazonian forests. The comparable ANPP and higher TBCF were unexpected, since higher water availability would suggest less fine root competition for water, giving higher ANPP and lower TBCF to GPP. Low nutrient availability may explain the comparable ANPP and higher TBCF. These data show that there are variations in C allocation patterns among mature tropical rainforests, and the variations cannot be explained solely by differences in soil water availability.     

Fluxes of nitrogen and phosphorus in a gallery forest in the Cerrado of central Brazil

The Gallery forests of the Cerrado biome play a critical role in controlling stream chemistry but little information about biogeochemical processes in these ecosystems is available. This work describes the fluxes of N and P in solutions along a topographic gradient in a gallery forest. Three distinct floristic communities were identified along the gradient: a wet community nearest the stream, an upland dry community adjacent to the woodland savanna and an intermediate community between the two. Transects were marked in the three communities for sampling. Fluxes of N from bulk precipitation to these forests resulted in deposition of 12.6 kg ha^?1 y^?1 of total N of which 8.8 kg ha^?1 was as inorganic N. The throughfall flux of total N was generally <8.4 kg ha^?1 year^?1. Throughfall NO₃?CN fluxes were higher (7?C32%) while NH₄?CN and organic N fluxes were lower (54?C69% and 5?C46%) than those in bulk precipitation. The throughfall flux was slightly lower for the wet forest community compared to other communities. Litter leachate fluxes differed among floristic communities with higher NH₄?CN in the wet community. The total N flux was greater in the wet forest than in the dry forest (13.5 vs. 9.4 kg ha^?1 year^?1, respectively). The stream water had total N flux of 0.3 kg ha^?1 year^?1. The flux of total P through bulk precipitation was 0.7 kg ha^?1 year^?1 while the mean fluxes of total P in throughfall (0.6 kg ha^?1 year^?1) and litter leachate (0.5 kg ha^?1 year^?1) declined but did not differ between communities. The low concentrations presented in soil solution and low fluxes in stream water (0.3 and 0.1 kg ha^?1 year^?1 for N and P, respectively) relative to other flowpaths emphasize the conservative nutrient cycling of these forests and the importance of internal recycling processes for the maintenance and conservation of riparian and stream ecosystems in the Cerrado.     

Losses of soil carbon by converting tropical forest to plantations: erosion and decomposition estimated by δ13C

Indonesia lost more tropical forest than all of Brazil in 2012, mainly driven by the rubber, oil palm, and timber industries. Nonetheless, the effects of converting forest to oil palm and rubber plantations on soil organic carbon (SOC) stocks remain unclear. We analyzed SOC losses after lowland rainforest conversion to oil palm, intensive rubber, and extensive rubber plantations in Jambi Province on Sumatra Island. The focus was on two processes: (1) erosion and (2) decomposition of soil organic matter. Carbon contents in the Ah horizon under oil palm and rubber plantations were strongly reduced up to 70% and 62%, respectively. The decrease was lower under extensive rubber plantations (41%). On average, converting forest to plantations led to a loss of 10 Mg C ha^?1 after about 15 years of conversion. The C content in the subsoil was similar under the forest and the plantations. We therefore assumed that a shift to higher δ¹³C values in plantation subsoil corresponds to the losses from the upper soil layer by erosion. Erosion was estimated by comparing the δ¹³C profiles in the soils under forest and under plantations. The estimated erosion was the strongest in oil palm (35 ± 8 cm) and rubber (33 ± 10 cm) plantations. The ¹³C enrichment of SOC used as a proxy of its turnover indicates a decrease of SOC decomposition rate in the Ah horizon under oil palm plantations after forest conversion. Nonetheless, based on the lack of C input from litter, we expect further losses of SOC in oil palm plantations, which are a less sustainable land use compared to rubber plantations. We conclude that δ¹³C depth profiles may be a powerful tool to disentangle soil erosion and SOC mineralization after the conversion of natural ecosystems conversion to intensive plantations when soils show gradual increase of δ¹³C values with depth.     

Indonesia’s blue carbon: a globally significant and vulnerable sink for seagrass and mangrove carbon

The global significance of carbon storage in Indonesia’s coastal wetlands was assessed based on published and unpublished measurements of the organic carbon content of living seagrass and mangrove biomass and soil pools. For seagrasses, median above- and below-ground biomass was 0.29 and 1.13 Mg C ha^?1 respectively; the median soil pool was 118.1 Mg C ha^?1. Combining plant biomass and soil, median carbon storage in an Indonesian seagrass meadow is 119.5 Mg C ha^?1. Extrapolated to the estimated total seagrass area of 30,000 km², the national storage value is 368.5 Tg C. For mangroves, median above- and below-ground biomass was 159.1 and 16.7 Mg C ha^?1, respectively; the median soil pool was 774.7 Mg C ha^?1. The median carbon storage in an Indonesian mangrove forest is 950.5 Mg C ha^?1. Extrapolated to the total estimated mangrove area of 31,894 km², the national storage value is 3.0 Pg C, a likely underestimate if these habitats sequester carbon at soil depths >1 m and/or sequester inorganic carbon. Together, Indonesia’s seagrasses and mangroves conservatively account for 3.4 Pg C, roughly 17 % of the world’s blue carbon reservoir. Continued degradation and destruction of these wetlands has important consequences for CO₂ emissions and dissolved carbon exchange with adjacent coastal waters. We estimate that roughly 29,040 Gg CO₂ (eq.) is returned annually to the atmosphere–ocean pool. This amount is equivalent to about 3.2 % of Indonesia’s annual emissions associated with forest and peat land conversion. These results highlight the urgent need for blue carbon and REDD+ projects as a means to stem the decline in wetland area and to mitigate the release of a significant fraction of the world’s coastal carbon stores.     

Importance of mangrove plantations for climate change mitigation in Bangladesh

Mangroves have been identified as blue carbon ecosystems that are natural carbon sinks. In Bangladesh, the establishment of mangrove plantations for coastal protection has occurred since the 1960s, but the plantations may also be a sustainable pathway to enhance carbon sequestration, which can help Bangladesh meet its greenhouse gas (GHG) emission reduction targets, contributing to climate change mitigation. As a part of its Nationally Determined Contribution (NDC) under the Paris Agreement 2016, Bangladesh is committed to limiting the GHG emissions through the expansion of mangrove plantations, but the level of carbon removal that could be achieved through the establishment of plantations has not yet been estimated. The mean ecosystem carbon stock of 5–42 years aged (average age: 25.5 years) mangrove plantations was 190.1 (±30.3) Mg C ha⁻¹, with ecosystem carbon stocks varying regionally. The biomass carbon stock was 60.3 (±5.6) Mg C ha⁻¹ and the soil carbon stock was 129.8 (±24.8) Mg C ha⁻¹ in the top 1 m of which 43.9 Mg C ha⁻¹ was added to the soil after plantation establishment. Plantations at age 5 to 42 years achieved 52% of the mean ecosystem carbon stock calculated for the reference site (Sundarbans natural mangroves). Since 1966, the 28,000 ha of established plantations to the east of the Sundarbans have accumulated approximately 76,607 Mg C year⁻¹ sequestration in biomass and 37,542 Mg C year⁻¹ sequestration in soils, totaling 114,149 Mg C year⁻¹. Continuation of the current plantation success rate would sequester an additional 664,850 Mg C by 2030, which is 4.4% of Bangladesh's 2030 GHG reduction target from all sectors described in its NDC, however, plantations for climate change mitigation would be most effective 20 years after establishment. Higher levels of investment in mangrove plantations and higher plantation establishment success could contribute up to 2,098,093 Mg C to blue carbon sequestration and climate change mitigation in Bangladesh by 2030.     

Soil Carbon Storage by Switchgrass Grown for Bioenergy

Life-cycle assessments (LCAs) of switchgrass (Panicum virgatum L.) grown for bioenergy production require data on soil organic carbon (SOC) change and harvested C yields to accurately estimate net greenhouse gas (GHG) emissions. To date, nearly all information on SOC change under switchgrass has been based on modeled assumptions or small plot research, both of which do not take into account spatial variability within or across sites for an agro-ecoregion. To address this need, we measured change in SOC and harvested C yield for switchgrass fields on ten farms in the central and northern Great Plains, USA (930 km latitudinal range). Change in SOC was determined by collecting multiple soil samples in transects across the fields prior to planting switchgrass and again 5 years later after switchgrass had been grown and managed as a bioenergy crop. Harvested aboveground C averaged 2.5?±?0.7 Mg C ha^?1 over the 5 year study. Across sites, SOC increased significantly at 0–30 cm (P?=?0.03) and 0–120 cm (P?=?0.07), with accrual rates of 1.1 and 2.9 Mg C ha^?1 year^?1 (4.0 and 10.6 Mg CO₂ ha^?1 year^?1), respectively. Change in SOC across sites varied considerably, however, ranging from ?0.6 to 4.3 Mg C ha^?1 year^?1 for the 0–30 cm depth. Such variation in SOC change must be taken into consideration in LCAs. Net GHG emissions from bioenergy crops vary in space and time. Such variation, coupled with an increased reliance on agriculture for energy production, underscores the need for long-term environmental monitoring sites in major agro-ecoregions.     

Drainage increases CO2 and N2O emissions from tropical peat soils

Tropical peatlands are vital ecosystems that play an important role in global carbon storage and cycles. Current estimates of greenhouse gases from these peatlands are uncertain as emissions vary with environmental conditions. This study provides the first comprehensive analysis of managed and natural tropical peatland GHG fluxes: heterotrophic (i.e. soil respiration without roots), total CO₂ respiration rates, CH₄ and N₂O fluxes. The study documents studies that measure GHG fluxes from the soil (n = 372) from various land uses, groundwater levels and environmental conditions. We found that total soil respiration was larger in managed peat ecosystems (median = 52.3 Mg CO₂ ha^?1 year^?1) than in natural forest (median = 35.9 Mg CO₂ ha^?1 year^?1). Groundwater level had a stronger effect on soil CO₂ emission than land use. Every 100 mm drop of groundwater level caused an increase of 5.1 and 3.7 Mg CO₂ ha^?1 year^?1 for plantation and cropping land use, respectively. Where groundwater is deep (≥0.5 m), heterotrophic respiration constituted 84% of the total emissions. N₂O emissions were significantly larger at deeper groundwater levels, where every drop in 100 mm of groundwater level resulted in an exponential emission increase (exp(0.7) kg N ha^?1 year^?1). Deeper groundwater levels induced high N₂O emissions, which constitute about 15% of total GHG emissions. CH₄ emissions were large where groundwater is shallow; however, they were substantially smaller than other GHG emissions. When compared to temperate and boreal peatland soils, tropical peatlands had, on average, double the CO₂ emissions. Surprisingly, the CO₂ emission rates in tropical peatlands were in the same magnitude as tropical mineral soils. This comprehensive analysis provides a great understanding of the GHG dynamics within tropical peat soils that can be used as a guide for policymakers to create suitable programmes to manage the sustainability of peatlands effectively.     

CH4 and N2O emissions from smallholder agricultural systems on tropical peatlands in Southeast Asia

There are limited data for greenhouse gas (GHG) emissions from smallholder agricultural systems in tropical peatlands, with data for non-CO₂ emissions from human-influenced tropical peatlands particularly scarce. The aim of this study was to quantify soil CH₄ and N₂O fluxes from smallholder agricultural systems on tropical peatlands in Southeast Asia and assess their environmental controls. The study was carried out in four regions in Malaysia and Indonesia. CH₄ and N₂O fluxes and environmental parameters were measured in cropland, oil palm plantation, tree plantation and forest. Annual CH₄ emissions (in kg CH₄ ha⁻¹ year⁻¹) were: 70.7 ± 29.5, 2.1 ± 1.2, 2.1 ± 0.6 and 6.2 ± 1.9 at the forest, tree plantation, oil palm and cropland land-use classes, respectively. Annual N₂O emissions (in kg N₂O ha⁻¹ year⁻¹) were: 6.5 ± 2.8, 3.2 ± 1.2, 21.9 ± 11.4 and 33.6 ± 7.3 in the same order as above, respectively. Annual CH₄ emissions were strongly determined by water table depth (WTD) and increased exponentially when annual WTD was above −25 cm. In contrast, annual N₂O emissions were strongly correlated with mean total dissolved nitrogen (TDN) in soil water, following a sigmoidal relationship, up to an apparent threshold of 10 mg N L⁻¹ beyond which TDN seemingly ceased to be limiting for N₂O production. The new emissions data for CH₄ and N₂O presented here should help to develop more robust country level ‘emission factors’ for the quantification of national GHG inventory reporting. The impact of TDN on N₂O emissions suggests that soil nutrient status strongly impacts emissions, and therefore, policies which reduce N-fertilisation inputs might contribute to emissions mitigation from agricultural peat landscapes. However, the most important policy intervention for reducing emissions is one that reduces the conversion of peat swamp forest to agriculture on peatlands in the first place.     

Linking Belowground Carbon Allocation to Anaerobic CH4 and CO2 Production in a Forested Peatland,New York State

Heterotrophic soil microorganisms rely on carbon (C) allocated belowground in plant production, but belowground C allocation (BCA) by plants is a poorly quantified part of ecosystem C cycling, especially, in peat soil. We applied a C balance approach to quantify BCA in a mixed conifer-red maple (Acer rubrum) forest on deep peat soil. Direct measurements of CH₄ and CO₂ fluxes across the soil surface (soil respiration), production of fine and small plant roots, and aboveground litterfall were used to estimate respiration by roots, by mycorrhizae and by free-living soil microorganisms. Measurements occurred in two consecutive years. Soil respiration rates averaged 1.2 bm μmol m^{? 2} s^{? 1} for CO₂ and 0.58 nmol m^{? 2} s^{? 1} for CH₄ (371 to 403 g C m^{? 2} year^{? 1}). Carbon in aboveground litter (144 g C m^{? 2} year^{? 1}) was 84% greater than C in root production (78 g C m^{? 2} year^{? 1}). Complementary in vitro assays located high rates of anaerobic microbial activity, including methanogenesis, in a dense layer of roots overlying the peat soil and in large-sized fragments within the peat matrix. Large-sized fragments were decomposing roots and aboveground leaf and twig litter, indicating that relatively fresh plant production supported most of the anaerobic microbial activity. Respiration by free-living soil microorganisms in deep peat accounted for, at most, 29 to 38 g C m^{? 2} year^{? 1}. These data emphasize the close coupling between plant production, ecosystem-level C cycling and soil microbial ecology, which BCA can help reveal.     

Biomass dynamics in a logged forest: the role of wood density

Wood density (WD) is believed to be a key trait in driving growth strategies of tropical forest species, and as it entails the amount of mass per volume of wood, it also tends to correlate with forest carbon stocks. Yet there is relatively little information on how interspecific variation in WD correlates with biomass dynamics at the species and population level. We determined changes in biomass in permanent plots in a logged forest in Vietnam from 2004 to 2012, a period representing the last 8 years of a 30 years logging cycle. We measured diameter at breast height (DBH) and estimated aboveground biomass (AGB) growth, mortality, and net AGB increment (the difference between AGB gains and losses through growth and mortality) per species at the individual and population (i.e. corrected for species abundance) level, and correlated these with WD. At the population level, mean net AGB increment rates were 6.47 Mg ha^?1 year^?1 resulting from a mean AGB growth of 8.30 Mg ha^?1 year^?1, AGB recruitment of 0.67 Mg ha^?1 year^?1 and AGB losses through mortality of 2.50 Mg ha^?1 year^?1. Across species there was a negative relationship between WD and mortality rate, WD and DBH growth rate, and a positive relationship between WD and tree standing biomass. Standing biomass in turn was positively related to AGB growth, and net AGB increment both at the individual and population level. Our findings support the view that high wood density species contribute more to total biomass and indirectly to biomass increment than low wood density species in tropical forests. Maintaining high wood density species thus has potential to increase biomass recovery and carbon sequestration after logging.     

Biomass accumulation and carbon storage of four different aged Sonneratia apetala plantations in Southern China

The objectives of this study were to examine plant biomass accumulation and carbon (C) storage in four different aged Sonneratia apetala plantations in the Leizhou Bay in South China. The allometric equations using diameter at breast height (DBH) and height (H) were developed to quantify plant biomass. The total forest biomass (TFB) of S. apetala plantation at 4, 5, 8, and 10 years old was 47.9, 71.7, 95.9, and 108.1 Mg ha^?1, respectively. The forest biomass C storage in aboveground (AGB) and roots at 4, 5, 8, and 10-year plantation was 19.9, 32.6, 42.0, 49.0 Mg ha^?1, respectively. Soil organic C (SOC) on the top 20 cm of sediments increased by 0.3, 6.8, 27.4, and 35.0 Mg ha^?1after 4, 5, 8, and 10 years of reforestation, respectively. The average annual rate of total carbon storage (TCS) accumulation at 4, 5, 8, and 10-year S. apetala plantation was 5.0, 7.9, 8.7, and 8.4 Mg ha^?1 yr^?1, respectively. The TCS values in this study were underestimated because we only estimated SOC storage on the top 20-cm sediments in these plantations. This study suggests these young S. apetala plantations have the characteristics of fast growth, high biomass accumulation, and high C storage capacity, especially in sediments. They sequestrated C at a high but varying rate over time. The large-scale reforestation of S. apetala plantations in the open coastal mudflats in southern China has great potential to sequestrate more C as well as restore the degraded coastal land. The potential ecological issues associated with the increasing monoculture plantations were discussed. More long-term monitoring and research are needed to further evaluate biomass and C accumulation of S. apetala plantations over time as well as how the increasing distribution of this monoculture plantation will influence the few native mangrove remnants.