High precipitation causes large fluxes of dissolved organic carbon and nitrogen in a subtropical montane <Emphasis Type="Italic">Chamaecyparis</Emphasis> forest in Taiwan

Fluxes of dissolved organic carbon (DOC) and nitrogen (DON) may play an important role for losses of C and N from the soils of forest ecosystems, especially under conditions of high precipitation. We studied DOC and DON fluxes and concentrations in relation to precipitation intensity in a subtropical montane Chamaecyparis obtusa var. formosana forest in Taiwan. Our objective was, to quantify DOC and DON fluxes and to understand the role of high precipitation for DOC and DON export in this ecosystem. From 2005 to 2008 we sampled bulk precipitation, throughfall, forest floor percolates and seepage (60 cm) and analyzed DOC, DON and mineral N concentrations. Average DOC fluxes in the soil were extremely high (962 and 478 kg C ha^?1 year^?1 in forest floor percolates and seepage, respectively) while DON fluxes were similar to other (sub)tropical ecosystems (16 and 8 kg N ha^?1 year^?1, respectively). Total N fluxes in the soil were dominated by DON. Dissolved organic C and N concentrations in forest floor percolates were independent of the water flux. No dilution effect was visible. Instead, the pool size of potentially soluble DOC and DON was variable as indicated by different DOC and DON concentrations in forest floor percolates at similar precipitation amounts. Therefore, we hypothesized, that these pools are not likely to be depleted in the long term. The relationship between water fluxes in bulk precipitation and DOC and DON fluxes in forest floor percolates was positive (DOC r = 0.908, DON r = 0.842, respectively, Spearman rank correlation). We concluded, that precipitation is an important driver for DOC and DON losses from this subtropical montane forest and that these DOC losses play an important role in the soil C cycle of this ecosystem. Moreover, we found that the linear relationship between bulk precipitation and DOC and DON fluxes in forest floor percolates of temperate ecosystems does not hold when incorporating additional data on these fluxes from (subtropical) ecosystems.     

Gaseous and fluvial carbon export from an Amazon forest watershed

The transfer of carbon (C) from Amazon forests to aquatic ecosystems as CO₂ supersaturated in groundwater that outgases to the atmosphere after it reaches small streams has been postulated to be an important component of terrestrial ecosystem C budgets. We measured C losses as soil respiration and methane (CH₄) flux, direct CO₂ and CH₄ fluxes from the stream surface and fluvial export of dissolved inorganic C (DIC), dissolved organic C (DOC), and particulate C over an annual hydrologic cycle from a 1,319-ha forested Amazon perennial first-order headwater watershed at Tanguro Ranch in the southern Amazon state of Mato Grosso. Stream pCO₂ concentrations ranged from 6,491 to 14,976 ??atm and directly-measured stream CO₂ outgassing flux was 5,994 ± 677 g C m^?2 y^?1 of stream surface. Stream pCH₄ concentrations ranged from 291 to 438 ??atm and measured stream CH₄ outgassing flux was 987 ± 221 g C m^?2 y^?1. Despite high flux rates from the stream surface, the small area of stream itself (970 m², or 0.007% of watershed area) led to small directly-measured annual fluxes of CO₂ (0.44 ± 0.05 g C m² y^?1) and CH₄ (0.07 ± 0.02 g C m² y^?1) per unit watershed land area. Measured fluvial export of DIC (0.78 ± 0.04 g C m^?2 y^?1), DOC (0.16 ± 0.03 g C m^?2 y^?1) and coarse plus fine particulate C (0.001 ± 0.001 g C m^?2 y^?1) per unit watershed land area were also small. However, stream discharge accounted for only 12% of the modeled annual watershed water output because deep groundwater flows dominated total runoff from the watershed. When C in this bypassing groundwater was included, total watershed export was 10.83 g C m^?2 y^?1 as CO₂ outgassing, 11.29 g C m^?2 y^?1 as fluvial DIC and 0.64 g C m^?2 y^?1 as fluvial DOC. Outgassing fluxes were somewhat lower than the 40?C50 g C m^?2 y^?1 reported from other Amazon watersheds and may result in part from lower annual rainfall at Tanguro. Total stream-associated gaseous C losses were two orders of magnitude less than soil respiration (696 ± 147 g C m^?2 y^?1), but total losses of C transported by water comprised up to about 20% of the ± 150 g C m^?2 (±1.5 Mg C ha^?1) that is exchanged annually across Amazon tropical forest canopies.     

Small scale variability of vertical water and dissolved organic matter fluxes in sandy Cambisol subsoils as revealed by segmented suction plates

Dissolved organic matter (DOM) is considered as a major carbon source in subsoils. As soil water fluxes are highly variable at small scale, and transport versus sorptive retention of DOM is related to water flux and associated contact time with minerals, knowledge of the small scale spatial variability of the dissolved organic carbon (DOC) concentrations and fluxes into the subsoil is decisive for a solid estimation of organic carbon (OC) translocation into the subsoil. Here, we made advantage of novel segmented suction plates (4 × 4 segments, each 36 cm²) to analyze the small scale spatial and temporal variability of DOC transport at 10, 50 and 150 cm depth of three subsoil observatories (approximately 50 m apart) in a sandy Dystric Cambisol under beech in the Grinderwald, 40 km northwest from Hannover, Germany. Water fluxes, DOC concentrations and fluxes as well as the specific UV absorbance (SUVA) at 280 nm were determined in weekly samples from August 2014 to November 2015 for each individual segment. The DOC fluxes decreased with depth (19.6 g C m^?2 year^?1, 10 cm; 1.2 g C m^?2 year^?1, 150 cm) and were strongly related to the water fluxes. The SUVA at 280 nm also decreased with depth (0.03 L mg C^?1 cm^?1, 10 cm; 0.01 L mg C^?1 cm^?1, 150 cm), indicating a selective retention of aromatic moieties, that was eased with increasing water flux at least in the subsoil. The proportion of temporal fluctuations and small scale variability on the total variance of each parameter where determined by the calculation of intra class correlations. The seasonal heterogeneity and the small scale spatial heterogeneity were identified to be of major importance. The importance of the small scale spatial heterogeneity strongly increased with depth, pointing towards the stability of flow paths and suggesting that at a given substrate hydrological processes rather than physicochemical processes are decisive for the sorptive retention of DOM and the variability of OC accumulation in the subsoil. Our results clearly show the demand of small scale sampling for the identification of processes regarding carbon cycling in the subsoil.     

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.     

Vulnerability of wetland soil carbon stocks to climate warming in the perhumid coastal temperate rainforest

The perhumid coastal temperate rainforest (PCTR) of southeast Alaska has some of the densest soil organic carbon (SOC) stocks in the world (>300 Mg C ha^?1) but the fate of this SOC with continued warming remains largely unknown. We quantified dissolved organic carbon (DOC) and carbon dioxide (CO₂) yields from four different wetland types (rich fen, poor fen, forested wetland and cedar wetland) using controlled laboratory incubations of surface (10 cm) and subsurface (25 cm) soils incubated at 8 and 15 °C for 37 weeks. Furthermore, we used fluorescence characterization of DOC and laboratory bioassays to assess how climate-induced soil warming may impact the quality and bioavailability of DOC delivered to fluvial systems. Soil temperature was the strongest control on SOC turnover, with wetland type and soil depth less important in controlling CO₂ flux and extractable DOC. The high temperature incubation increased average CO₂ yield by ~40 and ~25% for DOC suggesting PCTR soils contain a sizeable pool of readily biodegradable SOC that can be mineralized to DOC and CO₂ with future climate warming. Fluxes of CO₂ were positively correlated to both extractable DOC and percent bioavailable DOC during the last few months of the incubation suggesting mineralization of SOC to DOC is a strong control of soil respiration rates. Whether the net result is increased export of either carbon form will depend on the balance between the land to water transport of DOC and the ability of soil microbial communities to mineralize DOC to CO₂.     

Evolution of carbon fluxes during initial soil formation along the forefield of Damma glacier, Switzerland

Soil carbon (C) fluxes, soil respiration and dissolved organic carbon (DOC) leaching were explored along the young Damma glacier forefield chronosequence (7–128 years) over a three-year period. To gain insight into the sources of soil CO₂ effluxes, radiocarbon signatures of respired CO₂ were measured and a vegetation-clipping experiment was performed. Our results showed a clear increase in soil CO₂ effluxes with increasing site age from 9 ± 1 to 160 ± 67 g CO₂–C m^?2 year^?1, which was linked to soil C accumulation and development of vegetation cover. Seasonal variations of soil respiration were mainly driven by temperature; between 62 and 70 % of annual CO₂ effluxes were respired during the 4-month long summer season. Sources of soil CO₂ effluxes changed along the glacier forefield. For most recently deglaciated sites, radiocarbon-based age estimates indicated ancient C to be the dominant source of soil-respired CO₂. At intermediate site age (58–78 years), the contribution of new plant-fixed C via rhizosphere respiration amounted up to 90 %, while with further soil formation, heterotrophically respired C probably from accumulated ‘older’ soil organic carbon (SOC) became increasingly important. In comparison with soil respiration, DOC leaching at 10 cm depth was small, but increased similarly from 0.4 ± 0.02 to 7.4 ± 1.6 g DOC m^?2 year^?1 over the chronosequence. A strong rise of the ratio of SOC to secondary iron and aluminium oxides strongly suggests that increasing DOC leaching with site age results from a faster increase of the DOC source, SOC, than of the DOC sink, reactive mineral surfaces. Overall, C losses from soil by soil respiration and DOC leaching increased from 9 ± 1 to 70 ± 17 and further to 168 ± 68 g C m^?2 year^?1 at the <10, 58–78, and 110–128 year old sites. By comparison, total ecosystem C stocks increased from 0.2 to 1.1 and to 3.1 kg C m^?2 from the young to intermediate and old sites. Therefore, the ecosystem evolved from a dominance of C accumulation in the initial phase to a high throughput system. We suggest that the relatively strong increase in soil C stocks compared to C fluxes is a characteristic feature of initial soil formation on freshly exposed rocks.     

Decline in Net Ecosystem Productivity Following Canopy Transition to Late-Succession Forests

Boreal forests are critical to the global carbon (C) cycle. Despite recent advances in our understanding of boreal C budgets, C dynamics during compositional transition to late-succession forests remain unclear. Using a carefully replicated 203-year chronosequence, we examined long-term patterns of forest C stocks and net ecosystem productivity (NEP) following stand-replacing fire in the boreal forest of central Canada. We measured all C pools, including understorey vegetation, belowground biomass, and soil C, which are often missing from C budgets. We found a slight decrease in total ecosystem C stocks during early stand initiation, between 1 and 8 years after fire, at ?0.90 Mg C ha^?1 y^?1. As stands regenerated, live vegetation biomass increased rapidly, with total ecosystem C stocks reaching a maximum of 287.72 Mg C ha^?1 92 years after fire. Total ecosystem C mass then decreased in the 140- and 203-year-old stands, losing between ?0.50 and ?0.74 Mg C ha^?1 y^?1, contrasting with views that old-growth forests continue to maintain a positive C balance. The C decline corresponded with canopy transition from dominance of Populus tremuloides, Pinus banksiana, and Picea mariana in the 92-year-old stands to Betula papyrifera, Picea glauca, and Abies balsamea in the 203-year-old stands. Results from this study highlight the role of succession in long-term forest C dynamics and its importance when modeling terrestrial C flux.     

Radiocarbon-Based Assessment of Heterotrophic Soil Respiration in Two Mediterranean Forests

The amount of soil organic carbon (SOC) released into the atmosphere as carbon dioxide (CO₂), which is referred to as heterotrophic respiration (Rh), is technically difficult to measure despite its necessity to the understanding of how to protect and increase soil carbon stocks. Within this context, the aim of this study is to determine Rh in two Mediterranean forests dominated by pine and oak using radiocarbon measurements of the bulk SOC from different soil layers. The annual Rh was 3.22 Mg C ha^?1 y^?1 under pine and 3.13 Mg C ha^?1 y^?1 under oak, corresponding to 38 and 31% of the annual soil respiration, respectively. The accuracy of the Rh values was evaluated by determining the net primary production (NPP), as the sum of the Rh and the net ecosystem production measured by eddy covariance, then comparing it with the NPP obtained through independent biometric measurements. No significant differences were observed, which suggested the suitability of our methodology to infer Rh. Assuming the C inputs to soil to consist exclusively of the aboveground and belowground litter and the C output exclusively of the Rh, both soils were C sinks, which is consistent with a previous modeling study that was performed in the same stands. In conclusion, radiocarbon analysis of bulk SOC provided a reliable estimate of the average annual amount of soil carbon released to the atmosphere; hence, its application is convenient for calculating Rh because it utilizes only a single soil sampling and no time-consuming monitoring activities.     

Site‐to‐site variability and temporal trends of DOC concentrations and fluxes in temperate forest soils

Here, we report site‐to‐site variability and 12–14 year trends of dissolved organic carbon (DOC) from organic layers and mineral soils of 22 forests in Bavaria, Germany. DOC concentrations in the organic layer were negatively correlated with mean annual precipitation and elevation whereas air temperature had a positive effect on DOC concentrations. DOC fluxes in subsoils increased by 3 kg ha^?1 yr^?1 per 100 mm precipitation or per 100 m elevation. The highest DOC concentrations were found under pine stands with mor humus. Average DOC concentrations in organic layer leachates followed the order: pine>oak>spruce>beech. However, the order was different for mean DOC fluxes (spruce>pine>oak>beech) because of varying precipitation regimes among the forest types. In 12 of 22 sites, DOC concentrations of organic layer leachates significantly increased by 0.5 to 3.1 mg C L^?1 yr^?1 during the sampling period. The increase in DOC concentration coincided with decreasing sulfate concentration, indicating that sulfate concentration is an important driver of DOC solubility in the organic layer of these forest sites. In contrast to the organic layer, DOC concentrations below 60 cm mineral soil depth decreased by <0.1–0.4 mg C L^?1 yr^?1 at eight sites. The negative DOC trends were attributed to (i) increasing adsorption of DOC by mineral surfaces resulting from desorption of sulfate and (ii) increasing decay of DOC resulting from decreasing stabilization of DOC by organo‐Al complexes. Trends of DOC fluxes from organic layers were consistent with those of DOC concentrations although trends were only significant at seven sites. DOC fluxes in the subsoil were with few exceptions small and trends were generally not significant. Our results suggest that enhanced mobilization of DOC in forest floors contributed to the increase of DOC in surface waters while mineral horizons did not contribute to increasing DOC export of forest soils.     

Phosphorus cycling in a small watershed in the Brazilian Cerrado: impacts of frequent burning

Plant productivity in many tropical savannas is phosphorus limited. The biogeochemical cycling of P in these ecosystems, however, has not been well quantified. In the present study, we characterized P stocks and fluxes in a well-preserved small watershed in the Brazilian Cerrado. As the Cerrado is also a fire-dominated ecosystem, we measured the P stocks and fluxes in a cerrado stricto sensu plot with complete exclusion of fire for 26 years (unburned plot) and then tested some predictions about the impacts of fire impacts on P cycling in an experimental plot that was burned three times since 1992 (burned plot). The unburned area is an ecosystem with large soil stocks of total P (1,151 kg ha^?1 up to 50 cm depth), but the largest fraction is in an occluded form. Readily extractable P was found up to 3 m soil depth suggesting that deep soil is more important to the P cycle than has been recognized. The P stock in belowground biomass (0?C800 cm) was 9.9 kg ha^?1. Decomposition of fine litter released 0.97 kg P ha^?1 year^?1. Fluxes of P through bulk atmospheric deposition, throughfall and litter leachate were very low (0.008, 0.006 and 0.028 kg ha^?1 year^?1, respectively) as was stream export (0.001 kg ha^?1 year^?1). Immobilization of P by microbes during the rainy season seems to be an important mechanism of P conservation in this ecosystem. Fire significantly increased P flux in litter leachate to 0.11 kg ha^?1 year^?1, and added 1.2 kg ha^?1 of P in ash deposition after fire. We found an increase of P concentration in soil solution at 100 cm depth (from 0.03 ??g l^?1 in unburned plot to 0.3 ??g l^?1 in the burned plot). In surface soils (0?C10 cm) of the burned plot, fire decreased the concentrations of extractable organic-P fractions, but did not significantly increase inorganic-P fractions. The reduction of extractable soil organic P in the burned plot in topsoil and the increase of P in the soil solution at greater depths indicated a reduction of P availability and may increase P fixation in deep soils. Repeated fire events over the long term may result in significant net loss of available forms of phosphorus from this ecosystem.     

Seasonal variation in dissolved carbon concentrations and fluxes in the upper Purus River, southwestern Amazon

One of the less studied components of carbon cycling that could improve our understanding of how and how strongly Amazonian ecosystems act as sinks or sources of carbon is the amount that is carried downstream by rivers. In this paper, we show that a headwater river can carry from 25 to 130 % of the reported sink for Amazonian forests, therefore not being negligible for ecosystem-level carbon budgets. Based on monthly measurements from May 2004 to April 2005 of the upper Purus River, southwestern Amazonia, we found that: water pH, dissolved oxygen, specific electrical conductivity, and dissolved inorganic carbon (DIC) were inversely related to water discharge and precipitation; pCO₂ was directly and strongly related to discharge and precipitation, and to a lesser extent to pH and dissolved oxygen; and dissolved organic carbon (DOC) was not related to any measured variable. Annual flux of dissolved carbon (DIC + DOC) at the sampling site was estimated as 604 ± 55 Gg C a^?1. More than 75 % was in the form of bicarbonate, with the remainder as CO₂ and DOC. This amount is equivalent to 0.15 ± 0.01 Mg C ha^?1 a^?1 in the upstream drainage basin, which is on the same order of magnitude as terrestrial carbon fixation.     

Significance of Over-Mature and Decaying Trees for Carbon Stocks in a Central European Natural Spruce Forest

Old-growth forests are important stores for carbon as they may accumulate C for centuries. The alteration of biomass and soil carbon pools across the development stages of a forest dynamics cycle has rarely been quantified. We studied the above- and belowground C stocks in the five forest development stages (regeneration to decay stage) of a montane spruce (Picea abies) forest of the northern German Harz Mountains, one of Central Europe’s few forests where the natural forest dynamics have not been disturbed by man for several centuries. The over-mature and decay stages had the largest total (up to 480 Mg C ha^?1) and aboveground biomass carbon pools (200 Mg C ha^?1) with biomass C stored in dead wood in the decay stage. The soil C pool (220–275 Mg C ha^?1, 0–60 cm) was two to three times larger than in temperate lowland spruce forests and remained invariant across the forest dynamics cycle. On the landscape level, taking into account the frequency of the five forest development stages, the total carbon pool was approximately 420 Mg C ha^?1. The results evidence the high significance of over-mature and decaying stages of temperate mountain forests not only for conserving specialized forest organisms but also for their large carbon storage potential.     

Dissolved organic carbon production and flux under long-term litter manipulations in a Pacific Northwest old-growth forest

Dissolved organic carbon (DOC) flux is an important mechanism to convey soil carbon (C) from aboveground organic debris (litter) to deeper soil horizons and can influence the formation of stable soil organic C compounds. The magnitude of this flux depends on both infiltration and DOC production rates which are functions of the climatic, soil, topographic and ecological characteristics of a region. Aboveground litter quantity and quality was manipulated for 20 years in an old-growth Douglas fir forest under six treatments to study relationships among litter inputs, DOC production and flux, and soil C dynamics. DOC concentrations were measured at two depths using tension lysimeters, and a hydrologic model was created to quantify water and DOC flux through the soil profile. DOC concentrations ranged from 3.0–8.0 and 1.5–2.5 mg C/L among treatments at 30 and 100 cm below the soil surface, respectively. Aboveground detrital inputs did not have a consistent positive effect on soil solution DOC; the addition of coarse woody debris increased soil solution DOC by 58% 30 cm belowground, while doubling the mass of aboveground leaf litter decreased DOC concentrations by 30%. We suggest that high-quality leaf litter accelerated microbial processing, resulting in a “priming” effect that led to the lower concentrations. Annual DOC flux into groundwater was small (2.7–3.7 g C/m²/year) and accounts for < 0.1% of estimated litter C at the site. Therefore, direct DOC loss from surface litter to groundwater is relatively negligible to the soil C budget. However, DOC flux into the soil surface was much greater (73–210 g C/m²/year), equivalent to 1.4–2.4% of aboveground litter C. Therefore, DOC transport is an important source of C to shallow soil horizons.

     

The role of soil in storing carbon in tropical rainforests: the case of Ankasa Park, Ghana

Tropical primary rainforests of Africa are an enormous reservoir of carbon (C), most of which, in the common perception, is stored in the biomass. We studied one of these forests, Ankasa, in the south-western part of Ghana, in terms of quantity and ¹⁴C activity of soil organic carbon (SOC) to elucidate the little known important role of soil in storing carbon in such biomass-rich environments. The stock of carbon in the mineral soil to a depth of 1 m was measured to be 151?±?20 Mg C ha^?1, a similar value in magnitude to the one of the aboveground biomass being 138–170 Mg C ha^?1, including live and dead wood. Surface litter C is roughly 10% (15?±?9 Mg C ha^?1) of the C in the biomass and soil. The radiocarbon measurements indicate that SOC was significantly affected by “bomb C” enrichment, so that “Modern C”, namely with a mean radiocarbon age lower than 200 years, is present also deeper than 45 cm in the Bo2 horizon. The mean residence time (MRT) estimated from radiocarbon content are of the order of a few decades in the topsoil and a few centuries in the deeper horizons. Altogether, the MRT values indicate a fast recycle of C compared to temperate or boreal forests, but not as fast as usually believed for tropical forest soils. Making a pondered mean, in the Ankasa forest the time an atom of C resides in soil is not much different from one atom of C in the woody aboveground biomass. Hence, the contribution of soil in storing C is substantial, implying that in primary rainforests it is mandatory to determine the SOC stock and its dynamics, too often neglected or underestimated.     

Dynamics of oxidized and reduced iron in a northern hardwood forest

Iron (Fe) is ubiquitous in forest ecosystems and its cycle is thought to influence the development of soil, particularly Spodosols (podsolization), and the biogeochemistry of macronutrients such as carbon (C), nitrogen (N), and phosphorus (P), as well as many trace metals. The cycle of Fe in northern hardwood forests remains poorly understood. To address some of these uncertainties, we constructed a biogeochemical budget of Fe for a small catchment at the Hubbard Brook Experimental Forest in the White Mountains of New Hampshire, USA. Horizonal, temporal, and elevational patterns of concentrations and fluxes of oxidized and reduced Fe species were assessed in leaf litter, soil, soil solution, and stream water. The chemistry of dissolved Fe was evaluated in the context of its relationship with dissolved organic carbon, pH, and dissolved oxygen. Soil solution fluxes of Fe were highest in the organic (Oa, 52.5 mol ha^?1 year^?1) horizon and decreased with depth in the mineral (Bh, 50.5 mol ha^?1 year^?1, and Bs, 19.7 mol ha^?1 year^?1) horizons, consistent with podsolization theories predicting immobilization of Fe following downward transport to mineral soils. The export of Fe in stream water (1.8 mol ha^?1 year^?1) was lower than precipitation input (3.5 mol ha^?1 year^?1). The low stream flux indicates most Fe in drainage waters was immobilized in the soil and retained in the watershed. The portion of total Fe as Fe(II) was ~10?C60% in soil solutions, seemingly high for soils that are considered to be well-drained, oxidizing environments. Organic complexes likely stabilized Fe(II) in solution under oxidizing conditions that would otherwise promote considerably higher Fe(III)-to-Fe(II) ratios. Our study indicates that there are organic matter-derived sources of dissolved Fe(II) as well as substantial mobilization of Fe(II), possibly the result of the reduction of Fe-bearing soil minerals.     

Short-term responses of ecosystem carbon fluxes to experimental soil warming at the Swiss alpine treeline

Climatic warming will probably have particularly large impacts on carbon fluxes in high altitude and latitude ecosystems due to their great stocks of labile soil C and high temperature sensitivity. At the alpine treeline, we experimentally warmed undisturbed soils by 4 K for one growing season with heating cables at the soil surface and measured the response of net C uptake by plants, of soil respiration, and of leaching of dissolved organic carbon (DOC). Soil warming increased soil CO₂ effluxes instantaneously and throughout the whole vegetation period (+45%; +120 g C m y^?1). In contrast, DOC leaching showed a negligible response of a 5% increase (NS). Annual C uptake of new shoots was not significantly affected by elevated soil temperatures, with a 17, 12, and 14% increase for larch, pine, and dwarf shrubs, respectively, resulting in an overall increase in net C uptake by plants of 20–40 g C m^?2y^?1. The Q ₁₀ of 3.0 measured for soil respiration did not change compared to a 3-year period before the warming treatment started, suggesting little impact of warming-induced lower soil moisture (?15% relative decrease) or increased soil C losses. The fraction of recent plant-derived C in soil respired CO₂ from warmed soils was smaller than that from control soils (25 vs. 40% of total C respired), which implies that the warming-induced increase in soil CO₂ efflux resulted mainly from mineralization of older SOM rather than from stimulated root respiration. In summary, one season of 4 K soil warming, representative of hot years, led to C losses from the studied alpine treeline ecosystem by increasing SOM decomposition more than C gains through plant growth.     

Three-Year Soil Carbon and Nitrogen Responses to Sugarcane Straw Management

Green harvest sugarcane management has increased soil organic C and N stocks over time. However, emerging sugarcane straw removal to meet increasing bioenergy demands has raised concerns about soil C and N depletions. Thus, we conducted a field study in southeast Brazil over nearly three years (1100 days) for assessing soil C and N responses to increasing sugarcane straw removal rates. In order to detect the C input as a function of the different amounts of straw over three years, a field simulation was performed, where the original soil layer (0–0.30 m) was replaced by another from an adjacent area with low total C and δ¹³C. The treatments tested were as follows: (i) 0 Mg ha^?1 year^?1 (i.e., 100% removal), (ii) 3.5 Mg ha^?1 year^?1 (i.e., 75% removal), (iii) 7.0 Mg ha^?1 year^?1 (i.e., 50% removal), (iv) 14.0 Mg ha^?1 year^?1 (i.e., no removal), and (v) 21.0 Mg ha^?1 year^?1 (i.e., no removal + extra 50% of the straw left on the field). The results showed that sugarcane straw removal affected the soil C and total N pools. In the first 45 days of straw decomposition, a small but important straw-derived C portion enters into the soil as dissolved organic carbon (DOC). The lower the straw removal rate, the higher was straw-derived DOC content found into the soil, down to 0.50 m depth. After 3 years of management, keeping sugarcane straw on soil surface significantly increased C and N stocks within surface soil layer (0–0.025 m). Our findings suggest that under no straw removal management (i.e., 14 Mg ha^?1), approximately 364 kg ha^?1 of C and 23 kg ha^?1 of N are annually stored into this low-C soil. The contribution of the straw-derived C (C-C4) to the total soil C increases over time, which accounted for about 60% under no straw removal rate. The greatest contribution of the C storage preferentially occurs into the fraction of organic matter (<?0.53 μm) associated with soil clay minerals. We concluded that indiscriminate sugarcane straw removal to produce cellulosic ethanol or bioelectricity depletes soil C stocks and reduces N cycling in sugarcane fields, impairing environmental gains associated with bioenergy production. Therefore, this information, linked with other agronomic and environmental issues, should be taken into account towards a more sustainable straw removal management for bioenergy production in Brazil.     

Organic carbon transfers in the subtropical Red River system (Viet Nam): insights on CO<Subscript>2</Subscript> sources and sinks

The Red River, draining a 169,000 km² watershed, is the second largest river in Viet Nam and constitutes the main source of water for a large percentage of the population of North Viet Nam. Here we present the results of an investigation into the spatial distribution and temporal dynamics of particulate and dissolved organic carbon (POC and DOC, respectively) in the Red River Basin. POC concentrations ranged from 0.24 to 5.80 mg C L^?1 and DOC concentrations ranged from 0.26 to 5.39 mg C L^?1. The application of the Seneque/Riverstrahler model to monthly POC and DOC measurements showed that, in general, the model simulations of the temporal variations and spatial distribution of organic carbon (OC) concentration followed the observed trends. They also show the impact of high population densities (up to 994 inhab km^?2 in the delta area) on OC inputs in surface runoff from the different land use classes and from urban point sources. A budget of the main fluxes of OC in the whole river network, including diffuse inputs from soil leaching and runoff and point sources from urban centers, as well as algal net primary production and heterotrophic respiration was established using the model results. It shows the predominantly heterotrophic character of the river system and provides an estimate of CO₂ emissions from the river of 330 Gg C year^?1. This value is in reasonable agreement with the few available direct measurements of CO₂ fluxes in the downstream part of the river network.     

Controls on dissolved organic carbon composition and export from rice-dominated systems

Rice field outflow can contain high concentrations of dissolved organic carbon (DOC), which plays a crucial role in drinking water quality and aquatic ecosystem processes. This study examined the relationship between potential determining factors (i.e. rice area, outflow, drainwater reuse, soil properties, and time, measured as the day in the growing season) and the concentration and composition of DOC exported from 11 rice-dominated subwatersheds. Samples were collected from subwatershed inflow and outflow every 1–2 weeks from May through September 2008 and analyzed for DOC concentration, trihalomethane formation potential (THMFP), and also specific ultraviolet absorbance (SUVA₂₅₄) and the spectral slope parameter (S), which are indicators of DOC composition. Concentrations of DOC across all subwatersheds and sampling dates ranged from 1.56 to 14.43 mg L^?1 (mean = 4.32 mg L^?1). Linear mixed effects (LME) analysis indicated that DOC concentration decreased over time, and that THMFP, and DOC and THM flux, decreased over time, but increased with outflow. LME analysis of the SUVA₂₅₄ and S parameters indicated that the fraction of aromatic DOC moieties increased with time, outflow, and reuse. Additionally, apparent peaks in DOC concentrations, THMFP, and SUVA₂₅₄ coincided with the onsets of flooding and draining. Lastly, subwatersheds with outflow less than approximately 4,700 m³ ha^?1 behaved as sinks of DOC. Our findings suggest that water management factors such as outflow, reuse, and discrete irrigation events, all of which vary over the course of the growing season, were the dominant determinants of DOC concentration and composition.     

Dissolved carbon leaching from soil is a crucial component of the net ecosystem carbon balance

Estimates of carbon leaching losses from different land use systems are few and their contribution to the net ecosystem carbon balance is uncertain. We investigated leaching of dissolved organic carbon (DOC), dissolved inorganic carbon (DIC), and dissolved methane (CH₄), at forests, grasslands, and croplands across Europe. Biogenic contributions to DIC were estimated by means of its δ¹³C signature. Leaching of biogenic DIC was 8.3±4.9 g m^?2 yr^?1 for forests, 24.1±7.2 g m^?2 yr^?1 for grasslands, and 14.6±4.8 g m^?2 yr^?1 for croplands. DOC leaching equalled 3.5±1.3 g m^?2 yr^?1 for forests, 5.3±2.0 g m^?2 yr^?1 for grasslands, and 4.1±1.3 g m^?2 yr^?1 for croplands. The average flux of total biogenic carbon across land use systems was 19.4±4.0 g C m^?2 yr^?1. Production of DOC in topsoils was positively related to their C/N ratio and DOC retention in subsoils was inversely related to the ratio of organic carbon to iron plus aluminium (hydr)oxides. Partial pressures of CO₂ in soil air and soil pH determined DIC concentrations and fluxes, but soil solutions were often supersaturated with DIC relative to soil air CO₂. Leaching losses of biogenic carbon (DOC plus biogenic DIC) from grasslands equalled 5–98% (median: 22%) of net ecosystem exchange (NEE) plus carbon inputs with fertilization minus carbon removal with harvest. Carbon leaching increased the net losses from cropland soils by 24–105% (median: 25%). For the majority of forest sites, leaching hardly affected actual net ecosystem carbon balances because of the small solubility of CO₂ in acidic forest soil solutions and large NEE. Leaching of CH₄ proved to be insignificant compared with other fluxes of carbon. Overall, our results show that leaching losses are particularly important for the carbon balance of agricultural systems.