Clear-cutting of a Norway spruce stand: implications for controls on the dynamics of dissolved organic matter in the forest floor

Clear‐cutting of forest provides a unique opportunity to study the response of dynamic controls on dissolved organic matter. We examined differences in concentrations, fluxes and properties of dissolved organic matter from a control and a clear‐cut stand to reveal controlling factors on its dynamics. We measured dissolved organic C and N concentrations and fluxes in the Oi, Oe and Oa horizons of a Norway spruce stand and an adjacent clear‐cutting over 3 years. Aromaticity and complexity of organic molecules were determined by UV and fluorescence spectroscopy, and we measured δ¹³C ratios over 1 year. Annual fluxes of dissolved organic C and N remained unchanged in the thin Oi horizon (～ 260 kg C ha^?1, ～ 8.5 kg N ha^?1), despite the large reduction in fresh organic matter inputs after clear‐cutting. We conclude that production of dissolved organic matter is not limited by lack of resource. Gross fluxes of dissolved organic C and N increased by about 60% in the Oe and 40% in the Oa horizon upon clear‐cutting. Increasing organic C and N concentrations and increasing water fluxes resulted in 380 kg C ha^?1 year^?1 and 10.5 kg N ha^?1 year^?1 entering the mineral soil of the clear‐cut plots. We found numerous indications that the greater microbial activity induced by an increased temperature of 1.5°C in the forest floor is the major factor controlling the enhanced production of dissolved organic matter. Increasing aromaticity and complexity of organic molecules and depletion of ¹³C pointed to an accelerated processing of more strongly decomposed parts of the forest floor resulting in increased release of lignin‐derived molecules after clear‐cutting. The largest net fluxes of dissolved organic C and N were in the Oi horizon, yet dissolved organic matter sampled in the Oa horizon did not originate mainly from the Oi horizon. Largest gross fluxes in the Oa horizon (control 282 kg C ha^?1) and increased aromaticity and complexity of the molecules with increasing depth suggested that dissolved organic matter was derived mainly from decomposition, transformation and leaching of more decomposed material of the forest floor. Our results imply that clear‐cutting releases additional dissolved organic matter which is sequestered in the mineral soil where it has greater resistance to microbial decay.     

Drying–rewetting cycles release phosphorus from forest soils

Drying–rewetting cycles (D/W) occur frequently in topsoils and may mobilize phosphorus (P). We investigated the effect of repeated D/W on the release of dissolved inorganic (DIP) and organic P (DOP) from forest floors and A horizons. Samples were taken from 3 European beech sites and from 3 Norway spruce sites. Soils were desiccated up to pF 6 (–100 MPa) in three D/W cycles in the laboratory, while the controls were kept permanently at 50% water holding capacity. After each drying, P was extracted from the soils in water. D/W caused the release of DIP and DOP especially from O layers. There was no general difference in response to D/W between samples from beech and spruce. The net release of DIP after D/W was largest from the Oe horizons (average 50–60 mg P kg^?1) for both beech and spruce forest soils. The net release of DIP from Oi layers was on average 7.8 mg P kg^?1 and from spruce Oa layers 21.1 mg P kg^?1. In the A horizons, net DIP release was similar in beech and spruce soils with 0.4 mg P kg^?1. The release of DOP was less than the release of DIP except for the A horizons. Repeated cycles did not increase the release of DIP and DOP. The release of DIP and DOP was positively correlated with the microbial biomass in Oe and Oa layers but not in Oi layers. Our results suggest that D/W may significantly influence the short term availability of dissolved P in both beech and spruce forest soils.     

Long‐term development of nitrogen fluxes in a coniferous ecosystem: Does soil freezing trigger nitrate leaching?

In many forest ecosystems chronically large atmospheric deposition of N has caused considerable losses of inorganic N by seepage. Freezing and thawing of soil may alter the N turnover in soils and thereby the interannual variation of N seepage fluxes, which in turn makes it difficult to evaluate the N status of forest ecosystems. Here, we analyzed long‐term monitoring data of concentrations and fluxes of dissolved inorganic N (DIN) in throughfall and seepage from a Norway spruce stand at the Fichtelgebirge (SE Germany) between 1993 and 2004. Despite constant or even slightly increasing N inputs in throughfall, N losses with seepage at 90 cm declined from 15–32 kg N ha^–1 y^–1 in the first years of the study period (1993–1999) to 3–10 kg N ha^–1 y^–1 in 2000 to 2004. The large N losses in the first years coincided with extreme soil frost in the winter of 1995/96, ranging from –3.3°C to –1.0°C at 35 cm soil depth. Over the entire observation period, maximum fluxes of nitrate and ammonium were observed in the mineral soil following thawing of the soil. The elevated ammonium and nitrate fluxes resulted apparently from increased net ammonification and nitrification rates in the mineral soil, whereas mineral‐N fluxes in the O horizon were less affected by frost. Our data suggest that (1) extreme soil frost may cause substantial annual variations of nitrate losses with seepage and that (2) the assessment of the N status of forest ecosystems requires long periods of monitoring. Time series of biogeochemical data collected over the last 20–30 y include years with extreme cold winters and warm summers as well as unusual precipitation patterns. Analysis of such long‐term monitoring data should address climate extremes as a cause of variation in N outputs via leaching. The mean loss of 14.7 kg N with seepage water during 12 y of observation suggests that the forest ecosystem was saturated with N.     

Leaching of dissolved and particulate phosphorus via preferential flow pathways in a forest soil: An approach using zero‐tension lysimeters

Phosphorus (P) fluxes from forest soils are not well understood. For temperate zone forests, there is some evidence from watershed studies that P export occurs mainly in preferential flow pathways during storm events after dry periods. Therefore, we tested the practical applicability of a sampling approach, which should allow for quantifying P concentrations and fluxes. We used zero‐tension lysimeters, which were installed beneath the topsoil and in the subsoil at plots in the Tharandt Forest (Saxony, East Germany). Two storm events after dry periods were simulated by means of experimental sprinkler irrigation. Preferential flow water collected with the zero‐tension lysimeters was analyzed for total P (TP), particulate P (PP), dissolved organic P (DOP) and dissolved inorganic P (DIP), and the respective P fluxes were calculated. The results indicate that the experimental approach is applicable to estimate fluxes of different P fractions in preferential flow. Measured data point toward a distinct flushing of P in the first hours of heavy rainfall events with PP fraction playing a dominant role. In general, P concentrations decreased quickly during the first 2 h of irrigation and then remained constant. Initial concentrations and cumulative fluxes were highest in the subsoil samplers. For a better understanding of underlying processes, further research with a special focus on the PP fraction is necessary.     

Impact of anthropogenic induced nitrogen input and liming on phosphorus leaching in forest soils

Phosphorus (P) is essential for sustainable forest growth, yet the impact of anthropogenic impacts on P leaching losses from forest soils is hardly known. We conducted an irrigation experiment with 128 mesocosms from three forest sites representing a gradient of resin extractable P of the A‐horizon. On each site we selected a Fagus sylvatica and a Picea abies managed subsite. We simulated ambient rain (AR), anthropogenic nitrogen input (NI) of 100 kg (ha · a)^?1 and forest liming (FL) with a dolomite input of 0.3 Mg (ha · a)^?1. Soil solution was extracted from the organic layer, 10 cm depth and 20 cm depth of the mesocosms, and analyzed for molybdate reactive phosphorus (MRP) and molybdate unreactive phosphorus (MUP). Additionally, we separated colloids from the soil solution using Asymmetric Field Flow Fractionation for assessing the colloidal fraction of total element concentrations. NI increased MRP and MUP concentrations for all plots with one exception, while FL decreased MRP and MUP with the exception of another plot. While the irrigation treatments had little impact on the P‐richest site, MRP and MUP concentrations changed strongly at the poorer sites. The colloidal fraction of P in the soil solution equaled 38–47% of the total P load. Nitrogen input and liming also affected the Fe, Al, Ca, and Corg contents of the colloidal fraction.     

Assessing the bioavailability of dissolved organic phosphorus in pasture and cultivated soils treated with different rates of nitrogen fertiliser

A proportion of dissolved organic phosphorus (DOP) in soil leachates is readily available for uptake by aquatic organisms and, therefore, can represent a hazard to surface water quality. A study was conducted to characterise DOP in water extracts and soil P fractions of lysimeter soils (pasture before and after, and cultivated soil after leaching to simulate a wet winter-autumn) from a field trial. Data on DOP in drainage waters from the field trial were also generated. In water extracts, used as a surrogate for soil solution and drainage water, 70-90% of the total dissolved P (TDP) concentration was made up of DOP, of which 40% was hydrolysable by phosphatase enzymes. Proportions of hydrolysable DOP to TDP in drainage waters of the field trial were less than in water extracts due to enhanced DRP loss via dung inputs, but still large at 35% of DOP. Analysis of lysimeter soils by sequential fractionation indicated that several organic P fractions changed with land use and due to leaching. Further investigation using NaOH-EDTA extracts and ³¹P nuclear magnetic resonance spectroscopy indicated that the greatest changes were a decrease in the concentrations of orthophosphate diester P and an increase in orthophosphate monoester P. This was attributed to mineralization by cultivation and plant roots and also to the leaching of mobile diester P. This study suggests that in such soils with a dynamic soil organic P pool, the concentration of readily bioavailable P in soil solution and drainage waters and the potential to impair surface water quality cannot be determined from the DRP concentration alone.     

Phosphorus forms in forest soil colloids as revealed by liquid‐state 31P‐NMR

Nanoparticles and colloids affect the storage and hence the availability of P in forest ecosystems. We investigated the fine colloids present in forest soils and their association with inorganic and organic P. To differentiate between the different P forms, we performed liquid‐state ³¹P‐nucelar magnetic resonance (³¹P‐NMR) measurements on forest bulk soil extracts, on colloid extracts and on the electrolyte phase of their soil suspensions. The ³¹P‐NMR spectra indicated that soil nanoparticles and colloids were more enriched with organic than with inorganic P forms compared to the electrolyte phase. The P concentration was enriched in the colloidal fraction in comparison to the bulk soil and the phosphate diesters were more dominant in the colloidal fraction when compared to the bulk soil. The colloidal P‐diester to P‐monoester ratios were 2 to 3 times higher in the colloidal fraction than in the bulk soil. In contrast, relatively large percentages of inorganic P were found in the electrolyte phase. Supplementary (not shown) Data are available at the JuSER Server (juser.fz‐juelich.de, reference number: FZJ‐2016‐01739) https://juser.fz‐juelich.de/record/283057 .     

Effects of Lime and Phosphorus Application on Phosphorus Runoff Risk

Lime was investigated as a soil amendment to decrease phosphorus (P) loss in runoff from two Delaware sandy loam soils, one high and one low in P. Soils were limed at three rates (control and target pH values of 6 and 6.8, respectively), packed into runoff boxes (2,000?cm²) and received simulated rainfall (80?mm?h^?1 for 30?min). Lime showed potential to decrease P loss in runoff, but its effectiveness was soil specific and dependant on other management factors also. Lime decreased dissolved reactive P (DRP) and dissolved organic P (DOP) loss by 20?C25 and 52?C93?%, respectively, for the high-P soil and particulate P (PP) by 13?% for the low-P soil. The majority of P lost in runoff was DOP (3?C29?%) or PP (64?C96?%). Lime increased PP losses from the finer-textured soil following P application, indicating that increased P sorption can lead to increased losses if P is sorbed to more erodable particles. Initial soil P status was more important than liming in determining P loss. While amendments may decrease P losses in the short term, addressing nutrient imbalances at the field scale is clearly necessary in the long term. Losses increased significantly following inorganic P application. Although P was sorbed rapidly, with less than 2?% of added P removed in runoff, mean concentrations in excess of 700???g?l^?1 DRP, 2,500???g?l^?1 OP and 6,500???g?l^?1 PP were recorded for both soils immediately following P application.     

Dissolved phosphorus composition of grassland leachates following application of dairy‐slurry size fractions

Appropriate management of P from slurry can increase crop production and decrease nutrient loss to water bodies. The present study examined how the application of different size fractions of dairy slurry influenced the quantity and composition of P leached from grassland in a temperate climate. Soil blocks were amended (day 0 = start of the experiment) with either whole slurry (WS), the > 425 μm fraction (coarse slurry fraction, CSF), the < 45 μm slurry fraction (fine liquid slurry fraction, FLF), or not amended, i.e., the control soil (CON). Deionized water was added to the soil blocks to simulate six sequential rainfall events, equivalent to 250 mm (day 0.2, 1.2, 4.2, 11.2) or 500 mm of rainfall (day 18.2 and 25.2), with leachates collected the following day. The results showed that total dissolved P (TDP), dissolved reactive P (DRP), dissolved unreactive P (DUP), orthophosphate, phosphomonoester, and pyrophosphate concentrations generally decreased with the increasing number of simulated rain events. Total dissolved P was leached in the following order WS > FLF ≈ CSF > CON. Dissolved organic C was correlated with TDP, DRP, and DUP in leachates of all treatments. The highest concentrations of dissolved phosphomonoesters and pyrophosphate (147 μg P L^–1 and 57 μg P L^–1, respectively) were detected using solution ³¹P‐NMR spectroscopy in the WS leachates. Overall, there were significant differences observed between slurry treatments (e.g., relative contributions of inorganic P vs. organic P of dissolved P in leachates). Differences were independent from the rate at which slurry P was applied, because the highest dissolved P losses per unit of slurry P applied were measured in the FLF, i.e., the treatment that received the smallest amount of P. We conclude that the specific particle‐size composition of applied slurry influences dissolved P losses from grassland systems. This information should be taken in account in farm‐management approaches which aim to minimizing dissolved slurry P losses from grassland systems.     

Spatial variation in nitrogen deposition over five adjacent catchments in a larch forest

Abstract

In this report, we propose a new method of evaluating the effect of nitrogen deposition on forest ecosystems, namely the spatial variation in nitrogen deposition enables to detect readily the effect of anthropogenic N deposition on biogeochemical processes in forest ecosystems. We analyzed the nitrogen deposition (throughfall fluxes) and stream water chemistry over five adjacent small catchments in which soil types (Hapludants) and vegetation composition (50 to 60 years old larch plantation) were fairly identical. Thirty-two throughfall collectors were set up in the five catchments (six to eight collectors in each catchment) and throughfall samples were collected after a rain event, while stream water samples were collected once or twice a month. The monitoring was carried out during a period of 6 months (2002 June to 2002 November). Throughfall dissolved inorganic nitrogen (DIN) fluxes were highly variable: the highest N input, 1.32 kg N ha^?1 6 months^?1, was sixty-six times higher than the lowest input, 0.02 kg N ha^?1 6 months^?1. The mean DIN inputs and the mean nitrate concentrations in streams showed a three-time variation across the five catchments. In addition, the DIN inputs showed a high correlation with the stream nitrate concentrations (r = 0.88).     

Methane Fluxes from Alpine Wetlands of Zoige Plateau in Relation to Water Regime and Vegetation under Two Scales

Methane fluxes in alpine ecosystems remain insufficiently studied, especially in terms of the magnitude, temporal, and spatial patterns. To quantify the mean methane emission of alpine ecosystems, methane fluxes were measured among six ecosystems and microsites within each ecosystem at Zoige National Wetland Reserve. The average methane emission from Zoige Plateau was 2.25 mg CH₄ m^?2?h^?1, which fell into the range of methane emission rate reported by a number of studies in other alpine wetlands. Prevailing ecosystem types had important impacts on the methane flux on the landscape scale. In the wet ecosystems, the microsites had different methane emissions resulting from the differences in the depth of water table and associated vegetation characteristics. The identification of the microsites based on their vegetation characteristics thus allows upscaling of methane emissions in these ecosystems. However, in the dry ecosystems showing even methane uptake, the spatial variation in the methane fluxes was low and the vegetation has a poor predicative value for the methane fluxes. There, the soil porosity linked to the gas diffusion rate in soil would be the key factor explaining methane fluxes.     

Can ectomycorrhizal fungi circumvent the nitrogen mineralization for plant nutrition in temperate forest ecosystems?

Nitrogen (N) limits plant growth in many forest ecosystems. The largest N pool in the plant-soil system is typically organic, contained primarily within the living plants and in the humus and litter layers of the soil. Understanding the pathways by which plants obtain N is a priority for clarifying N cycling processes in forest ecosystems. In this review, the interactions between saprotrophic microorganisms and ectomycorrhizal fungi in N nutrition with a focus on the ability of ectomycorrhizal fungi to circumvent N mineralization for the nutrition of plants in forest ecosystems will be discussed. Traditionally, it is believed that in order for plants to fulfill their N requirements, they primarily utilize ammonium (NH₄⁺) and nitrate (NO₃⁻). In temperate forest ecosystems, many woody plants form ectomycorrhizas which significantly improves phosphorus (P) and N acquisition by plants. Under laboratory conditions, ectomycorrhizal fungi have also been proven to be able to obtain N from organic sources such as protein. It was thus proposed that ectomycorrhizal fungi potentially circumvent the standard N cycle involving N mineralization by saprotrophic microorganisms. However, in many forest ecosystems the majority of the proteins in the forest floor form complexes with polyphenols. Direct access of N by ectomycorrhizal fungi from a polyphenol-protein complex may be limited. Ectomycorrhizal fungi may depend on saprotrophic microorganisms to liberate organic N sources from polyphenol complexes. Thus, interactions between saprotrophic microorganisms and ectomycorrhizal fungi are likely to be essential in the cycling of N within temperate forest ecosystems.     

The importance of dissolved organic carbon fluxes for the carbon balance of a temperate Scots pine forest

Efforts to increase our understanding of the terrestrial carbon balance have resulted in a dense global network of eddy covariance towers, which are able to measure the net ecosystem exchange of CO₂, H₂O and energy between ecosystems and the atmosphere. However, the typical set-up on an eddy covariance tower does not monitor lateral CO₂- and carbon fluxes such as dissolved organic carbon (DOC). By ignoring DOC fluxes eddy covariance-based CO₂ balances overestimate the carbon sink of ecosystems as part of the DOC drains into the inland waters and get respired outside the footprint of the eddy covariance tower. In this study we quantify 7 years (2000-2006) of DOC fluxes from a temperate Scots pine forest in Belgium and analyse its inter-annual variability. On average, 10 gC m⁻² year⁻¹ is leached from the pine forest as DOC. If the DOC fluxes are considered relative to the gross ecosystem carbon fluxes we see that DOC fluxes are small: 0.8 ± 0.2% relative to gross primary productivity, 1.0 ± 0.3% relative to ecosystem respiration, and (2.4 ± 0.4%) relative to soil respiration. However, when compared to net fluxes such as net ecosystem productivity and net biome productivity the DOC flux is no longer negligible (11 ± 7% and 17%, respectively), especially because the DOC losses constitute a systematic bias and not a random error. The inter-annual variability of the DOC fluxes followed that of annual water drainage. Hence, drainage drives DOC leaching at both short and long time scales. Finally, it is noted that part of the carbon that is leached from the ecosystem as DOC is respired or sequestered elsewhere, so the physical boundaries of accounting should always be reported together with the carbon budget.     

洛桑试验站Broadbalk长期小麦试验地排水中磷组分研究

Total P (TP), total participate P (PP), total dissolved P (TDP), molybdate reactive P (MRP) and dissolved organic P (DOP) were determined in waters from pipe-drains (at 65-cm depth) from the Broadbalk Experiment at Rothamsted Research, UK. Average TP and PP exceeded 1 mg L^-1 in about half of the 12 plots receiving superphosphate for the 5 measurements taken between December 2000 and April 2001. Ranging between 33.8% and 87.3% of TP, PP was the largest P fraction in drainage waters, with DOP, ranging from 0.5% to 26.2% of TP, being the smallest fraction. Mean proportions of PP, MRP and DOP in TP in drainage waters were 63.4%, 32.5% and 4.1%, respectively. These findings support previous findings that P losses from soil to drainage waters were much larger than previously thought, and could therefore make a significant contribution to eutrophication.     

Multiple measurements constrain estimates of net carbon exchange by a Eucalyptus forest

Net ecosystem exchange of carbon (F_NEE) was estimated for a temperate broadleaf, evergreen eucalypt forest ecosystem at Tumbarumba in south-eastern Australia to investigate the processes controlling forest carbon sinks and their response to climate. Measurements at a range of temporal and spatial scales were used to make three different estimates of F_NEE based on: (1) the difference between fluxes of carbon input by photosynthesis and output by autotrophic plus heterotrophic respiration, (2) changes over time in the carbon pools in the above- and below-ground biomass, soil and litter, and (3) micrometeorological flux measurements that provide a continuous estimate of the net exchange. A rigorous comparison of aggregated component fluxes and the net eddy fluxes within a flux tower source area was achieved based on an inventory of the site and a detailed sampling strategy. Measurements replicated in space and time provided mean values, confidence limits and patterns of variation of carbon pools and fluxes that allowed comparisons within known limits of uncertainty. As a result of comparisons between nighttime eddy flux and chamber measurements of respiration, a revised micrometeorological method was developed for estimating nighttime carbon flux using flux tower measurements. Uncertainty in the final estimate of F_NEE was reduced through mutual constraints of each of these measurement approaches. F_NEE for the period October 2001–September 2002, with average rainfall, was an uptake of 6.7 (5.1–8.3) tC ha^?1 yr^?1 estimated from component fluxes, and 5.4 (3.0–7.5) tC ha^?1 yr^?1 estimated from the revised eddy flux method. Biomass increment was 4.5 (3.7–5.4) tC ha^?1 yr^?1 and the remaining 0.9–2.2 tC ha^?1 yr^?1 could represent a carbon sink in the soil and litter pools or lie within the confidence limits of the measured fluxes. F_NEE was reduced to ?0.1 to 2.4 tC ha^?1 yr^?1 during a period of drought and insect disturbance in October 2002–September 2003, with biomass increment being the main component reduced. The forest is a large carbon sink compared with other forest ecosystems, but this is subject to high-annual variability in response to climate variability and disturbance.     

Tropical forests: Their past,present, and potential future role in the terrestrial carbon budget

In this paper we review results of research to summarize the state-of-knowledge of the past, present, and potential future roles of tropical forests in the global C cycle. In the pre-industrial period (ca. 1850), the flux from changes in tropical land use amounted to a small C source of about 0.06 Pg yr^?1. By 1990, the C source had increased to 1.7 ± 0.5 Pg yr^?1. The C pools in forest vegetation and soils in 1990 was estimated to be 159 Pg and 216 Pg, respectively. No concrete evidence is available for predicting how tropical forest ecosystems are likely to respond to CO₂ enrichment and/or climate change. However, C sources from continuing deforestation are likely to overwhelm any change in C fluxes unless land management efforts become more aggressive. Future changes in land use under a “business as usual” scenario could release 41–77 Pg C over the next 60 yr. Carbon fluxes from losses in tropical forests may be lessened by aggressively pursued agricultural and forestry measures. These measures could reduce the magnitude of the tropical C source by 50 Pg by the year 2050. Policies to mitigate C losses must be multiple and concurrent, including reform of forestry, land tenure, and agricultural policies, forest protection, promotion of on-farm forestry, and establishment of plantations on non-forested lands. Policies should support improved agricultural productivity, especially replacing non-traditional slash-and-burn agriculture with more sustainable and appropriate approaches.     

Effect of plant-mediated oxygen supply and drainage on greenhouse gas emission from a tropical peatland in Central Kalimantan,Indonesia

Abstract

To evaluate the hypothesis that plant-mediated oxygen supplies decrease methane (CH₄) production and total global warming potential (GWP) in a tropical peatland, the authors compared the fluxes and dissolved concentrations of greenhouse gases [GHGs; CH₄, carbon dioxide (CO₂) and nitrous oxide (N₂O)] and dissolved oxygen (DO) at multiple peatland ecosystems in Central Kalimantan, Indonesia. Study ecosystems included tropical peat swamp forest and degraded peatland areas that were burned and/or drained during the rainy season. CH₄ fluxes were significantly influenced by land use and drainage, which were highest in the flooded burnt sites (5.75 ± 6.66 mg C m^?2 h^?1) followed by the flooded forest sites (1.37 ± 2.03 mg C m^?2 h^?1), the drained burnt site (0.220 ± 0.143 mg C m^?2 h^?1), and the drained forest site (0.0084 ± 0.0321 mg C m^?2 h^?1). Dissolved CH₄ concentrations were also significantly affected by land use and drainage, which were highest in the flooded burnt sites (124 ± 84 μmol L^?1) followed by the drained burnt site (45.2 ± 29.8 μmol L^?1), the flooded forest sites (1.15 ± 1.38 μmol L^?1) and the drained forest site (0.860 ± 0.819 μmol L^?1). DO concentrations were influenced by land use only, which were significantly higher in the forest sites (6.9 ± 5.6 μmol L^?1) compared to the burnt sites (4.0 ± 2.9 μmol L^?1). These results suggest that CH₄ produced in the peat might be oxidized by plant-mediated oxygen supply in the forest sites. CO₂ fluxes were significantly higher in the drained forest site (340 ± 250 mg C m^?2 h^?1 with a water table level of ?20 to ?60 cm) than in the drained burnt site (108 ± 115 mg C m^?2 h^?1 with a water table level of ?15 to +10 cm). Dissolved CO₂ concentrations were 0.6–3.5 mmol L^?1, also highest in the drained forest site. These results suggested enhanced CO₂ emission by aerobic peat decomposition and plant respiration in the drained forest site. N₂O fluxes ranged from ?2.4 to ?8.7 μg N m^?2 h^?1 in the flooded sites and from 3.4 to 8.1 μg N m^?2 h^?1 in the drained sites. The negative N₂O fluxes might be caused by N₂O consumption by denitrification under flooded conditions. Dissolved N₂O concentrations were 0.005–0.22 μmol L^?1 but occurred at < 0.01 μmol L^?1 in most cases. GWP was mainly determined by CO₂ flux, with the highest levels in the drained forest site. Despite having almost the same CO₂ flux, GWP in the flooded burnt sites was 20% higher than that in the flooded forest sites due to the large CH₄ emission (not significant). N₂O fluxes made little contribution to GWP.     

Trace element release from forest floor can be monitored by ion exchange resin tubes

Risk assessment of heavy metal input into forest ecosystems requires information about metal fluxes from the forest floor (organic layer) into the mineral soil. Common methods for the monitoring of element fluxes are generally time‐consuming and expensive. Additionally, the reliability of the results is in part contested especially for trace elements, showing very low concentrations which are sometimes even below analytical detection limit. We used ion exchange resin tubes installed below the forest floor to determine heavy metal and As fluxes at 25 forest monitoring sites in Germany. Chloride tracer experiments and the comparison of our data with throughfall and lysimeter data, determined within the Level II monitoring network, proved the accuracy of our method. Mean trace element fluxes based on the resin method were 50 g As ha^–1 yr^–1, 2 g Cd ha^–1 yr^–1, 168 g Cu ha^–1 yr^–1, 176 g Ni ha^–1 yr^–1, and 186 g Pb ha^–1 yr^–1.The results show that the organic layer may change into a source of heavy metals after emission has decreased.     

Enhancing the P trapping of pasture filter strips: successes and pitfalls in the use of water supply residue and polyacrylamide

In intensive pastoral systems the landscape at ground level is clad in dense, filtering vegetation – yet phosphorus losses in overland flow do occur, and pollution of surface waters is a serious consequence. The use of pre‐applied polyacrylamide (PAM) or chitosan to trap particulate phosphorus (PP) and P‐sorbing potable water treatment alum residue (PWTR) to enhance vegetative filtering effects is examined here using field and laboratory overland flow simulation (flows from 0.43 to 0.34 litres s^?1 (m width)^?1) and analysis. Fitted equations suggest that up to 40% of dissolved reactive P applied (0.75 mg P litre^?1) in overland flow could be captured in a flow length of 2.1 m (1 kg PWTR m^?2). Unfortunately, drying decreased PWTR effectiveness, though little of the P captured was readily desorbed. This effect did not appear to be the result of gibbsite formation. Compared with the other treatments, there was a strong treatment effect of pre‐applied PAM on the change in PP losses (P < 0.001) over time, though evidence suggests the PAM effect declined during a 44 minute flow period. We showed that the investigated two‐pronged approach to the enhancement of the effectiveness of P trapping by pasture had limitations. Laboratory sheet‐flow simulations suggest that a field‐stable P sorber with sorption characteristics similar to those of the un‐dried PWTR could be an effective retention enhancer for dissolved P. Pre‐applied PAM can have an effect on particulate‐P trapping but was rapidly dissolved and removed by flow.     

Preferential phosphorus leaching from an irrigated grassland soil

Intact lysimeters (50 cm diameter, 70 cm deep) of silt loam soil under permanent grassland were used to investigate preferential transport of phosphorus (P) by leaching immediately after application of dairy effluent. Four treatments that received mineral P fertilizer alone (superphosphate at 45 kg P ha^?1 year^?1) or in combination with effluent (at ～ 40–80 kg P ha^?1 year^?1) over 2 years were monitored. Losses of total P from the combined P fertilizer and effluent treatments were 1.6–2.3 kg ha^?1 (60% of overall loss) during eight drainage events following effluent application. The rest of the P lost (40% of overall loss) occurred during 43 drainage events following a significant rainfall or irrigation compared with 0.30 kg ha^?1 from mineral P fertilizer alone. Reactive forms of P (mainly dissolved reactive P: 38–76%) were the dominant fractions in effluent compared with unreactive P forms (mainly particulate unreactive P: 15–56%). In contrast, in leachate following effluent application, particulate unreactive P was the major fraction (71–79%) compared with dissolved reactive P (1–7%). The results were corroborated by ³¹P nuclear magnetic resonance analysis, which showed that inorganic orthophosphate was the predominant P fraction present in the effluent (86%), while orthophosphate monoesters and diesters together comprised up to 88% of P in leachate. This shows that unreactive P forms were selectively transported through soil because of their greater mobility as monoesters (labile monoester P and inositol hexakisphosphate) and diesters. The short‐term strategies for reducing loss of P after application of dairy effluent application should involve increasing the residence time of applied effluent in the soil profile. This can be achieved by applying effluent frequently in small amounts.