Dissolved organic carbon and nitrate concentrations in streams: a useful index indicating carbon and nitrogen availability in catchments

Dissolved organic carbon (DOC) and NO₃^– are important forms of C and N in stream water. Hypotheses concerning relationships between DOC and NO₃^– concentrations have been proposed, but there are no reports demonstrating a relationship between them in stream water. We observed 35 natural streams in the Lake Biwa watershed, central Japan, and found an inverse relationship between DOC and NO₃^– concentrations. This relationship was also found in observations of their seasonal variations in the Lake Biwa watershed. Moreover, this relationship was also found to apply to watersheds in other regions in Japan. These results suggest that forest biogeochemical processes which control DOC and NO₃^– concentrations in Japanese streams are closely related. Excess N availability together with a C (energy) deficit in a soil environment may explain this relationship. DOC and NO₃^– concentrations in streams will thus be a useful index indicating C and N availability in catchments.     

Soil N mineralization and nitrification in relation to nitrogen solution chemistry in a small forested watershed

Spatial variations in soil processes regulating mineral N losses to streams were studied in a small watershed near Toronto, Ontario. Annual net N mineralization in the 0–8 cm soil was measured in adjacent upland and riparian forest stands using in situ soil incubations from April 1985 to 1987. Mean annual rates of soil N mineralization and nitrification were higher in a maple soil (93.8 and 87.0 kg.ha^–1) than in a pine soil (23.3 and 8.2 kg.ha^–1 ). Very low mean rates of mineralization (3.3 kg.ha^–1) and nitrification (3.4 kg.ha^–1) were found in a riparian hemlock stand. Average NO₃-N concentrations in soil solutions were 0.3–1.0 mg.L^–1 in the maple stand and >0.06mg.L^–1 in the pine stand. Concentrations of NO₃–N in shallow ground water and stream water were 3–4× greater in a maple subwatershed than in a pine subwatershed. Rapid N uptake by vegetation was an important mechanism reducing solution losses of NO₃–N in the maple stand. Low rates of nitrification were mainly responsible for negligible NO₃–N solution losses in the pine stand.     

Predictability of streamflow and particulate organic matter concentration as indicators of stability in prairie streams

Predictability of stream discharge and particulate organic matter (POM) in the water column was estimated, using Colwell's indices of constancy and contingency, for 6 Texas prairie streams (1 each of 2nd, 3rd, and 4th order with intermittent or perennial discharge). Stream discharge in these 6 prairie streams varied between 0 and 36000 1 s^–1, depending on the stream and season. Predictability (P) of discharge in these streams ranged from 0.45 to 0.62, within the range of values expected for North American streams. Predictability of stream discharge was not significantly different between streams. Particulate organic matter concentrations in these prairie streams are relatively low, ranging from 0.25 to 4.00 mg AFDM 1^–1. Predictability of POM concentration in these streams was high, ranging from 0.75 to 0.85, and was largely the result of constancy of POM concentrations. Within the different POM size classes, Fine POM (FPOM) had the highest predictability (P = 0.89–0.96). In spite of relatively unpredictable stream discharge, POM remained fairly constant providing a measure of habitat predictability and stability.     

Groundwater nitrogen dynamics at the terrestrial-lotic interface of a small catchment in the Central Amazon basin

Processes operating at the terrestrial-lotic interface may significantly alter dissolved nitrogen concentrations in groundwater as a result of shifting redox conditions and microbial communities. We monitored concentrations of total dissolved nitrogen, NO ₄ ^– , NH ₄ ^– , O₂ and Fe²⁺ for 10 months along two transects tracing groundwater flow from an upland (terra firme) forest, beneath the riparian forest, and into the stream channel of a small Central Amazonian catchment. Our aim was to examine the role of near-stream processes in regulating groundwater transfers of dissolved nitrogen from terrestrial to lotic ecosystems in the Central Amazon. We found pronounced compositional differences in inorganic nitrogen chemistry between upland, riparian, and stream hydrologic compartments. Nitrate dominated (average 89% of total inorganic nitrogen; TIN) the inorganic nitrogen chemistry of oxygenated upland groundwater but decreased markedly upon crossing the upland-riparian margin. Conversely, NH ₄ ^– dominated (average 93% of TIN) the inorganic chemistry of apparently anoxic riparian groundwater; NH ₄ ^– and TIN concentrations decreased markedly across the riparian-stream channel margin. In the oxygenated streamwater, NO ₃ ^– again dominated (average 82% of TIN) inorganic nitrogen chemistry. Denitrification followed by continued ammonification is hypothesized to effect the shift in speciation observed at the upland-riparian margin, while a combination of several processes may control the shift in speciation and loss of TIN observed at the riparian-stream margin. Dissolved organic nitrogen concentrations did not vary significantly between upland and riparian groundwater, but decreased across the riparian-stream margin. Our data suggest that extensive transformation reactions focused at the upland and stream margins of the riparian zone strongly regulate and diminish transfers of inorganic nitrogen from groundwater to streamwater in the catchment. This suggestion questions the veracity of attempts in the literature to link stream nitrogen chemistry with nutrient status in adjacent forests of similar catchments in the Central Amazon. It also complicates efforts to model nitrogen transfers across terrestrial-lotic interfaces in response to deforestation and changing climate.     

Glucose-induced nitrate assimilation in prairie and cultivated soils

Native prairie and grassland soils are known to accumulate little inorganic N; however, N0₃ ^– is constantly being formed and re-immobilized. This suggests that microorganisms in prairie soils would be highly efficient in the assimilation of N0₃ ^– and would regularly have the assimilatory N0₃ ^– reductase (ANR) enzyme in an induced and active state. Aerated slurries and static systems prepared from prairie and cultivated soils amended with glucose and N0₃ ^– were observed for changes in N0₃ ^– concentration with time. Nitrate assimilation in the presence of glucose occurred more rapidly in cultivated than in prairie soils from the same soil map unit. Nitrate assimilation rates were not affected by inoculation of prairie soil with cultivated soil. It has been reported that the addition of glucose and NO₃ ^– to soils results in increased peptidase activity and a release of free amino acids. Mixing, sieving, and slurrying of prairie soils followed by treatment with glucose and NO₃ ^– may release free amino acids and other ANR inhibitors into the prairie soil slurries. Prairie soils had higher concentrations of soluble amino-N than cultivated soils with or without glucose and N0₃ ^– additions. Prairie soils also had greater concentrations of total Kjeldahl N and readily hydrolyzed amino acids than corresponding cultivated soils.     

Controlled release experiments to determine the effects of shade and plants on nutrient retention in a lowland stream

Understanding nutrient uptake and retention in streams remains an important challenge for lotic scientists. In this study a series of pulse and continuous releases of dissolved nutrients were made to shaded and unshaded (reference) reaches of a small lowland stream to determine whether suppression of macrophyte growth by riparian shade impaired nutrient retention. The nutrients were dissolved reactive phosphorus (DRP), total ammoniacal nitrogen (NH₄–N) and nitrate nitrogen (NO₃–N). Nutrient reductions ranged from 100% of DRP when stream water was anoxic, to 5–10% for NH₄–N and NO₃–N in the reference reach. Nutrient removals were affected by travel times in each reach. Percentage removals of NH₄–N (46 ± 10) and NO₃–N (52 ± 14) were higher in the shaded reach than in the swifter moving reference reach (15 ± 8 and 16 ± 10, respectively). DRP (%) removals were 75± 7 and 57 ± 12 for the shaded and reference reaches, respectively. The presence of emergent marginal macrophytes (Persicaria hydropiper) increased stream velocity in the reference reach by reducing the effective channel cross-section area. Shading reduced plant biomass, increased the channel cross-section and lowered velocity in the experimental reach, effecting dramatic reductions in nutrient concentrations over short distances. The opposite effect is more typical for larger, swifter streams having dense stands of submerged macrophytes, where lowering channel plant biomass will cause increased velocities and lower relative nutrient losses. Riparian shade does not necessarily impair nutrient uptake from small streams. Where invasive marginal species such as P. hydropiper dominate headwater streams shade may be beneficial to the protection of downstream waters from eutrophication. Where reduction of nutrient fluxes from small streams is a key objective for protection of downstream waters, active management of streams should seek to increase travel times, allowing greater potential for nutrient uptake. This will need to be weighed against the need for effective drainage in pastoral areas where reduced travel times are usually sought.     

Nitrate transformation and water movement in a wetland area

The NO₃ ^– transformation capacity of a riparian zone at Rabis stream, Denmark, was investigated for a period of 2 years. The riparian zone of 15–25 m received NO₃ ^–-containing groundwater from the adjoining agricultural areas. The water flows as surface runoff along the surface of the wetland and in the root zone towards the stream. Changes in water chemistry, water balance and mass transport were investigated. The riparian zone acted as a buffer zone for NO₃ ^–, PO₄ ^3– and dissolved Fe²⁺. The NO₃ ^–-transformation capacity of the wetland was about 400 kg N ha^–1 y^–1, but varied seasonally. A simple rearrangement of drain systems in wetland areas can probably reduce the NO₃ ^– content of Danish surface waters by 20 000–50 000 t N y^–1.     

15N evidence for the origin and cycling of inorganic nitrogen in a small Amazonian catchment

The ¹⁵N composition of the dominant form of dissolved inorganic nitrogen (DIN) was determined in upland groundwater, riparian groundwater, and stream water of the Barro Branco catchment, Amazônas, Brazil. The ¹⁵N composition of organic nitrogen in riparian and upland leaf litter was also determined. The data for these waters could be divided into three groups: upland groundwater DIN predominately composed of NO₃ ^– with ¹⁵N values averaging 6.25 ± 0.9 riparian groundwater DIN primarily composed of NH₄ ⁺ with ¹⁵N values averaging 9.17 ± 1.0 and stream water DIN predominately composed of NO₃ ^– with ¹⁵N values averaging 4.52 ± 0.8 Nitrate samples taken from the stream source and from the stream adjacent to the groundwater transects showed a downstream increase in ¹⁵N from 1.0to 4.5 Leaf litter samples averaged 3.5 ± 1.2The observed patterns in isotopic composition, together with previously observed inorganic nitrogen species and concentration shifts between upland, riparian and stream waters, suggest that groundwater DIN is not the primary source of DIN to the stream. Instead, the isotopic data suggest that remineralization of organic nitrogen within the stream itself may be a major source of stream DIN, and that the majority of DIN entering the stream via groundwater flowpaths is removed at the riparian-stream interface.     

Effects of urban stream burial on organic matter dynamics and reach scale nitrate retention

Nitrogen (N) retention in streams is an important ecosystem service that may be affected by the widespread burial of streams in stormwater pipes in urban watersheds. We predicted that stream burial suppresses the capacity of streams to retain nitrate (NO₃ ^?) by eliminating primary production, reducing respiration rates and organic matter availability, and increasing specific discharge. We tested these predictions by measuring whole-stream NO₃ ^? removal rates using ¹⁵NO₃ ^? isotope tracer releases in paired buried and open reaches in three streams in Cincinnati, Ohio (USA) during four seasons. Nitrate uptake lengths were 29 times greater in buried than open reaches, indicating that buried reaches were less effective at retaining NO₃ ^? than open reaches. Burial suppressed NO₃ ^? retention through a combination of hydrological and biological processes. The channel shape of two of the buried reaches increased specific discharge which enhanced NO₃ ^? transport from the channel, highlighting the relationship between urban infrastructure and ecosystem function. Uptake lengths in the buried reaches were further lengthened by low stream biological NO₃ ^? demand, as indicated by NO₃ ^? uptake velocities 17-fold lower than that of the open reaches. We also observed differences in the periphyton enzyme activity between reaches, indicating that the effects of burial cascade from the microbial to the ecosystem scale. Our results suggest that stream restoration practices involving “daylighting” buried streams have the potential to increase N retention. Further work is needed to elucidate the impacts of stream burial on ecosystem functions at the larger stream network scale.     

Patterns in groundwater nitrogen concentration in the floodplain of a subtropical stream (Wollombi Brook,New South Wales)

The sources of groundwater and the patterns in groundwater dissolved N and DOC concentration in the floodplain of a subtropical stream (Wollombi Brook, New South Wales) were studied over a 2-year period using three piezometer transects. While the stream was generally a discharge area for regional groundwater, this source represented only a small contribution to either the water or N budget of the alluvial aquifer. Groundwater–surface water interactions appeared mostly driven by cycles of bank recharge and discharge between the stream and the alluvial aquifer. DON and NH₄⁺ were the principal forms of dissolved N in groundwater, consistent with the primarily suboxic to anoxic conditions in the alluvial aquifer. A plume of groundwater NO₃⁻ was found at one transect where oxic conditions persisted within the riparian zone. The origin of the NO₃⁻ plume was hypothesized to be soil NO₃⁻ from the riparian zone flushed to the water table during recharge events. When present, NO₃⁻ did not reach surface water because conditions in the alluvial aquifer in the vicinity of the stream were always reduced. The concentration of groundwater DOC was variable across the floodplain and may be related to the extent of the vegetation cover. Overall, transformation and recycling of N during lateral exchange processes, as opposed to discharge of new N inputs from regional groundwater, appears to primarily control N cycling during groundwater–surface water interactions in this subtropical floodplain.     

Spatial variation in basic chemistry of streams draining a volcanic landscape on Costa Rica's Caribbean slope

Spatial variability in selected chemical, physical and biological parameters was examined in waters draining relatively pristine tropical forests spanning elevations from 35 to 2600 meters above sea level in a volcanic landscape on Costa Rica's Caribbean slope. Waters were sampled within three different vegetative life zones and two transition zones. Water temperatures ranged from 24–25 °C in streams draining lower elevations (35–250 m) in tropical wet forest, to 10 °C in a crater lake at 2600 m in montane forest. Ambient phosphorus levels (60–300 µg SRP L^–1; 66–405 µg TP L^–1) were high at sites within six pristine drainages at elevations between 35–350 m, while other undisturbed streams within and above this range in elevation were low (typically <30.0 µg SRP L^–1). High ambient phosphorus levels within a given stream were not diagnostic of riparian swamp forest. Phosphorus levels (but not nitrate) were highly correlated with conductivity, Cl, Na, Ca, Mg and SO₄. Results indicate two major stream types: 1) phosphorus-poor streams characterized by low levels of dissolved solids reflecting local weathering processes; and 2) phosphorus-rich streams characterized by relatively high Cl, SO₄, Na, Mg, Ca and other dissolved solids, reflecting dissolution of basaltic rock at distant sources and/or input of volcanic brines. Phosphorus-poor streams were located within the entire elevation range, while phosphorus-rich streams were predominately located at the terminus of Pleistocene lava flows at low elevations. Results indicate that deep groundwater inputs, rich in phosphorus and other dissolved solids, surface from basaltic aquifers at breaks in landform along faults and/or where the foothills of the central mountain range merge with the coastal plain.     

Dissolved phosphorus concentrations and sediment interactions in effluent–dominated Ozark streams

Phosphorus (P) loads from point sources have a significant influence on dissolved P concentrations in streams and sediment-water column dynamics. The goal of this study was to quantify dissolved P concentrations and sediment-P interactions in Ozark (USA) headwater streams with high point source P loads. Specifically, the objectives were to: (1) compare soluble reactive P (SRP) upstream and downstream from wastewater treatment plant (WWTP) effluent discharges; (2) examine longitudinal gradients in SRP downstream from WWTPs; (3) evaluate the effect of WTTP P inputs on sediment-water column P equilibrium and sediment exchangeable P. Water and sediment samples were collected, extracted and analyzed from July 2002 through June 2003 at these Ozark streams. Mean SRP concentrations in the select Ozark streams were significantly greater downstream from effluent discharges (0.08–2.10 mg L⁻¹) compared to upstream (0.02–0.12 mg L⁻¹). Effluent discharge from the WWTPs increased equilibrium concentrations between stream sediments and the water column; mean sediment equilibrium P concentration (EPC₀) was between 0.01–0.07 mg L⁻¹ upstream from WWTP and the increase downstream was proportional to that observed in water column SRP. Sediment exchangeable P (EXP) was greater downstream from the effluent discharges (0.3–6.8 mg kg⁻¹) compared to upstream (0.03–1.4 mg kg⁻¹), representing a substantial transient storage of P inputs from WWTPs. Furthermore, P was generally not retained in these stream reaches when dilution was considered using a hydrologic tracer and was released in one stream reach where effluent P concentrations decreased over the study period. Thus, the effect of the WWTPs was profound in these streams increasing water column and sediment-bound P, and also reducing the ability of these stream reaches to retain P. In P-enriched streams, effluent P discharges likely regulate sediment and aqueous phase P equilibrium and sediment bioavailable P, not the sediments.     

Nitrate reduction in sediments of lowland tropical streams draining swamp forest in Costa Rica: An ecosystem perspective

Nitrate reduction and denitrification were measured in swamp forest streams draining lowland rain forest on Costa Rica's Atlantic slope foothills using the C₂H₂-block assay and sediment-water nutrient fluxes. Denitrification assays using the C₂H₂-block technique indicated that the full suite of denitrifying enzymes were present in the sediment but that only a small fraction of the functional activity could be expressed without adding NO₃ ^–. Under optimal conditions, denitrification enzyme activity averaged 15 nmoles cm^–3 sediment h^–1. Areal NO₃ ^– reduction rates measured from NO₃ ^– loss in the overlying water of sediment-water flux chambers ranged from 65 to 470 umoles m^–2 h^–1. Oxygen loss rates accompanying NO₃ ^– depletion averaged 750 umoles m^–2 h^–1. Corrected for denitrification of NO₃ ^– oxidized from NH₄ ⁺ in the sediment, gross NO₃ ^– reduction rates increase by 130 umoles m^–2 h^–1, indicating nitrification may be the predominant source of NO₃ ^– for NO₃ ^– reduction in swamp forest stream sediments. Under field conditions approximately 80% of the increase in inorganic N mass along a 1250-m reach of the Salto River was in the form of NO₃ ^– with the balance NH₄ ⁺ . Scrutiny of potential inorganic N sources suggested that mineralized N released from the streambed was a major source of the inorganic N increase. Despite significant NO₃ ^– reduction potential, swamp forest stream sediments appear to be a source of inorganic N to downstream communities.     

Riparian control on NO3 −, DOC, and dissolved Fe concentrations in mountainous streams, northern Japan

We evaluated (1) the longitudinal pattern of stream chemistry and (2) the effects of the riparian zone on this longitudinal pattern for nitrate (NO₃ ⁻), dissolved organic carbon (DOC), and total dissolved iron (Fe). We selected two small watersheds; the “southern watershed” had an extending riparian wetland and the “northern watershed” had a narrow riparian area. Stream NO₃ ⁻ concentrations decreased from the spring to outlet of both watersheds. In the southern watershed, stream DOC concentration decreased from the spring to midstream and then increased to the outlet. Stream Fe concentration in the southern watershed longitudinally increased. On the other hand, the northern watershed exhibited no longitudinal pattern for DOC and Fe concentrations. In both watersheds, while NO₃ ⁻ concentrations in the soil and ground water were lower than those in the stream waters, DOC and Fe concentrations exhibited the opposite patterns. The longitudinal decreases of NO₃ ⁻ concentrations in both streams and increase of stream Fe in the southern watershed mainly resulted from the inflow of the soil and ground water to the stream. The decrease in stream DOC from the spring to midstream in the southern watershed was due to the deep groundwater having low DOC, while the subsequent increase to the surrounding soil and ground water. Moreover, considerations of stream solute flow with soil and ground water chemistry suggested other mechanisms adding NO₃ ⁻ and removing/diluting DOC and Fe, especially for the northern watershed; coexistence of oxidizing and reducing conditions in the riparian zone might control the longitudinal concentration change in the stream water chemistry.     

The effects of forest on stream water quality in two coastal plain watersheds of the Chesapeake Bay

Forest had varying effects on stream nutrients in two coastal plain basins of the Delmarva Peninsula, USA. In the Choptank basin, forest was strongly associated with low stream total nitrogen (TN) and nitrate (NO₃⁻) concentrations (r²0.70), and forest placement along first order streams was important in maintaining low stream nitrogen (N) concentrations (r²0.35). In addition, a multiple regression model explained 40% of the stream total phosphorus (TP) variance and indicated that forest directly adjacent to streams (0–100 m) acted as a TP source and forest further away (100–300 m) from streams acted as a TP sink. In contrast, stream nutrients in the nearby Chester basin demonstrated a strong relationship with soil hydrologic properties. Forest had no significant effect on stream N and P because the finer-textured soils, higher stream slopes, and higher runoff potential of the Chester basin appeared to result in less baseflow compared to that in the Choptank basin. This reduced the opportunity for forest to intercept N via plant uptake and denitrification in the high runoff potential soils of the Chester basin. The high percentage of stormflow (40%) coupled with high stream slopes resulted in high soil erosion potential, which may explain the higher TP stream concentrations measured in the Chester compared to that in the Choptank. Differences in the hydrologic pathway appear to explain the different effects of forest on water quality in these two basins.     

Nitrate removal in a first-order stream: reconciling laboratory and field measurements

A combination of laboratory and field experiments were carried out to evaluate nitrate(NO ₃ ^t- ) removal during stream transport in a first-order agricultural drainage stream. Intact stream sediment cores overlain with stream and NO ₃ ^– -amended stream water indicated NO ₃ ^– losses averaging 93 — 353 mg m^–2 day^–1, with NO ₃ ^– concentration exerting a primary control on loss rate. Isotopic data indicated enrichment of NO ₃ ^– - ¹⁵N over time as NO ₃ ^– concentrations decreased, indicating a denitrification loss. Field experiments were designed to evaluate dilution of streamwater with low-NO ₃ ^– groundwater in addition to other NO ₃ ^– removal processes during transport. A series of bromide tracer and NO ₃ ^– - addition experiments were carried out in the field; groundwater dilution dominated the downstream NO ₃ ^– concentration trends, accounting for all observed decreases in NO ₃ ^– concentration. Isotopic data did not point to denitrification downstream as a major NO ₃ ^– removal process. This apparent disparity between simulated laboratory and in-situ stream removal rates appears to be a function of the hydrological processes controlling exchanges between stream bottom sediments and the overlying water. These results suggest that caution must be exercised in extrapolating potentials for NO ₃ ^– removal measured in laboratory experiments to the field, as these rates could be overestimated in some watersheds.     

Nitrogen Transformations in Flowpaths Leading from Soils to Streams in Amazon Forest and Pasture

The modification of large areas of tropical forest to agricultural uses has consequences for the movement of inorganic nitrogen (N) from land to water. Various biogeochemical pathways in soils and riparian zones can influence the movement and retention of N within watersheds and affect the quantity exported in streams. We used the concentrations of NO₃ ⁻ and NH₄ ⁺ in different hydrological flowpaths leading from upland soils to streams to investigate inorganic N transformations in adjacent watersheds containing tropical forest and established cattle pasture in the southwestern Brazilian Amazon Basin. High NO₃ ⁻ concentrations in forest soil solution relative to groundwater indicated a large removal of N mostly as NO₃ ⁻ in flowpaths leading from soil to groundwater. Forest groundwater NO₃ ⁻ concentrations were lower than in other Amazon sites where riparian zones have been implicated as important N sinks. Based on water budgets for these watersheds, we estimated that 7.3–10.3 kg N ha⁻¹ y⁻¹ was removed from flowpaths between 20 and 100 cm, and 7.1–10.2 kg N ha⁻¹ y⁻¹ was removed below 100 cm and the top of the groundwater. N removal from vertical flowpaths in forest exceeded previously measured N₂O emissions of 3.0 kg N ha⁻¹ y⁻¹ and estimated emissions of NO of 1.4 kg N ha⁻¹ y⁻¹. Potential fates for this large amount of nitrate removal in forest soils include plant uptake, denitrification, and abiotic N retention. Conversion to pasture shifted the system from dominance by processes producing and consuming NO₃ ⁻ to one dominated by NH₄ ⁺, presumably the product of lower rates of net N mineralization and net nitrification in pasture compared with forest. In pasture, no hydrological flowpaths contained substantial amounts of NO₃ ⁻ and estimated N removal from soil vertical flowpaths was 0.2 kg N ha⁻¹ y⁻¹ below the depth of 100 cm. This contrasts with the extent to which agricultural sources dominate N inputs to groundwater and stream water in many temperate regions. This could change, however, if pasture agriculture in the tropics shifts toward intensive crop cultivation.     

Forest sources and pathways of organic matter transport to a blackwater stream: a hydrologic approach

Quantitative information regarding landscape sources and pathways of organic matter transport to streams is important for assessing impacts of terrestrial processes on aquatic ecosystems. We quantified organic C, a measure of organic matter, flowing from a blackwater stream draining a 12.6 km² watershed on the upper Atlantic Coastal Plain in South Carolina, and utilized a hydrologic approach to partition this outflow between its various pathways from upland and wetland forest sources. Results of this study indicate that 28.9 tonnes C yr^–1 were exported in stream flow, which was estimated to be 0.5% of the annual C input from forest detritus to the watershed. Upland forest, which covers 94% of the watershed area, contributed only 2.0 tonnes C yr^–1 to stream flow, which amounted to 0.04% of detritus annually produced by the upland forest. Organic matter was transported from uplands to the stream almost entirely through groundwater. Apparently, upland soils are too sandy to support overland flow, and the sloping topography insufficiently extensive or steep enough to drive important quantities of interflow. Riparian wetland forest, which covers only 6% of the watershed area, contributed 26.9 tonnes C yr^–1 to stream flow, amounting to about 10.2% of detritus annually produced by the wetland forest. Dissolved organic C leached from wetland soil accounted for 63% of all organic C entering the stream, and was transported chiefly in baseflow. These results indicate that upland detritus sources are effectively decoupled from the stream despite the sandy soils and quantitatively confirm that even small riparian wetland areas can have a dominant effect on the overall organic matter budget of a blackwater stream. In view of the recognized importance of dissolved organic matter in facilitating transport of other substances (e.g., cation nutrients, metals, and insoluble organic compounds), our results suggest that the potential for movement of these substances through wetland soils to streams in this region is high.     

Losses of inorganic carbon and nitrous oxide from a temperate freshwater wetland in relation to nitrate loading

We studied the export of inorganic carbon and nitrous oxide (N₂O) from a Danish freshwater wetland. The wetland is situated in an agricultural catchment area and is recharged by groundwater enriched with nitrate (NO₃ ^–) (1000 M). NO₃ ^– in recharging groundwater was reduced (57.5 mol NO₃ ^– m^–2 yr^–) within a narrow zone of the wetland. Congruently, the annual efflux of carbon dioxide (CO₂) from the sediment was 19.1 mol C m^–2 when estimated from monthly in situ measurements. In comparison the CO₂ efflux was 4.8 mol C m^–2 yr^–1 further out in the wetland, where no NO₃ ^– reduction occurred. Annual exports of inorganic carbon in groundwater and surface water was 78.4 mol C m^–2 and 6.1 mol C m^–2 at the two sites, respectively. N₂O efflux from the sedimenst was detectable on five out of twelve sampling dates and was significantly (P < 0.0001) higher in the NO₃ ^– reduction zone (0.35–9.40 mol m^–2 h^–1, range of monthly means) than in the zone without NO₃ ^– reduction (0.21–0.41 mol m^–2 h^–1). No loss of dissolved N₂O could be measured. Total annual export of N₂O was not estimated. The reduction of oxygen (O₂) in groundwater was minor throughout the wetland and did not exceed 0.2 mol 0₂ m^–2yr^–1. Sulfate (SO₄ ^––) was reduced in groundwater (2.1 mol SO₄ ^–– m^–2 yr^–1) in the zone without NO₃ ^– reduction. Although the NO₃ ^– in our wetland can be reduced along several pathways our results strongly suggest that NO₃ ^– loading of freshwater wetlands disturb the carbon balance of such areas, resulting in an accelerated loss of inorganic carbon in gaseous and dissolved forms.