Sources and sinks of dissolved organic carbon in a forested swamp catchment

Concentrations of dissolved organic carbon (DOC) were measured in precipitation, throughfall, stemflow, and soil, peat and stream water in a 50 ha catchment with a central 5 ha swamp at Mont St. Hilaire, Quebec. DOC concentrations in precipitation were low (2.0 mg L^–1), but increased in passage through the tree canopies as throughfall (9.1–14.6 mg L^–1) and stemflow (23.1–30.1 mg L^–1). For the period July 1–November 15, 1987, 0.5 g DOC m^–2 was imported as precipitation, and forest canopies contributed a further 1.4–1.7 g m^–2 2 to the soil surface. DOC concentrations were higher (46.0 and 67.6 mg L^–1) in upland soil organic horizons, but decreased with depth because subsoil mineral horizons acted as a major sink of DOC. A laboratory experiment using leaf leachate revealed that subsoil horizons were able to adsorb DOC, with equilibrium DOC concentrations ranging from 3 to 19 mg L^–1. Soil organic carbon appeared to be an important determinant of equilibrium DOC concentrations. The swamp was a major source of DOC, with an overall average DOC concentration of 58.6 mg L^–1 and showed strong spatial and temporal variations related to hydrologic and thermal regimes. During base flow periods, stream DOC concentrations were small (< 3 mg L^–1), dominated by water fed from springs draining upland soils. During high flows, stream DOC concentrations increased through the contribution of DOC-rich water originating in the swamp. Sources, sinks and transport of DOC are thus a function of a complex set of inter-related biotic and abiotic process.     

Ground water flow paths in relation to nitrogen chemistry in the near-stream zone

Interactions between ground water flow paths and water chemistry were studied in the riparian zone of a small headwater catchment near Toronto, Ontario. Significant variations in oxygen — 18 and chloride indicated the presence of distinct sources of water in the ground water flow system entering the near-stream zone. Shallow ground water at the upland perimeter of the riparian zone had nitrate-N, chloride and dissolved oxygen concentrations which ranged between 100–180 µg L^–1, 1.2–1.8 mg L^–1 and 4.6–9.1 mg L^–1 respectively. Concentrations of nitrate — N in deep ground water flowing upward beneath the riparian wetland were < 10 µg L^–1, whereas chloride and dissolved oxygen ranged between 0.6–0.9 mg L^–1 and 0.4–2.2 mg L^–1 respectively. Ammonium — N concentrations (20–60 µg L^–1) were similar in shallow and deep ground water. Ground water was transported through the wetland to the stream by three hydrologic pathways. 1) Shallow ground water emerged as springs near the base of the hillslope producing surface rivulets which crossed the riparian zone to the stream. 2) Deep ground water flowed upward through organic soils and entered the rivulets within the wetland. 3) Deep ground water reached the stream as bed and bank seepage. Springs were higher in nitrate and chloride than rivulets entering the stream, whereas bank seeps had lower concentrations of nitrate and chloride and considerably higher ammonium concentrations than the rivulets. These contrasts in nitrate and chloride concentrations were related to initial differences in the ion chemistry of shallow and deep ground water rather than to element transformations within the riparian wetland. Differences in ammonium concentration between seeps and rivulets were caused by immobilization of ammonium in the substrates of aerobic rivulets, whereas little ammonium depletion probably occurred in deep ground water flowing upward through reduced subsurface organic soils around the stream perimeter.     

Concentration and composition of dissolved organic carbon in streams in relation to catchment soil properties

Two adjacent catchments in the Otway Ranges of Victoria, Australia (Redwater and Clearwater) produce water with markedly different concentrations of dissolved organic carbon (DOC) during summer. Water from Redwater Creek had a DOC concentration of 32 mg L^–1, while water from Clearwater Creek had a DOC concentration of 3.8 mg L^–1. Examination of the catchments revealed that while climate, topography, vegetation and land use were similar, the soils were different. The objective of this study was to examine the relationship between the concentration and chemical composition of DOC in stream waters and the nature of soils in the two catchments. Soil mapping determined that clayey soils formed on Cretaceous sediments (Cretaceous soils) occurred throughout both catchments, but that Redwater Catchment also contained a large area (39%) of sandy soils formed on Tertiary sediments (Tertiary soils). The concentration of DOC in forest floor leachate was high in both the Tertiary and Cretaceous areas; however, the concentration of DOC in water draining areas dominated by Tertiary soils was greater than that in water draining areas dominated by Cretaceous soils. Laboratory experiments showed that the Cretaceous soils had higher adsorption capacities for forest floor leachate DOC than the Tertiary soils. The difference in DOC concentrations of the streams was therefore attributed to the difference in adsorption capacity of catchment soils for DOC. Adsorption capacities of the soils were found to be a function of their clay contents and specific surface areas.Solid-state³C nuclear magnetic resonance spectroscopy and pyrolysis-mass spectrometry were used to determine the chemical structure of DOC found in streams and forest floor leachate samples and that remaining in solution after interaction with soil. Chemistry of DOC in forest floor leachate was similar before and after interaction with soil, indicating no preferential adsorption of a particular type of carbon. Thus, differences between the chemical structure of stream DOC and forest floor leachate DOC could be attributed to microbial modifications during its movement through soils and into the streams, rather than losses by adsorption.     

Aluminum geochemistry in peatland waters

The chemical speciation of aluminum was examined in surface water samples from Sphagnum peatlands in north-central Minnesota, from peatlands along the Canadian east coast, and from bogs in the Pennine Mountain area of England. In highly organic ([DOC] 50 mg L^–1 ), low pH waters, 80–90% of total dissolved Al was complexed with organic matter (OM), while in waters with low DOC ([DOC] 5 mg L^–1) 54–86% of total dissolved Al existed as Al⁺³ or other inorganic Al species. Batch titrations of OM with Al revealed a high Al binding capacity, 1.4–2.8 mol (mg DOC)^–1, that generally was unsaturated with Al. Titrations of OM with Al in conjunction with a continuous distribution model were used to determine Al-OM conditional stability constants. Binding capacity (mol Al (mg DOC)^–1) and strength (formation constant) increased from pH 3 to 5 but decreased above pH 5 due to formation of AI-hydroxy species including A1(OH)₃ (s). The high binding capacity of OM in bog waters facilitates metal mobility, especially in low pH (< 5) wetlands where metal solubility is high and OM concentrations are highest. Results showed that the relative degree of organic matter saturation with metal ions was important in modeling AI speciation in bog waters.     

Controls on the dynamics of dissolved organic carbon and nitrogen in a Central European deciduous forest

Despite growing attention concerning therole of dissolved organic matter (DOM) inelement cycling of forest ecosystems, thecontrols of concentrations and fluxes of bothdissolved organic carbon (DOC) and nitrogen(DON) under field conditions in forest soilsremain only poorly understood. The goal ofthis project is to measure the concentrations and fluxes of DON, NH₄ ⁺, NO₃ ^–and DOC in bulkprecipitation, throughfall, forest floorleachates and soil solutions of a deciduousstand in the Steigerwald region (northernBavaria, Germany). The DOC and DONconcentrations and fluxes were highest inleachates originating from the Oa layer of theforest floor (73 mg C L^–1, 2.3 mg NL^–1 and about 200–350 kg C, 8–10 kg Nha^–1 yr^–1). They were observed to behighly variable over time and decreased in themineral topsoil (17 mg C L^–1, 0.6 mg NL^–1 and about 50–90 kg C, 2.0 to 2.4 kg Nha^–1 yr^–1). The annual variability ofDOC and DON concentrations and subsequentialDOC/DON ratios was substantial in allsolutions. The DOC and DON concentrations inthroughfall were positively correlated withtemperature. The DOC and DON concentrationsdid not show seasonality in the forest floorand mineral soil. Concentrations were notrelated to litterfall dynamics but didcorrespond in part to the input of DOC and DONfrom throughfall. The throughfall contributionto the overall element fluxes was higher forDON than for DOC. Concentrations and fluxes ofDON were significantly correlated to DOC inthroughfall and the Oi layer. However, thecorrelation was weak in Oa leachates. Inaddition, seasonal and annual variation ofDOC/DON ratios indicated different mechanismsand release rates from the forest floor forboth components. The concentrations of DOC andDON in forest floor leachates were in mostcases dependent neither on the pH value orionic strength of the solution, nor on thewater flux or temperature changes. As aconsequence, the DOC and DON fluxes from theforest floor into the mineral soil werelargely dependent on the water flux if annualand biweekly time scales are considered.     

Seasonal variability of dissolved organic carbon ina Mediterranean stream

The seasonal variability of dissolved organic carbon(DOC) flux in a Mediterranean stream subjected todischarges of wide range of intensities and variabledry period was studied as a function of the hydrologicconditions, and the relationship between surface andsubsurface (hyporheic and groundwater) DOCconcentration. DOC concentration in stream water(2.6 mg l^–1 ±1.5 SD) was higher thangroundwater (1.3 mg l^–1 ± 1.2 SD) and lower thanhyporheic water (3.8 mg l^–1 ±1.7 SD),suggesting that, at baseflow, stream DOC concentrationincreases when groundwater discharges through thehyporheic zone. Storms contributed to 39% of annualwater export and to 52% of the total annual DOCexport (220 kg km^–2). A positive relationship wasobserved between Discharge (Q) and stream DOCconcentration. Discharge explained only 40% of theannual variance in stream DOC, but explained up to93% of the variance within floods. The rate of streamDOC changes with discharge change during storms (dDOC/dQ), ranged between 0 and 0.0045 C mgl^–1 s l^–1, with minimum values during Springand Summer, and maxima values in Fall and Winter.These dynamics suggest that storm inputs ofterrigenous DOC vary between seasons. During floods inthe dormant season, DOC recession curves were alwayssteeper than discharge decline, suggesting shortflushing of DOC from the leaching of fresh detritusstored in the riparian zone.     

A long-term perspective of dissolved organic carbon transport in Sycamore Creek, Arizona, USA

Dissolved organic carbon (DOC) dynamics were examined over five years (1989–1993) in Sycamore Creek, a Sonoran Desert stream, specifically focusing on DOC concentration in surface and hyporheic waters, and rates of export. In 1989 and 1990, the years of lowest stream discharge (0.08 and 0.04 m³ s^–1 annual mean of daily discharge, respectively), DOC was high, averaging 7.37 and 6.22 mgC l^–1 (weighted annual means). In contrast, from 1991 through 1993, a period of increased flow (1.1, 1.2 and 4.3 m³ s^–1), concentration was significantly lower (P<0.001) with annual mean concentrations of 3.54, 3.49 and 3.39 mgC l^–1. Concentration exhibited little spatial variation between two sampling stations located 6 km apart along the mainstem or between surface and hyporheic waters. Annual export of DOC from Sycamore Creek varied 100-fold over the five-year period from a mean rate of only 24 kgC d^–1 in 1990 to 2100 kgC d^–1 in 1993. Ninety percent of DOC was exported by flows greater than 2.8 m³ s^–1, and 50% during flows greater than 27 m³ s^–1; flows of 2.8 and 24 m³ s^–1 occurred only 9 and 1% of the time. The export of organic matter in Sycamore Creek appears to be coupled to El Niño-Southern Oscillation phenomena. The years of highest export, 1991–1993, had El Niño conditions while 1989 and 1990 had medial conditions.     

Dissolved organic matter under native Cerrado and Pinus caribaea plantations in the Brazilian savanna

The transformation of native Cerrado into Pinus caribaea Morelet plantations changes the DOM dynamics including changed rates of mineralisation, denitrification, and C export to the groundwater. To examine the differences in quantity, temporal dynamics, and quality of DOM between Cerrado and Pine plantations we collected rainfall, throughfall, stemflow, litter leachate (under pine only) and soil solution at 15, 80, and 200 cm depth in weekly intervals during the rainy seasons 1997/98 and 1998/99. We determined total dissolved organic carbon (DOC) concentrations and assessed DOM quality by separating hydrophilic and hydrophobic fractions and by NMR analysis of organic layer extracts. The rainfall had a mean DOC concentration of 2.6 mg L^–1. The mean concentrations of DOC in the throughfall of the pine plantations (5.0–10.5 mg L^–1) were significantly above those of Cerrado (2.6–4.9 mg L^–1). During the first part of the rainy seasons (October–December), the concentrations of DOC in the soil solution (15–200 cm depth) under Cerrado and pine did not differ significantly. During the second part of both rainy seasons (January–April), the concentrations of DOC in the soil solution under Cerrado (4.4–5.1 mg L^–1) exceeded those under PI (1.4–2.7 mg L^–1). Possible explanations of the latter include higher DOM input into the Cerrado soil and a stronger retention and/or faster mineralisation of the pine DOM than of the Cerrado DOM in the mineral soil. As the structural composition of DOM extracted from the organic layer under Cerrado and pine did not differ significantly, faster mineralisation was the most likely explanation for partly lower DOC concentrations in the soil solution under pine than under Cerrado. This assumption was supported by increasing contributions of hydrophobic DOM to total DOM with increasing depth under pine while, under Cerrado, the DOM composition did not change with depth. The reason for DOM mineralisation under pine was probably the higher N availability because total N concentrations were 11–23 times higher under pine than under Cerrado.     

Seasonal and storm event nutrient removal by a created wetland in an agricultural watershed

This study examines the effectiveness of a 1.2-ha created/restored emergent marsh at reducing nutrients from a 17.0 ha agricultural and forested watershed in the Ohio River Basin in west central Ohio, USA, during base flow and storm flow conditions. The primary source of water to the wetland was surface inflow, estimated in water year 2000 (October 1999–September 2000) to be 646 cm/year. The wetland also received a significant amount of groundwater discharge at multiple locations within the site that was almost the same in quantity as the surface flow. The surface inflow had 2-year averages concentrations of 0.79, 0.033, and 0.16 mg L⁻¹ for nitrate + nitrite (as N), soluble reactive phosphorus (SRP), and total phosphorus (TP), respectively. Concentrations of nitrate–nitrite, SRP, and TP were 40, 56, and 59% lower, respectively, at the outflow than at the inflow to the wetland over the 2 years of the study. Concentrations of SRP and TP exported from the wetland increased significantly (α = 0.05) during precipitation events in 2000 compared to dry weather flows, but concentrations of nitrate–nitrite did not increase significantly. During these precipitation events the wetland retained 41% of the nitrate–nitrite, 74% of the SRP, and 28% of the TP (by mass). The wetland received an average of 50 g N m⁻² per year of nitrate–nitrite and 7.1 g m⁻² per year of TP in 2000. Retention rates for the wetland were 39 g N m⁻² per year of nitrates and 6.2 g P m⁻² per year. These are close to rates suggested in the literature for sustainable non-point source retention by wetlands. The design of this wetland appears to be suitable as it retained a significant portion of the influent nutrient load and did not lose much of its retention capacity during heavy precipitation events. Some suggestions are given for further design improvements.     

The impacts of a watershed CaCO3 treatment on stream and wetland biogeochemistry in the Adirondack Mountains

Temporal and longitudinal variations in the chemistry of two tributary streams of Woods Lake in the Adirondack Mountains of New York were monitored before and after a watershed CaCO₃ application. One subcatchment of the lake had a large beaver pond and wetland at its headwaters, while the second was free-flowing. Treatment of both subcatchments with CaCO₃ resulted in an immediate increase in acid neutralizing capacity (ANC) associated with Ca²⁺ release. The extent and duration of the response to the treatment were greater in the wetland-impacted stream. Aluminum was retained and complexed with organic solutes generated within the beaver-pond. In the free-flowing stream, NO ₃ ^– concentration increased significantly after the manipulation; this pattern was not evident in the wetland-impacted stream. Net retention of SOkinf4/sup2– was evident in the beaver pond prior to and following treatment, and this response was enhanced after the watershed liming. Comparisons of beaver pond inlet/outlet concentrations, mass balance calculations, and in-pond profiles of chemical parameters revealed patterns of retention of SO ₄ ^2– , NO ₃ ^– and Al, and release of Fe²⁺, dissolved organic carbon (DOC) and NH ₄ ⁺ in the wetland during the summer before CaCO₃ treatment. Post-treatment releases of Ca²⁺ from the near-sediment zone in the beaver pond corresponded to anoxic periods in mid- to late-summer and under ice in winter. These findings demonstrate the importance of increased microbial processing of organic matter, along with high partial pressure Of CO₂ (Pco₂) in facilitating the dissolution of the applied CaCO₃. Dissolved silica (H₄SiO₄) was retained in the wetland during the summer prior to treatment but was released after the manipulation. This phenomenon may reflect the dissolution of diatom frustules or silicate minerals in the wetland at higher pH and DOC concentrations. Within two years of the CaCO₃ treatment 60% of the CaCO₃ applied to the beaver pond and surrounding wetland was dissolved and transported from the pond, in contrast to only 2.2% of the CaCO₃ applied to the upland subcatchment draining into the wetland. These results, coupled with high quantities of exchangeable Ca²⁺ found in sediments and onSphagnums mosses in the pond, demonstrate the importance of hydrologic source areas and wetlands in facilitating the dissolution of added CaCO₃ and in regulating the production of chemical species important in ANC generation.     

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.     

Impacts of Tetracycline on Planktonic Bacterial Production in Prairie Aquatic Systems

In view of antibiotics being detected in surface waters, experiments were conducted to determine the impacts of tetracycline on planktonic bacteria in wetland and river waters. The minimum inhibitory concentration (MIC) method is often used to measure for resistance or susceptibility of microbes to antibiotics with typical concentrations of antibiotics being mg L⁻¹. Moreover, there is the belief that antibiotics in the lower μg L⁻¹ range are unlikely to affect bacteria. We examined this assumption by measuring the effects of a broad range of tetracycline concentrations on bacterial protein production by the incorporation of l-[4,5-³H]leucine method. Tetracycline significantly (P < 0.05) inhibited production in river water bacteria at a “free” concentration of 5 μg L⁻¹, but the inhibition was significant only at 1000 μg L⁻¹ in wetland water. The data indicate that planktonic bacteria can be very sensitive to tetracycline at extremely low concentrations and that microbial production is seriously affected.     

Kinetics and mechanisms of dissolved organic carbon retention in a headwater stream

Freeze-dried aqueous extracts of autumn-shed maple leaves, birch leaves, and spruce needles were added to a third-order reach of Bear Brook, New Hampshire at concentrations similar to those predicted to occur during peak leaf fall. Leachate from each species was rapidly removed from solution. With initial concentrations of added leachate of approximately 5 mgl^–1, dissolved organics (DOC) uptake ranged from 73 to 130 mg m^–2 h^–1 for the first five hours of travel downstream from the point of addition. There was no preferential removal of DOC of low molecular weight, or of monomeric carbohydrates relative to phenolics or unidentified DOC.Stream sediments and organic debris rapidly removed DOC from solution in laboratory experiments. No significant flocculation or microbial assimilation of sugar maple leachate occurred in stream water alone. Stream sediments showed small increases in respiration with addition of leaf leachate, but no increase in respiration occurred upon addition of leachate to organic debris. Abiotic adsorption due to the high concentrations of exchangeable iron and aluminium in stream sediments may be responsible for much of the rapid removal of leaf leachate observed in field experiments. Abiotic processes appear to retain DOC within the stream, thereby allowing subsequent metabolism of dissolved organic carbon by stream microflora.     

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.     

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.     

Relationship between DOC concentration and vadose zone thickness and depth below water table in groundwater of Cape Cod, U.S.A.

Changes in concentration ofdissolved organic carbon (DOC) reflectbiogeochemical processes that determinechemical composition of groundwater and othernatural waters. We found that the deeper thevadose zone, the lower the concentration of DOCin groundwater near the water table, indicatingthat considerable attenuation ofsurface-derived DOC occurred in the vadosezone. Under vadose zones <1.25 m, DOCconcentrations at the surface of the watertable ranged to >20 mg C l^–1, while forvadose zones >5.0 m, DOC never exceeded2.0 mg C l^–1. DOC concentrations alsodecreased exponentially with increasing depthbelow the water table, most notably in theupper two meters, implying continuedattenuation in the upper layer of the saturatedzone. Ninety-nine percent of the DOC wasattenuated by the time the water reached adepth of 19 m below the water table. A stronginverse relationship between DOC and nitrateconcentrations suggests that nitrate isdepleted where DOC supplies are high, providingevidence that some portion of the DOC losses ingroundwater are due to microbialtransformations, including denitrification. DOC concentrations in shallow groundwater showconsiderable spatial variability, butconcentration of DOC at any one site issurprisingly stable over time. The largestsource of variation in DOC concentration ingroundwater therefore is spatial rather thantemporal, suggesting that local heterogeneitiesplay an important role in DOC delivery toshallow groundwater. Our results highlightboth the importance of shallow vadose areas inDOC delivery to groundwater and the need todistinguish where samples are collected inrelation to flow paths before conclusions aremade about mean groundwater DOC concentrations. The substantial losses of DOC in the vadosezone and in shallow depths within the aquifersuggest quite active biogeochemical processesin these boundary environments.     

Nutrient cycling and productivity in a desert saline lake: observations from a dry,low-productivity year

Seasonal variability of nutrients and productivity were examined in Pyramid Lake, a hyposaline, N-deficient, terminal desert lake, during a dry period. River inflow and N-fixation during 1990 were minimal allowing internal nutrient cycling to be more closely studied. Nutrient cycling was strongly affected by seasonal thermal stratification that was typical for a warm monomictic lake. Concentrations of nitrate, phosphate, and silicate in surface waters were highest during winter mixing and decreased rapidly in the spring due to a diatom bloom. Maximum average chlorophyll concentration in surface waters was 2.7 ± 1.2 µg 1^–1 and occurred in April while surface nutrients were being depleted. In contrast to chlorophyll, maximum particulate carbon in surface waters occurred in July–August when areal productivity was highest (367–398 mg C m^–2 day^–1). Concurrent with spring nutrient depletion in surface waters was increasing N-deficiency in the plankton. After the spring bloom dissipated in May, particulate matter (POM) became increasingly N-deficient reaching maximum elemental C : N of > 18 during summer-fall. Profiles of the C : N ratio of POM were nearly constant with depth for individual sampling dates suggesting that the residence time of POM in the water column was short (< 1 month). While surface waters were nutrient depleted during summer stratification, nutrient concentrations of bottom waters progressively increased, presumably through the oxidation of POM sinking to the bottom (103 m). Converting the rate of oxygen depletion in bottom waters to carbon equivalents of POM suggests that 42 % of mean annual phytoplankton production in overlying waters during 1990 was mineralized in bottom waters.     

Bacterial response to extracellular dissolved organic carbon released from healthy and senescent Fragilaria crotonensis (Bacillariophyceae) in experimental systems

Responses of bacteria to dissolved organic carbon (DOC) released from healthy and senescent Fragilaria crotonensis (Bacillariophyceae) were examined in experimental systems. The alga released DOC actively, although the concentration fluctuated greatly in both the axenic (the alga alone) and the mixed (the alga plus the enriched bacteria) cultures. In the control (the bacteria alone) cultures, both DOC concentration and bacterial density were low and almost constant throughout the experiment: 5.0 mg C 1^–1 and 1.1 × 10⁵ cells ml^–1, respectively. In the mixed cultures, bacterial growth was negligible during the exponential growth phase of the alga, but rapid proliferation of the bacteria occurred after the onset of the stationary growth phase. As the bacterial population grew, the density of senescent algal cells also increased. When the bacteria were fed on the DOC from healthy algae, their growth rate was relatively low (0.44 d^–1), but the maximum cell density was high (6.4 × 10⁵ cells ml^–1). Conversely, when the bacteria fed on the DOC of senescent algae, they grew at a relatively high rate (0.51 d^–1), but the maximum cell density was low (2.8 × 10⁵ cells ml^–1). These results suggest that DOCs released from dominant phytoplankton species in different physiological states affect the biomass and activity of bacteria.     

Long-term trends in dissolved organic carbon concentration: a cautionary note

Dissolved organic carbon (DOC) plays an important role in surface water chemistry and ecology and trends in DOC concentration have been also associated with shifts in terrestrial carbon pools. Numerous studies have reported long-term trends in DOC concentration; however, some studies consider changes in average measured DOC whereas other compute discharge weighted concentrations. Because of differences in reporting methods and variable record lengths it is difficult to compare results among studies and make regional generalizations. Furthermore, changes in stream discharge may impact long-term trends in DOC concentration and the potentially subtle effect of shifts in stream flow may be missed if only measured DOC concentrations are considered. In this study we compare trends in volume-weighted vs. average measured DOC concentration between 1980 and 2001 at seven headwater streams in south-central Ontario, Canada that vary in wetland coverage and DOC (22-year mean vol. wt.) from 3.4 to 10.6 mg l⁻¹. On average, annual measured DOC concentrations were 13–34% higher than volume-weighted values, but differences of up to 290% occurred in certain years. Estimates of DOC flux were correspondingly higher using measured concentration values. Both measured and volume-weighted DOC concentrations increased significantly between 1980 and 2001, but slopes were larger in measured data (0.04–0.35 mg l⁻¹ year⁻¹ compared with 0.05–0.15 mg l⁻¹ year⁻¹) and proportional increases at the most wetland-influenced sites ranged from 32 to 43% in volume-weighted DOC and from 52 to 75% in measured DOC. In contrast, DOC flux did not change with time when estimated using either method, because of the predominant influence of stream flow on DOC export. Our results indicate that changes in stream flow have an important impact on trends in DOC concentration, and extrapolation of trend results from one region to another should be made cautiously and consider methodological and reporting differences among sites.     

Effects of forest clear-cutting on the carbon and nitrogen fluxes through podzolic soil horizons

Effects of clear-cutting on the dissolved fluxes of organic C (DOC), organic N (DON), NO₃ ^– and NH₄ ⁺ through surface soil horizons were studied in a Norway spruce dominated mixed boreal forest in eastern Finland. Bulk deposition, total throughfall and soil water from below the organic (including understorey vegetation and, after clear-cutting, also logging residues), eluvial and illuvial horizons were sampled weekly from 1993 to 1999. Clear-cutting was carried out in September 1996. The removal of the tree canopy decreased the deposition of DOC and DON to the forest floor and increased that of NH₄ ⁺ and NO₃ ^– but did not affect the deposition of total N (DTN, <3 kg ha^–1 a^–1). The leaching of DOC and DON from the organic horizon increased over twofold after clear-cutting (fluxes were on an average 168 kg C and 3.3 kg N ha^–1 a^–1), but the increased outputs were effectively retained in the surface mineral soil horizons. Inorganic N deposition was mainly retained by the logging residues and organic horizon indicating microbial immobilization. Increased NO₃ ^– formation reflected as elevated concentrations in the percolate from below the mineral soil horizons were observed especially in the third year after clear-cutting. However, the changes were small and the increased leaching of DTN from below the illuvial horizon remained small (<0.4 kg ha^–1 a^–1) and mainly DON. Effects of clear-cutting on the transport of C and N to surface waters will probably be negligible.